Survival, breeding probability and reproductive success in relation to population dynamics of Brandt's CormorantsPhalacrocorax penicillatus

Bird Study ◽  
1999 ◽  
Vol 46 (sup1) ◽  
pp. S92-S103 ◽  
Author(s):  
Nadav Nur ◽  
William J. Sydeman
2004 ◽  
Vol 26 (1) ◽  
pp. 45 ◽  
Author(s):  
AD Bilton ◽  
DB Croft

Female reproductive success and the recruitment of offspring to the next generation are key components of animal population dynamics. With an annual commercial harvest of between 13 and 22% of the red kangaroo (Macropus rufus) population, it is increasingly important that these processes are understood. We used data on the reproductive success of 33 free-ranging female M. rufus on Fowlers Gap station in far western New South Wales to determine the expected lifetime reproductive success (LRS) of females within an unharvested population. We also designed a model to generate predictions about female LRS incorporating empirical relationships between a mother?s reproductive success and maternal age, environmental conditions and the sex and survivorship of a previous reproductive attempt. Results from observations on female LRS (calculated from annual weaning rates) and those generated by the model predict that female M. rufus on ?Fowlers Gap? wean, on average, 3.7 young in a lifetime (ranges 0 - 11 and 0 - 20, respectively); representing only 41% of their maximum reproductive potential. Manipulation of initial starting conditions allowed the effect of varying environmental conditions on female LRS to be explored. The condition of the environment when females commence breeding does not appear to significantly affect their overall lifetime reproductive output. However, the occurrence of drought does. Females experiencing two droughts in a lifetime did not live as long and weaned fewer offspring and grandoffspring (from their daughters) than those females experiencing only one drought in a lifetime. In addition to the adverse effect of drought on the reproductive success of female M. rufus in this study, we suggest that, given the relatively high and stable population densities of M. rufus on ?Fowlers Gap?, other mechanisms (acting primarily on juvenile survival) must exist which limit population growth.


Author(s):  
Alita Pinter

A variety of hypotheses has been proposed to explain multiannual fluctuations in population density ("cycles") of small rodents (for reviews see Finerty 1980, Taitt and Krebs 1985). Doubtless, such cycles - known since antiquity (Elton 1942) - result from an interaction of a multitude of factors. However, the inability of extant hypotheses, alone or in combination, to explain the causality of cycles rests in no small measure with the fact that long-term studies of the phenomenon are notoriously uncommon.


2003 ◽  
Vol 81 (6) ◽  
pp. 994-1003 ◽  
Author(s):  
Jay E Clark ◽  
Eric C Hellgren ◽  
Eric E Jorgensen ◽  
Susan J Tunnell ◽  
David M Engle ◽  
...  

We conducted a mark–recapture experiment to examine the population dynamics of hispid cotton rats (Sigmodon hispidus) in response to low-level nitrogen amendments (16.4 kg nitrogen/ha per year) and exclosure fencing in an old-field grassland. The experimental design consisted of sixteen 0.16-ha plots with 4 replicates of each treatment combination. We predicted that densities, reproductive success, movement probabilities, and survival rates of cotton rats would be greater on nitrogen-amended plots because of greater aboveground biomass and canopy cover. Population densities of cotton rats tended to be highest on fenced nitrogen plots, but densities on unfenced nitrogen plots were similar to those on control and fenced plots. We observed no distinct patterns in survival rates, reproductive success, or movement probabilities with regard to nitrogen treatments. However, survival rates and reproductive success tended to be higher for cotton rats on fenced plots than for those on unfenced plots and this was likely attributable to decreased predation on fenced plots. As low-level nitrogen amendments continue to be applied, we predict that survival, reproduction, and population-growth rates of cotton rats on control plots, especially fenced plots with no nitrogen amendment, will eventually exceed those on nitrogen-amended plots as a result of higher plant-species diversity, greater food availability, and better quality cover.


Author(s):  
Aelita Pinter

Multiannual fluctuations in population density ("cycles") of small rodents have been known since antiquity (Elton 1942). Numerous hypotheses have been proposed to explain this phenomenon (for reviews see Finerty 1980, Taitt and Krebs 1985). However, none of these hypotheses, alone or in combination, have been able to explain the causality of cycles. The objectives of this long-term study are to determine whether environmental variables, possibly acting through reproductive responses, contribute to the multiannual fluctuations of the montane vole, Microtus montanus.


2021 ◽  
Author(s):  
◽  
Benjamin Moginie

<p>Identifying sources of variation in individual reproductive success is crucial to our understanding of population dynamics and evolutionary ecology. In many systems, the determinants of success are not well known. Where species have parental care, for example, determinants of success can be particularly challenging to partition between parents and offspring. In this thesis I investigate drivers and consequences of variable life histories, for a small reef fish that exhibits male parental care (the common triplefin Forsterygion lapillum). I examined the influence of individual life history, phenotype and behaviour on (1) the performance of recently settled juveniles, and (2) the reproductive success adult males.  I made field-based observations of adult males during the breeding season, measured their phenotypic traits (body size and condition) and used their otoliths to reconstruct life history characteristics (hatch dates and mean growth rates). My life history trait reconstructions suggested two alternate pathways to ’success’ for adult males. Successful males hatched earlier and therefore had a developmental ’head start’ over less successful males (i.e., males with eggs > male territory holders without eggs > floaters). Alternatively, males can apparently achieve success by growing faster: for males born in the same month, those with eggs grew faster than those with territories and no eggs, and both groups grew faster than floaters. These results suggest that accelerated growth rate may mediate the effects of a later hatch date, and that both hatch dates and growth rates influence the success of adult males, likely through proximate effects on individual phenotypes.  Identifying sources of variation in individual reproductive success is crucial to our understanding of population dynamics and evolutionary ecology. In many systems, the determinants of success are not well known. Where species have parental care, for example, determinants of success can be particularly challenging to partition between parents and offspring. Male parental care is common among fishes, where resources such as high quality territories and mates often may be limiting. In such systems, individual success of offspring may result from distinct life history pathways that are influenced by both parental effects (e.g., timing of reproduction) and by the offspring themselves (e.g., ’personalities’). These pathways, in turn, can induce phenotypic variation and affect success later in life. The drivers and consequences of variable life histories are not well understood in the context of reproductive success.  In this thesis I investigate drivers and consequences of variable life histories, for a small reef fish that exhibits male parental care (the common triplefin Forsterygion lapillum). I examined the influence of individual life history, phenotype and behaviour on (1) the performance of recently settled juveniles, and (2) the reproductive success adult males. I made field-based observations of adult males during the breeding season, measured their phenotypic traits (body size and condition) and used their otoliths to reconstruct life history characteristics (hatch dates and mean growth rates). Some males showed no evidence of territorial defence and were defined as ’floaters’; others defended territories, and a subset of these also had nests with eggs present. Adult male body size was significantly higher for males that defended breeding territories, and body condition was significantly higher for the males that had eggs (i.e., had successfully courted females). My otolith-based reconstructions of life history traits suggested two alternate pathways to ’success’ for adult males. Successful males hatched earlier and therefore had a developmental ’head start’ over less successful males (i.e., males with eggs > male territory holders without eggs > floaters). Alternatively, males can apparently achieve success by growing faster: for males born in the same month, those with eggs grew faster than those with territories and no eggs, and both groups grew faster than floaters. These results suggest that accelerated growth rate may mediate the effects of a later hatch date, and that both hatch dates and growth rates influence the success of adult males, likely through proximate effects on individual phenotypes.  I evaluated the effects of variable life history in a complimentary lab-based study. Specifically, I manipulated the developmental environments (feeding regime and temperature) for young fish and evaluated the direct effects on life history traits and phenotypes. Then, I conducted an assay to quantify the indirect effects of developmental environment, life history traits, and phenotypes on aggression and performance of young fish. These developmental environments did not have a clear, overall effect on juvenile phenotype or performance (i.e. behavioural aggression and the ability to dominate a resource). Instead, individuals (irrespective of developmental environment) that grew faster and/or longer pelagic larval durations had increased odds of dominating a limited resource. I attributed the non-significant direct effect of developmental environment to within-treatment mortality and variation among individuals in terms of their realised access to food (i.e., dominance hierarchies were apparent in rearing chambers, suggesting a non-uniform access to food). Fish that were more likely to dominate a resource were also more aggressive (i.e., more likely to engage in chasing behaviours). Fish that were larger and more aggressive established territories that were deemed to be of higher ’quality’ (inferred from percent cover of cobble resources). Overall, this study suggests a complex interplay between social systems, phenotype and life history. Developmental environments may influence phenotypes, although behavioural differences among individuals may moderate that effect, contributing to additional variation in phenotypes and life history traits which, in turn, shape the success of individuals.  Collectively, my thesis emphasises the consequences of life history variability on success at multiple life stages. These results may be relevant to other species that exhibit male parental care or undergo intense competition for space during early life stages. In addition, my results highlight interactions between life history, phenotype and behaviour that can have important implications for population dynamics and evolutionary ecology.</p>


Author(s):  
Aelita Pinter

Multiannual fluctuations in population density of small rodents have been known since antiquity. However, factors responsible for this phenomenon remain unknown (Krebs and Myers 1974, Finerty 1980, Taitt and Krebs 1985). The objectives of this long-term study are to determine whether environmental variables, possibly acting through reproductive responses, contribute to the multiannual fluctuations of the montane vole, Microtus montanus.


Author(s):  
Aelita Pinter

Multiannual fluctuations in population density ("cycles") of small rodents have been known since antiquity (Elton 1942). Numerous hypotheses have been proposed to explain this phenomenon (for reviews see Krebs and Myers 1974, Finery 1980, Taitt and Krebs 1985). However, none of these hypotheses, alone or in combination, can explain the causality of cycles. The objectives of this long-term study are to determine whether environmental variables, possibly acting through reproductive responses, contribute to the multiannual fluctuations of the montane vole, Microtus montanus.


1977 ◽  
Vol 34 (10) ◽  
pp. 1748-1763 ◽  
Author(s):  
William R. Nelson ◽  
Charles H. Walburg

Percid populations have generally increased in abundance relative to other groups of fishes in the 15–25 yr four large reservoirs have been operational on the Missouri River in South Dakota. Saugers (Stizostedion canadense) were initially the most abundant percid, but their numbers gradually declined, probably because of the reduction in river spawning habitat and the increase in water clarity. Yellow perch (Perca flavescens) increased to high population levels as the reservoirs filled but later decreased in abundance. Walleye (S. vitreum vitreum) populations were the slowest to develop in the reservoirs, probably because of initial lack of suitable spawning habitat; they later became well established.The yellow perch was one of the most important forage species in the reservoirs, and walleyes and saugers the primary predator and sport fishes. Sportfishing quality 15–25 yr after impoundment was good, but harvest remained low because of the large size of the reservoirs, inadequacy of facilities for anglers, and the relatively sparse human population. Reproductive success was the primary factor regulating the abundance of percids. Year-class strength was primarily determined by climatic rather than biological factors. Above-average precipitation presumably enhanced reproductive success, both directly by increasing the quantity and quality of spawning substrate through higher stream flows and water levels, and indirectly by providing a larger forage supply, thereby apparently reducing predation on young percids, as well as cannibalism. Kew words: Percidae, reservoirs, Missouri River, Stizostedion, Perca, population dynamics, ecology, precipitation, water level


Author(s):  
Aelita Pinter

Multiannual fluctuations in populations density ("cycles") of small rodents have been long recognized (Elton 1942). Numerous hypotheses have been proposed to explain this phenomenon (for reviews see Krebs and Myers 1974, Finery 1980, Taitt and Krebs 1985). However, none, alone or in combination, explain the causality of cycles.


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