Landscape Partnership Resources Library
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.
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
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.
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
Don't Blame the Beetles
Bark beetles have devastated western forests, but that may not mean more severe fires.
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.
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.
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.
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.
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.
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.
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.
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.
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
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
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.
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.
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
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.
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.
