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Ecosystem Processes and Human Influences Regulate Streamflow Response to Climate Change at Long-Term Ecological Research Sites
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Analyses of long-term records at 35 headwater basins in the United States and Canada indicate that climate change effects on streamflow are not as clear as might be expected, perhaps because of ecosystem processes and human influences. Evapotranspiration was higher than was predicted by temperature in water-surplus ecosystems and lower than was predicted in water-deficit ecosystems. Streamflow was correlated with climate variability indices (e.g., the El Niño–Southern Oscillation, the Pacific Decadal Oscillation, the North Atlantic Oscillation), especially in seasons when vegetation influences are limited. Air temperature increased significantly at 17 of the 19 sites with 20- to 60-year records, but streamflow trends were directly related to climate trends (through changes in ice and snow) at only 7 sites. Past and present human and natural disturbance, vegetation succession, and human water use can mimic, exacerbate, counteract, or mask the effects of climate change on streamflow, even in reference basins. Long-term ecological research sites are ideal places to disentangle these processes.
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Climate change and tropical biodiversity: a new focus
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Considerable efforts are focused on the consequences of climate change for tropical rainforests. However, potentially the greatest threats to tropical biodiversity (synergistic interactions between climatic changes and human land use) remain understudied. Key concerns are that aridification could increase the accessibility of previously non-arable or remote lands, elevate fire impacts and exacerbate ecological effects of habitat disturbance. The growing climatic change literature often fails to appreciate that, in coming decades, climate–land use interac- tions might be at least as important as abiotic changes per se for the fate of tropical biodiversity. In this review, we argue that protected area expansion along key ecological gradients, regulation of human-lit fires, strategic forest–carbon financing and re-evaluations of agricultural and biofuel subsidies could ameliorate some of these synergistic threats.
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Changes in Avian and Plant Communities of Aspen Woodlands over 12 Years after Livestock Removal in the Northwestern Great Basin
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Riparian and quaking aspen (Populus tremuloides) woodlands are centers of avian abundance and diversity in the western United States, but they have been affected adversely by land use practices, particularly livestock grazing. In 1990, cattle were removed from a 112,500-ha national wildlife refuge in southeastern Oregon. Thereafter, we monitored changes in vegetation and bird abundance in years 1–3 (phase 1) and 10–12 (phase 2) in 17 riparian and 9 snow-pocket aspen plots. On each 1.5-ha plot, we sampled vegetation in 6 transects. Three times during each breeding season, observers recorded all birds 50 m to each side of the plot’s 150-m centerline for 25 minutes. We analyzed data with multivariate analysis of variance and paired t tests with p values adjusted for multiple comparisons. In both periods, riparian and snow-pocket aspen produced extensive regeneration of new shoots ( x ̄ = 2646 stems/ha and 7079 stems/ha, respectively). By phase 2, a 64% increase in medium-diameter trees in riparian stands indicated successful recruitment into the overstory, but this pattern was not seen in snow-pocket stands, where the density of trees was over 2 times greater. By phase 2 in riparian and snow-pocket stands, native forb cover had increased by 68% and 57%, respectively, mesic shrub cover had increased by 29% and 58%, and sagebrush cover had decreased by 24% and 31%. Total avian abundance increased by 33% and 39% in riparian and snow-pocket aspen, respectively, ground or understory nesters increased by 133% and 67% and overstory nesters increased by 34% and 33%. Similarly, ground or understory foragers increased by 25% and 32%, aerial foragers by 55% and 57%, and overstory foragers by 66% and 43%. We interpreted the substantial regeneration of aspen shoots, increased densities of riparian forbs and shrubs, and increased avian abundances as a multitrophic-level response to the total removal of livestock and as substantial movement toward recovery of biological integrity.
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Evolution of climate niches in European mammals?
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Our ability to predict consequences of climate change is severely impaired by the lack of knowledge on the ability of species to adapt to changing environmental conditions. We used distribution data for 140 mammal species in Europe, together with data on climate, land cover and topography, to derive a statistical description of their realized climate niche. We then compared climate niche overlap of pairs of species, selected on the basis of phylogenetic information. In contrast to expectations, related species were not similar in their climate niche. Rather, even species pairs that had a common ancestor less than 1Ma already display very high climate niche distances. We interpret our finding as a strong inter- specific competitive constraint on the realized niche, rather than a rapid evolution of the fundamental niche. If correct, our results imply a very limited usefulness of climate niche models for the prediction of future mammal distributions.
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Citizen Involvement in the U.S. Endangered Species Act
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Data on listed species refute critiques of citizen involvement in the U.S. Endangered Species Act.
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CO2 emissions from land-use change affected more by nitrogen cycle, than by the choice of land-cover data
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The high uncertainty in land-based CO2 fluxes estimates is thought to be mainly due to uncertainty in not only quantifying historical changes among forests, croplands, and grassland, but also due to different processes included in calculation methods. Inclusion of a nitrogen (N) cycle in models is fairly recent and strongly affects carbon (C) fluxes. In this study, for the first time, we use a model with C and N dynamics with three distinct historical reconstructions of land-use and land-use change (LULUC) to quantify LULUC emissions and uncertainty that includes the integrated effects of not only climate and CO2 but also N. The modeled global average emissions including N dynamics for the 1980s, 1990s, and 2000–2005 were 1.8 ` 0.2, 1.7 ` 0.2, and 1.4 ` 0.2 GtC yr␣1, respectively, (mean and range across LULUC data sets). The emissions from tropics were 0.8 ` 0.2, 0.8 ` 0.2, and 0.7 ` 0.3 GtC yr␣1, and the non tropics were 1.1 ` 0.5, 0.9 ` 0.2, and 0.7 ` 0.1 GtC yr␣1. Compared to previous studies that did not include N dynamics, modeled net LULUC emissions were higher, particularly in the non tropics. In the model, N limitation reduces regrowth rates of vegetation in temperate areas resulting in higher net emissions. Our results indicate that exclusion of N dynamics leads to an underestimation of LULUC emissions by around 70% in the non tropics, 10% in the tropics, and 40% globally in the 1990s. The differences due to inclusion/exclusion of the N cycle of 0.1 GtC yr␣1 in the tro- pics, 0.6 GtC yr␣1 in the non tropics, and 0.7 GtC yr␣1 globally (mean across land-cover data sets) in the 1990s were greater than differences due to the land-cover data in the non tropics and globally (0.2 GtC yr␣1). While land-cover information is improving with satellite and inventory data, this study indicates the importance of accounting for different processes, in particular the N cycle.
Keywords: carbon cycle, carbon emissions, land-use change, model, nitrogen cycle
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Carbon Dynamics of the Forest Sector
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Main points: The basic ecosystem science behind carbon dynamics in forests is relatively straightforward (really!).This science doesn’t seem to be applied very routinely in the policy arena. This mismatch is undermining the potential of the forest sector in helping to mitigate greenhouse gases in the atmosphere
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Detection and Attribution of Streamflow Timing Changes to Climate Change in the Western United States
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This article applies formal detection and attribution techniques to investigate the nature of observed shifts in the timing of streamflow in the western United States. Previous studies have shown that the snow hy- drology of the western United States has changed in the second half of the twentieth century. Such changes manifest themselves in the form of more rain and less snow, in reductions in the snow water contents, and in earlier snowmelt and associated advances in streamflow ‘‘center’’ timing (the day in the ‘‘water-year’’ on average when half the water-year flow at a point has passed). However, with one exception over a more limited domain, no other study has attempted to formally attribute these changes to anthropogenic increases of greenhouse gases in the atmosphere. Using the observations together with a set of global climate model simulations and a hydrologic model (applied to three major hydrological regions of the western United States—the California region, the upper Colorado River basin, and the Columbia River basin), it is found that the observed trends toward earlier ‘‘center’’ timing of snowmelt-driven streamflows in the western United States since 1950 are detectably different from natural variability (significant at the p , 0.05 level). Furthermore, the nonnatural parts of these changes can be attributed confidently to climate changes induced by anthropogenic greenhouse gases, aerosols, ozone, and land use. The signal from the Columbia dominates the analysis, and it is the only basin that showed a detectable signal when the analysis was performed on individual basins. It should be noted that although climate change is an important signal, other climatic processes have also contributed to the hydrologic variability of large basins in the western United States.
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Effective Enforcement in a Conservation Area
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There are two primary approaches to wildlife conservation, the generation of economic benefits from wildlife to local communities, so that protecting wildlife is in their interest, and the enforcement of protected areas. Outside of protected areas, community- based conservation must be the cornerstone of protection (1). However, within protected areas there is debate as to whether enforcement can maintain wildlife and even whether protected areas as wildlife reserves are realistic or morally justified (2). Here, we present the history of illegal harvesting in Serengeti National Park (SNP), Tanzania; estimate the amount of antipoaching activity by park staff; and show how the level of funding for antipoaching has affected the trends in abundance of three severely affected species: African buffalo, elephant, and black rhino.
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Can forest management be used to sustain water-based ecosystem services in the face of climate change?
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Forested watersheds, an important provider of ecosystems services related to water supply, can have their structure, function, and resulting streamflow substantially altered by land use and land cover. Using a retrospective analysis and synthesis of long-term climate and streamflow data (75 years) from six watersheds differing in management histories we explored whether streamflow responded differently to variation in annual temperature and extreme precipitation than unmanaged watersheds. We show significant increases in temperature and the frequency of extreme wet and dry years since the 1980s. Response models explained almost all streamflow variability (adjusted R2 . 0.99). In all cases, changing land use altered streamflow. Observed watershed responses differed significantly in wet and dry extreme years in all but a stand managed as a coppice forest. Converting deciduous stands to pine altered the streamflow response to extreme annual precipitation the most; the apparent frequency of observed extreme wet years decreased on average by sevenfold. This increased soil water storage may reduce flood risk in wet years, but create conditions that could exacerbate drought. Forest management can potentially mitigate extreme annual precipitation associated with climate change; however, offsetting effects suggest the need for spatially explicit analyses of risk and vulnerability.
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