北京高校喜鹊巢址选择的主要生态因素

根据从2003～2005年每年一次关于北京近20所高校校园喜鹊（Pica pica sericea）巢址的分布情况的调查,对影响高校校园喜鹊巢址选择的因素进行了分析,结果表明营巢树因素（营巢树的高度、胸径、巢位高度、巢上方的植被盖度）和环境因素（嘈杂度和食物的丰富程度）都会影响喜鹊对巢址的选择。研究结果对如何进行校园绿地的规划以及鸟类保护具有一定的指导作用。     

新疆北部白冠攀雀的巢与巢址选择

2008年4—7月,在新疆北部对白冠攀雀巢址选择进行了研究。白冠攀雀的营巢习性特殊,巢呈囊袋状,结构甚为精致。对于白冠攀雀巢的研究,采用总面积调查法,进行地毯式的搜寻,并结合标图法对其进行标记,绘制分布图。研究结果共发现巢125个,营巢位于于临近湖泊、河流等水域附近的柳树、杨树、桦树等阔叶树上。营巢树种以柳树为主,占68.80%。巢的高度平均为(5.3±2.5)m,营巢于乔木的中下部（约1/3处）,约70%的巢离河边不足30 m。对于巢址选择的研究,将原始记录中与巢址选择有关的特征变量进行主成分分析,分析表明,影响白冠攀雀巢址选择的主要因素有4种,依次为：郁闭度因素（包括营巢树胸径、巢上郁闭度）、营巢树种因素(包括营巢树种、树高、巢位高度和乔木种类)、方位因素（包括距河边距离和巢向）、食物与巢材因素。     

芜湖市及附近地区三种鹭鸟巢址特征

2005年,对芜湖市及附近地区4个营巢地的3种主要营巢鹭鸟--白鹭(Egretta garzetta)、夜鹭(Nycticorax nycticorax)和池鹭(Ardeola bacchus)的巢址特征进行了抽样调查,选取了11个巢址变量,即营巢树种、巢高、巢树高、巢上方郁闭度、巢周围1m半径内植被郁闭度、巢树胸径、巢离树干距离、巢下最大支撑枝直径、巢离巢区边缘的距离、坡位、巢位海拔,运用单因素方差分析和主成分分析方法研究3种鹭乌的巢址特征.结果表明,巢位因子、巢树因子、保护因子、坡位因子等4个主成分描述了3种鹭鸟的巢址特征,其贡献率分别为25.51%、24.42%、13.19%和12.32%.影响鹭鸟巢址选择的最主要因素是微栖息地适合度和巢捕食压力.     

陇东地区金翅雀的巢址选择

为探究金翅雀(Chloris sinica)营巢是否偏好某些树种以及偏好原因,于2017—2019年4—8月,在陇东学院校园内,开展了金翅雀巢址选择调查。180个金翅雀巢址分析显示:金翅雀营巢利用圆柏(Juniperus chinensis)、刺柏(Juniperus formosana)、侧柏(Platycladus orientalis)、日本晚樱(Cerasus serrulata)等17种乔木,其中圆柏(χ2=13.6,df=1,P=0.000)和刺柏(χ2=9.8,df=1,P=0.002)是金翅雀选择的主要树种;与其他巢址比较,圆柏和刺柏巢址的巢树树冠直径(DNTC)、巢-缘距(DEC)和巢树-最近树距离(DT)显著小于其他树种巢址的相应参数,而圆柏和刺柏巢址的巢树树冠高度(HNTC)、巢-冠底距离(DBC)、巢树-草地距离(DM)、可利用林木数量(NT)和隐蔽度(CC)都显著大于其他树种巢址的相应参数(T或Mann-Whiteny U检验,全部P0.05);差异显著的8个巢址参数(DNTC、DEC、DT、HNTC、DBC、DM、NT和CC)的因子分析表明,环境隐蔽性、巢位隐蔽性和巢位不易接近性是导致金翅雀偏好在圆柏和刺柏上营巢的主要因素。本研究结果可为城市环境绿化中如何保护鸟类提供参考。     

哈尔滨市区灰喜鹊巢址选择研究

2010年6月至9月在哈尔滨市园林科学研究所实验基地采用样方法对灰喜鹊的巢址选择特征进行研究,并且利用主成分分析法对灰喜鹊巢址样方生境因子进行检验.结果表明,灰喜鹊主要选择针叶树筑巢;在同一生境中巢间距变化小,呈均匀分布;灰喜鹊巢址选择的主要因子包括营巢树高、距最近巢距离、样方内树均高、巢树胸径、距干扰源距离、距最近树距离.这说明灰喜鹊在巢址选择过程中选择巢树和其周围的小生境.     

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.     

荒漠伯劳巢址选择和繁殖成功

2011年5～7月对甘肃安西极旱荒漠国家级自然保护区(N40°21'～40°22',E96°13'～96°14',海拔1 306 m)荒漠伯劳(Lanius isabellinus)巢址选择和繁殖成功进行研究。调查了58巢的巢址因子,巢主要位于营巢树主枝上,巢距地面高度多为2.0～2.5 m。主成分分析结果表明,巢距地面高度、营巢树高度、营巢树胸径和营巢处树干直径是影响荒漠伯劳巢址选择的主要因素,这也是荒漠伯劳适应繁殖地大风天气的结果。既调查巢址数据又明确繁殖情况的49个巢中,红柳(Tamarix ramosissima)(5棵)上巢的繁殖成功率明显高于沙枣(Elaeagnus angusifolia)(43棵)和胡杨(Populus euphratica)(1棵)上的巢,原因可能是红柳郁闭度大。已知窝卵数和繁殖情况的30个巢中,窝卵数分别为2(1巢)、4(7巢)、5(18巢)、6(4巢)。卡方检验结果表明,窝卵数和繁殖成功率之间差异不显著(χ2=3.921,df=3,P0.05)。发现的63个巢中跟踪监测了54个巢(包括调查巢址数据的和未调查巢址数据的)的繁殖情况,54巢中37巢繁殖成功,成功率为68.52%。所有繁殖失败的巢均为产卵阶段或育雏早期阶段由于同类的破坏而导致繁殖失败,繁殖失败巢的数量随着相邻最近巢的距离的增加而减少,因而,繁殖失败可能与种群密度以及种内竞争有关。     

人造园林中斑文鸟和白腰文鸟的巢址选择

巢址选择对保证鸟类生存和繁殖成功、降低被捕食率和种间竞争至关重要。2016—2017年,在中国科学院西双版纳热带植物园选取3个研究区域对同域分布的斑文鸟Lonchura punctulata和白腰文鸟Lonchura striata进行调查。在记录的15个巢址特征因子中,14个数值型因子用于拟合Logistic回归模型,找出影响文鸟巢址选择的关键因子;使用独立样本t检验和Mann-Whitney U检验比较2种文鸟在巢址特征因子选择上的差异性;置换检验(Permutation test)用于检验2种文鸟对营巢树种选择偏好的差异性。研究发现,2种文鸟的巢址分布模式在3个研究区域中的差异很大。异种鸟巢间最小间距、营巢树胸径、营巢树与水源最近距离以及巢位高度都是影响巢址选择的关键因子。与白腰文鸟相比,斑文鸟通常选择在胸径更小、位置更高、距离异种鸟巢更远、距离水源更近的地方营巢。斑文鸟多选择枝条紧密的树,而白腰文鸟多选择枝干带刺的树营巢,这可能是二者不同的对抗捕食者的防御策略。     

四川南充农田区乌鸫的巢址选择

2007年3～5月在四川省南充市近郊农田区域对乌鸫Turdus merula sowerbyi的巢址选择进行了研究.共调查57个巢址样方,通过主成分分析(PCA)提取到影响乌鸫巢址选择的6个主要因子,其累积贡献率达74.44%, 其中乔木因子的贡献率最高,达26.58%.农田区中,乌鸫在4月中旬开始营巢,营巢树平均高度为16.02±2.29 m,主要巢树种类是白杨.     

盐城滨海海堤林中黑尾蜡嘴雀和黑卷尾的巢址选择与生态位

繁殖期鸟类的巢址选择受到很多因素的影响。许多雀形目鸟类选择在树上营巢,但开阔的沿海地区通常缺乏成片的自然林地,人工种植的廊道状海堤林则成为多种雀形目鸟类的营巢地。2018年4-8月在江苏省大丰麋鹿国家级自然保护区境内的海堤林中,对繁殖鸟类巢的分布及两种优势繁殖鸟类---黑尾蜡嘴雀(Eophona migratoria)和黑卷尾(Dicrurus macrocercus)的巢址选择进行了研究,分析了两种鸟类的生态位重叠情况。结果表明:海堤林生境中共发现10种繁殖鸟的127个巢,鸟巢多数位于5 m以上的空间;影响黑尾蜡嘴雀巢址选择的主要因素是巢树和灌木等,巢位置、乔木和安全等因素是次要因素(前5主分量累计贡献率为71.9%);影响黑卷尾巢址选择的主要是巢树因素和灌木因素,巢向、乔木因子是次要因素(前5主分量累计贡献率78.0%);在巢址生态位分化上:两种鸟类的巢向(Utest,Z=-3.013,P<0.01)、巢高(Utest,Z=-6.718,P<0.01)、巢位置(Utest,Z=-5.402,P<0.01)、隐蔽性(Utest,Z=-4.081,P<0.01)选择上存在极显著的差异,两者在这些因子存在生态位分化;两种鸟类在12个巢址因子选择上的生态位重叠值都较大(最小值为0.500,最大值为0.998),存在激烈的种间竞争;在滨海地区,海堤林是依赖树木筑巢繁殖鸟类的重要栖息地,需要加强保护与管理。     

Decaying trees improve nesting opportunities for cavity‐nesting birds in temperate and boreal forests: A meta‐analysis and implications for retention forestry

Many studies have dealt with the habitat requirements of cavity‐nesting birds, but there is no meta‐analysis on the subject and individual study results remain vague or contradictory. We conducted a meta‐analysis to increase the available evidence for nest‐site selection of cavity‐nesting birds. Literature was searched in Web of Science and Google Scholar and included studies that provide data on the habitat requirements of cavity‐nesting birds in temperate and boreal forests of varying naturalness. To compare nest and non‐nest‐tree characteristics, the following data were collected from the literature: diameter at breast height (DBH) and its standard deviation (SD), sample size of trees with and without active nest, amount of nest and available trees described as dead or with a broken crown, and amount of nest and available trees that were lacking these characteristics. Further collected data included bird species nesting in the cavities and nest‐building type (nonexcavator/excavator), forest type (coniferous/deciduous/mixed), biome (temperate/boreal), and naturalness (managed/natural). From these data, three effect sizes were calculated that describe potential nest trees in terms of DBH, vital status (dead/alive), and crown status (broken/intact). These tree characteristics can be easily recognized by foresters. The results show that on average large‐diameter trees, dead trees, and trees with broken crowns were selected for nesting. The magnitude of this effect varied depending primarily on bird species and the explanatory variables forest type and naturalness. Biome had lowest influence (indicated by ΔAIC). We conclude that diameter at breast height, vitality, and crown status can be used as tree characteristics for the selection of trees that should be retained in selectively harvested forests.     

Nest‐site selection by Slender‐billed Parakeets in a Chilean agricultural‐forest mosaic

ABSTRACT Species in the family Psittacidae may be particularly vulnerable to anthropogenic habitat transformations that reduce availability of suitable breeding sites at different spatial scales. In southern Chile, loss of native forest cover due to agricultural conversion may impact populations of Slender‐billed Parakeets (Enicognathus leptorhynchus), endemic secondary cavity‐nesting psittacids. Our objective was to assess nest‐site selection by Slender‐billed Parakeets in an agricultural‐forest mosaic of southern Chile at two spatial scales: nest trees and the habitat surrounding those trees. During the 2008–2009 breeding seasons, we identified nest sites (N= 31) by observing parakeet behavior and using information provided by local residents. Most (29/31) nests were in mature Nothofagus obliqua trees. By comparing trees used for nesting with randomly selected, unused trees, we found that the probability of a tree being selected as a nest site was positively related to the number of cavity entrances, less dead crown, and more basal injuries (e.g., fire scars). At the nesting‐habitat scale, nest site selection was positively associated with the extent of basal injuries and number of cavity entrances in trees within 50 m of nest trees. These variables are likely important because they allow nesting parakeets to minimize cavity search times in potential nesting areas, thereby reducing energetic demands and potential exposure to predators. Slender‐billed Parakeets may thus use a hierarchical process to select nest sites; after a habitat patch is chosen, parakeets may then inspect individual trees in search of a suitable nest site. Effective strategies to ensure persistence of Slender‐billed Parakeets in agricultural‐forest mosaics should include preservation of both individual and groups of scattered mature trees.     

Nesting preferences of common buzzard Buteo buteo and goshawk Accipiter gentilis in forest stands of different structure (Niepolomice Forest, Southern Poland)

Studies on nesting preferences of common buzzard and goshawk were carried out in two distinctly different parts of the Niepolomice Forest (S Poland): deciduous (oak-hornbeam wood) and coniferous. Characteristics of nest sites were determined on three spatial scales, separately for: (1) nest tree; (2) nest tree area (0.07 ha circle centred at nest tree) and (3) nest stand (15 ha circle centred at nest tree). Nesting preferences discovered for the nest tree and its surroundings, included height and diameter of trees, age of the forest stand, distance to the nearest open area or forest road and occurrence of open areas in the vicinity of the nest. In the diverse habitat of oak-hornbeam wood, more similar to natural woods, nest site selection operated on several levels, possibly starting at the most extensive end of the scale before narrowing to the selection of a particular nest tree. In the more homogeneous habitat of commercially exploited coniferous forest, the surrounding of the nest were found to be insignificant, and the nesting decisions were likely to be based principally on individual characteristics of a tree i.e. its shape and size, being suitable for nesting.     

斑翅山鹑巢址选择的研究

１９９１－１９９３年在山西宁武县对斑翅山鹑的巢址选择进行了研究,野外工作中共发现６０个巢,其中绝大多数位于远离林地的农田或灌丝地带,６６．６７％的巢位于向阳的东南坡和西南坡上,对巢址与随机选取的非巢样点所进行的对比分析发现,在１２个栖地参数中,影响巢址选择的５个因素依次为：落叶的数量、地缘宽度、干草的数量、灌丛宽度和梯田高度,判别分析的结果表明,落叶的数量和干草的数量是区别巢址与非巢样点的两个最重     

Managing ecological traps: Logging and sapsucker nest predation by bears

We tested the equal preference ecological trap hypothesis for breeding yellow-bellied sapsuckers (Sphyrapicus varius) along a time-since-harvest gradient (1–5 yr, 16–20 yr, 21–25 yr, and >60 yr) in selection system-logged hardwood forests in Algonquin Provincial Park, Ontario. Yellow-bellied sapsuckers preferred 1–5 year and >60-year-old cuts equally and more than 16–20 year and 21–25-year-old cuts. More-abundant arthropod food and/or higher-quality sap resources may have attracted yellow-bellied sapsuckers to 1–5 year and >60-year-old cuts. Only 52% of pairs raised fledglings in 1- to 5-year-old cuts during years when nest predation by American black bears (Ursus americanus) was common, the incidence of which was negatively related to increased availability of American beech (Fagus grandifolia) nuts from the previous autumn. By contrast, 88% of pairs raised fledglings in all years in >60-year-old cuts. One- to 5-year-old cuts were demographic sinks that represent equal-preference ecological traps in years when nest predation by bears was common, whereas >60-year-old cuts were always demographic sources. High-quality habitat cues for nesting yellow-bellied sapsuckers appear to be retained for 1–5 years after selection system logging but fail to deliver safe nest sites. Cavities excavated in heart-rot-infected nest trees are least likely to be depredated because cavity walls are typically harder and deter entry by depredating bears. Retaining more potential nest trees per ha at harvest (especially American beech with heart-rot) may increase the proportion of sapsucker nests that are excavated in bear-resistant trees, thereby reducing nest predation and increasing fecundity. © 2012 The Wildlife Society.     

A description of nesting behaviors,including factors impacting nest site selection,in black‐and‐white ruffed lemurs (Varecia variegata)

Nest site selection is at once fundamental to reproduction and a poorly understood component of many organisms’ reproductive investment. This study investigates the nesting behaviors of black‐and‐white ruffed lemurs, Varecia variegata, a litter‐bearing primate from the southeastern rainforests of Madagascar. Using a combination of behavioral, geospatial, and demographic data, I test the hypotheses that environmental and social cues influence nest site selection and that these decisions ultimately impact maternal reproductive success. Gestating females built multiple large nests throughout their territories. Of these, females used only a fraction of the originally constructed nests, as well as several parking locations as infants aged. Nest construction was best predicted by environmental cues, including the size of the nesting tree and density of feeding trees within a 75 m radius of the nest, whereas nest use depended largely on the size and average distance to feeding trees within that same area. Microhabitat characteristics were unrelated to whether females built or used nests. Although unrelated to nest site selection, social cues, specifically the average distance to conspecifics’ nest and park sites, were related to maternal reproductive success; mothers whose litters were parked in closer proximity to others’ nests experienced higher infant survival than those whose nests were more isolated. This is likely because nesting proximity facilitated communal crèche use by neighboring females. Together, these results suggest a complex pattern of nesting behaviors that involves females strategically building nests in areas with high potential resource abundance, using nests in areas according to their realized productivity, and communally rearing infants within a network of nests distributed throughout the larger communal territory.     

Nest site selection and patterns of nest re-use in the Hooded Crow Corvus cornix

Capsule: Hooded Crows Corvus cornix selected nesting trees based on species, height, grouping and distance from an occupied house. Nest re-use was common and pairs that re-used old nests produced more fledglings than those that built a new nest.

Aims: To determine the features of trees that influenced whether they were used by Hooded Crows as nest sites, to establish what factors influenced nest re-use between years and to explore potential costs or benefits of nest re-use.

Methods: In a large area of Orkney, Scotland, the features of trees that contained a Hooded Crow nest were compared to those of trees where nests were absent. Patterns of nest re-use between years were examined in relation to the availability of alternative sites, previous nesting success and the number of equivalent options to the tree used previously within 200?m of this site.

Results: Hooded Crows favoured spruce and pine trees as nest sites, above the most locally abundant tree species, elder and willow. Preference for trees increased with tree height, local tree density and distance from occupied houses. Over half of the crows studied re-used an old nest when one was available and crows that re-used an old nest fledged more offspring than those that built a new nest. The likelihood of a new nest being built increased as the number of potential locations to build increased. Territories where a nest survived the winter were more likely to be reoccupied the following year than those where nests fell, while territories with fewer trees around the old site were most likely to be abandoned, suggesting that those were territories of lower quality.

Conclusions: Hooded Crows displayed strong preferences for nest sites that might favour nesting success by offering concealment, shelter and protection from ground-based predators. Nest re-use was common, especially when alternative sites were scarce, and appeared to facilitate greater reproductive output.     

Social and Thermal Cues Influence Nest‐site Selection in a Nocturnal Gecko,Oedura lesueurii

In oviparous species lacking parental care, successful reproduction depends on females selecting nest sites that facilitate embryonic development. Such sites may be limited in the environment, which can lead to multiple females using the same nest site simultaneously. However, there are several alternative explanations for communal nesting, including natal homing, predator satiation, and adaptive benefits to offspring. We used laboratory experiments to evaluate three hypotheses about nest‐site selection in velvet geckos (Oedura lesueurii), which often nest communally. We investigated whether the trend to nest communally is influenced by the following: (1) evidence of previous nesting (hatched eggshells); (2) body size; and/or (3) thermal regimes. When given the choice, females laid their eggs in shelters containing hatched eggshells rather than in empty shelters, and this was not influenced by body size. Females selected nest sites that were cooler than their own mean selected body temperatures, suggesting that thermal requirements of their developing embryos could outweigh their own thermoregulatory preferences. Field observations of natal homing and high predation rates on gravid females suggest that imprinting on nest sites and/or predator swamping also play roles in communal nesting. Collectively, our results suggest that female velvet geckos use multiple cues to select appropriate nest sites, and hence that multiple mechanisms result in communal nesting behavior in this species.