南充雉鸡的巢址选择和春夏季栖息地选择

2006年3-6月,采用野外直接观察法和样方法,在四川省南充市太和白鹭自然保护区对雉鸡(Phasianus colchicus)的巢址选择和春夏季栖息地选择进行了研究。通过主成分分析和对比分析,巢址选择研究结果表明:雉鸡的巢都是选择在乔木盖度小、距水距离较近、草本高度和盖度都较大的白茅(Imperata cylindri-cal)干草丛中;影响雉鸡巢址选择的主要因子依次为:坡度、总盖度、乔木平均胸径、乔木盖度、郁闭度、距水距离、距路距离、灌木平均高度、巢周围干草比例、裸地面积、巢上方覆盖物厚、灌木盖度和巢所在草丛宽度等13个因子。春夏季栖息地选择研究结果表明:雉鸡在春夏季倾向于在植被总盖度大、坡度适中、乔木盖度适中、草本盖度和高度较大、灌木盖度较小、灌木高度较大、隐蔽度较大、距路距离较远和郁闭度较大等的生境栖息。     

南充雉鸡的巢址选择和春夏季栖息地选择

2006年3—6月，采用野外直接观察法和样方法，在四川省南充市太和白鹭自然保护区对雉鸡（Phasianus colchicus）的巢址选择和春夏季栖息地选择进行了研究。通过主成分分析和对比分析，巢址选择研究结果表明：雉鸡的巢都是选择在乔木盖度小、距水距离较近、草本高度和盖度都较大的白茅(Imperata cylindrical)干草丛中；影响雉鸡巢址选择的主要因子依次为：坡度、总盖度、乔木平均胸径、乔木盖度、郁闭度、距水距离、距路距离、灌木平均高度、巢周围干草比例、裸地面积、巢上方覆盖物厚、灌木盖度和巢所在草丛宽度等13个因子。春夏季栖息地选择研究结果表明：雉鸡在春夏季倾向于在植被总盖度大、坡度适中、乔木盖度适中、草本盖度和高度较大、灌木盖度较小、灌木高度较大、隐蔽度较大、距路距离较远和郁闭度较大等的生境栖息。     

人工巢箱条件下两种山雀鸟类的同域共存机制

种间竞争会导致鸟类对自身的生存策略进行多方面调整,将多种因素结合起来分析不同鸟类的同域共存机制具有十分重要的意义.2009-2011年的3-7月,在辽宁省东部山区以悬挂人工巢箱的方法招引杂色山雀(Parus varius)和大山雀(Parus major),通过比较这两种鸟类在繁殖时间、繁殖参数和巢址选择上的差异,分析其繁殖期的栖息地选择及繁殖对策,探讨这两种鸟类同域共存的机制.结果表明,生态位的部分分离是大山雀和杂色山雀能够长期共存的基础.两者都是在繁殖期到来立即开始繁殖,均出现两次繁殖高峰,采用消减窝卵数的对策来适应环境质量的下降.对繁殖参数的分析表明,两种鸟类的繁殖对策都为k-选择,但大山雀略偏向r端,大山雀倾向高窝卵数、低繁殖成功率的繁殖策略;杂色山雀倾向低窝卵数、高繁殖成功率的繁殖策略.两种鸟类都选择在林龄较长的森林中筑巢,但是大山雀较注重巢址的安全性能,巢距地面较高,周围乔木密集;杂色山雀较为注重植被类型的选择,巢址多选择在植被多样、灌木生长茂盛的针阔混交林中,推测可能与杂色山雀的食物构成有关.     

新疆阜康地区家麻雀的巢址选择

2013年7月和2014年5~7月,在新疆阜康地区对家麻雀(Passer domesticus)的巢址选择进行调查,以分析影响家麻雀巢址选择的生态因子。在研究区内共找到75个家麻雀的自然巢,筑巢生境为农田和防护林带,均在白杨(Populus adenopoda)林和胡杨(P.euphratica)林中的树上筑巢。其中,繁殖成功巢40个,繁殖失败巢20个,15个巢未记录到繁殖结果。在研究区内的居民房屋、墙洞等没有发现家麻雀的巢。采用逻辑斯蒂回归和主成分分析方法对筑巢地海拔(m)、筑巢树种、筑巢树高(m)、巢距路距离(m)、巢距地面高度(m)、巢上方盖度(%)、筑巢树胸径(m)、最近邻巢的距离(m)这些家麻雀的主要巢址参数进行分析,结果表明,影响新疆阜康地区家麻雀巢址利用的主要因素为巢距地面高度(m)、巢上方盖度(%)和巢距路距离(m)。对家麻雀繁殖成功巢(n=40)和繁殖失败巢(n=20)的巢址参数进行比较,两者差异不显著,因而推测,在研究区域的尺度内,家麻雀的巢址选择并不是影响其繁殖成效的主要因素。     

北京小龙门林场黄眉姬鹟的巢与巢址特征

2003—2006年,在北京小龙门林场共发现黄眉姬鹟(Ficedula narcissina elisae)巢43个。其中34巢筑于天然巢址:开放巢占29.4%,位于树枝间(10巢);洞巢占70.6%,位于树桩顶端凹坑中(10巢)和树洞中(14巢)。开放巢距地高度高于洞巢。黄眉姬鹟的主要营巢树种是棘皮桦(Betula dahurica)。在研究区内共悬挂了100个大洞口巢箱和130个小洞口巢箱,结果发现黄眉姬只利用大洞口巢箱(9巢),不利用小洞口巢箱。以巢为中心,取半径6m的样方测量巢址的植被特征。对海拔、坡向、林冠郁闭度、乔木数量、乔木高、乔木胸径、枯树数量、树桩数量和林下郁闭度等变量进行主成分分析。结果表明,黄眉姬鹟的巢址具有乔木高大、林冠郁闭度高、多枯树和树桩等特征。黄眉姬鹟的繁殖成功率为51.2%,天敌破坏是造成繁殖失败的主要原因。     

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。     

甘肃南部蓝马鸡的巢址选择

蓝马鸡(Crossoptilon auritum)是我国特有的雉类,仅分布在青海东部、东北部,甘肃西北部及南部,四川西北部以及宁夏西部。2007和2008年在甘肃南部林区对蓝马鸡巢址进行了研究。在发现的12个蓝马鸡巢中,4巢(33.3%)在乔木下,4巢(33.3%)在岩石上或者岩洞内,2巢(16.7%)在枯枝下,2巢(16.7%)在灌丛下。U检验和T检验表明,坡位、坡度、灌木高度、灌木数量、灌木盖度、0.5m植被盖度、1.0m植被盖度、2.0m植被盖度、干扰度等9个生态因子在巢址(n=12)与对照样方(n=24)中存在显著差异。对13个变量进行逐步判别分析,结果显示,高坡位、高林下植被盖度及低干扰度是蓝马鸡巢址优先选择的生态因子。     

东北地区北红尾鸲巢址选择及繁殖成效

北红尾鸲(Phoenicurus auroreus)是一种分布广泛的小型雀形目鸟类,主要分布于南亚东北部,东南亚北部、东亚及俄罗斯等地区,我国东北、华北、华中至西南等地也均有分布,是重要的食虫益鸟。为探究北红尾鸲巢址选择的影响因素,找到影响北红尾鸲繁殖成功率的主要巢址因子,于2017年4—7月,在辽宁仙人洞国家级自然保护区开展系统研究。共发现北红尾鸲自然巢44个,其中29巢繁殖成功,15巢繁殖失败。北红尾鸲主要筑巢于石墙缝、空心砖墙缝及废旧电表箱中。巢址参数的主成分分析结果表明:巢口因子(27.738%)、巢位因子(14.195%)、光照因子(12.145%)、人为干扰因子(10.440%)、安全因子(9.266%)和隐蔽因子(7.187%)是影响北红尾鸲巢址选择的重要因子。采用二元逻辑斯蒂回归分析繁殖成功巢与失败巢参数发现,成功巢的巢口最大高度显著小于失败巢(P=0.047),且其距顶的距离更近(P=0.043)。多元线性回归分析表明,巢上方盖度对繁殖成功率有极显著影响(t=2.883,P=0.009)。总的来说,北红尾鸲虽偏爱筑巢于人为干扰较大的村庄房屋附近,但较小的巢口能有效避免巢捕食者的捕食,更近的距顶距离和更大的巢上方盖度能有效降低巢上方的可视程度和降水等不利因素的影响,从而提高繁殖成功率。     

龙凤保护区普通鸬鹚巢特征与巢址选择

巢址选择作为鸟类繁殖的重要环节,是动物生态学关注的热点问题。为探究中等体型湿地鸟类普通鸬鹚的巢址选择偏好及主要影响因子,2019年4—10月运用秩和检验、主成分分析等方法对黑龙江龙凤保护区内普通鸬鹚巢特征、巢址特征、巢址选择进行了分析。结果表明：(1)普通鸬鹚偏好选择巢树乔木相对较矮(P<0.05)、周围灌木相对较矮(P<0.01)、植被盖度较低(P<0.01)、人为干扰距离较远(P<0.01)、距水面距离较远(P<0.05)的区域筑巢;(2)影响普通鸬鹚巢址选择的因子为隐蔽因子(20.634%)、巢稳定因子和干扰因子(27.614%)、植被因子(13.901%)、水因子(5.782%)和巢忠诚度(5.069%)。进一步分析表明：(1)普通鸬鹚倾向选择粗细适中的巢材,巢材来源于优势植被,巢深随纬度增高而增大;(2)巢区植被特征符合普通鸬鹚对能量支配的权衡,巢区粪便对该特征有强化作用。基于上述结果,建议龙凤保护区在巢区内加种高大乔木。     

四川洪雅县赤腹松鼠巢址选择研究

赤腹松鼠Callosciueus erythraeus在四川省洪雅县已经成为第一大森林害鼠.为了揭示赤腹松鼠巢址选择特征并为控制该物种的危害服务,2008年3～8月采取样线法对洪雅县赤腹松鼠的巢址选择状况进行了调查.共发现81棵巢树,对其巢位参数的统计显示,赤腹松鼠可在11种阔叶树和3种针叶树上营巢,对柏木Cpuressus funebris和楠木Phoebe zhennan有明显选择性,分别为营巢树数量的34.6%和33.3%.营巢树平均高度为18.6 m±0.6 m,巢距地面平均高度为16.2 m±0.5 m,巢位置一般靠近树的顶端,多朝东、南和东南方向,76.5%的巢位于树干与树枝的交界处.对无重复取样的巢址样方(n=65)和对照样方(n=65)中15个生境因子的对比分析表明,赤腹松鼠倾向在乔木平均高度较高、林下灌木盖度相对较高、坡度较大的生境中营巢.     

Building a home from foam—túngara frog foam nest architecture and three-phase construction process

Frogs that build foam nests floating on water face the problems of over-dispersion of the secretions used and eggs being dangerously exposed at the foam : air interface. Nest construction behaviour of túngara frogs, Engystomops pustulosus, has features that may circumvent these problems. Pairs build nests in periodic bursts of foam production and egg deposition, three discrete phases being discernible. The first is characterized by a bubble raft without egg deposition and an approximately linear increase in duration of mixing events with time. This phase may reduce initial over-dispersion of foam precursor materials until a critical concentration is achieved. The main building phase is marked by mixing events and start-to-start intervals being nearly constant in duration. During the final phase, mixing events do not change in duration but intervals between them increase in an exponential-like fashion. Pairs joining a colonial nesting abbreviate their initial phase, presumably by exploiting a pioneer pair''s bubble raft, thereby reducing energy and material expenditure, and time exposed to predators. Finally, eggs are deposited only in the centre of nests with a continuously produced, approximately 1 cm deep egg-free cortex that protectively encloses hatched larvae in stranded nests.     

白马雪山自然保护区灰头小鼯鼠的巢址特征

动物的巢为其育幼、避敌和休息等提供了适宜的空间,因此,了解其巢址特征对于物种的保护和管理有着重要的意义。灰头小鼯鼠是一种小型树栖、夜行性哺乳动物,在国内主要分布在中部、南部及西南地区。2012年4月至6月和2012年9月至12月在白马雪山国家级自然保护区对灰头小鼯鼠的巢址特征进行了初步研究。结果表明:灰头小鼯鼠共利用2种巢,在针叶树上,灰头小鼯鼠多利用树枝巢;在阔叶树上,灰头小鼯鼠仅利用树洞巢。巢多紧靠树干(0.2±0.1) m,平均巢高(11.3±0.8) m,巢口无方向偏好。灰头小鼯鼠喜欢选择冠幅更大、通道数更多的树上筑巢,此外,其对郁闭度大,灌木盖度高的生境有明显的选择性。     

Nest predators of woodland open-nesting songbirds in central Europe

I used time-lapse videotaping to identify predators of open songbird nests in fragmented deciduous woodland (nine plots, 2–10 ha each) in the Czech Republic from 2002 to 2006. I documented 22 species of predators at 171 nests of 13 species (mainly Blackcap Sylvia atricapilla , Song Thrush Turdus philomelos , Common Blackbird Turdus merula , Yellowhammer Emberiza citrinella and Chaffinch Fringilla coelebs ). The main predators were Pine Marten Martes martes (37% of 178 predation events), Jay Garrulus glandarius (29%), Buzzard Buteo buteo (7%) and Great Spotted Woodpecker Dendrocopos major (7%); mammals accounted for 48% of total predation. At least 3% of nests were depredated by multiple predators. In spite of their local abundance, Hooded Crows Corvus cornix did not present a serious threat for shrub nesting songbirds (< 1% of total predation). No predation by mice was recorded, suggesting that their importance has been overestimated in artificial nest studies. The proportional species composition of predators depended on which species occupied the monitored nest and location (study plot), but not on the year or the time of season. Corvids and raptors accounted for a relatively larger percentage of total predation of small ('warblers') and large ('thrushes') prey species, respectively, whereas carnivores were important predators of all prey species. Active nests of thrushes were only rarely robbed by Jays (< 4% of 52 events), presumably due to parental nest defence. Predation by woodpeckers was spatially clumped, probably due to individual foraging specialization. Predation by the other major predators was documented on most/all study plots.     

Nesting Success in Crimson Finches: Chance or Choice?

In avian systems, nest predation is one of the most significant influences on reproductive success. Selection for mechanisms and behaviours to minimise predation rates should be favoured. To avoid predation, breeding birds can often deter predators through active nest defence or by modifying behaviours around the nest (e.g. reducing feeding rates and vocalisations). Birds might also benefit from concealing nests or placing them in inaccessible locations. The relative importance of these strategies (behaviour vs. site selection) can be difficult to disentangle and may differ according to life history. Tropical birds are thought to experience higher rates of predation than temperate birds and invest less energy in nest defence. We monitored a population of crimson finches (Neochmia phaeton), in the Australian tropics, over two breeding seasons. We found no relationship between adult nest defence behaviour (towards a model reptile predator) and the likelihood of nest success. However, nest success was strongly related to the visibility of the nest and the structure of the vegetation. We found no evidence that adult nest building decisions were influenced by predation risk; individuals that re‐nested after a predation event did not build their nest in a more concealed location. Therefore, predator avoidance, and hence nest success, appears to be largely due to chance rather than due to the behaviour of the birds or their choice of nesting sites. To escape high predation pressures, multiple nesting attempts both within and between seasons may be necessary to increase reproductive success. Alternatively, birds may be limited in their nest‐site options; that is, high‐quality individuals dominate quality nest sites.     

Long-term familiarity promotes joining in neighbour nest defence

Familiarity plays an important role in the evolution of sociality and cooperation. Familiar individuals may gain a reputation for participating in, or defecting from, cooperative tasks. Previous research suggests that long-term familiarity with territorial neighbours benefits breeders. We tested the hypothesis that great tits (Parus major) are more likely to join in neighbours' nest defence if those neighbours are familiar from the previous year. We show that neighbours that shared a territory boundary the previous year are more likely to join their neighbours' nest defence than neighbours that did not share a boundary before. Closer neighbours did not differ from distant neighbours in their latency to join. For familiar neighbours that joined, there was no difference in call rate in relation to whether one or both members of the focal pair were familiar. First-time breeders (by definition unfamiliar) did not join each other's nest defence. This is the first evidence of a relationship between familiarity and joining in nest defence. Such direct benefits of familiarity may have important implications in the evolution of sociality.     

Nest survival in year‐round breeding tropical red‐capped larks Calandrella cinerea increases with higher nest abundance but decreases with higher invertebrate availability and rainfall

Nest survival is critical to breeding in birds and plays an important role in life‐history evolution and population dynamics. Studies evaluating the proximate factors involved in explaining nest survival and the resulting temporal patterns are biased in favor of temperate regions. Yet, such studies are especially pertinent to the tropics, where nest predation rates are typically high and environmental conditions often allow for year‐round breeding. To tease apart the effects of calendar month and year, population‐level breeding activity and environmental conditions, we studied nest survival over a 64‐month period in equatorial, year‐round breeding red‐capped larks Calandrella cinerea in Kenya. We show that daily nest survival rates varied with time, but not in a predictable seasonal fashion among months or consistently among years. We found negative influences of flying invertebrate biomass and rain on nest survival and higher survival of nests when nests were more abundant, which suggests that nest predation resulted from incidental predation. Although an increase in nest predation is often attributed to an increase in nest predators, we suggest that in our study, it may be caused by altered predator activity resulting from increased activity of the primary prey, invertebrates, rather than activity of the red‐capped larks. Our results emphasize the need to conduct more studies in Afro‐tropical regions because proximate mechanisms explaining nest predation can be different in the unpredictable and highly variable environments of the tropics compared with the relatively predictable seasonal changes found in temperate regions. Such studies will aid in better understanding of the environmental influences on life‐history variation and population dynamics in birds.