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Schimann, H., Ponton, S., Hattenschwiler, S., Ferry, B., Lensi, R., Domenach, A. M., et al. (2008). Differing nitrogen use strategies of two tropical rainforest late successional tree species in French Guiana: Evidence from N-15 natural abundance and microbial activities. Soil Biol. Biochem., 40(2), 487–494.
Abstract: Previous studies in lowland tropical rainforests of French Guiana showed that, among non-N-2-fixing trees, two groups of late successional species contrasting in their leaf N-15 natural abundance coexist, suggesting two different main ways of nitrogen acquisition. Two abundant late-successional species typically co-occurring in rainforests in French Guiana, namely Eperua falcata and Dicorynia guianensis, were chosen as representative of each group. Stable isotope techniques and measurements of potentials of microbial N transformation were performed to assess to what extent leaf N-15 natural abundance of these species could be related to (i) delta N-15 signatures of soil mineral N sources and (ii) the capacity of soil to express nitrification and denitrification (both processes being directly involved in the balance between NH4+ and NO3-). Soil delta N-15-NH4+ was roughly similar to leaf delta N-15 of D. guianensis (around 3.5 parts per thousand), suggesting a preferential use of NH4+, whereas in E. falcata, leaf delta N-15 values were closer to root delta N-15-NO3- values (0.2 and -2.0 parts per thousand, respectively), suggesting a preferential use of NO3-. These differences in N source utilization were not accompanied by differences in availability in soil NO3- or in intensity of microbial functions responsible for soil N mineral evolution. However, (i) under both tree species, these functions showed clear spatial partitioning, with denitrification occurring potentially in soil and nitrification in the litter layer, and (ii) E falcata fine roots colonized the litter layer much more strongly than D. guianensis fine roots. This strongly suggests that (i) the contrasted leaf delta N-15 values found in the two late-successional species reveal distinct N acquisition strategies and (ii) the ability of roots to predominantly exploit the litter layer (E falcata) or the soil (D. guianensis) may constitute an important explanation of the observed differences. A complementarity between tree species, based on mineral N resource partitioning (itself resulting from a spatially structured location of the microbial functions responsible for the balance between NH4+ and NO3-), n thus be supposed. (c) 2007 Elsevier Ltd. All rights reserved.
Keywords: soil; litter; nitrate; nitrification; tree rooting; N-15; Eperua falcata; Dicorynia guianensis; tropical forest
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Herault, B. (2007). Reconciling niche and neutrality through the Emergent Group approach. Perspect. Plant Ecol. Evol. Syst., 9(2), 71–78.
Abstract: Both niche and neutral theories have been suggested as potential frameworks for modelling biodiversity. Niche models assume that biological traits represent evolutionary adaptations and define individuals in terms of functional trade-offs. Neutral models assume that all individuals at a single trophic level are functionally equivalent on a per capita basis with respect to their birth, death, dispersal and speciation. The opinion of many researchers is that neutral and niche processes operate simultaneously to generate diversity without knowing how the unification of both models can be achieved. Recently, several theoretical papers have reported evidence on the evolutionary emergence of niche structures shaping the emergence of groups of similar species. In this way, an Emergent Group is defined as a set of species that have a similar functional niche owing to a convergent ecological strategy. Central to the Emergent Group concept are the assumptions of functional equivalence within and of functional divergence between Emergent Groups. Within an Emergent Group, species richness is subject to a zero-sum rule set by the balance between the rate of individual loss and of immigration. Between Emergent Groups, tradeoffs such as seed size/seedling competitivity, investment in reproductive system/investment in vegetative systems or competitive ability/predator invulnerability are cornerstones of the evolutionary divergence. Delineating Emergent Groups amounts to reaching a compromise between maximizing niche differentiation (i.e. maximizing differences in functional tradeoffs) between Emergent Groups and maximizing neutrality within Emergent Groups. Up to now, the Emergent Group concept has been mostly proposed by theoretical scientists but it should be tested by empirical ecologists. The way in which niche and neutral models could be combined provides a profitable opportunity for theoretical and empirical scientists to collaborate fruitfully. (c) 2007 Rubel Foundation, ETH Zurich. Published by Elsevier GmbH. All rights reserved.
Keywords: Biodiversity; ecological equivalency; biological traits; neutral theory; niche differentiation; redundancy
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Jaouen, G., Almeras, T., Coutand, C., & Fournier, M. (2007). How to determine sapling buckling risk with only a few measurements. Am. J. Bot., 94(10), 1583–1593.
Abstract: Tree buckling risk (actual height/critical buckling height) is an important biomechanical trait of plant growth strategies, and one that contributes to species coexistence. To estimate the diversity of this trait among wide samples, a method that minimizes damage to the plants is necessary. On the basis of the rarely used, complete version of Greenhill's model (1881, Proceedings of the Cambridge Philosophical Society 4(2): 65-73), we precisely measured all the necessary parameters on a sample of 236 saplings of 16 species. Then, using sensitivity (variance) analysis, regressions between successive models for risk factors and species ranks and the use of these models on samples of self- and nonself-supporting saplings, we tested different degrees of simplification up to the most simple and widely used formula that assumes that the tree is a cylindrical homogeneous pole. The size factor had the greatest effect on buckling risk, followed by the form factor and the modulus of elasticity of the wood. Therefore, estimates of buckling risk must consider not only the wood properties but especially the form factor. Finally, we proposed a simple but accurate method of assessing tree buckling risk that is applicable to a wide range of samples and that requires mostly nondestructive measurements.
Keywords: biomechanics; critical buckling height; French Guiana; risk factor; sapling; stem form; tropical rain forest; trunk volume
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Rockwell, C. A., Kainer, K. A., Staudhammer, C. L., & Baraloto, C. (2007). Future crop tree damage in a certified community forest in southwestern Amazonia. For. Ecol. Manage., 242(2-3), 108–118.
Abstract: Field studies in Acre, Brazil assessed logging impacts of a certified community timber management project. The main objectives of the study were: (1) to determine if damage incidence to future crop trees (FCTs; >= 20 cm diameter at breast height (dbh)) differs between (a) forest with and without bamboo (Guadua spp.), and (b) trees with and without lianas; (2) to what extent harvesting can be conducted more intensely (m(3)ha(-1)), without incurring greater FCT damage; and (3) to what extent marking diminishes FCT damage. Full inventories of FCTs of 50 commercial species complexes were conducted before and after logging in 50 m-radius zones of impact around each designated harvest tree in three 10 ha (200 m x 500 m) logging blocks. We also mapped all forested areas potentially influenced by logging, including skid trails, log landings and felling gaps, throughout the 30 ha logged. More than 28% of the forest area was disturbed by logging, with 12.1% in skid trails and 16.8% in gap clearings, indicating that the forest gap mosaic can be significantly altered even when reduced-impact logging guidelines are followed. Overall, 15% of FCTs inventoried were damaged. Damage rates were not significantly reduced by marking treatment, location in bamboo-dominated forest, or liana load on FCT damage. Harvest intensity did not influence the probability of FCT damage. For future studies, it would be prudent to address impacts of timber extraction on other livelihood activities, such as non-timber forest product collection, particularly in such regions as the Brazilian Amazon, where many communities are attempting to integrate a suite of income-generating activities. (C) 2007 Elsevier B.V. All rights reserved.
Keywords: bamboo; community forest management; forest certification; Guadua; liana; marking; reduced-impact logging; RIL; timber management; tropical forest
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Yamamoto, H., & Almeras, T. (2007). A mathematical verification of the reinforced-matrix hypothesis using the Mori-Tanaka theory. J. Wood Sci., 53(6), 505–509.
Abstract: This article presents a theoretical verification of the reinforced-matrix hypothesis derived from tensor equations, σ W = σ f + σ m and ε W = ε f = ε m (Wood Sci Technol 32:171–182, 1998; Wood Sci Technol 33:311–325, 1999; J Biomech Eng 124:432–440, 2002), using classical Mori-Tanaka theory on the micromechanics of fiber-reinforced materials (Acta Metall 21:571–574, 1973; Micromechanics — dislcation and inclusions (in Japanese), pp 141–147, 1976). The Mori-Tanaka theory was applied to a small fragment of the cell wall undergoing changes in its physical state, such as those arising from sorption of moisture, maturation of wall components, or action of an external force, to obtain 〈σ A〉D = ϕ·〈σ F〉I + (1−ϕ)·〈σ M〉D−I. When the constitutive equation of each constituent material was applied to the equation 〈σ A〉D = ϕ·〈σ F〉I + (1−ϕ)·〈σ M〉D−I, the equations σ W = σ f + σ m and ε W = ε f = ε m were derived to lend support to the concept that two main phases, the reinforcing cellulose microfibril and the lignin-hemicellulose matrix, coexist in the same domain. The constitutive equations for the cell wall fragment were obtained without recourse to additional parameters such as Eshelby’s tensor S and Hill’s averaged concentration tensors AF and AM. In our previous articles, the coexistence of two main phases and σ W = σ f + σ m and ε W = ε f =ε m had been taken as our starting point to formulate the behavior of wood fiber with multilayered cell walls. The present article provides a rational explanation for both concepts.
Keywords: Engineering
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Luyssaert, S., Inglima, I., Jung, M., Richardson, A. D., Reichsteins, M., Papale, D., et al. (2007). CO2 balance of boreal, temperate, and tropical forests derived from a global database. Glob. Change Biol., 13(12), 2509–2537.
Abstract: Terrestrial ecosystems sequester 2.1 Pg of atmospheric carbon annually. A large amount of the terrestrial sink is realized by forests. However, considerable uncertainties remain regarding the fate of this carbon over both short and long timescales. Relevant data to address these uncertainties are being collected at many sites around the world, but syntheses of these data are still sparse. To facilitate future synthesis activities, we have assembled a comprehensive global database for forest ecosystems, which includes carbon budget variables (fluxes and stocks), ecosystem traits (e.g. leaf area index, age), as well as ancillary site information such as management regime, climate, and soil characteristics. This publicly available database can be used to quantify global, regional or biome-specific carbon budgets; to re-examine established relationships; to test emerging hypotheses about ecosystem functioning [e.g. a constant net ecosystem production (NEP) to gross primary production (GPP) ratio]; and as benchmarks for model evaluations. In this paper, we present the first analysis of this database. We discuss the climatic influences on GPP, net primary production (NPP) and NEP and present the CO2 balances for boreal, temperate, and tropical forest biomes based on micrometeorological, ecophysiological, and biometric flux and inventory estimates. Globally, GPP of forests benefited from higher temperatures and precipitation whereas NPP saturated above either a threshold of 1500 mm precipitation or a mean annual temperature of 10 degrees C. The global pattern in NEP was insensitive to climate and is hypothesized to be mainly determined by nonclimatic conditions such as successional stage, management, site history, and site disturbance. In all biomes, closing the CO2 balance required the introduction of substantial biome-specific closure terms. Nonclosure was taken as an indication that respiratory processes, advection, and non-CO2 carbon fluxes are not presently being adequately accounted for.
Keywords: carbon cycle; CO2; forest ecosystems; global database; gross primary productivity; net ecosystem productivity; net primary productivity
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Almeras, T., & Gril, J. (2007). Mechanical analysis of the strains generated by water tension in plant stems. Part 1: stress transmission from the water to the cell walls. Tree Physiol., 27(11), 1505–1516.
Abstract: Plant tissues shrink and swell in response to changes in water pressure. These strains can be easily measured, e.g., at the surface of tree stems, to obtain indirect information about plant water status and other physiological parameters. We developed a mechanical model to clarify how water pressure is transmitted to cell walls and causes shrinkage of plant tissues, particularly in the case of thick-walled cells such as wood fibers. Our analysis shows that the stress inside the fiber cell walls is lower than the water tension. The difference is accounted for by a stress transmission factor that depends on two main effects. The first effect is the dilution of the stress through the cell wall, because water acts at the lumen border and is transmitted to the cuter border of the cell, which has a larger circumference. The second effect is the partial conversion of radial stress into tangential stress. Both effects are quantified as functions of parameters of the cell wall structure and its mechanical properties.
Keywords: biomechanics; cell mechanics; diurnal strains; mechanical model; multilayer cylinder; stress transtnissionjactor
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LaPierre, L., Hespenheide, H., & Dejean, A. (2007). Wasps robbing food from ants: a frequent behavior? Naturwissenschaften, 94(12), 997–1001.
Abstract: Food robbing, or cleptobiosis, has been well documented throughout the animal kingdom. For insects, intrafamilial food robbing is known among ants, but social wasps (Vespidae; Polistinae) taking food from ants has, to the best of our knowledge, never been reported. In this paper, we present two cases involving social wasps robbing food from ants associated with myrmecophytes. (1) Polybioides tabida F. (Ropalidiini) rob pieces of prey from Tetraponera aethiops Smith (Formicidae; Pseudomyrmecinae) specifically associated with Barteria fistulosa Mast. (Passifloraceae). (2) Charterginus spp. (Epiponini) rob food bodies from myrmecophytic Cecropia (Cecropiaceae) exploited by their Azteca mutualists (Formicidae; Dolichoderinae) or by opportunistic ants (that also attack cleptobiotic wasps). We note here that wasps gather food bodies (1) when ants are not yet active; (2) when ants are active, but avoiding any contact with them by flying off when attacked; and (3) through the coordinated efforts of two to five wasps, wherein one of them prevents the ants from leaving their nest, while the other wasps freely gather the food bodies. We suggest that these interactions are more common than previously thought.
Keywords: cleptobiosis; social wasps; charterginus; polybioides; plant-ants
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Schimann, H., Joffre, R., Roggy, J. C., Lensi, R., & Domenach, A. M. (2007). Evaluation of the recovery of microbial functions during soil restoration using near-infrared spectroscopy. Appl. Soil Ecol., 37(3), 223–232.
Abstract: Microbial-based indicators, such as C and N contents or microbial functions involved in C and N cycles, are currently used to describe the status of soils in disturbed areas. Microbial functions are more accurate indicators but their measurement for studies at the ecosystem level remains problematical because of the huge spatial variability of these processes and, consequently, of the large number of soil samples which must be analyzed. Our goal was to test the capacity of near-infrared reflectance spectroscopy (NIRS) to predict respiration and denitrification but also carbon and nitrogen contents of soils submitted to various procedures of restoration. To achieve this objective, we took advantage of an experiment conducted on a reforestation system established after open-cast gold mining in French Guiana. In this experimental station, plantations of various ages and various soil textures were at our disposal. Our results showed that both plantations and soil texture had a strong impact on the recovery of soil functioning: carbon and nitrogen contents, respiration and denitrification increased with age of plantation and clay content. Calibrations were performed between spectral data and microbial-based indicators using partial least squares regression (PLS). The results showed that C and N contents were accurately predicted. Microbial functions were less precisely predicted with results more accurate on clayey soils than on sandy soils. In clayey soils, perturbed or restored soils and the year of plantation were discriminated very efficiently through principal component analyses of spectral signatures (over 80% of variance explained on the first two axes). Near-infrared spectroscopy may thus be extended to the prediction of functional soil parameters, but the capacity of this method must be strengthened by expending the databases with other soils in other contexts. The possibility of using NIRS provides many opportunities for understanding both the temporal dynamics and the spatial variability of the recovery of key microbial functions during soil restoration. (c) 2007 Elsevier B.V. All rights reserved.
Keywords: NIRS; microbial activities; respiration; denitrification; carbon; nitrogen; soil functioning; restoration
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Fang, C. H., Clair, B., Gril, J., & Almeras, T. (2007). Transverse shrinkage in G-fibers as a function of cell wall layering and growth strain. Wood Sci. Technol., 41(8), 659–671.
Abstract: Transverse drying shrinkage was measured at microscopic and mesoscopic levels in poplar wood characterised by an increasing growth strain (GS), from normal to tension wood. Results show that: (a) the drying shrinkage, measured as a relative thickness decrease, was significantly higher for G-layer (GL) than for the other layers (OL), GL shrinkage was not significantly correlated with GS, and OL shrinkage was negatively correlated with GS. (b) In gelatinous fibre (G-fibre), lumen size increased during drying and this increase was positively related with GS, but in normal wood fibre, lumen size decreased during drying. These findings suggest that GL shrank outwards (i.e., its internal perimeter increases), so that its shrinkage weakly affected the total cell shrinkage and the mesoscopic shrinkage was controlled by the OL shrinkage which shrank inwards (i.e., its external perimeter decreases). (c) Measurements done on 7 x 7 mm(2) thin sections evidenced a negative correlation between transverse shrinkage and GS, significant in T direction but weak in R direction. These observations at both levels allow to discuss the contribution of GL to the mesoscopic shrinkage of tension wood.
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