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A safe operating space for humanity
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Identifying and quantifying planetary boundaries that must not be transgressed could help prevent human activities from causing unacceptable environmental change, argue Johan RockstrÖm and colleagues.
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El Nino in a changing climate
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El Nino events, characterized by anomalous warming in the eastern equatorial Pacific Ocean, have global climatic teleconnections and are the most dominant feature of cyclic climate variability on subdecadal timescales. Understanding changes in the frequency or characteristics of El Nino events in a changing climate is therefore of broad scientific and socioeconomic interest. Recent studies (1–5) show that the canonical El Nino has become less frequent and that a different kind of El Nino has become more common during the late twentieth century, in which warm sea surface temperatures (SSTs) in the central Pacific are flanked on the east and west by cooler SSTs. This type of El Nino, termed the central Pacific El Nino (CP-El Nino; also termed the dateline El Nino (2), El Nino Modoki (3) or a warm pool El Nino (5), differs from the canonical eastern Pacific El Nino (EP-El Nino) in both the location of maximum SST anomalies and tropical–midlatitude teleconnections. Here we show changes in the ratio of CP-El Nino to EP-El Nino under projected global EQ warming scenarios from the Coupled Model Intercomparison Project phase 3 multi-model data set (6). Using calculations based 10o S on historical El Nino indices, we find that projections of anthropogenic climate change are associated with an increased frequency of the CP-El Nino compared to the EP-El Nino. When restricted to the six climate models with the best representation of the twentieth-century ratio of CP-El Nino to EP-El Nino, the occurrence ratio of CP-El Nino/EP-El Nino is projected to increase as 10o N much as five times under global warming. The change is related to a flattening of the thermocline in the equatorial Pacific.
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CLIMATE’S SMOKY SPECTRE
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With their focus on greenhouse gases, atmospheric scientists have largely overlooked lowly soot particles. But black carbon is now a hot topic among researchers and politicians.
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COMMENTARY: Overshoot, adapt and recover
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We will probably overshoot our current climate targets, so policies of adaptation and recovery need much more attention, say Martin Parry, Jason Lowe and Clair Hanson. FROM THE TEXT: “We should be planning to adapt
to at least 4°C of warming.”
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ESSAY : The worst-case scenario
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Stephen Schneider explores what a world with 1,000 parts per million of CO2 in its atmosphere might look like.
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Approaching a state shift in Earth’s biosphere
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Localized ecological systems are known to shift abruptly and irreversibly from one state to another when they are forced across critical thresholds. Here we review evidence that the global ecosystem as a whole can react in the same way and is approaching a planetary-scale critical transition as a result of human influence. The plausibility of a planetary-scale ‘tipping point’ highlights the need to improve biological forecasting by detecting early warning signs of critical transitions on global as well as local scales, and by detecting feedbacks that promote such transitions. It is also necessary to address root causes of how humans are forcing biological changes.
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A global synthesis reveals biodiversity loss as a major driver of ecosystem change
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Evidence is mounting that extinctions are altering key processes important to the productivity and sustainability of Earth’s ecosystems (1–4). Further species loss will accelerate change in ecosystem processes (5–8), but it is unclear how these effects compare to the direct effects of other forms of environmental change that are both driving diversity loss and altering ecosystem function. Here we use a suite of meta-analyses of published data to show that the effects of species loss on productivity and decomposition—two processes important in all ecosystems—are of comparable magnitude to the effects of many other global environmental changes. In experiments, intermediate levels of species loss (21–40%) reduced plant production by 5–10%, comparable to previously documented effects of ultraviolet radiation and climate warming. Higher levels of extinction (41–60%) had effects rivalling those of ozone, acidification, elevated CO2 and nutrient pollution. At intermediate levels, species loss generally had equal or greater effects on decomposition than did elevated CO2 and nitrogen addition. The identity of species lost also had a large effect on changes in productivity and decomposition, generating a wide range of plausible outcomes for extinction. Despite the need for more studies on interactive effects of diversity loss and environmental changes, our analyses clearly show that the ecosystem consequences of local species loss are as quantitatively significant as the direct effects of several global change stressors that have mobilized major international concern and remediation efforts (9).
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Biodiversity loss and its impact on humanity
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The most unique feature of Earth is the existence of life, and the most extraordinary feature of life is its diversity. Approximately 9 million types of plants, animals, protists and fungi inhabit the Earth. So, too, do 7 billion people. Two decades ago, at the first Earth Summit, the vast majority of the world’s nations declared that human actions were dismantling the Earth’s ecosystems, eliminating genes, species and biological traits at an alarming rate. This observation led to the question of how such loss of biological diversity will alter the functioning of ecosystems and their ability to provide society with the goods and services needed to prosper.
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A large source of low-volatility secondary organic aerosol
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Forests emit large quantities of volatile organic compounds (VOCs) to the atmosphere. Their condensable oxidation products can form secondary organic aerosol, a significant and ubiquitous component of atmospheric aerosol 1,2, which is known to affect the Earth’s radiation balance by scattering solar radiation and by acting as cloud condensation nuclei 3. The quantitative assessment of such climate effects remains hampered by a number of factors, including an incom- plete understanding of how biogenic VOCs contribute to the formation of atmospheric secondary organic aerosol. The growth of newly formed particles from sizes of less than three nanometres up to the sizes of cloud condensation nuclei (about one hundred nanometres) in many continental ecosystems requires abundant, essentially non- volatile organic vapours4–6, but the sources and compositions of such vapours remain unknown. Here we investigate the oxidation of VOCs, in particular the terpene a-pinene, under atmospherically relevant conditions in chamber experiments. We find that a direct pathway leads from several biogenic VOCs, such as monoterpenes, to the for- mation of large amounts of extremely low-volatility vapours. These vapours form at significant mass yield in the gas phase and condense irreversibly onto aerosol surfaces to produce secondary organic aero- sol, helping to explain the discrepancy between the observed atmo- spheric burden of secondary organic aerosol and that reported by many model studies2. We further demonstrate how these low-volatility vapours can enhance, or even dominate, the formation and growth of aerosol particles over forested regions, providing a missing link between biogenic VOCs and their conversion to aerosol particles. Our findings could help to improve assessments of biosphere–aerosol– climate feedback mechanisms 6–8, and the air quality and climate effects of biogenic emissions generally.
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Carbon loss from an unprecedented Arctic tundra wildfire
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Arctic tundra soils store large amounts of carbon (C) in organic soil layers hundreds to thousands of years old that insulate, and in some cases maintain, permafrost soils1,2. Fire has been largely absent from most of this biome since the early Holocene epoch3, but its frequency and extent are increasing, probably in response to climate warming4. The effect of fires on the C balance of tundra landscapes, however, remains largely unknown. The Anaktuvuk River fire in 2007 burned 1,039 square kilometres of Alaska’s Arctic slope, making it the largest fire on record for the tundra biome and doubling the cumulative area burned since 1950 (ref. 5). Here we report that tundra ecosystems lost 2,016 6 435 g C m22 in the fire, an amount two orders of magnitude larger than annual net C exchange in undisturbed tundra6. Sixty per cent of this C loss was from soil organic matter, and radiocarbon dating of residual soil layers revealed that the maximum age of soil C lost was 50 years. Scaled to the entire burned area, the fire released approximately 2.1 teragrams of C to the atmosphere, an amount similar in magnitude to the annual net C sink for the entire Arctic tundra biome averaged over the last quarter of the twentieth century7. The mag- nitude of ecosystem C lost by fire, relative to both ecosystem and biome-scale fluxes, demonstrates that a climate-driven increase in tundra fire disturbance may represent a positive feedback, potentially offsetting Arctic greening 8 and influencing the net C balance of the tundra biome.
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