黄腹山鹪莺成鸟的秋季换羽

黄腹山鹪莺(Prinia flaviventris)具有冬羽尾羽长于繁殖羽尾羽的特点,可能意味着一种新的生存和繁殖策略。为此,从2006年9月～2007年2月,在广东省肇庆市江溪村对黄腹山鹪莺的秋季换羽进行研究。结果显示:(1)黄腹山鹪莺成鸟繁殖羽体长和尾羽长皆极显著短于冬羽(P<0.01),繁殖羽翼长显著短于冬羽(P<0.05),其余身体量度的差异均不显著(P>0.05)。(2)9月17日获得第一个黄腹山鹪莺换羽个体,初级飞羽已更换到P5,次级飞羽已更换到S6,11月20日后所获样本均已完成羽毛的更换。(3)初级飞羽的换羽模式为递降换羽,次级飞羽为递升换羽,尾羽为离心型换羽。(4)换羽期间,10月的个体平均体重最大,显著(P<0.01)重于11月的体重,其他各月无显著性差异(P>0.05)。据此,推测黄腹山鹪莺秋季种群换羽的持续时间约100d;相对其他羽毛而言,尾羽更换对黄腹山鹪莺生长发育的影响更为明显。     

Of squeezers and skippers: factors determining the age at moult of immature African Penguins Spheniscus demersus in Namibia

We used banding and resighting records of 391 African Penguins Spheniscus demersus banded as chicks and later resighted during immature moult to explain the roles of date of fledging and age at moult in determining the season of moult and its timing within the season. Breeding was continuous, but immature moult occurred mainly during spring and summer. Age at immature moult extended over 11 months, from 12 to 23 months after hatching. Birds that fledged during summer and early autumn generally moulted during the next moult season (squeezers), whereas birds that fledged in late autumn, winter and spring skipped the next moult season to moult only the following season (skippers). There was a significant relationship between age at moult and moult date, with young birds moulting later in the season than older birds. The age at moult of immature birds appears to be constrained by minimum age, moult seasonality and plumage wear. Birds that fledged over nearly 2 years moult during one season. Counts of moulting immature African Penguins have not been used to estimate year-class strength and post-fledging survival owing to the wide range of ages at immature moult. Our results provide the means of assigning recruits to specific age groups.     

The timing of breeding and moult of the Lesser Striped Swallow Hirundo abyssinica

The Lesser Striped Swallow seems to have two different breeding populations. The birds south of 10°S breed largely during the spring and summer (July to April) and moult from about April to August. Birds further north breed throughout the year, but mainly during the first seven months of the year. Moult in the birds north of 10°S is from July to February when few birds are breeding. There seem to be two clearly defined moulting populations, with the southern breeding population moulting largely south of 10°S and the east African breeding population moulting largely north of the equator. In both populations moult and breeding seem to be separated in time, at least at the individual level.     

Transition between moult and migration in a long-distance migratory passerine: organ flexibility in the African wintering area

Phenotypic flexibility of organs in migratory birds has been documented for a variety of species of different genera during the migratory period. However, very little is known about phenotypic mass changes of organs with respect to other events within the annual cycle. This seems particularly interesting when birds face different physiological challenges in quick succession. We investigated mass changes of 13 organs from garden warblers (Sylvia borin) during the transition from moult to migration. These long-distance migratory birds perform a complete moult within their wintering area just shortly before the onset of spring migration. Birds were sampled in three successive stages according to their moult status: group I consisted of birds with growing primary or secondary wing feathers, group II consisted of birds with completed wing moult but with still moulting body feathers, and group III consisted of birds that had completed wing moult and body moult. Size-corrected flight muscle, kidney mass, and pancreas mass differed significantly among the three groups. Flight muscle was heaviest in birds that were about to leave their wintering area (group III) compared with birds still in body moult (group II). Kidney and pancreas showed a pattern similar to each other, with the heaviest mass occurring in birds with moulting wing feathers (group I) and significantly reduced mass in birds that had completed wing moult (group II) or both wing and body moult (group III). Mass reductions of kidney and pancreas during the transition from moult to migration are considered to be related to the demands of moult, while increased flight muscle may be due to moult, migration, or both. Phenotypic mass changes of organs in birds occur during their migration, but they also occur during the transition between other phases of the annual cycle such as moult and migration and are not restricted to the flight muscle.     

The moult of the Little Stint Calidris minuta in the Kenyan rift valley

Moult data were collected during 1967–80 from some 6900 Little Stints in the southern Kenyan rift valley.
Adults typically moulted from summer to winter body and head plumage during September and early October, soon after arrival. The complete pre-winter wing and tail moult began in most adults between mid-September and early October. Some birds finished by December, but others continued until February and March. Individual duration was usually between 100 and 150 days. Adults which completed this moult early often remoulted outer primaries between January and early April.
Young birds acquired first-winter body plumage during October and early November. Some 90% had a complete pre-winter wing and tail moult. This usually began between December and early February, and finished during March or early April, taking about 70–100 days. In about 10% of young birds, flight feather moult was restricted to the outer primaries and inner secondaries. Birds adopting this strategy typically began moult late, during January or February. Short periods of suspension were common during pre-winter wing moult, particularly in adults. The difference in moult speed between adult arid first-winter birds was attributable in the primary, secondary and tail tracts to differences in numbers of growing feathers.
Practically all birds completed a pre-summer moult involving the entire body and head plumage, most of the tertials, some or all of the tail feathers and many wing coverts. Most birds began this moult between early February and late March, and finished between mid-April and early May. It was typically later and more rapid in first-year birds than adults. In late birds, the onset of pre-summer moult was linked to the final stages of pre-winter moult.
The wing moult of the Little Stint in different wintering areas is discussed. First-winter moult strategy is compared with that in other small Calidris species.     

MOULT OF BUDGERIGARS MELOPSZTTACUS UNDULATUS

In captive Budgerigars Melopsitticus undulatus moult of primaries started in the middle of the tract and moved progressively inwards and outwards, the inner feathers being replaced faster than the outer ones. Full replacement of primaries took six to eight months and a new cycle of moult usually started before completion of the old cycle. Moult of secondaries followed no clear pattern and occurred less frequently than moult of primaries. Moult of rectrices started with the middle pair and moved progressively outwards on both sides. Complete moult of rectrices took about six months and a new cycle often started before completion of the old. Moult of the head and body occurred intermittently throughout the year. Birds fledged in juvenal plumage, they passed into first basic plumage with a partial moult (head and body feathers) and into definitive basic plumage with a moult of all contour feathers.
In the field in inland mid-eastern Australia, there were some birds replacing feathers and some with complete plumage in most months of the year. Birds with complete plumage may have been between moults or within a moult and between replacement of feathers. The proportion of birds in moult did not increase in intensity after breeding, or cease during breeding or before movements. Some birds of both sexes with gonads in a reproductive condition were replacing feathers. Rirds that were replacing feathers had similar lipid deposits to birds that had a complete plumage.     

Breeding plumage honestly signals likelihood of tapeworm infestation in females of a long-distance migrating shorebird, the bar-tailed godwit

The indicator mechanism for sexual selection proposed by Hamilton and Zuk (i.e. that sexually selected ornaments signal parasite resistance) has received rather little observational support, and none in the case of long-distance migrant birds. Here we present a test by examining the association between helminth infestations and breeding plumage quality in bar-tailed godwits Limosa lapponica taymyrensis during their spring staging period in the Wadden Sea, The Netherlands. After a non-stop flight from West Africa, these shorebirds refuel in the Wadden Sea in preparation for a second flight to the central Siberian Arctic breeding grounds. Earlier studies have shown that only relatively heavy and well ornamented birds carry out a "top-up" moult during stopover, in which part of the contour feathers recently grown in West Africa are replaced by even fresher ones. Active body moult was therefore taken as the primary indicator of ornament quality. Of 78 birds collected between 1992 and 1997, 42% carried helminths, including four species of digenean trematodes (flukes), three species of cestodes (tapeworms) and an acanthocephalan (spiny-headed worm). Faecal samples examined for helminth eggs in another 92 birds in 1998 and 2000 showed similar rates of infestation. Actively moulting bar-tailed godwits were confirmed to be heavier and to show more extensive breeding plumage than non-moulting birds. In females, but not in males, active moult was associated with fewer cestodes and acanthocephalans. Also, breeding plumage and presence of cestodes were negatively associated in females. We argue that the quality of the breeding plumage reliably indicates parasite resistance in female godwits. The repeatability of plumage scores of females between years is consistent with such resistance having a heritable component. In contrast, male ornaments may demonstrate other qualities, e.g. an ability to combine adequate fuelling and flight performances with moult during the time-stress of migration.     

PTERYLOGRAPHY, PLUMAGE DEVELOPMENT AND MOULT OF JAPANESE QUAIL COTURNIX C. JAPONICA IN CAPTIVITY

Japanese Quail were kept in small cages under controlled conditions of temperature and light, and their pterylography and moult are described. There are 10 primaries, 14 secondaries and corresponding numbers of greater upper and lower wing coverts. The alula has four feathers and the tail from five to six pairs of feathers. There is an apterium in the dorso-pelvic tract similar to that in other quail genera. The arrangement of feathers in the ventral and cervical tracts appears to differ from that described for some North American quail.
The chicks hatch with a covering of natal down. Pre-juvenile moult can be seen when the chicks are three days old. Juvenile body plumage is complete in about 30 days; the sides of the face, around the eyes, are the last places to acquire feathers. The tenth and last juvenile primary to grow is mature when the chicks are 41 days old.
The moult in which the juvenile plumage is replaced overlaps the post-natal moult and in part of the ventral tract natal down is replaced by the first adult feathers. This makes it possible to sex the quail at 14 days old. The first adult moult is complete, in the body tracts, by the time the birds are five to six weeks old. The dropping of juvenile primaries commences at about three weeks old and ceases when about eight weeks old. Only from three to six primaries are replaced; most birds studied replaced five. The significance of this difference from other Galliformes is discussed; it is thought to be associated with the species' migratory behaviour. Quail which remained in the controlled laboratory environment did not undergo any further moult. All birds moulted when both temperature and light period were reduced and most birds moulted when the light period alone was reduced. Adult birds housed in small cages in an unheated, unlit shed underwent a complete moult between August and December in which all primaries were replaced. This moult took 8–14 weeks to complete.     

两种山鹪莺的春季换羽及尾羽变化

换羽是鸟类为保证持续生存的重要过程。换羽策略与鸟类进化及对环境的适应紧密相关,研究鸟类换羽特征,对于了解鸟类的分类、系统发育、进化历史及其对环境的适应性等方面都有重要意义。2007年3月至9月,在广东肇庆市江溪村对黄腹山鹪莺(Prinia flaviventris)和纯色山鹪莺(P.inornata)的春季换羽进行了研究。通过设置雾网捕捉2种山鹪莺,对捕捉到的成体进行体重及身体量度的测量;对飞羽及尾羽进行标记:初级飞羽以翅尖的第一枚羽毛标记为"P1",次级飞羽以翅中部最外一枚标记为"S1",向内依次递增标记;尾羽以中央两根最长尾羽为"T1",分别向两侧递增标记为"T2~T5"。采用单因素方差分析(One way ANOVA)对不同月份山鹪莺的体重值进行差异性检验,对体重与月份进行Pearson相关分析,对尾羽的长度和宽度进行Pearson偏相关分析(控制变量:体长)。研究结果表明:1)两种山鹪莺换羽期为3至5月,持续时间约为60 d;2)两种山鹪莺春季换羽仅更换尾羽,换羽模式均为离心型,即中央一对尾羽最先开始替换,然后向两侧由内到外逐次更替;3)两种山鹪莺的尾羽长度和宽度同步变化,但绝大部分山鹪莺非繁殖期尾羽长度与繁殖期尾羽长度之比大于非繁殖期尾羽宽度与繁殖期尾羽宽度之比,即繁殖期尾羽相对较宽;4)两种山鹪莺换羽期间体重大致呈现下降趋势,但变化不显著(P0.05)。推测两种山鹪莺通过增加食物的摄入来抵抗换羽期和繁殖期重叠而导致的能量消耗,这可能与该地区丰富的食物资源有关,并在一定程度上体现了两种山鹪莺换羽策略对环境的适应性。     

The Breeding Distribution and Habitats of the Pied Flycatcher (Muscicapa Hypoleuca) in Britain

Examination of the plumage of Palaearctic warblers as migrants or wintering birds at Kampala, Uganda, provided useful material for a consideration of moult in relation to the timing of spring and autumn migration. Reasons are suggested for observed interspecific differences in the moult pattern, and for the variation reported from different wintering areas in the African continent.     

黄腹山鹪莺稳定的配偶关系限制雄性欺骗者

多数鸟类通过性特征限制在同性竞争和配偶选择中的“欺骗者”存在,与此相反,雀形目扇尾莺科部分物种表现出繁殖季节性特征消退的身体特征变化模式.在广州市南沙区通过“目字笼”对黄腹山鹪莺配偶关系稳定性的限制机制进行研究,发现虽然雌性个体到访原配个体和对照个体的次数几乎相同,但是雌性个体对原配雄性的单次选择时间明显长于对照雄性个体,总计选择时间也明显长于对照雄性个体.选择实验过程中,原配雄性的跳动次数明显高于对照个体雄性,以竖尾扑哧和鸣声恐吓等为代表的威慑行为次数也明显高于对照雄性个体.结果说明,雌性更青睐于原配个体,配对时间越长,忠诚度越高,而且原配雄性比入侵雄性个体表现出更高的活跃度和威慑行为.繁殖季节性特征消退的物种可以通过保持稳定的配偶关系以限制“欺骗者”存在.可以推测繁殖的巨大投入和雌性之间的同性竞争可能是产生这种配偶稳定性的主要原因.     

Non‐moulted primary coverts correlate with rapid primary moulting

Time constraint is a main factor which affects the moult strategies in passerines, mainly during the first year of life. The variability of moult strategies between species is associated with the extent of the moult. In the first year of life, the extent of the moult is highly variable between species and individuals. In most passerine species, juveniles only renew some of their feathers, but the factors that govern which feathers are renewed and which are retained have been largely overlooked. Here we examine the common pattern of non‐moulted primary coverts (PC) in passerines during the first‐year moult cycle (post‐juvenile and first‐year pre‐breeding moults). On the interspecific level we found that among 63 species of passerines, PCs are the least commonly moulted feather tract. For five species (Hirundo rustica, Pycnonotus xanthopygos, Prinia gracilis, Acrocephalus stentoreus and Passer moabiticus) which perform a complete post‐juvenile moult, we found that the PC moult occurs over a longer period than greater coverts (GCs) and is sequential (non‐simultaneous). At the intraspecific level, we found that the main difference between a partial and complete moult in Prinia gracilis is the moulting or non‐moulting of the PCs. We also demonstrate that for Prinia gracilis 1) juveniles which do not moult their PCs, moult their primaries at a higher speed than those which moult their PCs and 2) area/mass ratio of PCs is lower than of GCs. These two findings may explain why many passerines skip PC renewal during the first year of life. Because the PC moult lasts a long time, forgoing this moult enables long term resource savings that allow for dealing with time constraints. Our results highlight the adaptive advantages of non‐moulted PCs in cases of time constraints.     

Migration and moult of Dunlin Calidris alpina wintering in the central Mediterranean

Dunlin migration in northeast Italy is described. An attempt to identify the main routes and staging areas used by birds wintering in the central Mediterranean is presented. The results of monthly counts from 1990–1995 revealed that the bulk of the population occupied the wintering area in October and left for the breeding grounds in April and May. The analysis of 342 Italian recoveries of foreign ringed birds showed that 65% were ringed during post-breeding migration through the Baltic Sea, whereas just a few birds had been ringed in western Europe. First-year birds arrived in autumn with a single migratory wave, peaking in October. Two categories of adults were identified during post-breeding migration: birds which directly reached Italian wintering sites and birds which arrived after they had suspended their migration for moulting: the Azov/Black Sea wetlands are suggested as possible moulting areas. Out of 2444 adults and 1627 first-years ringed between 1989 and 1996 at our study area, we obtained a total of 42 recoveries abroad and evidence of direct links between Azov/Black Sea and N Adriatic wetlands, both during autumn and spring migrations. Primary moult was observed only in adults arriving early, the second migratory wave being composed of moulted birds. Locally moulting adults adopted a moult strategy characterized by high raggedness scores, typical of resident moulters. Body mass was not affected by primary moult stage or intensity, winter mass values being reached two weeks after the average date of primary moult completion.     

The timing of breeding and moult of the Lesser Striped Swallow Hirundo abyssinica

The Lesser Striped Swallow seems to have two different breeding populations. The birds south of 10°s breed largely during the spring and summer (July to April) and moult from about April to August. Birds further north breed throughout the year, but mainly during the first seven months of the year. Moult in the birds north of 10°s is from July to February when few birds are breeding. There seem to be two clearly defined moulting populations, with the southern breeding population moulting largely south of 10°s and the east African breeding population moulting largely north of the equator. In both populationsmoult and breeding seem to be separated in time, at least at the individual level.     

The effects of delaying the start of moult on the duration of moult, primary feather growth rates and feather mass in Common Starlings Sturnus vulgaris

In many species of birds there is a close relationship between the end of breeding and the start of moult. Late-breeding birds therefore often start to moult late, but then moult more rapidly. This is an adaptive mechanism mediated by decreasing day lengths that allows late-breeding birds to complete moult in time. This study asked how these birds complete moult of the primary feathers more rapidly, and the consequences of this on the mass of primary feathers. Common Starlings Sturnus vulgaris were induced to moult rapidly in one of two ways. In the first experiment, one group was exposed to artificially decreasing photoperiods from the start of moult, whereas the control group remained on a constant long photoperiod. The second experiment was a more realistic simulation. Two groups were allowed to moult in an outdoor aviary. One group started to moult at the normal time. In the other, the start of moult was delayed by 3 weeks with an implant of testosterone. The duration of moult was significantly reduced in both the group experiencing artificially decreasing photoperiods and the group in which the start of moult was delayed. The faster moult rate was achieved by moulting more feathers concurrently. The rate of increase in length of each of the primary feathers, and their final length, did not differ between groups. The rate at which total new primary feather mass was accumulated was greater in more rapidly moulting birds, but this was insufficient to compensate for the greater numbers of feathers being grown concurrently. Consequently, the rate of increase in mass of individual feathers, and the final feather mass, were less in the rapidly moulting birds. A 3-week delay in the start of moult is not an unrealistic scenario. That this caused a measurable decrease in feather mass suggests that late-breeding birds are indeed likely to suffer a real decrease in the quality of plumage grown during the subsequent moult.     

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.     

GROWTH, AND ANNUAL CYCLES IN WEIGHTS, PLUMAGES AND REPRODUCTIVE ORGANS OF GOOSANDERS IN EASTERN CANADA

A study of Goosanders, in connection with a Fisheries shooting programme on Cape Breton Island, has shown the pattern of growth in young birds, and of plumage and other annual cycles in fully grown birds. The plumage cycles show little difference between the sexes in the first year, with males thereafter moulting about one month earlier than females. Virtually no moult occurs from January to March, nor in adults during April to mid-June, in this area. Weights and measurements permit ageing of flightless young of known sex, and sexing of all fully grown birds, but they do not distinguish first-year from older individuals. Gross examination suggests that males in the second calendar year (11 to 12 months old) may come into reproductive condition, at least under conditions of year-round hunting. Variations in annual moult cycles may be due to differing geographic origin of the birds; I suggest that birds killed in other Goosander shooting programmes should be used for comparative studies parallel to this one.     

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.     

The moults of captive Scottish ptarmigan (Lagopus mutus)

The moults of captive Scottish ptarmigan were studied at Banchory, north-east Scotland from December 1968 to February 1971. In the autumn moult (June to September) which included the primaries, cock ptarmigan moulted earlier and more completely than hens. In the winter moult (September to February) hens moulted earlier and both sexes moulted more completely than in spring. In the spring moult (February to June) cocks moulted more rapidly to begin with but by mid-April hens had caught up and thereafter moulted at least as rapidly as cocks. When kept indoors at slightly higher temperatures ptarmigan grew more pigmented feathers during the winter moult. In a colder winter the birds became whiter than in a milder one. First-winter ptarmigan completed the winter moult later than older birds. Birds from the Cairnwell hills had more dark feathers in winter than those from the eastern Cairngorms. There was no correlation between the start or finish of egg-laying and moulting.