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Competitive and demographic leverage points of community shifts under climate warming
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Accelerating rates of climate change and a paucity of whole-community studies of climate impacts limit our ability to forecast shifts in ecosystem structure and dynamics, particularly because climate change can lead to idiosyncratic responses via both demographic effects and altered species interactions. We used a multispecies model to predict which processes and species’ responses are likely to drive shifts in the composition of a space- limited benthic marine community. Our model was parametrized from experimental manipulations of the community. Model simulations indicated shifts in species dominance patterns as temperatures increase, with projected shifts in composition primarily owing to the temperature dependence of growth, mortality and competition for three critical species. By contrast, warming impacts on two other species (rendering them weaker competitors for space) and recruitment rates of all species were of lesser importance in determining projected community changes. Our analysis reveals the impor- tance of temperature-dependent competitive interactions for predicting effects of changing climate on such communities. Furthermore, by identify- ing processes and species that could disproportionately leverage shifts in community composition, our results contribute to a mechanistic understand- ing of climate change impacts, thereby allowing more insightful predictions of future biodiversity patterns.
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Anthropogenic environments exert variable selection on cranial capacity in mammals
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It is thought that behaviourally flexible species will be able to cope with novel and rapidly changing environments associated with human activity. However, it is unclear whether such environments are selecting for increases in behavioural plasticity, and whether some species show more pronounced evolutionary changes in plasticity. To test whether anthropogenic environ- ments are selecting for increased behavioural plasticity within species, we measured variation in relative cranial capacity over time and space in 10 species of mammals. We predicted that urban populations would show greater cranial capacity than rural populations and that cranial capacity would increase over time in urban populations. Based on relevant theory, we also predicted that species capable of rapid population growth would show more pronounced evolutionary responses. We found that urban populations of two small mammal species had significantly greater cranial capacity than rural populations. In addition, species with higher fecundity showed more pronounced differentiation between urban and rural populations. Contrary to expectations, we found no increases in cranial capacity over time in urban populations—indeed, two species tended to have a decrease in cranial capacity over time in urban populations. Furthermore, rural populations of all insectivorous species measured showed significant increases in relative cranial capacity over time. Our results provide partial support for the hypothesis that urban environments select for increased behavioural plasticity, although this selection may be most pronounced early during the urban colonization process. Furthermore, these data also suggest that behavioural plasticity may be simultaneously favoured in rural environments, which are also changing because of human activity.
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Disturbance−diversity models: what do they really predict and how are they tested?
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The intermediate disturbance hypothesis (IDH) and the dynamic equilibrium model (DEM) are influential theories in ecology. The IDH predicts large species numbers at intermediate levels of disturbance and the DEM predicts that the effect of disturbance depends on the level of productivity. However, various indices of diversity are considered more commonly than the predicted number of species in tests of the hypotheses. This issue reaches beyond the scientific community as the predictions of the IDH and the DEM are used in the management of national parks and reserves. In order to compare responses with disturbance among measures of biodiversity, we used two different approaches of mathematical modelling and conducted an extensive meta-analysis. Two-thirds of the surveyed studies present different results for different diversity measures. Accordingly, the meta-analysis showed a narrow range of negative quadratic regression components for richness, but not evenness. Also, the two models support the IDH and the DEM, respectively, when biodiversity is measured as species richness, but predict evenness to increase with increasing disturbance, for all levels of productivity. Consequently, studies that use compound indices of diversity should present logical arguments, a priori, to why a specific index of diversity should peak in response to disturbance.
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Diverse pollinator communities enhance plant reproductive success
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Understanding the functional consequences of biodiversity loss is a major goal of ecology. Animal-mediated pollination is an essential ecosystem function and service provided to mankind. However, little is known how pollinator diversity could affect pollination services. Using a substitutive design, we experimentally manipu- lated functional group (FG) and species richness of pollinator communities to investigate their consequences on the reproductive success of an obligate out-crossing model plant species, Raphanus sativus. Both fruit and seed set increased with pollinator FG richness. Furthermore, seed set increased with species richness in pol- linator communities composed of a single FG. However, in multiple-FG communities, highest species richness resulted in slightly reduced pollination services compared with intermediate species richness. Our analysis indicates that the presence of social bees, which showed roughly four times higher visitation rates than solitary bees or hoverflies, was an important factor contributing to the positive pollinator diversity–pollination service relationship, in particular, for fruit set. Visitation rate at different daytimes, and less so among flower heights, varied among social bees, solitary bees and hoverflies, indicating a niche complementarity among these pollinator groups. Our study demonstrates enhanced pollination services of diverse pollinator communities at the plant population level and suggests that both the niche complementarity and the presence of specific taxa in a pollinator community drive this positive relationship.
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Biotic Drivers of Stream Planform: Implications for Understanding the Past and Restoring the Future
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Traditionally, stream channel planform has been viewed as a function of larger watershed and valley-scale physical variables, including valley slope, the amount of discharge, and sediment size and load. Biotic processes serve a crucial role in transforming channel planform among straight, braided, meandering, and anabranching styles by increasing stream-bank stability and the probability of avulsions, creating stable multithread (anabranching) channels, and affecting sedimentation dynamics. We review the role of riparian vegetation and channel-spanning obstructions—beaver dams and logjams—in altering channel–floodplain dynamics in the southern Rocky Mountains, and we present channel planform scenarios for combinations of vegetation and beaver populations or old-growth forest that control logjam formation. These conceptual models provide understanding of historical planform variability throughout the Holocene and outline the implications for stream restoration or management in broad, low-gradient headwater valleys, which are important for storing sediment, carbon, and nutrients and for supporting a diverse riparian community.
Keywords: stream planform, riparian vegetation, beaver, old-growth forest, restoration
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Clone history shapes Populus drought responses
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Just as animal monozygotic twins can experience different environmental conditions by being reared apart, individual genetically identical trees of the genus Populus can also be exposed to contrasting environmental conditions by being grown in different locations. As such, clonally propagated Populus trees provide an opportunity to interrogate the impact of individual environmental history on current response to environmental stimuli. To test the hypothesis that current responses to an environmental stimulus, drought, are contingent on environmental history, the transcriptome- level drought responses of three economically important hybrid genotypes—DN34 (Populus deltoides × Populus nigra), Walker [P. deltoides var. occidentalis × (Populus laurifolia × P. nigra)], and Okanese [Walker × (P. laurifolia × P. nigra)]—derived from two different locations were compared. Strikingly, differences in transcript abundance patterns in response to drought were based on differences in geographic origin of clones for two of the three genotypes. This observation was most pronounced for the genotypes with the longest time since establishment and last common propagation. Differences in genome-wide DNA methylation paralleled the transcriptome level trends, whereby the clones with the most divergent transcriptomes and clone history had the most marked differences in the extent of total DNA methylation, suggesting an epigenomic basis for the clone history-dependent transcriptome divergence. The data provide insights into the interplay between genotype and environment in the ecologically and economically important Populus genus, with implications for the industrial application of Populus trees and the evolution and persistence of these important tree species and their associated hybrids.
epigenetics | forest trees | poplar
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Dispersal will limit ability of mammals to track climate change in the Western Hemisphere
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As they have in response to past climatic changes, many species will shift their distributions in response to modern climate change. However, due to the unprecedented rapidity of projected climatic changes, some species may not be able to move their ranges fast enough to track shifts in suitable climates and associated habitats. Here, we investigate the ability of 493 mammals to keep pace with projected climatic changes in the Western Hemisphere. We modeled the velocities at which species will likely need to move to keep pace with projected changes in suitable climates. We compared these velocities with the velocities at which species are able to move as a function of dispersal distances and dispersal frequencies. Across the Western Hemisphere, on average, 9.2% of mammals at a given location will likely be unable to keep pace with climate change. In some places, up to 39% of mammals may be unable to track shifts in suitable climates. Eighty-seven percent of mammalian species are expected to experience reductions in range size and 20% of these range reductions will likely be due to limited dispersal abilities as opposed to reductions in the area of suitable climate. Because climate change will likely outpace the response capacity of many mammals, mammalian vulnerability to climate change may be more extensive than previously anticipated.
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Carbon debt of Conservation Reserve Program (CRP) grasslands converted to bioenergy production
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Over 13 million ha of former cropland are enrolled in the US Conservation Reserve Program (CRP), providing well-recognized biodiversity, water quality, and carbon (C) sequestration benefits that could be lost on conversion back to agricultural production. Here we provide measurements of the greenhouse gas consequences of converting CRP land to continuous corn, corn–soybean, or perennial grass for biofuel production. No-till soybeans preceded the annual crops and created an initial carbon debt of 10.6 Mg CO2 equivalents (CO2e)·ha−1 that included agronomic inputs, changes in C stocks, altered N2O and CH4 fluxes, and foregone C sequestration less a fossil fuel offset credit. Total debt, which includes future debt created by additional changes in soil C stocks and the loss of substantial future soil C sequestration, can be constrained to 68 Mg CO2e·ha−1 if subsequent crops are under permanent no-till management. If tilled, however, total debt triples to 222 Mg CO2e·ha−1 on account of further soil C loss. Projected C debt repayment periods under no-till management range from 29 to 40 y for corn– soybean and continuous corn, respectively. Under conventional tillage repayment periods are three times longer, from 89 to 123 y, respectively. Alternatively, the direct use of existing CRP grasslands for cellulosic feedstock production would avoid C debt entirely and provide modest climate change mitigation immediately. Incentives for permanent no till and especially permission to harvest CRP biomass for cellulosic biofuel would help to blunt the climate impact of future CRP conversion.
land-use change | renewable energy | carbon balance | agriculture | nitrous oxide
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Assessing the impacts of livestock production on biodiversity in rangeland ecosystems
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Biodiversity in rangelands is decreasing, due to intense utilization for livestock production and conversion of rangeland into cropland; yet the outlook of rangeland biodiversity has not been considered in view of future global demand for food. Here we assess the impact of future livestock production on the global rangelands area and their biodiversity. First we formalized exist- ing knowledge about livestock grazing impacts on biodiversity, expressed in mean species abundance (MSA) of the original rangeland native species assemblages, through metaanalysis of peer-reviewed literature. MSA values, ranging from 1 in natural rangelands to 0.3 in man-made grasslands, were entered in the IMAGE-GLOBIO model. This model was used to assess the impact of change in food demand and livestock production on future rangeland biodiversity. The model revealed remarkable regional variation in impact on rangeland area and MSA between two agricultural production scenarios. The area of used rangelands slightly increases globally between 2000 and 2050 in the baseline scenario and reduces under a scenario of enhanced uptake of resource-efficient production technologies increasing production [high levels of agricultural knowledge, science, and technology (high-AKST)], particularly in Africa. Both scenarios suggest a global decrease in MSA for rangelands until 2050. The contribution of livestock grazing to MSA loss is, however, expected to diminish after 2030, in particular in Africa under the high-AKST scenario. Policies fostering agricultural intensification can reduce the overall pressure on rangeland biodiversity, but additional measures, addressing factors such as climate change and infrastructural development, are necessary to totally halt biodiversity loss.
dose-response model | intactness | land use
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Delayed detection of climate mitigation benefits due to climate inertia and variability
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Climate change mitigation acts by reducing greenhouse gas emissions, and thus curbing, or even reversing, the increase in their atmospheric concentration. This reduces the associated anthropogenic radiative forcing, and hence the size of the warming. Because of the inertia and internal variability affecting the climate system and the global carbon cycle, it is unlikely that a reduction in warming would be immediately discernible. Here we use 21st century simulations from the latest ensemble of Earth System Model experiments to investigate and quantify when mitigation becomes clearly discernible. We use one of the scenarios as a reference for a strong mitigation strategy, Representative Concentration Pathway (RCP) 2.6 and compare its outcome with either RCP4.5 or RCP8.5, both of which are less severe mitigation pathways. We analyze global mean atmospheric CO2, and changes in annually and seasonally averaged surface temperature at global and regional scales. For global mean surface temperature, the median detection time of mitigation is about 25–30 y after RCP2.6 emissions depart from the higher emission trajectories. This translates into detection of a mitigation signal by 2035 or 2045, depending on whether the comparison is with RCP8.5 or RCP4.5, respectively. The detection of climate benefits of emission mitigation occurs later at regional scales, with a median detection time between 30 and 45 y after emission paths separate. Requiring a 95% confidence level induces a delay of several decades, bringing detection time toward the end of the 21st century.
regional climate change | climate variability | signal detection
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