沙漠石蜂的筑巢材料和蜂巢结构

沙漠石蜂Megachile(Chalicodoma) desertorum Morawitz为多种植物的传粉昆虫,在西鄂尔多斯地区是多种濒危植物和荒漠建群植物的重要传粉者。在该地区研究沙漠石蜂的筑巢场所、筑巢材料和蜂巢结构。共调查统计5148个蜂巢的筑巢场所和朝向;选择4个土壤表层成分不同的筑巢地,分别测定其筑巢沙土的机械组成、pH值和土壤紧实度;定点连续观察整个筑巢过程。结果表明:沙漠石蜂95.80%的巢建于岩石表面;土墙、灌木枝条、水泥柱及钢窗框上的巢室数均较少。83.1%的巢室建在东向一面;南向14.2%,西向2.4%,北向仅0.3%;筑巢材料为沙土和唾液制成的泥浆,所用沙土的pH值在8.18～9.34之间、紧实度在1.28～1.84g/cm3之间,其中粒径为0.06～0.15mm的沙土比例最高;1个蜂巢一般由4～10个巢室组成。说明该蜂喜欢将巢室建在朝向东方的岩石表面;筑巢材料主要由唾液和以碱性的粒径为0.06～0.15mm左右的沙土构成。也说明是对干旱炎热的荒漠环境的适应。     

巨型褶翅小蜂的生活史和产卵行为

巨型褶翅小蜂Leucospis gigas Fabricius是小蜂总科中体型最大的物种之一,对野生传粉蜜蜂中的一些种类为害很大。在西鄂尔多斯地区首次发现其寄生当地多种植物的重要传粉昆虫沙漠石蜂Megachile(Chalicodoma)desertorum Cockerell后,对其在当地的生活史、成蜂的活动规律、寄主范围以及产卵行为进行了研究。结果表明:巨型褶翅小蜂在西鄂尔多斯地区1年发生1代,当地没有雄性个体,营孤雌生殖。雌蜂寿命30d左右,每年的6月中旬为成蜂活动高峰期。在当地只发现其寄生沙漠石蜂的老熟幼虫,其产卵行为分为3个阶段,即寻找寄主巢室、选择产卵位点与产卵、拉出产卵针。     

双斑切叶蜂的筑巢习性

【目的】明确双斑切叶蜂Megachile leachella在沙地上的筑巢环境及筑巢特点,旨在当地利用人工巢管诱引其筑巢。【方法】采用目测和拍照等方法对双斑切叶蜂的整个筑巢过程进行了连续观察; 采用挖掘、测量方法对双斑切叶蜂巢内结构进行了观测;在室内对蜂茧在土中和指形管中的羽化情况进行了初步观测。【结果】双斑切叶蜂一般在废弃的泥墙或者沙地上蚂蚁等废弃的巢穴中筑巢,有时候它也在沙地上挖掘新巢筑巢。双斑切叶蜂用叶片构建巢室,一巢多室,各巢室首尾相接排列在巢中,筑完巢后用叶片将巢口封住。双斑切叶蜂构建一个巢室需要切取11～14片叶子,为每巢室采集蜂粮6～9次,每巢室内产卵1粒;在内蒙古毛乌素沙地,该蜂一年2代,第1代在6月中下旬羽化,第2代大约在7月下旬至8月上旬羽化,主要寄生性天敌有尖腹蜂Coelioxy sp.、青蜂Chrysis sp.。双斑切叶蜂能在指形管中羽化。【结论】双斑切叶蜂不同个体之间的筑巢行为相似,雌蜂可以用人工巢管进行诱集和驯化。     

海切叶蜂的筑巢和访花行为

【目的】研究毛乌素沙地重要野生传粉昆虫海切叶蜂Megachile maritima的筑巢和访花行为对保护其栖息环境具有重要意义。【方法】采用目测及拍照等方法对海切叶蜂的整个筑巢过程进行了连续观测;以2 m×2 m 样方的方式观测海切叶蜂的访花频率、单花停留时间及日活动规律等访花行为,其中日活动规律每天连续观测,共观测7天。【结果】海切叶蜂在沙土中筑巢,每巢只有一个巢室,其筑巢过程为：寻找合适的筑巢地点,挖巢,构建巢室,采集蜂粮,产卵,封住巢室,筑完一个巢。它连续筑完一个巢大约需要9 h。海切叶蜂构建一个巢室需要切取26～29片叶子,为每巢室采集蜂粮11～12次,每巢室内产卵1粒;在塔落岩黄芪和细叶益母草上的平均访花频率分别为（13.23±6.49）朵/min和（16.72±4.84）朵/min,平均单花停留时间分别为（3.08±2.48）s和（2.49±1.31）s。晴天,海切叶蜂在12:00～14:00期间活动较活跃。【结论】海切叶蜂不同个体之间的筑巢行为相似。该蜂在塔落岩黄芪和细叶益母草上的访花过程、访花频率及单花停留时间具有显著的差异。     

沙漠石蜂的生物学特性

沙漠石蜂Megachile(Chalicodoma)desertorumMorawitz的成虫活动期与西鄂尔多斯地区多种植物的开花物候相适应,是多种荒漠植物(其中包括一些珍稀濒危植物)的重要传粉昆虫。该文报道了沙漠石蜂除成虫外各虫态的形态特征、生活史及幼虫和成虫的行为等生物学特性。该蜂在西鄂尔多斯地区1年发生1代。越冬成虫翌年4月中旬开始出巢活动;雄蜂早于雌蜂9 d左右出现,完成交尾后数日死亡,雄蜂出巢后寿命20 d左右,雌蜂约35 d。卵期约12 d。幼虫期85 d左右,老熟幼虫多数在6月中旬结茧,7月末开始化蛹,蛹期约18 d。成蜂于8月中旬陆续羽化,羽化后的成虫很快进入滞育状态,并在茧内越冬;滞育期长达235 d。     

赤足木蜂的形态和筑巢行为

【目的】研究绒木蜂亚属赤足木蜂Xylocopa rufipes Smith的形态特征和筑巢行为,为进一步保护和管理木蜂资源提供理论依据。【方法】采用网捕法采集赤足木蜂成虫;采用目测、拍照等方法记录赤足木蜂在不同地区的筑巢场所和筑巢基质;用游标卡尺测量赤足木蜂的形态指标和巢室结构指标;采用破坏巢室法和野外巢口观察法测定赤足木蜂的巢内行为。【结果】赤足木蜂雌雄形态区别明显。雌蜂后足胫节胫基板的二叉状分支是其所属的绒木蜂亚属区别其他木蜂的主要特征。赤足木蜂筑巢场所为旧房屋的木桁梁、临时木棚架的木梁或柴火堆,筑巢基质主要为干枯的杉木、泡桐和杨木等。巢建筑有不分枝型和分枝型两种类型,分别占26.09%和73.91%。巢口近圆形,从巢口向内挖掘的主隧道相对于木材纹理呈现一定弧度的夹角(锐角);每巢有1~10个分支隧道,每个分支隧道内巢室数为1~8个,平均3.63±2.08个。巢室长度为10.66±21.98 mm,平均为15.37±0.22 mm;巢室直径为9.79±14.40 mm,平均为12.33±1.08 mm;巢室隔板厚度为1.87±8.31 mm,平均为5.09±0.13 mm。解剖巢室法观察到每个巢内居住着0~6头繁殖后代的雌蜂(n=13巢),平均2.08±1.61头。观察雌蜂进出巢口的数量,发现每个巢室内居住有1~5头繁殖雌蜂(n=23巢),平均2.48±1.24头。【结论】同一种群的赤足木蜂具有独栖性到社会性生活的社会多态性。     

凹纹胡蜂与黑尾胡蜂蛋白氨基酸分析研究

为弄清胡蜂蛋白氨基酸(特别是人体必需氨基酸)的组成,探索利用胡蜂作食品,作者对凹纹胡蜂Vespa velutina auraria Smith与黑尾胡蜂Vespa tropica ducalisSmith成虫、蛹、幼虫、巢室、巢壳的氨基酸成分和含量进行了分析,结果报道如下:     

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%。     

长木蜂的筑巢和采粉贮粮行为

【目的】通过研究长木蜂Xylocopa tranquebarorum筑巢和贮粮行为, 为进一步查明独栖性蜂类行为特点、开发新的蜂类资源提供依据。【方法】采用目测和拍照等方法对长木蜂的整个筑巢过程进行了连续观察, 用游标卡尺对巢口大小进行测量, 采用室内解剖巢室对长木蜂贮蜂粮的大小和数量进行观测。【结果】长木蜂主要在竹子上筑巢, 偶尔也发现在芦苇上筑巢。最喜欢选择竹节直径1.2～2.5 cm的孝顺竹Bambusa multiplex和刚竹属 Phyllostachys的竹种上筑巢。其筑巢过程为：雌蜂寻找合适的筑巢地点, 咬巢口, 清理巢室, 采集花粉蜜制作蜂粮, 在蜂粮上产卵, 制作巢室隔板。筑巢地点主要位于离旧巢1 m以内的位置。雌蜂啃咬巢口平均用时（292±29）min, 制作一块蜂粮需采集粉蜜22～40次, 采集粉蜜平均用时（17.31±0.52）min/次, 携粉蜜回巢滞留时间平均为（16.45±1.08）min/次;巢中卸落粉蜜平均用时为（15.29±1.03）min/次, 一生贮蜂粮平均6块左右;蜂粮近长方形, 长12～18 mm, 宽6～10 mm, 平均重量（0.7140±0.0269）g。【结论】长木蜂雌蜂不同个体之间筑巢行为相似, 而采集粉蜜的次数和贮蜂粮所用时间均有显著差异。     

中国南部狭腹胡蜂的生物学与地理分布(膜翅目：胡蜂总科)

1989-1991年与日本京都大学合作,对我国南部狭腹胡蜂区系、生态、行为学等方面进行了研究。本文主要报道狭腹胡蜂的生物学与地理分布。研究结果表明狭腹胡蜂的栖息和巢室建筑分野外和住宅两种环境。密侧狭腹胡蜂Parischnogaster mellyi(Sau.)的蜂巢密度在30-100m²之间的住户内,平均为8.25巢,最高“巢,最低为2巢。巢室材料分植物纤维和土两类。在东径99‘15'一104°98',北纬20°06'-22°55'之间范围内,除分布在海拔1000m以上类群外,一年四季都可进行活动,无越冬现象。分布范围最北限止于贵州东北部。     

Old nests are cues for suitable breeding sites in the Eurasian penduline tit Remiz pendulinus

Nest-sites often have a major influence on avian reproductive success. The use of reliable cues that assist nest-site selection should thus be favoured by natural selection. The old nests have been known to serve as a cue in nest-site selection in several species. To find out whether the old nests act as cue in nest-site selection in the Eurasian penduline tit Remiz pendulinus , we carried out two experiments in southern Hungary, where the penduline tits breed around fishponds and build sophisticated pendulous nests on tree branches that often hang over water. In April 2006, we choose 20 groups of two nearby trees, and hung an old nest on one of the trees in each group. The male penduline tits choose 12 of these groups to build a new nest, and every of the twelve nests were built on trees with an old nest. This suggests that the old nests serve as a cue in the selection of breeding sites for males when they enter a habitat. To find out whether the old nests are cues of plentiful nest building material, or to signal high quality breeding areas, we carried out a second experiment in 2007 by selecting 13 groups of three nearby trees. A "worn-out" old nest was hung on one of the trees, a "re-utilize" type of old nest on another tree, whereas the third tree was left without an old nest in each group. The rationale was that while the worn-out material of the old nests is of no use in building the new nests, material of the "re-utilize" nests is good enough to be used for building new nests. Males built a new nest in 10 of the 13 groups, and eight of the new nests were built on trees with an old nest. Of the eight new nests, five were built on trees with a "worn-out" old nest and three on trees with a "re-utilize" type of old nest. It appears that for the penduline tit males it is the presence of an existing old nest and not the quality of the old nest material that serves as cue during the selection of the suitable breeding sites.     

Competition, predation and nest niche shifts among tropical cavity nesters: ecological evidence

I studied cavity-nesting birds in an undisturbed site in lowland Peru to determine the relative roles of competition and predation in favoring termitarium nesting over tree cavity nesting. Occupancy rates of both nest boxes and natural tree cavities near 2% suggest that competition for tree cavities is not favoring the use of termitaria. Artificial nests and bird nests in termitaria suffer significantly lower predation rates than similar nests in old tree cavities showing that predation is favoring the use of termitaria over old tree cavities. Bird nests in newly excavated tree cavities also show lower predation rates than older cavities suggesting that cavity age is more important than substrate (tree or termitaria) per se . This study suggests that nest predation has a greater influence than nest competition on life history evolution for many cavity-nesting birds.     

Flea burden and its influence on nest selection and use in Dryomys nitedula Pallas, 1778

Since dormice usually use natural tree hollows or artificial nest boxes as nest sites and these nests are reused from 1 year to another, the present study investigated how the parasite loads from old nests affected the behaviour of the forest dormouse Dryomys nitedula Pallas, 1778. Dormice were subjected to three different experiments: 1. They were given the choice of a nest box infected with ectoparasites and a new unused nest box; 2. Dormice were given the choice of a treated (uninfected) previously used nest boxes and previously used nest box that was infected; and 3. Using infrared motion sensor cameras, we tested weather they preferred to avoid nest boxes when only infected nests were available. The results revealed that the females with pups are pickier when choosing the nursery site. These preferred empty nest boxes or nest boxes with treated nests instead of the infested ones. However, non-breeding adults and sub-adults showed indifference to the flea infestation of the nest.     

Nest-dismantling behavior of yellow-bellied prinia in mainland and island populations

Nest-dismantling behavior in birds is considered a fitness-maximizing adaptive behavior. Here, we compared nest-dismantling behavior and associated predation rates and nest characteristics in yellow-bellied prinia (Prinia flaviventris) on mainland China and the island of Taiwan during the breeding season from 2010 to 2014. Our results indicated that the proportion of individuals showing nest-dismantling behavior was higher on the island than on the mainland (29.3 vs. 0.8%). Nest-dismantling behavior was most frequent at the peak of the breeding season and mainly involved removing the upper halves of the nests and reusing the materials to construct new nests. The time taken to dismantle old nests and use the materials to build new ones was shorter than the time needed to build completely new nests. Nest predation, fidelity to the nest site, distance between old and new nests, and the costs of searching for nest materials could influence nest-dismantling behavior. Our results suggested that saving time and energy searching for new nest materials was the primary motivation behind nest-dismantling behavior in yellow-bellied prinia.     

Individual variation in nest size and nest site features of the Bornean orangutans (Pongo pygmaeus)

Nest construction is a daily habit of independent orangutans for sleeping or resting. Data on their nests have been used in various ecological studies (e.g., density estimation, ranging behavior, evolution of material culture) because they are the most observable field signs. We investigated nest size and nest site features of Bornean orangutans in the wild during 10 months' fieldwork at three sites in East Kalimantan, Indonesia: Kutai National Park, Birawa, and Meratus. To examine individual variation, we followed 31 individual orangutans and recorded the 92 nests they made for nest size (diameter) and nest site features (height of nest above ground, tree species used for the nest site, the diameter and height of the tree, whether the nest was new or reused, and nest location within the tree). Analyses taking age–sex classes of the focal individuals into consideration showed significant age–sex differences in nest size and location, but not in nest height or nest tree features (diameter, height of tree, and height of lowest branch). Mature orangutans (adult females, unflanged and flanged males) made larger nests than immatures (juveniles and adolescents). Flanged male orangutans with larger nests used stable locations for nesting sites and reused old nests more frequently than immatures. The overall proportion of nests in open (exposed) locations was higher than in closed (sheltered) locations. Flanged males and immatures frequently made open nests, whereas adult females with an infant preferred closed locations. The good correspondence between nest size and age–sex classes indicates that nest size variation may reflect body size and therefore age–sex variation in the population. Am. J. Primatol. 71:393–399, 2009. © 2009 Wiley‐Liss, Inc.     

Do Fleas,and/or Old Nest Material,Influence Nest-site preference in Hole-nesting Passerines?

This study examined nest-site choice in a migratory population of pied flycatchers (Ficedula hypoleuca) and sympatric populations of three resident tit species (Parus major, P. caeruleus and P. palustris) in central Sweden. All four species are secondary-cavity nesters which naturally breed in pre-formed tree cavities but readily use artificial nest boxes. We asked whether flycatchers and tits discriminate between nest boxes that: 1. Are ‘empty’; 2. Contain old nests without ectoparasites (fleas Ceratophyllus sp.); or 3. Contain old nests with ectoparasites. We found that pied flycatchers preferred nest boxes containing old nests, regardless of whether these nests held parasites. In contrast, tits did not discriminate between the three types of boxes. Tits may pay a cost for their lack of choosiness: after the breeding season, tit nests contained more fleas than flycatcher nests. Nevertheless, parasites did not affect the choice of a nest site in any of the species studied. We suggest that the migratory flycatchers are in a hurry to start breeding upon arrival and use the presence of an old nest as a shortcut cue to assess nest-site quality. Also, they may save valuable time by copying the choice of previous breeders. Non-migratory tits may have more time to inspect nest sites, but do not seem to use the same cues in nest-site selection as the pied flycatcher.     

Repeatability of nest predation in passerines depends on predator species and time scale

It has been proposed that some specific locations of bird's nests have higher intrinsic chances of being depredated than other locations. This predicts that fates of consecutive nesting attempts at the same site should be repeatable. We used 20 pairs of old thrush nests to simulate repeated nesting attempts at the same sites, both within and between breeding seasons (n=40  sites×2  trials×2  years=160). Each nest was monitored by a camera to record multiple predation events and to identify predators. Predation by all predator species was repeatable during a 15-day trial. Predation by principal predators (jay Garrulus glandarius , marten Martes martes / foina ) and total predation (all species combined) was not correlated within pairs of simultaneously exposed nests or within samples of nests from particular study plot, and not repeatable for individual nests between-trials or between-years. These findings suggest short-term effect of predator memory causing revisitation of previously depredated nests during a current nesting trial (all predators); do not support an effect of nest site features on multiple nest discoveries and/or an effect of nest location on repeated random encounters with the same nest (principal predators). Long-term repeatability and correlation within pairs of simultaneously exposed nests was detectable only in occasional predators (great spotted woodpecker Dendrocopos major , possibly also squirrel Sciurus vulgaris ), which suggests effect of nest location combined with site fidelity and individual foraging specialization of these predators. We conclude that repeatability of nest predation depends on the time scale considered and the local predator community. We caution against spurious findings of repeatable nest predation resulting simply from statistical properties of correlation in binary data (nest fates).     

Nest site selection and predation driven despotic distribution of breeding long-eared owls Asio otus

Long-eared owls Asio otus do not build their own nests. They occupy old corvid nests in either coniferous or deciduous trees. In my study area owls favoured coniferous over deciduous trees for nesting and occupied nest sites in that order. Comparing overall breeding output, I found no difference between the two kinds of nest sites, but among early nests there was a higher proportion of unsuccessful nests in deciduous trees. This difference was due to differences in predation rate, indicating that the owls' pattern of nest site occupation followed predictions from the ideal despotic distribution model. I also show that, due to a seasonal change in habitat quality, predator driven despotism, although present, can be well masked and hence difficult to detect.     

Ants move to improve: colonies of Leptothorax albipennis emigrate whenever they find a superior nest site

A high-quality home can be a major factor determining fitness. However, when house hunting becomes necessary, animals might often face a speed-versus-accuracy trade-off and therefore be unable to survey their environment extensively for the optimum site. We found that the ant Leptothorax albipennis was able to correct errors made in such a hurried decision by continuing to survey even after a colony had settled in a nest site. Colonies moved from intact undisturbed nests to another nest site whenever the new nest site presented a sufficient improvement in nest quality. Thus, scout ants must be able to judge and compare the quality of the new, empty nest site with the one currently inhabited by the colony. Emigrations from intact nests were initiated by high numbers of ants recruited by tandem runs. This evidence may explain how a small number of scouts can motivate an entire colony to move when there is no immediate need to do so. Compared with their behaviour in emigrations from destroyed nests, the ants favoured even more strongly accuracy over speed, because they waited for a larger number of scouts to agree on one site before starting the emigration. They could do this without increased risk because the rest of the colony remained safely in the old nest.     

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.