Trombidium grandissimum
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Chelicerata
Class: Arachnida
Order: Trombidiformes
Family: Trombidiidae
Genus: Trombidium
Species:
T. grandissimum
Binomial name
Trombidium grandissimum
L. Koch, 1867

Trombidium grandissimum, commonly known as the giant red velvet mite, is a species of mite in the genus Trombidium in the family Trombidiidae.[1] This common mite is endemic to northern and central India, especially in the central plateau, and it primarily inhabits arid regions.[1][2] T. grandissimum live on the ground and often hidden among soil, but is commonly seen during the rainy season or after recent rain events, and therefore (along with some other red velvet mite species) has the nickname of "rain bug".[2]

Description

Trombidium grandissimum is one of the largest species of red velvet mite, with adults typically being about 1.2 cm (0.5 in) long.[2][3]

It is bright red and has a soft cushioning skin covered with fine hairs. A study of another species, the spider mite Tetranychus urticae, showed that the red color was caused by carotene, which was beneficial for their hibernation.[4] T. grandissimum, belonging to the same order as spider mites, spend an extensive period of time in hibernation under the soil. This might be the reason why they also depend on red pigmentation, by which their haemolymph is usually coloured.[1]

Microscopy

The mites were observed under stereo microscope for the detailed classification and analysis of different parts of their body,[1] and structural samples were processed using ESEM and FESEM.[5]

The FESEM images of the front leg sensilla hairs and claws at the tip usually measured around 500μm. Stalked eyes pointed with white arrows measured around 1mm. White arrows magnified by ESEM were measured around 400μm. The red velvet skin is shown to be covered by sensitive hairs. The whole body hairs showing the branches and arrangement measured around 50μm in size.[1]

Behavior

Trombidium grandissimum appears to be diurnal and will move into light, rather than darkness, if given the choice.[2] They feed on tiny animal prey, like insects and their eggs.[2][6] In the larval stage, T. grandissimum attach themselves to insects, most commonly crickets, and suck their fluids; they may occasionally even suck fluids from adults of their own species.[7]

In their natural habitat, they were found to move on a horizontal plane. They seemed to be reluctant to climb up against the gravitational force which may be due to their bulky body size and shorter legs. They can easily wriggle their bodies through small openings and thus can easily get inside the burrows of ants and other insects to feed on their eggs. Males and females of Trombidiidae mites perform encircling dances, after which they pair for mating.[8] A dead mite was found to be surrounded by ants, suggesting that they are non-toxic to other species and their cannibalistic nature suggests the same.[1]

Relationship with humans

T. grandissimum feed on insects and other mites, including species that are regarded as pests.[3]

In their native range in India, they are gathered in large numbers when they emerged during rains. They are made into an oil, a type of traditional medicine that is said to be useful for a wide range of things, including immunity related diseases, paralysis and as an aphrodisiac. Research is being conduced to confirm or refute whether it has potential for therapeutic treatments.[7]

References

  1. 1 2 3 4 5 6 George, Lighty; Padmalatha, C.; Ranjitsingh, A. J. A.; Dhasarathan, P. (2010-12-20). "Antifungl Efficiency of Haemolymph and Aqueous Extraction of Red Velvet Mite, T. Grandissimum". International Journal of Biology. 3 (1). doi:10.5539/ijb.v3n1p111. ISSN 1916-968X.
  2. 1 2 3 4 5 De, Sayantan (2020). "Red velvet mite (Trombidium grandissimum) and its extreme strategies for survival" (PDF). Species. 21 (67). Retrieved 23 November 2022.
  3. 1 2 "Trombidium grandissimum "Giant Red Velvet Mite" - Facts". bioweb.uwlax.edu. Retrieved 2023-07-16.
  4. Bryon, Astrid; Kurlovs, Andre H.; Dermauw, Wannes; Greenhalgh, Robert; Riga, Maria; Grbić, Miodrag; Tirry, Luc; Osakabe, Masahiro; Vontas, John; Clark, Richard M.; Van Leeuwen, Thomas (2017-07-18). "Disruption of a horizontally transferred phytoene desaturase abolishes carotenoid accumulation and diapause in Tetranychus urticae". Proceedings of the National Academy of Sciences. 114 (29): E5871–E5880. Bibcode:2017PNAS..114E5871B. doi:10.1073/pnas.1706865114. ISSN 0027-8424. PMC 5530703. PMID 28674017.
  5. Dracopoulos, Vassileios; Danilatos, Gerasimos (January 2013). "ESEM modifications to LEO SUPRA 35 VP FESEM". Micron. 44: 238–245. doi:10.1016/j.micron.2012.06.014. PMID 22841156.
  6. Ruppert, Edward E. (2004). Invertebrate zoology : a functional evolutionary approach. Robert D. Barnes, Richard S. Fox (Seventh ed.). Delhi, India. ISBN 978-81-315-0104-7. OCLC 970002268.{{cite book}}: CS1 maint: location missing publisher (link)
  7. 1 2 "T. grandissimum: Little With Big Interactions". bioweb.uwlax.edu. Retrieved 2022-11-23.
  8. Moss, W. Wayne (December 1960). "Description and Mating Behaviour of Allothrombium lerouxi, new species, (Acarina: Trombidiidae), a Predator of Small Arthropods in Quebec Apple Orchards". The Canadian Entomologist. 92 (12): 898–905. doi:10.4039/Ent92898-12. ISSN 1918-3240. S2CID 84189306.
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