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.     

NESTING DENSITY AND BREEDING SUCCESS IN THE HERRING GULL LARUS ARGENTATUS

The relationship between nesting density and breeding success of Herring Gulls Larus argentatus was studied on the Isle of May, Scotland, in 1968. Herring Gulls nesting at the most common density started laying earlier in the season than those nesting at lower or higher densities. Therefore, although the overall spacing of nests was uniform, the nest density of birds laying later in the season progressively approached a random distribution. The onset of laying occurred in synchronized groups within the colony. Late-laid clutches were commonly situated on the periphery of the colony where the density of nests was lowest. When the laying period was divided into four time periods, in each period the tendancy was for birds nesting at the most common density to have the highest clutch-size, hatching and fledging success, and to rear the most chicks per pair to fledging. In addition, birds which spaced their nests most uniformly, presumably as a consequence of territorial behaviour, were the most successful parents.     

Seasonal patterns of egg production in field colonies of the termite <Emphasis Type="Italic">Reticulitermes speratus</Emphasis> (Isoptera: Rhinotermitidae)

This is the first report on the annual egg production patterns in mature termite colonies in the field. Data on the seasonal patterns of egg production in field colonies are very important for understanding the annual colony growth schedule, resource allocation, and population dynamics of the termites. However, collecting the eggs from a sufficient number of colonies is extremely difficult in Reticulitermes termites because their multiple-site nesting makes it difficult to find the reproductive center of the colonies. Here, we first show the seasonal pattern of egg production in the subterranean termite Reticulitermes speratus by collecting the reproductive center of ten colonies each month from April through October. We had to destructively examine dozens of nests to find eggs from enough field colonies each month. Mature field colonies began to produce eggs in late May, soon after the swarming season, and the egg production rate (EPR) reached its maximum in early July. The eggs hatched until late October. The EPR was significantly correlated with the average monthly temperature. Additional investigation of the egg distributions in the nests showed that most eggs were kept around the royal cell, which contained the reproductives. The largest colony had 109 supplemental queens and 94,023 eggs, suggesting that each queen produced an average of 24.7 eggs per day, based on the known mean hatching period of an inseminated egg of 34.95±0.12 (SE) days.     

Breeding of the lappet-faced and white-headed vultures (Torgos tracheliotus Forster and Trigonoceps occipitalis Burchell) on the Serengeti Plains, Tanzania

The lappet-faced and white-headed vulture nests in a 1636 km² study area on the Serengeti Plains were kept under observation from June 1972 to August 1973. Active nests were inspected from a light aircraft at intervals of approximately 2 weeks. The inverse nesting densities were estimated as 43 km²/pair for the lappet-faced vulture and 409 km²/pair for the white-headed vulture. Nests were built of sticks in exposed sites on the crowns of trees, Acacia tortilis being the most popular species. Where the previous history was known, 44% of lappet-faced vulture nests were newly constructed, and the rest re-used from the previous year. The incubation period was about 55 days and the fledging period about 100 days in both species. Juveniles continued to frequent their nests after they could fly, sometimes for several months. Most lappet-faced vultures laid their eggs in April-May, the white-headed vultures in June-August. This means that the lappet-faced vultures raised their young during the dry season, when Grant's and Thomson's gazelles were the only animals present in any numbers on the plains. By contrast, the Ruppell's griffons nesting in the nearby Gol Escarpment colony raise their young during February-May, when the wildebeest and zebra herds are normally on the plains. The survival rate of lappet-faced vultures from laying to fledging was about 40%. The chicks are thought to be vulnerable to predation by tawny eagles, and one was known to have been killed by a leopard. Three adult vultures were killed on their nests, from unknown causes. Food remains from lappet-faced vulture nests showed a heavy preponderance of Grant's and Thomson's gazelles in all cases, with golden jackal the next most commonly occurring species. No food remains were obtained from white-headed vulture nests. The possibility of using aerial counts of vulture nests as an indicator of productivity is discussed.     

Breeding cycle of the Cape petrel Daption capense at Nelson Island, Antarctica

Timing and duration of the breeding cycle of the Cape petrel Daption capense were studied during two breeding seasons (1990/1991 and 1991/1992) at Nelson Island, South Shetland Islands, Antarctica. In 1991/1992 the copulatory period extended over 53 days, with median date and a peak about 28 and 19 days respectively, before the median date of laying. Laying began 85 days after arrival, with mean (= median) date on 2 December (SD = 2.5 days). The distributions of laying, hatching and fledging dates showed a similar degree of synchrony and did not differ between years. Incubation and chick period were equally long (46 days), the former being less variable (coefficient of variation = 2.8% and 4.6%, respectively). Mean completed nesting cycle (92 days) was about 2 days shorter at Nelson Island than elsewhere and tended to shorten as the breeding season progressed. Its mean length represented 86% of the whole nesting period (107 days), which in turn represented 56% of the period of continuous colony attendance. Timing and duration of nesting stages did not differ between colonies or sets of nests subjected to various levels of disturbance. Received: 8 July 1996 / Accepted: 11 November 1996     

Nest and breeding population abundance of Least Terns: assessing bias and variation in survey timing and methods

Methods commonly used to estimate the number of nests and size of the breeding population at colonies of Least Terns (Sternula antillarum) and other waterbirds include walk‐through counts of nests (ground‐nest counts) and counts of incubating adults from the colony perimeter (incubating‐adult counts). The bias and variance of different methods and the comparability of repeated surveys versus once‐annual censuses are poorly understood. Our objectives were to assess (1) the potential bias and variation of the more rapid incubating‐adult counts compared to the time‐intensive, and presumably more accurate, ground‐nest counts, and (2) how accurately a once‐annual census captured peak nesting abundance. We studied nine Least Tern colonies at Cape Lookout National Seashore (CALO), North Carolina, from April to August 2010–2012. We analyzed observer and survey method agreement with concordance correlation coefficients (ρ_c). We deployed time‐lapse cameras at 156 nests and used repeated‐measures logistic regression to determine if the proportion of time spent incubating varied with colony, time of day, or time of season. We found substantial agreement in abundance estimates of Least Tern nests and incubating adults between observers and survey methods, and among different times of day and seasons (all comparisons ρ_c > 0.97). Least Terns incubated eggs 94% of the time on average during daylight hours, irrespective of colony, nesting stage, or month. Although the nesting peak at CALO occurred during the recommended census period for Least Terns, abundance estimates for surveys conducted at different times during that period varied by as much as 39%. We recommend conducting incubating‐adult counts to estimate nest and breeding population abundance of Least Terns or other waterbirds when vegetation or dunes do not obstruct views of nesting colonies. In addition, given the variation in abundance estimates for surveys conducted at different times during the recommended survey period, incubating‐adult counts should be performed at least twice during the census period, with the maximum count reported as peak nest abundance.     

Nest survival and productivity of the critically endangered Sociable Lapwing Vanellus gregarius

The Sociable Lapwing Vanellus gregarius is a critically endangered species, probably declining from 5000 pairs to 500 pairs in 11 years. Fieldwork was conducted at two sites in Kazakhstan, May–August 2004, to identify causes of the species’ decline. In total, 58 nests and a minimum of 36 broods in 16 colonies were found: colonies consisted of 1–8 nests that were on average 154 m apart, with 2.1 km between colonies. Although classified as biparental, the total proportion of time both parents spent incubating was low (77 ± 2% se, n = 13 nests). Daily survival rates (Mayfield method) were very low during incubation (0.943 ± 0.009 se) but high during the chick stage (0.986 ± 0.004 se); incubation and chick‐stage durations were found to be 28.5 and 29 days, respectively, so that the overall probability of any breeding attempt fledging chicks was 0.124 (0.055–0.274 95% confidence interval). A breeding attempt that produced fledglings, fledged 2.2 ± 0.2 se chicks (n = 26) on average. Observed productivity predicted the population decline over the last 11 years well (using the maximum number of nesting attempts per pair of 1.4 that could have occurred in this study, and assuming an adult and first‐year survival rate of 0.74 and 0.60, respectively, based on the means for Northern Lapwing Vanellus vanellus and Golden Plover Pluvialis apricalia). Nest survival during incubation (controlling for colony effects) may have been longer for nests in predominantly Artemisia rather than grass habitat. Mean nest survival for a colony was higher in areas with more bare ground and more nest predators, suggesting that predators were relatively unimportant in nest (egg or chick) mortality, but was lower in areas with high numbers of cattle, suggesting that trampling was important (64% of known‐cause nest failures, n = 11, were trampled). Nests were preferentially sited in areas of Artemisia, where there was greater dung abundance, and probably shorter vegetation, suggesting that highly grazed vegetation is important for nesting. Chicks preferentially selected areas with a lower percentage of bare ground and possibly taller vegetation, suggesting that more vegetated areas are important for chicks. The results suggest that low egg survival due to nesting in areas of high grazer density may be responsible for the Sociable Lapwing's decline. Although grazers may create suitable vegetation for initial nesting, if those grazers remain at high density as in anthropogenic systems then they may reduce nest survival, probably through trampling. Experimentally maintaining grazing early but reducing it later in the breeding season is the logical first step in managing the species to increase egg survival and so to increase productivity.     

THE BREEDING OF HEUGLIN'S MASKED WEAVER AND ITS NESTING ASSOCIATION WITH THE RED WEAVER ANT

Grimes, L. G. 1973. The breeding of Heuglin's Masked Weaver and its nesting association with the Red Weaver Ant. Ostrich 44: 170–175.

The breeding season of Heuglin “s Masked Weaver Ploceus heuglini at Legon began in the latter half of the major dry season in January and February; continued through the main wet season and ceased in late August and for the rest of the year. The Accra colony had a similar breeding activity but in addition was active for a short period in November which had ended by mid-December. Although the majority of males formed colonies in which the number of males ranged from two to twenty, solitary breeding occurred equally frequently. Most males within the Legon colony, and possibly this is true for all colonies, were polygynous while most solitary males were monogamous. More nests were built by each male than the number of females involved in the polygyny.

A close nesting association with the Red Weaver Ant Oecophylla longinoda existed and the data suggested that the weaver sought the ant. Two cases were found of nesting association with the wasp Belanogaster grisens.     

Breeding biology of the Barn Owl Tyto alba in central Mali

Data were obtained on 178 clutches of African Barn Owls in central Mali from four breeding seasons during 1979–1983. Significantly more clutches were laid in 1979–1980 and significantly fewer in 1980– 1981 than the average for the 4 years and there were significantly more clutches laid in the middle period of the annual breeding season. The egg volume was significantly smaller at the beginning of the breeding season and significantly larger in the middle than the overall mean with eggs of second clutches being larger than those of first clutches. The clutch size was 605 eggs of which 479 hatched. The number of young fledged per successful nest was 319 and was 1 83 for all nesting attempts. The month was the only variable shown to affect significantly the clutch size, eggs hatched and fledging rate, the highest success rates being associated with the middle of the breeding period. The average interval between the hatching of eggs was 2–31 days. Survival rates (47'1%) to fledging were significantly affected by year (1981–1982 being the least) and month (mid-season birds the best). The order of hatching significantly affected age at death or disappearance, the first-hatched birds surviving the longest. The year significantly affected age at fledging, the young from the year in which most clutches were laid leaving the nest at the youngest age and those associated with the year having the least number of clutches remaining in the nest the longest. The month of hatching also affected fledging age, birds at the extremes of the breeding season fledging at older ages. The discussion compares these data with those from elsewhere.     

BREEDING OF SACRED IBIS THRESKIORNIS AETHIOPICA AT LAKE SHALA, ETHIOPIA

Data are based on more than 200 h of observation at Ethiopia's Lake Shala from 1966 to 1972. Except for differences in size of bill, there are no useful field characters separating male and female Sacred Ibis. The breeding plumage is described; vivid blood-red colour underneath the wings and the ornamental plumes are especially obvious when nesting commences. Physical and biological features of Lake Shala, Ethiopia, and its nesting islands are described; the species of birds nesting on the Shala islands are given. Ibises nest at Shah from March to August; no nesting has been recorded from September to February during the last months of the ‘big’ rains through the main dry season. Nesting normally begins in the ‘small’ rains (between 14 March-24 April), although instances were recorded as early as 1 March and as late as 20 August. The ibises normally nest once per year, although it is possible that occasionally a second nesting may occur after an unsuccessful first attempt. The ibises at Shala nest in discrete groups; several nesting groups may form on any or all of the islands; the number of groups attempting to nest varied from year to year. Nesting activity begins when males arrive and establish pairing territories, usually in a small tree but sometimes on the ground. When females and other males arrive at the pairing territories, pair formation ensues. At this time males perform forward threat, modified forward threat, pursuit flight, supplanting attack and modified snap displays, while both sexes perform stretch and bow displays. Once established, the pair abandons the pairing territory and moves to the nesting area, usually near but always distinct from the pairing territory, and establishes a nest-site territory. Most members of the nesting group move to the nesting area on the same day. Copulation then takes place, and is followed by collection of nest material, usually by the male. Nests are built close together. The average area of 10 nests measured was 0.09 m². Nests are usually less than 20 cm thick and are made of many small branches and sticks. The average clutch in 34 nests was 2.24 eggs; the average size of 34 eggs was 63.4×43.5 mm. Incubation probably begins when the clutch is complete. Both sexes incubate, and the incubation period probably lasts 28–29 days. The development of the young is described. The young leave the nest-site territory when 14–21 days old. Although they are capable of some flight when 35–40 days old, the young do not leave the colony until they are 44–48 days old. In the colony, both parents care for the young. Usually only one parent at a time is with the young. The parents recognize their own young and are usually recognized by them. The behavioural interactions between young and parents are described. Fledging success in 1968 was 1.06 young per pair. The number of pairs successfully rearing young varied annually from none to 81%, on average over six years (1966–70, 1972) 35%. Predation at the breeding colonies is minimal. The food of one one-month old chick consisted of beetle larvae, lepidopteran larvae and beetles. Feeding areas, although undetermined, must be widespread. Inter-specific competition between Sacred Ibis and other nesting birds at Shala is discussed. Among possible factors stimulating nesting at Shala one, fairly heavy rainfall, seems to be especially important. It is also suggested that especially heavy rain-storms cause ibises to abandon the colonies, and result in poor breeding success.     

Effects of the parasitic botfly Philornis carinatus on nestling house wrens,Troglodytes aedon,in Costa Rica

I studied the life cycle of a botfly (Diptera: Muscidae: Philornis carinatus) and examined the effects of botfly ectoparasitism on nestling house wrens (Passeriformes: Troglodytidae: Troglodytes aedon) during three years in Costa Rica. At three study sites, I found that nestlings were relatively unaffected by botflies, in contrast to all other studies of birds infected with philornid botflies. At Monteverde, the main study site, infected chicks grew slightly slower and had slightly shorter tarsi and wing chords than uninfected chicks, but both groups fledged at similar weights. Since weight at fledging is the only growth character associated with post-fledging survivorship, botfly infections likely cost wrens little in terms of fitness. At all sites, fledging success did not differ between infected and uninfected nests. Botfly infections were more prevalent at two lower elevation sites than at the high elevation Monteverde side. Infection prevalence increased during the nesting season at all study sites, which suggests a botfly life cycle in which adult population levels increase during the wren breeding season and then decline during a dormant period when wrens are not nesting. Finally, botflies may attack chicks throughout the period before fledging, but there is no indication they locate nests before hatching. In sum, botfly parasitism on wrens appears to be benign, perhaps because the study sites are at the edge of the botfly's range or because wrens are not a preferred host.     

Spatial patterns, temporal variability, and the role of multi-nest colonies in a monogynous Spanish desert ant

Abstract 1. The colonies of the Spanish desert ant Cataglyphis iberica are polydomous. This study describes the temporal and spatial patterns of the polydomy in this species at two different sites, and presents analyses of its role in reducing the attacks of the queen over sexual brood, and in allowing better habitat exploitation.
2. The spatial distribution of nests was clumped while colonies were distributed randomly. Mean nearest neighbour distance ranged from 3.4 to 7.0 m for nests and from 12.3 to 14.1 m for colonies. Distance of foragers searching for food varied among nests: mean values were between 6.1 and 12.6 m.
3. At both sites, the maximum number of nests per colony occurred in summer, during the maximum activity period of the species. Colonies regrouped at the end of this period but overwintered in several nests.
4. Nest renewal in C. iberica colonies was high and showed great temporal variability: nests changed (open, close, re-open) continuously through the activity season and/or among years. The lifetime of up to 55% of nests was only 1–3 months.
5. Polydomy in C. iberica might decrease the interactions between the queen and the sexual brood. In all colonies excavated just before the mating period, the nest containing the queen did not contain any virgin female. Females were in the queenless nests of the colony.
6. The results also suggest that polydomous C. iberica colonies may enhance habitat exploitation because foraging activity per colony increases with nest number. The relationship between total prey input and foraging efficiency and number of nests per colony attains a plateau or even decreases after a certain colony size (four to six nests). This value agrees with the observed mean number of nests per colony in C. iberica .     

Blue penguin (Eudyptula minor) nest distribution and breeding success on Otago Peninsula, 1992 to 1998

Abstract

Annual counts of nests with eggs or chicks (known nests) were made at blue penguin (Eudyptula minor) breeding sites on the Otago Peninsula in each November from 1994 to 1997. Although the population has doubled to an estimated 600 known nests over this period, the number of breeding sites on the Otago Peninsula has reduced since the 1970s. Breeding success at three areas at Taiaroa Head were monitored by regular nest checks in the breeding season from 1992 to 1998. At Taiaroa Head reproductive success ranged from 41 to 78% at the three sites during the seven‐year study and was generally higher for pairs nesting in nest boxes than for those in burrows. The percentage of breeding pairs that laid a second clutch after fledging at least one chick from their first clutch (double brooded) varied between seasons (0–48%) and was correlated with the date of the onset of breeding. Egg loss, possibly through predation by Norway rats (Rattus norvegicus), influenced the significantly lower reproductive success at one area (Area A) at Taiaroa Head during the 1996 season.     

TIMING AND SPACING OF BROODS IN THE BLACK-HEADED GULL LARUS RIDIBUNDUS

The nests of the Black-headed Gull Larus ridibundus are closely aggregated into dense colonies and their use synchronized, these two phenomena together tending to produce a maximal clumping effect. Within such a colony however, nests were found to be spaced out to produce a non-random uniform distribution. The commonest distance between neighbouring nests was found to be about one metre, in contrast to related species. This study was concerned with two aspects of this distribution pattern; its survival value and its behavioural causation.
It was found that pairs nesting just outside the colony had a much lower breeding success than those nesting in the colony and that nests on the colony fringe had a slightly lower success than those in the centre. Pairs laying during the peak laying period had a higher breeding success than pairs laying either earlier or later in the season. Since by far the most important mortality agent was predation, it seems likely that both clustering and synchronization of nesting function as antipredator systems and arguments in favour of this are discussed.
Variations in nest-spacing within the colony were not correlated with variations in breeding success.
In the causation of the spacing between nests, territorial aggression was demonstrated to be an effective dispersion mechanism and the way in which this mechanism works was investigated in detail.
This spacing mechanism was not sufficient by itself to explain the observed densities, which were higher than one would expect from the aggression alone; there was also some tendency for birds establishing a new nest-site to cluster close to others. The interaction between this, the territorial aggression of the residents and the subsequent avoidance responses of the settling birds, can explain the nest spacing pattern and probably also the observed densities.     

Early-season colony development of the paper wasp Ropalidia plebeiana (Hymenoptera: Vespidae) in Canberra, Australia

This study presents the first observations of early-season colony development of Ropalidia plebeiana in Canberra, Australia. The growth pattern of three R. plebeiana nests was measured during weekly observations from October 2006 to January 2007 and showed that nests steadily increase in size over the early summer to approximately 50 cells when the nest is newly established and to approximately 170 cells when nests from the previous season are re-used. A first generation of adult females is produced by December, and the bimodality of the curves of egg, larval and pupal numbers indicates that these three developmental stages last approximately 2–3 weeks each. The nesting cycle of R. plebeiana in Canberra commences approximately 2 weeks later than in coastal Australia, the shorter summers in this inland region restricting the length of the active season. R. plebeiana did not form dense nesting aggregations in Canberra as described elsewhere, with only small colonies consisting of a single or just a few nests. Characteristic comb-cutting behavior of the species was observed but this did not result in complete nest division as recorded from coastal populations.     

The post‐fledging period in a tropical bird: patterns of parental care and survival

How environmental conditions affect the timing and extent of parental care is a fundamental question in comparative studies of life histories. The post‐fledging period is deemed critical for offspring fitness, yet few studies have examined this period, particularly in tropical birds. Tropical birds are predicted to have extended parental care during the post‐fledging period and this period may be key to understanding geographic variation in avian reproductive strategies. We studied a neotropical passerine, the western slaty‐antshrike Thamnophilus atrinucha, and predicted greater care and higher survival during the post‐fledging period compared to earlier stages. Furthermore, we predicted that duration of post‐fledging parental care and survival would be at the upper end of the distribution for Northern Hemisphere passerines. Correspondingly, we observed that provisioning continued for 6–12 weeks after fledging. In addition, provisioning rate was greater after fledging and offspring survival from fledging to independence was 75%, greater than all estimates from north‐temperate passerines. Intervals between nesting attempts were longer when the first brood produced successful fledglings compared to nests where offspring died either in the nest or upon fledging. Parents delayed initiating second nests after the first successful brood until fledglings were near independence. Our results indicate that parents provide greater care after fledging and this extended care likely increased offspring survival. Moreover, our findings of extended post‐fledging parental care and higher post‐fledging survival compared to Northern Hemisphere species have implications for understanding latitudinal variation in reproductive effort and parental investment strategies.     

Brood raiding and the population dynamics of founding and incipient colonies of the fire ant, Solenopsis invicta

Abstract. 1. One of the first activities of minim workers in incipient fire ant nests is mutual brood raiding, the amalgamation of nests through the reciprocal stealing of brood and defection of workers.
2. Discrete mating flights created cohorts of incipient colonies. About 25% of founding nests survived the claustral period of 16–48 days (depending on season). Early incipient colony mortality was 5–6% per day. Over 60% of this mortality was accounted for through brood raiding. Most colonies raided when each cohort first became active, and many raided more than once. Raid size (number of nests, duration, distance) tended to increase during the summer as colonies grew through raiding. After the raiding period, nest mortality rate dropped 3–10-fold. Only 1–3% of founding nests were still alive at this time.
3. Queens from losing or failed nests tended to abandon their nests and attempted to enter successful ones, often following raiding trails to do so. This emigration was at least as successful as non-emigration in ultimately achieving the status of reproductrix of a successful nest (about 4%).
4. Brood raiding is a dominant process in early population dynamics, probably accounting for most of the early nest mortality. Its effect is to change the venue and unit of competition from nest-against-nest to a shifting aggregation of queens, workers and brood involving entire local populations. Nest thinning is thus very rapid, and the boost to the size of winning nests very large, allowing raiding colonies to win the competition for territory, and to achieve the early colony maturity so important to this, and other, weedy species. The importance of winning brood raids may also have driven increased minim production through the evolution of pleometrosis.     

Nourishment affects colony demographics in the paper wasp Polistes metricus

Abstract  1. Colony survivorship and numbers of nest cells, pupae, and adult females were monitored throughout the nesting season for a cohort of 78 colonies of the paper wasp Polistes metricus Say. Thirty-nine colonies received a twice-weekly nourishment supplement of honey during pre-emergence and early emergence phases of the colony cycle; 39 colonies were unsupplemented controls.
2. Colony survivorship was unaffected by the supplemental nourishment. Loss of colonies to predation differed among three sites but was unaffected by supplementation.
3. Honey-supplemented colonies constructed more nest cells than did control colonies but this effect was not expressed until after supplementation had ceased.
4. Honey-supplemented colonies produced more pupae than did control colonies but the number of adult females at nests did not differ between supplemented and control colonies. Because honey-supplemented colonies had more offspring but fewer of them remained as workers at the nest, honey supplementation led to a lower frequency of workers and corresponding higher frequency of reproductives than in control colonies.
5. In a second year of study, colony survivorship and numbers of nest cells, pupae, and adult females were monitored from late pre-emergence until the end of the nesting season for a cohort of 32 colonies of Polistes metricus . In 16 colonies, trophallactic saliva was taken from final-instar larvae on nine dates in the late pre-emergence and early emergence periods; 16 colonies served as controls.
6. Saliva-diminished colonies had lower survivorship, fewer nest cells, fewer pupae, and fewer adult females at the nest than did control colonies.
7. These results show that variation in nourishment in the early to mid phases of the colony cycle can have significant effects on the subsequent colony demographics of Polistes metricus paper wasps.     

THE BREEDING BIOLOGY OF THE GREAT WHITE PELICAN PELECANUS ONOCROTALUS ROSEUS AT LAKE SHALA, ETHIOPIA

Pelecanus onocrotalus roseus is known to breed more or less regularly in Africa at Lake Shala, Ethiopia; Lake Rukwa, Tanzania; St. Lucia Bay, Natal; Abou Tougour, Chad; Kapsikis, Northern Cameroons; and Wase Rock, Nigeria; and has been observed or reported breeding at Mweru Marsh, Zambia; Lake Ngami, Botswana; Seal and Dyers Islands, South Africa; and Lake Natron, Tanzania. The Shala colony, after Lake Rukwa's, is the largest known breeding colony in Africa and is probably of crucial importance to the species in Africa. For successful breeding regular colonies of P. onocrotalus must have an assured supply offish and an inaccessible breeding site. These conditions are met at the Lake Shala colony. Assuming that a Great White Pelican consumes about 10% of body weight or about 900-1,200 g per day, the Lake Shala breeding colony with 7,500-12,000 pairs would consume about 3,140-5,040 tonnes in the breeding seasons. The partially unsuccessful breeding of perhaps 10,000 pairs at Lake Natron in 1962 is described. Failure was attributed to sudden failure of the food supply. Breeding of the Great White Pelican on Lake Shala takes place throughout the year although there is a peak of numbers breeding from December to the end of March, which is in the dry season. Observations recorded in this paper cover two full breeding seasons, 1965-6 and 1966-7. Although during the peak period of breeding the flock at Shala is made up of 2,500-5,000 pairs, this mass is composed of smaller units, each made up of 300-1,200 pairs, laying more or less together with little overlap from one group to the next. Three changes occur in the plumage of the Great White Pelican towards the onset of the breeding season: (a) the development of a knob or swelling on the forehead at the base of the beak with associated expanses of brightly-coloured bare skin, pinkish yellow in males and bright orange in females; (b) the development of a crest; and (c) the development of a yellowish band across the chest or larger areas of darker brown in the plumage. Four distinct colour-types of breeding plumage were observed: the dark-brown type, the brown-breasted type, the yellow-banded type, and the type with scarcely any suggestion of a breast patch. No correlation was found between plumage type and sex, size, length of bill or any other obvious physical feature. Group display and individual displays of the adults are described. There appears to be no special pre-copulation display. Elaborate nests are not prepared; the male collects the nesting material, and both sexes build the nest. Nests are small, 35–60 cm in diameter (averaging 46-4 cm), and close together (364 nests averaged 1–55/m²). Average clutch-size is 1–88. Incubation begins with the first egg; both sexes incubate; the incubation period is probably about 38 days. The fledging period is 65–70 days, of which about the first 28–30 days are spent in the nesting area. After that the young form into groups or “pods”. The development of the young is described. When it is very small it is fed by either parent several times each day. When the young is 30–35 days or older, it is probably fed less than once per day. The bright red nail-like tip of the adult's upper mandible serves to direct the begging movements of the young chick, and it probably holds the liquid food on which the chick feeds. It is suggested that pod formation of young both in the middle of the day and at night possibly helps to avoid extremes of temperature, either of heat or cold. Parents recognise their own chicks; and young pelicans, at a later stage, recognise their parents. Indiscriminate feeding of young does not occur in P. o. roseus. Adults often are quiescent but not asleep at night. Activity is stimulated by the earliest light, and most pelicans begin leaving the island by 09.30-10.00 hrs. Most departures and arrivals take place from about 10.00 to 16.00 hrs. The distance from which food is brought to the colony is not known for certain, but most birds probably fly to and from Lake Abiata. It is not known where the young go once they leave the colony; most do not fly to the obvious place, Lake Abiata. Although difficult to determine, we suggest that the breeding success of the pelicans is on the average less than one young per nest. Egyptian Vultures were the most important predators at the colony, but all forms of predation together accounted for less than 10% of the nesting losses. The timing of breeding in relation to food supply, climatic factors and inaccessibility of the breeding site is discussed. Inaccessibility appears to override seasonal factors, but in permanently inaccessible sites the peak of breeding is in the dry season. It is suggested that the Great White Pelican nests in discrete breeding units within the main colony to minimise the effect of predation.     

Colony Foundation and Nestmate Recognition in the Social Wasp,Belonogaster petiolata

Emergence from hibernation and synchronized nest foundation by foundresses of B. petiolata in the southern Transvaal, appeared to be stimulated largely by a rise in temperature during early and mid August of each season. Initial foundresses on newly built nests were joined by other foundresses during the first few weeks of the nesting season to form foundress associations. Although females were strongly philopatric and able to discriminate between nestmates (from their natal nests) and non-nestmates, former nestmates did not reassociate to a significant degree on new nests. Thus, associated foundresses were, on average, not closely related. Rather than facilitating the reassociation of former nestmates, the advantage of philopatric behaviour appears to lie in ensuring that foundresses return to an area of relatively high nesting density, where their chances of being involved in multiple-foundress groups (irrespective of intra-colonial relatedness) are high. Non-philopatric females which nest away from localities of high nesting density have a low probability of being involved in associations, and may therefore have to attempt colony foundation alone, with little or no chance of reproducing successfully.