Abstract: A hyperelastic constitutive model is developed for textile composite reinforcement at large strain. A potential is proposed, which is the addition of two tension and one shear energies. The proposed potential is a function of the right Cauchy Green and structural tensor invariants whose choice corresponds to textile composite reinforcement mechanical behavior which exhibits weak elongations in the fiber directions and large angular variations in the fabric plane. The model is implemented in a Vumat user routine of ABAQUS/Explicit. Some elementary tests are performed in order to identify the model and verify its validity. It is then used to simulate the hemispherical punch forming of balanced and unbalanced fabrics. A correct agreement is obtained with experimental forming processes.

Abstract: P>1. As trees in a given cohort progress through ontogeny, many individuals die. This risk of mortality is unevenly distributed across species because of many processes such as habitat filtering, interspecific competition and negative density dependence. Here, we predict and test the patterns that such ecological processes should inscribe on both species and phylogenetic diversity as plants recruit from saplings to the canopy. 2. We compared species and phylogenetic diversity of sapling and tree communities at two sites in French Guiana. We surveyed 2084 adult trees in four 1-ha tree plots and 943 saplings in sixteen 16-m2 subplots nested within the tree plots. Species diversity was measured using Fisher's alpha (species richness) and Simpson's index (species evenness). Phylogenetic diversity was measured using Faith's phylogenetic diversity (phylogenetic richness) and Rao's quadratic entropy index (phylogenetic evenness). The phylogenetic diversity indices were inferred using four phylogenetic hypotheses: two based on rbcLa plastid DNA sequences obtained from the inventoried individuals with different branch lengths, a global phylogeny available from the Angiosperm Phylogeny Group, and a combination of both. 3. Taxonomic identification of the saplings was performed by combining morphological and DNA barcoding techniques using three plant DNA barcodes (psbA-trnH, rpoC1 and rbcLa). DNA barcoding enabled us to increase species assignment and to assign unidentified saplings to molecular operational taxonomic units. 4. Species richness was similar between saplings and trees, but in about half of our comparisons, species evenness was higher in trees than in saplings. This suggests that negative density dependence plays an important role during the sapling-to-tree transition. 5. Phylogenetic richness increased between saplings and trees in about half of the comparisons. Phylogenetic evenness increased significantly between saplings and trees in a few cases (4 out of 16) and only with the most resolved phylogeny. These results suggest that negative density dependence operates largely independently of the phylogenetic structure of communities. 6. Synthesis. By contrasting species richness and evenness across size classes, we suggest that negative density dependence drives shifts in composition during the sapling-to-tree transition. In addition, we found little evidence for a change in phylogenetic diversity across age classes, suggesting that the observed patterns are not phylogenetically constrained.

Abstract: 1. Plants often rely on external, mutualistic partners to survive and reproduce in resource-limited environments or for protection from enemies. Such interactions, including mycorrhizal symbioses and ant plant associations, are widespread and play an important role at the ecosystem and community levels. In ant-plant mutualisms, the plants may benefit from both the protection provided by the presence of ants and from the nutrients absorbed from insect debris. However, the role of third partners in plant nutrition, particularly ant-associated fungi, has never before been demonstrated. 2. We investigate this issue in the ant-plant Hirtella physophora. In this model system, Allomerus decemarticulatus ants are involved in two, highly specific interactions: first, with their host plant, and, secondly, with a fungus that they actively manipulate. Moreover, the ants combine both plant trichomes and fungal hyphae to make a trap to capture prey. 3. We empirically demonstrate the existence of a third type of interaction between the fungus and the plant through the use of both experimental enrichments with stable isotopes (N-15) and histological approaches. The fungus growing in the galleries plays a role in providing nutrients to the host plant, in addition to the structural role it plays for the ants. Fungus-facilitated nitrogen uptake occurs mainly in old domatia, where abundant hyphae are in close contact with the plant cells. Whether the fungi inside the domatia and those in the galleries are the same is still uncertain. 4. Synthesis. Together, our results show that a fungal partner in an ant-plant mutualism can benefit the plant by improving its nutrient uptake, and they demonstrate the existence of a true tripartite mutualism in this system. Our results add further evidence to the notion that interpretations of some ant plant symbioses as purely protective mutualisms have overlooked these nutritional aspects.

Abstract: 1.Regional above-ground biomass estimates for tropical moist forests remain highly inaccurate mostly because they are based on extrapolations from a few plots scattered across a limited range of soils and other environmental conditions. When such conditions impact biomass, the estimation is biased. The effect of soil types on biomass has especially yielded controversial results. 2.We investigated the relationship between above-ground biomass and soil type in undisturbed moist forests in the Central African Republic. We tested the effects of soil texture, as a surrogate for soil resources availability and physical constraints (soil depth and hydromorphy) on biomass. Forest inventory data were collected for trees ≥20cm stem diameter in 2754 0.5ha plots scattered over 4888km2. The plots contained 224 taxons, of which 209 were identified to species. Soil types were characterized from a 1:1000000 scale soil map. Species-specific values for wood density were extracted from the CIRAD's data base of wood technological properties. 3.We found that basal area and biomass differ in their responses to soil type, ranging from 17.8m2ha-1 (217.5tha-1) to 22.3m2ha-1 (273.3tha-1). While shallow and hydromorphic soils support forests with both low stem basal area and low biomass, forests on deep resource-poor soils are typically low in basal area but as high in biomass as forests on deep resource-rich soils. We demonstrated that the environmental filtering of slow growing dense-wooded species on resource-poor soils compensates for the low basal area, and we discuss whether this filtering effect is due to low fertility or to low water reserve. 4.Synthesis. We showed that soil physical conditions constrained the amount of biomass stored in tropical moist forests. Contrary to previous reports, our results suggest that biomass is similar on resource-poor and resource-rich soils. This finding highlights both the importance of taking into account soil characteristics and species wood density when trying to predict regional patterns of biomass. Our findings have implications for the evaluation of biomass stocks in tropical forests, in the context of the international negotiations on climate change. © 2011 The Authors. Journal of Ecology © 2011 British Ecological Society.

Abstract: 1.A recent article published by Toledo (2011b) investigates the effects of spatial variations in climate and soil, and of logging disturbance, on tree and forest growth in Bolivia. It concludes that climate is the strongest driver of tree and forest growth and that climate change may therefore have large consequences for forest productivity and carbon sequestration. However, serious methodological and conceptual discrepancies have been found that challenge these conclusions. 2.Because of an errant coding of 'time after logging' in the regression analysis, and because floristic changes induced by logging could not be incorporated into the analysis, the effect of logging on the average diameter growth is likely to have been strongly underestimated. 3.Basal area growth was improperly calculated as basal area change, and it displayed surprisingly high values, even among unlogged plots. We hypothesize that either these plots may be actually located in secondary forests recovering from past logging, or measurement biases may have hampered the data set. 4.Regardless of climate-growth relationships established across these plots, any inference concerning the potential effects of climate change on forest growth would require a specific quantitative assessment. 5.Synthesis. It is critical to re-assess the relative weight of climate and logging disturbance as driving factors of tree and forest growth, and to find an explanation for the very high basal area increment reported among the unlogged plots. We provide specific recommendations for further analyses of this and similar data sets. © 2012 British Ecological Society.