{"title":"Predation on scyphozoan polyps and selective hydrozoan nematocyst incorporation dynamics in an alien aeolid nudibranch","authors":"Hila Dror, Tamar Lotan, Dror Angel","doi":"10.1186/s12983-025-00589-9","DOIUrl":null,"url":null,"abstract":"Aeolid nudibranchs prey on various cnidarians and incorporate nematocysts from their prey into the cnidosac, located at the tip of their cerata for self-defense. This study examined the predator–prey interactions between two nudibranch species, Caloria militaris and Flabellina affinis, and various cnidarians, focusing on scyphozoan polyps from common eastern Mediterranean medusae, including Aurelia sp. Cassiopea andromeda, Phyllorhiza punctata, and Rhopilema nomadica. An initial short-term experiment assessed predation by both nudibranch species, after which subsequent experiments focused exclusively on C. militaris. Short-term experiments for 24 h and long-term experiments lasting up to 258 days were conducted to determine whether C. militaris consumes a variety of cnidarians, and if it incorporates the prey nematocysts into its cnidosacs. Laboratory experiments indicate that while F. affinis avoids scyphozoan polyps, C. militaris readily consumes all tested scyphozoan and hydrozoan species and can subsist on them for extended durations of up to 258 days. C. militaris predation rate, reaching 95 polyps day−1 increased with greater prey availability, but did not reach saturation even at very high prey abundances (> 80 polyps day−1), suggesting a higher predation capacity. Surprisingly, despite this intense predation, C. militaris did not incorporate any of the scyphozoan nematocysts in its cnidosac; only nematocysts from its known hydrozoan prey were identified in the cnidosac. C. militaris is a generalist that preys on hydrozoa and can extensively feed on a variety of scyphozoan polyps, yet it does not incorporate scyphozoan nematocysts into its cnidosacs. This is the first report to demonstrate complete selectivity in nematocyst sequestration over an extended feeding period in a nudibranch possessing a functional cnidosac. These findings contribute to understanding nudibranch feeding ecology and the potential role these predators may play in regulating jellyfish blooms. ","PeriodicalId":55142,"journal":{"name":"Frontiers in Zoology","volume":"13 1","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Zoology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12983-025-00589-9","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Aeolid nudibranchs prey on various cnidarians and incorporate nematocysts from their prey into the cnidosac, located at the tip of their cerata for self-defense. This study examined the predator–prey interactions between two nudibranch species, Caloria militaris and Flabellina affinis, and various cnidarians, focusing on scyphozoan polyps from common eastern Mediterranean medusae, including Aurelia sp. Cassiopea andromeda, Phyllorhiza punctata, and Rhopilema nomadica. An initial short-term experiment assessed predation by both nudibranch species, after which subsequent experiments focused exclusively on C. militaris. Short-term experiments for 24 h and long-term experiments lasting up to 258 days were conducted to determine whether C. militaris consumes a variety of cnidarians, and if it incorporates the prey nematocysts into its cnidosacs. Laboratory experiments indicate that while F. affinis avoids scyphozoan polyps, C. militaris readily consumes all tested scyphozoan and hydrozoan species and can subsist on them for extended durations of up to 258 days. C. militaris predation rate, reaching 95 polyps day−1 increased with greater prey availability, but did not reach saturation even at very high prey abundances (> 80 polyps day−1), suggesting a higher predation capacity. Surprisingly, despite this intense predation, C. militaris did not incorporate any of the scyphozoan nematocysts in its cnidosac; only nematocysts from its known hydrozoan prey were identified in the cnidosac. C. militaris is a generalist that preys on hydrozoa and can extensively feed on a variety of scyphozoan polyps, yet it does not incorporate scyphozoan nematocysts into its cnidosacs. This is the first report to demonstrate complete selectivity in nematocyst sequestration over an extended feeding period in a nudibranch possessing a functional cnidosac. These findings contribute to understanding nudibranch feeding ecology and the potential role these predators may play in regulating jellyfish blooms.
期刊介绍:
Frontiers in Zoology is an open access, peer-reviewed online journal publishing high quality research articles and reviews on all aspects of animal life.
As a biological discipline, zoology has one of the longest histories. Today it occasionally appears as though, due to the rapid expansion of life sciences, zoology has been replaced by more or less independent sub-disciplines amongst which exchange is often sparse. However, the recent advance of molecular methodology into "classical" fields of biology, and the development of theories that can explain phenomena on different levels of organisation, has led to a re-integration of zoological disciplines promoting a broader than usual approach to zoological questions. Zoology has re-emerged as an integrative discipline encompassing the most diverse aspects of animal life, from the level of the gene to the level of the ecosystem.
Frontiers in Zoology is the first open access journal focusing on zoology as a whole. It aims to represent and re-unite the various disciplines that look at animal life from different perspectives and at providing the basis for a comprehensive understanding of zoological phenomena on all levels of analysis. Frontiers in Zoology provides a unique opportunity to publish high quality research and reviews on zoological issues that will be internationally accessible to any reader at no cost.
The journal was initiated and is supported by the Deutsche Zoologische Gesellschaft, one of the largest national zoological societies with more than a century-long tradition in promoting high-level zoological research.