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Annals of Botany 2008 101(5):NP; doi:10.1093/aob/mcn037
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© The Author 2008. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

John Bryant takes a closer look at some of this month's Original Articles

J. A. Bryant, Professor

University of Exeter, UK
E-mail j.a.bryant{at}exeter.ac.uk

Dyeing to escape


Figure 1
As I glance out of my window at the rain being driven by 100-kph winds it is difficult to imagine ecosystems where fire is an essential factor. In such ecosystems, one of the effects of fire is the breakage of seed dormancy of many fire-dependent species. This phenomenon is discussed by Briggs and Morris, University of Western Sydney, Australia (pp. 623–632). Our knowledge of the mechanisms by which fire breaks seed dormancy is very ‘patchy’. For some species, for example, it is clear that smoke alters a seed-coat barrier so that a germination inhibitor may escape, but for many other species no obvious mechanism has been described. One such is Grevillea linearifolia, a native of eastern Australia. Dormancy is imposed by the seed coat; high germination rates are achieved in the absence of fire if the seed coat is removed. In the authors' experiments, 23 % of whole, untreated seeds germinated. This increased to 50 % in seeds exposed to heat, and to 67 % in seeds exposed to smoke. Seeds treated with both heat and smoke exhibited 80 % germination. The approach to detection of cell wall permeability changes was simple and effective, making use of the dye Lucifer Yellow (LY). The dye was applied either to the outside of the seed coat of whole seeds or to the inside of seed coats of partly dissected seeds. Permeation of the dye was observed by light microscopy in seed coats from control seeds and from seeds exposed to heat and/or smoke. The results were clear: smoke and/or heat treatment did not make the complex seed coat of G. linearifolia permeable to LY. The authors have therefore turned their attention to the possibility that heat and/or smoke alter the physical properties of the seed coat cells, as suggested by the ‘mechanical constraint’ model of seed coat dormancy.

Monkeyflowers, bees – but no birds


Figure 2
Working in a university department with a long-standing research interest in Mimulus, I noticed immediately the paper by Cooley et al.(Durham, USA and Santiago, Chile (pp. 641–650) who are interested in speciation mechanisms and reproductive isolation. In a recent paper (Hybridization as an invasion of the genome. Trends in Ecology and Evolution 20: 229–237; 2005), Mallet states that at least 25 % of plant species, mostly younger in evolutionary terms, are involved in hybridization. How then do reproductive barriers actually arise? Cooley et al. carried out a very careful, well-designed and thorough study based on the possibility that pollinator preference plays a role in floral diversification. They worked on Chilean populations of four Mimulus (sub)-species, M. luteus luteus, M. l. variegatus, and M. naiandinus and M. cupreus. The latter has orange flowers rather than the classic yellow with variable red spotting of the ‘monkeyflower’. In the field, pollinator visits were studied for large numbers of plants. Laboratory-based observations included floral morphology, floral anthocyanins and nectar contents. The three yellow (sub)species were all visited almost exclusively by the same generalist pollinator, a bumble bee, Bombus dahlbomii, which made no overall distinction between flowers based on the amount of red anthocyanin pigment spots when species were growing separately. However, observations in an area where both M. l. luteus and M. naiandinus (and hybrids) grow revealed that individual pollinators had different preferences but, overall, there was a bias towards luteus-type flowers. Mimulus cupreus differs from the other three, both in overall plant morphology and in possessing orange flowers. It received very few pollinator visits and, indeed, it exhibits a high degree of selfing. Low pollinator visitation was not caused by discrimination against orange flowers: a rare yellow morph was equally neglected. The authors have thus shown that the appearance of red-pigmented flowers in ‘yellow monkeyflower’ Mimulus species has not led to changes in pollinators and that we need to know more about non-pollinator mechanisms in the generation of floral diversity.

To boldly grow


Figure 3
In a recent book (Propitious esculent: the potato in world history. Heinemann, Oxford, 2008) John Reader suggests that in manned flights to Mars, the spacecraft should be able to accommodate a small stand of potatoes in order to feed the astronauts and to help maintain the CO2/O2 balance on board. However, if reliance is to be placed on plants grown in spacecraft then we need to know that plant growth and development are not unduly disrupted by the microgravity environment. Previous experiments to investigate plant growth in space have given conflicting results, as explained by De Micco et al. (Naples, Italy and Grenoble, France, pp. 661–669). In attempting to avoid some possible sources of variation, e.g. the intense gravitational changes that occur during re-entry, the authors set up an experiment in which soybean germination, seedling growth and then fixation of the seedlings after 5 d of growth were all performed automatically under microgravity during a 16-d orbit in the Foton-M2 capsule. After return to earth, seedlings were examined for general anatomical features and also by light, fluorescence and transmission electron microscopy. Particular attention was focused on the xylem and on the structure of xylem cell walls. Comparison was made with plants grown on earth but under otherwise identical conditions. Interestingly, growth under microgravity, albeit for only 5 d, had rather little effect on the seedlings. Clear effects were only seen at LM and EM levels: some xylem cell walls were thinner and there were perturbations in the orientation of cellulose microfibrils in the early stages of wall growth. However, this was not seen in the later stages of cellulose deposition when microfibrils assembled into normal lamellae. By the time secondary thickening occurred, xylem cell walls were similar (although sometimes thinner) to those in control plants. Returning to our opening theme, all this is good news for cosmic potato growers!

In the cold light of day


Figure 4
Many green plants are damaged by exposure to cold, sunny conditions. Not only is there the likelihood of freezing damage but also of damage to the photosynthetic machinery, such as photo-bleaching. The linkage between cold and light damage is discussed by Rapacz et al., Kraków and Czgestochowa, Poland (pp. 689–699) in relation to cereals. They point out that the cold-response gene COR14b is also involved with chloroplast redox metabolism: COR14b mRNA increases following cold treatment but accumulation of the protein is also regulated post-transcriptionally by the redox state of chloroplast plastocyanin. The authors thus investigated the effects of cold-acclimation on both cold-tolerance and tolerance to high light in four barley (Hordeum vulgare) cultivars. Acclimation at 2 °C for 14 d significantly increased the freezing tolerance of all four cultivars, such that the temperature causing 50 % lethality dropped in 14-d acclimation to –12 °C in the least cold-tolerant cultivar and to –15 °C in the most cold-tolerant. Cold-acclimation also led to increased tolerance of high light and an increased photosynthetic capacity when exposed to high light conditions after cold acclimation. The authors went on to study the expression of several proteins involved in cold acclimation and/or in photosynthetic metabolism; here we focus on Cor14b. In cultivars that had greater basic freezing tolerance and less basic light tolerance, COR14b mRNA and Cor14b protein accumulated quickly during acclimation but then declined (although not back to control levels). In cultivars with less basic freezing tolerance and greater basic light tolerance, mRNA and protein accumulated more slowly but higher levels were maintained through 14-d acclimation. We may conclude that the results obtained by the authors are symptoms of a network of interacting events enabling the plant to link together different aspects of its activity in response to environmental stresses – a nice example of what is now fashionably called systems biology.


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Related articles in Ann Bot:

Seed-coat Dormancy in Grevillea linearifolia: Little Change in Permeability to an Apoplastic Tracer after Treatment with Smoke and Heat
Candida L. Briggs and E. Charles Morris
Ann Bot 2008 101: 623-632. [Abstract] [Full Text]  

Is Floral Diversification Associated with Pollinator Divergence? Flower Shape, Flower Colour and Pollinator Preference in Chilean Mimulus
A. M. Cooley, G. Carvallo, and J. H. Willis
Ann Bot 2008 101: 641-650. [Abstract] [Full Text]  

Xylem Development and Cell Wall Changes of Soybean Seedlings Grown in Space
Veronica de Micco, Giovanna Aronne, Jean-Paul Joseleau, and Katia Ruel
Ann Bot 2008 101: 661-669. [Abstract] [Full Text]  

The Effects of Cold Acclimation on Photosynthetic Apparatus and the Expression of COR14b in Four Genotypes of Barley (Hordeum vulgare) Contrasting in their Tolerance to Freezing and High-light Treatment in Cold Conditions
Marcin Rapacz, Barbara Wolanin, Katarzyna Hura, and MirosLaw Tyrka
Ann Bot 2008 101: 689-699. [Abstract] [Full Text]  




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