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2.
Commun Biol ; 7(1): 647, 2024 May 27.
Article in English | MEDLINE | ID: mdl-38802506

ABSTRACT

Characterising how the totality of primate diversity is distributed across the order, and how it evolved, is challenging because diversity in individual traits often show opposing phylogenetic patterns. A species' combination of traits can be conceptualised as its 'niche'. Here, we describe and analyse seven-dimensional niche space, comprising 11 traits, for 191 primate species. Multifaceted diversity is distributed unequally among taxonomic groups. Cercopithecoidea and Hominidae occupy the largest areas of niche space, and are the most diverse families; platyrrhine families occupy small areas, and this space overlaps with strepsirrhines. The evolution of species' locations in niche space is regulated by selection for adaptive optima in trait combinations. Given that niche similarity results in interspecific competition, we quantify two measures of species' niche locations relative to others. We find that omnivores, frugivores, and species tolerating higher temperatures experience stronger interspecific competition. Hominidae occupation of niche space suggests competitive exclusion from niches by Cercopithecoidea over evolutionary time; but living great apes experience the lowest levels of interspecific competition. Callitrichids experience the highest levels of interspecific competition. Our results provide a standardised measure of primate niches that sheds light on the partitioning and evolution of primate diversity, and how this is driven by interspecific competition.


Subject(s)
Biological Evolution , Ecosystem , Primates , Animals , Primates/physiology , Phylogeny , Species Specificity
3.
Philos Trans R Soc Lond B Biol Sci ; 371(1690)2016 Mar 19.
Article in English | MEDLINE | ID: mdl-26926274

ABSTRACT

Young orangutans are highly neophobic, avoid independent exploration and show a preference for social learning. Accordingly, they acquire virtually all their learned skills through exploration that is socially induced. Adult exploration rates are also low. Comparisons strongly suggest that major innovations, i.e. behaviours that have originally been brought into the population through individual invention, are made where ecological opportunities to do so are propitious. Most populations nonetheless have large innovation repertoires, because innovations, once made, are retained well through social transmission. Wild orangutans are therefore not innovative. In striking contrast, zoo-living orangutans actively seek novelty and are highly exploratory and innovative, probably because of positive reinforcement, active encouragement by human role models, increased sociality and an expectation of safety. The explanation for this contrast most relevant to hominin evolution is that captive apes generally have a highly reduced cognitive load, in particular owing to the absence of predation risk, which strongly reduces the costs of exploration. If the orangutan results generalize to other great apes, this suggests that our ancestors could have become more curious once they had achieved near-immunity to predation on the eve of the explosive increase in creativity characterizing the Upper Palaeolithic Revolution.


Subject(s)
Behavior, Animal , Creativity , Phylogeny , Pongo/physiology , Animals , Animals, Wild , Animals, Zoo
4.
Thromb Res ; 74(4): 347-54, 1994 May 15.
Article in English | MEDLINE | ID: mdl-8085236

ABSTRACT

A monoclonal antibody purified factor VIII concentrate containing FVIII/vWF complex has been assayed by one-stage clotting (CA) and chromogenic substrate (CSA) methods. The influences of potassium iodide (KI) and albumin in combination with predilution buffers, standards and storage of samples have been examined. These components are compared for their effect on FVIII potencies in final product and in-process controls. FVIII:C purified by immunoaffinity chromatography can not be measured reliably by CA or CSA, because of KI which interfere on the assay. Overall yield of FVIII, efficiency of IAC step and purity of FVIII can be determined by assaying the desalted samples.


Subject(s)
Factor VIII/isolation & purification , von Willebrand Factor/isolation & purification , Albumins , Buffers , Chromatography, Affinity , Chromogenic Compounds/analysis , Factor VIII/chemistry , Humans , Potassium Iodide , Reference Standards , von Willebrand Factor/chemistry
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