Strepsirrhini

Strepsirrhines[1]
Temporal range: Early Eocene - Recent
Ring-tailed Lemur (Lemur catta)
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Primates
Suborder: Strepsirrhini
E. Geoffroy, 1812
Families

Cheirogaleidae
Lemuridae
Lepilemuridae
Indriidae
Daubentoniidae (Aye-aye)
Lorisidae
Galagidae

The clade Strepsirrhini (New Latin, from Greek strepsis, "a turning" and the stem of rhis, "nose")[2] is one of the two suborders of primates. Madagascar's only non-human primates are strepsirrhines, and others can be found in southeast Asia and Africa. The scientist given credit for the name, Étienne Geoffroy Saint-Hilaire, named it for the retention of the rhinarium, a trait characterized as a wet nose, generally present in mammals. In his catalog of features attributed to the Strepsirrhini, he lists "Les narines terminales et sinueuses" (translated "sinuous, twisted or curly nostrils").[3][Note 1] Strepsirrhines are often characterized by their wet noses, but the etymology of their group name refers to the sinuous openings of the rhinarium's nostrils.

Strepsirrhines are considered by primatologists to have more evolutionarily ancestral features and adaptations than their haplorhine ("dry-nose", in Greek "simple nose") cousins. Their moist nose is connected to the upper lip, which is connected to the gum, limiting the facial expressions they can manage. Their brain to body ratio tends to be smaller, indicating a lower intelligence. Their brain's olfactory lobes are larger, lending to the notion that they have a stronger reliance on smell. Their snouts are generally elongated, giving them a dog-like appearance, although this is true of some monkeys, too. Strepsirrhines have a postorbital bar, unlike haplorrhines. The strepsirrhines have also retained the ability to enzymatically manufacture ascorbic acid, which has been lost by all the haplorrhines, including the Tarsiidae.[4]

With the exception of the aye-aye, all strepsirrhines have a toothcomb—tightly clustered incisors and canine teeth—that is used for grooming. Another grooming adaptation is a toilet-claw on the second toe of all strepsirrhines, while the big toe is widely separated from the others, allowing a vise-like grip for locomotion.

About 75% of species are nocturnal and all of these have a tapetum, a shiny, reflective layer in the backs of their eyes, although several diurnal species, such as the ring-tailed lemur, have it, as well. Many of the nocturnal species also have very sensitive hearing and ears they can move independently, allowing them to capture sounds even better.

Strepsirrhine reproduction differs greatly from haplorrhine reproduction. Instead of an individual cycle, strepsirrhines have a breeding season. They also have a litter of offspring and the females have a Y-shaped (bicornate) uterus and multiple sets of nipples.

Contents

Classification and evolution

The suborder Strepsirrhini is composed of seven families split into two groups. The first group is the infraorder Lemuriformes, five families of primates typically called lemurs. The other two families are split with the lorises, pottos and the galagos in the infraorder Lorisiformes.

As recently as 2005, the aye-aye was tentatively placed in its own infraorder (Chiromyiformes). It was uncertain whether this unique primate split off from the ancestral strepsirrhine line before the lemurs and lorises, or after. If the aye-aye represents a group that is ancestral to all the rest of Strepsirrhini, then it evolved away from the strepsirrhine line between 63 million years ago (mya) (when the strepsirrhines split from the primitive primate line) and 50 mya (the lemur/loris split). If Chiromyiformes is to be considered as the sister only to the lemurs, then it must have evolved after the lemur/loris split 50 mya. In 2008, the aye-aye and its family, Daubentonia, were placed back in infraorder Lemuriformes, making it the fifth lemur family.[5] Molecular research had shown that Aye-ayes were basal to the lemuriform clade.[6]

Early classification schemes broke the Primate order into the suborders Prosimii (prosimians) and Anthropoidea (simians - monkeys and apes). However, the prosimian tarsiers have been shown to be more closely related to the simians. The remaining "prosimians" are now placed in Strepsirrhini, and tarsiers are now united with anthropoids (simians) in Haplorrhini.

Some classifications split Strepsirrhini directly into four superfamilies: Daubentonioidea, Lemuroidea, Loroidea (including Cheirogaleidae) and Indroidea. However, significant evidence suggests Cheirogaleidae is not related to the lorises, and that Indridae is sister-group to Lemuridae.

The strepsirrhine phylogeny has also been elucidated by retrotransposon presence/absence data.

The adapids are an extinct polyphyletic grouping that were most certainly prosimians and closely related to the strepsirrhines. The omomyids are another extinct group of prosmians, but they are believed to be haplorrhines, closely related to the tarsiers, but an outgroup to the rest of the haplorrhines.

As of 2010, there are 125 species of extant strepsirrhine primates, over three-quarters of which are lemurs from Madagascar.[5][7][8]

Notes

  1. ^ Some confuse the comb-shaped lower incisors with the nostrils to arrive at "comb-shaped", and some confuse the nostrils with the nose and strepsis with strephein, "to bend ot turn" to arrive at "bent nose." The nose is not bent, nor are the nostrils comb-shaped, but the nostrils of a rhinarium do generally feature sinuous openings.

References

  1. ^ Groves, C. (2005). "Strepsirrhini". In Wilson, D. E., & Reeder, D. M, eds. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. pp. 111–127. OCLC 62265494. ISBN 0-801-88221-4. http://www.bucknell.edu/msw3/browse.asp?id=12100002. 
  2. ^ "strepsi-". Webster's Third New International Dictionary (Unadbridged ed.). Encyclopædia Britannica, Inc.. 1986. 
  3. ^ Saint-Hilaire, E. Geoffroy (1812). "Suite au tableau de quadrumanes. Seconde famille. Lemuriens. Strepsirrini". Annales du Muséum d'Histoire naturelle (Paris) 19: 156–170. 
  4. ^ Pollock, J. I.; Mullin, R. J. (1987). "Vitamin C biosynthesis in prosimians: Evidence for the anthropoid affinity ofTarsius". American Journal of Physical Anthropology 73 (1): 65–70. doi:10.1002/ajpa.1330730106. PMID 3113259.  edit
  5. ^ a b Mittermeier, R. A.; Ganzhorn, J. U.; Konstant, W. R.; Glander, K.; Tattersall, I.; Groves, C. P.; Rylands, A. B.; Hapke, A. et al. (2008). "Lemur Diversity in Madagascar" (PDF). International Journal of Primatology 29 (6): 1607–1656. doi:10.1007/s10764-008-9317-y. http://www.aeecl.org/documents/28.pdf.  edit
  6. ^ Yoder, A. D.; Vilgalys, R.; Ruvolo, M. (1996). "Molecular evolutionary dynamics of cytochrome b in strepsirrhine primates: The phylogenetic significance of third-position transversions" (PDF). Molecular Biology and Evolution 13 (10): 1339–1350. PMID 8952078. http://mbe.oxfordjournals.org/content/13/10/1339.full.pdf.  edit
  7. ^ Groves, C. (2005). "Lorisidae". In Wilson, D. E., & Reeder, D. M, eds. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. OCLC 62265494. ISBN 0-801-88221-4. http://www.bucknell.edu/msw3/browse.asp?id=12100101. 
  8. ^ Groves, C. (2005). "Galagidae". In Wilson, D. E., & Reeder, D. M, eds. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. OCLC 62265494. ISBN 0-801-88221-4. http://www.bucknell.edu/msw3/browse.asp?id=12100126. 

Bibliography