Bruna Cama, Karl Heaton, Jane Thomas-Oates, Stefan Schulz, Kanchon K Dasmahapatra
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We focus on two different tissues: the wing androconia, responsible for MSPs used in courtship, and the genital tip, the production site for anti-aphrodisiac pheromones that affect post-mating behaviour. Gas chromatography-mass spectrometric analysis of tissue extracts from virgin males and females of both species from day 0 to 8 post-eclosion demonstrates the following. Some ubiquitous fatty acid precursors are already detectable at day 0. The complexity of the chemical blends increases with age regardless of tissue or sex. No obvious difference in the time course of blend production was evident between the two species, but female tissues in H. charithonia were more affected by age than in H. atthis. We suggest that compounds unique to male androconia and genitals and whose amount increases with age are potential candidates for future investigation into their roles as pheromones. While this analysis revealed some of the complexity in Heliconius chemical ecology, the effects of other factors, such as the time of day, remain unknown.</p>","PeriodicalId":15346,"journal":{"name":"Journal of Chemical Ecology","volume":" ","pages":"197-213"},"PeriodicalIF":2.2000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11233321/pdf/","citationCount":"0","resultStr":"{\"title\":\"Complexity of Chemical Emissions Increases Concurrently with Sexual Maturity in Heliconius Butterflies.\",\"authors\":\"Bruna Cama, Karl Heaton, Jane Thomas-Oates, Stefan Schulz, Kanchon K Dasmahapatra\",\"doi\":\"10.1007/s10886-024-01484-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Pheromone communication is widespread among animals. Since it is often involved in mate choice, pheromone production is often tightly controlled. 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The complexity of the chemical blends increases with age regardless of tissue or sex. No obvious difference in the time course of blend production was evident between the two species, but female tissues in H. charithonia were more affected by age than in H. atthis. We suggest that compounds unique to male androconia and genitals and whose amount increases with age are potential candidates for future investigation into their roles as pheromones. While this analysis revealed some of the complexity in Heliconius chemical ecology, the effects of other factors, such as the time of day, remain unknown.</p>\",\"PeriodicalId\":15346,\"journal\":{\"name\":\"Journal of Chemical Ecology\",\"volume\":\" \",\"pages\":\"197-213\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11233321/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Ecology\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1007/s10886-024-01484-z\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/3/13 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Ecology","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1007/s10886-024-01484-z","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/13 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
信息素交流在动物中非常普遍。由于费洛蒙通常与择偶有关,因此费洛蒙的产生通常受到严格控制。虽然已经对一些蝶类物种的雄性信息素(MSPs)和抗催情剂进行了研究,但对影响这些长寿蝶产生和释放信息素的因素知之甚少。在这里,我们研究了Heliconius atthis和Heliconius charithonia分别表现出的自由交配和蛹交配策略对其信息素释放时间的不同影响。我们重点研究了两种不同的组织:翅和生殖器顶端,翅和生殖器顶端是影响交配后行为的反催情信息素的产生部位。气相色谱-质谱法分析了两种雌雄蛙在孵化后第 0 天至第 8 天的组织提取物,结果如下。一些无处不在的脂肪酸前体在第 0 天就已经可以检测到。无论组织或性别如何,化学混合物的复杂性随着年龄的增长而增加。两个物种在产生混合物的时间过程上没有明显差异,但雌性 H. charithonia 组织受年龄的影响比 H. atthis 更大。我们认为,雄性雄冠花和生殖器中特有的、其含量随年龄增长而增加的化合物是未来研究其信息素作用的潜在候选物。尽管这项分析揭示了榛鸡化学生态学的一些复杂性,但其他因素(如一天中的时间)的影响仍然未知。
Complexity of Chemical Emissions Increases Concurrently with Sexual Maturity in Heliconius Butterflies.
Pheromone communication is widespread among animals. Since it is often involved in mate choice, pheromone production is often tightly controlled. Although male sex pheromones (MSPs) and anti-aphrodisiacs have been studied in some Heliconius butterfly species, little is known about the factors affecting their production and release in these long-lived butterflies. Here, we investigate the effect of post-eclosion age on chemical blends from pheromone-emitting tissues in Heliconius atthis and Heliconius charithonia, exhibiting respectively free-mating and pupal-mating strategies that are hypothesised to differently affect the timing of their pheromone emissions. We focus on two different tissues: the wing androconia, responsible for MSPs used in courtship, and the genital tip, the production site for anti-aphrodisiac pheromones that affect post-mating behaviour. Gas chromatography-mass spectrometric analysis of tissue extracts from virgin males and females of both species from day 0 to 8 post-eclosion demonstrates the following. Some ubiquitous fatty acid precursors are already detectable at day 0. The complexity of the chemical blends increases with age regardless of tissue or sex. No obvious difference in the time course of blend production was evident between the two species, but female tissues in H. charithonia were more affected by age than in H. atthis. We suggest that compounds unique to male androconia and genitals and whose amount increases with age are potential candidates for future investigation into their roles as pheromones. While this analysis revealed some of the complexity in Heliconius chemical ecology, the effects of other factors, such as the time of day, remain unknown.
期刊介绍:
Journal of Chemical Ecology is devoted to promoting an ecological understanding of the origin, function, and significance of natural chemicals that mediate interactions within and between organisms. Such relationships, often adaptively important, comprise the oldest of communication systems in terrestrial and aquatic environments. With recent advances in methodology for elucidating structures of the chemical compounds involved, a strong interdisciplinary association has developed between chemists and biologists which should accelerate understanding of these interactions in nature.
Scientific contributions, including review articles, are welcome from either members or nonmembers of the International Society of Chemical Ecology. Manuscripts must be in English and may include original research in biological and/or chemical aspects of chemical ecology. They may include substantive observations of interactions in nature, the elucidation of the chemical compounds involved, the mechanisms of their production and reception, and the translation of such basic information into survey and control protocols. Sufficient biological and chemical detail should be given to substantiate conclusions and to permit results to be evaluated and reproduced.