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Reproduction

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Although there is little or no information available describing specific mating systems within Rhinolophidae, a few inferences may be drawn from the patterns of association between males and females. Some species form small family groups, and monogamy may be the mating systems in these cases. Others form larger colonies, either of mixed or separate sexes. In bat families (e.g., Vespertilionidae) that have been more extensively studied, this colony structure is often correlated with a promiscuous mating system. Some rhinolophids are solitary, it is not clear what mating systems are associated with these bats.

All temperate rhinolophids are monestrous, having only a single reproductive cycle per year. These species typically mate in the fall before entering hibernation and undergo either delayed fertilization or delayed implantation to ensure that their young are born in the following spring, when resources are abundant. Tropical rhinolophids are probably monestrous but may be polyestrous. Adult females give birth to one offspring per breeding cycle. Young reach independence several weeks after birth and become sexually mature by 2 years of age.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous ; delayed fertilization ; delayed implantation

Parental care is provided exclusively by females in most rhinolophids (and in most bats in general). Males may provide some form of care or defense in those species that form family groups. Females that are near to giving birth bear a considerable burden; young may be up to 25% of the mother's weight when they are born. Heavily pregnant females are awkward flyers. Young are born in an altricial state, but develop rapidly. Females nurse their offspring for about a month before the young have learned to fly and hunt well enough to become independent. Juveniles may learn some aspects of foraging behaviors from their mothers. Females of many species of bats, including some rhinolophids, may use the same nursery roost site as their mothers when they have young of their own.

Parental Investment: altricial ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Male, Female); pre-independence (Provisioning: Female, Protecting: Male, Female); post-independence association with parents

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Untitled

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The earliest rhinolophids in the fossil record are known from the Middle Eocene in Europe.

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Behavior

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All rhinolophids use echolocation as a primary means of navigating and finding food. Rhinolophid echolocation calls typically have two components: a constant frequency portion and a frequency-modulated sweep. The constant-frequency portion is about 20 milliseconds long. Unlike many other microchiropterans, rhinolophids can tolerate considerable overlap between outgoing calls and returning echoes. This tolerance allows them to spend more time calling, thus increasing their chances of detecting prey. Rhinolophids emit calls through their nasal passages, which lets them continue calling as they chew. Their echolocation calls are directed using motions of the head and the physical attributes of their complex noseleaves. The calls of many species have several harmonics, which increases their frequency range and thus the size distribution of detectable targets.

Vision, olfaction, and touch are also important to varying degrees in bats. Scent plays an important role in many social interactions, such as in mating and in mother-infant bonding. Scent glands are common in many bats (as they generally are in mammals).

Communication Channels: visual ; tactile ; acoustic ; chemical

Other Communication Modes: pheromones

Perception Channels: visual ; tactile ; acoustic ; ultrasound ; echolocation ; chemical

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Conservation Status

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Many bats are declining worldwide, and this is true for many rhinolophids as well (e.g., Rhinolophus hipposideros and Rhinolophus ferrumequinum). Disturbance of roosts, particularly winter hibernacula, can threaten a large number of bats in a short time. Habitat destruction (e.g., the reduction of appropriate forest habitat) is also a problem. Many insectivorous species are threatend by widespread pesticide use. Individual bats can eat hundreds of insects in an evening. If those insects have ingested harmful chemicals, the bats may suffer as a result. The International Union for the Conservation of Nature and Natural Resources (IUCN) currently lists 5 species of rhinolophids as vulnerable, 6 as near threatened, 4 as endangerd, and 1 as critically endangered (Rhinolophus hilli). Data is insufficient to evaluate the status of many other species, so this may be an underestimate of the groups overall vulnerability.

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Comprehensive Description

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Rhinolophidae includes approximately 77 species in a single genus, Rhinolophus. Rhinolophidae has sometimes been considered to include members of the family Hipposideridae (Old World leaf-nosed bats, with 82 species in 9 genera) as well, with the two groups being considered subfamilies (Rhinolophinae and Hipposiderinae). There is little question that these two groups of bats are closely related, but current understanding suggests the two groups should be recognized as families.

Rhinolophids inhabit temperate and tropical regions of southern Europe, Africa, Asia, parts of Australasia, and many Pacific islands. All species are insectivorous, hawking insects in flight or gleaning them from surfaces. Their roost habits are diverse; some species are found in large colonies in caves, some prefer hollow trees; others sleep in the open, among the branches of trees. Members of northern populations may hibernate during the winter. Females of some rhinolophid species mate during the fall and store sperm over the winter, conceiving and gestating young beginning in the spring.

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Benefits

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Some rhinolophids may become household pests if they form large colonies in human dwellings. The buildup of guano from a large colony can produce a foul odor.

Negative Impacts: household pest

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Benefits

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Rhinolophids are all insectivorous and are likely to control populations of insect pests. Large guano deposits can be harvested commercially for fertilizer.

Positive Impacts: produces fertilizer; controls pest population

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Associations

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All bats in the family Rhinolophidae eat only insects and other small arthropods. Their primary ecosystem function is probably to limit populations of insects and spiders. Bats harbor parasites such as fleas, mites and trematodes; thus, rhinolophids also serve as a resource for parasites. Bats are not typically important prey for other animals, but they are preyed upon by nocturnal birds of prey and snakes.

Commensal/Parasitic Species:

  • fleas (Siphonaptera)
  • mites (Parasitiformes)
  • trematodes (Trematoda)
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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Trophic Strategy

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These bats either catch insects in flight or take insects and spiders from surfaces. Rhinolophids typically forage near the ground or near dense foliage, which allows them to detect non-flying prey. Rhinolophids are capable of extremely maneuverable flight, including the ability to hover. Bats that are capable of hovering can exploit prey sources on surfaces, a resource most bat species cannot exploit. Species in this family may use regular, well-defined foraging areas.

Primary Diet: carnivore (Insectivore , Eats non-insect arthropods)

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Distribution

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Rhinolophids are widely distributed throughout both temperate and tropical regions of the Old World. They inhabit southern Europe, Africa, Asia, northern and eastern Australia, and many Pacific islands.

Biogeographic Regions: palearctic (Native ); oriental (Native ); ethiopian (Native ); australian (Native ); oceanic islands (Native )

Other Geographic Terms: island endemic

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Habitat

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Rhinolophids are found in a variety of temperate, tropical and desert biomes at both high and low elevations. They forage both within forests and in open spaces. Their roosting habits are also diverse: rhinolophids use caves, tree holes, foliage, mines, and buildings. Species that hibernate may use different roost types in the summer and winter months. While a cave may be used for hibernation in the winter, a tree hole may be used as a summer roost.

Habitat Regions: temperate ; tropical ; terrestrial

Terrestrial Biomes: desert or dune ; forest ; rainforest ; mountains

Other Habitat Features: suburban ; agricultural

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Life Expectancy

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Rhinolophids, like many bats, can live exceptionally long lives for such small animals. The longest known lifespan of a wild rhinolophid is 30 years.

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Morphology

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All rhinolophids have leaf or spear-like protuberances on their noses. The projection beneath the nostrils is horse-shoe shaped and pronounced in rhinolophids. Echolocation calls are emitted through these nasal structures, which may serve to focus the sound. The ears of these bats vary in size and lack a tragus. Most rhinolophids are dull brown or reddish brown in color. Their fur has a tendency to become bleached, so some individuals may become a bright reddish-orange. They vary in size from small to moderately large (4 to 28 grams). Males may be slightly larger than females. Their wings are broad and rounded, making them highly maneuverable in flight in cluttered spaces.

Rhinolophids have distinctive premaxillae, with palatal branches only. The premaxillae on opposite sides of the skull are neither fused with each other nor are they fused with the maxillary bones. Rhinolophid skulls often have distinct sagittal and lambdoidal crests. The palate is unusually short due to deep indentations at both ends. The molars are dilambdodont, and the dental formula is 1/2, 1/1, 1-2/2-3, 3/3 = 28-32.

Other Physical Features: endothermic ; heterothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: sexes alike; male larger

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Associations

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Predation on bats generally appears to be low, and this probably is true for rhinolophids as well. Most knowledge of bat predators comes from anecdotal observation of predation events or bat remains in scat. Groups that are known to eat bats are owls and other birds of prey, many carnivores, other bats, snakes, and other opportunistic vertebrate scavengers that encounter an injured or juvenile bat. Bats are probably most vulnerable to predators while they roost or as they emerge in the evening to forage. Some predators (e.g., snakes or hawks) may wait near cave entrances at dusk, attacking bats as they emerge. Juvenile bats that cannot fly are also at risk if they fall to the ground and are not quickly retrieved by their mothers.

Known Predators:

  • owls
  • hawks
  • bats
  • Mammalian carnivores
  • snakes

Anti-predator Adaptations: cryptic

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Wund, M. and P. Myers 2009. "Rhinolophidae" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Rhinolophidae.html
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Horseshoe bat

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Rhinolophidae is a family of bats commonly known as horseshoe bats. In addition to the single living genus, Rhinolophus, one extinct genus, Palaeonycteris, has been recognized. Horseshoe bats are closely related to the Hipposideridae, which have sometimes been included in Rhinolophidae. Internally, the horseshoe bats are divided into six subgenera and many species groups. The common ancestor of all horseshoe bats lived 34–40 million years ago, though it is unclear where the geographic roots of the family are, and attempts to determine the biogeography of the family have been indecisive. Their taxonomy is complex, as genetic evidence shows the likely existence of many cryptic species, as well as species recognized as distinct that may, in fact, have little genetic divergence from previously recognized taxa. They are found in the Old World, mostly in tropical or subtropical areas, including Africa, Asia, Europe, and Oceania.

Horseshoe bats are considered small or medium-sized microbats, weighing 4–28 g (0.14–0.99 oz), with forearm lengths of 30–75 mm (1.2–3.0 in) and combined head and body lengths of 35–110 mm (1.4–4.3 in). Fur can be reddish-brown, blackish, or bright orange-red, with a majority of species having long, smooth fur. They get their common name from their large nose-leafs, which are shaped like horseshoes. The nose-leafs aid in echolocation; horseshoe bats have highly sophisticated echolocation, using constant frequency, high-duty calls to detect prey in areas of high environmental clutters. They hunt insects and spiders, swooping down on prey from a perch, or gleaning from foliage. Little is known about their mating systems, but at least one species is monogamous, while another is polygynous. Gestation is approximately seven weeks and one offspring is produced at a time. A typical lifespan is six or seven years, but one greater horseshoe bat lived more than thirty years.

Horseshoe bats are relevant to humans as a source of disease and as food and medicine in some regions. Several species are the natural reservoirs of SARS coronavirus, though masked palm civets were the intermediate hosts through which humans became infected. Some evidence suggests that some species could be the natural reservoir of SARS-CoV-2, which causes coronavirus disease 2019. They are hunted for food in several regions, particularly Sub-Saharan Africa, but also Southeast Asia. Some species or their guano are used in traditional medicine in Nepal, India, Vietnam, and Senegal.

Taxonomy and evolution

Taxonomic history

Rhinolophus was first described as a genus in 1799 by French naturalist Bernard Germain de Lacépède. Initially, all extant horseshoe bats were in Rhinolophus, as well as the species now in Hipposideros (roundleaf bats).[1](p xii) At first, Rhinolophus was within the family Vespertilionidae. In 1825, John Edward Gray subdivided Verspertilionidae into subfamilies, including what he called Rhinolophina.[2] English zoologist Thomas Bell is credited as the first to recognize horseshoe bats as a separate family, using Rhinolophidae in 1836.[3] While Bell is sometimes recognized as the authority for Rhinolophidae,[4] the authority is more often given as Gray, 1825.[3][5] Horseshoe bats are in the superfamily Rhinolophoidea, along with Craseonycteridae, Megadermatidae, Rhinonycteridae, and Rhinopomatidae.[6][7]

Attempts were made to divide Rhinolophus into other genera. In 1816, William Elford Leach proposed the genus name Phyllorhina; Gray proposed Aquias in 1847 and Phyllotis in 1866; and Wilhelm Peters proposed Coelophyllus in 1867. In 1876, George Edward Dobson returned all Asiatic horseshoe bats to Rhinolophus, additionally proposing the subfamilies Phyllorhininae (for the hipposiderids) and Rhinolophinae. Gerrit Smith Miller further divided the hipposiderids from the horseshoe bats in 1907, recognizing Hipposideridae as a distinct family.[1](p xii) Some authors have considered Hipposideros and associated genera as part of Rhinolophidae as recently as the early 2000s,[8] though they are now most often recognized as a separate family. After the split into Rhinolophidae and Hipposideridae, further divisions were proposed for Rhinolophus, with Rhinolphyllotis in 1934 and Rhinomegalophus in 1951, though both additional genera were returned to Rhinolophus.[1](p xii)

Knud Andersen was the first to propose species groups for Rhinolophus, doing so in 1905. He recognized six species groups: R. simplex (now R. megaphyllus), R. lepidus, R. midas (now R. hipposideros), R. philippinensis, R. macrotis, and R. arcuatus. The species have been frequently rearranged among the groups as new groups are added, new species are described, and relationships among species are revised.[1](p xiii) Fifteen species groups were given by Csorba et al. in 2003.[1][9] Various subgenera have been proposed as well, with six listed by Csorba et al. in 2003: Aquias, Phyllorhina, Rhinolophus, Indorhinolophus, Coelophyllus, and Rhinophyllotis.[1](p xvi) Informally, the rhinolophids can be split into two major clades: the mostly African clade, and the mostly Oriental clade.[8]

Evolutionary history

"
Upper and lower maxilla of the Lower Miocene fossil horseshoe bat, Palaeonycteris robustus

The most recent common ancestor of Rhinolophus lived an estimated 34–40 million years ago,[10] splitting from the hipposiderid lineage during the Eocene.[8] Fossilized horseshoe bats are known from Europe (early to mid-Miocene, early Oligocene), Australia (Miocene), and Africa (Miocene and late Pliocene).[11] The biogeography of horseshoe bats is poorly understood. Various studies have proposed that the family originated in Europe, Asia, or Africa. A 2010 study supported an Asian or Oriental origin of the family, with rapid evolutionary radiations of the African and Oriental clades during the Oligocene.[8] A 2019 study found that R. xinanzhongguoensis and R. nippon, both Eurasian species, were more closely related to African species than to other Eurasian species, suggesting that rhinolophids may have a complex biogeographical relationship with Asia and the Afrotropics.[10]

A 2016 study using mitochondrial and nuclear DNA placed the horseshoe bats within the Yinpterochiroptera as sister to the Hipposideridae.[7]

Chiroptera    

Yangochiroptera "Pteronotus

    Yinpterochiroptera

Pteropodidae (megabats) "Mariana

    Rhinolophoidea    

Rhinopomatidae "Lesser

     

Megadermatidae "Megaderma

   

Craseonycteridae

         

Rhinonycteridae "Rhinonicteris

     

Hipposideridae "Hipposideros

   

Rhinolophidae "Rhinolophus

                 

Rhinolophidae is represented by one extant genus, Rhinolophus. Both the family and the genus are confirmed as monophyletic (containing all descendants of a common ancestor). As of 2019, there were 106 described species in Rhinolophus, making it the second-most speciose genus of bat after Myotis. Rhinolophus may be undersampled in the Afrotropical realm, with one genetic study estimating that there could be up to twelve cryptic species in the region. Additionally, some taxa recognized as full species have been found to have little genetic divergence. Rhinolophus kahuzi may be a synonym for the Ruwenzori horseshoe bat (R. ruwenzorii), and R. gorongosae or R. rhodesiae may be synonyms of the Bushveld horseshoe bat (R. simulator). Additionally, Smithers's horseshoe bat (R. smithersi), Cohen's horseshoe bat (R. cohenae), and the Mount Mabu horseshoe bat (R. mabuensis) all have little genetic divergence from Hildebrandt's horseshoe bat (R. hildebrandtii). Recognizing the former three as full species leaves Hildebrandt's horseshoe bat paraphyletic.[10]

The second genus in Rhinolophidae is the extinct Palaeonycteris, represented by one species, Palaeonycteris robustus.[12] Palaeonycteris robustus lived during the Lower Miocene and its fossilized remains were found in Saint-Gérand-le-Puy, France.[13][14]

Description

Appearance

"
Nose-leaf diagram of a horseshoe bat

Horseshoe bats are considered small or medium microbats.[15] Individuals have a head and body length ranging from 35–110 mm (1.4–4.3 in) and have forearm lengths of 30–75 mm (1.2–3.0 in). One of the smaller species, the lesser horseshoe bat (R. hipposideros), weighs 4–10 g (0.14–0.35 oz), while one of the larger species, the greater horseshoe bat (R. ferrumequinum), weighs 16.5–28 g (0.58–0.99 oz). Fur color is highly variable among species, ranging from blackish to reddish brown to bright orange-red dorsal fur.[16][11] The underparts are paler than the back fur.[16] The majority of species have long, soft fur, but the woolly and lesser woolly horseshoe bats (R. luctus and R. beddomei) are unusual in their very long, woolly fur.[11]

Like most bats, horseshoe bats have two mammary glands on their chests. Adult females additionally have two teat-like projections on their abdomens, called pubic nipples or false nipples, which are not connected to mammary glands. Only a few other bat families have pubic nipples, including Hipposideridae, Craseonycteridae, Megadermatidae, and Rhinopomatidae; they serve as attachment points for their offspring.[17] In a few species, males have a false nipple in each armpit.[15]

Head and teeth

"
Skull of the greater horseshoe bat, showing the prominent rostral inflations on the snout

All horseshoe bats have large, leaf-like protuberances on their noses, which are called nose-leafs. The anterior portion of the nose-leaf has a horseshoe shape, earning them the common name of "horseshoe bats".[15] The nose-leafs are important in species identification, and are composed of several parts. The lancet is triangular, pointed, and pocketed, and points up between the bats' eyes.[18] The sella is a flat, ridge-like structure at the center of the nose, rising from behind the nostrils, that points out perpendicular from the head.[18] The sella usually has less hair than the lancet or the nose-leaf.[18] Their ears are large and leaf-shaped, nearly as broad as they are long, and lack tragi. The antitragi of the ears are conspicuous. Their eyes are very small.[15] The skull always has rostral inflations. The typical dental formula of a horseshoe bat is 1.1.2.32.1.3.3, but the middle lower premolars are often missing, as well as the anterior upper premolars.[1](p xi) The young lose their milk teeth while still in utero,[16] with the teeth resorbed into the body. They are born with the four permanent canine teeth erupted, which enables them to cling to their mothers.[19] This is atypical among bat families, as most newborns have at least some milk teeth at birth, which are quickly replaced by the permanent set.[20]

Postcrania

Several bones in their thoraxes are fused—the presternum, first rib, partial second rib, seventh cervical vertebra, first thoracic vertebra—making a solid ring.[1](p xi) This fusion is associated with the ability to echolocate while stationary.[21] Except for the first digit, which has two phalanges,[16] all of their toes have three phalanges.[1](p xi) This distinguishes them from hipposiderids, which have two phalanges in all toes.[15] The tail is completely enclosed in the uropatagium (tail membrane),[1](p xi) and the trailing edge of the uropatagium has calcars (cartilaginous spurs).[15]

Biology and ecology

Echolocation and hearing

"
The nose-leaf helps focus echolocation; pictured is Rüppell's horseshoe bat (R. fumigatus)

Horeshoe bats have very small eyes and their field of vision is limited by their large nose-leafs; thus, vision is unlikely to be a very important sense. Instead, they use echolocation to navigate.[11] Horseshoe bats have some of the most sophisticated echolocation of any bat group.[22] To echolocate, they produce sound through their nostrils. While some bats use frequency-modulated echolocation, horseshoe bats use constant-frequency echolocation (also known as single-frequency echolocation).[23] They have high duty cycles, meaning that when individuals are calling, sound production composes more than 30% of total time. The use of high-duty, constant-frequency echolocation aids in distinguishing prey items based on size. These echolocation characteristics are typical of bats that search for moving prey items in cluttered environments.[22] They echolocate at particularly high frequencies for bats, though not as high as hipposiderids relative to their body sizes, and the majority concentrate most of the echolocation energy into the second harmonic. The king horseshoe bat (R. rex) and the large-eared horseshoe bat (R. philippensis) are examples of outlier species that concentrate energy into the first harmonic rather than the second.[24] Their highly furrowed nose-leafs likely assist in focusing the emission of sound, reducing the effect of environmental clutter on sound.[23] The nose-leaf in general acts like a parabolic reflector, aiming the production of sound while simultaneously shielding the ear from some of it.[15]

Horseshoe bats have sophisticated senses of hearing via well-developed cochlea,[15] and are able to detect Doppler-shifted echoes. This allows them to produce and receive sounds simultaneously.[1](p xi) Within horseshoe bats, there is a negative relationship between ear length and echolocation frequency: Species with higher echolocation frequencies tend to have shorter ear lengths.[24] During echolocation, the ears can move independently of each other in a "flickering" motion characteristic of the family, while the head simultaneously moves up and down or side to side.[15]

Diet and foraging

"
Outline of Pearson's horseshoe bat (R. pearsonii) (top) compared to the European free-tailed bat (Tadarida teniotis), which is a molossid. In comparing the two families, horseshoe bats have lower aspect ratios, lower wing loading, larger wing areas, and rounder wing tips. Molossids are adapted for fast, less maneuverable flight.[25](pp387, 398–399)

Horseshoe bats are insectivorous, though consume other arthropods like spiders,[16] and employ two main foraging strategies. The first strategy is fly slow and low over the ground, hunting among trees and bushes. Some species who use this strategy are able to hover over prey and glean them from the substrate. The other strategy is known as perch feeding: Individuals roost on feeding perches and wait for prey to fly past, then fly out to capture it.[1](p xi) Foraging usually occurs 5.0–5.9 m (16.5–19.5 ft) above the ground.[11] While vesper bats may catch prey in their uropatagia and transfer it to their mouths, horseshoe bats do not use their uropatagia to catch prey. At least one species, the greater horseshoe bat, has been documented catching prey in the tip of its wing by bending the phalanges around it, then transferring it to its mouth.[15][26]

They have especially small and rounded wingtips, low wing loading (meaning they lave large wings relative to body mass), and high camber. These factors give them increased agility, and they are capable of making highly maneuverable, tight turns at slow speeds.[25](p361) The wingspans are typical for their body sizes, and their aspect ratios, which relate wingspan to wing area, are average or lower than average. Some species, like Rüppell's horseshoe bat (R. fumigatus), Hildebrandt's horseshoe bat, Lander's horseshoe bat (R. landeri), and Swinny's horseshoe bat (R. swinnyi), have particularly large total wing area, though most horseshoe bat species have average wing area.[25](p387)

Reproduction and life cycle

The mating systems of horseshoe bats are poorly understood. A review in 2000 noted that only about 4% of species had published information about their mating systems; along with the free-tailed bats (Molossidae), they had the least attention of any bat family relative to their species diversity. At least one species, the greater horseshoe bat, appears to have a polygynous mating system where males attempt to establish and defend territories, attracting multiple females. Rhinolophus sedulus, however, is a rare species of bat that is believed to be monogamous (only 17 bat species are recognized as such as of 2000).[27] Some species, particularly temperate species, have an annual breeding season in the fall, while other species mate in the spring.[16] Many horseshoe bat species have the adaptation of delayed fertilization through female sperm storage. This is especially common in temperate species. In hibernating species, the sperm storage timing coincides with hibernation.[1](p xi) Other species like Lander's horseshoe bat (R. landeri) have embryonic diapause, meaning that while fertilization occurs directly following copulation, the zygote does not implant into the uterine wall for an extended period of time.[15] The greater horseshoe bat has the adaptation of delayed embryonic development, meaning that growth of the embryo is conditionally delayed if the female enters torpor. This causes the interval between fertilization and birth to vary from two to three months.[28] Gestation takes approximately seven weeks before a single offspring is born, called a pup. Individuals reach sexual maturity by age two. While lifespans typically do not exceed six or seven years, some individuals may have extraordinarily long lives. A greater horseshoe bat individual was once banded and then rediscovered thirty years later.[16]

Behavior and social systems

Various levels of sociality are seen in horseshoe bats. Some species are solitary, with individuals roosting alone, while others are highly colonial, forming aggregations of thousands of individuals.[1](p xi) The majority of species are moderately social. In some species, the sexes segregate annually when females form maternity colonies, though the sexes remain together all year in others. Individuals hunt solitarily.[16] Because its hind limbs are poorly developed, it cannot scuttle on flat surfaces nor climb adeptly like other bats.[11][15]

Range and habitat

Horseshoe bats have a mostly Paleotropical distribution, though some species are in the southern Palearctic realm.[10] They are found in the Old World, including Africa, Australia, Asia, Europe, and Oceania.[8] The greater horseshoe bat has the greatest geographic range of any horseshoe bat, occurring across Europe, North Africa, Japan, China, and southern Asia. Other species are much more restricted, like the Andaman horseshoe bat (R. cognatus), which is only found on the Andaman Islands.[11] They roost in a variety of places, including buildings, caves, tree hollows, and foliage. They occur in both forested and unforested habitat,[16] with the majority of species occurring in tropical or subtropical areas.[15] For the species that hibernate, they select caves with an ambient temperature of approximately 11 °C (52 °F).[29]

Relationship to humans

As disease reservoirs

Coronaviruses

Number of SARS-related coronaviruses (SARSr-CoVs) by bat species[30] Bat species No. SARSr-CoVs Chinese rufous horseshoe bat
30
Greater horseshoe bat
9
Big-eared horseshoe bat
2
Least horseshoe bat
2
Intermediate horseshoe bat
1
Blasius's horseshoe bat
1
Stoliczka's trident bat
1
Wrinkle-lipped free-tailed bat
1
"
The rufous horseshoe bat (R. rouxii) has tested seropositive for Kyasanur Forest disease, which is transmitted to humans by ticks

Horseshoe bats are of particular interest to public health and zoonosis as a source of coronaviruses. Following the 2002–2004 SARS outbreak, several animal species were examined as possible natural reservoirs of the causative coronavirus, SARS-CoV. Several horseshoe bats were seropositive for SARS-related coronaviruses (testing positive for antibodies associated with it), tested positive for the viruses, or both. The least horseshoe bat (R. pusillus) was seropositive, the greater horseshoe bat tested positive for the virus only, and the big-eared horseshoe bat (R. macrotis), Chinese rufous horseshoe bat (R. sinicus), and Pearson's horseshoe bat (R. pearsoni) were seropositive and tested positive for the virus.[30][31] The bats' viruses were highly similar to SARS-CoV, with 88–92% similarity.[32] Though horseshoe bats appeared to be the natural reservoir of SARS-related coronaviruses, humans likely became sick through contact with infected masked palm civets, which were identified as intermediate hosts of the virus.[32] From 2003–2018, forty-seven SARS-related coronaviruses were detected in bats, forty-five of which were found in horseshoe bats. Thirty SARS-related coronaviruses were from Chinese rufous horseshoe bats, nine from greater horseshoe bats, two from big-eared horseshoe bats, two from the least horseshoe bat, and one each from the intermediate horseshoe bat (R. affinis), Blasius's horseshoe bat (R. blasii), Stoliczka's trident bat (Aselliscus stoliczkanus), and the wrinkle-lipped free-tailed bat (Chaerephon plicata).[30] In 2019, a coronavirus pandemic began in Wuhan, China. Researchers determined that the coronavirus is likely closely related to those found in horseshoe bats.[33]

Other viruses

They are also associated with viruses like orthoreoviruses, flaviviruses, and hantaviruses. They have tested positive for Mammalian orthoreovirus (MRV), including a type 1 MRV isolated from the lesser horseshoe bat and a type 2 MRV isolated from the least horseshoe bat (R. pusillus). The specific MRVs found in horseshoe bats have not been linked to human infection, though humans can become ill through exposure to other MRVs.[34] The rufous horseshoe bat (R. rouxii) has tested seropositive for Kyasanur Forest disease, which is a tick-borne viral hemorrhagic fever known from southern India. Kyasanur Forest disease is transmitted to humans through the bite of infected ticks, and has a mortality rate of 2–10%.[35] Longquan virus, a kind of hantavirus, has been detected in the intermediate horseshoe bat, Chinese rufous horseshoe bat, and the little Japanese horseshoe bat (R. cornutus).[36]

As food and medicine

Microbats are not hunted nearly as intensely as megabats: only 8% of insectivorous species are hunted for food, compared to half of all megabat species in the Old World tropics. Horseshoe bats are hunted for food, particularly in Sub-Saharan Africa. Species hunted in Africa include the halcyon horseshoe bat (R. alcyone), Guinean horseshoe bat (R. guineensis), R. hilli, Hills' horseshoe bat (R. hillorum), Maclaud's horseshoe bat (R. maclaudi), the Ruwenzori horseshoe bat, the forest horseshoe bat (R. silvestris), and the Ziama horseshoe bat (R. ziama). In Southeast Asia, Marshall's horseshoe bat (R. marshalli) is consumed in Myanmar and the large rufous horseshoe bat (R. rufus) is consumed in the Philippines.[37]

The Ao Naga people of Northeast India are reported to use the flesh of horseshoe bats to treat asthma. The Newar people of Nepal "almost certainly" use horseshoe bats, among other species, to prepare Cikā Lāpa Wasa ("bat oil"). Dead bats are rolled up and placed in tightly sealed jars of mustard oil; the oil is ready when it gives off a distinct and unpleasant smell. Traditional medicinal uses of the bat oil include removing "earbugs", reported to be millipedes that crawl into one's ears and gnaw at the brain, possibly a traditional explanation of migraines. It is also used as a purported treatment for baldness and partial paralysis.[38] In Senegal, there are anecdotal reports of horseshoe bats being used in potions to treat mental illness; in Vietnam, a pharmaceutical company reported using 50 t (50,000 kg) of horseshoe bat guano each year for medicinal uses.[39]

Conservation

Critically endangered (1.1%)
Endangered (8.0%)
Vulnerable (6.9%)
Near-threatened (9.2%)
Least concern (59.8%)
Data deficient (14.9%)

As of 2020, the IUCN had evaluated 87 species of horseshoe bat. They have the following IUCN statuses:[40]

Like all cave-roosting bats, cave-roosting horseshoe bats are vulnerable to disturbance of their cave habitats. Disturbance can include mining bat guano, quarrying limestone, and cave tourism.[29]

References

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  22. ^ a b Jones, G.; Teeling, E. (2006). "The evolution of echolocation in bats". Trends in Ecology & Evolution. 21 (3): 149–156. doi:10.1016/j.tree.2006.01.001. PMID 16701491.
  23. ^ a b Vanderelst, Dieter; Jonas, Reijniers; Herbert, Peremans (2012). "The furrows of Rhinolophidae revisited". Journal of the Royal Society Interface. 9 (70): 1100–1103. doi:10.1098/rsif.2011.0812. PMC 3306658. PMID 22279156.
  24. ^ a b Huihua, Zhao; Shuyi, Zhang; Mingxue, Zuo; Jiang, Zhou (2003). "Correlations between call frequency and ear length in bats belonging to the families Rhinolophidae and Hipposideridae". Journal of Zoology. 259 (2): 189–195. doi:10.1017/S0952836902003199.
  25. ^ a b c Norberg, U. M.; Rayner, J. M. V. (1987). "Ecological morphology and flight in bats (Mammalia; Chiroptera): Wing adaptations, flight performance, foraging strategy and echolocation". Philosophical Transactions of the Royal Society of London B, Biological Sciences. 316 (1179): 335–427. Bibcode:1987RSPTB.316..335N. doi:10.1098/rstb.1987.0030.
  26. ^ Webster, Frederic A.; Griffin, Donald R. (1962). "The role of the flight membranes in insect capture by bats". Animal Behaviour. 10 (3–4): 332–340. doi:10.1016/0003-3472(62)90056-8.
  27. ^ McCracken, Gary F.; Wilkinson, Gerald S. (2000). "Bat Mating Systems". Reproductive Biology of Bats. pp. 321–362. doi:10.1016/B978-012195670-7/50009-6. ISBN 9780121956707.
  28. ^ Gaisler, J. (2013). Kingdon, J.; Happold, D.; Butynski, T.; Hoffmann, M.; Happold, M.; Kalina, J. (eds.). Mammals of Africa. 4. A&C Black. pp. 327–328. ISBN 9781408189962.
  29. ^ a b Furey, Neil M.; Racey, Paul A. (2016). "Conservation Ecology of Cave Bats". Bats in the Anthropocene: Conservation of bats in a changing world. pp. 463–500. doi:10.1007/978-3-319-25220-9_15. ISBN 978-3-319-25218-6.
  30. ^ a b c Luk, Hayes K.H.; Li, Xin; Fung, Joshua; Lau, Susanna K.P.; Woo, Patrick C.Y. (2019). "Molecular epidemiology, evolution and phylogeny of SARS coronavirus". Infection, Genetics and Evolution. 71: 21–30. doi:10.1016/j.meegid.2019.03.001. PMID 30844511.
  31. ^ Shi, Zhengli; Hu, Zhihong (2008). "A review of studies on animal reservoirs of the SARS coronavirus". Virus Research. 133 (1): 74–87. doi:10.1016/j.virusres.2007.03.012. PMID 17451830.
  32. ^ a b Wang, Lin-Fa; Shi, Zhengli; Zhang, Shuyi; Field, Hume; Daszak, Peter; Eaton, Bryan (2006). "Review of Bats and SARS". Emerging Infectious Diseases. 12 (12): 1834–1840. doi:10.3201/eid1212.060401. PMC 3291347. PMID 17326933.
  33. ^ "Novel Coronavirus (2019-nCoV) Situation Report" (PDF). World Health Organization. 11 February 2020. Retrieved 15 February 2020.
  34. ^ Beltz, Lisa A. (2017). Bats and Human Health: Ebola, SARS, Rabies and Beyond. John Wiley & Sons. p. 155. ISBN 9781119150046.
  35. ^ Pattnaik, Priyabrata (2006). "Kyasanur forest disease: An epidemiological view in India". Reviews in Medical Virology. 16 (3): 151–165. doi:10.1002/rmv.495. PMID 16710839.
  36. ^ Guo, Wen-Ping; Lin, Xian-Dan; Wang, Wen; Tian, Jun-Hua; Cong, Mei-Li; Zhang, Hai-Lin; Wang, Miao-Ruo; Zhou, Run-Hong; Wang, Jian-Bo; Li, Ming-Hui; Xu, Jianguo; Holmes, Edward C.; Zhang, Yong-Zhen (2013). "Phylogeny and Origins of Hantaviruses Harbored by Bats, Insectivores, and Rodents". PLoS Pathogens. 9 (2): e1003159. doi:10.1371/journal.ppat.1003159. PMC 3567184. PMID 23408889.
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  38. ^ Tuladhar-Douglas, Will (2008). "The Use of Bats as Medicine Among the Newars". Journal of Ethnobiology. 28: 69–91. doi:10.2993/0278-0771(2008)28[69:TUOBAM]2.0.CO;2. ISSN 0278-0771.
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  40. ^ "Taxonomy=Rhinolophidae". IUCN. Retrieved 15 February 2020.
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Horseshoe bat: Brief Summary

provided by wikipedia EN

Rhinolophidae is a family of bats commonly known as horseshoe bats. In addition to the single living genus, Rhinolophus, one extinct genus, Palaeonycteris, has been recognized. Horseshoe bats are closely related to the Hipposideridae, which have sometimes been included in Rhinolophidae. Internally, the horseshoe bats are divided into six subgenera and many species groups. The common ancestor of all horseshoe bats lived 34–40 million years ago, though it is unclear where the geographic roots of the family are, and attempts to determine the biogeography of the family have been indecisive. Their taxonomy is complex, as genetic evidence shows the likely existence of many cryptic species, as well as species recognized as distinct that may, in fact, have little genetic divergence from previously recognized taxa. They are found in the Old World, mostly in tropical or subtropical areas, including Africa, Asia, Europe, and Oceania.

Horseshoe bats are considered small or medium-sized microbats, weighing 4–28 g (0.14–0.99 oz), with forearm lengths of 30–75 mm (1.2–3.0 in) and combined head and body lengths of 35–110 mm (1.4–4.3 in). Fur can be reddish-brown, blackish, or bright orange-red, with a majority of species having long, smooth fur. They get their common name from their large nose-leafs, which are shaped like horseshoes. The nose-leafs aid in echolocation; horseshoe bats have highly sophisticated echolocation, using constant frequency, high-duty calls to detect prey in areas of high environmental clutters. They hunt insects and spiders, swooping down on prey from a perch, or gleaning from foliage. Little is known about their mating systems, but at least one species is monogamous, while another is polygynous. Gestation is approximately seven weeks and one offspring is produced at a time. A typical lifespan is six or seven years, but one greater horseshoe bat lived more than thirty years.

Horseshoe bats are relevant to humans as a source of disease and as food and medicine in some regions. Several species are the natural reservoirs of SARS coronavirus, though masked palm civets were the intermediate hosts through which humans became infected. Some evidence suggests that some species could be the natural reservoir of SARS-CoV-2, which causes coronavirus disease 2019. They are hunted for food in several regions, particularly Sub-Saharan Africa, but also Southeast Asia. Some species or their guano are used in traditional medicine in Nepal, India, Vietnam, and Senegal.

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