1 Araneae |
All spiders |
Cosmopolitan; cheliceral venom glands, ability to produce silk from abdominal silk glands; male pedipalps modified for sperm transfer |
2 Mesothelae |
Plesiomorphic sister group to all living spiders |
SE Asia; mid ventrally positioned spinnerets; distinct dorsal abdominal tergites, very narrow sternum |
3 Opisthothelae |
The two major spider lineages |
Typical terminal spinneret placement and sternal morphology |
4 Mygalomorphae |
Trapdoor, baboon and funnel spiders, tarantulas, and their kin |
Paraxial chelicerae with venom glands; most lead sedentary lives in burrows; lack anterior median spinnerets; often large and hirsute; two pairs of book lungs |
5 Atypoidina |
Sister group to remaining mygalomorphs |
Most species with vestigial abdominal tergites and unique modifications to male pedipalp |
6 Avicularoidea |
All remaining mygalomorph taxa |
Includes major mygalomorph families, nearly half of which are likely not monophyletic |
7 Theraphosoidina |
Comprises families Theraphosidae and Barychelidae |
Includes the typically large and hirsute tarantulas and baboon spiders |
8 Araneomorphae |
Over 90% of all spider diversity |
Anterior median spinnerets fused to form a cribellum (later lost multiple times) |
9 Paleocribellatae |
Comprises single family Hypochilidae; hypothesized sister group to all other araneomorphs |
Hypochilid synapomorphies, e.g., cheliceral depression; also retain a number of primitive traits including two pairs of booklungs |
Neocribellatae |
Remaining spider lineages |
Paracribellum (complimentary spinning field to cribellum); extension of venom gland into prosoma |
Austrochiloidea |
Families Austrochilidae and Gradungulidae; sister group to all other neocribellate lineages |
Gondwanan taxa with notched tarsal organs; typically with two pairs of booklungs–posterior pair modified as tracheae in some taxa |
10 Haplogynae |
Neocribellate lineage with simple genitalia; includes spitting spiders and cellar spiders |
Spinnerets lack tartipores; mating with palps inserted simultaneously; in some taxa female genital opening lacks an epigynum; chelicerae fused at base, synspermia, male palpal organ simple |
11 Entelegynae |
Comprises all remaining spider lineages with complex genitalia |
Female genitalia with a flow through system of separate copulatory and fertilization ducts; male palpal organ typically under hydraulic control |
Palpimanoidea |
Comprises a number of enigmatic families |
Araneophages with lateral scopulae on anterior legs |
Eresoidea |
Includes 3 families: Eresidae, Hersiliidae, Oecobiidae; sister to remaining entelegynes |
Controversial superfamily; oecobiids and hersiliids share a unique attack behavior |
Orbiculariae |
Comprises the Deinopoidea and Araneoidea |
Members of this lineage include cribellate and ecribellate orb-web weavers as well as derived araneoids that use adhesive threads to construct sheet and cob-webs |
Deinopoidea |
Includes the cribellate orbicularian families Uloboridae and Deinopidae |
Construct cribellate orb web; long considered sister group to adhesive orb web weavers on basis of behavioral web construction data |
12 Araneoidea |
Spider superfamily that includes adhesive orb web weaving taxa and others |
Members of this lineage all use adhesive threads; monophyly supported by a number of spinning and other morphological characteristics |
13 RTA |
Large diverse lineage of spiders that includes wolf, jumping, running, fishing, and crab spiders |
Defined primarily by the presence of a projection on the male palp–the retrolateral tibial apophysis (RTA) |
14 Dionycha |
Subclade of the RTA lineage, comprises about 1/3 of all spider diversity |
Defined as a group based on their two clawed condition with flanking tufts of setae for adhesion to smooth surfaces |
Lycosoidea |
Large superfamily comprising 10 families including fishing and wolf spiders |
Monophyly of this superfamily is based on a number of morphological features (not universal) including a grate-shaped tapetum, an oval-shaped calamistrum, and male palpal features |