Predation on scyphozoan polyps and selective hydrozoan nematocyst incorporation dynamics in an alien aeolid nudibranch

IF 2.8 2区 生物学 Q1 ZOOLOGY
Hila Dror, Tamar Lotan, Dror Angel
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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.
外来海洋裸鳃动物对珊瑚虫的捕食和对水螅线虫囊的选择性结合动力学
羽状裸鳃捕食各种刺胞动物,并将猎物的刺丝囊吸收到刺胞囊中,刺胞囊位于它们角的尖端,用于自卫。本研究以地中海东部常见水母科(Aurelia sp. Cassiopea andromeda, Phyllorhiza punctata和Rhopilema nomadica)中的水螅类为研究对象,研究了两种裸鳃动物(Caloria militaris和Flabellina affinis)与多种刺胞动物之间的捕食-食饵相互作用。最初的短期实验评估了这两种裸鳃科动物的捕食行为,之后的实验只关注了蛹蛾。通过24 h的短期实验和258 d的长期实验,确定了军夜蛾是否消耗多种刺胞动物,以及是否将猎物的刺丝囊纳入其刺胞囊。实验室实验表明,虽然F. affinis避免珊瑚虫,但C. militaris很容易消耗所有被测试的珊瑚虫和水螅动物,并可以在长达258天的时间内生存。随着猎物数量的增加,蛹的捕食率达到95个,但即使在猎物丰度很高的情况下(80个),蛹的捕食率也没有达到饱和,表明蛹具有较高的捕食能力。令人惊讶的是,尽管如此激烈的捕食,军国棘球蚴并没有在其刺丝囊中加入任何孢子虫线虫囊;在刺胞体中只发现了来自其已知水生动物猎物的线虫囊。C. militaris是一种捕食水螅虫的多面手,可以广泛地以各种各样的孢子虫为食,但它不会将孢子虫的刺丝囊纳入其刺丝囊中。这是第一个证明具有功能刺丝囊的裸鳃动物在长时间取食期间对刺丝囊隔离完全选择性的报告。这些发现有助于了解裸鳃动物的摄食生态,以及这些捕食者在调节水母繁殖中可能发挥的潜在作用。
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
29
审稿时长
>12 weeks
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.
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