Abstract
Physiological and behavioural constraints hinder albino individuals. Albino animals are rare in the wild; this trait is associated with easy detection by predators, non-native or damaged environments, and exclusively aphotic environments in total darkness. The social aspect of albinism is reported only for human beings, and the effect is distinguishable in time and space when social benefits, are used to a limited the extent. Thus far, the social consequences of albinism for animals remain unknown. We used socially established groups of the pigmented catfish, (Silurus glanis), to observe space and temporal distance detachment of albino specimens in laboratory conditions. The albino fish were separated at larger distances from the group than pigmented individuals with the same social status determined by familiarity, and this asymmetry also varied in time. Albinism-related ostracism results in a solitary existence, usually followed by enhanced predation risk. The motivation for an individual’s exclusion from a group appears to be the avoidance of the predation risk that increases not only for an odd individual but also for conspecifics within a group. Our findings indicate a role for albinism in behavioural processes related to sociality in a group of conspecifics.
Highlights
Physiological and behavioural constraints hinder albino individuals [1,2]
Albino animals are rare in the wild; this trait is associated with easy detection by predators [3], non-native or damaged environments [3,4], and exclusively aphotic environments in total darkness [5]
The probability that an albino fish would be isolated in a separate sector of the artificial stream was two times higher than that for a pigmented individual (χ2 = 70.1293, P
Summary
Physiological and behavioural constraints hinder albino individuals [1,2]. Albino animals are rare in the wild; this trait is associated with easy detection by predators [3], non-native or damaged environments [3,4], and exclusively aphotic environments in total darkness [5]. Albinism encompasses genetically determined diseases that involve disorders of the melanin system, resulting in hypopigmentation [2]. Oculocutaneous albinism (OCA) is the result of a recessive mutation of the gene encoding the tyrosinase enzyme and is characterised by different levels of skin, hair, and eye pigmentation. Albinism has been recorded in plants [6], invertebrates [7], vertebrates, and human beings. The pleiotropic effect of albinism is considered to be PLOS ONE | DOI:10.1371/journal.pone.0128279. The pleiotropic effect of albinism is considered to be PLOS ONE | DOI:10.1371/journal.pone.0128279 May 27, 2015
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