首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   775篇
  免费   62篇
  国内免费   50篇
  2023年   4篇
  2022年   1篇
  2021年   14篇
  2020年   16篇
  2019年   20篇
  2018年   12篇
  2017年   18篇
  2016年   37篇
  2015年   40篇
  2014年   33篇
  2013年   51篇
  2012年   28篇
  2011年   47篇
  2010年   25篇
  2009年   48篇
  2008年   47篇
  2007年   51篇
  2006年   48篇
  2005年   32篇
  2004年   40篇
  2003年   21篇
  2002年   27篇
  2001年   28篇
  2000年   18篇
  1999年   29篇
  1998年   15篇
  1997年   16篇
  1996年   11篇
  1995年   7篇
  1994年   15篇
  1993年   12篇
  1992年   13篇
  1991年   6篇
  1990年   7篇
  1989年   5篇
  1988年   7篇
  1986年   8篇
  1985年   6篇
  1984年   8篇
  1983年   1篇
  1982年   7篇
  1981年   3篇
  1980年   2篇
  1979年   1篇
  1978年   2篇
排序方式: 共有887条查询结果,搜索用时 34 毫秒
21.
Two new species are added to the rare pompilid genus Abernessia Arlé. Abernessia capixaba sp. n. and A. giga sp. n. are described and illustrated. This is the first record of the genus from the states of Espírito Santo and Minas Gerais, Brazil. The genus now contains four species. A brief discussion of generic characters, illustrations, and a key to the known species of Abernessia are provided.  相似文献   
22.
The genera Odontacolus Kieffer and Cyphacolus Priesner are among the most distinctive platygastroid wasps because of their laterally compressed metasomal horn; however, their generic status has remained unclear. We present a morphological phylogenetic analysis comprising all 38 Old World and four Neotropical Odontacolus species and 13 Cyphacolus species, which demonstrates that the latter is monophyletic but nested within a somewhat poorly resolved Odontacolus. Based on these results Cyphacolus syn. n. is placed as a junior synonym of Odontacolus which is here redefined. The taxonomy of Old World Odontacolus s.str. is revised; the previously known species Odontacolus longiceps Kieffer (Seychelles), Odontacolus markadicus Veenakumari (India), Odontacolus spinosus (Dodd) (Australia) and Odontacolus hackeri (Dodd) (Australia) are re-described, and 32 new species are described: Odontacolus africanus Valerio & Austin sp. n. (Congo, Guinea, Kenya, Madagascar, Mozambique, South Africa, Uganda, Zimbabwe), Odontacolus aldrovandii Valerio & Austin sp. n. (Nepal), Odontacolus anningae Valerio & Austin sp. n. (Cameroon), Odontacolus australiensis Valerio & Austin sp. n. (Australia), Odontacolus baeri Valerio & Austin sp. n. (Australia), Odontacolus berryae Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus bosei Valerio & Austin sp. n. (India, Malaysia, Sri Lanka), Odontacolus cardaleae Valerio & Austin sp. n. (Australia), Odontacolus darwini Valerio & Austin sp. n. (Thailand), Odontacolus dayi Valerio & Austin sp. n. (Indonesia), Odontacolus gallowayi Valerio & Austin sp. n. (Australia), Odontacolus gentingensis Valerio & Austin sp. n. (Malaysia), Odontacolus guineensis Valerio & Austin sp. n. (Guinea), Odontacolus harveyi Valerio & Austin sp. n. (Australia), Odontacolus heratyi Valerio & Austin sp. n. (Fiji), Odontacolus heydoni Valerio & Austin sp. n. (Malaysia, Thailand), Odontacolus irwini Valerio & Austin sp. n. (Fiji), Odontacolus jacksonae Valerio & Austin sp. n. (Cameroon, Guinea, Madagascar), Odontacolus kiau Valerio & Austin sp. n. (Papua New Guinea), Odontacolus lamarcki Valerio & Austin sp. n. (Thailand), Odontacolus madagascarensis Valerio & Austin sp. n. (Madagascar), Odontacolus mayri Valerio & Austin sp. n. (Indonesia, Thailand), Odontacolus mot Valerio & Austin sp. n. (India), Odontacolus noyesi Valerio & Austin sp. n. (India, Indonesia), Odontacolus pintoi Valerio & Austin sp. n. (Australia, New Zealand, Norfolk Island), Odontacolus schlingeri Valerio & Austin sp. n. (Fiji), Odontacolus sharkeyi Valerio & Austin sp. n. (Thailand), Odontacolus veroae Valerio & Austin sp. n. (Fiji), Odontacolus wallacei Valerio & Austin sp. n. (Australia, Indonesia, Malawi, Papua New Guinea), Odontacolus whitfieldi Valerio & Austin sp. n. (China, India, Indonesia, Sulawesi, Malaysia, Thailand, Vietnam), Odontacolus zborowskii Valerio & Austin sp. n. (Australia), and Odontacolus zimi Valerio & Austin sp. n. (Madagascar). In addition, all species of Cyphacolus are here transferred to Odontacolus: Odontacolus asheri (Valerio, Masner & Austin) comb. n. (Sri Lanka), Odontacolus axfordi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus bhowaliensis (Mani & Mukerjee) comb. n. (India), Odontacolus bouceki (Austin & Iqbal) comb. n. (Australia), Odontacolus copelandi (Valerio, Masner & Austin) comb. n. (Kenya, Nigeria, Zimbabwe, Thailand), Odontacolus diazae (Valerio, Masner & Austin) comb. n. (Kenya), Odontacolus harteni (Valerio, Masner & Austin) comb. n. (Yemen, Ivory Coast, Paskistan), Odontacolus jenningsi (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus leblanci (Valerio, Masner & Austin) comb. n. (Guinea), Odontacolus lucianae (Valerio, Masner & Austin) comb. n. (Ivory Coast, Madagascar, South Africa, Swaziland, Zimbabwe), Odontacolus normani (Valerio, Masner & Austin) comb. n. (India, United Arab Emirates), Odontacolus sallyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tessae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus tullyae (Valerio, Masner & Austin) comb. n. (Australia), Odontacolus veniprivus (Priesner) comb. n. (Egypt), and Odontacolus watshami (Valerio, Masner & Austin) comb. n. (Africa, Madagascar). Two species of Odontacolus are transferred to the genus Idris Förster: Idris longispinosus (Girault) comb. n. and Idris amoenus (Kononova) comb. n., and Odontacolus doddi Austin syn. n. is placed as a junior synonym of Odontacolus spinosus (Dodd). Odontacolus markadicus, previously only known from India, is here recorded from Brunei, Malaysia, Sri Lanka, Thailand and Vietnam. The relationships, distribution and biology of Odontacolus are discussed, and a key is provided to identify all species.  相似文献   
23.
24.
25.
化学通讯是蜘蛛类群普遍使用的种内和种间信息交流方式,极可能是蜘蛛进化过程中最初用来进行个体之间信息交流的途径。本研究利用双向选择系统,测试了阴暗拟隙蛛(Pireneitega luctuosa)对同种其他个体的蛛网和蛛体挥发物的选择行为,采用卡方检验的统计学方法、利用SPSS 19.0和Origin Pro 8等软件对所测蜘蛛的选择数据进行了分析。结果显示:①阴暗拟隙蛛雄蛛和雌蛛对来自同种异性的蛛网(P 0.001)和蛛体挥发物(P 0.05)均具有显著的趋向性,雌、雄蛛在异性蛛网或蛛体挥发物所在的选择盒表现更长时间的停留、探索、织网等行为;②雄蛛和雌蛛对幼蛛蛛体释放出来的挥发物均表现出显著的回避行为(P 0.05),倾向于远离具有幼蛛挥发物的选择盒;③幼蛛对同种幼蛛和雄蛛的蛛网(P 0.001)以及同种幼蛛的蛛体挥发物(P 0.05)均具有选择偏好性,说明幼蛛倾向于与同种个体接近。我们的研究表明,阴暗拟隙蛛雄蛛、雌蛛及幼蛛的蛛网和蛛体挥发物能诱导种内其他个体的趋向或回避行为,阴暗拟隙蛛幼蛛对同种幼蛛的选择偏好性可能是该种个体在同一地域聚集分布的主要原因。我们的研究从行为学角度证实,阴暗拟隙蛛的蛛网及体表均携带有能够标识其性别和龄期的相关信息化学物质。  相似文献   
26.
The Australian redback spider, Latrodectus hasseltii preys on at least 10 endemic species in New Zealand, highlighting a need for control. Male redbacks are attracted to virgin females by an airborne pheromone. The aim of this study was to analyse the response of male redback spiders to two volatile chemicals found on the silk of virgin but not mated females, to determine whether these compounds constitute components of the airborne pheromone. Mature male redback spiders were placed in an olfactometer where they had a choice of two stimuli. We compared their response to paired combinations of a control, virgin silk, butyric acid and isovaleric acid. Male redbacks responded equally strongly to butyric acid and virgin silk, in terms of time spent near the stimulus. The identification of butyric acid as a component of the airborne sex pheromone of L. hasseltii provides the groundwork for developing a pheromone-based control.  相似文献   
27.
The present study introduces a new preparation of a spider vibration receptor that allows intracellular recording of responses to natural mechanical or electrical stimulation of the associated mechanoreceptor cells. The spider vibration receptor is a lyriform slit sense organ made up of 21 cuticular slits located on the distal end of the metatarsus of each walking leg. The organ is stimulated when the tarsus receives substrate vibrations, which it transmits to the organ’s cuticular structures, reducing the displacement to about one tenth due to geometrical reasons. Current clamp recording was used to record action potentials generated by electrical or mechanical stimuli. Square pulse stimulation identified two groups of sensory cells, the first being single-spike cells which generated only one or two action potentials and the second being multi-spike cells which produced bursts of action potentials. When the more natural mechanical sinusoidal stimulation was applied, differences in adaptation rate between the two cell types remained. In agreement with prior extracellular recordings, both cell types showed a decrease in the threshold tarsus deflection with increasing stimulus frequency. Off-responses to mechanical stimuli have also been seen in the metatarsal organ for the first time.  相似文献   
28.
When males fight for access to females, such conflict rarely escalates into lethal fight because the risks and costs involved, that is, severe injury or death, are too high. The social spider mite, Stigmaeopsis miscanthi, does exhibit lethal male fights, and this male–male aggressiveness varies among populations. To understand the evolution of lethal fighting, we investigated aggressiveness in 42 populations and phylogenetic relationships in 47 populations along the Japanese archipelago. By analysis of the male weapon morph, a proxy for aggressiveness, we confirmed the existence of a mildly aggressive (ML) form, besides the low aggression (LW) and high aggression (HG) forms reported earlier. To evaluate demographic history of these three forms, we employed the approximate Bayesian computation approach using mtCOI sequences and taking into consideration the postlast glacial expansion history of the host plant, Miscanthus sinensis. As results, hierarchical split models are more likely to explain the observed genetic pattern than admixture models, and the ML form in the subtropical region was considered the ancestral group. The inferred demographic history was consistent with the one reconstructed for the host plant in a previous study. The LW form was split from the ML form during the last glacial period (20,000–40,000 years BP), and subsequently, the HG form was split from the ML form at the end of or after the last glacial period (5,494–10,988 years BP). The results also suggest that the mite invaded Japan more than once, resulting in the present parapatric distribution of LW and HG forms in eastern Japan.  相似文献   
29.
Aglaoctenus lagotis (Lycosidae: Sosippinae) is a spider that, in contrast to the predominant wandering habit of the family, constructs funnel webs. The species is widely distributed throughout the Neotropics and is credited with high levels of intraspecific variation. Here, we evaluate whether reproductive isolating barriers operate between some populations of A. lagotis. We used heterotypic encounters between individuals from two distant localities: southern Uruguay (SU) and Central Argentina (CA). Additionally, we used spiders from an intermediate locality, western Uruguay (WU), where both forms of the species overlap (SU.WU was used to describe individuals from WU reminiscent of those from SU; and CA.WU was used to describe individuals from WU reminiscent of those from CA). No copulations occurred between SU and CA individuals, whereas a single and atypical copulation occurred between SU.WU and CA.WU individuals. Attacks (only by females on males) were rare. In tests of choice based on silk cues, SU males did not prefer homotypic cues but almost did not court CA females, whereas CA males preferred homotypic cues but usually courted heterotypic females. These findings, with a previously reported temporal asynchrony between populations, suggest the occurrence of reproductive isolation between both spider forms and a speciation process favoured by the wide distribution and plasticity of the species. © 2015 The Linnean Society of London, Biological Journal of the Linnean Society, 2015, 114 , 646–658.  相似文献   
30.
寄生蜂是蜘蛛的主要天敌类群之一,但寄生于漏斗蛛的寄生蜂种类较少,且缺乏相关寄生蜂的详细研究报道。我们研究了皱胸尖裂姬蜂(Oxyrrhexis rugosus)对机敏异漏斗蛛(Allagelena difficilis)的拟寄生,旨在揭示蜘蛛寄生蜂的拟寄生行为及其发育特征。显微镜下观察了12头机敏异漏斗蛛头胸部背面的皱胸尖裂姬蜂卵,并以均值法统计了皱胸尖裂姬蜂各发育阶段的历期,进一步观察了皱胸尖裂姬蜂寄生机敏异漏斗蛛后对寄主的影响。交配后的雌性皱胸尖裂姬蜂经过寻找、降落、蛰刺蛛体后伺机将卵产在机敏异漏斗蛛的头胸部背面后部;孵化后的皱胸尖裂姬蜂幼虫头部形成一个特殊摄食导管,通过摄食导管获取蛛体的营养;幼虫随着龄期增长,体色由浅变深,历期约10 d;幼虫老熟后在蛛网的漏斗状管道内结茧化蛹,蛹期约为12 d;成体雌、雄蜂寿命约为11 d,皱胸尖裂姬蜂的平均生活史周期约为33 d。皱胸尖裂姬蜂寄生后对寄主蜘蛛的行为和生活状态造成了严重的影响,随着幼虫龄期增长被寄生机敏异漏斗蛛不再进食、蜕皮,活动减少,蛛体逐渐萎缩,直至老熟幼虫离开蛛体时,蜘蛛死亡。该研究不仅增加了漏斗蛛寄生性天敌的已知种类,而且初步了解了以漏斗蛛为寄主的姬蜂的产卵行为、后代的发育特征以及对寄主蜘蛛的影响,这将为研究蜘蛛寄生蜂及其与寄主蜘蛛之间的化学通讯和协同进化提供重要的基础资料。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号