Petter's big-footed mouse

Petter's big-footed mouse
Scientific classification
M. petteri
Binomial name
Macrotarsomys petteri
Goodman and Soarimalala, 2005
Macrotarsomys petteri range.svg
Range of Macrotarsomys petteri on Madagascar. Red: find of a living animal; green: subfossil material; blue: subfossil material that is possibly referable to this species

Macrotarsomys petteri, also known as Petter's Big-footed Mouse,[1] is a Malagasy rodent in the genus Macrotarsomys. With a head and body length of 150 mm (5.9 in) and body mass of 105 g (3.7 oz), Macrotarsomys petteri is the largest species of its genus. The upperparts are brown, darkest in the middle of the back, and the underparts are white to yellowish. The animal has long whiskers, short forelimbs, and long hindfeet. The tail ends in a prominent tuft of long, light hairs. The skull is robust and the molars are low-crowned and cuspidate.

Macrotarsomys petteri is now found only in the Mikea Forest of southwestern Madagascar, but subfossil records indicate that it was previously more widely distributed in southern Madagascar. Climatic changes and competition with introduced species may have led to the shift in its distribution. The Mikea Forest, the only place where it is still known to occur, is threatened by human development.


During a 2003 biological inventory of the Mikea Forest, a forest region of southwestern Madagascar, a single specimen of the rodent genus Macrotarsomys was collected.[2] This animal turned out to be distinct from both previously known species of the genus—Macrotarsomys bastardi, which is widespread in western Madagascar, and the larger Macrotarsomys ingens, known only from the Ankarafantsika National Park. Accordingly, Steven Goodman and Voahangy Soarimalala named it in 2005 as a new species, Macrotarsomys petteri.[3] The specific name, petteri, honors French zoologist François Petter for his contributions to the study of Malagasy rodents.[4] M. petteri, the largest species in the genus, is most similar to M. ingens, which may be its closest relative.[5]


Macrotarsomys petteri is a terrestrial rodent with short forelimbs and long hindfeet.[6] With a head and body length of 150 mm (5.9 in) and body mass of 105 g (3.7 oz) in the only known complete specimen,[7] it is much larger than M. bastardi, and its measurements fall at or above the upper end of the known range of variation in M. ingens.[4] The upperparts are covered with soft and short, brown fur. Most cover hairs (the main part of the fur) are dark brown for the two-thirds closest to the base, then light brown, with a short dark brown tip. The middle of the back appears darker, because the cover hairs there are entirely dark brown. The hairs are 6 to 8 mm (0.2 to 0.3 in) long on the shoulders and 7 to 9 mm (0.3 to 0.4 in) on the back. The guard hairs are gray. Because the flanks lack entirely dark cover hairs, they are slightly lighter than the rest of the upperparts. They are sharply separated in color from the underparts, which are entirely white to buffish. The mystacial vibrissae (whiskers above the mouth) are long, up to 60 mm (2.4 in), and white or black in color. The pinnae (external ears) are dark brown and covered with fine gray hairs,[8] and ear length is 32 mm (1.3 in).[7]

Hindfoot length is 37 mm (1.5 in).[7] The upper sides of the feet are covered with grayish white fur, which extends around the claws to form ungual tufts. On the hindfeet, the fifth digit is relatively short at 6 mm (0.2 in); the hallux (first digit) is 8 mm (0.3 in) long, and the other digits 11 to 12 mm (0.4 to 0.5 in).[9] The tail is 238 mm (9.4 in) long[7] and naked in part.[8] At the base, it is dark brown both above and below, but slightly lighter below. The upper side remains dark brown for much of its length, though the color does become lighter towards the tip. The lower side becomes mottled at about 55 mm (2.2 in) from the tip and then whitish at about 65 mm (2.6 in). Macrotarsomys petteri has a well-developed tuft at its tail tip, consisting of whitish and occasional light brown hairs. This tuft commences at about 130 mm (5.1 in) from the base with fairly short hairs and becomes more pronounced at 180 mm (7.1 in).[10] In contrast, M. ingens has a weaker, dark brown tuft.[4]

Macrotarsomys petteri has a large and robust skull with well-developed zygomatic arches (cheekbones).[10] The interorbital region of the skull (between the eyes) is smooth, as in M. ingens, and lacks the shelves characteristic of M. bastardi. The palate is broad and the incisive foramina (openings in the front portion of the palate) are long and broad.[4] In the mandible (lower jaw), the root of the lower incisor is housed in a distinct capsular process, a protuberance at the back of the jawbone. The lower masseteric ridge (a crest on the outer side of the mandible) is prominent.[11] As is typical of Macrotarsomys, the molars are cuspidate and low-crowned.[4]

Distribution and ecology

The single known living specimen, a young adult male, was collected at 80 m (260 ft) altitude in the Andaladomo forest (part of the Mikea Forest).[6] The Andaladomo forest is different in vegetation from the rest of the Mikea Forest, and is similar to forests further to the north on Madagascar.[12] The animal was found in an isolated fragment of dry deciduous forest amid land cleared for maize cultivation. The trap was set at the foot of a tree surrounded by bushes and succulent plants.[6] Other small mammals known from the Mikea Forest include Macrotarsomys bastardi, the introduced black rat (Rattus rattus), several species of tenrecs, and the shrew Suncus madagascariensis.[5] Although only a single individual of M. petteri was caught during Goodman and Soarimalala's survey, which accrued 3100 trap-nights, they argue that this does not necessarily mean the species is rare, since trapping rates for rodents in the dry forests of Madagascar are often variable depending on year and season.[12] Nothing is known of its behavior, but the animal's morphology suggests it lives on the ground.[13]

Subsequent to its discovery at the Mikea Forest, Macrotarsomys petteri was also found as a subfossil in cave deposits at Andrahomana in far southeastern Madagascar, a find reported in 2006.[14] There, it was found together with more abundant remains of the introduced black rat and house mouse (Mus musculus), as well as indigenous rodents such as Macrotarsomys bastardi. Two M. petteri bones were radiocarbon dated to 790–410 BCE and 150–390 CE, respectively, a period when the local climate became drier and humans first appeared.[11] Macrotarsomys species are thought to burrow in sandy ground and would not be expected to enter caves; therefore, the subfossils are probably remains of animals eaten by birds of prey. Although M. petteri could conceivably persist in remnant pockets of wet habitat in southeastern Madagascar, searches at two sites near Andrahomana failed to confirm its presence. It may have become locally extinct in the area because of the drying climate and competition with the black rat.[15]

In 2009, Macrotarsomys petteri was also recorded from the cave of Ankilitelo in southwestern Madagascar.[16] Remains of a large Macrotarsomys had previously been reported from other southern Madagascar sites, and at least some of these may be M. petteri.[17] A karstic deposit near Lake Tsimanampetsotsa (dated to the Late Pliocene or Early Pleistocene on unclear grounds) contained three species of Macrotarsomys, including a very large one that may well be M. petteri. Remains identified as Macrotarsomys ingens have been reported from a cave at Ankazoabo in southern Madagascar; these may also be M. petteri.[5]

Conservation status

The IUCN Red List assesses Macrotarsomys petteri as "Data Deficient", but notes that the species will very probably qualify as threatened if its current distribution turns out to be restricted to primary forest in the Mikea Forest. The Mikea Forest is one of the largest remaining forests of southwestern Madagascar, but it is not protected and is threatened by logging, pasture, and conversion to agricultural land.[1]


  1. ^ a b c Goodman, 2008
  2. ^ Goodman and Soarimalala, 2005, p. 452
  3. ^ Goodman and Soarimalala, 2005, p. 453
  4. ^ a b c d e Goodman and Soarimalala, 2005, p. 457
  5. ^ a b c Goodman and Soarimalala, 2005, p. 459
  6. ^ a b c Goodman and Soarimalala, 2005, p. 454
  7. ^ a b c d Goodman and Soarimalala, 2006, table 1
  8. ^ a b Goodman and Soarimalala, 2005, p. 455
  9. ^ Goodman and Soarimalala, 2005, pp. 455–456
  10. ^ a b Goodman and Soarimalala, 2005, p. 456
  11. ^ a b Goodman et al., 2006, p. 957
  12. ^ a b Goodman and Soarimalala, 2005, p. 460
  13. ^ Garbutt, 2007, p. 242
  14. ^ Goodman et al., 2006, p. 753
  15. ^ Goodman et al., 2006, p. 960
  16. ^ Muldoon et al., 2009, p. 1120
  17. ^ Goodman and Soarimalala, 2005, p. 459; Goodman et al., 2006, p. 960

Literature cited