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Climate Science PDFs

Climate Science PDFs Collection
Functional response of U.S. grasslands to the early 21st-century drought
Grasslands across the United States play a key role in regional livelihood and national food security. Yet, it is still unclear how this important resource will respond to the prolonged warm droughts and more intense rainfall events predicted with climate change. The early 21st-century drought in the southwestern United States resulted in hydroclimatic conditions that are similar to those expected with future climate change. We investigated the impact of the early 21st-century drought on aboveground net primary production (ANPP) of six desert and plains grasslands dominated by C4 (warm season) grasses in terms of significant deviations between observed and expected ANPP. In desert grasslands, drought-induced grass mortality led to shifts in the functional response to annual total precipitation (PT), and in some cases, new species assemblages occurred that included invasive species. In contrast, the ANPP in plains grasslands exhibited a strong linear function of the current-year PT and the previous-year ANPP, despite prolonged warm drought. We used these results to disentangle the impacts of interannual total precipitation, intra-annual precipitation patterns, and grassland abundance on ANPP, and thus generalize the functional response of C4 grasslands to predicted climate change. This will allow managers to plan for predictable shifts in resources associated with climate change related to fire risk, loss of forage, and ecosystem services. Key words: climate change; desert; extreme events; grassland production; invasive species; plains; precipitation variability; resilience; warm drought.
A dispersal-induced paradox: synchrony and stability in stochastic metapopulations
Understanding how dispersal influences the dynamics of spatially distributed populations is a major priority of both basic and applied ecologists. Two well-known effects of dispersal are spatial synchrony (positively correlated population dynamics at different points in space) and dispersal-induced stability (the phenomenon whereby populations have simpler or less extinction-prone dynamics when they are linked by dispersal than when they are isolated). Although both these effects of dispersal should occur simultaneously, they have primarily been studied separately. Herein, I summarise evidence from the literature that these effects are expected to interact, and I use a series of models to characterise that interaction. In particular, I explore the observation that although dispersal can promote both synchrony and stability singly, it is widely held that synchrony paradoxically prevents dispersal-induced stability. I show here that in many realistic scenarios, dispersal is expected to promote both synchrony and stability at once despite this apparent destabilising influence of synchrony. This work demonstrates that studying the spatial and temporal impacts of dispersal together will be vital for the conservation and management of the many communities for which human activities are altering natural dispersal rates. Keywords Autoregressive model, correlated environmental stochasticity, dispersal, dispersal-induced stability, metapopulation, negative binomial model, Ricker model, spatial heterogeneity, synchrony.
Changes in forest productivity across Alaska consistent with biome shift
Global vegetation models predict that boreal forests are particularly sensitive to a biome shift during the 21st century. This shift would manifest itself first at the biome's margins, with evergreen forest expanding into current tundra while being replaced by grasslands or temperate forest at the biome's southern edge. We evaluated changes in forest productivity since 1982 across boreal Alaska by linking satellite estimates of primary productivity and a large tree-ring data set. Trends in both records show consistent growth increases at the boreal–tundra ecotones that contrast with drought-induced productivity declines throughout interior Alaska. These patterns support the hypothesized effects of an initiating biome shift. Ultimately, tree dispersal rates, habitat availability and the rate of future climate change, and how it changes disturbance regimes, are expected to determine where the boreal biome will undergo a gradual geographic range shift, and where a more rapid decline.
The cost of policy simplification in conservation incentive programs
Incentive payments to private landowners provide a common strategy to conserve biodiversity and enhance the supply of goods and services from ecosystems. To deliver cost-effective improvements in biodiversity, payment schemes must trade-off inefficiencies that result from over-simplified policies with the administrative burden of implementing more complex incentive designs. We examine the effectiveness of different payment schemes using field parameterized, ecological economic models of extensive grazing farms. We focus on profit maximising farm management plans and use bird species as a policy-relevant indicator of biodiversity. Common policy simplifications result in a 49–100% loss in biodiversity benefits depending on the conservation target chosen. Failure to differentiate prices for conservation improvements in space is particularly problematic. Additional implementation costs that accompany more complicated policies are worth bearing even when these constitute a substantial proportion (70% or more) of the payments that would otherwise have been given to farmers. Keywords Agriculture, agri-environment scheme, biodiversity, cost-effectiveness, ecological economics, grazing, incentive
Economic growth as the limiting factor for wildlife conservation
The concept of limiting factor includes the lack of welfare factors and the presence of decimating factors. Originally applied to populations and species, the concept may also be applied to wildlife in the aggregate. Because the decimating factor of economic growth eliminates welfare factors for virtually all imperiled species via the principle of competitive exclusion, economic growth may be classified as the limiting factor for wildlife conservation. The wildlife profes- sion has been virtually silent about this limiting factor, suggesting that the pro- fession has been laboring in futility. The public, exhorted by neoclassical economists and political leaders, supports economic growth as a national goal. To address the limiting factor for wildlife conservation, wildlife professionals need to become versed in the history of economic growth theory, neoclassical economic growth theory, and the alternative growth paradigm provided by ecological economics. The Wildlife Society should lead the natural resources professions in developing a position on economic growth. carrying capacity, competitive exclusion, ecological economics, economic growth, limiting factor, neoclassical economics, niche breadth, steady state economy
Interactions and Linkages among Ecosystems during Landscape Evolution
We synthesize our findings of studies in Glacier Bay National Park and Preserve, southeastern Alaska, to elucidate interactions and linkages among terrestrial, lake, stream, and marine intertidal ecosystems as the landscape evolves following ice recession. Development in each ecosystem is initially dominated by physical processes. Over time, biotic control becomes increasingly important, although the extent of biotic control varies among ecosystems. The changes occurring in the four ecosystems are linked by landscape processes, with the nature and strength of these linkages changing through time. Change in one ecosystem has a major influence on the nature and direction of change in other ecosystems. Soil development and woody biomass accumulation on land provide an inertia that is unmatched in stream, lake, or intertidal systems. It is important that researchers and managers understand this science of change, at different spatial and temporal scales, in order to predict future states of ecological systems. The dynamics of change that we document at Glacier Bay during primary succession have important implications for managing the system with respect to anthropogenic change. Keywords: landscape, development, ecosystems, succession, linkages
Effects of tree mortality caused by a bark beetle outbreak on the ant community in the San Bernardino National Forest
Ants are used as bioindicators of the effects of disturbance on ecosystems for several reasons. First, ants are generally responsive to alteration of the biomass and diversity of the local plant community (Kalif et al., 2001) and other environmental variables (Underwood & Fisher, 2006). Second, because they occupy fixed nest locations, ants are affected by conditions on a very small scale, so that their presence and abundance are a better indicator of local conditions than are the presence or abundance of more mobile animals (Stephens & Wagner, 2006; Underwood & Fisher, 2006). Ants play important ecosystem roles and are therefore often a relevant choice for monitoring (Ho ̈lldobler & Wilson, 1990). They make up a significant percentage of the animal biomass in many ecosystems, they can be crucial to processes such as soil mixing and nutrient transport (Gentry & Stiritz, 1972), and they are important players in nutrient cycling and energy flow. Ants can also strongly influence the plant community via seed dispersal and granivory (Christian, 2001; Barrow et al., 2007). While the diversity of a given taxon is often not a reliable indicator of the diversity of other groups (Lawton et al., 1998; Bennett et al., 2009; Maleque et al., 2009; Wike et al., 2010), ant diversity is known to reflect the diversity of other invertebrates in ecosystems recovering from a disturbance in some cases (Andersen & Majer, 2004).The use of ants as bioindicators must be undertaken with caution (Underwood & Fisher, 2006). Different ant communities do not always respond to a disturbance in the same way (Arnan et al., 2009). In addition, broad measures of a bioindicator taxon, such as species richness or abundance, are potentially misleading. For instance, while it is popular to measure the species richness of bioindicator groups, the ant species richness of different habitats has been observed to respond differently to similar disturbances (Farji-Brener et al., 2002; Ratchford et al., 2005; Barrow et al., 2007), and ant species richness often does not respond at all unless disturbances are extreme (Andersen & Majer, 2004).Nonetheless, changes in the ant community can provide useful information about the responses of the ecosystem as a whole.
Impacts of climate change on the future of biodiversity
Many studies in recent years have investigated the effects of climate change on the future of biodiversity. In this review, we first examine the different possible effects of climate change that can operate at individual, population, species, community, ecosystem and biome scales, notably showing that species can respond to climate change challenges by shifting their climatic niche along three non-exclusive axes: time (e.g. phenology), space (e.g. range) and self (e.g. physiology). Then, we present the principal specificities and caveats of the most common approaches used to estimate future biodiversity at global and sub- continental scales and we synthesise their results. Finally, we highlight several challenges for future research both in theoretical and applied realms. Overall, our review shows that current estimates are very variable, depending on the method, taxonomic group, biodiversity loss metrics, spatial scales and time periods considered. Yet, the majority of models indicate alarming consequences for biodiversity, with the worst- case scenarios leading to extinction rates that would qualify as the sixth mass extinction in the history of the earth. Keywords Biodiversity, climate change, species extinctions.
Energetic and biomechanical constraints on animal migration distance
Animal migration is one of the great wonders of nature, but the factors that determine how far migrants travel remain poorly understood. We present a new quantitative model of animal migration and use it to describe the maximum migration distance of walking, swimming and flying migrants. The model combines biomechanics and metabolic scaling to show how maximum migration distance is constrained by body size for each mode of travel. The model also indicates that the number of body lengths travelled by walking and swimming migrants should be approximately invariant of body size. Data from over 200 species of migratory birds, mammals, fish, and invertebrates support the central conclusion of the model – that body size drives variation in maximum migration distance among species through its effects on metabolism and the cost of locomotion. The model provides a new tool to enhance general understanding of the ecology and evolution of migration.
Biodiversity effects on ecosystem functioning change along environmental stress gradients
Positive relationship between biodiversity and ecosystem functioning has been observed in many studies, but how this relationship is affected by environmental stress is largely unknown. To explore this influence, we measured the biomass of microalgae grown in microcosms along two stress gradients, heat and salinity, and compared our results with 13 published case studies that measured biodiversity–ecosystem functioning relationships under varying environmental conditions. We found that positive effects of biodiversity on ecosystem functioning decreased with increasing stress intensity in absolute terms. However, in relative terms, increasing stress had a stronger negative effect on low-diversity communities. This shows that more diverse biotic communities are functionally less susceptible to environmental stress, emphasises the need to maintain high levels of biodiversity as an insurance against impacts of changing environmental conditions and sets the stage for exploring the mechanisms underlying biodiversity effects in stressed ecosystems.
Maximizing return on conservation investment in the conterminous USA
Efficient conservation planning requires knowledge about conservation targets, threats to those targets, costs of conservation and the marginal return to additional conservation efforts. Systematic conservation planning typically only takes a small piece of this complex puzzle into account. Here, we use a return-on- investment (ROI) approach to prioritise lands for conservation at the county level in the conterminous USA. Our approach accounts for species richness, county area, the proportion of species’ ranges already protected, the threat of land conversion and land costs. Areas selected by a complementarity-based greedy heuristic using our full ROI approach provided greater averted species losses per dollar spent compared with areas selected by heuristics accounting for richness alone or richness and cost, and avoided acquiring lands not threatened with conversion. In contrast to traditional prioritisation approaches, our results high- light conservation bargains, opportunities to avert the threat of development and places where conservation efforts are currently lacking. Keywords Benefit cost ratio, conservation planning, economic cost, habitat protection, heuristic, land prices, reserve selection, resource allocation.
Genetic diversity in widespread species is not congruent with species richness in alpine plant communities
The Convention on Biological Diversity (CBD) aims at the conservation of all three levels of biodiversity, that is, ecosystems, species and genes. Genetic diversity represents evolutionary potential and is important for ecosystem functioning. Unfortunately, genetic diversity in natural populations is hardly considered in conservation strategies because it is difficult to measure and has been hypothesised to co-vary with species richness. This means that species richness is taken as a surrogate of genetic diversity in conservation plan- ning, though their relationship has not been properly evaluated. We tested whether the genetic and species levels of biodiversity co-vary, using a large-scale and multi-species approach. We chose the high-mountain flora of the Alps and the Carpathians as study systems and demonstrate that species richness and genetic diversity are not correlated. Species richness thus cannot act as a surrogate for genetic diversity. Our results have important consequences for implementing the CBD when designing conservation strategies. Keywords alpine vascular plants, Alps, biodiversity conservation, Carpathians, genetic diversity, species richness.
How does climate change influence demographic processes of widespread species? Lessons from the comparative analysis of contrasted populations of roe deer
How populations respond to climate change depends on the interplay between life history, resource avail- ability, and the intensity of the change. Roe deer are income breeders, with high levels of allocation to reproduction, and are hence strongly constrained by the availability of high quality resources during spring. We investigated how recent climate change has influenced demographic processes in two populations of this widespread species. Spring began increasingly earlier over the study, allowing us to identify 2 periods with contrasting onset of spring. Both populations grew more slowly when spring was early. As expected for a long-lived and iteroparous species, adult survival had the greatest potential impact on population growth. Using perturbation analyses, we measured the relative contribution of the demographic parameters to observed variation in population growth, both within and between periods and populations. Within peri- ods, the identity of the critical parameter depended on the variance in growth rate, but variation in recruit- ment was the main driver of observed demographic change between periods of contrasting spring earliness. Our results indicate that roe deer in forest habitats cannot currently cope with increasingly early springs. We hypothesise that they should shift their distribution to richer, more heterogeneous landscapes to offset energetic requirements during the critical rearing stage. Keywords Age-structured populations, demographic change, income breeding, perturbation analysis, population growth, Recruitment, Stochastic environment, Survival.
Global shifts towards positive species interactions with increasing environmental stress
The study of positive species interactions is a rapidly evolving field in ecology. Despite decades of research, controversy has emerged as to whether positive and negative interactions predictably shift with increasing environmental stress as hypothesised by the stress-gradient hypothesis (SGH). Here, we provide a synthesis of 727 tests of the SGH in plant communities across the globe to examine its generality across a variety of ecological factors. Our results show that plant interactions change with stress through an outright shift to facilitation (survival) or a reduction in competition (growth and reproduction). In a limited number of cases, plant interactions do not respond to stress, but they never shift towards competition with stress. These findings are consistent across stress types, plant growth forms, life histories, origins (invasive vs. native), climates, ecosystems and methodologies, though the magnitude of the shifts towards facilitation with stress is dependent on these factors. We suggest that future studies should employ standardised defini- tions and protocols to test the SGH, take a multi-factorial approach that considers variables such as plant traits in addition to stress, and apply the SGH to better understand how species and communities will respond to environmental change. Keywords Biotic interactions, community ecology, ecosystems and climates, environmental stress, facilitation, invasive species, meta-analysis, plant traits, the stress-gradient hypothesis.
Persistent reduced ecosystem respiration after insect disturbance in high elevation forests
Amid a worldwide increase in tree mortality, mountain pine beetles (Dendroctonus ponderosae Hopkins) have led to the death of billions of trees from Mexico to Alaska since 2000. This is predicted to have important carbon, water and energy balance feedbacks on the Earth system. Counter to current projections, we show that on a decadal scale, tree mortality causes no increase in ecosystem respiration from scales of several square metres up to an 84 km2 valley. Rather, we found comparable declines in both gross primary productivity and respiration suggesting little change in net flux, with a transitory recovery of respiration 6–7 years after mortality associated with increased incorporation of leaf litter C into soil organic matter, followed by further decline in years 8–10. The mechanism of the impact of tree mortality caused by these biotic disturbances is consistent with reduced input rather than increased output of carbon. Keywords Carbon balance, disturbance, ecosystem respiration, gross primary productivity, insect outbreak, lodgepole pine, mountain pine beetle, mountain West, subalpine forest.
Alleles underlying larval foraging behaviour influence adult dispersal in nature
The dispersal and migration of organisms have resulted in the colonisation of nearly every possible habitat and ultimately the extraordinary diversity of life. Animal dispersal tendencies are commonly heterogeneous (e.g. long vs. short) and non-random suggesting that phenotypic and genotypic variability between individuals can contribute to population-level heterogeneity in dis- persal. Using laboratory and field experiments, we demonstrate that natural allelic variation in a gene underlying a foraging polymorphism in larval fruit flies (for), also influences their dispersal tendencies as adults. Rover flies (forR; higher foraging activity) have consistently greater dispersal tendencies and are more likely to disperse longer distances than sitter flies (fors; lower foraging activity). Increasing for expression in the brain and nervous system increases dispersal in sitter flies. Our study supports the notion that variation in dispersal can be driven by intrinsic variation in food-dependent search behaviours and confirms that single gene pleiotropic effects can contrib- ute to population-level heterogeneity in dispersal.
Rapid growth in CO2 emissions after the 2008–2009 global financial crisis.pdf
1st paragraph: Global carbon dioxide emissions from fossil-fuel combustion and cement production grew 5.9% in 2010, surpassed 9 Pg of carbon (Pg C) for the first time, and more than offset the 1.4% decrease in 2009. The impact of the 2008–2009 global financial crisis (GFC) on emissions has been short-lived owing to strong emissions growth in emerging economies, a return to emissions growth in developed economies, and an increase in the fossil-fuel intensity of the world economy.
Citizen Involvement in the U.S. Endangered Species Act
Data on listed species refute critiques of citizen involvement in the U.S. Endangered Species Act.
Elevated Eocene Atmospheric CO2 and Its Subsequent Decline
Closing paragraph: Estimates of early Eocene atmospheric CO2 from Green River sodium carbonates are in the same range as those predicted by geochemical models (7). By È20 Ma, all available data (8) suggest ECO2^atm was at or near modern concentrations.
The False Spring of 2012, Earliest in North American Record
2nd paragraph: As global climate warms, increasingly warmer springs may combine with the random climatological occurrence of advective freezes, which result from cold air moving from one region to another, to dramatically increase the future risk of false springs, with profound ecological and economic consequences [e.g., Gu et al., 2008; Marino et al., 2011; Augspurger, 2013]. For example, in the false spring of 2012, an event embedded in long-term trends toward earlier spring [e.g., Schwartz et al., 2006], the frost damage to fruit trees totaled half a billion dollars in Michigan alone, prompting the federal government to declare the state a disaster area [Knudson, 2012].