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Allowable carbon emissions lowered by multiple climate targets
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Climate targets are designed to inform policies that would limit the
magnitude and impacts of climate change caused by anthropogenic
emissions of greenhouse gases and other substances. The target
that is currently recognized by most world governments1 places a
limit of two degrees Celsius on the global mean warming since
preindustrial times. This would require large sustained reductions
in carbon dioxide emissions during the twenty-first century and
beyond2–4. Such a global temperature target, however, is not sufficient
to control many other quantities, such as transient sea level
rise5
, ocean acidification6,7 and net primary production on land8,9.
Here, using an Earth system model of intermediate complexity
(EMIC) in an observation-informed Bayesian approach, we show
that allowable carbon emissions are substantially reduced whenmultiple
climate targets are set. We take into account uncertainties in
physical and carbon cycle model parameters, radiative efficiencies10,
climate sensitivity11 and carbon cycle feedbacks12,13 along with a
large set of observational constraints. Within this framework, we
explore a broad range of economically feasible greenhouse gas scenarios
from the integrated assessment community14–17 to determine
the likelihood of meeting a combination of specific global
and regional targets under various assumptions. For any given
likelihood of meeting a set of such targets, the allowable cumulative
emissions are greatly reduced from those inferred from the temperature
target alone. Therefore, temperature targets alone are unable
to comprehensively limit the risks from anthropogenic emissions.
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Challenges in the conservation, rehabilitation and recovery of native stream salmonid populations: beyond the 2010 Luarca symposium
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– In May 2010, I chaired a session on challenges to salmonid conservation at the international symposium
‘Advances in the population ecology of stream salmonids’ in Luarca, Spain. I suggested that in addition to scientific challenges, a major challenge will be improving the links between ecologists, conservationists and policy makers. Because the Luarca symposium focused mainly on ecological research, little time was explicitly devoted to conservation. My objective in this paper is to further discuss the role of ecological research in informing salmonid conservation. I begin with a brief overview of research highlights from the symposium. I then use selected examples to show that ecological research has already contributed much towards informing salmonid conservation, but that ecologists will always be faced with limitations in their predictive ability. I suggest that conservation will need to move forward regardless of these limitations, and I call attention to some recent efforts wherein ecological research has played a crucial role. I conclude that ecologists should take urgent action to ensure that their results are availableto inform resource managers, conservation organisations and policy makers regarding past losses and present threats to native, locally-adapted salmonid stocks.
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Animal Versus Wind Dispersal and the Robustness of Tree Species to Deforestation
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Studies suggest that populations of different species do not decline equally after habitat loss. However, empirical tests have been confined to fine spatiotemporal scales and have rarely included plants. Using data from 89,365 forest survey plots covering peninsular Spain, we explored, for each of 34 common tree species, the relationship between probability of occurrence and the local cover of remaining forest. Twenty-four species showed a significant negative response to forest loss, so that decreased forest cover had
a negative effect on tree diversity, but the responses of individual species were highly variable. Animal-dispersed species were less vulnerable to forest loss, with six showing positive responses to decreased forest cover. The results imply that plant-animal interactions help prevent the collapse of forest communities that suffer habitat destruction.
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Carbon sequestration in the U.S. forest sector from 1990 to 2010
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From 1990 through 2005, the forest sector (including forests and wood products) sequestered an average 162 Tg C year1 . In 2005, 49% of the total forest sector sequestration was in live and dead trees, 27% was
in wood products in landfills, with the remainder in down dead wood, wood products in use, and forest floor and soil. The pools with the largest carbon stocks were not the same as those with the largest sequestration rates, except for the tree pool. For example, landfilled wood products comprise only 3% of total stocks but account for 27% of carbon sequestration. Conversely, forest soils comprise 48% of total stocks but account for only 2% of carbon sequestration. For the tree pool, the spatial pattern of carbon stocks was dissimilar to that of carbon flux. On an area basis, tree carbon stocks were highest in the Pacific Northwest, while changes were generally greatest in the upper Midwest and the Northeast. Net carbon sequestration in the forest sector in 2005 offset 10% of U.S. CO2 emissions. In the near future, we project that U.S. forests will continue to sequester carbon at a rate similar to that in recent years. Based on a comparison of our estimates to a compilation of land-based estimates of non-forest carbon sinks from the literature, we estimate that the conterminous U.S. annually sequesters 149–330 Tg C year1. Forests, urban trees, and wood products are responsible for 65–91% of this sink.
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A new, global, multi-annual (2000–2007) burnt area product at 1 km resolution Vol. 35
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This paper reports on the development and validation
of a new, global, burnt area product. Burnt areas are
reported at a resolution of 1 km for seven fire years (2000 to
2007). A modified version of a Global Burnt Area (GBA)
2000 algorithm is used to compute global burnt area. The
total area burnt each year (2000– 2007) is estimated to be
between 3.5 million km2 and 4.5 million km2
. The total
amount of vegetation burnt by cover type according to the
Global Land Cover (GLC) 2000 product is reported.
Validation was undertaken using 72 Landsat TM scenes
was undertaken. Correlation statistics between estimated
burnt areas are reported for major vegetation types. The
accuracy of this new global data set depends on vegetation
type.
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Animal migration amid shifting patterns of phenology and predation: lessons from a Yellowstone elk herd
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Migration is a striking behavioral strategy by which many animals enhance resource acquisition while reducing predation risk. Historically, the demographic benefits of such movements made migration common, but in many taxa the phenomenon is considered globally threatened. Here we describe a long-term decline in the productivity of elk (Cervus elaphus) that migrate through intact wilderness areas to protected summer ranges inside Yellowstone National Park, USA. We attribute this decline to a long-term reduction in the
demographic benefits that ungulates typically gain from migration. Among migratory elk, we observed a 21-year, 70% reduction in recruitment and a 4-year, 19% depression in their pregnancy rate largely caused by infrequent reproduction of females that were young or lactating. In contrast, among resident elk, we have recently observed increasing recruitment and a high rate of pregnancy. Landscape-level changes in habitat quality and predation appear to be responsible for the declining productivity of Yellowstone migrants. From 1989 to 2009, migratory elk experienced an increasing rate and shorter duration of green-up coincident with
warmer spring–summer temperatures and reduced spring precipitation, also consistent with observations of an unusually severe drought in the region. Migrants are also now exposed to four times as many grizzly bears (Ursus arctos) and wolves (Canis lupus) as resident elk. Both of these restored predators consume migratory elk calves at high rates in the Yellowstone wilderness but are maintained at low densities via lethal management and human disturbance in the year-round habitats of resident elk. Our findings suggest that large-carnivore recovery and drought, operating simultaneously along an elevation gradient, have disproportionately influenced the demography of migratory elk. Many migratory animals travel large geographic distances between their seasonal ranges. Changes in land use and climate that disparately
influence such seasonal ranges may alter the ecological basis of migratory behavior, representing an important challenge.
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Characterizing coal and mineral mines as a regional source of stress to stream fish assemblages
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Mining impacts on stream systems have historically been studied over small spatial scales, yet investigations over large areas may be useful for characterizing mining as a regional source of stress to stream fishes. The associations between co-occurring stream fish assemblages and densities of various “classes” of mining occurring in the same catchments were tested using threshold analysis. Threshold analysis identifies the point at which fish assemblages change substantially from best available habitat conditions with increasing disturbance. As this occurred over large regions, species comprising fish assemblages were represented by various functional traits as well as other measures of interest to management (characterizing reproductive ecology and life history, habitat preferences, trophic ecology, assemblage diversity and evenness, tolerance to anthropogenic disturbance and state-recognized game species). We used two threshold detection methods: change-point analysis with indicator analysis and piecewise linear regression. We accepted only those thresholds that were highly statistically significant (p 0.01) for both techniques and overlapped within 5% error. We found consistent, wedge-shaped declines in multiple fish metrics with increasing levels of mining in catchments, suggesting mines are a regional source of disturbance. Threshold responses were consistent across the three ecoregions occurring at low mine densities. For 47.2% of the significant thresholds, a density of only 0.01 mines/km2 caused a threshold response. In fact, at least 25% of streams in each of our three study ecoregions have mine densities in their catchments with the potential to affect fish assemblages. Compared to other anthropogenic impacts assessed over large areas (agriculture, impervious surface or urban land use), mining had a more pronounced and consistent impact on fish assemblages. Threshold analysis Fish functional traits Landscape influences Game fishes Mining Rivers
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Conservation threats: biofuel
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Biofuels: Europe’s largest conservation charity has launched a campaign to heighten the threat to wildlife habitats and biodiversity from plantations of fuel crops. Nigel Williams reports. 1st paragraph: Europe embraced the theoretical potential that biofuels might offer both in terms of climate change and renewable sources of energy, as enthusiastically as anywhere else, but the dawning reality has hit harder here than in many other areas with the realisation that it is a crowded continent with limited scope for home-grown material.
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Carbon debt and carbon sequestration parity in forest bioenergy production
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The capacity for forests to aid in climate change mitigation efforts is substantial but will ultimately depend on their management. If forests remain unharvested, they can further mitigate the increases in atmospheric CO2 that result from fossil fuel combustion and deforestation. Alternatively, they can be harvested for bioenergy production and serve as a substitute for fossil fuels, though such a practice could reduce terrestrial C storage and thereby increase atmospheric CO2 concentrations in the near-term. Here, we used an ecosystem simulation model to ascertain the effectiveness of using forest bioenergy as a substitute for fossil fuels, drawing from a broad range of land-use histories, harvesting regimes, ecosystem characteristics, and bioenergy conversion effi- ciencies. Results demonstrate that the times required for bioenergy substitutions to repay the C Debt incurred from biomass harvest are usually much shorter (< 100 years) than the time required for bioenergy production to substitute the amount of C that would be stored if the forest were left unharvested entirely, a point we refer to as C Sequestration Parity. The effectiveness of substituting woody bioenergy for fossil fuels is highly dependent on the factors that determine bioenergy conversion efficiency, such as the C emissions released during the har- vest, transport, and firing of woody biomass. Consideration of the frequency and intensity of biomass harvests should also be given; performing total harvests (clear-cutting) at high-frequency may produce more bioenergy than less intensive harvesting regimes but may decrease C storage and thereby prolong the time required to achieve C Sequestration Parity.
Keywords: bioenergy, biofuel, C cycle, C sequestration, forest management
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Changes in climate and land use have a larger direct impact than rising CO2 on global river runoff trends
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The significant worldwide increase in observed river runoff has been tentatively attributed to the stomatal ‘‘antitranspirant’’ response of plants to rising atmospheric CO2 [Gedney N, Cox PM, Betts RA, Boucher O, Huntingford C, Stott PA (2006) Nature 439: 835– 838]. However, CO2 also is a plant fertilizer. When allowing for the increase in foliage area that results from increasing atmospheric CO2 levels in a global vegetation model, we find a decrease in global runoff from 1901 to 1999. This finding highlights the importance of vegetation structure feedback on the water balance of the land surface. Therefore, the elevated atmospheric CO2 concentration does not explain the estimated increase in global runoff over the last century. In contrast, we find that changes in mean climate, as well as its variability, do contribute to the global runoff increase. Using historic land-use data, we show that land-use change plays an additional important role in controlling regional runoff values, particularly in the tropics. Land-use change has been strongest in tropical regions, and its contribution is substantially larger than that of climate change. On average, land-use change has increased global runoff by 0.08 mm/year2 and accounts for 50% of the reconstructed global runoff trend over the last century. Therefore, we emphasize the importance of land-cover change in forecasting future freshwater availability and climate.
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