Evidence map›Paper›PMID 42288841›Full record

ArticleFrontiers in zoology2026

Correlated evolution of core skin structures in freshwater fishes and challenges to epidermal club cells as the material basis of alarm responses.

Lu Li, Songtao Li, Haoyu Wang, Huan Xiong, Hongyan Wang, Haowen Wang, Zhijian Wang, Haoran Gu

Abstract read
In one paragraph

Article in Frontiers in zoology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Lu Li *Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China.
Songtao Li *Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China.
Haoyu WangIntegrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China.
Huan XiongIntegrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China.
Hongyan WangIntegrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China.
Haowen WangIntegrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China.
Zhijian WangIntegrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China. wangzj1969@126.com.
Haoran GuIntegrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, Key Laboratory of Freshwater Fish Reproduction and Development (Ministry of Education), Key Laboratory of Aquatic Science of Chongqing, School of Life Sciences, Southwest University, Chongqing, 400715, China. guhaoran@swu.edu.cm.

Funding

National Natural Science Foundation of China 32302987National Natural Science Foundation of China 32400382the New Doctoral Research Start-up Project of Southwest University SWU-KR25022
6 · The paper itself

Abstract

backgroundCorrelated evolution refers to the coordinated changes of multiple traits during species evolution. Fish skin exhibits diverse structures comprising the epidermis, dermis, scales, epidermal mucous cells (EMCs), and epidermal club cells (ECCs), yet the correlated evolution among these components remains unexplored. ECCs are classically hypothesized to be the source of chemical alarm cues in ostariophysan fishes, which are passively released during predator-inflicted skin damage to alert nearby conspecifics of active predation threats, this process known as the alarm response. However, we identified two critical exceptions from 53 freshwater fishes: naked carp (Gymnocypris, ostariophysans) have lost ECCs, while mandarin fish (Siniperca, non-ostariophysans) have acquired them. The established link between ECCs and alarm responses in ostariophysans may be confounded by phylogeny. Their consistent co-occurrence does not establish a causal relationship. The two evolutionary exceptions serve as ideal models to test this relationship.

resultsWe investigated correlated evolution across seven core skin structures, including epidermal thickness, dermal thickness, scale thickness, EMCs size/number, ECCs size/number in 53 freshwater fishes. Analysis revealed significant correlated evolution among skin structures. Epidermal thickness showed positive correlations with all other metrics, except for the relationship between scale thickness and EMCs number. Scale thickness exhibited antagonistic correlations with both epidermal and dermal thickness. Notably, scale thickness positively correlated with EMCs number, reflecting functional adaptation to reduce inter-scale friction. Critically, behavioral experiments demonstrated that naked carp, despite lacking ECCs, exhibited robust alarm responses. Furthermore, we tested six close relatives of the naked carp, all of which possessed ECCs and exhibited robust alarm responses. Conversely, mandarin fish, despite possessing ECCs, showed no alarm responses. This evidence does not support ECCs as the necessary source of chemical alarm cues.

conclusionsIn conclusion, our study demonstrates significant correlated evolution among core skin structures in freshwater fishes. Crucially, we challenge the prevailing paradigm by showing that chemical alarm cues can originate from integumentary components other than ECCs, evidenced by the robust alarm response in ECCs-lacking naked carp. Secondly, ECCs may play a multifunctional role evidenced by the absence of alarm response in ECCs-possessing mandarin fish. These insights advance our understanding of fish skin functional morphology and ecology.

Indexed as

Alarm responsesEpidermal club cellsInterspecific differenceSkin structure

Identifiers

PMID42288841
PMCPMC13440240

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.