THE PRESENT AND PAST DISTRIBUTION OF THE BALD IBIS IN THE PROVINCE OF THE CAPE OF GOOD HOPE

Tarboton, W. R. 1981. Cooperative breeding and group territoriality in the Black Tit. Ostrich 52:216-225.

In a small, colour-ringed population of Black Tits Parus niger in central Transvaal, 11 of 19 observed breeding units comprised pairs with one to three helper-males. These pairs and groups defended permanent territories, the size of which correlated with the size of the group. There were significantly more territorial disputes during winter when less food was available than in summer. Breeding occurred in summer and the female alone built the nest, incubated the eggs and brooded the young while they were small. During this time she was fed by the alpha male and helper males, although before egg-laying the alpha male prevented helpers from courtship-feeding her. On average, unassisted pairs reared 0,88 young/season whereas pairs with helpers reared 1,55 young/season. However the feeding rate of nestlings of pairs with helpers was not higher than that of unassisted pairs and the number of young reared per group did not correlate with the number of helpers within the group.

The helper system in Black Tits was associated with a skewed sex-ratio (1,7:1 males: females) in the adult population and the data are consistent with the “hopeful reproductive” hypothesis for cooperative breeding.     

A SOCIO-ECOLOGY OF MAGPIES PICA PICA

The behaviour and ecology of unmarked Magpies Pica pica living in the Cotswolds were investigated over 18 months. The spacing of nests was significantly more regular than random and breeding pairs defended territories throughout the year. In winter pairs occasionally left territories to feed with non-breeding birds which flocked throughout the year.
Magpies in flocks had a higher averiage feeding rate than birds alone or in pairs. Aggression rates in flocks increased as birds fed closer together and as food patches became richer.
Agonistic interactions between Crows Corvus corone and Magpies were common; Crows frequently dominated Magpies in disputes over food, and Crows also ate Magpie eggs and young. Single Magpies were most often chased by Crows while Magpies in flocks were able to feed longer in the presence of Crows.
Differences in fledgling success among breeding pairs were related to the location of nests; Magpie pairs breeding near Crow nests suffered higher rates of agonistic encounters with Crows and also produced fewer fledglings than did Magpies breeding at greater distances from Crow nests. Magpie nests were located nearer human habitations than were Crow nests.     

Population expansion and breeding success of Bearded Vultures Gypaetus barbatus in the French Pyrenees: results from long‐term population monitoring

Based on monitoring of Bearded Vultures over 24 years in the French Pyrenees, we assessed factors explaining temporal and spatial variations in numbers and breeding performance. The number of territorial pairs increased throughout the study period from 16 in 1994 to 44 in 2017. No significant negative trends in mean productivity (fledglings per territorial pair) were detected with increasing population size. Colonization probability increased significantly with breeding population size the previous year and with the regular provision of supplementary food in the territory the winter when colonization occurred. Colonization of new territories simultaneously increased the distribution range and local densities, but we found no effect of number of near neighbours on productivity. Pairs having bred less than 5 years together had a much lower probability of laying clutches, and higher lay rates were observed inside or close to protected areas after accounting for pair‐bond length, so productivity of territories inside protected areas was significantly higher. Nest success decreased with advanced lay date and increased with winter food abundance. Nesting failures in the study area were frequently associated with harsh weather. Additionally, disturbance by human activities was the second most important identified cause of breeding failure. The probability of failing due to disturbance was higher in western areas (where breeding areas are more accessible to humans), outside protected areas, and has increased with time. After a failure due to disturbance, there was a significantly higher probability of not producing a clutch the following year as compared with pairs that had not failed or had failed due to other causes, indicating deferred effects of disturbance. Our results show the benefits of conservation management actions, such as implementation of protected areas or designed supplementary food programmes in winter, to help range expansion. On the other hand, we did not find a significant effect of winter supplementary food on productivity. Management of feeding sites should be adapted to more specific planning, being used only in areas where natural food availability is scarce, avoiding its use close to breeding sites when juveniles disperse, and targeted mainly to help range expansion. Our results also highlight the importance of maintaining or enhancing good populations of wild ungulates and regulating human activities around nesting sites of this threatened species.     

Mate choice by marsh wrens: the influence of male and territory quality

If females choose breeding situations to maximize their fitness, then those features of the male and/or territory that are important in mate selection by females should affect female fitness, be assessable prior to mating, and vary among males. The purpose of this study was to identify characteristics of male quality and territory quality that fit these criteria for marsh wrens Cistothorus palustris. The male's contribution to nest defence appeared not to affect female success or choice. However, females that received male assistance with feeding young produced more and heavier fledglings than females without assistance. Males that fed young did not attract more mates. Few males in this population fed young, and no relationship was found between feeding effort and physical or behavioural features of the male. Results of multivariate analyses suggest that, within sites, the measures of territory quality used here cannot explain the variance in the number of young fledged per female or male harem size. The examination of arbitrary territories showed that male pairing success, female settlement order and predation patterns were not significantly correlated between years. The results suggest that territory quality does not influence female success or choice. These results are discussed in the light of earlier attempts to relate features of males and territories to mate selection by female passerines.     

Winter territoriality and its implications for the breeding ecology of White-throated Dippers Cinclus cinclus

Capsule: Pairs of White-throated Dippers Cinclus cinclus which defended winter territories bred earlier than non-territorial individuals, but there was no difference in reproductive success.

Aims: The effect of winter territoriality on breeding ecology has rarely been studied in resident birds. We carried out a preliminary investigation of whether winter territorial behaviour and territory size affect the timing of reproduction, breeding territory size and reproductive success in a riverine bird, the White-throated Dipper.

Methods: We monitored an individually marked population of White-throated Dippers in the UK. Wintering individuals were classified as either territorial or ‘floaters’ according to their patterns of occurrence and behaviour, and their nesting attempts were closely monitored in the subsequent months. Winter and breeding territory sizes were measured by gently ‘pushing’ birds along the river and recording the point at which they turned back.

Results: All birds defending winter territories did so in pairs, but some individuals changed partners before breeding. Territorial pairs that were together throughout the study laid eggs significantly earlier than pairs containing floaters and those comprising territorial birds that changed partners. However, there were no significant differences in clutch size, nestling mass or the number of chicks fledged. There was no relationship between winter territory length and lay date or any measure of reproductive success, although sample sizes were small. Winter territories were found to be significantly shorter than breeding territories.

Conclusion: Winter territoriality may be advantageous because breeding earlier increases the likelihood that pairs will raise a second brood, but further study is needed. Territories are shorter in winter as altitudinal migrants from upland streams increase population density on rivers, but this may also reflect seasonal changes in nutritional and energetic demands.     

Feeding territoriality and the reproductive consequences in brown skuas<Emphasis Type="Italic"> Catharacta antarctica lonnbergi</Emphasis>

In the maritime Antarctic, brown skuas (Catharacta antarctica lonnbergi) show two foraging strategies: some pairs occupy feeding territories in penguin colonies, while others can only feed in unoccupied areas of a penguin colony without defending a feeding territory. One-third of the studied breeding skua population in the South Shetlands occupied territories of varying size (48 to >3,000 penguin nests) and monopolised 93% of all penguin nests in sub-colonies. Skuas without feeding territories foraged in only 7% of penguin sub-colonies and in part of the main colony. Females owning feeding territories were larger in body size than females without feeding territories; no differences in size were found in males. Territory holders permanently controlled their resources but defence power diminished towards the end of the reproductive season. Territory ownership guaranteed sufficient food supply and led to a 5.5 days earlier egg-laying and chick-hatching. Short distances between nest and foraging site allowed territorial pairs a higher nest-attendance rate such that their chicks survived better (71%) than chicks from skua pairs without feeding territories (45%). Due to lower hatching success in territorial pairs, no difference in breeding success of pairs with and without feeding territories was found in 3 years. We conclude that skuas owning feeding territories in penguin colonies benefit from the predictable and stable food resource by an earlier termination of the annual breeding cycle and higher offspring survivorship.Research licence: Umweltbundesamt Bonn 13.4-94003-1/5-7.     

Sexual size dimorphism and positive assortative mating in red-backed shrike Lanius collurio: an adaptive value?

During field studies in 1997–1999 in South Bohemia (Czech Republic), we found significant differences in size between the sexes in a local breeding population of red-backed shrike Lanius collurio. Males were significantly larger than females for wing length and tarsus length, but had smaller body mass than females. However, there was considerable overlap in the ranges of these parameters between the sexes. Interestingly, pairs were formed at random with respect to wing length and tarsus length, but assortative mating was significant for body mass/body condition. Among tested variables, only male wing length correlated significantly with nestling body mass at day 7. However, clutch size and the number of fledglings strongly depended on differences in tarsus length between mates, but not on body size of mates. Individual improvements in foraging skills and/or courtship feeding rates are proposed as possible explanations for these findings.     

COOPERATIVE BREEDING OF THE NORTHWESTERN CROW CORVUS CAURINUS IN BRITISH COLUMBIA

The behaviour of helpers at nests of Northwestern Crows was studied on Mandarte Island and Mitlenatch Island, British Columbia. Not all nests had a helper and there was only one helper per nest. Helpers participated in varying degrees in the defence of the territory and nest, feeding of the nestlings and fledglings and they cached food on the territory. Adult males fed helpers, and helpers obtained most of their food on the adults' territory. Adults with helpers laid larger clutches and produced more fledglings per nest than adults without helpers. It is suggested that cooperative breeding in the Northwestern Crow is of recent origin.     

Geographical variation in reproductive ageing patterns and life‐history strategy of a short‐lived passerine bird

We investigated differences in ageing patterns in three measures of breeding performance in populations of barn swallows Hirundo rustica L. from Spain and Denmark differing in breeding latitude and hence migration distance and duration of the breeding season. We found differences in ageing patterns between populations. Generally, young (i.e. yearling) and old females (i.e. ≥ 5 years of age) laid their first eggs later and produced smaller clutches than middle‐aged females (i.e. 2–4 years of age) in both populations. The southernmost population (i.e. Spanish) showing the shorter migratory distance experienced a greater within‐individual increase in timing of breeding and clutch size in early life and a greater within‐individual decrease in laying date but not in clutch size during senescence compared with the northernmost population (i.e. Danish). We also found that the number of fledglings produced annually was related to the age of the two members of the breeding pairs with pairs composed of young and old females performing less well than breeding pairs composed of middle‐aged females. We did not find reproductive senescence for the age of the male while controlling for the age of the female on the number of fledglings produced annually by the breeding pair. Differential survival between individuals did not explain age effects on laying date or annual clutch size in neither population. However, the increase in the number of fledglings produced annually with age was partly explained by the disappearance of poor‐quality members of the pairs, mainly poor‐quality males. Age‐related breeding success (i.e. number of fledglings) was similar for barn swallows from Spain and Denmark. Therefore, the study of ageing patterns and life‐history strategies in free‐ranging animals from more than a single population can throw new light on life‐history theory, population dynamics and evolutionary studies of senescence.     

Spatial heterogeneity and structure of bird populations: a case example with the eagle owl

If individuals of the same population inhabit territories different in landscape structure and composition, experiencing habitat-specific demographic rates, then the landscape features become major determinants of the overall population characteristics. Few studies have tested how habitat-specific demography interacts with landscape heterogeneity to affect populations of territorial species. Here we report a 29-year study of an eagle owl (Bubo bubo) population in southern France. The aim of this study was to analyse how habitat heterogeneity could affect density and breeding performance. Mean productivity for the overall sample was 1.69±0.76 fledglings per breeding pair and, after controlling for year effect, significant differences between territories were detected for productivity. A positive correlation was found between the percentage of pairs producing 50% of the annual fledged young (an index of the distribution of fecundity among nesting territories) and the mean reproductive outputs, that is the heterogeneous structure of the population determined that most/all pairs contributed to the annual production of young during good years, but the opposite during poor years (i.e. fewer pairs produced the majority of fledglings). Mean reproductive output was positively affected by percentage of open country and diet richness. Although other factors different to territory quality could affect demography parameters (e.g. quality of breeders), our results clearly showed a significant correlation between landscape features and population productivity.     

BREEDING OF THE GREY WARBLER GERYGONE IGATA AT KAIKOURA, NEW ZEALAND

I studied the breeding of Grey Warblers Gerygone igata (Muscicapidae: Acanthizinae) in forest near Kaikoura, New Zealand, between 1976 and 1979. Only males sang and singing occurred all year. From late July to January pairs defended self-contained territories of 0·25–1·73 ha but they occupied larger home ranges when not breeding. Territorial adults were strictly sedentary all year. The average annual mortality of breeding adults was 18·5% and the predicted life-expectancy 4·9 years, which is remarkable in a bird weighing 6–7 g. The breeding season from first building to last fledging was six months long and it began early. Exceptionally, Grey Warblers may build and lay before the shortest day. As the season progressed warblers nested lower on average, both in absolute terms and relative to the tree nested in and canopy at the site. Warblers built in 7–27 days then delayed up to eight days before laying. Only females built and at no stage of breeding did males feed their mates. Both sexes fed the young. Grey Warblers laid for 15–16 weeks of the year and first clutches were laid asynchronously during 5–6 weeks. Eggs of a clutch appeared at two-day intervals and each egg weighed 1·5 g when fresh (23% of mean adult weight). Clutch size was nearly constant (mean 3·9, mode 4, range 3–5). The incubation period was 17–21 days (mean 19·5 days) and the nestling period 15–19 days (mean 17·2 days). On average the clutch hatched over 1·4 days, even though incubation commenced with the laying of the last egg. Nestlings reached maximum weight on Days 13–14 on average and then receded in weight by 4%, apparently through loss of water. All healthy nestlings exceeded mean adult weight during development by up to 39%. Nestlings from broods of two were at first lighter on average than those from larger broods, but in the second half of the nestling period twins were significantly the heaviest. Grey Warblers were fed for 28–35 days after fledging and they survived well while dependent on parents. Fledglings dispersed up to 3 km or more at independence and only 5% per annum joined the breeding population. Of nests that received eggs, 42% produced at least one fledgling. On average each breeding adult raised 2·0 fledglings per season. Of 265 eggs in 73 nests 70% hatched and 38% produced fledglings. Of 185 nestlings 54% fledged. Probably the main cause of mortality of eggs and nestlings was predation by introduced rodents and mustelids. Grey Warblers raise two small broods slowly during a long breeding season, rather than investing in one large quickly-reared brood. In New Zealand's mild climate the warbler's food supply may not decline severely in winter, and the population of warblers may remain so close to the limit set by food that extra for breeding is hard to obtain. Thus the breeding strategy may be adapted to a restricted food supply.     

A long-term large-scale study of the breeding biology of the Spanish imperial eagle (Aquila adalberti)

We present data from a 17-year study of the population biology of a growing population of Spanish imperial eagles Aquila adalberti across most of its breeding range. The objective of this study was to analyse the effects of age, supplemental feeding and rabbit haemorrhagic disease (RHD) on several breeding parameters of this population of eagles. Average clutch size was 2.2 eggs per clutch, and the average incubation time was 41.7 days per clutch. Fledging occurred an average of 76.8 days after hatching, the length of the fledgling period was not correlated to clutch size. The annual average percentage of pairs laying eggs was 88%. A significant reduction in the percentage of pairs laying eggs in the period 1992–1994 (from 91 to 81%) coincided with most of the eagles’ territories being affected by the rabbit epizootic disease, RHD, which reduced their food supply significantly. Average productivity was 1.23 chicks per monitored territory, average breeding success was 1.40 chicks in a clutch per territory and the average fledging rate was 1.69 chicks per territory with hatching success. The main known causes of breeding failure during incubation were nest collapse and human disturbance. During chick-rearing, total or partial chick losses were mainly caused by siblicide, disease, malnutrition or nest collapse. In 26.2% of the 1372 monitored breeding attempts, at least one of the breeding birds was a subadult (the male in 56.1% of the cases, the female in 15.5% and both sexes in 28.4% of cases). In cases of mixed-aged pairs (n = 205), 70.7% were the result of a substitution, and 29.3% were the result of the forming of a new pair. Egg laying took place significantly earlier and breeding success was higher in territories occupied by adults than in those occupied by subadults. Breeding parameters were higher in high-quality (rabbit-rich) territories than in low-quality (rabbit-poor) territories, but only for those territories occupied by adults. The values obtained in the territories occupied by adults were only significantly higher than in those of the subadults in high-quality territories. Age and territory quality thus simultaneously affected reproductive output.     

Shared parentage and incest avoidance in the cooperatively breeding acorn woodpecker

Social groups of acorn woodpeckers (Melanerpes formicivorus) range in size from unaided pairs to 15 adults. Behavioural indicators of mate guarding, assumed incest avoidance and observations of egg-laying indicate that social organization ranges from monogamous pairs to groups with up to seven male and three female putative cobreeders plus up to 10 nonbreeding helpers. In addition, groups occasionally lack a putative breeder throughout the breeding season. Here we report results from multilocus DNA fingerprinting of 372 nestlings from 123 nests in groups with putative cobreeders of one or both sexes. No extra-group fertilizations were found. Putative cobreeding males within social groups shared paternity. However, the most reproductively successful male was, on average, almost three times as successful as the next most successful and additional males only occasionally sired offspring. In contrast, cobreeding females shared parentage equally. Helpers never bred incestuously when their opposite-sex parent (or another relative, such as their uncle) held breeding status in the group. However, during breeding male vacancies, 14 nestlings were produced when helper males bred incestuously with their mother. Both male and female helpers usually became successful cobreeders with their same-sex parent following replacement of the opposite-sex breeder(s) by unrelated individuals.     

The role of male territories in the mating system of the Yellow-shouldered Widowbird Euplectes macrourus

The territorial system and breeding biology of the Yellow-shouldered Widowbird Euplectes macrourus (Ploceidae) was investigated in western Kenya. Yellow-shouldered Widowbirds had a resource-defence polygynous mating system: males defended large (mean = 0.95 ha) territories and built the coarse framing for the nests in tall grass. Males had up to five females nesting per territory. Females provided nearly all parental care except for a territorial male seen feeding a fledgling: the first observation of paternal care in the wild for this genus. There was considerable variation in territory size, but the cause of this variation remains unknown: territory size was not related to potential indicators of territory quality, such as grass height and abundance, did not relate to male morphology (mass, size and ornament size) or territorial behaviour (boundary displays and singing) and did not affect female preferences. Although resources (territories and nests) were defended by the males, observations that males frequently fed outside their territories and formed communal roosts during the breeding season suggest that this species represents a transitional stage between typical resource-defence polygyny and lek breeding.     

Long‐term breeding demography and density dependence in an increasing population of Golden Eagles Aquila chrysaetos

Few studies have quantified the dynamics of recovering populations of large raptors using long‐term, spatially explicit studies. Using data collected over 37 years in the western Italian Alps, we assessed the trends in distribution, abundance, fecundity and breeding population structure of Golden Eagles Aquila chrysaetos. Using the spatial distribution of territory centroids in 2007, we found that the spatial distribution of eagle territories was over‐dispersed up to 3 km. Although population size and total productivity increased from 1972 to 2008, the proportion of pairs that laid eggs showed a strong decline, falling to no more than 50% after 2003. On average, 15% of successful nests produced two fledglings, and productivity also declined over time. No significant relationship between population growth rate and total population size was detected, but the percentage of pairs that bred and breeding success showed evidence of density dependence, as they declined significantly with increasing density. Our results suggest that density dependence, operating across heterogeneous habitats, is currently regulating this population, while the carrying capacity may still be increasing. This may explain the apparent paradox of reduced breeding effort despite increasing total productivity.     

OBSERVATIONS OF GROUP BEHAVIOUR AND BREEDING BIOLOGY OF THE YELLOW-BILLED SHRIKE CORVINELLA CORVINA

Yellow-billed Shrikes were found to live in groups throughout the year. Within the group, each member helped to defend the group's territory, warn against predators and feed the breeding female, nestlings and fledglings.
During the study there was little change in the location of the boundaries and in the areas of the territories occupied by the majority of the groups. The densities of the larger groups were in general two to three times that of smaller groups. Numbers within one group varied by ±24% of the average (12) during a period of three years.
Progeny remained in a group for some years before dispersing, sometimes in parties of the same sex. Both sexes exchanged groups, the females moving on average further than males. During successive periods in the history of a group the representation of the sexes varied from a surplus of females to a surplus of males. In the population as a whole the sex ratio was probably parity.
Only one female bred in a group at a particular time and she alone incubated. Eggs were laid on consecutive days. Breeding started at the height of the dry season; the first peak in egg laying occurred at the beginning of the rains; laying continued through the wet season and ceased usually in August. The most frequent clutch size was four, and varied little within a breeding season or between seasons. The incubation period ranged from 15 to 18 days, the most frequently recorded being 17 days. The nestling period was 19 days. The percentage of total eggs laid that produced fledglings was 25% and yearlings 11%.
Young shrikes were independent in the seventh week, participated in group displays in their tenth week and fed fledglings in their fourteenth week.
The age of first breeding was not discovered. Two females in their sixth year were still helpers in a group at the end of the study.     

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.     

Positive effects of helpers on reproductive success in the brown treecreeper and the general importance of future benefits

1. Numerous studies of cooperatively breeding species have tested for effects of helpers on reproductive success to evaluate hypotheses for the evolution of cooperation, but relatively few have used experimental or statistical approaches that control for the confounding effects of breeder and territory quality. 2. In the brown treecreeper Climacteris picumnus, most helpers are male offspring of the breeding pair that have delayed dispersal. We analysed 5 years of data (97 territory-years) using hierarchical linear modelling to test for effects of helpers on reproductive success while controlling for confounding factors. 3. The number of helpers was related positively to reproductive success even after controlling for differences between territories and breeders. A threshold effect was observed, with success increasing most with the presence of a second helper (i.e. at group size of four). 4. Feeding at the nest was one mechanism responsible for this effect, as larger groups had higher total feeding rates at all nesting stages. Higher total feeding rates, as well as higher feeding rates by helpers, were correlated in turn with greater reproductive success. 5. An analysis of the effects of helper feeding rate on reproductive success in groups with just one helper produced only weak support for a positive effect of helpers. Controlled comparisons of this kind utilize only a small fraction of the total data available and thus have limited statistical power compared to hierarchical or mixed-modelling. 6. A number of hypotheses to explain the evolution and maintenance of helping behaviour are consistent with our results for brown treecreepers including kin selection and hypotheses based on future direct benefits. 7. A previous synthesis of studies of helper effects that controlled for confounding factors suggested a pattern in which male helpers rarely have positive effects on reproductive success. However, revising that synthesis to include recent hierarchical or mixed-modelling studies suggests that helpers of both sexes usually have positive effects, and that the relative importance of future direct benefits may have been underestimated.     

Seasonal change in Red-backed Shrike Lanius collurio territory quality - the role of nest predation

This paper examines the relationships between territory preference, reproductive performance and nest predation in a Red-backed Shrike Lanius collurio population breeding in rapidly changing farmland. Territory preference was measured by (a) the order of laying dates in territories within years and (b) territory occupation frequency over a five-year period. Seven environmental variables were tested but only the density of Sloe (Blackthorn) Prunus spinosa in territories was correlated positively with territory occupation frequency. Within years, Red-backed Shrikes started to breed earlier in territories with more Sloe, but reproductive performance was not related consistently to territory differences. A high proportion of Sloe-rich territories was vacant each year. Thus, the observed negative association between settlement order and amount of Sloe may reflect a seasonal change in habitat preference. Early breeders prefer Sloe-rich territories whereas late birds prefer Sloe-poor territories. Supporting evidence is that the proportion of occupied territories that was Sloe-rich was higher for early than for average or late first breeding attempts. Moreover, in contrast to early in the season, the probability of a replacement clutch following nest failure was not associated with the amount of Sloe, but increased with increasing densities of Juniper Juniperus communis. Late in the nesting season, pairs breeding in Sloe-rich territories suffered higher nest predation than those breeding in Sloe-poor territories. In early nesting attempts, however, the relationship was reversed. Nest predation is probably an important selective agent on habitat selection since it was the principal factor explaining variation in the numbers of fledglings produced among territories. Thus, the Red-backed Shrike may shift territorial preferences adaptively as the season progresses to match within-season changes in predation pressure in different types of territories.     

Seasonal reproductive success of the Moorhen Gallinula chloropus: the importance of male weight

During a three-year study of 82 pairs of Moorhens Gallinula chloropus, seasonal reproductive success (SRS) varied greatly between pairs. Pairs on big territories had a higher SRS than pairs on small territories, probably because clutch survival was higher on big territories. Pairs that began breeding early had a higher SRS than pairs that began late because early breeders laid larger clutches and could attempt more broods. Pairs with heavy males had bigger territories and began breeding earlier than pairs with light males. Heavy males therefore had a higher SRS than light males. Female weight did not affect territory size, timing of breeding, or female SRS. Assuming SRS to be a good predictor of lifetime reproductive success, selection should favour heavy males but not heavy females. Male Moorhens are significantly heavier than female Moorhens. Finally, pairs with breeding experience had a higher SRS than pairs without, because they had bigger territories and began breeding earlier. However, males in inexperienced pairs were not lighter than males in experienced pairs, so it is not clear why they defended smaller territories or laid later.