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Annals of Botany 2009 103(5):i; doi:10.1093/aob/mcp041
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© The Author 2009. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

ContentSnapshots

SXRF and metal homeostasis in plants (Botanical Briefing)
Figure 1
Synchrotron X-ray fluorescence microspectroscopy is a technique that allows the spatial distribution of multiple elements to be imaged simultaneously, without sample damage or preparation. Punshon et al. (pp. 665–672) describe its burgeoning use in the plant sciences, specifically in metal homeostasis research, and the exciting prospects for future applications.


Formation of clay pavements by eucalypts
Figure 2
Mallee eucalypts and proteaceous heath are colonizing a Pleistocene sand dune in Australia. Pate and Verboom (pp. 673–685) provide evidence of massive biogenic formation of columnar clay pavements in the lateral root catchments of the eucalypts. The findings are related to niche-building activities of the woody plants concerned, as described more generally in the recently proposed ‘phytotarium concept’.


Casparian bands of Iris roots
Figure 3
The multiseriate exodermis of Iris germanica roots has an unusual Casparian band (termed a ‘continuous circumferential Casparian band’) located in the tangential and anticlinal walls. Meyer et al. (pp. 687–702) trace the shape of this band to divisions in the apical meristem. Unique effects of culture conditions on exodermal maturation and a new correlation of Iris exodermis type with habitat are described.


Phylogenetic distribution of autumn colours
Figure 4
Some species of trees and shrubs change their leaf colour in autumn. Archetti (pp. 703–713) describes the autumn colours of 2368 species and their phylogenetic distribution. Autumn colours are present in less than 20% of the species examined, but evolved independently many times. These data can be used for a comparative analysis of hypotheses relating to co-evolutionary interaction or the need for photoprotection. (Featured article in ContentSelect on p. iii.)


Floral scent in a wasp-pollination system
Figure 5
Floral scent may play a key role as a selective attractant in plants that have specialized pollination but produce exposed nectar. In a study of two morphologically unspecialized Eucomis species, Shuttleworth and Johnson (pp. 715–725) find that the pompilid wasp pollinators are attracted exclusively by floral scent rather than visual cues, and these plants achieve specialization through a combination of cryptic colouring and floral scent.


Domestication syndrome in cardamom
Figure 6
Kuriakose et al. (pp. 727–733) provide the first analyses of the domestication syndrome of Elettaria cardamomum, an important spice. Domestication has brought about significant changes in several productive traits and a shift in effective pollinators from native solitary bees to social bees. This shift seems to be due to an increase in flower density and flowering duration rather than to co-evolution of the flower and the pollinator.


Ha-L1L gene and auxin in epiphylly
Figure 7
The clone EMB-2 of the interspecific hybrid Helianthus annuus x H. tuberosus produces epiphyllous leaves bearing embryos on the adaxial surface. Chiappetta et al. (pp. 735–747) demonstrate that localized Ha-L1L expression and IAA accumulation in leaf epidermis domains represent early events of somatic embryogenesis displayed by this clone. (Featured article in ContentSelect on p. iii.)


Transient callose in moss sporogenesis
Figure 8
Schuette et al. (pp. 749–756) provide the first immunocytochemical report of callose involvement in moss spore-wall development. Callose, present in the exine during early aperture formation of the spore wall, is absent during later stages of development. In addition, using phylogenomic techniques, an orthologous callose synthase gene (implicated in exine development of Arabidopsis pollen) is identified in moss.


Associations between leaf toughness and phenolics
Figure 9
Species investing heavily in mechanical defence have been suggested to invest less in chemical defence. Read et al. (pp. 757–767) instead find positive correlations between toughness and phenolics, but only on infertile soils. This suggests that additive investment in the two forms of defence is advantageous in nutrient-deficient environments where carbohydrate may be in surplus.


Stomatal density and climate change
Figure 10
Plant species will need to adapt to increased temperatures and altered precipitation due to global climate change. Fraser et al. (pp. 769–775) test the response of stomatal density in Pseudoroegneria spicata (bluebunch wheatgrass) to climate manipulations in the field. Although temperature did not affect stomatal density, it was increased by reducing water supply, and increasing water supply reduced leaf area.


Decreased genetic diversity after colonization
Figure 11
Land-use changes and associated extinction–colonization dynamics can have a large impact on population genetic diversity of plant species. Jacquemyn et al. (pp. 777–783) show that a small effective population size and genetic drift can lead to a rapid decline of genetic diversity of offspring in founding populations of the forest herb Primula elatior shortly after colonization. Considerable amounts of gene flow are thus required to sustain high levels of genetic diversity. (Featured article in ContentSelect on p. iii.)


Post-abscission seed development in Digitalis
Figure 12
The developmental progress of Digitalis purpurea seeds collected shortly before maturity is not terminated by desiccation ex planta. Butler et al. (pp. 785–794) show that maturation can continue at a wide range of relative humidities (RH) thereafter, leading to increased longevity; subsequent rehydration at 95 % RH, or priming, improves longevity further. However, individuals within the population differ in responsiveness, changing the survival curve shape. (Featured article in ContentSelect on p. iii.)


Optimal use of light by tree crowns
Figure 13
Posada et al. (pp. 795–805) show that individual leaves of adult trees use light with the same photosynthetic efficiency regardless of leaf position within the tree crown (e.g. sun/shade) or species' identity. Efficiency is maintained constant through co-ordinated adjustment in leaf angle and leaf physiology. This constant light use efficiency allows simple scaling of photosynthesis from leaves to canopies.


Lateral root initiation in plants
Figure 14
Positioning of newly initiated lateral-root primordia in plants is rather flexible. Nevertheless, Dubrovsky et al. (pp. 807–817) propose a new parameter – the average number of primordia per parent root portion comprising 100 elongated cortical cells – that is rather constant for Arabidopsis accessions and is age-independent. This parameter allows for a more precise analysis of lateral-root initiation under different growth conditions, treatments, genotypes and in different plant species.


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Using synchrotron X-ray fluorescence microprobes in the study of metal homeostasis in plants
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Ann Bot 2009 103: 665-672. [Abstract] [Full Text]  

Contemporary biogenic formation of clay pavements by eucalypts: further support for the phytotarium concept
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Environmental effects on the maturation of the endodermis and multiseriate exodermis of Iris germanica roots
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John Bryant takes a closer look at some of this month's Original Articles
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