Thomisidae

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Thomisidae
Temporal range: Palaeogene–present
Crab Spider 6299.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Chelicerata
Class: Arachnida
Order: Araneae
Infraorder: Araneomorphae
Family: Thomisidae
Sundevall, 1833 [1]
Diversity [2]
171 genera, 2,167 species
Distribution.thomisidae.1.png
Crab spider feeding on a Junonia atlites butterfly in a Zinnia elegans flower Crab spider feeding Junonia atlites in Kadavoor.jpg
Crab spider feeding on a Junonia atlites butterfly in a Zinnia elegans flower

The Thomisidae are a family of spiders, including about 170 genera and over 2,100 species. The common name crab spider is often linked to species in this family, but is also applied loosely to many other families of spiders. Many members of this family are also known as flower spiders or flower crab spiders. [3]

Contents

Description

Members of this family of spiders do not spin webs, and are ambush predators. The two front legs are usually longer and more robust than the rest of the legs. The back two legs are smaller, and are usually covered in a series of strong spines. [4] They have dull colorations such as brown, grey, or very bright green, pink, white or yellow. They gain their name from the shape of their body, and they usually move sideways or backwards. [5] These spiders are quite easy to identify and can very rarely be confused with Sparassidae family, though the crab spiders are usually smaller.

Etymology

Spiders in this family are called "crab spiders" due to their resemblance to crabs, the way such spiders hold their two front pairs of legs, and their ability to scuttle sideways or backwards. [3] [6] The Thomisidae are the family most generally referred to as "crab spiders", though some members of the Sparassidae are called "giant crab spiders", the Selenopidae are called "wall crab spiders", and various members of the Sicariidae are sometimes called "six-eyed crab spiders". [7] Some distantly related orb-weaver spider species such as Gasteracantha cancriformis also are sometimes called "crab spiders".

Behavior

Crab spider waiting in ambush, Behbahan, Iran Thomisus Onustus in Behbahan, Iran.jpg
Crab spider waiting in ambush, Behbahan, Iran
Crab spider on Queen Ann’s lace

Thomisidae do not build webs to trap prey, though all of them produce silk for drop lines and sundry reproductive purposes; some are wandering hunters and the most widely known are ambush predators. Some species sit on or beside flowers or fruit, where they grab visiting insects. Individuals of some species, such as Misumena vatia and Thomisus spectabilis , are able to change color over a period of some days, to match the flower on which they are sitting. Some species frequent promising positions among leaves or bark, where they await prey, and some of them sit in the open, where they are startlingly good mimics of bird droppings. However, these members of the family Thomisidae are not to be confused with the spiders that generally are called bird-dropping spiders, not all of which are close relatives of crab spiders.

Other species of crab spiders with flattened bodies either hunt in the crevices of tree trunks or under loose bark, or shelter under such crevices by day, and come out at night to hunt. Members of the genus Xysticus hunt in the leaf litter on the ground. In each case, crab spiders use their powerful front legs to grab and hold on to prey while paralysing it with a venomous bite.

The spider family Aphantochilidae was incorporated into the Thomisidae in the late 1980s. Aphantochilus species mimic Cephalotes ants, on which they prey.

The spiders of Thomisidae are not known to be harmful to humans. However, spiders of a distantly related genus, Sicarius , which are sometimes referred to as "crab spiders", or "six-eyed crab spiders", are close cousins to the recluse spiders, and are highly venomous, though human bites are rare.

Sexual dimorphism

Several different types of sexual dimorphism have been recorded in crab spiders. Some species exhibit color dimorphisms; [8] however, the most apparent dimorphism is the difference in size between males and females. In some species, this is relatively small; females of Misumena vatia are roughly twice the size of their male counterparts. [9] In other cases, the difference is extreme; on average, female Thomisus onustus are more than 60 times as massive as the males. [10]

Several hypothesized explanations are given for the evolution of sexual size dimorphisms in the Thomisidae and other sister taxa. [11] The most widely acknowledged hypothesis for female growth is the fecundity hypothesis: [12] selection favors larger females so they can produce more eggs and healthier offspring. Because males do not carry and lay eggs, a growth in size does not confer a fitness advantage. [13]

However, sexual size dimorphism may be a result of male dwarfism. The gravity hypothesis states that the smaller size allows the male to travel with greater ease, providing him with an increased opportunity to find mates. [14] Females are comparatively stationary, and their larger size allows them to capture larger prey, such as butterflies and bees, granting females the additional nutrients necessary for egg production. [10]

Other hypotheses propose that sexual size dimorphism evolved by chance, and no selective advantage exists to larger females or smaller males. [15]

Taxonomy

Misumena vatia female Misumena vatia female Luc Viatour 1.jpg
Misumena vatia female
Angaeus sp., Karnataka, India Angaeus sp.jpg
Angaeus sp., Karnataka, India
Ant-mimic Amyciaea sp., Karnataka, India Amyciaea sp..jpg
Ant-mimic Amyciaea sp., Karnataka, India
Phyrnarachne sp. mimicking bird-dropping, Karnataka, India Phyrnarachne sp.jpg
Phyrnarachne sp. mimicking bird-dropping, Karnataka, India
Camaricus sp., Goa, India Camaricus sp.jpg
Camaricus sp., Goa, India
Runcinia sp., Goa, India Runcinia sp.jpg
Runcinia sp., Goa, India

As of December 2021, this large family contains around 171 genera: [1]

See also

Related Research Articles

<span class="mw-page-title-main">Philodromidae</span> Family of spiders

Philodromidae, also known as philodromid crab spiders and running crab spiders, is a family of araneomorph spiders first described by Tord Tamerlan Teodor Thorell in 1870. It contains over 500 species in thirty genera.

<span class="mw-page-title-main">Orb-weaver spider</span> Family of spiders

Orb-weaver spiders are members of the spider family Araneidae. They are the most common group of builders of spiral wheel-shaped webs often found in gardens, fields, and forests. The English word "orb" can mean "circular", hence the English name of the group. Araneids have eight similar eyes, hairy or spiny legs, and no stridulating organs.

<i>Misumena</i> Genus of spiders

Misumena is a genus of crab spiders sometimes referred to as flower crab spiders. They are similar in appearance to several other genera in the family Thomisidae, such as Misumenoides and Mecaphesa.

<i>Misumenops</i> Genus of spiders

Misumenops is a common genus of crab spider with more than 50 described species.

<i>Misumenoides</i> Genus of spiders

Misumenoides is a genus of spiders in the family Thomisidae. Spiders in this family are commonly called "crab" or "flower" spiders.

<i>Xysticus</i> Genus of ground crab spiders

Xysticus is a genus of ground crab spiders described by C. L. Koch in 1835, belonging to the order Araneae, family Thomisidae. The genus name is derived from the Ancient Greek root xyst, meaning "scraped, scraper".

<i>Thanatus</i> Genus of spiders

Thanatus is a genus of false crab spiders described by Carl Ludwig Koch in 1837, belonging to the order Araneae, family Philodromidae.

<i>Micrathena</i> Genus of spiders

Micrathena, known as spiny orbweavers, is a genus of orb-weaver spiders first described by Carl Jakob Sundevall in 1833. Micrathena contains more than a hundred species, most of them Neotropical woodland-dwelling species. The name is derived from the Greek "micro", meaning "small", and the goddess Athena.

<i>Hogna</i> Genus of spiders

Hogna is a genus of wolf spiders with more than 200 described species. It is found on all continents except Antarctica.

<i>Tmarus</i> Genus of spiders

Tmarus is a genus of crab spiders, comprising 227 species:

<i>Tetragnatha</i> Genus of spiders

Tetragnatha is a genus of long-jawed orb-weavers found all over the world. It was first described by Pierre André Latreille in 1804, and it contains hundreds of species. Most occur in the tropics and subtropics, and many can run over water. They are commonly called stretch spiders in reference to their elongated body form and their ability to hide on blades of grass or similar elongated substrates by stretching their front legs forward and the others behind them. The name Tetragnatha is derived from Greek, tetra- a numerical prefix referring to four and gnatha meaning "jaw". Evolution to cursorial behavior occurred long ago in a few different species, the most studied being those found on the Hawaiian islands. One of the biggest and most common species is T. extensa, which has a holarctic distribution. It can be found near lakes, river banks or swamps. Large numbers of individuals can often be found in reeds, tall grass, and around minor trees and shrubs.

<i>Thomisus</i> Genus of spiders

Thomisus is a genus of crab spiders with around 142 species described. The genus includes species that vary widely in their ecology, with some that are ambush predators that feed on insects visiting flowers. Like several other genera in the family Thomisidae, they are sometimes referred to as flower crab spiders, from their crab-like motion and their way of holding their front legs, reminiscent of a crab spreading its claws as a threat.

<i>Euryopis</i> Genus of spiders

Euryopis is a genus of comb-footed spiders that was first described by Anton Menge in 1868.

<i>Synema</i> (spider) Genus of spiders

Synema is a genus of spider in the family Thomisidae, found in most parts of the world.

<span class="mw-page-title-main">Misumenini</span> Tribe of spiders

Misumenini is a tribe of spiders in the family Thomisidae.

References

  1. 1 2 "Family: Thomisidae Sundevall, 1833". World Spider Catalog. Natural History Museum Bern. Retrieved 4 December 2021.
  2. ↑ "Currently valid spider genera and species". World Spider Catalog. Natural History Museum Bern. Retrieved 4 December 2021.
  3. 1 2 Whyte, Robert; Anderson, Greg (2017). A field guide to spiders of Australia. Csiro Publishing. ISBN   9780643107083.
  4. ↑ "Thomisidae - General Information". www.arc.agric.za. Retrieved 2022-09-17.
  5. ↑ "crab spider | arachnid | Britannica". www.britannica.com. Retrieved 2022-09-17.
  6. ↑ Bradley, Richard A. (2012). Common Spiders of North America. University of California Press. ISBN   9780520954502.
  7. ↑ Filmer, Martin (1997). Southern African Spiders. City: BHB International / Struik. ISBN   1-86825-188-8.
  8. ↑ "BioKIDS - Kids' Inquiry of Diverse Species, Thomisidae: INFORMATION". www.biokids.umich.edu. Retrieved 2022-01-06.
  9. ↑ "Flower (a.k.a. Goldenrod) Crab Spider (Misumena vatia)". Woodland Park Zoo. Retrieved 2015-10-30.
  10. 1 2 Corcobado, G.; Rodríguez-Gironés, M.A.; De Mas, E. & Moya-Laraño, J. (2010). "Introducing the refined gravity hypothesis of extreme sexual size dimorphism". BMC Evolutionary Biology. 10: 236. doi: 10.1186/1471-2148-10-236 . PMC   2924870 . PMID   20682029.
  11. ↑ Hormiga, G; Scharff, N; Coddington, J.A. (2000). "The Phylogenetic Basis of Sexual Size Dimorphism in Orb-Weaving Spiders (Araneae, Obiculariae)". Systematic Biology. 49 (3): 435–462. doi: 10.1080/10635159950127330 . PMID   12116421.
  12. ↑ Head, G (1995). "Selection on Fecundity and Variation in the Degree of Sexual Size Dimorphism Among Spider Species (Class Araneae)". Evolution. 49 (4): 776–781. doi:10.2307/2410330. JSTOR   2410330. PMID   28565139.
  13. ↑ Head, G. (1995). "Selection on Fecundity and Variation in the Degree of Sexual Size Dimorphism Among Spider Species (Class Araneae)". Evolution. 49 (4): 776–781. doi:10.2307/2410330. JSTOR   2410330. PMID   28565139.
  14. ↑ Corcobado, G.; Rodríguez-Gironés, M.A.; De Mas, E.; Moya-Laraño, J. (2010). "Introducing the refined gravity hypothesis of extreme sexual size dimorphism". BMC Evolutionary Biology. 10: 236. doi: 10.1186/1471-2148-10-236 . PMC   2924870 . PMID   20682029.
  15. ↑ Prenter, J.; Elwood, R.W. & Montgomery, W.I. (1998). "No Association between Sexual Size Dimorphism and Life Histories in Spiders". Proceedings of the Royal Society of London B: Biological Sciences. 265 (1390): 57–62. doi:10.1098/rspb.1998.0264. PMC   1688762 .
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