Colour preferences in relation to diet in chimpanzees (Pan troglodytes), gorillas (Gorilla gorilla), and mandrills (Mandrillus sphinx)

2021 ◽  
Author(s):  
M. Carmen Hernández ◽  
Sandra González-Campos ◽  
Isabel Barja

Although trichromatic color vision has been extensively studied as it grants significant advantages for Old World primates, it is unknown which selective pressures were behind trait’s evolution. The leading hypothesis would be that colour vision arose as a foraging adaptation because it allowed individuals to spot food more efficiently. To test this, we exposed three chimpanzees (Pan troglodytes), five gorillas (Gorilla gorilla) and three mandrills (Mandrillus sphinx) to colour cardboard plates to assess if colours related to diet were the most preferred. Experimental setting was divided in two phases. During the first one, animals were provided with colour cardboard plates of only one colour per data collection session. The order of colour presentation was randomly determined: white, black, yellow, green and red. In phase two, primates were simultaneously provided with cardboard plates of all colours. Behavioural interactions with plates were measured using a one-zero group focal sampling (10 s sampling intervals and 20 m observation periods). Results showed that when animals were exposed to only one colour at a time, they exhibited different colour preferences depending on the species considered. Chimpanzees preferred red and yellow, the colours linked to fruits, while gorillas selected red and white. Mandrills exhibited fewer differences between colours preference, being red the most selected. Furthermore, when all colours were simultaneously provided, individuals chose colours related to diet over black and white. Although there were clear individual differences, our results support that trichromatic color vision is an advantage in detecting and selecting red items. In the wild, it could be important in the detection of reddish fruits and leaves.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lara M. Southern ◽  
Tobias Deschner ◽  
Simone Pika

AbstractIntraspecies violence, including lethal interactions, is a relatively common phenomenon in mammals. Contrarily, interspecies violence has mainly been investigated in the context of predation and received most research attention in carnivores. Here, we provide the first information of two lethal coalitionary attacks of chimpanzees (Pan troglodytes troglodytes) on another hominid species, western lowland gorillas (Gorilla gorilla gorilla), that occur sympatrically in the Loango National Park in Gabon. In both events, the chimpanzees significantly outnumbered the gorillas and victims were infant gorillas. We discuss these observations in light of the two most widely accepted theoretical explanations for interspecific lethal violence, predation and competition, and combinations of the two-intraguild predation and interspecific killing. Given these events meet conditions proposed to trigger coalitional killing of neighbours in chimpanzees, we also discuss them in light of chimpanzees’ intraspecific interactions and territorial nature. Our findings may spur further research into the complexity of interspecies interactions. In addition, they may aid in combining field data from extant models with the Pliocene hominid fossil record to better understand behavioural adaptations and interspecific killing in the hominin lineage.


Oryx ◽  
1988 ◽  
Vol 22 (4) ◽  
pp. 218-228 ◽  
Author(s):  
Michael J. S. Harrison

Little is known about the mandrill Mandrillus sphinx in the wild. It is an elusive primate and thus difficult to study in its rain-forest habitat in equatorial Africa. As human pressure on its habitat grows it has become increasingly urgent to discover more about the species so that appropriate conservation measures can be planned. The author made a 15-month study of the mandrill in Gabon and discovered that it was not as widely distributed as had been believed. Although it is threatened by hunting pressure and habitat disruption, populations still remain and five reserves protect some of these.


mBio ◽  
2015 ◽  
Vol 6 (2) ◽  
Author(s):  
Hannah J. Barbian ◽  
Julie M. Decker ◽  
Frederic Bibollet-Ruche ◽  
Rachel P. Galimidi ◽  
Anthony P. West ◽  
...  

ABSTRACTBroadly cross-reactive neutralizing antibodies (bNabs) represent powerful tools to combat human immunodeficiency virus type 1 (HIV-1) infection. Here, we examined whether HIV-1-specific bNabs are capable of cross-neutralizing distantly related simian immunodeficiency viruses (SIVs) infecting central (Pan troglodytestroglodytes) (SIVcpzPtt) and eastern (Pan troglodytesschweinfurthii) (SIVcpzPts) chimpanzees (n= 11) as well as western gorillas (Gorilla gorilla gorilla) (SIVgor) (n= 1). We found that bNabs directed against the CD4 binding site (n= 10), peptidoglycans at the base of variable loop 3 (V3) (n= 5), and epitopes at the interface of surface (gp120) and membrane-bound (gp41) envelope glycoproteins (n= 5) failed to neutralize SIVcpz and SIVgor strains. In addition, apex V2-directed bNabs (n= 3) as well as llama-derived (heavy chain only) antibodies (n= 6) recognizing both the CD4 binding site and gp41 epitopes were either completely inactive or neutralized only a fraction of SIVcpzPttstrains. In contrast, one antibody targeting the membrane-proximal external region (MPER) of gp41 (10E8), functional CD4 and CCR5 receptor mimetics (eCD4-Ig, eCD4-Igmim2, CD4-218.3-E51, and CD4-218.3-E51-mim2), as well as mono- and bispecific anti-human CD4 (iMab and LM52) and CCR5 (PRO140, PRO140-10E8) receptor antibodies neutralized >90% of SIVcpz and SIVgor strains with low-nanomolar (0.13 to 8.4 nM) potency. Importantly, the latter antibodies blocked virus entry not only in TZM-bl cells but also in Cf2Th cells expressing chimpanzee CD4 and CCR5 and neutralized SIVcpz in chimpanzee CD4+T cells, with 50% inhibitory concentrations (IC50s) ranging from 3.6 to 40.5 nM. These findings provide new insight into the protective capacity of anti-HIV-1 bNabs and identify candidates for further development to combat SIVcpz infection.IMPORTANCESIVcpz is widespread in wild-living chimpanzees and can cause AIDS-like immunopathology and clinical disease. HIV-1 infection of humans can be controlled by antiretroviral therapy; however, treatment of wild-living African apes with current drug regimens is not feasible. Nonetheless, it may be possible to curb the spread of SIVcpz in select ape communities using vectored immunoprophylaxis and/or therapy. Here, we show that antibodies and antibody-like inhibitors developed to combat HIV-1 infection in humans are capable of neutralizing genetically diverse SIVcpz and SIVgor strains with considerable breadth and potency, including in primary chimpanzee CD4+T cells. These reagents provide an important first step toward translating intervention strategies currently developed to treat and prevent AIDS in humans to SIV-infected apes.


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