Is resource overlap disadvantageous to three sympatric legumes?

Abstract The sympatric legumes Dillwynia hispida, Dillwynia uncinata and Pultenaea densifolia overlap in flowering phenology, floral characters and native bee pollinators. Tests for pollen-limitation were conducted to determine whether or not the overlap in pollinator use was detrimental to individuals of these species. Pollen limitation was only detected in D. hispida. Pollen loads on bees were examined and it was found that pollen loads from Dillwynia and P. densifolia were spatially segregated on the pollinator's body reducing the likelihood of pollen transfer between these species. The pollen of D. hispida and D. uncinata overlapped on the heads of bees suggesting that interspecific pollinations may be responsible for lowered fruit-set in D. hispida. However, hand pollinations involving heterospecific pollen and controlled floral visits by bees to the two Dillwynia species revealed that heterospecific pollen loads did not significantly depress fruit-set in either D. hispida or D. uncinata. Pollinator preferences were examined in detail and it was found that D. uncinata flowers received twice as many bees in a day compared with D. hispida and P. densifolia. Competition through pollinator preference is implicated here as a mechanism of competition. Intraspecific competition is also implicated as D. hispida was pollen limited in the absence of D. uncinata and P. densifolia.     

A dynamic model of photosynthesis in varying light taking account of stomatal conductance, C3-cycle intermediates, photorespiration and Rubisco activation

Abstract. A dynamic model of whole leaf C₃ photosynthesis is constructed using a modified version of the Farquliar-von Caemmerer approach. The model is designed to provide a physiological basis to understand observations of assimilation in environments with varying photon flux densities, including induction phenomena. The model couples the effect of light activation and dark deactivation of enzymes, stomatal conductance responses, and variations in the pools of carbon cycle intermediates. The dynamic components are viewed on three time scales, the slowest of which (min to h) involves changes in stomatal conductance and the activation stale of Rubisco. On a time scale of seconds to a few minutes, adjustments in pools of biochemical components of the photosynthetic pathway occurs. The most rapid time scale corresponds to the equilibration time of intercelluar CO₂ concentration through gaseous diffusion and is here assumed to occur instantaneously. The model form includes a single pool for reduced intermediates including RuBP, a single pool for components of the glycolate pathway, and a third component corresponding to the activation state of Rubisco. This is coupled to a previously described model for the dynamics of stomatal conductance, giving a final model form consisting of six non-linear ordinary differential equations, of which three control conductance dynamics and three control assimilation. The coupling between these occurs through the variable p_i, the intercellular partial pressure of CO_2. Only three of the parameters for the assimilation portion of the model require dynamic data to estimate. The remaining parameters are estimated from steady-state data. The model is calibrated using previously collected data on the tropical understory plant Alocasia macrorrhiza and is shown to have qualitatively similar behaviour to that of experimental measurements using simple changes in PFD, as well as a complex sequence of such changes.     

An improved dynamic model of photosynthesis for estimation of carbon gain in sunfleck light regimes

A dynamic model of leaf photosynthesis for C₃ plants has been developed for examination of the role of the dynamic properties of the photosynthetic apparatus in regulating CO₂ assimilation in variable light regimes. The model is modified from the Farquhar-von Caemmerer-Berry model by explicitly including metabolite pools and the effects of light activation and deactivation of Calvin cycle enzymes. It is coupled to a dynamic stomatal conductance model, with the assimilation rate at any time being determined by the joint effects of the dynamic biochemical model and the stomatal conductance model on the intercellular CO₂ pressure. When parametrized for each species, the model was shown to exhibit responses to step changes in photon flux density that agreed closely with the observed responses for both the understory plant Alocasia macrorrhiza and the crop plant Glycine max. Comparisons of measured and simulated photosynthesis under simulated light regimes having natural patterns of lightfleck frequencies and durations showed that the simulated total for Alocasia was within ±4% of the measured total assimilation, but that both were 12–50% less than the predictions from a steady–state solution of the model. Agreement was within ±10% for Glycine max, and only small differences were apparent between the dynamic and steady–state predictions. The model may therefore be parametrized for quite different species, and is shown to reflect more accurately the dynamics of photosynthesis than earlier dynamic models.     

Genomic affinities in Arachis section Arachis (Fabaceae): molecular and cytogenetic evidence

Section Arachis is the largest of nine sections in the genus Arachis and includes domesticated peanut, A. hypogaea L. Most species are diploids (x=10) with two tetraploids and a few aneuploids. Three genome types have been recognized in this section (A, B and D), but the genomes are not well characterized and relationships of several newly described species are uncertain. To clarify genomic relationships in section Arachis, cytogenetic information and molecular data from amplified fragment length polymorphism (AFLP) and the trnT-F plastid region were used to provide an additional insight into genome composition and species relationships. Cytogenetic information supports earlier observations on genome types of A. cruziana, A. herzogii, A. kempff-mercadoi and A. kuhlmannii but was inconclusive about the genome composition of A. benensis, A. hoehnei, A. ipaensis, A. palustris, A. praecox and A. williamsii. An AFLP dendrogram resolved species into four major clusters and showed A. hypogaea grouping closely with A. ipaensis and A. williamsii. Sequence data of the trnT-F region provided genome-specific information and showed for the first time that the B and D genomes are more closely related to each other than to the A genome. Integration of information from cytogenetics and biparentally and maternally inherited genomic regions show promise in understanding genome types and relationships in Arachis.     

Protein evolution in different cellular environments: cytochrome b in sharks and mammals

DNA sequences for the mitochondrial cytochrome b gene were determined for 13 species of sharks. Rates and patterns of amino acid replacement are compared for sharks and mammals. Absolute rates of cytochrome b evolution are six times slower in sharks than in mammals. Bivariate plots of the number of nonsynonymous and silent transversions are indistinguishable in the two groups, however, suggesting that the differences in amino acid replacement rates are due primarily to differences in DNA substitution rates. Patterns of amino acid replacement are also similar in the two groups. Conserved and variable regions occur in the same parts of the cytochrome b gene, and there is little evidence that the types of amino acid changes are significantly different between the groups. Similarity in the relative rates and patterns of protein change between the two groups prevails despite dramatic differences in the cellular environments of sharks and mammals. Poor penetrance of physiological differences through to rates of protein evolution provides support for the neutral theory and suggests that, for cytochrome b, patterns of evolution have been relatively constant throughout much of vertebrate history.