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Committed terrestrial ecosystem changes due to climate change
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Targets for stabilizing climate change are often based on considerations of the impacts of different levels of global warming, usually assessing the time of reaching a particular level of warming. However, some aspects of the Earth system, such as global mean temperatures1 and sea level rise due to thermal expansion2 or the melting of large ice sheets3 , continue to respond long after the stabilization of radiative forcing. Here we use a coupled climate–vegetation model to show that in turn the terrestrial biosphere shows significant inertia in its response to climate change. We demonstrate that the global terrestrial biosphere can continue to change for decades after climate stabilization. We suggest that ecosystems can be committed to long-term change long before any response is observable: for example, we find that the risk of significant loss of forest cover in Amazonia rises rapidly for a global mean temperature rise above 2 ◦ C. We conclude that such committed ecosystem changes must be considered in the definition of dangerous climate change, and subsequent policy development to avoid it.
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Editorial : Beyond forest carbon
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The preservation of forests, both on land and in mangrove swamps, has received much attention in the move to protect biological carbon stores. Less conspicuous communities of organisms deserve some scrutiny, too.
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Continuous flux of dissolved black carbon from a vanished tropical forest biome
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Humans have used fire extensively as a tool to shape Earth’s vegetation. The slash-and-burn destruction of Brazil’s Atlantic forest, which once covered over 1.3 million km2 of present-day Brazil and was one of the largest tropical forest biomes on Earth1, is a prime example. Here, we estimate the amount of black carbon generated by the burning of the Atlantic forest, using historical records of land cover, satellite data and black carbon conversion ratios. We estimate that before 1973, destruction of the Atlantic forest generated 200–500 million tons of black carbon. We then estimate the amount of black carbon exported from this relict forest between 1997 and 2008, using measurements of polycyclic aromatic black carbon collected from a large river draining the region, and a continuous record of river discharge. We show that dissolved black carbon (DBC) continues to be mobilized from the watershed each year in the rainy season, despite the fact that widespread forest burning ceased in 1973. We estimate that the river exports 2,700 tons of DBC to the ocean each year. Scaling our findings up, we estimate that 50,000–70,000 tons of DBC are exported from the former forest each year. We suggest that an increase in black carbon production on land could increase the size of the refractory pool of dissolved organic carbon in the deep ocean.
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Autopsy of two mega-heatwaves
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Record-breaking heatwaves in 2003 and 2010 surprised both the public and experts. Observations provide new insights into how temperatures escalated to unprecedented values through the interaction of boundary-layer dynamics and land surface drying.
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Brownness of organics in aerosols from biomass burning linked to their black carbon content
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Atmospheric particulate matter plays an important role in the Earth’s radiative balance. Over the past two decades, it has been established that a portion of particulate matter, black carbon, absorbs significant amounts of light and exerts a warming effect rivalling that of anthropogenic carbon dioxide1,2. Most climate models treat black carbon as the sole light-absorbing carbonaceous particulate. However, some organic aerosols, dubbed brown carbon and mainly associated with biomass burning emissions3–6 , also absorbs light7 . Unlike black carbon, whose light absorption properties are well understood8, brown carbon comprises a wide range of poorly characterized compounds that exhibit highly variable absorptivities, with reported values spanning two orders of magnitude3–6,9,10. Here we present smog chamber experiments to characterize the effective absorptivity of organic aerosol from biomass burning under a range of conditions. We show that brown carbon in emissions from biomass burning is associated mostly with organic compounds of extremely low volatility11. In addition, we find that the effective absorptivity of organic aerosol in biomass burning emissions can be parameterized as a function of the ratio of black carbon to organic aerosol, indicating that aerosol absorptivity depends largely on burn conditions, not fuel type. We conclude that brown carbon from biomass burning can be an important factor in aerosol radiative forcing.
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Elevation-dependent influence of snow accumulation on forest greening
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Rising temperatures and declining water availability have influenced the ecological function of mountain forests over the past half-century. For instance, warming in spring and summer and shifts towards earlier snowmelt are associated with an increase in wildfire activity and tree mortality in mountain forests in the western United States (1,2). Temperature increases are expected to continue during the twenty-first century in mountain ecosystems across the globe (3,4), with uncertain consequences. Here, we examine the influence of interannual variations in snowpack accumulation on forest greenness in the Sierra Nevada Mountains, California, between 1982 and 2006. Using observational records of snow accumulation and satellite data on vegetation greenness we show that vegetation greenness increases with snow accumulation. Indeed, we show that variations in maximum snow accumulation explain over 50% of the interannual variability in peak forest greenness across the Sierra Nevada region. The extent to which snow accumulation can explain variations in greenness varies with elevation, reaching a maximum in the water-limited mid- elevations, between 2,000 and 2,600 m. In situ measurements of carbon uptake and snow accumulation along an elevational transect in the region confirm the elevation dependence of this relationship. We suggest that mid-elevation mountain forest ecosystems could prove particularly sensitive to future increases in temperature and concurrent changes in snow accumulation and melt.
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Comment:Nuclear winter is a real and present danger
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Models show that even a ‘small’ nuclear war would cause catastrophic climate change. Such findings must inform policy, says Alan Robock.
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Ecological and Evolutionary Responses to Recent Climate Change
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Ecological changes in the phenology and distribution of plants and animals are occurring in all well-studied marine, freshwater, and terrestrial groups. These observed changes are heavily biased in the directions predicted from global warming and have been linked to local or regional climate change through correlations between climate and biological variation, field and laboratory experiments, and physiological research. Range-restricted species, particularly polar and mountaintop species, show severe range contractions and have been the first groups in which entire species have gone extinct due to recent climate change. Tropical coral reefs and amphibians have been most negatively affected. Predator-prey and plant-insect interactions have been disrupted when interacting species have responded differently to warming. Evolutionary adaptations to warmer conditions have occurred in the interiors of species’ ranges, and resource use and dispersal have evolved rapidly at expanding range margins. Observed genetic shifts modulate local effects of climate change, but there is little evidence that they will mitigate negative effects at the species level.
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A globally coherent fingerprint of climate change impacts across natural systems
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Causal attribution of recent biological trends to climate change is complicated because non-climatic influences dominate local, short-term biological changes. Any underlying signal from climate change is likely to be revealed by analyses that seek systematic trends across diverse species and geographic regions; however, debates within the Intergovernmental Panel on Climate Change (IPCC) reveal several definitions of a ‘systematic trend’. Here, we explore these differences, apply diverse analyses to more than 1,700 species, and show that recent biological trends match climate change predictions. Global meta-analyses documented significant range shifts averaging 6.1 km per decade towards the poles (or metres per decade upward), and significant mean advancement of spring events by 2.3 days per decade. We define a diagnostic fingerprint of temporal and spatial ‘sign-switching’ responses uniquely predicted by twentieth century climate trends. Among appropriate long-term/large-scale/multi-species data sets, this diagnostic fingerprint was found for 279 species. This suite of analyses generates ‘very high confidence’ (as laid down by the IPCC) that climate change is already affecting living systems.
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Decline of Leaf Hydraulic Conductance with Dehydration: Relationship to Leaf Size and Venation Architecture
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Across plant species, leaves vary enormously in their size and their venation architecture, of which one major function is to replace water lost to transpiration. The leaf hydraulic conductance (Kleaf) represents the capacity of the transport system to deliver water, allowing stomata to remain open for photosynthesis. Previous studies showed that Kleaf relates to vein density (vein length per area). Additionally, venation architecture determines the sensitivity of Kleaf to damage; severing the midrib caused Kleaf and gas exchange to decline, with lesser impacts in leaves with higher major vein density that provided more numerous water flow pathways around the damaged vein. Because xylem embolism during dehydration also reduces Kleaf, we hypothesized that higher major vein density would also reduce hydraulic vulnerability. Smaller leaves, which generally have higher major vein density, would thus have lower hydraulic vulnerability. Tests using simulations with a spatially explicit model confirmed that smaller leaves with higher major vein density were more tolerant of major vein embolism. Additionally, for 10 species ranging strongly in drought tolerance, hydraulic vulnerability, determined as the leaf water potential at 50% and 80% loss of Kleaf, was lower with greater major vein density and smaller leaf size (|r| = 0.85–0.90; P , 0.01). These relationships were independent of other aspects of physiological and morphological drought tolerance. These findings point to a new functional role of venation architecture and small leaf size in drought tolerance, potentially contributing to well-known biogeographic trends in leaf size.
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