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<title><![CDATA[ContentSnapshots]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/i?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:25 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp277</dc:identifier>
<dc:title><![CDATA[ContentSnapshots]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>iii</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>i</prism:startingPage>
<prism:section>ContentSnapshots</prism:section>
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<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/ix?rss=1">
<title><![CDATA[Plants at the margin. Ecological limits and climate change]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/ix?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[le Roux, P.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp220</dc:identifier>
<dc:title><![CDATA[Plants at the margin. Ecological limits and climate change]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>ix</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>ix</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
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<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/ix-a?rss=1">
<title><![CDATA[Phytochemicals: aging and health]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/ix-a?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Larsson, S.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp222</dc:identifier>
<dc:title><![CDATA[Phytochemicals: aging and health]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>x</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>ix</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/v?rss=1">
<title><![CDATA[John Bryant takes a closer look at some of this month's Original Articles]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/v?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Bryant, J.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:25 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp279</dc:identifier>
<dc:title><![CDATA[John Bryant takes a closer look at some of this month's Original Articles]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>vi</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
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<prism:section>ContentSelect</prism:section>
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<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/vii?rss=1">
<title><![CDATA[An orchard invisible. A natural history of seeds]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/vii?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Matthews, S.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp224</dc:identifier>
<dc:title><![CDATA[An orchard invisible. A natural history of seeds]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>viii</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>vii</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
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<title><![CDATA[Plant genomes. Genome dynamics vol. 4]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/viii?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Leitch, A. R., Leitch, I. J.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp221</dc:identifier>
<dc:title><![CDATA[Plant genomes. Genome dynamics vol. 4]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>viii</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>viii</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/x?rss=1">
<title><![CDATA[Advances in haploid production in higher plants]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/x?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Davey, M. R.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp248</dc:identifier>
<dc:title><![CDATA[Advances in haploid production in higher plants]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>x</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>x</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/x-a?rss=1">
<title><![CDATA[Plant systems biology. Annual Plant Reviews, Volume 35]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/x-a?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Hilson, P., Inze, D.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp249</dc:identifier>
<dc:title><![CDATA[Plant systems biology. Annual Plant Reviews, Volume 35]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>xi</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>x</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1255?rss=1">
<title><![CDATA[Myco-heterotrophy: when fungi host plants]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1255?rss=1</link>
<description><![CDATA[
<sec><st>Background</st>
<p>Myco-heterotrophic plants are partly or entirely non-photosynthetic plants that obtain energy and nutrients from fungi. These plants form a symbiosis with arbuscular mycorrhizal, ectomycorrhizal or saprotrophic fungi to meet their nutrient demands.</p>
</sec>
<sec><st>Scope</st>
<p>This Botanical Briefing summarizes current knowledge about myco-heterotrophy, discusses its controversial aspects and highlights future directions for research.</p>
</sec>
<sec><st>Conclusions</st>
<p>Considerable recent progress has been made in terms of understanding the evolutionary history, germination and nutrition of myco-heterotrophic plants. Myco-heterotrophic plants: (1) are diverse and often ancient lineages that have coevolved with fungi, (2) often demonstrate unusually high specificity towards fungi during germination and maturity, and (3) can either cheat common mycorrhizal networks supported by neighbouring photosynthetic plants to satisfy all or part of their energetic and nutritional needs, or recruit free-living saprotrophic fungi into novel mycorrhizal symbioses. However, several fundamental aspects of myco-heterotrophy remain controversial or unknown, such as symbiotic costs and physiology.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Merckx, V., Bidartondo, M. I., Hynson, N. A.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp235</dc:identifier>
<dc:title><![CDATA[Myco-heterotrophy: when fungi host plants]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1261</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1255</prism:startingPage>
<prism:section>BOTANICAL BRIEFING</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1263?rss=1">
<title><![CDATA[Arbuscular mycorrhizal fungi in alleviation of salt stress: a review]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1263?rss=1</link>
<description><![CDATA[
<sec><st>Background</st>
<p>Salt stress has become a major threat to plant growth and productivity. Arbuscular mycorrhizal fungi colonize plant root systems and modulate plant growth in various ways.</p>
</sec>
<sec><st>Scope</st>
<p>This review addresses the significance of arbuscular mycorrhiza in alleviation of salt stress and their beneficial effects on plant growth and productivity. It also focuses on recent progress in unravelling biochemical, physiological and molecular mechanisms in mycorrhizal plants to alleviate salt stress.</p>
</sec>
<sec><st>Conclusions</st>
<p>The role of arbuscular mycorrhizal fungi in alleviating salt stress is well documented. This paper reviews the mechanisms arbuscular mycorrhizal fungi employ to enhance the salt tolerance of host plants such as enhanced nutrient acquisition (P, N, Mg and Ca), maintenance of the K<sup>+</sup> : Na<sup>+</sup> ratio, biochemical changes (accumulation of proline, betaines, polyamines, carbohydrates and antioxidants), physiological changes (photosynthetic efficiency, relative permeability, water status, abscissic acid accumulation, nodulation and nitrogen fixation), molecular changes (the expression of genes: <I>PIP</I>, Na<sup>+</sup>/H<sup>+</sup> antiporters, <I>Lsnced</I>, <I>Lslea</I> and <I>LsP5CS</I>) and ultra-structural changes. Theis review identifies certain lesser explored areas such as molecular and ultra-structural changes where further research is needed for better understanding of symbiosis with reference to salt stress for optimum usage of this technology in the field on a large scale. This review paper gives useful benchmark information for the development and prioritization of future research programmes.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Evelin, H., Kapoor, R., Giri, B.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp251</dc:identifier>
<dc:title><![CDATA[Arbuscular mycorrhizal fungi in alleviation of salt stress: a review]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1280</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1263</prism:startingPage>
<prism:section>INVITED REVIEW</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1281?rss=1">
<title><![CDATA[Adaptive significance and ontogenetic variability of the waxy zone in Nepenthes rafflesiana]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1281?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The slippery waxy zone in the upper part of pitchers has long been considered the key trapping structure of the <I>Nepenthes</I> carnivorous plants; however, the presence of wax is reported to be variable within and between species of this species-rich genus. This study raises the question of the adaptive significance of the waxy zone and investigates the basis for an ontogenetic cause of its variability and correlation with pitcher shape.</p>
</sec>
<sec><st>Methods</st>
<p>In Brunei (Borneo) the expression of the waxy zone throughout plant ontogeny was studied in two taxa of the <I>Nepenthes rafflesiana</I> complex, <I>typica</I> and <I>elongata</I>, which differ in pitcher shape and size. We also tested the adaptive significance of this zone by comparing the trapping efficiency and the number of prey captured of wax-bearing and wax-lacking plants.</p>
</sec>
<sec><st>Key Results</st>
<p>In <I>elongata</I>, the waxy zone is always well expanded and the elongated pitchers change little in form during plant development. Wax efficiently traps experimental ants but the number of captured prey in pitchers is low. In contrast, in <I>typica</I>, the waxy zone is reduced in successively produced pitchers until it is lost at the end of the plant's juvenile stage. The form of pitchers thus changes continuously throughout plant ontogeny, from elongated to ovoid. In <I>typica</I>, the number of captured prey is greater, but the role of wax in trapping is minor compared with that of the digestive liquid, and waxy plants do not show a higher insect retention and prey abundance as compared with non-waxy plants.</p>
</sec>
<sec><st>Conclusions</st>
<p>The waxy zone is not always a key trapping structure in <I>Nepenthes</I> and can be lost when supplanted by more efficient features. This study points out how pitcher structure is submitted to selection, and that evolutionary changes in developmental mechanisms could play a role in the morphological diversity of <I>Nepenthes</I>.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Gaume, L., Di Giusto, B.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp238</dc:identifier>
<dc:title><![CDATA[Adaptive significance and ontogenetic variability of the waxy zone in Nepenthes rafflesiana]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1291</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1281</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1293?rss=1">
<title><![CDATA[Stem growth habit affects leaf morphology and gas exchange traits in soybean]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1293?rss=1</link>
<description><![CDATA[
<sec><st>Backgrounds and Aims</st>
<p>The stem growth habit, determinate or indeterminate, of soybean, <I>Glycine max</I>, varieties affects various plant morphological and developmental traits. The objective of this study is to identify the effect of stem growth habit in soybean on the stomatal conductance of single leaves in relation to their leaf morphology in order to better understand the ecological and agronomic significance of this plant trait.</p>
</sec>
<sec><st>Methods</st>
<p>The stomatal conductance of leaves on the main stem was measured periodically under favourable field conditions to evaluate <I>g</I><SUB>max</SUB>, defined as the maximum stomatal conductance at full leaf expansion, for four varieties of soybean and their respective determinate or indeterminate near isogenic lines (NILs). Leaf morphological traits including stomatal density, guard cell length and vein density were also measured.</p>
</sec>
<sec><st>Key Results</st>
<p>The value of <I>g</I><SUB>max</SUB> ranged from 0&middot;383 to 0&middot;754 mol H<SUB>2</SUB>O m<sup>&ndash;2</sup> s<sup>&ndash;1</sup> across all the genotypes for both years. For the four pairs of varieties, the indeterminate lines exhibited significantly greater <I>g</I><SUB>max</SUB>, stomatal density, numbers of epidermal cells per unit area and total vein length per unit area than their respective determinate NILs in both years. The guard cell length, leaf mass per area and single leaf size all tended to be greater in the determinate types. The variation of <I>g</I><SUB>max</SUB> across genotypes and years was well explained by the product of stomatal density and guard cell length (<I>r</I> = 0&middot;86, <I>P</I> &lt; 0&middot;01).</p>
</sec>
<sec><st>Conclusions</st>
<p>The indeterminate stem growth habit resulted in a greater maximum stomatal conductance for soybean than the determinate habit, and this was attributed to the differences in leaf structure. This raises the further hypothesis that the difference in stem growth habit results in different water use characteristics of soybean plants in the field. Stomatal conductance under favourable conditions can be modified by leaf morphological traits.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Tanaka, Y., Shiraiwa, T.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp240</dc:identifier>
<dc:title><![CDATA[Stem growth habit affects leaf morphology and gas exchange traits in soybean]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1299</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1293</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1301?rss=1">
<title><![CDATA[Hanging by a coastal strand: breeding system of a federally endangered morning-glory of the south-eastern Florida coast, Jacquemontia reclinata]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1301?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Coastal development has led to extensive habitat destruction and the near extinction of the beach clustervine, <I>Jacquemontia reclinata</I> (Convolvulaceae), an endangered, perennial vine endemic to dune and coastal strand communities in south-eastern Florida. We examined the breeding system of this rare species, and observed visitors to its flowers, as part of a larger effort to document its status and facilitate its recovery.</p>
</sec>
<sec><st>Methods</st>
<p>Reproductively mature experimental plants were grown from seed collected from wild plants in two of the largest remaining populations. Controlled hand pollinations on potted plants were conducted to determine the level of compatibility of the species and to investigate compatibility within and between populations. Seeds from the hand pollinations were planted in soil, and they were monitored individually, recording time to seed germination (cotyledon emergence). Wild plants were observed in several of the remaining populations to determine which species visited the flowers.</p>
</sec>
<sec><st>Key Results</st>
<p>Hand pollination and seed planting experiments indicate that <I>J. reclinata</I> has a mixed mating system: flowers are able to set fruit with viable seeds with self-pollen, but outcross pollen produces significantly greater fruit and seed set than self-pollen (&ge;50 % for crosses vs. &lt;25 % for self-pollinations). Visitors included a wide array of insect species, primarily of the orders Diptera, Hymenoptera and Lepidoptera. All visitors captured and examined carried <I>J. reclinata</I> pollen, and usually several other types of pollen.</p>
</sec>
<sec><st>Conclusions</st>
<p>Remnant populations of beach clustervine will have greater reproductive success not only if floral visitor populations are maintained, but also if movement of either pollen or seed takes place between populations. Restoration efforts should include provisions for the establishment and maintenance of pollinator populations.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Pinto-Torres, E., Koptur, S.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp241</dc:identifier>
<dc:title><![CDATA[Hanging by a coastal strand: breeding system of a federally endangered morning-glory of the south-eastern Florida coast, Jacquemontia reclinata]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1311</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1301</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1313?rss=1">
<title><![CDATA[Isolated populations of a rare alpine plant show high genetic diversity and considerable population differentiation]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1313?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Gene flow and genetic variability within and among alpine plant populations can be greatly influenced by the steep environmental gradients and heterogeneous topography of alpine landscapes. In this study, the effects are examined of natural isolation of alpine habitats on genetic diversity and geographic structure in populations of <I>C. thyrsoides</I>, a rare and isolated European Alpine monocarpic perennial with limited seed dispersal capacity.</p>
</sec>
<sec><st>Methods</st>
<p>Molecular diversity was analysed for 736 individuals from 32 populations in the Swiss Alps and adjacent Jura mountains using five polymorphic microsatellite loci. Pollen flow was estimated using pollen grain-sized fluorescent powder. In addition, individual-based Bayesian approaches were applied to examine population structure.</p>
</sec>
<sec><st>Key Results</st>
<p>High within-population genetic diversity (<I>H</I><SUB>E</SUB> = 0&middot;76) and a relatively low inbreeding coefficient (<I>F</I><SUB>IS</SUB> = 0&middot;022) were found. Genetic differentiation among populations measured with a standardized measure was considerable (<I>G</I>'<SUB>ST</SUB> = 0&middot;53). A significant isolation-by-distance relationship was found (<I>r</I> = 0&middot;62, <I>P</I> &lt; 0&middot;001) and a significant geographic sub-structure, coinciding with proposed postglacial migration patterns. Altitudinal location and size of populations did not influence molecular variation. Direct measures of pollen flow revealed that insect-mediated pollen dispersal was restricted to short distances within a population.</p>
</sec>
<sec><st>Conclusions</st>
<p>The natural isolation of suitable habitats for <I>C. thyrsoides</I> restricts gene flow among the populations as expected for a monocarpic species with very limited seed dispersal capacities. The observed high within-population genetic diversity in this rare monocarpic perennial is best explained by its outcrossing behaviour, long-lived individuals and overlapping generations. Despite the high within-population genetic diversity, the considerable genetic differentiation and the clear western&ndash;eastern differentiation in this species merits consideration in future conservation efforts.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Aegisdottir, H. H., Kuss, P., Stocklin, J.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp242</dc:identifier>
<dc:title><![CDATA[Isolated populations of a rare alpine plant show high genetic diversity and considerable population differentiation]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1322</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1313</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1323?rss=1">
<title><![CDATA[Natural variation reveals relationships between pre-stress carbohydrate nutritional status and subsequent responses to xenobiotic and oxidative stress in Arabidopsis thaliana]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1323?rss=1</link>
<description><![CDATA[
<sec><st>Background</st>
<p>Soluble sugars are involved in responses to stress, and act as signalling molecules that activate specific or hormone cross-talk transduction pathways. Thus, exogenous sucrose treatment efficiently induces tolerance to the herbicide atrazine in <I>Arabidopsis thaliana</I> plantlets, at least partially through large-scale modifications of expression of stress-related genes.</p>
</sec>
<sec><st>Methods</st>
<p>Availability of sugars <I>in planta</I> for stress responses is likely to depend on complex dynamics of soluble sugar accumulation, sucrose&ndash;starch partition and organ allocation. The question of potential relationships between endogenous sugar levels and stress responses to atrazine treatment was investigated through analysis of natural genetic accessions of <I>A. thaliana</I>. Parallel quantitative and statistical analysis of biochemical parameters and of stress-sensitive physiological traits was carried out on a set of 11 accessions.</p>
</sec>
<sec><st>Key Results</st>
<p>Important natural variation was found between accessions of <I>A. thaliana</I> in pre-stress shoot endogenous sugar levels and responses of plantlets to subsequent atrazine stress. Moreover, consistent trends and statistically significant correlations were detected between specific endogenous sugar parameters, such as the pre-stress end of day sucrose level in shoots, and physiological markers of atrazine tolerance.</p>
</sec>
<sec><st>Conclusions</st>
<p>These significant relationships between endogenous carbohydrate metabolism and stress response therefore point to an important integration of carbon nutritional status and induction of stress tolerance in plants. The specific correlation between pre-stress sucrose level and greater atrazine tolerance may reflect adaptive mechanisms that link sucrose accumulation, photosynthesis-related stress and sucrose induction of stress defences.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ramel, F., Sulmon, C., Gouesbet, G., Couee, I.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp243</dc:identifier>
<dc:title><![CDATA[Natural variation reveals relationships between pre-stress carbohydrate nutritional status and subsequent responses to xenobiotic and oxidative stress in Arabidopsis thaliana]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1337</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1323</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1339?rss=1">
<title><![CDATA[BcMF9, a novel polygalacturonase gene, is required for both Brassica campestris intine and exine formation]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1339?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The polygalacturonase (PG) gene family has been found to be enriched in pollen of several species; however, little is currently known about the function of the PG gene in pollen development. To investigate the exact role that the PG gene has played in pollen development and about this family in general, one putative PG gene, <I>Brassica campestris Male Fertility 9</I> (<I>BcMF9</I>), was isolated from Chinese cabbage (<I>Brassica campestris</I> ssp. <I>chinensis</I>, syn. <I>B. rapa</I> ssp. <I>chinensis</I>) and characterized.</p>
</sec>
<sec><st>Methods</st>
<p>RT-PCR, northern blotting and <I>in situ</I> hybridization were used to analyse the expression pattern of <I>BcMF9</I>, and antisense RNA technology was applied to study the function of this gene.</p>
</sec>
<sec><st>Key Results</st>
<p><I>BcMF9</I> is expressed in particular in the tapetum and microspore during the late stages of pollen development. Antisense RNA transgenic plants that displayed decreased expression of <I>BcMF9</I> showed pollen morphological defects that resulted in reduced pollen germination efficiency. Transmission electron microscopy revealed that the homogeneous pectic exintine layer of pollen facing the exterior was over-developed and predominantly occupied the intine, reversing the normal proportional distribution of the internal endintine layer and the external exintine in transgenic pollen. Inhibition of <I>BcMF9</I> also resulted in break-up of the previously formed tectum and baculae from the beginning of the binucleate stage, as a result of premature degradation of tapetum.</p>
</sec>
<sec><st>Conclusions</st>
<p>Several lines of evidence, including patterns of <I>BcMF9</I> expression and phenotypic defects, suggest a sporophytic role in exine patterning, and a gametophytic mode of action of <I>BcMF9</I> in intine formation. <I>BcMF9</I> might act as a co-ordinator in the late stages of tapetum degeneration, and subsequently in the regulation of wall material secretion and, in turn, exine formation. <I>BcMF9</I> might also play a role in intine formation, possibly via regulation of the dynamic metabolism of pectin.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Huang, L., Ye, Y., Zhang, Y., Zhang, A., Liu, T., Cao, J.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp244</dc:identifier>
<dc:title><![CDATA[BcMF9, a novel polygalacturonase gene, is required for both Brassica campestris intine and exine formation]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1351</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1339</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1353?rss=1">
<title><![CDATA[Developmental morphology of strap-shaped gametophytes of Colysis decurrens: a new look at meristem development and function in fern gametophytes]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1353?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The gametophytes of most homosporous ferns are cordate&ndash;thalloid in shape. Some are strap- or ribbon-shaped and have been assumed to have evolved from terrestrial cordate shapes as an adaptation to epiphytic habitats. The aim of the present study was to clarify the morphological evolution of the strap-shaped gametophyte of microsoroids (Polypodiaceae) by precise analysis of their development.</p>
</sec>
<sec><st>Methods</st>
<p>Spores of <I>Colysis decurrens</I> collected in Kagoshima, Japan, were cultured and observed microscopically. Epi-illuminated micrographs of growing gametophytes were captured every 24 h, allowing analysis of the cell lineage of meristems. Light microscopy of resin-sections and scanning electron microscopy were also used.</p>
</sec>
<sec><st>Key Results</st>
<p>Contrary to previous assumptions that strap-shaped <I>Colysis</I> gametophytes have no organized meristem, three different types of meristems are formed during development: (1) apical-cell based &ndash; responsible for early growth; (2) marginal &ndash; further growth, including gametophyte branching; and (3) multicellular &ndash; formation of cushions with archegonia. The cushion is two or three layers thick and intermittent. The apical-cell and multicellular meristems are similar to those of cordate gametophytes of other ferns, but the marginal meristem is unique to the strap-shaped gametophyte of this fern.</p>
</sec>
<sec><st>Conclusions</st>
<p>The strap-shaped gametophytes of <I>C. decurrens</I> may have evolved from ancestors with a cordate shape by insertion of the marginal meristem phase between the first apical-cell-based meristem and subsequent multicellular meristem phases. Repeated retrieval of the marginal meristem at the multicellular meristem phase would result in indefinite prolongation of gametophyte growth, an ecological adaptation to epiphytic habitats.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Takahashi, N., Hashino, M., Kami, C., Imaichi, R.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp245</dc:identifier>
<dc:title><![CDATA[Developmental morphology of strap-shaped gametophytes of Colysis decurrens: a new look at meristem development and function in fern gametophytes]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1361</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1353</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1363?rss=1">
<title><![CDATA[Temporal regulation of cell-wall pectin methylesterase and peroxidase isoforms in cadmium-treated flax hypocotyl]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1363?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>In hypocotyls of flax (<I>Linum usitatissimum</I>) cadmium-induced reorientation of growth (i.e. an increase in expansion and a decrease in elongation) coincides with marked changes in the methylesterification and cross-linking of homogalacturonans within various cell-wall (CW) domains. The aim of the present study was to examine the involvement of pectin methylesterase (PME) and peroxidase (PER) in this cadmium-induced CW remodelling.</p>
</sec>
<sec><st>Methods</st>
<p>CW proteins were extracted from hypocotyls of 10- and 18-d-old flax that had been treated or not treated with 0&middot;5 m<scp>m</scp> Cd(NO<SUB>3</SUB>)<SUB>2</SUB>. PME and PER expression within these extracts was detected by LC/MS, by isoelectric focusing and enzyme activity assays. Transcript expression by RT-PCR of known flax PME and PER genes was also measured in corresponding samples.</p>
</sec>
<sec><st>Key Results</st>
<p>In cadmium-treated seedlings, PME activity increased as compared with controls, particularly at day 10. The increased activity of PME was accompanied by increased abundance of both a basic protein isoform (B2) and a particular transcript (<I>Lupme</I>5). In contrast, induction of PER activity by cadmium was highest at day 18. Among the four reported PER genes, <I>Flxper</I>1 and 3 increased in abundance in the presence of cadmium at day 18.</p>
</sec>
<sec><st>Conclusions</st>
<p>The temporal regulation of <I>Lupme</I> and <I>Flxper</I> genes and of their respective enzyme activities fits the previously reported cadmium-induced structural changes of homogalacturonans within the CWs. After PME-catalysed de-esterification of homogalacturonans, their cross-linking would depend on the activity of PERs interacting with calcium-dimerized blocks and reinforce the cell cohesion during the cadmium-induced swelling.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Paynel, F., Schaumann, A., Arkoun, M., Douchiche, O., Morvan, C.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp254</dc:identifier>
<dc:title><![CDATA[Temporal regulation of cell-wall pectin methylesterase and peroxidase isoforms in cadmium-treated flax hypocotyl]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1372</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1363</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1373?rss=1">
<title><![CDATA[The role of callose in guard-cell wall differentiation and stomatal pore formation in the fern Asplenium nidus]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1373?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The pattern of callose deposition was followed in developing stomata of the fern <I>Asplenium nidus</I> to investigate the role of this polysaccharide in guard cell (GC) wall differentiation and stomatal pore formation.</p>
</sec>
<sec><st>Methods</st>
<p>Callose was localized by aniline blue staining and immunolabelling using an antibody against (1 -&gt; 3)-&beta;-<scp>d</scp>-glucan. The study was carried out in stomata of untreated material as well as of material treated with: (1) 2-deoxy-<scp>d</scp>-glucose (2-DDG) or tunicamycin, which inhibit callose synthesis; (2) coumarin or 2,6-dichlorobenzonitrile (dichlobenil), which block cellulose synthesis; (3) cyclopiazonic acid (CPA), which disturbs cytoplasmic Ca<sup>2+</sup> homeostasis; and (d) cytochalasin B or oryzalin, which disintegrate actin filaments and microtubules, respectively.</p>
</sec>
<sec><st>Results</st>
<p>In post-cytokinetic stomata significant amounts of callose persisted in the nascent ventral wall. Callose then began degrading from the mid-region of the ventral wall towards its periphery, a process which kept pace with the formation of an &lsquo;internal stomatal pore&rsquo; by local separation of the partner plasmalemmata. In differentiating GCs, callose was consistently localized in the developing cell-wall thickenings. In 2-DDG-, tunicamycin- and CPA-affected stomata, callose deposition and internal stomatal pore formation were inhibited. The affected ventral walls and GC wall thickenings contained membranous elements. Stomata recovering from the above treatments formed a stomatal pore by a mechanism different from that in untreated stomata. After coumarin or dichlobenil treatment, callose was retained in the nascent ventral wall for longer than in control stomata, while internal stomatal pore formation was blocked. Actin filament disintegration inhibited internal stomatal pore formation, without any effect on callose deposition.</p>
</sec>
<sec><st>Conclusions</st>
<p>In <I>A. nidus</I> stomata the time and pattern of callose deposition and degradation play an essential role in internal stomatal pore formation, and callose participates in deposition of the local GC wall thickenings.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Apostolakos, P., Livanos, P., Nikolakopoulou, T. L., Galatis, B.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp255</dc:identifier>
<dc:title><![CDATA[The role of callose in guard-cell wall differentiation and stomatal pore formation in the fern Asplenium nidus]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1387</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1373</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1389?rss=1">
<title><![CDATA[Vesicle formation in the membrane of onion cells (Allium cepa) during rapid osmotic dehydration]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1389?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Optimization of osmotic dehydration in different plant cells has been investigated through the variation of parameters such as the nature of the sugar used, the concentration of osmotic solutions and the processing time. In micro-organisms such as the yeast, <I>Saccharomyces cerevisiae</I>, the exposure of a cell to a slow increase in osmotic pressure preserves cell viability after rehydration, while sudden dehydration involves a lower rate of cell viability, which could be due to membrane vesiculation. The aim of this work is to study cytoplasmic vesicle formation in onion epidermal cells (<I>Allium cepa</I>) as a function of the kinetics of osmotic pressure variation in the external medium.</p>
</sec>
<sec><st>Methods</st>
<p>Onion epidermal cells were submitted either to an osmotic shock or to a progressive osmotic shift from an osmotic pressure of 2 to 24 MPa to induce plasmolysis. After 30 min in the treatment solution, deplasmolysis was carried out. Cells were observed by microscopy during the whole cycle of dehydration&ndash;rehydration.</p>
</sec>
<sec><st>Key Results</st>
<p>The application of an osmotic shock to onion cells, from an initial osmotic pressure of 2 MPa to a final one of 24 MPa for &lt;1 s, led to the formation of numerous exocytotic and osmocytic vesicles visualized through light and confocal microscopy. In contrast, after application of a progressive osmotic shift, from an initial osmotic pressure of 2 MPa to a final one of 24 MPa for 30 min, no vesicles were observed. Additionally, the absence of Hechtian strand connections led to the bursting of vesicles in the case of the osmotic shock.</p>
</sec>
<sec><st>Conclusions</st>
<p>It is concluded that the kinetics of osmotic dehydration strongly influence vesicle formation in onion cells, and that Hechtian strand connections between protoplasts and exocytotic vesicles are a prerequisite for successful deplasmolysis. These results suggest that a decrease in the area-to-volume ratio of a cell could cause cell death following an osmotic shock.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Assani, A., Moundanga, S., Beney, L., Gervais, P.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp256</dc:identifier>
<dc:title><![CDATA[Vesicle formation in the membrane of onion cells (Allium cepa) during rapid osmotic dehydration]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1395</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1389</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1397?rss=1">
<title><![CDATA[Pollination biology of fruit-bearing hedgerow plants and the role of flower-visiting insects in fruit-set]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1397?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>In the UK, the flowers of fruit-bearing hedgerow plants provide a succession of pollen and nectar for flower-visiting insects for much of the year. The fruits of hedgerow plants are a source of winter food for frugivorous birds on farmland. It is unclear whether recent declines in pollinator populations are likely to threaten fruit-set and hence food supply for birds. The present study investigates the pollination biology of five common hedgerow plants: blackthorn (<I>Prunus spinosa</I>), hawthorn (<I>Crataegus monogyna</I>), dog rose (<I>Rosa canina</I>), bramble (<I>Rubus fruticosus</I>) and ivy (<I>Hedera helix</I>).</p>
</sec>
<sec><st>Methods</st>
<p>The requirement for insect pollination was investigated initially by excluding insects from flowers by using mesh bags and comparing immature and mature fruit-set with those of open-pollinated flowers. Those plants that showed a requirement for insect pollination were then tested to compare fruit-set under two additional pollination service scenarios: (1) reduced pollination, with insects excluded from flowers bagged for part of the flowering period, and (2) supplemental pollination, with flowers hand cross-pollinated to test for pollen limitation.</p>
</sec>
<sec><st>Key Results</st>
<p>The proportions of flowers setting fruit in blackthorn, hawthorn and ivy were significantly reduced when insects were excluded from flowers by using mesh bags, whereas fruit-set in bramble and dog rose were unaffected. Restricting the exposure of flowers to pollinators had no significant effect on fruit-set. However, blackthorn and hawthorn were found to be pollen-limited, suggesting that the pollination service was inadequate in the study area.</p>
</sec>
<sec><st>Conclusions</st>
<p>Ensuring strong populations of insect pollinators may be essential to guarantee a winter fruit supply for birds in UK hedgerows.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Jacobs, J. H., Clark, S. J., Denholm, I., Goulson, D., Stoate, C., Osborne, J. L.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp236</dc:identifier>
<dc:title><![CDATA[Pollination biology of fruit-bearing hedgerow plants and the role of flower-visiting insects in fruit-set]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1404</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1397</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1405?rss=1">
<title><![CDATA[Female reproductive success decreases with display size in monkshood, Aconitum kusnezoffii (Ranunculaceae)]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1405?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Reduction in female fitness in large clones can occur as a result of increased geitonogamous self-fertilization and its influence through inbreeding depression. This possibility was investigated in the self-compatible, bee-pollinated perennial herb <I>Aconitum kusnezoffii</I> which varies in clone size.</p>
</sec>
<sec><st>Methods</st>
<p>Field investigations were conducted on pollinator behaviour, flowering phenology and variation in seed set. The effects of self-pollination following controlled self- and cross-pollination were also examined. Selfing rates of differently sized clones were assessed using allozyme markers.</p>
</sec>
<sec><st>Key Results</st>
<p>High rates of geitonogamous pollination were associated with large display size. Female fitness at the ramet level decreased with clone size. Fruit and seed set under cross-pollination were significantly higher than those under self-pollination. The pre-dispersal inbreeding depression was estimated as 0&middot;502 based on the difference in seed set per flower between self- and cross-pollinated flowers. Selfing rates of differently sized clones did not differ.</p>
</sec>
<sec><st>Conclusions</st>
<p>It is concluded that in <I>A. kusnezoffii</I> the negative effects of self-pollination causing reduced female fertility with clone size arise primarily from a strong early-acting inbreeding depression leading to the abortion of selfed embryos prior to seed maturation.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Liao, W.-J., Hu, Y., Zhu, B.-R., Zhao, X.-Q., Zeng, Y.-F., Zhang, D.-Y.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp237</dc:identifier>
<dc:title><![CDATA[Female reproductive success decreases with display size in monkshood, Aconitum kusnezoffii (Ranunculaceae)]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1412</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1405</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1413?rss=1">
<title><![CDATA[High variation in clonal vs. sexual reproduction in populations of the wild strawberry, Fragaria virginiana (Rosaceae)]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1413?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Many plants reproduce both clonally and sexually, and the balance between the two modes of reproduction will vary among populations. Clonal reproduction was characterized in three populations of the wild strawberry, <I>Fragaria virginiana</I>, to determine the extent that reproductive mode varied locally between sites. The study sites were fragmented woodlands in Cook County, Illinois, USA.</p>
</sec>
<sec><st>Methods</st>
<p>A total of 95 strawberry ramets were sampled from the three sites via transects. Ramets were mapped and genotyped at five variable microsatellite loci. The variability at these five loci was sufficient to assign plants to clones with high confidence, and the spatial pattern of genets was mapped at each site.</p>
</sec>
<sec><st>Key Results</st>
<p>A total of 27 distinct multilocus genotypes were identified. Of these, 18 genotypes were detected only once, with the remaining nine detected in multiple ramets. The largest clone was identified in 16 ramets. No genets were shared between sites, and each site exhibited markedly different clonal and sexual recruitment patterns, ranging from two non-overlapping and widespread genets to 19 distinct genets. Only one flowering genet was female; the remainder were hermaphrodites.</p>
</sec>
<sec><st>Conclusions</st>
<p>Local population history or fine-scale ecological differences can result in dramatically different reproductive patterns at small spatial scales. This finding may be fairly widespread among clonal plant species, and studies that aim to characterize reproductive modes in species capable of asexual reproduction need to evaluate reproductive modes in multiple populations and sites.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Wilk, J. A., Kramer, A. T., Ashley, M. V.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp239</dc:identifier>
<dc:title><![CDATA[High variation in clonal vs. sexual reproduction in populations of the wild strawberry, Fragaria virginiana (Rosaceae)]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1419</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1413</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1421?rss=1">
<title><![CDATA[Paternity analysis-based inference of pollen dispersal patterns, male fecundity variation, and influence of flowering tree density and general flowering magnitude in two dipterocarp species]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1421?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Knowledge of pollen dispersal patterns and variation of fecundity is essential to understanding plant evolutionary processes and to formulating strategies to conserve forest genetic resources. Nevertheless, the pollen dispersal pattern of dipterocarp, main canopy tree species in palaeo-tropical forest remains unclear, and flowering intensity variation in the field suggests heterogeneity of fecundity.</p>
</sec>
<sec><st>Methods</st>
<p>Pollen dispersal patterns and male fecundity variation of <I>Shorea leprosula</I> and <I>Shorea parvifolia</I> ssp. <I>parvifolia</I> on Peninsular Malaysian were investigated during two general flowering seasons (2001 and 2002), using a neighbourhood model modified by including terms accounting for variation in male fecundity among individual trees to express heterogeneity in flowering.</p>
</sec>
<sec><st>Key Results</st>
<p>The pollen dispersal patterns of the two dipterocarp species were affected by differences in conspecific tree flowering density, and reductions in conspecific tree flowering density led to an increased selfing rate. Active pollen dispersal and a larger number of effective paternal parents were observed for both species in the season of greater magnitude of general flowering (2002).</p>
</sec>
<sec><st>Conclusions</st>
<p>The magnitude of general flowering, male fecundity variation, and distance between pollen donors and mother trees should be taken into account when attempting to predict the effects of management practices on the self-fertilization and genetic structure of key tree species in tropical forest, and also the sustainability of possible management strategies, especially selective logging regimes.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Tani, N., Tsumura, Y., Kado, T., Taguchi, Y., Lee, S. L., Muhammad, N., Ng, K. K. S., Numata, S., Nishimura, S., Konuma, A., Okuda, T.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp252</dc:identifier>
<dc:title><![CDATA[Paternity analysis-based inference of pollen dispersal patterns, male fecundity variation, and influence of flowering tree density and general flowering magnitude in two dipterocarp species]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1434</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1421</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/7/1435?rss=1">
<title><![CDATA[Photosynthetic acclimation is important for post-submergence recovery of photosynthesis and growth in two riparian species]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/7/1435?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Concomitant increases in O<SUB>2</SUB> and irradiance upon de-submergence can cause photoinhibition and photo-oxidative damage to the photosynthetic apparatus of plants. As energy and carbohydrate supply from photosynthesis is needed for growth, it was hypothesized that post-submergence growth recovery may require efficient photosynthetic acclimation to increased O<SUB>2</SUB> and irradiance to minimize photo-oxidative damage. The hypothesis was tested in two flood-tolerant species: a C<SUB>3</SUB> herb, <I>Alternanthera philoxeroides</I>; and a C<SUB>4</SUB> grass, <I>Hemarthria altissima</I>. The impact of low O<SUB>2</SUB> and low light, typical conditions in turbid floodwater, on post-submergence recovery was assessed by different flooding treatments combined with shading.</p>
</sec>
<sec><st>Methods</st>
<p>Experiments were conducted during 30 d of flooding (waterlogging or submergence) with or without shading and subsequent recovery of 20 d under growth conditions. Changes in dry mass, number of branches/tillers, and length of the longest internodes and main stems were recorded to characterize growth responses. Photosynthetic parameters (photosystem II efficiency and non-photochemical quenching) were determined in mature leaves based on chlorophyll <I>a</I> fluorescence measurements.</p>
</sec>
<sec><st>Key Results</st>
<p>In both species growth and photosynthesis recovered after the end of the submergence treatment, with recovery of photosynthesis (starting shortly after de-submergence) preceding recovery of growth (pronounced on days 40&ndash;50). The effective quantum yield of photosystem II and non-photochemical quenching were diminished during submergence but rapidly increased upon de-submergence. Similar changes were found in all shaded plants, with or without flooding. Submerged plants did not suffer from photoinhibition throughout the recovery period although their growth recovery was retarded.</p>
</sec>
<sec><st>Conclusions</st>
<p>After sudden de-submergence the C<SUB>3</SUB> plant <I>A. philoxeroides</I> and the C<SUB>4</SUB> plant <I>H. altissima</I> were both able to maintain the functionality of the photosynthetic apparatus through rapid acclimation to changing O<SUB>2</SUB> and light conditions. The ability for photosynthetic acclimation may be essential for adaptation to wetland habitats in which water levels fluctuate.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Luo, F.-L., Nagel, K. A., Zeng, B., Schurr, U., Matsubara, S.]]></dc:creator>
<dc:date>Tue, 17 Nov 2009 06:46:26 PST</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp257</dc:identifier>
<dc:title><![CDATA[Photosynthetic acclimation is important for post-submergence recovery of photosynthesis and growth in two riparian species]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1444</prism:endingPage>
<prism:publicationDate>2009-12-01</prism:publicationDate>
<prism:startingPage>1435</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/i?rss=1">
<title><![CDATA[ContentSnapshots]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/i?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:27 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp263</dc:identifier>
<dc:title><![CDATA[ContentSnapshots]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>iii</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>i</prism:startingPage>
<prism:section>ContentSnapshots</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/ix?rss=1">
<title><![CDATA[Association mapping in plants]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/ix?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Gonzalez-Martinez, S. C., Grivet, D.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp218</dc:identifier>
<dc:title><![CDATA[Association mapping in plants]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>x</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>ix</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/ix-a?rss=1">
<title><![CDATA[Grasses and grassland ecology]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/ix-a?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Wilson, S.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp219</dc:identifier>
<dc:title><![CDATA[Grasses and grassland ecology]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>ix</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>ix</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/v?rss=1">
<title><![CDATA[John Bryant takes a closer look at some of this month's Original Articles]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/v?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Bryant, J. A.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:27 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp264</dc:identifier>
<dc:title><![CDATA[John Bryant takes a closer look at some of this month's Original Articles]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>vi</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>v</prism:startingPage>
<prism:section>ContentSelect</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/vii?rss=1">
<title><![CDATA[Breeding plantation tree crops. Tropical species]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/vii?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Rival, A.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:27 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp206</dc:identifier>
<dc:title><![CDATA[Breeding plantation tree crops. Tropical species]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>viii</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>vii</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/viii?rss=1">
<title><![CDATA[Breeding plantation tree crops. Temperate species]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/viii?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Dosba, F.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:27 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp205</dc:identifier>
<dc:title><![CDATA[Breeding plantation tree crops. Temperate species]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>ix</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>viii</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/x?rss=1">
<title><![CDATA[Introduction to statistics for biology, 3rd edn]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/x?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Gee, J.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp223</dc:identifier>
<dc:title><![CDATA[Introduction to statistics for biology, 3rd edn]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>xi</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>x</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1017?rss=1">
<title><![CDATA[The evolution of bat pollination: a phylogenetic perspective]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1017?rss=1</link>
<description><![CDATA[
<sec><st>Background</st>
<p>Most tropical and subtropical plants are biotically pollinated, and insects are the major pollinators. A small but ecologically and economically important group of plants classified in 28 orders, 67 families and about 528 species of angiosperms are pollinated by nectar-feeding bats. From a phylogenetic perspective this is a derived pollination mode involving a relatively large and energetically expensive pollinator. Here its ecological and evolutionary consequences are explored.</p>
</sec>
<sec><st>Scope and Conclusions</st>
<p>This review summarizes adaptations in bats and plants that facilitate this interaction and discusses the evolution of bat pollination from a plant phylogenetic perspective. Two families of bats contain specialized flower visitors, one in the Old World and one in the New World. Adaptation to pollination by bats has evolved independently many times from a variety of ancestral conditions, including insect-, bird- and non-volant mammal-pollination. Bat pollination predominates in very few families but is relatively common in certain angiosperm subfamilies and tribes. We propose that flower-visiting bats provide two important benefits to plants: they deposit large amounts of pollen and a variety of pollen genotypes on plant stigmas and, compared with many other pollinators, they are long-distance pollen dispersers. Bat pollination tends to occur in plants that occur in low densities and in lineages producing large flowers. In highly fragmented tropical habitats, nectar bats play an important role in maintaining the genetic continuity of plant populations and thus have considerable conservation value.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Fleming, T. H., Geiselman, C., Kress, W. J.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp197</dc:identifier>
<dc:title><![CDATA[The evolution of bat pollination: a phylogenetic perspective]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1043</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1017</prism:startingPage>
<prism:section>INVITED REVIEW</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1045?rss=1">
<title><![CDATA[The distribution of cell wall polymers during antheridium development and spermatogenesis in the Charophycean green alga, Chara corallina]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1045?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The production of multicellular gametangia in green plants represents an early evolutionary development that is found today in all land plants and advanced clades of the Charophycean green algae. The processing of cell walls is an integral part of this morphogenesis yet very little is known about cell wall dynamics in early-divergent green plants such as the Charophycean green algae. This study represents a comprehensive analysis of antheridium development and spermatogenesis in the green alga, <I>Chara corallina</I>.</p>
</sec>
<sec><st>Methods</st>
<p>Microarrays of cell wall components and immunocytochemical methods were employed in order to analyse cell wall macromolecules during antheridium development.</p>
</sec>
<sec><st>Key Results</st>
<p>Cellulose and pectic homogalacturonan epitopes were detected throughout all cell types of the developing antheridium including the unique cell wall protuberances of the shield cells and the cell walls of sperm cell initials. Arabinogalactan protein epitopes were distributed only in the epidermal shield cell layers and anti-xyloglucan antibody binding was only observed in the capitulum region that initially yields the sperm filaments. During the terminal stage of sperm development, no cell wall polymers recognized by the probes employed were found on the scale-covered sperm cells.</p>
</sec>
<sec><st>Conclusions</st>
<p>Antheridium development in <I>C. corallina</I> is a rapid event that includes the production of cell walls that contain polymers similar to those found in land plants. While pectic and cellulosic epitopes are ubiquitous in the antheridium, the distribution of arabinogalactan protein and xyloglucan epitopes is restricted to specific zones. Spermatogenesis also includes a major switch in the production of extracellular matrix macromolecules from cell walls to scales, the latter being a primitive extracellular matrix characteristic of green plants.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Domozych, D. S., Sorensen, I., Willats, W. G. T.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp193</dc:identifier>
<dc:title><![CDATA[The distribution of cell wall polymers during antheridium development and spermatogenesis in the Charophycean green alga, Chara corallina]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1056</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1045</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1057?rss=1">
<title><![CDATA[Intraspecific variation in the magnitude and pattern of flooding-induced shoot elongation in Rumex palustris]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1057?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Intraspecific variation in flooding tolerance is the basic pre-condition for adaptive flooding tolerance to evolve, and flooding-induced shoot elongation is an important trait that enables plants to survive shallow, prolonged flooding. Here an investigation was conducted to determine to what extent variation in flooding-induced leaf elongation exists among and within populations of the wetland species <I>Rumex palustris</I>, and whether the magnitude of elongation can be linked to habitat characteristics.</p>
</sec>
<sec><st>Methods</st>
<p>Offspring of eight genotypes collected in each of 12 populations from different sites (ranging from river mudflats with dynamic flooding regimes to areas with stagnant water) were submerged, and petioles, laminas and roots were harvested separately to measure traits related to elongation and plant growth.</p>
</sec>
<sec><st>Key Results</st>
<p>We found strong elongation of petioles upon submergence, and both among- and within-population variation in this trait, not only in final length, but also in the timing of the elongation response. However, the variation in elongation responses could not be linked to habitat type.</p>
</sec>
<sec><st>Conclusions</st>
<p>Spatio-temporal variation in the duration and depth of flooding in combination with a presumably weak selection against flooding-induced elongation may have contributed to the maintenance of large genetic variation in flooding-related traits among and within populations.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Chen, X., Huber, H., de Kroon, H., Peeters, A. J. M., Poorter, H., Voesenek, L. A. C. J., Visser, E. J. W.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp198</dc:identifier>
<dc:title><![CDATA[Intraspecific variation in the magnitude and pattern of flooding-induced shoot elongation in Rumex palustris]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1067</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1057</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1069?rss=1">
<title><![CDATA[Relevance of genetics for conservation policies: the case of Minorcan cork oaks]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1069?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Marginal populations of widely distributed species can be of high conservation interest when they hold a significant or unique portion of the genetic diversity of the species. However, such genetic information is frequently lacking. Here the relevance of genetic surveys to develop efficient conservation strategies for such populations is illustrated using cork oak (<I>Quercus suber</I>) from Minorca (Balearic Islands, Spain) as a case study. Cork oak is highly endangered on the island, where no more than 67 individuals live in small, isolated stands in siliceous sites. As a consequence, it was recently granted protected status.</p>
</sec>
<sec><st>Methods</st>
<p>Two Bayesian clustering approaches were used to analyse the genetic structure of the Minorcan population, on the basis of nuclear microsatellite data. The different groups within the island were also compared with additional island and continental populations surrounding Minorca.</p>
</sec>
<sec><st>Key Results</st>
<p>Very high genetic diversity was found, with values comparable with those observed in continental parts of the species' range. Furthermore, the Minorcan oak stands were highly differentiated from one another and were genetically related to different continental populations of France and Spain.</p>
</sec>
<sec><st>Conclusions</st>
<p>The high levels of genetic diversity and inter-stands differentiation make Minorcan cork oak eligible for specific conservation efforts. The relationship of Minorcan stands to different continental populations in France and Spain probably reflects multiple colonization events. However, discrepancy between chloroplast DNA- and nuclear DNA-based groups does not support a simple scenario of recent introduction. Gene exchanges between neighbouring cork oak stands and with holm oak have created specific and exceptional genetic combinations. They also constitute a wide range of potential genetic resources for research on adaptation to new environmental conditions. Conservation guidelines that take into account these findings are provided.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lorenzo, Z., Burgarella, C., de Heredia, U. L., Lumaret, R., Petit, R. J., Soto, A., Gil, L.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp200</dc:identifier>
<dc:title><![CDATA[Relevance of genetics for conservation policies: the case of Minorcan cork oaks]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1076</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1069</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1077?rss=1">
<title><![CDATA[On the roles of colour and scent in a specialized floral mimicry system]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1077?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Sexually deceptive orchids achieve cross-pollination by mimicking the mating signals of female insects, generally hymenopterans. This pollination mechanism is often highly specific as it is based primarily on the mimicry of mating signals, especially the female sex pheromones of the targeted pollinator. Like many deceptive orchids, the Mediterranean species <I>Ophrys arachnitiformis</I> shows high levels of floral trait variation, especially in the colour of the perianth, which is either green or white/pinkinsh within populations. The adaptive significance of perianth colour polymorphism and its influence on pollinator visitation rates in sexually deceptive orchids remain obscure.</p>
</sec>
<sec><st>Methods</st>
<p>The relative importance of floral scent versus perianth colour in pollinator attraction in this orchid pollinator mimicry system was evaluated by performing floral scent analyses by gas chromatography-mass spectrometry (GC-MS) and behavioural bioassays with the pollinators under natural conditions were performed.</p>
</sec>
<sec><st>Key Results</st>
<p>The relative and absolute amounts of behaviourally active compounds are identical in the two colour morphs of <I>O. arachnitiformis</I>. Neither presence/absence nor the colour of the perianth (green versus white) influence attractiveness of the flowers to <I>Colletes cunicularius</I> males, the main pollinator of <I>O. arachnitiformis</I>.</p>
</sec>
<sec><st>Conclusion</st>
<p>Chemical signals alone can mediate the interactions in highly specialized mimicry systems. Floral colour polymorphism in <I>O. arachnitiformis</I> is not subjected to selection imposed by <I>C. cunicularius</I> males, and an interplay between different non-adaptive processes may be responsible for the maintenance of floral colour polymorphism both within and among populations.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Vereecken, N. J., Schiestl, F. P.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp208</dc:identifier>
<dc:title><![CDATA[On the roles of colour and scent in a specialized floral mimicry system]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1084</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1077</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1085?rss=1">
<title><![CDATA[Shifts in leaf vein density through accelerated vein formation in C4 Flaveria (Asteraceae)]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1085?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Leaf venation in many C<SUB>4</SUB> species is characterized by high vein density, essential in facilitating rapid intercellular diffusion of C<SUB>4</SUB> photosynthetic metabolites between different tissues (mesophyll, bundle sheath). Greater vein density has been hypothesized to be an early step in C<SUB>4</SUB> photosynthesis evolution. Development of C<SUB>4</SUB> vein patterning is thought to occur from either accelerated or prolonged procambium formation, relative to ground tissue development.</p>
</sec>
<sec><st>Methods</st>
<p>Cleared and sectioned tissues of phylogenetically basal C<SUB>3</SUB> <I>Flaveria robusta</I> and more derived C<SUB>4</SUB> <I>Flaveria bidentis</I> were compared for vein pattern in mature leaves and vein pattern formation in developing leaves.</p>
</sec>
<sec><st>Key Results</st>
<p>In mature leaves, major vein density did not differ between C<SUB>3</SUB> and C<SUB>4</SUB> <I>Flaveria</I> species, whereas minor veins were denser in C<SUB>4</SUB> species than in C<SUB>3</SUB> species. The developmental study showed that both major and minor vein patterning in leaves of C<SUB>3</SUB> and C<SUB>4</SUB> species were initiated at comparable stages (based on leaf length). An additional vein order in the C<SUB>4</SUB> species was observed during initiation of the higher order minor veins compared with the C<SUB>3</SUB> species. In the two species, expansion of bundle sheath and mesophyll cells occurred after vein pattern was complete and xylem differentiation was continuous in minor veins. In addition, mesophyll cells ceased dividing sooner and enlarged less in C<SUB>4</SUB> species than in C<SUB>3</SUB> species.</p>
</sec>
<sec><st>Conclusions</st>
<p>Leaf vein pattern characteristic to C<SUB>4</SUB> <I>Flaveria</I> was achieved primarily through accelerated and earlier offset of higher order vein formation, rather than other modifications in the timing of vein pattern formation, as compared with C<SUB>3</SUB> species. Earlier cessation of mesophyll cell division and reduced expansion also contributed to greater vein density in the C<SUB>4</SUB> species. The relatively late expansion of bundle sheath and mesophyll cells shows that vein patterning precedes ground tissue development in C<SUB>4</SUB> species.</p>
</sec>
]]></description>
<dc:creator><![CDATA[McKown, A. D., Dengler, N. G.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp210</dc:identifier>
<dc:title><![CDATA[Shifts in leaf vein density through accelerated vein formation in C4 Flaveria (Asteraceae)]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1098</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1085</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1099?rss=1">
<title><![CDATA[Evolution of petal epidermal micromorphology in Leguminosae and its use as a marker of petal identity]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1099?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The legume flower is highly variable in symmetry and differentiation of petal types. Most papilionoid flowers are zygomorphic with three types of petals: one dorsal, two lateral and two ventral petals. Mimosoids have radial flowers with reduced petals while caesalpinioids display a range from strongly zygomorphic to nearly radial symmetry. The aims are to characterize the petal micromorphology relative to flower morphology and evolution within the family and assess its use as a marker of petal identity (whether dorsal, lateral or ventral) as determined by the expression of developmental genes.</p>
</sec>
<sec><st>Methods</st>
<p>Petals were analysed using the scanning electron microscope and light microscope. A total of 175 species were studied representing 26 tribes and 89 genera in all three subfamilies of the Leguminosae.</p>
</sec>
<sec><st>Key Results</st>
<p>The papilionoids have the highest degree of variation of epidermal types along the dorsiventral axis within the flower. In Loteae and genistoids, in particular, it is common for each petal type to have a different major epidermal micromorphology. Papillose conical cells are mainly found on dorsal and lateral petals. Tabular rugose cells are mainly found on lateral petals and tabular flat cells are found only in ventral petals. Caesalpinioids lack strong micromorphological variation along this axis and usually have only a single major epidermal type within a flower, although the type maybe either tabular rugose cells, papillose conical cells or papillose knobby rugose cells, depending on the species.</p>
</sec>
<sec><st>Conclusions</st>
<p>Strong micromorphological variation between different petals in the flower is exclusive to the subfamily Papilionoideae. Both major and minor epidermal types can be used as micromorphological markers of petal identity, at least in papilionoids, and they are important characters of flower evolution in the whole family. The molecular developmental pathway between specific epidermal micromorphology and the expression of petal identity genes has yet to be established.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ojeda, I., Francisco-Ortega, J., Cronk, Q. C. B.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp211</dc:identifier>
<dc:title><![CDATA[Evolution of petal epidermal micromorphology in Leguminosae and its use as a marker of petal identity]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1110</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1099</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1111?rss=1">
<title><![CDATA[The role of carbohydrates in seed germination and seedling establishment of Himatanthus sucuuba, an Amazonian tree with populations adapted to flooded and non-flooded conditions]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1111?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>In the Amazonian floodplains plants withstand annual periods of flooding which can last 7 months. Under these conditions seedlings remain submerged in the dark for long periods since light penetration in the water is limited. <I>Himatanthus sucuuba</I> is a tree species found in the &lsquo;v&aacute;rzea&rsquo; (VZ) floodplains and adjacent non-flooded &lsquo;terra-firme&rsquo; (TF) forests. Biochemical traits which enhance flood tolerance and colonization success of <I>H. sucuuba</I> in periodically flooded environments were investigated.</p>
</sec>
<sec><st>Methods</st>
<p>Storage carbohydrates of seeds of VZ and TF populations were extracted and analysed by HPAEC/PAD. Starch was analysed by enzyme (glucoamylase) degradation followed by quantification of glucose oxidase. Carbohydrate composition of roots of VZ and TF seedlings was studied after experimental exposure to a 15-d period of submersion in light versus darkness.</p>
</sec>
<sec><st>Key Results</st>
<p>The endosperm contains a large proportion of the seed reserves, raffinose being the main non-structural carbohydrate. Around 93 % of the cell wall storage polysaccharides (percentage dry weight basis) in the endosperm of VZ seeds was composed of mannose, while soluble sugars accounted for 2&middot;5%. In contrast, 74 % of the endosperm in TF seeds was composed of galactomannans, while 22 % of the endosperm was soluble sugars. This suggested a larger carbohydrate allocation to germination in TF populations whereas VZ populations allocate comparatively more to carbohydrates mobilized during seedling development. The concentration of root non-structural carbohydrates in non-flooded seedlings strongly decreased after a 15-d period of darkness, whereas flooded seedlings were less affected. These effects were more pronounced in TF seedlings, which showed significantly lower root non-structural carbohydrate concentrations.</p>
</sec>
<sec><st>Conclusions</st>
<p>There seem to be metabolic adjustments in VZ but not TF seedlings that lead to adaptation to the combined stresses of darkness and flooding. This seems to be important for the survival of the species in these contrasting environments, leading these populations to different directions during evolution.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ferreira, C. d. S., Piedade, M. T. F., Tine, M. A. S., Rossatto, D. R., Parolin, P., Buckeridge, M. S.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp212</dc:identifier>
<dc:title><![CDATA[The role of carbohydrates in seed germination and seedling establishment of Himatanthus sucuuba, an Amazonian tree with populations adapted to flooded and non-flooded conditions]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1119</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1111</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1121?rss=1">
<title><![CDATA[Arabidopsis plants harbouring a mutation in AtSUC2, encoding the predominant sucrose/proton symporter necessary for efficient phloem transport, are able to complete their life cycle and produce viable seed]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1121?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p><I>AtSUC2</I> encodes a sucrose/proton symporter that localizes throughout the collection and transport phloem and is necessary for efficient transport of sucrose from source to sink tissues in <I>Arabidopsis thaliana</I>. Plants harbouring homozygous <I>AtSUC2</I> null alleles accumulate sugar, starch, and anthocyanin in mature leaves, have severely delayed development and stunted growth and, in previous studies, failed to complete their life cycle by producing viable seed.</p>
</sec>
<sec><st>Methods</st>
<p>An <I>AtSUC2</I> allele with a T-DNA insertion in the second intron was analysed. Full-length transcript from this allele is not produced, and a truncated protein translated from sequences upstream of the insertion site did not catalyse sucrose uptake into yeast, supporting the contention that this is a null allele. Mutant plants were grown in a growth chamber with a diurnal light/dark cycle, and growth patterns recorded.</p>
</sec>
<sec><st>Key Results</st>
<p>This allele (SALK_038124, designated <I>AtSUC2-4</I>) has the hallmarks of previously described null alleles but, despite compromised carbon partitioning and growth, produces viable seeds. The onset of flowering was chronologically delayed but occurred at the same point in the plastochron index as wild type.</p>
</sec>
<sec><st>Conclusions</st>
<p><I>AtSUC2</I> is important for phloem loading and is therefore fundamental to phloem transport and plant productivity, but plants can complete their life cycle and produce viable seed in its absence. Arabidopsis appears to have mechanisms for mobilizing reduced carbon from the phloem into developing seeds independent of <I>AtSUC2</I>.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Srivastava, A. C., Dasgupta, K., Ajieren, E., Costilla, G., McGarry, R. C., Ayre, B. G.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp215</dc:identifier>
<dc:title><![CDATA[Arabidopsis plants harbouring a mutation in AtSUC2, encoding the predominant sucrose/proton symporter necessary for efficient phloem transport, are able to complete their life cycle and produce viable seed]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1128</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1121</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1129?rss=1">
<title><![CDATA[Reproductive biology of the andromonoecious Cucumis melo subsp. agrestis (Cucurbitaceae)]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1129?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p><I>Cucumis melo</I> subsp. <I>agrestis</I> (Cucurbitaceae) is cultivated in many African regions for its edible kernels used as a soup thickener. The plant, an annual, andromonoecious, trailing-vine species, is of high social, cultural and economic value for local communities. In order to improve the yield of this crop, the first step and our aim were to elucidate its breeding system.</p>
</sec>
<sec><st>Methods</st>
<p>Eight experimental pollination treatments were performed during three growing seasons to assess spontaneous selfing, self-compatibility and effects of pollen source (hermaphroditic vs. male flowers). Pollination success was determined by pollen tube growth and reproductive success was assessed by fruit, seed and seedling numbers and characteristics. The pollinator guild was surveyed and the pollination distance determined both by direct observations and by indirect fluorescent dye dispersal.</p>
</sec>
<sec><st>Key Results</st>
<p>The species is probably pollinated by several Hymenoptera, principally by <I>Hypotrigona para.</I> Pollinator flight distances varied from 25 to 69 cm. No evidence for apomixis or spontaneous self-pollination in the absence of insect visitors was found. The self-fertility index (SFI = 0) indicated a total dependence on pollinators for reproductive success. The effects of hand pollination on fruit set, seed number and seedling fitness differed among years. Pollen tube growth and reproductive success did not differ between self- and cross-pollinations. Accordingly, a high self-compatibility index for the fruit set (SCI = 1&middot;00) and the seed number (SCI = 0&middot;98) and a low inbreeding depression at all developmental stages (cumulative <I></I> = 0&middot;126) suggest a high selfing ability. Finally, pollen origin had no effect on fruit and seed sets.</p>
</sec>
<sec><st>Conclusions</st>
<p>This andromonoecious species has the potential for a mixed mating system with high dependence on insect-mediated pollination. The selfing rate through geitonogamy should be important.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kouonon, L. C., Jacquemart, A.-L., Zoro Bi, A. I., Bertin, P., Baudoin, J.-P., Dje, Y.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp196</dc:identifier>
<dc:title><![CDATA[Reproductive biology of the andromonoecious Cucumis melo subsp. agrestis (Cucurbitaceae)]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1139</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1129</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1141?rss=1">
<title><![CDATA[Elaiophores in Gomesa bifolia (Sims) M.W. Chase & N.H. Williams (Oncidiinae: Cymbidieae: Orchidaceae): structure and oil secretion]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1141?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Oils are an unusual floral reward in Orchidaceae, being produced by specialized glands called elaiophores. Such glands have been described in subtribe Oncidiinae for a few species. The aims of the present study were to identify the presence of elaiophores in <I>Gomesa bifolia</I>, to study their structure and to understand how the oil is secreted. Additionally, elaiophores of <I>G. bifolia</I> were compared with those of related taxa within the Oncidiinae.</p>
</sec>
<sec><st>Methods</st>
<p>Elaiophores were identified using Sudan III. Their structure was examined by using light, scanning electron and transmission electron microscopy.</p>
</sec>
<sec><st>Key Results</st>
<p>Secretion of oils was from the tips of callus protrusions. The secretory cells each had a large, centrally located nucleus, highly dense cytoplasm, abundant plastids containing lipid globules associated with starch grains, numerous mitochondria, an extensive system of rough and smooth endoplasmatic reticulum, and electron-dense dictyosomes. The outer tangential walls were thick, with a loose cellulose matrix and a few, sparsely distributed inconspicuous cavities. Electron-dense structures were observed in the cell wall and formed a lipid layer that covered the cuticle of the epidermal cells. The cuticle as viewed under the scanning electron microscope was irregularly rugose.</p>
</sec>
<sec><st>Conclusions</st>
<p>The elaiophores of <I>G. bifolia</I> are of the epithelial type. The general structure of the secretory cells resembles that described for other species of Oncidiinae, but some unique features were encountered for this species. The oil appears to pass through the outer tangential wall and the cuticle, covering the latter without forming cuticular blisters.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Aliscioni, S. S., Torretta, J. P., Bello, M. E., Galati, B. G.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp199</dc:identifier>
<dc:title><![CDATA[Elaiophores in Gomesa bifolia (Sims) M.W. Chase & N.H. Williams (Oncidiinae: Cymbidieae: Orchidaceae): structure and oil secretion]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1149</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1141</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1151?rss=1">
<title><![CDATA[Litter quality and decomposability of species from a Mediterranean succession depend on leaf traits but not on nitrogen supply]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1151?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The rate of plant decomposition depends on both the decomposition environment and the functional traits of the individual species (e.g. leaf and litter quality), but their relative importance in determining interspecific differences in litter decomposition remains unclear. The aims of this study were to: (<I>a</I>) determine if species from different successional stages grown on soils with low and high nitrogen levels produce leaf and litter traits that decompose differently under identical conditions; and (<I>b</I>) assess which trait of living leaves best relates to litter quality and litter decomposability</p>
</sec>
<sec><st>Methods</st>
<p>The study was conducted on 17 herbaceous species representative of three stages of a Mediterranean successional sere of Southern France. Plants were grown in monocultures in a common garden under two nitrogen levels. To elucidate how different leaf traits affected litter decomposition a microcosm experiment was conducted to determine decomposability under standard conditions. Tests were also carried out to determine how successional stage and nitrogen supply affected functional traits of living leaves and how these traits then modified litter quality and subsequent litter decomposability.</p>
</sec>
<sec><st>Key Results</st>
<p>The results demonstrated that leaf traits and litter decomposability varied according to species and successional stage. It was also demonstrated that while nitrogen addition affected leaf and litter traits, it had no effect on decomposition rates. Finally, leaf dry matter content stood out as the leaf trait best related to litter quality and litter decomposability</p>
</sec>
<sec><st>Conclusions</st>
<p>In this study, species litter decomposability was affected by some leaf and litter traits but not by soil nitrogen supply. The results demonstrated the strength of a trait-based approach to predict changes in ecosystem processes as a result of species shifts in ecosystems.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kazakou, E., Violle, C., Roumet, C., Pintor, C., Gimenez, O., Garnier, E.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp202</dc:identifier>
<dc:title><![CDATA[Litter quality and decomposability of species from a Mediterranean succession depend on leaf traits but not on nitrogen supply]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1161</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1151</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1163?rss=1">
<title><![CDATA[Escape from water or remain quiescent? Lotus tenuis changes its strategy depending on depth of submergence]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1163?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Two main strategies that allow plants to cope with soil waterlogging or deeper submergence are: (1) escaping by means of upward shoot elongation or (2) remaining quiescent underwater. This study investigates these strategies in <I>Lotus tenuis</I>, a forage legume of increasing importance in areas prone to soil waterlogging, shallow submergence or complete submergence.</p>
</sec>
<sec><st>Methods</st>
<p>Plants of <I>L. tenuis</I> were subjected for 30 d to well-drained (control), waterlogged (water-saturated soil), partially submerged (6 cm water depth) and completely submerged conditions. Plant responses assessed were tissue porosity, shoot number and length, biomass and utilization of water-soluble carbohydrates (WSCs) and starch in the crown.</p>
</sec>
<sec><st>Key Results</st>
<p><I>Lotus tenuis</I> adjusted its strategy depending on the depth of submergence. Root growth of partially submerged plants ceased and carbon allocation prioritized shoot lengthening (32 cm vs. 24&middot;5 cm under other treatments), without depleting carbohydrate reserves to sustain the faster growth. These plants also developed more shoot and root porosity. In contrast, completely submerged plants became quiescent, with no associated biomass accumulation, new shoot production or shoot elongation. In addition, tissue porosity was not enhanced. The survival of completely submerged plants is attributed to consumption of WSCs and starch reserves from crowns (concentrations 50&ndash;75 % less than in other treatments).</p>
</sec>
<sec><st>Conclusions</st>
<p>The forage legume <I>L. tenuis</I> has the flexibility either to escape from partial submergence by elongating its shoot more vigorously to avoid becoming totally submerged or to adopt a non-elongating quiescent strategy when completely immersed that is based on utilizing stored reserves. The possession of these alternative survival strategies helps to explain the success of <I>L. tenuis</I> in environments subjected to unpredictable flooding depths.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Manzur, M. E., Grimoldi, A. A., Insausti, P., Striker, G. G.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp203</dc:identifier>
<dc:title><![CDATA[Escape from water or remain quiescent? Lotus tenuis changes its strategy depending on depth of submergence]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1169</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1163</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1171?rss=1">
<title><![CDATA[Phenology and growth adjustments of oil palm (Elaeis guineensis) to photoperiod and climate variability]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1171?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Oil palm flowering and fruit production show seasonal maxima whose causes are unknown. Drought periods confound these rhythms, making it difficult to analyse or predict dynamics of production. The present work aims to analyse phenological and growth responses of adult oil palms to seasonal and inter-annual climatic variability.</p>
</sec>
<sec><st>Methods</st>
<p>Two oil palm genotypes planted in a replicated design at two sites in Indonesia underwent monthly observations during 22 months in 2006&ndash;2008. Measurements included growth of vegetative and reproductive organs, morphology and phenology. Drought was estimated from climatic water balance (rainfall &ndash; potential evapotranspiration) and simulated fraction of transpirable soil water. Production history of the same plants for 2001&ndash;2005 was used for inter-annual analyses.</p>
</sec>
<sec><st>Key Results</st>
<p>Drought was absent at the equatorial Kandista site (0&deg;55'N) but the Batu Mulia site (3&deg;12'S) had a dry season with variable severity. Vegetative growth and leaf appearance rate fluctuated with drought level. Yield of fruit, a function of the number of female inflorescences produced, was negatively correlated with photoperiod at Kandista. Dual annual maxima were observed supporting a recent theory of circadian control. The photoperiod-sensitive phases were estimated at 9 (or 9 + 12 <FONT FACE="arial,helvetica">x</FONT> <I>n</I>) months before bunch maturity for a given phytomer. The main sensitive phase for drought effects was estimated at 29 months before bunch maturity, presumably associated with inflorescence sex determination.</p>
</sec>
<sec><st>Conclusion</st>
<p>It is assumed that seasonal peaks of flowering in oil palm are controlled even near the equator by photoperiod response within a phytomer. These patterns are confounded with drought effects that affect flowering (yield) with long time-lag. Resulting dynamics are complex, but if the present results are confirmed it will be possible to predict them with models.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Legros, S., Mialet-Serra, I., Caliman, J.-P., Siregar, F. A., Clement-Vidal, A., Dingkuhn, M.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp214</dc:identifier>
<dc:title><![CDATA[Phenology and growth adjustments of oil palm (Elaeis guineensis) to photoperiod and climate variability]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1182</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1171</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1183?rss=1">
<title><![CDATA[Phenology, growth and physiological adjustments of oil palm (Elaeis guineensis) to sink limitation induced by fruit pruning]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1183?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Despite its simple architecture and small phenotypic plasticity, oil palm has complex phenology and source&ndash;sink interactions. Phytomers appear in regular succession but their development takes years, involving long lag periods between environmental influences and their effects on sinks. Plant adjustments to resulting source&ndash;sink imbalances are poorly understood. This study investigated oil palm adjustments to imbalances caused by severe fruit pruning.</p>
</sec>
<sec><st>Methods</st>
<p>An experiment with two treatments (control and complete fruit pruning) during 22 months in 2006&ndash;2008) and six replications per treatment was conducted in Indonesia. Phenology, growth of above-ground vegetative and reproductive organs, leaf morphology, inflorescence sex differentiation, dynamics of non-structural carbohydrate reserves and light-saturated net photosynthesis (<I>A</I><SUB>max</SUB>) were monitored.</p>
</sec>
<sec><st>Key Results</st>
<p>Artificial sink limitation by complete fruit pruning accelerated development rate, resulting in higher phytomer, leaf and inflorescence numbers. Leaf size and morphology remained unchanged. Complete fruit pruning also suppressed the abortion of male inflorescences, estimated to be triggered at about 16 months before bunch maturity. The number of female inflorescences increased after an estimated lag of 24&ndash;26 months, corresponding to time from sex differentiation to bunch maturity. The most important adjustment process was increased assimilate storage in the stem, attaining nearly 50 % of dry weight in the stem top, mainly as starch, whereas glucose, which in controls was the most abundant non-structural carbohydrate stored in oil palm, decreased.</p>
</sec>
<sec><st>Conclusions</st>
<p>The development rate of oil palm is in part controlled by source&ndash;sink relationships. Although increased rate of development and proportion of female inflorescences constituted observed adjustments to sink limitation, the low plasticity of plant architecture (constant leaf size, absence of branching) limited compensatory growth. Non-structural carbohydrate storage was thus the main adjustment process.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Legros, S., Mialet-Serra, I., Caliman, J.-P., Siregar, F. A., Clement-Vidal, A., Fabre, D., Dingkuhn, M.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp216</dc:identifier>
<dc:title><![CDATA[Phenology, growth and physiological adjustments of oil palm (Elaeis guineensis) to sink limitation induced by fruit pruning]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1194</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1183</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1195?rss=1">
<title><![CDATA[Annual and spatial variation in shoot demography associated with masting in Betula grossa: comparison between mature trees and saplings]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1195?rss=1</link>
<description><![CDATA[
<sec><st>Backgrounds and Aims</st>
<p>Shoot demography affects the growth of the tree crown and the number of leaves on a tree. Masting may cause inter-annual and spatial variation in shoot demography of mature trees, which may in turn affect the resource budget of the tree. The aim of this study was to evaluate the effect of masting on the temporal and spatial variations in shoot demography of mature <I>Betula grossa</I>.</p>
</sec>
<sec><st>Methods</st>
<p>The shoot demography was analysed in the upper and lower parts of the tree crown in mature trees and saplings over 7 years. Mature trees and saplings were compared to differentiate the effect of masting from the effect of exogenous environment on shoot demography. The fate of different shoot types (reproductive, vegetative, short, long), shoot length and leaf area were investigated by monitoring and by retrospective survey using morphological markers on branches. The effects of year and branch position on demographic parameters were evaluated.</p>
</sec>
<sec><st>Key Results</st>
<p>Shoot increase rate, production of long shoots, bud mortality, length of long shoots and leaf area of a branch fluctuated periodically from year to year in mature trees over 7 years, in which two masting events occurred. Branches within a crown showed synchronized annual variation, and the extent of fluctuation was larger in the upper branches than the lower branches. Vegetative shoots varied in their bud differentiation each year and contributed to the dynamic shoot demography as much as did reproductive shoots, suggesting physiological integration in shoot demography through hormonal regulation and resource allocation.</p>
</sec>
<sec><st>Conclusions</st>
<p>Masting caused periodic annual variation in shoot demography of the mature trees and the effect was spatially variable within a tree crown. Since masting is a common phenomenon among tree species, annual variation in shoot demography and leaf area should be incorporated into resource allocation models of mature masting trees.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ishihara, M. I., Kikuzawa, K.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp217</dc:identifier>
<dc:title><![CDATA[Annual and spatial variation in shoot demography associated with masting in Betula grossa: comparison between mature trees and saplings]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1205</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1195</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1207?rss=1">
<title><![CDATA[How yield relates to ash content, {Delta}13C and {Delta}18O in maize grown under different water regimes]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1207?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Stable isotopes have proved a valuable phenotyping tool when breeding for yield potential and drought adaptation; however, the cost and technical skills involved in isotope analysis limit its large-scale application in breeding programmes. This is particularly so for <sup>18</sup>O despite the potential relevance of this trait in C<SUB>4</SUB> crops. The accumulation of minerals (measured as ash content) has been proposed as an inexpensive way to evaluate drought adaptation and yield in C<SUB>3</SUB> cereals, but little is known of the usefulness of this measure in C<SUB>4</SUB> cereals such as maize (<I>Zea mays</I>). The present study investigates how yield relates to ash content, <sup>13</sup>C and <sup>18</sup>O, and evaluates the use of ash content as an alternative or complementary criterion to stable isotopes in assessing yield potential and drought resistance in maize.</p>
</sec>
<sec><st>Methods</st>
<p>A set of tropical maize hybrids developed by CIMMYT were subjected to different water availabilities, in order to induce water stress during the reproductive stages under field conditions. Ash content and <sup>13</sup>C were determined in leaves and kernels. In addition, <sup>18</sup>O was measured in kernels.</p>
</sec>
<sec><st>Key Results</st>
<p>Water regime significantly affected yield, ash content and stable isotopes. The results revealed a close relationship between ash content in leaves and the traits informing about plant water status. Ash content in kernels appeared to reflect differences in sink&ndash;source balance. Genotypic variation in grain yield was mainly explained by the combination of ash content and <sup>18</sup>O, whilst <sup>13</sup>C did not explain a significant percentage of such variation.</p>
</sec>
<sec><st>Conclusions</st>
<p>Ash content in leaves and kernels proved a useful alternative or complementary criterion to <sup>18</sup>O in kernels for assessing yield performance in maize grown under drought conditions.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Cabrera-Bosquet, L., Sanchez, C., Araus, J. L.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp229</dc:identifier>
<dc:title><![CDATA[How yield relates to ash content, {Delta}13C and {Delta}18O in maize grown under different water regimes]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1216</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1207</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1217?rss=1">
<title><![CDATA[Plant morphometric traits and climate gradients in northern China: a meta-analysis using quadrat and flora data]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1217?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The collection of field data on plant traits is time consuming and this makes it difficult to examine changing patterns of traits along large-scale climate gradients. The present study tests whether trait information derived from regional floras can be used in conjunction with pre-existing quadrat data on species presence to derive meaningful relationships between specific morphometric traits and climate.</p>
</sec>
<sec><st>Methods</st>
<p>Quadrat records were obtained for 867 species in 404 sites from northern China (38&ndash;49&deg;N, 82&ndash;132&deg;E) together with information on the presence/absence of key traits from floras. Bioclimate parameters for each site were calculated using the BIOME3 model. Principal component analysis and correlation analysis were conducted to determine the most important climate factors. The Akaike Information Criterion was used to select the best relationship between each trait and climate. Canonical correspondence analysis was used to explore the relationships between climate and trait occurrence.</p>
</sec>
<sec><st>Key Results</st>
<p>The changing abundance of life form, leaf type, phenology, photosynthetic pathway, leaf size and several other morphometric traits are determined by gradients in plant-available moisture (as measured by the ratio of actual to potential evapotranspiration: <I></I>), growing-season temperature (as measured by growing degree-days on a 0 &deg; base: GDD<SUB>0</SUB>) or a combination of these. Different plant functional types (PFTs, as defined by life form, leaf type and phenology) reach maximum abundance in distinct areas of this climate space: for example, evergreen trees occur in the coldest, wettest environments (GDD<SUB>0</SUB> &lt; 2500 &deg;Cd, <I></I> &gt; 0&middot;38), and deciduous scale-leaved trees occur in drier, warmer environments than deciduous broad-leaved trees. Most leaf-level traits show similar relationships with climate independently of PFT: for example, leaf size in all PFTs increases as the environment becomes wetter and cooler. However, some traits (e.g. petiole length) display different relationships with climate in different PFTs.</p>
</sec>
<sec><st>Conclusions</st>
<p>Based on presence/absence species data and flora-based trait assignments, the present study demonstrates ecologically plausible trends in the occurrence of key plant traits along climate gradients in northern China. Life form, leaf type, phenology, photosynthetic pathway, leaf size and other key traits reflect climate. The success of these analyses opens the possibility of using quadrat- and flora-based trait analyses to examine climate&ndash;trait relationships in other regions of the world.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Meng, T.-T., Ni, J., Harrison, S. P.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp230</dc:identifier>
<dc:title><![CDATA[Plant morphometric traits and climate gradients in northern China: a meta-analysis using quadrat and flora data]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1229</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1217</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1231?rss=1">
<title><![CDATA[Small effect of fragmentation on the genetic diversity of Dalbergia monticola, an endangered tree species of the eastern forest of Madagascar, detected by chloroplast and nuclear microsatellites]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1231?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The oriental forest ecosystem in Madagascar has been seriously impacted by fragmentation. The pattern of genetic diversity was analysed on a tree species, <I>Dalbergia monticola</I>, which plays an important economic role in Madagascar and is one of the many endangered tree species in the eastern forest.</p>
</sec>
<sec><st>Methods</st>
<p>Leaves from 546 individuals belonging to 18 small populations affected by different levels of fragmentation were genotyped using eight nuclear (nuc) and three chloroplast (cp) microsatellite markers.</p>
</sec>
<sec><st>Key Results</st>
<p>For nuclear microsatellites, allelic richness (<I>R</I>) and heterozygosity (<I>H</I><SUB>e,nuc</SUB>) differed between types of forest: <I>R =</I> 7&middot;36 and <I>R =</I> 9&middot;55, <I>H</I><SUB>e,nuc</SUB> = 0&middot;64 and <I>H</I><SUB>e,nuc</SUB> = 0&middot;80 in fragmented and non-fragmented forest, respectively, but the differences were not significant. Only the mean number of alleles (<I>N</I><SUB>a,nuc</SUB>) and the fixation index <I>F</I><SUB>IS</SUB> differed significantly: <I>N</I><SUB>a,nuc</SUB> = 9&middot;41 and <I>N</I><SUB>a,nuc</SUB> = 13&middot;18, <I>F</I><SUB>IS</SUB> = 0&middot;06 and <I>F</I><SUB>IS</SUB> = 0&middot;15 in fragmented and non-fragmented forests, respectively. For chloroplast microsatellites, estimated genetic diversity was higher in non-fragmented forest, but the difference was not significant. No recent bottleneck effect was detected for either population. Overall differentiation was low for nuclear microsatellites (<I>F</I><SUB>ST,nuc</SUB> = 0&middot;08) and moderate for chloroplast microsatellites (<I>F</I><SUB>ST,cp</SUB> = 0&middot;49). A clear relationship was observed between genetic and geographic distance (<I>r</I> = 0&middot;42 P &lt; 0&middot;01 and <I>r</I> = 0&middot;42 <I>P</I> = 0&middot;03 for nuclear and chloroplast microsatellites, respectively), suggesting a pattern of isolation by distance. Analysis of population structure using the neighbor-joining method or Bayesian models separated southern populations from central and northern populations with nuclear microsatellites, and grouped the population according to regions with chloroplast microsatellites, but did not separate the fragmented populations.</p>
</sec>
<sec><st>Conclusions</st>
<p>Residual diversity and genetic structure of populations of <I>D. monticola</I> in Madagascar suggest a limited impact of fragmentation on molecular genetic parameters.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Andrianoelina, O., Favreau, B., Ramamonjisoa, L., Bouvet, J.-M.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:28 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp231</dc:identifier>
<dc:title><![CDATA[Small effect of fragmentation on the genetic diversity of Dalbergia monticola, an endangered tree species of the eastern forest of Madagascar, detected by chloroplast and nuclear microsatellites]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1242</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1231</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/6/1243?rss=1">
<title><![CDATA[Early reproductive developmental anatomy in Decaisnea (Lardizabalaceae) and its systematic implications]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/6/1243?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p><I>Decaisnea insignis</I>, known as &lsquo;dead man's fingers&rsquo; (Lardizabalaceae), is widely distributed in China and the Himalayan foothill countries. This economically important plant, which is the only species in the genus, has not been the subject of any embryological studies aside from one brief, older paper that lacks micrographs. Data on <I>Decaisnea</I> are also important because its systematic position has been unstable since the genus was established in 1855. Therefore, the objectives of this study were: (<I>a</I>) to use modern microscopy to document early reproductive anatomical development in <I>Decaisnea</I>; and (<I>b</I>) to compare qualitatively these early embryological characters with allied taxa in a systematic context.</p>
</sec>
<sec><st>Methods</st>
<p><I>Decaisnea insignis</I> floral buds and inflorescences were regularly collected from Shaanxi Province, China and prepared for light microscopy. The embryological characters studied were qualitatively compared with those of allied taxa via a thorough examination of the existing literature.</p>
</sec>
<sec><st>Key Results</st>
<p>Early reproductive anatomy in <I>Decaisnea</I> was documented and novel revelations made. It was discovered that the pollen is shed when three-celled (not two-celled, as previously reported), and that endosperm formation is nuclear (not cellular or helobial, as previously reported). These two newly revealed embryological characters are not found in any other members of Lardizabalaceae. Furthermore, neither are persistent antipodal cells, which we confirmed to be present in <I>Decaisnea</I>.</p>
</sec>
<sec><st>Conclusions</st>
<p><I>Decaisnea</I> and other Lardizabalaceae characteristically have tetrasporangiate anthers, a secretory tapetum, simultaneous microsporocyte cytokinesis, primarily bitegmic, crassinucellate ovules, and a <I>Polygonum</I> type embryo sac. However, in the family, persistent antipodals, nuclear endosperm, and pollen shed at the three-celled stage are only found in <I>Decaisnea</I>. These embryological data prompted the suggestion that <I>Decaisnea</I> needs elevation above the level of genus.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Wang, H.-F., Friedman, C. R., Zhu, Z.-X., Qin, H.-N.]]></dc:creator>
<dc:date>Thu, 22 Oct 2009 08:58:29 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp232</dc:identifier>
<dc:title><![CDATA[Early reproductive developmental anatomy in Decaisnea (Lardizabalaceae) and its systematic implications]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1253</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1243</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/i?rss=1">
<title><![CDATA[ContentSnapshots]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/i?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:51 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp247</dc:identifier>
<dc:title><![CDATA[ContentSnapshots]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>iii</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>i</prism:startingPage>
<prism:section>ContentSnapshots</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/v?rss=1">
<title><![CDATA[John Bryant takes a closer look at some of this month's Original Articles]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/v?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Bryant, J. A.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:51 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp246</dc:identifier>
<dc:title><![CDATA[John Bryant takes a closer look at some of this month's Original Articles]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>vi</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>v</prism:startingPage>
<prism:section>ContentSelect</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/vii?rss=1">
<title><![CDATA[Biology and evolution of ferns and lycophytes]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/vii?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Dyer, A.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:51 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp194</dc:identifier>
<dc:title><![CDATA[Biology and evolution of ferns and lycophytes]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>x</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>vii</prism:startingPage>
<prism:section>BOOK REVIEW</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/789?rss=1">
<title><![CDATA[Calibrating the Tree of Life: fossils, molecules and evolutionary timescales]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/789?rss=1</link>
<description><![CDATA[
<sec><st>Background</st>
<p>Molecular dating has gained ever-increasing interest since the molecular clock hypothesis was proposed in the 1960s. Molecular dating provides detailed temporal frameworks for divergence events in phylogenetic trees, allowing diverse evolutionary questions to be addressed. The key aspect of the molecular clock hypothesis, namely that differences in DNA or protein sequence between two species are proportional to the time elapsed since they diverged, was soon shown to be untenable. Other approaches were proposed to take into account rate heterogeneity among lineages, but the calibration process, by which relative times are transformed into absolute ages, has received little attention until recently. New methods have now been proposed to resolve potential sources of error associated with the calibration of phylogenetic trees, particularly those involving use of the fossil record.</p>
</sec>
<sec><st>Scope and Conclusions</st>
<p>The use of the fossil record as a source of independent information in the calibration process is the main focus of this paper; other sources of calibration information are also discussed. Particularly error-prone aspects of fossil calibration are identified, such as fossil dating, the phylogenetic placement of the fossil and the incompleteness of the fossil record. Methods proposed to tackle one or more of these potential error sources are discussed (e.g. fossil cross-validation, prior distribution of calibration points and confidence intervals on the fossil record). In conclusion, the fossil record remains the most reliable source of information for the calibration of phylogenetic trees, although associated assumptions and potential bias must be taken into account.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Forest, F.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:51 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp192</dc:identifier>
<dc:title><![CDATA[Calibrating the Tree of Life: fossils, molecules and evolutionary timescales]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>794</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>789</prism:startingPage>
<prism:section>BOTANICAL BRIEFING</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/795?rss=1">
<title><![CDATA[Ploidy manipulation of the gametophyte, endosperm and sporophyte in nature and for crop improvement: a tribute to Professor Stanley J. Peloquin (1921-2008)]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/795?rss=1</link>
<description><![CDATA[
<sec><st>Background</st>
<p>Emeritus Campbell-Bascom Professor Stanley J. Peloquin was an internationally renowned plant geneticist and breeder who made exceptional contributions to the quantity, quality and sustainable supply of food for the world from his innovative and extensive scientific contributions. For five decades, Dr Peloquin merged basic research in plant reproduction, cytology, cytogenetics, genetics, potato (<I>Solanum tuberosum</I>) improvement and education at the University of Wisconsin-Madison. Successive advances across these five decades redefined scientific comprehension of reproductive variation, its genetic control, genetic effects, evolutionary impact and utility for breeding. In concert with the International Potato Center (CIP), he and others translated the advances into application, resulting in large benefits on food production worldwide, exemplifying the importance of integrated innovative university research and graduate education to meet domestic and international needs.</p>
</sec>
<sec><st>Scope</st>
<p>Dr Peloquin is known to plant breeders, geneticists, international agricultural economists and potato researchers for his enthusiastic and incisive contributions to genetic enhancement of potato using haploids, 2<I>n</I> gametes and wild <I>Solanum</I> species; for his pioneering work on potato cultivation through true seed; and as mentor of a new generation of plant breeders worldwide. The genetic enhancement of potato, the fourth most important food crop worldwide, benefited significantly from expanded germplasm utilization and advanced reproductive genetic knowledge, which he and co-workers, including many former students, systematically transformed into applied breeding methods. His research on plant sexual reproduction included subjects such as haploidization and polyploidization, self- and cross-incompatibility, cytoplasmic male sterility and restorer genes, gametophytic/sporophytic heterozygosity and male fertility, as well as endosperm dosages and seed development. By defining methods of half-tetrad analysis and new cytological techniques, he elucidated modes, mechanisms and genetic controls and effects of 2<I>n</I> gametes in <I>Solanum</I>. Ramifications extend to many other crops and plants, in both basic and applied sciences.</p>
</sec>
<sec><st>Achievements</st>
<p>Based upon a foundation of genetics, cytogenetics and plant reproductive biology, Dr Peloquin and co-workers developed methods to use 2<I>n</I> gametes and haploids for breeding, and used them to move genes for important horticultural traits from wild tuber-bearing <I>Solanum</I> species to cultivated potato for the betterment of agriculture. The resulting potato germplasm included combinations of yield, adaptation, quality and disease resistance traits that were previously unavailable. This elite plant germplasm was utilized and distributed to 85 countries by the CIP, because it not only increased potato yields and quality, it also broadened the adaptation of potato to lowland tropical regions, where humanity has benefited from this addition to their food supply.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ortiz, R., Simon, P., Jansky, S., Stelly, D.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:51 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp207</dc:identifier>
<dc:title><![CDATA[Ploidy manipulation of the gametophyte, endosperm and sporophyte in nature and for crop improvement: a tribute to Professor Stanley J. Peloquin (1921-2008)]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>807</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>795</prism:startingPage>
<prism:section>INVITED REVIEW</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/809?rss=1">
<title><![CDATA[Establishment of zygomorphy on an ontogenic spiral and evolution of perianth in the tribe Delphinieae (Ranunculaceae)]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/809?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Ranunculaceae presents both ancestral and derived floral traits for eudicots, and as such is of potential interest to understand key steps involved in the evolution of zygomorphy in eudicots. Zygomorphy evolved once in Ranunculaceae, in the speciose and derived tribe Delphinieae. This tribe consists of two genera (<I>Aconitum</I> and <I>Delphinium s.l.</I>) comprising more than one-quarter of the species of the family. In this paper, the establishment of zygomorphy during development was investigated to cast light on the origin and evolution of this morphological novelty.</p>
</sec>
<sec><st>Methods</st>
<p>The floral developmental sequence of six species of Ranunculaceae, three actinomorphic (<I>Nigella damascena</I>, <I>Aquilegia alpina</I> and <I>Clematis recta</I>) and three zygomorphic (<I>Aconitum napellus</I>, <I>Delphinium staphisagria</I> and <I>D. grandiflorum</I>), was compared. A developmental model was elaborated to break down the successive acquisitions of floral organ identities on the ontogenic spiral (all the species studied except <I>Aquilegia</I> have a spiral phyllotaxis), giving clues to understanding this complex morphogenesis from an evo-devo point of view. In addition, the evolution of symmetry in Ranunculaceae was examined in conjunction with other traits of flowers and with ecological factors.</p>
</sec>
<sec><st>Key Results</st>
<p>In the species studied, zygomorphy is established after organogenesis is completed, and is late, compared with other zygomorphic eudicot species. Zygomorphy occurs in flowers characterized by a fixed merism and a partially reduced and transformed corolla.</p>
</sec>
<sec><st>Conclusions</st>
<p>It is suggested that shifts in expression of genes controlling the merism, as well as floral symmetry and organ identity, have played a critical role in the evolution of zygomorphy in Delphinieae, while the presence of pollinators able to exploit the peculiar morphology of the flower has been a key factor for the maintenance and diversification of this trait.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Jabbour, F., Ronse De Craene, L. P., Nadot, S., Damerval, C.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:51 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp162</dc:identifier>
<dc:title><![CDATA[Establishment of zygomorphy on an ontogenic spiral and evolution of perianth in the tribe Delphinieae (Ranunculaceae)]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>822</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>809</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/823?rss=1">
<title><![CDATA[Floral thermogenesis of three species of Hydnora (Hydnoraceae) in Africa]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/823?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Floral thermogenesis occurs in at least 12 families of ancient seed plants. Some species show very high rates of respiration through the alternative pathway, and some are thermoregulatory, with increasing respiration at decreasing ambient temperature. This study assesses the intensity and regulation of respiration in three species of African <I>Hydnora</I> that represent the Hydnoraceae, an unusual family of holoparasitic plants from arid environments.</p>
</sec>
<sec><st>Methods</st>
<p>Long-term respirometry (CO<SUB>2</SUB> production) and thermometry were carried out on intact flowers of <I>H. africana</I>, <I>H. abyssinica</I> and <I>H. esculenta</I> in the field, and short-term measurements were made on floral parts during the protogynous flowering sequence.</p>
</sec>
<sec><st>Key Results</st>
<p>For <I>H. africana</I>, there was no temperature elevation in either the osmophores or the gynoecial chamber in any phase, and mass-specific respiration rates of the flower parts were low (maximum 8&middot;3 nmol CO<SUB>2</SUB> g<sup>&ndash;1</sup> s<sup>&ndash;1</sup> in osmophore tissue). Respiration tracked ambient and floral temperatures, eliminating the possibility of the inverse relationship expected in thermoregulatory flowers. <I>Hydnora abyssinica</I> flowers had higher respiration (maximum 27&middot;5 nmol g<sup>&ndash;1</sup> s<sup>&ndash;1</sup> in the osmophores) and a slight elevation of osmophore temperature (maximum 2&middot;8 &deg;C) in the female stage. Respiration by gynoecial tissue was similar to that of osmophores in both species, but there was no measurable elevation of gynoecial chamber temperature. Gynoecial chamber temperature of <I>H. esculenta</I> could reach 3&middot;8 &deg;C above ambient, but there are no respiration data available. Antheral tissue respiration was maximal in the male phase (4&middot;8 nmol g<sup>&ndash;1</sup> s<sup>&ndash;1</sup> in <I>H. africana</I> and 10&middot;3 nmol g<sup>&ndash;1</sup> s<sup>&ndash;1</sup> in <I>H. abyssinica</I>), but it did not raise the antheral ring temperature, which showed that thermogenesis is not a by-product of pollen maturation or release.</p>
</sec>
<sec><st>Conclusions</st>
<p>The exceptionally low thermogenesis in <I>Hydnora</I> appears to be associated with scent production and possibly gynoecial development, but has little direct benefit to beetle pollinators.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Seymour, R. S., Maass, E., Bolin, J. F.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp168</dc:identifier>
<dc:title><![CDATA[Floral thermogenesis of three species of Hydnora (Hydnoraceae) in Africa]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>832</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>823</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/833?rss=1">
<title><![CDATA[Identification and characterization of the water gap in the physically dormant seeds of Dodonaea petiolaris: a first report for Sapindaceae]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/833?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The Sapindaceae is one of 17 plant families in which seed dormancy is caused by a water-impermeable seed or fruit coat (physical dormancy, PY). However, until now the water gap in Sapindaceae had not been identified. The primary aim of this study was to identify the water gap in <I>Dodonaea petiolaris</I> (Sapindaceae) seeds and to describe its basic morphology and anatomy.</p>
</sec>
<sec><st>Methods</st>
<p>Seed fill, viability, water-uptake (imbibition) and other characteristics were assessed for <I>D. petiolaris</I> seeds. The location and structure of the water gap were investigated using a blocking experiment, time series photography, scanning electron microscopy and light microscopy. <I>Dodonaea petiolaris</I> seeds with PY also were assessed for loss of PY at four ecologically significant temperatures under moist and dry conditions. Seeds of three other species of Sapindaceae were examined for presence of a water gap.</p>
</sec>
<sec><st>Key Results</st>
<p>The water gap in <I>D. petiolaris</I> seeds was identified as a small plug in the seed coat adjacent to the hilum and opposite the area where the radicle emerges. The plug was dislodged (i.e. water gap opened = dormancy break) by dipping seeds in boiling water for 2&middot;5 min or by incubating seeds on a moist substrate at 20/35 &deg;C for 24 weeks. Layers of cells in the plug, including palisade and subpalisade, are similar to those in the rest of the seed coat. The same kind of water gap was found in three other species of Sapindaceae, <I>Diplopeltis huegelii</I>, <I>Distichostemon hispidulus</I> and <I>Dodonaea aptera</I>.</p>
</sec>
<sec><st>Conclusions</st>
<p>Following dormancy break (opening of water gap), initial uptake of water by the seed occurs only through the water gap. Thus, the plug must be dislodged before the otherwise intact seed can germinate. The anatomy of the plug is similar to water gaps in some of the other plant families with PY.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Turner, S. R., Cook, A., Baskin, J. M., Baskin, C. C., Tuckett, R. E., Steadman, K. J., Dixon, K. W.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp171</dc:identifier>
<dc:title><![CDATA[Identification and characterization of the water gap in the physically dormant seeds of Dodonaea petiolaris: a first report for Sapindaceae]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>844</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>833</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/845?rss=1">
<title><![CDATA[Effective pollinators of Asian sacred lotus (Nelumbo nucifera): contemporary pollinators may not reflect the historical pollination syndrome]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/845?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>If stabilizing selection by pollinators is a prerequisite for pollinator-mediated floral evolution, spatiotemporal variation in the pollinator assemblage may confuse the plant&ndash;pollinator interaction in a given species. Here, effective pollinators in a living fossil plant <I>Nelumbo nucifera</I> (Nelumbonaceae) were examined to test whether beetles are major pollinators as predicted by its pollination syndrome.</p>
</sec>
<sec><st>Methods</st>
<p>Pollinators of <I>N. nucifera</I> were investigated in 11 wild populations and one cultivated population, and pollination experiments were conducted to examine the pollinating role of two major pollinators (bees and beetles) in three populations.</p>
</sec>
<sec><st>Key Results</st>
<p>Lotus flowers are protogynous, bowl shaped and without nectar. The fragrant flowers can be self-heating during anthesis and produce around 1 million pollen grains per flower. It was found that bees and flies were the most frequent flower visitors in wild populations, contributing on average 87&middot;9 and 49&middot;4 % of seed set in Mishan and Lantian, respectively. Beetles were only found in one wild population and in the cultivated population, but the pollinator exclusion experiments showed that beetles were effective pollinators of Asian sacred lotus.</p>
</sec>
<sec><st>Conclusions</st>
<p>This study indicated that in their pollinating role, beetles, probable pollinators for this thermoregulating plant, had been replaced by some generalist insects in the wild. This finding implies that contemporary pollinators may not reflect the pollination syndrome.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Li, J.-K., Huang, S.-Q.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp173</dc:identifier>
<dc:title><![CDATA[Effective pollinators of Asian sacred lotus (Nelumbo nucifera): contemporary pollinators may not reflect the historical pollination syndrome]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>851</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>845</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/853?rss=1">
<title><![CDATA[Mesophyll distribution of 'antioxidant' flavonoid glycosides in Ligustrum vulgare leaves under contrasting sunlight irradiance]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/853?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Flavonoids have the potential to serve as antioxidants in addition to their function of UV screening in photoprotective mechanisms. However, flavonoids have long been reported to accumulate mostly in epidermal cells and surface organs in response to high sunlight. Therefore, how leaf flavonoids actually carry out their antioxidant functions is still a matter of debate. Here, the distribution of flavonoids with effective antioxidant properties, i.e. the orthodihydroxy B-ring-substituted quercetin and luteolin glycosides, was investigated in the mesophyll of <I>Ligustrum vulgare</I> leaves acclimated to contrasting sunlight irradiance.</p>
</sec>
<sec><st>Methods</st>
<p>In the first experiment, plants were grown at 20 % (shade) or 100% (sun) natural sunlight. Plants were exposed to 100 % sunlight irradiance in the presence or absence of UV wavelengths, in a second experiment. Fluorescence microspectroscopy and multispectral fluorescence microimaging were used in both cross sections and intact leaf pieces to visualize orthodihydroxy B-ring-substituted flavonoids at inter- and intracellular levels. Identification and quantification of individual hydroxycinnamates and flavonoid glycosides were performed via HPLC-DAD.</p>
</sec>
<sec><st>Key Results</st>
<p>Quercetin and luteolin derivatives accumulated to a great extent in both the epidermal and mesophyll cells in response to high sunlight. Tissue fluorescence signatures and leaf flavonoid concentrations were strongly related. Monohydroxyflavone glycosides, namely luteolin 4'-<I>O</I>-glucoside and two apigenin 7-<I>O</I>-glycosides were unresponsive to changes in sunlight irradiance. Quercetin and luteolin derivatives accumulated in the vacuoles of mesophyll cells in leaves growing under 100 % natural sunlight in the absence of UV wavelengths.</p>
</sec>
<sec><st>Conclusions</st>
<p>The above findings lead to the hypothesis that flavonoids play a key role in countering light-induced oxidative stress, and not only in avoiding the penetration of short solar wavelengths in the leaf.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Agati, G., Stefano, G., Biricolti, S., Tattini, M.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp177</dc:identifier>
<dc:title><![CDATA[Mesophyll distribution of 'antioxidant' flavonoid glycosides in Ligustrum vulgare leaves under contrasting sunlight irradiance]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>861</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>853</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/863?rss=1">
<title><![CDATA[Comparative molecular cytogenetics of major repetitive sequence families of three Dendrobium species (Orchidaceae) from Bangladesh]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/863?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p><I>Dendrobium</I> species show tremendous morphological diversity and have broad geographical distribution. As repetitive sequence analysis is a useful tool to investigate the evolution of chromosomes and genomes, the aim of the present study was the characterization of repetitive sequences from <I>Dendrobium moschatum</I> for comparative molecular and cytogenetic studies in the related species <I>Dendrobium aphyllum</I>, <I>Dendrobium aggregatum</I> and representatives from other orchid genera.</p>
</sec>
<sec><st>Methods</st>
<p>In order to isolate highly repetitive sequences, a <I>c</I><SUB><I>0</I></SUB><I>t-1</I> DNA plasmid library was established. Repeats were sequenced and used as probes for Southern hybridization. Sequence divergence was analysed using bioinformatic tools. Repetitive sequences were localized along orchid chromosomes by fluorescence <I>in situ</I> hybridization (FISH).</p>
</sec>
<sec><st>Key Results</st>
<p>Characterization of the <I>c</I><SUB><I>0</I></SUB><I>t-1</I> library resulted in the detection of repetitive sequences including the (GA)<SUB>n</SUB> dinucleotide DmoO11, numerous <I>Arabidopsis</I>-like telomeric repeats and the highly amplified dispersed repeat DmoF14. The DmoF14 repeat is conserved in six <I>Dendrobium</I> species but diversified in representative species of three other orchid genera. FISH analyses showed the genome-wide distribution of DmoF14 in <I>D. moschatum</I>, <I>D. aphyllum</I> and <I>D. aggregatum</I>. Hybridization with the telomeric repeats demonstrated <I>Arabidopsis</I>-like telomeres at the chromosome ends of <I>Dendrobium</I> species. However, FISH using the telomeric probe revealed two pairs of chromosomes with strong intercalary signals in <I>D. aphyllum</I>. FISH showed the terminal position of 5S and 18S&ndash;5&middot;8S&ndash;25S rRNA genes and a characteristic number of rDNA sites in the three <I>Dendrobium</I> species.</p>
</sec>
<sec><st>Conclusions</st>
<p>The repeated sequences isolated from <I>D. moschatum c<SUB>0</SUB>t-1</I> DNA constitute major DNA families of the <I>D. moschatum</I>, <I>D. aphyllum</I> and <I>D. aggregatum</I> genomes with DmoF14 representing an ancient component of orchid genomes. Large intercalary telomere-like arrays suggest chromosomal rearrangements in <I>D. aphyllum</I> while the number and localization of rRNA genes as well as the species-specific distribution pattern of an abundant microsatellite reflect the genomic diversity of the three <I>Dendrobium</I> species.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Begum, R., Alam, S. S., Menzel, G., Schmidt, T.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp178</dc:identifier>
<dc:title><![CDATA[Comparative molecular cytogenetics of major repetitive sequence families of three Dendrobium species (Orchidaceae) from Bangladesh]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>872</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>863</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/873?rss=1">
<title><![CDATA[Comparative cytogenetic analysis of the genomes of the model grass Brachypodium distachyon and its close relatives]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/873?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p><I>Brachypodium</I> is a small genus of temperate grasses that comprises 12&ndash;15 species. <I>Brachypodium distachyon</I> is now well established as a model species for temperate cereals and forage grasses. In contrast to <I>B. distachyon</I>, other members of the genus have been poorly investigated at the chromosome level or not at all.</p>
</sec>
<sec><st>Methods</st>
<p>Twenty accessions comprising six species and two subspecies of <I>Brachypodium</I> were analysed cytogenetically. Measurements of nuclear genome size were made by flow cytometry. Chromosomal localization of 18&ndash;5&middot;8&ndash;25S rDNA and 5S rDNA loci was performed by dual-colour fluorescence <I>in situ</I> hybridization (FISH) on enzymatically digested root-tip meristematic cells. For comparative phylogenetic analyses genomic <I>in situ</I> hybridization (GISH) applied to somatic chromosome preparations was used.</p>
</sec>
<sec><st>Key Results</st>
<p>All <I>Brachypodium</I> species examined have rather small genomes and chromosomes. Their chromosome numbers and genome sizes vary from 2<I>n</I> = 10 and 0&middot;631 pg/2C in <I>B. distachyon</I> to 2<I>n</I> = 38 and 2&middot;57 pg/2C in <I>B. retusum</I>, respectively. Genotypes with 18 and 28 chromosomes were found among <I>B. pinnatum</I> accessions. GISH analysis revealed that <I>B. pinnatum</I> with 28 chromosomes is most likely an interspecific hybrid between <I>B. distachyon</I> (2<I>n</I> = 10) and <I>B. pinnatum</I> (2<I>n</I> = 18). Two other species, <I>B. phoenicoides</I> and <I>B. retusum</I>, are also allopolyploids and <I>B. distachyon</I> or a close relative seems to be one of their putative ancestral species. In chromosomes of all species examined the 45S rDNA loci are distally distributed whereas loci for 5S rDNA are pericentromeric.</p>
</sec>
<sec><st>Conclusions</st>
<p>The increasing significance of <I>B. distachyon</I> as a model grass emphasizes the need to understand the evolutionary relationships in the genus <I>Brachypodium</I> and to ensure consistency in the biological nomenclature of its species. Modern molecular cytogenetic techniques such as FISH and GISH are suitable for comparative phylogenetic analyses and may provide informative chromosome- and/or genome-specific landmarks.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Wolny, E., Hasterok, R.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp179</dc:identifier>
<dc:title><![CDATA[Comparative cytogenetic analysis of the genomes of the model grass Brachypodium distachyon and its close relatives]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>881</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>873</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/883?rss=1">
<title><![CDATA[Identifying ontogenetic, environmental and individual components of forest tree growth]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/883?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>This study aimed to identify and characterize the ontogenetic, environmental and individual components of forest tree growth. In the proposed approach, the tree growth data typically correspond to the retrospective measurement of annual shoot characteristics (e.g. length) along the trunk.</p>
</sec>
<sec><st>Methods</st>
<p>Dedicated statistical models (semi-Markov switching linear mixed models) were applied to data sets of Corsican pine and sessile oak. In the semi-Markov switching linear mixed models estimated from these data sets, the underlying semi-Markov chain represents both the succession of growth phases and their lengths, while the linear mixed models represent both the influence of climatic factors and the inter-individual heterogeneity within each growth phase.</p>
</sec>
<sec><st>Key Results</st>
<p>On the basis of these integrative statistical models, it is shown that growth phases are not only defined by average growth level but also by growth fluctuation amplitudes in response to climatic factors and inter-individual heterogeneity and that the individual tree status within the population may change between phases. Species plasticity affected the response to climatic factors while tree origin, sampling strategy and silvicultural interventions impacted inter-individual heterogeneity.</p>
</sec>
<sec><st>Conclusions</st>
<p>The transposition of the proposed integrative statistical modelling approach to cambial growth in relation to climatic factors and the study of the relationship between apical growth and cambial growth constitute the next steps in this research.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Chaubert-Pereira, F., Caraglio, Y., Lavergne, C., Guedon, Y.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp189</dc:identifier>
<dc:title><![CDATA[Identifying ontogenetic, environmental and individual components of forest tree growth]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>896</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>883</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/897?rss=1">
<title><![CDATA[Pollination biology of Eulophia alta (Orchidaceae) in Amazonia: effects of pollinator composition on reproductive success in different populations]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/897?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Spatial variation in pollinator composition and abundance is a well-recognized phenomenon. However, a weakness of many studies claiming specificity of plant&ndash;pollinator interactions is that they are often restricted to a single locality. The aim of the present study was to investigate pollinator effectiveness of the different flower visitors to the terrestrial orchid <I>Eulophia alta</I> at three different localities and to analyse whether differences in pollinator abundance and composition effect this plant's reproductive success.</p>
</sec>
<sec><st>Methods</st>
<p>Natural pollination was observed <I>in vivo</I>, and manipulative experiments were used to study the pollination biology and breeding system of <I>E. alta</I> at three sites near Manaus, Brazil. To gain a better understanding of the underlying mechanisms of pollinator attraction, nectar composition and secretion patterns were also studied, floral scent composition was analysed and a bioassay was conducted.</p>
</sec>
<sec><st>Key Results</st>
<p>Flower visitors, pollinator composition, pollinia transfer efficiency of particular pollinator species and natural fruit set differed among the investigated populations of <I>E. alta</I>. Flowers were self-compatible, partially autogamous and effectively pollinated by five bee species (four <I>Centris</I> species and <I>Xylocopa muscaria</I>). Visiting insects appeared to imbibe small amounts of hexose-rich nectar. Nectar sugar content was highest on the third day after flower opening. Floral fragrance analyses revealed 42 compounds, of which monoterpenes and benzenoids predominated. A bioassay using floral parts revealed that only floral tissue from the labellum chamber and labellum tip was attractive to flower visitors.</p>
</sec>
<sec><st>Conclusions</st>
<p>The data suggest that observed differences in reproductive success in the three populations cannot be explained by absolute abundance of pollinators alone. Due to behavioural patterns such as disturbance of effective pollinators on flowers by male <I>Centris varia</I> bees defending territory, pollinia transfer efficiencies of particular pollinator species also vary between study sites and result in differing reproductive success.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Jurgens, A., Bosch, S. R., Webber, A. C., Witt, T., Frame, D., Gottsberger, G.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp191</dc:identifier>
<dc:title><![CDATA[Pollination biology of Eulophia alta (Orchidaceae) in Amazonia: effects of pollinator composition on reproductive success in different populations]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>912</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>897</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/913?rss=1">
<title><![CDATA[Floral development and anatomy of Salvadoraceae]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/913?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>This study is an investigation into the floral development and anatomy of two genera of the small family Salvadoraceae, which belongs to the Brassicales in a clade with <I>Batis</I> and <I>Koeberlinia</I>. Salvadoraceae remains little known, despite its wide distribution in arid areas of the globe. Floral morphological data are scarce, and information on floral anatomy is limited to a single study, although morphological and anatomical characters are now used increasingly as a counterpart of molecular data. There remain a number of controversial morphological questions, such as the fusion of the petals, the number of carpels and the nature of the nectaries.</p>
</sec>
<sec><st>Methods</st>
<p>Floral anatomy and ontogeny were studied in two species of <I>Salvadora</I> and one species of <I>Dobera</I>. Only for <I>S. persica</I> could a full floral developmental sequence be done.</p>
</sec>
<sec><st>Key Results</st>
<p>The floral development demonstrates that the ovary of Salvadoraceae is basically bicarpellate and pseudomonomerous with a single locule and parietal placenta. The ovary of <I>Dobera</I> resembles <I>Azima tetracantha</I> in the presence of a false apical septum. Evidence for a staminodial nature of the nectaries is not decisive. In <I>Salvadora</I> petals and stamens are lifted by a short hypanthium.</p>
</sec>
<sec><st>Conclusions</st>
<p>Salvadoraceae share several morphological and developmental synapomorphies with <I>Batis</I> (Bataceae) and possibly <I>Koeberlinia</I> (Koeberliniaceae), supporting their close relationship as indicated by molecular phylogeny.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ronse De Craene, L., Wanntorp, L.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp170</dc:identifier>
<dc:title><![CDATA[Floral development and anatomy of Salvadoraceae]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>923</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>913</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/925?rss=1">
<title><![CDATA[Abscisic acid has contrasting effects on salt excretion and polyamine concentrations of an inland and a coastal population of the Mediterranean xero-halophyte species Atriplex halimus]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/925?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Different populations of the Mediterranean xerohalophyte species <I>Atriplex halimus</I> exhibit different levels of resistance to salt and osmotic stress depending on the nature of the osmocompatible solute they accumulate. There is, however, no conclusive description of the involvement of abscisic acid (ABA) in the plant response to NaCl or osmotic stress in this species.</p>
</sec>
<sec><st>Methods</st>
<p>Seedlings issued from an inland water-stress-resistant population (Sbikha) and from a coastal salt-resistant one (Monastir) were exposed in nutrient solutions to NaCl (40 or 160 m<scp>m</scp>) or to 15 % PEG for 1 d and 10 d in the presence or absence of 50 &micro;<scp>m</scp> ABA.</p>
</sec>
<sec><st>Key Results</st>
<p>Plants from Sbikha accumulated higher amounts of ABA in response to osmotic stress than those of Monastir, while an opposite trend was recorded for NaCl exposure. Exogenous ABA improved osmotic stress resistance in Monastir through an improvement in the efficiency of stomatal conductance regulation. It also improved NaCl resistance in Sbikha through an increase in sodium excretion through the external bladders. It is suggested that polyamines (spermidine and spermine) are involved in the salt excretion process and that ABA contributes to polyamine synthesis as well as to the conversion from the bound and conjugated to the free soluble forms of polyamine. Proline accumulated in response to osmotic stress and slightly increased in response to ABA treatment while glycinebetaine accumulated in response to salinity and was not influenced by ABA.</p>
</sec>
<sec><st>Conclusions</st>
<p>It is concluded that ABA is involved in both salt and osmotic stress resistance in the xerohalophyte species <I>Atriplex halimus</I> but that it acts on different physiological cues in response to those distinct environmental constraints.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ben Hassine, A., Ghanem, M. E., Bouzid, S., Lutts, S.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp174</dc:identifier>
<dc:title><![CDATA[Abscisic acid has contrasting effects on salt excretion and polyamine concentrations of an inland and a coastal population of the Mediterranean xero-halophyte species Atriplex halimus]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>936</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>925</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/937?rss=1">
<title><![CDATA[Ultrastructure and post-floral secretion of the pericarpial nectaries of Erythrina speciosa (Fabaceae)]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/937?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>The occurrence of nectaries in fruits is restricted to a minority of plant families and consistent reports of their occurrence are not found associated with Fabaceae, mainly showing cellular details. The present study aims to describe the anatomical organization and ultrastructure of the pericarpial nectaries (PNs) in <I>Erythrina speciosa</I>, a bird-pollinated species, discussing functional aspects of these unusual structures.</p>
</sec>
<sec><st>Methods</st>
<p>Samples of floral buds, ovaries of flowers at anthesis and fruits at several developmental stages were fixed and processed by the usual methods for studies using light, and scanning and transmission electron microscopy. Nectar samples collected by filter paper wicks were subjected to chemical analysis using thin-layer chromatography.</p>
</sec>
<sec><st>Key Results</st>
<p>The PNs are distributed in isolation on the exocarp. Each PN is represented by a single hyaline trichome that consists of a basal cell at epidermal level, stalk cell(s) and a small secretory multicellular head. The apical stalk cell shows inner periclinal and anticlinal walls impregnated by lipids and lignin and has dense cytoplasm with a prevalence of mitochondria and endoplasmic reticulum. The secretory cells show voluminous nuclei and dense cytoplasm, which predominantly has dictyosomes, rough endoplasmic reticulum, plastids, mitochondria and free ribosomes. At the secretory stage the periplasmic space is prominent and contains secretion residues. Tests for sugar indicate the presence of non-reducing sugars in the secretory cells. Nectar samples from PNs contained sucrose, glucose and fructose.</p>
</sec>
<sec><st>Conclusions</st>
<p>The secretory stage of these PNs extends until fruit maturation and evidence suggests that the energetic source of nectar production is based on pericarp photosynthesis. Patrolling ants were seen foraging on fruits during all stages of fruit development, which suggests that the PNs mediate a symbiotic relationship between ants and plant, similar to the common role of many extrafloral nectaries.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Paiva, E. A. S.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp175</dc:identifier>
<dc:title><![CDATA[Ultrastructure and post-floral secretion of the pericarpial nectaries of Erythrina speciosa (Fabaceae)]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>944</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>937</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/945?rss=1">
<title><![CDATA[Influence of plant maturity, shoot reproduction and sex on vegetative growth in the dioecious plant Urtica dioica]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/945?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Stinging nettle (<I>Urtica dioica</I>) is a herbaceous, dioecious perennial that is widely distributed around the world, reproduces both sexually and asexually, and is characterized by rapid growth. This work was aimed at evaluating the effects of plant maturity, shoot reproduction and sex on the growth of leaves and shoots.</p>
</sec>
<sec><st>Methods</st>
<p>Growth rates of apical shoots, together with foliar levels of phytohormones (cytokinins, auxins, absicisic acid, jasmonic acid and salicylic acid) and other indicators of leaf physiology (water contents, photosynthetic pigments, -tocopherol and <I>F</I><SUB>v</SUB>/<I>F</I><SUB>m</SUB> ratios) were measured in juvenile and mature plants, with a distinction made between reproductive and non-reproductive shoots in both males and females. Vegetative growth rates were not only evaluated in field-grown plants, but also in cuttings obtained from these plants. All measurements were performed during an active vegetative growth phase in autumn, a few months after mature plants reproduced during spring and summer.</p>
</sec>
<sec><st>Key Results</st>
<p>Vegetative growth rates in mature plants were drastically reduced compared with juvenile ones (48 % and 78 % for number of leaves and leaf biomass produced per day, respectively), which was associated with a loss of photosynthetic pigments (up to 24 % and 48 % for chlorophylls and carotenoids, respectively) and increases of -tocopherol (up to 2&middot;7-fold), while endogenous levels of phytohormones did not differ between mature and juvenile plants. Reductions in vegetative growth were particularly evident in reproductive shoots of mature plants, and occurred similarly in both males and females.</p>
</sec>
<sec><st>Conclusions</st>
<p>It is concluded that (<I>a</I>) plant maturity reduces vegetative growth in <I>U. dioica</I>, (<I>b</I>) effects of plant maturity are evident both in reproductive and non-reproductive shoots, but particularly in the former, and (<I>c</I>) these changes occur similarly in both male and female plants.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Onate, M., Munne-Bosch, S.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp176</dc:identifier>
<dc:title><![CDATA[Influence of plant maturity, shoot reproduction and sex on vegetative growth in the dioecious plant Urtica dioica]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>956</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>945</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/957?rss=1">
<title><![CDATA[Genetic differences in fruit-set patterns are determined by differences in fruit sink strength and a source : sink threshold for fruit set]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/957?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Fruit set in indeterminate plant species largely depends on the balance between source and sink strength. Plants of these species show fluctuations in fruit set during the growing season. It was tested whether differences in fruit sink strength among the cultivars explained the differences in fruit-set patterns.</p>
</sec>
<sec><st>Methods</st>
<p><I>Capsicum</I> was chosen as a model plant. Six cultivars with differences in fruit set, fruit size and plant growth were evaluated in a greenhouse experiment. Fruit-set patterns, generative and vegetative sink strength, source strength and the source : sink ratio at fruit set were determined. Sink strength was quantified as potential growth rate. Fruit set was related to total fruit sink strength and the source : sink ratio. The effect of differences observed in above-mentioned parameters on fruit-set patterns was examined using a simple simulation model.</p>
</sec>
<sec><st>Key Results</st>
<p>Sink strengths of individual fruits differed greatly among cultivars. Week-to-week fruit set in large-fruited cultivars fluctuated due to large fluctuations in total fruit sink strength, but in small-fruited cultivars, total fruit sink strength and fruit set were relatively constant. Large variations in week-to-week fruit set were correlated with a low fruit-set percentage. The source : sink threshold for fruit set was higher in large-fruited cultivars. Simulations showed that within the range of parameter values found in the experiment, fruit sink strength and source : sink threshold for fruit set had the largest impact on fruit set: an increase in these parameters decreased the average percentage fruit set and increased variation in weekly fruit set. Both were needed to explain the fruit-set patterns observed. The differences observed in the other parameters (e.g. source strength) had a lower effect on fruit set.</p>
</sec>
<sec><st>Conclusions</st>
<p>Both individual fruit sink strength and the source : sink threshold for fruit set were needed to explain the differences observed between fruit-set patterns of the six cultivars.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Wubs, A. M., Ma, Y., Heuvelink, E., Marcelis, L. F. M.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp181</dc:identifier>
<dc:title><![CDATA[Genetic differences in fruit-set patterns are determined by differences in fruit sink strength and a source : sink threshold for fruit set]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>964</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>957</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/965?rss=1">
<title><![CDATA[Distribution and diversity of cytotypes in Dianthus broteri as evidenced by genome size variations]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/965?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Studying the spatial distribution of cytotypes and genome size in plants can provide valuable information about the evolution of polyploid complexes. Here, the spatial distribution of cytological races and the amount of DNA in <I>Dianthus broteri</I>, an Iberian carnation with several ploidy levels, is investigated.</p>
</sec>
<sec><st>Methods</st>
<p>Sample chromosome counts and flow cytometry (using propidium iodide) were used to determine overall genome size (2C value) and ploidy level in 244 individuals of 25 populations. Both fresh and dried samples were investigated. Differences in 2C and 1Cx values among ploidy levels within biogeographical provinces were tested using ANOVA. Geographical correlations of genome size were also explored.</p>
</sec>
<sec><st>Key Results</st>
<p>Extensive variation in chromosomes numbers (2<I>n</I> = 2<I>x</I> = 30, 2<I>n</I> = 4<I>x</I> = 60, 2<I>n</I> = 6<I>x</I> = 90 and 2<I>n</I> = 12<I>x</I> =180) was detected, and the dodecaploid cytotype is reported for the first time in this genus. As regards cytotype distribution, six populations were diploid, 11 were tetraploid, three were hexaploid and five were dodecaploid. Except for one diploid population containing some triploid plants (2<I>n</I> = 45), the remaining populations showed a single cytotype. Diploids appeared in two disjunct areas (south-east and south-west), and so did tetraploids (although with a considerably wider geographic range). Dehydrated leaf samples provided reliable measurements of DNA content. Genome size varied significantly among some cytotypes, and also extensively within diploid (up to 1&middot;17-fold) and tetraploid (1&middot;22-fold) populations. Nevertheless, variations were not straightforwardly congruent with ecology and geographical distribution.</p>
</sec>
<sec><st>Conclusions</st>
<p><I>Dianthus broteri</I> shows the highest diversity of cytotypes known to date in the genus <I>Dianthus</I>. Moreover, some cytotypes present remarkable internal genome size variation. The evolution of the complex is discussed in terms of autopolyploidy, with primary and secondary contact zones.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Balao, F., Casimiro-Soriguer, R., Talavera, M., Herrera, J., Talavera, S.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp182</dc:identifier>
<dc:title><![CDATA[Distribution and diversity of cytotypes in Dianthus broteri as evidenced by genome size variations]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>973</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>965</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/975?rss=1">
<title><![CDATA[Expression of ABA signalling genes and ABI5 protein levels in imbibed Sorghum bicolor caryopses with contrasting dormancy and at different developmental stages]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/975?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Pre-harvest sprouting susceptibility in grain sorghum (<I>Sorghum bicolor</I>) is related to low seed dormancy and reduced embryo sensitivity to inhibition of germination by abscisic acid (ABA). Intra-specific variability for pre-harvest sprouting might involve differential regulation of ABA signalling genes.</p>
</sec>
<sec><st>Methods</st>
<p>Sorghum genes encoding homologues for ABA signalling components from other species (<I>ABI5</I>, <I>ABI4</I>, <I>VP1</I>, <I>ABI1</I> and <I>PKABA1</I>) were studied at the transcriptional and protein level (ABI5) during grain imbibition for two sorghum lines with contrasting sprouting phenotypes and in response to hormones.</p>
</sec>
<sec><st>Key Results</st>
<p>Transcript levels of these genes and protein levels of ABI5 were higher in imbibed immature caryopses of the more dormant line. Dormancy loss was related to lower transcript levels of these genes and lower ABI5 protein levels in both genotypes. Exogenous ABA inhibited germination of isolated embryos but failed to prevent ABI5 rapid decrease supporting a role for the seed coat in regulating ABI5 levels.</p>
</sec>
<sec><st>Conclusions</st>
<p>Several genes involved in ABA signalling are regulated differently in imbibed caryopses from two sorghum lines with contrasting pre-harvest sprouting response before &ndash; but not after &ndash; physiological maturity. A role for ABI5 in the expression of dormancy during grain development is discussed.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Rodriguez, M. V., Mendiondo, G. M., Maskin, L., Gudesblat, G. E., Iusem, N. D., Benech-Arnold, R. L.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp184</dc:identifier>
<dc:title><![CDATA[Expression of ABA signalling genes and ABI5 protein levels in imbibed Sorghum bicolor caryopses with contrasting dormancy and at different developmental stages]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>985</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>975</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/987?rss=1">
<title><![CDATA[Costs of height gain in rainforest saplings: main-stem scaling, functional traits and strategy variation across 75 species]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/987?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Height gain plays an important role in plant life-history strategies and species coexistence. Here main-stem costs of height gain of saplings across species within a rainforest community are compared.</p>
</sec>
<sec><st>Methods</st>
<p>Scaling relationships of height to diameter at the sapling stage were compared among 75 woody rainforest plant species in subtropical eastern Australia using standardized major axis regression. Main-stem costs of height gain were then related to other functional traits that reflect aspects of species ecological strategies.</p>
</sec>
<sec><st>Key Results</st>
<p>Slopes (<I>&beta;</I>) for the height&ndash;diameter (<I>H&ndash;D</I>) scaling relationship were close to 1&middot;3, in line with previous reports and with theory. Main-stem volume to achieve 5 m in height varied substantially between species, including between species within groups based on adult height and successional status. The variation was largely independent of other species traits, being uncorrelated with mature plant height (<I>H</I><SUB>max</SUB>) and with leaf size, and weakly negatively correlated with wood density and seed size. The relationship between volume to reach 5 m and wood density was too weak to be regarded as a trade-off. Estimated main-stem dry mass to achieve 5 m height varied almost three-fold across species, with wood density and stem volume contributing roughly equally to the variation.</p>
</sec>
<sec><st>Conclusion</st>
<p>The wide range in economy of sapling height gain reported here is presumed to be associated with a trade-off between faster growth and higher mortality rates. It is suggested that wide diameters would have a stronger effect in preventing main-stem breakage in the short term, while high wood density would have a stronger effect in sustaining stem strength over time.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kooyman, R. M., Westoby, M.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:subject><![CDATA[Ecology]]></dc:subject>
<dc:identifier>info:doi/10.1093/aob/mcp185</dc:identifier>
<dc:title><![CDATA[Costs of height gain in rainforest saplings: main-stem scaling, functional traits and strategy variation across 75 species]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>993</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>987</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/995?rss=1">
<title><![CDATA[Population dynamics of epiphytic orchids in a metapopulation context]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/995?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Populations of many epiphytes show a patchy distribution where clusters of plants growing on individual trees are spatially separated and may thus function as metapopulations. Seed dispersal is necessary to (re)colonize unoccupied habitats, and to transfer seeds from high- to low-competition patches. Increasing dispersal distances, however, reduces local fecundity and the probability that seeds will find a safe site outside the original patch. Thus, there is a conflict between seed survival and colonization.</p>
</sec>
<sec><st>Methods</st>
<p>Populations of three epiphytic orchids were monitored over three years in a Mexican humid montane forest and analysed with spatially averaged and with spatially explicit matrix metapopulation models. In the latter, population dynamics at the scale of the subpopulations (epiphytes on individual host trees) are based on detailed stage-structured observations of transition probabilities and trees are connected by a dispersal function.</p>
</sec>
<sec><st>Key Results</st>
<p>Population growth rates differed among trees and years. While ignoring these differences, and averaging the population matrices over trees, yields negative population growth, metapopulation models predict stable or growing populations because the trees that support growing subpopulations determine the growth of the metapopulation. Stochastic models which account for the differences among years differed only marginally from deterministic models. Population growth rates were significantly lower, and extinctions of local patches more frequent in models where higher dispersal results in reduced local fecundity compared with hypothetical models where this is not the case. The difference between the two models increased with increasing mean dispersal distance. Though recolonization events increased with dispersal distance, this could not compensate the losses due to reduced local fecundity.</p>
</sec>
<sec><st>Conclusions</st>
<p>For epiphytes, metapopulation models are useful to capture processes beyond the level of the single host tree, but local processes are equally important to understand epiphyte population dynamics.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Winkler, M., Hulber, K., Hietz, P.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp188</dc:identifier>
<dc:title><![CDATA[Population dynamics of epiphytic orchids in a metapopulation context]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1004</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>995</prism:startingPage>
<prism:section>ORIGINAL ARTICLES</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/1005?rss=1">
<title><![CDATA[Counting pollen grains using readily available, free image processing and analysis software]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/1005?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Although many methods exist for quantifying the number of pollen grains in a sample, there are few standard methods that are user-friendly, inexpensive and reliable. The present contribution describes a new method of counting pollen using readily available, free image processing and analysis software.</p>
</sec>
<sec><st>Methods</st>
<p>Pollen was collected from anthers of two species, <I>Carduus acanthoides</I> and <I>C. nutans</I> (Asteraceae), then illuminated on slides and digitally photographed through a stereomicroscope. Using ImageJ (NIH), these digital images were processed to remove noise and sharpen individual pollen grains, then analysed to obtain a reliable total count of the number of grains present in the image. A macro was developed to analyse multiple images together. To assess the accuracy and consistency of pollen counting by ImageJ analysis, counts were compared with those made by the human eye.</p>
</sec>
<sec><st>Key Results and Conclusions</st>
<p>Image analysis produced pollen counts in 60 s or less per image, considerably faster than counting with the human eye (5&ndash;68 min). In addition, counts produced with the ImageJ procedure were similar to those obtained by eye. Because count parameters are adjustable, this image analysis protocol may be used for many other plant species. Thus, the method provides a quick, inexpensive and reliable solution to counting pollen from digital images, not only reducing the chance of error but also substantially lowering labour requirements.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Costa, C. M., Yang, S.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp186</dc:identifier>
<dc:title><![CDATA[Counting pollen grains using readily available, free image processing and analysis software]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1010</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1005</prism:startingPage>
<prism:section>TECHNICAL ARTICLE</prism:section>
</item>

<item rdf:about="http://aob.oxfordjournals.org/cgi/content/short/104/5/1011?rss=1">
<title><![CDATA[Release of developmental constraints on tetrad shape is confirmed in inaperturate pollen of Potamogeton]]></title>
<link>http://aob.oxfordjournals.org/cgi/content/short/104/5/1011?rss=1</link>
<description><![CDATA[
<sec><st>Background and Aims</st>
<p>Microsporogenesis in monocots is often characterized by successive cytokinesis with centrifugal cell plate formation. Pollen grains in monocots are predominantly monosulcate, but variation occurs, including the lack of apertures. The aperture pattern can be determined by microsporogenesis features such as the tetrad shape and the last sites of callose deposition among the microspores. <I>Potamogeton</I> belongs to the early divergent Potamogetonaceae and possesses inaperturate pollen, a type of pollen for which it has been suggested that there is a release of the constraint on tetrad shape. This study aimed to investigate the microsporogenesis and the ultrastructure of pollen wall in species of <I>Potamogeton</I> in order to better understand the relationship between microsporogenesis features and the inaperturate condition.</p>
</sec>
<sec><st>Methods</st>
<p>The microsporogenesis was investigated using both light and epifluorescence microscopy. The ultrastructure of the pollen grain was studied using transmission electron microscopy.</p>
</sec>
<sec><st>Key Results</st>
<p>The cytokinesis is successive and formation of the intersporal callose wall is achieved by centrifugal cell plates, as a one-step process. The microspore tetrads were tetragonal, decussate, T-shaped and linear, except in <I>P. pusillus</I>, which showed less variation. This species also showed a callose ring in the microsporocyte, and some rhomboidal tetrads. In the mature pollen, the thickening observed in a broad area of the intine was here interpreted as an artefact.</p>
</sec>
<sec><st>Conclusions</st>
<p>The data support the view that there is a correlation between the inaperturate pollen production and the release of constraint on tetrad shape. However, in <I>P. pusillus</I> the tetrad shape may be constrained by a callose ring. It is also suggested that the lack of apertures in the pollen of <I>Potamogeton</I> may be due to the lack of specific sites on which callose deposition is completed. Moreover, inaperturate pollen of <I>Potamogeton</I> would be better classified as omniaperturate.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Nunes, E. L. P., Bona, C., Moco, M. C. d. C., Coan, A. I.]]></dc:creator>
<dc:date>Wed, 23 Sep 2009 09:22:52 PDT</dc:date>
<dc:identifier>info:doi/10.1093/aob/mcp160</dc:identifier>
<dc:title><![CDATA[Release of developmental constraints on tetrad shape is confirmed in inaperturate pollen of Potamogeton]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>104</prism:volume>
<prism:endingPage>1015</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1011</prism:startingPage>
<prism:section>SHORT COMMUNICATION</prism:section>
</item>

</rdf:RDF>