Climate Science Documents
Rebuilding Soils on Mined Land for Native Forests in Appalachia
The eastern U.S. Appalachian region supports the world’s most extensive temperate forests, but surface mining for coal has caused forest loss. New reclamation methods are being employed with the intent of restoring native forest on Appalachian mined lands. Mine soil construction is essential to the reforestation process. Here, we review scientific literature concerning selection of mining materials for mine soil construction where forest ecosystem restoration is the reclamation goal. Successful establishment and productive growth of native Appalachian trees has been documented on mine soils with coarse fragment contents as great as 60% but with low soluble salt levels and slightly to moderately acidic pHs, properties characteristic of the region’s native soils. Native tree productivity on some Appalachian mined lands where weathered rock spoils were used to reconstruct soils was found comparable to productivity on native forest sites. Weathered rock spoils, however, are lower in bioavailable N and P than native Appalachian soils and they lack live seed banks which native soils contain. The body of scientific research suggests use of salvaged native soils for mine soil construction when forest ecosystem restoration is the reclamation goal, and that weathered rock spoils are generally superior to unweathered rock spoils when constructing mine soils for this purpose.
Amazon Basin climate under global warming: the role of the sea surface temperature
The Hadley Centre coupled climate–carbon cycle model (HadCM3LC) predicts loss of the Amazon rainforest in response to future anthropogenic greenhouse gas emissions. In this study, the atmospheric component of HadCM3LC is used to assess the role of simulated changes in midtwenty-first century sea surface temperature (SST) in Amazon Basin climate change. When the full HadCM3LC SST anomalies (SSTAs) are used, the atmosphere model reproduces the Amazon Basin climate change exhibited by HadCM3LC, including much of the reduction in Amazon Basin rainfall. This rainfall change is shown to be the combined effect of SSTAs in both thetropical Atlantic and the Pacific, with roughly equal contributions from each basin. The greatest rainfall reduction occurs from May to October, outside of the mature South American monsoon (SAM) season. This dry season response is the combined effect of a more rapid warming of the tropical North Atlantic relative to the south, and warm SSTAs in the tropical east Pacific. Conversely, a weak enhancement of mature SAM season rainfall in response to Atlantic SST change is suppressed by the atmospheric response to Pacific SST. This net wet season response is sufficient to prevent dry season soil moisture deficits from being recharged through the SAM season, leading to a perennial soil moisture reduction and an associated 30% reduction in annual Amazon Basin net primary productivity (NPP). A further 23% NPP reduction occurs in response to a 3.58C warmer air temperature associated with a global mean SST warming.
Allowable carbon emissions lowered by multiple climate targets
Climate targets are designed to inform policies that would limit the magnitude and impacts of climate change caused by anthropogenic emissions of greenhouse gases and other substances. The target that is currently recognized by most world governments1 places a limit of two degrees Celsius on the global mean warming since preindustrial times. This would require large sustained reductions in carbon dioxide emissions during the twenty-first century and beyond2–4. Such a global temperature target, however, is not sufficient to control many other quantities, such as transient sea level rise5 , ocean acidification6,7 and net primary production on land8,9. Here, using an Earth system model of intermediate complexity (EMIC) in an observation-informed Bayesian approach, we show that allowable carbon emissions are substantially reduced whenmultiple climate targets are set. We take into account uncertainties in physical and carbon cycle model parameters, radiative efficiencies10, climate sensitivity11 and carbon cycle feedbacks12,13 along with a large set of observational constraints. Within this framework, we explore a broad range of economically feasible greenhouse gas scenarios from the integrated assessment community14–17 to determine the likelihood of meeting a combination of specific global and regional targets under various assumptions. For any given likelihood of meeting a set of such targets, the allowable cumulative emissions are greatly reduced from those inferred from the temperature target alone. Therefore, temperature targets alone are unable to comprehensively limit the risks from anthropogenic emissions.
Managing Forests and Fire in Changing Climates
With projected climate change, we expect to face much more forest fi re in the coming decades. Policymakers are challenged not to categorize all fires as destructive to ecosystems simply because they have long fl ame lengths and kill most of the trees within the fi re boundary. Ecological context matters: In some ecosystems, high-severity regimes are appropriate, but climate change may modify these fi re regimes and ecosystems as well. Some undesirable impacts may be avoided or reduced through global strategies, as well as distinct strategies based on a forest’s historical fi re regime. SCIENCE VOL 342 4 OCTOBER 2013
Rate of tree carbon accumulation increases continuously with tree size
Forests are major components of the global carbon cycle, providing substantial feedback to atmospheric greenhouse gas concentrations1 . Our ability to understand and predict changes in the forest carbon cycle—particularly net primary productivity and carbon storage— increasingly relies on models that represent biological processes across several scales of biological organization, from tree leaves to forest stands2,3. Yet, despite advances in our understanding of productivity at the scales of leaves and stands, no consensus exists about the nature of productivity at the scale of the individual tree4–7, in part because we lack a broad empirical assessment of whether rates of absolute treemass growth (and thus carbon accumulation) decrease, remain constant, or increase as trees increase in size and age. Here we present a global analysis of 403 tropical and temperate tree species, showing that for most species mass growth rate increases continuously with tree size. Thus, large, old trees do not act simply as senescent carbon reservoirs but actively fix large amounts of carbon compared to smaller trees; at the extreme, a single big tree can add the same amount of carbon to the forest within a year as is contained in an entire mid-sized tree. The apparent paradoxes of individual tree growth increasing with tree size despite declining leaf-level8–10 and stand-level10 productivity can be explained, respectively, by increases in a tree’s total leaf area that outpace declines in productivity per unit of leaf area and, among other factors, age-related reductions in population density. Our results resolve conflicting assumptions about the nature of tree growth,inform efforts to undertand and model forest carbon dynamics, and have additional implications for theories of resource allocation11 and plant senescence1
Risk Communication on Climate: Mental Models and Mass Balance
Public confusion about the urgency of reductions in greenhouse gas emissions results from a basic misconception.
When the river runs dry: human and ecological values of dry riverbeds
Temporary rivers and streams that naturally cease to flow and dry up can be found on every continent. Many other water courses that were once perennial now also have temporary flow regimes due to the effects of water extraction for human use or as a result of changes in land use and climate. The dry beds of these temporary rivers are an integral part of river landscapes. We discuss their importance in human culture and their unique diversity of aquatic, amphibious, and terrestrial biota. We also describe their role as seed and egg banks for aquatic biota, as dispersal corridors and temporal ecotones linking wet and dry phases, and as sites for the storage and processing of organic matter and nutrients. In light of these valuable functions, dry riverbeds need to be fully integrated into river management policies and monitoring programs. We also identify key knowledge gaps and suggest research questions concerning the values of dry riverbeds.
The energetic implications of curtailing versus storing solar- and wind-generated electricity
We present a theoretical framework to calculate how storage affects the energy return on energy investment (EROI) ratios of wind and solar resources. Our methods identify conditions under which it is more energetically favorable to store energy than it is to simply curtail electricity production. Electrochemically based storage technologies result in much smaller EROI ratios than large-scale geologically based storage technologies like compressed air energy storage (CAES) and pumped hydroelectric storage (PHS). All storage technologies paired with solar photovoltaic (PV) generation yield EROI ratios that are greater than curtailment. Due to their low energy stored on electrical energy invested (ESOIe) ratios, conventional battery technologies reduce the EROI ratios of wind generation below curtailment EROI ratios. To yield a greater net energy return than curtailment, battery storage technologies paired with wind generation need an ESOIe > 80. We identify improvements in cycle life as the most feasible way to increase battery ESOIe. Depending upon the battery's embodied energy requirement, an increase of cycle life to 10 000–18 000 (2–20 times present values) is required for pairing with wind (assuming liberal round-trip efficiency [90%] and liberal depth-of-discharge [80%] values). Reducing embodied energy costs, increasing efficiency and increasing depth of discharge will also further improve the energetic performance of batteries. While this paper focuses on only one benefit of energy storage, the value of not curtailing electricity generation during periods of excess production, similar analyses could be used to draw conclusions about other benefits as well
Ecologists Report Huge Storm Losses in China’s Forests
From delicate orchids and magnolias to rare Chinese yews and Kwangtung pines, the flora of Guangdong Nanling National Nature Reserve is considered so precious that ecologists call the reserve “a treasure trove of species.” But winter storms have reduced the biological hot spot to a splintered ruin. Snow, sleet, and ice laid waste to 90% of the 58,000- hectare reserve’s forests, says He Kejun, director of Guangdong Forestry
Challenges in the conservation, rehabilitation and recovery of native stream salmonid populations: beyond the 2010 Luarca symposium
– In May 2010, I chaired a session on challenges to salmonid conservation at the international symposium ‘Advances in the population ecology of stream salmonids’ in Luarca, Spain. I suggested that in addition to scientific challenges, a major challenge will be improving the links between ecologists, conservationists and policy makers. Because the Luarca symposium focused mainly on ecological research, little time was explicitly devoted to conservation. My objective in this paper is to further discuss the role of ecological research in informing salmonid conservation. I begin with a brief overview of research highlights from the symposium. I then use selected examples to show that ecological research has already contributed much towards informing salmonid conservation, but that ecologists will always be faced with limitations in their predictive ability. I suggest that conservation will need to move forward regardless of these limitations, and I call attention to some recent efforts wherein ecological research has played a crucial role. I conclude that ecologists should take urgent action to ensure that their results are availableto inform resource managers, conservation organisations and policy makers regarding past losses and present threats to native, locally-adapted salmonid stocks.
Climate change impacts on the biophysics and economics of world fisheries
Global marine fisheries are underperforming economically because of overfishing, pollution and habitat degradation. Added to these threats is the looming challenge of climate change. Observations, experiments and simulation models show that climate change would result in changes in primary productivity, shifts in distribution and changes in the potential yield of exploited marine species, resulting in impacts on the economics of fisheries worldwide. Despite the gaps in understanding climate change effects on fisheries, there is sufficient scientific information that highlights the need to implement climate change mitigation and adaptation policies to minimize impacts on fisheries.
Dissecting insect responses to climate warming: overwintering and post-diapause performance in the southern green stink bug, Nezara viridula, under simulated climate-change conditions
The effect of simulated climate change on overwintering and postdiapause reproductive performance is studied in Nezara viridula (L.) (Heteroptera: Pentatomidae) close to the species’ northern range limit in Japan. Insects are reared from October to June under quasi-natural (i.e. ambient outdoor) conditions and in a transparent incubator, in which climate warming is simulated by adding 2.5 ◦ C to the ambient temperatures. Despite the earlier assumption that females of N. viridula overwinter in diapause, whereas males do so in quiescence, regular dissections show that the two sexes overwinter in a state of true diapause. During winter, both sexes are dark-coloured and have undeveloped reproductive organs. Resumption of development does not start until late March. During winter, the effect of simulated warming on the dynamics and timing of physiological processes appears to be limited. However, the warming significantly enhances winter survival (from 27–31% to 47–70%), which is a key factor in range expansion of N. viridula. In spring, the effect of simulated warming is complex. It advances the post-diapause colour change and transition from dormancy to reproduction. The earlier resumption of development is more pronounced in females: in April, significantly more females are already in a reproductive state under the simulated warming than under quasi-natural conditions. In males, the tendency is similar, although the difference is not significant. Warming significantly enhances spring survival and percentage of copulating adults, although not the percentage of ovipositing females and fecundity. The results suggest that, under the expected climate-warming conditions, N. viridula will likely benefit mostly as a result of increased winter and spring survival and advanced post-diapause reproduction. Further warming is likely to allow more adults to survive the critical cold season and contribute (both numerically and by increasing heterogeneity) to the post-overwintering population growth, thus promoting the establishment of this species in newly-colonized area
The Holocene`
Combining nine tree growth proxies from four sites, from the west coast of Norway to the Kola Peninsula of NW Russia, provides a well replicated (> 100 annual measurements per year) mean index of tree growth over the last 1200 years that represents the growth of much of the northern pine timberline forests of northern Fennoscandia. The simple mean of the nine series, z-scored over their common period, correlates strongly with mean June to August temperature averaged over this region (r = 0.81), allowing reconstructions of summer temperature based on regression and variance scaling. The reconstructions correlate significantly with gridded summer temperatures across the whole of Fennoscandia, extending north across Svalbard and south into Denmark. Uncertainty in the reconstructions is estimated by combining the uncertainty in mean tree growth with the uncertainty in the regression models. Over the last seven centuries the uncertainty is < 4.5% higher than in the 20th century, and reaches a maximum of 12% above recent levels during the 10th century. The results suggest that the 20th century was the warmest of the last 1200 years, but that it was not significantly different from the 11th century. The coldest century was the 17th. The impact of volcanic eruptions is clear, and a delayed recovery from pairs or multiple eruptions suggests the presence of some positive feedback mechanism. There is no clear and consistent link between northern Fennoscandian summer temperatures and solar forcing.
The Wheel of Life Food, Climate, Human Rights, and the Economy
The links between climate change and industrial agriculture create a nexus of crises—food insecurity, natural resource depletion and degradation, as well as human rights violations and inequities. While it is widely recognized that greenhouse gas (GHG) emissions due to human activity are detrimental to the natural environment, it can be difficult to untangle the cascading effects on other sectors. To unravel some of the effects, this paper focuses on three interrelated issues: 1) What are the critical links between climate change and agriculture? 2) How is the nexus of agriculture and climate change affecting human societies particularly regarding food and water, livelihoods, migration, gender equality, and other basic survival and human rights? 3) What is the interplay between economic and finance systems, on the one hand, and food security, climate change, and fundamental human rights, on the other? In the process of drawing connections among these issues, the report will identify the commonality of drivers, or “push” factors, that lead to adverse impacts. A central theme throughout this report is that policies and practices must begin with the ecological imperative in order to ensure authentic security and stability on all fronts including food, water, livelihoods and jobs, climate, energy, and economic. In turn this engenders equity, social justice, and diverse cultures. This imperative, or ethos of nature, is a foundation that serves as a steady guide when reviewing mitigation and adaptation solutions to climate change. Infused within this theme is the sobering recognition that current consumption and production patterns are at odds with goals of reducing GHGs and attaining global food security. For instance, consumption and production levels, based on the global average, are 25 percent higher than the earth’s ecological capacity.1 As societies address the myriad ecological and social issues at the axis of global warming, a central task will be to re-align consumption and production trends in a manner that can fulfill economic and development requirements. This will require a major shift away from present economic growth paradigms based on massive resource extraction and toward creating prosperous and vital societies and economies that preserve the planet’s environmental capacity
Missing feedbacks, asymmetric uncertainties, and the underestimation of future warming
Historical evidence shows that atmospheric greenhouse gas (GhG) concentrations increase during periods of warming, implying a positive feedback to future climate change. We quantified this feedback for CO2 and CH4 by combining the mathematics of feedback with empirical icecore information and general circulation model (GCM) climate sensitivity, finding that the warming of 1.5 –4.5C associated with anthropogenic doubling of CO2 is amplified to 1.6– 6.0C warming, with the uncertainty range deriving from GCM simulations and paleo temperature records. Thus, anthropogenic emissions result in higher final GhG concentrations, and therefore more warming, than would be predicted in the absence of this feedback. Moreover, a symmetrical uncertainty in any component of feedback, whether positive or negative, produces an asymmetrical distribution of expected temperatures skewed toward higher temperature. For both reasons, the omission of key positive feedbacks and asymmetrical uncertainty from feedbacks, it is likely that the future will be hotter than we think. Citation: Torn, M. S., and J. Harte (2006), Missing feedbacks, asymmetric uncertainties, and the underestimation of future warming.
TRY – a global database of plant traits
Plant traits – the morphological, anatomical, physiological, biochemical and phenological characteristics of plants and their organs – determine how primary producers respond to environmental factors, affect other trophic levels, influence ecosystem processes and services and provide a link from species richness to ecosystem functional diversity. Trait data thus represent the raw material for a wide range of research from evolutionary biology, community and functional ecology to biogeography. Here we present the global database initiative named TRY, which has united a wide range of the plant trait research community worldwide and gained an unprecedented buy-in of trait data: so far 93 trait databases have been contributed. The data repository currently contains almost three million trait entries for 69 000 out of the world’s 300 000 plant species, with a focus on 52 groups of traits characterizing the vegetative and regeneration stages of the plant life cycle, including growth, dispersal, establishment and persistence. A first data analysis shows that most plant traits are approximately log-normally distributed, with widely differing ranges of variation across traits. Most trait variation is between species (interspecific), but significant intraspecific variation is also documented, up to 40% of the overall variation. Plant functional types (PFTs), as commonly used in vegetation models, capture a substantial fraction of the observed variation – but for several traits most variation occurs within PFTs, up to 75% of the overall variation. In the context of vegetation models these traits would better be represented by state variables rather than fixed parameter values. The improved availability of plant trait data in the unified global database is expected to support a paradigm shift from species to trait-based ecology, offer new opportunities for synthetic plant trait research and enable a more realistic and empirically grounded representation of terrestrial vegetation in Earth system models.
U.S. Forest Carbon and Climate Change Controversies and Win-Win Policy Approaches
As consensus grows about the serious impacts of global climate change, the role of forests in carbon storage is increasingly recognized. Terrestrial vegetation worldwide currently removes about 24 percent of the greenhouse gases released by industrial processes. Unfortunately, this contribution is approximately cancelled out by carbon released as a result of global deforestation and other ecosystem changes. Slowing or halting the rate of deforestation is thus one of the prime strategies to mitigate global climate change. The U.S. situation differs from the global one in several ways. Since both forest acres and average biomass per forest acre are currently increasing, as U.S. forests recover from past clearing or heavy harvest, our forest carbon stores are growing larger over time. However, our high rate of industrial emissions means that only about 10 percent of the carbon released from burning fossil fuels in the United States is captured by our forests. Moreover, net U.S. forest carbon sequestration has begun to slow in recent years as reforestation reaches its limits and development sprawls into more rural forested areas. U.S. forests could possibly capture a much higher portion of our industrial emissions, but only if we prevent forest conversion and development and manage our forests to maximize carbon stores.
Unburnable Carbon – Are the world’s financial markets carrying a carbon bubble?
The Carbon Tracker initiative is a new way of looking at the carbon emissions problem. It is focused on the fossil fuel reserves held by publically listed companies and the way they are valued and assessed by markets. Currently financial markets have an unlimited capacity to treat fossil fuel reserves as assets. As governments move to control carbon emissions, this market failure is creating systemic risks for institutional investors, notably the threat of fossil fuel assets becoming stranded as the shift to a low-carbon economy accelerates.
Scenario Planning: a Tool for Conservation in an Uncertain World
: Conservation decisions about how, when, and where to act are typically based on our expectations for the future. When the world is highly unpredictable and we are working from a limited range of expectations, however, our expectations will frequently be proved wrong. Scenario planning offers a framework for developing more resilient conservation policies when faced with uncontrollable, irreducible uncertainty. A scenario in this context is an account of a plausible future. Scenario planning consists of using a few contrasting scenarios to explore the uncertainty surrounding the future consequences of a decision. Ideally, scenarios should be constructed by a diverse group of people for a single, stated purpose. Scenario planning can incorporate a variety of quantitative and qualitative information in the decision-making process. Often, consideration of this diverse information in a systemic way leads to better decisions. Furthermore, the participation of a diverse group of people in a systemic process of collecting, discussing, and analyzing scenarios builds shared understanding. The robustness provided by the consideration of multiple possible futures has served several groups well; we present examples from business, government, and conservation planning that illustrate the value of scenario planning. For conservation, major benefits of using scenario planning are (1) increased understanding of key uncertainties, (2) incorporation of alternative perspectives into conservation planning, and (3) greater resilience of decisions to surprise.
Call Off the Quest
Over the past 30 years, the climate research community has made valiant efforts to answer the “climate sensitivity” question: What is the long-term equilibrium warming response to a doubling of atmospheric carbon dioxide? Earlier this year, the Intergovernmental Panel on Climate Change (1) concluded that this sensitivity is likely to be in the range of 2° to 4.5°C, with a 1-in-3 chance that it is outside that range. The lower bound of 2°C is slightly higher than the 1.6°C proposed in the 1970s (2). 26 OCTOBER 2007 VOL 318 SCIENCE
Why Is Climate Sensitivity So Unpredictable?
Uncertainties in projections of future climate change have not lessened substantially in past decades. Both models and observations yield broad probability distributions for long-term increases in global mean temperature expected from the doubling of atmospheric carbon dioxide, with small but finite probabilities of very large increases. We show that the shape of these probability distributions is an inevitable and general consequence of the nature of the climate system, and we derive a simple analytic form for the shape that fits recent published distributions very well. We show that the breadth of the distribution and, in particular, the probability of large temperature increases are relatively insensitive to decreases in uncertainties associated with the underlying climate processes. VOL 318 26 OCTOBER 2007
Volcanic cause of catastrophe
From the timing, it looks as if an episode of marked oceanic oxygen deficiency during the Cretaceous was the result of undersea volcanism. Studies of such events are relevant to the warming world of today. NATURE|Vol 454|17 July 2008
Are we in the midst of the sixth mass extinction? A view from the world of amphibians
Many scientists argue that we are either entering or in the midst of the sixth great mass extinction. Intense human pressure, both direct and indirect, is having profound effects on natural environments. The amphibians—frogs, salamanders, and caecilians—may be the only major group currently at risk globally. A detailed worldwide assessment and subsequent updates show that onethird or more of the 6,300 species are threatened with extinction. This trend is likely to accelerate because most amphibians occur in the tropics and have small geographic ranges that make them susceptible to extinction. The increasing pressure from habitat destruction and climate change is likely to have major impacts on narrowly adapted and distributed species. We show that salamanders on tropical mountains are particularly at risk. A new and significant threat to amphibians is a virulent, emerging infectious disease, chytridiomycosis, which appears to be globally distributed, and its effects may be exacerbated by global warming. This disease, which is caused by a fungal pathogen and implicated in serious declines and extinctions of >200 species of amphibians, poses the greatest threat to biodiversity of any known disease. Our data for frogs in the Sierra Nevada of California show that the fungus is having a devastating impact on native species, already weakened by the effects of pollution and introduced predators. A general message from amphibians is that we may have little time to stave off a potential mass extinction. 11466–11473 PNAS August 12, 2008 vol. 105 suppl. 1
Phylogenetic patterns of species loss in Thoreau’s woods are driven by climate change
Climate change has led to major changes in the phenology (the timing of seasonal activities, such as flowering) of some species but not others. The extent to which flowering-time response to temperature is shared among closely related species might have important consequences for community-wide patterns of species loss under rapid climate change. Henry David Thoreau initiated a dataset of the Concord, Massachusetts, flora that spans !150 years and provides information on changes in species abundance and flowering time. When these data are analyzed in a phylogenetic context, they indicate that change in abundance is strongly correlated with flowering-time response. Species that do not respond to temperature have decreased greatly in abundance, and include among others anemones and buttercups [Ranunculaceae pro parte (p.p.)], asters and campanulas (Asterales), bluets (Rubiaceae p.p.), bladderworts (Lentibulariaceae), dogwoods (Cornaceae), lilies (Liliales), mints (Lamiaceae p.p.), orchids (Orchidaceae), roses (Rosaceae p.p.), saxifrages (Saxifragales), and violets (Malpighiales). Because flowering-time response traits are shared among closely related species, our findings suggest that climate change has affected and will likely continue to shape the phylogenetically biased pattern of species loss in Thoreau’s woods PNAS ! November 4, 2008 ! vol. 105 ! no. 44 ! 17029–17033
A westward extension of the warm pool leads to a westward extension of the Walker circulation, drying eastern Africa
Observations and simulations link anthropogenicgreenhouse and aerosol emissions with rapidly increasing Indian Ocean sea surface temperatures (SSTs). Over the past 60 years, the Indian Ocean warmed two to three times faster than the central tropical Pacific, extending the tropical warm pool to the west by *40 longitude ([4,000 km). This propensity toward rapid warming in the Indian Ocean has been the dominant mode of interannual variability among SSTs throughout the tropical Indian and Pacific Oceans (55E–140W) since at least 1948, explaining more variance than anomalies associated with the El Nin˜o-Southern Oscillation (ENSO). In the atmosphere, the primary mode of variability has been a corresponding trend toward greatly increased convection and precipitation over the tropical Indian Ocean. The temperature and rainfall increases in this region have produced a westward extension of the western, ascending branch of the atmospheric Walker circulation. Diabatic heating due to increased mid-tropospheric water vapor condensation elicits a westward atmospheric response that sends an easterly flow of dry air aloft toward eastern Africa. In recent decades (1980–2009), this response has suppressed convection over tropical eastern Africa, decreasing precipitation during the ‘long-rains’ season of March–June. This trend toward drought contrasts with projections of increased rainfall in eastern Africa and more ‘El Nin˜o-like’ conditions globally by the Intergovernmental Panel on Climate Change. Increased Indian Ocean SSTs appear likely to continue to strongly modulate the Warm Pool circulation, reducing precipitation in eastern Africa, regardless of whether the projected trend in ENSO is realized. These results have important food security implications, informing agricultural development, environmental conservation, and water resource planning.
Ecological responses to recent climate change
There is now ample evidence of the ecological impacts of recent climate change, from polar terrestrial to tropical marine environments. The responses of both flora and fauna span an array of ecosystems and organizational hierarchies, from the species to the community levels. Despite continued uncertainty as to community and ecosystem trajectories under global change, our review exposes a coherent pattern of ecological change across systems. Although we are only at an early stage in the projected trends of global warming, ecological responses to recent climate change are already clearly visible.
Predicting satellite-derived patterns of large-scale disturbances in forests of the Pacific Northwest Region in response to recent climatic variation
Across the Pacific Northwest, the climate between 1950 and 1975 was exceptionally cool and wet compared with more recent conditions (1995–2005). We reasoned that the changes in climate could result in expanded outbreaks of insects, diseases, and fire. To test this premise, we first modeled monthly variation in photosynthesis and growth of the most widely distributed species, Douglas-fir (Pseudotsuga menziesii), using a process-based model (3-PG) for the two periods. To compare with remotely sensed variables, we converted modeled growth potential into maximum leaf area index (LAImax), which was predicted to range from 1 to 9 across the region. On most sites, varying soil moisture storage capacity (θcap) from 200 to 300 mm while holding soil fertility constant, made slight but insignificant difference in simulated LAImax patterns. Both values of θcap correlated well with LAI estimates acquired from NASA's MODIS satellites in June, 2005 (r2= 0.7). To evaluate where 15 coniferous tree species might be prone to wide-scale disturbance, we used climatically-driven decision-tree models, calibrated in the 1950–1975 period, to identify vulnerable areas in 1995–2005. We stratified predictions within 34 recognized ecoregions and compared these results with large-scale disturbances recorded on MODIS imagery acquired between 2005 and 2009. The correlation between the percent of species judged as vulnerable within each ecoregion and the percent of forested areas recorded as disturbed with a MODIS-derived Global Disturbance Index was linear and accounted for 65 to 73% of the observed variation, depending on whether or not disturbance by fire was excluded from the analysis. Based on climate projections through the rest of the rest of the 21st century, we expect continued high levels of disturbance in ecoregions located beyond the climatically buffering influence of the Pacific Ocean.
How Much More Rain Will Global Warming Bring?
Climate models and satellite observations both indicate that the total amount of water in the atmosphere will increase at a rate of 7% per kelvin of surface warming. However, the climate models predict that global precipitation will increase at a much slower rate of 1 to 3% per kelvin. A recent analysis of satellite observations does not support this prediction of a muted response of precipitation to global warming. Rather, the observations suggest that precipitation and total atmospheric water have increased at about the same rate over the past two decades. SCIENCE VOL 317 13 JULY 2007
Slowly Warming
A chart about global Warming
Spatial patterns and policy implications for residential water use
The front yard makes a powerful visual statement about the occupants of the residence. As visible statements, yards are likely to induce a behavioral response on the part of neighboring residents. As an example, residents may strive to keep their yard as green and lush as their neighbors. For Kelowna, British Columbia, a highly significant positive spatial lag for summer water use implies some degree of spatial emulation in water using behavior. Other variables such as lot size, building size, assessed value, presence of a pool, etc. impact on water use as expected. The presence of a spatial lag implies a spatial multiplier for water saving innovations. If local water managers and policy makers can influence the spatial pattern of water saving innovations, they may be able to increase the size of the multiplier effect. Similar spatial policies may also be applicable to other socially influenced behaviors that leave a spatial signature, such as protecting ecologically significant habitats in urban areas
Columbia Water Center White Paper America’s Water Risk: Water Stress and Climate Variability
The emerging awareness of the dependence of business on water has resulted in increasing awareness of the concept of “Water Risk” and the diverse ways in which water can pose threats to businesses in certain regions and sectors. Businesses seek to secure sustainable income. To do so, they need to maintain a competitive advantage and brand differentiation. They need secure and stable supply chains. Their exposure risks related to increasing scarcity of water can come in a variety of forms at various points in the supply chain. Given increasing water scarcity and the associated deterioration of the quantity and quality of water sources in many parts of the world, many “tools” have been developed to map water scarcity riskor water risk. Typically, these tools are based on estimates of the average water supply and demand in each unit of analysis.Often, they are associated with river basins, while business is associated with cities or counties. They provide a useful first look at the potential imbalance of supply and demand to businesses.
Safe Havens, Safe Passages for Vulnerable Fish and Wildlife
Some of the best-known and most-cherished mountains on Earth are set in the Canadian Rockies of British Columbia and Alberta. Indeed, the mention of Banff, Jasper, Kootenay or Yoho National Parks evokes images of snow-capped peaks, thundering falls and turquoise waters, numerous natural wonders and majestic wildlife. The adjoining Provincial Parks in British Columbia – Mount Robson, Mount Assiniboine, and Hamber – are just as spectacular, if not quite as renowned. Waterton Lakes National Park in Alberta and Glacier National Park in Montana – brought together in 1931 as an International Peace Park by the respective Rotary Clubs – exemplify international cooperation and wilderness and wildlife without borders. All 9 of these parks have been designated as World Heritage Sites in recognition of their outstanding natural importance to the common heritage of humanity.
Conservation VALUE OF ROADLESS AREAS FOR VULNERABLE FISH AND Wildlife Species in the Crown of the Continent Ecosystem, Montana
The Crown of the Continent Ecosystem is one of the most spectacular landscapes in the world and most ecologically intact ecosystem remaining in the contiguous United States. Straddling the Continental Divide in the heart of the Rocky Mountains, the Crown of the Continent Ecosystem extends for >250 miles from the fabled Blackfoot River valley in northwest Montana north to Elk Pass south of Banff and Kootenay National Parks in Canada. It reaches from the short-grass plains along the eastern slopes of the Rockies westward nearly 100 miles to the Flathead and Kootenai River valleys. The Crown sparkles with a variety of dramatic landscapes, clean sources of blue waters, and diversity of plants and animals.Over the past century, citizens and government leaders have worked hard to save the core of this splendid ecosystem in Montana by establishing world-class parks and wildernesses – coupled with conservation of critical wildlife habitat on state and private lands along the periphery. These include jewels such as Glacier National Park, the Bob Marshall-Scapegoat-Great Bear Wilderness, the first-ever Tribal Wilderness in the Mission Mountains, numerous State of Montana Wildlife Management Areas (WMAs), and vital private lands through land trusts such as The Nature Conservancy. Their combined efforts have protected 3.3 million acres and constitute a truly impressive commitment to conservation. It was a remarkable legacy and great gift …but, in the face of new challenges, it may not have been enough.
Projections of Future Drought in the Continental United States and Mexico
Using the Palmer drought severity index, the ability of 19 state-of-the-art climate models to reproduce observed statistics of drought over North America is examined. It is found that correction of substantial biases in the models’ surface air temperature and precipitation fields is necessary. However, even after a bias correction, there are significant differences in the models’ ability to reproduce observations. Using metrics based on the ability to reproduce observed temporal and spatial patterns of drought, the relationship between model performance in simulating present-day drought characteristics and their differences in projections of future drought changes is investigated. It is found that all models project increases in future drought frequency and severity. However, using the metrics presented here to increase confidence in the multimodel projection is complicated by a correlation between models’ drought metric skill and climate sensitivity. The effect of this sampling error can be removed by changing how the projection is presented, from a projection based on a specific time interval to a projection based on a specified temperature change. This modified class of projections has reduced intermodel uncertainty and could be suitable for a wide range of climate change impacts projections.
When It Rains, It Pours Global Warming and the Increase in Extreme Precipitation from 1948 to 2011
Global warming is happening now and its effects are being felt in the United States and around the world. Among the expected consequences of global warming is an increase in the heaviest rain and snow storms, fueled by increased evaporation and the ability of a warmer atmosphere to hold more moisture. An analysis of more than 80 million daily precipitation records from across the contiguous United States reveals that intense rainstorms and snowstorms have already become more frequent and more severe. Extreme downpours are now happening 30 percent more often nationwide than in 1948. In other words, large rain or snowstorms that happened once every 12 months, on average, in the middle of the 20th century now happen every nine months. Moreover, the largest annual storms now produce 10 percent more precipitation, on average.
‘As Earth’s testimonies tell’: wilderness conservation in a changing world
Too often, wilderness conservation ignores a temporal perspective greater than the past 50 years, yet a long-term perspective (centuries to millennia) reveals the dynamic nature of many ecosystems. Analysis of fossil pollen, charcoal and stable isotopes, combined with historical analyses and archaeology can reveal how ongoing interactions between climatic change, human activities and other disturbances have shaped today’s landscapes over thousands of years. This interdisciplinary approach can inform wilderness conservation and also contribute to interpreting current trends and predicting how ecosystems might respond to future climate change. In this paper, we review literature that reveals how increasing collaboration among palaeoecologists, archaeologists, historians, anthropologists and ecologists is improving understanding of ecological complexity. Drawing on case studies from forested and non-forested ecosystems in Europe, the Americas, Africa and Australia, we discuss how this integrated approach can inform wilderness conservation and ecosystem management.
Wildfire and fuel treatment effects on forest carbon dynamics in the western United States
Sequestration of carbon (C) in forests has the potential to mitigate the effects of climate change by offsetting future emissions of greenhouse gases. However, in dry temperate forests, wildfire is a natural disturbance agent with the potential to release large fluxes of C into the atmosphere. Climate-driven increases in wildfire extent and severity are expected to increase the risks of reversal to C stores and affect the potential of dry forests to sequester C. In the western United States, fuel treatments that successfully reduce surface fuels in dry forests can mitigate the spread and severity of wildfire, while reducing both tree mortality and emissions from wildfire. However, heterogeneous burn environments, site-specific variability in post-fire ecosystem response, and uncertainty in future fire frequency and extent complicate assessments of long-term (decades to centuries) C dynamics across large landscapes. Results of studies on the effects of fuel treatments and wildfires on long-term C retention across large landscapes are limited and equivocal. Stand-scale studies, empirical and modeled, describe a wide range of total treatment costs (12–116 Mg C ha1 ) and reductions in wildfire emissions between treated and untreated stands (1–40 Mg C ha1 ). Conclusions suggest the direction (source, sink) and magnitude of net C effects from fuel treatments are similarly variable (33 Mg C ha1 to +3 Mg C ha1 ). Studies at large spatial and temporal scales suggest that there is a low likelihood of high-severity wildfire events interacting with treated forests, negating any expected C benefit from fuels reduction. The frequency, extent, and severity of wildfire are expected to increase as a result of changing climate, and additional information on C response to management and disturbance scenarios is needed improve the accuracy and usefulness of assessments of fuel treatment and wildfire effects on C dynamics. 20
The anatomy of predator–prey dynamics in a changing climate
1. Humans are increasingly influencing global climate and regional predator assemblages, yet a mechanistic understanding of how climate and predation interact to affect fluctuations in prey populations is currently lacking. 2. Here we develop a modelling framework to explore the effects of different predation strategies on the response of age-structured prey populations to a changing climate. 3. We show that predation acts in opposition to temporal correlation in climatic conditions to suppress prey population fluctuations. 4. Ambush predators such as lions are shown to be more effective at suppressing fluctuations in their prey than cursorial predators such as wolves, which chase down prey over long distances, because they are more effective predators on prime-aged adults. 5. We model climate as a Markov process and explore the consequences of future changes in climatic autocorrelation for population dynamics. We show that the presence of healthy predator populations will be particularly important in dampening prey population fluctuations if temporal correlation in climatic conditions increases in the future.
Animal Versus Wind Dispersal and the Robustness of Tree Species to Deforestation
Studies suggest that populations of different species do not decline equally after habitat loss. However, empirical tests have been confined to fine spatiotemporal scales and have rarely included plants. Using data from 89,365 forest survey plots covering peninsular Spain, we explored, for each of 34 common tree species, the relationship between probability of occurrence and the local cover of remaining forest. Twenty-four species showed a significant negative response to forest loss, so that decreased forest cover had a negative effect on tree diversity, but the responses of individual species were highly variable. Animal-dispersed species were less vulnerable to forest loss, with six showing positive responses to decreased forest cover. The results imply that plant-animal interactions help prevent the collapse of forest communities that suffer habitat destruction.
Large in-stream wood studies: a call for common metrics
During the past decade, research on large in-stream wood has expanded beyond North America’s Pacifi c Northwest to diverse environments and has shifted toward increasingly holistic perspectives that incorporate processes of wood recruitment, retention, and loss at scales from channel segments to entire watersheds. Syntheses of this rapidly expanding literature can be facilitated by agreement on primary variables and methods of measurement. In this paper we address these issues by listing the variables that we consider fundamental to studies of in-stream wood, discussing the sources of variability in their measurement, and suggesting more consistency in future studies. We recommend 23 variables for all studies of in-stream wood, as well as another 12 variables that we suggest for studies with more specifi c objectives. Each of these variables relates either to the size and characteristics of in-stream wood, to the geomorphic features of the channel and valley, or to the ecological characteristics of the riparian zone adjacent to the study reach. The variables were derived from an overview of those cited in the literature and from our collective fi eld experiences.
Landscape-scale carbon storage associated with beaver dams
Beaver meadows form when beaver dams promote prolonged overbank flooding and floodplain retention of sediment and organic matter. Extensive beaver meadows form in broad, low-gradient valley segments upstream from glacial terminal moraines. Surveyed sediment volume and total organic carbon content in beaver meadows on the eastern side of Rocky Mountain National Park are extrapolated to create a first-order approximation of landscape-scale carbon storage in these meadows relative to adjacent uplands. Differences in total organic carbon between abandoned and active beaver meadows suggest that valley-bottom carbon storage has declined substantially as beaver have disappeared and meadows have dried. Relict beaver meadows represent ~8% of total carbon storage within the landscape, but the value was closer to 23% when beaver actively maintained wet meadows. These changes reflect the general magnitude of cumulative effects in heterotrophic respiration and organic matter oxidation associated with historical declines in beaver populations across the continent
Carbon sequestration in the U.S. forest sector from 1990 to 2010
From 1990 through 2005, the forest sector (including forests and wood products) sequestered an average 162 Tg C year1 . In 2005, 49% of the total forest sector sequestration was in live and dead trees, 27% was in wood products in landfills, with the remainder in down dead wood, wood products in use, and forest floor and soil. The pools with the largest carbon stocks were not the same as those with the largest sequestration rates, except for the tree pool. For example, landfilled wood products comprise only 3% of total stocks but account for 27% of carbon sequestration. Conversely, forest soils comprise 48% of total stocks but account for only 2% of carbon sequestration. For the tree pool, the spatial pattern of carbon stocks was dissimilar to that of carbon flux. On an area basis, tree carbon stocks were highest in the Pacific Northwest, while changes were generally greatest in the upper Midwest and the Northeast. Net carbon sequestration in the forest sector in 2005 offset 10% of U.S. CO2 emissions. In the near future, we project that U.S. forests will continue to sequester carbon at a rate similar to that in recent years. Based on a comparison of our estimates to a compilation of land-based estimates of non-forest carbon sinks from the literature, we estimate that the conterminous U.S. annually sequesters 149–330 Tg C year1. Forests, urban trees, and wood products are responsible for 65–91% of this sink.
A new, global, multi-annual (2000–2007) burnt area product at 1 km resolution Vol. 35
This paper reports on the development and validation of a new, global, burnt area product. Burnt areas are reported at a resolution of 1 km for seven fire years (2000 to 2007). A modified version of a Global Burnt Area (GBA) 2000 algorithm is used to compute global burnt area. The total area burnt each year (2000– 2007) is estimated to be between 3.5 million km2 and 4.5 million km2 . The total amount of vegetation burnt by cover type according to the Global Land Cover (GLC) 2000 product is reported. Validation was undertaken using 72 Landsat TM scenes was undertaken. Correlation statistics between estimated burnt areas are reported for major vegetation types. The accuracy of this new global data set depends on vegetation type.
Animal migration amid shifting patterns of phenology and predation: lessons from a Yellowstone elk herd
Migration is a striking behavioral strategy by which many animals enhance resource acquisition while reducing predation risk. Historically, the demographic benefits of such movements made migration common, but in many taxa the phenomenon is considered globally threatened. Here we describe a long-term decline in the productivity of elk (Cervus elaphus) that migrate through intact wilderness areas to protected summer ranges inside Yellowstone National Park, USA. We attribute this decline to a long-term reduction in the demographic benefits that ungulates typically gain from migration. Among migratory elk, we observed a 21-year, 70% reduction in recruitment and a 4-year, 19% depression in their pregnancy rate largely caused by infrequent reproduction of females that were young or lactating. In contrast, among resident elk, we have recently observed increasing recruitment and a high rate of pregnancy. Landscape-level changes in habitat quality and predation appear to be responsible for the declining productivity of Yellowstone migrants. From 1989 to 2009, migratory elk experienced an increasing rate and shorter duration of green-up coincident with warmer spring–summer temperatures and reduced spring precipitation, also consistent with observations of an unusually severe drought in the region. Migrants are also now exposed to four times as many grizzly bears (Ursus arctos) and wolves (Canis lupus) as resident elk. Both of these restored predators consume migratory elk calves at high rates in the Yellowstone wilderness but are maintained at low densities via lethal management and human disturbance in the year-round habitats of resident elk. Our findings suggest that large-carnivore recovery and drought, operating simultaneously along an elevation gradient, have disproportionately influenced the demography of migratory elk. Many migratory animals travel large geographic distances between their seasonal ranges. Changes in land use and climate that disparately influence such seasonal ranges may alter the ecological basis of migratory behavior, representing an important challenge.
The Gift of the Dying: The Tragedy of AIDS and the Welfare of Future African Generations
This paper simulates the impact of the AIDS epidemic on future living standards in South Africa. I emphasize two competing effects. On the one hand, the epidemic is likely to have a detrimental impact on the human capital accumulation of orphaned children. On the other hand, widespread community infection lowers fertility, both directly, through a reduction in the willingness to engage in unprotected sexual activity, and indirectly, by increasing the scarcity of labor and the value of a woman’s time. I find that even with the most pessimistic assumptions concerning reductions in educational attainment, the fertility effect dominates. The AIDS epidemic, on net, enhances the future per capita consumption possibilities of the South African economy.
Don't Blame the Beetles
Bark beetles have devastated western forests, but that may not mean more severe fires.
Characterizing coal and mineral mines as a regional source of stress to stream fish assemblages
Mining impacts on stream systems have historically been studied over small spatial scales, yet investigations over large areas may be useful for characterizing mining as a regional source of stress to stream fishes. The associations between co-occurring stream fish assemblages and densities of various “classes” of mining occurring in the same catchments were tested using threshold analysis. Threshold analysis identifies the point at which fish assemblages change substantially from best available habitat conditions with increasing disturbance. As this occurred over large regions, species comprising fish assemblages were represented by various functional traits as well as other measures of interest to management (characterizing reproductive ecology and life history, habitat preferences, trophic ecology, assemblage diversity and evenness, tolerance to anthropogenic disturbance and state-recognized game species). We used two threshold detection methods: change-point analysis with indicator analysis and piecewise linear regression. We accepted only those thresholds that were highly statistically significant (p 0.01) for both techniques and overlapped within 5% error. We found consistent, wedge-shaped declines in multiple fish metrics with increasing levels of mining in catchments, suggesting mines are a regional source of disturbance. Threshold responses were consistent across the three ecoregions occurring at low mine densities. For 47.2% of the significant thresholds, a density of only 0.01 mines/km2 caused a threshold response. In fact, at least 25% of streams in each of our three study ecoregions have mine densities in their catchments with the potential to affect fish assemblages. Compared to other anthropogenic impacts assessed over large areas (agriculture, impervious surface or urban land use), mining had a more pronounced and consistent impact on fish assemblages. Threshold analysis Fish functional traits Landscape influences Game fishes Mining Rivers
Nonrandom, diversifying processes are disproportionately strong in the smallest size classes of a tropical forest
Here, we use one of the world’s longest-running, plot-based forest dynamics projects to compare nonrandom outcomes across stage classes. We considered a cohort of 7,977 individuals in 186 species that were alive in 1971 and monitored in 13 mortality censuses over 42 y to 2013. Nonrandom mortality with respect to species identity occurred more often in the smaller rather than the larger size classes. Furthermore, observed nonrandom mortality in the smaller size classes had a diversifying influence; species richness of the survivors was up to 30% greater than expected in the two smallest size classes, but not greater than expected in the larger size classes. These results highlight the importance of early life cycle stages in tropical forest community dynamics. More generally, they add to an accumulating body of evidence for the importance of early-stage nonrandom outcomes to community structure in marine and terrestrial environments. diversity | early life-cycle stages | nonrandom | tropical forest
Saturation-state sensitivity of marine bivalve larvae to ocean acidification
Ocean acidification results in co-varying inorganic carbon system variables. Of these, an explicit focus on pH and organismal acid–base regulation has failed to distinguish the mechanism of failure in highly sensitive bivalve larvae. With unique chemical manipulations of seawater we show definitively that larval shell development and growth are dependent on seawater saturation state, and not on carbon dioxide partial pressure or pH. Although other physiological processes are affected by pH, mineral saturation state thresholds will be crossed decades to centuries ahead of pH thresholds owing to nonlinear changes in the carbonate system variables as carbon dioxide is added. Our findings were repeatable for two species of bivalve larvae could resolve discrepancies in experimental results, are consistent with a previous model of ocean acidification impacts due to rapid calcification in bivalve larvae, and suggest a fundamental ocean acidification bottleneck at early life-history for some marine keystone species.
Microhabitats in the tropics buffer temperature in a globally coherent manner
Vegetated habitats contain a variety of fine-scale features that can ameliorate temperate extremes. These buffered microhabitats may be used by species to evade extreme weather and novel climates in the future. Yet, the magnitude and extent of this buffering on a global scale remains unknown. Across all tropical continents and using 36 published studies, we assessed temperature buffering from within microhabitats across various habitat strata and structures (e.g. soil, logs, epiphytes and tree holes) and compared them to non-buffered macro-scale ambient temperatures (the thermal control). Microhabitats buf- fered temperature by 3.98C and reduced maximum temperatures by 3.58C. Buffering was most pronounced in tropical lowlands where temperatures were most variable. With the expected increase in extreme weather events, microhabitats should provide species with a local layer of protection that is not captured by traditional climate assessments, which are typically derived from macro-scale temperatures (e.g. satellites). Our data illustrate the need for a next generation of predictive models that account for species’ ability to move within microhabitats to exploit favourable buffered microclimates.
Managing the whole landscape: historical, hybrid, and novel ecosystems
The reality confronting ecosystem managers today is one of heterogeneous, rapidly transforming landscapes, particularly in the areas more affected by urban and agricultural development. A landscape management framework that incorporates all systems, across the spectrum of degrees of alteration, provides a fuller set of options for how and when to intervene, uses limited resources more effectively, and increases the chances of achieving management goals. That many ecosystems have departed so substantially from their historical trajectory that they defy conventional restoration is not in dispute. Acknowledging novel ecosystems need not constitute a threat to existing policy and management approaches. Rather, the development of an integrated approach to management interventions can provide options that are in tune with the current reality of rapid ecosystem change.
Challenges of ecological restoration: Lessons from forests in northern Europe
The alarming rate of ecosystem degradation has raised the need for ecological restoration throughout different biomes and continents. North European forests may appear as one of the least vulnerable ecosystems from a global perspective, since forest cover is not rapidly decreasing and many ecosystem services remain at high level. However, extensive areas of northern forests are heavily exploited and have lost a major part of their biodiversity value. There is a strong requirement to restore these areas towards a more natural condition in order to meet the targets of the Convention on Biological Diversity. Several northern countries are now taking up this challenge by restoring forest biodiversity with increasing intensity. The ecology and biodiversity of boreal forests are relatively well understood making them a good model for restoration activities in many other forest ecosystems. Here we introduce northern forests as an ecosystem, discuss the historical and recent human impact and provide a brief status report on the ecological restoration projects and research already conducted there. Based on this discussion, we argue that before any restoration actions commence, the ecology of the target ecosystem should be established with the need for restoration carefully assessed and the outcome properly monitored. Finally, we identify the most important challenges that need to be solved in order to carry out efficient restoration with powerful and long-term positive impacts on biodiversity: coping with unpredictability, maintaining connectivity in time and space, assessment of functionality, management of conflicting interests and social restrictions and ensuring adequate funding.
Rising air and stream-water temperatures in Chesapeake Bay region, USA
Monthly mean air temperature (AT) at 85 sites and instantaneous stream-water temperature (WT) at 129 sites for 1960–2010 are examined for the mid-Atlantic region, USA. Temperature anomalies for two periods, 1961–1985 and 1985–2010, relative to the climate normal period of 1971–2000, indicate that the latter period was statistically signifi- cantly warmer than the former for both mean AT and WT. Statistically significant temporal trends across the region of 0.023 °C per year for AT and 0.028 °C per year for WT are detected using simple linear regression. Sensitivity analyses show that the irregularly sampled WT data are appropriate for trend analyses, resulting in conservative estimates of trend magnitude. Relations between 190 landscape factors and significant trends in AT-WT relations are examined using principal components analysis. Measures of major dams and deciduous forest are correlated with WT increasing slower than AT, whereas agriculture in the absence of major dams is correlated with WT increasing faster than AT. Increasing WT trends are detected despite increasing trends in streamflow in the northern part of the study area. Continued warming of contributing streams to Chesapeake Bay likely will result in shifts in distributions of aquatic biota and contribute to worsened eutrophic conditions in the bay and its estuaries.
Effect of Risk Aversion on Prioritizing Conservation Projects
Agencies making decisions about what threat mitigation actions to take to save which species frequently face the dilemma of whether to invest in actions with high probability of success and guaranteed benefits or to choose projects with a greater risk of failure that might provide higher benefits if they succeed. The answer to this dilemma lies in the decision maker’s aversion to risk—their unwillingness to accept uncertain outcomes. Little guidance exists on how risk preferences affect conservation investment priorities. Using a prioritization approach based on cost effectiveness, we compared 2 approaches: a conservative probability threshold approach that excludes investment in projects with a risk of management failure greater than a fixed level, and a variance-discounting heuristic used in economics that explicitly accounts for risk tolerance and the probabilities of management success and failure. We applied both approaches to prioritizing projects for 700 of New Zealand’s threatened species across 8303 management actions. Both decision makers’ risk tolerance and our choice of approach to dealing with risk preferences drove the prioritization solution (i.e., the species selected for management). Use of a probability threshold minimized uncertainty, but more expensive projects were selected than with variance discounting, which maximized expected benefits by selecting the management of species with higher extinction risk and higher conservation value. Explicitly incorporating risk preferences within the decision making process reduced the number of species expected to be safe from extinction because lower risk tolerance resulted in more species being excluded from management, but the approach allowed decision makers to choose a level of acceptable risk that fit with their ability to accommodate failure. We argue for transparency in risk tolerance and recommend that decision makers accept risk in an adaptive management framework to maximize benefits and avoid potential extinctions due to inefficient allocation of limited resources. Keywords: conservation decisionmaking,cost-effectiveness analysis, management effectiveness,Project Prioritization Protocol, risk analysis, risk tolerance, threatened species, uncertainty
Using and improving the social cost of carbon: Regular, institutionalized updating and review are essential
The social cost of carbon (SCC) is a crucial tool for economic analysis of climate policies. The SCC estimates the dollar value of reduced climate change damages associated with a one-metric-ton reduction in carbon dioxide (CO2) emissions. Although the con-ceptual basis, challenges, and merits of the SCC are well established, its use in government cost-benefit analysis (CBA) is relatively new. In light of challenges in constructing the SCC, its newness in government regulation, and the importance of updating, we propose an institutional process for regular SCC review and revision when used in government policy-making and suggest how scientists might contribute to improved SCC estimates.
Ten years of vegetation assembly after a North American mega fire
Altered fuels and climate change are transforming fire regimes in many of Earth’s biomes. Postfire reassembly of vegetation – paramount to C storage and biodiversity conservation – frequently remains unpredictable and complicated by rapid global change. Using a unique data set of pre and long-term postfire data, combined with long-term data from nearby unburned areas, we examined 10 years of understory vegetation assembly after the 2002 Hayman Fire. This fire was the largest wildfire in recorded history in Colorado, USA. Resistance (initial postfire deviance from pre- fire condition) and resilience (return to prefire condition) declined with increasing fire severity. However, via both resistance and resilience, ‘legacy’ species of the prefire community constituted >75% of total plant cover within 3 years even in severely burned areas. Perseverance of legacy species, coupled with new colonizers, created a persis- tent increase in community species richness and cover over prefire levels. This was driven by a first-year increase (maintained over time) in forbs with short life spans; a 2–3-year delayed surge in long-lived forbs; and a consistent increase in graminoids through the 10th postfire year. Burning increased exotic plant invasion relative to prefire and unburned areas, but burned communities always were >89% native. This study informs debate in the literature regarding whether these increasingly large fires are ‘ecological catastrophes.’ Landscape-scale severe burning was catastrophic from a tree overstory perspective, but from an understory perspective, burning promoted rich and productive native understories, despite the entire 10-year postfire period receiving below-average precipitation. Keywords: disturbance, exotic species, fire severity, Hayman Fire, Pinus ponderosa, resilience, resistance, succession, vegetation change
Untangling human and environmental effects on geographical gradients of mammal species richness: a global and regional evaluation
1. Different hypotheses (geographical, ecological, evolutionary or a combination of them) have been suggested to account for the spatial variation in species richness. However, the relative importance of environment and human impacts in explaining these patterns, either globally or at the biogeographical region level, remains largely unexplored. 2. Here, we jointly evaluate how current environmental conditions and human impacts shape global and regional gradients of species richness in terrestrial mammals. 3. We processed IUCN global distributional data for 3939 mammal species and a set of seven environmental and two human impact variables at a spatial resolution of 965 9 965 km. We used simple, multiple and partial regression techniques to evaluate environmental and human effects on species richness. 4. Actual evapotranspiration (AET) is the main driver of mammal species richness globally. Together with our results at the biogeographical realm level, this lends strong support for the water-energy hypothesis (i.e. global diversity gradients are best explained by the interaction of water and energy, with a latitudinal shift in the relative importance of ambient energy vs. water availability as we move from the poles to the equator). 5. While human effects on species richness are not easily detected at a global scale due to the large proportion of shared variance with the environment, these effects significantly emerge at the regional level. In the Nearctic, Palearctic and Oriental regions, the independent contribu- tion of human impacts is almost as important as current environmental conditions in explain- ing richness patterns. The intersection of human impacts with climate drives the geographical variation in mammal species richness in the Palearctic, Nearctic and Oriental regions. Using a human accessibility variable, we show, for the first time, that the zones most accessible to humans are often those where we find lower mammal species richness. Key-words: human accessibility, human footprint, macroclimate, macroecology, terrestrial vertebrates, water–energy dynamics
Physiological plasticity increases resilience of ectothermic animals to climate change
Understanding how climate change affects natural populations remains one of the greatest challenges for ecology and management of natural resources. Animals can remodel their physiology to compensate for the effects of temperature variation, and this physiological plasticity, or acclimation, can confer resilience to climate change1,2. The current lack of a comprehensive analysis of the capacity for physiological plasticity across taxonomic groups and geographic regions, however, constrains predictions of the impacts of climate change. Here, we assembled the largest database to date to establish the current state of knowledge of physiological plasticity in ectothermic animals. We show that acclimation decreases the sensitivity to temperature and climate change of freshwater and marine animals, but less so in terrestrial animals. Animals from more stable environments have greater capacity for acclimation, and there is a significant trend showing that the capacity for thermal acclimation increases with decreasing latitude. Despite the capacity for acclimation, climate change over the past 20 years has already resulted in increased physiological rates of up to 20%, and we predict further future increases under climate change. The generality of these predictions is limited, however, because much of the world is drastically undersampled in the literature, and these undersampled regions are the areas of greatest need for future research efforts.
Dramatically increasing chance of extremely hot summers since the 2003 European heatwave
Socio-economic stress from the unequivocal warming of the global climate system(1)could be mostly felt by societies through weather and climate extremes (2). The vulnerability of European citizens was made evident during the summer heatwave of 2003 (refs 3,4) when the heat-related death toll ran into tens of thousands (5). Human influence at least doubled the chances of the event according to the first formal event attribution study (6), which also made the ominous forecast that severe heatwaves could become commonplace by the 2040s. Here we investigate how the likelihood of having another extremely hot summer in one of the worst affected parts of Europe has changed ten years after the original study was published, given an observed summer temperature increase of 0.81 K since then. Our analysis benefits from the availability of new observations and data from several new models. Using a previously employed temperature threshold to define extremely hot summers, we find that events that would occur twice a century in the early 2000s are now expected to occur twice a decade. For the more extreme threshold observed in 2003, the return time reduces from thousands of years in the late twentieth century to about a hundred years in little over a decade.
Livelihood resilience in the face of climate change
The resilience concept requires greater attention to human livelihoods if it is to address the limits to adaptation strategies and the development needs of the planet’s poorest and most vulnerable people. Although the concept of resilience is increasingly informing research and policy, its transfer from ecological theory to social systems leads to weak engagement with normative, social and political dimensions of climate change adaptation. A livelihood perspective helps to strengthen resilience thinking by placing greater emphasis on human needs and their agency, empowerment and human rights, and considering adaptive livelihood systems in the context of wider transformational changes.
Global protected area expansion is compromised by projected land-use and parochialism
Protected areas are one of the main tools for halting the continuing global biodiversity crisis1–4 caused by habitat loss, fragmentation and other anthropogenic pressures5–8. According to the Aichi Biodiversity Target 11 adopted by the Convention on Biological Diversity, the protected area network should be expanded to at least 17% of the terrestrial world by 2020 (http://www.cbd.int/sp/targets). To max- imize conservation outcomes, it is crucial to identify the best expan- sion areas. Here we show that there is a very high potential to increase protection of ecoregions and vertebrate species by expanding the pro- tected area network, but also identify considerable risk of ineffective outcomes due to land-use change and uncoordinated actions between countries. We use distribution data for 24,757 terrestrial vertebrates assessed under the International Union for the Conservation of Nature (IUCN) ‘red list of threatened species’9, and terrestrial eco- regions10 (827), modified by land-use models for the present and 2040, and introduce techniques for global and balanced spatial con- servation prioritization. First, we show that with a coordinated global protected area network expansion to 17% of terrestrial land, average protection of species ranges and ecoregions could triple. Second, if projected land-use change by 2040 (ref. 11) takes place, it becomes infeasible to reach the currently possible protection levels, and over 1,000 threatened species would lose more than 50% of their present effective ranges worldwide. Third, we demonstrate a major efficiency gap between national and global conservation priorities. Strong evi- dence is shown that further biodiversity loss is unavoidable unless international action is quickly taken to balance land-use and biodiversity conservation. The approach used here can serve as a framework for repeatable and quantitative assessment of efficiency, gaps and expansion of the global protected area network globally, regionally and nationally, considering current and projected land-use pressures.
Critical slowing down as early warning for the onset of collapse in mutualistic communities
Tipping points are crossed when small changes in external conditions cause abrupt unexpected responses in the current state of a system. In the case of ecological communities under stress, the risk of approaching a tipping point is unknown, but its stakes are high. Here, we test recently developed critical slowing-down indicators as early-warning signals for detecting the proximity to a potential tipping point in structurally complex ecological communities. We use the structure of 79 empirical mutualistic networks to simulate a scenario of gradual environmental change that leads to an abrupt first extinction event followed by a sequence of species losses until the point of complete community collapse. We find that critical slowing-down indicators derived from time series of bio- masses measured at the species and community level signal the proximity to the onset of community collapse. In particular, we identify specialist species as likely the best-indicator species for mon- itoring the proximity of a community to collapse. In addition, trends in slowing-down indicators are strongly correlated to the timing of species extinctions. This correlation offers a promising way for map- ping species resilience and ranking species risk to extinction in a given community. Our findings pave the road for combining theory on tipping points with patterns of network structure that might prove useful for the management of a broad class of ecological networks under global environmental change. resilience | critical transition | mutualism | ecological networks | pollinator decline
Rapid deposition of oxidized biogenic compounds to a temperate forest
We report fluxes and dry deposition velocities for 16 atmospheric compounds above a southeastern United States forest, including: hydrogen peroxide (H2O2), nitric acid (HNO3), hydrogen cyanide (HCN), hydroxymethyl hydroperoxide, peroxyacetic acid, organic hydroxy nitrates, and other multifunctional species derived from the oxidation of isoprene and monoterpenes. The data suggest that dry deposition is the dominant daytime sink for small, satu- rated oxygenates. Greater than 6 wt %C emitted as isoprene by the forest was returned by dry deposition of its oxidized products. Peroxides account for a large fraction of the oxidant flux, possibly eclipsing ozone in more pristine regions. The measured organic nitrates comprise a sizable portion (15%) of the oxidized nitrogen input into the canopy, with HNO3 making up the balance. We ob- serve that water-soluble compounds (e.g., strong acids and hydro- peroxides) deposit with low surface resistance whereas compounds with moderate solubility (e.g., organic nitrates and hydroxycarbon- yls) or poor solubility (e.g., HCN) exhibited reduced uptake at the surface of plants. To first order, the relative deposition velocities of water-soluble compounds are constrained by their molecular diffu- sivity. From resistance modeling, we infer a substantial emission flux of formic acid at the canopy level (∼1 nmol m−2·s−1). GEOS−Chem, a widely used atmospheric chemical transport model, currently under- estimates dry deposition for most molecules studied in this work. Reconciling GEOS−Chem deposition velocities with observations resulted in up to a 45% decrease in the simulated surface con- centration of trace gases. biosphere−atmosphere exchange | isoprene | dry deposition | OVOCs | fluxes
Recovery of large carnivores in Europe’s modern human-dominated landscapes
The conservation of large carnivores is a formidable challenge for biodiversity conservation. Using a data set on the past and current status of brown bears (Ursus arctos), Eurasian lynx (Lynx lynx), gray wolves (Canis lupus), and wolverines (Gulo gulo) in European countries, we show that roughly one-third of mainland Europe hosts at least one large carnivore species, with stable or increasing abundance in most cases in 21st-century records. The reasons for this overall conservation success include protective legislation, supportive public opinion, and a variety of practices making coexistence between large carnivores and people possible. The European situation reveals that large carnivores and people can share the same landscape.
Temporal stability in forest productivity increases with tree diversity due to asynchrony in species dynamics
Theory predicts a positive relationship between biodiversity and stability in ecosystem properties, while diversity is expected to have a negative impact on stability at the species level. We used virtual experiments based on a dynamic simulation model to test for the diversity–stability relationship and its underlying mechanisms in Central European forests. First our results show that variability in productivity between stands differing in species composition decreases as species richness and functional diversity increase. Second we show temporal stability increases with increasing diversity due to compensatory dynamics across species, supporting the biodiversity insurance hypothesis. We demonstrate that this pattern is mainly driven by the asynchrony of spe- cies responses to small disturbances rather than to environmental fluctuations, and is only weakly affected by the net biodiversity effect on productivity. Furthermore, our results suggest that com- pensatory dynamics between species may enhance ecosystem stability through an optimisation of canopy occupancy by coexisting species. Keywords Asynchrony, biodiversity, ecosystem functioning, ecosystem predictability, forests, gap model, insurance hypothesis, productivity, stability, structural equation model.
Controls on Annual Forest Carbon Storage: Lessons from the Past and Predictions for the Future
The temperate forests of North America may play an important role in future carbon (C) sequestration strategies. New, multiyear, ecosystem-scale C cycling studies are providing a process-level understanding of the factors controlling annual forest C storage. Using a combination of ecological and meteorological methods, we quantified the response of annual C storage to historically widespread disturbances, forest succession, and climate variation in a common forest type of the upper Great Lakes region. At our study site in Michigan, repeated clear-cut harvesting and fire disturbance resulted in a lasting decrease in annual forest C storage. However, climate variation exerts a strong control on C storage as well, and future climate change may substantially reduce annual C storage by these forests. Annual C storage varies through ecological succession by rising to a maximum and then slowly declining in old-growth stands. Effective forest C sequestration requires the management of all C pools, including traditionally managed pools such as bole wood and also harvest residues and soils. Keywords: forests, carbon, climate change, succession, disturbance
Conservation threats: biofuel
Biofuels: Europe’s largest conservation charity has launched a campaign to heighten the threat to wildlife habitats and biodiversity from plantations of fuel crops. Nigel Williams reports. 1st paragraph: Europe embraced the theoretical potential that biofuels might offer both in terms of climate change and renewable sources of energy, as enthusiastically as anywhere else, but the dawning reality has hit harder here than in many other areas with the realisation that it is a crowded continent with limited scope for home-grown material.
Impacts of plant diversity on biomass production increase through time because of species complementarity
We summarize the results of 44 experiments that have manipulated the richness of plants to examine how plant diversity affects the production of biomass. We show that mixtures of species produce an average of 1.7 times more biomass than species monocultures and are more productive than the average monocul- ture in 79% of all experiments. However, in only 12% of all experiments do diverse polycultures achieve greater biomass than their single most productive species. Previously, a positive net effect of diversity that is no greater than the most productive species has been interpreted as evidence for selection effects, which occur when diversity maximizes the chance that highly productive species will be included in and ultimately dominate the biomass of polycultures. Contrary to this, we show that although productive species do indeed contribute to diversity effects, these contributions are equaled or exceeded by species complementar- ity, where biomass is augmented by biological processes that involve multiple species. Importantly, both the net effect of diver- sity and the probability of polycultures being more productive than their most productive species increases through time, because the magnitude of complementarity increases as experiments are run longer. Our results suggest that experiments to date have, if anything, underestimated the impacts of species extinction on the productivity of ecosystems.
Forest fuel reduction alters fire severity and long-term carbon storage in three Pacific Northwest ecosystems
Abstract. Two forest management objectives being debated in the context of federally managed landscapes in the U.S. Pacific Northwest involve a perceived trade-off between fire restoration and carbon sequestration. The former strategy would reduce fuel (and therefore C) that has accumulated through a century of fire suppression and exclusion which has led to extreme fire risk in some areas. The latter strategy would manage forests for enhanced C sequestration as a method of reducing atmospheric CO2 and associated threats from global climate change. We explored the trade-off between these two strategies by employing a forest ecosystem simulation model, STANDCARB, to examine the effects of fuel reduction on fire severity and the resulting long-term C dynamics among three Pacific Northwest ecosystems: the east Cascades ponderosa pine forests, the west Cascades western hemlock–Douglas-fir forests, and the Coast Range western hemlock–Sitka spruce forests. Our simulations indicate that fuel reduction treatments in these ecosystems consistently reduced fire severity. However, reducing the fraction by which C is lost in a wildfire requires the removal of a much greater amount of C, since most of the C stored in forest biomass (stem wood, branches, coarse woody debris) remains unconsumed even by high-severity wildfires. For this reason, all of the fuel reduction treatments simulated for the west Cascades and Coast Range ecosystems as well as most of the treatments simulated for the east Cascades resulted in a reduced mean stand C storage. One suggested method of compensating for such losses in C storage is to utilize C harvested in fuel reduction treatments as biofuels. Our analysis indicates that this will not be an effective strategy in the west Cascades and Coast Range over the next 100 years. We suggest that forest management plans aimed solely at ameliorating increases in atmospheric CO2 should forgo fuel reduction treatments in these ecosystems, with the possible exception of some east Cascades ponderosa pine stands with uncharacteristic levels of understory fuel accumulation. Balancing a demand for maximal landscape C storage with the demand for reduced wildfire severity will likely require treatments to be applied strategically throughout the landscape rather than indiscriminately treating all stands. Key words: biofuels; carbon sequestration; fire ecology; fuel reduction treatment; Pacific Northwest, USA; Picea sitchensis; Pinus ponderosa; Pseudotsuga menziesii.
Carbon debt and carbon sequestration parity in forest bioenergy production
The capacity for forests to aid in climate change mitigation efforts is substantial but will ultimately depend on their management. If forests remain unharvested, they can further mitigate the increases in atmospheric CO2 that result from fossil fuel combustion and deforestation. Alternatively, they can be harvested for bioenergy production and serve as a substitute for fossil fuels, though such a practice could reduce terrestrial C storage and thereby increase atmospheric CO2 concentrations in the near-term. Here, we used an ecosystem simulation model to ascertain the effectiveness of using forest bioenergy as a substitute for fossil fuels, drawing from a broad range of land-use histories, harvesting regimes, ecosystem characteristics, and bioenergy conversion effi- ciencies. Results demonstrate that the times required for bioenergy substitutions to repay the C Debt incurred from biomass harvest are usually much shorter (< 100 years) than the time required for bioenergy production to substitute the amount of C that would be stored if the forest were left unharvested entirely, a point we refer to as C Sequestration Parity. The effectiveness of substituting woody bioenergy for fossil fuels is highly dependent on the factors that determine bioenergy conversion efficiency, such as the C emissions released during the har- vest, transport, and firing of woody biomass. Consideration of the frequency and intensity of biomass harvests should also be given; performing total harvests (clear-cutting) at high-frequency may produce more bioenergy than less intensive harvesting regimes but may decrease C storage and thereby prolong the time required to achieve C Sequestration Parity. Keywords: bioenergy, biofuel, C cycle, C sequestration, forest management
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 emissions2, and forest thinning to reduce wildfire emissions3. 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.
From plant to power
Petrol might yet survive the green revolution. Some investors are taking seriously the con- cept of ‘green gasoline’ — transforming the woody remains of plants into exact replicas of today’s transportation fuels. Many see promise because, unlike other biofuels, this product would blend smoothly into today’s petrol-driven infrastructure. “This is one I like. It’s got a chance of making it,” says Lanny Schmidt, a chemical engineer who works on combustion processes and alternative fuels at the University of Minnesota in Minneapolis. Yet this ‘biomass-to-liquid’ approach is one of the least known in the biofuels portfolio, and barely makes a dent in alternative fuel quotas.
Do alternative energy sources displace fossil fuels?
A fundamental, generally implicit, assumption of the Intergov- ernmental Panel on Climate Change reports and many energy analysts is that each unit of energy supplied by non-fossil-fuel sources takes the place of a unit of energy supplied by fossil- fuel sources (1–4). However, owing to the complexity of economic systems and human behaviour, it is often the case that changes aimed at reducing one type of resource consumption, either through improvements in efficiency of use or by developing substitutes, do not lead to the intended outcome when net effects are considered (5–9). Here, I show that the average pattern across most nations of the world over the past fifty years is one where each unit of total national energy use from non- fossil-fuel sources displaced less than one-quarter of a unit of fossil-fuel energy use and, focusing specifically on electricity, each unit of electricity generated by non-fossil-fuel sources displaced less than one-tenth of a unit of fossil-fuel-generated electricity. These results challenge conventional thinking in that they indicate that suppressing the use of fossil fuel will require changes other than simply technical ones such as expanding non-fossil-fuel energy production.
The Biofuels Landscape Through the Lens of Industrial Chemistry
Replacing petroleum feedstock with biomass in the production of fuels and value-added chemicals carries considerable appeal. As in industrial chemistry more broadly, high-throughput experimentation has greatly facilitated innovation in small-scale exploration of biomass production and processing. Yet biomass is hard to transport, potentially hindering the integration of manufacturing-scale processes. Moreover, the path from laboratory breakthrough to commercial production remains as tortuous as ever.
Beneficial Biofuels—The Food, Energy, and Environment Trilemma
Exploiting multiple feedstocks, under new policies and accounting rules, to balance biofuel production, food security, and greenhouse-gas reduction.
Implications of Limiting CO2 Concentrations for Land Use and Energy
Limiting atmospheric carbon dioxide (CO2) concentrations to low levels requires strategies to manage anthropogenic carbon emissions from terrestrial systems as well as fossil fuel and industrial sources. We explore the implications of fully integrating terrestrial systems and the energy system into a comprehensive mitigation regime that limits atmospheric CO2 concentrations. We find that this comprehensive approach lowers the cost of meeting environmental goals but also carries with it profound implications for agriculture: Unmanaged ecosystems and forests expand, and food crop and livestock prices rise. Finally, we find that future improvement in food crop productivity directly affects land-use change emissions, making the technology for growing crops potentially important for limiting atmospheric CO2 concentrations.
Virtual Hot Spots
Physiological ecologists who design computer models to predict how animals handle heat are forecasting the effects of climate change
Roles and Effects of Environmental Carbon Dioxide in Insect Life
Key Words behavior, olfaction, antennal lobe, herbivory, oviposition Abstract Carbon dioxide (CO2) is a ubiquitous sensory cue that plays mul- tiple roles in insect behavior. In recent years understanding of the well-known role of CO2 in foraging by hematophagous insects (e.g., mosquitoes) has grown, and research on the roles of CO2 cues in the foraging and oviposition behavior of phytophagous insects and in behavior of social insects has stimulated interest in this area of insect sensory biology. This review considers those advances, as well as some of the mechanistic bases of the modulation of behavior by CO2 and important progress in our understanding of the detection and CNS processing of CO2 information in insects. Finally, this review briefly addresses how the ongoing increase in atmospheric CO2 levels may affect insect life.
Can Plants Adapt? New Questions in Climate Change Research
As it becomes increasingly apparent that human activities are partly responsible for global warming, the focus of climate change research is shifting from the churning out of assessments to the pursuit of science that can test the robustness of existing models. The questions now being addressed are becoming more challenging:The questions now being addressed are becoming more challenging: Can water-use efficiency of plants keep up with rising temperatures? Will we see a greening period for some decades, even a century, before facing a rapid browndown as threshold temperatures are reached? Or could the thresholds be reached much sooner because of interactions of biophysical processes? Is the carbon storage issue missing the point?
Montane meadow change during drought varies with background hydrologic regime and plant functional group
Key words:drought; forbs; hydrological gradient; plant community; woody plants. Abstract. Climate change models for many ecosystems predict more extreme climatic events in the future, including exacerbated drought conditions. Here we assess the effects of drought by quantifying temporal variation in community composition of a complex montane meadow landscape characterized by a hydrological gradient. The meadows occur in two regions of the Greater Yellowstone Ecosystem (Gallatin and Teton) and were classified into six categories (M1–M6, designating hydric to xeric) based upon Satellite pour l’Observation de la Terre (SPOT) satellite imagery. Both regions have similar plant communities, but patch sizes of meadows are much smaller in the Gallatin region. We measured changes in the percent cover of bare ground and plants by species and functional groups during five years between 1997 and 2007. We hypothesized that drought effects would not be manifested evenly across the hydrological gradient, but rather would be observed as hotspots of change in some areas and minimally evident in others. We also expected varying responses by plant functional groups (forbs vs. woody plants). Forbs, which typically use water from relatively shallow soils compared to woody plants, were expected to decrease in cover in mesic meadows, but increase in hydric meadows. Woody plants, such as Artemisia, were expected to increase, especially in mesic meadows. We identified several important trends in our meadow plant communities during this period of drought: (1) bare ground increased significantly in xeric meadows of both regions (Gallatin M6 and Teton M5) and in mesic (M3) meadows of the Teton, (2) forbs decreased significantly in the mesic and xeric meadows in both regions, (3) forbs increased in hydric (M1) meadows of the Gallatin region, and (4) woody species showed increases in M2 and M5 meadows of the Teton region and in M3 meadows of the Gallatin region. The woody response was dominated by changes in Artemisia spp. and Chrysothamnus viscidiflorus. Thus, our results supported our expectations that community change was not uniform across the landscape, but instead could be predicted based upon functional group responses to the spatial and temporal patterns of water availability, which are largely a function of plant water use and the hydrological gradient.
A Large-Scale Deforestation Experiment: Effects of Patch Area and Isolation on Amazon Birds
As compared with extensive contiguous areas, small isolated habitat patches lack many species. Some species disappear after isolation; others are rarely found in any small patch, regardless of isolation. We used a 13-year data set of bird captures from a large landscape-manipulation experiment in a Brazilian Amazon forest to model the extinction-colonization dynamics of 55 species and tested basic predictions of island biogeography and metapopulation theory. From our models, we derived two metrics of species vulnerability to changes in isolation and patch area. We found a strong effect of area and a variable effect of isolation on the predicted patch occupancy by birds.
From Individual Dispersal to Species Ranges: Perspectives for a Changing World
Dispersal is often risky to the individual, yet the long-term survival of populations depends on having a sufficient number of individuals that move, find each other, and locate suitable breeding habitats. This tension has consequences that rarely meet our conservation or management goals. This is particularly true in changing environments, which makes the study of dispersal urgently topical in a world plagued with habitat loss, climate change, and species introductions. Despite the difficulty of tracking mobile individuals over potentially vast ranges, recent research has revealed a multitude of ways in which dispersal evolution can either constrain, or accelerate, species’ responses to environmental changes.
How Does It Feel to Be Like a Rolling Stone? Ten Questions About Dispersal Evolution
This review proposes ten tentative answers to frequently asked ques- tions about dispersal evolution. I examine methodological issues, model assumptions and predictions, and their relation to empirical data. Study of dispersal evolution points to the many ecological and genetic feedbacks affecting the evolution of this complex trait, which has contributed to our better understanding of life-history evolution in spatially structured populations. Several lines of research are suggested to ameliorate the exchanges between theoretical and empirical studies of dispersal evolution.
The effect of changing climate on the frequency of absolute extreme events
n some areas of climate impact analysis, the possible impact of a changing mean climate has been dismissed by some writers either because of a belief that society can adapt to a slowly changing mean and/or because expected rates of future changes lie within or not far outside those experienced in the past. The two standard counter arguments to this optimistic view are: (1) the future will lead to much longer periods of protracted change in one direction, with final conditions well into the no-analogue region; and/or (2) the main impacts will accrue through changes in the frequency of extremes. In the literature on greenhouse effect, lip service is often paid to the effect of changes in the frequency of extremes. But just how will a slowly changing mean affect the frequency of extremes?
Vegetation Responses to Extreme Hydrological Events: Sequence Matters
Extreme hydrological events such as flood and drought drive vegetation dynamics and are projected to increase in frequency in association with climate change, which could result in sequences of extreme events. However, experimental studies of vegetation re- sponses to climate have largely focused on responses to a trend in climate or to a single extreme event but have largely overlooked the potential for complex responses to specific sequences of extreme events. Here we document, on the basis of an experiment with seed- lings of three types of subtropical wetland tree species, that mortality can be amplified and growth can even be stimulated, depending on event sequence. Our findings indicate that the impacts of multiple extreme events cannot be modeled by simply summing the projected effects of individual extreme events but, rather, that models should take into account event sequences.
Climatic extremes improve predictions of spatial patterns of tree species
Understanding niche evolution, dynamics, and the response of species to climate change requires knowledge of the determinants of the environmental niche and species range limits. Mean values of climatic variables are often used in such analyses. In contrast, the increasing frequency of climate extremes suggests the importance of understanding their additional influence on range limits. Here, we assess how measures representing climate extremes (i.e., interannual variability in climate parameters) explain and predict spatial patterns of 11 tree species in Switzerland. We find clear, although comparably small, improvement (20% in adjusted D2, 8% and 3% in cross-validated True Skill Statistic and area under the receiver operating characteristics curve values) in models that use measures of extremes in addition to means. The primary effect of including information on climate extremes is a correction of local overprediction and underprediction. Our results demonstrate that measures of climate extremes are important for understanding the climatic limits of tree species and assessing species niche characteristics. The inclusion of climate variability likely will improve models of species range limits under future conditions, where changes in mean climate and increased variability are expected.
Tree spatial patterns in fire-frequent forests of western North America, including mechanisms of pattern formation and implications for designing fuel reduction and restoration treatments
Restoring characteristic fire regimes and forest structures are central objectives of many restoration and fuel reduction projects. Within-stand spatial pattern is a fundamental attribute of forest structure and influences many ecological processes and ecosystem functions. In this review we synthesize the available spatial reference information for fire-frequent pine and mixed-conifer forests in western North America; interpret this information in the context of restoration and fuel reduction treatment design; and identify areas for future research, including recommended approaches for quantifying within-stand tree spatial patterns. We identified 50 studies of tree spatial patterns in fire-frequent pine and mixed conifer forests, 25 of which documented spatial reference conditions. The characteristic structure of fire-frequent forests is a mosaic of three elements: openings, single trees, and clumps of trees with adjacent or interlocking crowns. This mosaic structure typically manifests at scales <0.4 ha, but sometimes extends to scales as large as 4 ha, particularly on sites with fire regimes that include both low- and moderate-severity fires. We documented preferential use of global pattern analysis techniques (90% of analyses) relative to local analysis techniques (10% of analyses). Ripley’s K statistic, an example of global spatial pattern analysis, was the most frequently used analytic technique (38% of analyses). These findings are important because global pattern analysis does not explicitly quantify spatial heterogeneity within a pattern, the very thing spatial reference studies seek to characterize and one of the core structural attributes treatments aim to restore. Based on these findings, we encourage managers to consciously adopt a view of forest structure that accommodates spatial heterogeneity within forest stands, and to use this conceptualization of forest structure to guide prescription development. Restoration prescriptions and marking guidelines that explicitly incorporate within-stand spatial heterogeneity—such as by specifying the numbers and sizes of openings and tree clumps, and the number of widely-spaced single trees to retain per unit area—will improve the likelihood of restoring characteristic forest structures and the ecological processes such structures support. We infer that the near-exclusive use of global pattern analysis has limited the quan- tity and usability of spatial reference information available to managers, has also likely limited the development and testing of novel ecological hypotheses about pattern-generating mechanisms. Consequently, we recommend that forest scientists change how they quantify tree spatial patterns by complimenting the traditional global analysis methods with local pattern analysis techniques, which quantify spatial heterogeneity within a study area.
Are there basic physical constraints on future anthropogenic emissions of carbon dioxide?
Here, it is shown both theoretically and observationally how the evolution of the human system can be considered from a surprisingly simple thermodynamic perspective in which it is unnecessary to explicitly model two of the emissions drivers: population and standard of living. Specifically, the human system grows through a self-perpetuating feedback loop in which the consumption rate of primary energy resources stays tied to the historical accumulation of global economic production—or p × g—through a time-independent factor of 9.7 ± 0.3 mW per inflation-adjusted 1990 US dollar. This important constraint, and the fact that f and c have historically varied rather slowly, points towards substantially narrowed visions of future emissions scenarios for implementation in GCMs.
Stability and Diversity of Ecosystems
Understanding the relationship between diversity and stability requires a knowledge of how species interact with each other and how each is affected by the environment. The relationship is also complex, because the concept of stability is multifaceted; different types of stability describing different properties of ecosystems lead to multiple diversity-stability relationships. A growing number of empirical studies demonstrate positive diversity-stability relationships. These studies, however, have emphasized only a few types of stability, and they rarely uncover the mechanisms responsible for stability. Because anthropogenic changes often affect stability and diversity simultaneously, diversity-stability relationships cannot be understood outside the context of the environmental drivers affecting both. This shifts attention away from diversity-stability relationships toward the multiple factors, including diversity, that dictate the stability of ecosystems.
Projected climate-induced faunal change in the Western Hemisphere
Climate change is predicted to be one of the greatest drivers of ecological change in the coming century. Increases in temperature over the last century have clearly been linked to shifts in species distributions. Given the magnitude of projected future climatic changes, we can expect even larger range shifts in the coming century. These changes will, in turn, alter ecological communities and the functioning of ecosystems. Despite the seriousness of predicted climate change, the uncertainty in climate-change projections makes it difficult for conservation managers and planners to proactively respond to climate stresses. To address one aspect of this uncertainty, we identified predictions of faunal change for which a high level of consensus was exhibited by different climate models. Specifically, we assessed the potential effects of 30 coupled atmosphere–ocean general circulation model (AOGCM) future-climate simulations on the geographic ranges of 2954 species of birds, mammals, and amphibians in the Western Hemisphere. Eighty percent of the climate projections based on a relatively low greenhouse-gas emissions scenario result in the local loss of at least 10% of the vertebrate fauna over much of North and South America. The largest changes in fauna are predicted for the tundra, Central America, and the Andes Mountains where, assuming no dispersal constraints, specific areas are likely to experience over 90% turnover, so that faunal distributions in the future will bear little resemblance to those of today.
Early warning signals of extinction in deteriorating environments
During the decline to extinction, animal populations may present dynamical phenomena not exhibited by robust populations (1,2). Some of these phenomena, such as the scaling of demographic variance, are related to small size (3–6) whereas others result from density- dependent nonlinearities (7). Although understanding the causes of population extinction has been a central problem in theoretical biology for decades (8), the ability to anticipate extinction has remained elusive (9). Here we argue that the causes of a population’s decline are central to the predictability of its extinction. Specifically, environmental degradation may cause a tipping point in population dynamics, corresponding to a bifurcation in the underlying population growth equations, beyond which decline to extinction is almost certain. In such cases, imminent extinction will be signalled by critical slowing down (CSD) critical slowing down
Space observations of inland water bodies show rapid surface warming since 1985
Surface temperatures were extracted from nighttime thermal infrared imagery of 167 large inland water bodies distributed worldwide beginning in 1985 for the months July through September and January through March. Results indicate that the mean nighttime surface water temperature has been rapidly warming for the period 1985–2009 with an average rate of 0.045 ± 0.011°C yr−1 and rates as high as 0.10 ± 0.01°C yr−1. Worldwide the data show far greater warming in the mid‐ and high latitudes of the northern hemisphere than in low latitudes and the southern hemisphere.
Non-equilibrium succession dynamics indicate continued northern migration of lodgepole pine
This study provides evidence of range expansion under current climatic conditions of an indigenous species with strong ecosystem effects. Surveys of stands along the northern distribution limit of lodgepole pine (Pinus contorta var. latifolia) in central Yukon Territory, Canada showed consistent increases in pine dominance following fire. These patterns differed strongly from those observed at sites where pine has been present for several thousand years. Differences in species thinning rates are unlikely to account for the observed increases in pine dominance. Rates of pine regeneration at its range limits were equivalent to those of spruce, indicating a capacity for rapid local population expansion. The study also found no evidence of strong climatic limitation of pine population growth at the northern distribution limit. We interpret these data as evidence of current pine expansion at its range limits and conclude that the northern distribution of lodgepole pine is not in equilibrium with current climate. This study has implications for our ability to predict vegetation response to climate change when populations may lag in their response to climate.
Rapid shifts in plant distribution with recent climate change
A change in climate would be expected to shift plant distribution as species expand in newly favorable areas and decline in increas- ingly hostile locations. We compared surveys of plant cover that were made in 1977 and 2006–2007 along a 2,314-m elevation gradient in Southern California’s Santa Rosa Mountains. Southern California’s climate warmed at the surface, the precipitation vari- ability increased, and the amount of snow decreased during the 30-year period preceding the second survey. We found that the average elevation of the dominant plant species rose by 65 m between the surveys. This shift cannot be attributed to changes in air pollution or fire frequency and appears to be a consequence of changes in regional climate. plant migration range shift
Impact of terrestrial biosphere carbon exchanges on the anomalous CO2 increase in 2002–2003
Concluding paragraphs: In general, we find that the remarkable feature of the 2002– 2003 anomaly seems to be that climate fluctuations, not only related to El Nin ̃o and occurring across all latitudes, acted together to create an unusually strong outgasing of CO2 of the terrestrial biosphere. Further research will be required to investigate if this fluctuation carries features of projected future climate change and the CO2 growth rate anomaly has been a first indicator of a developing positive feedback between climate warming and the global carbon cycle.
Another reason for concern: regional and global impacts on ecosystems for different levels of climate change
Between 1C and 2C increases in global mean temperatures most species, ecosystems and landscapes will be impacted and adaptive capacity will become limited. With the already ongoing high rate of climate change, the decline in biodiversity will therefore accelerate and simultaneously many ecosystem services will become less abundant.
A long-term association between global temperature and biodiversity, origination and extinction in the fossil record
We analysed the fossil record for the last 520 Myr against estimates of low latitude sea surface temperature for the same period. We found that global biodiversity (the richness of families and genera) is related to temperature and has been relatively low during warm ‘greenhouse’ phases, while during the same phases extinction and origination rates of taxonomic lineages have been relatively high. These findings are consistent for terrestrial and marine environments and are robust to a number of alternative assumptions and potential biases. Our results provide the first clear evidence that global climate may explain substantial variation in the fossil record in a simple and consistent manner. Our findings may have implications for extinction and biodiversity change under future climate warming.
Keeping up with a warming world; assessing the rate of adaptation to climate change
The pivotal question in the debate on the ecological effects of climate change is whether species will be able to adapt fast enough to keep up with their changing environment. If we establish the maximal rate of adaptation, this will set an upper limit to the rate at which temperatures can increase without loss of biodiversity.The rate of adaptation will primarily be set by the rate of microevolution since (i) phenotypic plasticity alone is not sufficient as reaction norms will no longer be adaptive and hence microevolution on the reaction norm is needed, (ii) learning will be favourable to the individual but cannot be passed on to the next generations, (iii) maternal effects may play a role but, as with other forms of phenotypic plasticity, the response of offspring to the maternal cues will no longer be adaptive in a changing environment, and (iv) adaptation via immigration of individuals with genotypes adapted to warmer environments also involves microevolution as these genotypes are better adapted in terms of temperature, but not in terms of, for instance, photoperiod.Long-term studies on wild populations with individually known animals play an essential role in detecting and understanding the temporal trends in life-history traits, and to estimate the heritability of, and selection pressures on, life-history traits. However, additional measurements on other trophic levels and on the mechanisms underlying phenotypic plasticity are needed to predict the rate of microevolution, especially under changing conditions. Using this knowledge on heritability of, and selection on, life-history traits, in combination with climate scenarios, we will be able to predict the rate of adaptation for different climate scenarios. The final step is to use ecoevolutionary dynamical models to make the link to population viability and from there to biodiversity loss for those scenarios where the rate of adaptation is insufficient. Keywords: climate change; phenology; microevolution; phenotypic plasticity; intergovernmental panel on climate change; scenario
Quantifying the Extent of North American Mammal Extinction Relative to the Pre-Anthropogenic Baseline
Earth has experienced five major extinction events in the past 450 million years. Many scientists suggest we are now witnessing a sixth, driven by human impacts. However, it has been difficult to quantify the real extent of the current extinction episode, either for a given taxonomic group at the continental scale or for the worldwide biota, largely because comparisons of pre-anthropogenic and anthropogenic biodiversity baselines have been unavailable. Here, we compute those baselines for mammals of temperate North America, using a sampling-standardized rich fossil record to reconstruct species-area relationships for a series of time slices ranging from 30 million to 500 years ago. We show that shortly after humans first arrived in North America, mammalian diversity dropped to become at least 15%–42% too low compared to the ‘‘normal’’ diversity baseline that had existed for millions of years. While the Holocene reduction in North American mammal diversity has long been recognized qualitatively, our results provide a quantitative measure that clarifies how significant the diversity reduction actually was. If mass extinctions are defined as loss of at least 75% of species on a global scale, our data suggest that North American mammals had already progressed one-fifth to more than halfway (depending on biogeographic province) towards that benchmark, even before industrialized society began to affect them. Data currently are not available to make similar quantitative estimates for other continents, but qualitative declines in Holocene mammal diversity are also widely recognized in South America, Eurasia, and Australia. Extending our methodology to mammals in these areas, as well as to other taxa where possible, would provide a reasonable way to assess the magnitude of global extinction, the biodiversity impact of extinctions of currently threatened species, and the efficacy of conservation efforts into the future.
Changes in climate and land use have a larger direct impact than rising CO2 on global river runoff trends
The significant worldwide increase in observed river runoff has been tentatively attributed to the stomatal ‘‘antitranspirant’’ response of plants to rising atmospheric CO2 [Gedney N, Cox PM, Betts RA, Boucher O, Huntingford C, Stott PA (2006) Nature 439: 835– 838]. However, CO2 also is a plant fertilizer. When allowing for the increase in foliage area that results from increasing atmospheric CO2 levels in a global vegetation model, we find a decrease in global runoff from 1901 to 1999. This finding highlights the importance of vegetation structure feedback on the water balance of the land surface. Therefore, the elevated atmospheric CO2 concentration does not explain the estimated increase in global runoff over the last century. In contrast, we find that changes in mean climate, as well as its variability, do contribute to the global runoff increase. Using historic land-use data, we show that land-use change plays an additional important role in controlling regional runoff values, particularly in the tropics. Land-use change has been strongest in tropical regions, and its contribution is substantially larger than that of climate change. On average, land-use change has increased global runoff by 0.08 mm/year2 and accounts for 50% of the reconstructed global runoff trend over the last century. Therefore, we emphasize the importance of land-cover change in forecasting future freshwater availability and climate.
