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At least 19 recordsLinked to original sources
PubMed1980

[Comparative anatomical studies on the Jacobson organs of Nycticebus coucang Boddaert, 1785 (Prosimiae, Lorisidae) and Galago crassicaudatus E. Geoffroy, 1812 (Prosimiae, Lorisidae). I. Nycticebus coucang].

The goal of this research was to study the macroscopic and microscopic anatomy of the vomeronasal organ in Nycticebus coucang. Based on numerous measurements in cross-sections of all parts of the organ, three-dimensional graphs of the vomeronasal cartilage, the organ and the system of blood-vessels, situated around the organ, were drawn. Nycticebus has a well developed vomeronasal organ exhibiting a well developed sensory epithelium. The oral end of the organ opens into the middle part of the nasopalatine duct, which has an open connection with the cavum nasi and the cavum oris. The cartilago paraseptalis is connected with the cartilago ductus nasopalatini by the sickle-shaped part of the cartilago paraseptalis. An "outer bar", which is present in the vomeronasal cartilage of Tupaia, is absent in Nycticebus. The oral part of the organ contains nonciliated, pseudostratified epithelium with secretory crypts and goblet cells. In the main part of the organ the dorso-lateral wall consists of nonsensory, nonciliated, pseudostratified epithelium, while the sensory epithelium is situated in the dorsolateral wall. Serous glands, which are situated dorsal to the organ, open into the organ at its dorsal margin. Caudal to this part there is a long part of the organ without sensory epithelium. At its caudal end the organ is branched. The sensory epithelium of the vomeronasal organ is thicker than the sensory epithelium of the nose. It contains a nucleus-free space between the nuclei of supporting cells and the nuclei of sensory cells. The sensory epithelium contains about 92 000 receptor cells/mm2. Capillaries could not be seen in the epithelia of the organ. The vessels, which accompany the organ, are veins and capillaries. The dorsal veins exhibit thicker walls and a wider lumen than the ventral ones and are therefore better suited for the pumping-mechanism, as suggested by BROMAN (1920). Connective tissue, surrounding the organ, aids the pumping-mechanism of the veins.

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PubMed1979

[Cytogenetics of two Lorisidae (Nycticebus coucang and Perodicticus potto). Comparison with the lemurs and the simians (author's transl)].

The karyotypes of two Lorisidae (Prosimians) Nycticebus coucang and Perodicticus potto have been studied, using many banding techniques. These karyotypes are compared with each other and also with those of Microcebus murinus (Lemur) and of Cebus capucinus (Simian, platyrrhine). The karyotype of M. murinus appears ancestral to the other. That of the Lorisidae cannot be an intermediatry stage between the karyotypes of the lemurs and of the simians. An important part (12 p. cent) of the genome of N. coucang is comprised of heterochromatin ; it and the juxta centromeric heterochromatin stain negatively with C-banding techniques. C-banding therefore is insufficient to delineate constitutive heterochromatin, late replication being the only universal criterion.

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PubMed1988

Scaling of growth and life history traits relative to body size, brain size, and metabolic rate in lorises and galagos (Lorisidae, primates).

A broad range of variation in body size, brain size, and metabolic rate occurs within the primate family Lorisidae, thus providing an opportunity to examine the relationship of these three parameters to variation in growth and life history traits. Data on adult body weight, gestation length, lactation length, age at first estrus, litter size, and growth parameters were collected from a captive colony of four lorisid species, Loris tardigradus, Nycticebus coucang, Galago crassicaudatus, and G. senegalensis. The data presented here constitute the most complete life history information available for these poorly understood prosimian species. Correlation and allometric analyses were performed to determine the relationships between variables. Among the lorisids studied, adult body weight, adult cranial capacity, and relative cranial capacity did not predict variation in life history traits. Adult basal metabolic rate predicted most of the variability in gestation length, lactation length, and growth parameters. Lorisines differ from similarly sized galagines in having lower basal metabolic rates, slower growth rates, slower developmental rates, and smaller litter sizes, resulting in reduced reproductive potential. This may be a consequence of lorisine adaptation to a diet of toxic insects. Metabolic rate and diet may be among the most important parameters to examine in any study of life history evolution.

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PubMed2005

Reconstructing the evolutionary history of the Lorisidae using morphological, molecular, and geological data.

Major aspects of lorisid phylogeny and systematics remain unresolved, despite several studies (involving morphology, histology, karyology, immunology, and DNA sequencing) aimed at elucidating them. Our study is the first to investigate the evolution of this enigmatic group using molecular and morphological data for all four well-established genera: Arctocebus, Loris, Nycticebus, and Perodicticus. Data sets consisting of 386 bp of 12S rRNA, 535 bp of 16S rRNA, and 36 craniodental characters were analyzed separately and in combination, using maximum parsimony and maximum likelihood. Outgroups, consisting of two galagid taxa (Otolemur and Galagoides) and a lemuroid (Microcebus), were also varied. The morphological data set yielded a paraphyletic lorisid clade with the robust Nycticebus and Perodicticus grouped as sister taxa, and the galagids allied with Arctocebus. All molecular analyses maximum parsimony (MP) or maximum likelihood (ML) which included Microcebus as an outgroup rendered a paraphyletic lorisid clade, with one exception: the 12S + 16S data set analyzed with ML. The position of the galagids in these paraphyletic topologies was inconsistent, however, and bootstrap values were low. Exclusion of Microcebus generated a monophyletic Lorisidae with Asian and African subclades; bootstrap values for all three clades in the total evidence tree were over 90%. We estimated mean genetic distances for lemuroids vs. lorisoids, lorisids vs. galagids, and Asian vs. African lorisids as a guide to relative divergence times. We present information regarding a temporary land bridge that linked the two now widely separated regions inhabited by lorisids that may explain their distribution. Finally, we make taxonomic recommendations based on our results.

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PubMed1979

A quantitative approach to cytoarchitectonics. IV. The areal pattern of the cortex of Galago demidovii (e. Geoffroy, 1796), (lorisidae, primates).

The boundaries of neo- and allocortical areas of Galago demidovii are analyzed with an automatic quantitative procedure using an image analyzer. The results are summarized in a cortical map and compared with a cortical map of Tupaia. Galago shows a highly differentiated temporal lobe and no homogeneous peristriate area comparable to the classical concept of Brodmann's Area 19. Primary motor, somatosensory, auditory, and visual areas are delineated and shown to be surrounded by distinct secondary areas.

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PubMed1979

Concentrating capacity of the kidney and nitrogen partition in the urine in Perodicticus potto (Prosimii, Lorisidae, Lorisinae).

The concentrating ability of the kidney in Perodicticus potto was investigated. As the relation between this capacity and the thickness of the medulla has been stressed by Schmidt-Nielsen & O'Dell, the size of the various layers in the kidney was measured. Based on our observation that the potto may excrete uric acid in fairly high concentrations, the partition of nitrogen in the urine was also explored.

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PubMed1982

Chromosomal evolution in "lemurs". VI. Chromosomal banding studies of Galago senegalensis, Galago alleni, Galago demidovii and Euoticus elegantulus.

The karyotype of four Galagidae (Galago senegalensis, G. demidovii, G. alleni and Euoticus elegantulus) are studied and compared with the aid of various banding techniques. Many common chromosome segments were found, and it was possible to reconstruct a hypothetical ancestral karyotype for the family. It was also possible to show the relation between the chromosomes of Galagidae with those of two Lorisidae. The general scheme of chromosomal evolution of the Lorisiforms can be proposed, resulting from a common populational evolution followed by an accumulation of translocations, mostly of the Robertsonian type. Several pericentric inversions have also occurred in the trunk of the Lorisidae, emerging from this common population. Then, Galagidae have evolved, each species independently, by an accumulation of translocations, mostly Robertsonian, whereas Lorisidae have accumulated pericentric inversions prior diverging.

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PubMed2007

Phylogenetic relationships among the Lorisoidea as indicated by craniodental morphology and mitochondrial sequence data.

The phylogeny of the Afro-Asian Lorisoidea is controversial. While postcranial data attest strongly to the monophyly of the Lorisidae, most molecular analyses portray them as paraphyletic and group the Galagidae alternately with the Asian or African lorisids. One of the problems that has bedevilled phylogenetic analysis of the group in the past is the limited number of taxa sampled for both ingroup families. We present the results of a series of phylogenetic analyses based on 635 base pairs (bp) from two mitochondrial genes (12S and 16S rRNA) with and without 36 craniodental characters, for 11 galagid and five lorisid taxa. The outgroup was the gray mouse lemur (Microcebus murinus). Analyses of the molecular data included maximum parsimony (MP), neighbor joining (NJ), maximum likelihood (ML), and Bayesian methods. The model-based analyses and the combined "molecules+morphology" analyses supported monophyly of the Lorisidae and Galagidae. The lorisids form two geographically defined clades. We find no support for the taxonomy of Galagidae as proposed recently by Groves [Primate Taxonomy, Washington, DC: Smithsonian Institution Press. 350 p, 2001]. The taxonomy of Nash et al. [International Journal of Primatology 10:57-80, 1989] is supported by the combined "molecules+morphology" analysis; however, the model-based analyses suggest that Galagoides may be an assemblage of species united by plesiomorphic craniodental characters.

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