Predation by mustelids and rodents on the eggs and chicks of native and introduced birds in Kowhai Bush, New Zealand

Prior to human settlement the endemic New Zealand avifauna evolved in the absence of mammalian predators. Subsequently mustelids, rodents and feral cats have become established and frequently prey on birds and nests. It has been suggested that, because of their evolutionary history, the endemic birds are especially susceptible to such predators. In this paper predation by mustelids and rodents on the eggs and nestlings of eight species of native bird is compared with that on five species of introduced European passerine inhabiting the same lowland forest.
Final outcomes were known for 101 nests of native birds and 48 nests of introduced birds found during three breeding seasons. There was no significant difference between the two groups in frequency of predation. Native birds lost 70-1% of their nests to predators and introduced birds 64-6%. Most predations occurred during the egg stage. Clutch size did not influence frequency of predation, but brood size did for Fantails and introduced birds. Stoats and weasels were responsible for 77-9% of predations on native birds and 77-4% on introduced birds; corresponding percentages for rodents (principally ship rats) were 14-7% and 19-4%. Mustelids destroyed proportionately more nests with chicks than with eggs, whereas rodents did the reverse. Predation on both groups of birds was not influenced by their nesting habitat, the species of tree used for nesting, or the height and position of the nest. The vulnerability to introduced predators of native New Zealand birds is discussed in relation to the historical declines of many species, and also their life-history patterns.     

Causes of morbidity and mortality and their effect on reproductive success in double-crested cormorants from Saskatchewan

The objectives of this study were to describe causes of morbidity and mortality in a breeding colony of double-crested cormorants (Phalacrocorax auritus) on Doré Lake (Saskatchewan, Canada), and to determine cause-specific mortality rates of juvenile birds. Morbidity and mortality were monitored every third day during the breeding season from 1994 to 1996 from inside a tunnel-and-blind system. Affected eggs and birds were collected for examination and diagnosis. The cause of mortality was determined for 105 eggs, 178 nestlings (< or = 4-wk-old), 1393 post-nestling chicks (> 4-wk-old), and 10 adults. The main causes of mortality were infertility or embryonal death, avian predation, displacement of eggs and chicks from the nest, starvation from sibling competition, Newcastle disease, coyote predation, human-induced suffocation, and entrapment. In 49% of the cases, avian predation and displacement from the nest of eggs or nestlings was associated with human disturbance. Thirty-six nestlings, 40 post-nestling chicks, and three adults were examined for the presence of parasites. Contracaecum spiculigerum was found in the proventriculus; Amphimerus elongatus in the liver. Piagetiella incomposita in the gular pouch; Eidmanniella pellucida, Pectinopygus farallonii, and Ceratophyllus lari in the plumage; and Theromyzon sp. in the nasal and oral cavity. Contracaecum spiculigerum was associated with ulcerative gastritis, A. elongatus with multifocal hepatitis and bile duct hyperplasia, and P. incomposita with ulcerative stomatitis, but these lesions were not considered fatal. Other diseases included beak deformity, abnormal rotation of the carpal joint, hypopigmentation, and eye loss. Overall mortality of cormorant chicks between hatching and the end of the breeding season varied from 25 to 48%. The most important causes of mortality were Newcastle disease, which killed 21% of hatched chicks in 1995, sibling competition (maximum 12% in 1994), and coyote predation (2% in 1994).     

THE BREEDING BIOLOGY OF THE BLACK-FACED DIOCH QUELEA QUELEA IN NIGERIA

A study of the breeding biology of Quelea quelea in Nigeria, and particularly at a large breeding colony near Lake Chad, showed that losses of eggs and young were extremely small. 95% of eggs laid hatched successfully, and 87% give rise to fledglings. Nestling deaths were density-dependent and apparently due to starvation.
The incubation period was 10 days or less. By day, eggs were heated to 34°- 37° C. by the sun; at night the females incubated. The nestlings were initially fed mainly on insects, their diet gradually changing to one of seeds—mostly of the grass Echinochloa pyramidalis . The deep body temperatures of young birds were determined. It is suggested that the nestlings left the nest after, on average, 11¹/₂ days to escape intolerable temperature conditions in the nest.
Fat reserves were accumulated by nestlings and fledglings, and were utilized when the young became independent. The adults put on fat during the incubation period and lost it during the time spent feeding nestlings.
It is concluded that the most common clutch-size of Q. quelea , which is everywhere three, corresponds to the largest number of young the parents can normally nourish. This conforms to Lack's theory on the significance of clutch-size, and gives no support to Skutch's opinion that the theory does not apply to tropical birds.     

Can redistribution of breeding colonies on a landscape mitigate changing predation danger?

The reproductive success of colonially breeding species depends in part upon a trade‐off between the benefit of a dilution effect against nestling predation within larger colonies and colony conspicuousness. However, there may be no net survivorship benefit of dilution if smaller colonies are sufficiently inconspicuous. This raises the question about how the size distribution of breeding colonies on a landscape might change as the predation danger for nestlings changes. In southwest British Columbia, Canada, bald eagle Haliaeetus leucocephalus populations have increased exponentially at ～5% per year in recent decades and prey upon nestlings of colonial breeding great blue herons Ardea herodias faninni. Motivated by field data on reproductive success in relation to colony size, modeling is used to ask under which circumstances trading off a dilution benefit against colony conspicuousness can improve population reproductive success. That is, which colonial nesting distribution, dispersed and cryptic versus clumped and conspicuous, best mitigates predation danger on nestlings? When predators are territorial, the modeling predicts a dispersed nesting strategy as attack rate increases, but not as predator numbers increase. When predators are non‐territorial, the modeling predicts a dispersed nesting strategy as predator numbers and/or attack rates increase. When predators are both territorial and non‐territorial, colonial nesting within a predator's territory improves reproductive success when attack rates are low. This suggests nesting in association with territorial predators may offer decreased levels of predation when compared with nesting amongst non‐territorial predators. Thus a change in the colony size distribution of colonially breeding species might be anticipated on a landscape experiencing a change in predation danger.     

Breeding biology of rooks (Corvus frugilegus L.) in Hawke's Bay,New Zealand

Abstract

Three rookeries in Hawke's Bay were studied during 1966–68. First or replacement clutches were started between 26 August and 23 October. First clutches averaged 4.3 eggs and replacements 3.7 eggs. The mean size of first clutches varied between years from 4.1 to 4.6 eggs. Incubation took 17–18 days. Most losses occurred around hatching, when about 40% of the eggs or young were lost. Incubated eggs and small nestlings incurred losses of 20% and 10% respectively, and all nestlings older than 10 days survived to at least 20 days. On average, 1.4 young were reared per nest in which eggs were laid; successful nests averaged 2.2 young. First clutches averaged 1.3 young (2.4 per successful first clutch). During the season, mean clutch size declined from 4.2 to 3.5, the mean number of young hatched declined from 2.0 to 0.6 per clutch, and the mean number of young fledged from all clutches declined from 1.3 to 0.4 per clutch. Mean nestling weight increased with age from 14 g on the first day after hatching to 360 g on the 19th day. The causes of egg and nestling mortality and the adaptiveness of clutch size are discussed.     

Predators and the breeding bird: behavioral and reproductive flexibility under the risk of predation

A growing body of work suggests that breeding birds have a significant capacity to assess and respond, over ecological time, to changes in the risk of predation to both themselves and their eggs or nestlings. This review investigates the nature of this flexibility in the face of predation from both behavioural and reproductive perspectives, and also explores several directions for future research. Most available work addresses different aspects of nest predation. A substantial change in breeding location is perhaps the best documented response to nest predation, but such changes are not always observed and not necessarily the best strategy. Changes in nesting microhabitat (to more concealed locations) following predation are known to occur. Surprisingly little work addresses the proactive avoidance of areas with many nest predators, but such avoidance is probably widespread. Individual birds could conceivably adopt anti‐predator strategies based on the nest predators actually present in an area, but such effects have yet to be demonstrated. In fact, the ways in which birds assess the risk of nest predation is unclear. Nest defence in birds has historically received much attention, but little is known about how it interacts with other aspects of decision‐making by parents. Other studies concentrate on predation risk to adults. Some findings suggest that risk to adults themselves influences territory location, especially relative to raptor nests. An almost completely unexplored area concerns the sorts of social protection from predators that might exist during the breeding season. Flocking typical of the non‐breeding season appears unusual while breeding, but a mated pair may sometimes act as a “flock of two”. Opportunistic heterospecific sociality may exist, with heterospecific protector species associations more prevalent than currently appreciated. The dynamics of singing during the breeding season may also respond to variation in predation risk, but empirical research on this subject is limited. Furthermore, a few theoretical and empirical studies suggest that changes in predation risk also influence the behaviour of lekking males. The major influence of predators on avian life histories is undoubtedly expressed at a broad phylogenetic scale, but several studies hint at much flexibility on an ecological time scale. Some species may forgo breeding completely if the risk of nest predation is too high, and a few studies document smaller clutch sizes in response to an increase in nest predation. Recent evidence suggests that a female may produce smaller eggs rather than smaller clutches following an increase in nest predation risk. Such an increase may also influence decisions about intraspecific brood parasitism. There are no clear examples of changes in clutch/egg size with changes in risk experienced by adults, but parental responses to predators have clear consequences for offspring fitness. Changes in risk to adults may also influence body mass changes across the breeding season, although research here is sparse. The topics highlighted herein are all in need more empirical attention, and more experimental field work whenever feasible.     

The causes of the mortality of eggs and nestlings ofPasser sp.

In the world-wide literature the role of predators and food shortage are considered as responsible for mortality of eggs and nestlings. In synantropic altricial hole-nestling birds such as sparrowsPasser domesticus (L.) andPasser montanus (L.) the predation plays unimportant role and in spite of this, mortality of eggs and nestlings can exceeded 50%. The role of microorganisms, heavy metals, pesticides and food shortage were investigated as possible causes of embryo and nestling deaths. About 70% of eggs that not hatched were infested with such pathogens asEscherichia coil, Staphylococcus epidermitis and several, more rarely occurring others. Considerable percentage of nestlings died due to pathogenic impact of such factors asEscherichia coli, Isospora lacazei, Candida spp., heavy metals and pesticides. As one effect of such interaction, the level of sublethal doses of heavy metals and pesticides are much lower that reported in the literature.     

Anti-social and social behaviour of adolescent yellow-rumped caciques (Icterinae: Cacicus cela)

In an individually marked population in southeastern Peru, males and females of the polygynous, colonial yellow-rumped cacique delayed successful breeding until they were 3 years old. Adolescent (2-year-old) females competed for nest sites, built nests, laid fertile eggs, incubated, and sometimes fed nestlings, but always abandoned nests before they fledged young. Females that completed nests during their adolescent years were also more successful in establishing nest sites the following year. Adolescent females that failed to establish nest sites and those that lost nests to predators tended to leave the study area altogether. By attempting to nest early, adolescent females may facilitate future nesting attempts by forming coalitions with other females and assessing nest site quality in an area. Adolescent males, on the other hand, avoided aggressive interactions with other males, but were very aggressive towards adult females and fledglings. Adolescent males attacked females in nests, chased females to and from the colony, pecked and mounted recent fledglings, and, rarely, pulled nestlings out of nests. This harassment resulted in the death of nestlings and fledglings and was energetically costly to females, which often fought adolescent males while defending their young. Adolescent males preferentially harassed nestling-feeding females, avoided egg-laying females and were never observed attempting to mate with females. Adult males rarely interfered during any of these interactions. Such anti-social behaviour may function as a way of practising adult behaviour, as a means of eliminating future competitors, or may be an epiphenomenon of rising hormone levels and therefore of no adaptive significance.     

Differences in reproductive seasonality of the Central American cichlid Cichlasoma urophthalmus from three 'cenotes' (sinkholes)

A total of 966 cichlids, Cichlasoma urophthalmus , was sampled from three karstic water bodies ('cenotes') in the Yucatan Peninsula. Sex ratio was not different from 1. Specimens with ripe eggs were found during the dry and rainy seasons in the inland cenote and during the dry, rainy, and north winds seasons in the two wetland cenotes. With respect to relative fecundity, data show the C . urophthalmus inland population as two- to three-fold greater (53.1 ± 27.7) than the wetland populations (15.7 ± 5.1 and 18.2 ± 3.1). This is attributable to the different breeding strategies of C . urophthalmus populations inhabiting these two types of cenotes. In particular, the ichthyofauna from the two wetlands showed not only higher species richness (17 and 16 species) but also a higher number of potential predators (nine and eight species) as compared to the inland cenote (six species; two potential predators). It is hypothesized that C . urophthalmus adjusts its clutch size and extends its breeding periods as a response to riskier sites as compared to more secure ones; a higher competition for breeding sites and to increased fishing mortality.     

Mate desertion by male Great Reed Warblers Acrocephalus arundinaceus at the end of the breeding season

Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains. Male Great Reed Warblers usually take part in the care of offspring as nest defenders and by feeding young, but at the end of the breeding season they desert their mates with eggs or nestlings. Deserted females continue offspring care. Desertion does not depend on the male's mated status (polygynous or monogamous) nor on his past breeding success. Deserted females compensate for the loss of their partners by increasing the frequency of food-bringing, resulting in a reduction in the amount of time the nestlings are brooded. Although desertion may lead to increased rates of offspring mortality through predation, breeding success of deserted females was high, especially if the male assisted during the early stages. Deserters pay costs by giving up the chance of additional matings and by lowering the reproductive success of existing mates. Male warblers reduce the former cost by choosing the season of desertion and the latter is lowered by the female's high parental ability. A deserter was found to start moulting while his mate was still feeding his nestlings, and an earlier start to the moult may be the primary benefit that he gains.     

The nest defence by the red‐backed shrike Lanius collurio – support for the vulnerability hypothesis

The majority of altricial bird species defend their brood against predators more intensively in nestlings rather than eggs stage. Several hypotheses have been proposed to explain this difference. The majority of existing experimental studies have recorded a gradually increasing intensity of nest defence supporting the reproductive value hypothesis. We have compared nest defence in two nesting stages of the red‐backed shrike against two predators of adult birds and against two predators of nests. While the nests with nestlings were defended by parents against three out of four predators, nests with eggs were almost not defended at all. This rapid change in parent nest defence supports rather the vulnerability hypothesis, predicting that the threat to nests with nestlings increases rapidly after hatching, as they became more conspicuous due to their begging and parental provisioning. Unlike most of the species tested previously, the red‐backed shrike uses very vigorous mobbing towards predators. We suggest that the occurrence of this active mobbing (strikes, including physical contact) is a good proxy of the current threat to the nest.     

洋县野生朱Huan的繁殖

朱鹮(Nipponia nippon)的繁殖状况 ,尤其是种群数量的变化 ,一直受到国内外的关注。本文收集分析了 1 981～ 1 997年 1 7年朱繁殖资料 ,进一步研究了朱的繁殖及其数量 ,以期为朱保护 ,采取行之有效的措施 ,提供科学依据。1　研究方法自 1 981年朱被重新发现后 ,至 1 997年 ,每年3～ 6月繁殖期 ,固定人员 ,2～ 3人为 1组 ,在每个巢区设立观察点 ,进行跟踪观察 ,并详细统计每窝产卵数、孵化数、雏鸟成活数和死亡数。并结合平常的跟踪监护 ,调查分析种群数量动态 ,统计成鸟死亡数 ,然后进行整理分析。2　结果与讨论2 .1　种群数量1 98…     

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.     

Tawny Owls Strix aluco with reliable food supply produce male-biased broods

Tawny Owls Strix aluco have been reported to skew the sex ratio of their offspring towards males when facing food shortage during the nestling period (and vice versa), because female fitness is more compromised by food shortage during development than male fitness. To test the generality of these results we used a DNA marker technique to determine the sex ratio in broods of Tawny Owls in Danish deciduous woodland during two years of ample food supply (rodent population outbreak) and two years of poor food supply. Of 268 nestlings, 59% were males (95% CI: 53–65%). This proportion was higher than previously reported for the species (49% in Northumberland, UK, and 52% in Hungary), but consistent with Fisherian sex allocation, which predicts a male bias of c . 57% based on inferred differences in energy requirements of male and female chicks. Contrary to previous results, brood sex ratios were not correlated with the resource abundance during the breeding seasons, despite considerable variation in breeding frequency, brood size or hatching date across years. Brood sex ratios were unaffected by brood reduction prior to DNA sampling, and nestling mortality rates after DNA sampling were not related to gender. The inconsistency between the sex ratio allocation patterns in our study and previous investigations suggests that adaptive sex allocation strategies differ across populations. These differences may relate to reproductive constraints in our population, where reproductive decisions seem primarily to concern whether to lay eggs at all, rather than adjust the sex ratio to differences in starvation risk of nestlings.     

The behavioural response of Great Tits to novel environment and handling is affected by the DRD4 gene

Studies have provided inconsistent evidence regarding the effects on behaviour of nucleotide polymorphism at the DRD4 gene. For instance, the DRD4 gene affects exploratory behaviour in some bird species and populations but not in others. Our earlier experiment with a wild Great Tit Parus major population revealed an important impact of the DRD4 gene on behavioural variation during the breeding season. The aim of this study was to clarify these results by measuring individual behavioural differences (exploration and anxiety) in Great Tits under controlled conditions before the beginning of egg‐laying in order to exclude the potential impacts of breeding (egg‐laying, motivation to feed nestlings, the potential effect of a partner) and the natural environment (e.g. the presence of predators). Birds were caught from their natural habitat and their behaviour was tested in a trial room the following morning. Individuals with the CT heterozygous genotype (SNP830) performed more actively in different contexts (visiting a novel object in the trial room and vocal behaviour during handling) compared with homozygotes, and the relationships were consistent in males and females. In light of the results from our previous study (heterozygous males, but not females, had a shorter latency to feed nestlings than CC homozygotes), we conclude that the same DRD4 gene variants affect behavioural responses in a controlled environment and wild contexts in the same directions, but that these relationships are not sex‐specific under standardized conditions.     

Nest losses of cavity nesting birds caused by dormice (Gliridae, Rodentia)

Mammals are common predators on bird nests. However, their species identity frequently remains unknown. Here we present long-term data (1975–2005) from a central European woodland on the predatory effect of three dormice species (Rodentia, Gliridae) on cavity-nesting birds. Dormice are mostly frugivorous during the active late-summer season, but shortly after they terminate hibernation, they frequently depredate cavity-nesting-bird nests. The seven bird species studied, lost on average between 2.9 to 18.4% of their broods. MigratoryFicedula flycatchers suffered the highest brood losses, while the residentParus titmice and the nuthatchSitta europaea had much lower brood losses. The three dormice species differed significantly in their predatory effect during different avian breeding stages. The edible dormouseGlis glis (Linnaeus, 1766) depredated both eggs and nestlings equally, while the common dormouseMuscardinus avellanarius (Linnaeus, 1758) and the forest dormouseDryomys nitedula (Pallas, 1778) destroyed more nests during egg laying and the incubation period. Among adult birds, females were taken more frequently by dormice than males. Among avian species, adultFicedula flycatchers were more often depredated than the titmice and nuthatch. Our study provided further evidence, that among the traditional studies on the costs of reproduction, parental mortality at the nests needs to be considered and that incubating or brooding females might be under higher predation risk than the males.     

Factors affecting the cost of polygynous breeding for female Great Reed Warblers Acrocephalus arundinaceus

The male's role in feeding young and his effect on the mortality of eggs and nestlings of the Great Reed Warbler Acrocephalus arundinaceus were studied in Kahokugata, central Japan, during eight breeding seasons. Three potential costs of polygynous breeding for females were examined:(i) a reduction of male parental care per brood, (ii) an attraction of predators due to concentration of nests, and (iii) an increase of unfertilized eggs due to the reduced frequency of copulation per female. Only the first cost was found to occur:polygynous males fed their young, especially of their second broods, less frequently than monogamous ones. The lowered paternal feeding frequency, however, did not increase the mortality by starvation in second-hatched broods. This was because the warm climate emancipated females from brooding and enabled them to compensate for the deficiency of feeding by males. The paper discusses possible roles of the staggering of the time of laying among harem mates and the shift of breeding status of females caused by nesting failure, in reducing potential costs of polygynous breeding for females.     

Breeding success of the Great Bustard Otis tarda in Zamora Province, Spain, in 1984

Great Bustards are still fairly abundant (5-2 nests/1000 ha) in Zamora. Overall fecundity was high (92% of adult females attempt to nest; 2–47 eggs/clutch; 89% egg fertility), but pre- and post-hatching mortality were also high (50% of eggs laid; 57% of nestlings hatched), due mainly to agricultural machinery but also to natural predators. Calculated annual yields per 100 adult females were: 227 eggs, 102 hatchlings, 44 fledglings. Production of 44 fledglings/y could sustain a stable adult population (mortality approx. 8%/y) if mortality of immatures is not more than 18–22%/y.     

Predation on amphibian eggs and tadpoles by common predators in acidified lakes

Eggs and three different stages of premetamorphic tadpoles of moor frog Rana arvalis and common toad Bufo bufo were offered to the following potential predators in acidified lakes: newt Triturus vulgaris , water beetles Rhantus exoletus and Dytiscus lapponicus , dragonfly larvae Leucorrhinia dubia and Aeshna spp., water boatman Notonecta glauca and water bugs, Cymatia bonsdorffi, Glaenocorisa p. propinqua , and Corixa dentipes.
The predation pressure on eggs of R. arvalis was low due to thick jelly. The eggs of B. bufo were not attractive to predators with chewing mouth parts due to unpalatability but predators with sucking mouth parts were not repulsed. Tadpoles of R. arvalis were eaten by all predators but tadpoles of B. bufo were unpalatable to most predators. The predators used in the experiments are the new top predators in acidified fishless lakes. They may contribute to the reduction of populations of R. arvalis in acidified areas.     

Body weight,energy metabolism,and time in the life of birds

The breeding of birds, both large and small, is affected by two specific factors: (1) hypometry of egg weight relative to female body weight and (2) seasonality of breeding, with the favorable period being limited and almost equal for birds of different body sizes. Dozens of published allometric formulas describing the dependence of energy parameters of eggs and nestlings at different growth stages and the energy cost of parental care on the body weight of parents, eggs, and nestlings, respectively, are reviewed. It is shown that birds, especially species with a large body weight, repeatedly change their metabolic parameters during ontogeny in order to shorten the period of breeding and growth. In most species, the energy costs of breeding in both sexes are approximately equal. Bringing food in the bill allows birds to supply nestlings with the amount of energy that is dozens of times greater than that expended for obtaining the food. In placental mammals, only females are involved in offspring development. Therefore, the growth rate of embryos and energy expenditures for milk feeding are limited by the metabolic potential of the mother. As a consequence, mammalian offspring grow ten times slower than bird nestlings, the body weights of females being equal.