ritual jousting by horned parisoschoenus expositus weevils (coleoptera, curculionidae, baridinae)仪式由角parisoschoenus比赛expositus象鼻虫(鞘翅目,象甲科,baridinae).pdfVIP
- 8
- 0
- 约 31页
- 2017-09-01 发布于上海
- 举报
ritual jousting by horned parisoschoenus expositus weevils (coleoptera, curculionidae, baridinae)仪式由角parisoschoenus比赛expositus象鼻虫(鞘翅目,象甲科,baridinae)
RITUAL JOUSTING BY HORNED PAMSOSCHOENUSEXPOSI-
TUSWEEVILS (COLEOPTERA,CURCULIONIDAE, BARIDINAE)
2
BY WILLIAM G. EBERHARD AND J. MAURICIO GARCIA-C.
1Smithsonian Tropical Research Institute, and Escuela de Biologia,
Universidad de Costa Rica, Ciudad Universitaria, Costa Rica;
email: weberhar@cariari.ucr.ac.cr
2Apdo. 1179-2100, Guadalupe, San Jose, Costa Rica;
email: mgarciac@solracsa.co.cr
ABSTRACT
Males of the weevil Parisoschoenus expositus use their prothoracic
horns as weapons in stylized battles with other males over females that
are drilling oviposition holes in palm leaves. The unusual sheath-like
structures that penetrate deep into the male prothorax function to
receive the horns of opponents during battles. Horn size is dimorphic
with respect to body size, and small and large males also differ behav-
iorally. Small males that have mated with a drilling female are some-
times able to impede a large male’s access to the female until after she
has oviposited, but they are not able to take over females from larger
males.
INTRODUCTION
Beetle horns are extremely diverse in size and shape (e.g., Arrow
1951; Eberhard 1979). Despite occasional claims to the contrary
(Moller 1992), observations oftheir use in natural contexts suggest that
they function as weapons in battles between conspecifics (Mor6n 1976;
Bechtle 1977; Eberhard 1977, 1979, 1981, 1987; Palmer 1978; Brown
and Siegfried 1983; Otronen 1988; Connor 1988; Siva-Jothy 1989;
Rasmussen 1994; Emlen 1994, 1997), rather than as visual display
devices as do the horns and antlers of some ungulates (Geist 1966,
1978; Lincoln 1994). Three common functional designs have been
documented among beetle horns: a dorso-ventrally mobile head horn
which serves as a lever to lift the oppo
您可能关注的文档
- notch lineages and activity in intestinal stem cells determined by a new set of knock-in mice血统和肠道干细胞的活动由一组新的敲入小鼠.pdf
- notch mrna expression in drosophila embryos is negatively regulated at the level of mrna 3′ processing切口mrna表达在果蝇胚胎负监管层面的mrna 3u2032处理.pdf
- notch pathway modulation on bone marrow-derived vascular precursor cells regulates their angiogenic and wound healing potential来源于血管前体细胞的notch通路调制在骨调节血管生成和伤口愈合的潜力.pdf
- notch1, hif1a and other cancer-related proteins in lung tissue from uranium miners—variation by occupational exposure and subtype of lung cancernotch1 hif1a和其他癌症相关的蛋白在肺组织从铀miners-variation职业暴露和肺癌亚型.pdf
- notch signaling activation suppresses v-src-induced transformation of neural cells by restoring tgf-β-mediated differentiationnotch信号激活抑制v-src-induced变换恢复tgf-β-mediated分化的神经细胞.pdf
- not all scale-free networks are born equal the role of the seed graph in ppi network evolution并不是所有的无标度网络生来平等的角色在ppi网络进化的种子图.pdf
- notch signalling synchronizes the zebrafish segmentation clock but is not needed to create somite boundariesnotch信号同步斑马鱼分割时钟但不需要创建体节的界限.pdf
- notch2 is neither rearranged nor mutated in t(1;19) positive oligodendrogliomasnotch2既不重新安排也不突变在t(1;19)正少突神经胶质瘤.pdf
- notch2 signaling sensitizes endothelial cells to apoptosis by negatively regulating the key protective molecule survivinnotch2信号糖分会让内皮细胞凋亡的负调节的关键保护分子存活素.pdf
- notch3 is dispensable for thymocyte β-selection and notch1-induced t cell leukemogenesisnotch3是可有可无的胸腺细胞β-selection notch1-induced t细胞白血病生成.pdf
- 2025年版汽车趋势报告 The 2025 EPA Automotive Trends Report.docx
- 2026年边缘计算开源平台EdgeX Foundry入门与二次开发.docx
- 2026年超声内镜放大内镜早癌诊断AI辅助识别系统临床评价.docx
- 2026年报废汽车回收与再制造逆向物流体系.docx
- 2026年产品碳足迹核算方法学:从摇篮到大门与从摇篮到坟墓.docx
- 2026年城乡要素平等交换双向流动政策创新试点申报材料.docx
- 2026年超导半导体接口电路架构与电平转换驱动器设计.docx
- 2026年财政贴息不再以再贷款支持为前提后的风险防范与合规要点.docx
- 2026年不动产信托登记试点政策对遗嘱信托支持.docx
- 2026年城乡有机废弃物协同处理技术方案.docx
原创力文档

文档评论(0)