THE MOULT OF THE BULLFINCH PYRRHULA PYRRHULA

The distribution of feather tracts and their sequence of moult in the Bullfinch is described. The adult post-nuptial moult, which is complete, lasted 10–12 weeks, and the post-juvenile moult, which is partial, 7–9 weeks. Adult moult began with the shedding of the first (innermost) primary and ended with the replacement of the last. Variations in the rate of moult in the flight feathers were mainly achieved, not by changes in the growth rates of individual feathers, but in the number of feathers growing concurrently. The primaries were shed more slowly, and the onset of body moult delayed, in birds which were still feeding late young. In 1962, the onset of moult in the adults was spread over 11 weeks from thc end of July to the beginning of October, and in the two following years over the six weeks, from the end of July to the beginning of September. The onset of moult was delayed by late breeding, which itself occurred in response to a comparative abundance of food in late summer, markedly in 1962. In all years, the first juveniles to moult started at the end of July, and the last, three weeks after the latest adults. Juveniles moulting late in the season retained more juvenile feathers than those moulting earlier. During moult, adult and juvenile Bullfinches produce feathers equivalent to 40% and 33% respectively of their dry weights. In both, for much of the moult, an average of nearly 40 mgm. of feather material—some 0.6% of their dry-weight–is laid down each day. The remiges of the adult comprise only a seventh of the weight of the entire plumage, and it is suggested that their protracted moult results not so much from their energy requirements, as from the need to maintain efficient flight. Variation in the rate of moult in the remiges was much less pronounced than in the body feathers. Bullfinches were less active during moult than at other times of the year. The weights of both adults and juveniles increased during moult. The food during the moult period is described. In all years, most Bullfinches finished moulting just before food became scarce, even though this occurred at different times in different years. In one year, adults moulting latest in the season probably survived less well than those moulting earlier; the same was apparently true of the juveniles in all years. The timing of moult in the Bullfinch, and the factors initiating it, are discussed in relation to the breeding season and foodsupply near Oxford.     

MOULT IN FIVE SPECIES OF CORVIDAE IN BRITAIN

This paper presents objective methods for measuring moult and uses them to describe the pattern and rate of the complete moult as a component of the annual cycle in Corvus corone, C. frugilegus, C. monedula, Pica pica and Garrulus glandarius in Britain. The basis of the methods used to measure the rate of moult was the dry weight of the whole plumage and its component tracts and feathers. Within whole tracts of flight feathers showing diversity of size, the longer feathers grew in length a little faster than the others by accumulating feather material very much faster. Thus, for the flight feathers at least length by itself was a poor indicator of size, but, if first related to weight, could be used to predict weight. Hence, to enable realistic comparisons to be made between different flight feathers and tracts of flight feathers on a given individual bird or on individuals of different species, a ‘units’ system was created which would take account of such variations in size. This information provided a standard against which the growth of new flight feathers in a specimen collected in the field could be measured. The progress of moult in each tract was indicated by the sum of the units. In addition, for both the flight feathers and all other tracts, the duration of moult was measured from the start and finish in each tract as indicated by the proportion of birds having either growing or entirely fully-grown feathers in each tract. In the annual cycle body weight and abdominal fat weight were at a maximum in mid-winter and at a minimum in mid-summer in Corvus; variations in these items were apparently absent in G. glandarius. In Corvus probably only post-second-year birds breed, but in P. pica some second-year individuals do so as well; also, increase in testes size in second-year males was greatest in P. pica. The patterns of the relative seasonal timing of the start and finish of moult in each tract were most similar in the three Corvus species, in which moult in the whole plumage began in the primary tract and finished in tracts on the body; P. pica differed principally in the extended growth of the secondary tract; G. glandarius differed in that moult began in the dorsal tract. By summing the data from individual tracts, a measure of the rate of growth in the whole plumage was obtained: all five species moulted at essentially the same time of year. In the primary, secondary, tertiary and rectricial tracts the seasonal accumulation of dry weight of feather material in each tract followed a sigmoid pattern; in the alula tract dry weight increased most rapidly at the beginning. These patterns were correlated with the numbers of feathers growing at different stages in each tract. The primary tract accumulated dry matter at the highest relative rate, while the rectricial, secondary, tertiary and alula tracts did so at successively lower rates. The maximum relative rate of increase in dry weight in any given tract of flight feathers was fairly similar in all five species, but was possibly related inversely to body weight. Maximum absolute rates of increase in dry tract weight were also calculated. During the springtime period when non-moulting and moulting birds were present simultaneously in the population, no difference could be detected between these groups in any species in body and fat weights; in individuals obtained together with evidence of reproductive activity, few had begun primary moult, but in post-second-year C. frugilegus with branchers, males began before females; in C. corone and C. frugilegus testes weight was lower in moulting than in non-moulting birds. In conclusion, some aspects of moult for further research are suggested.     

MOULT OF THE PURPLE SANDPIPER CALIDRIS MARITIMA IN ICELAND

The autumn moult pattern of adult Purple Sandpipers Calidris maritima in Iceland is described. The duration of the moult was estimated to be c. 5½-7 weeks (c. 40–50 days). Females generally started moult before males and moult did not appear to overlap breeding. Information from other areas is reviewed. A mechanism by which the duration of moult is shortened amongst various species is by an increase in the number of feathers growing concurrently during the moult. Likely reasons for the placing of the moult in the annual cycle of the Purple Sandpiper are discussed, and appear to be related to the exceptionally northerly wintering distribution of the species.     

MOULT AND MENSURAL DATA OF RUFF ON THE WITWATERSRAND

Schmitt. M. B. & Whitehouse, P. J. 1976. Moult and mensural data of Ruff on the Witwatersrand. Ostrich 47: 179–190

During a five-and-a-half year study 1 600 Ruffs Philomachus pugnux were captured on the southern and eastern Witwatersrand, South Africa. Mensural data for these birds are given and the moult cycle discussed. Birds in the study area appear to moult much later than elsewhere, but the moulting sequence appears similar. Recaptures and leg colour are discussed.     

DISTRIBUTION,MIGRATION AND TIMING OF MOULT IN THE SOUTH AFRICAN CLIFF SWALLOW

Earle, R. A. 1987. Distribution, migration and timing of moult in the South African Cliff Swallow. Ostrich 58:118-121. The South African Cliff Swallow Hirundo spilodera breeds in South Africa mainly between 25 and 31S and 24 and 31E. In some years with exceptionally high rainfall the breeding range is more extensive. Man has probably had a pronounced influence on the present-day distribution of this species. Seven winter recovery/collecting localities are known from the lower Congo basin in Zaire. Possible migrating birds were observed in Zambia and Malawi in the east, and on the Namibian coast in the west. The few sight records suggest a direct migrational route over Botswana. Moult takes place between March and September primarily in the winter quarters, but about 2% of the birds handled during March and April started moult before migrating.     

褐马鸡雏鸟的换羽研究

对我国特产珍禽——褐马鸡雏鸟的羽毛生长及脱换即“稚后换羽”进行了观察研究。褐马鸡有小翼羽4枚,初级飞羽10枚,次级飞羽13枚,三级飞羽4枚,尾羽22枚。稚后换羽是飞羽和尾羽全部脱换,仅第一枚初级飞羽当年保留。 褐马鸡羽毛的脱换规律是:飞羽是先生长者先脱换;尾羽是由外向内的“向心型”。     

FACTORS AFFECTING EGG-WEIGHT, BODY-WEIGHT AND MOULT OF THE WOODPIGEON COLUMBA PALUMBUS

The heaviest clutches (2 eggs) laid by Woodpigeons Columba palumbus in a Cambridgeshire study area weighed 30% more than the lightest. Yet the variation in egg-weight within clutches was less than 1 %. Irrespective of initial weight, eggs lost weight at the same constant rate during incubation. Heavy eggs hatched more successfully than light eggs and none weighing less than 16 g hatched. There was no correlation between chicks' weight at hatching and their weight at day 6 during the July-September part of the breeding season. The ability to feed crop milk at this stage could compensate for low chick-weight, but this might not be true early in the season. Weight at day 6 was correlated with the weight at day 16 or 17. The growth pattern is discussed. Chicks in broods of one achieved a higher weight at day 17 than those in broods of two. The survival rate both in and after leaving the nest was the same in both brood-sizes. Chick-weight in artificially created broods of three was almost as high as in broods of two, but again data refer to the July-September period when abundant cereal food is available. Survival before and after fledging was lower in broods of three. Clutch- and egg-weight declined from April until September. It is suggested that this is adaptive, in that the adults produce heavier eggs when food supplies are most difficult to collect. The critical period probably occurs during the few days when the adult must produce crop milk and the young cannot be left unattended. Thus egg-weight depends on the female's capacity to acquire nutrients, and is related to the needs of embryonic development and the amount of compensation in nutrient supply which can be provided immediately after hatching. But clutch-size is more related to the bird's ability to feed and rear young to the point of fledging, thereby influencing the number of offspring which survive to leave progeny. Egg-weight and female body-weight were positively correlated in females weighing less than 480 g but not in heavier females. First-year birds did not acquire adult weight until midsummer and they would probably produce light eggs if they could breed before this month. However, their gonads do not recrudesce until July and this prevents them breeding in the spring. Seasonal changes in body-weight and fat content of adults and first-year birds are described and discussed; differences were noted between adult males and females which were considered to be adaptive. The moult is described. It begins in April and continues until November, approximately one pair of primaries being replaced per month. The moult ceases during the winter months, when it is known that food supplies become limiting. Woodpigeons lay light eggs relative to their body-weight but can achieve the extra parental care needed for the altricial chicks by producing crop milk. Because the moult is extended, the energy demands of moulting and breeding combined are relatively low and this enables the Woodpigeon to have a long breeding season and to moult coincidentally.     

TAXONOMY,DISTRIBUTION, MIGRATION AND MOULT OF THE REDBREASTED SWALLOW HIRUNDO SEMIRUFA

Earlé R. A. & Brooke, R. K. 1989. Taxonomy, distribution, migration and moult of the Redbreasted Swallow Hirundo semirufa. Ostrich: 60:151-158.

There are two well defined races of the Redbreasted Swallow Hirundo semirufa, the nominate and gordoni. H. s. neumanni is a synonym of gordoni. The breeding ranges of the two races do not meet. The Redbreasted Swallow has extended its range south and southeast following the construction of concrete road culverts which provide nest sites, together with bush clearance. The strongly migratory southern populations reach their southern limits by August each ear and depart again mainly in March-April although there are some records for May. Males are significantly larger than females in wing length and the length of the longest rectrix but not in other measurements. Moulting birds were found in each month of the year but the moults of the two races are largely separated in time. Moulting birds were found only between 10S and 10N with the majority close to the equator.     

THE WINTERING AND MOULT OF RUFFS PHILOMACHUS PUGNAX IN THE KENYAN RIFT VALLEY

Some 5700 Ruffs were ringed in the southern Kenyan rift valley during 1967–79, mainly at Lakes Nakuru and Magadi. These have produced 15 recoveries outside East Africa, 14 in Siberia between 73° and 154°E and one in India. Adult males returned to Kenya mainly during August, and females during late August and early September. Females greatly outnumbered males at all times. Most wintering males departed late in March and early in April, but females not until about a month later. First-year birds appeared from the end of August, but remained in low numbers until late October or November. Most departed during April and May, but a few females oversummered. First-year birds typically accounted for about 25% of the wintering Nakuru females, but about 50% of those at Magadi. At both sites they accounted for a higher proportion of male birds than females. Most of the birds at Nakuru throughout late August to May appeared to be local winterers, and many individuals remained in the area for many months each year. Retrapping indicated that approximately 60% of each season's birds returned the following season. Adult males and most adult females commenced pre-winter wing moult before arrival, but completed most of it in Kenya. Males moulted 3–4 weeks ahead of females, and most had finished before December. Females typically finished during December and early January. Most second year birds timed their pre-winter moult similarly to older adults. Suspension was recorded in over 15% of all moulting birds examined. Adult pre-summer moult involved most or all of the tertials, some or all of the tail feathers, most of the inner wing coverts and the body and head plumage. It occurred mainly during January to March (males) or February to April (females), although tertial renewal commonly began a month earlier. Males showed no sign in Kenya of the supplementary prenuptial moult. First-year birds moulted from juvenile into first winter body plumage during late September to November. They underwent a pre-summer moult similar in extent and timing to that of adults, and again about a month earlier in males than females. Spring feathers acquired were often as brightly coloured as those of adults. About 15% of first-year birds renewed their outer 2–4 pairs of large primaries during January to April. Adult and first-year birds fattened before spring departure, commonly reaching weights 30–60% above winter mean. Weights of adult males peaked early in April, those of adult females early in May, and those of first-winter females later in May. Weights were relatively high also during August and September. This was due to the arrival of wintering birds carrying ‘spare’ reserves, and also apparently to the presence of a late moulting fattening passage contingent. The wing length of newly moulted adults was about 3 mm longer than that of newly arrived first-year birds, but there was no evidence of an increase in the wing kngth of adults with successive moults. Adult wing length decreased by 4–5 mm between the completion of one moult and the middle stages of the next. The migrations and annual timetable of Kenyan wintering Ruffs are discussed, and their moult strategy is compared with that of other Holarctic waders.