Stem straightness is an important selection trait in Pinus pinaster Ait. breeding programs. Despite the stability of stem straightness rankings in provenance trials, the efficiency of breeding programs based on a quantitative index of stem straightness remains low. An alternative approach is to analyze biomechanical processes that underlie stem form. The rationale for this selection method is that genetic differences in the biomechanical processes that maintain stem straightness in young plants will continue to control stem form throughout the life of the tree. We analyzed the components contributing most to genetic differences among provenances in stem straightening processes by kinetic analysis and with a biomechanical model defining the interactions between the variables involved (Fournier's model). This framework was tested on three P. pinaster provenances differing in adult stem straightness and growth. One-year-old plants were tilted at 45 degrees, and individual stem positions and sizes were recorded weekly for 5 months. We measured the radial extension of reaction wood and the anatomical features of wood cells in serial stem cross sections. The integral effect of reaction wood on stem leaning was computed with Fournier's model. Responses driven by both primary and secondary growth were involved in the stem straightening process, but secondary-growth-driven responses accounted for most differences among provenances. Plants from the straight-stemmed provenance showed a greater capacity for stem straightening than plants from the sinuous provenances mainly because of (1) more efficient reaction wood (higher maturation strains) and (2) more pronounced secondary-growth-driven autotropic decurving. These two process-based traits are thus good candidates for early selection of stem straightness, but additional tests on a greater number of genotypes over a longer period are required.

International audienceKey messageWe present a comprehensive database of 478 allometric equations to estimate biomass of trees and other life forms in Mexican forest and scrubland ecosystems.ContextAccurate estimation of standing biomass in forests is a prerequisite for any approach to carbon storage and a number of additional applications.AimsTo provide a comprehensive database with allometric equations applicable to a large number of tree and shrub species of Mexico.MethodsAn intensive literature search was carried out to pull together all publications related to allometric equations in the libraries of the most important forest research institutes across Mexico and the neighboring countries.ResultsA total of 478 equations were compiled. Four hundred fourteen equations included a detailed analysis of all compartments of the trees; 7 equations applied to shrubs, 15 to bamboos, and 2 to palms. The collected equations are applicable to a wide variety of forest ecosystems in Mexico ranging from desert scrublands in the North to lowland evergreen rainforests in the South. The attached database of allometric equations is possibly the most extensive compilation of equations currently available for Mexico.ConclusionThe database covers almost 100 % of the individuals recorded in the National Forest Inventory

Deforestation of tropical forests for the establishment of grass monoculture for livestock production is responsible for about 30 % of CO 2 emissions. This issue is particularly severe in degraded pastures because degraded soils favor CO 2 flow to the soil surface. Silvopastoral systems could reduce CO 2 emissions, notably by using live fences. Here, we hypothesized that live fences of Gliricidia sepium in livestock systems should reduce variations in environmental relative humidity and soil temperature and, in turn, reduce soil CO 2 emissions. Here, we studied two livestock systems: (1) grass monoculture of Brachiaria decumbens with live fences of G. sepium and (2) grass monoculture of B. decumbens without live fences. We measured soil CO 2 seasonal emissions at different times of the day, soil temperature, and environmental relative humidity. Nine 600-m 2 plots were established in each system. All variables were measured over four 6-h period during a 24-h period, twice a month from April to September. Our results show that soil CO 2 emissions showed less variability with G. septum live fences than without live fences. This lower variability is explained by the creation of a microclimate with a higher and more stable environmental relative humidity, provided by the shade of trees. Results also show, however, that global soil CO 2 emissions did not differ between the two systems, with and without live fence. Moreover, soil CO 2 emissions varied according to season, as shown by 1.082 g CO 2 m −2 h −1 in the wet season versus 0.871 g CO 2 m −2 h −1 in the dry season. Soil CO 2 emissions varied also according to sampling time, as shown by 1.116 g CO 2 m −2 h −1 in the night versus 0.960 CO 2 m −2 h −1 in the morning.

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