Climate Science Documents
Conservation value of forests attacked by bark beetles: Highest number of indicator species is found in early successional stages
Heavy natural disturbance in large protected areas of former commercial forests increasingly evokes European parliaments to call for management intervention because a loss of habitats and species is feared. In contrast, natural early successional habitats have recently been recognised as important for conservation. Current knowledge in this field mostly results from studies dealing only with selected taxa. Here we analyse the success of species across 24 lineages of three kingdoms in the Bavarian Forest National Park (Germany) after 15 years of a European spruce bark beetle (Ips typographus L.) outbreak that led to rapid canopy opening. Using indicator species analysis, we found 257 species with a significant preference for open forests and 149 species with a preference for closed forests, but only 82 species with a preference for the stand conditions transitional between open and closed forests. The large number of species with a preference for open forests across lineages supports the role of this bark beetle as a keystone species for a broad array of species. The slowdown of the outbreak after 15 years in the core zone of the national park resulted in less than half of the area being affected, due to variability in stand ages and tree species mixtures. Our case study is representative of the tree species composition and size of many large protected montane areas in Central European countries and illustrates that (1) natural disturbances increase biodiversity in formerly managed forests and (2) a montane protected area spanning 10,000 ha of low range mountains is likely sufficient to allow natural disturbances without a biased loss of closed-forest species.
Effects of Management on Carbon Sequestration in Forest Biomass in Southeast Alaska
The Tongass National Forest (Tongass) is the largest national forest and largest area of old-growth forest in the United States. Spatial geographic informa- tion system data for the Tongass were combined with forest inventory data to estimate and map total carbon stock in the Tongass; the result was 2.8±0.5PgC,or8%of the total carbon in the forests of the conterminous USA and 0.25% of the carbon in global forest vegetation and soils. Cumulative net carbon loss from the Tongass due to management of the forest for the period 1900–95 was estimated at 6.4–17.2 Tg C. Using our spatially explicit data for carbon stock and net flux, we modeled the potential effect of five management regimes on future net carbon flux. Estimates of net carbon flux were sensitive to projections of the rate of carbon accumulation in second-growth forests and to the amount of carbon left in standing biomass after harvest. Projections of net carbon flux in the Tongass range from 0.33 Tg C annual sequestration to 2.3 Tg C annual emission for the period 1995–2095. For the period 1995–2195, net flux estimates range from 0.19 Tg C annual sequestra- tion to 1.6 Tg C annual emission. If all timber harvesting in the Tongass were halted from 1995 to 2095, the economic value of the net carbon sequestered during the 100-year hiatus, assuming $20/Mg C, would be $4 to $7 million/y (1995 US dollars). If a prohibition on logging were extended to 2195, the annual economic value of the carbon sequestered would be largely unaffected ($3 to $6 million/y). The potential annual economic value of carbon sequestration with management maxi- mizing carbon storage in the Tongass is comparable to revenue from annual timber sales historically authorized for the forest. Key words: carbon sequestration; geographic information system; climate change; forest management; Alaska.
Impacts of climate change on August stream discharge in the Central-Rocky Mountains
In the snowmelt dominated hydrology of arid western US landscapes, late summer low streamflow is the most vulnerable period for aquatic ecosystem habitats and trout populations. This study analyzes mean August discharge at 153 streams throughout the Central Rocky Mountains of North America (CRMs) for changes in discharge from 1950–2008. The purpose of this study was to determine if: (1) Mean August stream discharge values have decreased over the last half-century; (2) Low discharge values are occurring more frequently; (3) Climatic variables are influencing August discharge trends. Here we use a strict selection process to characterize gauging stations based on amount of anthropogenic impact in order to identify heavily impacted rivers and understand the relationship between climatic variables and discharge trends. Using historic United States Geologic Survey discharge data, we analyzed data for trends of 40–59 years. Combining of these records along with aerial photos and water rights records we selected gauging stations based on the length and continuity of discharge records and categorized each based on the amount of diversion. Variables that could potentially influence discharge such as change in vegetation and Pacific Decadal Oscillation (PDO) were examined, but we found that that both did not significantly influence August discharge patterns. Our analyses indicate that non-regulated watersheds are experiencing substantial declines in stream discharge and we have found that 89% of all non-regulated stations exhibit a declining slope. Additionally our results here indicate a significant (α≤0.10) decline in discharge from 1951–2008 for the CRMs. Correlations results at our pristine sites show a negative relationship between air temperatures and discharge and these results coupled with increasing air temperature trends pose serious concern for aquatic ecosystems in CRMs.
Divergent global precipitation changes induced by natural versus anthropogenic forcing
As a result of global warming, precipitation is likely to increase in high latitudes and the tropics and to decrease in already dry sub-tropical regions (1). The absolute magnitude and regional details of such changes, however, remain intensely debated (2,3). As is well known from El Nino studies, sea-surface-temperature gradients across the tropical Pacific Ocean can strongly influence global rainfall (4,5). Palaeoproxy evidence indicates that the difference between the warm west Pacific and the colder east Pacific increased in past periods when the Earth warmed as a result of increased solar radiation (6–9). In contrast, in most model projections of future greenhouse warming this gradient weakens (2,10,11). It has not been clear how to reconcile these two findings. Here we show in climate model simulations that the tropical Pacific sea-surface-temperature gradient increases when the warming is due to increased solar radiation and decreases when it is due to increased greenhouse-gas forcing. For the same global surface temperature increase the latter pattern produces less rainfall, notably over tropical land, which explains why in the model the late twentieth century is warmer than in the Medieval Warm Period (around AD 1000–1250) but precipitation is less. This difference is consistent with the global tropospheric energy budget (12), which requires a balance between the latent heat released in precipitation and radiative cooling. The tropospheric cooling is less for increased greenhouse gases, which add radiative absorbers to the troposphere, than for increased solar heating, which is concentrated at the Earth’s surface. Thus warming due to increased greenhouse gases produces a climate signature different from that of warming due to solar radiation changes.
The Role of Livestock Production in Carbon and Nitrogen Cycles
This review looks at the role of the livestock sector in carbon (C) and nitrogen (N) cycles from a global perspective and considers impacts at the various stages of the commodity chain. With regard to livestock, N and C cycles are closely connected to livestock’s role in land use and land-use change. Livestock’s land use includes grazing land and cropland dedicated to the production of feed crops and fodder. Considering emissions along the entire commodity chain, livestock currently contribute about 18% to the global warming effect. Live- stock contribute about 9% of total carbon dioxide (CO2) emissions, but 37% of methane (CH4), and 65% of nitrous oxide (N2O). The latter will substantially increase over the coming decades, as the pasture land is currently at maximum expanse in most regions; future expansion of the livestock sector will increasingly be crop based. The chapter also reviews mitigation options to reduce C and N emissions from livestock’s land use, production, and animal waste.
A paradigm shift in understanding and quantifying the effects of forest harvesting on floods in snow environments
A well-established precept in forest hydrology is that any reduction of forest cover will always have a progressively smaller effect on floods with increasing return period. The underlying logic in snow environments is that during the largest snowmelt events the soils and vegetation canopy have little additional storage capacity and under these conditions much of the snowmelt will be converted to runoff regardless of the amount or type of vegetation cover. Here we show how this preconceived physical understanding, reinforced by the outcomes of numerous paired watershed studies, is indefensible because it is rationalized outside the flood frequency distribution framework. We conduct a meta-analysis of postharvest data at four catchments (3–37 km2) with moderate level of harvesting (33%–40%) to demonstrate how harvesting increases the magnitude and frequency of all floods on record (19–99 years) and how such effects can increase unchecked with increasing return period as a consequence of changes to both the mean (þ11% to þ35%) and standard deviation (12% to þ19%) of the flood frequency distribution. We illustrate how forest harvesting has substantially increased the frequency of the largest floods in all study sites regardless of record length and this also runs counter to the prevailing wisdom in hydrological science. The dominant process responsible for these newly emerging insights is the increase in net radiation associated with the conversion from longwave-dominated snowmelt beneath the canopy to shortwave-dominated snowmelt in harvested areas, further amplified or mitigated by basin characteristics such as aspect distribution, elevation range, slope gradient, amount of alpine area, canopy closure, and drainage density. Investigating first order environmental controls on flood frequency distributions, a standard research method in stochastic hydrology, represents a paradigm shift in the way harvesting effects are physically explained and quantified in forest hydrology literature.
Frequent Long-Distance Plant Colonization
The ability of species to track their ecological niche after climate change is a major source of uncertainty in predicting their future distribution. By analyzing DNA fingerprinting (amplified fragment-length polymorphism) of nine plant species, we show that long-distance colonization of a remote arctic archipelago, Svalbard, has occurred repeatedly and from several source regions. Propagules are likely carried by wind and drifting sea ice. The genetic effect of restricted colonization was strongly correlated with the temperature requirements of the species, indicating that establishment limits distribution more than dispersal. Thus, it may be appropriate to assume unlimited dispersal when predicting long-term range shifts in the Arctic.
Long term climate implications of 2050 emission reduction targets
A coupled atmosphere-ocean-carbon cycle model is used to examine the long term climate implications of various 2050 greenhouse gas emission reduction targets. All emission targets considered with less than 60% global reduction by 2050 break the 2.0°C threshold warming this century, a number that some have argued represents an upper bound on manageable climate warming. Even when emissions are stabilized at 90% below present levels at 2050, this 2.0°C threshold is eventually broken. Our results suggest that if a 2.0°C warming is to be avoided, direct CO2 capture from the air, together with subsequent sequestration, would eventually have to be introduced in addition to sustained 90% global carbon emissions reductions by 2050.
Wildfire and forest harvest disturbances in the boreal forest leave different long-lasting spatial signatures
Natural disturbances leave long-term legacies that vary among landscapes and ecosystem types, and which become integral parts of successional pro- cesses at a given location. As humans change land use, not only are immediate post-disturbance patterns altered, but the processes of recovery themselves are likely altered by the disturbance. We assessed whether short-term effects on soil and vegetation that distinguish wildfire from forest harvest persist over 60 years after disturbance in boreal black spruce forests, or post-disturbance processes of recovery promote convergence of the two disturbance types.
Untangling the confusion around land carbon science and climate change mitigation policy
Depletion of ecosystem carbon stocks is a significant source of atmospheric CO2 and reducing land-based emissions and maintaining land carbon stocks contributes to climate change mitigation. We summarize current understanding about human perturbation of the global carbon cycle, examine three scientific issues and consider implications for the interpretation of international climate change policy decisions, concluding that considering carbon storage on land as a means to ‘offset’ CO2 emissions from burning fossil fuels (an idea with wide currency) is scientifically flawed. The capacity of terrestrial ecosystems to store carbon is finite and the current sequestration potential primarily reflects depletion due to past land use. Avoiding emissions from land carbon stocks and refilling depleted stocks reduces atmospheric CO2 concentration, but the maximum amount of this reduction is equivalent to only a small fraction of potential fossil fuel emissions.
Interactions between climate and habitat loss effects on biodiversity: a systematic review and meta-analysis
Climate change and habitat loss are both key threatening processes driving the global loss in biodiversity. Yet little is known about their synergistic effects on biological populations due to the complexity underlying both processes. If the combined effects of habitat loss and climate change are greater than the effects of each threat individually, current conservation management strategies may be inefficient and at worst ineffective. Therefore, there is a pressing need to identify whether interacting effects between climate change and habitat loss exist and, if so, quantify the magnitude of their impact. In this article, we present a meta-analysis of studies that quantify the effect of habitat loss on biologi- cal populations and examine whether the magnitude of these effects depends on current climatic conditions and his- torical rates of climate change. We examined 1319 papers on habitat loss and fragmentation, identified from the past 20 years, representing a range of taxa, landscapes, land-uses, geographic locations and climatic conditions. We find that current climate and climate change are important factors determining the negative effects of habitat loss on spe- cies density and/or diversity. The most important determinant of habitat loss and fragmentation effects, averaged across species and geographic regions, was current maximum temperature, with mean precipitation change over the last 100 years of secondary importance. Habitat loss and fragmentation effects were greatest in areas with high maxi- mum temperatures. Conversely, they were lowest in areas where average rainfall has increased over time. To our knowledge, this is the first study to conduct a global terrestrial analysis of existing data to quantify and test for inter- acting effects between current climate, climatic change and habitat loss on biological populations. Understanding the synergistic effects between climate change and other threatening processes has critical implications for our ability to support and incorporate climate change adaptation measures into policy development and management response. Keywords: climate change, habitat fragmentation, habitat loss, interactions, meta-analysis, mixed-effects logistic regression
Effects of grazing on grassland soil carbon: a global review
Soils of grasslands represent a large potential reservoir for storing CO2, but this potential likely depends on how grasslands are managed for large mammal grazing. Previous studies found both strong positive and negative grazing effects on soil organic carbon (SOC) but explanations for this variation are poorly developed. Expanding on previous reviews, we performed a multifactorial meta-analysis of grazer effects on SOC density on 47 independent experimen- tal contrasts from 17 studies. We explicitly tested hypotheses that grazer effects would shift from negative to positive with decreasing precipitation, increasing fineness of soil texture, transition from dominant grass species with C3 to C4 photosynthesis, and decreasing grazing intensity, after controlling for study duration and sampling depth. The six variables of soil texture, precipitation, grass type, grazing intensity, study duration, and sampling depth explained 85% of a large variation (`150 g m␣2 yr␣1) in grazing effects, and the best model included significant interactions between precipitation and soil texture (P = 0.002), grass type, and grazing intensity (P = 0.012), and study duration and soil sampling depth (P = 0.020). Specifically, an increase in mean annual precipitation of 600 mm resulted in a 24% decrease in grazer effect size on finer textured soils, while on sandy soils the same increase in precipitation pro- duced a 22% increase in grazer effect on SOC. Increasing grazing intensity increased SOC by 6–7% on C4-dominated and C4–C3 mixed grasslands, but decreased SOC by an average 18% in C3-dominated grasslands. We discovered these patterns despite a lack of studies in natural, wildlife-dominated ecosystems, and tropical grasslands. Our results, which suggest a future focus on why C3 vs. C4-dominated grasslands differ so strongly in their response of SOC to grazing, show that grazer effects on SOC are highly context-specific and imply that grazers in different regions might be managed differently to help mitigate greenhouse gas emissions. Keywords: carbon sequestration, grasslands, grazing, grazing intensity, precipitation, soil organic carbon, soil texture
Millennium Ecosystem Assessment: Research Needs
The research community needs to develop analytical tools for projecting future trends and evaluating the success of interventions as well as indicators to monitor biological, physical, and social changes.
Migration and Dispersal: Science Special Section
INTRODUCTION: When to Go, Where to Stop THE ABILITY TO MOVE, AT SOME STAGE IN THE LIFE CYCLE, IS FUNDAMENTAL TO SUCCESS in life. Passive drift in water columns conferred a selective advantage for early life, offering an escape from starvation and genetic uniformity. Since then, organisms have evolved many ways to disperse and migrate in response to the pressures of finding resources, escaping predators, seeking out mates and suitable breeding grounds, and distancing themselves from family. Dispersal in its broadest sense means movement away from the birthplace. Strictly speaking, migration involves travel in a periodically and geographically predictable way, whether it occurs just once or many times. In this issue, Science deals with what we know, what we need to know, and how we are going to find out more about both of these movement types. In plants, the spore, seed, or fruit is typically the unit of dispersal. Although the many morphological adaptations for their dispersal are known, until now, researchers have been unable to determine the distances traveled or the proportion of dispersal events that lead to seedlings. In one Perspective (p. 786), Nathan describes recent developments in the modeling and measurement of the long-distance dispersal of plants. A News story by Holden (p. 779) discusses the push to come up with a theoretical framework, not just for plants, but for all moving organisms. Organisms also disperse in reaction to changing habitats and climate. The Perspective by Kokko and López-Sepulcre (p. 789) discusses the selective forces affecting this ability in animals and how dispersal translates into range expansions and contractions. Kintisch (p. 776) describes the challenges for marine scientists assessing how climate change may affect oceangoing species. Humans have been great dispersers. Colonizing new habitat has been a hallmark of human ecology over the past million years or so. In a Review (p. 796), Mellars considers recent advances in archaeology and genetics that are illuminating the controversies over the routes taken by ancient peoples in the colonization of Asia 40,000 to 60,000 years ago. Two Perspectives consider migration: Holland et al. (p. 794) focus on migrating insects, which tend to travel in established geographical patterns across several generations rather than returning to their birthplace, and Alerstam (p. 791) discusses the accumulating and sometimes conflicting evidence about the navigational mechanisms used by animals (particularly birds) in long-distance annual migrations. In a related Report (p. 837), Muheim et al. describe the role of polarized light at dawn and sunset in calibrating the magnetic compasses of migrating birds. A News story by Morell (p. 783) describes a new model that will clarify the mix of genes and environmental responses underlying successful bird migration. As News stories by Blackburn and Holden (p. 780) and Unger (p. 784) point out, ingenuity and persistence are beginning to pay off in new techniques for following organisms, be they fish, crabs, jellyfish, rhinos, or polar bears. Thanks to these advances, the study of the ecology and evolution of movement is charging ahead and unearthing the challenges faced by organisms in dispersing and migrating in a world undergoing anthropogenic change.
On the Hydrologic Adjustment of Climate-Model Projections: The Potential Pitfall of Potential Evapotranspiration
Hydrologic models often are applied to adjust projections of hydroclimatic change that come from climate models. Such adjustment includes climate-bias correction, spatial refinement (‘‘downscaling’’), and consideration of the roles of hydrologic processes that were neglected in the climate model. Described herein is a quantitative analysis of the effects of hydrologic adjustment on the projections of runoff change associated with projected twenty-first-century climate change. In a case study including three climate models and 10 river basins in the contiguous United States, the authors find that relative (i.e., fractional or percentage) runoff change computed with hydrologic adjustment more often than not was less positive (or, equivalently, more negative) than what was pro- jected by the climate models. The dominant contributor to this decrease in runoff was a ubiquitous change in runoff (median 211%) caused by the hydrologic model’s apparent amplification of the climate-model-implied growth in potential evapotranspiration. Analysis suggests that the hydrologic model, on the basis of the empirical, temperature-based modified Jensen–Haise formula, calculates a change in potential evapotranspiration that is typically 3 times the change implied by the climate models, which explicitly track surface energy budgets. In com- parison with the amplification of potential evapotranspiration, central tendencies of other contributions from hydrologic adjustment (spatial refinement, climate-bias adjustment, and process refinement) were relatively small. The authors’ findings highlight the need for caution when projecting changes in potential evapotranspiration for use in hydrologic models or drought indices to evaluate climate change impacts on water. KEYWORDS: Hydrologic model; Climate change; Potential evapotranspi- ration
Temperature Mediated Moose Survival in Northeastern Minnesota
The earth is in the midst of a pronounced warming trend and temperatures in Minnesota, USA, as elsewhere, are projected to increase. Northern Minnesota represents the southern edge to the circumpolar distribution of moose (Alces alces), a species intolerant of heat. Moose increase their metabolic rate to regulate their core body temperature as temperatures rise. We hypothesized that moose survival rates would be a function of the frequency and magnitude that ambient temperatures exceeded the upper critical temperature of moose. We compared annual and seasonal moose survival in northeastern Minnesota between 2002 and 2008 with a temperature metric. We found that models based on January temperatures above the critical threshold were inversely correlated with subsequent survival and explained .78% of variability in spring, fall, and annual survival. Models based on late-spring temperatures also explained a high proportion of survival during the subsequent fall. A model based on warm-season temperatures was important in explaining survival during the subsequent winter. Our analyses suggest that temperatures may have a cumulative influence on survival. We expect that continuation or acceleration of current climate trends will result in decreased survival, a decrease in moose density, and ultimately, a retreat of moose northward from their current distribution.
CARBON CYCLE : Fertilizing change
Carbon cycle–climate feedbacks are expected to diminish the size of the terrestrial carbon sink over the next century. Model simulations suggest that nitrogen availability is likely to play a key role in mediating this response.
First signs of carbon sink saturation in European forest biomass
European forests are seen as a clear example of vegetation rebound in the Northern Hemisphere; recovering in area and growing stock since the 1950s, after centuries of stock decline and deforestation. These regrowing forests have shown to be a persistent carbon sink, projected to continue for decades, however, there are early signs of saturation. Forest policies and management strategies need revision if we want to sustain the sink.
Earth system sensitivity inferred from Pliocene modelling and data
Here we use a coupled atmosphere–ocean general circulation model to simulate the climate of the mid-Pliocene warm period (about three million years ago), and analyse the forcings and feedbacks that contributed to the relatively warm temperatures. Furthermore, we compare our simulation with proxy records of mid-Pliocene sea surface temperature. Taking these lines of evidence together, we estimate that the response of the Earth system to elevated atmospheric carbon dioxide concentrations is 30–50% greater than the response based on those fast-adjusting components of the climate system that are used traditionally to estimate climate sensitivity. We conclude that targets for the long-term stabilization of atmospheric greenhouse gas concentrations aimed at preventing a dangerous human interference with the climate system should take into account this higher sensitivity of the Earth system.
A general integrative model for scaling plant growth, carbon flux, and functional trait spectra
Linking functional traits to plant growth is critical for scaling attributes of organisms to the dynamics of ecosystems (1,2) and for understanding how selection shapes integrated botanical phenotypes (3). However, a general mechanistic theory showing how traits specifically influence carbon and biomass flux within and across plants is needed. Building on foundational work on relative growth rate (4–6), recent work on functional trait spectra (7–9), and metabolic scaling theory (10,11), here we derive a generalized trait-based model of plant growth. In agreement with a wide variety of empirical data, our model uniquely predicts how key functional traits interact to regulate variation in relative growth rate, the allometric growth normalizations for both angiosperms and gymnosperms, and the quantitative form of several functional trait spectra relationships. The model also provides a general quantitative framework to incorporate additional leaf-level trait scaling relationships (7,8) and hence to unite functional trait spectra with theories of relative growth rate, and metabolic scaling. We apply the model to calculate carbon use efficiency. This often ignored trait, which may influence variation in relative growth rate, appears to vary directionally across geographic gradients. Together, our results show how both quantitative plant traits and the geometry of vascular transport networks can be merged into a common scaling theory. Our model provides a framework for predicting not only how traits covary within an integrated allometric phenotype but also how trait variation mechanistically influences plant growth and carbon flux within and across diverse ecosystems.
Snowball Earth termination by destabilization of equatorial permafrost methane clathrate
The start of the Ediacaran period is defined by one of the most severe climate change events recorded in Earth history—the recov- ery from the Marinoan ‘snowball’ ice age, ,635 Myr ago (ref. 1). Marinoan glacial-marine deposits occur at equatorial palaeolati- tudes2, and are sharply overlain by a thin interval of carbonate that preserves marine carbon and sulphur isotopic excursions of about 25 and 115 parts per thousand, respectively3–5; these deposits are thought to record widespread oceanic carbonate precipitation during postglacial sea level rise1,3,4. This abrupt transition records a climate system in profound disequilibrium3,6 and contrasts shar- ply with the cyclical stratigraphic signal imparted by the balanced feedbacks modulating Phanerozoic deglaciation. Hypotheses accounting for the abruptness of deglaciation include ice albedo feedback3, deep-ocean out-gassing during post-glacial oceanic overturn7 or methane hydrate destabilization8–10. Here we report the broadest range of oxygen isotope values yet measured in mar- ine sediments (225% to 112%) in methane seeps in Marinoan deglacial sediments underlying the cap carbonate. This range of values is likely to be the result of mixing between ice-sheet-derived meteoric waters and clathrate-derived fluids during the flushing and destabilization of a clathrate field by glacial meltwater. The equatorial palaeolatitude implies a highly volatile shelf permafrost pool that is an order of magnitude larger than that of the present day. A pool of this size could have provided a massive biogeochem- ical feedback capable of triggering deglaciation and accounting for the global postglacial marine carbon and sulphur isotopic excur- sions, abrupt unidirectional warming, cap carbonate deposition, and a marine oxygen crisis. Our findings suggest that methane released from low-latitude permafrost clathrates therefore acted as a trigger and/or strong positive feedback for deglaciation and warming. Methane hydrate destabilization is increasingly suspected as an important positive feedback to climate change11–13 that coincides with critical boundaries in the geological record14,15 and may represent one particularly important mechanism active during conditions of strong climate forcing.
Strong effect of dispersal network structure on ecological dynamics
A central question in ecology with great importance for management, conservation and biological control is how changing connectivity affects the persistence and dynamics of interacting species. Researchers in many disciplines have used large systems of coupled oscillators to model the behaviour of a diverse array of fluctuating systems in nature1–4. In the well-studied regime of weak coupling, synchronization is favoured by increases in coupling strength and large-scale network structures (for example ‘small worlds’) that produce short cuts and clustering5–9. Here we show that, by contrast, randomizing the structure of dispersal networks in a model of predators and prey tends to favour asyn- chrony and prolonged transient dynamics, with resulting effects on the amplitudes of population fluctuations. Our results focus on synchronization and dynamics of clusters in models, and on time- scales, more appropriate for ecology, namely smaller systems with strong interactions outside the weak-coupling regime, rather than the better-studied cases of large, weakly coupled systems. In these smaller systems, the dynamics of transients and the effects of changes in connectivity can be well understood using a set of methods including numerical reconstructions of phase dynamics, examinations of cluster formation and the consideration of important aspects of cyclic dynamics, such as amplitude.
Using (brain)temperature to analyse temporal dynamics in the songbird motor pathway
Here we address these issues by using temperature to manipulate the biophysical dynamics in different regions of the songbird forebrain involved in song production. We find that cooling the premotor nucleus HVC (formerly known as the high vocal centre) slows song speed across all timescales by up to 45 per cent but only slightly alters the acoustic structure, whereas cooling the downstream motor nucleus RA (robust nucleus of the arcopallium) has no observable effect on song timing. Our observations suggest that dynamics within HVC are involved in the control of song timing, perhaps through a chain-like organization. Local manipulation of brain temperature should be broadly applicable to the identification of neural circuitry that controls the timing of behavioural sequences and, more generally, to the study of the origin and role of oscillatory and other forms of brain dynamics in neural systems.
vegetation controlled by tropical sea surface temperatures in the mid-Pleistocene period
The dominant forcing factors for past large-scale changes in vegetation are widely debated. Changes in the distribution of C4 plants—adapted to warm, dry conditions and low atmospheric CO2 concentrations1—have been attributed to marked changes in environmental conditions, but the relative impacts of changes in aridity, temperature2,3 and CO2 concentration4,5 are not well understood. Here, we present a record of African C4 plant abundance between 1.2 and 0.45 million years ago, derived from compound-specific carbon isotope analyses of wind-trans- ported terrigenous plant waxes. We find that large-scale changes in African vegetation are linked closely to sea surface temperatures in the tropical Atlantic Ocean. We conclude that, in the mid- Pleistocene, changes in atmospheric moisture content—driven by tropical sea surface temperature changes and the strength of the African monsoon—controlled aridity on the African continent, and hence large-scale vegetation changes.
Acceleration of global warming due to carbon-cycle feedbacks in a coupled climate model
The continued increase in the atmospheric concentration of carbon dioxide due to anthropogenic emissions is predicted to lead to significant changes in climate1. About half of the current emissions are being absorbed by the ocean and by land ecosystems2, but this absorption is sensitive to climate3,4 as well as to atmospheric carbon dioxide concentrations5, creating a feedback loop. General circulation models have generally excluded the feedback between climate and the biosphere, using static vegetation distributions and CO2 concentrations from simple carbon-cycle models that do not include climate change6. Here we present results from a fully coupled, three-dimensional carbon±climate model, indicating that carbon-cycle feedbacks could signi®cantly accelerate climate change over the twenty-®rst century. We ®nd that under a `business as usual' scenario, the terrestrial biosphere acts as an overall carbon sink until about 2050, but turns into a source thereafter. By 2100, the ocean uptake rate of 5 Gt C yr-1 is balanced by the terrestrial carbon source, and atmospheric CO2 concentrations are 250 p.p.m.v. higher in our fully coupled simulation than in uncoupled carbon models2, resulting in a global-mean warming of 5.5 K, as compared to 4 K without the carbon-cycle feedback.
CO2 emissions from forest loss
Deforestation is the second largest anthropogenic source of carbon dioxide to the atmosphere, after fossil fuel combustion. Following a budget reanalysis, the contribution from deforestation is revised downwards, but tropical peatlands emerge as a notable carbon dioxide source.
Global warmth with little extra co2
Most climate models consider only short-term processes such as cloud and sea-ice formation when assessing Earth’s sensitivity to greenhouse-gas forcing. Mounting evidence indicates that the response could be stronger if boundary conditions change drastically.
Importance of methane and nitrous oxide for Europe’s terrestrial greenhouse-gas balance
Concluding sentence of the abstract: The trend towards more intensive agriculture and logging is likely to make Europe’s land surface a significant source of greenhouse gases. The development of land management policies which aim to reduce greenhouse-gas emissions should be a priority.
Statistically derived contributions of diverse human influences to twentieth-century temperature changes
The warming of the climate system is unequivocal as evidenced by an increase in global temperatures by 0.8 ◦ C over the past century. However, the attribution of the observed warming to human activities remains less clear, particularly because of the apparent slow-down in warming since the late 1990s. Here we analyse radiative forcing and temperature time series with state-of-the-art statistical methods to address this question without climate model simulations. We show that long-term trends in total radiative forcing and temperatures have largely been determined by atmospheric greenhouse gas concentrations, and modulated by other radiative factors. We identify a pronounced increase in the growth rates of both temperatures and radiative forcing around 1960, which marks the onset of sustained global warming. Our analyses also reveal a contribution of human interventions to two periods when global warming slowed down. Our statistical analysis suggests that the reduction in the emissions of ozone-depleting substances under the Montreal Protocol, as well as a reduction in methane emissions, contributed to the lower rate of warming since the 1990s. Furthermore, we identify a contribution from the two world wars and the Great Depression to the documented cooling in the mid-twentieth century, through lower carbon dioxide emissions. We conclude that reductions in greenhouse gas emissions are effective in slowing the rate of warming in the short term.
Biodiversity and ecosystem multifunctionality
Biodiversity loss can affect ecosystem functions and services1–4. Individual ecosystem functions generally show a positive asymptotic relationship with increasing biodiversity, suggesting that some species are redundant5–8. However, ecosystems are managed and conserved for multiple functions, which may require greater biodiversity. Here we present an analysis of published data from grassland biodiversity experiments9–11, and show that ecosystem multifunctionality does require greater numbers of species. We analysed each ecosystem function alone to identify species with desirable effects. We then calculated the number of species with positive effects for all possible combinations of functions. Our results show appreciable differences in the sets of species influ- encing different ecosystem functions, with average proportional overlap of about 0.2 to 0.5. Consequently, as more ecosystem pro- cesses were included in our analysis, more species were found to affect overall functioning. Specifically, for all of the analysed experiments, there was a positive saturating relationship between the number of ecosystem processes considered and the number of species influencing overall functioning. We conclude that because different species often influence different functions, studies focus- ing on individual processes in isolation will underestimate levels of biodiversity required to maintain multifunctional ecosystems.
Subtropical to boreal convergence of tree-leaf temperatures
The oxygen isotope ratio (d18O) of cellulose is thought to provide a record of ambient temperature and relative humidity during per- iods of carbon assimilation1,2. Here we introduce a method to resolve tree-canopy leaf temperature with the use of d18O of cellulose in 39 tree species. We show a remarkably constant leaf temperature of 21.4 6 2.2 6C across 506 of latitude, from subtropical to boreal biomes. This means that when carbon assimilation is maximal, the physiological and morphological properties of tree branches serve to raise leaf temperature above air temperature to a much greater extent in more northern latitudes. A main assumption underlying the use of d18O to reconstruct climate history is that the temperature and relative humidity of an actively photosynthesizing leaf are the same as those of the surrounding air3,4. Our data are contrary to that assumption and show that plant physiological ecology must be considered when reconstructing climate through isotope analysis. Furthermore, our results may explain why climate has only a modest effect on leaf economic traits5 in general.
The effect of permafrost thaw on old carbon release and net carbon exchange from tundra
Permafrost soils in boreal and Arctic ecosystems store almost twice as much carbon1,2 as is currently present in the atmosphere3. Permafrost thaw and the microbial decomposition of previously frozen organic carbon is considered one of the most likely positive climate feedbacks from terrestrial ecosystems to the atmosphere in a warmer world1,2,4–7. The rate of carbon release from permafrost soils is highly uncertain, but it is crucial for predicting the strength and timing of this carbon-cycle feedback effect, and thus how important permafrost thaw will be for climate change this century and beyond1,2,4–7. Sustained transfers of carbon to the atmosphere that could cause a significant positive feedback to climate change must come from old carbon, which forms the bulk of the perma- frost carbon pool that accumulated over thousands of years8–11. Here we measure net ecosystem carbon exchange and the radio- carbon age of ecosystem respiration in a tundra landscape under- going permafrost thaw12 to determine the influence of old carbon loss on ecosystem carbon balance. We find that areas that thawed over the past 15 years had 40 per cent more annual losses of old carbon than minimally thawed areas, but had overall net eco- system carbon uptake as increased plant growth offset these losses. In contrast, areas that thawed decades earlier lost even more old carbon, a 78 per cent increase over minimally thawed areas; this old carbon loss contributed to overall net ecosystem carbon release despite increased plant growth. Our data document significant losses of soil carbon with permafrost thaw that, over decadal timescales, overwhelms increased plant carbon uptake13–15 at rates that could make permafrost a large biospheric carbon source in a warmer world.
The role of stomata in sensing and driving environmental change
Stomata, the small pores on the surfaces of leaves and stalks, regulate the flow of gases in and out of leaves and thus plants as a whole. They adapt to local and global changes on all timescales from minutes to millennia. Recent data from diverse fields are establishing their central importance to plant physiology, evolution and global ecology. Stomatal morphology, distribution and behaviour respond to a spectrum of signals, from intracellular signalling to global climatic change. Such concerted adaptation results from a web of control systems, reminiscent of a ‘scale-free’ network, whose untangling requires integrated approaches beyond those currently used.
rainfall preceded by air passage over forests
Vegetation affects precipitation patterns by mediating moisture, energy and trace-gas fluxes between the surface and atmosphere1. When forests are replaced by pasture or crops, evapotranspiration of moisture from soil and vegetation is often diminished, leading to reduced atmospheric humidity and potentially suppressing precipitation2,3. Climate models predict that large-scale tropical deforestation causes reduced regional precipitation4–10, although the magnitude of the effect is model9,11 and resolution8 dependent. In contrast, observational studies have linked deforestation to increased precipitation locally12–14 but have been unable to explore the impact of large-scale deforestation. Here we use satellite remote-sensing data of tropical precipitation and vegetation, combined with simulated atmospheric transport patterns, to assess the pan-tropical effect of forests on tropical rainfall. We find that for more than 60 per cent of the tropical land surface (latitudes 30 degrees south to 30 degrees north), air that has passed over extens- ive vegetation in the preceding few days produces at least twice as much rain as air that has passed over little vegetation. We demonstrate that this empirical correlation is consistent with evapotranspiration maintaining atmospheric moisture in air that passes over extensive vegetation. We combine these empirical rela- tionships with current trends of Amazonian deforestation to estimate reductions of 12 and 21 per cent in wet-season and dry- season precipitation respectively across the Amazon basin by 2050, due to less-efficient moisture recycling. Our observation-based results complement similar estimates from climate models4–10, in which the physical mechanisms and feedbacks at work could be explored in more detail.
New particle formation in forests inhibited by isoprene emissions
It has been suggested that volatile organic compounds (VOCs) are involved in organic aerosol formation, which in turn affects radiative forcing and climate1. The most abundant VOCs emitted by terrestrial vegetation are isoprene and its derivatives, such as monoterpenes and sesquiterpenes 2. New particle formation in boreal regions is related to monoterpene emissions3 and causes an estimated negative radiative forcing4 of about 20.2 to 20.9 W m22. The annual variation in aerosol growth rates during particle nucleation events correlates with the seasonality of mono- terpene emissions of the local vegetation, with a maximum during summer5. The frequency of nucleation events peaks, however, in spring and autumn5. Here we present evidence from simulation experiments conducted in a plant chamber that isoprene can sig- nificantly inhibit new particle formation. The process leading to the observed decrease in particle number concentration is linked to the high reactivity of isoprene with the hydroxyl radical (OH). The suppression is stronger with higher concentrations of iso- prene, but with little dependence on the specific VOC mixture emitted by trees. A parameterization of the observed suppression factor as a function of isoprene concentration suggests that the number of new particles produced depends on the OH concentra- tion and VOCs involved in the production of new particles undergo three to four steps of oxidation by OH. Our measure- ments simulate conditions that are typical for forested regions and may explain the observed seasonality in the frequency of aero- sol nucleation events, with a lower number of nucleation events during summer compared to autumn and spring5. Biogenic emissions of isoprene are controlled by temperature and light2, and if the relative isoprene abundance of biogenic VOC emissions increases in response to climate change or land use change, the new particle formation potential may decrease, thus damping the aerosol negative radiative forcing effect.
Successful range-expanding plants experience less above-ground and below-ground enemy impact
Many species are currently moving to higher latitudes and altitudes1–3. However, little is known about the factors that influence the future performance of range-expanding species in their new habitats. Here we show that range-expanding plant species from a riverine area were better defended against shoot and root enemies than were related native plant species growing in the same area. We grew fifteen plant species with and without non-coevolved polyphagous locusts and cosmopolitan, polyphagous aphids. Contrary to our expectations, the locusts performed more poorly on the range-expanding plant species than on the congeneric native plant species, whereas the aphids showed no difference. The shoot herbivores reduced the biomass of the native plants more than they did that of the congeneric range expanders. Also, the range-expanding plants developed fewer pathogenic effects4,5 in their root-zone soil than did the related native species. Current predictions forecast biodiversity loss due to limitations in the ability of species to adjust to climate warming conditions in their range 6–8. Our results strongly suggest that the plants that shift ranges towards higher latitudes and altitudes may include potential invaders, as the successful range expanders may experience less control by above-ground or below- ground enemies than the natives.
Attributing physical and biological impacts to anthropogenic climate change
Significant changes in physical and biological systems are occurring on all continents and in most oceans, with a concentration of available data in Europe and North America. Most of these changes are in the direction expected with warming temperature. Here we show that these changes in natural systems since at least 1970 are occurring in regions of observed temperature increases, and that these temperature increases at continental scales cannot be explained by natural climate variations alone. Given the conclusions from the Intergovernmental Panel on Climate Change (IPCC) Fourth Assessment Report that most of the observed increase in global average temperatures since the mid-twentieth century is very likely to be due to the observed increase in anthropogenic greenhouse gas concentrations, and furthermore that it is likely that there has been significant anthropogenic warming over the past 50 years averaged over each continent except Antarctica, we conclude that anthropogenic climate change is having a significant impact on physical and biological systems globally and in some continents.
Warming caused by cumulative carbon emissions towards the trillionth tonne
Global efforts to mitigate climate change are guided by projections of future temperatures1. But the eventual equilibrium global mean temperature associated with a given stabilization level of atmospheric greenhouse gas concentrations remains uncertain1–3, complicating the setting of stabilization targets to avoid poten- tially dangerous levels of global warming4–8. Similar problems apply to the carbon cycle: observations currently provide only a weak constraint on the response to future emissions9–11. Here we use ensemble simulations of simple climate-carbon-cycle models constrained by observations and projections from more compre- hensive models to simulate the temperature response to a broad range of carbon dioxide emission pathways. We find that the peak warming caused by a given cumulative carbon dioxide emission is better constrained than the warming response to a stabilization scenario. Furthermore, the relationship between cumulative emissions and peak warming is remarkably insensitive to the emis- sion pathway (timing of emissions or peak emission rate). Hence policy targets based on limiting cumulative emissions of carbon dioxide are likely to be more robust to scientific uncertainty than emission-rate or concentration targets. Total anthropogenic emissions of one trillion tonnes of carbon (3.67 trillion tonnes of CO2), about half of which has already been emitted since industrialization began, results in a most likely peak carbon-dioxide- induced warming of 2 6C above pre-industrial temperatures, with a 5–95% confidence interval of 1.3–3.9 6C.
Greenhouse-gas emission targets for limiting global warming to 2 C
More than 100 countries have adopted a global warming limit of 2 6C or below (relative to pre-industrial levels) as a guiding principle for mitigation efforts to reduce climate change risks, impacts and damages1,2. However, the greenhouse gas (GHG) emissions corresponding to a specified maximum warming are poorly known owing to uncertainties in the carbon cycle and the climate response. Here we provide a comprehensive probabilistic analysis aimed at quantifying GHG emission budgets for the 2000–50 period that would limit warming throughout the twenty-first century to below 2 6C, based on a combination of published distributions of climate system properties and observational con- straints. We show that, for the chosen class of emission scenarios, both cumulative emissions up to 2050 and emission levels in 2050 are robust indicators of the probability that twenty-first century warming will not exceed 26C relative to pre-industrial temperatures. Limiting cumulative CO2 emissions over 2000–50 to 1,000Gt CO2 yields a 25% probability of warming exceeding 2 6C—and a limit of 1,440 Gt CO2 yields a 50% probability—given a representative estimate of the distri- bution of climate system properties. As known 2000–06 CO2 emissions3 were234 Gt CO2, less than half the proven economi-cally recoverable oil, gas and coal reserves 4–6 can still be emitted up to 2050 to achieve such a goal. Recent G8 Communique ́s7 envisage halved global GHG emissions by 2050, for which we estimate a 12– 45% probability of exceeding 2 6C—assuming 1990 as emission base year and a range of published climate sensitivity distributions. Emissions levels in 2020 are a less robust indicator, but for the scenarios considered, the probability of exceeding 26C rises to 53–87% if global GHG emissions are still more than 25% above 2000 levels in 2020.
Increasing carbon storage in intact African tropical forests
The response of terrestrial vegetation to a globally changing environment is central to predictions of future levels of atmospheric carbon dioxide1,2. The role of tropical forests is critical because they are carbon-dense and highly productive3,4. Inventory plots across Amazonia show that old-growth forests have increased in carbon storage over recent decades5–7, but the response of one-third of the world’s tropical forests in Africa8 is largely unknown owing to an absence of spatially extensive observation networks9,10. Here we report data from a ten-country network of long-term monitoring plots in African tropical forests. We find that across 79 plots (163ha) above-ground carbon storage in live trees increased by 0.63 Mg C ha21 yr21 between 1968 and 2007 (95% confidence inter- val (CI), 0.22–0.94; mean interval, 1987–96). Extrapolation to unmeasured forest components (live roots, small trees, necromass) and scaling to the continent implies a total increase in carbon storage in African tropical forest trees of 0.34 Pg C yr21 (CI, 0.15–0.43). These reported changes in carbon storage are similar to those reported for Amazonian forests per unit area6,7, providing evidence that increasing carbon storage in old-growth forests is a pan-tropical phenomenon. Indeed, combining all standardized inventory data from this study and from tropical America and Asia5,6,11 together yields a comparable figure of 0.49 Mg C ha21 yr21 (n 5 156; 562 ha; CI, 0.29–0.66; mean interval, 1987–97). This indicates a carbon sink of 1.3 Pg C yr21 (CI, 0.8–1.6) across all tropical forests during recent decades. Taxon-specific analyses of African inventory and other data12 suggest that widespread changes in resource availability, such as increasing atmospheric carbon dioxide concentrations, may be the cause of the increase in carbon stocks13, as some theory14 and models2,10,15 predict.
Reconstruction of the history of anthropogenic CO2 concentrations in the ocean
The release of fossil fuel CO2 to the atmosphere by human activity has been implicated as the predominant cause of recent global climate change1. The ocean plays a crucial role in mitigating the effects of this perturbation to the climate system, sequestering 20 to 35 per cent of anthropogenic CO2 emissions2–4. Although much progress has been made in recent years in understanding and quantifying this sink, considerable uncertainties remain as to the distribution of anthropogenic CO2 in the ocean, its rate of uptake over the industrial era, and the relative roles of the ocean and terrestrial biosphere in anthropogenic CO2 sequestration. Here we address these questions by presenting an observationally based reconstruction of the spatially resolved, time-dependent history of anthropogenic carbon in the ocean over the industrial era. Our approach is based on the recognition that the transport of tracers in the ocean can be described by a Green’s function, which we estimate from tracer data using a maximum entropy deconvo- lution technique. Our results indicate that ocean uptake of anthro- pogenic CO2 has increased sharply since the 1950s, with a small decline in the rate of increase in the last few decades. We estimate the inventory and uptake rate of anthropogenic CO2 in 2008 at 140 6 25 Pg C and 2.3 6 0.6 Pg C yr21, respectively. We find that the Southern Ocean is the primary conduit by which this CO2 enters the ocean (contributing over 40 per cent of the anthro- pogenic CO2 inventory in the ocean in 2008). Our results also suggest that the terrestrial biosphere was a source of CO2 until the 1940s, subsequently turning into a sink. Taken over the entire industrial period, and accounting for uncertainties, we estimate that the terrestrial biosphere has been anywhere from neutral to a net source of CO2, contributing up to half as much CO2 as has been taken up by the ocean over the same period.
Carbon in idle croplands
The collapse of the Soviet Union had diverse consequences, not least the abandonment of crop cultivation in many areas. One result has been the vast accumulation of soil organic carbon in the areas affected.
A BURDEN BEYOND BEARING
The climate situation may be even worse than you think. In the first of three features, Richard Monastersky looks at evidence that keeping carbon dioxide beneath dangerous levels is tougher than previously thought.
Carbon respiration from subsurface peat accelerated by climate warming in the subarctic
Among the largest uncertainties in current projections of future climate is the feedback between the terrestrial carbon cycle and climate1. Northern peatlands contain one-third of the world’s soil organic carbon, equivalent to more than half the amount of carbon in the atmosphere2. Climate-warming-induced acceleration of carbon dioxide (CO2) emissions through enhanced respiration of thick peat deposits, centuries to millennia old, may form a strong positive carbon cycle–climate feedback. The long-term temperature sensitivity of carbon in peatlands, especially at depth, remains uncertain, however, because of the short duration or correlative nature of field studies3–5 and the disturbance associated with respiration measurements below the surface in situ or during laboratory incubations6,7. Here we combine non-disturbing in situ measurements of CO2 respiration rates and isotopic (13C) composition of respired CO2 in two whole-ecosystem climate- manipulation experiments in a subarctic peatland. We show that approximately 1 6C warming accelerated total ecosystem respira- tion rates on average by 60% in spring and by 52% in summer and that this effect was sustained for at least eight years. While warm- ing stimulated both short-term (plant-related) and longer-term (peat soil-related) carbon respiration processes, we find that at least 69% of the increase in respiration rate originated from carbon in peat towards the bottom (25–50 cm) of the active layer above the permafrost. Climate warming therefore accelerates respiration of the extensive, subsurface carbon reservoirs in peat- lands to a much larger extent than was previously thought6,7. Assuming that our data from a single site are indicative of the direct response to warming of northern peatland soils on a global scale, we estimate that climate warming of about 1 6C over the next few decades could induce a global increase in heterotrophic respiration of 38–100 megatonnes of C per year. Our findings suggest a large, long-lasting, positive feedback of carbon stored in northern peatlands to the global climate system.
Call for a climate culture shift
A new book describes the rapid reshaping of human priorities needed to save the planet from global warming. Some of that change is already under way at the community level, explains Robert Costanza.
Increase in Agulhas leakage due to poleward shift of Southern Hemisphere westerlies
The transport of warm and salty Indian Ocean waters into the Atlantic Ocean—the Agulhas leakage—has a crucial role in the global oceanic circulation1 and thus the evolution of future climate. At present these waters provide the main source of heat and salt for the surface branch of the Atlantic meridional overturning circulation (MOC)2. There is evidence from past glacial-to-interglacial variations in foraminiferal assemblages3 and model studies4 that the amount of Agulhas leakage and its corresponding effect on the MOC has been subject to substantial change, potentially linked to latitudinal shifts in the Southern Hemisphere westerlies5. A pro- gressive poleward migration of the westerlies has been observed during the past two to three decades and linked to anthropogenic forcing6, but because of the sparse observational records it has not been possible to determine whether there has been a concomitant response of Agulhas leakage. Here we present the results of a high- resolution ocean general circulation model7,8 to show that the transport of Indian Ocean waters into the South Atlantic via the Agulhas leakage has increased during the past decades in response to the change in wind forcing. The increased leakage has contri- buted to the observed salinification 9 of South Atlantic thermocline waters. Both model and historic measurements off South America suggest that the additional Indian Ocean waters have begun to invade the North Atlantic, with potential implications for the future evolution of the MOC.
A safe operating space for humanity
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.
El Nino in a changing climate
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.
The El Nino with a difference
Patterns of sea-surface warming and cooling in the tropical Pacific seem to be changing, as do the associated atmospheric effects. Increased global warming is implicated in these shifts in El Niño phenomena.
CLIMATE’S SMOKY SPECTRE
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.
The late Precambrian greening of the Earth
Many aspects of the carbon cycle can be assessed from temporal changes in the 13C/12C ratio of oceanic bicarbonate. 13C/12C can temporarily rise when large amounts of 13C-depleted photosyn- thetic organic matter are buried at enhanced rates1, and can decrease if phytomass is rapidly oxidized2 or if low 13C is rapidly released from methane clathrates3. Assuming that variations of the marine 13C/12C ratio are directly recorded in carbonate rocks, thousands of carbon isotope analyses of late Precambrian examples have been published to correlate these otherwise undatable strata and to document perturbations to the carbon cycle just before the great expansion of metazoan life. Low 13C/12C in some Neoproterozoic carbonates is considered evidence of carbon cycle perturbations unique to the Precambrian. These include complete oxidation of all organic matter in the ocean2 and complete produc- tivity collapse such that low-13C/12C hydrothermal CO2 becomes the main input of carbon4. Here we compile all published oxygen and carbon isotope data for Neoproterozoic marine carbonates, and consider them in terms of processes known to alter the isotopic composition during transformation of the initial precipitate into limestone/dolostone. We show that the combined oxygen and carbon isotope systematics are identical to those of well- understood Phanerozoic examples that lithified in coastal pore fluids, receiving a large groundwater influx of photosynthetic carbon from terrestrial phytomass. Rather than being perturba- tions to the carbon cycle, widely reported decreases in 13C/12C in Neoproterozoic carbonates are more easily interpreted in the same way as is done for Phanerozoic examples. This influx of terrestrial carbon is not apparent in carbonates older than 850 Myr, so we infer an explosion of photosynthesizing communities on late Precambrian land surfaces. As a result, biotically enhanced weathering generated carbon-bearing soils on a large scale and their detrital sedimentation sequestered carbon 5. This facilitated a rise in O2 necessary for the expansion of multicellular life.
Opinion : No quick switch to low-carbon energy
In the first of two pieces on reducing greenhouse-gas emissions, Gert Jan Kramer and Martin Haigh analyse historic growth in energy systems to explain why deploying alternative technologies will be a long haul.
COMMENTARY: Overshoot, adapt and recover
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.”
Too much of a bad thing
There are various — and confusing — targets to limit global warming due to emissions of greenhouse gases. Estimates based on the total slug of carbon emitted are possibly the most robust, and are worrisome.
ESSAY : The worst-case scenario
Stephen Schneider explores what a world with 1,000 parts per million of CO2 in its atmosphere might look like.
The proportionality of global warming to cumulative carbon emissions
The global temperature response to increasing atmospheric CO2 is often quantified by metrics such as equilibrium climate sensitivity and transient climate response1. These approaches, however, do not account for carbon cycle feedbacks and therefore do not fully represent the net response of the Earth system to anthropogenic CO2 emissions. Climate–carbon modelling experiments have shown that: (1) the warming per unit CO2 emitted does not depend on the background CO2 concentration2; (2) the total allowable emissions for climate stabilization do not depend on the timing of those emissions3–5; and (3) the temperature response to a pulse of CO2 is approximately constant on timescales of decades to centuries3,6–8. Here we generalize these results and show that the carbon–climate response (CCR), defined as the ratio of temper- ature change to cumulative carbon emissions, is approximately independent of both the atmospheric CO2 concentration and its rate of change on these timescales. From observational constraints, we estimate CCR to be in the range 1.0–2.1 6C per trillion tonnes of carbon (TtC) emitted (5th to 95th percentiles), consistent with twenty-first-century CCR values simulated by climate–carbon models. Uncertainty in land-use CO2 emissions and aerosol forcing, however, means that higher observationally constrained values cannot be excluded. The CCR, when evaluated from climate– carbon models under idealized conditions, represents a simple yet robust metric for comparing models, which aggregates both climate feedbacks and carbon cycle feedbacks. CCR is also likely to be a useful concept for climate change mitigation and policy; by combining the uncertainties associated with climate sensitivity, carbon sinks and climate–carbon feedbacks into a single quantity, the CCR allows CO2-induced global mean temperature change to be inferred directly from cumulative carbon emissions.
Warming experiments underpredict plant phenological responses to climate change
Warming experiments are increasingly relied on to estimate plant responses to global climate change1,2. For experiments to provide meaningful predictions of future responses, they should reflect the empirical record of responses to temperature variability and recent warming, including advances in the timing of flowering and leafing3–5. We compared phenology (the timing of recurring life history events) in observational studies and warming experiments spanning four continents and 1,634 plant species using a common measure of temperature sensitivity (change in days per degree Celsius). We show that warming experiments underpredict advances in the timing of flowering and leafing by 8.5-fold and 4.0-fold, respectively, compared with long-term observations. For species that were common to both study types, the experimental results did not match the observational data in sign or magnitude. The observational data also showed that species that flower earliest in the spring have the highest temperature sensitivities, but this trend was not reflected in the experimental data. These significant mismatches seem to be unrelated to the study length or to the degree of manipulated warming in experiments. The discrepancy between experiments and observations, however, could arise from complex interactions among multiple drivers in the observational data, or it could arise from remediable artefacts in the experiments that result in lower irradiance and drier soils, thus dampening the phenological responses to manipulated warming. Our results introduce uncertainty into ecosystem models that are informed solely by experiments and suggest that responses to climate change that are predicted using such models should be re-evaluated.
Approaching a state shift in Earth’s biosphere
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.
A global synthesis reveals biodiversity loss as a major driver of ecosystem change
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).
International trade drives biodiversity threats in developing nations
Human activities are causing Earth’s sixth major extinction event1— an accelerating decline of the world’s stocks of biological diversity at rates 100 to 1,000 times pre-human levels2. Historically, low-impact intrusion into species habitats arose from local demands for food, fuel and living space3. However, in today’s increasingly globalized economy, international trade chains accelerate habitat degradation far removed from the place of consumption. Although adverse effects of economic prosperity and economic inequality have been confirmed4,5, the importance of international trade as a driver of threats to species is poorly understood. Here we show that a signifi- cant number of species are threatened as a result of international trade along complex routes, and that, in particular, consumers in developed countries cause threats to species through their demand of commodities that are ultimately produced in developing countries. We linked 25,000 Animalia species threat records from the International Union for Conservation of Nature Red List to more than 15,000 commodities produced in 187 countries and evaluated more than 5billion supply chains in terms of their biodiversity impacts. Excluding invasive species, we found that 30% of global species threats are due to international trade. In many developed countries, the consumption of imported coffee, tea, sugar, textiles, fish and other manufactured items causes a biodiversity footprint that is larger abroad than at home. Our results emphasize the importance of examining biodiversity loss as a global systemic phe- nomenon, instead of looking at the degrading or polluting producers in isolation. We anticipate that our findings will facilitate better regulation, sustainable supply-chain certification and consumer product labelling.
Biodiversity loss and its impact on humanity
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.
Probabilistic cost estimates for climate change mitigation
For more than a decade, the target of keeping global warming below 2 6C has been a key focus of the international climate debate1. In response, the scientific community has published a number of scenario studies that estimate the costs of achieving such a target 2–5. Producing these estimates remains a challenge, particularly because of relatively well known, but poorly quantified, uncertainties, and owing to limited integration of scientific knowledge across disciplines6. The integrated assessment community, on the one hand, has extensively assessed the influence of technological and socio-economic uncertainties on low-carbon scenarios and asso- ciated costs2–4,7. The climate modelling community, on the other hand, has spent years improving its understanding of the geo- physical response of the Earth system to emissions of greenhouse gases8–12. This geophysical response remains a key uncertainty in the cost of mitigation scenarios but has been integrated with assess- ments of other uncertainties in only a rudimentary manner, that is, for equilibrium conditions6,13. Here we bridge this gap between the two research communities by generating distributions of the costs associated with limiting transient global temperature increase to below specific values, taking into account uncertainties in four factors: geophysical, technological, social and political. We find that political choices that delay mitigation have the largest effect on the cost–risk distribution, followed by geophysical uncertainties, social factors influencing future energy demand and, lastly, technological uncertainties surrounding the availability of greenhouse gas miti- gation options. Our information on temperature risk and mitigation costs provides crucial information for policy-making, because it clarifies the relative importance of mitigation costs, energy demand and the timing of global action in reducing the risk of exceeding a global temperature increase of 2 6C, or other limits such as 3 6C or 1.5 6C, across a wide range of scenarios.
Terrestrial water fluxes dominated by transpiration
Renewable fresh water over continents has input from precipitation and losses to the atmosphere through evaporation and transpiration. Global-scale estimates of transpiration from climate models are poorly constrained owing to large uncertainties in stomatal conductance and the lack of catchment-scale measurements required for model calibration, resulting in a range of predictions spanning 20 to 65 per cent of total terrestrial evapotranspiration (14,000 to 41,000 km3 per year) (refs 1–5). Here we use the distinct isotope effects of transpiration and evaporation to show that transpiration is by far the largest water flux from Earth’s continents, representing 80 to 90 per cent of terrestrial evapotranspiration. On the basis of our analysis of a global data set of large lakes and rivers, we conclude that transpiration recycles 62,000 6 8,000 km3 of water per year to the atmosphere, using half of all solar energy absorbed by land surfaces in the process. We also calculate CO2 uptake by terrestrial vegetation by connecting transpiration losses to carbon assimilation using water-use efficiency ratios of plants, and show the global gross primary productivity to be 129 6 32 giga- tonnes of carbon per year, which agrees, within the uncertainty, with previous estimates6. The dominance of transpiration water fluxes in continental evapotranspiration suggests that, from the point of view of water resource forecasting, climate model development should prioritize improvements in simulations of biological fluxes rather than physical (evaporation) fluxes.
A large source of low-volatility secondary organic aerosol
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.
Carbon loss from an unprecedented Arctic tundra wildfire
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.
Coastal habitats shield people and property from sea-level rise and storms
Extreme weather, sea-level rise and degraded coastal ecosystems are placing people and property at greater risk of damage from coastal hazards 1–5. The likelihood and magnitude of losses may be reduced by intact reefs and coastal vegetation 1, especially when those habitats fringe vulnerable communities and infrastructure. Using five sea-level-rise scenarios, we calculate a hazard index for every 1 km2 of the United States coastline. We use this index to identify the most vulnerable people and property as indicated by being in the upper quartile of hazard for the nation’s coastline. The number of people, poor families, elderly and total value of residential property that are most exposed to hazards can be reduced by half if existing coastal habitats remain fully intact. Coastal habitats defend the greatest number of people and total property value in Florida, New York and California. Our analyses deliver the first national map of risk reduction owing to natural habitats and indicates where conservation and restoration of reefs and vegetation have the greatest potential to protect coastal communities.
Delayed phenology and reduced fitness associated with climate change in a wild hibernator
The most commonly reported ecological effects of climate change are shifts in phenologies, in particular of warmer spring temperatures leading to earlier timing of key events 1,2. Among animals, however, these reports have been heavily biased towards avian phenologies, whereas we still know comparatively little about other seasonal adaptations, such as mammalian hibernation. Here we show a significant delay (0.47 days per year, over a 20-year period) in the hibernation emergence date of adult females in a wild population of Columbian ground squirrels in Alberta, Canada. This finding was related to the climatic conditions at our study location: owing to within-individual phenotypic plasticity, females emerged later during years of lower spring temperature and delayed snowmelt. Although there has not been a significant annual trend in spring temperature, the date of snowmelt has become progressively later owing to an increasing prevalence of late-season snowstorms. Importantly, years of later emergence were also associated with decreased individual fitness. There has consequently been a decline in mean fitness (that is, population growth rate) across the past two decades. Our results show that plastic responses to climate change may be driven by climatic trends other than increasing temperature, and may be associated with declines in individual fitness and, hence, population viability.
Forests fuel fish growth in freshwater deltas
Aquatic ecosystems are fuelled by biogeochemical inputs from surrounding lands and within- lake primary production. Disturbances that change these inputs may affect how aquatic ecosystems function and deliver services vital to humans. Here we test, using a forest cover gradient across eight separate catchments, whether disturbances that remove terrestrial biomass lower organic matter inputs into freshwater lakes, thereby reducing food web productivity. We focus on deltas formed at the stream-lake interface where terrestrial-derived particulate material is deposited. We find that organic matter export increases from more forested catchments, enhancing bacterial biomass. This transfers energy upwards through communities of heavier zooplankton, leading to a fourfold increase in weights of plankti- vorous young-of-the-year fish. At least 34% of fish biomass is supported by terrestrial primary production, increasing to 66% with greater forest cover. Habitat tracers confirm fish were closely associated with individual catchments, demonstrating that watershed protection and restoration increase biomass in critical life-stages of fish.
Genealogy of nature conservation: a political perspective
Modern nature conservation is a product of post-Enlightenment modernity; I explore the heterogeneity of its conceptual and ideological background. The 19th century legacy comprises concern over human-caused extinctions; protests against excessive hunting and cruelty toward animals; utilitarian care for natural resources; and romantic sensibility concerning the value of nature for human health and spirituality. The 20th century added into conservation thinking increasing consciousness about human biospheric dependence; efforts to identify appropriate conservation targets; and most recently concern over the loss of biodiversity. The politics of nature conservation has taken shape within the framework of politics of nature, that is, choices vis-á-vis nature that have been made either as deliberate decisions on resource use or as side-effects of subsistence practices of various types. Because of tensions and conflicts with alternative ways of using nature, formulating realistic conservation policies has been a complicated task. Problems and uncertainties emerge: pursuing material aspirations of the current world society will necessarily bring about damage to ecological systems of the Earth. The way forward is to identify feasible alternatives in the midst of the tensions and ambiguities that arise, and to open up space for carrying through conservation initiatives. Keywords conservation thought, conservation policy, conservation governance, utilitarian conservation, romanticism, genealogy, framing, normativity, normative order, action space
Observed increase in local cooling effect of deforestation at higher latitudes
Deforestation in mid- to high latitudes is hypothesized to have the potential to cool the Earth’s surface by altering biophysical processes1–3. In climate models of continental-scale land clearing, the cooling is triggered by increases in surface albedo and is reinforced by a land albedo–sea ice feedback 4,5. This feedback is crucial in the model predictions; without it other biophysical processes may overwhelm the albedo effect to generate warming instead5. Ongoing land-use activities, such as land management for climate mitigation, are occurring at local scales (hectares) presumably too small to generate the feedback, and it is not known whether the intrinsic biophysical mechanism on its own can change the surface temperature in a consistent manner6,7. Nor has the effect of deforestation on climate been demonstrated over large areas from direct observations. Here we show that surface air temper- ature is lower in open land than in nearby forested land. The effect is 0.85 6 0.44 K (mean 6 one standard deviation) northwards of 456N and 0.2160.53K southwards. Below 356N there is weak evidence that deforestation leads to warming. Results are based on comparisons of temperature at forested eddy covariance towers in the USA and Canada and, as a proxy for small areas of cleared land, nearby surface weather stations. Night-time temperature changes unrelated to changes in surface albedo are an important contributor to the overall cooling effect. The observed latitudinal dependence is consistent with theoretical expectation of changes in energy loss from convection and radiation across latitudes in both the daytime and night-time phase of the diurnal cycle, the latter of which remains uncertain in climate models8.
The Next Dust Bowl
Drought is the most pressing problem caused by climate change. It receives too little attention, says Joseph Romm.
The rebound effect is overplayed
Increasing energy efficiency brings emissions savings. Claims that it backfires are a distraction, say Kenneth Gillingham and colleagues.
Comment: The end of cheap coal
New forecasts suggest that coal reserves will run out faster than many believe. Energy policies relying on cheap coal have no future, say Richard Heinberg and David Fridley.
Civil conflicts are associated with the global climate
It has been proposed that changes in global climate have been responsible for episodes of widespread violence and even the collapse of civilizations 1,2. Yet previous studies have not shown that violence can be attributed to the global climate, only that random weather events might be correlated with conflict in some cases 3–7. Here we directly associate planetary-scale climate changes with global patterns of civil conflict by examining the dominant inter- annual mode of the modern climate 8–10, the El Nino/Southern Oscillation (ENSO). Historians have argued that ENSO may have driven global patterns of civil conflict in the distant past11–13, a hypothesis that we extend to the modern era and test quantitatively. Using data from 1950 to 2004, we show that the probability of new civil conflicts arising throughout the tropics doubles during El Nino years relative to La Nina years. This result, which indicates that ENSO may have had a role in 21% of all civil conflicts since 1950, is the first demonstration that the stability of modern societies relates strongly to the global climate.
A reality check on the shale revolution
The production of shale gas and oil in the United States is overhyped and the costs are underestimated, says J. David Hughes.
Ecohydrologic separation of water between trees and streams in a Mediterranean climate
Water movement in upland humid watersheds from the soil surface to the stream is often described using the concept of translatory flow (1,2), which assumes that water entering the soil as precipitation displaces the water that was present previously, pushing it deeper into the soil and eventually into the stream (2). Within this framework, water at any soil depth is well mixed and plants extract the same water that eventually enters the stream. Here we present water-isotope data from various pools throughout a small watershed in the Cascade Mountains, Oregon, USA. Our data imply that a pool of tightly bound water that is retained in the soil and used by trees does not participate in translatory flow, mix with mobile water or enter the stream. Instead, water from initial rainfall events after rainless summers is locked into small pores with low matric potential until transpiration empties these pores during following dry summers. Winter rainfall does not displace this tightly bound water. As transpiration and stormflow are out of phase in the Mediterranean climate of our study site, two separate sets of water bodies with different isotopic characteristics exist in trees and streams. We conclude that complete mixing of water within the soil cannot be assumed for similar hydroclimatic regimes as has been done in the past (3,4) .
Activation of old carbon by erosion of coastal and subsea permafrost in Arctic Siberia
The future trajectory of greenhouse gas concentrations depends on interactions between climate and the biogeosphere1,2. Thawing of Arctic permafrost could release significant amounts of carbon into the atmosphere in this century3. Ancient Ice Complex deposits outcropping along the 7,000-kilometre-long coastline of the East Siberian Arctic Shelf (ESAS)4,5, and associated shallow subsea permafrost6,7, are two large pools of permafrost carbon8, yet their vulnerabilities towards thawing and decomposition are largely unknown9–11. Recent Arctic warming is stronger than has been predicted by several degrees, and is particularly pronounced over the coastal ESAS region12,13. There is thus a pressing need to improve our understanding of the links between permafrost carbon and climate in this relatively inaccessible region. Here we show that extensive release of carbon from these Ice Complex deposits dominates (57 6 2 per cent) the sedimentary carbon budget of the ESAS, the world’s largest continental shelf, over- whelming the marine and topsoil terrestrial components. Inverse modelling of the dual-carbon isotope composition of organic carbon accumulating in ESAS surface sediments, using Monte Carlo simulations to account for uncertainties, suggests that 44 6 10 teragrams of old carbon is activated annually from Ice Complex permafrost, an order of magnitude more than has been suggested by previous studies14. We estimate that about two-thirds (66 6 16 per cent) of this old carbon escapes to the atmosphere as carbon dioxide, with the remainder being re-buried in shelf sediments. Thermal collapse and erosion of these carbon-rich Pleistocene coastline and seafloor deposits may accelerate with Arctic amplification of climate warming 2,13.
Has the Earth’s sixth mass extinction already arrived?
Palaeontologists characterize mass extinctions as times when the Earth loses more than three-quarters of its species in a geologically short interval, as has happened only five times in the past 540 million years or so. Biologists now suggest that a sixth mass extinction may be under way, given the known species losses over the past few centuries and millennia. Here we review how differences between fossil and modern data and the addition of recently available palaeontological information influence our understanding of the current extinction crisis. Our results confirm that current extinction rates are higher than would be expected from the fossil record, highlighting the need for effective conservation measures.
Natural and anthropogenic variations in methane sources during the past two millennia
Methane is an important greenhouse gas that is emitted from multiple natural and anthropogenic sources. Atmospheric methane concentrations have varied on a number of timescales in the past, but what has caused these variations is not always well understood1–8. The different sources and sinks of methane have specific isotopic signatures, and the isotopic composition of methane can therefore help to identify the environmental drivers of variations in atmo- spheric methane concentrations9. Here we present high-resolution carbon isotope data (d13C content) for methane from two ice cores from Greenland for the past two millennia. We find that the d13C content underwent pronounced centennial-scale variations between 100 BC and AD 1600. With the help of two-box model calculations, we show that the centennial-scale variations in isotope ratios can be attributed to changes in pyrogenic and biogenic sources. We find correlations between these source changes and both natural climate variability—such as the Medieval Climate Anomaly and the Little Ice Age—and changes in human population and land use, such as the decline of the Roman empire and the Han dynasty, and the population expansion during the medieval period.
Comment: Time to Model all Life on Earth
To help transform our understanding of the biosphere, ecologists — like climate scientists — should simulate whole ecosystems, argue Drew Purves and colleagues. FROM THE TEXT: General circulation models, which simulatethe physics and chemistry of Earth’s land, ocean and atmosphere, embody scientists’ best understanding of how the climate system works and are crucial to making predictions and shaping policies. We think that analogous general ecosystem models (GEMs) could radically improve understanding of the biosphere and inform policy decisions about biodiversity and conservation.
Comment: Don’t judge species on their origins
SUMMARY: Conservationists should assess organisms on environmental impact rather than on whether they are natives, argue Mark Davis and 18 other ecologists. FROM THE TEXT: Nativeness is not a sign of evolutionary fitness or of a species having positive effects.The insect currently suspected to be killing more trees than any other in North Americais the native mountain pine beetle Dendroctonus ponderosae. Classifying biota according to their adherence to cultural standards of belonging, citizenship, fair play and morality does not advance our understanding of ecology. Over the past few decades, this perspective has led many conservation and restoration efforts down paths that make little ecological or economic sense
Shifts in Season
Is the rising heat forcing change on the seasons? To find out, observed data may be superior to model projections.
Atmospheric CO2 forces abrupt vegetation shifts locally, but not globally
It is possible that anthropogenic climate change will drive the Earth system into a qualitatively different state1. Although different types of uncertainty limit our capacity to assess this risk 2, Earth system scientists are particularly concerned about tipping elements, large-scale components of the Earth system that can be switched into qualitatively different states by small perturbations. Despite growing evidence that tipping elements exist in the climate system1,3, whether large-scale vegetation systems can tip into alternative states is poorly understood4. Here we show that tropical grassland, savanna and forest ecosystems, areas large enough to have powerful impacts on the Earth system, are likely to shift to alternative states. Specifically, we show that increasing atmospheric CO2 concentration will force transitions to vegetation states characterized by higher biomass and/or woody-plant dominance. The timing of these critical transitions varies as a result of between-site variance in the rate of temperature increase, as well as a dependence on stochastic variation in fire severity and rainfall. We further show that the locations of bistable vegetation zones (zones where alternative vegetation states can exist) will shift as climate changes. We conclude that even though large-scale directional regime shifts in terrestrial ecosystems are likely, asynchrony in the timing of these shifts may serve to dampen, but not nullify, the shock that these changes may represent to the Earth system.
Increased soil emissions of potent greenhouse gases under increased atmospheric CO2
Increasing concentrations of atmospheric carbon dioxide (CO2) can affect biotic and abiotic conditions in soil, such as microbial activity and water content 1,2. In turn, these changes might be expected to alter the production and consumption of the important greenhouse gases nitrous oxide (N2O) and methane (CH4) (refs 2, 3). However, studies on fluxes of N2O and CH4 from soil under increased atmo- spheric CO2 have not been quantitatively synthesized. Here we show, using meta-analysis, that increased CO2 (ranging from 463 to 780 parts per million by volume) stimulates both N2O emissions from upland soils and CH4 emissions from rice paddies and natural wetlands. Because enhanced greenhouse-gas emissions add to the radiative forcing of terrestrial ecosystems, these emissions are expected to negate at least 16.6 per cent of the climate change mitigation potential previously predicted from an increase in the terrest- rial carbon sink under increased atmospheric CO2 concentrations4. Our results therefore suggest that the capacity of land ecosystems to slow climate warming has been overestimated.
Asymmetric effects of economic growth and decline on CO2 emissions
Letter to Editor: Excerpt: "Why does economic decline not have an effect on CO2 emissions that is symmetrical with the effect of economic growth? There are various reasons that this may occur, but the asymmetry is probably due to the fact that economic growth produces durable goods, such as cars and energy-intensive homes, and infrastructure, such as manufacturing facilities and transportation networks, that are not removed by economic decline and that continue to contribute to CO2 emissions even after growth is curtailed."
Global diversity of drought tolerance and grassland climate-change resilience
Drought reduces plant productivity, induces widespread plant mortality and limits the geographic distribution of plant species1–7. As climates warm and precipitation patterns shift in the future8,9, understanding the distribution of the diversity of plant drought tolerance is central to predicting future ecosystem function and resilience to climate change10–12 . These questions are especially pressing for the world’s 11,000 grass species13, which dominate a large fraction of the terrestrial biosphere14, yet are poorly characterized with respect to re- sponses to drought. Here, we show that physiological drought tolerance, which varied tenfold among 426 grass species, is well distributed both climatically and phylogenetically, sug- gesting most native grasslands are likely to contain a high diversity of drought tolerance. Consequently, local species may help maintain ecosystem functioning in response to changing drought regimes without requiring long-distance migrations of grass species. Furthermore, physiologically drought-tolerant species had higher rates of water and carbon dioxide exchange than intolerant species, indicating that severe droughts may generate legacies for ecosystem functioning. In all, our findings suggest that diverse grasslands throughout the globe have the potential to be resilient to drought in the face of climate change through the local expansion of drought-tolerant species.
The temperature response of soil microbial efficiency and its feedback to climate
Soils are the largest repository of organic carbon (C) in the terrestrial biosphere and represent an important source of carbon dioxide (CO2)totheatmosphere,releasing60–75PgC an- nually through microbial decomposition of organic materials1,2. A primary control on soil CO2 flux is the efficiency with which the microbial community uses C. Despite its critical importance to soil–atmosphere CO2 exchange, relatively few studies have examined the factors controlling soil microbial efficiency. Here, we measured the temperature response of microbial efficiency in soils amended with substrates varying in lability. We also examined the temperature sensitivity of microbial efficiency in response to chronic soil warming in situ. We find that the efficiency with which soil microorganisms use organic matter is dependent on both temperature and substrate quality, with efficiency declining with increasing temperatures for more recalcitrant substrates. However, the utilization efficiency of a more recalcitrant substrate increased at higher temperatures in soils exposed to almost two decades of warming 5 ◦ C above ambient. Our work suggests that climate warming could alter the decay dynamics of more stable organic matter compounds, thereby having a positive feedback to climate that is attenuated by a shift towards a more efficient microbial community in the longer term.
Shrinking body size as an ecological response to climate change
Determining how climate change will affect global ecology and ecosystem services is one of the next important frontiers in environmental science. Many species already exhibit smaller sizes as a result of climate change and many others are likely to shrink in response to continued climate change, following fundamental ecological and metabolic rules. This could negatively impact both crop plants and protein sources such as fish that are important for human nutrition. Furthermore, heterogeneity in response is likely to upset ecosystem balances. We discuss future research directions to better understand the trend and help ameliorate the trophic cascades and loss of biodiversity that will probably result from continued decreases in organism size.
Regional carbon dioxide implications of forest bioenergy production
Strategies for reducing carbon dioxide emissions include substitution of fossil fuel with bioenergy from forests1, where carbon emitted is expected to be recaptured in the growth of new biomass to achieve zero net emissions 2, and forest thinning to reduce wildfire emissions 3. Here, we use forest inventory data to show that fire prevention measures and large-scale bioenergy harvest in US West Coast forests lead to 2–14% (46–405 Tg C) higher emissions compared with current management practices over the next 20 years. We studied 80 forest types in 19 ecoregions, and found that the current carbon sink in 16 of these ecoregions is sufficiently strong that it cannot be matched or exceeded through substitution of fossil fuels by forest bioenergy. If the sink in these ecoregions weakens below its current level by 30–60 g C m−2 yr−1 owing to insect infestations, increased fire emissions or reduced primary production, management schemes including bioenergy production may succeed in jointly reducing fire risk and carbon emissions. In the remaining three ecoregions, immediate implementation of fire prevention and biofuel policies may yield net emission savings. Hence, forest policy should consider current forest carbon balance, local forest conditions and ecosystem sustainability in establishing how to decrease emissions.
Analysing fossil-fuel displacement
It is commonly assumed that fossil fuels can be replaced by alternative forms of energy. Now research challenges this assumption, and highlights the role of non-technological solutions to reduce fossil-fuel consumption.
Enhanced poleward moisture transport and amplified northern high-latitude wetting trend
Observations and climate change projections forced by greenhouse gas emissions have indicated a wetting trend in northern high latitudes, evidenced by increasing Eurasian Arctic river discharges (1–3). The increase in river discharge has accelerated in the latest decade and an unprecedented, record high discharge occurred in 2007 along with an extreme loss of Arctic summer sea-ice cover (4–6). Studies have ascribed this increasing discharge to various factors attributable to local global warming effects, including intensifying precip- itation minus evaporation, thawing permafrost, increasing greenness and reduced plant transpiration7–11. However, no agreement has been reached and causal physical processes remain unclear. Here we show that enhancement of poleward atmospheric moisture transport (AMT) decisively contributes to increased Eurasian Arctic river discharges. Net AMT into the Eurasian Arctic river basins captures 98% of the gauged climatological river discharges. The trend of 2.6% net AMT increase per decade accounts well for the 1.8% per decade increase in gauged discharges and also suggests an increase in underlying soil moisture. A radical shift of the atmospheric circulation pattern induced an unusually large AMT and warm surface in 2006–2007 over Eurasia, resulting in the record high discharge.
Anthropogenic influence on multidecadal changes in reconstructed global evapotranspiration
Global warming is expected to intensify the global hydrological cycle1, with an increase of both evapotranspiration (EVT) and precipitation. Yet, the magnitude and spatial distribution of this global and annual mean response remains highly uncertain2. Better constraining land EVT in twenty-first-century climate scenarios is critical for predicting changes in surface climate, including heatwaves3 and droughts4, evaluating impacts on ecosystems and water resources5, and designing adaptation policies. Continental scale EVT changes may already be underway6,7, but have never been attributed to anthropogenic emissions of greenhouse gases and sulphate aerosols. Here we provide global gridded estimates of annual EVT and demonstrate that the latitudinal and decadal differentiation of recent EVT variations cannot be understood without invoking the anthropogenic radiative forcings. In the mid-latitudes, the emerging picture of enhanced EVT confirms the end of the dimming decades 8 and highlights the possible threat posed by increasing drought frequency to managing water resources and achieving food security in a changing climate.
Focus on poleward shifts in species’ distribution underestimates the fingerprint of climate change
Species are largely predicted to shift poleward as global temperatures increase, with this fingerprint of climate change being already observed across a range of taxonomic groups and, mostly temperate, geographic locations1–5. However, the assumption of uni-directional distribution shifts does not account for complex interactions among temperature, precipitation and species-specific tolerances 6, all of which shape the direction and magnitude of changes in a species’ climatic niche. We analysed 60 years of past climate change on the Australian continent, assessing the velocity of changes in temperature and precipitation, as well as changes in climatic niche space for 464 Australian birds. We show large magnitude and rapid rates of change in Australian climate over the past 60 years resulting in high-velocity and multi-directional, including equatorial, shifts in suitable climatic space for birds (ranging from 0.1 to 7.6kmyr−1, mean 1.27kmyr−1). Overall, if measured only in terms of poleward distribution shifts, the fingerprint of climate change is underestimated by an average of 26% in temperate regions of the continent and by an average of 95% in tropical regions. We suggest that the velocity of movement required by Australian species to track their climatic niche may be much faster than previously thought and that the interaction between temperature and precipitation changes will result in multi-directional distribution shifts globally.
Response of snow-dependent hydrologic extremes to continued global warming
Snow accumulation is critical for water availability in the Northern Hemisphere 1,2, raising concern that global warming could have important impacts on natural and human systems in snow-dependent regions1,3. Although regional hydrologic changes have been observed (for example, refs 1,3–5), the time of emergence of extreme changes in snow accumulation and melt remains a key unknown for assessing climate- change impacts3,6,7. We find that the CMIP5 global climate model ensemble exhibits an imminent shift towards low snow years in the Northern Hemisphere, with areas of western North America, northeastern Europe and the Greater Himalaya showing the strongest emergence during the near- term decades and at 2 ◦ C global warming. The occurrence of extremely low snow years becomes widespread by the late twenty-first century, as do the occurrences of extremely high early-season snowmelt and runoff (implying increasing flood risk), and extremely low late-season snowmelt and runoff (implying increasing water stress). Our results suggest that many snow-dependent regions of the Northern Hemisphere are likely to experience increasing stress from low snow years within the next three decades, and from extreme changes in snow-dominated water resources if global warming exceeds 2 ◦ C above the pre-industrial baseline.
The challenge to keep global warming below 2 °C
The latest carbon dioxide emissions continue to track the high end of emission scenarios, making it even less likely global warming will stay below 2 °C. A shift to a 2 °C pathway requires immediate significant and sustained global mitigation, with a probable reliance on net negative emissions in the longer term.
Projections of declining surface-water availability for the southwestern United States
Global warming driven by rising greenhouse-gas concentrations is expected to cause wet regions of the tropics and mid to high latitudes to get wetter and subtropical dry regions to get drier and expand polewards 1–4. Over southwest North America, models project a steady drop in precipitation minus evapotranspiration, P − E, the net flux of water at the land surface5–7, leading to, for example, a decline in Colorado River flow8–11. This would cause widespread and important social and ecological consequences12–14. Here, using new simulations from the Coupled Model Intercomparison Project Five, to be assessed in Intergovernmental Panel on Climate Change As- sessment Report Five, we extend previous work by examining changes in P, E, runoff and soil moisture by season and for three different water resource regions. Focusing on the near future, 2021–2040, the new simulations project declines in surface-water availability across the southwest that translate into reduced soil moisture and runoff in California and Nevada, the Colorado River headwaters and Texas.
Impacts of biofuel cultivation on mortality and crop yields
Ground-level ozone is a priority air pollutant, causing ∼22,000 excess deaths per year in Europe1, significant reductions in crop yields2 and loss of biodiversity3. It is produced in the troposphere through photochemical reactions involving oxides of nitrogen (NOx) and volatile organic compounds (VOCs). The biosphere is the main source of VOCs, with an estimated 1,150 TgC yr−1 (∼90% of total VOC emissions) released from vegetation globally4 . Isoprene (2-methyl-1,3-butadiene) is the most significant biogenic VOC in terms of mass (around 500 TgC yr−1 ) and chemical reactivity4 and plays an important role in the mediation of ground-level ozone concentrations5. Concerns about climate change and energy security are driving an aggressive expansion of bioenergy crop production and many of these plant species emit more isoprene than the traditional crops they are replacing. Here we quantify the increases in isoprene emission rates caused by cultivation of 72 Mha of biofuel crops in Europe. We then estimate the resultant changes in ground-level ozone concentrations and the impacts on human mortality and crop yields that these could cause. Our study highlights the need to consider more than simple carbon budgets when considering the cultivation of biofuel feedstock crops for greenhouse-gas mitigation.
Energy consumption and the unexplained winter warming over northern Asia and North America
The worldwide energy consumption in 2006 was close to 498 exajoules. This is equivalent to an energy convergence of 15.8 TW into the populated regions, where energy is consumed and dissipated into the atmosphere as heat. Although energy consumption is sparsely distributed over the vast Earth surface and is only about 0.3% of the total energy transport to the extratropics by atmospheric and oceanic circulations, this anthropogenic heating could disrupt the normal atmospheric circulation pattern and produce a far-reaching effect on surface air temperature. We identify the plausible climate impacts of energy consumption using a global climate model. The results show that the inclusion of energy use at 86 model grid points where it exceeds 0.4 W m−2 can lead to remote surface temperature changes by as much as 1K in mid- and high latitudes in winter and autumn over North America and Eurasia. These regions correspond well to areas with large differences in surface temperature trends between observations and global warming simulations forced by all natural and anthropogenic forcings 1. We conclude that energy consumption is probably a missing forcing for the additional winter warming trends in observations.
Shifts in Arctic vegetation and associated feedbacks under climate change
Climate warming has led to changes in the composition, density and distribution of Arctic vegetation in recent decades1–4. These changes cause multiple opposing feedbacks between the biosphere and atmosphere5–9, the relative magnitudes of which will have globally significant consequences but are unknown at a pan-Arctic scale10. The precise nature of Arctic vegetation change under future warming will strongly influence climate feedbacks, yet Earth system modelling studies have so far assumed arbitrary increases in shrubs (for example, +20%; refs 6,11), highlighting the need for predictions of future vegetation distribution shifts. Here we show, using climate scenarios for the 2050s and models that utilize statistical associations between vegetation and climate, the potential for extremely widespread redistribution of vegetation across the Arctic. We predict that at least half of vegetated areas will shift to a different physiognomic class, and woody cover will increase by as much as 52%. By incorporating observed relationships between vegetation and albedo, evapotranspiration and biomass, we show that vegetation distribution shifts will result in an overall positive feedback to climate that is likely to cause greater warming than has previously been predicted. Such extensive changes to Arctic vegetation will have implications for climate, wildlife and ecosystem services.
Observed and predicted effects of climate change on species abundance in protected areas
The dynamic nature and diversity of species’ responses to climate change poses significant difficulties for developing robust, long-term conservation strategies. One key question is whether existing protected area networks will remain effective in a changing climate. To test this, we developed statistical models that link climate to the abundance of internationally important bird populations in northwestern Europe. Spatial climate–abundance models were able to predict 56% of the variation in recent 30-year population trends. Using these models, future climate change resulting in 4.0 ◦C global warming was projected to cause declines of at least 25% for more than half of the internationally important populations considered. Nonetheless, most EU Special Protection Areas in the UK were projected to retain species in sufficient abundances to maintain their legal status, and generally sites that are important now were projected to be important in the future. The biological and legal resilience of this network of protected areas is derived from the capacity for turnover in the important species at each site as species’ distributions and abundances alter in response to climate. Current protected areas are therefore predicted to remain important for future conservation in a changing climate.
