Hubbry Logo
TetrapulmonataTetrapulmonataMain
Open search
Tetrapulmonata
Community hub
Tetrapulmonata
logo
8 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Tetrapulmonata
Tetrapulmonata
Tetrapulmonata
View on Wikipedia
from Wikipedia

Tetrapulmonata
Temporal range: Devonian–Holocene
Clockwise from top left: Araneus diadematus (Araneae) Phrynus (Amblypygi) Hubbardia briggsi (Schizomida) Mastigoproctus scabrosus (Uropygi)
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Chelicerata
Class: Arachnida
Clade: Arachnopulmonata
Clade: Pantetrapulmonata
Clade: Tetrapulmonata
Shultz, 1990
Orders

Tetrapulmonata is a non-ranked supra-ordinal clade of arachnids. It is composed of the extant orders Uropygi (whip scorpions), Schizomida (short-tailed whip scorpions), Amblypygi (tail-less whip scorpions) and Araneae (spiders). It is the only supra-ordinal group of arachnids that is strongly supported in molecular phylogenetic studies.[1] Two extinct orders are also placed in this clade, Haptopoda and Uraraneida.[2] In 2016, a newly described fossil arachnid, Idmonarachne, was also included in the Tetrapulmonata; as of March 2016 it has not been assigned to an order.[3]

Etymology

[edit]

It receives its name from the presence of paired book lungs occupying the second and third opisthosomal segments, although the posterior pair is absent in Schizomida and most araneomorph spiders. Previous synonyms of this lineage are rejected; "Caulogastra Pocock, 1893" refers to pedicel, which is symplesiomorphic for the lineage and convergent with Solifugae, and "Arachnidea Van der Hammen, 1977" is easily confused with Arachnida. The clade is referred to as Pantetrapulmonata when the extinct trigonotarbid arachnids are included.[2]

The name "Pulmonata" has been used for this group as recently as 2000, in the first paragraph of an article in Journal of Paleontology,[4] but this creates ambiguity because Pulmonata is a group of gastropods.

Characteristics

[edit]

In addition to the two pairs of book lungs, other synapomorphies of Tetrapulmonata include a large postcerebral pharynx (reduced in Uropygi), prosomal endosternite with four segmental components, subchelate chelicerae, a complex coxotrochanteral joint in the walking legs, a pretarsal depressor muscle arising in the patella (convergent with Dromopoda, lost in Amblypygi), a pedicel formed, in part, by ventral elements of the second opisthomal segment and a spermatozoon axoneme with a 9+3 microtubule arrangement.[5]

Phylogeny

[edit]

A cladogram published in 2014 divides the Tetrapulmonata into two clades, the Schizotarsata and the Serikodiastida. The Schizotarsata have walking legs II–IV with the tarsus having a specific pattern of three subsegments (tarsomeres). The Serikodiastida (Greek for "silk workers") share the ability to produce and use silk. The sister clade to Tetrapulmonata is the extinct order Trigonotarbida; together they form a clade that has been called "Pantetrapulmonata", to which the Carboniferous genus Douglassarachne was also referred in 2024.[2][6]

Pantetrapulmonata

†Trigonotarbida

Tetrapulmonata
Schizotarsata

†Haptopoda

Pedipalpi
Thelyphonida s.l. or Uropygi s.l.

Amblypygi

Serikodiastida

In 2016, a fossil arachnid from the Late Carboniferous (Pennsylvanian) age was described in the genus Idmonarachne. Based on its overall morphology, it was considered to belong to the Serikodiastida, although the presence of silk-producing spigots was not demonstrated. Like uraraneids, it lacked spinnerets, but it also lacked a flagellum, thus resembling spiders. A cladogram based on morphology placed Idmonarachne between uraraneids and spiders:[3]

Serikodiastida

The Late Carboniferous appears to be a time when there was a greater diversity of tetrapulmonate arachnids.[3]

References

[edit]

Sources

[edit]

Jeffrey W. Shultz. 2007. "A phylogenetic analysis of the arachnid orders based on morphological characters". Zoological Journal of the Linnean Society 150(?):221-265. (See External links below).

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Tetrapulmonata

View on Grokipedia
from Grokipedia
Tetrapulmonata is a monophyletic within the arachnids (subphylum ), comprising four extant orders: Araneae (spiders), Amblypygi (), Uropygi (), and Schizomida (). Named for the two pairs of book lungs (four book lungs total) characteristic of their ground pattern—a stacked, leaf-like respiratory organ enabling efficient oxygen uptake in air—this represents a key evolutionary adaptation to terrestrial life among arthropods. While schizomids and some derived spiders retain fewer pairs (one or two), the ancestral configuration underscores their shared pulmonary homology. Tetrapulmonates exhibit remarkable morphological and ecological diversity, with spiders dominating the group's at over 52,000 described species worldwide (as of November 2025), far exceeding the hundreds in each of the other orders—approximately 260 in , 350 in , and 120 in . Most non-spider tetrapulmonates are tropical or subtropical nocturnal predators, featuring pedipalps for prey capture, elongated first legs functioning as sensory whips, and no silk-producing spinnerets (except in spiders). They lack venomous fangs or stings, relying instead on mechanical subduing, and many display complex social behaviors, such as vibration-based communication in amblypygids. Phylogenetically, Tetrapulmonata forms part of the larger Arachnopulmonata alongside scorpions, with molecular and morphological evidence supporting the divergence of Tetrapulmonata from scorpions within Arachnopulmonata around 400 million years ago during the period, and Arachnopulmonata itself diverging from other arachnids earlier, around 450–500 million years ago. records, including early whip spider-like forms from the , reveal a rich evolutionary history marked by ancient terrestrialization and adaptive radiations, though non-spider lineages remain relatively depauperate compared to the explosive diversification of spiders. This clade highlights the evolutionary success of pulmonate respiration in shaping arachnid and .

Taxonomy and Etymology

Definition

Tetrapulmonata is a non-ranked supra-ordinal within the class Arachnida, first proposed by Shultz in 1990 through a cladistic analysis of morphological characters across euchelicerate genera. This unites the orders Araneae (spiders), (whip spiders), (short-tailed whip scorpions), and (whip scorpions), which share derived morphological features distinguishing them from other arachnids. The name Tetrapulmonata derives from the Greek roots tetra- (four) and (lung-bearing), emphasizing the primitive condition of two pairs of book lungs—one pair on the second opisthosomal segment and another on the third—resulting in four total book lungs in the ground pattern of the . Although the posterior pair is often reduced or lost in derived lineages, this respiratory configuration serves as a key diagnostic trait. Defining synapomorphies of Tetrapulmonata include a reduced preoral chamber formed by anterior projections of the coxae, with a mediolateral articulation between the fixed and movable digits, and four pulmonary opercula covering the openings. These features support the of the group and reflect adaptations linked to terrestrial lifestyles. The exhibits substantial extant diversity, comprising approximately 54,320 across its four orders as of November 2025, dominated by the hyperdiverse Araneae with 53,545 described , alongside smaller numbers in (approximately 265 ), Schizomida (approximately 380 ), and (approximately 130 ).

Historical Classification

Early arachnid classifications in the 19th and early 20th centuries often grouped taxa based on respiratory structures, distinguishing those with book lungs—termed pulmonates—from those relying on tracheae or other systems, such as tracheates like . This distinction highlighted the evolutionary significance of book lungs as adaptations for terrestrial respiration, with pulmonates including scorpions, spiders, and certain pedipalp-like orders. A key milestone came in 1893 when Reginald Innes Pocock proposed an informal grouping of arachnids characterized by two pairs of book lungs, encompassing the orders Araneae (spiders), Amblypygi (whip spiders), Uropygi (whip scorpions), and Schizomida (short-tailed whip scorpions), based on shared morphological features including respiratory and appendage structures. Pocock's arrangement, published in the Annals and Magazine of Natural History, reflected a shift toward more systematic comparisons within Arachnida, foreshadowing modern phylogenetic hypotheses by emphasizing synapomorphies like book lung configuration. The concept was formalized in 1990 by Jeffrey W. Shultz, who established Tetrapulmonata as a monophyletic clade through a cladistic analysis of 28 morphological characters, including details of book lung anatomy, cheliceral structure, and opisthosomal segmentation, confirming the inclusion of Araneae, Amblypygi, Uropygi, and Schizomida. Shultz's work in Cladistics marked a transition from descriptive taxonomy to rigorous phylogenetic methods, building directly on earlier proposals like Pocock's while incorporating outgroup comparisons with other chelicerates. Throughout the 1990s and 2000s, debates persisted regarding the precise inclusion and internal relationships of and within Tetrapulmonata, with some morphological analyses questioning their or suggesting alternative placements due to reductive traits and convergent adaptations. These uncertainties were resolved in the by phylogenomic studies using extensive molecular datasets, which consistently supported Tetrapulmonata's with high statistical confidence, affirming the clade's composition and rejecting earlier dissenting views through analyses of hundreds of genes across diverse taxa. For instance, Sharma et al. (2014) and Ballesteros et al. (2022) demonstrated robust support for the group via transcriptomic data and advanced modeling, overcoming long-branch attraction artifacts. This historical progression paralleled a broader shift in arachnid taxonomy from Linnaean hierarchies—such as the outdated "Pedipalpi," a traditional order uniting , , and as sister to Araneae—to cladistic s emphasizing shared derived characters over artificial groupings.

Included Orders

Tetrapulmonata encompasses four extant orders: Araneae, , , and . These orders share membership in the , unified by morphological traits such as book lungs, though each exhibits distinct adaptations. The order Araneae, comprising spiders, includes 53,545 described species as of November 2025 and represents the vast majority of tetrapulmonate diversity. Spiders are characterized by their ability to produce silk from abdominal spinnerets, used for web-building, prey capture, and other functions, with Araneae positioned as the basal lineage within the clade despite high derivation in silk-related behaviors. Amblypygi, known as whip spiders or tailless whip scorpions, consists of approximately 265 species as of 2025. These nocturnal predators are primarily tropical and feature elongated, antenniform first legs modified for sensory exploration, covered in mechanoreceptors that aid in navigation and prey detection. Uropygi, or whip scorpions (also called vinegaroons), encompasses approximately 130 species. They are distinguished by a long, flagelliform extension on the abdomen's posterior end and possess defense glands that secrete acetic acid to deter predators. Schizomida, the short-tailed whip scorpions, includes approximately 380 species as of 2025. These soil- and litter-dwelling arachnids have robust, pedipalps for prey capture and a short, flagelliform opisthosoma, adapting them to subterranean habitats. Overall, Tetrapulmonata harbors more than 54,000 species as of November 2025, overwhelmingly dominated by Araneae, with the remaining orders contributing modest diversity. The clade also includes extinct stem-group taxa, such as the order Haptopoda, which shares early tetrapulmonate features like tactile legs but lacks modern derivations. ===== END CLEANED SECTION =====

Morphology and Anatomy

General Body Plan

Tetrapulmonata exhibit a typical body plan divided into two distinct tagmata: the anterior prosoma and the posterior opisthosoma, connected by a narrow articulation. The prosoma bears the , pedipalps, and four pairs of walking legs, which are used for locomotion and prey capture. The are two-segmented appendages located anteriorly on the prosoma, functioning primarily in feeding; in some taxa, such as certain spiders, they feature a rastellum—a row of strong spines—for manipulating prey. The pedipalps, positioned between the and walking legs, are elongated and primarily sensory in non-Araneae members like Amblypygi and Uropygi, aiding in exploration and prey detection, whereas in Araneae, they are often sexually dimorphic and modified for sperm transfer in males. The opisthosoma is segmented, typically comprising 12 somites in primitive forms, and houses the digestive, reproductive, and respiratory systems; ventrally, it bears two pairs of book lungs in basal taxa, though these are reduced or absent in derived groups such as Amblypygi. Members of Tetrapulmonata vary widely in size, with Schizomida reaching as small as 1 mm in body length, Uropygi up to 10 cm including the flagellum, and Araneae exhibiting leg spans up to 30 cm in large species like the Goliath birdeater.

Respiratory Structures

The primitive respiratory system of Tetrapulmonata features two pairs of book lungs, an anterior pair on the second abdominal segment and a posterior pair on the third, representing the defining characteristic of the clade. Each book lung consists of numerous thin, stacked lamellae filled with , forming a book-like structure that maximizes surface area for between air in the atrium and the circulatory fluid. These organs open externally via spiracles and are protected by opercula, which regulate airflow and prevent . Homology among book lungs in Tetrapulmonata is evidenced by conserved developmental pathways involving shared genes, such as those regulating lamellar formation, and ultrastructural similarities including pillar cells that support the lamellae and chitinous hairs that maintain air channels. These features indicate a single evolutionary origin from ancestral book gills during a terrestrialization event in the common stem lineage around 400–450 million years ago, in the Silurian-Devonian period. Diversity in respiratory structures has arisen through modifications across orders. In Araneae, the posterior pair is frequently reduced or lost, with many derived species relying on a single anterior pair supplemented by tracheae for enhanced oxygen delivery to tissues. and exhibit further simplification, lacking functional posterior book lungs while retaining the anterior pair for basic . In contrast, preserve the primitive condition with two functional pairs (four book lungs total), supporting their active, nocturnal lifestyles in moist microhabitats. Physiologically, book lungs enable efficient oxygen diffusion via across thin, moist lamellae, optimized for humid environments where prevents hemolymph dehydration and maintains high permeability. This adaptation supports metabolic demands in terrestrial settings with variable oxygen levels, though efficiency declines in arid conditions, influencing preferences across the .

Sensory and Locomotory Adaptations

Tetrapulmonates exhibit a range of sensory adaptations that reflect their diverse lifestyles, with vision generally reduced in non-araneid lineages compared to the more developed visual systems in spiders. In Araneae, the principal eyes (anterior median pair) provide high for hunting and , featuring everted retinas without a reflective tapetum, while the three pairs of secondary lateral eyes possess a tapetum layer that enhances low-light sensitivity through light reflection. In contrast, , , and typically retain eight eyes—comprising one median pair and three lateral pairs—but with reduced functionality; the lateral eyes often show simplified structures and limited resolution, emphasizing reliance on other sensory modalities over vision. Tactile and chemosensory capabilities are prominent in Tetrapulmonata, particularly through modifications to the appendages. In and , the first pair of legs is elongated into antenniform structures that function as primary sensory organs for chemotactile exploration, bearing dense arrays of chemoreceptors, mechanoreceptors, and contact chemosensilla to detect chemical cues, textures, and prey vibrations in dark or cluttered environments. These antenniform legs enable precise environmental sampling without locomotion involvement, distinguishing them from the walking legs. Additionally, trichobothria—fine, hair-like setae distributed across the legs and body—serve as sensitive detectors of airborne vibrations and air currents, aiding in prey localization and predator avoidance across all tetrapulmonate orders. Locomotory adaptations in Tetrapulmonata support their primarily nocturnal and terrestrial habits, with variations tied to sensory integration. Araneae are predominantly , utilizing all eight legs for rapid running and agile maneuvers during predation, often guided by visual and vibratory cues. In , , and , locomotion is ambulatory using six legs, as the antenniform first pair is reserved for sensing; Schizomida further adapt with elongated, forward-oriented pedipalps that assist in through narrow crevices and substrate probing, enhancing stability in confined spaces. These modifications integrate with sensory systems to facilitate efficient movement in low-visibility habitats. supplement locomotion-related defense with pygidial glands that secrete acetic acid (up to 84% concentration), triggered by tactile or vibratory stimuli to deter pursuers during evasion.

Phylogeny and Evolution

Phylogenetic Relationships

The of Tetrapulmonata, comprising the orders Araneae, , , and , is robustly supported by more than 20 morphological synapomorphies, including the primitive presence of two pairs of book lungs, specific modifications to the and pedipalps, and shared genital opercula structures. This was first formally proposed based on these anatomical features in a comprehensive morphological analysis of orders. Molecular evidence, including 18S rRNA sequences and phylogenomic datasets from nuclear and mitochondrial genes, consistently reinforces this across studies from 2014 to 2023. A 2024 molecular phylogeny of further supports the internal , while 2025 cytogenetic studies confirm shared chromosomal features such as holokinetic chromosomes across the . Within Tetrapulmonata, the internal positions Araneae as the to a clade formed by and the Pedipalpi ( + ), with and forming a monophyletic sister pair based on multi-locus molecular phylogenies. This arrangement reflects shared derivations in respiratory and locomotor adaptations, though some lineages exhibit secondary reductions in book lungs. , often used synonymously but more narrowly defined here to exclude certain derived forms with reduced pulmonary structures, emerges as a within this framework, highlighting evolutionary convergence in air-breathing mechanisms. In the broader context of Arachnida, Tetrapulmonata forms the core of Arachnopulmonata alongside Scorpiones as its sister group, a relationship established through phylogenomic analyses resolving earlier morphological debates on respiratory organ homologies. Initial uncertainties regarding the inclusion of Thelyphonida (the primary lineage within Uropygi) have been clarified by 2020s genomic datasets, confirming its placement within Tetrapulmonata and Arachnopulmonata without requiring reclassification. Recent karyotype analyses, incorporating chromosome mapping and fluorescence in situ hybridization of markers like 18S rDNA, further validate these relationships by identifying shared cytogenetic features such as holokinetic chromosomes across the clade.

Fossil Record

The fossil record of Tetrapulmonata is relatively sparse compared to that of other clades, with most discoveries dating from the period onward and preserving key morphological features such as book lungs and pedipalps. The clade's evolutionary history is illuminated by over 1,400 described fossil species across its included orders and stem groups, dominated by arachnids attributable to Araneae (over 1,400 species), with far fewer records for the pedipalpate lineages (approximately 35 species combined). The earliest confirmed tetrapulmonate fossils appear in the Late Carboniferous (Pennsylvanian, approximately 315–305 million years ago), including stem-group representatives that exhibit transitional features between modern orders. Idmonarachne brasieri, from the Stephanian deposits of Montceau-les-Mines in (ca. 305 Ma), is a notable example of a spider-like lacking spinnerets but possessing a similar , including and book lungs, positioning it as a basal member of the Tetrapulmonata stem. In the Measures (Westphalian, ca. 310 Ma), madeleyi represents the extinct order Haptopoda, characterized by four pairs of book lungs—a unique trait among —and robust, pedipalps adapted for prey capture, suggesting close affinities to the Uropygi-Schizomida lineage. Similarly, Graeophonus anglicus from the same British deposits exhibits elongated first legs and a flattened body, traits linking it to early , with tomographic reconstructions revealing well-preserved cheliceral structures indicative of predatory behavior. Permian records (ca. 299–252 Ma) are limited but include additional pedipalpate forms, such as fragmentary remains from European and North American coal deposits that show continuity in morphology and limb segmentation with taxa. discoveries, primarily from inclusions, bridge gaps in the pedipalpate and araneid lineages. Chimerarachne yingi from mid- Burmese amber (ca. 100 Ma) preserves silk-producing glands and a flagelliform spinneret-like structure alongside a whip-like , marking it as a stem-tetrapulmonate that retains primitive features while foreshadowing araneid silk use. Other amber specimens from the and further document Idmonarachne-like forms, emphasizing the persistence of transitional morphologies into the . Significant gaps persist in the tetrapulmonate fossil record, particularly for , which has only a handful of confirmed specimens—such as Graeophonus—despite potential Middle (ca. 390 Ma) cuticle fragments hinting at earlier origins. Taphonomic biases, including the poor preservation of delicate book lungs and structures in sedimentary deposits, likely contribute to these absences, as and lagerstätten provide the best evidence for internal .

Evolutionary Origins

The evolutionary origins of Tetrapulmonata trace back to the Silurian-Devonian transition, a pivotal period marking the shift from marine to terrestrial environments among early arachnids. During this interval, approximately 443–358 million years ago, ancestral arachnids adapted to land, with book lungs emerging as a key respiratory innovation derived from gill-like structures in a common aquatic . evidence from deposits, such as the Rhynie Cherts in (ca. 410 million years ago), reveals preserved book lungs in trigonotarbids, primitive relatives of Tetrapulmonata, confirming their early terrestrial adaptation for gas exchange in atmospheric oxygen. A defining innovation in Tetrapulmonata was the development of four book lungs—two pairs opening via genital opercula—enabling efficient oxygen uptake in low-oxygen terrestrial habitats. This quadrupulmonary condition likely arose in a common ancestor, distinguishing Tetrapulmonata from other pulmonate like scorpions, which possess only two. Following the Late Devonian extinction event around 350 million years ago, which disrupted marine ecosystems and facilitated terrestrial colonization, Tetrapulmonata underwent significant radiation, exploiting newly available habitats amid recovering vegetation and communities. Diversification within Tetrapulmonata accelerated in the , with Araneae (spiders) experiencing a major explosive radiation during the (ca. 252–201 million years ago), coinciding with the recovery from the Permian-Triassic mass extinction and the proliferation of insect prey. In contrast, the non-spider orders—Uropygi, , and —showed patterns of tropical specialization during the mid-Cretaceous (ca. 100–90 million years ago), aligning with the breakup of and the expansion of humid, forested environments that favored their nocturnal, predatory lifestyles. Recent embryological and molecular studies have reinforced the homology of book lungs across Tetrapulmonata, supporting a single evolutionary origin around 420 million years ago in the . Detailed analyses of developmental patterns in and whip scorpion embryos reveal conserved formation from opisthosomal limb buds, akin to ancestral gills, underscoring a unified terrestrialization event in the stem lineage.

Ecology and Diversity

Habitats and Distribution

Tetrapulmonata exhibit a broad range of habitat preferences and distributions, with the order Araneae (spiders) achieving a cosmopolitan presence across all continents except continental , including regions where species inhabit and polar ecosystems. In contrast, the non-spider orders— (whip spiders), (whip scorpions), and (short-tailed whip scorpions)—are predominantly confined to tropical and subtropical zones between approximately 40°N and 40°S latitudes, reflecting their sensitivity to cooler climates and reliance on warm, humid environments. While Araneae have diversified into nearly every terrestrial habitat through and human-mediated invasions, such as the widespread establishment of species like in urban and agricultural areas across multiple continents, the other orders remain largely restricted to equatorial and near-equatorial regions without such invasive expansions. Microhabitats within these tropical and subtropical ranges are typically moist and sheltered, supporting the respiratory demands of book lungs. favor leaf litter, layers, nests, and entrances, where constant high humidity prevents and facilitates foraging. commonly occupy bark crevices, walls, and debris in humid forests, using these refuges for predation and . prefer similar concealed spots, such as under logs, rotting wood, rocks, and in seasonally moist forest floors, often excavating shallow burrows to maintain moisture levels. Araneae, by comparison, exploit a wider array of microhabitats, including silk-based webs in foliage, orb structures in open areas, and ground burrows, enabling occupancy of diverse settings from deserts to high-altitude meadows. Biogeographically, the non-spider orders trace origins to the ancient supercontinent , with showing particularly strong ties through high diversity in and the , indicative of vicariance following continental breakup. A high proportion of described in and occur in the Neotropics and Indo-Malaya hotspots, underscoring these realms as centers of and diversification driven by humid tropical conditions. Araneae, while globally distributed, also concentrate high diversity in these same tropical regions but extend further via natural dispersal and invasions. The book lungs characteristic of Tetrapulmonata impose a strong dependence on high environmental to minimize respiratory loss, limiting non-spider orders to areas with adequate and rendering them vulnerable to . exacerbates this by fragmenting humid forest habitats, prompting observed range contractions and shifts toward remaining moist refugia in affected tropical landscapes. Sensory adaptations, such as elongated antenniform legs in non-spiders, further aid navigation through these dense, humid microhabitats.

Behavioral Traits

Tetrapulmonata exhibit a range of behavioral adaptations shaped by their predatory lifestyles and environmental pressures, with many displaying nocturnal activity patterns that align with their reliance on tactile and chemosensory cues for and . Across the , individuals are predominantly active at night, retreating to refuges such as crevices or burrows during the day to avoid diurnal predators, a strategy facilitated by their sensitive antenniform first legs in non-araneid groups and detection in Araneae. This temporal partitioning enhances survival while enabling opportunistic hunting of nocturnal prey. Predatory strategies in Tetrapulmonata vary by order but emphasize and tactile hunting over visual pursuit, leveraging specialized appendages for prey capture. In , species employ sit-and-wait tactics, using pedipalps to grasp , other arachnids, and occasionally small vertebrates like or hummingbirds, with some capturing aerial prey such as moths via elevated perches. , such as Mastigoproctus species, are nocturnal hunters that actively patrol substrates, employing large pedipalps to seize and crush small arthropods like crickets and isopods, often detecting vibrations through their flagelliform tails. demonstrate active predation, using elongated antenniform legs to explore and pedipalps to immobilize prey up to 75% of their body length, including springtails and mites, with juveniles targeting even larger relative prey sizes. In contrast, Araneae display diverse approaches, including web-based where orb-weavers detect vibrations transmitted through to ensnare flying , and active stalking by (Lycosidae) that pursue ground-dwelling prey using keen vision and speed. Reproductive behaviors in Tetrapulmonata highlight indirect sperm transfer in non-araneid orders via spermatophores, contrasting with the direct in spiders, often accompanied by elaborate to reduce sexual cannibalism risks. In , males deposit stalked spermatophores on substrates after antennal contact and leg-waving displays, with females subsequently picking them up; females then brood 10–90 eggs in a ventral sac and carry protonymphs dorsally for weeks, providing protection and transport. Uropygi reproduction involves prolonged lasting hours to days, where males use pedipalps to position females over deposited spermatophores, as observed in Mastigoproctus brasilianus with multiple depositions per mating; females attach 12–40 eggs to their ventral in a brood sac, guarding them in burrows without feeding for up to five weeks. Schizomida similarly use spermatophores with distinct sperm masses, with females exhibiting maternal care by carrying protonymphs on their backs, a behavior that supports juvenile survival during dispersal. Araneae feature complex rituals, such as vibratory signaling on webs or nuptial presentation in some species, followed by direct sperm transfer via the male's embolus-tipped ; many families, like theridiids, show extended maternal care, with females guarding sacs and sometimes feeding young. Defense mechanisms in Tetrapulmonata are diverse, focusing on chemical, behavioral, and structural deterrents to counter predation from vertebrates and conspecifics. deploy a potent spray of acetic and caprylic acids from pygidial glands, projecting up to 80 cm to irritate attackers like mammals or birds, with the mixture's wetting agents enhancing skin penetration without harming the emitter. In , individuals adopt defensive postures with raised antenniform legs and pedipalps, and some employ thanatosis—feigning death by immobility—to deter predators, alongside potential glandular secretions for territorial marking. rely on of long legs to escape grasps, combined with aggressive pedipalp displays and refuge territoriality to ward off intruders. Araneae utilize silk webs not only for capture but also as barriers or retreats, supplemented by injection, , and in some cases, deimatic displays like leg-waving to startle threats. While most Tetrapulmonata are solitary, with interactions limited to mating or territorial disputes, exceptions occur in social Araneae species, and limited gregariousness appears in some . Araneae include communal spiders like Anelosimus studiosus, where colonies cooperate in web construction, prey capture, and brood care, though often with high intraspecific aggression and skewed reproduction. In , species such as Phrynus marginemaculatus form kin-based groups in refuges, showing individual recognition via antennal contacts and reduced cannibalism, potentially conferring benefits like shared vigilance. and remain largely solitary, with agonistic encounters resolved through antennal fencing or avoidance, emphasizing the clade's general asocial nature despite these derived social traits in select lineages.

Conservation Status

The conservation status of Tetrapulmonata varies significantly across its constituent orders, with the vast majority of species remaining unevaluated by the International Union for Conservation of Nature (IUCN). In Araneae, the largest order within Tetrapulmonata comprising over 50,000 described species, most assessed taxa are classified as Least Concern due to their widespread distributions and adaptability, though endemic island species face heightened vulnerability from localized threats. Among the non-Araneae orders—, , and —fewer than 50 species have been formally assessed globally, with approximately 20 categorized as , Endangered, or Critically Endangered; for instance, only two species are listed as Vulnerable, while several exhibit Critically Endangered status in regional evaluations, and remain entirely unevaluated. This paucity of assessments underscores the overall status for these smaller orders, which include approximately 260 , 126 , and 380 species— the latter seeing recent increases due to new descriptions, particularly in the Neotropics—many of which are short-range endemics susceptible to extinction. Major threats to Tetrapulmonata diversity, particularly in the non-Araneae orders, stem from through tropical , which fragments leaf litter and soil microhabitats essential for these nocturnal predators. Climate change exacerbates risks by altering humidity levels in tropical forests, rendering species in and particularly vulnerable due to their dependence on moist environments. Additionally, collection for the international pet trade poses a targeted threat to , with at least 11 species detected in unregulated markets, potentially leading to of wild populations in regions like the and . Conservation efforts for Tetrapulmonata are limited but focused on protecting key habitats, such as national parks and reserves in the and , where ongoing deforestation monitoring indirectly benefits endemic and through broader arachnid-inclusive initiatives. However, significant research gaps persist, especially in , where taxonomic uncertainty and incomplete inventories have resulted in only about 10% of species being evaluated for IUCN status as of 2025, hindering targeted protections. hotspots, including the for (with over 50 endemic species in alone) and for (home to unique taxa like Charinus madagascariensis), highlight priorities for intensified surveys and habitat safeguards to prevent undetected declines.

References

  1. https://pmc.ncbi.nlm.nih.gov/articles/PMC8614469/
  2. http://assets.press.princeton.edu/chapters/s11293.pdf
  3. https://www.researchgate.net/publication/7384242_The_book_lungs_of_Scorpiones_and_Tetrapulmonata_Chelicerata_Arachnida_Evidence_for_homology_and_a_single_terrestrialisation_event_of_a_common_arachnid_ancestor
  4. https://wsc.nmbe.ch/statistics/
  5. https://pubmed.ncbi.nlm.nih.gov/18931924/
  6. https://bmcbiol.biomedcentral.com/articles/10.1186/s12915-017-0399-x
  7. https://www.researchgate.net/profile/Thomas-Hegna/publication/316346672_The_phylogeny_of_fossil_whip_spiders/links/58fea9070f7e9bcf654417e8/The-phylogeny-of-fossil-whip-spiders.pdf
  8. https://pubmed.ncbi.nlm.nih.gov/16386884/
  9. https://www.gbif.org/species/165843060
  10. https://www.european-arachnology.org/esa/wp-content/uploads/2015/08/009-016_Dunlop.pdf
  11. https://academic.oup.com/zoolinnean/article/150/2/221/2607396
  12. https://animalfact.com/tailless-whip-scorpions-amblypygi/
  13. https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/schizomida
  14. https://www.researchgate.net/figure/Grades-25-and-26-There-are-presently-126-living-species-of-whipscorpions-Uropygi-and_fig6_378037817
  15. https://www.britannica.com/animal/arachnid/Respiration
  16. https://link.springer.com/article/10.1007/s13127-021-00524-w
  17. https://www.biodiversitylibrary.org/item/88432#page/7/mode/1up
  18. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1096-0031.1990.tb00523.x
  19. https://pmc.ncbi.nlm.nih.gov/articles/PMC8845124/
  20. https://doi.org/10.1093/molbev/msac021
  21. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1096-3642.2007.00284.x
  22. https://pmc.ncbi.nlm.nih.gov/articles/PMC3563967/
  23. https://www.sciencedirect.com/science/article/abs/pii/B978012415919800001X
  24. https://repository.si.edu/bitstream/handle/10088/8114/CoddingtonSystStatusArachnidaNAmer90.pdf?sequence=1
  25. https://pubmed.ncbi.nlm.nih.gov/15813383/
  26. https://zookeys.pensoft.net/article/9337/
  27. https://mapress.com/zt/article/view/53811
  28. https://www.sciencedirect.com/science/article/abs/pii/S0944200605000796
  29. https://pmc.ncbi.nlm.nih.gov/articles/PMC10409265/
  30. https://www.americanarachnology.org/about-arachnids/arachnid-orders/thelyphonida/
  31. https://www.britannica.com/animal/spider-arachnid/Size-range
  32. https://pmc.ncbi.nlm.nih.gov/articles/PMC2429929/
  33. https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/amblypygi
  34. http://research.amnh.org/users/lorenzo/PDF/Kamenz.2008.Bul.Booklungs.pdf
  35. https://www.sciencedirect.com/science/article/pii/S0960982224008042
  36. https://www.biorxiv.org/content/10.1101/2020.04.28.067199v2.full-text
  37. https://pmc.ncbi.nlm.nih.gov/articles/PMC6299927/
  38. https://www.sciencedirect.com/science/article/abs/pii/S1467803919300210
  39. https://ojs.akademperiodyka.org.ua/index.php/Zoodiversity/article/view/521
  40. https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/trichobothria
  41. https://digitalcommons.unl.edu/cgi/viewcontent.cgi?article=1056&context=bioscihebets
  42. https://onlinelibrary.wiley.com/doi/full/10.1002/jmor.21260
  43. https://www.sciencedirect.com/science/article/abs/pii/S0022191099001304
  44. https://academic.oup.com/sysbio/article/73/3/495/7669116
  45. https://www.mdpi.com/2073-4425/16/2/207
  46. https://onlinelibrary.wiley.com/doi/10.1111/jbi.13076
  47. https://academic.oup.com/mbe/article/31/11/2963/2925668
  48. https://wsc.nmbe.ch/resources/fossils/Fossils23.5.pdf
  49. https://royalsocietypublishing.org/doi/10.1098/rspb.2016.0125
  50. https://www.cambridge.org/core/journals/earth-and-environmental-science-transactions-of-royal-society-of-edinburgh/article/redescription-of-the-carboniferous-arachnid-plesiosiro-madeleyi-pocock-1911-arachnida-haptopoda/DCEE767A0E10E4563ADDB3BA7BB06FEC
  51. https://www.cambridge.org/core/journals/earth-and-environmental-science-transactions-of-royal-society-of-edinburgh/article/affinities-of-the-carboniferous-whip-spider-graeophonus-anglicus-pocock-1911-arachnida-amblypygi/667AD606539C43C587242C7702657CAC
  52. https://www.nature.com/articles/s41559-017-0449-3
  53. https://bmcecolevol.biomedcentral.com/articles/10.1186/s12862-017-0931-1
  54. https://evolution-outreach.biomedcentral.com/articles/10.1007/s12052-011-0357-y
  55. https://pubmed.ncbi.nlm.nih.gov/25936921/
  56. https://royalsocietypublishing.org/doi/10.1098/rsbl.2007.0597
  57. https://pmc.ncbi.nlm.nih.gov/articles/PMC2890420/
  58. https://www.sciencedirect.com/science/article/pii/S0960982218304226
  59. https://www.researchgate.net/publication/319186286_First_global_molecular_phylogeny_and_biogeographical_analysis_of_two_arachnid_orders_Schizomida_and_Uropygi_supports_a_tropical_Pangean_origin_and_mid-Cretaceous_diversification
  60. https://arthropod-systematics.arphahub.com/article/31986/
  61. https://zookeys.pensoft.net/article/140810/
  62. https://www.americanarachnology.org/journal-joa/joa-all-articles/article/download/arac-30-02-357.pdf
  63. https://pubmed.ncbi.nlm.nih.gov/28028084/
  64. https://link.springer.com/article/10.1007/s10841-024-00565-4
  65. https://edis.ifas.ufl.edu/publication/IN890
  66. https://pmc.ncbi.nlm.nih.gov/articles/PMC3926130/
  67. https://bioone.org/journals/american-museum-novitates/volume-2023/issue-4000/4000.1/Systematic-Revision-of-the-Whip-Spider-Family-Paracharontidae-Arachnida/10.1206/4000.1.pdf
  68. https://www.sciencedirect.com/science/article/abs/pii/S0195667123002306
  69. https://www.biorxiv.org/content/10.1101/2024.03.01.582919v1.full.pdf
  70. https://pmc.ncbi.nlm.nih.gov/articles/PMC9120460/
Add your contribution
Related Hubs
User Avatar
No comments yet.