Annual cycle in female minnows Phoxinus phoxinus (L.) from an upland Welsh lake

A population of Phoxinus phoxinus in a small, upland, Welsh lake was sampled at monthly intervals between February 1976 and January 1977. Mature females belonged to the 1972, 1973 and 1974 year classes. Spawning took place in May and June over gravel at the lake's edge. Regression analysis provided estimates of the mean carcase, ovary and liver weights expected for a female of length 65 mm. The ovarian weight increased rapidly in spring but dropped sharply between May and August. Carcase and liver weight declined during the breeding season, but recovered rapidly on completion of breeding. The increase in the weight of the ovary was accompanied by an increase in the proportion of dry matter, while the carcase and liver became relatively hydrated during the breeding season. Also at this time, the energy and lipid content of the carcase was low, but the ash content was high. Thus ovarian maturation and breeding were associated with a depletion of the carcase and liver, but this was quickly reversed at the end of the breeding season. Preliminary estimates of the changes in total energy in the ovary and carcase during ovarian maturation were made which suggested that the decline in the energy content of the carcase represented a significant proportion of the gain in energy content of the ovary. The sampling period coincided with an unusually severe drought and the possible consequences of this on the population are considered.     

Delayed female reproduction in equilibrium and chaotic populations

Behavioural and life history polymorphisms are often observed in animal populations. We analyse the timing of maturation and reproduction in risky and resource-limited environments. Field and laboratory evidence suggests that female voles and mice, for example, can adjust their breeding according to the level of risk to their own survival and to survival probabilities and recruitment of young produced under different environmental conditions. Under risky or harsh conditions breeding can be postponed until later in the current breeding season or even to the next breeding season. We develop a population dynamics and life history model for polymorphism in reproduction (co-existence of breeding and non-breeding behaviours) of females in an age-structured population, with two temporally distinct mating events within the breeding season. We assume that, after overwintering, the females can breed in spring and again in summer or they can delay breeding in spring and breed in summer only. Young females born in spring can either mature and breed in summer or stay immature and postpone breeding over the winter to the next breeding season. We show that an evolutionarily stable breeding strategy is either an age-structured combination of pure breeding behaviours (old females breed and young delay maturity) or a mixed breeding behaviour within age-classes (a fraction of females breed and the rest of the age class postpones breeding). Co-occurrence of mixed reproductive behaviour in spring and summer within a single breeding season is observed in fluctuating populations only. The reproductive patterns depend on intraspecific, possibly interspecific, and ecological factors. The density dependence (e.g. social suppression) and predation risk are shown to be possible evolutionary mechanisms in adjusting the relative proportions of the different but co-existing reproductive behaviours.     

Population ecology of Mus musculus on Mana Island, New Zealand

Feral house mice ( Mus musculus ) living on 217 ha Mana Island, New Zealand, with no mammalian predators, were snap-trapped and autopsied. A 7-month breeding season took the population from a spring low to extremely high density in autumn. Litters were largest in the middle of the breeding season, and significantly larger on Mana than on the New Zealand mainland. Litter size in early pregnancy was similar for young and old mice but more embryos were resorbed by old females. The breeding season ended in April when adult females stopped ovulating and young failed to mature. When the population declined over winter no animals bred, they all lost weight, and even previously mature males lost their reproductive ability. Mice continue to grow throughout life and become larger than mice in most populations on the New Zealand mainland. The regular and pronounced seasonal pulse in Mana's mouse population contrasts with longer-term fluctuations generally seen in mainland populations at lower density in indigenous forest. These differences may be explained by absence of predators, habitat features or lack of any chance to disperse on the island.     

Age, growth and rate of food consumption in an upland population of the three-spined stickleback, Gasterosteus aculeatus L.

In a population of Gasterosteus aculeatus living in an infertile, upland lake, the fish bred at the age of one year and few survived to breed again. The highest growth rates were achieved in the first month of life, but in comparison with other populations of G. aculeatus growth was slow during the autumn and ceased during the winter. But in spring and early summer, there was a spurt in the growth rate.
Laboratory studies provided regression models for the prediction of the rate of food consumption from measurements of growth. The estimates of the consumption rate indicated the effect of the growth in body size and seasonal variations during the first year of life. It was estimated that a fish of mean length in the population consumed 3150 mg of food in a year in which it grew from 65.8 to 552.0 mg, with an overall gross growth efficiency of 15.4%.
The study illustrated the integration of laboratory and field studies to obtain reasonable estimates of the rate of food consumption by fish throughout their first year of life.     

Life cycles of Gammarus oceanicus and G. salinus (Amphipoda) in the Oslofjord, Norway

In the Oslofjord the amphipods Gammarus oceanicus Segerstråle, 1947 and G. salinus Spooner, 1947 were estimated to live for a maximum of 15 months. All specimens which survived during winter died in spring, mainly in May. A G. oceanicus population living on a freshwater influenced shore contained smaller specimens, had a lower proportion of the female population in breeding condition and probably produced fewer broods than a population living on a fully marine shore. The differences are discussed in relation to environmental factors and the distribution of G. salinus. Gammarus oceanicus possibly was breeding from December to May, some females even in June, resulting in an estimated maximum of three broods from December to May. Gammarus salinus showed two breeding periods, the first from December to May, a few of these females even bred in June, while new females bred from June to October, giving estimated maxima of respectively three (December to May) and five broods. Gammarus salinus females entered a reproductive resting stage in September-October. The sex ratio was mostly female dominated. A shift to male dominance was noted in one population and was related to possible infections. Information from the literature on longevity and breeding periods was compiled and compared to the Oslofjord data.     

Some population dynamics of the Bank vole, Clethrionomys glareolus and the Wood mouse, Apodemus sylvaticus in mixed woodland

The population dynamics of Clethrionomys glareolus Schr.and Apodemus sylvaticus (L.) in mixed woodland in County Durham, were studied from March 1963 to January 1965. Two areas of 0.9 ha (2.25 acres) each were trapped monthly and information was obtained on population size, reproduction, survival and growth from marked animals.
Clethrionomys populations increased from June to an autumn peak; then declined, at first rapidly, but then more slowly in winter, before reaching a spring trough. The breeding season of Clethrionomys was from May to December; juveniles were caught from mid-June to December. Survival was in general poor during the breeding season but good at other times. Survival of young born early in the summer was particularly good on one of the areas and some individuals lived long enough to breed in two successive years. On both areas young born early in the year matured rapidly and bred in the year of their birth. Young born in late summer and early autumn ceased growing at a weight of about 14.5 g, remained immature, and formed the bulk of the overwintering population. Growth was completed at the time of sexual maturation the following spring.
Trapping failed to provide adequate samples of juvenile Apodemus in summer to account for subsequent recruitment. The possibility that a substantial proportion of the adult population of this species was also either trap shy or had emigrated temporarily is discussed. Breeding occurred from April until the following January, but the numbers trapped remained very low throughout the early months of the breeding season. Large scale recruitment of young fecund animals into the trap-revealed population occurred during the autumn. Apodemus males continued to grow rapidly during the winter.     

Do intrinsic or extrinsic factors limit reproduction in cyclic populations of Clethrionomys glareolus and C. rufocanus?

Changes in reproduction and functional age structure of females in cyclic populations of Clethrionomys glareolus and C. rufocanus were studied by live-trapping individually marked voles during 1980 to 1984 in northern Sweden. A complete population cycle was observed in both species, with a synchronous 'summer-decline' in 1982. In both species, the length of the breeding season became successively shorter towards the peak, and it was extremely short at the decline. When the populations expanding, the density of breeding females increased in a sigmoid way, and thereafter it remained fairly constant throughout the summer. At the decline, the density of breeding females decreased successively from spring to autumn. Year-born females matured and bred in all years except at the decline. Intrinsic factors, such as spacing behaviour of breeding females, are thought to limit the density of breeders in general, but only when the populations are expanding. Other factors such as deteriorating food conditions are more likely to operate at the decline.     

The breeding population of Peregrine Falcon Falco peregrinus in the United Kingdom,Isle of Man and Channel Islands in 2014

Capsule: Overall numbers of Peregrines are higher than previously recorded, due primarily to the growth of lowland populations, despite declines in many upland areas.

Aims: To estimate the breeding population of Peregrines, and changes in this population over time, as well as to relate variation in trends and observed breeding success to variation in region, breeding site type and other ecological influences.

Methods: Two types of survey methods were used. Site-based visits focussed on locations where Peregrines were known to have bred previously, while area-based searches aimed to find all Peregrines breeding in randomly chosen 5?km?×?5?km squares. Findings from each method were used to estimate population size in different parts of the survey area. Breeding outcome and site type were assessed for most of the pairs found during either survey.

Results: In 2014, the breeding population of Peregrines in the UK, Isle of Man and Channel Islands was estimated at 1769 pairs. This is 22% larger than the population estimate from the previous survey in 2002. Most of this increase is accounted for by increases in lowland England. Populations in some upland areas have declined.

Conclusions: The gap between the fortunes of lowland and upland Peregrines has continued to grow, along with the overall UK population. Likely reasons for the continued success of Peregrines in the lowlands include increasing uptake of breeding sites on human structures, abundant availability of prey in many lowland situations and, in many areas, a relative lack of conflict with humans. Factors likely to be limiting upland Peregrine populations vary between different regions, and include ongoing illegal killing and deliberate disturbance, and food supply.     

Family-based winter territoriality in western bluebirds, Sialia mexicana: the structure and dynamics of winter groups

Winter residency is characteristic of the majority of cooperatively breeding birds, but the composition and dynamics of winter groups have been examined in relatively few. In 1996-1998, we examined winter territoriality in the western bluebird, a year-round resident that shows a limited degree of helping behaviour in central coastal California, U.S.A. In spring, most western bluebirds breed as socially monogamous pairs, but a small proportion of pairs (3-16%) have additional breeding-age males helping at the nest, usually assisting parents or brothers. We found that year-round residents commonly wintered in family groups that defended territories similar to those used in spring. Winter groups had an even sex ratio and formed early in the autumn, when hatch-year birds dispersed. More females than males left their natal groups to be replaced by an influx of immigrant hatch-year birds. Winter groups typically consisted of breeders and one or two sons from the prior breeding season along with one or more immigrant females. A second period of dispersal occurred in spring when winter groups broke up and most birds other than the breeding pair left the winter territory. When they bred, yearling males and females often bred with unrelated individuals from their winter groups. Sons were more likely to remain on the study area as yearlings when they wintered with both parents than when they wintered with just one parent. We suggest that young males stay the winter due to benefits of remaining in family groups on mistletoe-based winter territories. Subsequent localized dispersal of sons then leads to opportunistic kin-based interactions later in life. Copyright 2001 The Association for the Study of Animal Behaviour.     

Population dynamics of an outbreak of house mice (Mus domesticus) in the mallee wheatlands of Australia—hypothesis of plague formation

A plague of mice ( Mus domesticus ) in the Victorian mallee wheatlands of south-eastern Australia in autumn 1984 appeared to be generated by a sequence of rainfall events: high autumn (March), mid winter and late winter rainfall in 1983, and high summer rainfall in 1983/84. The March rainfall in 1983 ended a drought; mice began to breed and bred until the end of May. Relatively high survival of mice for 12 months after March 1983, together with early onset of breeding and high reproductive performance throughout the 1983/84 breeding season, including summer, were key demographic processes during the formation of the plague. Temporal differences in mouse abundance and breeding performance between habitats highlighted the relevance of specific habitats to the dynamics of mouse populations in the wheatlands. Fencelines were the most important habitat of mice because they were foci for breeding at the start of the breeding season, good nesting sites which were rarely disturbed, and widespread and in close proximity to crops. Cereal crops were colonized in spring 1983 and in autumn 1984; they became important habitats in 1983 when mice dispersed and bred there in early spring. Redhead's (1988) model was sufficient to explain the 1984 plague, but not the magnitude of the decline of mouse numbers in 1984, nor the absence of a further outbreak in 1985. A new model is proposed based on a sequence of rainfall events beginning at least 10 months prior to a plague.     

Asynchronous male and female life cycles in the sexually dimorphic, harem-forming isopod Paragnathia formica (Crustacea: Isopoda)

The complex life history of the sexually dimorphic, harem-forming isopod Paragnathia formica Hesse is described, combining published information with new observations. The results of a two-and-a-half year field study, carried out within the animal's saltmarsh habitat, are presented, revealing significant differences in the life cycles of males and females. Settlement to the breeding habitat of final stage male and female larvae, derived from the same annual generation, was recorded at very different times of the year. The total lifespan of males was shown to be twice that of females.
The larvae, temporary ectoparasites of estuarine fish, and the non-feeding, burrow-living adults are described and categorized into several developmental phases, whose numbers were recorded during the course of the study.
The annual production of larvae during a limited period in the autumn, and the subsequent settlement of final stage larval females and males the following year, were monitored. Larval females entered the burrows of adult males in the spring to breed, and died after releasing viviparous broods in the autumn. Larval males settled later in the summer, reaching adulthood in the autumn and overwintering before breeding some 18 months after their birth and dying at the end of the breeding season. Adult males thus bred with females from the next generation. The differences in male and female life cycles led to great seasonal variations in adult sex ratios, a huge winter bias towards males contrasting with a brief excess of females in the summer.     

Latitudinal differences in somatic energy storage: adaptive responses to seasonality in an estuarine fish (Atherinidae: Menidia menidia)

This study focuses on the seasonal accumulation and depletion of somatic energy in the Atlantic silverside (Menidia menidia), an annual estuarine fish. Previous research revealed that northern silversides are subject to strong size-dependent winter mortality, while southern fish suffer no appreciable winter mortality. To examine whether there was geographic differentiation in allocation strategies, we compared temporal patterns of energy storage and utilization among three populations along this gradient in seasonality. The comparative design used monthly or biweekly samples of fish collected in the wild, as well as samples of fish from each population reared in a common environment, where genetic differences can be clarified. Somatic energy stores were quantified via gravimetric analysis of neutral storage lipids and lean tissue. Analysis revealed that small individuals maintained relatively low levels of lipid reserves, which may account for their lower survival in winter. Wild fish in the north rapidly accumulated large somatic reserves, which were depleted over the winter and then increased again during the subsequent spring breeding season. In wild southern fish, relatively small reserves accumulated slowly until breeding commenced in the spring. The common-environment comparison of somatic storage patterns revealed a genetic basis for among-population differences in reserve accumulation rates, but no differences in the amount of reserves stored. We conclude that the overwinter depletion of somatic reserves has a significant selective impact on energy accumulation and allocation strategies in seasonal environments. Received: 1 November 1995 / Accepted: 13 September 1996     

Age structure and reproduction in feral New Zealand populations of the house mouse (Mus musculus), in relation to seedfall of southern beech

Abstract

After good seedfalls by southern beech (Nothofagus spp.), density indices for mice increased, the breeding season for adult females was brought forward, and winter breeding was observed. The end of the breeding season of the following summer was brought forward only slightly if the maximum density achieved was not great; incomplete data on 2 very high-density populations suggested a much earlier end to breeding. In early winter following a good seedfall the recruitment of juveniles was temporarily increased. After spring, few young mice entered the population, though breeding continued. The distribution of age classes shifted steadily upwards as population density rose. The peak population of 1976–77 comprised mainly old mice, still breeding, but without significant recruitment. No effects of density on sex ratio, litter size, or body weight could be detected from these data. In all populations studied, density decreases were ultimately due to failure of recruitment and the disappearance of ageing, non-breeding mice. The proximate causes of this mortality were probably the onset of cold weather in 1976–77 and predation by stoats in 1979–80.     

Age variation in a fluctuating population of the common vole

We analysed variation in age in a fluctuating population of the common vole (Microtus arvalis) in southern Moravia, Czech Republic, to test the assumption of the senescence hypothesis that the age of voles increases with increasing population density. Between 1996 and 1998, we monitored the demographic changes by snap-trapping and live-trapping in a field population passing through the increase, peak and decline phase of the population cycle. We used the eye lens mass method to determine the age of snap-trapped animals and those that died in live-traps. The average age of winter males was clearly higher after the peak phase breeding season than before it. No such phase-dependent shift in age, however, was observed in the female component. Male age continued to increase from autumn to spring over the pre-peak winter, and the highest age was in spring of the peak phase year. However, after the peak phase breeding season the highest age was achieved in winter, with the decline phase males during the next spring tending to be younger. The average age of females in spring populations was always lower than in winter populations. The average age of voles from live-traps was always higher than voles from snap-traps, particularly in winter and spring populations, suggesting the presence of senescent animals. Although the density-dependent changes in age are consistent with those observed for other voles, they provide only weak evidence that population cycles in the common vole are accompanied by pronounced shifts in individual age, particularly in female voles.Due to an error in the citation line, this revised PDF (published in December 2003) deviates from the printed version, and is the correct and authoritative version of the paper.     

Annual productivity and individual female reproductive success in a Great Bustard Otis tarda population

The reproductive success of Great Bustards Otis tarda in north-western Spain was studied between 1987 and 1998, both at the population ( c . 700 adult females breeding in our study area) and the individual level (sample of 32 marked females). Overall productivity was low, with a population mean of only 0.14 chicks reared per adult female, and an average breeding success of 0.15 chicks per year in the sample of marked females, but interannual variability was high (0.04–0.29). Population productivity was positively correlated with winter (October–March) precipitation prior to each breeding season, and negatively correlated with the number of days of rain during the hatching period. High annual productivity resulted from a high proportion of females rearing two chicks. Reproductive success was higher in females older than 6 years than in younger birds. The proportion of females in the marked sample that failed in breeding after having bred successfully the previous season was significantly higher than the proportion of those that did not. Finally, females with a higher than average breeding success tended to breed successfully in years of both low and high population productivity, whereas those with lower than average breeding success did so only in years of high productivity.     

WEIGHTS OF SOME PALAEARCTIC WADERS WINTERING IN KENYA

Palaearctic waders were caught and weighed at Lake Nakuru in the Kenyan rift valley on 22 occasions in the non-breeding season between March 1967 and May 1969. The weights of four species are presented:Curlew Sandpiper, Little Stint, Ruff and Marsh Sandpiper.
Winter weights were relatively low and varied little. It is thought that waders had very little fat reserve at this time.
The mean weights of early autumn samples tended to be higher than corresponding mean winter weights, and autumn populations included some markedly heavy birds.
An increase in the mean weight, and a dramatic rise in the maximum weights of each species occurred shortly before its main spring departure time. The great majority of waders apparently gained considerable weight before migration from the area in April and May.
The spring migration of waders from Kenya is briefly discussed.     

Reproductive changes in fluctuating house mouse populations in southeastern Australia

House mice (Mus domesticus) in the Victorian mallee region of southeastern Australia show irregular outbreaks. Changes in reproductive output that could potentially drive changes in mouse numbers were assessed from 1982 to 2000. Litter size in females is positively correlated with body size. When standardized to an average size female, litter size changes seasonally from highest in spring to lowest in autumn and winter. Litter size is depressed throughout breeding seasons that begin when the abundance of mice is high, but is similar in breeding seasons over which the abundance of mice increases rapidly or remains low. Breeding begins early and is extended on average by about five weeks during seasons when mouse abundance increases rapidly. The size at which females begin to reproduce is larger during breeding seasons that begin when mouse abundance is high. An extended breeding season that begins early in spring is necessary for the generation of a house mouse plague, but it is not in itself sufficient. Reproductive changes in outbreaks of house mice in Australia are similar but not identical to reproductive changes that accompany rodent population increases in the Northern Hemisphere. We conclude that food quality, particularly protein, is a probable mechanism driving these reproductive changes, but experimental evidence for field populations is conflicting.     

Kin-related social organization in a winter population of the voleClethrionomys rufocanus

Kinship amongClethrionomys rufocanus was investigated during the winter of 1992/93 in a 3-ha enclosure using both molecular and catch-mark-release techniques. Forty-six adult voles (22 males and 24 females) having high heterozygosities, which were collected from several natural populations, were released into the enclosure on 29 September 1992. Most fall-born individuals of both sexes stayed in their natal site during the non-breeding period (December–March), although reproductively active females dispersed during the fall breeding season (October–November). These philopatric individuals aggregated and formed an maternal family in the winter. Several females which failed to reproduce were solitary during this season. Some individuals which were derived from several families also aggregated into a mixed lineage group. Survival rate of fall-born voles from earlier litters was higher than that from later ones. Maternal families broke up soon after the onset of spring reproduction. Most females established a territory near the wintering site and made a kincluster, in which close relatives neighbored each other. Maternal families in winter bring about female kin-clusters in spring, which may influence reproductive output in the breeding season.     

Effect of food on the growth of carcase, liver and ovary in female Gasterosteus aculeatus L.

The effect of ration size on the growth of the carcase, liver and ovary in female three-spined sticklebacks, Gasterosteus aculeatus L., was studied experimentally at monthly intervals throughout the annual reproductive cycle. Temperature and photoperiod during each experiment corresponded to the average, natural conditions for that month.
Growth of the carcase was sensitive to ration in all months. At a given ration, the growth rate of the carcase was relatively constant. The water content of the carcase was inversely correlated with ration size. Growth of the liver was also sensitive to ration, but the sensitivity varied in different phases of the reproductive cycle. High rates of weight loss occurred in the liver under starvation, but at maximum rations the liver showed high rates of weight gain particularly in the post-spawning period. Growth of the ovary was relatively insensitive to ration but directly reflected the changes occurring naturally in the reproductive cycle.
It is suggested that the liver acts as a buffer between the carcase and the ovary and this helps to insulate the ovary from the immediate effects of fluctuations in food supply.
The growth rates of the carcase and liver may provide useful indices of the rate of food consumption in natural populations. Although, if the liver is used, its growth has to be interpreted in the context of the annual reproductive cycle.     

The reproductive biology of Common frog (Rana temporaria) populations from different altitudes in northern England

The study investigated the ecophysiological differences between populations of the Common frog( Rana temporaria L.) from different altitudes in northern England. Frog embryos in upland northern ponds experience very low temperatures during the period of embryonic development. These embryos were found to have a lower lethal limit for 50% normal development of2–8 °C, compared with3–8 °C for lowland embryos. These values are below most of the lower limiting temperature estimates previously obtained for R. temporaria . Embryos from upland ponds developed faster at low temperatures than embryos from lowland ponds. This may be an adaptation to the shorter growing season and lower temperatures at higher altitudes. Upland female frogs were found to be shorter and produced fewer eggs than lowland females. The differences found between lowland and upland frogs are discussed in terms of their potential adaptive significance.