scholarly journals A fish for all seasons: Spatial and temporal variation in patterns of demographic heterogeneity for Retropinna retropinna

2021 ◽  
Author(s):  
◽  
Christopher McDowall

<p>Demographic heterogeneity can have big effects on population dynamics, but for most species we have limited understanding of how and why individuals vary. Variation among individuals is of particular importance for stage-structured populations, and/or where species have ‘complex life-cycles’. This is especially relevant in the case of amphidromous fishes that typically spawn in river mouths and estuaries, develop at sea and return to freshwater to finish development. These fish face strong selection pressures as they negotiate challenges around dispersal and development in order to reproduce successfully. Quantifying variation amongst individual fish can improve understanding of their population dynamics and suggest possible drivers of variation.  I evaluate patterns and sources of variation in demographic attributes of the New Zealand smelt (Retropinna retropinna). R. retropinna is an amphidromous fish that is endemic to New Zealand. While most populations have a sea-going larval stage, a number of landlocked freshwater populations occur, with the largest landlocked population residing in Lake Taupo. Here R. retropinna are presented with a variety of littoral feeding/spawning habitats and environmental conditions that may vary across distinct regions of the lake. In addition, the protracted spawning period for this species in Lake Taupo (occurring over eight months of the year) provides additional scope for seasonal variation to influence demographic attributes of individuals.  I sampled R. retropinna from discrete coastal habitats (beach or river) that were located in the eastern, southern and western regions of the lake. I evaluated patterns of variation in the size-structure, age-structure and morphology of R. retropinna among habitats and/or regions across Lake Taupo. I used otoliths to reconstruct demographic histories (ages, growth rates, hatch dates) of individuals, and used a set of statistical models to infer spatial variation in demographic histories. I found differences in size and age structure between regions, and a temporal effect of hatch date on larval/juvenile growth rates.  In addition, I obtained samples of R. retropinna from a sea-going population at the Hutt river mouth (sampled fish were presumed to be migrating upstream after their development period in Wellington Harbour and/or adjacent coastal environments). While Lake Taupo is large, deep, fresh, oligotrophic and strongly stratified for 8-9 months outside of winter, Wellington Harbour is less than a sixth of the area, shallow, saline, eutrophic and never stratified. These greatly differing environmental conditions led me to expect that these systems’ R. retropinna populations would carry significantly different demographic attributes. I compared the hatching phenology, recruitment age, body morphology, and individual growth histories (reconstructed from otoliths) of R. retropinna sampled from Lake Taupo and Wellington Harbour. I explored the relationships between demographic variation and environmental variation (water temperature, chlorophyll a) for the two systems and found that this additional environmental information could account for much of the seasonal variation in daily otolith increment widths of R. retropinna. My results also suggest that while the two sampled populations likely share similar hatching and spawning phenologies, individuals from Lake Taupo tend to grow more slowly, particularly during winter, and end up smaller than sea-going fish sampled near Wellington. I speculate that these differences reflect variation in food supply (zooplankton may be limited in Lake Taupo over winter).  Overall, my results demonstrate a high degree of variation in morphological and life-history traits within a single species, potentially driven by an interaction between environmental variation and timing of development. My work contributes to a growing body of literature on demographic heterogeneity, and may help to inform the management of landlocked populations of R. retropinna in Lake Taupo.</p>

2021 ◽  
Author(s):  
◽  
Christopher McDowall

<p>Demographic heterogeneity can have big effects on population dynamics, but for most species we have limited understanding of how and why individuals vary. Variation among individuals is of particular importance for stage-structured populations, and/or where species have ‘complex life-cycles’. This is especially relevant in the case of amphidromous fishes that typically spawn in river mouths and estuaries, develop at sea and return to freshwater to finish development. These fish face strong selection pressures as they negotiate challenges around dispersal and development in order to reproduce successfully. Quantifying variation amongst individual fish can improve understanding of their population dynamics and suggest possible drivers of variation.  I evaluate patterns and sources of variation in demographic attributes of the New Zealand smelt (Retropinna retropinna). R. retropinna is an amphidromous fish that is endemic to New Zealand. While most populations have a sea-going larval stage, a number of landlocked freshwater populations occur, with the largest landlocked population residing in Lake Taupo. Here R. retropinna are presented with a variety of littoral feeding/spawning habitats and environmental conditions that may vary across distinct regions of the lake. In addition, the protracted spawning period for this species in Lake Taupo (occurring over eight months of the year) provides additional scope for seasonal variation to influence demographic attributes of individuals.  I sampled R. retropinna from discrete coastal habitats (beach or river) that were located in the eastern, southern and western regions of the lake. I evaluated patterns of variation in the size-structure, age-structure and morphology of R. retropinna among habitats and/or regions across Lake Taupo. I used otoliths to reconstruct demographic histories (ages, growth rates, hatch dates) of individuals, and used a set of statistical models to infer spatial variation in demographic histories. I found differences in size and age structure between regions, and a temporal effect of hatch date on larval/juvenile growth rates.  In addition, I obtained samples of R. retropinna from a sea-going population at the Hutt river mouth (sampled fish were presumed to be migrating upstream after their development period in Wellington Harbour and/or adjacent coastal environments). While Lake Taupo is large, deep, fresh, oligotrophic and strongly stratified for 8-9 months outside of winter, Wellington Harbour is less than a sixth of the area, shallow, saline, eutrophic and never stratified. These greatly differing environmental conditions led me to expect that these systems’ R. retropinna populations would carry significantly different demographic attributes. I compared the hatching phenology, recruitment age, body morphology, and individual growth histories (reconstructed from otoliths) of R. retropinna sampled from Lake Taupo and Wellington Harbour. I explored the relationships between demographic variation and environmental variation (water temperature, chlorophyll a) for the two systems and found that this additional environmental information could account for much of the seasonal variation in daily otolith increment widths of R. retropinna. My results also suggest that while the two sampled populations likely share similar hatching and spawning phenologies, individuals from Lake Taupo tend to grow more slowly, particularly during winter, and end up smaller than sea-going fish sampled near Wellington. I speculate that these differences reflect variation in food supply (zooplankton may be limited in Lake Taupo over winter).  Overall, my results demonstrate a high degree of variation in morphological and life-history traits within a single species, potentially driven by an interaction between environmental variation and timing of development. My work contributes to a growing body of literature on demographic heterogeneity, and may help to inform the management of landlocked populations of R. retropinna in Lake Taupo.</p>


2014 ◽  
Vol 71 (8) ◽  
pp. 1198-1208 ◽  
Author(s):  
Douglas C. Braun ◽  
John D. Reynolds

Understanding linkages among life history traits, the environment, and population dynamics is a central goal in ecology. We compared 15 populations of sockeye salmon (Oncorhynchus nerka) to test general hypotheses for the relative importance of life history traits and environmental conditions in explaining variation in population dynamics. We used life history traits and habitat variables as covariates in mixed-effect Ricker models to evaluate the support for correlates of maximum population growth rates, density dependence, and variability in dynamics among populations. We found dramatic differences in the dynamics of populations that spawn in a small geographical area. These differences among populations were related to variation in habitats but not life history traits. Populations that spawned in deep water had higher and less variable population growth rates, and populations inhabiting streams with larger gravels experienced stronger negative density dependence. These results demonstrate, in these populations, the relative importance of environmental conditions and life histories in explaining population dynamics, which is rarely possible for multiple populations of the same species. Furthermore, they suggest that local habitat variables are important for the assessment of population status, especially when multiple populations with different dynamics are managed as aggregates.


Parasitology ◽  
1987 ◽  
Vol 94 (1) ◽  
pp. 181-197 ◽  
Author(s):  
M. G. Roberts ◽  
J. R. Lawson ◽  
M. A. Gemmell

SUMMARYIt is shown that under the conditions that prevailed in New Zealand in the late 1950s, Taenia hydatigena was hyperendemic, the life-cycle being regulated by a density-dependent constraint in the form of acquired immunity, and T. ovis was rare. The control measures that caused Echinococcus granulosus, which was endemic at the time, to decline towards extinction reduced T. hydatigena and T. ovis to endemic status only. A non-linear integrodifferential equation model, which was previously linearized to describe the life-cycle of E. granulosus in dogs and sheep in New Zealand, is used to describe the life-cycles of T. hydatigena and T. ovis. The model is then used to compare and contrast the population dynamics of these three species. The model is used to demonstrate that the endemic steady state is structurally unstable, and may be asymptotically unstable to small perturbations. It is also shown that despite the lower infection pressure experienced by the intermediate host in the endemic state, the numbers of larvae in sheep may be higher than in the hyperendemic state. Finally it is shown that the partial success of the control measures against T. hydatigena may have caused an increase in the numbers and prevalence of T. ovis larvae in sheep due to the reciprocal immunity between the two species.


PLoS ONE ◽  
2021 ◽  
Vol 16 (6) ◽  
pp. e0252748
Author(s):  
Nathan J. Hostetter ◽  
Nicholas J. Lunn ◽  
Evan S. Richardson ◽  
Eric V. Regehr ◽  
Sarah J. Converse

Understanding the influence of individual attributes on demographic processes is a key objective of wildlife population studies. Capture-recapture and age data are commonly collected to investigate hypotheses about survival, reproduction, and viability. We present a novel age-structured Jolly-Seber model that incorporates age and capture-recapture data to provide comprehensive information on population dynamics, including abundance, age-dependent survival, recruitment, age structure, and population growth rates. We applied our model to a multi-year capture-recapture study of polar bears (Ursus maritimus) in western Hudson Bay, Canada (2012–2018), where management and conservation require a detailed understanding of how polar bears respond to climate change and other factors. In simulation studies, the age-structured Jolly-Seber model improved precision of survival, recruitment, and annual abundance estimates relative to standard Jolly-Seber models that omit age information. Furthermore, incorporating age information improved precision of population growth rates, increased power to detect trends in abundance, and allowed direct estimation of age-dependent survival and changes in annual age structure. Our case study provided detailed evidence for senescence in polar bear survival. Median survival estimates were lower (<0.95) for individuals aged <5 years, remained high (>0.95) for individuals aged 7–22 years, and subsequently declined to near zero for individuals >30 years. We also detected cascading effects of large recruitment classes on population age structure, which created major shifts in age structure when these classes entered the population and then again when they reached prime breeding ages (10–15 years old). Overall, age-structured Jolly-Seber models provide a flexible means to investigate ecological and evolutionary processes that shape populations (e.g., via senescence, life expectancy, and lifetime reproductive success) while improving our ability to investigate population dynamics and forecast population changes from capture-recapture data.


Parasitology ◽  
1974 ◽  
Vol 69 (3) ◽  
pp. 361-371 ◽  
Author(s):  
G. A. Boxshall

The ectoparasitic copepod Lepeophtheirus pectoralis exhibited a regular annual cycle of abundance on its hosts. Both the incidence and intensity of infection were greatest in August or September and both declined over winter to their minimum values in April. Very similar cycles were observed in both 1972 and 1973. Analysis of the age structure of the parasite population showed that the increase in abundance coincided with the onset of the breeding season. Although females always outnumbered males the sex ratio approached unity during the breeding season, which extended from May to October. Copulating pairs were most commonly observed during this period.There was a marked bimodal peak of egg production each year, with the first mode occurring around May and the second mode around August or September. This pattern was produced by a system of alternation of generations operating within the parasite population, with a summer type generation (distinguishable by its rapid maturation rate and reduced longevity) alternating with an overwintering type of generation.


2014 ◽  
Vol 8 ◽  
Author(s):  
Sinéad Murphy ◽  
Matthew Perrott ◽  
Jill McVee ◽  
Fiona L Read ◽  
Karin A Stockin

Knowledge of age structure and longevity (maximum age) are essential for modelling marine mammal population dynamics. Estimation of age in common dolphins (Delphinus spp.) is primarily based on counting Growth Layer Groups (GLGs) in the dentine of thin, decalcified and stained sections of teeth. An annual incremental deposition rate was validated for Delphinus spp. 30-years ago through the use of tetracycline. However, it is not known if the pulp cavity becomes occluded in older individuals or GLGs continue to be deposited in dentine tissue. To investigate the deposition of GLGs in dentine tissue, teeth samples were obtained during the necropsies of two short-beaked common dolphins (Delphinus delphis) that were held in captivity for 31 and 33 years in New Zealand. Individuals were captured together in Hawkes Bay, North Island, New Zealand and classified as juveniles based on physical appearance. Teeth were processed in two ageing laboratories, using four different bone decalcifiers, two sectioning techniques incorporating the use of both a freezing microtome (-20°C) and paraffin microtome, and two different stains. An age was estimated for one of the dolphins, in line with that proposed based on estimated age at capture and period in captivity. However, a hypomineralised area was observed in the dentine tissue close to the pulp cavity of the second individual, preventing estimation of maximum age. The presence and structure of this anomaly is explored further within the study. 


Respirology ◽  
2000 ◽  
Vol 5 (3) ◽  
pp. 241-246 ◽  
Author(s):  
Mona Kimbell‐Dunn ◽  
Neil Pearce ◽  
Richard Beasley

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