Prosimii

原猿亜目

関

Propithecus、prosimian、Strepsirhini

　

WordNet

1. not used in all classifications; in some classifications considered coextensive with the Lemuroidea; in others includes both Lemuroidea and Tarsioidea (同)suborder Prosimii
2. in some classifications either coextensive with the Lemuroidea or comprising the true lemurs (同)suborder Strepsirhini
3. primitive primates having large ears and eyes and characterized by nocturnal habits

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/02/15 03:11:59」(JST)

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Strepsirrhines Temporal range: Early Eocene–Recent PreЄ Є O S D C P T J K Pg N
A sample of extant strepsirrhine diversity; 8 biological genera are depicted (from top, left to right): Lemur, Propithecus, Daubentonia, Varecia, Microcebus, Nycticebus, Loris, Otolemur.
Scientific classification
Kingdom:	Animalia
Phylum:	Chordata
Class:	Mammalia
Order:	Primates
Suborder:	Strepsirrhini É. Geoffroy, 1812
Infraorders
†Adapiformes Lemuriformes (See text)
Range of living strepsirrhine primates (green) and Eocene-Miocene fossil sites (red)

Strepsirrhini or Strepsirhini (ⁱ/ˌstrɛpsəˈraɪniː/; STREP-sə-RY-nee) is a suborder of primates that includes the lemuriform primates, which consist of the lemurs of Madagascar, galagos ("bushbabies") and pottos from Africa, and the lorises from India and southeast Asia. Also belonging to the suborder are the extinct adapiform primates, a diverse and widespread group that throve during the Eocene (56 to 34 million years ago [mya]) in Europe, North America, and Asia, but disappeared from most of the Northern Hemisphere as the climate cooled. The last of the adapiforms died out at the end of the Miocene (~7 mya). Adapiforms are sometimes referred to as being "lemur-like", although the diversity of both lemurs and adapiforms do not support this comparison. The two leading taxonomic classifications for the suborder divide living strepsirrhine primates into either two superfamilies (Lemuroidea and Lorisoidea) within the infraorder Lemuriformes or two infraorders, Lemuriformes and Lorisiformes. The suborder represents a related group, and replaced the widely used and now obsolete suborder Prosimii ("prosimians"), which included strepsirrhines and tarsiers, a grouping based primarily on shared anatomical traits. Today, Strepsirrhini excludes the tarsiers, which are now grouped in the other major primate suborder, Haplorhini, along with the monkeys and apes (simians or anthropoids). Strepsirrhines are often inappropriately referred to as "living fossils". Instead, they have evolved for millions of years under natural selection, and have diversified to fill many ecological niches. Some of their traits may be derived from ancestral primates, while others are unique to strepsirrhines.

Strepsirrhines are defined by their wet nose or rhinarium. They also have a smaller brain than comparably sized simians, large olfactory lobes for smell, a vomeronasal organ to detect pheromones, and a bicornuate uterus with an epitheliochorial placenta. Their eyes contain a reflective layer to improve their night vision, and their eye sockets include a ring of bone around the eye, but they lack a wall of thin bone behind it. Strepsirrhine primates produce their own vitamin C, whereas haplorhine primates must obtain it from their diets. Lemuriform primates are characterized by a toothcomb, a specialized set of teeth in the front, lower part of the mouth mostly used for combing fur during grooming. Often, the toothcomb is incorrectly used to characterize all strepsirrhines. Instead, it is unique to lemuriforms and is not seen among adapiforms. Lemuriforms groom orally, and also possess a grooming claw on the second toe of each foot for scratching in areas that are inaccessible to the mouth and tongue. It is unclear whether adapiforms possessed grooming claws.

The taxonomy of strepsirrhines is controversial and has a complicated history. Confused taxonomic terminology and oversimplified anatomical comparisons have created misconceptions about primate and strepsirrhine phylogeny, illustrated by the media attention surrounding the single "Ida" fossil in 2009. Strepsirrhines diverged from the haplorhine primates near the beginning of the primate radiation between 55 and 90 mya. Older divergence dates are based on genetic analysis estimates, while younger dates are based on the scarce fossil record. Lemuriform primates may have evolved from either cercamoniines or sivaladapids, both of which were adapiforms that may have originated in Asia. They were once thought to have evolved from adapids, a more specialized and younger branch of adapiform primarily from Europe. Lemurs rafted to Madagascar between 47 and 54 mya, whereas the lorises split from the African galagos around 40 mya and later colonized Asia. Both living and extinct strepsirrhines are behaviorally diverse, although all are primarily arboreal (tree-dwelling). Most living lemuriforms are nocturnal, while most extinct adapiforms were diurnal. Both living and extinct groups primarily fed on fruit, leaves, and insects. Many of today's strepsirrhines are endangered due to habitat destruction, hunting for bushmeat, and live capture for the exotic pet trade.

Etymology

The taxonomic name Strepsirrhini derives from the Greek στρεψίς (strepsis or "a turning [inward])" and ῥινός (rhinos or "nose"), which refers to the appearance of the sinuous (comma-shaped) nostrils on the rhinarium or wet nose. The name was first used by French naturalist Étienne Geoffroy Saint-Hilaire in 1812 as a subordinal rank comparable to Platyrrhini (New World monkeys) and Catarrhini (Old World monkeys). In his description, he mentioned "Les narines terminales et sinueuses" ("Nostrils terminal and winding").

When British zoologist Reginald Innes Pocock revived Strepsirrhini and defined Haplorhini in 1918, he omitted the second "r" from both ("Strepsirhini" and "Haplorhini" instead of "Strepsirrhini" and "Haplorrhini"), although he did not remove the second "r" from Platyrrhini or Catarrhini, both of which were also named by É. Geoffroy in 1812. Following Pocock, many researchers continued to spell Strepsirrhini with a single "r" until primatologists Paulina Jenkins and Prue Napier pointed out the error in 1987.

Evolutionary history

Primate phylogeny

Euarchonta  Scandentia (treeshrews)  Primatomorpha  Dermoptera (colugos)  Primates  †Plesiadapiformes  Euprimates   Haplorhini  Simians Tarsiers †Omomyiformes  Strepsirrhini  †Adapiformes  Lemuriformes  Lorisoids Lemurs

Strepsirrhines and haplorhines diverged shortly after the emergence of the first true primates (euprimates). The relationship between euprimates, treeshrews, colugos, and plesiadapiforms is less certain. Sometimes plesiadapiforms are grouped with the euprimates under the order Primates, colugos are grouped with primates under Primatomorpha, and all four are grouped under Euarchonta.

Strepsirrhines include the extinct adapiforms and the lemuriform primates, which include lemurs and lorisoids (lorises, pottos, and galagos). The lemuriforms, and particularly the lemurs of Madagascar, are often portrayed inappropriately as "living fossils" or as examples of "basal", or "inferior" primates. These views have historically hindered the understanding of mammalian evolution and the evolution of strepsirrhine traits, such as their reliance on smell (olfaction), characteristics of their skeletal anatomy, and their brain size, which is relatively small. In the case of lemurs, natural selection has driven this isolated population of primates to diversify significantly and fill a rich variety of ecological niches, despite their smaller and less complex brains compared to simians.

The origin of the earliest primates, from which both the strepsirrhines and haplorhines (simians and tarsiers) evolved, is a mystery. Both their place of origin and the group from which they evolved are uncertain. Although the fossil record demonstrating their initial radiation across the Northern Hemisphere is very detailed, the fossil record from the tropics—where primates most likely evolved—is very poor, particularly around the time that primates and other major clades (groups consisting of an ancestor and all its descendants) of eutherian mammals were first appearing. Consequently, geneticists and primatologists have used genetic analyses to determine the relatedness between primate lineages and the amount of time since they diverged. Using this molecular clock, divergence dates for the major primate lineages have suggested that primates evolved more than 80–90 mya, nearly 40 million years before the first primates appear in the fossil record.

Early primates possessed adaptations for arboreal locomotion that enabled maneuvering along fine branches, as seen in this slender loris.

The early primates include both nocturnal and diurnal small-bodied species, and all were arboreal, with hands and feet specially adapted for maneuvering on small branches. Plesiadapiforms from the early Paleocene are sometimes considered "archaic primates" because their teeth resembled those of early primates, and because they possessed arboreal adaptations, such as a divergent hallux (big toe). Although plesiadapiforms were closely related to primates, they may represent a paraphyletic group from which primates may or may not have directly evolved, and some genera may have been more closely related to colugos, also known as dermopterans or "flying lemurs", which are thought to be closely related to primates.

The first true primates (euprimates) do not appear in the fossil record until the early Eocene (~55 mya), at which point they radiated across the Northern Hemisphere during a brief period of rapid global warming known as the Paleocene–Eocene Thermal Maximum. These first primates included Cantius, Donrussellia, Altanius, and Teilhardina on the northern continents, as well as the more questionable (and fragmentary) fossil Altiatlasius from Paleocene Africa. These earliest fossil primates are often divided into two groups, adapiforms (sometimes called adapids, or adapoids) and omomyiforms (or omomyids—suspected relatives of tarsiers). Both appeared suddenly in the fossil record without transitional forms to indicate ancestry, and both groups were rich in diversity and were widespread throughout the Eocene. Although few fossils of extant primate groups—lemuriforms, tarsiers, or simians—are known from the Early to Middle Eocene, evidence from genetics and newer fossil finds suggest they may have been present during this early adaptive radiation. The divergence between strepsirrhines, simians, and tarsiers likely followed almost immediately after primates first evolved.

Adapiform evolution

Notharctus, a type of North American adapiform, resembled lemurs but it did not give rise to them.

Adapiforms are extinct strepsirrhines that shared many anatomical similarities with lemuriforms. They are sometimes referred to as lemur-like primates, although the diversity of both lemurs and adapiforms do not support this analogy. Like living strepsirrhines, adapiforms were extremely diverse, with at least 30 genera and 80 species known from the fossil record as of the early 2000s. They diversified across Laurasia during the Eocene, some reaching North America via a land bridge. They were among the most common mammals found in the fossil beds from that time. A few rare species have also been found in northern Africa. The most basal of the adapiforms include the genera Cantius from North America and Europe and Donrussellia from Europe. The latter bears the most ancestral traits, so it is often considered a sister group or stem group of the other adapiforms.

Adapiforms are often divided into three major groups:

• Adapids were most commonly found in Europe, although the oldest specimens (Adapoides from middle Eocene China) indicate that they most likely evolved in Asia and immigrated. They died out in Europe during the Grande Coupure, part of a significant extinction event at the end of the Eocene.

• Notharctids, which most closely resembled some of Madagascar's lemurs, come from Europe and North America. The European branch is often referred to as cercamoniines. The North American branch thrived during the Eocene, but did not survive into the Oligocene. Like the adapids, the European branch were also extinct by the end of the Eocene.

• Sivaladapids of southern and eastern Asia are best known from the Miocene, and the only adapiforms to survive past the Eocene/Oligocene boundary (~34 mya). Their relationship to the other adapiforms remains unclear. They had vanished before the end of the Miocene (~7 mya).

The relationship between adapiform and lemuriform primates has not been clearly demonstrated, so the position of adapiforms as a paraphyletic stem group is questionable. Both molecular clock data and new fossil finds suggest that the lemuriform divergence from the other primates and the subsequent lemur-lorisoid split both predate the appearance of adapiforms in the early Eocene. Yet new calibration methods may reconcile the discrepancies between the molecular clock and the fossil record, favoring more recent divergence dates. The fossil record suggests that the strepsirrhine adapiforms and the haplorhine omomyiforms had been evolving independently before the early Eocene, although their most basal members share enough dental similarities to suggest that they diverged during the Paleocene (66–55 mya).

Lemuriform evolution

The earliest primates, including early strepsirrhines, diversified across the northern continents during the early Eocene during a period of global warming.

See also: Evolutionary history of lemurs

Lemuriform origins are unclear and debated. American paleontologist Philip Gingerich proposed that lemuriform primates evolved from one of several genera of European adapids based on similarities between the front lower teeth of adapids and the toothcomb of extant lemuriforms; however, this view is not strongly supported due to a lack of clear transitional fossils. Instead, lemuriforms may be descended from a very early branch of Asian cercamoniines or sivaladapids that immigrated to northern Africa.

Until discoveries of three 40-million-year-old fossil lorisoids (Karanisia, Saharagalago, and Wadilemur) in the El Fayum deposits of Egypt between 1997 and 2005, the oldest known lemuriforms had come from the early Miocene (~20 mya) of Kenya and Uganda. These newer finds demonstrate that lemuriform primates were present during the middle Eocene in Afro-Arabia and that the lemuriform lineage and all other strepsirrhine taxa had diverged before then. Djebelemur from Tunisia dates to the late early or early middle Eocene (52 to 46 mya) and has been considered a cercamoniine, but also may have been a stem lemuriform. Azibiids from Algeria date to roughly the same time and may be a sister group of the djebelemurids. Together with Plesiopithecus from the late Eocene Egypt, the three may qualify as the stem lemuriforms from Africa.

Molecular clock estimates indicate that lemurs and the lorisoids diverged in Africa during the Paleocene, approximately 62 mya. Between 47 and 54 mya, lemurs dispersed to Madagascar by rafting. In isolation, the lemurs diversified and filled the niches often filled by monkeys and apes today. In Africa, the lorises and galagos diverged during the Eocene, approximately 40 mya. Unlike the lemurs in Madagascar, they have had to compete with monkeys and apes, as well as other mammals.

Taxonomic classification

The suborder Strepsirrhini was proposed by É. Geoffroy in 1812.

Strepsirrhine primates were first grouped under the genus Lemur by Swedish taxonomist Carl Linnaeus in the 10th edition of Systema Naturae published in 1758. At the time, only three species were recognized, one of which (the colugo) is no longer recognized as a primate. In 1785, Dutch naturalist Pieter Boddaert divided the genus Lemur into two genera: Prosimia for the lemurs, colugos, and tarsiers and Tardigradus for the lorises. Ten years later, É. Geoffroy and Georges Cuvier grouped the tarsiers and galagos due to similarities in their hindlimb morphology, a view supported by German zoologist Johann Karl Wilhelm Illiger, who placed them in the family Macrotarsi while placing the lemurs and tarsiers in the family Prosimia (Prosimii) in 1811. The use of the tarsier-galago classification continued for many years until 1898, when Dutch zoologist Ambrosius Hubrecht demonstrated two different types of placentation (formation of a placenta) in the two groups.

English comparative anatomist William Henry Flower created the suborder Lemuroidea in 1883 to distinguish these primates from the simians, which were grouped under English biologist St. George Jackson Mivart's suborder Anthropoidea (=Simiiformes). According to Flower, the suborder Lemuroidea contained the families Lemuridae (lemurs, lorises, and galagos), Chiromyidae (aye-aye), and Tarsiidae (tarsiers). Lemuroidea was later replaced by Illiger's suborder Prosimii. Many years earlier, in 1812, É. Geoffroy first named the suborder Strepsirrhini, in which he included the tarsiers. This taxonomy went unnoticed until 1918, when Pocock compared the structure of the nose and reinstated the use of the suborder Strepsirrhini, while also moving the tarsiers and the simians into a new suborder, Haplorhini. It was not until 1953, when British anatomist William Charles Osman Hill wrote an entire volume on strepsirrhine anatomy, that Pocock's taxonomic suggestion became noticed and more widely used. Since then, primate taxonomy has shifted between Strepsirrhini-Haplorhini and Prosimii-Anthropoidea multiple times.

Most of the academic literature provides a basic framework for primate taxonomy, usually including several potential taxonomic schemes. Although most experts agree upon phylogeny, many disagree about nearly every level of primate classification.

Competing strepsirrhine taxonomic nomenclature

2 infraorders

3 infraorders

Suborder Strepsirrhini Infraorder †Adapiformes Superfamily †Adapoidea Family †Adapidae Family †Notharctidae Family †Sivaladapidae Infraorder Lemuriformes Superfamily Lemuroidea Family †Archaeolemuridae Family Cheirogaleidae Family Daubentoniidae Family Indriidae Family Lemuridae Family Lepilemuridae Family †Megaladapidae Family †Palaeopropithecidae Superfamily Lorisoidea Family Lorisidae Family Galagidae

Suborder Strepsirrhini Infraorder †Adapiformes Superfamily †Adapoidea Family †Adapidae Family †Notharctidae Family †Sivaladapidae Infraorder Lemuriformes Superfamily Lemuroidea Family †Archaeolemuridae Family Cheirogaleidae Family Daubentoniidae Family Indriidae Family Lemuridae Family Lepilemuridae Family †Megaladapidae Family †Palaeopropithecidae Infraorder Lorisiformes Superfamily Lorisoidea Family Lorisidae Family Galagidae

Subordinal controversies

The most commonly recurring debate in primatology during the 1970s, 1980s, and early 2000s concerned the phylogenetic position of tarsiers compared to both simians and the other prosimians. Tarsiers are most often placed in either the suborder Haplorhini with the simians or in the suborder Prosimii with the strepsirrhines. Prosimii is one of the two traditional primate suborders and is based on evolutionary grades (groups united by anatomical traits) rather than phylogenetic clades, while the Strepsirrhini-Haplorrhini taxonomy was based on evolutionary relationships. Yet both systems persist because the Prosimii-Anthropoidea taxonomy is familiar and frequently seen in the research literature and textbooks.

Strepsirrhines are traditionally characterized by several symplesiomorphic (ancestral) traits not shared with the simians, particularly the rhinarium. Other symplesiomorphies include long snouts, convoluted maxilloturbinals, relatively large olfactory bulbs, and smaller brains. The toothcomb is a synapomorphy (shared, derived trait) seen among lemuriforms, although it is frequently and incorrectly used to define the strepsirrhine clade. Strepsirrhine primates are also united in possessing an epitheliochorial placenta. Unlike the tarsiers and simians, strepsirrhines are capable of producing their own vitamin C and do not need it supplied in their diet. Further genetic evidence for the relationship between tarsiers and simians as a haplorhine clade is the shared possession of three SINE markers.

Because of their historically mixed assemblages which included tarsiers and close relatives of primates, both Prosimii and Strepsirrhini have been considered wastebasket taxa for "lower primates". Regardless, the strepsirrhine and haplorrhine clades are generally accepted and viewed as the preferred taxonomic division. Yet, tarsiers still closely resemble both strepsirrhines and simians in different ways, and since the early split between strepsirrhines, tarsiers, and simians is ancient and hard to resolve, a third taxonomic arrangement with three suborders is sometimes used: Prosimii, Tarsiiformes, and Anthropoidea. More often, the term "prosimian" is no longer used in official taxonomy, but is still used to illustrate the behavioral ecology of tarsiers relative to the other primates.

In addition to the controversy over tarsiers, the debate over the origins of simians once called the strepsirrhine clade into question. Arguments for an evolutionary link between adapiforms and simians made by paleontologists Gingerich, Elwyn Simons, Tab Rasmussen, and others could have potentially excluded adapiforms from Strepsirrhini. In 1975, Gingerich proposed a new suborder, Simiolemuriformes, to suggest that strepsirrhines are more closely related to simians than tarsiers. However, no clear relationship between the two had been demonstrated by the early 2000s. The idea reemerged briefly in 2009 during the media attention surrounding Darwinius masillae (dubbed "Ida"), a cercamoniine from Germany that was touted as a "missing link between humans and earlier primates" (simians and adapiforms). However, the cladistic analysis was flawed and the phylogenetic inferences and terminology were vague. Although the authors noted that Darwinius was not a "fossil lemur", they did emphasize the absence of a toothcomb, which adapiforms did not possess.

Infraordinal classification and clade terminology

Strepsirrhini phylogeny

†Adapiformes stem lemuriforms lemuriforms or  crown strepsirrhines   lemuroid clade  Daubentoniidae other lemurs  lorisoid clade  lorises galagos

Within Strepsirrhini, two common classifications include either two infraorders (Adapiformes and Lemuriformes) or three infraorders (Adapiformes, Lemuriformes, Lorisiformes). A less common taxonomy places the aye-aye (Daubentoniidae) in its own infraorder, Chiromyiformes. In some cases, plesiadapiforms are included within the order Primates, in which case Euprimates is sometimes treated as a suborder, with Strepsirrhini becoming an infraorder, and the Lemuriformes and others become parvorders. Regardless of the infraordinal taxonomy, Strepsirrhini is composed of three ranked superfamilies and 14 families, seven of which are extinct. Three of these extinct families included the recently extinct giant lemurs of Madagascar, many of which died out within the last 1,000 years following human arrival on the island.

The media attention over "Ida" played upon confused terminology and misconceptions about strepsirrhines.

When Strepsirrhini is divided into two infraorders, the clade containing all toothcombed primates can be called "lemuriforms". When it is divided into three infraorders, the term "lemuriforms" refers only to Madagascar's lemurs, and the toothcombed primates are referred to as either "crown strepsirrhines" or "extant strepsirrhines". Confusion of this specific terminology with the general term "strepsirrhine", along with oversimplified anatomical comparisons and vague phylogenetic inferences, can lead to misconceptions about primate phylogeny and misunderstandings about primates from the Eocene, as seen with the media coverage of Darwinius. Because the skeletons of adapiforms share strong similarities with those of lemurs and lorises, researchers have often referred to them as primitive strepsirrhines, lemur ancestors, or a sister group to the living strepsirrhines. They are included in Strepsirrhini, and are considered basal members of the clade. Although their status as true primates is not questioned, the questionable relationship between adapiforms and other living and fossil primates leads to multiple classifications within Strepsirrhini. Often, adapiforms are placed in their own infraorder due to anatomical differences with lemuriforms and their unclear relationship. When shared traits with lemuriforms (which may or may not be synapomorphic) are emphasized, they are sometimes reduced to families within the infraorder Lemuriformes (or superfamily Lemuroidea).

The first fossil primate described was the adapiform Adapis parisiensis by French naturalist Georges Cuvier in 1821, who compared it to a hyrax ("le Daman"), then considered a member of a now obsolete group called pachyderms. It was not recognized as a primate until it was reevaluated in the early 1870s. Originally, adapiforms were all included under the family Adapidae, which was divided into two or three subfamilies: Adapinae, Notharctinae, and sometimes Sivaladapinae. All North American adapiforms were lumped under Notharctinae, while the Old World forms were usually assigned to Adapinae. Around the 1990s, two distinct groups of European "adapids" began to emerge, based on differences in the postcranial skeleton and the teeth. One of these two European forms was identified as cercamoniines, which were allied with the notharctids found mostly in North America, while the other group falls into the traditional adapid classification. The three major adapiform divisions are now typically regarded as three families within Adapiformes (Notharctidae, Adapidae and Sivaladapidae), but other divisions ranging from one to five families are used as well.

Anatomy and physiology

Strepsirrhines have a reflective layer in the eye, called a tapetum lucidum that helps them see better at night.

All lemuriforms possess a specialized dental structure called a toothcomb, with the exception of the aye-aye, in which the structure has been modified into two continually growing (hypselodont) incisors (or canine teeth), similar to those of rodents. The toothcomb consists of either two or four procumbent lower incisors and procumbent lower canine teeth followed by a canine-shaped premolar. It is used to comb the fur during oral grooming. Shed hairs that accumulate between the teeth of the toothcomb are removed by the sublingua or "under-tongue". Lemuriforms also possess a grooming claw on the second digit of each foot for scratching. Adapiforms did not possess a toothcomb. Instead, their lower incisors varied in orientation—from somewhat procumbent to somewhat vertical—and the lower canines were projected upwards and were often prominent. Adapiforms may have had a grooming claw, but there is little evidence of this.

Like all primates, strepsirrhine orbits (eye sockets) have a postorbital bar, a protective ring of bone created by a connection between the frontal and zygomatic bones. Both living and extinct strepsirrhines lack a thin wall of bone behind the eye, referred to as postorbital closure, which is only seen in haplorhine primates. Although the eyes of strepsirrhines point forward, giving stereoscopic vision, the orbits do not face fully forward. Among living strepsirrhines, most or all species are thought to possess a reflective layer behind the retina of the eye, called a tapetum lucidum, which improves vision in low light, but they lack a fovea, which improves day vision. This differs from tarsiers, which lack a tapetum lucidum but possess a fovea.

Strepsirrhines are characterized by a typically longer snout and wet nose compared to haplorhine primates.

Strepsirrhine primates have a brain relatively comparable to or slightly larger in size than most mammals. Compared to simians, however, they have a relatively small brain-to-body size ratio. Strepsirrhines are also traditionally noted for their unfused mandibular symphysis (two halves of the lower jaw), however, fusion of the mandibular symphysis was common in adapiforms, notably Notharctus. Also, several extinct giant lemurs exhibited a fused mandibular symphysis.

Many nocturnal species have large, independently movable ears, although there are significant differences in sizes and shapes of the ear between species. The structure of the middle and inner ear of strepsirrhines differs between the lemurs and lorisoids. In lemurs, the tympanic cavity, which surrounds the middle ear, is expanded. This leaves the ectotympanic ring, which supports the eardrum, free within the auditory bulla. This trait is also seen in adapiforms. In lorisoids, however, the tympanic cavity is smaller and the ectotympanic ring becomes attached to the edge of the auditory bulla. The tympanic cavity in lorisoids also has two accessory air spaces, which are not present in lemurs. Both lorisoids and cheirogaleid lemurs have replaced the internal carotid artery with an enlarged ascending pharyngeal artery. Strepsirrhines also possess distinctive features in their tarsus (ankle bones) that differentiate them from haplorhines, such as a sloping talo-fibular facet (the face where the talus bone and fibula meet) and a difference in the location of the position of the flexor fibularis tendon on the talus. These differences give strepsirrhines the ability to make more complex rotations of the ankle and indicate that their feet are habitually inverted, or turned inward, an adaptation for grasping vertical supports.

Sexual dichromatism (different coloration patterns between males and females) can be seen in most brown lemur species, but otherwise lemurs show very little if any difference in body size or weight between sexes. This lack of sexual dimorphism is not characteristic of all strepsirrhines. Some adapiforms were sexually dimorphic, with males bearing a larger sagittal crest (a ridge of bone on the top of the skull to which jaw muscles attach) and canine teeth. Lorisoids exhibit some sexual dimorphism, but males are typically no more than 20 percent larger than females.

Rhinarium and olfaction

The noses of five prosimian primates: A) dwarf lemur, B) greater galago, C) lesser galago, D) aye-aye, and E) a tarsier.

A through D possess a rhinarium and are strepsirrhines, whereas E does not and is a haplorhine.

Strepsirrhines have a long snout that ends in a moist and touch-sensitive rhinarium, similar to that of dogs and many other mammals. The rhinarium is surrounded by vibrissae that are also sensitive to touch. Convoluted maxilloturbinals on the inside of their nose filter, warm, and moisten the incoming air, while olfactory receptors of the main olfactory system lining the ethmoturbinals detect airborne smells. The olfactory bulbs of lemurs are comparable in size to those of other arboreal mammals.

The surface of the rhinarium does not have any olfactory receptors, so it is not used for smell in terms of detecting volatile substances. Instead, it has sensitive touch receptors (Merkel cells). The rhinarium, upper lip, and gums are tightly connected by a fold of mucous membrane called the philtrum, which runs from the tip of the nose to the mouth. The upper lip is constrained by this connection and has fewer nerves to control movement, which leaves it less mobile than the upper lips of simians. The philtrum creates a gap (diastema) between the roots of the first two upper incisors.

The strepsirrhine rhinarium can collect relatively non-volatile, fluid-based chemicals (traditionally categorized as pheromones) and transmit them to the vomeronasal organ (VNO), which is located below and in front of the nasal cavity, above the mouth. The VNO is an encased duct-like structure made of cartilage and is isolated from the air passing through the nasal cavity. The VNO is connected to the mouth through nasopalatine ducts (also known as the incisive foramen), which pass through the hard palate at the top, front of the mouth. Fluids traveling from the rhinarium to the mouth and then up the nasopalatine ducts to the VNO are detected, and information is relayed to the accessory olfactory bulb, which is relatively large in strepsirrhines. From the accessory olfactory bulb, information is sent to the amygdala, which handles emotions, and then to the hypothalamus, which handles basic body functions and metabolic processes. This neural pathway differs from that used by the main olfactory system.

All lemuriforms have a VNO, as do tarsiers and some New World monkeys. Adapiforms exhibit the gap between the upper incisors, which indicates the presence of a VNO, but there is some disagreement over whether or not they possessed a rhinarium.

Reproductive physiology

Extant strepsirrhines have an epitheliochorial placenta, where the maternal blood does not come in direct contact with the fetal chorion like it does in the hemochorial placenta of haplorhines. The strepsirrhine uterus has two distinct chambers (bicornuate). Despite having similar gestation periods to comparably sized haplorhines, fetal growth rates are generally slower in strepsirrhines, which results in newborn offspring that are as little as one-third the size of haplorhine newborns. Extant strepsirrhines also have a lower basal metabolic rate, which elevates in females during gestation, putting greater demands on the mother.

Most primates have two mammary glands, but the number and positions vary between species within strepsirrhines. Lorises have two pairs, while others, like the ring-tailed lemur, have one pair on the chest (pectoral). The aye-aye also has two mammary glands, but they are located near the groin (inguinal). In females, the clitoris is sometimes enlarged and pendulous, resembling the male penis, which can make gender identification difficult for human observers. The clitoris may also have a bony structure in it, similar to the baculum (penis bone) in males. Most male primates have a baculum, but it is typically larger in strepsirrhines and usually forked at the tip.

Behavior

Like other primates, infants often cling to their mother's fur.

Approximately three-quarters of all extant strepsirrhine species are nocturnal, sleeping in nests made from dead leaves or tree hollows during the day. All of the lorisoids from continental Africa and Asia are nocturnal, a circumstance that minimizes their competition with the simian primates of the region, which are diurnal. The lemurs of Madagascar, living in the absence of simians, are more variable in their activity cycles. The aye-aye, mouse lemurs, woolly lemurs, and sportive lemurs are nocturnal, while ring-tailed lemurs and most of their kin, sifakas, and indri are diurnal. Yet some or all of the brown lemurs (Eulemur) are cathemeral, which means they may be active during the day or night, depending on factors such as temperature and predation. Many extant strepsirrhines are well adapted for nocturnal activity due to their relatively large eyes; large, movable ears; sensitive tactile hairs; strong sense of smell; and the tapetum lucidum behind the retina. Among the adapiforms, most are considered diurnal, with the exception of Pronycticebus and Godinotia from Middle Eocene Europe, both of which had large orbits that suggest nocturnality.

Reproduction in most strepsirrhine species tends to be seasonal, particularly in lemurs. Key factors that affect seasonal reproduction include the length of the wet season, subsequent food availability, and the maturation time of the species. Like other primates, strepsirrhines are relatively slow breeders compared to other mammals. Their gestation period and interbirth intervals are usually long, and the young develop slowly, just like in haplorhine primates. Unlike simians, some strepsirrhines produce two or three offspring, although some produce only a single offspring. Those that produce multiple offspring tend to build nests for their young. These two traits are thought to be plesiomorphic (ancestral) for primates. The young are precocial (relatively mature and mobile) at birth, but not as coordinated as ungulates (hoofed mammals). Infant care by the mother is relatively prolonged compared to many other mammals, and in some cases, the infants cling to the mother's fur with their hands and feet.

Despite their relatively smaller brains compared to other primates, lemurs have demonstrated levels of technical intelligence in problem solving that are comparable to those seen in simians. However, their social intelligence differs, often emphasizing within-group competition over cooperation, which may be due to adaptations for their unpredictable environment. Although lemurs have not been observed using objects as tools in the wild, they can be trained to use objects as tools in captivity and demonstrate a basic understanding about the functional properties of the objects they are using.

Social systems and communication

The nocturnal strepsirrhines have been traditionally described as "solitary", although this term is no longer favored by the researchers who study them. Many are considered "solitary foragers", but many exhibit complex and diverse social organization, often overlapping home ranges, initiating social contact at night, and sharing sleeping sites during the day. Even the mating systems are variable, as seen in wooly lemurs, which live in monogamous breeding pairs. Because of this social diversity among these solitary but social primates, whose level of social interaction is comparable to that of diurnal simians, alternative classifications have been proposed to emphasize their gregarious, dispersed, or solitary nature.

Among extant strepsirrhines, only the diurnal and cathemeral lemurs have evolved to live in multi-male/multi-female groups, comparable to most living simians. This social trait, seen in two extant lemur families (Indriidae and Lemuridae), is thought to have evolved independently. Group sizes are smaller in social lemurs than in simians, and despite the similarities, the community structures differ. Female dominance, which is rare in simians, is fairly common in lemurs. Strepsirrhines spend a considerable amount of time grooming each other (allogrooming). When lemuriform primates groom, they lick the fur and then comb it with their toothcomb. They also use their grooming claw to scratch places they cannot reach with their mouth.

Like New World monkeys, strepsirrhines rely on scent marking for much of their communication. This involves smearing secretions from epidermal scent glands on tree branches, along with urine and feces. In some cases, strepsirrhines may anoint themselves with urine (urine washing). Body postures and gestures may be used, although the long snout, non-mobile lips, and reduced facial enervation restrict the use of facial expressions in strepsirrhines. Short-range calls, long-range calls, and alarm calls are also used. Nocturnal species are more constrained by the lack of light, so their communication systems differ from those of diurnal species, often using long-range calls to claim their territory.

Locomotion

Dwarf lemurs (top) are arboreal quadrupeds while galagos (bottom) favor vertical clinging and leaping.

Living strepsirrhines are predominantly arboreal, with only the ring-tailed lemur spending considerable time on the ground. Most species move around quadrupedally (on four legs) in the trees, including five genera of smaller, nocturnal lemurs. Galagos, indriids, sportive lemurs, and bamboo lemurs leap from vertical surfaces, and the indriids are highly specialized for vertical clinging and leaping. Lorises are slow-moving, deliberate climbers.

Analyses of extinct adapiforms postcranial skeletons suggest a variety of locomotor behavior. The European adapids Adapis, Palaeolemur, and Leptadapis shared adaptations for slow climbing like the lorises, although they may have been quadrupedal runners like small New World monkeys. Both Notharctus and Smilodectes from North America and Europolemur from Europe exhibit limb proportions and joint surfaces comparable to vertical clinging and leaping lemurs, but were not as specialized as indriids for vertical clinging, suggesting that they ran along branches and did not leap as much. Notharctids Cantius and Pronycticebus appear to have been agile arboreal quadrupeds, with adaptations comparable to the brown lemurs.

Diet

Primates primarily feed on fruits (including seeds), leaves (including flowers), and animal prey (arthropods, small vertebrates, and eggs). Diets vary markedly between strepsirrhine species. Like other leaf-eating (folivorous) primates, some strepsirrhines can digest cellulose and hemicellulose. Some strepsirrhines, such as the galagos, slender lorises, and angwantibos are primarily insectivorous. Other species, such as fork-marked lemurs and needle-clawed bushbabies, specialize on tree gum, while indriids, sportive lemurs, and bamboo lemurs are folivores. Many strepsirrhines are frugivores (fruit eaters), and others, like the ring-tailed lemur and mouse lemurs, are omnivores, eating a mix of fruit, leaves, and animal matter.

Among the adapiforms, frugivory seems to have been the most common diet, particularly for medium-sized to large species, such as Cantius, Pelycodus and Cercamonius. Folivory was also common among the medium and large-sized adapiforms, including Smilodectes, Notharctus, Adapis and Leptadapis. Sharp cusps on the teeth of some of the smaller adapiforms, such as Anchomomys and Donrussellia, indicate that they were either partly or primarily insectivorous.

Distribution and habitat

Before their extinction, adapiform primates were primarily found across North America, Asia, and Europe, with a few species in Africa. They flourished during the Eocene when those regions were more tropical in nature, and they disappeared when the climate became cooler and drier. Today, the lemuriforms are confined in the tropics, ranging between 28° S to 26° N latitude. Lorises are found both in equatorial Africa and Southeast Asia, while the galagos are limited to the forests and woodlands of sub-Saharan Africa. Lemurs are endemic to Madagascar, although much of their diversity and habitat has been lost due to recent human activity.

As with nearly all primates, strepsirrhines typically reside in tropical rainforests. These habitats allow strepsirrhines and other primates to evolve diverse communities of sympatric species. In the eastern rainforests of Madagascar, as many as 11 or 12 species share the same forests, and prior to human arrival, some forests had nearly double that diversity. Several species of lemur are found in drier, seasonal forests, including the spiny forest on the southern tip of the island, although the lemur communities in these regions are not as rich.

Conservation

Strepsirrhines are threatened by deforestation in tropical regions.

See also: Conservation of slow lorises and Lemur#Conservation

Like all other primates, strepsirrhines face an elevated risk of extinction due to human activity, particularly deforestation in tropical regions. Much of their habitat has been converted for human use, such as agriculture and pasture. The threats facing strepsirrhine primates fall into three main categories: habitat destruction, hunting (for bushmeat or traditional medicine), and live capture for export or local exotic pet trade. Although hunting is often prohibited, the laws protecting them are rarely enforced. In Madagascar, local taboos known as fady sometimes help protect lemur species, although some are still hunted for traditional medicine.

In 2012, the International Union for Conservation of Nature (IUCN) announced that lemurs were the "most endangered mammals", due largely to elevated illegal logging and hunting following a political crisis in 2009. In Southeast Asia, slow lorises are threatened by the exotic pet trade and traditional medicine, in addition to habitat destruction. Both lemurs and slow lorises are protected from commercial international trade under CITES Appendix I.

Notes

References

Literature cited

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English Journal

• Characterizing cryptic species: A morphometric analysis of craniodental characters in the dwarf galago genus Galagoides.

• Masters JC1, Couette S2.
• American journal of physical anthropology.Am J Phys Anthropol.2015 Jul 14. doi: 10.1002/ajpa.22792. [Epub ahead of print]
• OBJECTIVES: The true dwarf galagos of the genus Galagoides, G. demidoff and G. thomasi, are difficult to distinguish morphologically at a specific or subspecific level, and most taxonomic designations are based primarily on geographic localities. We used morphometrics to investigate the morphologica
• PMID 26173582

• MHC class II variation in a rare and ecological specialist mouse lemur reveals lower allelic richness and contrasting selection patterns compared to a generalist and widespread sympatric congener.

• Pechouskova E1, Dammhahn M, Brameier M, Fichtel C, Kappeler PM, Huchard E.
• Immunogenetics.Immunogenetics.2015 Apr;67(4):229-45. doi: 10.1007/s00251-015-0827-4. Epub 2015 Feb 18.
• The polymorphism of immunogenes of the major histocompatibility complex (MHC) is thought to influence the functional plasticity of immune responses and, consequently, the fitness of populations facing heterogeneous pathogenic pressures. Here, we evaluated MHC variation (allelic richness and divergen
• PMID 25687337

• Species-specific transmission of novel picornaviruses in lemurs.

• Lim ES1, Deem SL2, Porton IJ3, Cao S1, Wang D4.
• Journal of virology.J Virol.2015 Apr;89(7):4002-10. doi: 10.1128/JVI.03342-14. Epub 2015 Jan 28.
• The roles of host genetics versus exposure and contact frequency in driving cross-species transmission remain the subject of debate. Here, we used a multitaxon lemur collection at the Saint Louis Zoo in the United States as a model to gain insight into viral transmission in a setting of high intersp
• PMID 25631076

• Hearing and age-related changes in the gray mouse lemur.

• Schopf C1, Zimmermann E, Tünsmeyer J, Kästner SB, Hubka P, Kral A.
• Journal of the Association for Research in Otolaryngology : JARO.J Assoc Res Otolaryngol.2014 Dec;15(6):993-1005. doi: 10.1007/s10162-014-0478-4. Epub 2014 Aug 12.
• In order to examine auditory thresholds and hearing sensitivity during aging in the gray mouse lemur (Microcebus murinus), suggested to represent a model for early primate evolution and Alzheimer research, we applied brainstem-evoked response audiometry (BERA), traditionally used for screening heari
• PMID 25112886

Japanese Journal

• Introduction to diversity and speciation in the Prosimii

• ZIMMERMANN E
• Int J Primatol 21, 789-791, 2000
• NAID 30012156854

• スロ-ロリスの浅指屈筋の2元性〔英文〕

• 山田 格
• Bulletin of the National Science Museum Ser. A Zoology 21(3), p189-201, 1995-09
• … This last branch, with which the exact identification of the muscle is achieved, has not been described in Prosimii by any preceding authors. …
• NAID 110004311833

• A remarkable cranium of Pleisopithecus teras (Primates, Prosimii) from the Eocene of Egypt

• SIMONS E. L.
• Proceedings of National Academy of Science of the United States of America 91, 9946-9950, 1994
• NAID 30016297535

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リンク元	「Strepsirhini」「Propithecus」「原猿亜目」「prosimian」

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