新疆木垒波斑鸨的繁殖成功率

作者于 1998～ 2 0 0 0年 4～ 7月 ,采用野外直接观察、栖息地植被样方调查和无线电跟踪等方法对分布于新疆木垒的波斑鸨 (Chlamydotiundulatamacqueenii)种群的繁殖生态进行了初步观察与研究。考察中共发现45个巢、 84窝幼雏。研究结果表明 ,木垒波斑鸨有两个产卵高峰期 ,表明雌鸟第一次繁殖失败后可能再次产卵。雌鸟营巢成功率平均为 0 5 0 5。波斑鸨的窝卵数在 2～ 6枚之间 ,出现 4枚卵的频率最高。第一产卵期内的平均窝卵数 ( 4 0± 0 8枚 /窝 )大于第二产卵期内的平均窝卵数 ( 3 3± 0 8枚 /窝 )。木垒波斑鸨种群三年间卵孵化率分别为 0 84、 0 80和 1,繁殖成功率为 0 45 6。种群在繁殖期几乎不受人类活动干扰 ,巢卵及幼雏损失主要来自天敌捕食 ,如沙狐、大和棕尾等.     

吉林白城地区草原栗斑腹(巫鸟)窝卵数、营巢成功率和繁殖成功率的研究

对分布于吉林白城地区草原生境中栗斑腹巫鸟的窝卵数、营巢成功率和繁殖成功率的初步研究结果表明 ,繁殖期栗斑腹巫鸟种群的平均窝卵数为 5 .0 9± 0 .5 8枚 /巢 ;窝卵数与产卵期、出巢数与产卵期、窝卵数与卵大小之间呈负相关 ,产卵期与孵化率之间存在极显著的负相关关系 ,巢外径与窝卵数之间存在显著的正相关关系 ,巢的其余指标均与窝卵数呈正相关 ;平均孵化期为 12± 0 .4 9d ,孵化率为 36 .3% ,繁殖成功率为 11.11% ;7日龄以上的雏鸟群体大小为 2 .5 6± 1.5 3只 ,栗斑腹巫鸟的雏鸟存活率为 2 7.6 9% .     

四川瓦屋山金色林鸲的繁殖生态及孵卵节律

20 0 3年 4～ 7月 ,在四川省瓦屋山自然保护区对金色林鸲 (Tarsigerchrysaeus)的繁殖生态和孵卵节律进行了较为深入的研究。金色林鸲营巢期从 4月下旬～ 6月中旬 ,孵卵期一般为 1 6～ 1 7d,育雏期为1 6d。窝卵数一般为 3～ 4枚 ,平均为 (3 . 75± 0. 45 )枚 (n =1 2 ) ,孵化率为 60 0 % ,育雏成功率为 85 2 %。仅雌鸟孵卵 ,根据对 3巢的监测 ,发现雌鸟早晨 6:0 0时左右首次离巢 ,晚上 2 0 :0 0时左右回到巢中 ,每天出巢次数 1 8～ 1 9次。孵卵雌鸟每次出巢时间一般少于 2 0min ,异常离巢时最长达到 65 6min。雌鸟出巢时间的长度和环境温度呈明显的正相关 (Spearman,r=0 . 1 1 8,P =0 . 0 0 7,n =5 3 1 )。金色林鸲雄鸟存在羽毛延迟成熟现象 ,亚成体雄鸟可以繁殖。     

虎纹伯劳的巢生境选择与繁殖行为

2005年3~7月通过焦点动物取样法(focal animal sampling)和完全记录法(all-occur rencerecording)对四川南充地区虎纹伯劳的繁殖行为进行了研究。结果表明,虎纹伯劳喜在5~12m的高大阔叶乔木的冠部分叉处营巢。对15个巢址主成分分析表明,前5个主成分特征值均大于1,累积贡献率高达83.15%,说明前5个主成分已经基本包含了所有参数的总信息量。4月下旬开始陆续有虎纹伯劳迁到,初到时并未配对。5月上旬开始出现求偶行为,并伴有递食行为。5月中旬首次见到营巢,两性参与营巢,营巢期5~7d。营巢结束一两天后开始产卵,一天一枚,窝卵数4~6枚。营巢期和产卵期都有求偶和交配行为。产完最后1枚卵后即开始由雌鸟单独孵卵,孵卵期13~14d。两性育雏,育雏期13~15d。     

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。     

青海湖鸬鹚繁殖习性的初步观察

1999年 4～ 7月和 2 0 0 0年 3～ 8月 ,对青海湖地区的鸬鹚繁殖过程进行了观察 ,初步掌握了鸬鹚的迁移、营巢、产卵、孵卵、育雏和扩散等生态习性。结果表明 :鸬鹚每年 3月中、下旬迁来青海湖繁殖 ,两性共同营巢 ,营巢期集中在每年 4月上旬至 6月中旬 ;产卵高峰期为 4月下旬至 5月中旬。平均卵重是(5 7 5± 2 0 2 )g ,卵的大小为 67 2 9mm× 40 2mm ,平均窝卵数为 (3 61± 0 3 4)枚。鸬鹚孵卵期为 (2 8 0 7±0 5 3 )d ,孵化期间的卵重损失 (Y)与孵卵天数 (X)之间的线性回归方程为Y =0 997-0 0 0 68X(r=0 990 ,df=8,P <0 0 1 )。     

北戴河朱鹮野化训练种群的繁殖和婚外配北大核心CSCD

为了扩大朱鹮(Nipponia nippon)种群的数量和分布区,于2018年7月从洋县引进20只朱鹮在北戴河建立了朱鹮野化种群。2020年繁殖期,北戴河共有22只朱鹮,其中成年朱鹮17只,雌雄性比为1.1;实际繁殖密度为37.8只/hm2;人工巢的密度为40.0巢/hm2,人工巢筐内径为50 cm。2020年繁殖期,北戴河朱鹮共配对8对,其中6对繁殖成功,营巢成功率为75%;共产卵33枚,平均窝卵数为(4.1±1.8)枚;出壳18只,孵化率54.5%;出飞13只,出飞率72.2%,繁殖成功率为39.4%,繁殖生产力为2.2±1.2。与洋县饲养种群相比,北戴河种群首枚卵的产卵时间晚17 d,与两地温差相吻合。北戴河朱鹮的窝卵数显著高于洋县种群,这可能是由种内巢寄生所致。监控录像表明,北戴河1巢朱鹮的窝卵数高达6枚,超过野生种群平均窝卵数(2或3枚)的2倍,推测发生了种内巢寄生行为。此外,还观察到8号巢朱鹮同时发生了婚外配和种内巢寄生行为,婚外配雌鸟将卵产在该雄鸟的巢中,使得窝卵数高达7枚。此后在该巢中发现3只朱鹮轮流孵卵,以及2只雌性朱鹮并排孵于同一巢中的异常情况。北戴河朱鹮的种内巢寄生行为可能是因网笼内人工巢址密度较高但隐蔽性较低所致,而婚外配行为可能与种群密度和繁殖密度过高有关。本文有关朱鹮异常繁殖行为的研究结果可为野化网笼内人工巢筐的设置和野化种源的选择提供参考,并提示我们进一步关注朱鹮在环境压力下的表型可塑性和生态适应能力。     

四川南充崖沙燕的洞巢生物学

20 0 3年 2～ 6月 ,通过观察法对崖沙燕福建亚种的洞巢进行了考察。崖沙燕巢多筑于水边沙质硬土悬壁的沙土与黄壤交错的沙土层 ,且主要选择在沙土顶部与黄壤交界的部位啄洞营巢 ,喜利用旧巢洞。巢洞呈椭圆形、坑道状 ,多单洞道 ,洞末端扩大成椭球形巢室 ,具巢的洞深 ( 64 3 8± 1 1 73 )cm(n =5 0 )。巢室内外温度差异大 ,而巢室内昼夜温度稳定。繁殖力高、体型大的个体占据中心区深洞繁殖 ,巢多呈半圆状。窝卵数 ( 3 89± 0 92 )枚 (n =3 6) ;多数巢内有一枚卵未孵出 ( 63 3 %) ,孵化率 83 0 4%。     

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。     

笼养冠斑犀鸟繁殖生态的初步观察

2002~2004年通过对笼养冠斑犀鸟的繁殖生态进行观察,结果表明:冠斑犀鸟的发情期为3月中旬至4月初,求偶的追求者为雌鸟,雌鸟占据选巢营巢主导地位,从入巢到破巢的整个营巢期雌鸟始终把自己封闭在巢洞内,雄鸟担负了运送巢料和食物的所有任务直到雌鸟出巢,出巢后幼鸟在未具有觅食能力前,绝大部分的哺育任务仍由雄鸟承担。冠斑犀鸟的繁殖封巢期为89.0±12.99天,首次营巢的时间较长达15天左右,从第二年起营巢时间缩短为3天,孵化期为25.25±3.86天,育雏期为45.75±2.87天,繁殖成功率为100%。繁殖期除了人工投料外,冠斑犀鸟仍可从生态园中获得多种食物,以满足幼鸟的生长需要。     

Evolution of single-chick broods in the Swallow-tailed Gull Creagrus furcatus

Swallow-tailed Gulls lay single-egg clutches, and so raise single-chick broods. As they are pelagic seabirds, this small brood size is expected to relate to proximate food limitation owing to infrequent food deliveries. However, a previous brood doubling experiment detected an 82% increase in fledging success from experimentally doubled broods compared to controls. We repeated the brood doubling experiment, and found that none of 50 enlarged broods produced more than one independent offspring. Control and experimental parents produced fledglings of similar body size, which also had indistinguishable rates of fledging and subsequent survival and reproduction. A variety of parameters estimating survival and breeding costs of reproduction showed no treatment effect. Since two-chick broods yield dramatically higher fledging rates at some times, apparently without excess costs of reproduction, selection on brood size appears to favour a two-chick brood. However, selection may not favour a two-egg clutch if egg production is very costly. Additionally, our estimates of reproductive success do not incorporate the performance of experimental and control offspring as adults, which could differ, since growth of chicks differed slightly by treatment.     

Reproductive success of the Kittiwake Rissa tridactyla: the roles of clutch size, chick growth rates and parental quality

Kittiwake growth rates and breeding success are examined in relation to survival between fledging and breeding and to adult survival rates. High chick growth rates lead to increased survival after fledging. Broods of three (the maximum brood size) did not suffer lower fledging success than broods of two and clutches of three fledged appreciably more chicks per pair than did clutches of two or one. On average, the a- and b -chicks in broods of three grew at a faster rate and had a higher survival before breeding than those from smaller broods. Chicks from broods of two with experienced female parents grew at a faster rate than those of inexperienced female parents. Female parents which laid three egg clutches had a higher survival rate than those which laid clutches of two or one. We contend that three egg clutches were laid by higher quality individuals. We believe that clutch size indicates the condition of the Kittiwakes forming the pair. This condition probably has a genetical component, but is modified by environmental factors.     

The significance of clutch overlap in Great Tits Parus major

We studied the effects of manipulation of the size of first broods in the Great Tit Parus major on the size and breeding success of second clutches and its relation to the degree of clutch overlap. The rearing of first brood fledglings always overlapped with the laying of the second clutch and in most cases also with the incubation period of the latter. The degree of clutch overlap depended on the size of the first brood, being less when the first brood was large. Clutch overlap also increased with season. Mechanisms affecting the timing of laying of second clutches are discussed. A large first brood imposed reproductive costs. It affected the size of the second clutch by causing it to be delayed; second clutch size decreases with season. It affected the post-fledging survival of second brood young as, in this population, this decreases with fledging date. The breeding success of second clutches was, however, not affected by the size of the first brood, but instead by the weight of the female when rearing the first brood.     

人工巢箱条件下白眉姬鹟的繁殖参数

2005～2006年,在吉林省左家自然保护区的次生林中,对人工巢箱条件下白眉姬鹟(Ficedulazanthopygia)的繁殖参数开展了初步研究.结果表明,人工巢箱中自眉姬鹟的窝卵数为5～7枚,平均6.0枚;卵重平均为1.6 g.卵大小平均为17.0 mm×13.1 mm.孵化期平均为13.1 d,每巢平均出雏5.4只,育雏期平均为12.8 d,每巢平均出飞雏鸟5.3只.白眉姬鹟的营巢成功率为70.0%,繁殖成功率为81.3%.     

Larger clutch size increases fledging success and offspring quality in a precocial species

1. We tested the hypothesis that the ability of parents to raise viable offspring limits clutch size in the greater snow goose ( Anser caerulescens atlanticus L.), a precocial bird.
2. We manipulated clutch size by exchanging complete clutches between pairs of nests to increase or decrease the clutch size by zero (control), one, two or three eggs in 314 nests over 2 years.
3. Pre-fledging survival of goslings increased in enlarged broods and decreased in reduced broods compared to control. Consequently, enlarged broods fledged more offspring and the reverse was true for reduced broods.
4. Size and mass of goslings near fledging was also higher in enlarged broods than in control, which suggests that offspring quality was also enhanced by the manipulation. This is contrary to the common trade-off between offspring numbers and quality.
5. Large families were dominant over smaller ones in feeding sites, which could explain the increased survival and growth of enlarged broods.
6. Our results suggest that the ability to raise young does not limit clutch size in this species and that parents could be more successful (i.e. increase both the number and quality of their offspring) by laying more eggs. However, the time required to lay additional eggs reduces the viability of all offspring and may explain why females do not lay more eggs.     

Reproduction in a population of the hooded crow Corvus cornix

Nest density was stable during the 8-year study period. The mean clutch size was 4.3, and the production of fledglings was 2.0 per pair. Incubation started, on average, when there were still two eggs to be laid and lasted for 18 days. Few eggs were lost but 23% of all broods of nestlings were lost to predators. Single nestlings in a brood were not lost to predators but often starved to death, this applied to 25% of all nestlings. A large proportion of the nestlings were probably infected by Syngamus tracheae , and some of these succumbed during the first weeks after fledging. A comparison with other studies of crow populations shows that the major causes of breeding failure are different in different populations. The causes of variation in breeding success between populations are discussed, especially considering the role of nonbreeding crows.     

No effect of the ectoparasite Crataerina pallida on reproduction of Common Swifts Apus apus

Previous studies have failed to ascertain negative effects of the Swift Lousefly Crataerina pallida parasitism on Common Swifts Apus apus. Abundances of C. pallida were experimentally manipulated to create broods experiencing either enhanced or reduced parasitism, and host life‐history traits were examined. No significant differences in clutch and brood size, rate of growth, asymptotic and fledging mass and size, or the number of fledglings per nest were observed. Reductions in parasite virulence may have developed due to the connection of C. pallida and host success, or costs may be borne by traits not influencing immediate fledging success.     

Effects of maternal quality and mating status on female reproductive success in the polygynous spotless starling

Female mating status may affect reproductive success in avian polygynous mating systems through a combination of differences in female parental quality and status-dependent male assistance in parental care. Traditionally the literature has emphasized male assistance, neglecting evidence for consistency in female parental quality independent of mating status or repeatability in status. We studied the effects of male assistance on breeding success and its association with female mating status in a population of the polygynous spotless starling, Sturnus unicolor, during 3 years. Nestling provisioning by males improved the fledging success of late (mostly second) but not early (mostly first) broods. Reproductive success of females was affected mainly by female maternal quality: (1) primary and secondary females did not differ in output for early broods and in seasonal output despite a greater male assistance at primary nests; (2) monogamous females were more successful despite receiving no more help than other females; and (3) primary and secondary females had different clutch sizes before male assistance in parental care could operate. Female mating status was not significantly repeatable within seasons or between years. Females who changed status between years were as successful when rearing broods as secondary females as they were as primary or monogamous females. Breeding success (proportion of eggs resulting in fledglings) and clutch size were significantly repeatable between years for late but not for early clutches. Performance showed no strong association with female age or condition. Female breeding success seems to be weakly affected by male assistance in this sedentary, colonial species, and more dependent on inherent differences between females. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

Are incubation costs in female pied flycatchers expressed in humoral immune responsiveness or breeding success?

Although clutch size variation has been a key target for studies of avian life history theory, most empirical work has only focused on the ability of parents to raise their altricial young. In this study, we test the hypothesis that costs incurred during incubation may be an additional factor constraining clutch size in altricial birds. In the pied flycatcher (Ficedula hypoleuca), we manipulated the incubation effort of the female by enlarging and reducing clutch sizes. To manipulate incubation effort only, the original clutch sizes were restored shortly after hatching. We found that fledging success was lower among broods whose clutches were enlarged during incubation. There was, however, no effect of manipulation on female body condition or on their ability to mount a humoral immune response to diphtheria or tetanus toxoid during the incubation or nestling provisioning period. Instead, we found that the original clutch size was related to the immune response so that females with seven eggs had significantly lower primary antibody responses against tetanus compared to those with six eggs. Our results suggest that incubating females are not willing to jeopardise their own condition and immune function, but instead pay the costs of incubating a larger clutch by lower offspring production. The results support the view that costs of producing and incubating eggs may be substantial and hence that these costs are likely to contribute to shaping the optimal clutch size in altricial birds.     

Seasonal variation in reproductive measures of tropical Roseate Terns Sterna dougallih previously undescribed breeding patterns in a seabird

Seasonal variation in egg-laying, egg size, hatching success, hatchling mass, fledging success and chick growth of Roseate Terms Sterna dougallii breeding on Aride Island (Seychelles), Indian Ocean, were studied in 1997 and 1998. I investigated to what extent two patterns, common in a range of species, were followed by tropical Roseate Terns: (a) seasonal decrease in clutch size, egg size and breeding success and (b) an increase in breeding success with increasing egg weight. In 1997 (a poor year), the earliest nesting birds laid significantly smaller eggs, and chicks were lighter at hatching than those of peak nesting birds. The mean clutch size, of 1.04 eggs, showed no seasonal variation and no 'b'-eggs hatched. In 1998 (a good year) the earliest nesting birds laid eggs of similar size and their chicks were of similar weight to those of peak nesting birds. Mean clutch size, of 1.25 eggs, increased significantly through the season and about 60% of the 'b'-eggs hatched. In 1997, hatching success was 57% whereas in 1998 it was 80%. In both years, breeding success declined significantly through the season. The fact that the earliest breeding birds laid smaller eggs in a poor year and smaller clutches in a good year is in marked contrast to a range of other species, and to temperate-nesting Roseate Terns. Egg volume explained about half of the variance in hatchling mass in both years, but only 15% of the variation in linear growth rate. Hatching date was the only variable with a significant effect on fledging success. Roseate Terns on Aride seemed to sacrifice egg size and clutch size for earliness of laying. Presumably it is a strategy of older birds to lay as early as possible and may be regarded as a response of tropical Roseate Terns to breeding under relatively poor, and seasonally declining, food conditions.