Mammals < Bats & flying foxes > Birds
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4.3.1.1 — Mammals: Bats and flying foxes (Chiroptera and Megachiroptera)

Most bat species of temperate zones disappear during winter when insects are not available. Many of them hibernate in caves or retreats, but others migrate considerable distances to wintering sites or insect-rich hunting grounds. Griffin (1970) differentiates between cave and tree bats, such as the North American species of the genera Lasiurus spp. (silver-haired and red bat) and Lasionycteris borealis, which spend their life in trees during summer and winter. From November to April they are only found south of approximately 37º N. Subtropical and tropical regions are the home of frugivorous and flower-visiting bats and flying foxes. Most species follow flowering patterns, and several of them cover considerable distances.

From the 124 bat species covered by the GROMS, 3 are classified as "Endangered", 15 as "Vulnerable" and 17 as "Lower Risk/near threatened" by the International Red List 2000 (Hilton-Taylor 2000). Among these, the Mexican free-tailed bat (Tadarida brasiliensis) is the only species listed on CMS Appendix I (Figure A2.3). Some subspecies migrate between North and South America, and distances up to 1300 km have been observed. All European bat populations are listed on CMS Appendix II, and are covered by a CMS agreement on European bats (EUROBATS: Figure A2.2), regardless of their migratory status. Among them is the noctule bat Nyctalus noctula (Schreber 1774). Females migrate further than males, and North Eastern populations move up to 2000 km in south-western direction (Figure A2.4).

Baker (1978) has compiled maps and migration distances for 20 bat species in a compact format (l.c., pp. 566 ff.). They show a complex picture with considerable variation of migration distances between sexes and different populations (demes). As shown by Figure 4.4, there is still considerable uncertainty about the migratory status of bats. Most information about migration patterns is based on the

Fig. 4.4: Migratory status of 124 bat species listed by the GROMS. Non-migratory bats are included because they are listed on CMS Appendix II and covered by the EUROBATS agreement. Note the high number of species for which a reliable assessment was impossible. Abb. 4.4: Wanderverhalten der 124 von GROMS erfaßten Fledermausarten. Berücksichtigt wurden auch nicht wandernde Arten, da diese im CMS Anhang II enthalten sind und durch das EUROBATS Abkommen geschützt werden. Man beachte die hohe Zahl von Arten, für die eine zuverlässige Einteilung nicht möglich war.

results of ringing studies, beginning with Eisentraut’s extensive banding of Myotis myotis in minetunnels in Berlin from 1932 to 1950 (Eisentraut,1935). Roer (1995) has summarised the results of bat banding in Europe, and banding schemes are still carried out in Australia (Baker et al. 1997). However, banding has been criticised as being harmful for bats (Hutson 1999). Today, it is substituted and complemented by genetic fingerprinting (cf. Webb & Tidemann 1996; Wilkinson & Fleming 1996). Hopefully, such studies will help to improve our scanty knowledge, in particular about tropical migration patterns. The IUCN/SSC Chiroptera Specialist Group planned a symposium on migration for the 12th International Bat Research Conference (Malaysia 2001) with a workshop to identify potential and priorities for future research and conservation and the potential of the development of further international collaboration, especially in South America (Hutson 2001).

Migration patterns among New World bats are less well studied, but several species do exhibit transboundary migrations, mainly from the U.S. to Mexico, and therefore qualify for CMS listing (Table 4.2). These 4 species are all threatened because of "severe declines in area of occupancy" (criteria A1c, A2c), due to habitat destruction. The western long-nose bat (Leptonycteris curasoae), and in particular the subspecies L. c. yerbabuenae (lesser long-nosed bat), pollinates the saguaro, organ-pipe cacti and the agave, the plant from which tequila is made. It suffers from degradation of the Sonoran desert ecosystem, over-exploitation of Agave and modification or destruction of roost sites, which also affect its congener, the Mexican long-nosed bat (Leptonycteris nivalis). Both species are migratory. Wilkinson & Fleming (1996) suggest two migration routes for Leptonycteris curasoae, based on genetic analysis of unique haplotypes at distant sites, 1) along the Pacific coast ranging from at least Juxtlahuaca in Guerrero to south-western Arizona and (2) inland along the Sierra Madre possibly ranging from as far south as Chiapas to south-eastern Arizona. Leptonyceris nivalis (considered conspecific with L. curasoae). No such detailed studies are available for the other species listed in Table 4.2, but they all seem to migrate.

Several species of flying foxes (Pteropodidae: Megachiroptera) are known to migrate in response to flowering and fruiting of their fruit plants, but direct observation of movement patterns is difficult.

Tab. 4.2: Threatened migratory bat species, CMS status and migratory behaviour. Threat status is given according to Red List 2000 (Hilton-Taylor 2000). Note that only European populations are covered by the CMS through the EUROBATS agreement (Figure A2.2) Tab. 4.2: Bedrohte wandernde Fledermausarten, ihr Schutzstatus gemäß der Bonner Konvention und Wanderverhalten (Gefährdung nach Hilton-Taylor 2000). Man beachte, daß nur europäische Populationen durch die Bonner Konvention und das EUROBATS-Abkommen (Figure A2.2) geschützt sind.
Family Scientific name Common name RL 2000 CMS Migration
Mormoopidae Pteronotus macleayii MacLeay's moustached bat VU N.L. possibly
migratory
Phyllostomidae Artibeus hirsutus Hairy Fruit-eating bat VU N.L. possibly
migratory
Phyllostomidae Leptonycteris curasoae Western long-nosed bat VU N.L. intra-
continental
Phyllostomidae Leptonycteris
nivalis
Mexican long-nosed bat EN N.L. possibly
migratory
Phyllostomidae Macrotus
californicus
California leaf-nosed bat VU N.L. possibly
migratory
Phyllostomidae Musonycteris
harrisoni
Trumped-nosed bat VU N.L. data
deficient
Rhinolophidae Rhinolophus
euryale
Mediterranean horseshoe bat VU App. II (Pop) technical
migrant
Rhinolophidae Rhinolophus
hipposideros
Lesser horseshoe bat VU App. II (Pop) intra-
continental
Rhinolophidae Rhinolophus
mehelyi
Mehely's horseshoe bat VU App. II (Pop) technical
migrant
Vespertilionidae Barbastella
barbastellus
Barbastelle bat VU App. II (Pop) partial
Vespertilionidae Myotis bechsteini Bechstein's bat VU App. II (Pop) technical
migrant
Vespertilionidae Myotis capaccinii Long-fingered bat VU App. II (Pop) data
deficient
Vespertilionidae Myotis dasycneme Pond bat VU App. II (Pop) intra-
continental
Vespertilionidae Myotis
emarginatus
Geoffroy's bat VU App. II (Pop) partial
Vespertilionidae Myotis grisescens Grey myotis EN App. II (Pop) data
deficient
Vespertilionidae Myotis sodalis Indiana bat EN N.L. intra-
continental
Vespertilionidae Plecotus
rafinesquii
Rafinesque's big-eared bat VU N.L. data
deficient
Vespertilionidae Plecotus
townsendii
Townsend's big-eared bat VU App. II (Pop) data
deficient

Indirect evidence by an analysis of genetic subdivisions between populations indicates that Australian Pteropus spp. (e.g. Pteropus poliocephalus Grey headed flying-fox) should be considered migratory (Webb & Tidemann 1996), at least within large ranges in coastal north and eastern Australia. The African straw-coloured fruit bat (Eidolon helvum) occurs in large seasonal concentrations near Kampala, Uganda, but their migratory movements are not understood (Kingdon 1974).

Habitat degradation affects bat species worldwide. Destruction of roosting sites and cave colonies takes place even in remote areas, due to mining and cave tourism (cf. Johnson et al. 1997) Deliberate destruction of fruit-eating bat colonies is reported from Central American banana plantation, to prevent bats from leaving claw prints on fruit. Herbicides and pesticide application affect all species directly, and indirectly by destroying food resources for insectivorous bats. High organochlorine content in bat tissue has been reported worldwide (North America: Thies 1994, Thies et al. 1996, Thies & Thies 1997; Clark et al. 1987; Thailand: Kruthanut 1986; Spain: Fernandez et al. 1993), and in particular in industrialised countries due to roof timber treatment (Shore et al. 1989). For Germany, causes of threat have been carefully compiled by Boye et al. (1999). They list:

Mammals < Bats & flying foxes > Birds
Terrestrial mammals
Marine mammals

This document should be quoted as part of the publication "Riede, K. (2001): The Global Register of Migratory Species ­ Database, GIS Maps and Threat Analysis. Münster (Landwirtschaftsverlag), 400 pp." + CD

 by Klaus Riede