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At least 271 records · Page 15Linked to original sources

Landscape change, fire and erosion

New Mexico has a dynamic landscape, which will become even more so in response to climate change over the next 50 years, in part because of increasing incidence of wildfire. As the climate changes to warmer conditions, less rainfall will infiltrate into aquifers, leading to increased overland runoff. Landform processes can be complex, but in general, the predicted changes in climate and precipitation will lead to increased flooding, increased upland erosion caused by runoff, and increased downstream sediment deposition. Canyons and mesas, small basins or valleys filled with sediment will be particularly affected. Rapid rearrangement of sediments by water is disruptive and potentially hazardous to ecosystems and societies. Dramatic examples of accelerated erosion following the Whitewater-Baldy, Las Conchas and other wildfires here in New Mexico illustrate the types of hazards created when forested landscapes are severely burned. Post-wildfire erosion is typically initiated by intense rainfall events. Given that both the number of wildfires, and rainfall intensities are likely to increase as the climate warms, New Mexico can expect to see increases in widespread erosion and sedimentation across and downstream from upland forested areas in the state. The large volume of sediment predicted to be on the move will be of concern for many reasons including filling reservoirs, choking channels, blocking or destroying infrastructure and positive feedback loops that lead to further reductions in slope stability.

New Mexico↗

A global assessment of environmental and climate influences on wetland macroinvertebrate community structure and function

Estimating organisms' responses to environmental variables and taxon associations across broad spatial scales is vital for predicting their responses to climate change. Macroinvertebrates play a major role in wetland processes, but studies simultaneously exploring both community structure and community trait responses to environmental gradients are still lacking. We compiled a global dataset (six continents) from 756 depressional wetlands, including the occurrence of 96 macroinvertebrate families, their phylogenetic tree, and 19 biological traits. Using Bayesian hierarchical joint species distribution models (JSDMs), we estimated macroinvertebrate associations and compared the influences of local and climatic predictors on both individual macroinvertebrate families and their traits. While macroinvertebrate families were mainly related to broad-scale factors (maximum temperature and precipitation seasonality), macroinvertebrate traits were strongly related to local wetland hydroperiod. Interestingly, macroinvertebrate families and traits both showed positive and negative associations to the same environmental variables. As expected, many macroinvertebrate family occurrences were positively associated with temperature, but a few showed the opposite pattern and were found in cooler or montane regions. We also found that wetland macroinvertebrate communities would likely be affected by changing climates through alterations in traits related to precipitation seasonality, temperature seasonality, and wetland area. Temperature increases may negatively affect collector and shredder functional groups. A decrease in precipitation could lead to reductions in wetland area benefiting drought-tolerant macroinvertebrates, but it may negatively affect macroinvertebrates lacking those adaptations. Wetland processes may be compromised through broad-scale environmental changes altering macroinvertebrate family distributions and local hydroperiod shifts altering organism traits. Our complementary family-based and trait-based approaches elucidate the complex effects that climate change may produce on wetland ecosystems.

Global Change Biology↗

Global synthesis of the documented and projected effects of climate change on inland fishes

Although climate change is an important factor affecting inland fishes globally, a comprehensive review of how climate change has impacted and will continue to impact inland fishes worldwide does not currently exist. We conducted an extensive, systematic primary literature review to identify English-language, peer-reviewed journal publications with projected and documented examples of climate change impacts on inland fishes globally. Since the mid-1980s, scientists have projected the effects of climate change on inland fishes, and more recently, documentation of climate change impacts on inland fishes has increased. Of the thousands of title and abstracts reviewed, we selected 624 publications for a full text review: 63 of these publications documented an effect of climate change on inland fishes, while 116 publications projected inland fishes’ response to future climate change. Documented and projected impacts of climate change varied, but several trends emerged including differences between documented and projected impacts of climate change on salmonid abundance ( P = 0.0002). Salmonid abundance decreased in 89.5% of documented effects compared to 35.7% of projected effects, where variable effects were more commonly reported (64.3%). Studies focused on responses of salmonids (61% of total) to climate change in North America and Europe, highlighting major gaps in the literature for taxonomic groups and geographic focus. Elucidating global patterns and identifying knowledge gaps of climate change effects on inland fishes will help managers better anticipate local changes in fish populations and assemblages, resulting in better development of management plans, particularly in systems with little information on climate change effects on fish.

Reviews in Fish Biology and Fisheries↗

Dry forest decline is driven by both declining recruitment and increasing mortality in response to warm, dry conditions

Aim: Anticipating when and where changes in species' demographic rates will lead to range shifts in response to changing climate remains a major challenge. Despite evidence of increasing mortality in dry forests across the globe in response to drought and warming temperatures, the overall impacts on the distribution of dry forests are largely unknown because we lack comparable large-scale data on tree recruitment rates. Here, our aim was to develop range-wide population models for dry forest tree species (pinyon pine and juniper), quantifying both mortality and recruitment, to better understand where and under what conditions species range contractions are occurring. Location: Western United States. Major taxa studied: Two pinyon pine ( Pinus spp . ) and three juniper ( Juniperus spp . ) species. Methods: We developed range-wide demographic models for five species using forest inventory data from across the western United States and estimated population trends and climate vulnerability. Results: We find that four of the five species are declining in parts of their range, with Pinus edulis having the largest proportion of populations declining (24%). Population vulnerability increases with aridity and temperature, with up to ~50% of populations declining in the warmest and driest conditions. Mortality and recruitment were both essential to explaining where populations are declining. Main conclusions: Our results suggest that dry forest species are undergoing an active range shift driven by both changing recruitment and mortality, and that increasing temperatures and drought threaten the long-term viability of many of these species in their current range. While four of the five species examined were experiencing some declines, P. edulis is currently most vulnerable. Management actions such as reducing tree density may be able to mitigate some of these impacts. The framework we present to estimate range-wide demographic rates can be applied to other species to determine where range contractions are most likely.

Colorado, Idaho, Kansas, Montana, Nebraska, New Me↗

Collapsing avian community on a Hawaiian island

The viability of many species has been jeopardized by numerous negative factors over the centuries, but climate change is predicted to accelerate and increase the pressure of many of these threats, leading to extinctions. The Hawaiian honeycreepers, famous for their spectacular adaptive radiation, are predicted to experience negative responses to climate change, given their susceptibility to introduced disease, the strong linkage of disease distribution to climatic conditions, and their current distribution. We document the rapid collapse of the native avifauna on the island of Kaua‘i that corresponds to changes in climate and disease prevalence. Although multiple factors may be pressuring the community, we suggest that a tipping point has been crossed in which temperatures in forest habitats at high elevations have reached a threshold that facilitates the development of avian malaria and its vector throughout these species’ ranges. Continued incursion of invasive weeds and non-native avian competitors may be facilitated by climate change and could also contribute to declines. If current rates of decline continue, we predict multiple extinctions in the coming decades. Kaua‘i represents an early warning for the forest bird communities on the Maui and Hawai‘i islands, as well as other species around the world that are trapped within a climatic space that is rapidly disappearing.

Science Advances↗

A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests

Greenhouse gas emissions have significantly altered global climate, and will continue to do so in the future. Increases in the frequency, duration, and/or severity of drought and heat stress associated with climate change could fundamentally alter the composition, structure, and biogeography of forests in many regions. Of particular concern are potential increases in tree mortality associated with climate-induced physiological stress and interactions with other climate-mediated processes such as insect outbreaks and wildfire. Despite this risk, existing projections of tree mortality are based on models that lack functionally realistic mortality mechanisms, and there has been no attempt to track observations of climate-driven tree mortality globally. Here we present the first global assessment of recent tree mortality attributed to drought and heat stress. Although episodic mortality occurs in the absence of climate change, studies compiled here suggest that at least some of the world's forested ecosystems already may be responding to climate change and raise concern that forests may become increasingly vulnerable to higher background tree mortality rates and die-off in response to future warming and drought, even in environments that are not normally considered water-limited. This further suggests risks to ecosystem services, including the loss of sequestered forest carbon and associated atmospheric feedbacks. Our review also identifies key information gaps and scientific uncertainties that currently hinder our ability to predict tree mortality in response to climate change and emphasizes the need for a globally coordinated observation system. Overall, our review reveals the potential for amplified tree mortality due to drought and heat in forests worldwide.

Forest Ecology and Management↗

The physiology of mangrove trees with changing climate

Mangrove forests grow on saline, periodically flooded soils of the tropical and subtropical coasts. The tree species that comprise the mangrove are halophytes that have suites of traits that confer differing levels of tolerance of salinity, aridity, inundation and extremes of temperature. Here we review how climate change and elevated levels of atmospheric CO2 will influence mangrove forests. Tolerance of salinity and inundation in mangroves is associated with the efficient use of water for photosynthetic carbon gain which unpins anticipated gains in productivity with increasing levels of CO2. We review evidence of increases in productivity with increasing CO2, finding that enhancements in growth appear to be similar to trees in non-mangrove habitats and that gains in productivity with elevated CO2 are likely due to changes in biomass allocation. High levels of trait plasticity are observed in some mangrove species, which potentially facilitates their responses to climate change. Trait plasticity is associated with broad tolerance of salinity, aridity, low temperatures and nutrient availability. Because low temperatures and aridity place strong limits on mangrove growth at the edge of their current distribution, increasing temperatures over time and changing rainfall patterns are likely to have an important influence on the distribution of mangroves. We provide a global analysis based on plant traits and IPCC scenarios of changing temperature and aridity that indicates substantial global potential for mangrove expansion.

Book chapter↗

Divergent climate impacts on C3 versus C4 grasses imply widespread 21st century shifts in grassland functional composition

Aim Grasslands cover a third of Earth's landmass and provide critical ecosystem services. Anticipating how perennial C 3 (cool-season) and C 4 (warm-season) grasses respond to climate change will be key to predicting future composition and functioning of grasslands. Here, we evaluate environmental drivers of C 3 and C 4 perennial distributions and assess how C 3 and C 4 grass distributions shift in response to future climate change. Location Western United States. Methods We developed integrated species distribution models to identify climate and soil drivers of relative abundance of C 3 and C 4 perennial grasses. We then created projections of species abundances under future climate and evaluated when and where projected shifts in relative abundance were robust across climate models. Results Historically, C 3 grasses occupied areas with lower temperature and more variable precipitation regimes, while C 4 grasses occupied areas of higher temperature, greater temperature variability and greater warm-season precipitation. C 4 species also occupied narrower soil texture niches. In response to future climate change, C 3 grass abundance declined across 74% of areas, while C 4 abundance increased across 66% of areas. C 3 grasses expanded in mid- to higher-latitude areas with increasing temperature and decreasing seasonality of precipitation. In contrast, C 4 grasses increased in higher-latitude regions, but declined in lower-latitude, dryer regions. Results were surprisingly robust across climate scenarios, suggesting high confidence in the direction of these future changes. Main Conclusions Findings imply C 3 and C 4 perennial grasses will have highly divergent responses to climate change that may result in grassland functional compositional changes. Increasing temperatures and precipitation variability may favour some C 4 grasses, but C 4 habitat expansion may be constrained by soil conditions in western USA. Results provide actionable insights for anticipating the impacts of climate change on grass-dominated and co-dominated ecosystems and improving large-scale conservation and restoration efforts.

Diversity and Distributions↗

Areas contributing recharge to production wells and effects of climate change on the groundwater system in the Chipuxet River and Chickasheen Brook Basins, Rhode Island

The Chipuxet River and Chickasheen Brook Basins in southern Rhode Island are an important water resource for public and domestic supply, irrigation, recreation, and aquatic habitat. The U.S. Geological Survey, in cooperation with the Rhode Island Department of Health, began a study in 2012 as part of an effort to protect the source of water to six large-capacity production wells that supply drinking water and to increase understanding of how climate change might affect the water resources in the basins. Soil-water-balance and groundwater-flow models were developed to delineate the areas contributing recharge to the wells and to quantify the hydrologic response to climate change. Surficial deposits of glacial origin ranging from a few feet to more than 200 feet thick overlie bedrock in the 24.4-square mile study area. These deposits comprise a complex and productive aquifer system. Simulated areas contributing recharge to the production wells covered a total area of 0.63 square miles for average well withdrawal rates from 2007 through 2011 (total rate of 583 gallons per minute). Simulated areas contributing recharge for the maximum well pumping capacities (total rate of 3,700 gallons per minute) covered a total area of 2.55 square miles. Most simulated areas contributing recharge extend upgradient of the wells to morainal and upland till deposits and to groundwater divides. Some simulated areas contributing recharge include small, isolated areas remote from the wells. Relatively short groundwater traveltimes from recharging locations to discharging wells indicated that the wells are vulnerable to contamination from land-surface activities; median traveltimes ranged from 3.5 to 8.6 years for the production wells examined, and 57 to 91 percent of the traveltimes were 10 years or less. Land cover in the areas contributing recharge includes a substantial amount of urban and agriculture land use for five wells adjacent to the Chipuxet River; for one well adjacent to a tributary stream, land use is less developed. The calibrated groundwater-flow model provided a single, best representation of the areas contributing recharge to a production well. The parameter variance-covariance matrix from model calibration was used to create parameter sets that reflect the uncertainty of the parameter estimates and the correlation among parameters to evaluate the uncertainty associated with the predicted contributing areas to the wells. A Monte Carlo analysis led to contributing areas expressed as a probability distribution that differed from a single deterministic contributing area. Because of the effects of parameter uncertainty, the size of the probabilistic contributing areas for both average and maximum pumping rates was larger than the size of the deterministic contributing areas for the wells. Thus, some areas not in the deterministic contributing area might actually be in the contributing area, including additional areas of urban and agricultural land use that has the potential to contaminate groundwater. Additional areas that might be in the contributing area included recharge originating near the pumping wells that have relatively short groundwater-flow paths and traveltimes. At the maximum pumping rates, areas associated with low probabilities extended long distances along groundwater divides in the uplands remote from the wells. Climate projections for the Chipuxet River and Chickasheen Brook Basins from downscaled output from general circulation models indicate that mean annual temperature might increase by 4.7 degrees Fahrenheit and 8.0 degrees Fahrenheit by the late 21st century (2070–99) compared with the late 20th century (1970–99) under scenarios of lower and higher emissions of greenhouse gases, respectively. By the late 21st century, winter and spring precipitation is projected to increase by 12 to 17 percent, summer precipitation to increase by about the same as mean annual precipitation (8 percent), and fall precipitation to decrease by 5 percent for both emission scenarios compared with the late 20th century. Soil-water-balance simulations indicate that, although precipitation is expected to increase in three seasons, only in winter do precipitation increases exceed actual evapotranspiration increases. Recharge is projected to decrease in fall and generally change little in spring and summer. By the late 21st century, winter recharge is expected to increase by 13 percent for the lower emissions scenario and by 15 percent for the higher emissions scenario. In fall, recharge is projected to diminish by 13 percent for the lower emissions scenario and by 24 percent for the higher emissions scenario. Although recharge is projected to change seasonally in the 21st century, mean annual recharge changes minimally. Soil moisture is projected to decrease in the 21st century from spring through fall because of increases in potential evapotranspiration, and in fall because of decreases in precipitation in addition to increases in potential evapotranspiration. By the late 21st century, soil moisture for the lower emissions scenario is expected to decrease by 11 percent in summer and 15 percent in fall, and for the higher emissions scenario, decrease by 23 percent for both seasons. These decreases in soil moisture during the growing season might have implications for agriculture in the study area. Predicted changes in the magnitude and seasonal distribution of recharge in the 21st century increase simulated base flows and groundwater levels in the winter months for both emission scenarios, but because of less recharge in the fall and less or about the same recharge in the preceding months of spring and summer, base flows and groundwater levels in the fall months decrease for both emission scenarios. October has the largest base flow and groundwater level decreases. By the late 21st century, base flows at the Chipuxet River in October are projected to decrease by 9 percent for the lower emissions scenario and 18 percent for the higher emissions scenario. For a headwater stream in the upland till with shorter groundwater-flow paths and lower storage properties in its drainage area, base flows in October are projected to diminish by 28 percent and 42 percent for the lower and higher emissions scenarios by the late 21st century. Groundwater level changes in the uplands show substantial decreases in fall, but because of the large storage capacity of stratified deposits, water levels change minimally in the valley. By the late 21st century, water levels in large areas of upland till deposits in October are projected to decrease by up to 2 feet for the lower emissions scenario, whereas large areas decrease by up to 5 feet, with small areas with decreases of as much as 10 feet, for the higher emissions scenario. For both emission scenarios, additional areas of till go dry in fall compared with the late 20th century. Thus projected changes in recharge in the 21st century might extend low flows and low water levels for the year later in fall and there might be more intermittent headwater streams compared with the late 20th century with corresponding implications to aquatic habitat. Finally, the size and location of the simulated areas contributing recharge to the production wells are minimally affected by climate change because mean annual recharge, which is used to determine the contributing areas to the production wells, is projected to change little in the 21st century.

Rhode Island↗

Targeting climate diversity in conservation planning to build resilience to climate change

Climate change is raising challenging concerns for systematic conservation planning. Are methods based on the current spatial patterns of biodiversity effective given long-term climate change? Some conservation scientists argue that planning should focus on protecting the abiotic diversity in the landscape, which drives patterns of biological diversity, rather than focusing on the distribution of focal species, which shift in response to climate change. Climate is one important abiotic driver of biodiversity patterns, as different climates host different biological communities and genetic pools. We propose conservation networks that capture the full range of climatic diversity in a region will improve the resilience of biotic communities to climate change compared to networks that do not. In this study we used historical and future hydro-climate projections from the high resolution Basin Characterization Model to explore the utility of directly targeting climatic diversity in planning. Using the spatial planning tool, Marxan, we designed conservation networks to capture the diversity of climate types, at the regional and sub-regional scale, and compared them to networks we designed to capture the diversity of vegetation types. By focusing on the Conservation Lands Network (CLN) of the San Francisco Bay Area as a real-world case study, we compared the potential resilience of networks by examining two factors: the range of climate space captured, and climatic stability to 18 future climates, reflecting different emission scenarios and global climate models. We found that the climate-based network planned at the sub-regional scale captured a greater range of climate space and showed higher climatic stability than the vegetation and regional based-networks. At the same time, differences among network scenarios are small relative to the variance in climate stability across global climate models. Across different projected futures, topographically heterogeneous areas consistently show greater climate stability than homogenous areas. The analysis suggests that utilizing high-resolution climate and hydrological data in conservation planning improves the likely resilience of biodiversity to climate change. We used these analyses to suggest new conservation priorities for the San Francisco Bay Area.

Ecosphere↗

Projecting species’ vulnerability to climate change: Which uncertainty sources matter most and extrapolate best?

Species distribution models (SDMs) are commonly used to assess potential climate change impacts on biodiversity, but several critical methodological decisions are often made arbitrarily. We compare variability arising from these decisions to the uncertainty in future climate change itself. We also test whether certain choices offer improved skill for extrapolating to a changed climate and whether internal cross-validation skill indicates extrapolative skill. We compared projected vulnerability for 29 wetland-dependent bird species breeding in the climatically dynamic Prairie Pothole Region, USA. For each species we built 1,080 SDMs to represent a unique combination of: future climate, class of climate covariates, collinearity level, and thresholding procedure. We examined the variation in projected vulnerability attributed to each uncertainty source. To assess extrapolation skill under a changed climate, we compared model predictions with observations from historic drought years. Uncertainty in projected vulnerability was substantial, and the largest source was that of future climate change. Large uncertainty was also attributed to climate covariate class with hydrological covariates projecting half the range loss of bioclimatic covariates or other summaries of temperature and precipitation. We found that choices based on performance in cross-validation improved skill in extrapolation. Qualitative rankings were also highly uncertain. Given uncertainty in projected vulnerability and resulting uncertainty in rankings used for conservation prioritization, a number of considerations appear critical for using bioclimatic SDMs to inform climate change mitigation strategies. Our results emphasize explicitly selecting climate summaries that most closely represent processes likely to underlie ecological response to climate change. For example, hydrological covariates projected substantially reduced vulnerability, highlighting the importance of considering whether water availability may be a more proximal driver than precipitation. However, because cross-validation results were correlated with extrapolation results, the use of cross-validation performance metrics to guide modeling choices where knowledge is limited was supported.

Prairie Pothole Region↗

Framework for using downscaled climate model projections in ecological experiments to quantify plant and soil responses

Soil and plant responses to climate change can be quantified in controlled settings. However, the complexity of climate projections often leads researchers to evaluate ecosystem response based on general trends, rather than specific climate model outputs. Climate projections capture spatial and temporal climate extremes and variability that are lost when using mean climate trends. In addition, application of climate projections in experimental settings remains limited. Our objective was to develop a framework to incorporate statistically downscaled climate model projections into the design of temperature and precipitation treatments for ecological experiments. To demonstrate the utility of experimental treatments derived from climate projections, we used wetlands in the Great Plains as a model ecosystem for evaluating plant and soil responses. Spatial and temporal projections were selected to capture variability and intensity of projected future conditions for exemplary purposes. To illustrate climate projection application for ecological experiments, we developed temperature and precipitation treatments based on moderate-emissions scenario climate outputs (i.e., RCP4.5–650 ppm CO 2 equivalent). Our temperature treatments captured weekly trends that represented cool, average, and warm temperature predictions, and our daily precipitation treatments mimicked various seasonal precipitation trends and extreme events projected for the late 21st century. Treatments were applied to two short-term controlled experiments evaluating (1) plant germination (temperature treatment applied in growth chamber) and (2) soil nitrogen cycling (precipitation treatment applied in greenhouse) responses to projected future conditions in the Great Plains. Our approach provides flexibility for selecting appropriate and precise climate model outputs to design experimental treatments. Using these techniques, ecologists can better incorporate variation in climate model projections for experimentally evaluating ecosystem responses to future climate conditions, reduce uncertainty in predictive ecological models, and apply predicted outcomes when making management and policy decisions.

Nebraska, Texas↗

Ecology of urban climates: The need for landscape biophysics in cities

In this chapter we will review and evaluate the climatic and ecological parallels between urbanization and climate change, with an emphasis on temperature and its effects on terrestrial ectotherms, a group of organisms thought to be particularly sensitive to climate change. We will summarize patterns of urban warming and how they relate to global climate change projections, then discuss the potential strengths and limitations of urban climates as a source of insight into biotic responses to climate change and highlight future research directions. Future work will benefit from explicit consideration of the mechanisms by which urbanization and urban warming drive ectotherms’ body temperatures and activity periods. Urban ecosystems may provide a valuable first approximation of the dramatic effects of warming on certain terrestrial systems, and continued advances in urban thermal biology will promote a mechanistic understanding of how organisms use, respond to, and adapt to the unique thermal landscapes of cities.

Book chapter↗

Biological communities in San Francisco Bay track large‐scale climate forcing over the North Pacific

Long‐term observations show that fish and plankton populations in the ocean fluctuate in synchrony with large‐scale climate patterns, but similar evidence is lacking for estuaries because of shorter observational records. Marine fish and invertebrates have been sampled in San Francisco Bay since 1980 and exhibit large, unexplained population changes including record‐high abundances of common species after 1999. Our analysis shows that populations of demersal fish, crabs and shrimp covary with the Pacific Decadal Oscillation (PDO) and North Pacific Gyre Oscillation (NPGO), both of which reversed signs in 1999. A time series model forced by the atmospheric driver of NPGO accounts for two‐thirds of the variability in the first principal component of species abundances, and generalized linear models forced by PDO and NPGO account for most of the annual variability of individual species. We infer that synchronous shifts in climate patterns and community variability in San Francisco Bay are related to changes in oceanic wind forcing that modify coastal currents, upwelling intensity, surface temperature, and their influence on recruitment of marine species that utilize estuaries as nursery habitat. Ecological forecasts of estuarine responses to climate change must therefore consider how altered patterns of atmospheric forcing across ocean basins influence coastal oceanography as well as watershed hydrology.

California↗

Simulating 2,368 temperate lakes reveals weak coherence in stratification phenology

Changes in water temperatures resulting from climate warming can alter the structure and function of aquatic ecosystems. Lake-specific physical characteristics may play a role in mediating individual lake responses to climate. Past mechanistic studies of lake-climate interactions have simulated generic lake classes at large spatial scales or performed detailed analyses of small numbers of real lakes. Understanding the diversity of lake responses to climate change across landscapes requires a hybrid approach that couples site-specific lake characteristics with broad-scale environmental drivers. This study provides a substantial advancement in lake ecosystem modeling by combining open-source tools with freely available continental-scale data to mechanistically model daily temperatures for 2,368 Wisconsin lakes over three decades (1979-2011). The model accurately predicted observed surface layer temperatures (RMSE: 1.74°C) and the presence/absence of stratification (81.1% agreement). Among-lake coherence was strong for surface temperatures and weak for the timing of stratification, suggesting individual lake characteristics mediate some - but not all - ecologically relevant lake responses to climate.

Ecological Modelling↗

Microbiome assembly in thawing permafrost and its feedbacks to climate

The physical and chemical changes that accompany permafrost thaw directly influence the microbial communities that mediate the decomposition of formerly frozen organic matter, leading to uncertainty in permafrost–climate feedbacks. Although changes to microbial metabolism and community structure are documented following thaw, the generality of post-thaw assembly patterns across permafrost soils of the world remains uncertain, limiting our ability to predict biogeochemistry and microbial community responses to climate change. Based on our review of the Arctic microbiome, permafrost microbiology, and community ecology, we propose that Assembly Theory provides a framework to better understand thaw-mediated microbiome changes and the implications for community function and climate feedbacks. This framework posits that the prevalence of deterministic or stochastic processes indicates whether the community is well-suited to thrive in changing environmental conditions. We predict that on a short timescale and following high-disturbance thaw (e.g., thermokarst), stochasticity dominates post-thaw microbiome assembly, suggesting that functional predictions will be aided by detailed information about the microbiome. At a longer timescale and lower-intensity disturbance (e.g., active layer deepening), deterministic processes likely dominate, making environmental parameters sufficient for predicting function. We propose that the contribution of stochastic and deterministic processes to post-thaw microbiome assembly depends on the characteristics of the thaw disturbance, as well as characteristics of the microbial community, such as the ecological and phylogenetic breadth of functional guilds, their functional redundancy, and biotic interactions. These propagate across space and time, potentially providing a means for predicting the microbial forcing of greenhouse gas feedbacks to global climate change.

Global Change Biology↗

Distributional changes in the western Burrowing Owl ( Athene cunicularia hypugaea ) in North America from 1967 to 2008

The quantification of shifts in bird distributions in response to climate change provides an opportunity to gain a deeper understanding of the processes that influence species persistence. We used data from the North American Breeding Bird Survey (BBS) to document changes in the distributional limits of the western Burrowing Owl ( Athene cunicularia hypugaea ) from 1967 to 2008. We used logistic regression to model presence probability ( p ) as a function of longitude, latitude, and year. We modeled a linear trend in logit( p ) through time with slope and intercept modeled as a double Fourier series of longitude and latitude. We found that the western Burrowing Owl has experienced an intriguing southward shift in the northern half of its breeding range, contrary to what is predicted by most species niche models and what has been observed for many other species in North America. The breeding range of the Burrowing Owl has been shrinking near its northern, western, and eastern edges. Our model detected the population declines that were observed in California and eastern Washington, in locations where maps based on route-specific estimating equations had predicted significant population increases. We suggest that the northern boundary of the breeding distribution of the western Burrowing Owl has contracted southward and the southern boundary of the species' breeding distribution has expanded southward into areas of northern Mexico that were formerly used only by wintering migrants.

Journal of Raptor Research↗

How will East African maize yields respond to climate change and can agricultural development mitigate this response?

We analyze the response of Kenyan maize yields to near-term climate change and explore potential mitigation options. We model county level yields as a function of rainfall and temperature during a period of increased regional warming and drying (1989–2008). We then do a counter factual analysis by comparing existing maize yields from 2000 to 2008 to what yields might have been if observed warming and drying trends had not occurred. We also examine maize yields based on projected 2026–2040 climate trends. Without the observed warming and drying trends, Eastern Kenya would have had an 8% increase in maize yields, which in turn would have led to a net production increase of 500,000 metric tons. In Western Kenya, the magnitude of change is higher but the relative changes in predicted values are smaller. If warming and drying trends continue, we expect future maize yields to decline by 11% in Eastern Kenya (vs. 7% in Western Kenya). We also examine whether these future losses might be offset through agricultural development. For that analysis, we use a household panel dataset (2000, 2005) with measurements of individual farm plot yields, inputs, and outputs. We find that under a scenario of aggressive adoption of hybrid seeds and fertilizer usage coupled with warming and drying trends, yields in Western Kenya might increase by 6% while those in Eastern Kenya could increase by 14%. This increase in yields might be larger if there is a corresponding increase in usage of drought-tolerant hybrids. However, wide prediction intervals across models highlight the uncertainty in these outcomes and scenarios.

Climatic Change↗