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PubMedDate not supplied

Activity budget and positional behavior of the Mysore slender loris (Loris tardigradus lydekkerianus): implications for slow climbing locomotion.

Both predator defense and feeding ecology models have been proposed to explain the relatively slow climbing locomotion of the Lorisinae. During a study of the socioecology of the Mysore slender loris (Loris tardigradus lydekkerianus) in Tamil Nadu, India, six categories of behavior and eleven different postures were recorded to estimate a general activity budget for the slender loris, and are examined here particularly in relation to slow climbing locomotor strategies. Reactions to potential predators are also described. The main study population was composed of 15 animals. Activity budgets were compiled in three ways: all instantaneous point samples collected over 1,173 h pooled (n = 13,717), the means of individual lorises (n = 15) and behavior at the moment of first contact (n = 357). No significant difference was found between these three data sets. Approximately 45% of the activity budget was spent in inactive behaviors including sitting vigilant, resting and sleeping. Foraging and traveling comprised nearly half the activity budget, with the rest of the time spent grooming. The most common postures assumed by lorises were sitting and quadrupedal walking. Individual lorises were relatively gregarious and spent up to half their activity budget with other animals. Unlike pottos and angwantibos, lorises did not freeze, head butt or drop from branches in reaction to potential predators, but either ignored them, fled or made loud calls. Cryptic and slow climbing locomotion were used before traveling on open ground between discontinuous substrates, thereby supporting hypotheses relating to predator pressure, and also before capturing fast moving insect prey, supporting hypotheses relating to diet. It is proposed that a divergence in foraging strategies between bushbabies and lorisines may be the best adaptive explanation for their behavioral and morphological differences, including predator defense mechanisms.

Animals↗
PubMed1998

Evolutionary history of lorisiform primates.

We integrate information from the fossil record, morphology, behavior and molecular studies to provide a current overview of lorisoid evolution. Several Eocene prosimians of the northern continents, including both omomyids and adapoids, have been suggested as possible lorisoid ancestors, but these cannot be substantiated as true strepsirhines. A small-bodied primate, Anchomomys, of the middle Eocene of Europe may be the best candidate among putative adapoids for status as a true strepsirhine. Recent finds of Eocene primates in Africa have revealed new prosimian taxa that are also viable contenders for strepsirhine status. Plesiopithecus teras is a Nycticebussized, nocturnal prosimian from the late Eocene, Fayum, Egypt, that shares cranial specializations with lorisoids, but it also retains primitive features (e.g. four premolars) and has unique specializations of the anterior teeth excluding it from direct lorisiform ancestry. Another unnamed Fayum primate resembles modern cheirogaleids in dental structure and body size. Two genera from Oman, Omanodon and Shizarodon, also reveal a mix of similarities to both cheirogaleids and anchomomyin adapoids. Resolving the phylogenetic position of these Africa primates of the early Tertiary will surely require more and better fossils. By the early to middle Miocene, lorisoids were well established in East Africa, and the debate about whether these represent lorisines or galagines is reviewed. Neontological data are used to address the controversial branching sequences among extent lorisid clades. Data from the skin and scent glands, when integrated with other lines of evidence, suggest that Asian and African lorisines share a common lorisine ancestry. The hypothesis of an African clade containing both pottos and galagos to the exclusion of Asian lorisines is less tenable. True galagines are found in the fossil record of Namibia, while true lorisines are known from the Miocene of Asia. The hypothetical branching sequences can be integrated with behavioral and morphological features to develop an adaptive model of lorisoid divergence. By specializing on two different foraging modes early in their radiation, lorisines and galagines subsequently underwent a chain of integrated evolutionary changes eventually having an impact on many components of locomotor behavior, anatomy, physiology, reproduction, life history, and social behavior. Ongoing evolutionary studies of extant galagines are illuminating population phenomena and processes of speciation in an ecological context.

Africa↗
PubMedDate not supplied

Social behaviour of the slender Loris (Loris tardigradus lydekkerianus).

The social behaviour of the nocturnal prosimian Loris tardigradus lydekkerianus in its natural habitat was studied for 21 months in a scrub jungle in Dindigul, southern India. A total of 22834 scans were collected during 2656 hours of observation on identified and unidentified lorises. Social interactions were observed between individuals of all age-sex classes, both during the night and at dawn, when the animals met to sleep together. The majority of aggressive encounters between individuals occurred in territorial and mating contexts. Individuals also communicated with each other through chemical and vocal signals. Adults and sub-adults of both sexes were observed to immigrate into the study area, leading to social interactions with resident individuals.

Aggression↗
PubMedDate not supplied

Mother-infant interactions in slow lorises (Nycticebus bengalensis) and pygmy lorises (Nycticebus pygmaeus).

The study had three purposes: (1) to obtain information about mother-infant interactions in a rarely studied nocturnal prosimian, the pygmy loris (Nycticebus pygmaeus); (2) to compare pygmy lorises with a closely related and better-studied nocturnal prosimian, the Bengal slow loris (Nycticebus bengalensis); and (3) to determine how the presence of a second offspring affected mother-infant interactions in pygmy lorises. Three Bengal slow loris mothers and 3 pygmy loris mothers served as subjects, along with their 10 offspring (4 Bengal slow loris singletons, 2 pygmy loris singletons and 2 sets of pygmy loris twins). Observations were carried out in a zoo research facility for the first 24 weeks of the infants' lives. Although the two species differ in size and reproductive patterns, mother-infant interactions were similar. The primary modes of infant and adult contact were ventral and passive contact, respectively. Mothers parked their infants from the first week, and infants followed from the second week. Mothers displayed little protection or rejection, and there was little aggression. Infants solicited play and social grooming from their mothers. Pygmy loris mothers engaged in social grooming and play with their infants more frequently and for longer periods if the infant was a singleton rather than a twin.

Animals↗
PubMedDate not supplied

Observations of mating, birthing and parental behaviour in three subspecies of slender loris (Loris tardigradus and Loris lydekkerianus ) in India and Sri Lanka.

Studies of the life history parameters of slender lorises in captivity have led to conflicting results regarding gestation length, birth seasonality, interspecies variation in litter size and the degree of parental care given to offspring. During the course of field studies of Loris lydekkerianus lydekkerianus, L. l. nordicus and L. tardigradus tardigradus, data were collected on these life history variables, as well as on behaviours relating to mating. All 3 taxa displayed courtship behaviour involving the pursuit of a female by multiple males. Mating corresponded closely with captive observations, with a period of prolonged single intromissions lasting 3-11 min. One gestation period of 163 days was calculated for L. l. lydekkerianus. Births for all 3 taxa were distributed throughout the year, and males were seen mating throughout the year. All 3 taxa gave birth to singletons and twins; no subspecific pattern in litter size was evident. Females carried infants for the first 4 weeks of life and were regularly attended by males, which groomed both the mother and her offspring. After infants had been parked, female L. l. lydekkerianus and L. l. nordicus rarely returned before dawn, though males visited and played with infants. Female L. t. tardigradus maintained proximity with their infants, whilst males were not observed in proximity to infants during the night. All 3 taxa slept in social groups. High-energy milk, in combination with male care, may aid in the potentially high reproductive output of 4 infants per year.

Animals↗
PubMedDate not supplied

Reproductive biology of the slender loris (Loris lydekkerianus lydekkerianus).

The slender loris (Loris lydekkerianus lydekkerianus), a nocturnal prosimian, was studied for 21 months in its natural habitat of scrub jungle in Dindigul, south India. Here we report on its reproductive biology. Identified and unidentified lorises were observed for a total of 2,656 h. Reproductive seasonality was seen, with births and oestrus observed to be highest in April-June and October-December. The mating system was promiscuous with 1 female mating successively with 3-4 males. A gestation period of 5.5 months and an inter-birth interval of 7 months were recorded. Adult females had a reproductive potential of 4 infants per year. The findings presented in this paper constitute the first information on the life history parameters of wild slender lorises.

Animals↗
PubMed2005

Fluorescence in situ hybridization to chromosomes as a tool to understand human and primate genome evolution.

For the last 15 years molecular cytogenetic techniques have been extensively used to study primate evolution. Molecular probes were helpful to distinguish mammalian chromosomes and chromosome segments on the basis of their DNA content rather than solely on morphological features such as banding patterns. Various landmark rearrangements have been identified for most of the nodes in primate phylogeny while chromosome banding still provides helpful reference maps. Fluorescence in situ hybridization (FISH) techniques were used with probes of different complexity including chromosome painting probes, probes derived from chromosome sub-regions and in the size of a single gene. Since more recently, in silico techniques have been applied to trace down evolutionarily derived chromosome rearrangements by searching the human and mouse genome sequence databases. More detailed breakpoint analyses of chromosome rearrangements that occurred during higher primate evolution also gave some insights into the molecular changes in chromosome rearrangements that occurred in evolution. Hardly any "fusion genes" as known from chromosome rearrangements in cancer cells or dramatic "position effects" of genes transferred to new sites in primate genomes have been reported yet. Most breakpoint regions have been identified within gene poor areas rich in repetitive elements and/or low copy repeats (segmental duplications). The progress in various molecular and molecular-cytogenetic approaches including the recently launched chimpanzee genome project suggests that these new tools will have a significant impact on the further understanding of human genome evolution.

Animals↗
PubMed2006

A re-evaluation of the role of vision in the activity and communication of nocturnal primates.

This paper examines the importance of vision in the lives of nocturnal primates in comparison to diurnal and cathemeral species. Vision is the major sense in all primates and there is evidence that the eyesight of nocturnal species is more acute and variable than has previously been recognized. Case studies of the behaviour of a galago and a loris in open woodland habitats in relation to ambient light show that Galago moholi males are more likely to travel between clumps of vegetation along the ground when the moon is up, and during periods of twilight, whereas they retreat to more continuous vegetation and travel less when the moon sets. This is interpreted as a strategy for avoiding predators that hunt on the ground when it is dark. The travel distances of Loris lydekkerianus are not affected by moonlight but this species reduces its choice of food items from more mobile prey to mainly ants when the moon sets, indicating the importance of light when searching for high-energy supplements to its staple diet. Evidence is presented for the first time to indicate key aspects of nocturnal vision that would benefit from further research. It is suggested that the light and dark facial markings of many species convey information about species and individual identity when animals approach each other at night. Differences in the colour of the reflective eye-shine, and behavioural responses displayed when exposed to white torchlight, point to different kinds of nocturnal vision that are suited to each niche, including the possibility of some degree of colour discrimination. The ability of even specialist nocturnal species to see well in broad daylight demonstrates an inherent flexibility that would enable movement into diurnal niches. The major differences in the sensitivity and perceptual anatomy of diurnal lemurs compared to diurnal anthropoids, and the emergence of cathemerality in lemurs, is interpreted as a reflection of evolution from different ancestral stocks in very different ecosystems, and not a recent shift towards diurnality due to human disturbance.

Animals↗
PubMed1993

Areal, modular, and connectional organization of visual cortex in a prosimian primate, the slow loris (Nycticebus coucang).

Slow lorises (Nycticebus coucang) are nocturnal prosimian (i.e. strepsirhine) primates, closely related to bushbabies (Galago spp.). We examined the organization of visual cortex in four hemispheres from two slow lorises, using connectional and architectonic techniques. All hemispheres were flattened and sections stained for myelin and cytochrome oxidase (CO). Our results indicate, first, that the primary visual area (V1) in slow lorises has a system of small CO-dense blobs, as has been described in most other anthropoid and prosimian primates examined to date. The second visual area (V2) is characterized by broad, stripe-like zones of dense CO staining separated by zones of lighter staining. Loris V2 stripes are less distinct than those of anthropoid primates, and separate classes of thin and thick dark stripes are not apparent. However, V2 stripes are much better developed than in Galago, where they are virtually absent. Injections of wheat-germ agglutinin conjugated to horseradish peroxidase (WGA-HRP) in area V1 revealed reciprocal connections with area V2, and the middle temporal (MT) and dorsolateral (DL) extrastriate areas. Area MT was also identified by its distinctive, dense myelination. As has been reported in anthropoids, DL can be divided into separate caudal and rostral divisions, which differ in myelin and CO staining, and in the strength of their connections with V1. Taken together, our results suggest that many of the features that characterize visual cortex organization in anthropoid primates are present in prosimians and thus probably evolved early in primate history, prior to the diversification of modern primate groups.

Animals↗
PubMed1990

Ontogeny of relationship of middle ear and temporomandibular (squamomandibular) joint in mammals. III. Morphology and ontogeny in scandentia and primates.

The ontogeny of the mandibular joint and the middle ear region was studied in Tupaia javanica, Microcebus murinus, Nycticebus coucang and Tarsius bancanus. During development, a passage connection was found between the mandibular condyle and Meckel's cartilage that is produced by the primordium of the lateral pterygoid muscle. The articular disk is formed separately, and it appears later in development. A theory is presented on the interpretation of these findings.

Animals↗
PubMed1981

The anatomy and phylogenetic significance of the carotid arteries and nerves in strepsirhine primates.

The internal carotid artery in lorisiform primates was identified on the basis of its close association with the internal carotid nerve (postsynaptic sympathetic trunk). An atrophic vessel in the lorisine Arctocebus resembles the internal carotid artery of Lemur in that it enters the tympanic bulla and promontory tube closely associated with the internal carotid nerve. According to this criterion of homology, the enigmatic lorisiform extrabullar carotid artery is not homologous with the internal carotid (promontory) artery of lemuriform primates or the medial internal carotid artery of the dog. Hypotheses about strepsirhine evolution must take these morphological facts into account.

Animals↗
PubMed1983

The karyotype of Galago crassicaudatus is ancestral for lorisiforms.

The karyotype, comprised of 62 chromosomes, of Galago crassicaudatus is described. It is compared to the karyotype of Galago senegalensis and to that of the presumed common ancestor to Lorisiforms, previously reconstructed. Most of the reconstructed chromosomes were found, unmodified, in G. crassicaudatus, strengthening the validity of the reconstruction.

Animals↗
PubMed1983

Learning set formation in slow lorises (Nycticebus coucang).

In primates, learning set formation has been reported in various simian species, but in only few prosimian species. The formation of visual discrimination learning set was tested on a nocturnal prosimian species, slow lorises (Nycticebus coucang). Their performance was higher than that of some New World monkeys. This confirmed the suggestion from the data on black lemurs (Lemur macaco) that there is an overlap between prosimians and simians in learning set ability.

Activity Cycles↗
PubMed1984

Gustatory threshold values of xylitol in primates.

The gustatory threshold values of xylitol solutions were determined in some nonhuman primates and compared with those of humans. Furthermore, the threshold values of xylitol and sucrose were compared.

Animals↗