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Record W4242794810 · doi:10.2307/3504373

Mormopterus petrophilus

2002· article· en· W4242794810 on OpenAlexaboutno aff
David S. Jacobs, M. Brock Fenton

Bibliographic record

VenueMammalian Species · 2002
Typearticle
Languageen
FieldAgricultural and Biological Sciences
TopicFish Biology and Ecology Studies
Canadian institutionsnot available
Fundersnot available
KeywordsEnvironmental scienceChemistry

Abstract

fetched live from OpenAlex

NyctinomusGeoffroy Saint-Hillaire, 1818:114. Type species Nyctinomus aegyptiacus. MolossusGray, 1839:7. Type species Molossus norfolkensis. Mormopterus Peters in Sclater, 1865:468. Type species Nyctinomus jugularis Peters. PlatymopsRoberts, 1917:5. Type species Platymops petrophilus. MicronomusIredale and Troughton, 1934:100. Type species Molossus norfolkensis Gray. SauromysPeterson, 1965:12. Based on Platymops petrophilus Roberts. Order Chiroptera, suborder Microchiroptera, family Molossidae. The genus Mormopterus contains 11 species. Classification of Mormopterus species from Australia is in flux because undescribed taxa may be present (Churchill 1998). Skull extremely flattened; occurs in Africa ----------------------------------------------------- 2 Skull not extremely flattened; mostly not in Africa ----------------------------------------------------- 3 Forearm with wartlike granulations; length of forearm 29–36 mm ----------------------------------------------------- M. setiger Forearm lacking wartlike granulations; length of forearm 38–48 mm ----------------------------------------------------- M. petrophilus Known from the New World ----------------------------------------------------- 4 Not known from the New World ----------------------------------------------------- 6 Recorded from Cuba; length of forearm 29–31 mm ----------------------------------------------------- M. minutus Recorded from southwestern South America; length of forearm 34–49 mm ----------------------------------------------------- 5 Length of forearm 34–49 mm; skull not flattened; 1 upper premolar per quadrat; basisphenoid pits present; palate not domed ----------------------------------------------------- M. kalinowski Length of forearm 33–34 mm; skull flattened; 2 upper premolars per quadrat; no basisphenoid pits; palate domed ----------------------------------------------------- M. phrudus Recorded from Madagascar; some records from Africa ----------------------------------------------------- 7 Only known from locations east of Madagascar ----------------------------------------------------- 8 Madagascar; 2 African records; ears triangular in shape; length of forearm 38–39 mm ----------------------------------------------------- M. acetabulosus Madagascar; ears rounded; length of forearm 35–37 mm ----------------------------------------------------- M. jugularis Recorded from Sumatra; not known from Australia and/or New Guinea; length of forearm 32–34 mm ----------------------------------------------------- M. doriae Not known from Sumatra; occurs in Australia and/or New Guinea; length of forearm 33–40 mm ----------------------------------------------------- 9 Length of forearm ≤33 mm ----------------------------------------------------- M. planiceps (= loriae) Length of forearm >33 mm ----------------------------------------------------- 10 Gular gland lacking; heavy build; length of forearm 33–39 mm ----------------------------------------------------- M. beccarii Gular gland present; light build; length of forearm 36–40 mm ----------------------------------------------------- M. norfolkensis Platymops petrophilusRoberts, 1917:5. Type locality “Bleskop, near Rustenburg.” Sauromys petrophilusPeterson, 1965:12. Based on Platymops petrophilus Roberts. Mormopterus petrophilusFreeman, 1981:78, figure 16. First use of current name combination. Generic context given above. M. petrophilus was treated as a separate genus, Sauromys, by Peterson (1965). Wilson and Reeder (1993) follow Freeman (1981) and do not recognize Sauromys as a genus, although Freeman distinguished Sauromys as a subgenus and thought it 1 of the 2 most derived members of Mormopterus along with M. setiger. Corbet and Hill (1991) recognized Sauromys as a genus, a view persistently held by Peterson (Peterson 1985; Peterson et al. 1995) and followed by Nowak (1999). Although 5 subspecies (erongensis, fitzsinonsi, haagneri, petrophilus, and umbratus) have been proposed based on minor variations in pelage color, morphometric data do not support these divisions and we consider M. petrophilus monotypic. Lips of sympatric species of Chaerephon, Mops, and Tadarida are wrinkled unlike those of M. petrophilus (Fig. 1), which also has stiff hairs on the upper lips. Unlike M. setiger, males of M. petrophilus lack a gular gland, and their forearms lack wartlike granulations (Peterson 1965). M. petrophilus is 1 of 2 species of African molossids with a distinctively flattened skull lacking any sagittal crest (Fig. 2). In M. petrophilus, ears arise from a common point on top of head but are not connected by a flap of skin. Other species of Mormopterus have ears arising from separate points on the head. Mormopterus petrophilus captured at the Algeria Forestry Station in South Africa. Photograph by D. S. Jacobs Dorsal, ventral, and lateral views of cranium and lateral view of mandible of Mormopterus petrophilus from Zimbabwe (19°56′S, 32°24′E; male, Royal Ontario Museum # 65 007). Greatest length of cranium 12.65 mm. Photograph by M. B. Fenton Mormopterus petrophilus is a small- to medium-sized, flat-headed molossid with a light gray-brown dorsum, although pelage may be dark brown in some areas. Venter is lighter in color: throat, chest, and belly are creamy white with some lateral light-brown wash. Thoracoabdominal stripes, typical of some other African molossids, are absent. External and skull measurements that follow (ranges; in mm) are from specimens from the Transvaal taken from Rautenbach (1978) via Smithers (1983): length of forearm, 34.0–40.4; length of head and body, 86–100; length of ear, 10–15; length of tail, 26–40; condylobasal length, 16.7–178.3; zygomatic breadth, 10.3–11.1; c–m, 5.8–6.3; and length of mandible, 11.7–12.3. Roberts' flat-headed bats range in body mass from 9 to 22 g. Mormopterus petrophilus has a wide and deep palatal emargination between upper incisors and a small secondary cusp on lateral side of upper incisors just below gum line (Peterson 1965). Ears are simple ovoid and subtriangular in form, with a well-developed antitragal lobe. Tragus is small. Outer aspects of 1st and 4th toes are adorned with short recurved hairs. Wings are relatively broad. Mormopterus petrophilus is known from southern Africa, with records from the Cape region of South Africa, north and east through Namibia, Botswana, Zimbabwe, and Mozambique (Fig. 3; Peterson 1965; Rautenbach et al. 1979; Smithers 1983). Although Meester et al. (1986) referred to a specimen from Ghana in the Smithsonian collection, a check of the collections in October 2000 (D. E. Wilson, pers. comm.) revealed that the 38 specimens in that collection were from Botswana (2), Mozambique (14), Namibia (9), and South Africa (13). No fossils are known. Specimen records (crosses) of Mormopterus petrophilus and distribution in Zimbabwe and adjacent South Africa (solid area) Wing span of 4 individuals (3 females, 1 male) from the Cape region of South Africa ranged from 25.1 to 27.5 cm, and wing area was relatively low, ranging from 81.0 to 96.9 cm2 (D. S. Jacobs, in litt.). Relatively high wing loading (11.6–12.7 N/m2) with moderately high aspect ratio (7.6–8.3) suggests that Roberts' flat-headed bat is a relatively fast flyer in open space. This agrees with the fact that M. petrophilus is most often captured over open water (Jacobs and Fenton, in press). At Nyashato in Zimbabwe, pregnant and lactating females were taken in November (W. Cotterill, pers. comm.). Roberts' flat-headed bats were caught in mist nets, often set over or near water, or were taken during the day from under slabs of exfoliated rock or in narrow crevices. Up to 4 individuals have been found roosting together, although at least 10 individuals may use a single roost (Rautenbach 1978). When disturbed in their roosts, Roberts' flat-headed bats scramble back into the crevices. Roosting Roberts' flat-headed bats are often tightly packed together but scatter when disturbed. In Zimbabwe, Roberts' flat-headed bats roost in the same crevices as Tadarida aegyptiaca (Irwin and Donelly 1962). Both species are often caught together at the Algeria Forestry Station in Cape Province, South Africa (Jacobs and Fenton, in press). Based on skull and mandible morphology, M. petrophilus may feed mainly on small-sized, soft-bodied prey (Freeman 1981). However, stomach contents of 11 specimens contained both soft- and hard-bodied prey (moths and beetles—Freeman 1981). Hard-bodied prey also were present in fecal pellets. Diet of 14 specimens (71 pellets from 14 bats—D. S. Jacobs, in litt.) from the Cape region of South Africa was dominated by hard-bodied insects (43% Coleoptera, 29% Hemiptera, 18% Hymenoptera). Soft-bodied prey constituted about 10% of the diet (Lepidoptera, Diptera, and Neuroptera). In Namibia, M. petrophilus does not require regular access to water, presumably acquiring water from its insect prey (Roer 1971). Like other molossids, M. petrophilus is a low-duty cycle echolocator. An analysis of 30 calls from 8 individuals recorded at the Algeria Forestry Station in South Africa reveals the use of frequency-modulated, narrow-band calls (bandwidth ranged from 3.9 to 14.7 kHz) typically sweeping from a maximum frequency of 31.4–43.5 kHz to a minimum frequency of 26.7–30.9 kHz. Call duration ranged from 5.0 to 10.2 ms, and frequency at the heel of the call ranged from 28.0 to 37.5 kHz. The heel of the call corresponds to the frequency of maximum intensity (Taylor 1999). In 26 specimens, the chromosomal complement (2n = 48; FN = 62) consists of 1 pair of large metacentric, 3 pairs of medium metacentric, 4 pairs of medium subtelocentric, and 15 pairs of medium-to-small acrocentric chromosomes (Rautenbach et al. 1993). The X chromosome is a medium-sized submetacentric, and the Y chromosome, a small acrocentric. Mormopterus petrophilus is rare in the Cape Province of South Africa (Herselman and Norton 1985). However, M. petrophilus was not distinguished from Chaerephon pumila (Jacobs and Fenton, in press). M. petrophilus is commonly captured at some sites in the Cape Province, is not listed by the International Union for the Conservation of Nature, and is identified as lower risk by Hutson et al. (2001). The generic name Mormopterus means winged goblin. The species name petrophilus means rock-loving, reflecting the fact that the 1st specimens were found by people looking for scorpions under rocks. Used with Sauromys (sauros meaning lizard, mys meaning mouse), the name Sauromys petrophilus means rock-loving lizard mouse. The number of upper premolars varies in Mormopterus, making the taxonomic value of this feature questionable (Harrison 1962). We thank I. L. Rautenbach and D. E. Wilson for sharing with us information about specimens in their care and W. Cotterill for information about the species distribution and reproduction in Zimbabwe. We thank P. W. Freeman and I. L. Rautenbach for commenting on this manuscript.

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How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesInsufficient payload (model declined to judge)
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.109
Threshold uncertainty score0.999

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0130.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.035
GPT teacher head0.174
Teacher spread0.139 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; both teacher heads agree on what is shown here.

Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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