灰喜鹊的行为生态学研究 Ⅰ．生殖行为

在从南到北的地理分布上,灰喜鹊的繁殖期相应有所推迟．在它们的繁殖区域,人类的影响越大,其巢也建得越高、越隐蔽．这种很强的适应性使得它们在城区和近郊区能够更好地生存和繁殖．北京地区的灰喜鹊在４月中、下旬开始建巢,５月底是产卵高峰期．在孵卵期它们不断地翻动卵,以使其受热均匀．灰喜鹊对卵的数量比对卵的颜色和大小更敏感．孵卵期约１５—１７天,幼鸟１８—２０天出巢．在北京大学校园内的灰喜鹊的繁殖成功率约为６９．０５％．建立了灰喜鹊的发育行为谱．在繁殖期,灰喜鹊的巢彼此靠得较近,形成一个集体生殖领域,共同进行集体防御．     

灰喜鹊繁殖习性的初步观察

2002～2004年在山西历山保护区对灰喜鹊的繁殖习性进行了观察。结果表明,该鸟在我区为留鸟,营巢始于4月下旬,5月中旬产卵,窝卵数4-7枚,孵卵期17-18天,育雏期18～20天。食物以动物性食物为主,占88．96％,植物性食物占11．04％。     

四川雉鹑孵卵行为初步观察

2009年4～5月,在四川省雅江县对四川雉鹑Tetraophasis szechenyii的孵卵行为进行了观察.在孵化过程中,卵重与孵卵剩余天数呈明显的正相关(r=0.939,F=59.585,P<0.001).卵在巢中的位置是不断变化的.雌鸟坐巢的行为主要是孵卵行为(78.7%),其次是离巢(17.4%)和翻卵(3.1%),其他行为(如鸣叫和梳理)偶尔发生(0.8%).孵卵行为全天发生,离巢行为主要发生在7:30～11:30,翻卵行为多发生在13:30～15:30.雌鸟从巢的一个固定位置进出巢.雏鸟出巢时只由雌鸟带领活动.     

栗头鹟莺繁殖生态的初步观察

鹟莺属(Seicercus)鸟类的繁殖资料十分缺乏。2015年4~8月,采用录像全程监控的方法,在贵州宽阔水国家级自然保护区,对4巢栗头鹟莺(S.castaniceps)的繁殖过程进行了完整观察。栗头鹟莺的繁殖期主要集中在5~7月,巢址选择专一性较强,均筑巢于公路边的土坎内壁,距路(1.3±1.2)m,巢为球状侧开口,巢材主要为新鲜苔藓及细草根,巢高(2.2±0.6)m,巢宽(10.9±1.5)cm,杯宽(3.3±0.5)cm,巢深(9.5±1.9)cm,杯深(5.5±1.0)cm。窝卵数(4.5±0.6)枚(4~5枚),卵重(0.92±0.04)g,卵长(14.30±0.30)mm,卵宽(11.22±0.23)mm,卵体积(0.92±0.05)mm3(n=18)。亲鸟在产满窝卵后开始孵卵,孵卵期12~13 d,在孵卵中期(第5~9天)亲鸟的孵卵时间开始增加,翻卵次数增多,在孵卵后期(第10~13天)亲鸟的孵卵时间和翻卵次数基本保持不变。育雏期13~14 d。雌、雄共同育雏,雏鸟在3日龄时,体重和跗跖开始显著增长,在7日龄时,增长速度变缓。孵化率为88.9%(16/18),营巢成效为100%,出飞成效为3.3只/巢。     

四川雉鹑繁殖习性初报

2005～2008年,在四川省雅江县对四川雉鹑(Tetraophasis szechenyii)的繁殖习性,包括巢、卵、孵卵时间、生长量度和日行为节律进行了初步观察.四川雉鹑同时营树上巢和地面巢,以树上巢为主,占68%(n=25);产卵期集中在4月,正常窝卵数2～5枚(n=9),窝卵孵化率为63.89%(n=12);雌鸟在孵卵期每天离巢1次,离巢平均时间(63.0±22.6)min(n=18),孵卵期24～29 d(n=4);150日龄幼鸟的体重接近成体.在繁殖期,四川雉鹑6:30～7:00时从夜栖树上飞下,行至觅食地觅食,17:00时左右返回夜栖地,19:00～19:30时上树夜栖.     

莲花山云南柳莺的孵卵行为

20 0 2年 6～ 7月 ,在甘肃省莲花山自然保护区对云南柳莺的孵卵行为进行了研究。结果表明 ,雌鸟孵卵的日活动期为 (80 0 5± 42 8)min (n =1 5 ) ,每天离巢 (3 2 7± 3 9)次 (n =1 5 ) ,每次离巢时间 (6 6±1 8)min (n =5 99) ,每次坐巢时间 (1 8 4± 9 2 )min (n =5 83 ) ,坐巢率为 (73 1± 1 9) %。雌鸟每次坐巢时间和离巢时间的长度均与气温显著相关。日活动期雌鸟在巢的平均卵温为 3 2 3℃ ,夜晚的平均卵温为3 2 7℃。整个孵卵期卵温在发育临界值 2 8℃以上的时间比例为 92 7%。在孵卵后期卵温有逐渐上升的趋势。     

云雀的生态与繁殖

云雀于5月中旬开始产卵,每窝卵4—5枚,卵重3.25克。雌雄鸟均参加孵卵,孵化期11—12天,留巢期9.5天。食物以草籽为主,繁殖期主要食鳞翅目幼虫,鞘翅目和直翅目昆虫等。     

乌鸫的繁殖行为与坐巢行为初步观察

于2009年3～7月、2010年3～6月,采用焦点动物观察法和全事件行为记录法对乌鸫(Turdusmerula)的孵卵及育雏行为进行了研究。结果表明,乌鸫是雌鸟孵卵,在孵卵期出现卵损失现象,具补卵行为;孵卵前期与后期的坐巢行为存在差异,且其坐巢时间、频次和坐巢率有随孵卵数递增的趋势。双亲育雏但以雌鸟为主,喂食模式3种:雌鸟喂食、雄鸟喂食、雄鸟将食物递给雌鸟由雌鸟喂食。随着雏鸟日龄的增长,喂食次数增多,暖雏行为减少,至育雏后期未观察到暖雏行为。为权衡孵卵期和育雏前期的能量分配,乌鸫在孵卵期及育雏前期分别采取时间长而频次少和时间短而频次多的坐巢策略。     

内蒙古赛罕乌拉国家级自然 保护区黑鹳繁殖记述

黑鹳(Ciconia nigra)种群数量稀少,成活率低,为国家Ⅰ级重点保护物种,加强对黑鹳的保护已刻不容缓。内蒙古赛罕乌拉国家级自然保护区是黑鹳的重要繁殖栖息地,开展繁殖行为研究有助于提高对黑鹳的保护成效。2012至2015年对2处黑鹳繁殖巢址进行了繁殖期观察。2012年5月15日首次发现1巢内有4枚卵并有亲鸟在巢中孵卵,6月7日孵化出4只幼雏,8月底全部成功离巢。2013年4月黑鹳利用该巢产卵5枚,孵化1只雏鸟,孵卵期约33 d,后期卵、雏鸟均消失,推测为来自蛇类的捕食。2014、2015年该巢未被利用。2014年4月24日发现另外一处巢址,8月12日观察到3只幼鸟已开始练习飞行,至8月19日全部离巢。2015年该巢孵化雏鸟4只,6月初死于恶劣天气。通过监测发现黑鹳连续多年在保护区内栖息繁殖,所发现的两巢成功出雏7只个体。本研究初步获得保护区境内黑鹳的繁殖信息,为后续促进黑鹳种群恢复与栖息地保护提供了基础数据。     

黑翅长脚鹬繁殖生态的研究

据黑翅长脚鹬繁殖生态的调查发现它的巢主要选择芦苇丛生的小土岛上,于5月末开始产卵,每窝卵4—5枚,卵重19.6;雌雄亲鸟均参加孵卵,孵化期17—19天。食物以鞘翅目昆虫,双翅目幼虫,半翅目的蚜虫等为食。此外还吃少量植物藻类。黑翅长脚鹬的天敌主要是猛禽和家犬,在繁殖期对卵和雏鸟危害较大,因此,在黑翅长脚鹬的繁殖期严禁放牧和捕鱼的生产活动,为黑翅长脚鹬的栖息与繁殖提供良好的环境条件。     

Eavesdropping cuckoos: further insights on great spotted cuckoo preference by magpie nests and egg colour

Reproductive success of brood parasites largely depends on appropriate host selection and, although the use of inadvertent social information emitted by hosts may be of selective advantage for cuckoos, this possibility has rarely been experimentally tested. Here, we manipulated nest size and clutch colouration of magpies (Pica pica), the main host of great spotted cuckoos (Clamator glandarius). These phenotypic traits may potentially reveal information about magpie territory and/or parental quality and could hence influence the cuckoo’s choice of host nests. Experimentally reduced magpie nests suffered higher predation rate, and prevalence of cuckoo parasitism was higher in magpie nests with the densest roofs, which suggests a direct advantage for great spotted cuckoos choosing this type of magpie nest. Colouration of magpie clutches was manipulated by adding one artificial egg (blue or cream colouration) at the beginning of the egg-laying period. We found that host nests holding an experimental cream egg experienced a higher prevalence of cuckoo parasitism than those holding a blue-coloured egg. Results from these two experiments suggest that great spotted cuckoos cue on magpie nest characteristics and the appearance of eggs to decide parasitism, and confirm, for the first time, the ability of cuckoos to distinguish between eggs of different colours within the nest of their hosts. Several hypothetical scenarios explaining these results are discussed.     

Host sexual selection and cuckoo parasitism: an analysis of nest size in sympatric and allopatric magpie Pica pica populations parasitized by the great spotted cuckoo Clamator glandarius

Magpies (Pica pica) build large nests that are the target of sexual selection, since males of early breeding pairs provide many sticks for nests and females mated to such males enjoy a material fitness benefit in terms of better quality territory and parental care of superior quality. Great spotted cuckoos (Clamator glandarius) preferentially parasitize large magpie nests and sexual selection for large nests is thus opposed by natural selection due to brood parasitism. Consistent with the hypothesized opposing selection pressures, in a comparative analysis of 14 magpie populations in Europe we found that nest volume was consistently smaller in sympatry than in allopatry with the great spotted cuckoo, in particular in areas with a high parasitism rate and high rates of rejection of mimetic model cuckoo eggs. These observations are consistent with the suggestion that magpies have evolved a smaller nest size in areas where cuckoos have exerted strong selection pressures on them in the recent past.     

Unusual incubation rhythms the Spotted Barbtail, Premnoplex brunnescens

The Spotted Barbtail (Premnoplex brunnescens) inhabits the understory of humid montane forests in Central and South America. Apart from basic information on eggs and nest form, little has been published on its breeding ecology. Using temperature sensors in nest cups, I have collected data on the diurnal patterns of egg-coverage from three nests in eastern Ecuador and reveal a remarkable incubation rhythm. After providing near-constant coverage during the morning, adults leave the eggs unattended for most of the afternoon, returning to the nest only in the late afternoon. The mean duration (±standard deviation) of this period of absence, across the entire incubation period at three nests, was 6.4 ± 1.9 h. These results are discussed in relation to their physiological and ecological significance.     

朱鹮(Nipponia nippon)的繁殖习性

文章概述了朱鹮的濒危状况及陕西省洋县1981—1986年的繁殖数量,计6年9窝27幼,已知死亡4只,人工喂养3只。 朱鹮在洋县为留鸟,越冬期间偶尔返回繁殖地,2月中旬后不再离开。有显著的领域性。3月上旬开始营巢,中旬至4月初产卵,多数3枚(1—4枚)。孵卵期30天左右,育雏期约为40天,均由雌雄亲鸟共同承担。6月中下旬全窝育成后一起飞离巢区。     

ECOLOGY OF THE RED-NECKED FALCON FALCO CHICQUERA IN ZAMBIA

The Red-necked Falcon in southern Zambia is a year-long resident in its breeding territory. The study was conducted on a floodplain and the adjacent acacia savannah in an undisturbed natural environment. The falcon principally nests in natural depressions on frond bases on the leeward side of Borassus Palms but also utilizes old crow and raptor nests. Incubation averaged 33 days and was undertaken by the female. The young fledged after a 36-day nestling period and remained under parental care for up to three weeks after that. Nesting success averaged 1.3 young per nest or 44% of the eggs laid. The post-juvenal moult commenced when the young were five to six months old and continued for six months. Birds comprised 98% of the diet of the falcons. The adults selected larger prey as the nestlings increased in size. The 69-day incubation and nesting period is up to 14 days longer than in similar-sized falcons.     

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.     

Effects of stimuli emanating from the nest on the reproductive cycle in the ring dove. III: building in the postlaying period and effects on the success of the cycle.

Nest-building as a functional activity is shown to continue well into the incubation period of the ring dove (Streptopelia risoria), its intensity depending on the state of the nest. The presence of a nest has profound consequences on breeding success: pairs with no nests did not incubate well and did not hatch their eggs. Pre-laying disruption of the nest or of the usual roles of the male and female had no effect on incubation as long as a nest was present when the eggs were laid. It is concluded that the presence of a nest is necessary for the proper establishment of incubation. The possible role of the nest in incubation is discussed.     

Breeding biology and social behaviour of Magellanic Woodpeckers (<Emphasis Type="Italic">Campephilus magellanicus</Emphasis>) in Argentine Patagonia

The Magellanic Woodpecker (Campephilus magellanicus) is a poorly known species endemic of the Austral Temperate Forests of South America, where it is a potential keystone habitat modifier. Here, I summarize data on the social and breeding biology of this woodpecker, based on 22 active nests located from 1998–2002 in forests from northwestern Argentine Patagonia. Woodpeckers normally traveled in pairs or family parties. In late Austral winter, one to three cavities were selected for completion at each territory. Breeding occurred between mid- to late spring and early to mid-summer, and took about 65 days. Monogamous parents shared duties in nest excavation, incubation and young rearing. Egg length (±SD) measured 34.13±0.79 mm and egg breadth 23.91±0.67 mm, and incubation took roughly 20 days. Nestlings were altricial and remained at the nest for about 45 days. Clutch size was one, occasionally two eggs, and one nestling was produced at all successful nests. Young remained with their family group for up to 2 years or more, and were fed by adults, who normally bred every second year. Nest re-use, nest predation and helpers at the nest were not recorded. Holes were placed (±SD) 8.84±3.71 m high and were 32.3±5.32 cm deep. Entrances (±SD) were 8.92±0.46 cm wide and 15.59±2.54 cm high and mostly oval in shape. Peculiarities of the breeding biology and social behaviour of this species are discussed in the light of patterns common to picids, especially Campephilus spp.     

Breeding of the bellbird on the Poor Knights Islands,New Zealand

Abstract

The breeding of the bellbird (Anthornis melanura) was studied intensively over three seasons on Aorangi Island, Poor Knights Islands. Adult males defended territories all year but ventured beyond them to exploit localised food resources and to obtain water; some adults defended the same territory for at least 5 years. Adult females shared a territory with a male only during the breeding season. At other times of the year adult females were joined by juveniles and immatures and formed feeding flocks. The breeding season extended from late September to late December. A few nests were built on the ground but most were in dense vegetation, usually near the canopy. Peak egg-laying extended from mid-October to mid-November and only one clutch of two to four eggs was laid. Nest building and incubation were completed by the female alone but both parents fed nestlings. Fledglings stayed in the vicinity of the nest for several days, and were fed by both parents. Incubation and nestling periods were about 15 and 19 days respectively. Comparisons are made with the breeding biology of bellbirds and other native passerines on mainland New Zealand, and the importance of the predator-free enviomment of the Poor Knights Islands is stressed.