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。     

棕背黑头鸫繁殖习性初步观察

2008年和2009年的4～8月,在四川省雅江县帕姆岭对棕背黑头鸫Turdus kessleri的繁殖生态进行了初步观察.该鸟繁殖期在4月下旬至7月上旬,营树上巢,营巢树种为高山栎Quercus aquifolioides和鳞皮冷杉Abies squamata.窝卵数为2~3枚(n=7),平均卵重(7.96±0.03)g(n=8),卵长径(32.7±0.17)mm,短径(21.9±0.13)mm(n=13),雌雄共同孵卵,以雌性为主,孵化期为15~17 d(n=2),孵化率为83.3%(n=18).雌雄共同育雏,以雄性为主,雏鸟出飞后主要在巢周围的林下或灌从活动,这时亲鸟仍会对幼鸟喂食.在同一繁殖季对巢有重复利用的现象.     

甘肃安西荒漠伯劳的繁殖生态

2010年4～8月在甘肃安西极旱荒漠国家级自然保护区,采用样点法对荒漠伯劳(Lanius isabellinus isabellinus)的繁殖生态进行了研究,采用单因素方差分析(ANVON)对荒漠伯劳卵体积与卵序之间的关系进行了研究,用二元Logistic回归对雏鸟生长曲线进行拟合。结果表明,荒漠伯劳的繁殖时间为4月底至8月初,每巢产卵3～6枚,平均窝卵数为4.67±0.57(n=21),卵体积为(3.14±0.32)cm3(n=95),卵鲜重(3.48±0.20)g(n=20),卵体积随着产卵顺序显著减小(R=-0.427,P=0.021,n=29),其采取的是"窝雏减少"的繁殖策略。雌鸟产首枚卵后即开始孵卵,雄鸟负责情饲及警戒。温度自动记录仪测量平均孵卵温度为(38.19±0.77)℃(n=2),雌鸟在巢率为93.95%。平均孵卵时间为(15.33±0.52)d(n=6)。荒漠伯劳雏鸟留巢期12～15 d,幼鸟离巢后亲鸟继续饲喂幼鸟,整个育雏期最长达31 d。研究地区荒漠伯劳种群的孵卵率为82.50%(n=80),卵成功率为46.25%(n=80),雏鸟离巢率为56.06%(n=66),巢成功率58.62%(n=29)。在2010年环志标记的12对繁殖鸟中只有1对繁殖了第二窝。     

甘肃莲花山黑冠山雀繁殖生态的初步研究

2017和2018年每年的4至8月在甘肃莲花山国家级自然保护区,对人工巢箱中黑冠山雀（Periparus rubidiventris）的繁殖生态进行了研究。共悬挂100个巢箱,两年共计招引到15巢黑冠山雀。此外,还记录到4个自然巢,分别位于干枯的糙皮桦（Betula utilise）树洞（1巢）、土坡的缝隙（1巢）和路边水泥护坡的出水管中（2巢）。黑冠山雀雌雄亲鸟共同筑巢,巢内壁为兽毛夹杂少量绒羽,外壁为草茎须根和苔藓。5月中下旬为黑冠山雀的产卵高峰期,清晨产卵,日产1枚,产下最后1枚卵后开始孵卵。平均窝卵数为6枚（4 ~ 7 枚,n = 15）,平均卵重（1.12 ± 0.02）g,卵长径（15.30 ± 0.10）mm,卵短径（12.09 ± 0.11）mm（n = 86）。孵卵由雌鸟承担,孵卵期为15 d（14 ~ 16 d,n = 5）。产卵期,雌鸟离巢时有用巢材盖卵的行为,开始孵卵后则不再盖卵。双亲共同育雏,育雏期为16 d和17 d（n = 2）。所记录的18巢黑冠山雀的繁殖成功率为83.3%,人工巢箱（15巢）中繁殖成功率为86.7%,巢捕食者主要为鼠类。     

湖北兴山县龙门河地区灰林（即鸟）繁殖习性

2004年5月~2005年7月,在湖北省兴山县龙门河村,对灰林(Saxicola ferrea)的繁殖习性进行了初步研究。研究结果显示,灰林在湖北兴山龙门河地区的繁殖时间为4月中旬至7月下旬。主要在农田边、公路旁、河岸边、山间小路旁等山坡草丛中营巢,巢址选择在牲畜较少光顾的、较陡的土坡上,上方往往有茅草等遮挡,较为隐蔽。筑巢工作全部由雌鸟承担,一般需要5~7 d即可完成。雌鸟每天产一枚卵,产卵时间一般在清晨。窝卵数5枚(n=15),第4枚卵产出后即开始孵化,孵卵工作全部由雌鸟承担。雌鸟的孵卵行为有明显的节律性。孵化期13~14 d。雏鸟晚成性,雌雄共同育雏,育雏期12~13 d。雏鸟离巢前体重有所下降。     

内蒙古达赉湖国家级自然保护区短趾百灵繁殖生态学初报

本文对内蒙古达赉湖国家级自然保护区短趾百灵繁殖生态进行了初步研究,共记录到短趾百灵繁殖巢37个。筑巢期7~10 d。巢外径91.95 mm±3.85 mm(n=37),巢内径53.89 mm±3.29 mm(n=37),巢深43.62 mm±5.36 mm(n=37)。平均窝卵数3.05枚±0.51枚。孵卵期10~12 d。孵化率、离巢率和繁殖成功率分别为83.3%、94.1%和54.1%。雏鸟食性以直翅目昆虫幼虫为主。     

广西防城港黑翅长脚鹬的繁殖行为

本研究于2021年3～9月,采用目标观察和全事件记录法,对广西防城港市钦州湾八路水湿地黑翅长脚鹬（Himantopus himantopus）的繁殖习性进行全过程观察记录。黑翅长脚鹬的栖息生境主要在盐田、虾塘和鱼塘,而巢主要分布在盐田生境。共发现39巢,雌雄共同营巢,按照主要巢材将其巢分为干草巢、碎石巢、泥皮巢和牛毛毡草巢4种;巢材包括禾本科（Gramineae）和莎草科（Cyperaceae）植物以及碎石、贝壳等;巢外径为（23.3±10.7）cm,巢内径为（11.2±1.9）cm,巢深为（1.6±0.5）cm,巢高为（6.5±4.3）cm(n=39);筑巢需（3±2）d(n=6)。窝卵数2～4枚,1～2 d产1枚卵,7 d内产完满窝卵（n=6）。雌雄均参与孵卵,雄性孵卵时间比雌性长,但二者差异不显著（P> 0.05）,雄性（8 550±245.9）min,雌性（7 530±263.3）min,孵卵期为（25±2）d(n=6)。育雏期（26±3）d(n=6),雌雄轮流育雏,育雏前、中期（雏鸟1～20d日龄）,雌性育雏时间比雄性长,是雄性的2倍,育雏后期（雏鸟大于20 d日龄）,...     

河南董寨寿带鸟繁殖生态及雌雄个体形态类型

寿带（Terpsiphone incei）是雀形目王鹟科的鸟类,在我国大部分地区均有分布。以往研究曾对我国部分地区寿带的繁殖习性进行了报道,但对其雌雄个体的形态类型缺少描述。为进一步了解寿带的繁殖习性及其雌雄个体的形态类型,本研究于2014至2017年每年的5至7月在河南董寨国家级自然保护区对其进行了观察。观察发现,寿带在董寨国家级自然保护区一般于5月下旬开始筑巢繁殖,雌雄亲鸟均参与筑巢、孵卵和育雏。寿带巢多位于刺槐（Robinia pseudoacacia）、麻栎（Quercus acutissima）、枫杨（Pterocarya stenoptera）等几种植物上,平均窝卵数（± SD）为（3.8 ± 0.6）枚（n = 25巢）,孵卵期12 ~ 13 d（n = 4巢）,各巢卵的平均孵化率（± SD）为91.7% ± 17.7%（n = 9巢）,窝雏数（± SD）为（3.6 ± 0.8）只（n = 19巢）,巢内育雏期约10 d,巢成功率为34.5%（n = 29巢）,弃巢和天敌捕食是巢失败的主要原因。寿带雌鸟具有栗色短尾型和栗色长尾型2种形态,而雄鸟具有栗色长尾型、白色长尾型和栗色短尾型3种常见形态,且雄鸟以栗色长尾型所占比例最高,为69.4%（n = 36巢）。此外还记录到1只栗色身体但具有白色长尾羽的雄鸟。本研究的结果有助于进一步了解寿带的繁殖习性及其雌雄个体的形态类型。     

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.     

湖北巴东寿带鸟繁殖行为观察

20 0 2年 5月～ 2 0 0 4年 8月 ,在湖北省巴东县沿渡河镇的东圩口、小溪、锯锯湾、两河口等 4个村 ,对寿带鸟 (Terpsiphoneparadisiincei)的繁殖生态进行了初步研究。研究结果显示 ,寿带鸟在湖北巴东的繁殖时间为 5月下旬～ 7月上旬 ,主要在农田居民区附近的阔叶树上营巢 ,巢材主要有青苔、草叶、草茎、细草根、棕丝、树耳、蜘蛛网等。筑巢工作主要由雌鸟承担 ,一般需要 5～ 7d即可完成。巢距离地面高度1 72～ 6 45m ,巢外径 6 0～ 8 8cm ,巢内径 4 9～ 6 4cm ,巢深 2 9～ 4 1cm ,巢高 6 3～ 9 5cm。雌鸟每天产 1枚卵 ,产卵时间均在清晨。窝卵数 4枚 (n =1 1 ) ,卵产齐后即开始孵化 ,雌雄鸟轮流孵卵 ,孵化期 1 3d。雏鸟晚成性 ,雌雄共同育雏 ,育雏期 9d。寿带鸟对不同的外界干扰反应明显不同 ,当有对其卵和雏鸟构成威胁的动物接近时 ,护巢行为表现十分强烈 ;而对其没有威胁的物种接近其巢时则无动于衷。面对同样的干扰 ,雌雄亲鸟的反应存在显著差异。     

Incubation and rearing-effort partitioning of wing-banded hornero Furnarius figulus (Passeriformes: Furnariidae).

We studied incubation and feeding rates in two of five broods in two oven nests of Furnarius figulus at Lagoa Rodrigo de Freitas. During incubation, the number of visits and time spent in the nest did not differ between the adults. The number of feeding visits was significantly different between members of the breeding pair of the first but not of the second nest. Nestlings received arthropods, fishes, and larvae in the first nest and, in the second, arthropods, larvae, and fruits. The nestlings stayed about 23 days in the nests.     

Breeding biology of Eared Quetzals in the Sierra Madre Occidental, Mexico

ABSTRACT.   Eared Quetzals ( Euptilotis neoxenus ), a threatened species, are one of the least studied trogons in Mexico. We monitored 29 Eared Quetzal nests in the Chihuahuan portion of the Sierra Madre Occidental from 1998 to 2003. All nests were in tree cavities, and the mean tree and nest cavity heights ( N = 14) were 16.9 ± 7.8 m and 11.4 ± 4.1 m, respectively. The mean clutch size was 2.8 ± 0.9 eggs ( N = 28), the incubation period lasted 22 d ( N = 1), and nestling periods ranged from 29 to 31 d ( N = 5). Both adults incubated eggs and fed nestlings. Of 80 eggs, 70 hatched (87.5%) and 67 of 70 young fledged (95.7%). Twenty-five of 29 nests (86.2%) produced at least one fledgling. One nest was predated, and two failed when nest trees fell. Higher rates of nest predation have been reported for other species of trogons. However, fewer potential predators, such as snakes and mammals, are present in the Sierra Madre than in tropical zones where most trogon species occur. In addition, antipredator behaviors, including nestlings with calls resembling a snake and nests with an unpleasant odor, may contribute to the high nesting success. The main limiting factors for Eared Quetzals in the northern Chihuahua may be competition for cavities with other secondary cavity-nesters, and the failure of nests when snags fall.     

绿翅鸭繁殖生态初报

2007～2009年在黑龙江中南部地区对绿翅鸭(Anas crecca)繁殖生态习性进行了观察。绿翅鸭在黑龙江属夏候鸟,每年3月末4月初迁来,10月上旬迁离,所观察的4对绿翅鸭居留期约6个月。迁来时成群停留在湖泊及江的冰面上,开江以后散去,繁殖期间,绿翅鸭的配偶关系为一雄一雌,巢址多选择离水域较近的草丛或灌木丛中,所观察的4巢,巢都比较简单,筑巢时间为(5.5±1.0)d(n=4)。巢筑成后的(3.25±0.50)d开始产卵。每窝70～12枚不等,平均(9.80±2.21)枚(n=4)。卵重平均(28.70±0.72)g(n=39),最后一枚卵产出后(2.50±0.577)d(n=4),开始孵卵,孵卵期约为22～26 d不等,平均孵卵期为(24.25±1.17)d(n=4),平均孵化率为79.5%±29.98%。幼鸟为早成鸟,育雏期为(29.75±1.70)d。     

云南云县黑喉山鹪莺繁殖生态初报

2016年3~9月对云南云县中岭岗村(24°15′42″N,100°02′42″E,平均海拔1 650 m)的黑喉山鹪莺(Prinia atrogularis)繁殖生态进行了研究。研究期间共发现42巢,主要位于杂草丛中(n=37)和灌木丛(茶树)中(n=5),筑巢期一般5~6 d,巢材有蜘蛛丝、苔藓植物、茅草花、茅草叶、铁线莲花、竹根须、枯枝、棕丝、干枯草穗等。巢呈球状,中上部侧方开口,巢重为(8.3±1.7)g,巢长为(13.2±0.9)cm,宽为(8.2±0.5)cm,巢口长(4.9±0.7)cm,巢口宽为(4.0±0.5)cm(n=25)。窝卵数为(3.9±0.4)枚(n=21,3~4枚)。卵的底色为白色、淡绿或者淡粉,遍布褐红色斑点,有的在钝端呈环状。卵重为(1.38±0.09)g,卵长为(17.3±0.7)mm,宽为(12.6±0.3)mm,卵体积为(1.4±0.1)cm3(n=65)。孵卵期(13.9±0.9)d(n=5,13~15 d),育雏期为(13.5±1.3)d(n=4,12~15 d)。利用Logistic曲线拟合雏鸟体重及外部器官增长,雏鸟的体重和嘴峰在5日龄左右增长最快,体长、翼长、跗跖在7日龄增长最快。对繁殖时间和地点较近的28巢进行连续观察,其中有7巢成功、21巢失败。造成繁殖失败的主要原因分别是巢捕食(62%)、亲鸟弃巢(14%)、人为破坏(14%)。     

Nest position,breeding success and diet of the Black-crowned Night Heron,Nycticorax nycticorax in the Anzali Wetland,Northern Iran (Aves: Ardeidae)

Breeding ecology of the Black-crowned Night Heron (Nycticorax nycticorax) was studied in a mono-specific colony in the Anzali wetland, Northern Iran during the breeding season of 2016. The breeding period lasted from mid-May to late July. The average clutch size was 3.1±0.6 eggs and the breeding success 77.6%. No significant differences were found between nests built on trunks and those built on branches of trees. The clutch size and breeding success appeared to be independent of the structural variables of the nesting site (diameter of trees, height from the ground, height of nests from the canopy, nest number per tree, location of nests on trunks and branches). No significant difference was found between the timing of the start of incubation and the height of nests above the ground. The average vertical and horizontal distances between nests was one metre. Fish, particularly Carassius gibelio, dominated the diet of the nestlings.     

云南纳帕海湿地越冬黑鹳种群动态和迁徙

掌握种群动态以及迁徙习性对濒危候鸟的保护至关重要。2004~2005、2007~2008、2008~2009年的冬季(10月~次年4月),采用夜栖地直接计数法对云南省纳帕海湿地黑鹳(Ciconia nigra)的种群数量进行了监测。结果表明,在2004~2005、2007~2008、2008~2009年冬季,纳帕海湿地越冬黑鹳种群平均数量分别为39.6、128.6、181.8只,呈逐年增加的趋势;通常黑鹳10月下旬迁来,至次年3月中下旬迁离;纳帕海同时也是繁殖于蒙古国的黑鹳迁往印度越冬地的重要停歇地,过境时间集中在 11月中上旬。纳帕海湿地已经成为国内最为重要的黑鹳越冬地和迁徙停歇地,建议当地管理部门加强湿地管理,维持适当的浅水区域作为黑鹳的觅食地,另外需加强旅游管理,减少游客对黑鹳的干扰。     

Sex-related parental care strategies in the lesser spotted woodpecker Picoides minor: of flexible mothers and dependable fathers

We investigated sex-specific parental care behaviour of lesser spotted woodpeckers Picoides minor in the low mountain range Taunus, Germany. Observed parental care included incubation, nest sanitation as well as brooding and feeding of nestlings. Contributions of the two sexes to parental care changed in progress of the breeding period. During incubation and the first half of the nestling period, parental care was divided equally between partners. However, in the late nestling stage, we found males to feed their nestlings irrespective of brood size while females considerably decreased feeding rate with the number of nestlings. This behaviour culminated in desertion of small broods by females shortly before fledging. The fact that even deserted nests were successful indicates that males were able to compensate for the females' absence. Interestingly, the mating of one female with two males with separate nests could be found in the population, which confirms earlier findings of polyandry in the lesser spotted woodpecker. We conclude that biparental care is not essential in the later stage and one partner can reduce effort and thus costs of parental care, at least in small broods where the mate is able to compensate for that behaviour. Reduced care and desertion appears only in females, which might be caused by a combination of two traits: First, females might suffer higher costs of investment in terms of mortality and secondly, male-biased sex ratio in the population generally leads to higher mating probabilities for females in the following breeding season. The occurrence of polyandry seems to be a result of these conditions.     

The process of fledging in the Mountain Bluebird

Fledging is a critical event in the avian breeding cycle, but remains unstudied in almost all species. As a result, little is known about factors that cause nestlings to leave nests. We documented fledging behavior in a box‐nesting population of Mountain Bluebirds (Sialia currucoides) using radio‐frequency identification. We attached a passive integrated transponder (PIT tag) to the leg of each nestling in 40 nests. An antenna checked for the presence of a transponder signal (i.e., a nestling) at nest‐box entrances every 2 s. The time of last detection of a nestling was taken as the time that nestling fledged. We found that fledging began when the oldest nestlings were 15–22 d old. Broods that were ahead in development, as measured by primary feather length, fledged at relatively younger ages. All nestlings fledged on the same day at 33 nests (83%) and over 2 d at remaining nests. When all nestlings fledged on the same day, fledging usually began in the morning and median time between the first and last fledging was 55 min (range = 2.3 min–10.6 h). When young fledged over 2 d, fledging always began >8 h after sunrise and usually just one nestling fledged the first day, suggesting that this fledging may have been accidental. Clutches in our population often hatch asynchronously, which sets up a hierarchy within broods in developmental state, size, and competitive ability. In such situations, fledging may be initiated by one of the most‐developed and hence most‐competitive nestlings in a brood, presumably when it reaches a certain threshold state of development. Alternatively, fledging may begin when a less‐developed, less‐competitive, and probably hungrier nestling leaves the nest, presumably to gain better access to food. We used the proportion of time that a nestling was able to occupy the nest‐box entrance late in the nestling stage, waiting to intercept parents with food, as an index of nestling competitive ability. Assuming that the number of nest entrance detections reliably indicates nestling competitive ability, we found that the most‐competitive nestling fledged first at over half of all nests, supporting the notion that fledging usually begins when oldest nestlings reach a threshold state of development.     

Breeding cycle of the Southern Bald Ibis,Geronticus calvus

Kopij, G., Kok, O.B. & Nuttall, R.J. 2000. Breeding cycle of the Southern Bald lbis, Geronticus calvus. Ostrich 71(3&4): 393-399. The breeding cycle of the Southern Bald lbis, Geronticus calvus, was studied at a colony in the eastern Free State. Birds were paired before breeding commenced and nest bulding began regularly two weeks before the first eggs were laid. Nesting material was collected chiefly by the male. Incubation statted with the first egg and lasted 26-32 days. Both sexes incubated, the female usually in the morning, the male around noon, and both sexes in the afternoon. Hatching is asynchronous with intervals between eggs ranging from one to four days. Bothe parents participate in rearing the young; the female broods more often, while the male brings the bulk of the food for the nestlings that were fed 3-4 times a day. Strong competition for food between nestlings was recorded. Nestlings remain in nests for at least 35 days.