人工巢箱繁殖鸟类主要巢捕食者及其影响因素

巢捕食是影响鸟类繁殖成功率的一个重要因素,也是鸟类繁殖生态研究中的一项重要内容。确定鸟类的主要巢捕食者及影响巢捕食的因素对于了解鸟类繁殖成功率、种群增长率及种群数量等具有重要意义。2009—2012年,对辽宁仙人洞国家级自然保护区人工巢箱中繁殖的杂色山雀(Parus varius)、沼泽山雀(P.palustris)、大山雀(P.major)和白眉姬鹟(Ficedula zanthopygia)四种鸟类的巢捕食率及影响巢捕食的因素进行了研究。研究共记录到238个繁殖巢(杂色山雀74巢、沼泽山雀21巢、大山雀118巢、白眉姬鹟25巢),其中35巢被捕食,捕食率为14.7%,雏鸟期被捕食占91.4%。巢捕食率在4种鸟类之间无差异(x~2=0.429,df=3,P=0.934)。以锦蛇(Elaphe spp.)为代表的蛇类是该地区小型森林洞巣鸟类繁殖期主要捕食者,占总捕食率的94.3%。对影响巢捕食的22个相关因子进行二元逻辑斯蒂回归分析发现,坡度、地面裸露率、草本盖度对巢捕食具有显著性影响;出雏时间、坡位、距碎石块距离对巢捕食的影响接近显著水平;而巢高、树粗、巢箱年龄、窝卵数、距路距离等对巢捕食无显著影响。因此,处于坡度较陡,坡位较高,草本覆盖率较高,地面裸露率较低,距碎石块距离较近,且出雏时间较晚的巢更容易被捕食。     

长白山中华秋沙鸭的种内巢寄生

雁形目鸟类的种内巢寄生现象十分普遍,但有关中华秋沙鸭(Mergussquamatus)的种内巢寄生现象未见报道。2019年4和5月,从长白山1个中华秋沙鸭人工巢的视频监控发现,1只雌鸭在亲鸟孵卵时强行进入巢箱趴卧约29 min。其后根据该巢窝卵数的增加、超常窝卵数和窝卵不同步孵化3个指标,确认该巢存在种内巢寄生现象。宿主对进入巢内寄生的个体表现出强烈的攻击行为,但对寄生卵未表现出明显的拒卵行为。由于区域内仍有较多巢箱未被利用,中华秋沙鸭的种内巢寄生行为是否源于对有限巢址资源的竞争,有待进一步研究。     

两种山鹪莺的繁殖参数比较

生活史是鸟类生态学研究的重要内容之一,分析生活史的影响因子对于研究鸟类的生态适应具有重要意义。2007年3~9月,在广东省肇庆市江溪村对黄腹山鹪莺(Prinia flaviventris)和纯色山鹪莺(P.inornata)的繁殖参数进行了比较研究。结果表明:1)除筑巢集中期、窝卵数、巢捕食率和割草毁巢率外,两种山鹪莺各繁殖参数均存在显著性差异;2)黄腹山鹪莺的窝卵数相对较小,但卵重较大,而纯色山鹪莺则相反;3)与体重相似的9种雀形目鸟类相比,两种山鹪莺具有相对较高的年生产力;4)两种山鹪莺在部分繁殖参数上出现了分化,这可能是它们对不同巢捕食风险的响应,黄腹山鹪莺的巢捕食率相对较高,采取低窝卵数和高的卵重,而纯色山鹪莺则为高的窝卵数和低的卵重。     

人工巢箱中大山雀和褐头山雀的繁殖比较

2009年3-7月,在北京小龙门森林公园悬挂人工巢箱,对大山雀(Parus major)和褐头山雀(P.montanus;)的繁殖进行比较研究.野外共悬挂100个巢箱,其中19巢(19.0%)被大山雀、11巢(11.0%)被褐头山雀进驻,总利用率为30.0%.同域繁殖的大山雀和褐头山雀在窝卵数、孵化期上有极显著差异(P＜0.01),其中大山雀的窝卵数(8.21枚±0.25枚,n=19)极显著大于褐头山雀(6.18枚±0.23枚,n=11),而褐头山雀的孵化期(14.22d±0.44d,n=10)极显著长于大山雀(13.17 d±O.83 d,n=12).两者在卵重、卵大小、出雏数、雏鸟出飞数上无显著差异(P＞0.05).大山雀的繁殖成功率(27.0%)和营巢成效(63.2%)均显著低于褐头山雀(54.5%和100%)(P＜0.01).表明大山雀可能采取高产卵数、低存活率的繁殖对策,而褐头山雀的繁殖策略则可能为低产卵数、高存活率.     

营巢类型、巢捕食和窝卵数对高寒草甸雀形目雏鸟生长期的影响

根据1998—2001年高寒草甸10种雀形目鸟类的窝卵数、雏期和巢捕食数据,以Logistic方程拟合雏鸟生长过程,并计算出有关生长率参数;根据营巢类型将10种雀形目鸟划分为开放或半开放类群(GOB)和全封闭穴居类群(HCB)两类,将把雏鸟的生长过程划分为3个生长期(缓增期、快增期和渐增期)。3个生长期占雏期的比例因营巢类型而异,GOB类群快增期>渐增期>缓增期;HCB类群渐增期>快增期>缓增期。分析营巢类型、巢捕食和窝卵数与各生长期之间的关系,结果表明3个生长期的体重积累占离巢时体重的比例因巢型不同而有显著差异;营巢类型和巢捕食显著影响各生长期占雏期的比例和体重积累占离巢时体重的比例;窝卵数影响快增期和渐增期长度,而不影响缓增期长度。快增期体重积累与渐增期的生长率不相关,但与渐增期长度显著相关。因此,前期的能量积累不影响后期生长率,而影响后期生长的长度。该结果进一步印证在晚成鸟中不存在补偿性生长。     

人工巢箱条件下白眉姬鹟的繁殖习性和巢址选择

2005年2月—2006年7月,通过悬挂人工巢箱,对白眉姬鹟(Ficedula zanthopygia)的繁殖习性和巢址选择进行了初步研究。结果表明:2年间,共悬挂人工巢箱226个,其中25个巢箱被白眉姬鹟利用,以小型山雀式巢箱为主(96%),白眉姬鹟对巢大小有选择性;在人工巢箱条件下,白眉姬鹟的窝卵数为(6.00±0.17)枚,卵长径为(17.45±0.07)mm,卵短径为(13.20±0.06)mm,卵重为(1.54±0.02)g,孵化期为12～14d,孵化率为88.76%,育雏期为12～14d,出飞率为96.22%。影响白眉姬鹟巢址选择的主要因素有巢位因子(31.46%)、巢下隐蔽因子(24.67%)、光照因子(15.70%)和食物因子(11.32%)等,其中巢位因子是白眉姬鹟巢址选择中首要考虑的因素;其次是隐蔽性,它可以减少白眉姬鹟被捕食的几率;光照可以提高巢内温度,对于白眉姬鹟的孵化也起到重要作用;食物则保证了繁殖期亲、幼鸟的食物要求。白眉姬鹟的巢材较为广泛,与当地环境密切相关,反映了白眉姬鹟对生境有较强的适应性。     

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%.     

千岛湖栖息地片段化效应对鸟类巢捕食风险的影响

为了解栖息地片段化对鸟类巢捕食风险的影响,我们于2010年4-8月,在千岛湖地区选取16个岛屿,分别在岛屿边缘和内部区域用放置鸡蛋(大型卵)和鹌鹑(Coturnix japonica)蛋(小型卵)的方法进行人工模拟地面巢试验,研究不同体积大小鸟卵的巢捕食率及其差异,分析巢捕食率与岛屿面积、隔离度、形状指数和植物物种丰富...     

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% .     

大山雀对巢箱颜色的识别和繁殖功效

为了确定大山雀对巢箱颜色是否能够识别和对繁殖功效的影响,以利于更好的进行保护,于2007—2010年3—7月,在吉林省左家自然保护区,通过悬挂黑、蓝、绿、白和红色巢箱,对大山雀的入住状况和繁殖参数进行了调查和分析。结果显示:2007、2008、2010年红色巢箱的入住率最高,2009年低于平均值;窝卵数除2010年红色巢箱组略低于其它颜色组平均值外,其它年份略高于其它组,而各年份的出飞数红色组均高于其它组。将其它组的合并均值与红色组进行了方差分析,结果表明,窝卵数之间无显著差异,而出飞数之间则有显著差异(F=17.65,df=1,P=0.04),表明红色组的出飞数高于其他组的平均值。     

Experimental enlargement of nest size does not increase risk of predation or brood parasitism in the Great Reed Warbler Acrocephalus arundinaceus

We assessed whether nest size affects the probability of nest loss using dyads of large and small (large being twice the size of small) inactive Great Reed Warbler Acrocephalus arundinaceus nests placed at similar sites in Great Reed Warbler territories. Large nests were not predated significantly more frequently than small nests. Experimentally enlarged active Great Reed Warbler nests suffered non‐significantly higher predation compared with non‐manipulated control nests. Our experiments did not support the nest‐size hypothesis and suggested that nest size does not appear to be a factor affecting the risk of nest predation in this species. The probability of brood parasitism by the Common Cuckoo Cuculus canorus was also unaffected by experimental nest enlargement, supporting the commonly accepted hypothesis that the Common Cuckoo searches for suitable host nests by host activity during nest building rather than nest size.     

Habitat-specific clutch size and cost of incubation in eiders reconsidered

The energetic incubation constraint hypothesis (EICH) for clutch size states that birds breeding in poor habitat may free up resources for future reproduction by laying a smaller clutch. The eider (Somateria mollissima) is considered a candidate for supporting this hypothesis. Clutch size is smaller in exposed nests, presumably because of faster heat loss and higher incubation cost, and, hence, smaller optimal clutch size. However, an alternative explanation is partial predation: the first egg(s) are left unattended and vulnerable to predation, which may disproportionately affect exposed nests, so clutch size may be underestimated. We experimentally investigated whether predation on first-laid eggs in eiders depends on nest cover. We then re-evaluated how nesting habitat affects clutch size and incubation costs based on long-term data, accounting for confounding effects between habitat and individual quality. We also experimentally assessed adult survival costs of nesting in sheltered nests. The risk of egg predation in experimental nests decreased with cover. Confounding between individual and habitat quality is unlikely, as clutch size was also smaller in open nests within individuals, and early and late breeders had similar nest cover characteristics. A trade-off between clutch and female safety may explain nest cover variation, as the risk of female capture by us, mimicking predation on adults, increased with nest cover. Nest habitat had no effect on female hatching weight or weight loss, while lower temperature during incubation had an unanticipated positive relationship with hatching weight. There were no indications of elevated costs of incubating larger clutches, while clutch size and colony size were positively correlated, a pattern not predicted by the ‘energetic incubation constraint’ hypothesis. Differential partial clutch predation thus offers the more parsimonious explanation for clutch size variation among habitats in eiders, highlighting the need for caution when analysing fecundity and associated life-history parameters when habitat-specific rates of clutch predation occur.     

Winter territoriality in migrant Black Redstarts Phoenicurus ochrurus in the Mediterranean area

The nest predation hypothesis predicts that clutch size should be inversely related to the risk of nest predation. In this paper we analyse data on nest predation, clutch size and fledgling production in 128 Jackdaw nests in order to test if clutches are larger in the safer sites. The predation rate was positively correlated with the minimum nest-entrance dimensions (predation is greater in nests with large entrances). Clutch size was not related to the risk of nest predation, and our data do not therefore support the nest predation hypothesis.     

Nest predation in hole-nesting birds in relation to habitat edge: an experiment

We experimentally tested the hypothesis that nest predation rate in hole-nesting birds, especially the common goldeneye Bucephala clangula , was related to the edge between aquatic and terrestrial habitats We also studied whether nest predation rate was related to habitat patch (lake) size In three study areas nest-boxes were erected in pairs one nest-box was erected at the shoreline and the other one inside the forest at a varying distance (range from 14 to 140 m) from the shoreline One chicken egg was placed in each nest-box (dummy nest) Overall predation rate on dummy nests varied from 34 6% to 52 6% depending on the study area The pine marten Martes manes was the primary nest predator m all study areas Daily predation rates did not differ between natural and dummy nests Predation rate on dummy nests was not related to the distance of the nest-box from the shoreline in any study area Predation rate was not related to lake size in two study areas but in one area predation rate on dummy nests was lower around largest lakes However, the result may be accidental and not because of lake size per se because the proportion of forest was exceptionally low in that part of the study area     

Anti-predator adaptations in nesting Marsh Tits Parus palustris: the role of nest-site security

A proposal that nest predation is the most important selective pressure shaping nest-site use of Marsh Tits Parus palustris was checked in a long-term study (almost 500 nests) carried out in the Białowieża National Park (eastern Poland) in primeval conditions, where the birds breed in natural holes and their nests are at risk from a variety of predators. It was predicted that predation rates would depend on hole attributes, so that Marsh Tits should use the most secure holes. Predation was responsible for 70% of total nest losses. Predation risk depended on hole attributes. Nests in dead wood were predated significantly more often than those in live wood. Nests in old woodpecker holes were predated more frequently than nests in holes of other origin, and nests situated closer to the entrance were more at risk than ones further from it. The entrance size did not influence overall predation risk, but small entrance size was important in preventing access by larger predators. These differences can account for the very rare use of holes in dead wood or of woodpecker holes, the fact that they nest in holes with small entrances and relatively far from the entrance. It is concluded that the patterns of nest-site use found in this species are best explained as anti-predator adaptations, which have evolved and are maintained by the pressure of nest predators. This study also indicates the possible limits of, and constraints on, these adaptations.     

Age-specific nest-site preference and success in eiders

Variation in nest concealment is puzzling given the expected strong selection for safe nest sites. Selecting a concealed nest may decrease the risk of clutch predation but hinder parents from escaping predators, providing a possible solution to this paradox. Because the relative value of current versus future reproduction may vary with breeder age or state, nest concealment may also vary as a function of these attributes. We tested four predictions of the female and clutch safety trade-off hypothesis in eiders (Somateria mollissima): (1) nest concealment is negatively related to escape possibilities, (2) our capture rate of females is higher in covered nests, (3) egg predation is higher in open nests, and (4) overall nest success is unrelated to nest habitat. We also analysed nest microhabitat preferences and nest success relative to breeder age and body condition, controlling for nest spatial centrality. As expected, nest concealment and potential escape angle were negatively related, and capture by us, indicating female predation vulnerability, increased with nest cover. Clutch size was smaller in open nests, suggesting higher partial clutch predation, while it was larger among experienced and good-condition breeders. The probability of successful hatching was unrelated to nest habitat, positively associated with breeder experience, and negatively associated with hatching date. Experienced females selected more concealed and centrally located nests without sacrificing potential escape angles. The age-specific spatial distribution of nests on islands was unrelated to nest initiation dates, indicating no apparent competition. The age-specific preference of eiders for concealed nests may reflect declining reproductive value with age or confidence in surviving despite selecting a concealed nest. The apparently positive relationship between female age and survival and fecundity in eiders refutes the former alternative. Individual improvement in choosing safe nest sites, coupled with differential survival of individuals performing well, most likely explains age-specific nest-site preference and success.     

Fear factor: prey habitat selection and its consequences in a predation risk landscape

Predation risk influences prey use of space. However, little is known about how predation risk influences breeding habitat selection and the fitness consequences of these decisions. The nest sites of central-place foraging predators may spatially anchor predation risk in the landscape. We explored how the spatial dispersion of avian predator nests influenced prey territory location and fitness related measures. We placed 249 nest boxes for migrant pied flycatchers Ficedula hypoleuca , at distances between 10 and 630 m, around seven different sparrowhawk nests Accipiter nisus . After closely monitoring flycatcher nests we found that flycatcher arrival dates, nest box occupation rates and clutch size showed a unimodal relationship with distance from sparrowhawk nests. This relationship suggested an optimal territory location at intermediate distances between 330 and 430 m from sparrowhawk nests. Furthermore, pied flycatcher nestling quantity and quality increased linearly with distance from sparrowhawk nests. These fitness related measures were between 4 and 26% larger in flycatcher nestlings raised far from, relative to those raised nearby, sparrowhawk nests. Our results suggest that breeding sparrowhawk affected both flycatcher habitat selection and reproductive success. We propose that nesting predators create predictable spatial variation in predation risk for both adult prey and possibly their nests, to which prey individuals are able to adaptively respond. Recognising predictable spatial variation in perceived predation risk may be fundamental for a proper understanding of predator-prey interactions and indeed prey species interactions.     

Plasticity of nest-site selection in the trumpeter finch: A comparison between two different habitats

In habitats with more predators, a species is expected to breed in safer sites and be less successful than in predator-impoverished habitats. We tested this hypothesis by studying nest-habitat selection and nest predation in two populations of Trumpeter finch (Bucanetes githagineus). One breeds in a predator-rich habitat (Tabernas, Iberian Peninsula), and the other is found on an island with fewer predators (La Oliva, Canary Islands). In both localities, we studied the features of nests in two different substrates, on the ground and in cliffs, including visibility and position in the cliff. We measured the habitat characteristics in a series of plots around the ground nests and compared them to random points. We also studied the influence of nest features and habitat selection on predation of both nest types. Trumpeter finches built more nests in cliffs in Tabernas, probably because there are more cliffs available there. In this locality, the patches selected for ground nesting had below-average vegetation cover, lower vegetation height, and were on steeper slopes. In La Oliva, they selected above-average vegetation height and steeper slopes. Cliff nests were less predated than ground nests in La Oliva, but not in Tabernas. The only variable that affected survival rates in Tabernas was the height of vegetation around ground nests, with nests in lower vegetation having higher survival rates. These results suggest that locality-related differences in habitat selection by vegetation height could be related to the different predator assemblages present in any given area, though we cannot rule out confounding influences of other differences between the two sites.