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At least 469 records · Page 26Linked to original sources

Interaction of rearing environment and reproductive tactic on gene expression profiles in Atlantic salmon

Organisms that share the same genotype can develop into divergent phenotypes, depending on environmental conditions. In Atlantic salmon, young males of the same age can be found either as sneakers or immature males that are future anadromous fish. Just as the organism-level phenotype varies between divergent male developmental trajectories, brain gene expression is expected to vary as well. We hypothesized that rearing environment can also have an important effect on gene expression in the brain and possibly interact with the reproductive tactic adopted. We tested this hypothesis by comparing brain gene expression profiles of the two male tactics in fish from the same population that were reared in either a natural stream or under laboratory conditions. We found that expression of certain genes was affected by rearing environment only, while others varied between male reproductive tactics independent of rearing environment. Finally, more than half of all genes that showed variable expression varied between the two male tactics only in one environment. Thus, in these fish, very different molecular pathways can give rise to similar macro-phenotypes depending on rearing environment. This result gives important insights into the molecular underpinnings of developmental plasticity in relationship to the environment. ?? 2005 The American Genetic Association.

Conference Paper↗

Life-history organization of Yellowstone cutthroat trout (Oncorhynchus clarki bouvieri) in Yellowstone Lake

Life-history organization of the cutthroat trout (Oncorhynchus clarki) may be viewed at various levels, including species, subspecies, metapopulation, population, or individual. Each level varies in spatial scale and temporal persistence, and components at each level continually change with changes in environment. Cutthroat trout are widely distributed throughout the western United States, occurring in such diverse environments as coastal rivers of the Pacific Northwest and interior streams of the Great Basin. During its evolution the species has organized into 14 subspecies with many different life-history characteristics and habitat requirements. Within subspecies, organization is equally complex. For example, life-history traits, such as average size and age, migration strategy, and migration timing, vary among individual spawning populations of Yellowstone cutthroat trout (Oncorhynchus clarki bouvieri) in tributary streams of Yellowstone Lake. Understanding the effects of human perturbations on life-history organization is critical for management of the cutthroat trout and other polytypic salmonid species. Loss of diversity at any hierarchical level jeopardizes the long-term ability of the species to adapt to changing environments, and it may also lead to increased fluctuations in abundance and yield and increase the risk of extinction.

Canadian Journal of Fisheries and Aquatic Sciences↗

Shifting species interactions in terrestrial dryland ecosystems under altered water availability and climate change

Species interactions play key roles in linking the responses of populations, communities, and ecosystems to environmental change. For instance, species interactions are an important determinant of the complexity of changes in trophic biomass with variation in resources. Water resources are a major driver of terrestrial ecology and climate change is expected to greatly alter the distribution of this critical resource. While previous studies have documented strong effects of global environmental change on species interactions in general, responses can vary from region to region. Dryland ecosystems occupy more than one-third of the Earth's land mass, are greatly affected by changes in water availability, and are predicted to be hotspots of climate change. Thus, it is imperative to understand the effects of environmental change on these globally significant ecosystems. Here, we review studies of the responses of population-level plant-plant, plant-herbivore, and predator-prey interactions to changes in water availability in dryland environments in order to develop new hypotheses and predictions to guide future research. To help explain patterns of interaction outcomes, we developed a conceptual model that views interaction outcomes as shifting between (1) competition and facilitation (plant-plant), (2) herbivory, neutralism, or mutualism (plant-herbivore), or (3) neutralism and predation (predator-prey), as water availability crosses physiological, behavioural, or population-density thresholds. We link our conceptual model to hypothetical scenarios of current and future water availability to make testable predictions about the influence of changes in water availability on species interactions. We also examine potential implications of our conceptual model for the relative importance of top-down effects and the linearity of patterns of change in trophic biomass with changes in water availability. Finally, we highlight key research needs and some possible broader impacts of our findings. Overall, we hope to stimulate and guide future research that links changes in water availability to patterns of species interactions and the dynamics of populations and communities in dryland ecosystems.

Biological Reviews↗

Pollution and wildlife health

Pollution is a pervasive and growing threat to wildlife health. This chapter discusses two broad groups of pollution, those whose abatement could have immediate beneficial effects including light, air, and noise pollution, and those that will take relatively longer to address due to their environmental persistence or their continuing discharge. Whilst we are very good at detecting the presence of pollutants in tissues or the environment, making a convincing link between the presence of these compounds and mortality events in the field or population effects will remain a challenge for the foreseeable future. Creative new approaches are also being considered to mitigate the effects of pollution on wildlife and ecosystems. Depending on the source of pollution, the beneficial outcomes of mitigation measures, if properly implemented, could have immediate effects. Given the plethora of potential adverse pollution effects, frameworks to prioritize which threats are most likely to cause adverse effects and develop means to address or manage them are an imperative. In the interim, focusing on preserving existing habitats and reducing our footprint by adjusting human activities to minimize the release of pollutants into the environment will go a long way toward promoting healthy wildlife and ecosystems.

Book chapter↗

Remaining populations of an upland stream fish persist in refugia defined by habitat features at multiple scales

Aim Conserving stream biota could require strategies that preserve habitats conveying resistance to ecological impacts of changing land use and climate. Retrospective analyses of species’ responses to anthropogenic disturbances can inform such strategies. We developed a hierarchical framework to contrast environmental conditions underlying persistence versus extirpation of an imperilled stream fish, Candy Darter ( Etheostoma osburni ), over decades of changing land use. The decline of E. osburni may broadly represent the challenge of conserving sensitive freshwater species in intensively used upland environments. Location New River drainage, Appalachian Mountains, USA. Methods We surveyed fish and habitat in historically occupied sites to identify population refugia, and used multivariate and spatial analyses to address three questions: (a) what are the environmental correlates of refugia? (b) are the pathways by which land use impacts instream habitat constrained by catchment- and/or segment-scale features? and (c) are E. osburni distributional dynamics spatially structured and explained by fine sediment and warm stream temperatures? Results We confirmed a recently localized distribution similar to other upland species, marked by at least seven extirpations from streams throughout E. osburni 's southern range. Catchment-scale features primarily constrained land use and finer-scale habitat, leading to either extirpations or population-supporting refugia defined by features at multiple scales. Refugium habitats contained cooler temperatures and less fine sediment. Rare mismatches between persistence and habitat suitability were explained by network location , suggesting unmeasured environmental gradients and/or dispersal contributed to distributional dynamics. Main conclusions We provided insight at multiple spatial scales into how aquatic species’ distributions become fragmented and localized. Our results demonstrate that natural landscape heterogeneity imparts spatially variable resistance of sensitive species to intensive land uses. By recognizing the scale-specific features that buffer populations from extirpation, conservation strategies could be tailored to protect naturally occurring refugium habitats and focus restoration in systems where such habitats are broadly lacking.

Virginia, West Virginia↗

Survival of female wood ducks during brood rearing in Mississippi and Alabama

Knowledge of survival of female ducks is important for understanding population dynamics and managing hunted species. We estimated survival of female wood ducks ( Aix sponsa ) during brood rearing in different wetland environments in Mississippi (1996-1999) and Alabama (1998-1999). Survival was 0.90 ± 0.05 (Ŝ ± SE) in Mississippi and 0.92 ± 0.07 in Alabama. A composite estimate of female survival for all years and both areas was 0.90 ± 0.04. High survival of females during brood rearing in our study areas suggests that this factor may be less important than other population factors (e.g., duckling survival) influencing fall recruitment in these wood duck populations.

Alabama, Mississippi↗

Amphibians of the northern Great Plains

No cry of alarm has been sounded over the fate of amphibian populations in the northern grasslands of North America, yet huge percentages of prairie wetland habitat have been lost, and the destruction continues. Scarcely 30% of the original mixedgrass prairie remains in Nebraska, South Dakota, and North Dakota (See Table 1 in this chapter). If amphibian populations haven’t declined, why haven’t they? Or, have we simply failed to notice? Amphibians in the northern grasslands evolved in a boom-or-bust environment: species that were unable to survive droughts lasting for years died out long before humans were around to count them. Species we find today are expert at seizing the rare, wet moment to rebuild their populations in preparation for the next dry season. When numbers can change so rapidly, who can say if a species is rare or common? A lot depends on when you look.

Book chapter↗

Rapid simulation of wave runup on morphologically diverse, reef-lined coasts with the BEWARE-2 (Broad-range Estimator of Wave Attack in Reef Environments) meta-process model

Low-lying, tropical, coral-reef-lined coastlines are becoming increasingly vulnerable to wave-driven flooding due to population growth, coral reef degradation, and sea-level rise. Early-warning systems (EWSs) are needed to enable coastal authorities to issue timely alerts and coordinate preparedness and evacuation measures for their coastal communities. At longer timescales, risk management and adaptation planning require robust assessments of future flooding hazard considering uncertainties. However, due to diversity in reef morphologies and complex reef hydrodynamics compared to sandy shorelines, there have been no robust analytical solutions for wave runup to allow for the development of large-scale coastal wave-driven flooding EWSs and risk assessment frameworks for reef-lined coasts. To address the need for fast, robust predictions of runup that account for the natural variability in coral reef morphologies, we constructed the BEWARE-2 (Broad-range Estimator of Wave Attack in Reef Environments) meta-process modeling system. We developed this meta-process model using a training dataset of hydrodynamics and wave runup computed by the XBeach Non-Hydrostatic process-based hydrodynamic model for 440 combinations of water level, wave height, and wave period with 195 representative reef profiles that encompass the natural diversity in real-world fringing coral reef systems. Through this innovation, BEWARE-2 can be applied in a larger range of coastal settings than meta-models that rely on a parametric description of the coral reef geometry. In the validation stage, the BEWARE-2 modeling system produced runup results that had a relative root mean square error of 13% and relative bias of 5% relative to runup simulated by XBeach Non-Hydrostatic for a large range of oceanographic forcing conditions and for diverse reef morphologies (root mean square error and bias 0.63 and 0.26 m, respectively, relative to mean simulated wave runup of 4.85 m). Incorporating parametric modifications in the modeling system to account for variations in reef roughness and beach slope allows for systematic errors (relative bias) in BEWARE-2 predictions to be reduced by a factor of 1.5–6.5 for relatively coarse or smooth reefs and mild or steep beach slopes. This prediction provided by the BEWARE-2 modeling system is faster by 4–5 orders of magnitude than the full, process-based hydrodynamic model and could therefore be integrated into large-scale EWSs for tropical, reef-lined coasts and used for large-scale flood risk assessments.

Natural Hazards and Earth System Sciences↗

Overview on the effects of parasites on fish health

It is believed by many that parasites are only as important as the fish they infect. Parasites are ubiquitous, primarily surviving in a dynamic equilibrium with their host(s) and they are often overlooked in fish health assessments. Changes in the environment, both anthropogenic and environmental, can alter the parasite/host equilibrium and cause disease or mortality in fish. Therefore it is imperative that we have knowledge of both parasites and parasitic communities within a given population. When fish kills occur, it can often be associated with changes in parasite density and community composition. Often the damage associated with these fish is relative to the rate of infestation with the parasite; a fish that is lightly infected will show few signs of the parasite, while a heavily infected fish may become physiologically impaired and even die. Parasites can cause mechanical damage (fusion of gill lamellae, tissue replacement), physiological damage (cell proliferation, immunomodulation, detrimental behavioral responses, altered growth) and reproductive damage. As parasitism is the most common lifestyle on the planet, understanding its role in the environment may help researchers understand changes in a given fish population or stream ecosystem.

Conference Paper↗

Global volcanic hazards and risk

An estimated 800 million people live within 100 km of an active volcano in 86 countries and additional overseas territories worldwide [see Chapter 4 and Appendix B]1. Volcanoes are compelling evidence that the Earth is a dynamic planet characterised by endless change and renewal. Humans have always found volcanic activity fascinating and have often chosen to live close to volcanoes, which commonly provide favourable environments for life. Volcanoes bring many benefits to society: eruptions fertilise soils; elevated topography provides good sites for infrastructure (e.g. telecommunications on elevated ground); water resources are commonly plentiful; volcano tourism can be lucrative; and volcanoes can acquire spiritual, aesthetic or religious significance. Some volcanoes are also associated with geothermal resources, making them a target for exploration and a potential energy resource. Much of the time volcanoes are not a threat because they erupt very infrequently or because communities have become resilient to frequently erupting volcanoes. However, there is an everpresent danger of a long-dormant volcano re-awakening or of volcanoes producing anomalously large or unexpected eruptions. Volcanic eruptions can cause loss of life and livelihoods in exposed communities, damage or disrupt critical infrastructure and add stress to already fragile environments. Their impacts can be both short-term, e.g. physical damage, and long-term, e.g. sustained or permanent displacement of populations. The risk from volcanic eruptions and their attendant hazards is often underestimated beyond areas within the immediate proximity of a volcano. For example, volcanic ash hazards can have effects hundreds of kilometres away from the vent and have an adverse impact on human and animal health, infrastructure, transport, agriculture and horticulture, the environment and economies. The products of volcanism and their impacts can extend beyond country borders, to be regional and even global in scale. Although known historical loss of life from volcanic eruptions (since 1600 AD about 280,000 fatalities are recorded, Auker et al. (2013)) is modest compared to other major natural hazards, volcanic eruptions can be catastrophic for exposed communities. In 1985 the town of Armero in Colombia was buried by lahars (volcanic mudflows) with more than 21,000 fatalities due to relatively small explosive eruptions at the summit of Nevado del Ruiz volcano that partially melted a glacier (Voight, 1990).

Book chapter↗

An overview of agent-based models in plant biology and ecology

Agent-based modeling (ABM) has become an established methodology in many areas of biology, ranging from the cellular to the ecological population and community levels. In plant science, two different scales have predominated in their use of ABM. One is the scale of populations and communities, through the modeling of collections of agents representing individual plants, interacting with each other and with the environment. The other is the scale of the individual plant, through the modeling, by functional-structural plant models (FSPMs), of agents representing plant building blocks, or metamers, to describe the development of plant architecture and functions within individual plants. The purpose of this review is to show key results and parallels in ABM for growth, mortality, carbon allocation, competition, and reproduction across the scales from the plant organ to populations and communities on a range of spatial scale to the whole landscape. Several areas of application of ABMs are reviewed, showing that some issues are addressed by both population-level ABMs and FSPMs. Continued increase in the relevance of ABM to environmental science and management will be helped by greater integration of ABMs across these two scales.

Annals of Botany↗

Demography of Dall's sheep in northwestern Alaska

Dall’s sheep in northwestern Alaska declined in the early 1990s following the severe 1989-90 and 1990-91 winters. In the Baird Mountains of Noatak National Preserve, estimates of adult sheep declined by 50% from 800 in 1989 to under 400 in 1991. Population counts remained low throughout 1991 to 1996, reaching a minimum of 244 adult sheep in 1996. Few lambs were observed during annual midsummer aerial surveys in 1991 to 1994. We suspect that these declines resulted from a combination of poorer nutritional condition and increased vulnerability of sheep to predation resulting from severe winter conditions. As a result of these declines, both subsistence and sport hunting seasons were closed by emergency order in 1991, resulting in substantial management controversy. The affected publics, although willing to accept the closures, questioned the validity of the sheep survey data and strongly emphasized their interest in restoring harvests as soon as populations increased sufficiently. In 1995 the Northwest Arctic Regional Advisory Council, the local advisory committee for the Federal Subsistence Board, passed a motion supporting efforts to initiate research on sheep populations in the region to better understand the factors limiting sheep populations and to evaluate sheep survey methodologies. Currently estimates of Dall’s sheep population size and composition in the western Brooks Range are based on intensive fixed-wing aerial surveys conducted annually since 1986 in areas including the Baird Mountains. The annual variation in recent Baird Mountains aerial counts cannot be explained with reasonable assumptions about reproduction and survival, suggesting that there is some variability in the proportion of the population observed each year or that a substantial number of sheep move during the survey. Prior to our research, no attempt had been made to estimate visibility bias or precision for these surveys. Our understanding of Dall’s sheep population biology comes largely from studies in central or southern Alaska and the southern Yukon. However, sheep in northwestern Alaska are at the northwestern extreme of their range and live in a less hospitable environment characterized by short growing seasons and long, severe winters. We expect patterns of productivity and survival for sheep in Noatak National Preserve to differ from the more southerly populations. To adequately manage sheep harvests in northwestern Alaska, we need a better understanding of sheep demography. Along with unbiased population estimates, understanding the dynamics of sheep populations in the region will allow population models to be developed that can provide focus for a useful dialog on management goals and strategies and facilitate a cooperative strategy for managing sheep harvests in northwestern Alaska.

Alaska↗

Morphologic and transport properties of natural organic floc

The morphology, entrainment, and settling of suspended aggregates (“floc”) significantly impact fluxes of organic carbon, nutrients, and contaminants in aquatic environments. However, transport properties of highly organic floc remain poorly understood. In this study detrital floc was collected in the Florida Everglades from two sites with different abundances of periphyton for use in a settling column and in racetrack flume entrainment experiments. Although Everglades flocs are similar to other organic aggregates in terms of morphology and settling rates, they tend to be larger and more porous than typical mineral flocs because of biostabilization processes and relatively low prevailing shear stresses typical of wetlands. Flume experiments documented that Everglades floc was entrained at a low bed shear stress of 1.0 × 10 −2 Pa, which is considerably smaller than the typical entrainment threshold of mineral floc. Because of similarities between Everglades floc and other organic floc populations, floc transport characteristics in the Everglades typify the behavior of floc in other organic‐rich shallow‐water environments. Highly organic floc is more mobile than less organic floc, but because bed shear stresses in wetlands are commonly near the entrainment threshold, wetland floc dynamics are often transport‐limited rather than supply limited. Organic floc transport in these environments is therefore governed by the balance between entrainment and settling fluxes, which has implications for ecosystem metabolism, materials cycling, and even landscape evolution.

Water Resources Research↗

The effectiveness of non-native fish removal techniques in freshwater ecosystems: a systematic review

In aquatic systems, biological invasions can result in adverse ecological effects. Management techniques available for non-native fish removal programs (including eradication and population size control) vary widely, but include chemicals, harvest regimes, physical removal, or biological control. For management agencies, deciding on what non-native fish removal program to use has been challenging because there is little reliable information about the relative effectiveness of these measures in controlling or eradicating non-native fish. We conducted a systematic review, including a critical appraisal of study validity, to assess the effectiveness of different non-native fish removal methods, and to identify the factors that influence the overall success rate of each type of method. We found 95 relevant studies, generating 158 data sets. The evidence base was dominated by poorly documented studies with inadequate experimental designs (76% of removal projects). When the management goal was non-native fish eradication, chemical treatments were relatively successful (antimycin 75%; rotenone 89%) compared to other interventions. Electrofishing and passive removal measure studies indicated successful eradication was possible (58% each respectively) but required intensive effort and multiple treatments over a number of years. Of these studies with sufficient information, electrofishing had the highest success for population size control (56% of data sets). Overall, inadequate data quality and completeness severely limited our ability to make strong conclusions about the relationships between non-native fish abundance and different methods of eradication and population control, and the factors influencing the overall success rate of each method. Our review highlights that there is considerable scope for improving our evaluations of non-native fish removal methods. It is recommended that programs should have explicitly stated objectives, better data reporting, and study designs that (when possible and appropriate) incorporate replicated and controlled investigations with rigorous, long-term quantitative monitoring. Future research on the effectiveness of non-native fish removal methods should focus on: (1) the efficacy of existing or potentially new removal measures in larger, more complex environments; (2) a broader range of removal measures in general, and (3) phenotypic characteristics of individual fish within a population that fail to be eradicated or controlled.

Environmental Reviews↗

Population assessment and potential functional roles of native mussels in the Upper Hudson River

General Electric Company (GE) directly and indirectly released polychlorinated biphenyls (PCBs) into the Hudson River and the surrounding environment starting in the late 1940’s, making it one of the most PCB-contaminated rivers in North America. Source control at two GE plant sites was implemented in 2009 to stem the influx of PCBs into the river (NYSDEC 2004; Farrar 2013; NYSDEC 2015). The Hudson River, like many other rivers, contains populations of native freshwater mussels—a group of animals that perform vital functions in freshwater systems. While there was anecdotal evidence of mussels residing in the Upper Hudson River (north of Troy, NY; GE 2005, GE 2009), quantitative data on mussel assemblages was lacking. Systematic, quantitative surveys for native mussels were completed in 2013 and 2015 in a total of six pools of the Upper Hudson River including one reference pool (Feeder Dam) located upstream of the former GE plant sites and five contaminated pools downstream of the GE plant sites (Thompson Island, Fort Miller, Northumberland, Stillwater, and Upper Mechanicville). Surveys were designed to estimate species composition, relative abundance, population size, population structure, and ecological services (i.e., biomass and filtration) of mussel communities prior to and after remedial actions to remove PCB contaminated sediments (i.e., dredged and subsequently capped or backfilled). In most pools, the experimental design incorporated stratification on remediated (before or after remedial activities were completed) and non-remediated areas. ... (access to the full abstract is restricted)

New York↗

Homogenization of large-scale movement models in ecology

A difficulty in using diffusion models to predict large scale animal population dispersal is that individuals move differently based on local information (as opposed to gradients) in differing habitat types. This can be accommodated by using ecological diffusion. However, real environments are often spatially complex, limiting application of a direct approach. Homogenization for partial differential equations has long been applied to Fickian diffusion (in which average individual movement is organized along gradients of habitat and population density). We derive a homogenization procedure for ecological diffusion and apply it to a simple model for chronic wasting disease in mule deer. Homogenization allows us to determine the impact of small scale (10–100 m) habitat variability on large scale (10–100 km) movement. The procedure generates asymptotic equations for solutions on the large scale with parameters defined by small-scale variation. The simplicity of this homogenization procedure is striking when compared to the multi-dimensional homogenization procedure for Fickian diffusion,and the method will be equally straightforward for more complex models.

Bulletin of Mathematical Biology↗

Genetic variation, relatedness, and effective population size of polar bears (Ursus maritimus) in the southern Beaufort Sea, Alaska

Polar bears ( Ursus maritimus ) are unique among bears in that they are adapted to the Arctic sea ice environment. Genetic data are useful for understanding their evolution and can contribute to management. We assessed parentage and relatedness of polar bears in the southern Beaufort Sea, Alaska, with genetic data and field observations of age, sex, and mother–offspring and sibling relationships. Genotypes at 14 microsatellite DNA loci for 226 bears indicate that genetic variation is comparable to other populations of polar bears with mean number of alleles per locus of 7.9 and observed and expected heterozygosity of 0.71. The genetic data verified 60 field-identified mother–offspring pairs and identified 10 additional mother–cub pairs and 48 father–offspring pairs. The entire sample of related and unrelated bears had a mean pairwise relatedness index ( r xy ) of approximately zero, parent–offspring and siblings had r xy of approximately 0.5, and 5.2% of the samples had r xy values within the range expected for parent-offspring. Effective population size ( N e = 277) and the ratio of N e to total population size ( N e / N = 0.182) were estimated from the numbers of reproducing males and females. N e estimates with genetic methods gave variable results. Our results verify and expand field data on reproduction by females and provide new data on reproduction by males and estimates of relatedness and N e in a polar bear population.

Journal of Heredity↗

Effect of climate change on disease spread in wildlife

A growing body of evidence indicates that climate change alone, or acting synergistically with current anthropogenic threats, is affecting the health of wild populations of aquatic and terrestrial wildlife. Measurable by-products of climate change include elevated atmospheric concentrations of greenhouse gases, higher average global temperatures; variations in global precipitation patterns, rising and warming oceans, altered hydrographs of rivers, and increased mid-continental drying during summer. These consequences affect the terrestrial environment through shifts in phenology, vegetation cover, and fire regimes. Warmer ocean temperatures, increased acidification, rise in sea levels, and reduction in sea ice cover are also leading to widespread ecological changes in marine systems. Wildlife populations face a variety of climate-related pressures, such as changes in animal distribution or density, limitation of food resources, and alteration to critical habitats. The increased potential for emergence and resurgence of diseases that are responsive to environmental conditions also has implications for wildlife populations. Shifts in temperature or other climatic factors may directly affect the incidence of disease in wildlife by altering host-pathogen interactions, promoting vector populations or allowing new ranges for vectors, or reducing development times for parasites. A number of examples from both field and laboratory studies have demonstrated a clear link between warming environments and disease spread. Many climate-related environmental changes also influence wildlife health indirectly. For example, increasing temperatures, in combination with shifts in rainfall and humidity, may aggravate current trends for water resource limitation and habitat degradation or destruction and lead to increased crowding of animal populations, thereby promoting transmission opportunities of pathogens within populations or across species. Although it may be difficult to disentangle the influences of other anthropogenic changes from the direct effects of warming, some ecosystems provide especially useful models for studying climate-related disease spread in wildlife. For example, the effects of climate change on parasite dynamics may be easily observed in the Arctic, where environmental changes are occurring rapidly, anthropogenic influences are relatively limited, and biodiversity is generally low. Marine ecosystems are also undergoing rapid rates of change and may be vulnerable to a variety of natural and anthropogenic perturbations. Although many factors affect the health of organisms in ocean environments, temperature has been clearly linked to an increase in disease prevalence among sessile organisms such as corals. In this chapter, we discuss observed and predicted changes to wildlife health resulting from climate change. Our review will not include all aspects of wildlife health, but will instead focus on established or suspected links between climate drivers and disease spread and discuss examples from the current literature. Here, we define disease spread to include: 1) change in geographical or altitudinal distribution of pathogens, parasites, and vectors and the diseases they cause; 2) change in prevalence or severity of disease; and 3) emergence of novel diseases. Additionally, because wildlife species serve as reservoirs for zoonotic diseases that affect both animals and humans, we include select examples of the effect of climate change on the capacity of wildlife to harbor and spread these disease agents.

Book chapter↗