AMERICAN MUSEUM NOVITATES

Number 3842: 23 pp. November 23, 2015

Copyright © American Museum of Natural History 2015

ISSN 0003-0082

New records of flying foxes (Chiroptera: Pteropus sp.) from Seram, Indonesia, with notes on ecology and conservation status

Susan M. Tsang,[1],[2] Sigit Wiantoro,[3] and Nancy B. Simmons[4]

ABSTRACT

Bat species in the genus Pteropus (flying foxes) occur throughout most of Southeast Asia, but little is known about their distribution and patterns of local diversity across much of Indonesia. To help address this problem, a field survey of Pteropus species in Central and West Seram, Maluku Province, Indonesia, was conducted in 2012 and 2013. This study resulted in new records of rare Moluccan bats, including new locality records for four near-endemic species: P. chrysoproctus, P. melanopogon, P. ocularis, and P. temminckii. Together with data from additional specimens, these records provide new information about morphological variation in Moluccan Pteropus. High local diversity of large-bodied bats with restricted geographic ranges raises interesting questions about evolution in Pteropus and about ecological niche partitioning in Paleotropical pteropodid communities. More monitoring efforts in Maluku are needed, as the roosts located during the 2012–2013 survey are some of the only known sites where these species may be found, and none of these sites are located in protected areas. Without updated natural history data and taxonomic revision, proper management decisions cannot be made for any of these threatened species despite mounting anthropogenic pressure on their populations.

INTRODUCTION

The genus Pteropus (Chiroptera: Pteropodidae) includes over 60 species of large fruit bats commonly known as flying foxes. These bats inhabit Paleotropical regions ranging from Madagascar to Australia and the South Pacific, with highest species diversity occurring in Southeast Asia (Mickleburgh et al., 1992; Simmons, 2005). Although some species occupy extensive ranges on continental landmasses, the majority of Pteropus species are endemic to islands and coastal areas (Simmons, 2005; Helgen et al., 2009; Almeida et al., 2014). The rarity of and difficulty in locating Pteropus in the wild has led to a paucity of data on their occurrence, particularly in island archipelagos that comprise much of Indonesia. This is particularly true in poorly studied areas such as Seram, Maluku Province, Indonesia, where even local forestry rangers may be unfamiliar with these bats. Data on local species diversity, distributions, and roost sites are fragmentary. These data are necessary to any future conservation and research efforts for all Pteropus species, many of which are intensely threatened by burgeoning development in Indonesia.

Maluku (= the Moluccas, or Spice Islands) is a large island archipelago between Sulawesi and New Guinea (fig. 1). There is no agreement as to the exact number of islands in Maluku (77,990 km2), which is part of the country of Indonesia, but Maluku is often described as “having 999 islands and being 90% sea” (Monk et al., 1997). As a whole, the region is broken into two administrative provinces: North Maluku (including Bacan, Halmahera, Morotai, Obi, the Sula Islands, Ternate, and Tidore) and Maluku (including Ambon, the Aru Islands, Buru, the Kai Islands [= Kei Islands], and Seram). Seram is the largest (17,429 km2) and highest (3027 m) island in Maluku Province, and it is located centrally in the biogeographically complex region of Wallacea on its own microplate (Linthout and Helmers, 1994). Its geological isolation, size, elevation, and biological diversity have contributed to the recognition of Seram as a hotspot of endemism for vertebrate taxa including birds (Smiet, 1982) and rodents (Helgen, 2003).

Little bat research has been done in Maluku in recent decades despite its recognition as a priority region in the IUCN Old World Fruit Bat Action Plan (Mickleburgh et al., 1992). This has led to a lack of understanding of current levels of chiropteran diversity in the region, which are likely underestimated. Pteropodid species have not been monitored at all for almost two decades in Maluku, a period in which human development has likely changed the landscape significantly. The handful of studies conducted in the 20th century have primarily focused on pteropodids other than Pteropus because this genus requires dedicated sampling efforts beyond those usually employed for other bats (e.g., canopy netting and active hunting from roost sites). This has resulted in relatively low representation of Maluku Pteropus in museum collections (table 1) (Koopman and Gordon, 1992; Kitchener et al., 1993, 1994, 1995; Kitchener and Maryanto, 1995; Kompanje and Moeliker, 2001). Research on Moluccan pteropodids has primarily focused on smaller species of the genera Syconycteris and Nyctimene (Kitchener et al., 1993, 1994; Kompanje and Moeliker, 2001). Pteropodid specimens, including Pteropus, deposited in the collection of the Zoölogisch Museum of Amsterdam were discussed in detail in Bergmans (2001), though some of these were collected in the earlier part of the 20th century and do not represent more recent survey efforts of the species to determine their population status.

Studies on Seram have been few and mostly focused solely on areas in or near Manusela National Park in Central Seram Regency (Kitchener and Maryanto, 1995; Kitchener et al., 1995). West Seram Regency is of particular interest to conservationists because of its biodiversity combined with high levels of human activity due to its proximity to Ambon and other urban centers and ports, leading to its popularity as a domestic tourism destination. The regency also faces environmental issues related to blast fishing and overexploitation of live reef fish species, such as grouper (Epinephelinae), coral trout (Plectropomus spp.), and wrasse (Cheillinus undulatus) for the international fish market (Fanli Marine and Consultancy Sendirian Berhad, 2012). Hunting of wild animals as a preferred protein source, particularly mammals like bats and phalangers, is still prevalent in Central Maluku (Latinis, 1996). The true cumulative effects of hunting on biodiversity are largely unknown, however, because of the lack of taxonomic work conducted in the region. Seram remains a relatively unexplored island, largely because transportation is dependent on unreliable marine means, but plans to further develop roads and bridges on the island will threaten its biota as access increases to allow for further natural resource exploitation.

Four species of Pteropus (see below) are known from the islands of Seram (17,100 km2) and Buru (9505 km2). This level of diversity is exceptional, as most similarly sized islands in Southeast Asia usually support only two species of Pteropus (Mickleburgh et al., 1992). In comparison, Sulawesi (174,600 km2), more than 10 times larger in area, supports five Pteropus species, as does the entire Philippines archipelago (298,170 km2) (Mickleburgh et al., 1992). The evolutionary or ecological drivers behind this species diversity cannot be determined given the paucity of phylogenetic studies or natural history data available currently.

The goal of this study was to review the population and conservation statuses of the near-endemic Pteropus species on Seram, Maluku. Four Pteropus species are native to Seram: P. chrysoproctus, P. melanopogon, P. ocularis, and P. temminckii (Mickleburgh et al., 1992; Simmons, 2005). Little is known about these taxa because they have very restricted ranges. Pteropus chrysoproctus is known only from Ambon, Buru, Seram, and small islands east of Seram, and may include more than one species (Simmons, 2005; K. Helgen, personal commun.). Similarly, Pteropus melanopogon occurs on Ambon, Buru, Seram, the Banda Islands, Yamdena (in the Tanimbar Islands), and adjacent small islands, and probably also contains more than one species (Simmons, 2005; K. Helgen, personal commun.). Pteropus temminckii occurs on Ambon, Buru, Seram, and nearby small islands, perhaps including Timor (Simmons, 2005). Pteropus ocularis is recorded from just Ambon, Buru, and Seram (Simmons, 2005). Here we present new data on localities, roost sites, and morphology of the Seram Pteropus species. Tissue samples collected as part of this project will contribute to ongoing work on diversity, phylogeography, and evolution in this genus.

FIG. 1. Map of Maluku Province, Indonesia, showing major islands. Points mark localities visited on Seram in this study: (1) Pulau Marsegu, (2) Sipa, (3) Pulau Raja, and (4) Mosso.

MATERIALS AND METHODS

All protocols followed the guidelines from the American Society of Mammalogists for collection (Sikes et al., 2011) and were approved by IACUC Committee at City College of New York (protocol no. 896.2). We conducted Pteropus surveys from 2012 to 2013 in Central and West Seram regencies, Maluku Province. Bats were captured using a system of two 12 and 6 m canopy mistnets at four sites on Seram as follows: Pulau Marsegu (mangrove near Pulau Osi, West Seram), Sipa (orchard near Pelita Jaya, West Seram), Pulau Raja (mangrove near Sawai, Central Seram), and near Mosso (montane secondary forest, Central Seram). The sites were chosen based on recent sightings of Pteropus in the area, and all other pteropodids opportunistically captured were also recorded. Due to permit limitations, only representative individuals were collected as vouchers while others were identified and released.

All pteropodid species captured were identified to species and measurements were taken prior to release or vouchering. Four specimens of P. chrysoproctus, one of P. melanopogon, one of P. ocularis, and three of P. temminckii were captured, measured, weighed, and vouchered. Voucher specimens (two males and two females where possible) were skinned, with remaining samples preserved in 8%–10% formalin in the field, and subsequently transferred to 70% ethanol for preservation. A 4 mm2 biopsy wing punch was taken along with muscle and liver samples and preserved in 95% ethanol. Associated ectoparasites were collected if present. The specimens are housed at the Museum Zoologicum Bogoriense–LIPI (MZB) in Bogor, Indonesia. Skulls were extracted and measured upon return from the field to MZB. Duplicate tissue samples are housed in the Ambrose Monell Cryo Collection at the American Museum of Natural History in New York.

The following external, cranial, and dental characters were taken using digital calipers: head and body length (HB), ear length (EAR), forearm length (FA), tibia length (TIB), hind foot length (HF), greatest skull length (GSL), zygomatic breadth (ZB), least interorbital width (LIOW), postorbital width (POW), braincase width (BW), condylobasal length (CBL), condylocanine length (CCL), upper canine to second molar length (CM2), outside upper canine breadth (C1–C1), breadth across the second upper molars (M2–M2), lower canine to third molar length (C–M3). Weight (WT) was measured in grams using Pesola scales. We also measured specimens available in the collections at MZB, AMNH, and FMNH (see below), and extracted available measurements from the literature for comparative purposes. Comparative photos of skulls and jaws of representatives of each of the four Pteropus species from Seram are provided in figures 2–6.

Museum collections are abbreviated as follows: AMNH, American Museum of Natural History, New York; AM, Australian Museum, Sydney; BMNH, British Museum of Natural History, London; FMNH, Field Museum of Natural History, Chicago; MZB, Museum Zoologicum Bogoriense, Indonesian Institute of Sciences, Bogor; NMNL, National Museum of Natural History Naturalis Leiden; ZMB, Universität Humboldt Museum für Naturkunde, Berlin.

RESULTS AND DISCUSSION

All 10 species of pteropodids known to be native to Seram (Mickleburgh et al., 1992; Simmons, 1995) were captured and identified during our surveys: Dobsonia moluccensis, D. viridis, Macroglossus minimus, Nyctimene cephalotes, Pteropus chrysoproctus, P. melanopogon, P. ocularis, P. temminckii, Rousettus amplexicaudatus, and Syconycteris australis (table 1). Since the primary targets of the study were Pteropus species, we describe here only vouchered Pteropus individuals. No Pteropus were found at the Sipa site despite earlier reports by forestry officials and local people that the flying foxes foraged there. We did, however, find bite marks on overripe jambu fruit (Syzygium sp.) at the Sipa site that suggest that flying foxes had been there recently.

Craniodental measurements (table 2) and external measurements (table 3) of Moluccan Pteropus specimens from the MZB, FMNH, and AMNH were compared with those captured during our survey. The newly captured adult specimens fall well within the expected range of forearm and cranial measurements for each species, as suggested by data from Flannery (1995), Bergmans (2001), and historical specimens.

TABLE 1. Sites where each pteropodid species was captured from our surveys.

“X” indicates that individuals were captured, “O” indicates that individuals were noted but not captured at each site.

Sites

Species

P. Marsegu

Sipa

P. Raja

Mosso

Dobsonia moluccensis

X

X

Dobsonia viridis

X

Macroglossus minimus

X

X

Nyctimene cephalotes

X

X

Pteropus chrysoproctus

X

O

Pteropus melanopogon

X

O

O

Pteropus ocularis

X

Pteropus temminckii

X

X

Rousettus amplexicaudatus

X

X

Syconycteris australis

X

X

TABLE 2. Skull and dental measurements of Moluccan Pteropus.

All measurements in mm, blanks represent unavailable data. Asterisks indicate type specimens.

Coll.ID

Age/Sex

GSL

ZB

LIOW

POW

BW

CBL

CCL

CM2

C-C

M2-M2

CM3

Pteropus chrysoproctus

MZB 1077

A ♂

71.5

38.7

10.2

6.5

23.4

66.8

62.5

27.2

12.3

18.1

31.1

MZB 13568

A ♂

73.4

41.0

9.3

7.9

23.1

71.8

66.3

28.9

13.5

17.3

32.0

ZMA 16.369a

A ♂

73.6

MZB 1076

SA ♂

59.1

29.4

7.6

9.8

23.3

56.5

52.5

23.9

10.5

14.3

26.0

MZB 36911

SA ♂

68.4

34.5

10.4

10.7

23.7

67.6

61.6

26.4

11.6

16.2

28.7

MZB 36909

A ♀

76.6

41.4

10.0

7.9

24.4

76.2

69.4

29.1

13.6

19.5

32.5

MZB 1078

A ♀

67.6

38.3

9.3

7.5

22.8

66.8

61.8

26.1

12.5

16.5

ZMA 16.370a

A ♀

76.5

MZB 36908

SA ♀

60.7

30.7

8.7

11.3

23.5

58.0

52.9

24.6

11.9

16.0

27.6

MZB 36910

SA ♀

67.0

33.4

9.1

9.6

24.8

65.8

59.5

26.2

11.9

16.3

28.4

MZB 0219

A

63.3

31.3

8.4

8.8

21.8

61.1

55.7

25.2

9.8

15.2

27.5

Pteropus melanopogon

MZB 13566

A ♂

79.3

40.4

10.7

8.2

24.3

80.0

73.6

30.9

14.1

18.6

35.0

MZB 13569

A ♂

81.3

45.0

11.4

7.4

24.1

81.0

75.0

31.9

15.3

19.4

36.3

MZB 13570

A ♂

80.6

45.0

11.7

11.7

23.6

78.4

71.4

30.4

16.1

19.5

34.7

MZB 1075

A ♂

85.5

46.9

11.4

7.9

28.1

83.0

76.3

32.5

16.0

36.3

MZB 36927

Juv ♂

48.8

26.0

7.6

11.1

22.0

45.0

MZB 1074

A ♀

79.5

45.4

11.0

7.9

25.0

30.6

14.7

20.0

34.7

ZMA 16.368a

A ♀

78.8

FMNH 8228

SA

71.7

38.2

9.7

9.9

23.4

71.7

65.8

26.1

13.7

4.2

32.7

MZB 1059

A

84.4

45.4

11.4

7.5

24.9

82.7

76.5

31.8

14.9

19.7

36.2

var. keyensis

*ZMB 4752

A ♂

46.3

11.0

7.6

26.3

14.6

*ZMB 4701

A ♀

74.9

41.1

9.3

7.4

26.2

73.3

67.6

29.4

14.5

19.4

33.3

var. aruensis

*ZMB 4703

A ♂

76.4

40.3

10.7

10.2

26.3

74.4

68.6

30.3

15.2

18.0

34.8

*ZMB 4962

A ♂

11.4

9.1

31.4

15.7

21.1

34.9

Pteropus ocularis

*ZMB 2958

A ♂

35.0

7.0

7.5

22.3

24.5

11.9

15.8

27.4

MZB 36928

SA ♂

62.3

33.4

6.9

7.5

22.1

61.6

56.5

23.3

11.7

16.2

26.7

MZB 13361

A ♀

59.9

32.1

7.7

21.9

57.9

53.7

23.0

11.3

14.7

25.3

Pteropus temminckii

*ZMB 4964

A ♂

28.8

7.5

9.1

20.2

18.7

10.2

13.2

21.3

*ZMB 3473

A ♂

18.6

9.5

12.6

20.8

MZB 36925

A ♂

51.4

28.1

6.6

9.8

20.3

49.1

44.8

18.8

9.3

12.9

20.5

MZB 2155

A ♀

50.8

26.8

6.7

7.9

19.7

49.7

44.5

17.0

9.1

11.8

20.0

MZB 15597

A ♀

53.8

29.8

7.0

7.5

19.9

51.6

47.4

20.0

10.0

13.7

21.9

TABLE 2 (continued).

Coll.ID

Age/Sex

GSL

ZB

LIOW

POW

BW

CBL

CCL

CM2

C-C

M2-M2

CM3

MZB 36924

A ♀

51.7

29.1

7.8

9.2

20.3

50.1

45.6

19.2

9.4

13.9

21.8

MZB 36926

A ♀

51.2

28.1

6.8

9.1

20.2

48.5

43.6

18.3

9.4

13.1

20.1

MZB 8341

A ♀

29.3

6.9

9.9

28.3

48.0

43.9

19.0

9.8

13.1

20.9

ZMA 3080a

SA ♀

44.9

ZMA 3084a

A ♀

50.4

a From Bergmans 2001.

TABLE 3. External measurements of Moluccan Pteropus.

Most external character data are not available for the specimen, as skins are difficult to manipulate. Weight is in grams, all other measurements are in mm, blanks represent unavailable data. Asterisks indicate type specimens.

Coll.ID

Age/Sex

WT

FA

HB

EAR

TIB

HF

Pteropus chrysoproctus

*ZMB 2626

A ♂

145

52

MZB 13568

A ♂

174

82.00

ZMA 16.369a

A ♂

166

MZB 36911

SA ♂

420

144

220

30.91

65.72

52.66

MZB 36909

A ♀

780

180

265

30.81

79.91

52.00

MZB 1078

A ♀

670

ZMA 16.370a

A ♀

170

MZB 36908

SA ♀

290

138

190

27.08

62.39

48.73

MZB 36910

SA ♀

380

150

210

32.09

66.14

49.26

MZB 0219

A

140

Pteropus melanopogon

MZB 13566

A ♂

510

188

MZB 13569

A ♂

882

205

MZB 13570

A ♂

900

204

MZB 1075

A ♂

192

MZB 36927

Juv ♂

150

91

146

23.71

38.31

45.33

MZB 1074

A ♀

192

FMNH 8228

SA

169

MZB 1059

A

198

var. keyensis

*ZMB 4752

A ♂

172

55

*ZMB 4701

A ♀

174

31

80

53

var. aruensis

*ZMB 4703

A ♂

181

38

87

66

*ZMB 4962

A ♂

183

Pteropus ocularis

*ZMB 2958

A ♂

138

AMNH 234939

A ♂

118

MZB 36928

SA ♂

400

144

195

26.29

60.89

44.38

MZB 13361

A ♀

220

142

24

37

MZB 0112

A ♀

132

18.41

Pteropus temminckii

*ZMB 2633

A ♂

96

30

*ZMB 4964

A ♂

101

30

*ZMB 3473

A ♂

97

MZB 36925

A ♂

150

97

160

23.92

45.59

30.09

MZB 14839

A ♂

150

100

155

22

22

MZB 36924

A ♀

200

106

155

22.71

47.10

32.38

MZB 36926

A ♀

160

102

140

22.88

44.86

31.51

MZB 8341

A ♀

175

100

MZB 15597

A ♀

105

46

MZB 2155

A ♀

104

ZMA 3084a

A ♀

101

a From Bergmans, 2001.

Pteropus chrysoproctus (Temminck, 1837)

Moluccan flying fox

Type Locality: Ambon, Central Maluku, Indonesia.

New Material: Pulau Raja, offshore from Sawai, Maluku Tengah Regency, Maluku Province, Indonesia. Collected by Sigit Wiantoro and Susan M. Tsang, 3 females: MZB 36908, MZB 36909, MZB 36910, 1 male MZB 36911.

Other Specimens Examined: MZB 0219, MZB 1076, MZB 1077, MZB 1078, MZB 13568, and ZMB 2626.

Occurrence and Identification: Pteropus chrysoproctus is rare in collections, but likely not uncommon despite anecdotal evidence of historical decline according to the IUCN red list assessment (Huston and Helgen, 2013). The individuals encountered at Pulau Raja in Seram resemble specimens from older collections purportedly from Ambon and Seram, including the poorly preserved syntype in Berlin (ZMB 2626). Unlike the other three sympatric species, the ears (>30 mm) are distinctly longer than the CM2 length. The pelage is dark reddish brown over most of the body, appearing a bit brighter on the ruff and darker red on the belly—another unique characteristic among Moluccan species. Compared to the sympatric P. melanopogon, P. chrysoproctus is smaller in size and has a much narrower skull: FA 170–180 mm, GSL 63–77 mm, ZB 31–42 mm, LIOW 8–10.5 mm (compared to FA >185 mm, GSL >75 mm, ZB >40 mm, LIOW >10 mm in P. melanopogon) (tables 2 and 3). Similarity between individuals from Ambon and Seram is important to note, as populations of P. chrysoproctus from different Moluccan islands may represent distinct subspecies or species (K. Helgen, personal commun.).

Human Disturbance: Hunting of P. chrysoproctus, along with habitat loss, threatens the species. Thought to occur only in small groups, our survey found a roost of approximately 300 individuals in a patch of mangrove trees (primarily Rhizophora sp.) near Manusela National Park. According to the local villagers in Sawai and forestry rangers, the roost is present year-round and will likely not be lost to development in the near future since it is protected as an ecotourism attraction by local resorts. However, according to forestry rangers, this is the only roost site for this species currently known on Seram. There were no indications of presence of P. chyrsoproctus colonies at any of the other sites we surveyed.

Anecdotal evidence suggests that these bats have been hunted intensely and have either moved permanently or are locally extirpated at other sites. According to the local people, P. chrysoproctus, along with P. temminckii, were once the most commonly encountered species by hunting parties seeking Pteropus, particularly at their foraging sites. Patchy forests near villages such as Mosso in Central Seram were known to be foraging areas for many pteropodids, including Pteropus, Nyctimene, and Syconycteris. Through interviews with local residents, we learned that Muslim villagers do not enter the forest to forage because of their belief that it is a sacred area, but Christian villagers from the other side of the forest enter often to hunt bats. The Christian villagers stated that there were more bats in the area in the past decades than there are now, and described three distinct types: the “red one” (likely P. chrysoproctus), the “white one” (likely P. temminckii), and the “black one” (likely P. melanopogon). We concluded that the “black one” was P. melanopogon and not P. ocularis based on size descriptions (“very big”) and distinct markings (“white belly”), and we were able to confirm this visually when we were shown a small group of P. melanopogon by villagers in the nearby forest.

Villagers near Manusela National Park customarily go into stands of kapok trees (Ceiba pentandra) where Pteropus were known to forage in order to shoot bats for food. It is customary for the men to hunt Pteropus as an appetizer for drinking parties. Even if roosting sites are within the limits of a national park, there is no guarantee of protection for Pteropus species because the bats may be vulnerable to hunters when foraging outside park boundaries. Forestry rangers indicated that after severe storms battered the mangroves in 2010, the colony of P. chrysoproctus temporarily moved to areas surrounding the national park, including villages where bat consumption is common. The P. chrysoproctus population was purportedly much larger prior to this storm.

Conservation: Pteropus chrysoproctus is currently listed as Near Threatened by the IUCN, but our data suggests that the species should be listed as Vulnerable under criteria B1a, b (iii, iv). This categorization means that the extent of the species occurrence is less than 20,000 km2, with fewer than 10 known localities, and continuing decline in both habitat and number of subpopulations. It is extremely unlikely P. chrysoproctus is still on Ambon since its colonial behavior would attract the attention of the local forestry rangers. While the colony of P. chrysoproctus in Sawai is an ecotourism attraction and will likely remain undisturbed, it is not under the protection of Manusela National Park nor local forestry services. The site merits some official level of recognition for its uniqueness and high conservation value.

Pteropus melanopogon (Peters, 1867)

Black-bearded flying fox

Type Locality: Amboina (= Ambon), Central Maluku, Indonesia.

New Material: Pulau Marsegu, Seram Bagian Barat Regency, Maluku Province, Indonesia. Collected by Sigit Wiantoro and Susan M. Tsang, 1 female MZB 36927.

Other Specimens Examined: MZB 1059, MZB 1074, MZB 1075, MZB 13566, MZB 13569, MZB 13570, FMNH 8228, ZMB 4752, ZMB 4701, ZMB 4703, and ZMB 4962.

Occurrence and Identification: Pteropus melanopogon were found roosting in a colony of approximately 200 individuals in two patches of mangrove trees (Rhizophora sp.) on Pulau Marsegu, an island named for the presence of the bat colony (marsegu is the local word for “flying fox”). Only a single injured juvenile was captured, meaning we could not corroborate species identity by using available adult craniodental or external measurements. Photographic and video documentation of the roosting groups were collected to corroborate species identity by SMT since no adults were captured at this site. The adult P. melanopogon we observed in the colony in Seram fit the description of the nominotypical form of this species provided by Andersen (1912): “blackish back, chestnut head and collar, golden-buffy underside of body.” These individuals all appear to be part of a single colony of bats that moves between trees on the island of Pulau Marsegu throughout the course of the day; at dusk, there is only one large group that was observed exiting from the roost. We are confident that the juvenile we collected is P. melanopogon because we opportunistically collected this individual from under the roosting tree after the main colony of adult P. melanopogon had departed.

Occasionally, P. melanopogon were spotted roosting with the main P. chrysoproctus colony, though they remained on separate trees. When we visited the Sawai site in June 2012, a small group of P. melanopogon was seen roosting a short distance away from the main P. chrysoproctus colony. The P. melanopogon colony we located on Pulau Marsegu has previously been seen feeding on flowers of durian trees (Durio sp.), which are very abundant in this part of Seram. No colonies of P. melanopogon are currently known from Ambon, but more surveys are needed to verify this claim. As indicated in the earlier discussion of P. chrysoproctus, a small group of P. melanopogon was found roosting in disturbed forest near Mosso, but none were captured nor seen emerging at dusk.

Pteropus melanopogon and P. chrysoproctus are sympatric but are easily distinguished from one another. While P. melanopogon has highly variable pelage coloration across its geographic range, its massive size (FA >185 mm) and robust skull (GSL >75 mm, ZB >40 mm, LIOW >10 mm) make it unmistakable (tables 2 and 3, fig. 2). Like the colony sighted in our survey, the specimens at MZB are similar to the nominotypical form according to Andersen (1912) in both coloration and size with a brownish-yellow head, darker brown mantle, pale yellowish-buff abdomen, massive overall body size, ears shorter than CM2 length, an interfemoral membrane that is short in the center, and a practically naked forearm and tibia. Given its size, it is likely that P. melanopogon is one of the heavier pteropodid species; one of our specimens weighed 900 g (table 3).

Despite being abundant in the 19th century, previous modern survey efforts had failed to locate a single colony of P. melanopogon on either Buru or Seram (Flannery, 1995). Morphological similarities of previously collected specimens suggest an affinity between the populations of P. melanopogon on Buru and Seram, but comparisons with specimens from other Moluccan islands, especially Aru and Kai, are needed for a thorough review. A comprehensive analysis of the P. melanopogon complex (inclusive of P. keyensis and P. aruensis) is a high priority since P. aruensis is severely threatened by conversion of the Aru Islands into corporate plantations (Amianti, 2015). Like P. chrysoproctus, P. melanopogon is also likely no longer extant on Ambon, as there have been no recent reports of colonies, but more surveys are needed.

Human Disturbance: The roosting colony of P. melanopogon in West Seram is extremely vulnerable to hunting. While the local fishermen do not hunt bats, the site is easily accessible to bushmeat hunters from other provinces. Disturbance from hunting affects both the numbers and distribution of the bats. We were unsuccessful in capturing any individuals during our 2012 visit because a hunter from a different province had apparently killed many bats with a gun at the roost a few days prior to our arrival, and this proved enough of a disturbance to disperse the colony. We were informed by the local villagers that disturbed bat colonies moved from their original isolated roosts to suboptimal sites (e.g. shorter trees in the forest closer to villages), which were often actually easier for hunters to reach. Clearly such events can threaten the stability of the colony.

Conservation: Currently, IUCN lists P. melanopogon as Endangered under criteria A3c, d since it has not been recorded within the entirety of its range on any Moluccan islands in the past 20 years (Helgen and Salas, 2013a). This threat categorization means that there is a projected decline of ≥50% of the population in the next three generations due to deforestation and hunting. Our results indicate that the Pulau Marsegu roost is the only known colony found on Seram within the past several decades. But the Pulau Marsegu roost is not in a protected area and merits protection for its high conservation value.

Pteropus ocularis (Peters, 1867)

Seram flying fox

Type Locality: Seram, Central Maluku, Indonesia.

New Material: Pulau Marsegu, Seram Bagian Barat Regency, Maluku Province, Indonesia. Collected by Sigit Wiantoro and Susan M. Tsang, 1 male MZB 36928.

Other Specimens Examined: MZB 0112, MZB 13361, AMNH 234939, ZMB 2958. Additional specimens that we did not examine for this study are housed at the AM and BMNH.

Occurrence and Identification: Pteropus ocularis is a species that is very rare in collections. We suspect P. ocularis is unlikely to be found in colonies based on our inability to locate any colonies, the lack of historical or current colony information from local forestry rangers, and having captured an individual under similar circumstances as the other noncolonial Pteropus species, P. temminckii. The IUCN red list assessment of P. ocularis states that it has been collected only four times (Helgen and Salas, 2013b) although we are aware of six previous records: the holotype collected by Alfred Russel Wallace (at ZMB), two females (one collected in 1915 and another from 1982) housed at MZB, a series at BMNH, a series from Ambon at NMNL, a female at AM in Sydney (Flannery, 1995), and a male at AMNH with vague locality data (“Moluccas”). The MZB and BMNH specimens are from Buru, whereas the AM specimen is from an area near Manusela National Park, Seram. Unfortunately, the tag on the holotype and the original description by Peters (1867) only states that it is from Wallace’s “Ceram” collection. We are doubtful of the species identity of the AMNH specimen because the forearm length (FA = 118 mm) is significantly smaller than expected, and we also ruled out the possibility that it was not a mature adult. Additionally, the ventral fur has a distinct, large, light blond patch that is not characteristic of P. ocularis. We could not further investigate because the skin is in such poor condition with the skull still inside.

Our collection of P. ocularis is likely the first record from West Seram. Our identification of this specimen is based on pelage pattern and morphological measurements. Dobson (1878) noted that that P. ocularis has distinctive light reddish-brown rings around the eyes similar to P. conspicillatus, however, P. ocularis is much smaller in size and the body shape of P. ocularis is “Pteropus griseus-like” with an interfemoral membrane that is narrow in the middle. Our specimen conforms to this description. Our specimen also falls within the expected range of measurements for this species: FA 130 to 145 mm, GSL 59 to 63 mm, ZB 32 to 34 mm, LIOW 6 to 7 mm (tables 2 and 3, fig. 2).

Our specimen was captured in a mangrove forest. The IUCN red list assessment states that P. ocularis “probably occurs only in old growth forest,” but the habitat of this specimen indicates that more extensive surveying is necessary to understand the habitat preferences of this species.

Human Disturbance: It remains unclear whether P. ocularis faces persistent, targeted hunting pressure like P. chrysoproctus and P. melanopogon since it is a solitary species and relatively rarely encountered. There were no indications that the local villagers knew this species very well from any particular location, but they may consume it as a result of incidental capture.

Conservation: P. ocularis is currently listed by the IUCN as Vulnerable B1 a, b (iii, v). This categorization means that the extent of the species occurrence is less than 20,000 km2, with fewer than 10 known localities, and continuing decline in both habitat and number of subpopulations. Deforestation in and around Manusela National Park probably affects this species. It is unclear whether the apparent rarity of P. ocularis is due to low relative abundance or cryptic behavior or whether populations are declining. Further monitoring is necessary to determine whether an IUCN Endangered status may be more appropriate for P. ocularis than its current one of Vulnerable.

Pteropus temminckii (Peters, 1867)

Temminck’s flying fox

Type Locality: Amboina (= Ambon), Central Maluku, Indonesia.

New Material: Pulau Marsegu, Seram Bagian Barat Regency, Maluku Province, Indonesia. Collected by Sigit Wiantoro and Susan M. Tsang, 1 female MZB 36926, 1 male MZB 36925. Mosso Village, Maluku Tengah Regency, Maluku Province, Indonesia. Collected by Sigit Wiantoro and Susan M. Tsang, 1 female MZB 36924.

Other Specimens Examined: MZB 15597, MZB 8341, MZB 2155, MZB 14839, ZMB 2633, ZMB 4964, and ZMB 3473.

Occurrence and Identification: Pteropus temminckii was captured in both West and Central Seram, in both mangrove (Pulau Marsegu) and secondary forest (Mosso) habitats. A foliage rooster that is unlikely to occur in large colonies (Helgen and Bonaccorso, 2013), P. temminckii is not easily detected. Of the four Moluccan Pteropus species, P. temminckii is best represented by previous collection efforts throughout its range. Combined records from our expeditions and previous collection efforts suggest that P. temminckii is relatively common compared to P. ocularis. Flannery (1995) states that P. temminckii likely prefers primary forest based on a report that researchers from AM captured large numbers in primary forests at ~800 m elevation in Ambon. However, in Seram P. temminckii is apparently most commonly encountered today in secondary forest. Local villagers describe encountering these bats relatively often in the small patches of secondary forest that frequently occur between villages, and we were able to capture a female in this habitat. These fragmented forests are used as orchards or hunting areas by Christian villagers. The mangrove habitat where one male and one female P. temminckii were captured was also unexpected, as this species has not been previously reported in mangrove forest and our mistnets were set with the goal of capturing the P. melanopogon.

Pteropus temminckii is significantly smaller than other Pteropus species on Seram, and comparatively easy to identify. Adults have a forearm length <110 mm and GSL <55mm, which is significantly smaller than the next largest species found on Seram, P. ocularis (tables 2 and 3, fig. 2). Our specimens all exhibit uniquely dense pale yellowish-buff silky fur described by Dobson (1878) as diagnostic for the species. The coloration and fur thickness are similar to P. personatus, a North Moluccan species, but P. temminckii does not have a black facial mask.

Human Disturbance: P. temminckii is threatened by habitat loss and by bushmeat hunting (Helgen and Bonaccorso, 2013). As a species commonly encountered by hunters, more data is needed to determine how intensely hunting has affected population trends.

Conservation: Currently, the IUCN lists P. temminckii as Vulnerable under criteria A2c, meaning a projected decline of ≥30% of the population in the next three generations due to a decline in habitat. Pteropus temminckii was the only species that we found at multiple survey sites and habitats (including disturbed areas), and it was the most commonly encountered of the four Pteropus found in Seram during our survey. Our observations indicate that this species has broader habitat preferences than previously reported. We did not directly observe or capture the species in Manusela National Park, though it has previously been recorded there according to park staff. We found foraging sites with telltale bite marks on fruits for P. temminckii within Manusela National Park, but did not find any foliage roosts. Pteropus temminckii will likely face increased extinction pressure as habitat continues to be degraded, but our observations suggest it is likely the least threatened of the four Pteropus species in Seram.

FIG. 2. Dorsal views of skulls of A, Pteropus chrysoproctus (MZB 36909♀); B, Pteropus melanopogon (MZB 1075♂); C, Pteropus ocularis (MZB 36928♂); D, Pteropus temminckii (MZB 36925♂).

FIG. 3. Ventral views of skulls of A, Pteropus chrysoproctus (MZB 36909♀); B, Pteropus melanopogon (MZB 1075♂); C, Pteropus ocularis (MZB 36928♂); D, Pteropus temminckii (MZB 36925♂).

FIG. 4. Lateral views of skulls of A, Pteropus chrysoproctus (MZB 36909♀); B, Pteropus melanopogon (MZB 1075♂); C, Pteropus ocularis (MZB 36928♂); D, Pteropus temminckii (MZB 36925♂).

FIG. 5. Dorsal views of lower jaws of A, Pteropus chrysoproctus (MZB 36909♀); B, Pteropus melanopogon (MZB 1075♂); C, Pteropus ocularis (MZB 36928♂); D, Pteropus temminckii (MZB 36925♂).

FIG. 6. Lateral views of lower jaws of A, Pteropus chrysoproctus (MZB 36909♀); B, Pteropus melanopogon (MZB 1075♂); C, Pteropus ocularis (MZB 36928♂); D, Pteropus temminckii (MZB 36925♂).

DIRECTIONS FOR FUTURE RESEARCH

Our surveys confirmed the occurrence of four native Pteropus species on Seram, and resulted in documentation of several roosting colonies of high conservation value. Voucher specimens we collected were compared to available specimens from other islands available from historic collection to confirm characteristics of each species, but we did not attempt a complete revision of these taxa, which in most cases have ranges extending far beyond Seram. Future systematic studies should include a comprehensive revision of P. melanopogon, which likely represents a complex of more than one species. The original variants recorded in Dobson (1878) are now recognized as separate species (P. neohibernicus, P. aruensis, and P. keyensis), but the species status of populations occurring on other remote Indonesian islands is unknown (Simmons, 2005). Poor understanding of variation within Moluccan Pteropus species may result in an underestimated level of phylogenetic diversity, a measure often used by biodiversity management and conservation biologists to evaluate of areas of endemism, which in turn influences priorities for establishing new protected areas. Oceanic islands such as those in Maluku have a mammal fauna composed primarily of bats and rodents, and updated data on all species is needed to inform management decisions. Many Moluccan Pteropus species likely have unrecognized endemic subspecies, but incomplete collections have resulted in hypotheses of geographically widespread species complexes with vague species limits. Additional research likely with result in many distinct, new threatened taxa with small, circumscribed geographic ranges.

The current study represents the first effort in decades to comprehensively review all known Pteropus from Seram. We provide comparisons of their occurrences, particularly in light of recent anthropogenic disturbance. More detailed studies of the effect of anthropogenic change on six other pteropodid species, as well as the four Pteropus species, are needed. At the two disturbed sites that we sampled (Sipa and Mosso), we were able to capture all pteropodid species other than Pteropus known to be present on the island (table 1). Comparisons to previously collected specimens of these taxa from throughout their ranges should be made to evaluate variation and species/subspecies limits. For example, a comparison to other P. chrysoproctus specimens deposited at the Australian Museum from Buru (AM 29985) and Bisa in the Obi Group (AM 28901 and AM 28902)—something unfortunately beyond the scope of this study—would help in understanding variation throughout Maluku (Flannery, 1995). Unfortunately, no tissue samples are available from these specimens.

Determining the level of molecular diversity within each population and connectivity between island populations is recommended to further assess the status of these bats. This has already started through genetic analyses of the tissue samples collected during the surveys reported here. Using next-generation sequencing methods, historical specimens may be able to provide genetic information previously unavailable to determine whether human encroachment has had any effect on genetic diversity and population connectivity. More information about the foraging and roosting ecology of these bats are needed to understand potential localized migration patterns as it pertains to their demographic histories. If observation conditions do not permit adequate sampling of feeding behavior, a metagenomic study of food remains from feces is recommended to provide a preliminary understanding of their diets.

Our data suggest that Pteropus temminckii may adapt to light disturbance, as these bats are found in gardens, orchards, and disturbed secondary broadleaf forests. Determining which species occur in mangrove forests in addition to primary forests is also important, as we found large roosting colonies of P. chrysoproctus and P. melanopogon along with a single P. ocularis in mangroves. The degree of prevalence of Pteropus in disturbed areas or mangroves is unknown, especially for poorly known Moluccan species. It remains unclear whether these two habitats are highly seasonal and timed to the flowering of a few tree species or they are alternate roosts following previous human disturbance in primary forests. More concerted survey efforts will be needed in the future to corroborate population trends and habitat preferences of all pteropodid species since our data are not fully representative of occurrence patterns and could be misleading. Due to the small sample size, we could not determine whether habitat preference was statistically correlated with other traits (e.g. body size or feeding ecology). Estimating these characteristics may be possible when more data are available from future surveys on Seram and other Moluccan islands. Information from such surveys could thus assist planners in assessing where protected areas should be situated to encompass both the foraging and the roosting sites for bats.

ACKNOWLEDGMENTS

We thank the Ministry of Research and Technology (RISTEK), the Ministry of Forestry of the Republic of Indonesia, and BKSDA Ambon for research permissions, access, and field assistance. We thank L.R. Heaney for providing measurements for specimens at FMNH. We thank R.S. Voss for measuring type material and other specimens in Berlin, and we are grateful to Christiane Funk (manager of the ZMB mammal collection) for making this work possible. This research was funded by the Fulbright Indonesia Student Research Fellowship and the National Geographic Society Young Explorers Grant (9272-13) awarded to S.M.T. and in part by the National Institute of Allergy and Infectious Diseases under Grant No. 1R21A105050 to D.J. Lohman and N.B.S. We are grateful to all local assistants and informants in the field.

REFERENCES

Almeida, F. C., N.P. Giannini, N.B. Simmons, and K.M. Helgen. 2014. Each flying fox on its own branch: a phylogenetic tree for Pteropus and related genera (Chiroptera: Pteropodidae). Molecular Phylogenetics and Evolution 77: 83–95.

Amianti, G.D. 2015. Govt prepares areas for sugar, cattle investors. Jakarta Post. 18 June 2015. Internet resource (http://www.thejakartapost.com/news/2015/06/18/govt-prepares-areas-sugar-cattle-investors.html), accessed August 17, 2015.

Andersen, K. 1912. Catalogue of the Chiroptera in the collection of the British Museum. Vol. 1: Megachiroptera. London: British Museum.

Bergmans, W. 2001. Notes on distribution and taxonomy of Australasian bats. I. Pteropodinae and Nyctimeninae (Mammalia, Megachiroptera, Pteropodidae). Beaufortia 51: 119–152.

Dobson, G.E. 1878. Catalogue of the Chiroptera in the collection of the British Museum. London: British Museum.

Fanli Marine and Consultancy Sendirian Berhad 2012. Proposal for a multi-stakeholder forum on the live reef food fish trade – final report. Selangor, Malaysia.

Flannery, T.F. 1995. Mammals of the south-west Pacific and the Moluccan Islands. Ithaca, NY: Cornell University Press.

Helgen, K.M. 2003. A review of the rodent fauna of Seram, Moluccas, with the description of a new subspecies of mosaic-tailed rat, Melomys rufescens paveli. Journal of Zoology 261: 165–172.

Helgen, K.M., and L. Salas. 2013a. Pteropus melanopogon: IUCN red list of threatened species. Internet resource (http://www.iucnredlist.org/details/18739), accessed December 27, 2014.

Helgen, K.M., and L. Salas. 2013b. Pteropus ocularis: IUCN red list of threatened species. Internet resource (http://www.iucnredlist.org/details/18745), accessed December 27, 2014.

Helgen, K.M., and F. Bonaccorso. 2013. Pteropus temminckii: IUCN red list of threatened species. Internet resource (http://www.iucnredlist.org/details/18762), accessed December 27, 2014.

Helgen, K.M., L.E. Helgen, and D.E. Wilson. 2009. Pacific flying foxes (Mammalia: Chiroptera): two new species of Pteropus from Samoa, probably extinct. American Museum Novitates 3646: 1–37.

Huston, M.A., and K.M. Helgen. 2013. Pteropus chrysoproctus: IUCN red list of threatened species. Internet resource (http://www.iucnredlist.org/details/18720), accessed December 27, 2014.

Kitchener, D.J., and I. Maryanto. 1995. Small Pteropus (Chiroptera: Pteropodidae) from Timor and surrounding islands, Indonesia. Records of the Western Australian Museum 152: 147–152.

Kitchener, D.J., W.C. Packer, and I. Maryanto. 1993. Taxonomic status of Nyctimene (Chiroptera: Pteropodidae) from the Banda, Kai and Aru Islands, Maluku, Indonesia – implications for biogeography. Record of the Western Australian Museum 16: 399–417.

Kitchener, D.J., W.C. Packer, and I. Maryanto. 1994. Morphological variation in Maluku populations of Syconycteris australis (Peters, 1867) (Chiroptera: Pteropodidae). Record of the Western Australian Museum 16: 485–498.

Kitchener, D.J., W.C. Parker, and A. Suyanto. 1995. Systematic review of Nyctimene cephalotes and N. albiventer (Chiroptera: Pteropodidae) in the Maluku and Sulawesi regions, Indonesia. Record of the Western Australian Museum 142: 125–142.

Kompanje, E.J.O., and C.W. Moeliker. 2001. Some fruit bats from remote Moluccan and West-Papuan Islands, with the description of a new subspecies of Macroglossus minimus (Megachiroptera: Pteropodidae). Deinsea 8: 143–167.

Koopman, K.F., and L.K. Gordon. 1992. Systematic notes on a collection of bats from Halmahera (Indonesia: Moluccas). American Museum Novitates 3035: 1–8.

Latinis, K. 1996. Hunting the cuscus in western Seram: the role of the phalanger in subsistence economies in Central Maluku. Cakalele 7: 17–32.

Linthout, K., and H. Helmers. 1994. Pliocene obducted, rotated and migrated ultramafic rocks and obduction-induced anatectic granite, SW Seram and Ambon, Eastern Indonesia. Journal of Southeast Asian Earth Sciences 9: 95–109.

Mickleburgh, S.P., P.A. Racey, and IUCN/SSC Chiroptera Specialist Group. 1992. Old World fruit bats: an action plan for their conservation. Gland, Switzerland: IUCN Press.

Monk, K.A., Y. de Fretes, and G. Reksodiharjo-Lilley. 1997. The ecology of Nusa Tenggara and Maluku. Singapore: Periplus.

Peters, M.B. 1867. Pteropus ocularis. Monatsberichte der Königlichen Preussische Akademie des Wissenschaften zu Berlin 1867: 331.

Sikes, R.S., W.L. Gannon, and the Animal Care and Use Committee of the American Society of Mammalogists. 2011. Guidelines of the American Society of Mammalogists for the use of wild mammals in research. Journal of Mammalogy 92: 235–253.

Simmons, N.B. 1995. Bat relationships and the origin of flight. Symposium of the Zoological Society London 67: 27–43.

Simmons, N.B. 2005. Order Chiroptera. In D.E. Wilson and D.M. Reeder (editors), Mammal species of the world: a taxonomic and geographic reference, 3rd ed.: 312–529. Baltimore, MD: Johns Hopkins University Press.

Smiet, F. 1982. Threats to the Spice Islands. Oryx 16: 323–328.

APPENDIX

Specimens Examined

Coll.ID

Year

Site Name

Island

Collector(s)

Latitude

Longitude

Pteropus chrysoproctus

MZB 1077

1921

Leksula

Buru

L.J. Toxopeus

3°46’S

126°35’E

MZB 13568

1982

Wamlana

Buru

Asep & J. Hardjono

3°7’41’’S

126°33’46’’E

ZMA 16.369

1922

Buru

MZB 1076

1921

Leksula

Buru

L.J. Toxopeus

3°46’S

126°35’E

MZB 36911

2014

Pulau Raja

Seram

S. Wiantoro & S.M. Tsang

2°55’7’’S

129°9’46’’E

MZB 36909

2014

Pulau Raja

Seram

S. Wiantoro & S.M. Tsang

2°55’7’’S

129°9’46’’E

MZB 1078

1921

Leksula

Buru

L.J. Toxopeus

3°46’S

126°35’E

ZMA 16.370

1922

Buru

MZB 36908

2014

Pulau Raja

Seram

S. Wiantoro & S.M. Tsang

2°55’7’’S

129°9’46’’E

MZB 36910

2014

Pulau Raja

Seram

S. Wiantoro & S.M. Tsang

2°55’7’’S

129°9’46’’E

MZB 0219

1913

Buru

*ZMB 2626

1828

Ambon

S. Müller

Pteropus melanopogon

MZB 13566

1983

Wamlana

Buru

Asep & J. Hardjono

3°7’41’’S

126°33’46’’E

MZB 13569

1983

Wamlana

Buru

Asep & J. Hardjono

3°7’41’’S

126°33’46’’E

MZB 13570

1983

Wamlana

Buru

Asep & J. Hardjono

3°7’41’’S

126°33’46’’E

MZB 1075

1921

Nal-Besi

Buru

L.J. Toxopeus

3°26’S

126°32’E

MZB 36927

2014

Pulau Marsegu

Seram

S. Wiantoro & S.M. Tsang

3°0’45’’S

128°2’60’’E

MZB 1074

1921

Rana-Meer

Buru

L.J. Toxopeus

3°25’60’’S

126°34’1’’E

ZMA 16.368

1921

Leksula

Buru

L.J. Toxopeus

3°46’S

126°35’E

FMNH 8228

1898

Kajeli

Buru

A. Everett

3°22’60’’S

127°5’60’’E

MZB 1059

1918

Kali Toam

Seram

var. keyensis

*ZMB 4752

1865

Kai

von Rosenberg

*ZMB 4701

1865

Kai

O. Beccari

var. aruensis

*ZMB 4703

1865-1867

Aru

O. Beccari

*ZMB 4962

Aru

Bernstein

Pteropus ocularis

*ZMB 2958

1860

Seram

A.R. Wallace

AMNH 234939

1973

“Moluccas”

A.S. Bickmore

MZB 36928

2014

Pulau Marsegu

Seram

S. Wiantoro & S.M. Tsang

3°0’45’’S

128°2’60’’E

MZB 13361

1982

Wamlana

Buru

Asep & J. Hardjono

3°7’41’’S

126°33’46’’E

MZB 0112

1915

Buru

Denin

APPENDIX (continued).

Coll.ID

Year

Site Name

Island

Collector(s)

Latitude

Longitude

Pteropus temminckii

*ZMB 2633

Ambon

S. Müller

*ZMB 4964

Ambon

Bernstein

*ZMB 3473

Ambon

von Rosenberg

MZB 36925

2014

Pulau Marsegu

Seram

S. Wiantoro & S.M. Tsang

3°0’45’’S

128°2’60’’E

MZB 2155

1921

Buru

L.J. Toxopeus

MZB 15597

1984

Seram

Djafar

MZB 14839

1987

Solea

Seram

B.J. Christiansen

MZB 36924

2014

Mosso

Seram

S. Wiantoro & S.M. Tsang

3°18’30’’S

129°35’60’’E

MZB 36926

2014

Pulau Marsegu

Seram

S. Wiantoro & S.M. Tsang

3°0’45’’S

128°2’60’’E

MZB 8341

1969

Waii

Ambon

Saan

ZMA 3080a

1922

Buru

L.J. Toxopeus

3°27’S

126°40’E

ZMA 3084a

1913

Ambon

Willemsz Geerooms

3°41’S

128°01’E

a From Bergmans 2001.

[1] Department of Biology, City College and the Graduate Center, City University of New York.

[2] Department of Mammalogy, Division of Vertebrate Zoology, American Museum of Natural History.

[3]3 Museum Zoologicum Bogoriense, Research Center for Biology, Indonesian Institute of Sciences (LIPI), West Java, Indonesia.

[4] Department of Mammalogy, Division of Vertebrate Zoology, American Museum of Natural History.