Reduced Rainfall Increases Metabolic Rates in Upper Mixed Layers of Tropical Lakes

Ecosystems - Ecosystem-level metabolism is a good sentinel for human and natural disturbances in freshwater systems, responding from local changes (for example, land use) to regional and global...     

Invasive Temperate Species are a Threat to Tropical Island Biodiversity

To protect the remaining biodiversity on tropical islands it is important to predict the elevational ranges of non-native species. We evaluated two hypotheses by examining land snail faunas on the eastern (windward) side of the island of Hawaii: (1) the latitude of a species' native region can be used to predict its potential elevational range and (2) non-native temperate species, which experience greater climatic fluctuations in their native range, are more likely to become established at higher elevations and to extend over larger elevational ranges than non-native tropical species. All non-native tropical species were distributed patchily among sites ≤500 m and occupied small elevational ranges, whereas species introduced from temperate regions occupied wide elevational ranges and formed a distinct fauna spanning elevations 500–2000 m. Most native land snail species and ecosystems occur >500 m in areas dominated by temperate non-native snail and slug species. Therefore, knowing the native latitudinal region of a non-native species is important for conservation of tropical island ecosystems because it can be translated into potential elevational range if those species are introduced. Because temperate species will survive in tropical locales particularly at high elevation, on many tropical islands the last refuges of the native species, preventing introduction of temperate species should be a conservation priority.     

Relative Importance of Vital Rates to Population Dynamics of Wood Ducks

The wood duck (Aix sponsa) is a common and important cavity-nesting duck in North America; however, we know very little about how changes in vital rates influence population growth rate (λ). We used estimates of fertility and survival of female wood ducks from our nest-box studies in South Carolina, Alabama, and Georgia, USA, to create a stage-based matrix population model. We conducted perturbation analyses and ranked elasticity values to examine the relative importance of 17 component vital rates to λ. Female survival is influenced by nest success, so we recognized this female heterogeneity in our analyses. Four vital rates showed the greatest importance to λ. Analytic elasticities were greatest for breeding season and nonbreeding season survival of females that nested successfully, followed by nest success and female recruitment to the breeding population. Differences in female quality were important to λ. Next, we used process variation of vital rates and conducted life-stage simulation analyses (LSA) followed by variance decomposition to determine the amount of variation in λ explained by each vital rate. Female recruitment to the breeding population explained 57.7% of the variation in λ followed by nest success (11.4%), and breeding and nonbreeding season survival of females that nested successfully (9.3% and 9.4%, respectively). Together these 4 vital rates explained 88% of the variation in λ. Mean asymptotic population growth rate (λ = 0.80 ± 0.08 [SD]) from LSA revealed a declining population. Recruitment of females hatched from nest boxes was insufficient to sustain the nest-box population. However, including yearling (SY) females that were produced outside of nest boxes (i.e., immigrants) increased recruitment rates 1.5 to 2 times more than when only SY females recruited from nest boxes were included. Future research that examines how emigration and immigration interact with survival and reproduction to influence local population dynamics of wood ducks will be important for identifying the value of nest-box programs to wood duck conservation and management. © 2019 The Wildlife Society.     

Nasal Discs and the Vital Rates of Lesser Scaup

Nasal discs have been used to identify ducks in studies of survival and reproduction. To date, there has not been a comprehensive assessment of nasal-disc effects on the vital rates of wild ducks. We applied nasal discs to 603 juvenile and 784 adult lesser scaup (Aythya affinis) females from a population breeding in southwest Montana, USA, and released 1,399 juvenile and 71 adult females wearing only metal leg bands between June 2005 and September 2016. Using resighting, recapture, and hunter-recovery data collected from those individuals, we estimated survival and recovery probability with multistate capture-recapture models in Program MARK. We also assessed if recovery distance from our study site and pre-breeding and brood-rearing body condition were diminished for females wearing nasal discs. Model-averaged survival probabilities were 0.231 ± 0.035 (SE) for juveniles and 0.482 ± 0.019 for adults released with nasal discs. Survival was 1.8–3.4 times higher for females released with metal leg bands when compared to those released with nasal discs; survival of these juveniles was 0.433 ± 0.049 and 0.693 ± 0.039 for adults. We did not find evidence for recovery probability or recovery distance varying between females that wore nasal discs and those that did not. During the pre-breeding and brood-rearing seasons, we did not find females wearing nasal discs to be in lower body condition when compared to unmarked females. Our comprehensive assessment of nasal discs on wild lesser scaup suggests that survival probabilities estimated from nasal-marked study populations should be cautiously interpreted as minimum estimates. © 2021 The Wildlife Society.     

Growth of Juvenile Centropomus undecimalis in a Tropical Island

Age, growth rates and hatching dates were determined for juvenile common snook, Centropomus undecimalis, collected in several Puerto Rican estuarine systems. Two growth models (von Bertalanffy and power curve) were used and compared based on the fitting, the residual distribution and homogeneity of variances. A multiple linear regression was also fit to predict age from otolith weight, fish weight and standard length. Hatching dates back-calculated from age estimates, suggested that spawning occurs throughout the year but peaks from May to October. Early juveniles (age < 100d) recruited during the wet season (August to November) showed a significantly higher growth rate (0.67mmd^–1) than the dry season (December to July) recruits (0.41mmd^–1). These results are compared with snook collected in west Florida.     

Vegetation Structure,Composition, and Species Richness Across a 56‐year Chronosequence of Dry Tropical Forest on Providencia Island,Colombia1

We compared vegetation structure and species richness across a 56‐yr chronosequence of six replicated age classes of dry tropical forest on the island of Providencia, Colombia, in the Southwest Caribbean. Stand age classes were determined using sequential, orthorectified panchromatic aerial photos acquired between 1944 and 1996 and Landsat 7 ETM + satellite imagery from 2000. Along the chronosequence we established 59 plots of 2 × 50 m (0.01 ha) to document changes in species richness, basal area, tree height, stem density, and sprouting ability. All woody trees and shrubs >2.5 cm diameter at breast height (DBH) were censused and measured. Although woody species density reached a peak in stands from 32 to 56 yr old, rarefaction analysis showed that species richness increased linearly with stand age and was highest in stands 56 yr old or greater. Nonparametric, abundance‐based estimators of species richness also showed positive and linear associations with age. Basal area and mean tree height were positively associated with age since abandonment, while sprouting ability showed a negative relationship. Our results indicate rapid recovery of woody species richness and structural characteristics along this tropical dry forest chronosequence.     

Linking White-Tailed Deer Density,Nutrition, and Vegetation in a Stochastic Environment

Density-dependent behavior underpins white-tailed deer (Odocoileus virginianus) theory and management application in North America, but strength or frequency of the phenomenon has varied across the geographic range of the species. The modifying effect of stochastic environments and poor-quality habitats on density-dependent behavior has been recognized for ungulate populations around the world, including white-tailed deer populations in South Texas, USA. Despite the importance of understanding mechanisms influencing density dependence, researchers have concentrated on demographic and morphological implications of deer density. Researchers have not focused on linking vegetation dynamics, nutrition, and deer dynamics. We conducted a series of designed experiments during 2004–2012 to determine how strongly white-tailed deer density, vegetation composition, and deer nutrition (natural and supplemented) are linked in a semi-arid environment where the coefficient of variation of annual precipitation exceeds 30%. We replicated our study on 2 sites with thornshrub vegetation in Dimmit County, Texas. During late 2003, we constructed 6 81-ha enclosures surrounded by 2.4-m-tall woven wire fence on each study site. The experimental design included 2 nutrition treatments and 3 deer densities in a factorial array, with study sites as blocks. Abundance targets for low, medium, and high deer densities in enclosures were 10 deer (equivalent to 13 deer/km²), 25 deer (31 deer/km²), and 40 deer (50 deer/km²), respectively. Each study site had 2 enclosures with each deer density. We provided deer in 1 enclosure at each density with a high-quality pelleted supplement ad libitum, which we termed enhanced nutrition; deer in the other enclosure at each density had access to natural nutrition from the vegetation. We conducted camera surveys of deer in each enclosure twice per year and added or removed deer as needed to approximate the target densities. We maintained >50% of deer ear-tagged for individual recognition. We maintained adult sex ratios of 1:1–1:1.5 (males:females) and a mix of young and older deer in enclosures. We used reconstruction, validated by comparison to known number of adult males, to make annual estimates of density for each enclosure in analysis of treatment effects. We explored the effect of deer density on diet composition, diet quality, and intake rate of tractable female deer released into low- and high-density enclosures with natural nutrition on both study sites (4 total enclosures) between June 2009 and May 2011, 5 years after we established density treatments in enclosures. We used the bite count technique and followed 2–3 tractable deer/enclosure during foraging bouts across 4 seasons. Proportion of shrubs, forbs, mast, cacti, and subshrubs in deer diets did not differ (P > 0.57) between deer density treatments. Percent grass in deer diets was higher (P = 0.05) at high deer density but composed only 1.3 ± 0.3% (SE) of the diet. Digestible protein and metabolizable energy of diets were similar (P > 0.45) between deer density treatments. Likewise, bite rate, bite size, and dry matter intake did not vary (P > 0.45) with deer density. Unlike deer density, drought had dramatic (P ≤ 0.10) effects on foraging of tractable deer. During drought conditions, the proportion of shrubs and flowers increased in deer diets, whereas forbs declined. Digestible protein was 31%, 53%, and 54% greater (P = 0.06) during non-drought than drought during autumn, winter, and spring, respectively. We studied the effects of enhanced nutrition on the composition and quality of tractable female deer diets between April 2007 and February 2009, 3 years after we established density treatments in enclosures. We also estimated the proportion of supplemental feed in deer diets. We used the 2 low-density enclosures on each study site, 1 with enhanced nutrition and 1 with natural nutrition (4 total enclosures). We again used the bite count technique and 2–3 tractable deer living in each enclosure. We estimated proportion of pelleted feed in diets of tractable deer and non-tractable deer using ratios of stable isotopes of carbon. Averaged across seasons and nutrition treatments, shrubs composed a majority of the vegetation portion of deer diets (44%), followed by mast (26%) and forbs (15%). Enhanced nutrition influenced the proportion of mast, cacti, and flowers in the diet, but the nature and magnitude of the effect varied by season and year. The trend was for deer in natural-nutrition enclosures to eat more mast. We did not detect a statistical difference (P = 0.15) in the proportion of shrubs in diets between natural and enhanced nutrition, but deer with enhanced nutrition consumed 7–24% more shrubs in 5 of 8 seasons. Deer in enhanced-nutrition enclosures had greater (P = 0.03) digestible protein in their overall diet than deer in natural-nutrition enclosures. The effect of enhanced nutrition on metabolizable energy in overall diets varied by season and was greater (P < 0.04) for enhanced-nutrition deer during summer and autumn 2007 and winter 2008. In the enhanced-nutrition treatment, supplemental feed averaged 47–80% of the diet of tractable deer. Of non-tractable deer in all density treatments with enhanced nutrition, 97% (n = 128 deer) ate supplemental feed. For non-tractable deer averaged across density treatments, study sites, and years, percent supplemental feed in deer diets exceeded 70% for all sex and age groups. We determined if increasing deer density and enhanced nutrition resulted in a decline in preferred forbs and shrubs and an increase in plants less preferred by deer. We sampled all 12 enclosures via 20, 50-m permanent transects in each enclosure. Percent canopy cover of preferred forbs was similar (P = 0.13) among deer densities averaged across nutrition treatments and sampling years (low density: = 8%, SE range 6–10; medium density: 5%, 4–6; high density: 4%, 3–5; SE ranges are presented because SEs associated with backtransformed means are asymetrical). Averaged across deer densities, preferred forb canopy cover was similar between nutrition treatments in 2004; but by 2012 averaged 20 ± 17–23% in enhanced-nutrition enclosures compared to 10 ± 8–13% in natural-nutrition enclosures (P = 0.107). Percent canopy cover of other forbs, preferred shrubs, other shrubs, and grasses, as well as Shannon's index, evenness, and species richness were similar (P > 0.10) among deer densities, averaged across nutrition treatments and sampling years. We analyzed fawn:adult female ratios, growth rates of fawns and yearlings, and survival from 6 to 14 months of age and for adults >14 months of age. We assessed adult body mass and population growth rates (lambda apparent, λ_APP) to determine density and nutrition effects on deer populations in the research enclosures during 2004–2012. Fawn:adult female ratios declined (P = 0.04) from low-medium density to high density in natural-nutrition enclosures but were not affected (P = 0.48) by density in enhanced nutrition enclosures although, compared to natural nutrition, enhanced nutrition increased fawn:adult female ratios by 0.15 ± 0.12 fawns:adult female at low-medium density and 0.44 ± 0.17 fawns:adult female at high density. Growth rate of fawns was not affected by deer density under natural or enhanced nutrition (P > 0.17) but increased 0.03 ± 0.01 kg/day in enhanced-nutrition enclosures compared to natural nutrition (P < 0.01). Growth rate of yearlings was unaffected (P > 0.71) by deer density, but growth rate increased for males in some years at some density levels in enhanced-nutrition enclosures. Adult body mass declined in response to increasing deer density in natural-nutrition enclosures for both adult males (P < 0.01) and females (P = 0.10). Enhanced nutrition increased male body mass, but female mass did not increase compared to natural nutrition. Survival of adult males was unaffected by deer density in natural- (P = 0.59) or enhanced- (P = 0.94) nutrition enclosures. Survival of adult females was greatest in medium-density enclosures with natural nutrition but similar at low and high density (P = 0.04). Enhanced nutrition increased survival of females (P < 0.01) and marginally for males (P = 0.11). Survival of fawns 6–14 months old was unaffected (P > 0.35) by density in either natural- or enhanced-nutrition treatments but was greater (P = 0.04) under enhanced nutrition. Population growth rate declined (P = 0.06) with increasing density in natural-nutrition enclosures but not (P = 0.55) in enhanced nutrition. Enhanced nutrition increased λ_APP by 0.32. Under natural nutrition, we found only minor effects of deer density treatments on deer diet composition, nutritional intake, and plant communities. However, we found density-dependent effects on fawn:adult female ratios, adult body mass, and population growth rate. In a follow-up study, deer home ranges in our research enclosures declined with increasing deer density. We hypothesized that habitat quality varied among home ranges and contributed to density-dependent responses. Variable precipitation had a greater influence on deer diets, vegetation composition, and population parameters than did deer density. Also, resistance to herbivory and low forage quality of the thornshrub vegetation of our study sites likely constrained density-dependent behavior by deer. We posit that it is unlikely that, at our high-density (50 deer/km²) and perhaps even medium-density (31 deer/km²) levels, negative density dependence would occur without several wet years in close association. In the past century, this phenomenon has only happened once (1970s). Thus, density dependence would likely be difficult to detect in most years under natural nutrition in this region. Foraging by deer with enhanced nutrition did not result in a reduction in preferred plants in the vegetation community and had a protective effect on preferred forbs because ≤53% of deer diets consisted of vegetation. However, enhanced nutrition improved fitness of individual deer and deer populations, clearly demonstrating that nutrition is limiting for deer populations under natural conditions in western South Texas. © 2019 The Authors. Wildlife Monographs published by Wiley Periodicals, Inc. on behalf of The Wildlife Society.     

海南岛尖峰岭热带植被类型垂直分布与水热状况

本文阐述了海南岛尖峰岭各植被类型特征及分布,其分布是决定海拔与水热状况的变化。文中试用气候指标确立我国热带地区植被类型随海拔变化的模式,建立了指数、线性方程。本研究的目的在于加深对我国热带植被类型生境特点的认识,对合理利用和经营,起到应有的作用。     

Modeled Effects of Climate Change and Plant Invasion on Watershed Function Across a Steep Tropical Rainfall Gradient

Climate change is anticipated to affect freshwater resources, but baseline data on the functioning of tropical watersheds is lacking, limiting efforts that seek to predict how watershed processes, water supply, and streamflow respond to anticipated changes in climate and vegetation change, and to management. To address this data gap, we applied the distributed hydrology soil vegetation model (DHSVM) across 88 watersheds spanning a highly constrained, 4500 mm mean annual rainfall (MAR) gradient on Hawai‘i Island to quantify stream flow at 3-h time-steps for eight years in response to the independent and interactive effects of (1) large observed decrease in MAR; (2) projected warming and altered precipitation; and (3) four scenarios of forest invasion by the high water-demanding non-native tree species Psidium cattleianum. The model captured 62% of variability in measured flow at daily time scales, 95% at monthly time scales, and 98% at annual time scales. We found that low DHSVM modeled flow (Q ₉₀) and storm flow (Q ₁₀) responses to observed declines in rainfall dwarfed those of projected temperature increase or invasion, with flow decline positively correlated with MAR. As a percentage of streamflow, temperature and invasion reductions were negatively correlated with MAR. By comparison, warming alone had little effect on Q ₉₀ or Q ₁₀, but both decreased with increasing P. cattleianum cover, and projected effects of declining MAR were accentuated when combined with P. cattleianum and warming. Restoration mitigated some effects of climate warming by increasing stream base flows, with the relative effects of restoration being larger in drier versus wetter watersheds. We conclude that potential changes in climate in tropical environments are likely to exert significant effects on streamflow, but managing vegetation can provide mitigating benefits.     

西沙群岛主要岛屿不同植被类型对土壤理化性质的影响

为了解海岛植被恢复过程中植物群落对土壤理化性质的影响,对西沙群岛的永兴岛和东岛上不同植被群落的土壤主要理化性质进行测定。结果表明,随着岛屿植被由藤草经灌木向乔木群落的过渡,土壤含水量由5.9%显著升高至14.2%;土壤微生物生物量碳、生物量氮分别由176.2和41.2 mg kg~(-1)显著升高至391.5和98.8 mg kg~(-1);而pH呈下降趋势。这表明随着植被的恢复,海岛土壤质量不断提高,生态系统渐趋稳定。     

Low Redox Decreases Potential Phosphorus Limitation on Soil Biogeochemical Cycling Along a Tropical Rainfall Gradient

Ecosystems - Humid tropical forests on highly weathered soils are often characterized by low bioavailable phosphorus (P) concentrations. These ecosystems also often experience low and fluctuating...     

Occurrence of Plant Growth Inhibitors in Tropical and Subtropical Vegetation

Acetone, ethanol and water extracts of mature fruits of yaupon (llex vomitoria Ait.) inhibited germination of mesquite (Prosopis juliflora Swartz DC. var. glandulosa (Torr.) Cockerell and sorghum (Sorghum bicolor (L.) Moench). Extracts of guava fruit (Psidium guajava L.) inhibited cucumber (Cucumis sativus L.) seed germination. Water soluble inhibitors were found in fruits, leaves, roots and bark of several tropical species representing 10 different families. Strong inhibition of cucumber seed germination and growth did not occur in sand when water extracts containing inhibitors were applied. Growth of corn, sorghum, cucumber and bean was reduced in soils collected beneath Malay apple (Eugenia malaccensis L.) trees. Plant growth-inhibitors occurred in all species studied in various plant parts, and some apparently affect the growth and ecology of other plant species.     

The Effect of Macroinvertebrate Exclusion on Leaf Breakdown Rates in a Tropical Headwater Stream1

The role of macroinvertebrates in the process of leaf breakdown is well studied in temperate streams, but less is known about their role in the tropics. We investigated the effect of reducing macroinvertebrate access to leaf material on leaf breakdown rates in a forested headwater stream in the Luquillo Experimental Forest, Puerto Rico. We measured leaf mass loss using fine and coarse mesh bags over 12 weeks for two common riparian species: Cecropia schreberiana (Moraceae) and Dacryodes excelsa (Burseraceae). Coarse mesh allowed freshwater shrimp and other macroinvertebrates to access leaf material, while fine mesh did not. Leaf breakdown rates did not differ between C. schreberiana and D. excelsa in coarse mesh bags (?0.0375/day vs. ?0.0395/day, respectively), but C. schreberiana breakdown was significantly slower than D. excelsa in fine mesh bags (?0.0159/day vs. ?0.0266/day). Additionally, breakdown in fine mesh bags was significantly slower compared to coarse mesh bags for C. schreberiana, but less so for D. excelsa. Breakdown rates for all treatments were fast relative to those in temperate‐zone streams indicating that both macroinvertebrates and macroinvertebrate‐independent processing can strongly influence leaf decomposition in tropical streams. The difference between C. schreberiana and D. excelsa indicates that the effect of macroinvertebrate exclusion can change with leaf type.     

Soil Bacterial Community Shift Correlated with Change from Forest to Pasture Vegetation in a Tropical Soil

The change in vegetative cover of a Hawaiian soil from forest to pasture led to significant changes in the composition of the soil bacterial community. DNAs were extracted from both soil habitats and compared for the abundance of guanine-plus-cytosine (G+C) content, by analysis of abundance of phylotypes of small-subunit ribosomal DNA (SSU rDNA) amplified from fractions with 63 and 35% G+C contents, and by phylogenetic analysis of the dominant rDNA clones in the 63% G+C content fraction. All three methods showed differences between the forest and pasture habitats, providing evidence that vegetation had a strong influence on microbial community composition at three levels of taxon resolution. The forest soil DNA had a peak in G+C content of 61%, while the DNA of the pasture soil had a peak in G+C content of 67%. None of the dominant phylotypes found in the forest soil were detected in the pasture soil. For the 63% G+C fraction SSU rDNA sequence analysis of the three most dominant members revealed that their phyla changed from Fibrobacter and Syntrophomonas assemblages in the forest soil to Burkholderia and Rhizobium–Agrobacterium assemblages in the pasture soil.     

Tracking Human Disturbance in Mangroves: Estimating Harvest Rates on a Micronesian Island

Disturbance is an integral component in mangrove forest dynamics, influencing forest structure, composition, and function. The impacts of human disturbance, however, threaten mangrove forests throughout the world. Small-scale wood harvesting on the small Pacific island of Kosrae, Federated States of Micronesia, provided an instructive scenario for exploring the dynamics of human disturbance. Natural disturbances on the island are rare, but the growing island population harvests mangrove trees for firewood and construction materials, placing pressure on the forest. In order to determine recent harvest rates, we estimated gap ages by developing a time scale for mangrove wood decomposition and by quantifying growth rates for Rhizophora apiculata and Bruguiera gymnorhiza seedlings. Stump and log decomposition patterns were useful in aging gaps, although some patterns were more reliable than others. Seedlings of both species added approximately 5 nodes/year depending on light conditions. The island-wide harvest rate was 10% over the last 10 years, but the rates varied widely among different parts of the island. Rhizophora apiculata has been harvested preferentially, and a dearth of young trees where harvesting has been heaviest portends a decline of this highly desired species in the forest. Socio-economic data substantiated some but not all of the trends we observed. Even on a small island, local differences in both natural and anthropogenic factors are important to understanding forest dynamics.     

Effects of Vegetation Thinning on Above- and Belowground Carbon in a Seasonally Dry Tropical Forest in Mexico

Mature tropical forests are disappearing and secondary forests are becoming more abundant, thus there is an increasing need to understand the ecology and management of secondary forests. In the Yucatan Peninsula, Mexico, seasonally dry tropical forests are subject to frequent fire, and early-successional stands are extremely dense. We applied vegetation thinning (removal of all stems < 2 cm in diameter) to hasten secondary succession and open the understory to reduce the fire ladder in an 11-yr-old stand. We quantified the effect of vegetation thinning on above- and belowground carbon over 5 yr. Aboveground carbon included all standing vegetation and belowground carbon included fine roots and organic carbon in the Oi, Oe, and Oa soil horizons. Trees with diameter of 2–10 cm and > 10 cm had higher carbon accumulation rates in thinned plots than in control plots. Carbon stored in the Oi-horizon and the Oe > 2 mm fraction remained significantly higher in thinned plots even 5 yr after treatment. Carbon in fine roots was significantly higher in thinned plots, and radiocarbon (¹⁴C) data suggest that fine roots in thinned plots were recently produced in comparison with fine roots in control plots. We did not find significant differences in total ecosystem carbon after 5 yr (126 ± 6 and 136 ± 8 Mg C/ha, respectively). These results suggest rapid carbon recovery and support the hypothesis that young tropical forests thinned to hasten succession and reduce the fire hazard may have only a short-term negative impact on carbon accumulation in vegetation and soils.     

Rates of Dry-matter Production in Some Tropical Forest-tree Seedlings

An analysis of growth in full daylight of four tropical forest-treeseedlings and Helianthus was made with the view of ascertainingwhether woody plants in the tropics have a lower net assimilationrate than herbaceous plants as has been demonstrated in otherenvironments. Significant differences in net assimilation ratewere found between Helianthus and three of the woody speciestested: Chlorophora excelsa, Musanga cecropioides, and Terminaliaivorensis; the fourth woody plant, Ceiba pentandra, had an unusuallyhigh net assimilation rate which, in one experiment, did notdiffer significantly from the value found for Helianthus. The data are discussed in relation to the general problems ofcomparative growth-rates of herbaceous and woody plants andof factors contributing to differences in forest productivitybetween climates.     

Redox Fluctuations Frame Microbial Community Impacts on N-cycling Rates in a Humid Tropical Forest Soil

Fluctuating soil redox regimes may facilitate the co-occurrence of microbial nitrogen transformations with significantly different sensitivities to soil oxygen availability. In an upland humid tropical forest, we explored the impact of fluctuating redox regimes on gross nitrogen cycling rates and microbial community composition. Our results suggest that the rapidly fluctuating redox conditions that characterize these upland soils allow anoxic and oxic N processing to co-occur. Gross nitrogen mineralization was insensitive to soil redox fluctuations. In contrast, nitrifiers in this soil were directly affected by low redox periods, yet retained some activity even after 3–6 weeks of anoxia. Dissimilatory nitrate reduction to ammonium (DNRA) was less sensitive to oxygen exposure than expected, indicating that the organisms mediating this reductive process were also tolerant of unfavorable (oxic) conditions. Denitrification was a stronger sink for NO₃⁻ in consistently anoxic soils than in variable redox soils. Microbial biomass and community composition were maintained with redox fluctuation, but biomass decreased and composition changed under static oxic and anoxic soil regimes. Bacterial community structure was significantly correlated with rates of nitrification, denitrification and DNRA, suggesting that redox-control of soil microbial community structure was an important determinant of soil N-cycling rates. Specific nitrogen cycling functional groups in this environment (such as nitrifiers, DNRA organisms, and denitrifiers) appear to have adapted to nutrient resources that are spatially and temporally variable. In soils where oxygen is frequently depleted and re-supplied, characteristics of microbial tolerance and resilience can frame N cycling patterns.