Early springs and breeding performance in two sympatric duck species with different migration strategies

The capacity of migratory species to adapt to climate change may depend on their migratory and reproductive strategies. For example, reproductive output is likely to be influenced by how well migration and nesting are timed to temporal patterns of food abundance, or by temperature variations during the brood rearing phase. Based on two decades (1988–2009) of waterfowl counts from a boreal catchment in southern Finland we assessed how variation in ice break‐up date affected nesting phenology and breeding success in two sympatric duck species, Mallard Anas platyrhynchos and Eurasian Teal Anas crecca. In Fennoscandia these species have similar breeding habitat requirements but differ in migration distance; Teal migrate roughly seven times as far as do Mallard. Annual ice break‐up date was used as a proxy of spring ‘earliness’ to test the potential effect of climate change on hatching timing and breeding performance. Both species were capable of adapting their nesting phenology, and bred earlier in years when spring was early. However, the interval from ice break‐up to hatching tended to be longer in early springs in both species, so that broods hatched relatively later than in late springs. Ice break‐up date did not appear to influence annual number of broods per pair or annual mean brood size in either species. Our study therefore does not suggest that breeding performance in Teal and Mallard is negatively affected by advancement of ice break‐up at the population level. However, both species showed a within‐season decline in brood size with increasing interval between ice break‐up and hatching. Our study therefore highlights a disparity between individuals in their capacity to adjust to ice break‐up date, late breeders having a lower breeding success than early breeders. We speculate that breeding success of both species may therefore decline should a consistent trend towards earlier springs occur.     

Seasonal variation in reproductive measures of tropical Roseate Terns Sterna dougallih previously undescribed breeding patterns in a seabird

Seasonal variation in egg-laying, egg size, hatching success, hatchling mass, fledging success and chick growth of Roseate Terms Sterna dougallii breeding on Aride Island (Seychelles), Indian Ocean, were studied in 1997 and 1998. I investigated to what extent two patterns, common in a range of species, were followed by tropical Roseate Terns: (a) seasonal decrease in clutch size, egg size and breeding success and (b) an increase in breeding success with increasing egg weight. In 1997 (a poor year), the earliest nesting birds laid significantly smaller eggs, and chicks were lighter at hatching than those of peak nesting birds. The mean clutch size, of 1.04 eggs, showed no seasonal variation and no 'b'-eggs hatched. In 1998 (a good year) the earliest nesting birds laid eggs of similar size and their chicks were of similar weight to those of peak nesting birds. Mean clutch size, of 1.25 eggs, increased significantly through the season and about 60% of the 'b'-eggs hatched. In 1997, hatching success was 57% whereas in 1998 it was 80%. In both years, breeding success declined significantly through the season. The fact that the earliest breeding birds laid smaller eggs in a poor year and smaller clutches in a good year is in marked contrast to a range of other species, and to temperate-nesting Roseate Terns. Egg volume explained about half of the variance in hatchling mass in both years, but only 15% of the variation in linear growth rate. Hatching date was the only variable with a significant effect on fledging success. Roseate Terns on Aride seemed to sacrifice egg size and clutch size for earliness of laying. Presumably it is a strategy of older birds to lay as early as possible and may be regarded as a response of tropical Roseate Terns to breeding under relatively poor, and seasonally declining, food conditions.     

Resource partitioning in sympatric arctic-breeding geese: summer habitat use, spatial and dietary overlap of Barnacle and Pink-footed Geese in Svalbard

The spatial, habitat and dietary overlap of two breeding goose species was studied in Sassendalen, Svalbard, in summer 2003 based on abundance within 500 × 500‐m grid squares and faecal diet analyses during pre‐breeding, nesting and post‐hatching periods. More than half of all Pink‐footed Geese Anser brachyrhynchus occurred in the absence of Barnacle Geese Branta leucopsis during nesting and post‐hatching periods compared to c. 20% when concentrated by pre‐breeding snow cover. In contrast, only 5% of Barnacle Geese were observed in the absence of Pink‐footed Geese pre‐breeding, 15% during nesting, and 35% post‐hatching. Among six defined habitat types, Barnacle Geese resorted more to ‘upland’ habitats during pre‐breeding and nesting and to lowland lakes post‐hatching when compared to Pink‐footed Geese. Although Pink‐footed Geese showed less change in seasonal habitat preference, many shifted to the river valley bottom post‐hatching, giving access to open water (predator avoidance) and lush green vegetation (foraging for goslings). The smallest extent of distributional overlap between the two species occurred post‐hatching, but each species was also highly restricted by snow cover during pre‐nesting. The greatest extent of overlap in distribution and diet occurred during incubation, when large dietary variation between different breeding valleys reflected local food availability around nests (probably a result of nest‐site preference rather than food selection per se). Whether this means that increased interactions within and between the two goose species with future increases in local density are most likely to be manifest at this stage of the summer is impossible to determine without knowledge of available food resources and manipulative experiments. More detailed investigations of the effects of foraging by both species on plant structure, quality and community composition are necessary to predict likely outcomes of future changes in population densities of both species.     

Causes and consequences of fine-scale breeding dispersal in a female-philopatric species

The potentially confounded effects of factors affecting breeding dispersal have rarely been simultaneously examined. The consequences of breeding dispersal are even less studied, presenting a paradox: breeding dispersal seldom seems to improve breeding success, despite its presumed adaptiveness. We studied the causes and consequences of breeding dispersal in female-philopatric eiders (Somateria mollissima) in relation to the spatiotemporal predictability of nest success. Previous nest fate, breeding experience, and breeding density simultaneously affected breeding dispersal. Dispersal distances were longer among inexperienced breeders and after failed breeding. Individual dispersal distances decreased with increasing nest-site-specific breeding density, whereas island-specific nesting success peaked at intermediate densities. The fate of neighbouring nests (‘public information’) did not influence dispersal. Breeding dispersal was unrelated to subsequent hatching success, controlling for individual quality (body condition, breeding experience, previous nest fate), while it delayed hatch date, which is likely to impair reproductive success. This delay may result from the loss of acquired information of local breeding conditions, prolonging nest prospecting and establishment, also helping explain why breeding dispersal did not increase at high breeding densities, despite a potential reduction in nesting success. In long-lived species, however, dispersal-induced reductions in reproductive output in one season could be offset by improved parental survival prospects. Careful nest prospecting may be profitable, because overall nest success had a strong island-specific component but showed weak temporal variation, and successive individual nest fates were predictable between years. Once a safe nest site is found, females may breed at the same place successfully for many years.     

The breeding biology of the Dalmatian Pelican Pelecanus crispus

The breeding biology of the Dalmatian Pelican Pelecanus crispus , a vulnerable bird species in the Palaearctic, has been studied for 7 years at Lake Mikri Prespa, a continental wetland and Tsoukalio lagoon, a coastal wetland within the Amvrakikos Gulf. The two colonies showed stability, with fluctuations in the number of breeding attempts each year varying by about 30% over a period of 7 years. The date of arrival at the breeding sites and the date of laying of the first egg varied between mid-February and mid-March. The egglaying period (including renesting) varied between 18 and 114 days between years. The annual average clutch size varied between 1.60 and 1.94 eggs per nest. The incubation period averaged 31.4 ± 1.4 days. The overall hatching success varied from 36% to 70%. Egg losses were mainly due to nest abandonment, infertile eggs and eggs rolled from the nests. The Dalmatian Pelican chicks took 11–12 weeks to fledge. Nestling mortality was very low in contrast to other species of pelican. Such a low nestling mortality explains why the breeding success each year is largely explained by the hatching success.     

3. THE GOLDEN ORIOLE (Oriolus oriolus) IN HOLLAND

Even though Sfax salina in Tunisia hosts a significant part of the Mediterranean population of Pied Avocet Recurvirostra avosetta, data on the breeding ecology of this species in this area are lacking. Such data are nonetheless necessary, not only for the understanding of the ecology and dynamics of this species in general, but also for conservation purposes. In this paper we use the results of a one-year monitoring of nests in Sfax salina to provide information on its nesting parameters, in particular nesting phenology, colony size and hatching success. Our results show that Pied Avocets formed dense colonies at the beginning of the nesting season, but colony size decreased as the nesting season advanced. Clutch size varied between 1 and 7 eggs, similar to other Mediterranean and European populations. Hatching success, estimated by the Mayfield method, was relatively low, mainly due to predation by stray dogs. Overall, our work shows that relatively high nest losses occur here. It also highlights the need for management efforts aiming to enhance the reproductive success in this artificial habitat. Creation of suitable and safe nesting sites is proposed.     

Aspects of the breeding ecology of the Purple Swamphen Porphyrio porphyrio in the wetland complex of Guerbes-Sanhadja,north-east Algeria

The Purple Swamphen Porphyrio porphyrio is a common rail that previously was little investigated in North Africa. From 2011 to 2013, its breeding ecology was studied at two natural wetlands in north-east Algeria, namely Garaet Hadj Tahar and Garaet Messaoussa. Numbers of Purple Swamphens at both localities peaked in late April and early May. Egg-laying started in early March, whereas hatching started in late March. Peak egg-laying took place in late March and early April, and peak hatching from mid-April to early May. There were significant differences in the size and weight of eggs between years and localities. The mean clutch size was 2.75 ± 0.70 eggs and it was not signifi- cantly different between localities and years. Mean hatching success was 51% and it was positively correlated to nest depth only at Garaet Hadj Tahar. Most nests were built in dense tufts of Typha angustifolia and Phragmites australis. The main nesting materials were Phragmites australis and Scirpus maritimus.     

Breeding success and chronology of Wood Storks Mycteria americana in northern and central Florida, U.S.A.

The breeding success and chronology of Wood Storks Mycteria americana were studied at eight colonies in northern and central Florida during 1981–1985. Mean ± s.d. clutch size for all colony-years was 3.07 ± 0.56 (n = 2694 nests), with three-egg clutches (72%) most frequent. Mean clutch size among all colonies and years ranged from 2.73 ± 0.55 to 3.41 ± 0.61. Many colonies exhibited significant negative trends in clutch size with, hatching date because of a proportional decrease in four-egg clutches later in the season. Mean colony clutch size was not correlated with nest numbers, nesting density or mean hatching date within most years. Mean ± s.d. number of fledglings for all colonies and years was 1.29 ± 1.16 fledglings per nest (n = 2812 nests). Mean annual fledging rates in colonies ranged from 0 (colony failed) to 2.66 fledglings per nest. Most breeding failure occurred prior to egg hatching, and the second highest mortality occurred between hatching and 2 weeks of age. Four-egg clutches fledged more storks than three-egg clutches, which in turn were more successful than two-egg clutches. However, all clutch sizes showed similar fledgling per egg rates. The seasonal decline in productivity was associated proportionally with smaller clutch sizes later in the breeding season. An increase in mean hatching date was correlated with an increase in latitude. There was greater within-year breeding synchrony among colonies than interyear breeding synchrony within each colony. Breeding synchrony was not correlated with mean hatching date, latitude, longitude, nest numbers or nesting density.     

Interactive effects of time and vegetation on reproduction of redshanks (Tringa totanus) breeding in Wadden Sea salt marshes

As shown for various species, nesting waders are non-randomly distributed on wetlands and preferentially select riparian nest-sites adjacent to limnic or marine waterbodies. Studying the redshank Tringa totanus, we tested the hypotheses that, in a coastal wader species which conceals its clutch in vegetation, predation and hatching success are affected by vegetation zonation, and that breeding in lower salt marsh areas has negative consequences for reproduction. We further predicted effects of timing of breeding and breeding experience/age of adults potentially reflected by egg biometrics both on nest-site selection and reproduction. Effects of vegetation, space, time and individual quality on hatching success of redshanks were studied in the German part of the Wadden Sea. Dominant plant species, vertical vegetation structure and nest concealment varied significantly between nests. Variation in nest concealment was relatively low: about 90% of clutches were classified as being well concealed. This variation was explainable by vegetation structure but not by vegetation composition at the nest-site, distance to shoreline, and time of clutch initiation. Vertical vegetation structure varied by dominant plant species but not by distance to shoreline and time of clutch initiation. Hatching success of clutches was low (10.6%) due to high predation (daily predation rate: 7.4%). Hatching success and duration of clutch survival were negatively and predation positively related to the date of clutch initiation. Furthermore, negative relationships were found between egg size and predation and duration of survival, respectively. We assume that concealed nests, early breeding and breeding experience diminish predation in salt marsh breeding redshanks. Thus, redshank reproduction appears to be affected by interactive effects of timing of breeding and vegetation facilitating early breeding. In contrast to open-nesting species, breeding in riparian habitats next to waterbodies may be disadvantageous for species breeding concealed in vegetation if these are covered by less structured vegetation.     

Use of time‐lapse photography and digital image analysis to estimate breeding success of a cliff‐nesting seabird

Development of new methods for obtaining basic demographic data from difficult‐to‐access breeding colonies and easily disturbed species is an important challenge in studies of seabirds. We describe a method that can generate data concerning annual breeding success of cliff‐nesting seabirds or other colonial birds with open nests. Our method requires only a single visit to a colony every second or third year, and is based on the use of automated time‐lapse photography. To test our method, we used time‐lapse photos to examine the breeding success of Thick‐billed Murres (Uria lomvia) in two breeding colonies in Greenland during the years 2011, 2012, and 2014. Based on the analysis of time‐lapse photos, we found that hatching success during the 3 yr of our study ranged from 60% to 81%, fledging success from 89% to 95%, and breeding success from 53% to 74% (Table 1). Use of digital image analysis made it possible to differentiate between breeding and non‐breeding birds and determine if and when breeding attempts failed or succeeded. The key to making our method a realistic long‐term monitoring technique is the use of an automated, formal image analysis to process the thousands of photos from the time‐lapse cameras and, more specifically, to reduce a large number of photos to a manageable number. Using our method, we needed 12–22 h per study plot, depending on the number of breeding sites per plot (range = 47–127) and whether it was the first or the second time the plot was analyzed, to obtain our estimates of hatching, fledging, and breeding success. This included time for data preparation, image analyses, visual inspections, and summarizing data in a spreadsheet. We found that our estimates of breeding success were comparable to those obtained by direct observation in the field. An important aspect of using time‐lapse technology is to foresee potential reasons why time‐lapse cameras might stop taking pictures, for example, equipment failure (camera, timer, or battery) or interference by visitors (e.g., vandalism or theft). As such, thorough testing of time‐lapse systems and selecting camera locations less likely to be disturbed are most important. We believe that use of time‐lapse photography in combination with digital image analysis to estimate breeding success can be useful for determining the breeding success of other cliff‐nesting seabirds and, more generally, other birds that breed in colonies, especially those located in remote areas and where direct observation may disturb birds.