FOOD SIZE AND AGGRESSIVE INTERACTIONS BETWEEN TWO SPECIES OF GULLS: AN EXPERIMENTAL APPROACH TO RESOURCE PARTITIONING

Duffy, D. C., Heseltine, S. & La Cock, G. D. 1987. Food size and aggressive interactions between two species of gulls: an experimental approach to resource partitioning. Ostrich 58: 164–167.

In feeding experiments with different sizes offish, Hartlaub's Gulls Larus hartlaubi reached prey first, but lost larger items to the larger, dominant Kelp Gull L. dominicanus. Hartlaub's Gulls took longer than Kelp Gulls to consume prey of the same size.     

DIET OF HARTLAUB'S GULL LARUS HARTLAUBU AND THE KELP GULL L. DOMINICANUS IN THE SOUTHWESTERN CAPE PROVINCE,SOUTH AFRICA

Steele, W.K. 1992. Diet of Hartlaub's Gull Larus hartlaubii and the Kelp Gull L. dominicanus in the southwestern Cape Province, South Africa. Ostrich 63:68-82.

Hartlaub's Larus hartlaubii and Kelp Gulls L. dominicanus in the southwestern Cape feed on a wide range of prey species. On average, Kelp Gulls feed on larger-sized prey than do the smaller Hartlaub's Gulls. In an undisturbed environment the preferred foraging habitats of Hartlaub's and Kelp Gulls are rocky shores and open, sandy beaches (where sand mussels Donax serra are common) respectively. However, as a result of man's activities, several new foraging habitats have become available including croplands, fishing harbours and refuse dumps. The provision of supplementary food at these new foraging habitats is likely to be the cause of a recent population increase. Kelp Gull chicks are fed predominantly “natural” prey which indicates that the population increase may not be due to enhanced reproductive success, but to improved post-fledging survival of juveniles, which are known to aggregate at sites where supplementary food is provided.     

THE LAYING INTERVAL AND INCUBATION PERIOD OF ROCKHOPPER AND MACARONI PENGUINS

Williams, A. J. 1981. The laying interval and incubation period of Rockhopper and Macaroni Penguins. Ostrich 52: 226–229.

The laying interval and incubation period of Rockhopper Penguins Eudyptes chrysocome and Macaroni Penguins E. chrysolophus were studied at Marion Island in 1974–75 and 1976–77. On average, the laying interval was 4,4 and 4,5 days, the incubation period of second-laid eggs was 34,2 and 35,9 days and that of first-laid eggs was 39,1 and 38,0 days in Rock-hopper and Macaroni Penguins respectively. The laying interval in this genus is longer than that in other penguins. The incubation period is similar to that of most other penguins but the second-laid egg normally hatches before the first-laid egg. The long laying interval and the hatching sequence of the eggs both have important affects upon the mortality of eggs in the genus Eudyptes.     

DISTRIBUTION,POPULATION SIZE AND CONSERVATION OF HARTLAUB'S GULL LARUS HARTLAUBIL

Williams, A. J., Steele, W. K., Cooper, J. & Crawford, R. J. M. 1990. Distribution, population size and conservation of Hartlaub's Gull Lorus hurtlaubii. Ostrich 61: 66–76.

Hartlaub's Gull Larus hartlaubii is endemic to southern Africa, where it breeds between Swakopmund, Namibia and Dyer Island, southwestern Cape Province, South Africa. The species has been re breeding at 48 localities within this range. Between 1984 and 1989 an estimated 12000 pain brered at 31 localities. Twenty-eet percent of the population breeds at Robben Island off the Cape Peninsula, sQuth Africa. Hartlaub's Gull frequently has low breeding success and is considered endangered in Narmbia, where 12% of the poulation occurs. However, the population is increaslng around the urbanmd Cape Peninsula where HartLub's Gull has the potential to become a pest species.     

1. A CENSUS AND STUDY OF BIRDS IN ALBANY OPEN THORNBUSHVELD

Williams, A. J. &; Cooper, J. 1983. The Crowned Cormorant: breeding biology, diet, and offspring reduction strategy. Ostrich 54:213-219.

Crowned Cormorants Phalacrocorax coronatus were studied at Dassen and Marcus Islands. The most frequent clutch was three eggs. Egg size varied within clutches with first-laid eggs being largest and heaviest and subsequent eggs progressively smaller and lighter, The mean laying interval was 2,2 days, the mean laying-to-hatching interval was 23,0 days, and the hatching interval was one day. The normal incubation period was 22.4 days. The weight of hatchings was related to the position of the originating egg in the laying sequence. Chicks were fed within 24 h of hatching. Chick development is described over the first 35 days. One chick could fly at 35 days. Hatching success was 48,2%. Hatching success was greatest in second-laid eggs, least in last-laid eggs. The mean number of chicks hatched at a nest was two. Mean diving time was 23,5 s. Most food was fish, particularly klipfish Clinidae and pipefish Syngnathus, 60–160 mm long. The number of offspring produced can be related to food availability by interaction of difference in egg size, hatching asynchrony, and the preferential feeding by adults of the strongest-begging chick. There is a trend towards producing two chicks, normally those from the first two eggs to be laid.     

THE BREEDING BIOLOGY OF AN URBAN POPULATION OF ROCK PIGEONS COLUMBA GUINEA

Elliott, C. C. H. & Cooper, J. 1980. The breeding biology of an urban population of Rock Pigeons Columba guinea. Ostrich 51:198-203.

The breeding biology of the Rock Pigeon Columba guinea was studied for three seasons from 1972 to 1975 at the University of Cape Town, southwestern Cape, South Africa. Nests were visited at approximately weekly intervals. The breeding season (September to February) coincided with the end of the winter rainy season and the presence of cereal crops. Clutch size was two eggs in 99% of cases. Mean incubation period was 14,8 days. Incubation was shared as two continuous shifts per day. Growth rate was similar to that in other studies. The mean nestling period was 23,6 days. Second broods after the successful departure of chicks were frequent, the interval between nest departure and re-laying being as little as five days. Hatching success was 66%, chick rearing success 83% and overall breeding success 49%, similar to other Columba pigeons. It is suggested that the production of pigeon's milk is the limiting factor controlling the invariable clutch size.     

4. CLIMPSES OF THE NARINA TROGON

Bertram, B. C. R. &; Burger, A. E. 1981. Aspects of incubation in Ostriches. Ostrich 52:36-43.

We studied incubation in domesticated Ostriches Struthio camelus in South Africa and wild Ostriches in Kenya. Although the eggs were large, with relatively high thermal capacities, unattended eggs exposed to the sun reached dangerously high temperatures (40,5°C). Experimental exposure of fresh eggs to the sun for seven days prior to incubation greatly reduced the percentage of embryos which developed, and no embryos survived 15 days of exposure. In the wild. Ostriches frequently shade their eggs in the pre-incubation period to prevent overheating.

During natural incubation, temperatures in the eggs (range 30,8-33,8°C) and of nest-air (31,9-34,6°C) were remarkably constant, despite the daily ambient fluctuations of air temperatures (17,8-38,9°C). Similarly the humidity of the nest-air (39–52%) was lower and less variable than the ambient air (39–72%). Water loss during 42 days of incubation was 11–12% of initial egg weight and, in addition, early laid eggs lost 3–4% during the 2½-3 week pre-incubation period. The water vapour conductivity and the daily water loss of Ostrich eggs were similar to those of other birds, in proportion to epg size, despite the arid environment inhabited by Ostriches. Some of the constraints on the feeding and breeding behaviour of Ostriches imposed by the physical requirements of their eggs are discussed.     

The comparative breeding behaviour of two sympatric cuckoos, Horsfield's Bronze-Cuckoo Chrysococcyx basalts and the Shining Bronze-Cuckoo C. lucidus, in Western Australia: a new model for the evolution of egg morphology and host specificity in avian brood parasites

The breeding behaviour of two similarly sized sympatric cuckoos, Horsfield's Bronze-Cuckoo Chrysococcyx basalts and the Shining Bronze-Cuckoo C. lucidus, was studied over four breeding seasons at Gooseberry Hill, Western Australia. Both cuckoos usually began laying in late August; Shining Bronze-Cuckoos laid for up to 13 weeks and Horsfield's Bronze-Cuckoos for up to 15 weeks. Four host species were parasitized and major hosts were parasitized throughout most of their laying periods. The frequency of parasitism varied between hosts and between years, but Splendid Fairy-wrens Malurus splendens and Yellow-rumped Thornbills Acanthiza chrysorrhoa (major hosts) were always parasitized more heavily than Western Thornbills A. inornata and Scarlet Robins Petroica multicolor. Western Thornbills were parasitized by both cuckoos. Horsfield's and Shining Bronze-Cuckoos laid monomorphic eggs; those of Horsfield's Bronze-Cuckoos were highly mimetic whereas those of Shining Bronze-Cuckoos were non-mimetic and dark in colour. Both cuckoos laid one egg per host nest, deposited eggs directly into the nest, laid very quickly in the early morning, removed at least one host egg at laying, laid eggs small for the size of the birds, hatched after 12 days and evicted nest companions shortly after hatching. Laying was well synchronized with the start of incubation by hosts. Field observations and experiments with egg models indicated that neither of the major hosts, nor the secondary host in common, discriminate against foreign eggs. The nestling period for Horsfield's Bronze-Cuckoo was 17 days, and for the Shining Bronze-Cuckoo 20 days. There was a corresponding difference in nestling growth rate between the cuckoo species. About 50% of cuckoo eggs produced fledglings. Reproductive success for both cuckoos was highest in nests of the secondary host in common, the Western Thornbill. Young cuckoos reached independence 5–6 weeks after hatching. The adaptive significance of competition between cuckoos as a selective agent for cuckoo egg morphology and host specificity is discussed.     

VARIATION IN THE CAPPED WHEATEAR

Williams, A. J. 1980. Aspects of the breeding biology of the Subantarctic Skua at Marion Island. Ostrich 51:160-167.

The breeding biology of the Subantarctic Skua Catharacta antarctica lonnbergi was studied in two austral summers at Marion Island. Eggs were laid between 23 October and 19 December. The clutch size was one (6%) or two (94%) eggs. The laying interval was two (20%) or three (80%) days and the incubation period was 29 days. Chicks could fly at 50–65 days after hatching. Chicks from first and second hatched eggs in the same brood had similar growth rates. Chicks in one- and two-chick broods had similar growth rates until 50 days after hatching when chicks reared singly were heavier. Egg mortality was 15,8%, chick mortality was 34,8% and the overall breeding success was 50,9%. The results are discussed in comparison with previous studies of Subantarctic and South Polar C. maccormicki Skuas.     

Mate provisioning, nutritional requirements for egg production, and primary reproductive effort of female Common Terns Sterna hirundo

We assessed the nutritional importance of mate provisioning to females during egg production and its effects on clutch parameters (egg size, length of the laying period) in Common Terns Sterna hirundo: (1) we estimated the costs of egg production by modeling the daily protein, lipid, and energy requirements of laying females, and (2) compared these costs to both the amount, and the timing, of the male's contribution via mate provisioning. Net lipid, net protein, and gross energy requirements for a three‐egg clutch were estimated to be 5.4 g, 8.6 g, and 569 kJ respectively. Peak protein and lipid requirements occurred one (day ?1) and two (day ?2) days before laying, respectively. Peak energy requirement occurred on day ?1; a cost of 127% to 157% above maintenance. Variation in male provisioning effort (in terms of energy and nutrients delivered) paralleled variation in predicted female requirements for egg production at the level of individual pairs. Males delivered protein in excess of the female's requirements on all days investigated. Male lipid delivery accounted for 45% of female net requirement on the day when demand was greatest (day ?2), but exceeded requirements on all other days. However, the proportion of the female's total energy budget (egg production, maintenance, and activity costs) that was supplied by her mate rose from an average of 29% on day ?2 to 76% during the interval between second and third eggs. Paradoxically, females that were fed at higher rates during the interval between first and second eggs produced clutches with lower total volumes, smaller last‐laid eggs, and clutches with a greater egg‐size hierarchy than conspecifics receiving less food from their mates. Also, females fed at higher rates during the interval between second and third eggs took longer to produce their clutch. These negative relationships between mate provisioning and clutch parameters contrast with previous studies in this and other species.     

BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART I: THE PRELAYING AND INCUBATION PERIODS

Brown, C. J. 1990. Breeding biolo of the Bearded Vulture in southern Africa, Part I: The pre-laying and incubation periods. Ostrich 61: 24–32.

In southern Africa the Bearded Vulture Gpaetus barbatus lays its eggs in mid-winter. between the second half of May and the first week of July. Pairs became more active in their nesting areas about six weeks before laying and usually roosted there at night. Courtship flights were less frequent and demonstrative than in Eurasian birds and took place mainly in the late afternoons. During the pre-laying period most nest visits (77%) were to bring nesting material, 92% by the male. All nesting material was arranged by the female. Copulation was always preceded by allopreening, and occurred most frequently in the mornings. No copulation or courtship display took place after the first egg had been laid. Of 18 clutches, 16 (89%) contained two eggs and the remainder one egg. The laying interval was usually 3–5 days (range 2–9 days). Incubation started with the first egg and was evenly shared by both parents during the day, but only the female incubated at night, individual pairs maintained distinctive nest attendance and foraging period timetables, which allowed sufficient time for self-foraging by both parentes. No food was brought into the nest during the pre-laying and incubation periods, but in some pairs food was cached in nearby potholes in cliffs. The incubation period was 56–57 days.     

When should Common Cuckoos Cuculus canorus lay their eggs in host nests?

Capsule Brood parasitic Common Cuckoo Cuculus canorus chicks hatch earlier than the nestlings of their Great Reed Warbler Acrocephalus arundinaceus hosts, but hatching priority is less consistent when Cuckoo eggs are laid after the onset of host incubation.

Aim To reveal by field observations what the optimal stage is for Cuckoos to lay their eggs in relation to the host laying cycle to ensure prior hatching of the parasitic chicks.

Methods We monitored the hatching of Cuckoo chicks in relation to the hosts’ laying stage at which the Cuckoo eggs appeared and also monitored host incubation behaviour.

Results Great Reed Warblers incubated more on day 5 after the host's onset of laying relative to day 3. All Cuckoo eggs hatched earlier than hosts when they were laid prior to the onset of host incubation (day 4). Cuckoo eggs also maintained hatching priority in about 2/3 of the nests when laid on days 5–6.

Conclusions Most Cuckoo eggs are laid prior to the onset of host incubation and this, together with other adaptive mechanisms, ensures the prior hatching of Cuckoo eggs. Cuckoo eggs laid after the onset of incubation lose the advantage of prior hatching in approximately 30% of nests.     

SOME NOTES ON THE CAPE GANNET,Morus capensis

Tarboton, W. R. 1978. Breeding of the Little Banded Goshawk. Ostrich 49:132-143.

The behaviour and vocalizations of a pair of Little Banded Goshawks Accipiter badius during part of their breeding cycle is described. Both sexes built the nest. Two eggs were laid three days apart. The first egg was incubated for 52% of the day, but this increased to 90% when the clutch was complete, of which the female's share was 86% and the male's 4%. The second egg hatched after 29 days, 18 h. The female did not hunt during the incubation or early nestling period and was fed by the male who brought her, on average, 7,0 food objects per day. Lizards formed 73% of the 91 identified prey objects, and small birds, 24%. The female and chick, when 16 days old, were killed by a predator on the nest at night.     

4. UNUSUAL EXPERIENCES WITH BIRDS

Earlé, R. A. 1989. Breeding biology of the Redbreasted Swallow Hirundo semirufa. Ostrich 60: 13–21.

The two races of the Redbreasted Swallow Hirundo semirufa seem to have separate breeding seasons with the northern race H. s. gordoni breeding April-July, while most records for the nominate race fall in October-February. All nests studied were in concrete culverts less than 1 m high. Eggs laid in second clutches by individual females weighed significantly less than eggs laid in first clutches. Eggs hatched on average 16,2 days after incubation started or 18–21 days after the eggs were laid. Only females incubated. Chicks fledged 23–25 days after hatching and reached a maximum body mass of about 31,5 g on day 18 before a steady decline in mass until fledging. Most nesting failures resulted from infertile eggs or starvation of young in the nest (16,2% of all young starved). Overall breeding success was 60,6%. In all, 81,8% of first clutches produced fledglings but only 44,4% of second clutches. Over a three year period 4,9 young were produced per pair breeding in the area (1,6 young/pair/breeding season).     

Parasitization by Edovum puttleri (Hymenoptera: Eulophidae) in relation to host density in the field

Abstract.

• 1 The relationship between parasitization by Edovum puttleri Grissell and density of eggs of the Colorado potato beetle, Leptinotarsa decemlineata Say (Coleoptera: Chrysomelidae), was studied on two spatial scales (eggs mass and 6 m² cage).
• 2 For both scales, rates of parasitism were generally inversely related to host density for periods ranging from 2 to 8 days after parasitoid release. Thereafter, parasitism became independent of host density.
• 3 The initial inverse-density relationship and subsequent shift to density independence may result from several factors: (1) ambient temperatures, (2) the parasitoid's limited egg production, (3) differential times of exposure of egg masses to parasitoids, and/or (4) the parasitoid's patterns of host feeding and oviposition.
• 4 Although overall levels of parasitism were relatively low, total mortality of L.decemlineata eggs (including nonviable and cannibalized eggs, and those killed by parasitoid feeding) in parasitized egg masses was consistently high (?70–90%).

     

FIELD OBSERVATIONS ON CENTROPUS TOULOU INSULARIS ON ALDABRA ATOLL

Frith, C. B. 1975. Field observations on Centropus toulou insularis on Aldabra Atoll. Ostrich 46:251-257.

Details are presented of the nesting of a pair of Malagasy Coucals on Aldabra, with incidental observations of other pairs and nests. Courtship and copulation behaviour is very similar to that of the black Coucal Centropus grillii of Africa. Both sexes net build and incubate the eggs but these activities are performed very predominately by the male. Eggs are white and average 27,5 x 23.5 mm and 8,3 g. Two complete clutches of two and one of thee egg; were found and a doubtful early record of a four egg clutch is considered unlikely. There was an interval of at least 9 days between the laying of the two egg;, which hatched 7–8 days apart, incubation commencing with the first egg. The incubation of the second egg was 14 days, and the fledging period of both young about 19 days. Nestlings in the chamber produce a snake-like hissing noise, excrete a foul-smelling sticky fluid when handled and burst through the rear chamber wall as means of avoiding predation.

Both members of the pair were in the brown plumage generally considered to be the non-breeding plumage. It is suggested that the plumages of the Aldabran population of Centropus toulou are possibly more complex than previously considered or that the population may be dimorphic.     

Breeding systems of New Zealand Snipe Coenocorypha aucklandica and Chatham Island Snipe C. pusilla; are they food limited?

New Zealand Snipe Coenocorypha aucklandica were studied over six breeding seasons on the Snares Islands. The study area (7.5 ha) held about 20 pairs at a density of 3.2 ± O.5 pairs/ha, plus 5 to 25 nonterritorial birds. Most matings were monogamous but simultaneous polygyny was recorded in one territory (by two different males) in four consecutive seasons. Males courtship fed females before egg-laying. The typical clutch was two eggs, laid three days apart. Incubation was shared equally by the sexes in monogamous pairs and took 22 days. Some females with polygynous mates attempted to incubate unaided, which took about 38 days. Broods were split at hatching, with the male caring for the first chick to leave the nest. Chicks were fed by adults for at least 41 days, and did not become independent until about 65 days old. Growth rates were slow compared to Common Snipe Gallinago gallinago and full plumage took about 54 days to attain. No pairs were double-brooded but 43% of pairs that failed during incubation or early chick-rearing renested together. Some breeders of both sexes who had lost their dependent chick bred a second time with a new mate while their first mate continued rearing the surviving chick (sequential polygyny and polyandry). Hatching success was 80%, and fledging success was 48%. Each pair produced, on average, O.6 fledglings per year. Chatham Island Snipe C. pusilla were studied on Rangatira Island during the 1983–84 breeding season. Breeding density was about 5.6 pairs/ha. The breeding system was very similar to that for C. aucklandica but chicks became independent at about 41 days old. Hatching success was 89%. Compared to Common Snipe, Coenocorypha snipes occurred at high densities, had courtship feeding, large eggs, a long interegy interval, a small clutch, shared incubation and a long incubation period. Nest desertion rates were high, but overall hatching success was also high, chick growth rates were slow, there was a long period of chick dependence and a long relaying interval following nest failure or chick loss. Survival rates of both adults and chicks were high. These differences are attributed to the absence of predation, and to intense intraspecific competition for food in a stable environment.     

Artificial incubation of trumpeter swan eggs: Selected factors affecting hatchability

Eggs collected from captive trumpeter swans (Cygnus buccinator) in 1993 (n = 33) and 1994 (n = 42) were artificially incubated with careful monitoring to identify factors contributing to the low hatch success reported by the Ontario Trumpeter Swan Restoration Program. Fertility was > 80% in both years, whereas hatch success of fertile eggs was 14.3% (n = 4) of 28 eggs in 1993 and 37.1% (n = 13) of 35 eggs in 1994. Necropsy of non‐viable eggs indicated a high incidence of embryonic mortality during early and late incubation. Early embryonic mortality was associated with egg storage times exceeding 7 days (P < 0.05) and bacterial contamination of eggs (P < 0.01). Late mortality was associated with (P < 0.001) increased weight loss during incubation period and may have resulted from incubator temperature and humidity fluctuations. We established patterns of weight loss for eggs and determined that hatched eggs lost 11–15% of initial mass and that weight loss >15% resulted in embryo mortality. Results from this study indicate that collection and handling of eggs before incubation and precise control of the incubator environment are critical to hatchability of eggs. Zoo Biol 18:403–414, 1999. © 1999 Wiley‐Liss, Inc.     

How incubation temperature influences the physiology and growth of embryonic lizards

Eggs of two small Australian lizards, Lampropholis guichenoti and Bassiana duperreyi, were incubated to hatching at 25 °C and 30 °C. Incubation periods were significantly longer at 25 °C in both species, and temperature had a greater effect on the incubation period of B. duperreyi (41.0 days at 25 °C; 23.1 days at 30 °C) than L. guichenoti (40.1 days at 25 °C; 27.7 days at 30 °C). Patterns of oxygen consumption were similar in both species at both temperatures, being sigmoidal in shape with a fall in the rate of oxygen consumption just prior to hatching. The higher incubation temperature resulted in higher peak and higher pre-hatch rates of oxygen consumption in both species. Total amount of oxygen consumed during incubation was independent of temperature in B. duperreyi, in which approximately 50 ml oxygen was consumed at both temperatures, but eggs of L. guichenoti incubated at 30 °C consumed significantly more (32.6 ml) than eggs incubated at 25 °C (28.5 ml). Hatchling mass was unaffected by either incubation temperature or the amount of water absorbed by eggs during incubation in both species. The energetic production cost of hatchling B. duperreyi (3.52 kJ · g⁻¹) was independent of incubation temperature, whereas in L. guichenoti the production cost was greater at 30 °C (4.00 kJ · g⁻¹) than at 25 °C (3.47 kJ · g⁻¹). Snout-vent lengths and mass of hatchlings were unaffected by incubation temperature in both species, but hatchling B. duperreyi incubated at 30 °C had longer tails (29.3 mm) than those from eggs incubated at 25 °C (26.2 mm). These results indicate that incubation temperature can affect the quality of hatchling lizards in terms of embryonic energy consumption and hatchling morphology. Accepted: 27 January 2000