Habitat preference, breeding success and the effect of primary productivity on Tawny Eagles Aquila rapax in the tropics

Breeding success of 176 Tawny Eagle pairs nesting on basalt (4724 km²– 92 pairs) and kalahari sand (9876 km²– 84 pairs) was monitored from 1973 to 1984 in Hwange National Park, Zimbabwe. Flat-topped trees were preferred for nesting but kalahari sand pairs used round-crowned trees more often, probably due to tree availability. Mean inter-nest distances on both biomes were significantly different (3–5 km on basalt, 59 km on kalahari sand). Clutch size and frequency of one-egg clutches in both biomes were similar and many more one-egg clutches were laid in the drier period of the study (1979–1984). There was no correlation between laying date and breeding success. More basalt pairs laid synchronously, probably due to the smaller inter-nest distances. Breeding success in both biomes was similar and significantly more chicks were reared during 1973–1978 than during 1979–1984 (wet and dry periods, respectively). Some districts produced more chicks than others, suggesting good and marginal areas within both biomes. The greater inter-nest distances and ability to breed successfully in round-crowned trees by kalahari sand Tawny Eagles resulted in a similar number of chicks reared per breeding attempt as basalt pairs, in spite of the lower primary production of the sand area.     

ASPECTS OF THE BREEDING STATUS AND ECOLOGY OF THE BATELEUR AND TAWNY EAGLE IN THE KALAHARI GEMSBOK NATIONAL PARK,SOUTH AFRICA

Herholdt, J.J., Kemp, A.C. & Du Plessis, D. 1996. Aspects of the breeding status and ecology of the Bateleur and Tawny Eagle in the Kalahari Gemsbok National Park. Ostrich 67:126-137.

The nesting success at 13 nesting territories of Bateleur Terathopius ecaudatus and 19 nesting territorites of Tawny Eagle Aquila rapax was monitored for seven successive years (1988–1994) in a protected area in the Kalahari desert of South Africa. On average Bateleurs laid one year in two (51/95 pair-years) and fledged 0.33 young/pair/year (31/95). Tawny Eagles laid, on average, in two out of three years (66/105), and fledged 0.4 young/pair/year (42/105). Most Bateleurs laid eggs in January and February, while Tawny Eagles mostly laid from May to June. Almost all Bateleur and Tawny Eagle nesting territories located were in the Acacia erioloba savanna in the dry Auob and Nossob riverbeds. Bateleur nesting territories were spaced at intervals of 7.2 km (2.5–14.6 km; n = 9) along the Nossob River. Tawny Eagle nesting territories were spaced at intervals of 17.6 km (6.1–32.7 km) in the Nossob River and 11.3 km (8–14 km) in the Auob River respectively. A total of 13 Bateleur and 30–40 Tawny Eagle nesting territories (27 known active nesting territories) respectively occurred in the Kalahari Gemsbok National Park during the study period. There was evidence of a 13% decline in active nesting territories of Bateleur during the seven year study, and at least a 40% decline over the previous 10 years. Vacated nesting territories were not reoccupied. There was no safe buffer zone around the Kalahari Gemsbok National Park and persecution in the adjacent farmlands, when foraging Bateleur from the protected Park enter these areas, as well as nesting site disturbance, could have been part of the reason for this decline. Poisoned and suspected poisoned Bateleurs have been found in the Park during the study period. There was no obvious decline in active Tawny Eagle nesting territories.     

Breeding success of the Eurasian eagle owl (<Emphasis Type="Italic">Bubo bubo</Emphasis>) and rodent population dynamics

The dependence of the breeding success of the eagle owl on the population dynamics of rodents, which are a staple of its diet in Mordovia, was traced. At peak numbers of rodents, large clutches and a high survival rate of fledglings were observed in the breeding pairs; after a year of depression of rodent populations, in the following year, the pairs do not nest at all or their breeding success is reduced to a minimum due to the death of the clutches. In 52% of the cases, the nesting pairs laid three eggs; in 31%, two eggs; in 9%, four eggs; in 4%, one egg or five eggs. The average clutch size was 2.78 ± 0.17. The average number of chicks grown from a successful nest was 2.41 ± 0.27. The nests in Mordovia were located at a distance of 1.1–3.7 km from residential areas.     

A 13-YEAR POPULATION STUDY OF THE BLACK EAGLES IN THEMATOPOS,RHODESIA, 1964–1976

Gargett, V. 1977. A 13-year population study of the Black Eagles in the Matopos, Rhodesia, 1964–1976. Ostrich 48:17-27.

The resident black Eagle Aquila verreauxi population in approximately 620 km² of the Matopos, Rhodesia, underwent changes from 1971 and appeared less stable than in the first five years. Six new territories were established in the National Park; two territories in Tribal Trust Land were abandoned; one territory in the National Park vacant for five years and one in Tribal Land vacant for at least 11 years were reoccupied. breeding data covering 13 years confirm the five-year findings. In 652 pair-years 442 breeding attempts were made with 339 young eagles f edging: a reproductive success rate of 0,52 young per pair per year. On average 68 % of the population bred every year, each pair attempted breeding in two years out of three, and one attempt in four was unsuccessful. Annual and individual variations in breeding performance were considerable, from 46% to 89% of the population breeding, and from two successes in six attempts for one pair to 12 successes in 12 attempts for two pairs. Over 13 years the percentage of the population breeding annually followed the form of a sine curve with a ten year period.

Fourteen factors that might affect annual and/or individual performance are considered. Below average rainfall years were followed by above average breeding; and generally fewer clutches were laid early after heavy rainfall in the three months preceding laying. Clutches laid late were less successful than those laid early. Breeding was affected by the proximity and intervisibility of nests, the previous year's performance and intraspecific disturbance. Appropriation of nests by other species prevented breeding and no new pair bred while establishing or re-establishing its territory. Building a new nest was followed by laying in the same season only if the nest was completed by mid-May, the peak laying period, building or partly building two nests in one season did not prevent breeding in the following year. At least 76% of clutches were c/2. The causes of two eaglets' deaths were ascertained and the remains of two adults were found. Pairs with territories in Tribal Trust Land had a significantly lower breeding performance than pairs in the protected National Park. Only traces of pesticide residues were found in four eggs. Observers' visits did not affect reproductive success.     

THE INFLUENCE OF THE ENVIRONMENT ON BREEDING SUCCESS OF A SUBURBAN POPULATION OF CRESTED BARBETS TRACHYPHONUS VAILLANTII

Van Zyl, A.J. 1994. The influence of the environment on the breeding success of a suburban population of Crested Barbets Trachyphonus vaillantii. Ostrich 65: 291–296.

I studied the breeding biology of the Crested Barbet Trachyphonus vaillantii in Colbyn, a suburb east of Pretoria, South Africa, for nine breeding seasons from 1981 to 1989 to examine patterns in annual breeding success, breeding attempt success in multiple broods, and rainfall. The modal incubation period was 14 days and the nestling period ranged from 28 to 31 days. Average clutch size for all the years was 3,3 eggs/clutch and there was no significant difference in clutch size or number of young fledged/nest between years. On average, Crested Barbet pairs made 2,4 breeding attempts/season. There was no difference in clutch size or breeding success between the breeding attempts. Crested Barbets nesting in natural nests laid on average larger clutches than those in artificial nestboxes, but had non-signficantly lower breeding success. Failure to raise Crested Barbet chicks was attributed to parasitism by Lesser Honeyguides Indicator minor, bee swarms occupying nestboxes, and flooding of natural nests. Breeding performance was not correlated with rainfall or adult body size. The suburban environment may be less variable than a natural environment, resulting in a stable breeding Crested Barbet population.     

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).     

3. NOTES OF THE BIRDS OF THE KRUGER NATIONAL PARK

Mundy. P. J. &; Cook. A. W. 1975. Hatching and rearing of two chicks by the Hooded Vulture. Ostrich 46:45-50

The single-egg clutches of 10 pairs of Hooded Vultures Necrosyrtes monachus were doubled by the addition of one egg to each in the breeding season of 1971/72 at Sokoto, Nigeria. Three pairs hatched both eggs and a further two pairs hatched one egg each. Only one pair raised both chicks to fledging and, apart from a depressed weight gain and tail growth of the younger “sibling”, the chicks grew at approximately the average rate for the species. The average rate was determined by following 27 normal nests in the study area. There was no evidence of aggression between the “siblings”. It was suggested that the success of one adult pair in raising two chicks was partly occasioned by the chicks' ages being only four days apart, and by the unusually rich food supply available from nearby human activities.     

Observations on the breeding biology and behaviour of the Lesser Jacana,Microparra capensis

Two Lesser Jacana nests were found in Hwange National Park, Zimbabwe and were observed over a period of four months beginning in March 2000. Both sexes were involved in preparing the breeding platform, incubation, and caring for the chicks, which were not carried by the adults. Both nests had three eggs. The incubation period for one clutch of eggs was not less than 19 days. The chicks all hatched on the same day and remained in the vicinity ofthe nest for the first few days where they were brooded by an adult. Initially the adults brought food to the chicks but the chicks started feeding themselves when they moved away from the nest. Ten days after hatching the chicks had doubled in size and were walking confidently with the attending adult some distance from the nest. First flight was seen at 32 days old, and the chicks appeared to be independent 63 days after hatching.     

Breeding performance of Indian Sarus Crane Grus antigone antigone in the paddy crop agroecosystem

The breeding performance of the Indian Sarus Crane Grusantigone antigone Linn. was studied in the agriculturallandscape of Gujarat, India during 1996. Detailed records of a total of22 nests were compiled from egg-laying till fledging. Eleven clutches(50.0%) produced at least one chick. Ten clutches (45.45%) weredestroyed due to various mortality factors, and one clutch (4.50%)failed to hatch. Of the 10 pairs whose clutches were destroyed, at leastfour renested. Renesting in the wild was reported for the first time.Egg destruction was mainly due to flooding (12.20%), predation (21.95%)and conflicts with farmers (14.64%). Predation accounted for 31.58% ofchick mortality. The egg and chick mortality factors identified wereunique to the agricultural ecosystem. The number of chicks that hatched andof chicks fledged per nest did not differ significantly in differentmicrohabitats. Hatching success was higher in non-cultivableagricultural marshland (68.18%) compared to paddy cultivated marshland(38.48%), mainly due to human disturbance and higher predation risk.Overall breeding success was 19.51%. Juveniles comprised only 8.96% ofthe total number of Sarus Cranes sighted during the post-breedingperiod. One of the causes of poor breeding performance in theagricultural landscape was increasing conflict with the farmers, whosuffer economic loss due to nesting in the crop field. If compensated,farmers may help in Sarus Crane conservation efforts.     

BREEDING NOTES ON THE BLACK-NECKED GREBE PODICEPS NIGRICOLLIS BREHM

Summary

Tarboton, W. R. &; Fry, C. H. 1986. Breeding and other behaviour of the Lesser Jacana. Ostrich 57: 233–243.

Breeding Lesser Jacanas were studied briefly at Lake St Lucia (Zululand), Hwange (Zimbabwe) and the Okavango Delta (Botswana). The species is monogamous and breeding birds are dispersed as territorial pairs. Male and female share incubation nearly equally, alternating at the nest in shifts averaging 39min; the eggs are attended (incubated or shaded), on average, for 82% of the daylight hours. Eggs are incubated by holding them against the breast with the underside of the wings; at least one chick was seen carried under a parent's wing. The pullus, foraging behaviour, courtship and vocalisations are described. It is suggested that the Lesser Jacana's small egg necessitates a high rate of nest attendance which could account for the sociosexual differences between this species and other jacanas.     

Increased survival and breeding performance of double breeders in little penguins Eudyptula minor,New Zealand: evidence for individual bird quality?

The little penguin Eudyptula minor is unique among penguin species in being able to fledge chicks from two clutches in one breeding season. Pairs laying two clutches in a given season make a higher reproductive investment, and may be rewarded by a higher reproductive success as they may raise twice as many chicks as pairs laying one clutch. The higher effort made by pairs laying two clutches could correlate negatively with survival, future reproductive performance or offspring survival, indicating a cost of reproduction. Conversely, a positive relationship between the number of clutches produced in a given breeding season and survival, future reproductive performance or offspring survival would indicate that birds laying two clutches belonged to a category of birds with higher fitness, compared to birds laying only one clutch in the season. In this study we used a long‐term data set taken from an increasing population of little penguins in Otago, SE New Zealand. We modelled the relationship between the number of clutches laid in a breeding season and survival probability, reproductive performance in the next breeding season and first year survival of offspring using capture‐recapture modelling.
Birds laying two clutches produced 1.7 times more fledglings during a breeding season than pairs laying one clutch. We found that birds laying two clutches had a higher probability of breeding in the following breeding season, a higher probability of laying two clutches in the following breeding season and a higher survival probability. There was no overall difference in post‐fledging survival between the young of birds producing one clutch and the young of birds producing two clutches. However, the survival of young of single clutch breeders declined with laying date, whereas the young of double clutch breeders had the same survival rate irrespective of laying date. For a subset of data with birds of known age, we found evidence that the probability of laying two clutches increased with age. However, there were also indications for differences among birds in the tendency to lay two clutches that could not be attributed to age. We tentatively interpret our results as evidence of quality difference among little penguin breeders.     

BREEDING BIOLOGY OF THE BATELEUR

Watson, R. T. 1990. Breeding biology of the Bateleur. Ostrich 61: 13–23.

Observations were made on the breeding biology of the Bateleur Terathpoius ecaudataus between 1981 and 1984, in the central region of the Kruger Nabonal Park. Nests were uniformly distributed with a mean inter-nest distance of 5,1 km and density of 3,1 nests/100km². Single-egg clutches were laid from January to June, and laying appeared to be suressed by unusually high rainfall events. The mean productivity was 0,47 young per pair per year, an a breeding failures were mainly due to failure to lay or predation. Breeding adults chaned nest sites within their territory on average once every 2,8 years, but territories and pairs were stable from year to year. Both members of a pair put equal time into care of the young.     

Breeding biology of the Redwing Francolin in the highland grasslands of Mpumalanga Province,South Africa

We studied the breeding biology of the Redwing Francolin, Francolinus levaillantii, in the highland grasslands of Mpumalanga Province, South Africa, from 1995–1996. The breeding season is from August to March. Clutches were incubated by hens only and all nests were located in rank grass close to surface water. Mean clutch size was 4.3 eggs (S.D. = 0.78, n = 10) and mean egg dimensions were 40.1 × 32.3 mm (S.D. = 1.07 and 0.81, n = 44). Hatching success was 83.7% and clutch survival rate to 22 days of incubation was 82.8%. A mean of 3 chicks was produced per clutch; observed mean production (counts of hens with chicks) was 2.6 chicks per brood (n = 24 clutches; 62 chicks). The hunting season for Redwing Francolin in Mpumalanga should be from 15 April to 15 July.     

Do marine birds use environmental cues to optimize egg production? An experimental test based on relaying propensity

According to the environmental cues hypothesis, female birds use information available to them in the early‐season environment to fine‐tune egg production annually. However, support for the hypothesis derives largely from correlational studies. In each year from 2002 to 2006, which spanned a period of extreme variation in environmental conditions, we removed eggs from early‐laying rhinoceros auklets Cerorhinca monocerata, burrow‐nesting seabirds that lay a single‐egg clutch. We then measured their relaying rates, relaying intervals, and breeding success. We also monitored the timing and success of breeding in control pairs, and control chick diets. If the experimental females base their relaying decision on early‐season cues, then we predict that few will relay in years in which early‐laying control birds breed unsuccessfully, and in which a preferred prey species, Pacific sandlance Ammodytes hexapterus, is in short supply in nestling diets. Results matched neither prediction. In each year, almost all (88–90%) of the experimental females relaid, despite that the control pairs’ breeding success (32–87% fledged chicks), and their chicks’ diets (twofold variation in proportion of sandlance), varied markedly. We conclude that female rhinoceros auklets did not modify their relaying decision in response to variation in environmental conditions, although relaying intervals and their own breeding success (0–78%) covaried negatively. Our results may have important implications related to using seabirds as monitors of the marine environment.     

Proceedings of the New Zealand Society for Parasitology Inc.

Abstract

A study of the nesting habits and breeding biology of blue penguin Eudyptula minor was undertaken over the 1995–96 and 1996–97 breeding seasons on Matiu‐Somes Island, Wellington, New Zealand. Male and female blue penguins tended to be faithful to both mates and nest sites, although there was insufficient evidence to detect any association between a bird's breeding success in 1995 and a subsequent change of mate or nest in 1996. Over the 1995 and 1996 seasons the recorded hatching success (0.51 ±0.11 and 0.63 ± 0.10 respectively), fledging success (0.81 ±0.12 and 0.85 ±0.10 respectively) and reproductive success (0.41 + 0.11 and 0.54 ± 0.11 respectively) were similar each season. There was no significant difference between the proportion of eggs laid, or eggs hatched and chicks fledged, between the two seasons. The mean number of chicks raised over the two seasons was 0.94 ± 0.05 per nest. Replacement clutches were laid by 11 per cent of failed breeders in each season, but only in 1996 were they successful in fledging chicks.

No significant difference was found between the breeding success of the Matiu‐Somes Island blue penguin colony recorded during this study and a previous study undertaken on the island 40 years ago.     

Breeding success and nest-site characteristics of Red-breasted Flycatchers Ficedula parva in a primeval forest

Capsule Predation is a major factor influencing the breeding success of Red-breasted Flycatchers under natural conditions.

Aims To examine the breeding success of Red-breasted Flycatchers in relation to nest-site characteristics and time of breeding.

Methods Data were collected during seven breeding seasons under natural conditions in Bia?owie?a National Park. We used survival time analysis to estimate changes in survival probability over time and breeding success in relation to first-egg date and nest-site characteristics.

Results Offspring fledged successfully from 51% of clutches, but the Kaplan–Meier estimate of survival was lower at 0.43. Of the unsuccessful clutches, 82% were lost to predators. The highest probability of loss was during egg-laying and in the second half of incubation. Breeding success was influenced by the height of the nest above the ground, but no relation to other nest-site characteristics was found.

Conclusion To avoid predation Red-breasted Flycatchers build nests in various sites that are more open than most cavity-nesting species. The position of the nest-sites allows the sitting female to observe her surroundings and to escape rapidly from the nest, giving the chance for a replacement clutch.     

Drought mortality of bush elephants in Hwange National Park, Zimbabwe

African bush elephants inhabiting the undeveloped Kalahari Sands region of Hwange National Park, Zimbabwe are subject to episodic mortality during droughts. We monitored the drought‐related mortality of elephants in Hwange National Park over the course of an extended drought between 1993 and 1995. The drought‐related mortality of elephants was higher during 1994 than 1995, despite significantly higher rainfall in 1994 than 1995. We found significant differences in the age‐specific mortality of elephants during 1994 and 1995. The cumulative mortality profile from this study differed significantly from previous die‐offs at this site, with a higher mortality among adult age classes than that reported from earlier studies in Hwange National Park. The effective duration of the rainy season, not total annual precipitation, appears to be the best predictor for the potential severity of drought mortality among elephants in the Kalahari Sands habitats of Hwange National Park.     

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.     

Effects of clutch size and egg-laying order on the breeding success in the Little Tern Sterna albifrons on the Nakdong Estuary, Republic of Korea

Survivorship of Little Tern Sterna albifrons eggs and chicks was followed on an islet in the Nakdong Estuary, Republic of Korea, in 1995 and 1996. Mean egg size and incubation period were significantly different between the 2 years. The maximum clutch size was three eggs, and the second egg in the clutch often hatched earlier than the first, while most of the third eggs hatched last. In 1996, when the fate of 249 eggs from 106 nests was followed for 40 days, hatching success, fledging success and breeding success were 77%, 40% and 31%, respectively. High mortality occurred in the early chick stage, mostly because of rain and predation by Weasels Mustela sibirica. The breeding success per egg was 14% in one-egg clutches, 28% in two-egg clutches and 34% in three-egg clutches. This difference was mainly attributed to the lower hatching success in the smaller clutches. In three-egg clutches, the third egg showed significantly lower breeding success than siblings. The main foods of the Little Tern were Tridentiger obscurus, Engraulis japonicus, Hyporhamphus intermedius, Acanthogobius flavimanus (all fish), Palaemon sp. and Crangon affinis (shrimps). The feeding frequency was, apparently, not affected by time of day and age of chicks but was probably influenced by weather conditions. Newly hatched chicks failed to eat 25% of the prey brought to them, although this decreased with the age of the chicks.     

Breeding success in a Houbara Bustard Chlamydotis [undulata] macqueenii population on the eastern fringe of the Jungar Basin, People's Republic of China

Nesting success and chick survival of a migratory population of Houbara Bustard Chlamydotis [undulata] macqueenii were studied during three consecutive years (1998–2000) in the Xinjiang province of north‐west China. A total of 45 nests was monitored and 85 broods comprising 227 chicks were captured, of which 82 chicks were radio‐tracked. Start of laying varied between 6 and 17 April between years but the laying mode fell consistently between 26 and 30 April. Mean clutch size was 4.0 (sd = 0.8) (range 2–6) for early clutches and 3.3 (sd = 1.1) for late clutches (range 2–5). The average nesting success was 0.588 (sd = 0.270) but great variations were observed between years –0.882 in 1998, 0.530 in 1999 and 0.351 in 2000. This was related to increased predation in 1999 and 2000, which is reflected by increased predator density (chiefly Corsac Fox Vulpes corsac and Long‐legged Buzzards Buteo rufinus). The overall hatchability, defined as the proportion of eggs hatched in successful nests was 0.839 sd = 0.238). The average brood size at hatching varied from 2.9 (sd = 0.8) to 3.3 (sd = 0.9) according to years, and no significant decrease in brood size was observed in the first 5 days post‐hatching. In 1999 and 2000 the brood size diminished sharply (14% and 27%, respectively) in prefledging chicks. A further severe decrease (37%) was observed in fledglings in 2000, probably due to predation by raptors. For the 3 years of the study, a successful female Houbara would bring on average 2.3 (sd = 0.9) chicks to fledging and would have lost 30.2% (sd = 14.9%) of its brood to adversity during the rearing process. The proportion of females that lost their entire brood was 0.181 in 1998, 0.708 in 1999 and 0.453 in 2000. For the 3 years of the study, only 55.3% (sd = 26.3%) of the females hatching eggs brought chicks to fledging. The overall chick production was 0.827 per breeding female per year and the probability of an egg laid producing a fledgling of 8 weeks old was 0.190.