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Bolas spider
Bolas spider
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Bolas spiders
Mastophora phrynosoma with bolas, Virginia, US
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Chelicerata
Class: Arachnida
Order: Araneae
Infraorder: Araneomorphae
Family: Araneidae
Subfamily: Cyrtarachninae s.l.
Informal group: Bolas spiders
Genera[1][2][3]

A bolas spider is a member of the orb-weaver spider (family Araneidae) that, instead of spinning a typical orb web, hunts by using one or more sticky "capture blobs" on the end of a silk line, known as a "bolas". By swinging the bolas at flying male moths or moth flies nearby, the spider may snag its prey rather like a fisherman snagging a fish on a hook. Because of this, they are also called angling or fishing spiders[4] (although the remotely related genus Dolomedes is also called a fishing spider). The prey is lured to the spider by the production of up to three sex pheromone-analogues.

Bolas spiders have been treated as either the whole or part of either the tribe "Mastophoreae" or Mastophorini, the subfamily Mastophorinae, or the informal group mastophorines. Recent studies show that the genus Celaenia, which does not use a bolas, belongs in the same taxonomic group.

Description

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Mastophora bisaccata resembles a snail when at rest

Bolas spiders are small nocturnal animals with conspicuous outgrowths on the upper (dorsal) surface of the cephalothorax. Mature females have a body length of 10–20 mm (1234 in), while the males, which are much smaller, have a body length usually less than 2 mm (116 in). The abdomen of adult females is large relative to the cephalothorax, partially covering it. In some species, the female's abdomen is comparatively smooth, while in others it has humps and tubercules. The females of some bolas spiders (e.g. Mastophora cornigera) look remarkably like a bird dropping, thanks to their large, globular abdomen and brownish cephalothorax. This is a form of defensive mimicry as the animals that prey on spiders pay little attention to bird droppings, which enables the spiders to rest unnoticed during the day in fairly exposed places. M. bisaccata resembles the shell of a snail that is abundant in the spider's habitat. While the bird dropping mimics rest on the upper surface of leaves, M. bisaccata rests on the undersides. If removed from the surface, Mastophora females produce a pungent odor, which is highly unusual for spiders (other than bolas spiders, only one species of Cyrtarachne is known to do this). They do not attempt to flee when handled. Some species of Cladomelea also rest exposed on leaves during the day. However, the Australian Ordgarius magnificus, which displays eye spots on its back that make it resemble the moth it hunts, ties leaves together with silk to form a retreat.[5][6]

Taxonomy

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Genera

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Bolas-using spiders are species of four related genera.[1][2][3] (Distributions are from the World Spider Catalog.[7])

  • Cladomelea Simon, 1895 – Central and South Africa
  • Exechocentrus Simon, 1889Madagascar
  • Mastophora Holmberg, 1876 (syn. Agathostichus) – North and South America
  • Ordgarius Keyserling, 1886 (syn. Dicrostichus) – Australia north to India, China and Japan

The use of a bolas by the Madagascan genus Exechocentrus was not reported until 2012,[3] so the genus is not included in earlier accounts of bolas spiders.

Classification

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Bolas spiders are members of the family Araneidae, the orb-weaver spiders, although they do not weave webs. They may be treated as a group within the subfamily Cyrtarachninae sensu lato,[8] or as the whole or part of a separate taxon. In 1931, Mello-Leitão created a tribe under the name Mastophoreae, which included genera now known to use a bolas as well the genus Acantharachne.[9] Gertsch in 1955 also placed bolas spiders in the tribe Mastophoreae, again including Acantharachne (under the synonym Acantharanea).[10] Article 29.2 of the International Code of Zoological Nomenclature states that the ending "-ini" should be used for tribes, so the correct name for the tribe is now "Mastophorini".[11] The tribe has been elevated to a separate subfamily Mastophorinae.[12] The informal name "mastophorines" has also been used, including both bolas-using spiders and a related genus.[13]

A 2014 molecular phylogenetic study of a representative set of genera placed in Cyrtarachninae s.l. showed that the species of the two bolas spider genera included in the study formed a strongly supported clade nested within Cyrtarachninae s.l.[8] A wider study of the family Araneidae published in 2020 reached a similar conclusion, separating Cyrtarachninae s.l. into two informal sister groups "mastophorines" and "cyrtarachines". Mastophorines included the genus Celaenia that does not use a bolas.[13] Bolas-using spiders thus form a subgroup within the narrowly defined mastophorines or the broadly defined Cyrtarachninae.

Phylogeny and web evolution

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The Cyrtarachninae, defined broadly, construct several kinds of web, which differ from the orb webs of other Araneidae. Some construct "spanning-thread webs", which have a small number of radii and widely spaced sticky threads that do not form spirals. Others construct triangular webs. These are formed in the same way as spanning-thread webs, but with only three radii, so that they appear triangular. Bolas spiders do not spin webs at all, adult females catching their prey on single sticky threads. Finally, some species capture their prey without a web, using their outstretched legs, as do juvenile and male bolas spiders.[8]

One hypothesis was that the evolution of the web types involved successive reduction: spanning-thread webs → triangular webs → bolas → no web. However, the 2014 molecular phylogenetic study by Tanikawa et al. showed that this hypothesis did not fit with the evolutionary relationships they derived. Their cladogram is shown below.[8] (The dashed line shows where the genus Exechocentrus would be expected to fall based on a 2020 study.[13]) Triangular webs could have been derived from spanning-thread webs, but spiders with no webs or that used bolas formed a completely separate monophyletic group.[8]

Cyrtarachninae s.l.

Scharff et al. in a molecular phylogenetic study of the family Araneidae published in 2020 reached a similar conclusion concerning the relationships within the broadly defined Cyrtarachninae. They included the bolas-using genus Exechocentrus in their analysis (which has been added to the cladogram above), dividing Cyrtarachninae s.l. into "mastophorines" and "cyrtarachnines".[13]

Distribution

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Bolas spiders are found in America, Africa including Madagascar, and Australasia northwards into Asia. They do not occur in temperate Eurasia. About half of the known Mastophora species occur in South America. The genus is distributed from southern Chile to the northern US (to 45° north latitude in Minnesota). M. archeri, M. bisaccata, M. hutchinsoni and M. phrynosoma occur widely in the US east of the Great Plains. M. cornigera occurs from Alabama to California, as well as in northern Mexico.

Life-cycle

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Mastophora phrynosoma resting in full view, resembling a bird dropping; egg sac under the leaf

The life-cycle of the North American Mastophora hutchinsoni is best known. As is probably the case for other Mastophora species in temperate regions, mating takes place in late summer or early fall, after which egg cases are produced. Adults do not survive the winter, males typically dying before females. A similar pattern is observed for bolas spiders in the Southern Hemisphere, depending on the climate. In the subtropical climate of Edmonton in north Queensland, Australia, a female Ordgarius monstrosus matured in June and produced egg cases between late June and early September. In Pietermaritzburg, South Africa, adult females of Cladomelea akermani were observed with egg cases during July. The number of egg cases varies widely among species, with temperate species producing fewer than tropical ones (e.g. one to three for Mastophora species in temperate regions of the United States, and up to 11 for M. dizzydeani near the equator). The number of eggs per case also varies depending on the climate, so that the total number of spiderlings produced by one female ranges from several hundred in the temperate US to several thousand in Colombia.[6]

Some male bolas spiders, such as those of Mastophora cornigera and Ordgarius magnificus, appear to be mature on emergence from their egg cases and so capable of inseminating females. Others, such as those of M. dizzydeani, M. hutchinsoni and M. phrynosoma require one or two moults before becoming mature. By contrast, Mastophora females may require up to eight moults to reach maturity.[6]

Prey capture

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Cladomelea sp. from South Africa with multiple drops on its bolas line

Bolas spiders are defined by the way in which adults catch their prey. Like other members of the subfamily Cyrtarachninae sensu lato, bolas spiders specialize in catching moths. The scales covering moth wings are detachable, so that most ordinary orb webs are not effective at capturing moths. Adult female bolas spiders spend the day resting, disguised in various ways, including as bird droppings. At night, they feed on male moths which they attract by producing a scent that mimics the sex pheromones emitted by the female of one or more species of moth. They capture approaching male moths by using a "bolas", a silken thread with one or more sticky drops at the end which they swing, rather than throw, at the moth.[2][6] Other spiders in the subfamily Cyrtarachninae, including Celaenia species from Australia and Taczanowskia species from South America, also use chemical lures to attract moths, but they catch them with their front legs.[6]

Bolas spiders will try and often succeed in catching any insect that is flying nearby. They seem able to detect prey by the sound of their approaching flight. In experiments, M. cornigera attacked a hand-held moth whose wings were fluttering, but did not attack if the moth's wings were immobilized.[6]

Left: Mastophora cornigera attracting a moth while holding its bolas; right: with captured moth

The manner in which the bolas is used differs among the genera. Mastophora species hold the bolas stationary with a front leg until a moth approaches, and then cock the leg and swing the bolas towards the prey with a rapid pendulum-like stroke. Other genera use their second leg. Ordgarius species begin to whirl the bolas rapidly when detecting an incoming moth. Cladomelea akermani whirls the bolas immediately after it has been prepared for about 15 minutes, even when there is no moth present.[6] Instead of preparing a single bolas, at least four Mastophora species are known to sometimes hang up to nine droplets on one horizontal line. This has not been observed to result in prey capture, but is remarkably similar to the midline of a Pasilobus web in which the spanning threads have been broken.[6]

Spiderlings of both sexes and adult males hunt without a bolas. This might be because the small globule these spiders could produce would dry out rapidly. Rather, they position themselves at edges of leaves and grab prey with their frontal pair of legs. Juvenile females and males of all ages of M. hutchinsoni have a row of strong bristles on the prolateral surface of the tibiae and metatarsi of each of their first two pairs of legs which may aid in prey capture. Females lose these bristles after a few moults. Moth flies of the genus Psychoda are prominent prey of juvenile and adult male Mastophora.[14][15]

Drop structure

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The sticky drops of the bolas have a diameter of about 2.5 mm (110 in). Their internal structure is complex, consisting of a mass of curled or folded fibre embedded in a viscid matrix which is in turn surrounded by a less viscous layer. This results in the low viscosity liquid flowing past the moth's scales to reach the cuticle below, while the more viscous liquid forms a bond to the thread to sustain the moth's weight. The folded thread inside the ball permits elastic elongations which extend the spider's striking range. Ordgarius sometimes has smaller droplets above the terminal one.[6] Exechocentrus lancearius uses a bolas with two globules.[3] The other genera usually produce only one terminal globule. The drop shrinks over time, thus presumably reducing its effectiveness in catching prey. Bolas spiders consume unused bolas after at most half an hour if the hunt was fruitless.[6]

Prey variety

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Female Mastophora catch an average of two moths per night, but as many as six or seven catches during a single night have been observed. Bolas spiders vary in the range of moth species they capture, with 20 moth species recorded for Mastophora cornigera females, mostly noctuids, and four for Mastophora hutchinsoni females, three of which were noctuids.[6] A study of M. hutchinsoni showed that the blend of chemicals produced by the spider was very similar to that produced by the female of the bristly cutworm, Lacinipolia renigera, whose males make up about two thirds of the biomass consumed by the spider.[16] A study by K.F. Haynes showed that M. hutchinsoni females adapt to changes in prey availability, with one major prey species flying from early evening until 10:30 pm or so and the other only after 11:00 pm. The first moth ignores the pheromone of the second, so the spider produces a mix of both pheromones early in the evening. However, since the second moth is repulsed by the other moth's pheromone, the spider ceases to produce the first pheromone later at night.[17][16]

Natural enemies

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Yeargan noted that records of natural enemies of bolas spiders all concern predators or parasitoids of the egg stage. A gryllacridid was observed feeding on the eggs of Ordgarius magnificus, and a flesh fly parasitoid has been reared from egg cases of the same species. Five species of hymenopteran parasitoids are known to attack Mastophora eggs. Tromatobia notator parasitizes M. cornigera, M. bisaccata and M. phrynosoma; a Gelis species parasitizes M. cornigera. Eupelmids in the genus Arachnophaga also parasitize Mastophora species.[6]

References

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Bibliography

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Bolas spiders (Mastophora spp.) are a of orb-weaver spiders in the family Araneidae, renowned for their specialized in which adult females construct and swing a —a small, sticky globule of suspended from a short dragline—to capture airborne prey, particularly male attracted by the spider's chemical of female moth sex pheromones. The Mastophora was established by Eduardo Ladislao Holmberg in 1876 and encompasses 47 valid species, with a distribution spanning the Americas from southern through the , , , and into as far as and . These spiders belong to the Cyrtarachninae and exhibit extreme sexual size dimorphism, with females typically much larger than males—females can reach body lengths of up to 2 cm, while mature males are often under 5 mm. During the day, females remain inactive on foliage or branches, their globular abdomens and pale coloration providing that resembles bird droppings. Hunting occurs primarily at night in humid conditions, when females emit blends of volatile compounds—such as (Z)-9-tetradecenyl , (Z)-9-tetradecenal, and (Z)-11-hexadecenal—that precisely imitate the sex pheromones of target species, drawing males within 1-2 meters. Once a moth is detected via air currents or visual cues, the spider forms the bolas by coiling a specialized "windlass" thread within a glue droplet nearly 2 mm in diameter and flicks it in a rapid, targeted swing, often achieving capture in a multi-stage process that includes resistance to the prey's escape attempts followed by reeling and subduing. This represents an evolutionary departure from typical orb-weaving, as bolas spiders forgo full webs in favor of this active, pheromone-assisted method, preying almost exclusively on s in habitats ranging from forests to scrublands.

Description

Morphology

Bolas spiders, belonging to genera such as Mastophora, Cladomelea, and Ordgarius, display extreme characteristic of many orb-weaving spiders in the family Araneidae, with females being substantially larger and more robust than males to support egg production and hunting activities. Adult females typically measure 10–20 mm in body length, while adult males are diminutive, usually under 2 mm, and juveniles are proportionally smaller across life stages. Males possess smaller relative to their body size compared to females, reflecting their reduced predatory role as adults. The of bolas spiders often features conspicuous outgrowths on its dorsal surface, a morphological trait that distinguishes them from typical araneids and may aid in by mimicking natural debris. Females exhibit a bulbous , wider than long, adapted for accommodating developing eggs and contributing to their overall robust form, whereas males have a more slender abdominal profile. This extends to the lightweight build of both sexes, optimized for mobility and minimal reliance on extensive web structures. Their legs are notably long and thin, enabling females to grip and swing the bolas effectively during prey capture, with specialized silk glands in the abdomen producing the adhesive droplets essential for this hunting method. These glands generate aggregate silk for the sticky component, distinct from the radial threads used in limited web anchoring, underscoring the spiders' evolutionary adaptations for a reduced web-building lifestyle. Many species also show brief camouflage patterns on the abdomen, resembling bird droppings to evade predators.

Camouflage and Sensory Adaptations

Bolas spiders, particularly females of genera such as Mastophora, exhibit remarkable visual that enhances their survival by resembling innocuous environmental elements. Adult females often display white or mottled coloration combined with a hunched posture that closely imitates bird droppings, allowing them to blend seamlessly with foliage during periods of inactivity. In certain species like Mastophora bisaccata, this extends to resembling the shells of local snails, further aiding concealment on leaf surfaces where such debris is common. As a secondary line of defense, bolas spiders employ chemical repellents when threatened. When disturbed or forcibly removed from their resting substrate, females emit a distinctive pungent , typically produced via a droplet of regurgitant rather than specialized glands, which serves to deter potential predators. This disagreeable emission is a rare trait among spiders and underscores their reliance on olfactory deterrence outside of predatory contexts. Sensory adaptations in bolas spiders support their non-web-based lifestyle, emphasizing detection of airborne cues over substrate vibrations typical of orb-weavers. Chemoreceptors, in the form of sensilla on the walking legs, facilitate the perception of environmental chemical signals, though their precise role in Mastophora remains underexplored beyond general mechanoreceptive and chemoreceptive functions. Due to their active , these spiders show reduced dependence on web-transmitted vibrations, instead utilizing trichobothria—vibration-sensitive hairs on the legs—to detect distant airborne disturbances like wingbeats from up to 30 cm away. To maximize the efficacy of their , bolas spiders engage in diurnal resting , remaining motionless and withdrawn on surfaces throughout the day. This inactivity, often on the upper or lower sides of leaves depending on , minimizes visibility and movement that could betray their presence to diurnal predators.

Taxonomy and Evolution

Genera and Classification

Bolas spiders belong to the family Araneidae, the orb-weaver spiders, and are placed in the Cyrtarachninae lato, which encompasses genera exhibiting reduced web structures and specialized hunting behaviors; alternatively, some classifications elevate the bolas-using taxa to the distinct Mastophorinae as a to Cyrtarachninae based on molecular phylogenetic analyses. The primary genera of bolas spiders include Mastophora, which is distributed across the and contains approximately 50 , Ordgarius, found from to with about 12 , Cladomelea, restricted to and comprising a few , and Exechocentrus, endemic to with 1–2 ; this group also incorporates the non-bolas genus Celaenia, which shares morphological and phylogenetic affinities but lacks the bolas-hunting . Historically, bolas spiders were largely classified under the genus Mastophora following early revisions that emphasized shared morphological traits like reduced webs and chemical lures, but molecular data from multi-gene phylogenies have prompted splits into these separate genera to reflect evolutionary divergences. In total, approximately 70 of bolas spiders have been described, with Mastophora cornigera frequently serving as a model for on their unique predatory strategies due to its well-documented in the Neotropics.

Phylogenetic Relationships

Bolas spiders are positioned within the family Araneidae, derived from orb-weaving ancestors that typically construct wheel-shaped webs, but have evolved specialized hunting strategies involving reduced or modified silk structures. They belong to the Cyrtarachninae subfamily, a characterized by moth-specialized predation and varying degrees of web reduction, which includes both bolas-using genera and close relatives with spanning-thread or triangular webs. Molecular phylogenetic analyses have clarified inter-generic relationships among bolas spiders, placing Mastophora and Ordgarius as sister groups within a monophyletic or webless that diverged early from the spanning-thread web spiders such as Cyrtarachne and Paraplectana. Cladomelea is considered closely related based on morphological traits, though it has not been included in molecular analyses. Post-2010 molecular studies, utilizing markers like COI, 18S-rRNA, and 28S-rRNA, confirm the of the analyzed bolas-using genera, supporting their shared evolutionary origin from a common ancestor specialized for luring via pheromones. In relation to non-bolas Araneidae, bolas spiders retain core orb-weaver traits such as aggregate silk glands for sticky capture threads and a triad spigot configuration, but exhibit reduced web complexity, often limited to a single thread or none at all, representing an for active prey rather than passive ensnarement. Recent phylogenomic advancements in the , incorporating multi-gene datasets for over 150 Araneidae taxa, have refined these classifications by confirming the inclusion of Exechocentrus as a bolas-user within the monophyletic Mastophorines alongside Mastophora and Celaenia, thus updating earlier morphological-based groupings and highlighting in pheromone-based hunting across the subfamily.

Web and Hunting Evolution

Bolas spiders, belonging to genera such as Mastophora within the family Araneidae, trace their evolutionary origins to ancestors that constructed elaborate two-dimensional orb-webs, a defining trait of most orb-weaving spiders. Over evolutionary time, these structures underwent progressive reduction, simplifying from full orb-webs to a minimal setup consisting of a single thread bearing a sticky globule, or bolas, at its tip. This transition is interpreted as an energy-conserving adaptation, as producing a complete orb-web demands substantial production and maintenance costs, whereas the bolas method requires far less material while retaining efficacy for capturing flying prey. Phylogenetic analyses place the emergence of bolas-using behavior early within the moth-specialized Cyrtarachninae, diverging from clades that retained more extensive spanning-thread webs. A pivotal innovation in this lineage was the development of chemical , where spiders produce volatile compounds imitating female sex pheromones to lure male moths into striking range of the . This sensory likely coevolved with web simplification, enhancing the selective pressure for reduced web architectures in moth-focused predation. Parallel evolutionary trends toward web reduction appear in other Araneidae subgroups, such as the Cyrtarachneae, which exhibit intermediate forms like triangular or beaded spanning-threads, and the Celaenieae, with similar specializations. These convergences suggest that bolas hunting occupies an evolutionary midpoint between passive orb-webbing and fully active pursuit strategies, allowing spiders to exploit aerial with minimal structural investment. No direct fossils document bolas spiders, as their delicate silk-based traits rarely preserve; instead, their evolutionary is inferred from molecular phylogenies, comparative morphology, and behavioral homologies across Araneidae, revealing multiple independent losses of complex webs within the family.

Distribution and Habitat

Geographic Range

spiders, belonging to the tribe Mastophoreae within the family Araneidae, exhibit a primarily and subtropical distribution across the , , and extending northward into southern . The genus Mastophora predominates in the , with species ranging from southern , including where M. gasteracanthoides occurs, northward through and into . In , Mastophora species such as M. hutchinsoni extend to the temperate edges, reaching southern in provinces like and Québec, and as far north as in the United States; M. cornigera occurs in the southern United States and northern . In , bolas spiders are represented by genera such as Cladomelea and Exechocentrus. Cladomelea species, including C. longipes, C. akermani, and C. debeeri, are distributed across the Afrotropical region, with records primarily from but extending beyond type localities in recent surveys. Exechocentrus lancearius is known from , with limited additional records from nearby areas. The genus Ordgarius occurs in and , spanning eastern from southward, and extending through , , , and . Bolas spiders are notably absent from and northern , with no verified records in temperate Eurasian regions. Their distribution patterns suggest Gondwanan origins, aligned with the broader phylogenetic history of the Araneidae family, which shows ancient divergences consistent with continental fragmentation. No confirmed evidence exists for recent human-mediated introductions beyond their natural ranges. Regional species richness remains unevenly documented, with Mastophora comprising the most widespread and diverse genus, while and show gaps due to understudied areas; for instance, new records of Cladomelea in highlight ongoing discoveries, and Southeast Asian spider faunas, including Ordgarius, are generally less surveyed compared to the .

Preferred Environments

Bolas spiders of the genus Mastophora primarily inhabit open habitats such as woodlands, grasslands, shrublands, meadows, and gardens across the , where provides suitable perches for hunting and resting. These environments typically feature low to mid-height , with individuals often selecting woody plants or for attachment sites. The species favor warm, humid climates in tropical and subtropical regions, exhibiting multivoltine life cycles with year-round activity in such areas; in temperate zones, they are univoltine, overwintering as eggs to tolerate cooler conditions but remaining absent from colder temperate . This distribution reflects an to environments supporting abundant nocturnal populations, their primary prey. In microhabitats, adult females perch on stems, leaves, or twigs at heights of approximately 1.5–3 m during nocturnal hunting, aligning their activity with peak flight times after . Diurnally, they rest exposed on the upper or underside of leaves, utilizing morphological that mimics bird droppings or shells to evade predators. Egg cases are typically suspended on woody vegetation in similar low-to-mid strata, ensuring protection while maintaining proximity to hunting sites.

Life Cycle

Reproduction and Mating

Bolas spiders exhibit reproductive cycles that align with climatic conditions. In temperate regions, mating occurs primarily from late summer to fall; for instance, in Mastophora hutchinsoni from , males reach maturity in late June to early July, while females mature in early September, facilitating copulation soon after. In tropical and subtropical environments, reproduction is often year-round, as demonstrated by Mastophora cornigera in , where egg cases are produced monthly throughout the year. Mating in bolas spiders involves males cautiously approaching mature females, though specific details for bolas species remain sparsely documented. Copulation is brief, lasting only seconds to minutes, during which the male inserts his pedipalps into the female's to transfer sperm directly into her spermathecae for storage and later use in fertilization. Unlike some araneid relatives where is common, the risk appears low in bolas spiders, likely due to the extreme sexual size dimorphism that minimizes male vulnerability during this rapid process. In certain species, males die shortly after , coinciding with the end of their adult lifespan. Post-mating, varies by and . In temperate zones, females typically produce 1–3 egg sacs per season, each containing 150–300 eggs. Tropical species exhibit higher output; for example, Mastophora dizzydeani from can lay up to 11 sacs, with one documented case holding 826 eggs (averaging 0.40 mg per egg). Egg sac numbers and sizes depend on climate and resources, enabling total progeny from hundreds to thousands per .

Development Stages

Bolas spiders exhibit a univoltine life cycle in temperate regions, with development progressing through distinct stages from egg to adult over approximately one year. lay eggs in the fall, enclosing 150 to 300 in a single tough, camouflaged egg sac that resembles plant structures such as buds or berries, as observed in Mastophora hutchinsoni. These eggs overwinter within the sac, undergoing embryonic development during the cold months, with spiderlings typically hatching in around May in locations like . Upon hatching, the tiny spiderlings disperse from the egg sac, often via ballooning, where they release silk threads caught by the wind to travel aerially and colonize new areas, a common dispersal mechanism among juvenile orb-weaver spiders. During early juvenile instars, they hunt actively by ambushing small such as and flies using specialized bristles on their legs to grab prey, rather than employing the bolas technique. As juveniles grow, they undergo multiple molts; females typically require up to eight or more to reach maturity, enabling substantial body size increase to 10–20 mm, while males, emerging nearly mature, need only one or two molts and remain diminutive at under 2 mm. This disparity allows males to mature rapidly by late or early , preceding female maturation in early September and aligning with mating opportunities. The transition to bolas hunting begins in later juvenile stages for females, typically by early after initial molts, coinciding with the loss of leg bristles and adoption of the adhesive silk droplet method. Adult lifespan is short, lasting weeks to months post-maturation, with females dying shortly after egg sac production and males perishing soon after ; no adults survive winter. Overwintering occurs exclusively in the stage in temperate populations, ensuring survival through and addressing stage-specific vulnerabilities in harsh conditions.

Hunting Behavior

Prey Capture Mechanism

Bolas spiders utilize a specialized apparatus known as a for prey capture, consisting of a single thread of measuring 5–30 cm in length, depending on the and individual, with 1–3 glue droplets attached, each approximately 2–2.5 mm in . The thread is primarily produced from major ampullate glands, while the sticky globules derive from aggregate glands that secrete a viscoelastic glue optimized for adhering to flying ; pyriform glands contribute to the structural attachment of the globules to the thread. This construction allows the spider to create a portable, targeted trap rather than a fixed web. The adult female spider grasps the proximal end of the bolas in her forelegs and swings it in rapid circular or flicking motions toward approaching prey, primarily moths drawn within striking range. This technique generates a conical zone, with rotational speeds reaching up to 1.5 m/s in like Cladomelea akermani, enabling the globule to intercept the target at close range (often within 2 cm). Observed success rates for strikes that result in adhesion are high, around 83% in controlled video analyses of Mastophora hutchinsoni, though overall encounter-to-capture efficiency varies with prey behavior and environmental factors. The glue's formulation effectively counters moth defenses by penetrating and anchoring to the loose scales, preventing the shedding that often allows escape from traditional orb webs. Upon adhesion, the reels in the bolas at a deliberate pace of approximately 0.017 m/s, typically completing retrieval in 2–3 seconds, before injecting to immobilize the prey. This post-capture process minimizes energy expenditure and ensures secure handling. In contrast, juvenile females, males, and early-instar forgo the bolas, opting instead for an ambush tactic where they extend their forelegs to grasp passing directly. Through this mechanism, bolas spiders achieve moderate nightly efficiency, capturing an average of 2–3 moths per night, with occasional peaks up to 6–7 in optimal conditions.

Lure Production and Prey Variety

Bolas spiders employ aggressive chemical , in which adult females release volatile compounds that imitate the pheromones of female to attract males of specific . For instance, in Mastophora cornigera, these include (Z)-9-tetradecenyl acetate, (Z)-9-tetradecenal, and (Z)-11-hexadecenal, which match components used by multiple prey moth . This deception exploits the moths' mating behavior, drawing them into striking distance without alerting non-target , as the pheromones are highly species-specific. The pheromones are produced endogenously by the spider and emitted either directly from the body or incorporated into the adhesive droplet of the bolas. Emission often occurs via the sticky globule on the thread, where the volatile compounds are concentrated to create a localized plume that mimics a female moth's calling signal. Production varies by species; for example, Mastophora hutchinsoni releases blends such as (Z)-9-tetradecenyl acetate and (Z,E)-9,12-tetradecadienyl acetate to target moths. This method allows precise control, with females adjusting release rates to optimize attraction during nocturnal hunting. Temporal variation in emission enhances prey diversity, as females can switch blends over the course of a night to match the activity patterns of different moth . Recent observations indicate that M. hutchinsoni alters its chemical output, potentially emitting one blend at for early-flying and another near for later ones, thereby accessing a broader range of prey without fixed specialization. This multi-pheromone strategy, documented in 2022 field studies, addresses limitations of single-blend and supports sustained efficiency. The prey spectrum consists primarily of male from the family , though bolas spiders target a diverse array across genera and families. In M. cornigera, at least 19 species from 10 genera in five families have been recorded as prey, with a focus on comprising the majority. M. hutchinsoni attracts four species but relies on two species—such as the bristly cutworm () and smoky bomolocha (Hypena scabra)—for over 90% of its diet. Juveniles may also capture male (Psychodidae), but adult females avoid non- insects due to the pheromones' specificity.

Ecology

Natural Enemies

Bolas spiders encounter threats primarily from parasitoids and predators that target their egg sacs, with fewer documented attacks on adults or juveniles. Records indicate that natural enemies focus on the vulnerable egg stage, where mortality can be substantial due to infestation. For instance, hymenopteran parasitoids such as Tromatobia notator () attack egg sacs of species including Mastophora cornigera, M. bisaccata, and M. phrynosoma, laying s that develop by consuming the spider embryos. Similarly, wasps of the genus Arachnophaga (Eupelmidae) infest Mastophora egg sacs, with larvae feeding on the s; in one examined sac, all spider eggs were consumed, resulting in 100% offspring mortality. Flesh flies (Sarcophagidae) also parasitize egg cases in related bolas spiders like Ordgarius magnificus, emerging after feeding on the contents and contributing to high larval loss. Insects such as gryllacridids have been observed preying on eggs within sacs of Ordgarius magnificus, directly consuming the developing spiderlings. Egg sacs may additionally face predation from , which can breach the enclosure to access the contents, though specific rates for Mastophora remain undocumented. Adults and juveniles experience stage-specific risks, with juveniles potentially vulnerable to opportunistic predators like during their active hunting phase on foliage, while adults face threats from generalist hunters. Bolas spiders employ behavioral and chemical defenses to mitigate these threats. Their drab coloration and provide effective , reducing detection by visual predators such as birds and that patrol . When disturbed, females release a pungent , which acts as a repellent against certain attackers, including some predators. Studies underscore the specificity of parasitoids like Arachnophaga to Mastophora egg sacs, highlighting how structure and placement influence infestation success.

Ecosystem Role

Bolas spiders contribute to pest regulation in their native habitats by selectively preying on male , including species from the family that are significant agricultural pests. For instance, Mastophora hutchinsoni captures noctuid s such as the bristly cutworm (Lacinipolia renigera) and pale-legged dart (Tetanolita mynesalis), both of which can damage crops as larvae. This predation reduces local densities, thereby limiting potential crop damage in tropical and subtropical agricultural areas where these spiders occur. Species like Mastophora cornigera have been observed targeting up to 20 species, many of which are polyphagous noctuids that pose economic threats to . Although their impact is localized and not sufficient for large-scale control, they serve as natural allies against pests like the in subtropical ecosystems. Within the , bolas spiders function as mid-level predators that control populations while serving as prey for higher trophic levels, including hymenopteran parasitoids such as Tromatobia notator, which target their egg sacs. Five species of these parasitoids are documented to attack Mastophora eggs, integrating the spiders into broader parasitic interactions. The reliance of bolas spiders on diverse moth prey and their role in functional diversity highlight their contribution to predator-prey dynamics in ecosystems like tropical forests. Bolas spiders hold relevance for human applications through their pheromone mimicry, which has informed research into synthetic attractants for in agriculture. Studies on Mastophora species' chemical lures, which replicate moth sex pheromones, have advanced techniques for trapping pests without broad-spectrum pesticides. They face no formal conservation designations but are vulnerable to habitat loss from and land conversion in their native ranges, which disrupts moth-spider interactions.

References

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