FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2014648748> ?p ?o ?g. }

• W2014648748 endingPage "475" @default.
• W2014648748 startingPage "425" @default.
• W2014648748 abstract "This paper examines the structure and role of visual signals in African forest guenons with particular attention to face pattern. Anatomical and genetic configuration is sufficiently similar in Cercupithecus for hybridisation to be possible between most species and they share a large common repertory of gestures and expressions, yet cross-breeding is relatively rare in the wild, even along allopatric boundaries and in localities with up to six sympatric species. The most obvious differences between species are in voice and coat colour, It has been found that each of the major species making up a sympatric guenon community employs a different mode of visual signalling, each employing a distinct arrangement of pattern. The following types of pattern can be distinguished. 1 Dull agouti pattern, minimal contrasts, possibly in interest of full repertoire of postures and facial expressions plus greater reliance on voice. Typified by large unspecialised monkeys of “blue monkey” or mitis group. Normally in relatively stable one-male groups, medium to low densities. 2 Dull coat and face pattern, perhaps secondarily reduced in the interest of crypsis. Principal visual signal sex, and age-linked to scrotal area of adult male. Typified by sexually dimorphic C. hamlyni. Specialised, largely terrestrial; one-male groups at low densities. 3 Bold, strongly simplified pattern. Signal over longer ranges. Genital and facial poles well differentiated. Typified by C. (diana), high canopy specialist, one-male groups at relatively high densities. 4 Complex patterns concentrated in head, correlated with stereotyped head-flagging over medium ranges. Typified by C. (cephus) group, small, highly arboreal secondary growth specialists; high densities with relatively unstable male membership. 5 Patterns with mosaic of separate features or mixture of earlier types (further categorisation probably possible here). C. (mona) group, C. neglectus and others. Ecological strategies and the environment especially influence the structuring of rally signals (which need to be species-specific in multi-specific communities). Correlations between a species' ecological/behavioural adaptations and the relative visibility in its favoured habitat are exemplified in comparisons between three divergent but related species, C. (diana), C. neglectus and C. hamlyni. (a). In arboreal C. (diana) reliance on visual communication evident in elaborate design while sharp tonal contrasts correlate with relatively long transmission ranges. Differentiated patterns at the front and back ends of the animal suggest facial and genital signals are functionally separate. (b). The flag-like chin panel of C. neglectus is appropriate to advertise rally call and ritualised side-to-side head movements with which it is associated. Beard matches white buttock patches of approximately similar shape and size, implying poor discrimination between genital and facial signals. (c). In more terrestrial and vulnerable C. hamlyni principal visual advertisement of caller is scrotal area. Discreet but eccentric design of the face pattern appropriate to short-range communication and staged movements. Examples of species-specific stereotypy in behaviour correlating with patterns in appropriate parts of the body or face are given for some other species. It is suggested that minor variations in a common cercopithecine behavioural repertoire are translated into highly specific visual signals through the elaboration of patterns. Effective transmission demands selection for maximum optical clarity in the signal. The patterns of isolates with a common ancestry suggest that this principle determines how “traits” evolve into “patterns” but they also suggest numerous options for the elaboration of signals. A concentration of pattern in the faces of the spot-nosed, red-tailed monkey group can be correlated with a transfer of signals from the genital to the facial pole. Factors influencing this development are size, diet, spatial dispersal and social organisation. Detailed examination of their signalling behaviour and the structure of their facial patterns has indicated that these very diverse monkeys belong to a single allopatric species group which has necessitated a minor taxonomic revision and the allocation of all forms to the super-species Cercopithecus (cephus). Stereotyped head movements in five members of this group have been filmed and subjected to time and motion analysis. They are unlike those observed and recorded in other species groups and appear to have a distinct derivation. Head “flagging” appears in the context of courtship and appeasement in all observed members of C. (cephus). Variations in their motor patterns suggest that there may be regional (and in captives, individual) dialects which can, in some cases, be correlated with the structure and type of face marking. It is suggested that the diversity of this group derives from past climatic changes and isolation at a critical time in their evolution. It is significant that genetic distinctness has been maintained in a large number of forms, despite the absence of contemporary geographic barriers. The association of face patterns and idiosyncratic signalling with reproductive behaviour may constitute a major mechanism reinforcing the genetic isolation of a population. In this way the mechanism for reproductive isolation may be already operative in the contemporary allopatric populations of this species group." @default.
• W2014648748 created "2016-06-24" @default.
• W2014648748 creator A5047488634 @default.
• W2014648748 date "1980-12-01" @default.
• W2014648748 modified "2023-09-25" @default.
• W2014648748 title "The role of visual signals and face patterns in African forest monkeys (guenons) of the genus <i>Cercopithecus</i>" @default.
• W2014648748 cites W1648764661 @default.
• W2014648748 cites W1829900417 @default.
• W2014648748 cites W1971313190 @default.
• W2014648748 cites W1982685823 @default.
• W2014648748 cites W1995338505 @default.
• W2014648748 cites W1996506098 @default.
• W2014648748 cites W2021746991 @default.
• W2014648748 cites W2022296898 @default.
• W2014648748 cites W2025293667 @default.
• W2014648748 cites W2026645680 @default.
• W2014648748 cites W2041282488 @default.
• W2014648748 cites W2043748922 @default.
• W2014648748 cites W2059085538 @default.
• W2014648748 cites W2066726873 @default.
• W2014648748 cites W2067815382 @default.
• W2014648748 cites W2084273744 @default.
• W2014648748 cites W2093080235 @default.
• W2014648748 cites W2095525009 @default.
• W2014648748 cites W2103867598 @default.
• W2014648748 cites W2150765739 @default.
• W2014648748 cites W2156000508 @default.
• W2014648748 cites W2318491337 @default.
• W2014648748 cites W2329532206 @default.
• W2014648748 cites W2331925520 @default.
• W2014648748 cites W2746869860 @default.
• W2014648748 cites W2796960048 @default.
• W2014648748 doi "https://doi.org/10.1111/j.1096-3642.1980.tb00062.x" @default.
• W2014648748 hasPublicationYear "1980" @default.
• W2014648748 type Work @default.
• W2014648748 sameAs 2014648748 @default.
• W2014648748 citedByCount "62" @default.
• W2014648748 countsByYear W20146487482012 @default.
• W2014648748 countsByYear W20146487482013 @default.
• W2014648748 countsByYear W20146487482014 @default.
• W2014648748 countsByYear W20146487482015 @default.
• W2014648748 countsByYear W20146487482016 @default.
• W2014648748 countsByYear W20146487482017 @default.
• W2014648748 countsByYear W20146487482018 @default.
• W2014648748 countsByYear W20146487482019 @default.
• W2014648748 countsByYear W20146487482020 @default.
• W2014648748 countsByYear W20146487482021 @default.
• W2014648748 countsByYear W20146487482022 @default.
• W2014648748 countsByYear W20146487482023 @default.
• W2014648748 crossrefType "journal-article" @default.
• W2014648748 hasAuthorship W2014648748A5047488634 @default.
• W2014648748 hasConcept C115225378 @default.
• W2014648748 hasConcept C121332964 @default.
• W2014648748 hasConcept C144024400 @default.
• W2014648748 hasConcept C149923435 @default.
• W2014648748 hasConcept C15744967 @default.
• W2014648748 hasConcept C18903297 @default.
• W2014648748 hasConcept C24890656 @default.
• W2014648748 hasConcept C2778473898 @default.
• W2014648748 hasConcept C2780509455 @default.
• W2014648748 hasConcept C2908647359 @default.
• W2014648748 hasConcept C46312422 @default.
• W2014648748 hasConcept C53889494 @default.
• W2014648748 hasConcept C78458016 @default.
• W2014648748 hasConcept C86803240 @default.
• W2014648748 hasConcept C90856448 @default.
• W2014648748 hasConceptScore W2014648748C115225378 @default.
• W2014648748 hasConceptScore W2014648748C121332964 @default.
• W2014648748 hasConceptScore W2014648748C144024400 @default.
• W2014648748 hasConceptScore W2014648748C149923435 @default.
• W2014648748 hasConceptScore W2014648748C15744967 @default.
• W2014648748 hasConceptScore W2014648748C18903297 @default.
• W2014648748 hasConceptScore W2014648748C24890656 @default.
• W2014648748 hasConceptScore W2014648748C2778473898 @default.
• W2014648748 hasConceptScore W2014648748C2780509455 @default.
• W2014648748 hasConceptScore W2014648748C2908647359 @default.
• W2014648748 hasConceptScore W2014648748C46312422 @default.
• W2014648748 hasConceptScore W2014648748C53889494 @default.
• W2014648748 hasConceptScore W2014648748C78458016 @default.
• W2014648748 hasConceptScore W2014648748C86803240 @default.
• W2014648748 hasConceptScore W2014648748C90856448 @default.
• W2014648748 hasIssue "4" @default.
• W2014648748 hasLocation W20146487481 @default.
• W2014648748 hasOpenAccess W2014648748 @default.
• W2014648748 hasPrimaryLocation W20146487481 @default.
• W2014648748 hasRelatedWork W1972217528 @default.
• W2014648748 hasRelatedWork W2000699432 @default.
• W2014648748 hasRelatedWork W2074460143 @default.
• W2014648748 hasRelatedWork W2097490023 @default.
• W2014648748 hasRelatedWork W2135630539 @default.
• W2014648748 hasRelatedWork W2313369403 @default.
• W2014648748 hasRelatedWork W2320113063 @default.
• W2014648748 hasRelatedWork W4241023053 @default.
• W2014648748 hasRelatedWork W4246159404 @default.
• W2014648748 hasRelatedWork W4253041405 @default.
• W2014648748 hasVolume "35" @default.
• W2014648748 isParatext "false" @default.
• W2014648748 isRetracted "false" @default.

• next