潜在洞巢资源差异对次级洞巢鸟及繁殖鸟类群落的影响

为了解次生林中潜在洞巢资源(包括各种啄木鸟的啄洞和人工巢箱)的多寡对次级洞巢鸟集团及繁殖鸟类群落结构的影响, 2007年11月至2008年7月, 我们在吉林省吉林市大岗林场选择洞巢密度不同的样地, 对其次级洞巢鸟及鸟类群落结构进行了比较研究。根据洞巢资源密度我们将9块样地分为3组, 即巢箱区(啄洞密度最低, 悬挂人工巢箱使其潜在洞巢资源总密度大幅提高)、低密度区(啄洞密度较低, 无巢箱)和高密度区(啄洞密度较高, 无巢箱), 调查了3组样地内鸟类的组成和密度、潜在洞巢资源的利用情况等。3组样地中均调查到4种初级洞巢鸟, 其种类组成略有不同; 4种次级洞巢鸟在3组样地广泛分布, 分别为白眉姬鹟(Ficedula zanthopygia)、大山雀(Parus major)、沼泽山雀(P. palustris)和普通鳾(Sitta europaea)。巢箱区和高密度区的次级洞巢鸟总密度显著高于低密度区。巢箱区同高密度区一样, 大山雀和白眉姬鹟的密度显著高于低密度区, 这是由于大山雀和白眉姬鹟是人工巢箱的主要利用鸟种, 而沼泽山雀和普通鳾的密度在三组样地间差异不显著。初级洞巢鸟总密度与啄洞密度、次级洞巢鸟总密度与潜在洞巢资源总密度都呈显著正相关关系。潜在洞巢资源丰富的样地中鸟类群落多样性指数显著高于潜在洞巢资源贫乏样地中的鸟类群落多样性指数, 人为增加洞巢资源可以改变鸟类群落组成并显著提高群落的多样性指数。三组样地中鸟类群落的均匀性、丰富度指数和种间相遇率没有显著差异, 群落相似性指数也相近。高密度区和低密度区鸟类群落集团结构相似。次级洞巢鸟密度的增加短时期内未对群落内其他主要鸟种的密度产生显著影响。研究结果显示, 初级洞巢鸟的密度决定了啄洞的丰富程度, 而洞巢资源的差异会对次级洞巢鸟集团的分布模式产生影响, 进而影响整个繁殖鸟类群落的结构。     

人工巢箱对次级洞巢鸟类多样性及繁殖鸟类群落稳定性的作用

人工巢箱在鸟类研究与保护中的使用越来越广泛, 但是人工巢箱对鸟类群落的影响并不清楚, 人工巢箱在鸟类群落保护过程中所扮演的角色仍然值得商榷。我们于2007年3–8月, 在北京门头沟区小龙门国家森林公园选择两块海拔及植被情况相似的样地, 一块悬挂50个人工巢箱, 另一块作为对照。我们调查了巢箱利用情况、巢箱内鸟类的繁殖情况及两样地的植被群落和鸟类群落。50个巢箱中有20个分别被褐头山雀(Parus songarus)、白眉姬鹟(Ficedula zanthopygia)、普通鳾(Sitta europaea)及大山雀(Parus major)占用。通过比较分析得知, 人工巢箱使实验样地白眉姬鹟的种群密度显著增加, 使实验样地次级洞巢鸟类群落的多样性指数(H’)和群落种间相遇率(PIE)显著高于对照样地, 而优势度指数(λ)显著低于对照样地。同时, 繁殖鸟类群落的相应指数也呈现出相同变化。这种变化更多地应该归因于人工巢箱的调节作用。通过这次研究, 我们认为人工巢箱影响了一部分次级洞巢鸟的分布模式, 并通过影响鸟类多度影响了次级洞巢鸟的多样性, 增加了一部分利用巢箱鸟类的种群密度, 进而使得实验样地繁殖鸟类多样性增加, 个体数量差异降低, 而群落均匀性增加。巢箱的悬挂对次生林鸟类群落保护产生了积极的影响。     

不同纬度洞巢鸟类对人工巢箱的利用及差异

迄今对洞巢鸟类生活史特征的纬度变异（特别是热带洞巢鸟类的繁殖）了解还十分有限。我们于2018年3至8月,分别在海南吊罗山（热带）、河南董寨（亚热带）和河北塞罕坝（温带）的林缘地带,悬挂相同规格的人工巢箱招引洞巢鸟类繁殖,用以比较不同地理区域的洞巢鸟类对人工巢箱的利用情况及其孵化成效和繁殖成功率。野外共悬挂577个木制巢箱,3个研究地的利用率在海南吊罗山为最低（32.6%）,河南董寨最高（92.0%）。3个地点均有大山雀（Parus cinereus）入住（占总巢数的84.3%）,其孵化成效和繁殖成功率在3个地点不存在显著差异（P > 0.05）。但在河北塞罕坝,大山雀的孵化成效（75.7%）和繁殖成功率（65.7%）显著低于同域繁殖的褐头山雀（Poecile montanus）（97.7% 和97.7%）和煤山雀（Periparus ater）（93.5%和90.3%）（P < 0.05）。研究表明,3个地理区域利用巢箱繁殖的洞巢鸟的种类、数量以及对巢箱的利用率均存在差异,但对于广布种大山雀来说,地理位置的差异并不影响其孵化成效和繁殖成功率。     

次级洞巢鸟对次生林天然树洞的利用

1996年 3～ 7月对吉林省左家自然保护区次生阔叶混交林中的 5种次级洞巢鸟的巢位选择进行了研究 ,所涉及的 5种次级洞巢鸟为大山雀 (Parusmajor)、沼泽山雀 (Paruspalustris)、普通 (Sittaeuropacea)、白眉姬 (Ficedulazanthopygia)、灰椋鸟 (Sturnuscineraceus)。研究表明 :5种次级洞巢鸟在位巢选择中 ,对洞口横径、洞口纵径、洞内径、洞深和洞口方向的选择具有共性。利用的洞口 ,方向在 180°～ 2 2 5°和 315°～ 36 0°分布最少 ;而未利用的洞口 ,方向在这 2个区间的分布恰好相反。利用和未利用的巢洞特征因子差异显著。人为堵塞后又打开的巢洞会迅速被再利用 ,结果说明次生林中天然树洞资源成为次级洞巢鸟巢位选择的限制因子。     

利用天然树洞繁殖的五种鸟的巢位特征及繁殖成功率

对吉林省左家自然保护区次生阔叶林中的大山雀 ( Parusmajor)、沼泽山雀 ( Paruspalustris)、普通跓( Sitta europacea)、白眉姬? ( Ficedula zanthopygia)和灰椋鸟 ( Sturnus cineraceus) 5种利用天然树洞繁殖的次级洞巢鸟进行了巢位选择和繁殖成功率研究。本研究中共发现 1 41巢。五种鸟对树洞类型的选择存在种间差异 ,普通跓不利用裂洞 ,沼泽山雀不利用啄洞 ,其它 3种鸟对 3种洞均有利用 ,但有一定的倾向性。对 5种鸟 9个巢位变量的比较中 ,只有洞口方向差异不显著 ( p >0 .0 5 ) ,其它 8个变量均差异显著 ( p<0 .0 5 ) ,该结果说明 5种次级洞巢鸟对巢位的选择具有其各自的需求。洞口横径、洞口纵径、洞处树直径、洞内径、巢距地高是巢位选择重要变量 ,它们决定不同种类对树洞的利用。巢损失多数出现在产卵之前和孵化阶段 ,44个繁殖失败的巢中有 35个在这两个阶段损失。大山雀的巢成功率最低 ,灰椋鸟的巢成功率最高。 5种鸟的孵化率都超过 90 %。人为破坏和动物捕食是繁殖失败的主要原因 ,占总数的 61 .4%。洞巢鸟巢位选择中的重要变量影响繁殖成功。普通跓繁殖是否成功受洞口横径和巢高影响 ,沼泽山雀受洞口纵径、树胸径和洞内径影响 ,大山雀受洞口横径、巢高和洞内径影响 ,灰椋鸟受洞内径和洞深影     

祁连山东段高原鼢鼠洞道土壤微生物和土壤酶

高原鼢鼠繁杂的洞道系统对高寒草甸土壤的理化性质有着重要影响。本研究采集高原鼢鼠活动洞道土壤样本,并以无鼢鼠扰动的同深度土层土壤作为对照。对比分析了2个处理土壤微生物（细菌、真菌、放线菌）、土壤酶（脲酶、蔗糖酶、碱性磷酸酶）活性以及土壤全氮、有机质、速效磷含量的差异。结果表明：高原鼢鼠洞道土壤速效磷和全氮的含量均高于对照,其中春季和秋季的速效磷达到显著水平（P<0.05）;秋季无鼢鼠扰动的土壤有机质和真菌的含量显著高于洞道土壤（P<0.05）;3种酶活性各处理间无显著差异（P>0.05）;对照区春季土壤的细菌和秋季真菌的含量显著高于洞道土壤（P<0.05）;洞道和对照区土壤的细菌、放线菌、速效磷、全氮和有机质的含量均在夏季达到最大值,各种指标其它月份差异不显著（P>0.05）。基于以上结果,本研究发现高原鼢鼠活动洞道土壤微生物和土壤酶与对照区土壤无显著差异（P>0.05）。     

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。     

人工巢箱条件下杂色山雀的巢位选择及其对繁殖成功率的影响

杂色山雀(Parus varius)是一种分布区域极其狭窄的小型森林洞巢鸟类,种群数量稀少,在中国大陆仅见繁殖于辽宁省的东南部山区和毗邻辽宁的吉林省西南部山区,为当地留鸟.为了探讨巢址选择对杂色山雀繁殖的影响,找出影响杂色山雀繁殖成功率的巢址选择方面的主要因子,于2009-2011年3-7月,在辽宁省仙人洞国家级自然保护区通过悬挂人工巢箱,进行杂色山雀对人工巢箱的巢址选择以及不同的巢址对杂色山雀繁殖成功率的影响研究.研究表明:杂色山雀多在针阔混交林中活动和繁殖,对位于赤松与蒙古栎混交林中的巢箱有一定偏好.野外共发现24巢杂色山雀在人工巢箱中繁殖,其中15巢繁殖成功,9巢繁殖失败.对杂色山雀利用的巢址样方主成分分析表明,巢位因子( 19.826％)、乔木因子(17.571％)、灌木因子(13.11％)、光照因子(11.587％)、隐蔽因子(10.562％)和边缘效应因子(7.572％)是影响杂色山雀对人工巢箱选择的重要因子.利用巢箱与对照巢箱相比,两者在距水源距离、距路距离、乔木平均高度、灌木平均高度和植被类型这5个环境变量上存在显著差异.繁殖成功巢与繁殖失败巢相比,繁殖成功的巢箱所在位置距路稍远,坡度较高,乔木最大高度较高,灌木盖度略低于繁殖失败巢箱.人为干扰和天敌捕食是造成杂色山雀繁殖失败的主要原因.以上研究结果表明,巢向偏南、距地面2 m以上、周围乔木高大、灌木平均高度大于1.5m、盖度在45％-55％之间、距水源20 m左右、距路20 m以外的位于针阔混交林边缘的巢箱是杂色山雀繁殖的最优巢址.目前杂色山雀的种群数量还很稀少,希望本研究能对这一珍稀鸟类的保护提供重要参考.     

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。     

普通鳾的巢位选择和繁殖成功巢特征

普通对巢位具有选择性,利用树种共7种,利用率不同,利用树洞类型有两种,啄洞利用率高,结洞低。洞口朝向在西至西偏北45°方向的树洞利用率最低,其它方向差异不大。洞口处树的直径、洞口纵径、洞内径、洞深和洞周围10m范围,树的密度5个巢位变量在利用和未利用树洞之间差异极显著(P<001),洞口横径,洞口处树干与垂直方向夹角和洞口方向90°角10m范围树的密度差异显著(P<005),其余变量差异不显著(P>005)。23巢平均窝卵数778±095,孵化率8994%,出飞率9627%。30个巢中成功巢和失败巢的11个巢位特征比较发现,洞高和洞口方向90°角10m范围内树的密度差异极显著,洞口纵径和洞口横径差异显著,其余变量差异不显著。     

Nest boxes for Cape Parrots Poicephalus robustus in the Hogsback area,Eastern Cape,South Africa

Breeding propensity of tree-cavity nesting bird species are often limited by a shortage of natural nesting sites. Artificial nests can be used to provide alternative nest sites. Cape Parrots Poicephalus robustus are nationally endangered and nest in existing tree-cavities in high-altitude fragmented Afromontane forests in South Africa, assumed to be in short supply due to historic and current logging practices. To increase nest site availability, 179 wooden bird boxes and 28 bee boxes (to ‘pull’ bees) were erected during 2011–2012 in Hogsback, Eastern Cape. In 2016, no bird boxes were occupied by Cape Parrots. A total of 43% were used by other species, 51% were unused and 6% could not be inspected due to tree instability and inaccessibility. Two bird boxes were inspected by two pairs of Cape Parrots, but were never occupied. Occupancy of boxes by birds was not associated with nest, tree or habitat characteristics. However, occupancy of boxes by bees was associated with habitat type and tree species. Future conservation efforts will include locating natural Cape Parrot nesting sites and reforestation efforts to ensure the long-term availability of natural nesting sites.     

Specific nest box designs can improve habitat restoration for cavity‐dependent arboreal mammals

Tree‐cavity‐dependent wildlife faces future shortages of cavities due to a decline in the abundance of large, old trees in many parts of the world. Nest boxes are proposed as a tool to restore habitat value but evidence of their effectiveness for arboreal mammals remains equivocal. This may arise from a poor understanding of design preferences. We conducted investigations in two landscapes in eastern Australia to determine whether species show a preference for specific designs. We observed a preference by some mammal species for particular designs (33–78% occupied/used), suggesting that design refinement can improve the frequency with which nest boxes are used. Although feral species may out‐compete target species for nest boxes, we did not observe this. We recorded feral honeybees (Apis mellifera) in 6–9% of nest boxes but they did not remain, and many occupied boxes were later used by mammals. The introduced common myna bird (Acridotheres tristis) was prevalent in one landscape, but competition for nest boxes was localized. For nest boxes to be an effective habitat restoration tool, they must be able to be occupied over long periods of time. We investigated this for the squirrel glider (Petaurus norfolcensis), an arboreal marsupial threatened through part of its geographic range. Squirrel gliders occupied and bred within nest boxes (100% used) at two locations continuously over a 10‐year period with minimal nest box maintenance. Individuals occupied boxes for up to 7 years. This confirms that targeted nest box programs can be an effective restoration tool for cavity‐dependent arboreal mammals.     

Avian conservation practices strengthen ecosystem services in California vineyards

Insectivorous Western Bluebirds (Sialia mexicana) occupy vineyard nest boxes established by California winegrape growers who want to encourage avian conservation. Experimentally, the provision of available nest sites serves as an alternative to exclosure methods for isolating the potential ecosystem services provided by foraging birds. We compared the abundance and species richness of avian foragers and removal rates of sentinel prey in treatments with songbird nest boxes and controls without nest boxes. The average species richness of avian insectivores increased by over 50 percent compared to controls. Insectivorous bird density nearly quadrupled, primarily due to a tenfold increase in Western Bluebird abundance. In contrast, there was no significant difference in the abundance of omnivorous or granivorous bird species some of which opportunistically forage on grapes. In a sentinel prey experiment, 2.4 times more live beet armyworms (Spodoptera exigua) were removed in the nest box treatment than in the control. As an estimate of the maximum foraging services provided by insectivorous birds, we found that larval removal rates measured immediately below occupied boxes averaged 3.5 times greater than in the control. Consequently the presence of Western Bluebirds in vineyard nest boxes strengthened ecosystem services to winegrape growers, illustrating a benefit of agroecological conservation practices. Predator addition and sentinel prey experiments lack some disadvantages of predator exclusion experiments and were robust methodologies for detecting ecosystem services.     

Ousting of the Common Redstart (Aves: Turdidae: Phoenicurus phoenicurus) from its nests by the bumblebee Bombus niveatus vorticosus (Hymenoptera: Apidae)

During a study of bird nesting in SW. Anatolia, 125 man-made nest boxes have been installed, 3 m high, in the trees. These nest boxes have been occupied by several bird species (Phoenicurus phoenicurus, Parus major, Parus ater, Sitta krueperi, Certhia brachydactyla). Of the 48 Redstart nests, 19 (40 %) had been successfully invaded by the bumblebee Bombus niveatus vorticosus. This invasion occurred at different times in the nest building cycle: - during the building of the nest, - during the incubation or - after the hatching of the young. Once installed in the nest of the Redstart, the bumblebee does not directly attack the bird, but disturbs it by continuously rearranging the nesting material and by covering the bird’s brood. Eventually, the bird deserts its nest and brood. The Redstart does not display any agonistic behaviour towards the bumblebee. Nests of other bird species are never invaded.     

Avian Nest Box Selection and Nest Success in Burned and Unburned Southwestern Riparian Forest

ABSTRACT Riparian forest communities in the southwestern United States were historically structured by a disturbance regime of annual flooding. In recent decades, however, frequency of flooding has decreased and frequency of wildfires has increased. Riparian forests provide important breeding habitat for a large variety of bird species, and the effects of this altered disturbance regime on birds and their breeding habitat is largely unknown. To evaluate effects of high-intensity spring and summer wildfire on the quality of breeding bird habitat in the Middle Rio Grande valley, we measured vegetation structure and composition, avian nest use, and nest success at 4 unburned plots and 4 wildfire plots over a 3-year period. We measured avian nest use and success at nest boxes located in unburned riparian forest plots and plots recently burned by wildfire. Recent wildfire plots (<7 yr after fire) had a much different vegetation structure than unburned plots; an older (>7 yr after fire) wildfire plot more closely resembled its paired unburned plot than did recently burned plots. Ash-throated flycatchers (Myiarchus cinerascens) and Bewick's wrens (Thryomanes bewickii; hereafter, flycatchers and wrens, respectively) used nest boxes in most of the plots. A model selection procedure applied to logistic regressions showed that frequency of nest box use by flycatchers was positively associated with wildfire, although flycatchers used boxes in unburned plots as well. Wrens showed a preferential use of nest boxes that were in unburned sites and in close proximity to vegetative cover. Growth rates, feeding rates, and fledging mass of flycatchers were similar in wildfire and unburned plots. Growth rates for wrens were slower in wildfire plots, while feeding rates and fledging mass were similar. Nest predation varied between years, was higher for flycatchers than for wrens, and was not directly influenced by wildfire. Model selection showed that predation increased with grass cover, an indicator of forest openness, and decreased with distance to habitat edge. Recovery of dense vegetation appears important in maintaining populations of Bewick's wrens, whereas ash-throated flycatchers were less sensitive to vegetative structure and composition of postfire succession. Postfire management that maintains nest sites in large forest strips would enhance nesting density and success of these cavity-nesting birds in riparian zones.     

Nest Mosquito Trap quantifies contact rates between nesting birds and mosquitoes

Accurate estimates of host-vector contact rates are required for precise determination of arbovirus transmission intensity. We designed and tested a novel mosquito collection device, the Nest Mosquito Trap (NMT), to collect mosquitoes as they attempt to feed on unrestrained nesting birds in artificial nest boxes. In the laboratory, the NMT collected nearly one-third of the mosquitoes introduced to the nest boxes. We then used these laboratory data to estimate our capture efficiency of field-collected bird-seeking mosquitoes collected over 66 trap nights. We estimated that 7.5 mosquitoes per trap night attempted to feed on nesting birds in artificial nest boxes. Presence of the NMT did not have a negative effect on avian nest success when compared to occupied nest boxes that were not sampled with the trap. Future studies using the NMT may elucidate the role of nestlings in arbovirus transmission and further refine estimates of nesting bird and vector contact rates.     

Do nest boxes in restored woodlands promote the conservation of hollow‐dependent fauna?

Vegetation restoration is considered as an important strategy for reversing biodiversity decline in agricultural areas. However, revegetated areas often lack key vegetation attributes like large old hollow‐bearing trees. As these trees take a long time to develop, artificial cavities such as nest boxes are sometimes provided to address lag effects. We conducted a 3‐year experiment using 150 nest boxes with 4 designs to quantify patterns of occupancy within 16 replanted areas and 14 patches of remnant old‐growth eucalypt woodland. We quantified patterns of occupancy of nest boxes in physically connected versus isolated remnants and plantings, and multiple covariate effects on nest box occupancy at the nest box, tree, patch, and landscape levels. Our analyses revealed a lower probability of nest box occupancy within remnants (vs. plantings) for 2 of the 6 response variables examined: any species and the Feral Honeybee. Nest boxes in connected remnants and plantings were more likely to be occupied than those in isolated plantings and remnants by any mammal and the Common Brushtail Possum. Nest boxes in restored woodlands are used by some hollow‐dependent fauna but principally already common species and not taxa of conservation concern. Nest boxes were also used by pest species. A key management consideration must be to create connected habitat to facilitate colonization of nest boxes by mammals. Approximately 15% of the cavity‐dependent vertebrates within the study area used next boxes, possibly because the diverse requirements of the array of other species were not met by the range of nest boxes deployed.     

Nest quality limits the number of hole-nesting passerines in their natural cavity-rich habitat

We experimentally tested whether the lack of high-quality nest holes may limit the number of secondary cavity-nesters in cavity-rich habitats. We mapped and measured natural tree-holes in 10 mature aspen forests in Estonia. In five experimental plots, we provided nest-boxes on trees having suitable cavities for hole-nesting passerines. This improved the quality of available cavities but retained their total number (due to territoriality, sites in the same tree could not be occupied simultaneously) and location on the landscape. In the next breeding season, the density of hole-nesting passerines increased in experimental plots but remained at the same level in control plots. The increase was due to the species that used boxes: Parus major that preferred these over natural cavities, and Ficedula hypoleuca that used both nest types more opportunistically. We concluded that the quality of cavities can influence the numbers of hole-nesting birds in old cavity-rich forests, also; probably, adaptive habitat selection is the proximate mechanism in this case.     

Ability to assess nest predation risk in secondary hole-nesting birds: an experimental study

Because nest predation is the major source of nesting mortality in birds, site-specific predation risk may play an important role in determining birds' ability to select nest sites that reduce predation risk. This possibility has not been adequately tested. Here we report on 5-year experiments by which we studied, independently from birds' earlier experience with specific nest boxes, both the selection and predation risk of nest sites in the common goldeneye (Bucephala clangula). New, previously unoccupied nest boxes were erected in two habitat types on three study areas. Experimentally measured predation risk in the nest boxes varied between 0 and 1.0, i.e. goldeneye females could select a nest site along a wide gradient of possible predation-risk values. We did not find a difference in predation risk between occupied and unoccupied nest boxes, nor was the order of nest box occupation associated with predation risk. A power analysis revealed that our test had reasonably high power to reject a false null hypothesis. Our results suggest that common goldeneye females likely have not evolved an ability to assess predation risk of new, previously unoccupied nest sites.