Drought exerts a strong influence on tropical forest metabolism, carbon stocks, and ultimately the flux of carbon to the atmosphere. Satellite-based studies have suggested that Amazon forests green up during droughts because of increased sunlight, whereas field studies have reported increased tree mortality during severe droughts. In an effort to reconcile these apparently conflicting findings, we conducted an analysis of climate data, field measurements, and improved satellite-based measures of forest photosynthetic activity. Wet-season precipitation and plant-available water (PAW) decreased over the Amazon Basin from 1996−2005, and photosynthetically active radiation (PAR) and air dryness (expressed as vapor pressure deficit, VPD) increased from 2002-2005. Using improved enhanced vegetation index (EVI) measurements (2000)(2001)(2002)(2003)(2004)(2005)(2006)(2007)(2008), we show that gross primary productivity (expressed as EVI) declined with VPD and PAW in regions of sparse canopy cover across a wide range of environments for each year of the study. In densely forested areas, no climatic variable adequately explained the Basin-wide interannual variability of EVI. Based on a site-specific study, we show that monthly EVI was relatively insensitive to leaf area index (LAI) but correlated positively with leaf flushing and PAR measured in the field. These findings suggest that production of new leaves, even when unaccompanied by associated changes in LAI, could play an important role in Basin-wide interannual EVI variability. Because EVI variability was greatest in regions of lower PAW, we hypothesize that drought could increase EVI by synchronizing leaf flushing via its effects on leaf bud development.drought | enhanced vegetation index | moderate-resolution imaging spectroradiometer | tropical | carbon cycling
Large-scale wildfires are expected to accelerate forest dieback in Amazô nia, but the fire vulnerability of tree species remains uncertain, in part due to the lack of studies relating fire-induced mortality to both fire behavior and plant traits. To address this gap, we established two sets of experiments in southern Amazonia. First, we tested which bark traits best predict heat transfer rates (R) through bark during experimental bole heating. Second, using data from a large-scale fire experiment, we tested the effects of tree wood density (WD), size, and estimated R (inverse of cambium insulation) on tree mortality after one to five fires. In the first experiment, bark thickness explained 82% of the variance in R, while the presence of water in the bark reduced the difference in temperature between the heat source and the vascular cambium, perhaps because of high latent heat of vaporization. This novel finding provides an important insight for improving mechanistic models of fire-induced cambium damage from tropical to temperate regions. In the second experiment, tree mortality increased with increasing fire intensity (i.e. as indicated by bark char height on tree boles), which was higher along the forest edge, during the 2007 drought, and when the fire return interval was 3 years instead of one. Contrary to other tropical studies, the relationship between mortality and fire intensity was strongest in the year following the fires, but continued for 3 years afterwards. Tree mortality was low ( 20%) for thick-barked individuals ( ! 18 mm) subjected to medium-intensity fires, and significantly decreased as a function of increasing tree diameter, height and wood density. Hence, fire-induced tree mortality was influenced not only by cambium insulation but also by other traits that reduce the indirect effects of fire. These results can be used to improve assessments of fire vulnerability of tropical forests.
The effect of Ca and phytase on phytate phosphorus (PP) hydrolysis was studied in vitro and in vivo. In vitro, PP hydrolysis by a 3-phytase and a 6-phytase was studied at pH 2.5 and 6.5 with Ca added at levels equivalent to 0, 0.1, 0.2, 0.4, 0.7, or 0.9% of the diet. Irrespective of enzyme, Ca at a level as low as 0.1% reduced (P < 0.05) PP hydrolysis at pH 6.5. To test these effects in vivo, 22-d-old male broilers were fed 1 of 6 diets (10 replicate pens of 4 birds per diet) for 30 h. The experimental design was a 3 x 2 factorial arrangement of 3 phytase treatments (0, 500 U of phytase A/kg of diet, and 500 U of phytase B/kg of diet) and 2 added Ca levels (0 and 0.5% from CaCO3) to a corn-soy basal diet. Adding Ca to the diet resulted in a reduction (P < 0.05) in ileal PP disappearance from 69.2 to 25.4% when the 0 and 0.5% added Ca diets were fed, respectively, and in apparent ileal Ca and P absorption (46.3 to 33.6% and 67.9 to 29.4% when 0 and 0.5% Ca were added, respectively). Inclusion of a 3-phytase improved (P < 0.05) ileal PP disappearance from 25.4 to 58.9% in diets containing 0 and 0.5% added Ca, but the improvement was less pronounced with a 6-phytase. Apparent ileal Ca absorption was improved (P < 0.05) when Ca, phytase, or both were added to the diet.
We assembled a list of obligate cave‐dwelling species and subspecies, their county distribution, and their provisional global conservation rank. A total of 927 species and 46 additional subspecies in 96 families exclusively from cave and associated subterranean habitats have been described in the 48 contiguous states of the United States. The terrestrial (troglobitic) species are concentrated in northeast Alabama (especially Jackson County), with other concentrations in Kentucky, Texas, Virginia, and West Virginia. Only 23 counties, comprising less than 1% of the land area of the 48 contiguous states, account for over 50% of the terrestrial species and subspecies. The aquatic (stygobitic) species are concentrated in Hays County, Texas, with other concentrations in Florida, Oklahoma, Texas, Virginia, and West Virginia. Only 18 counties, comprising less than 1% of the land area, account for over 50% of the aquatic species and subspecies. Endemism is high, with 54% of the species known from a single county. Approximately 95% of the species are listed by The Nature Conservancy as vulnerable or imperiled in the United States. These cave species comprise 50% of all vulnerable or imperiled species listed in databases of the Natural Heritage Program. Less than 4% of these subterranean species have federal status. Conservation can best be accomplished through habitat protection, which must include protection of the associated surface habitat.
Aim Over 250 species of obligate terrestrial cave‐dwelling animals (troglobionts) are known from single caves in the eastern United States. We investigate their geographical distribution, especially in relation to other troglobionts. We relate these patterns to taxonomic group, opportunities for dispersal and geographical location. Location Caves of the United States east of the Mississippi River. Methods We associated over 3000 records of more than 450 troglobiotic species and subspecies with hexagons of 1000, 5000 and 10,000 km2 in size. We calculated Moran's I, black–white joins and cubic regression of endemics on non‐endemics at all three spatial scales. For 5000 km2 hexagons, we modelled the spatial autocorrelation of the residuals of the cubic regression of endemics on non‐endemics. Results Differences among orders in percentage single‐cave endemism were not significant, except for Pseudoscorpionida, which was higher (69%) than any other order. At all three scales, Moran's I and black–white joins were significant, indicating a clumped distribution of both single‐cave endemics and other troglobionts. Spatial patterns were similar at all three scales and Moran's I was highest at 5000 km2. The cubic fit of endemics to non‐endemics was consistently better, with less systematic error or residuals, than were linear or quadratic models. Residuals showed a significant geographical pattern with excess endemics in more southerly locations. Main conclusions There was both a non‐spatial and spatial component to the pattern of single‐cave endemism. The non‐spatial component was the association of high levels of single‐cave endemism with areas of high diversity of non‐endemics. It may be that both are high because of high secondary productivity. Spatially, single‐cave endemism is high in central rather than peripheral areas and in the southern part of the range. It is not higher in areas of more dissected limestone, which would reduce migration rates; if anything endemism is lower. Regional spatial effects are important, indicating that cave communities cannot be understood (or protected) in isolation.
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