scholarly journals Effects of life history stage and climatic conditions on fecal egg counts in plains zebras (Equus quagga) in the Serengeti National Park

2020 ◽  
Vol 119 (10) ◽  
pp. 3401-3413
Author(s):  
Peter A. Seeber ◽  
Tetiana A. Kuzmina ◽  
Alex D. Greenwood ◽  
Marion L. East

Abstract In wildlife, endoparasite burden can be affected by host life history stage, environmental conditions, host abundance, and parasite co-infections. We tested the effects of these factors on gastrointestinal parasite infection in plains zebras (Equus quagga) in the Serengeti ecosystem, Tanzania, using fecal egg counts of two nematode families (Strongylidae and Ascarididae) and the presence/absence of cestode (Anoplocephalidae) eggs. We predicted higher egg counts of Strongylidae and Ascarididae, and increased likelihood of Anoplocephalidae infection in individuals (1) during energetically costly life history stages when resource allocation to immune processes may decrease and in young zebras after weaning because of increased uptake of infective stages with forage, (2) when climatic conditions facilitate survival of infective stages, (3) when large zebra aggregations increase forage contamination with infective stages, and (4) in individuals co-infected with more than one parasite group as this may indicate reduced immune competence. Strongylidae egg counts were higher, and the occurrence of Anoplocephalidae eggs was more likely in bachelors than in band stallions, whereas Ascarididae egg counts were higher in band stallions. Strongylidae and Ascarididae egg counts were not increased in lactating females. Strongylidae egg counts were higher in subadults than in foals. Regardless of sex and age, Ascarididae infections were more likely under wet conditions. Co-infections did not affect Strongylidae egg counts. Ascarididae egg counts in adult females were higher when individuals were co-infected with Anoplocephalidae. We present evidence that parasite burdens in plains zebras are affected by life history stage, environmental conditions, and co-infection.

2007 ◽  
Vol 363 (1490) ◽  
pp. 425-441 ◽  
Author(s):  
John C Wingfield

The majority of vertebrates have a life span of greater than one year. Therefore individuals must be able to adapt to the annual cycle of changing conditions by adjusting morphology, physiology and behaviour. Phenotypic flexibility, in which an individual switches from one life history stage to another, is one way to maximize fitness in a changing environment. When environmental variation is low, few life history stages are needed. If environmental variation is large, there are more life history stages. Each life history stage has a characteristic set of sub-stages that can be expressed in various combinations and patterns to determine state at any point in the life of the individual. Thus individuals have a finite number of states that can be expressed over the spectrum of environmental conditions in their life spans. Life history stages have three phases–development, mature capability (when characteristic sub-stages can be expressed) and termination. Expression of a stage is time dependent (probably a minimum of one month), and termination of one stage overlaps development of the next stage. It follows that the more life history stages an individual expresses, the less flexibility it will have in timing those stages. Having fewer life history stages increases flexibility in timing, but less tolerance of variation in environmental conditions. To varying degrees it is possible to overlap mature capability of some life history stages to effectively reduce ‘finite stage diversity’ and maximize flexibility in timing. Theoretical ways by which this can be done, and the implications for neuroendocrine and endocrine control mechanisms are discussed. Twelve testable hypotheses are posed that relate directly to control mechanisms.


2017 ◽  
Vol 372 (1723) ◽  
pp. 20160140 ◽  
Author(s):  
John C. Wingfield ◽  
Jonathan H. Pérez ◽  
Jesse S. Krause ◽  
Karen R. Word ◽  
Paulina L. González-Gómez ◽  
...  

As global climate change progresses, the occurrence of potentially disruptive climatic events such as storms are increasing in frequency, duration and intensity resulting in higher mortality and reduced reproductive success. What constitutes an extreme climatic event? First we point out that extreme climatic events in biological contexts can occur in any environment. Focusing on field and laboratory data on wild birds we propose a mechanistic approach to defining and investigating what extreme climatic events are and how animals cope with them at physiological and behavioural levels. The life cycle of birds is made up of life-history stages such as migration, breeding and moult that evolved to match a range of environmental conditions an individual might expect during the year. When environmental conditions deteriorate and deviate from the expected range then the individual must trigger coping mechanisms (emergency life-history stage) that will disrupt the temporal progression of life-history stages, but enhance survival. Using the framework of allostasis, we argue that an extreme climatic event in biological contexts can be defined as when the cumulative resources available to an individual are exceeded by the sum of its energetic costs—a state called allostatic overload. This allostatic overload triggers the emergency life-history stage that temporarily allows the individual to cease regular activities in an attempt to survive extreme conditions. We propose that glucocorticoid hormones play a major role in orchestrating coping mechanisms and are critical for enduring extreme climatic events. This article is part of the themed issue ‘Behavioural, ecological and evolutionary responses to extreme climatic events’.


2020 ◽  
Vol 639 ◽  
pp. 185-197 ◽  
Author(s):  
MJ Malick ◽  
ME Hunsicker ◽  
MA Haltuch ◽  
SL Parker-Stetter ◽  
AM Berger ◽  
...  

Environmental conditions can have spatially complex effects on the dynamics of marine fish stocks that change across life-history stages. Yet the potential for non-stationary environmental effects across multiple dimensions, e.g. space and ontogeny, are rarely considered. In this study, we examined the evidence for spatial and ontogenetic non-stationary temperature effects on Pacific hake Merluccius productus biomass along the west coast of North America. Specifically, we used Bayesian additive models to estimate the effects of temperature on Pacific hake biomass distribution and whether the effects change across space or life-history stage. We found latitudinal differences in the effects of temperature on mature Pacific hake distribution (i.e. age 3 and older); warmer than average subsurface temperatures were associated with higher biomass north of Vancouver Island, but lower biomass offshore of Washington and southern Vancouver Island. In contrast, immature Pacific hake distribution (i.e. age 2) was better explained by a nonlinear temperature effect; cooler than average temperatures were associated with higher biomass coastwide. Together, our results suggest that Pacific hake distribution is driven by interactions between age composition and environmental conditions and highlight the importance of accounting for varying environmental effects across multiple dimensions.


2015 ◽  
Vol 66 (5) ◽  
pp. 399 ◽  
Author(s):  
Peter M. Yates ◽  
Michelle R. Heupel ◽  
Andrew J. Tobin ◽  
Stephen K. Moore ◽  
Colin A. Simpfendorfer

Effective conservation and management of shark populations is complicated by our limited understanding of their spatial ecology. For example, there are scarce data on diversity in community structure and nursery function across broader geographic scales (e.g. across multiple inshore systems) and the implications of this diversity for shark populations. Accordingly, fishery-independent surveys were undertaken to investigate shark communities along ~400km of the tropical eastern coast of Australia (18.1–20.6°S, 146.0–148.8°E). A variety of shark species were encountered, with 19 species of Carcharhiniformes contributing 99.2% of the total shark catch. Of the 1806 sharks captured, 567 were immature, including 336 young-of-the-year individuals. Immature sharks from 18 species were present; however, interspecific variation in the proportions of life-history stages was apparent. Multivariate analyses identified significant spatial heterogeneity in immature-shark communities. Results also highlighted the importance of tropical coastal habitats for numerous shark species, and indicated community-wide spatial structuring of sharks on the basis of body size rather than life-history stage. In addition to building on traditional shark-nursery paradigms, these results demonstrated that data on nursery function from restricted areas may not accurately portray patterns occurring over broader geographic scales, and this diversity may provide population-level benefits for sharks.


<em>Abstract.</em>—Pacific salmon <em>Oncorhynchus </em>spp. are important components of numerous food webs throughout their life history, yet we know very little about the historic and current abundance of these life history stages. We used past cannery records, recent harvest and hatchery records, and salmon life history information drawn from the literature to construct a simple bioregional model of historic and recent salmon abundance at egg, fry, smolt, ocean adult, and spawning stages for five species of Pacific salmon from Alaska to California. We found a historic-to-recent bioregional decline in salmon biomass in all life history stages. Recent salmon egg, fry, smolt, ocean-going adult, and escapement biomass estimates for northwestern North America are 74%, 55%, 59%, 86%, and 35%, respectively, of historic levels. Recent high productivity in Alaskan waters, however, masks a precipitous decline south of Alaska, where recent egg, fry, smolt, ocean-going adult, and escapement biomass levels are 34%, 23%, 50%, 40%, and 15% that of historic levels. Adult production and harvest levels are no longer sufficient measures of salmon management success. Researchers need to quantify and elucidate the ecosystem effects of historic biomass changes in life history stages of Pacific salmon on a watershed basis. Fisheries managers must set and meet specific targets for salmon life history stage abundance—from egg to spawning adult—to restore and maintain ecosystem function.


2021 ◽  
Author(s):  
◽  
Melissa Marquez

<p>Over the last few decades, much effort has been devoted towards evaluating and reducing bycatch in marine fisheries. There has been a particular focus on quantifying the risk to chondrichthyans, primarily because of their relatively high vulnerability to overfishing. A key part of risk assessment is evaluating the distributional overlap of the fish with the fisheries, where fish distribution is influenced by habitat use. I synthesised published observations of habitat use for different life history stages of chondrichthyans and hypothesised the associated catch composition in terms of fish sex, size, and maturity. I then searched for these catch compositions, and thereby locations, using New Zealand research vessel catch data. Results show that some life history stages and habitats for certain species can be identified, whereas others could not. Pupping ground criteria were met for Callorhynchus milii (ELE), Hydrolagus novaezealandiae (GSH), and Hydrolagus bemisi (GSP); nursery ground criteria were met for Callorhynchus milii (ELE), mating ground criteria were met for Callorhynchus milii (ELE), Hydrolagus novaezealandiae (GSH), Hydrolagus bemisi (GSP), and Harriotta raleighana (LCH); lek-like mating criteria were met for Hydrolagus novaezealandiae (GSH). For those life-history stage habitats not found, this may be because these are outside of the coverage of the data set (and likely also commercial fisheries), or because they do not actually exist for some chondrichthyans. On the basis of results, I propose to change the order of species in the New Zealand qualitative (Level 1) risk assessment, and rise the relative risk for Hydrolagus bemisi (GSP), given the species vulnerability of pupping grounds.</p>


Author(s):  
Gary M. Fellers ◽  
Patrick M. Kleeman ◽  
David A. W. Miller

We estimated wetland occupancy and population trends for three species of pond-breeding anurans in Yosemite National Park from 2007 – 2011. We used a double survey technique in which two observers independently surveyed each site on the same day. Double surveys allowed us to calculate detectability for the three most common anurans within the park: Rana sierrae, Anaxyrus canorus, and Pseudacris regilla. Annual estimates of detectability were generally high; mean detectability ranged from 73.7% + 0.6 (SE) for any life history stage of A. canorus to 86.7% + 0.7 for sites with P. regilla reproduction (eggs or larvae present). Detectability was most variable for Anaxyrus canorus, which ranged from 45.9% to 99.7%. The probability of occupancy for R. sierrae was highest in larger, low-elevation wetlands that lacked fish. Anaxyrus canorus were more common in shallow high-elevation ponds; their occurrence was minimally impacted by the presence of fish. Finally, occurrence of P. regilla was largely unrelated to wetland size and elevation, but like R. sierrae, they were less likely to occupy sites with fish. Occupancy showed no trend over the five years of our study for R. sierrae or A. canorus when considering either sites with any life stage or only sites with reproduction. However, P. regilla showed a modest downward trend for sites with any life stage and sites with reproduction. Our results for R. sierrae run counter to expectations given recent concern about the decline of this species, while our findings for P. regilla raise concerns for this widespread and generally common species.


2001 ◽  
Vol 58 (2) ◽  
pp. 375-385 ◽  
Author(s):  
Katriona Shea ◽  
Marc Mangel

Populations of coho salmon (Oncorhynchus kisutch) in California are listed as threatened under the U.S. Endangered Species Act. Such listings refer to adult populations, but often, juvenile life history stages are censused, so it is important to understand what affects the relationship between true adult and observed juvenile numbers. We present models to address how observational uncertainty, census length, and autocorrelation in vital rates affect our ability to observe trends. We ask two questions about our ability to detect declines in one life history stage from censuses of another. First, given an observed decline in parr numbers, what is the chance that this reflects a decline in adults? Second, given that adult numbers are declining, what is the chance that we see that decline in parr? Our results indicate that statistical power decreases with increasing observational uncertainty and decreasing census lengths and demonstrate how these two parameters interact. Power increases as the level of autocorrelation in mortality rates increases. Management recommendations include obtaining more accurate estimates of autocorrelation in mortality and of observational uncertainty.


2008 ◽  
Vol 4 (5) ◽  
pp. 468-471 ◽  
Author(s):  
Jonathan H Pérez ◽  
Daniel R Ardia ◽  
Elise K Chad ◽  
Ethan D Clotfelter

Investment in one life-history stage can have delayed effects on subsequent life-history stages within a single reproductive bout. We experimentally heated tree swallow ( Tachycineta bicolor ) nests during incubation to test for effects on parental and nestling conditions. Females incubating in heated boxes maintained higher body condition and fed nestlings at higher rates. We cross-fostered nestlings and found that young nestlings (4–7 days old) incubated in heated nests had higher body condition and body mass, regardless of treatment status of their rearing parent. However, older nestlings which were fed by heated females maintained higher condition and body mass regardless of treatment status of their incubating parent. These results indicate that investment in one life-history stage can have multiple pathways of carry-over effects on future life-history stages.


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