Diet of sympatrically breeding Southern Carmine Bee-eater Merops nubicoides and White-fronted Bee-eater Merops bullockoides

The Southern Carmine Bee-eater Merops nubicoides and White-fronted Bee-eater Merops bullockoides are insectivore, cavity-nesting bird species, both of which occur in the Zambezi Region, north-eastern Namibia. I examined there the diet composition of these species by an analysis of prey remnants. The Southern Carmine Bee-eater chick's diet consisted of exclusively insects, represented by seven orders. The most numerous were orthopterans and beetles (40.9% and 26.1%, respectively; n = 582 prey items). Hymenopterans (18.7%) and bugs (12.9%) supplemented the diet, whereas dragonflies (Odonata) and moths (Lepidoptera) were preyed only occasionally. In the diet of the White-fronted Bee-eater, nesting at the same site, beetles were the most important prey (81.2% of all 101 prey items identified), with scarabaeids comprising more than half of the beetle diet. In comparison with the White-fronted Bee-eater, a lower proportion of beetles, but much larger proportion of orthopterans were recorded in the diet of the Southern Carmine Bee-eater. In both bee-eater species, hymenopterans appear to be less important than was expected. The essential difference in the proportion of main prey groups recorded in Southern Carmine and White-fronted Bee-eaters breeding at the same site may represent a shift in food niche due to both temporal segregation in breeding, and differences in food preferences (feeding sites).     

蓝喉蜂虎的捕食行为与食性

在我国有分布的7种蜂虎科鸟类中,蓝喉蜂虎(Merops viridis)分布范围最广,但相关野外研究还比较少。2011~2016年,我们以江西省吉安市郊区的一个蓝喉蜂虎种群为研究对象,在观察野外捕食行为的基础上,记录了其食物种类,研究了该鸟的食性。蓝喉蜂虎的食物主要是蜂类、蝶类和蜻蜓类昆虫,其被捕食频次的百分比分别为26.0%、26.3%和38.3%。其中,繁殖前期以蜂类居多,繁殖后期以蜻蜓类居多,数量比例存在显著的季节性差异。这种差异可能是昆虫生活史差异造成的。网络图片资料佐证了其食物种类主要为以上3类昆虫。在吞食食物前,蓝喉蜂虎会对不同类群的昆虫进行不同时长和不同方式的处理。此外,野外研究发现,产卵期蓝喉蜂虎巢室中散布着可能被吞食过带有食物残渣的小型贝类碎片。通过实验筛选营巢河滩地的沙土,发现这些贝壳碎片是外来。这表明,蓝喉蜂虎可能通过取食小型贝类贝壳,在产卵期获取短期额外的钙质补偿。蓝喉蜂虎在其分布区内属不常见鸟类,但其捕食的主要昆虫类群在我国南方比较常见,这说明食物不是限制该鸟分布的原因。蓝喉蜂虎是一个极具观赏价值的美丽小鸟,当前亟需深入研究,为该鸟的保护提供决策依据。     

Cytochrome c oxidase subunit I barcoding of the green bee-eater (Merops orientalis)

DNA barcoding using mitochondrial cytochrome c oxidase subunit I (COI) is regarded as a standard method for species identification. Recent reports have also shown extended applications of COI gene analysis in phylogeny and molecular diversity studies. The bee-eaters are a group of near passerine birds in the family Meropidae. There are 26 species worldwide; five of them are found in Saudi Arabia. Until now, GenBank included a COI barcode for only one species of bee-eater, the European bee-eater (Merops apiaster). We sequenced the 694-bp segment of the COI gene of the green bee-eater M. orientalis and compared the sequences with those of M. apiaster. Pairwise sequence comparison showed 66 variable sites across all the eight sequences from both species, with an interspecific genetic distance of 0.0362. Two and one within-species variable sites were found, with genetic distances of 0.0005 and 0.0003 for M. apiaster and M. orientalis, respectively. This is the first study reporting barcodes for M. orientalis.     

The discriminant power of biometrics for sex determination in European Bee-eaters Merops apiaster

ABSTRACT

Capsule A combination of several biometric measures enables the reliable sexing of the European Bee-eater Merops apiaster, a species with subtle sex differences in plumage and morphometry.

Aims To explore variation in biometrics and their suitability to discriminate sex in adult European Bee-eaters Merops apiaster.

Methods We sampled populations of a long-distance migratory species with low sexual size dimorphism, the European Bee-eater Merops apiaster, from colonies in western Iberia (Portugal) and Central Europe (Germany) to investigate body size variation and derive population-specific and general sex discriminant functions.

Results Overall, male Bee-eaters were larger than females while Bee-eaters from Germany and Portugal did not differ in size, except for primary length and tail length. The best single measurement to discriminate sex was wing length for Portuguese birds and tail tip length for German birds, as in the combined dataset. Multivariate discriminant functions of head-bill, wing and tail tip lengths provided the highest discriminant accuracy, discriminating sex for 91% of the birds from Portugal, 96% from Germany and 94% when using the combined dataset. Nonetheless, the discriminant accuracy remained high in the functions using only two variables for Portugal (head-bill and tail tip 91%, head-bill and wing 88%, wing and tail tip 88%), Germany (head-bill and tail tip 95%, wing and tail tip 97%) and in the combined dataset (head-bill and tail tip 92%, wing and tail tip 93%).

Conclusions Population specific discriminant functions allow sexing of European Bee-eaters by morphometry with high degree of accuracy at least for Iberia and Central European populations. Such discriminant functions can be used to assign the sex of adult Bee-eaters reliably and swiftly while the bird is still in the hand, highlighting the potential of these functions for rapidly sexing species with low degrees of sexual size and plumage dimorphism.     

Range-wide migration corridors and non-breeding areas of a northward expanding Afro-Palaearctic migrant,the European Bee-eater Merops apiaster

Across their ranges, different populations of migratory species often use separate routes to migrate between breeding and non-breeding grounds. Recent changes in climate and land-use have led to breeding range expansions in many species but it is unclear whether these populations also establish new migratory routes, non-breeding sites and migration phenology. Thus, we compared the migration patterns of European Bee-eaters Merops apiaster from two established western (n = 5) and eastern (n = 6) breeding populations in Europe, with those from a newly founded northern population (n = 19). We aimed to relate the breeding populations to the two known non-breeding clusters in Africa, and to test for similarities of migration routes and timing between the old and new populations. Western Bee-eaters used the western flyway to destinations in West Africa; the eastern birds uniformly headed south to southern African non-breeding sites, confirming a complete separation in time and space between these long-established populations. The recently founded northern population, however, also used a western corridor, but crossed the Mediterranean further east than the western population and overwintered mainly in a new non-breeding area in southern Congo/northern Angola. The migration routes and the new non-breeding range overlapped only slightly with the western, but not with the eastern, population. In contrast, migration phenology appeared to differ between the western and both the northern and the eastern populations, with tracked birds from the western population migrating 2–4 weeks earlier. The northern population thus shares some spatial traits with western Bee-eaters, but similar phenology only with eastern population. This divergence highlights the adjustments in the timing of migration to local environmental conditions in newly founded populations, and a parallel establishment of new breeding and non-breeding sites.     

Assimilation efficiency and growth of nestling insectivores

The efficiency of energy assimilation by Pacific Swallows Hirundo tahitica and Blue-throated Bee-eaters Merops viridis was measured in captive nestlings fed on their natural diets. Assimilation efficiency (AE) was 68% in Pacific Swallows, similar to published values for altricial nestlings, including other hirundines. AE was unusually low in Blue-throated Bee-eaters, conforming to results with the European Bee-eater Merops apiaster , at around 57%. As expected, nestling growth was positively correlated with daily metabolized energy. Estimates of daily metabolized energy for captive reared nestlings, closely resembled estimates obtained for wild youngsters in an earlier study using different methods.     

Territorial Organization of the White Fronted Bee-eater in Kenya

White fronted bee-eaters (Merops bullockoides) live in extended family clans that aggregate to roost and nest in large colonies. Members of a given clan also share a common foraging territory, spatially segregated from the colony, to which they commute daily. The size of this foraging territory is positively related to clan size. Clan foraging territories are divided into a number of loosely overlapping foraging home ranges (FHRs), each occupied by an individual or mated pair of birds. Bee-eaters feed solitarily, flycatching to snap up large insects from widely dispersed perches. Each bird tolerates intrusion on its FHR by various members of its own clan, but aggressively excludes individuals belonging to other clans. Birds defend only their own FHR; however, because of the high amount of FHR overlap, the result is a loose form of group defense of the larger clan feeding area. For this reason we refer to the system as one of clan foraging territories. Birds occupying clan foraging territories located more than 1.5 to 2 km from a colony temporarily abandoned them while feeding nestlings. At such times, these birds provisioned their young by foraging near the colony. Birds that abandoned territories foraged less efficiently, provisioned nestlings at a lower rate, and had lower breeding success than did birds that continued use of their foraging territories. A model is developed relating territory abandonment to the energetics of central place foraging. Bee-eaters typically shift colony locations between successive breeding seasons. Foraging territory locations, in contrast, remain largely stable, resulting in large and unpredictable changes in the quality of any given foraging territory across years (quality being defined as distance from the currently active nesting colony). When a pair bond forms in bee-eaters, one member typically remains in its natal clan while the other moves into the clan of its partner. At this time, the new pair also establishes its own FHR, generally located within or on the periphery of the clan foraging territory of the natal member. The result of this settlement pattern is that white fronted bee-eaters live their lives spatially surrounded by members of their natal or their matrimonial clan. This, in turn, increases the likelihood of both mutualistic and nepotistic interactions among clan members. Such benefits include shared territory defense, enhanced security against predation, and maintenance of close social bonds with potential helpers. We hypothesize that the adaptive value of clan foraging territories lies in long-term familiarity with a foraging area. Such familiarity was demonstrated to lead to improved foraging efficiency and hypothesized to provide both increased security from predation and a more accurate means of monitoring temporal changes in environmental quality. The system of clan foraging territories found in white fronted bee-eaters differs from the all-purpose group territories of most other cooperative breeders studied to date in two important ways. First, foraging territories were not limiting in the sense of restricting dispersal and “forcing” offspring to remain with their natal clans. Unoccupied areas of seemingly suitable habitat were present throughout the study area at all times. Birds also showed no tendency to expand their boundaries or move into areas vacated when neighboring clans decreased in size or died off. Second, breeding status and foraging territory ownership are not linked in Merops bullockoides. All pairs defended foraging areas, yet only about 3/4 of them bred in any given year. This percentage did not differ significantly between pairs occupying high quality foraging territories (located near the active nesting colony) and pairs forced to abandon low quality foraging territories located more distantly. We conclude that foraging territories are not a critical ecological constraining factor for white fronted bee-eaters in Kenya.     

怒江河谷栗喉蜂虎的繁殖行为观察

2007年3月26日—7月16日,采用典型野外记录法和所有事件取样法对云南省保山市道街怒江河谷栗喉蜂虎繁殖行为进行了观察。结果表明：1）产卵期雄性栗喉蜂虎求偶喂食的食物以蜻蜓目和膜翅目昆虫为主,占83.56%;雌鸟接受喂食的可能性为96.83%,接受喂食后仅有17.49%的雌鸟与雄鸟进行交配。2）在孵卵期昼间,雄鸟每次坐巢的时间为（23.521.6）min,每日坐巢的时间占54.4%;雌鸟每次坐巢的时间为（25.811.5）min,每日坐巢的时间占42.1%,雌雄鸟每次坐巢的时间无明显差异。3）幼雏出壳后亲鸟对幼雏的暖雏时间逐日减少,至第20 d亲鸟不再暖雏。栗喉蜂虎的育雏期为29～33 d,在繁殖过程中帮助喂食的鸟确实能提高被助鸟的繁殖成功率。     

Synchronization of host-parasite cycles by means of diapause: host influence and parasite response to involuntary host shifting

Many parasites require synchronization of their infective phases with the appearance of susceptible host individuals and, for many species, diapause is one of the mechanisms contributing to such coincidence. A variety of ecological factors, like changes in host temperature produced by involuntary host shifting (substitution of the usual host by an infrequent one), can modify host-parasite synchronization of diapausing ectoparasites of endothermic species. To understand the influence of host shifting on the mechanisms of parasite synchronization, we conducted experiments using the system formed by the ectoparasitic fly Carnus hemapterus and its avian hosts. We simulated the occurrence of the usual host and natural cases of host shifting by exposing overwintering carnid pupae from Bee-eater nests (Merops apiaster) to the earlier incubation periods of two Carnus host species that frequently reoccupy Bee-eater nests. Pupae exposed to host shifting treatments advanced the mean date of emergence and produced an earlier and faster rate of emergence in comparison with pupae exposed both to the control (absence of any host) and Bee-eater treatments. The effect was more evident for the treatment resembling the host with the most dissimilar phenology to the one of the usual host. Our results show that host temperature is an environmental cue used by this nest-dwelling haematophagous ectoparasite and reveal that Carnus hemapterus has some potential to react to involuntary host shifting by means of plasticity in the termination of diapause.     

Incidence and Geographical Distribution of Honeybee (Apis mellifera L.) Pests in Jordan

The occurrence and distribution of pests of honeybee (Apis mellifera L.) in Jordan were surveyed during the agricultural seasons of 1999 and 2000. A total of 800 colonies in 112 apiaries were chosen from different geographical regions that support beekeeping in Jordan. Honeybee colonies are attacked by 21 pest species in different areas of Jordan. The most distributed pests which cause considerable damage are Varroa destructor, Vespa orientalis, Galleria melonella, Dorylus fulvus, Braula orientalis, Merops apiaster, Hirundo rustica, Hirundo daurica and Merops orientalis. Other pests of minor importance to beekeeping were also recorded. Most of the recorded pests were appeared in both the Jordan Valley and Irbid regions.     

Microsatellite loci in the European bee‐eater,Merops apiaster

Twelve polymorphic microsatellite markers have been developed for the European bee‐eater, Merops apiaster (Coraciiformes: Meropidae). Screening of eight individuals at these loci showed that the average allelic diversity was 5.8, with a range of two to 11 alleles per locus. The loci reported here will provide insight into the levels of extra‐pair parentage, kin selection and dispersal in this species, which has co‐operative breeding and nests in large colonies.     

The dilemma of where to nest: influence of spring snow cover,food proximity and predator abundance on reproductive success of an arctic-breeding migratory herbivore is dependent on nesting habitat choice

Pink-footed geese Anser brachyrhynchus nest in two contrasting but commonly found habitats: steep cliffs and open tundra slopes. In Svalbard, we compared nest densities and nesting success in these two environments over ten breeding seasons to assess the impact of spring snow cover, food availability to nesting adults and arctic fox Vulpes lagopus (main terrestrial predator) abundance. In years with extensive spring snow cover, fewer geese at both colonies attempted to breed, possibly because snow cover limited pre-nesting feeding opportunities, leaving adults in poor breeding condition. Nesting success at the steep cliff colony was lower with extensive spring snow cover; such conditions force birds to commit to repeated and prolonged recess periods at far distant feeding areas, leaving nests open to predation. By contrast, nesting success at the open tundra slope was not affected by spring snow cover; even if birds were apparently in poor condition they could feed immediately adjacent to their nests and defend them from predators. Foxes were the main nest predator in the open tundra slopes but avian predators likely had a larger impact at the steep cliffs colony. Thus, the relative inaccessibility of the cliffs habitat may bring protection from foxes but also deprives geese from readily accessing feeding areas, with the best prospects for successful nesting in low spring snow cover years. Our findings indicate that spring snow cover, predator abundance and food proximity did not uniformly influence nesting success of this herbivore, and their effects were dependent on nesting habitat choice.     

Division of labor in post-emergence colonies of the primitively eusocial waspPolistes instabilis de Saussure (Hymenoptera: Vespidae)

Polyethism was quantified in post-emergence colonies of the primitively eusocial wasp,Polistes instabilis, and compared to polyethism in a sympatric advanced eusocial wasp,Polybia occidentalis. Like P.occidentalis, P. instabilis foragers collected food (nectar and prey) and nest materials (wood pulp and water).P. instabilis foragers showed some evidence of specialization with respect to which materials they gathered, but most foragers, divided their effort among food and nest materials, a pattern that is rarely seen inP. occidentalis. In colonies of both species, more foragers collected nectar than any other material; in contrast, most water foraging was performed by one or two workers. Upon returning to the nest,P. instabilis foragers gave up part or all of most nectar, prey, and pulp loads to nestmates, while water was rarely partitioned. Prey loads were most likely to be given up entirely.P. instabilis workers show evidence of conflict over the handling of materials at the nest. The frequency with which workers took portions of nectar loads from forgers was positively correlated with their frequency of aggressive dominant behavior, and with their frequency of taking other foraged materials. Compared to polyethism inP. occidentalis P. instabilis showed less individual specialization on foraging tasks and less partitioning of foraged materials with nestmates, suggesting that these characteristics of polyethism have been modified during the evolution of advanced insect societies.     

Constrained by available raptor hosts and islands: density-dependent reproductive success in red-breasted geese

In this paper we aim to explain the distribution of red-breasted geese Branta ruficollis over different nesting habitats. To be safe from land predators red-breasted goose colonies were restricted to i) islands on rivers, ii) cliffs with peregrine falcons Falco peregrinus , and iii) the close proximity of snowy owl Nyctea scandiaca and rough-legged buzzard Buteo lagopus nests. Among years nest site availability varied by fluctuations in numbers of owls and buzzards in association with cycles in lemming abundance, but the total number of goose nests found in the study area did not vary. The distribution of geese, in combination with data on reproductive success, suggested a despotic mechanism: at cliffs, goose numbers were constant among years with an invariably high reproductive success, whereas large fluctuations in numbers on islands coincided with opposite trends in success. Apparently, geese nesting with owls or buzzards moved to the few islands present in the study area during years when these birds of prey were absent. Consequently, in such years the average density of geese on islands was more than twice as high as at cliff colonies (5.4 and 2.3 pairs per ha of foraging habitat, respectively). Colony size at cliffs may have been restricted by territorial behaviour of the geese, though there is evidence that, additionally, the host falcons also limited the number of nesting geese. Apparently rare in closely related species, we observed a negative density-dependent effect on reproductive success during the nest phase, and attribute this to limited food resources, reinforced by the high frequency of territorial interactions. This leads to the conclusion that, in addition to predation pressure, nesting density is an important agent in the link between lemming cycles and goose breeding success.     

SOCIAL ORGANIZATION AND NEST-BUILDING IN THE FOREST WEAVER BIRDS OF THE GENUS MALIMBUS (PLOCEINAE)

A comparative study was made of social organization during breeding among the genus Malimbus. In M. nitens, the male chooses the nest site, builds the nest alone, guards the nest during incubation, and feeds the young; the female incubates, broods alone and with the male feeds the young. In M. malimbicus, the male chooses the nest site, builds the nest with the female and guards the nest; the female builds the nest with the male, but incubates alone. In M. racheliae and M. cassini, the nest is built by one female and a multi-male party of two or three. One male drives off the other males when the nest is completed. One male and one female incubate alternately. The female seems to be the leader of the building group, and works like a male. In M. coronatus, the nest is built by a mixed party of males and females (3–6 birds), all working together without any overt leadership. Only one male and one female however, incubate, brood and feed the young. In their morphology and behaviour, Malimbus spp. are close to the weaver birds of the genus Ploceus. M. nitens seems the least evolved species while M. cassini and M. coronatus are behaviourally the most evolved. In the last species, which has a very elaborate nest, the pair of breeding birds is helped by one to four other birds. These helpers are birds in full adult plumage, and are probably capable of breeding and may do so at another period in the long breeding season of at least six months.     

Breeding ecology and behaviour of the last wild oriental Northern Bald Ibises (Geronticus eremita) in Syria

A relict colony of Northern Bald Ibis (Geronticus eremita), a critically endangered species, was unexpectedly discovered in Syria in 2002. During six subsequent breeding seasons (2002–2007), the 3, and then 2, breeding pairs of Northern Bald Ibises have shown to be still vital and, when intensively protected, showed a higher average breeding success than that recorded in Morocco, the only other country where these birds still breed in the wild. During the six breeding seasons, a total of 24 chicks fledged and left the breeding area successfully. Between 2004 and 2007, a total of 5 immature ibises have made a return to the colony, separately and later than adults. As a consequence, two recruitment events have taken place (2006 and 2007), partly compensating for the gradual decrease in the number of adults. Breeding adults arrive from migration during the second half of February, separately, and leave together around mid-July. They nest in cavities and ledges of two limestone cliffs of the central Syria desert, located 20 km apart, well protected from the predominant wind. Breeding behaviour and the cycle are described, summarised and compared with data from the wild colonies of Morocco and the colony of Turkey before the extinction. Key threats still in place at the Syrian breeding quarters are human disturbance during settling and incubation, chick depredation by ravens, uncontrolled hunting and habitat degradation. Recommendations on how to enhance the breeding performance and ensure the survival of this colony in the future are given.     

Colonial breeding reduces nest predation in the common gull (Larus canus)

It is often suggested that colonial breeding reduces nest predation for birds with a high defence capacity, but experimental comparison of predation at solitary and colonial nests is seldom feasible within a single species. We here report on such a test in the common gull (Larus canus). The rate of predation on experimental eggs was significantly lower near colonies than near solitary gull nests, and the eggs survived longer at the edge of a colony than farther away. Communal mobbing of nest predators is the likely reason. In both of two years, almost all nests of solitary gulls were destroyed by predators, while most clutches survived in colonies. Nest predation hence selects strongly for colonial breeding in the present population of common gulls.     

SYNCHRONY AND SOCIAL STIlMULATION IN COLONIES OF THE BLACK-HEADED WEAVER PLOCEUS CUCULLATUS AND VIEILLOT'S BLACK WEAVER MELANOPTERYX NIGERRIMUS

The paper is concerned with the relative importance of environmental changes and social stimulation in bringing about synchronized social breeding in Ploceus cucullatus and Melanopteryx (Ploceus) nigerrimus . Field work was carried out in central Uganda.
Observations on a single colony of each species extending over a complete breeding period showed that breeding started abruptly with the arrival of a large number of males and the construction of new nests. The majority of females arrived later within a relatively short space of time. Subsequently the number of birds and the amount of activity declined gradually. Nests were repeatedly destroyed and reconstructed in the same positions. In P. cucullatus an entrance funnel was generally added only after occupation of the nest by a female.
Studies extending over a large number of colonies showed that main breeding seasons correspond approximately with the two rainy seasons each year. Isolated colonies may be active between seasons, however.
Nest-building and breeding are highly synchronized within colonies. Uniform responses to rain may partly account for this synchrony, but fluctuations of activity in neighbouring colonies are relatively unsynchronized, suggesting that social stimulation is also an important factor. This is supported by direct observations of social interactions and by the fact that small colonies are relatively less successful than larger ones, apparently because the pair-formation process may fail in the absence of sufficient social stimulation.