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Bat Predation by Spiders


In this paper more than 50 incidences of bats being captured by spiders are reviewed. Bat-catching spiders have been reported from virtually every continent with the exception of Antarctica (∼90% of the incidences occurring in the warmer areas of the globe between latitude 30° N and 30° S). Most reports refer to the Neotropics (42% of observed incidences), Asia (28.8%), and Australia-Papua New Guinea (13.5%). Bat-catching spiders belong to the mygalomorph family Theraphosidae and the araneomorph families Nephilidae, Araneidae, and Sparassidae. In addition to this, an attack attempt by a large araneomorph hunting spider of the family Pisauridae on an immature bat was witnessed. Eighty-eight percent of the reported incidences of bat catches were attributable to web-building spiders and 12% to hunting spiders. Large tropical orb-weavers of the genera Nephila and Eriophora in particular have been observed catching bats in their huge, strong orb-webs (of up to 1.5 m diameter). The majority of identifiable captured bats were small aerial insectivorous bats, belonging to the families Vespertilionidae (64%) and Emballonuridae (22%) and usually being among the most common bat species in their respective geographic area. While in some instances bats entangled in spider webs may have died of exhaustion, starvation, dehydration, and/or hyperthermia (i.e., non-predation death), there were numerous other instances where spiders were seen actively attacking, killing, and eating the captured bats (i.e., predation). This evidence suggests that spider predation on flying vertebrates is more widespread than previously assumed.


Bats have few natural enemies [1]. The most prominent bat enemies mentioned in the scientific literature are owls, hawks, and snakes [1][3]. Predation by a few large arthropods is occasionally documented in the literature as well [3][5]. In a cave in Venezuela, giant centipedes (Scolopendridae) have been observed killing and eating mormoopid and phyllostomid bats [5]. Whip spiders (Phrynidae) were observed feeding on dead phyllostomid bats in caves of the Caribbean, but it is not known whether this were cases of predation or scavenging ([6]; B. Fenton, pers. comm.). Despite their name, whip spiders do not belong to the order “spiders” (Araneae); instead they belong to the Amblypygi which is a separate arachnid order. Furthermore, cockroaches have been seen feeding on bat pups which have fallen to the floor [7][8]. In several technical books on chiropterology, accidental deaths of bats in spider webs have been reported [3], [9][12]. The observation of bat-catching by spiders is not that peculiar if we consider the fact that a number of larger-sized spiders are known to supplement their arthropod diet by occasionally preying on vertebrates. Fishing spiders (Pisauridae) have been reported capturing and devouring fish and frogs [13][14]. Some species of wolf spiders (Lycosidae), huntsman spiders (Sparassidae), tarantulas (Theraphosidae) and other mygalomorph spiders were observed killing and eating frogs and lizards [13], [15][19]. Predation on snakes and mice by tarantulas and comb-footed spiders (Theridiidae) has been mentioned in the literature [13], [20]. Furthermore, there are numerous reports of birds being killed in the large orb-webs of araneid and nephilid spiders, whereby the birds were either eaten by the spiders or not [21][29].

Deaths of bats in spider webs have been considered to occur very rarely. In two more recent papers, a web-building spider, Argiope savignyi, and a theraphosid spider, Poecilotheria rufilata, were each reported to predate on a small bat [30][31]. These authors hypothesized that bat captures and kills due to spiders might be more frequent than previously thought. To test this hypothesis, an extensive global literature survey on bat-catching spiders was conducted, along with an attempt to use web-based sources as well. The insights from this research are reviewed here.


An extensive bibliographic search was conducted in order to find any information available on bat-catching spiders. The search was based largely on the Thomson-Reuters data base (Web of Science), Google Scholar, Google Books, ProQuest Dissertations & Theses, and Flickr image-hosting website (hosting more than 6 billion images). In addition to this, an internet search for blogger information on this topic was conducted. Bloggers who had posted photographs and reports on bat-catching spiders on the internet were contacted to get detailed information on their observations. Furthermore, the staff of bat hospitals was contacted to get information on bats rescued from spider webs. Finally, an inquiry among fellow arachnologists and chiropterologists was carried out to get access to unpublished reports on this topic. Many of these experts had conducted field studies for decades, and their feedback provided valuable information needed to assess how frequent incidences of bat catches by spiders might be. Altogether, 52 reports on bat-catching spiders could be gathered (Table 1). Twenty-three of these reports have previously been published in scientific journals, books, and a doctoral thesis.

Table 1. Fifty-two reports of bat-catching spiders based on literature and unpublished data (for more details see File S1).

During these inquiries we got access to several previously unpublished photographs of bat-catching spiders. These photographs were shown to established bat and spider taxonomists for identification of the bats and spiders, respectively. In a few cases photographs of habitats were sent to vegetation specialists for proper habitat classification. Nomenclature follows [32][33]. Spiders reported in this paper are divided into two major groups based on foraging mode (sensu Gertsch [14]): “Hunting spiders” (i.e., spiders that forage without the use of a catching web) and “Web-building spiders” (i.e., spiders that forage using a catching web). Data on spider weight and size as well as bat weight, wingspan, foraging mode and echolocation call frequency were taken from the literature when available. Report numbers used in the results, tables and figures refer to the respective detailed report description (see File S1).


Geographic Distribution of Bat Catches by Spiders

Incidences of bats being captured by spiders have been reported from virtually every continent with the exception of Antarctica (Table 1). Seventy-seven percent of the incidences listed in Table 1 were witnessed in regions of tropical climate between latitude 23° N and 23° S (∼90% of the cases occurred between latitude 30° N and 30° S; Fig. 1). The prevalence of such events in the warmer areas of the globe may be explained, among others, by the fact that the vast majority of spider species capable of catching bats are giant theraphosids, nephilids, and araneids who have their main area of distribution in the tropical and subtropical regions [20], [33][35].

Figure 1. Geographic distribution of bat catching spiders worldwide.

The map depicts the locations were spiders were observed catching bats (red dots). Large red dots indicate that several reports originated from the same geographic region. Numbers refer to the detailed report description (see File S1).

There are six reports on bats being captured by hunting spiders. Tarantulas (Theraphosidae) of the genus Avicularia have been observed eating small bats in tropical rainforest areas in Peru (Fig. 2A; report # 1) and eastern Ecuador (report # 2), respectively ([18]; Rick West, pers. website; G. Schmid, flickr image hosting website). A large tarantula of the genus Lasiodora was observed eating a bat on the forest floor in northeastern Brazil (R. West, pers. comm.; report # 3). Moreover, a large Reddish Parachute tarantula, Poecilotheria rufilata, was reported to predate on a small bat in Kerala, India ([31]; report # 4). Furthermore, a huntsman spider Heteropoda venatoria (Sparassidae) was observed capturing and killing a small bat in a shed near Kolkata, India ([36]; report # 5). This spider had apparently not fed on the bat which may be explained by the fact that the observer interfered by capturing spider and bat and placing them into a glass jar (see File S1). An attempt by a large fishing spider Dolomedes triton (Pisauridae) to kill a bat pup has been witnessed below a bridge in Indiana, USA (P. Clem & V. Brack, pers. comm.; report # 6). However, in this latter case the predation attempt failed probably because the spider was frightened by the presence of the photographing observers (see File S1). All other reports refer to web-building spiders.

Figure 2. Bats caught by spiders. A -

Adult female Avicularia urticans feeding on a Greater Sac-winged Bat (Saccopteryx bilineata) on the side of a palm tree near the Rio Yarapa, Peru (photo by Rick West, Victoria, Canada; report # 1). B - Adult Proboscis Bat (Rhynchonycteris naso) entangled in a web of Argiope savignyi at the La Selva Biological Station, northern Costa Rica (photo by Mirjam Knörnschild, Ulm, Germany; report # 14). C - Dead bat (presumably Centronycteris centralis) entangled in an orb-web in Belize (photo by Carol Farneti-Foster, Belice City, Belize; report # 12). D - Dead bat (Myotis sp.) entangled in a web of Nephila clavipes in La Sirena, Corcovado National Park, Costa Rica (photo by Harald & Gisela Unger, Köln, Germany; report # 17). E - A bat caught in the web of an araneid spider (possibly Eriophora sp.) in Tortuguero National Park, Costa Rica (photo by Cassidy Metcalf, USA; report # 18). F - Live bat trapped in web of Nephilengys cruentata in a thatch roof at Nisela Lodge, Swaziland (photo by Donald Schultz, Hollywood, USA; report # 47). G - Volant juvenile Proboscis Bat (Rhynchonycteris naso) entangled in web of Nephila clavipes photographed in a palm swamp forest near Madre de Dios, Peru (photo by Sam Barnard, Colorado Springs, USA; report # 7). H - Dead bat entangled in web of a female Nephila clavipes in tropical rainforest in the middle of the Rio Dulce River Canyon near Livingston, Guatemala (photo by Sam & Samantha Bloomquist, Indianapolis, USA; report # 11). I - Dead bat (Rhinolophus cornutus orii) caught in the web of a female Nephila pilipes on Amami-Oshima Island, Japan (photo by Yasunori Maezono, Kyoto University, Japan; report # 35). J, K - A small bat (superfamily Rhinolophoidea) entangled in web of Nephila pilipes at the top of the Cockatoo Hill near Cape Tribulation, Queensland, Australia (photo by Carmen Fabro, Cockatoo Hill, Australia; report # 39). The spider pressed its mouth against the dead, wrapped bat, indicating that it was feeding on it. A Nephila pilipes male also present in the web (K) may have been feeding on the bat as well. L - Dead vespertilionid bat entangled in the web of a female Nephila pilipes in the Aberdeen Country Park, Hong Kong (photo by Carol S.K. Liu from AFCD Hong Kong, China; report # 32).

There are 19 reports of Neotropical bats being captured in orb-webs of large araneids or nephilinids. These reports refer to incidences witnessed in Peru (report # 7), Colombia (report # 8–10), Guatemala (report # 11), Belize (report # 12–13), Costa Rica (report # 14–20), Panama (report # 21–24), or elsewhere in Central America (report # 25) and are depicted in Fig. 2B–E, G and H. Several of these observations were made by researchers stationed at the Los Amigos Biological Station in Peru, the Biological Stations La Selva and La Sirena in Costa Rica and the Smithsonian Tropical Research Station Barro Colorado Island in Panama, which are all located in lowland tropical rainforest ([8], [30], [37][38]; M. Knörnschild, unpubl. data; M. Eckenweber, pers. comm.; M. Mallo & C. Díez, pers. comm.; M. Nagy, pers. comm.; H & G. Unger, pers. comm.; M. Weber, pers. comm.). In the incidences witnessed in Costa Rica and Panama, the spiders had constructed their webs on the outside of or in close proximity to buildings inhabited by bat colonies ([8]; M. Knörnschild, unpubl. data; C. Metcalf, pers. comm.).

A second geographic region where bat-catching by web-building spiders has frequently been reported (13 reports; 2I and L) is eastern and southeastern Asia including locations in China (report # 26–34), Japan (report # 35), Vietnam (report # 36), Malaysia (report # 37), and Sri Lanka (report # 38). Here, bat-catching by spiders have been witnessed particularly often in the eastern coastal area of China, specifically in parks and forests of the Greater Hong Kong area ([39][40]; G. Ades, pers. comm.; C.S.K. Liu, pers. comm.; Fig. 2L).

A third geographic region where bat-catching by web-building spiders was repeatedly witnessed (seven reports) is the area of Australia (report # 39–44) and Papua New Guinea (report # 45). Most Australian incidences were observed in the coastal areas of New South Wales and Queensland (Fig. 2J–K).

Three incidences of bat captures by web-building spiders have been reported from Africa ([41][42]; D. Schultz, pers. comm.; Fig. 2F; report # 46–48). Only two incidences of bat catches by web-building spiders witnessed in North America have been reported so far ([43][44]; report # 49–50), and these both refer to warm areas in the southern USA. Incidences of bat catches by orb-weaving spiders are unknown from the northern part of North America (B. Fenton, pers. comm.). Likewise, incidences of this type have not been reported in the Ukrainian and Russian scientific literature (A.T. Bashta, pers. comm.). Only two incidences of bats being captured in spider webs have been reported from Europe (report # 51–52). In one case, a dead bat was found entangled in the web of an orb-weaving spider on a building site near Stuttgart, Germany (German tabloid BILD, May 2011). Another incidence of a bat caught in a spider web was observed on the Isle of Wight, South East England (G. Street, pers. comm.).

Which Spider Species are Involved in Bat Catches?

Bat-catching spiders belong to the araneomorph families Nephilidae (golden silk orb-weavers), Araneidae (orb-weaver spiders), Sparassidae (huntsman spiders), and the mygalomorph family Theraphosidae (tarantulas). Furthermore, an attack attempt by an araneomorph hunting spider of the family Pisauridae (fishing spiders) was witnessed. Seventy-three percent of the known incidences of bat catches were attributable to orb-weaving spiders, 15% to unidentified web-building spiders, and 12% to hunting spiders (Table 1).

The dominant group of bat-catching spiders are giant orb-weavers of the genus Nephila (Nephilidae). These spiders are forest-dwellers that reach a legspan of 10–15 cm and a weight of ∼1–7 g ([34], [45]; Table 2). They are diurnally and nocturnally hunting [46][47]; feeding was found to be most intense in the time between sundown and midnight [46]. Nephila spp. spin strong webs with a diameter of up to 1.5 m at a height of 1 to 6 m above the ground [34], [47][48]. On certain locations, where females aggregate, several webs are built connected to each other, which may result in a web area of many square meters [49]. Of the 15 valid species in the genus Nephila (see [34]) only two species - namely Nephila clavipes and Nephila pilipes - have been reported so far to be engaged in bat catching. It can be assumed, however, that other Nephila spp. catch bats as well. Up to the present, the Neotropical Nephila clavipes has not been proven to feed on the bats captured in its webs. This species is, on average, significantly smaller than the Asia-Pacific species Nephila pilipes [50][52]. One might speculate that the smaller-sized N. clavipes perhaps is less successful in subduing bats (H. Höfer, pers. comm.). It appears that the female Nephila spiders depicted in Fig. 2H, I, and L were each missing a leg. Leg loss in adult female Nephila spiders is a well-known phenomenon [53]. It cannot be ruled out that some of the leg losses occurred during aggressive encounters between spiders and bats trying to defend themselves after being entangled in spider webs.

Table 2. Fresh weight and body length (cephalothorax plus abdomen) of adult spiders reported to catch bats (arranged in alphabethical order).

A second dominant group of bat-catching spiders are large orb-weavers of the genus Eriophora (Araneidae) that spin strong vertical orb-webs of up to 1.5 m diameter [8], [37][38], [54][55]. These spiders, that reach a legspan of 5–8 cm and a weight of >1 g at favourable web sites (Table 2), are forest-dwellers like the Nephila spp. The Eriophora spp. are nocturnal spiders that hide in a leaf retreat during the daytime hours and start spinning their webs just after sunset [8], [37], [54]. They stay at the hub of the web all night long, the majority of their feeding activity taking place at the beginning of the night [56]. The genus Eriophora is represented in the Neotropics with four species [33]. A congener from Australia, Eriophora transmarina, has been witnessed catching bats as well (Table 1). Several araneids (genera Eriophora and Caerostris) spin orb-webs of extraordinary size and tensile strength suspended upon bridge lines of several meters, which led to the assumption that such web gigantism might have evolved as an adaptation for capturing flying vertebrates such as bats and birds [57][59]. In the case of Caerostris darwini, an araneid which spins giant orb-webs of up to 2 m diameter across rivers in Madagascar suspended upon bridge lines exceeding 20 meters in length, chiropterophagy could not be evidenced so far [58][59]. However, in this latter study the sample size of recorded predation events was rather small [58][59]. In the habitats of Caerostris darwini, several species of small riverine bats of the families Vespertilionidae and Emballonuridae occur who would be available as potential prey at least for a few weeks per year during which time their volant juveniles (weighing ∼2.5–4 g) are within the spiders’ prey size range (S. Goodman, pers. comm.; P.A. Racey, pers. comm.). Quantitative prey analyses of Caerostris darwini at various seasons (with a high enough sample size to not miss rare events) are urgently needed to answer the question whether this spider is preying exclusively on larger-sized flying insects (as suggested by [58][59]) or whether it supplements its diet by occasional catches of flying vertebrates.

Nephilengys cruentata, another bat-catching nephilid (Table 1), weighs 0.5–1.6 g (Table 2). It is a synanthrophic spider that spins orb webs (with up to 1 m diameter) on the corners of walls and ceilings of buildings [60][62]. Nephilengys might be less efficient in bat catching. The only reported incidence where a bat got entangled in a Nephilengys web ended with the bat’s successful escape. Nevertheless this spider species should not be ruled out as a potential predator of small bats; it is known to catch and eat various types of vertebrates including small birds [25][26], [62].

Other orb-weavers reported to have caught bats in their webs are found in the araneid genera Argiope and Parawixia (Table 1). These lighter spiders, in comparison to Nephila spp. and Eriophora spp., spin webs of much smaller size and may be engaged in bat catches less frequently, although it must be noted that Argiope spp. have repeatedly been observed killing (and sometimes eating) small birds in North America and elsewhere (e.g. [21], [29]).

Heteropoda venatoria, a sparassid spider reported capturing a pipistrelle in India, has an adult legspan of 7–12 cm and weighs between 2–6.5 g [63][64]. Other larger-sized cave-dwelling Heteropoda spp. (with a legspan of 20–30 cm), likewise suspected to be predators of bats, are expected to be even heavier though body mass data for these latter species are missing [65][66]. Based on their estimated size, the theraphosids Avicularia spp. engaged in bat-eating may have weighed between 10–30 g (compare [67] for body mass data of theraphosids), whereas Lasiodora parahybana, another bat-eating theraphosid, may have weighed even more [68]. The theraphosid Poecilotheria rufilata that was observed preying on a bat in India may have weighted between 28–85 g [31]. These giant sparassids and theraphosids are fully equipped with the toxins and enzymes needed to subdue and devour small vertebrate prey [14][18], [20]. The occasional capture of a bat should therefore come as no surprise, though these spiders are actually known to feed predominantly on arthropods [14], [64], [69]. Another group of hunting spiders that might be capable of attacking and killing small bats are a few large-sized species in the superfamily Lycosoidea (e.g., genera Hogna and Dolomedes) whose adult females weigh between 1–2 g [70]. Such huge hunters might occasionally attack neonatal bats fallen from the roost. An incident of this type, where a large pisaurid (Dolomedes triton) was attacking an immature bat, was witnessed in Indiana, USA (report # 6).

Which Bat Species are Captured by Spiders?

So far, microbats from five families are known to have been captured by spiders in the field (Table 1): Vespertilionidae (plain-faced bats), Emballonuridae (sheath-tailed bats), Rhinolophidae (horseshoe bats), Hipposideridae (Old World leaf-nosed bats) and Phyllostomidae (New World leaf-nosed bats). In 31% of the reported incidences the captured bats remained unidentified. The majority of identifiable captured bats belonged to the families Vespertilionidae (64% of reports) or Emabllonuridae (22%), whereas only few reports existed for Hipposideridae (8%) and one for Rhinolophidae (3%). The capture of phyllostomid bats was only reported once (report # 20) or maybe twice (report # 11). In the latter, uncertain report, concerning a small brown-coloured bat entangled in a spider web in Guatemala (Fig. 2H; report # 11), the captured bat might have been a juvenile fruit-eating phyllostomid bat though the features needed for a positive identification were not sufficiently recognizable in the photo (A. Gardner, pers. comm.). The Old World flying foxes (Pteropodidae) have never been reported to get captured or killed by spiders except for one report from captivity. Liat [71] reported that neonates of the Lesser Dawn Bat, Eonycteris spelaea were offered to a theraphosid, Coremiocnemis brachyramosa (subfamily Selenocosmiinae), in captivity. The neonatal bats were eaten readily by this theraphosid. It is therefore possible that small or immature flying foxes are caught and eaten by spiders in the field as well. Due to the fact that the incidence reported by Liat [71] was not witnessed in the field, it was not included in Table 1.

The majority of bats captured by spiders represented species that are among the most common bats in their respective geographic region (e.g., Pipistrellus spp. in various parts of the world; Myotis nigricans and Rhynchonycteris naso in the Neotropics). Nevertheless, rare species may sometimes get caught in spider webs as well (e.g., Centronycteris centralis; compare [72]).

The majority of bats entangled in spider webs were small species with a wingspan of 10–24 cm and an adult weight of 3–8 g (Table 3). It is noteworthy that adult bat weight can vary by several grams depending on the bat’s feeding status and it is plausible that only the lightest individuals of any given bat species get entangled in spider webs; moreover, some of the captured bats were juveniles or subadults (reports # 7, 15–16, 20–23, and 50) and thus presumably much lighter than the weights for adults presented in Table 3. Some of the entangled bats are among the smallest bats on earth (e.g., Tylonycteris pachypus weighs only 3 g; [73]). Likewise, the neonatal Myotis austroriparius bats found entangled in spider webs in a study in Florida (see [43]) weighed only 3 g [74]. Large bats are missing in Table 3 because of these bats’ capability to fly right through a web (see below). Most of the species listed in Table 3 are known to roost in buildings, caves, and tree holes.

Table 3. Fresh weight and wingspan of bat species reported to be captured by spiders (arranged in alphabethical order).

Eighty-five percent of the reports with identifiably bats entangled in spider webs refer to species classified as “aerial insectivorous bats” (Table 4). Such bats (e.g., Pipistrellus spp. and Myotis nigricans) feed aerially on flying insects; non-volant prey such as spiders is almost entirely missing in their diets [75][77]. In contrast, there are some bats that feed heavily on web-building spiders (e.g., Phoniscus papuensis, Myotis emarginatus, Myotis nattereri, Myotis bechsteinii, Myotis keenii, Myotis lucifugus, Myotis aurascens; see [78][85]). These are all bats with an average adult weight of 5–10 g and a wingspan of 21–27 cm [81], [86]. In particular, the Golden-tipped Bat (Phoniscus papuensis [formerly termed Kerivoula papuensis]) and Geoffroy’s Myotis (Myotis emarginatus) are considered to be true spider specialists with spiders making up>75% of their total prey [81], [85], [87]. These bats, which glean spiders from webs are characterized by high flight agility and manoeuvrability at low speed, using high frequency echolocation calls (>100 kHz start frequency) to detect spider prey and to avoid accidential crashes ([81]; [88]; G. Jones, pers. comm.). One might expect such highly specialized foragers to be sufficiently well adapted to avoid collisions with spider webs. However, studies in New South Wales (Australia) and Bavaria (Germany) revealed that gleaning insectivorous bats (i.e., Phoniscus papuensis and Myotis emarginatus) captured in harp traps and mist nets, had often spider web material attached to their body fur and wing membrane, indicating that these bats frequently strike spider webs while gleaning spiders suspended in webs or while accidentally encountering webs during their flights through the cluttered forest vegetation [87], [89]. In these latter studies, the web material must have originated from smaller-sized spider webs that were not strong enough to withstand the bats’ kinetic energy without breaking (“low energy absorbing webs” sensu Craig [90]). Analyses of faecal pellets likewise confirm that these bats prey on orb-weavers of rather small size (∼2–10 mm in length; [80], [91]), suggesting that they select smaller-sized webs for their gleaning attempts. Quite a number of studies on spider-eating Myotis bats were conducted in geographic areas such as Europe and northern parts of North America [78][79], [82][83], [85], [89], [91][94] where huge araneid and nephilid spiders do not occur (compare [33]), implying that in these areas gleaning bats presumably face little danger of being caught and killed by web-building spiders. But in some tropical areas of Australia, where Phoniscus papuensis does occur sympatrically with huge nephilid spiders, incidences of Phoniscus papuensis being accidentally ensnared and killed in Nephila webs would be imaginable, though nothing has been reported about this so far.

Table 4. Foraging mode and echolocation call frequency of adult bat species reported to be captured in spider webs (arranged in order of increasing peak frequency).

Size Ratio of Web-building Spiders Versus Bats

Bats trapped in spider webs are usually small-sized (3–8 g adult weight; Table 3), whereas the spiders capable of overpowering bats are giant orb-weavers (∼0.5–7 g weight; Table 2). The largest bat species reported to have been captured in spider webs were an adult male Nyctophilus gouldi (a species with a known adult weight of 11 g) and a Chalinolobus gouldii of unknown age (a species with a known adult weight of 15 g; Table 3). The tensile strength and elasticity of silk produced by large nephilid and araneid orb-weavers is high (e.g. [95]), enabling such “high energy absorbing webs” to retain flying vertebrates whose weight exceeds by far the spiders’ own weight. Large orb-weaving spiders are generally capable of trapping and killing prey that is much larger than themselves [96]. For instance, a Nephila sp. was reported to have captured a 30–35 g bird, a Lewin’s Honeyeater, Meliphaga lewinii [24]. Furthermore it has been reported that an 18 g Grasshopper Sparrow, Ammodramus savannarum, was trapped in a spider web in New York [24], while a 90–110 g Black-faced Cuckoo-Shrike, Coracina novaehollandiae, was ensnared in a spider web in Australia [24]. The exact circumstances under which these relatively heavy birds were trapped in spider webs are not reported. Flying vertebrates of fairly large size might be retained if such an animal crashes into an entire aggregation of large, strong Nephila webs.


Are the Witnessed Incidences Real Predation Attempts?

It is arguable whether all incidences reported in this paper are real predation attempts or whether some are just deaths by web ensnarement without the active involvement of the spider (non-predation deaths). Begon et al. [97] define the term predation as follows “…Predation, put simply, is consumption of one organism (the prey) by another organism (the predator), in which the prey is alive when the predator first attacks it…” With other words, the definition of predation implies that a prey item must have been killed and eaten by the predator.

With regard to bat-eating theraphosids photographed in the Neotropics and in India, the actual killing of the bats was not witnessed. However, it has been proven by means of observations in captivity that large theraphosids are capable of killing bats. This is shown in a YouTube video where a Grammostola rosea (subfamily Theraphosinae) is killing a small bat offered to it in a cage environment (; this report was not included in Table 1 because it occurred in captivity). The Grammostola rosea shown in this video was identified for us by R. West (pers. comm.). Theraphosid venom has been proven to be active on small mammals [20]. One can therefore assume that theraphosid predation on bats is taking place in the field as well and that the incidences witnessed in the Neotropics and in India may have been cases of predation and not scavenging.

With regard to the sparassid Heteropoda venatoria, reported to have killed a small bat in India [36], the situation is somewhat different. Here the spider did catch and kill the bat, but the sequence of behavioral units naturally displayed during a predation event - starting with the attack of the prey and ending with the cessation of feeding - was disrupted as the observer interfered by capturing spider and bat and placing them into a glass jar. As it appears, the dead bat was subsequently not preyed upon (non-predation death). The spider in question might have preyed on the bat had it not been disturbed by the observer. Heteropoda spp. often occur in high abundance in close proximity to bat roost sites in places like caves, buildings, and trees [63], [98]. Especially in caves in Southeast Asia, large-sized Heteropoda spp. cohabit with different species of bats [63], [65][66], [69]. Large-sized Heteropoda spp. are powerful enough to subdue small bats, especially if one takes into consideration that they possess impressive chelicerae, potent venom against small vertebrates, and the ability to move at high speed [17], [19], [64]. Furthermore, these spiders show morphological characteristics suggesting that they may be highly adapted to climb vertical surfaces and walk on cave ceilings [69], [99]. The spiders may climb cave walls and ceilings to catch perching bats or they may search for bat pups fallen from the roost to the floor. It is readily imaginable that the Heteropoda spp. supplement their staple diet, made up of arthropods (i.e., in particular cave crickets, cockroaches, arachnids, and centipedes; e.g. [64], [69]), by the occasional catch of a small bat. One way to find out whether Heteropoda spp. feed on bats would be to video record the behavior of these spiders at locations where they forage in close proximity to bat colonies. In 2006 (April to December), such a study was undertaken at several pipistrelle roost sites in the Christmas Islands, Australia; there, five video cameras were deployed for a total of 663 trap nights [98]. Sparassid spiders, Heteropoda venatoria, were the most frequently recorded potential predators on the trunks of the roost trees, with 43 individual records. The video recordings, however, did not reveal any of these spiders preying on bats, disturbing them or entering their roost sites. Currently we cannot confirm whether Heteropoda spp. are habitually engaged in bat predation or whether the incidence witnessed by Bhattacharya [36] was just a chance occurrence. Further studies on possible interactions between sparassid spiders and small-sized bats are therefore of considerable interest (also see [100]).

The Neotropical orb-weaving spider Eriophora fuliginea has been observed to kill and eat small bats that got entangled in its webs [8], [37], [101]. When a bat got caught in a web, the spider immobilized the bat by attack-wrapping and subsequently biting it [101]. Following this, the spiders fed on the dead bats for many hours (D.E. Wilson, pers. comm.). The incidences of bats being caught, killed, and eaten in webs of Eriophora spp. are without any doubt predation events.

Likewise, the orb-weaving spider Nephila pilipes, occurring in Asia and Australia, has many times been observed to attack, kill and eat small bats. Contrary to Eriophora, Nephila pilipes immobilizes its prey by always first biting and subsequently wrapping it [38], [102]. The immediate attack bite of Nephila towards bats has been witnessed by two authors [11], [103], whereas the consumption of bats was repeatedly observed/photographed ([39][40], [104]; C. Fabro, pers. comm.; C.S.K. Liu, pers. comm.). There are several reports where Nephila pilipes was seen killing and eating small birds as well (e.g. [28]). Thus, the behavior of Nephila pilipes towards small bats (catching, killing, and eating them), clearly complies with the definition of predation.

The Neotropical orb-weaving spider Nephila clavipes has been witnessed catching bats quite frequently (9 reports), but in none of these cases was it seen biting, wrapping or eating a bat. Likewise, birds trapped in the webs of this spider species were apparently not consumed [22]–. Only once has a Neotropical Nephila been observed biting a bird, but without subsequent consumption of the prey [22]. It has been suggested that Nephila clavipes might be unable to deal with large, aggressive prey such as bats and birds [24], [27]. If this latter assumption is true, then the captures of bats in the webs of Nephila clavipes would be cases of non-predation deaths (the bats dying of exhaustion, starvation, dehydration, and/or hyperthermia). The two European incidences where bats were killed in spider webs without the spiders feeding on them must be considered to have been cases of non-predation deaths as well.

In conclusion, some of the bats entangled in spider webs are actively killed and consumed by the spiders (i.e., predation), whereas in other instances the entangled bats are not consumed by the spiders (i.e., non-predation deaths). In several of the incidences, where dead bats were found suspended in spider webs, it could not be determined whether predation had taken place because of the bats’ desiccated condition (e.g. [44]).

How Frequent are Bat Catches by Spiders?

We conducted a survey of a large number of chiropterologists and arachnologists who had conducted extensive field investigations in the tropics/subtropics to find out how many of them have ever witnessed a spider catching a bat. A bat trapped in a spider web is a fairly conspicuous sight that an experienced biologist will hardly overlook, especially since it takes a spider several hours to handle a bat prey. Only very few bat scientists (e.g. [8], [30], [105]) have ever witnessed an incidence of a bat caught by a spider, while many others who also spent decades in the field (e.g., B. Fenton, pers. comm.) have never seen this. Likewise, very few orb-weaving spider experts (e.g. Robinson [101]) have witnessed spiders catching bats. The 52 incidences reported in our review, which refers to a time period of more than 100 years (starting with Cantor’s report in 1842 [106]), is very low if this figure is compared to estimates of bat mortality attributable to the bats’ chief natural enemies. For instance, Speakman [2] estimated that ∼200,000 bats per year are killed as a result of predation by owls and kestrels in Great Britain alone. The fact that bat catching by spiders has been witnessed so infrequently suggests that this type of bat fatality is extremely rare. This is surprising because in tropical/subtropical areas the millions of huge webs of Nephila spp. and Eriophora spp. stretched across the bats’ flight paths pose an enormous risk to bats (especially in locations where such orb-webs are aggregated) and, actually, one would expect large numbers of bats being killed each night. It appears that bats are evolutionarily well-adapted to detect and avoid spider webs [107][108]. Bats are likely capable of detecting spider webs by means of echolocation. Though single silk strands of spiders (∼0.002–0.005 mm in diameter; [109]) are probably below the detection threshold of echolocating bats (∼0.16 mm for the aerial insectivore Eptesicus fuscus; [110]; H.-U. Schnitzler, pers. comm.), the webs as a whole, often containing additional conspicuous, densely-woven silk decorations or silk barriers [54], [107], may present themselves as tangible objects that presumably bounce back echolocation calls emitted by the bats with enough intensity to be detectable by the bats [107]. Not only the webs, but also the spiders (in particular the huge adult females of Nephila spp. and Eriophora spp. staying at the hub of the web all night long) presumably generate strong echoes that the echolocating bats should be able to detect, advertising to them the presence of obstacles that need to be avoided. In a study in Australia, Schultz & Wainer [87] captured more than 1200 bats (representing eleven species) and checked them for the presence of spider web fragments around their wing membrane and/or on the body fur. These authors found that the vast majority of bats did not have any traces of spider web fragments attached to their body, strongly confirming the above-mentioned hypothesis that bats are able to largely avoid encounters with spider webs. This is also confirmed by a study conducted in British Columbia where no spider web material was found attached to the body of two species of Myotis bats trapped in mist nets [83]. However, even if some bats collide with spider webs, a considerable proportion of these bats may be able to elude ensnarement by the following reasons: First, only large webs from a limited number of giant orb-weaving spider species (especially Nephila spp. and Eriophora spp.) are strong enough to withstand the tremendous kinetic energy of a flying bat without breaking. Such webs that intercept heavy and fast flying prey have been termed “high energy absorbing webs” (sensu Craig [90]). If bats strike a smaller web (i.e., “low energy absorbing webs”, designed to intercept light and slow flying prey), the bats fly right through it, leaving behind a damaged or destroyed web (also see [87], [89]). Second, only small bats can be retained in orb webs. If a larger-sized bat strikes a web of any size, the kinetic energy is too high to be absorbed and the web will break. Thus, larger-sized bats will usually fly right through a web, leaving behind a big hole. The same happens when larger-sized birds fly through spider webs [54]. Third, even if small bats get entangled in large webs, a certain percentage of violently struggling bats is able to escape (D.E. Wilson, pers. comm.). The same is true for small birds that may get temporarily entangled in spider webs but are often able to free themselves after a short time of struggling [23]. It should be noted that various species of bats behave differently when trapped in a web, resulting in differing chances to escape. This is known from experience with trapping bats in mist nets, which may be looked upon as “huge artificial spider webs”. For instances, Rhynchonycteris naso does not defend itself if trapped in a net, whereas other sympatric bats of comparable size (e.g., Rhogeessa io) struggle violently (M. Knörnschild, unpubl. data). Accordingly, chances for a Rhynchonycteris naso to escape from a large spider web are slim compared to other bat species. Adaptation for escape from spider webs also exists in various taxa of flying insects (e.g. [111][112]).

Nevertheless, some bats get caught and killed in spider webs. Such cases might be considered to be “accidents”. Why do such accidents happen? There may be several possible reasons for this:

First, it is noteworthy that the majority of the identifiable bats (65% of reports) that accidentally crashed into spider webs echolocate at frequencies of only ∼36–72 kHz (Table 4). It could be that the echolocation calls of these aerial insectivorous species (e.g., Pipistrellus spp. and Myotis nigricans) are less well-adapted to detecting spider webs compared to the high frequency echolocating species (G. Jones, pers. comm.). Bats such as the pipistrelles and Myotis nigricans are relatively fast flying and may not always be able to avoid the webs if detected only at close range (G. Jones, pers. comm.). Thus, though we hypothesize that most bats are able to largely avoid encounters with spider webs (see above), accidents do happen and bats echolocating with lower frequencies might be engaged in these accidents with a higher likelihood. Second, Griffin [113] theorized that bats flying in familiar territory rely heavily on spatial memory and not on echolocation. This might be the case when bats fly in proximity to the roost or when they use “flyways” from the roost to the hunting ground and vice versa [114]. In such situations of heavy reliance on spatial memory, the bats might not notice a spider web until they have already hit it. Indeed several incidences reported in this paper (27% of reports) occurred while the bats were flying in proximity to their roost (i.e., buildings, caves, and forest trees [30], [44]; M. Knörnschild, unpubl. data) and thus in spots where the bats presumably did not rely heavily on echolocation. Third, some bats found entangled in spider webs were juveniles or inexperienced subadults (reports # 7, 15–16, 20–23, and 50). As unskilled flyers, young bats may be more susceptible to accidents than adults [115][117]. A special case was the incidence observed in Florida where bat pups of the Southeastern Brown Bat got entangled in spider webs after falling from the roost [43]. Bat pups falling from the roost frequently become prey of various predators [7]. Fourthly, some bats may get captured when they crash into an aggregation of large orb-webs. Large orb-weavers of the genus Nephila tend do aggregate under circumstances of high prey availability [49], [118]. Blackledge et al. [119] states: “…While reducing the overall number of prey that might be intercepted, these spiders gain access to larger insects that would normally break through a web as the insects either ricochet off or slow down as they pass through exterior webs…” This is exemplified by Sue Churchill’s observation at Tolmer Falls, Australia, where an adult Hipposideros ater had apparently got partially tangled in one web and then fallen into the other webs before being fully caught (report # 44). Fifthly, bats that habitually glean insects from spider webs while hovering in front of them [120] may sometimes get entangled after accidentially striking the web. This evidently happens despite the fact that these bats, echolocating at high frequencies (>100 kHz start frequency [81], [88]), are thought to be evolutionarily adapted to avoid collision with spider webs. The Rhinolophus cornutus orii captured in a Nephila web in Japan (Fig. 2I) may exemplify an incidence of this type (report # 35). Bats from this genus sometimes strike spider webs, evidenced by the fact that 4 out of 58 specimens of Rhinolophus megaphyllus captured in harp traps in Australia had spider web fragments attached to their wing membrane and body fur [87]. The spider webs in this latter study were obviously not strong enough to withstand the bats’ kinetic energy without breaking (“low energy absorbing webs”). Sixly, during periods of food scarcity, weakened small bats might be unable to free themselves if trapped in spider webs, even if the webs are not as strong as those spun by tropical large orb-weavers. The incidences witnessed in Germany and England, where small pipistrelle bats were killed in webs without any involvement of the spiders, might present examples for this type of non-predation deaths.

At the present time nothing is known about the frequency with which theraphosids and sparassids catch bats. The cryptic life habits of these predominantly nocturnal hunters make them difficult animals to study. Likewise, nothing is known about the frequency of predation on bats by pisaurids.

Are Nephilid Webs at Cave Entrances a Threat to Cave-roosting Bats?

In the tropics, huge nephilid orb-webs (genera Nephila and Nephilengys) sometimes block the entrances to bat caves ([61]; C. Dietz, pers. comm.). Such cave entrance inhabiting nephilid populations have been discovered in East and South East Asia as well as in the Neotropics. So far it is unknown to what extend cave-roosting bats flying back and forth between caves and foraging areas are able to detect and avoid these webs. Since it is hypothesized that the bats might navigate by spatial memory while passing through cave entrances [121], it is conceivable that some of them may crash into nephilid webs within the cave’s entrance zone, given the fact that in some areas they leave caves at dusk in gigantic swarms. Monitoring nephild webs at cave entrances by means of video recording devices could bring an answer to this question.

How Important is Chiropterophagy from a Point of View of Spider Nutritional Ecology?

All five groups of bat-catching spider taxa (Nephilidae, Araneidae, Theraphosidae, Sparassidae, and Pisauridae) are known to be predominantly predaceous on insects [14], [53], [64], [69], [101]. With regard to large-sized theraphosids, sparassids, and pisaurids, their feeding behavior in the field has not been thoroughly investigated and one cannot currently judge whether predation on bats is of significance to them from a feeding ecological point of view.

Our current knowledge of orb-weaver feeding ecology suggests that these spiders depend on flying insects as main prey, whereas bats and also birds occasionally entangled in spider webs might be considered to be by-catch [45]. It can take a large orb-weaver many hours to consume a bat or bird prey ([26], [28], [30]; D.E. Wilson, pers. comm.) indicating that spiders might extract a substantial amount of energy while feeding on such a large prey. Based on field observations in Papua New Guinea, Robinson & Robinson [53] estimated the average capture rate of Nephila pilipes at ∼0.19 g wet weight prey killed per spider per day (which corresponds to ∼0.015 g dry weight food ingested per spider per day). According to Higgins [46], the average prey capture rate of the significantly smaller-sized Nephila clavipes in Texas was ∼1.5–2.5 times lower than the estimate by Robinson & Robinson [53]. Thus, the catch of a ∼2 g bat yields a Nephila pilipes a potential prey biomass that is about 10 times the average daily prey catch.

In recent years, the idea has been proposed that the occasional catch of large, energetically rewarding prey may be essential in order to fulfil the reproductive needs of large orb-weaving spiders (“rare, large prey” hypothesis; see [122][123]). While large orb-weavers such as Nephila spp. capture predominantly small insects of little energetic value, they derive the bulk of their energy from a few rare, large prey items (see [46], [49], [53], [122]). In this context “rare, large prey” encompasses large insects (e.g., cicadas, moths, coleopterans, orthopterans, and odonates) as well as small flying vertebrates (bats and birds). In our opinion, the examples of bat-eating orb-weavers reported in this paper are consistent with the "rare, large prey" hypothesis, though one may object to this given the rarity of such events.

Supporting Information


Many people have contributed greatly to this review paper. First we wish to thank all those who kindly provided us with unpublished information and/or photographs of incidences of bat-catching spiders. Second we wish to thank all those scientists who identified bats or spiders based on photographs. Alfred Gardner, Don Wilson, Richard Laval, and Adriana Bravo identified Neotropical bats. Marc Holderied and Tigga Kingston identified a bat from Hong Kong. A group of Australian bat scientists - including Kyle Armstrong, Mike Craig, Chris Pavey, Terry Reardon, Martin Rhodes, and Christopher Tidemann - identified a bat from Queensland, Australia. Nephilid spiders depicted in photographs were identified by Matjaz Kuntner and I-Min Tso. We wish to acknowledge William Eberhard and G.B. Edwards for commenting on araneid spiders depicted in photographs or shown in film clips. Samuel Zschokke identified spider webs based on photographs and a film clip. Rick West identified a theraphosid spider shown in a film clip. Monika Rhodes was very helpful by posting an information request on the listserver of the Australasian Bat Society. Appreciation is also expressed to the following people who helped us in various ways: Brock Fenton, Thierry Gasnier, Steve Goodman, Hubert Höfer, Gareth Jones, Brad Law, Markus Metz, Tadashi Miyashita, Paul A. Racey, Hans-Ulrich Schnitzler, Chung-Tong Shek, John Speakman, Erik Thorn, John O. Whitaker Jr. and many others who cannot all be named here. Special thanks to Derek Yalden for valuable suggestions and comments that helped to improve the manuscript.

Author Contributions

Conceived and designed the experiments: MN. Performed the experiments: MN. Analyzed the data: MN MK. Contributed reagents/materials/analysis tools: MN. Wrote the paper: MN MK.


  1. 1. Whitaker JO, Hamilton WJ (1998) Mammals of the Eastern United States, 3rd edition. Ithaca, New York: Cornell University Press. 608 p.
  2. 2. Speakman JR (1991) The impact of predation by birds on bat populations in the British Isles. Mammal Rev 21: 123–142.
  3. 3. Altringham JD (1996) Bats: Biology and Behaviour. Oxford, UK: Oxford University Press. 262 p.
  4. 4. Gillette DD, Kimbrough JD (1970) Chiropteran mortality. In: Slaughter BH, Walton DW, editors. About Bats. Dallas: Southern Methodist University Press. pp. 262–283.
  5. 5. Molinari J, Gutiérrez EE, Ascenção AA, Nassar JM, Arends A, et al. (2005) Predation by giant centipedes, Scolopendra gigantea, on three species of bats in a Venezuelan cave. Caribb J Sci 41: 340–346.
  6. 6. Rivera LG, Espin RM, De Armas LF, Hernandez NH (2009) Necrofagia en Amblypygi (Arachnida: Pedipalpi). Boletín Sociedad Entomológica Aragonesa 45: 505–507.
  7. 7. Rice DW (1957) Life history and ecology of Myotis austroriparius in Florida. J Mammal 38: 15–32.
  8. 8. Wilson DE (1971) Ecology of Myotis nigricans (Mammalia: Chiroptera) on Barro Colorado Island, Panama Canal Zone. J Zool 163: 1–13.
  9. 9. Leen N, Novick A (1969) The World of Bats. New York: Holt, Rinehart and Winston. 171 p.
  10. 10. Yalden DW, Morris PA (1975) The Lives of Bats. Newton Abbot, UK: David and Charles. 247 p.
  11. 11. Hill JE, Smith JD (1984) Bats: A Natural History. Austin: University of Texas Press. 243 p.
  12. 12. Allen GM (2004) Bats: Biology, Behavior, and Folklore. New York: Dover Publications, Inc. 368 p.
  13. 13. Kaston BJ (1965) Some little known aspects of spider behavior. Am Mid Nat 73: 336–356.
  14. 14. Gertsch WJ (1979) American Spiders, 2nd edition. New York: Van Nostrand Reinhold. 196 p.
  15. 15. Formanowicz DR Jr, Stewart MM, Townsend P, Brussard DF (1981) Predation by giant crab spiders on the Puerto Rican frog Eleutherodactylus coqui. Herpetologica 37: 125–129.
  16. 16. Stewart MM (1985) Arboreal habitat use and parachuting by a subtropical forest frog. J Herpetol 19: 391–401.
  17. 17. Brown RM, Ferner JW, Sison RV, Gonzales PC, Kennedy RS (1996) Amphibians and reptiles of the Zambales mountains of Luzon Island, Philippines. Herpetol Nat Hist 4: 1–17.
  18. 18. Conniff R (1996) Tarantulas: earth tigers and bird spiders. National Geographic 190: 99–115.
  19. 19. Hamidy A, Matsui M, Nishikawa K, Belabut D, Ahmad N (2010) Rana picturata (Yellow-spotted frog) predation. Herpetol Rev 41: 66–67.
  20. 20. Marshall SD (2001) Tarantulas and Other Arachnids. Hauppauge, New York: Barron’s Educational Series, Inc. 111 p.
  21. 21. Mackay GH (1929) A spider (Argiope aurantia) and a bird (Astragalinus tristis tristis). Auk 46: 123–124.
  22. 22. Teixeira DM, Luigi G, Schloemp IM (1991) Aves brasileiras como presas de artrópodes. Ararajuba (Rev Bras Ornitol) 2: 69–74.
  23. 23. Graham DL (1997) Spider webs and windows as potentially important sources of hummingbird mortality. J Field Ornithol 68: 98–101.
  24. 24. Cox JA, NeSmith CC (2007) Acadian flycatcher caught in the web of a golden silk orb-weaver. Fla Field Nat 35: 46–48.
  25. 25. Duca C, Modesto W (2007) Spider web as a natural trap for small birds. Rev Bras Ornitol 15: 615–616.
  26. 26. Peloso PL, de Sousa VP (2007) Predation on Todirostrum cinereum (Tyrannidae) by the orb-web spider Nephilengys cruentata (Araneae, Nephilidae). Rev Bras Ornitol 15: 461–463.
  27. 27. Sakai WH (2007) Long-billed Hermit (Phaethornis superciliosus) caught in Golden Orb-spider (Nephilia clavipes) Web. Ornitol Neotrop 18: 117–119.
  28. 28. Manchi S, Sankaran R (2009) Predators of swiftlets and their nests in the Andaman and Nicobar Islands. Indian Birds 5: 118–120.
  29. 29. Deans A (2011) Spider captures a bird. Insect Museum (Website), Dept. of Entomology, North Carolina State University, Raleigh, USA. Available: Accessed 2011 September 3.
  30. 30. Timm RM, Losilla M (2007) Orb-weaving spider, Argiope savignyi (Araneidae), Predation on the proboscis bat Rhynchonycteris naso (Emballonuridae). Caribb J Sci 43: 282–284.
  31. 31. Das KSA, Sreekala LK, Abdurahiman O (2012) Predation on the Kelaart’s Pipistrelle Bat Pipistrellus ceylonicus Keelart (Chiroptera: Vespertilionidae), by the Reddish Parachute Tarantula, Poecilotheria rufilata Pockock (Araneae: Theraphosidae) in Chinnar Wildlife Sanctuary, Kerala, India. Tropical Natural History 12: 257–260.
  32. 32. Wilson DE, Reeder DM (2005) Mammal Species of the World: A taxonomic and geographic reference, 3rd edition. Baltimore: Johns Hopkins University Press. 142 p.
  33. 33. Platnick NI (2012) The world spider catalog, v12.5. American Museum of Natural History. Available: DOI:10.5531/db.iz.0001.
  34. 34. Kuntner M, Coddington JA (2009) Discovery of the largest orbweaving spider species: The evolution of gigantism in Nephila. PLOS ONE 4: e7516.
  35. 35. Kuntner M, Agnarsson I (2011) Phylogeography of a successful aerial disperser: the golden orb spider Nephila on Indian Ocean islands. BMC Evol Biol 11: 119.
  36. 36. Bhattacharya GC (1941) Heteropoda venatoria preying on a pipistrelle bat. Curr Sci 10: 183.
  37. 37. Levi HW (1970) The Ravilla group of the orb weaver genus Eriophora in North America (Araneae: Araneidae). Psyche 77: 280–302.
  38. 38. Robinson MH, Mirick H (1971) The predatory behavior of the golden-web spider Nephila clavipes (Araneae: Araneidae). Psyche 78: 123–139.
  39. 39. Kershaw JCW (1905) II. Butterfly-destroyers in Southern China. T Roy Ent Soc London 53: 5–8.
  40. 40. Hill DS, Hore PM, Thornton IWB (1982) Insects of Hong Kong. Hong Kong: Hong Kong University Press. 540 p.
  41. 41. Rosevear DR (1965) The Bats of West Africa. London: Publications British Museum (Natural History). 418 p.
  42. 42. Happold DCD, Happold M, Hill JE (1987) The bats of Malawi. Mammalia 51: 337–414.
  43. 43. Hermanson JW, Wilkins KT (1986) Pre-weaning mortality in a Florida maternity roost of Myotis austroriparius and Tadarida brasiliensis. J Mammal 67: 751–754.
  44. 44. Laduc TJ (1993) Accidental death by web entanglement in the Western Pipistrelle, Pipistrellus hesperus. Bat Research News 34: 58–59.
  45. 45. Selden PA, Shih C, Ren D (2011) A golden orb-weaver spider (Araneae: Nephilidae: Nephila) from the Middle Jurassic of China. Biol Lett 7: 775–778.
  46. 46. Higgins LE (1987) Time budget and prey of Nephila clavipes (Linnaeus) (Araneae, Araneidae) in southern Texas. J Arachnol 15: 401–417.
  47. 47. Levi HW (1980) The orb-weaver genus Mecynogea, the subfamily Metinae and the genera Pachygnatha, Glenognatha and Azilia of the subfamily Tetragnathinae North of Mexico (Araneae: Araneidae). Bull Mus Comp Zool 149: 1–74.
  48. 48. Weems HV, Edwards GB (2011) Golden Silk Spider, Nephila clavipes (Linnaeus) (Arachnida: Araneae: Tetragnathidae). Entomology and Nematology Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. EENY-229, 5 pp.
  49. 49. Harvey MS, Austin AD, Adams M (2007) The systematics and biology of the spider genus Nephila (Araneae: Nephilidae) in the Australasian region. Invertebr Syst 21: 407–451.
  50. 50. Hormiga G, Scharff N, Coddington JA (2000) The phylogenetic basis of sexual size dimorphism in orb-weaving spiders (Araneae, Orbiculariae). Syst Biol 49: 435–462.
  51. 51. Higgins L (2002) Female gigantism in a New Guinea population of the spider Nephila maculata. Oikos 99: 377–385.
  52. 52. Higgins L, Coddington J, Goodnight C, Kuntner M (2011) Testing ecological and developmental hypotheses of mean and variation in adult size in nephild orb-weaving spiders. Evol Ecol 25: 1289–1306.
  53. 53. Robinson MH, Robinson B (1973) The ecology and behavior of the giant wood spider Nephila marculata (Fabricius) in New Guinea. Smith Cont Zool 149: 1–76.
  54. 54. Eisner T, Nowicki S (1983) Spider web protection through visual advertisement: role of the stabilimentum. Science 219: 185–187.
  55. 55. Stowe MK (1986) Prey specialization in the Araneidae. In: Shear WA, editor. Spiders: Webs, Behavior, and Evolution. Stanford, California: Stanford University Press. pp. 101–131.
  56. 56. Ceballos L, Hénaut Y, Legal L (2005) Foraging strategies of Eriophora edax (Araneae, Araneidae): A nocturnal orb-weaving spider. J Arachnol 33: 509–515.
  57. 57. Kuntner M, Agnarsson I (2010) Web gigantism in Darwin's bark spider, a new species from Madagascar (Araneidae: Caerostris). J Arachnol 38: 346–356.
  58. 58. Gregorič M, Agnarsson I, Blackledge TA, Kuntner M (2011a) Darwin's bark spider: Giant prey in giant orb webs (Caerostris darwini, Araneae: Araneidae)? J Arachnol 39: 287–295.
  59. 59. Gregorič M, Agnarsson I, Blackledge TA, Kuntner M (2011b) How did the spider cross the river? Behavioral adaptations for river-bridging webs in Caerostris darwini (Araneae: Araneidae). PLOS ONE 6: e26847.
  60. 60. Schuck-Paim C (2000) Orb-webs as extended-phenotypes: Web design and size assessment in contests between Nephilengys cruentata females (Araneae, Tetragnathidae). Behaviour 137: 1331–1347.
  61. 61. Kuntner M (2007) A monograph of Nephilengys, the pantropical ‘hermit spiders’ (Araneae, Nephilidae, Nephilinae). Syst Entomol 32: 95–135.
  62. 62. Diniz S (2011) Predation and feeding on the tropical house gecko Hemidactylus mabouia (Squamata: Gekkonidae) by the giant orb-weaver spider Nephilengys cruentata (Araneae: Nephilidae). Herpetol Notes 4: 357–358.
  63. 63. Huang CY (2000) Cave structure and cave faunal diversity in Kenting Area. Master’s Thesis, Department of Biological Sciences, National Sun Yat-Sen University, Kaohsiung, Taiwan.
  64. 64. Edwards GB (2009) Huntsman Spider, Heteropoda venatoria (Linnaeus) (Arachnida: Araneae: Sparassidae). Entomology and Nematology Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. EENY-160, 3 pp.
  65. 65. Jaeger P (2001) A new species of Heteropoda (Araneae, Sparassidae, Heteropodinae) from Laos, the largest huntsman spider? Zoosyst 23: 461–465.
  66. 66. Jaeger P (2005) New large-sized cave-dwelling Heteropoda species from Asia, with notes on their relationships (Araneae: Sparassidae: Heteropodinae). Rev Suisse Zool 112: 87–114.
  67. 67. Baerg WJ (1963) Tarantula life history records. J New York Entomol Soc 71: 233–238.
  68. 68. World Association of Zoos and Aquariums (WAZA) (2011) Brazilian salmon pink (Lasiodora parahybana). Available: Accessed 2011 January.
  69. 69. Harries DB, Ware FJ, Fisher CW, Biswas J, Kharpran-Daly BD (2008) A review of the biospeleology of Meghalaya, India. J Cave Karst Stud 70: 163–176.
  70. 70. Nicholas AC, Stratton GE, Reed DH (2011) Reproductive allocation in female wolf and nursery-web spiders. J Arachnol 39: 22–29.
  71. 71. Liat LB (1964) The bird-eating spider. Malay Nat J 18: 20–25.
  72. 72. Woodman N (2003) New record of the rare emballonurid bat Centronycteris centralis Thomas, 1912 in Costa Rica, with notes on feeding habits. Caribb J Sci 39: 399–402.
  73. 73. Zhang L, Liang B, Parsons S, Wei L, Zhang S (2007) Morphology, echolocation and foraging behaviour in two sympatric sibling species of bat (Tylonycteris pachypus and Tylonycteris robustula) (Chiroptera: Vespertilionidae). J Zool 271: 344–351.
  74. 74. Hermanson JW, Wilkins KT (2008) Growth and development of two species of bats in a shared maternity roost. Cells Tiss Org 187: 24–34.
  75. 75. Barlow KE (1997) The diets of two phonic types of the bat Pipistrellus pipistrellus in Britain. J Zool 243: 597–609.
  76. 76. Lee YF, Lee LL (2005) Food habits of Japanese pipistrelles Pipistrellus abramus (Chiroptera: Vespertilionidae) in northern Taiwan. Zool Stud 44: 95–101.
  77. 77. Aguiar LMS, Antonini Y (2008) Diet of two sympatric insectivores bats (Chiroptera : Vespertilionidae) in the Cerrado of Central Brazil. Rev Bras Zool 25: 28–31.
  78. 78. Whitaker JO, Lawhead B (1992) Foods of Myotis lucifugus in maternity colony in central Alaska. J Mammal 73: 646–648.
  79. 79. Parker DI, Lawhead BE, Cook JA (1997) Distributional limits of bats in Alaska. Arctic 50: 256–265.
  80. 80. Funakoshi K, Takeda Y (1998) Food habits of sympatric insectivorous bats in southern Kyushu, Japan. Mamm Stud 23: 49–62.
  81. 81. Schulz M (2000) Diet and foraging behavior of the golden-tipped bat, Kerivoula papuensis: a spider specialist? J Mammal 81: 948–57.
  82. 82. Siemers BM, Swift SM (2006) Differences in sensory ecology contribute to resource partitioning in the bats Myotis bechsteinii and Myotis nattereri (Chiroptera: Vespertilionidae). Behav Ecol Sociobiol 59: 373–380.
  83. 83. Burles DW, Brigham RM, Ring RA, Reimchen TE (2008) Diet of two insectivorous bats, Myotis lucifugus and Myotis keenii, in relation to arthropod abundance in a temperate Pacific Northwest rainforest environment. Can J Zool 86: 1367–1375.
  84. 84. Whitaker JO, Karatas A (2009) Food and feeding habits of some bats from Turkey. Acta Chiropterol 11: 393–403.
  85. 85. Goiti U, Aihartza J, Guiu M, Salsamendi E, Almenar D, et al. (2011) Geoffroy's bat, Myotis emarginatus, preys preferentially on spiders in multistratified dense habitats: a study of foraging bats in the Mediterranean. Folia Zool 60: 17–24.
  86. 86. Norberg UM, Rayner JMV (1987) Ecological morphology and flight in bats (Mammalia; Chiroptera): Wing adaptations, flight performance, foraging strategy and echolocation. Phil Trans R Soc 316: 335–427.
  87. 87. Schultz M, Wainer J (1997) Diet of the golden-tipped bat Kerivoula papuensis (Microchiroptera) from north-eastern New South Wales, Australia. J Zool 243: 653–658.
  88. 88. Siemers BM, Schnitzler H-U (2004) Echolocation signals reflect niche differentiation in five sympatric congeneric bat species. Nature 429: 657–661.
  89. 89. Krull D, Schumm A, Metzner W, Neuweiler G (1991) Foraging areas and foraging behavior in the notch-eared bat, Myotis emarginatus (Vespertilionidae). Behav Ecol Sociobiol 28: 247–253.
  90. 90. Craig CL (1987) The ecological and evolutionary interdependence between web architecture and web silk spun by orb weaving spiders. Biol J Linn Soc 30: 135–162.
  91. 91. Swift SM, Racey PA (2002) Gleaning as a foraging strategy in Natterer's bat, Myotis nattereri. Behav Ecol Sociobiol 52: 408–416.
  92. 92. Bauerova Z (1986) Contribution to the trophic bionomics of Myotis emarginatus. Folia Zool 35: 305–310.
  93. 93. Parker DI, Cook JA (1996) Keen's long-eared bat, Myotis keenii, confirmed in southeast Alaska. Can Field Nat 110: 611–614.
  94. 94. Steck C, Brinkmann R (2006) The trophic niche of the Geoffroy's bat (Myotis emarginatus) in south-western Germany. Acta Chiropterol 8: 445–450.
  95. 95. Agnarsson I, Kuntner M, Blackledge TA (2010) Bioprospecting finds the toughest biological material: Extraordinary silk from a giant riverine orb spider. PLOS ONE 5: e11234.
  96. 96. Nyffeler M, Dean DA, Sterling WL (1987) Feeding ecology of the orb-weaving spider Argiope aurantia (Araneae, Araneidae) in a cotton agroecosystem. Entomophaga 32: 367–375.
  97. 97. Begon M, Townsend CR, Harper JL (2005) Ecology: From Individuals to Ecosystems, 4th edition. Oxford, UK: Blackwell Publishing. 752 p.
  98. 98. James DJ (2007) Christmas Island biodiversity monitoring programme: summary report, December 2003 to April 2006. Report to Department of Finance & Administration and Department of the Environment & Water Resources, Canberra.
  99. 99. Moya-Laraño J, Vinković D, Allard CM, Foellmer MW (2009) Optimal climbing speed explains the evolution of extreme sexual size dimorphism in spiders. J Evol Biol 22: 954–963.
  100. 100. LaVal RK, LaVal ML (1977) Reproduction and behaviour of the African banana bat, Pipistrellus nanus. J Mammal 58: 403–410.
  101. 101. Robinson MH, Robinson B, Graney W (1971) The predatory behavior of the nocturnal orb web spider Eriophora fuliginea (C.L. Koch) (Araneae: Araneidae). Rev Per Entomol 14: 304–315.
  102. 102. Eisner T, Dean J (1976) Ploy and counterploy in predator-prey interactions: Orb-weaving spiders versus bombardier beetles. Proc Nat Acad Sci USA 73: 1365–1367.
  103. 103. Banfield EJ (1918) Tropic Days. London: T. Fisher Unwin Ltd. 313 p.
  104. 104. Sherriffs WR (1934) Hong Kong spiders. I. Hong-Kong Naturalist 5: 85–90.
  105. 105. Churchill S (2008) Australian Bats, 2nd edition. Sydney: New Holland. 255 p.
  106. 106. Cantor T (1842) General Features of Chusan, with remarks on the Flora and Fauna of that Island. Animals Observed at Chusan. Ann Mag Nat Hist 9: 481–493.
  107. 107. Neet CR (1990) Function and structural variability of the stabilimenta of Cyclosa insulana (Costa) (Araneae, Araneidae). Bull Brit Arachnol Soc 8: 161–164.
  108. 108. Kilgore CH (2008) Ecological associations of bats (Mammalia: Chiroptera) in the upper Mobile-Tensaw river delta, Alabama. M.Sc. Thesis, Auburn University, Auburn, Alabama, USA.
  109. 109. Ebenstein DM, Wahl KJ (2006) Anisotropic nanomechanical properties of Nephila clavipes dragline silk. J Mat Res 21: 2035–2044.
  110. 110. Sümer S, Denzinger A, Schnitzler H-U (2009) Spatial unmasking in the echolocating Big Brown Bat, Eptesicus fuscus. J Comp Physiol A 195: 463–472.
  111. 111. Eisner T, Alsop R, Ettershank G (1964) Adhesiveness of spider silk. Science 146: 1058–1061.
  112. 112. Masters WM, Eisner T (1990) The escape strategy of green lacewings from orb webs. J Insect Behav 3: 143–157.
  113. 113. Griffin DR (1958) Listening in the Dark. New Haven: Yale University Press. 413 p.
  114. 114. Schnitzler H-U, Moss CF, Denzinger A (2003) From spatial orientation to food acquisition in echolocating bats. Trends Ecol Evol 18: 386–394.
  115. 115. Gould E (1955) The feeding efficiency of insectivorous bats. J Mammal 36: 399–407.
  116. 116. Manville RH (1963) Accidential mortality in bats. Mammalia 27: 361–366.
  117. 117. Wilhide JD, Rick V, Harvey MJ, White DR (1998) Telemetric observations of foraging Ozark big-eared bats in Arkansas. J Ark Acad Sci 52: 113–116.
  118. 118. Rypstra AL (1985) Aggregations of Nephila clavipes (L.) (Araneae, Araneidae) in relation to prey availability. J Arachnol 13: 71–78.
  119. 119. Blackledge TA, Kuntner M, Agnarsson I (2011) The form and function of spider orb webs: evolution from silk to ecosystems. Adv Insect Physiol 41: 175–262.
  120. 120. Kunz TH, Braun de Torrez E, Bauer D, Lobova T, Fleming TH (2011) Ecosystem services provided by bats. Ann New York Acad Sci 1223: 1–38.
  121. 121. Ulanovsky N, Moss CF (2008) What the bat's voice tells the bat's brain. Proc Nat Acad Sci USA 105: 8491–8498.
  122. 122. Blackledge TA (2011) Prey capture in orb weaving spiders: are we using the best metric? J Arachnol 39: 205–210.
  123. 123. Higgins L, Goodnight C (2011) Developmental response to low diets by giant Nephila clavipes females (Araneae: Nephilidae). J Arachnol 39: 399–408.
  124. 124. Le Souef D (1915) North Queensland birds. Emu 14: 163–166.
  125. 125. McKeown KC (1952) Australian Spiders. Sydney: Angus and Robertson. 274 p.
  126. 126. Threlfall C (2011) Conserving biodiversity in urban landscapes. Mechanisms influencing the distribution, community assembly and resource use of insectivorous bats in Sydney, Australia. Ph.D. Thesis, Evolution & Ecology Research Centre, School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, Australia.
  127. 127. Ochoa JG, Soriano PJ, Hernandez-Camacho J (1994) Sobre la presencia de Cyttarops alecto (Chiroptera: Emballonuridae) en Colombia. Trianea 5: 411–414.
  128. 128. Medway L (1972) Reproductive cycles of the flat-headed bats Tylonycteris pachypus and T. robustula (Chiroptera: Vespertilioninae) in a humid equatorial environment. Zool J Linn Soc 51: 33–61.
  129. 129. Levi HW (2004) Comments and new records for the American genera Gea and Argiope with the description of new species (Araneae: Areneidae). Bull Mus Comp Zool 158: 47–66.
  130. 130. Suter RB, Gruenwald J (2000) Spider size and locomotion on the water surface (Araneae, Pisauridae). J Arachnol 28: 300–308.
  131. 131. Koh JKH (2000) A Guide to Common Singapore Spiders. Singapore: Singapore Science Centre. 160 p.
  132. 132. Robinson MH, Robinson B (1970) Prey caught by a sample population of the spider Argiope argentata (Araneae: Araneidae) in Panama: a year's census data. Zool J Linn Soc 49: 345–358.
  133. 133. Simmons NB, Handley CO (1998) A revision of Centronycteris Gray (Chiroptera: Emballonuridae) with notes on natural history. Am Mus Novit 3239: 1–28.
  134. 134. Bhat HR, Sreenivasan MA, Jacobs PG (1980) Breeding cycle of Eonycteris spelaea (Dobson, 1871) (Chiroptera, Pteropodidae, Macroglossinae) in India. Mammalia 44: 343–347.
  135. 135. Menkhorst P, Knight F (2001) A Field Guide to the Mammals of Australia. Melbourne, Australia: Oxford University Press. 278 p.
  136. 136. Srinivasulu C, Srinivasulu B (2006) First record of Hipposideros ater Templeton 1848 from Andhra Pradesh, India with a description of a new subspecies. Zoos' Print Journal 21: 2241–2245.
  137. 137. Douangboubpha B, Bumrungsri S, Soisook P, Satasook C, Thomas NM, et al. (2010) A Taxonomic Review of the Hipposideros bicolor Species Complex and H. pomona (Chiroptera: Hipposideridae) in Thailand. Acta Chiropterol 12: 415–438.
  138. 138. Lin AQ, Jin LR, Shi LM, Sun KP, Berquist SW, et al. (2011) Postnatal development in Andersen's leaf-nosed bat Hipposideros pomona: flight, wing shape, and wing bone lengths. Zoology (Jena) 114: 69–77.
  139. 139. Lausen CL, Barclay RMR (2005) Pipistrellus nanus. Mammalian Species 784: 1–7.
  140. 140. Hiryu S, Hagino T, Riquimaroux H, Watanabe Y (2007) Echo-intensity compensation in echolocating bats (Pipistrellus abramus) during flight measured by a telemetry microphone. J Acoust Soc Am 121: 1749–1757.
  141. 141. Fitzinger LJFJ (1870) Kritische Durchsicht der Ordnung der Flatterthiere oder Handflügler (Chiroptera). Familie der Kammnasen (Rhinolophi). II. Abteilung. In: Sitzungsberichte der Akademie der Wissenschaften mathematisch-naturwissenschaftlicher Klasse 61: 123–198.
  142. 142. Huihua Z, Shuyi Z, Mingxue Z, Jiang Z (2003) Correlations between call frequency and ear length in bats belonging to the families Rhinolophidae and Hipposideridae. J Zool 259: 189–195.
  143. 143. Jung K, Kalko EKV, von Helversen O (2007) Echolocation calls in Central American emballonurid bats: Signal design and call frequency alternation. J Zool 272: 125–137.
  144. 144. Fullard JH, Koehler C, Surlykke A, McKenzie NL (1991) Echolocation ecology and flight morphology of insectivorous bats (Chiroptera) in South-western Australia. Aust J Zool 39: 427–438.
  145. 145. Schoeman CM, Jacobs DS (2008) The relative influence of competition and prey defenses on the phenotypic structure of insectivorous bat ensembles in Southern Africa. PLOS ONE 3: e3715.
  146. 146. Jones G, van Parijs SM (1993) Bimodal echolocation in pipistrelle bats: Are cryptic species present? Proc R Soc Lond B 251: 119–125.
  147. 147. Ma J, Jones G, Zhu G-J, Metzner W (2010) Echolocation behaviour of the Japanese pipistelle bat Pipistrellus abramus during foraging flight. Acta Theriol 55: 315–332.
  148. 148. Siemers BM, Kalko EKV, Schnitzler H-U (2002) Echolocation behavior and signal plasticity in the Neotropical bat Myotis nigricans (Schinz, 1821) (Vespertilionidae): a convergent case with European species of Pipistrellus? Behav Ecol Sociobiol 50: 317–328.
  149. 149. Fenton MB, Bell GP (1981) Recognition of species of insectivorous bats by their echolocation calls. J Mammal 62: 233–243.
  150. 150. Guppy A, Coles RB (1988) Acoustical and neural aspects of hearing in the Australian gleaning bats, Macroderma gigas and Nyctophilus gouldi. J Comp Physiol A 162: 653–658.
  151. 151. Funakoshi K, Nomura E, Matsukubo M, Wakita Y (2010) Postnatal growth and vocalization development of the Lesser Horseshoe Bat, Rhinolophus cornutus, in the Kyushu District, Japan. Mamm Stud 35: 65–78.
  152. 152. Grundwald J-E (2004) Echo-acoustic evaluation of real and phantom objects in phyllostomid bats. Ph.D. Thesis, LMU Munich, Germany.
  153. 153. Zubaid A (1988) Food habits of Hipposideros pomona (Chiroptera: Rhinolophidae) from Peninsular Malaysia. Mammalia 52: 134–137.
  154. 154. Pavey CR, Burwell CJ (2000) Foraging ecology of three species of hipposiderid bats in tropical rainforest in north-east Australia. Wildlife Res 27: 283–287.