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At least 775 records · Page 43Linked to original sources

Costs of living for juvenile Chinook salmon ( Oncorhynchus tshawytscha ) in an increasingly warming and invaded world

Rapid environmental change in freshwater ecosystems has created a need to understand the interactive effects of multiple stressors, with temperature and invasive predators identified as key threats to imperiled fish species. We tested the separate and interactive effects of water temperature and predation by non-native smallmouth bass ( Micropterus dolomieu ) on the lethal (mortality) and sublethal (behavior, physiology, and growth) effects for juvenile Chinook salmon ( Oncorhynchus tshawytscha ) in seminatural stream channel experiments. Over 48 h trials, there was no difference in direct predation with warmer temperatures, but significant interactive effects on sublethal responses of juvenile salmon. Warmer temperatures resulted in significantly stronger and more variable antipredator responses (surface shoaling and swimming activity), while physiological indicators (plasma glucose, plasma cortisol) suggested suppression of physiological mechanisms in response to the combined stressors. These patterns corresponded with additive negative growth in predation, temperature, and combined treatments. Our results suggest that chronic increases in temperature may not increase direct predation over short periods, but can result in significant sublethal costs with negative implications for long-term development, disease resistance, and subsequent size-selective mortality of Pacific salmon.

Canadian Journal of Fisheries and Aquatic Sciences↗

A sigmoid model to predict gastric evacuation rates of smallmouth bass Micropterus dolomieui fed juvenile salmon

Laboratory experiments were conducted to examine the effects of water temperature, predator size, prey size, and prey number on gastric evacuation of smallmouth bass ( Micropterus dolomieui ) fed juvenile salmon. The smallmouth bass were allowed to feed voluntarily after 24–48 h of starvation and stomachs were pumped at intervals of 1–4 h until 90% of the stomach contents were evacuated ( E 90 ). Evacuation approximated an S -shaped curve over time, and a sigmoid model was developed to predict evacuation at varying water temperatures, total meal weights, predator sizes, and prey number. The rate of evacuation increased with increasing water temperature, meal weight, or predator size. The E 90 increased with larger meal weights but decreased with increasing temperature or predator size. E 90 ranged between 4 and 95 h, depending upon conditions. E 90 was slower than those estimated previously for another predator of salmon, the stomachless northern squawfish ( Ptychocheilus oregonensis ).

Canadian Journal of Fisheries and Aquatic Sciences↗

Effect of lake-wide planktivory by the pelagic prey fish community in Lakes Michigan and Ontario

We compared predatory demand by pelagic planktivorous prey fish with invertebrate production in Lake Michigan during 1987 and in Lake Ontario during 1990. Predation by the planktivores in Lake Ontario was nearly fourfold higher than in Lake Michigan (approx. 87 g wet weight∙m −2 ∙year −1 ). Predation rates on Mysis were comparable in Lakes Michigan and Ontario (approx. 21 g∙m −2 ∙year −1 ), while predation on Diporeia was markedly higher in Lake Michigan than in Lake Ontario (21.3 vs. 8.5 g wet weight∙m −2 ∙year −1 ). In Lake Ontario, predatory demand on zooplankton exceeded our best estimate of production by a factor of 1.7. Similarly, predation estimates on Mysis in Lake Ontario were 1.2–2.0 times the estimated rate of production, depending on the production model used. Lake Michigan planktivores consumed approximately 55% of available zooplankton production in 1987, indicating that competition for prey resources, if operating, was not as intense as that in Lake Ontario in 1990. It is unclear how to resolve the paradox that predation could markedly exceed available prey production in some cases. There could be sources of error in the estimates of both the supply and demand sides of these trophic relationships.

Canadian Journal of Fisheries and Aquatic Sciences↗

Black carp Mylopharyngodon piceus (Richardson, 1846) mouth gape and size preference of a bivalve prey

Black carp Mylopharyngodon piceus (Richardson, 1846) have been widely used as biological control of snails in aquaculture and were imported to the United States in the 1970s and 1980s for this purpose. Prior research emphasizes the species’ propensity to control gastropods, but since subsequent escape and establishment of black carp in portions of the Mississippi River Basin, concerns now focus on the numerous endangered and endemic bivalve species upon which black carp may predate. Black carp mouth gape may limit predation on larger bivalves, but bite force is also a factor. We used regression of fish length to mouth gape of wild-caught black carp and compared these results to tank forage size preference trials with bivalve prey Corbicula fluminea clams. Wild-caught black carp ranged from 429 to 1580 mm total length, a size range larger than measured in previous studies. Regression of fish length and mouth gape indicated greater variability among sizes, as expected from wild versus cultured populations. Clam consumption was size-dependent. Black carp commonly engulfed but did not consume the largest clams in tank feeding trials. Shell width was a better predictor of successful consumption than length or height. Predation was restricted at sizes less than the mouth gape of test black carp as observed by individuals engulfing but failing to consume prey. This result indicates that either bite force or the pharyngeal apparatus gape (i.e., the distance between the pharyngeal teeth and keratinous pad) limited successful crushing of engulfed shells. Bivalve predation by black carp is limited by both a fish’s ability to engulf prey and the ability to fracture the shell of larger prey items that cannot be broken or swallowed whole. The results of this research may be used to assess potential prey sizes of wild black carp and anticipated effects of predation on bivalve communities.

Journal of Applied Ichthyology↗

Comparing mechanisms of host manipulation across host and parasite taxa

Parasites affect host behavior in several ways. They can alter activity, microhabitats or both. For trophically transmitted parasites (the focus of our study), decreased activity might impair the ability of hosts to respond to final-host predators, and increased activity and altered microhabitat choice might increase contact rates between hosts and final-host predators. In an analysis of trophically transmitted parasites, more parasite groups altered activity than altered microhabitat choice. Parasites that infected vertebrates were more likely to impair the host’s reaction to predators, whereas parasites that infected invertebrates were more likely to increase the host’s contact with predators. The site of infection might affect how parasites manipulate their hosts. For instance, parasites in the central nervous system seem particularly suited to manipulating host behavior. Manipulative parasites commonly occupy the body cavity, muscles and central nervous systems of their hosts. Acanthocephalans in the data set differed from other taxa in that they occurred exclusively in the body cavity of invertebrates. In addition, they were more likely to alter microhabitat choice than activity. Parasites in the body cavity (across parasite types) were more likely to be associated with increased host contact with predators. Parasites can manipulate the host through energetic drain, but most parasites use more sophisticated means. For instance, parasites target four physiological systems that shape behavior in both invertebrates and vertebrates: neural, endocrine, neuromodulatory and immunomodulatory. The interconnections between these systems make it difficult to isolate specific mechanisms of host behavioral manipulation.

Journal of Experimental Biology↗

Forage species in lakes and reservoirs of the western United States

Fisheries management in the western United States has concentrated on salmonid species, particularly in streams. Forage‐fish management in lakes and reservoirs is not highly developed, and has emphasized introductions of both predators and prey. In coldwater lakes, kokanees Oncorhynchus nerka have been established widely as the principal forage for salmonids and often support a sport fishery themselves. Introductions of other forage organisms in coldwater lakes and reservoirs, notably the opossum shrimp Mysis relicta and redside shiner Richardsonius balteatus have had mixed results due in part to food competition with resident species. A variety of exotic predator and prey species have been introduced in coolwater and warmwater reservoirs. Results have varied greatly, and include establishment of successful sport fisheries, elimination of native fishes, failure of introduced predators or prey, and predation on stocked salmonids. Native forage species generally have been overlooked by management, although there appears to be a large potential for their utilization, particularly with coadapted salmonid species. Better screening procedures for exotic introductions and a concerted investigation of the ecological requirements of both native and introduced predator‐prey combinations are required for intelligent management of western lakes and reservoirs.

western United States↗

Multiple factors affect a population of Agassiz's desert tortoise ( Gopherus agassizii ) in the Northwestern Mojave Desert

Numerous factors have contributed to declines in populations of the federally threatened Agassiz's Desert Tortoise ( Gopherus agassizii ) and continue to limit recovery. In 2010, we surveyed a low-density population on a military test facility in the northwestern Mojave Desert of California, USA, to evaluate population status and identify potential factors contributing to distribution and low densities. Estimated densities of live tortoises ranged spatially from 1.2/km 2 to 15.1/km 2 . Although only one death of a breeding-age tortoise was recorded for the 4-yr period prior to the survey, remains of 16 juvenile and immature tortoises were found, and most showed signs of predation by Common Ravens ( Corvus corax ) and mammals. Predation may have limited recruitment of young tortoises into the adult size classes. To evaluate the relative importance of different types of impacts to tortoises, we developed predictive models for spatially explicit densities of tortoise sign and live tortoises using topography (i.e., slope), predators (Common Raven, signs of mammalian predators), and anthropogenic impacts (distances from paved road and denuded areas, density of ordnance fragments) as covariates. Models suggest that densities of tortoise sign increased with slope and signs of mammalian predators and decreased with Common Ravens, while also varying based on interaction effects involving these predictors as well as distances from paved roads, denuded areas, and ordnance. Similarly, densities of live tortoises varied by interaction effects among distances to denuded areas and paved roads, density of ordnance fragments, and slope. Thus multiple factors predict the densities and distribution of this population.

California;Nevada↗

Functional response models to estimate feeding rates of wading birds

Forager (predator) abundance may mediate feeding rates in wading birds. Yet, when modeled, feeding rates are typically derived from the purely prey-dependent Holling Type II (HoII) functional response model. Estimates of feeding rates are necessary to evaluate wading bird foraging strategies and their role in food webs; thus, models that incorporate predator dependence warrant consideration. Here, data collected in a mangrove swamp in Puerto Rico in 1994 were reanalyzed, reporting feeding rates for mixed-species flocks after comparing fits of the HoII model, as used in the original work, to the Beddington-DeAngelis (BD) and Crowley-Martin (CM) predator-dependent models. Model CM received most support (AIC c wi = 0.44), but models BD and HoII were plausible alternatives (AIC c ??? 2). Results suggested that feeding rates were constrained by predator abundance. Reductions in rates were attributed to interference, which was consistent with the independently observed increase in aggression as flock size increased (P < 0.05). Substantial discrepancies between the CM and HoII models were possible depending on flock sizes used to model feeding rates. However, inferences derived from the HoII model, as used in the original work, were sound. While Holling's Type II and other purely prey-dependent models have fostered advances in wading bird foraging ecology, evaluating models that incorporate predator dependence could lead to a more adequate description of data and processes of interest. The mechanistic bases used to derive models used here lead to biologically interpretable results and advance understanding of wading bird foraging ecology.

Waterbirds↗

Fishing for lobsters indirectly increases epidemics in sea urchins

Two ecological paradigms, the trophic cascade and the host-density threshold in disease, interact in the kelp-forest ecosystem to structure the community. To investigate what happens when a trophic cascade pushes a host population over a host-threshold density, I analyzed a 20-year data set of kelp forest communities at 16 sites in the region of the Channel Islands National Park, California, USA. Historically, lobsters, and perhaps other predators, kept urchin populations at low levels and kelp forests developed a community-level trophic cascade. In geographic areas where the main predators on urchins were fished, urchin populations increased to the extent that they overgrazed algae and starvation eventually limited urchin-population growth. Despite the limitation of urchin population size by food availability, urchin densities, at times, well exceeded the host-density threshold for epidemics. An urchin-specific bacterial disease entered the region after 1992 and acted as a density-dependent mortality source. Dense populations were more likely to experience epidemics and suffer higher mortality. Disease did not reduce the urchin population at a site to the density that predators previously did. Therefore, disease did not fully replace predators in the trophic cascade. These results indicate how fishing top predators can indirectly favor disease transmission in prey populations.

Ecological Applications↗

Savanna tree density, herbivores, and the herbaceous community: Bottom-up vs. top-down effects

Herbivores choose their habitats both to maximize forage intake and to minimize their risk of predation. For African savanna herbivores, the available habitats range in woody cover from open areas with few trees to dense, almost‐closed woodlands. This variation in woody cover or density can have a number of consequences for herbaceous species composition, cover, and productivity, as well as for ease of predator detection and avoidance. Here, we consider two alternative possibilities: first, that tree density affects the herbaceous vegetation, with concomitant “bottom‐up” effects on herbivore habitat preferences; or, second, that tree density affects predator visibility, mediating “top‐down” effects of predators on herbivore habitat preferences. We sampled sites spanning a 10‐fold range of tree densities in an Acacia drepanolobium‐dominated savanna in Laikipia, Kenya, for variation in (1) herbaceous cover, composition, and species richness; (2) wild and domestic herbivore use; and (3) degree of visibility obstruction by the tree layer. We then used structural equation modeling to consider the potential influences that tree density may have on herbivores and herbaceous community properties. Tree density was associated with substantial variation in herbaceous species composition and richness. Cattle exhibited a fairly uniform use of the landscape, whereas wild herbivores, with the exception of elephants, exhibited a strong preference for areas of low tree density. Model results suggest that this was not a response to variation in herbaceous‐community characteristics, but rather a response to the greater visibility associated with more open places. Elephants, in contrast, preferred areas with higher densities of trees, apparently because of greater forage availability. These results suggest that, for all but the largest species, top‐down behavioral effects of predator avoidance on herbivores are mediated by tree density. This, in turn, appears to have cascading effects on the herbaceous vegetation. These results shed light on one of the major features of the “landscape of fear” in which African savanna herbivores exist.

Laikipia County↗

Co-occurence of Chiricahua leopard frogs (Lithobates chiricahuensis) with sunfish (Lepomis)

Invasive species are a major threat to the persistence of native species, particularly in systems where ephemeral aquatic habitats have been replaced by permanent water and predators, such as fish, have been introduced. Within the Altar Valley, Arizona, the invasive American bullfrog, Lithobates catesbeianus (formerly Rana catesbeianus ), has been successfully eradicated to help recover Chiricahua leopard frogs ( Lithobates chiricahuensis ). However, other nonnative predators including sunfish ( Lepomis ) are present in some permanent water bodies. During four consecutive years (2014–2017), we detected both the federally threatened Chiricahua leopard frog and sunfish at one permanent water body in the Altar Valley. This suggests that despite the potential negative effect of predatory fish on amphibians, there may be conditions where the Chiricahua leopard frog can co-occur with this nonnative predator. A better understanding of rare situations of co-occurrence with nonnative predators may contribute to our understanding of why co-occurrence happens in some, but not all, systems and whether conservation strategies can be developed in situations where eradication of nonnative predators is infeasible.

Arizona↗

Caribou calf mortality in Denali National Park, Alaska

Calf mortality is a major component of caribou (Rangifer tarandus) population dynamics, but little is known about the timing or causes of calf losses, or of characteristics that predispose calves to mortality. During 1984-87, we radiocollared 226 calves (≤3 days old) in the Denali Caribou Herd (DCH), an unhunted population utilized by a natural complement of predators, to determine the extent, timing, and causes of calf mortality and to evaluate influences of year, sex, birthdate, and birth mass on those losses. Overall, 39% of radio-collared calves died as neonates (≤15 days old), and 98% of those deaths were attributed to predation. Most neonatal deaths (85%) occurred within 8 days of birth. Few deaths occurred after the neonatal period (5, 10, and 0% of calves instrumented died during 16-30, 31-150, and >150 days of age, respectively). Survival of neonates was lower (P = 0.038) in 1985, following a severe winter, than during the other 3 years. In years other than 1985, calves born during the peak of calving (approx 50% of the total, born 5-8 days after calving onset) experienced higher (P < 0.001) neonatal survival than did other calves. Grizzly bears (Ursus arctos), wolves (Canis lupus), and unknown large predators (i.e., grizzly bears or wolves) accounted for 49, 29, and 16% of the neonatal deaths, respectively. The rate of bear-caused mortalities declined (P < 0.001) with calf age, and bears killed few calves >10 days old. Wolf predation was not related (P > 0.05) to calf age and peaked 10 days after onset of calving. Grizzly bear and wolf predation on neonates during the calving season was a limiting factor for the Denali Caribou Herd.

Journal of Wildlife Management↗

Assessing the efficacy of using a parentage-based tagging survival model to evaluate two sources of mortality for juvenile Chinook salmon (Oncorhynchus tshawytscha) in Lookout Point Reservoir, Oregon

We conducted a study to assess the efficacy of using a parentage-based tagging survival model (PBT N-mixture model) to evaluate two sources of mortality for juvenile Chinook salmon ( Oncorhynchus tshawytscha ) in Lookout Point Reservoir, Oregon. The model was originally developed to evaluate reservoir mortality because of predation from piscivorous fish. However, recent studies have also found that juvenile Chinook salmon experience high infection rates from parasitic copepods ( Salmincola californiensis ), which are known to negatively affect performance and survival. Our study was conducted to determine if the PBT N-mixture model could separately estimate mortality because of predation from non-native fish and mortality resulting from copepod infection. This assessment was conducted in two parts: (1) data collected in Lookout Point Reservoir during 2018 were re-analyzed; and (2) a simulation was conducted to evaluate a multi-year study that included inter-annual variation in copepod infection rate and two subsampling strategies (10 fish per month, 30 fish per month) to characterize monthly copepod infection rate. Results from each of these efforts suggest that the survival model is unlikely to provide reliable survival estimates for the two mortality sources that we evaluated. The re-analysis of 2018 data showed that “predation only” and “copepod only” models estimated a negative coefficient for the respective covariate, but the model that included both covariates provided coefficient estimates that differed from the other models and were highly uncertain. Similarly, the simulation results showed that most models failed to correctly estimate the magnitude and direction of mortality due to predation and copepods. These results suggest that additional data will be required if a model is desired that can separately estimate mortality effects due to both predation and copepods in the future. The existing data are limited by factors including low detection probabilities from previous field studies, existing uncertainties about copepod effects on mortality in a natural setting and expected limitations in the number of years that a field study could realistically be expected to receive funding.

Oregon↗

Effects of Coralliophila violacea on tissue loss in the scleractinian corals Porites spp. depend on host response

We investigated interactions between the corallivorous gastropod Coralliophila violacea and its preferred hosts Porites spp. Our objectives were to experimentally determine whether tissue loss could progress in Porites during or after Coralliophila predation on corals with and without tissue loss and to histologically document snail predation. In 64% of feeding scars, tissue regenerated within 3 wk, leaving no trace of predation. However, in roughly 28% of scars, lesions progressed to subacute tissue loss resembling white syndrome. In feeding experiments, scars from snails previously fed diseased tissue developed progressive tissue loss twice as frequently as scars from snails previously fed healthy tissue. Scars from previously healthy-fed snails were 3 times as likely to heal as those from previously diseased-fed snails. Histology revealed marked differences in host responses to snails; P. cylindrica manifested a robust inflammatory response with fewer secondary colonizing organisms such as algae, sponges, and helminths, whereas P. rus showed no evident inflammation and more secondary colonization. We conclude that lesion progression associated with Coralliophila may be associated with secondary colonization of coral tissues damaged by predator-induced trauma and necrosis. Importantly, variation at the cellular level should be considered when explaining interspecific differences in host responses in corals impacted by phenomena such as predation.

Diseases of Aquatic Organisms↗

Effects of marine reserves and urchin disease on southern Californian rocky reef communities

While the species level effects of marine reserves are widely recognized, community level shifts due to marine reserves have only recently been documented. Protection from fishing of top predators may lead to trophic cascades, which have community-wide implications. Disease may act in a similar manner, regulating population levels of dominant species within a community. Two decades of data from the Channel Islands National Park Service's Kelp Forest Monitoring database allowed us to compare the effects of fishing and urchin disease on rocky reef community patterns and dynamics. Different size-frequency distributions of urchins inside and outside of reserves indicated reduced predation on urchins at sites where fishing removes urchin predators. Rocky reefs inside reserves were more likely to support kelp forests than were fished areas. We suggest that this results from cascading effects of the fishery on urchin predators outside the reserves, which releases herbivores (urchins) from predation. After periods of prevalent urchin disease, the reef community shifted more towards kelp forest assemblages. Specific groups of algae and invertebrates were associated with kelp forest and barrens communities. The community dynamics leading to transitions between kelp forests and barrens are driven by both fishing and disease; however the fishery effect was of greater magnitude. This study further confirms the importance of marine reserves not only for fisheries conservation, but also for the conservation of historically dominant community types.

Marine Ecology Progress Series↗

Effect of invasive plant removal on the density of Peromyscus sonoriensis (western deer mice) in Point Reyes National Seashore, California, USA.

Non-native plants can affect communities through direct competition, and by providing refuge to seed predators, creating apparent competition with native plants. Ammophila arenaria (European beachgrass) has been introduced to coastal dune habitats throughout the western United States where it forms dense monocultures, stabilizes dunes, and alters abiotic and biotic conditions. The dominance of European beachgrass has been linked to declines of Lupinus tidestromii (Tidestrom’s lupine), an herb endemic to coastal dune communities in central and northern California. Peromyscus sonoriensis (western deer mice), a native seed predator, use beachgrass as refuge from predators. Tidestrom’s lupine plants near European beachgrass stands experience greater predation pressure from deer mice. At Point Reyes National Seashore, California, USA (PRNS), mechanical removal, manual pulling, and herbicide treatment have been used to reduce the density of European beachgrass near Tidestrom’s lupine populations. We trapped deer mice at five sites in PRNS that experienced different management regimes and used spatially-explicit capture-recapture models to estimate deer mouse density as a function of site and habitat treatment. We found that deer mouse density was lowest in areas where European beachgrass was mechanically removed and in herbicide-treated foredunes, and highest in areas highly invaded by European beachgrass and Carpobrotus spp. (iceplant). The density of deer mice increased from 2021 to 2022 at every site except one that underwent extensive mechanical removal of European beachgrass from 2010-2011. This study shows enduring effects of European beachgrass removal on the density of a native seed predator and highlights the importance of habitat management for conservation of Tidestrom’s lupine.

California↗

Learning to be different: Acquired skills, social learning, frequency dependence, and environmental variation can cause behaviourally mediated foraging specializations

Question: How does the ability to improve foraging skills by learning, and to transfer that learned knowledge, affect the development of intra-population foraging specializations? Features of the model: We use both a state-dependent life-history model implemented by stochastic dynamic programming (SDPM) and an individual-based model (IBM) to capture the dynamic nature of behavioural preferences in feeding. Variables in the SDPM include energy reserves, skill levels, energy and handling time per single prey item, metabolic rate, the rates at which skills are learned and forgotten, the effect of skills on handling time, and the relationship between energy reserves and fitness. Additional variables in the IBM include the probability of successful weaning, the logistic dynamics of the prey species with stochastic recruitment, the intensity of top-down control of prey by predators, the mean and variance in skill levels of new recruits, and the extent to which learned Information can be transmitted via matrilineal social learning. Key range of variables: We explore the effects of approaching the time horizon in the SDPM, changing the extent to which skills can improve with experience, increasing the rates of learning or forgetting of skills, changing whether the learning curve is constant, accelerating (T-shaped) or decelerating ('r'-shaped), changing both mean and maximum possible energy reserves, changing metabolic costs of foraging, and changing the rate of encounter with prey. Conclusions: The model results show that the following factors increase the degree of prey specialization observed in a predator population: (1) Experience handling a prey type can substantially improve foraging skills for that prey. (2) There is limited ability to retain complex learned skills for multiple prey types. (3) The learning curve for acquiring new foraging skills is accelerating, or J-shaped. (4) The metabolic costs of foraging are high relative to available energy reserves. (5) Offspring can learn foraging skills from their mothers (matrilineal social learning). (6) Food abundance is limited, such that average individual energy reserves are low Additionally, the following factors increase the likelihood of alternative specializations co-occurring in a predator population: (1) The predator exerts effective top-down control of prey abundance, resulting in frequency-dependent dynamics. (2) There is stochastic Variation in prey population dynamics, but this Variation is neither too extreme in magnitude nor too 'slow' with respect to the time required for an individual forager to learn new foraging skills. For a given predator population, we deduce that the degree of specialization will be highest for those prey types requiring complex capture or handling skills, while prey species that are both profitable and easy to capture and handle will be included in the diet of all individuals. Frequency-dependent benefits of selecting alternative prey types, combined with the ability of foragers to improve their foraging skills by learning, and transmit learned skills to offspring, can result in behaviourally mediated foraging specialization, and also lead to the co-existence of alternative specializations. The extent of such specialization is predicted to be a variable trait, increasing in locations or years when intra-specific competition is high relative to inter-specific competition. ?? 2009 M. Tim Tinker.

Evolutionary Ecology Research↗

Loss and modification of habitat

Amphibians live in a wide variety of habitats around the world, many of which have been modified or destroyed by human activities. Most species have unique life history characteristics adapted to specific climates, habitats (e.g., lentic, lotic, terrestrial, arboreal, fossorial, amphibious), and local conditions that provide suitable areas for reproduction, development and growth, shelter from environmental extremes, and predation, as well as connectivity to other populations or habitats. Although some species are entirely aquatic or terrestrial, most amphibians, as their name implies, lead a dual life and require a mosaic of habitats in both aquatic and terrestrial ecosystems. With over 6 billion people on Earth, most species are now persisting in habitats that have been directly or indirectly influenced by human activities. Some species have disappeared where their habitats have been completely destroyed, reduced, or rendered unsuitable. Habitat loss and degradation are widely considered by most researchers as the most important causes of amphibian population decline globally (Barinaga 1990; Wake and Morowitz 1991; Alford and Richards 1999). In this chapter, a background on the diverse habitat requirements of amphibians is provided, followed by a discussion of the effects of urbanization, agriculture, livestock grazing, timber production and harvesting, fire and hazardous fuel management, and roads on amphibians and their habitats. Also briefly discussed is the influence on amphibian habitats of natural disturbances, such as extreme weather events and climate change, given the potential for human activities to impact climate in the longer term. For amphibians in general, microhabitats are of greater importance than for other vertebrates. As ectotherms with a skin that is permeable to water and with naked gelatinous eggs, amphibians are physiologically constrained to be active during environmental conditions that provide appropriate body temperatures and adequate water balance (Thorson and Svihla 1943; Brattstrom 1963; Tracy 1976). Hence, individuals require and seek specific microhabitats that maintain their preferred body temperature while at the same time reducing water loss or allowing individuals to re-hydrate. Amphibians also possess relatively few physical attributes that protect them from predators. Although they may avoid predators behaviourally or deter them by skin toxins, amphibians lack defensive shells or hardened cuticles, do not have protective teeth or claws, and most are insufficiently fast to escape predators. Hence, they are relatively dependent on sites that conceal or protect them from predation. Most amphibians also differ significantly from other vertebrates in possessing a complex two-phase life cycle: the pre-metamorphic larval (tadpole) stage and the post-metamorphic juvenile and adult stage (Wilbur 1980, 1984). Most amphibian species have two distinct econes (Heatwole 1989), each with different habitat requirements, the larvae being aquatic and the post-metamorphic animals more terrestrial. The habitats required by the two phases can differ greatly, but both are essential to the survival of a species. However, amphibian diversity is great and exceptions to this general pattern exist. For example, some species have direct development without going through a larval stage and are fully terrestrial, whereas the larvae of other species can reach sexual maturity without going through metamorphosis (i.e., neoteny) and are fully aquatic.

Book chapter↗