Tag Archives: flies

Friday Fellow: Damaging Black Fly

by Piter Kehoma Boll

If you live in tropical and subtropical areas, or even in forested temperate areas, you may have had the “opportunity” to meet a black fly. Those annoying little dipterans sneak toward you and bite you without you even noticing. After they fly away they let a small round red mark on your skin that will itch like hell in the next hours or days. But this is the least comparing to all the damage those annoying flies can cause.

And talking about damage, we will focus on a black fly named Simulium damnosum. It does not have a specific popular name, but I decided to call it the damaging black fly.

A damaging black fly on human skin. Credits to Otis Historical Archives of “National Museum of Health & Medicine”**.

The damaging black fly is very similar to other black flies and it is very hard to differentiate them morphologically. Thus, the name Simulium damnosum is often used in the sense of what is identified as the Simulium damnosum complex, a group of very similar species that can only be differentiated through genetic and cytological aspects. Thus, this article will focus mostly on the complex and not the species Simulium damnosum specifically. They are, afterall, basically identical in all relevant aspects, including their ecology.

Adult damaging black flies measure less than 5 mm in length and have a black chubby body. Females feed on both nectar and mammal blood, while males feed only on nectar. The damaging black fly is found in Subsaharian Africa, especially near rivers. Females lay their eggs in well-oxygenated running water, which larvae need to survive. They are very sensitive to pollution and larvae need immersed substrates, such as rocks or vegetation, to which they anchor themselves using small hooks. Females can lay up to 250 eggs per day and they hatch between 36 and 48 hours after laying.

The life cycle is very fast. The larvae feed on floating organic particles and under favorable conditions turn into pupae after about 8 to 10 days. The pupae remains encased in a coccoon, attached to the substrate and does not move. About three days later the adults emerge from the pupae and move toward the surface, taking flight as soon as they leave the water. The adults mate a few hours after emerging from water, but females continue alive for several days, laying hundred, thousands of eggs, and feeding on mammal blood daily.

Pupae and larvae of a species of black fly (probably not S. damnosum) in South Africa. Photo by Rob Palmer.*

As a blood-sucking insect, the damaging black fly is the vector of one of the most serious tropical diseases, onchocerciasis or river blindess. This disease is caused by a nematode that spends part of their life cycle in mammals and part in the flies. Onchocerciasis leads to several debilitating symptoms in humans, especially skin problems and glaucoma, which can cause blindness. It is, in fact, the second most common cause of blindness worldwide, making around 250 thousand people become blind every year.

Since damaing black flies cause such a serious disease to humans and since they live near water courses, such areas are almost uninhabitable in many regions of Subsaharan Africa. However, these areas are the most suitable for agriculture, which causes serious economical problems.

Until now, most attempts to reduce the number of black flies have been unsuccessful. The most effective method until now is the use of inseticides but, as you may guess, this does not only kill the black flies, but many other beneficial insects as well and, as soon as an area is free of black flies, it is colonized again by populations for the surrounding areas. Other alternative to reduce the ability of black flies to reproduce is to build dams that will reduce water flow in rivers, turning the water unsuitable for the larvae, but this, of course, can lead to an even worse ecological disaster.

While the countries affected by the disease lack resources to promote research on the subject, the rich countries couldn’t care less about the human population of such places, as we all know. This is a problem that, in a capitalist world, will hardly find a quick and effective solution.

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References:

Jacob, B. G., Novak, R. J., Toe, L. D., Sanfo, M., Griffith, D. A., Lakwo, T. L., … & Unnasch, T. R. (2013). Validation of a remote sensing model to identify Simulium damnosum sl breeding sites in sub-Saharan Africa. PLoS Negl Trop Dis7(7), e2342.]

Le Berre, R. (1974). Simulium damnosum. In Control of Arthropods of Medical and Veterinary Importance (pp. 55-63). Springer, Boston, MA.

Post, R. J., Onyenwe, E., Somiari, S. A. E., Mafuyai, H. B., Crainey, J. L., & Ubachukwu, P. O. (2011). A guide to the Simulium damnosum complex (Diptera: Simuliidae) in Nigeria, with a cytotaxonomic key for the identification of the sibling species. Annals of Tropical Medicine & Parasitology105(4), 277-297.

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*Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

**Creative Commons License This work is licensed under a Creative Commons Attribution-Share Alike 2.0 Generic License.

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Friday Fellow: Hippo Fly

by Piter Kehoma Boll

If you ever lived in the countryside or visited the country side often, you may be aware of the existence of an annoying group of flies that bite humans and other animals, the so-called horseflies that make up the family Tabanidae. Today’s fellow is a member of this family and is known scientifically as Tabanus biguttatus and commonly as the hippo fly.

This species is found throughout Africa and some areas of Middle East, being, apparently, much more common in eastern and southeastern Africa. As with all tabanid flies, the hippo fly has an aquatic to semiaquatic larva that lives in muddy areas. They are ferocious predators and prey on other animals living in the same habitat, such as larvae of crane flies, and can also feed on dead animals. When the larvae are about the pupate, they construct a mud cylinder, cover it with a circular lid with only a small hole to allow them to breathe, and remain there until they turn into adults. This is, apparently, a strategy to avoid desiccation.

Male hippo fly in South Africa. Photo by Ryan Tippett.*

Adult hippo flies measure about 2 cm in length, being relatively large tabanids, and show a considerable sexual dimorphism. As all tabanids, males are smaller but have larger compound eyes than females. The eyes of the males are so large that they touch each other, covering the whole top of the head. Females, on the other hand, have smaller eyes with a considerable space between them. The body of both males and females is predominantly black. Males have two white triangular spots on the abdomen while females have the thorax covered with white to golden hair with a small heart-shaped black spot in the middle.

Female hippo fly in South Africa. Photo by iNaturalist user bgwright.*

Male adult hippo flies are harmless and feed only on nectar. Females, on the other hand, need mammal blood to obtain enough protein for egg development. They attack many large mammal species, including humans, cattle and even dogs, but they have a strong preference for hippos, hence the common name.

Two female hippo flies feeding on a southern warthog (Phacocerus africanus spp. sundevallii). Photo by iNaturalist user happyasacupake.*

Hippo flies, like all tabanids, are diurnal flies and love sunny places. They avoid shaded areas, so animals in open areas are much more vulnerable. To get blood, a female approach animals and cut their skin with her sharp mouthparts, making them bleed and licking up the blood. This bite is very painful, which you may know if you have ever been bitten by a horsefly. If undisturbed, the fly can remain up to three minutes drinking blood.

Closeup of the two flies on the warthog’s back. Photo by iNaturalist user happyasacupake.*

The blood-drinking activity of female hippo flies, and of tabanids in general, make them likely mechanical vectors of some parasites, including species of the flagellate genus Tripanossoma, as well as Bacillus anthracis, the bacteria that causes anthrax, which is a considerably common disease in hippos.

Hippo flies are such a nuisance for hippos that their behavior is heavily affected by the flies’ presence, much more than by the presence of any large predator. Most of the time, hippos remain in the water solely to get rid of these annoying insects.

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More Dipterans:

Friday Fellow: Housefly (on 12 October 2012)

Friday Fellow: Cute Bee Fly (on 29 July 2016)

Friday Fellow: Bathroom Moth Midge (on 5 April 2019)

Friday Fellow: Blue Paddled Mosquito (on 27 September 2019)

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References:

Callan EM (1980) Larval feeding habits of Tabanus biguttatus and Amanella emergens in South Africa (Diptera: Tabanidae). Revue de Zoologie Africaine 94(4): 791-794.

Tinley KL (2009) Some observations on certain tabanid flies in North-Eastern Zululand (Diptera: Tabanidae). Proceedings of the Royal Entomological Society of London. Series A, General Entomology, 39(4-6), 73–75. doi: 10.1111/j.1365-3032.1964.tb00789.x

Tremlett JG (2009) Mud cylinders formed by larvae of Tabanus biguttatus Wied. (Diptera: Tabanidae) in Kenya. Proceedings of the Royal Entomological Society of London. Series A, General Entomology, 39(1-3), 23–24. doi: 10.1111/j.1365-3032.1964.tb00779.x

Wiesenhütter E (1975) Research into the relative importance of Tabanidae (Diptera) in mechanical disease transmission. Journal of Natural History, 9(4), 385–392. doi: 10.1080/00222937500770281 

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Friday Fellow: Bathroom Moth Midge

by Piter Kehoma Boll

No matter where you live, you probably have seen, at least once in your life, these little insects that love bathroom walls. They belong to the species Clogmia albipunctata, popularly known as bathroom moth midge, drain fly and other names.

A bathroom moth midge in Curitiba, Brazil. Photo by Evandro Maia.*

The bathroom moth midge and is found all around the world, being more common in tropical areas, but is also found frequently in temperate zones. They are often associated with humans and are found in bathrooms and, to a less extent, in kitchens. In warmer areas, they may also be seen in the wild, especially near small water ponds with plenty of organic matter, such as water stored in holes of dead trees.

Bathroom moth midge in Matara, Sri Lanka. Photo by iNaturalist user rvp.*

It is very easy to recognize the bathroom moth midge. They are gray and small, with a length of about 5 mm, and have two relatively large wings that make them look like an inverted heart shape. The body and the wings are covered with a thick grayish hair, which makes them look like moths. They are, however, part of the order Diptera and thus closely related to mosquitos and flies. With a close inspection, it is possible to notice some very small white spots on the wings. The antennae are long and each segment has a separate whorl of hair.

The larvae of the bathroom moth midge are aquatic and feed on organic decaying matter. They find the ideal habitat in the drains of bathrooms, in which there is enough organic matter and humidity and a good protection against predators, as well as a good stability in temperature. The larva passes through four instars during a period of about 18 days and then changes into the pupa, which takes about 5 days to turn into an adult. The adults do not eat and their main function is reproduction. The complete life cycle takes about a month.

Life cycle of the bathroom moth midge. Credits to Jiménez-Guri et al. (2014).**

The bathroom moth midge is mostly harmless and can even be useful by reducing the accumulation of organic matter that could clog drainage systems. There are a few reports of urinary myiasis, i.e., parasitism by fly larvae in the urinary tract, caused by this species, but they are associated with environments with poor sanitary conditions and very poor personal hygiene. The main concern with this species occurs in hospitals, as its presence in hospital bathrooms makes it a possible vector of pathogenic bacteria carried from the drainage system to the patients.

During the past years, the bathroom moth midge has been studied as a model for embryonic development and gene expression, especially for comparative studies with the well-known fruit fly model, Drosophila melanogaster.

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References:

El-Dib NA, Wahab WMAE, Hamdy DA, Ali MI (2017) Case Report of Human Urinary Myiasis Caused by Clogmia albipunctata (Diptera: Psychodidae) with Morphological Description of Larva and Pupa. Journal of Arthropod-Borne Diseases 11(4): 533–538.

Faulde M, Spiesberger M (2012) Hospital infestations by the moth fly, Clogmia albipunctata (Diptera: Psychodinae), in Germany. Journal of Hospital Infection 81(2): 134–136. doi: 10.1016/j.jhin.2012.04.006

Faulde M, Spiesberger M (2013) Role of the moth fly Clogmia albipunctata (Diptera: Psychodinae) as a mechanical vector of bacterial pathogens in German hospitals. Journal of Hospital Infection 83(1): 51–60. doi: 10.1016/j.jhin.2012.09.019

Jiménez-Guri E, Wolton KR, Gavilán B, Jaeger J (2014) A staging schefor the development of the moth midge Clogmia albipunctata. PLoS One 9(1): e84422. doi: 10.1371/journal.pone.0084422

Oboňa J, Ježek J (2012) Range expansion of the invasive moth midge Clogmia albipunctata (Williston, 1893) in Slovakia (Diptera: Psychodidae). Folia faunistica Slovaca 17(4): 387–391.

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*Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

**Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 International License.

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New Species: September 11 to 20

by Piter Kehoma Boll

Here is a list of species described from September 11 to September 20. It certainly does not include all described species. Most information comes from the journals Mycokeys, Phytokeys, Zookeys, Phytotaxa, Zootaxa, International Journal of Systematic and Evolutionary Microbiology, and Systematic and Applied Microbiology, as well as journals restricted to certain taxa.

petrolisthes-paulayi

Petrolisthes paulayi is a new crab described in the past 10 days.

SARs

Plants

Amoebozoans

Fungi

Sponges

Cnidaria

Flatworms

Annelids

Nematodes

Arachnids

Myriapods

Crustaceans

Hexapods

Cartilaginous fishes

Ray-finned fishes

Lissamphibians

Reptiles

Mammals

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New Species: July 11 to July 20

by Piter Kehoma Boll

Here is a list of species described from July 11 to July 20. It certainly does not include all described species. Most information comes from the journals Mycokeys, Phytokeys, Zookeys, Phytotaxa, Zootaxa, International Journal of Systematic and Evolutionary Microbiology, and Systematic and Applied Microbiology, as well as journals restricted to certain taxa.

Pseudoechthistatus sinicus(top) and P. pufujiae are two of the more than 40 new species of beetles described in the last 10 days.

Pseudoechthistatus sinicus (top) and P. pufujiae (bottom) are two of the 40 new species of beetles described in the last 10 days.

Archaea

Bacteria

SARs

Plants

Excavates

Fungi

Sponges

Flatworms

Annelids

Mollusks

Roundworms

Arachnids

Myriapods

Crustaceans

Hexapods

Cartilaginous fishes

Ray-finned fishes

Reptiles

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The history of Systematics: Animals in Systema Naturae, 1758 (part 3)

by Piter Kehoma Boll

This is the third part of this series of posts. See here part 1part 2 and part 4.

In this post I’ll present a single class: Insecta. At that time, however, Insecta included not only what we call insects today, but all arthropods.

5. Insecta (Insects)

Heart with one ventricle and one auricle; cold pus.
Spiracles: pores at the sides of the body.
Jaws lateral.
Penises entering.
Senses: tongue, eyes, antennae in head without brain (no ears and nostrils).
Covering: armored sustaining bony skin.
Support: feet, in some wings.

Insects were classified according to the number and aspect of the wings and included 7 orders: Coleoptera, Hemiptera, Lepidoptera, Neuroptera, Hymenoptera, Diptera, and Aptera.

5.1 Coleoptera (case wings), with four wings, the forewings fully hardened: Scarabeus (scarab beetles), Dermestes (larder beetles), Hister (clown beetles), Attelabus (leaf-rolling weevils), Curculio (true weevils), Silpha (carrion beetles), Coccinella (ladybugs), Cassida (tortoise beetles), Chrysomela (leaf beetles), Meloe (blister beetles), Tenebrio (darkling beetles), Mordella (tumbling flower beetles), Staphylinus (rove beetles), Cerambyx (longhorn beetles), Leptura (flower longhorn beetles), Cantharis (soldier beetles, glowworms), Elater (click beetles), Cicindela (tiger beetles), Buprestis (jewel beetles), Dytiscus (diving beetles), Carabus (ground beetles), Necydalis (wasp beetles), Forficula (earwigs), Blatta (cockroaches), Gryllus (crickets, locusts, grasshoppers, mantises, stick bugs).

1758Linnaeus_coleoptera

Species grouped by Linnaeus under Coleoptera (from left to right, top to bottom): sacred scarab (Scarabaeus sacer), larder beetle (Dermestes lardarius), four-spotted clown beetle (Hister quadrimaculatus), hazel-leaf roller weevil (Attelabus coryli, currently Apoderus coryli), nut weevil (Curculio nucum), dark carrion beetle (Silpha obscura), seven-spotted ladybug (Coccinella septempunctata), green tortoise beetle (Cassida viridis), red poplar leaf beetle (Chrysomela populi), black blister beetle (Meloe proscarabaeus), mealworm beetle (Tenebrio molitor), pointed tumbling flower beetle (Mordella aculeata), red-winged rove beetle (Staphylinus erythropterus), great capricorn beetle (Cerambyx cerdo), banded flower longhorn beetle (Leptura quadrifasciata), dull soldier beetle (Cantharis fusca), red click beetle (Elater ferrugineus), green tiger beetle (Cicindela campestris), eight-spotted jewel beetle (Buprestis octoguttata), broad diving beetle (Dytiscus latissimus), hard ground beetle (Carabus coriaceus), greater wasp beetle (Necydalis major), European earwig (Forficula auricularia), common cockroach (Blatta orientalis), and common field cricket (Gryllus campestris). Credits to Wikimedia user Sarefo (scarab), Guttorm Flatabø (larder beetle), Didier Descouens (clown beetle, tumbling flower beetle), entomart [www.entomart.be] (weevils, tortoise beetle), Dominik Stodulski (ladybug), Wikimedia user Quartl (leaf beetle, flower longhorn beetle), Václav Hanzlík (rove beetle), Franz Xaver (capricorn beetle), James K. Lindsey (soldier beetle), Stanislav Krejčik (click beetle), Olaf Leillinger (tiger beetle), Biopix [www.biopix.com] (diving beetle), Gyorgy Csoka (wasp beetle), Miroslav Deml (earwig), K Schneider (cockroach), Gilles San Martin (cricket).

5.2 Hemiptera (half wings): with four wings, the forewings half-hardened: Cicada (cicadas),  Notonecta (backswimmers), Nepa (water scorpions), Cimex (shield bugs and bedbugs), Aphis (aphids), Chermes (wooly aphids), Coccus (scale insects), Thrips (thrips).

Linnaeus’ Hemiptera included the following species (from left to right, top to bottom): ash cicada (Cicada orni), common backswimmer (Notonecta glauca), common water scorpion (Nepa cinerea), common bedbug (Cimex lectularius), elder aphid (Aphis sambuci), pineapple gall aldegid (Chermes abietis, currently Adelges abietis), brown soft scale (Coccus hesperidum), dandelion thrips (Thrips physapus). Credits to Wikimedia user Hectonichus (cicada), Holger Gröschl (backswimmer), Wikimedia user XenonX3 (water scorpion), James K. Lindsey (aphid), Magne Flåten (aldegid), Whitney Cranshaw (soft scale), thrips.w.interiowo.pl (thrips).

Linnaeus’ Hemiptera included the following species (from left to right, top to bottom): ash cicada (Cicada orni), common backswimmer (Notonecta glauca), common water scorpion (Nepa cinerea), common bedbug (Cimex lectularius), elder aphid (Aphis sambuci), pineapple gall aldegid (Chermes abietis, currently Adelges abietis), brown soft scale (Coccus hesperidum), and dandelion thrips (Thrips physapus). Credits to Wikimedia user Hectonichus (cicada), Holger Gröschl (backswimmer), Wikimedia user XenonX3 (water scorpion), James K. Lindsey (aphid), Magne Flåten (aldegid), Whitney Cranshaw (soft scale), thrips.w.interiowo.pl (thrips).

5.3 Lepidoptera (scale wings), with four scaly wings: Papilio (butterflies), Phalaena (moths), Sphinx (hawk moths).

Among the species put by Linnaeus under Lepidoptera, there were (from left to right, top to bottom): paris peacock (Papilio paris), gothic moth (Phalaena typical, now Naenia typical), privet hawk moth (Sphinx ligustri). Creditos to Wikimedia user Peellden (paris peacock), Danny Chapman (gothic moth), Wikimedia user Jdiemer (hawk moth).

Among the species put by Linnaeus under Lepidoptera, there were (from left to right): paris peacock (Papilio paris), gothic moth (Phalaena typica, now Naenia typica), and privet hawk moth (Sphinx ligustri). Credits to Wikimedia user Peellden (paris peacock), Danny Chapman (gothic moth), Wikimedia user Jdiemer (hawk moth).

5.4 Neuroptera (veined wings), with four membranous wings and an unarmed tail: Libellula (dragonflies and damselflies), Ephemera (mayflies), Phryganea (caddislies), Hemerobius (lacewings, antlions, alderflies), Panorpa (scorpionflies), Raphidia (snakeflies).

Linnaeus order Neuroptera included (from left to right, top to bottom) the four-spotted chaser (Libellula quadrimaculata), common mayfly (Ephemera vulgata), greater caddisly (Phryganea grandis), common brown lacewing (Hemerobius humulinus), common scorpionfly (Panorpa communis), common snakefly (Raphidia ophiopsis). Credits to Wikimedia user Bj.schoenmakers (mayfly), Donald Hobern (caddisfly), Wikimedia user AfroBrazilian (lacewing), André Karwath (scorpionfly).

Linnaeus order Neuroptera included (from left to right, top to bottom) the four-spotted chaser (Libellula quadrimaculata), common mayfly (Ephemera vulgata), greater caddisly (Phryganea grandis), common brown lacewing (Hemerobius humulinus), common scorpionfly (Panorpa communis), and common snakefly (Raphidia ophiopsis). Credits to Wikimedia user Bj.schoenmakers (mayfly), Donald Hobern (caddisfly), Wikimedia user AfroBrazilian (lacewing), André Karwath (scorpionfly).

5.5 Hymenoptera (membranous wings), with four membranous wings and an armed tail: Cynips (gall wasps), Tenthredo (sawflies), Ichneumon (parasitoid wasps), Sphex (digger wasps and potter wasps), Vespa (hornets and wasps), Apis (bees), Formica (ants), Mutilla (velvet ants).

Linnaeus order Neuroptera included (from left to right, top to bottom) the common gall wasp (Cynips quercusfolii), figwort sawfly (Tenthredo scrophulariae), common parasitoid wasp (Ichneumon sarcitorius), South American potter wasp (Sphex argillacea, now Zeta argillaceum), European hornet (Vespa crabro), Western honey bee (Apis mellifera), red wood ant (Formica rufa), European velvet ant (Mutilla europaea). Credits to Wikimedia user Wofl (gall wasp), James K. Lindsey (sawfly, parasitoid wasp), Sean McCann (potter wasp), Wikipedia user Flugwapsch62 (hornet), Böhringer Friedrich (bee), Adam Opio¬ła (ant), Valter Jacinto (velvet ant).

Linnaeus order Hymenoptera included (from left to right, top to bottom) the common gall wasp (Cynips quercusfolii), figwort sawfly (Tenthredo scrophulariae), common parasitoid wasp (Ichneumon sarcitorius), South American potter wasp (Sphex argillacea, now Zeta argillaceum), European hornet (Vespa crabro), Western honey bee (Apis mellifera), red wood ant (Formica rufa), and European velvet ant (Mutilla europaea). Credits to Wikimedia user Wofl (gall wasp), James K. Lindsey (sawfly, parasitoid wasp), Sean McCann (potter wasp), Wikimedia user Flugwapsch62 (hornet), Böhringer Friedrich (bee), Adam Opioła (ant), Valter Jacinto (velvet ant).

5.6 Diptera (two wings), with two wings: Oestrus (botflies), Tipula (craneflies and midges), Musca (houseflies, hoverflies, blowflies, snipe flies), Tabanus (horse-flies), Culex (mosquitoes), Empis (dance flies), Conops (thick-headed flies, hornflies, stable flies), Asilus (robber flies), Bombylius (beeflies), Hippobosca (louse flies).

In Diptera, Linnaeus included the sheep botly (Oestrus ovis), garden cranefly (Tipula hortorum), common housefly (Musca domestica), pale giant horse-fly (Tabanus bovinus), common house mosquito (Culex pipiens), northern dance fly (Empis borealis), yellow thick-headed fly (Conops flavipes), hornet robberfly (Asilus crabroniformis), large beefly (Bombylius major), forest fly (Hippobosca equina). Credits to picotverd user from diptera.info (botfly), James K. Lindsey (cranefly, horse-fly, dance fly), Kamran Iftikhar (housefly), David Barillet-Portal (mosquito), Martin Harvey (robberfly), Richard Bartz (beefly), Wikimedia user Janswart (forest fly).

In Diptera, Linnaeus included the sheep botly (Oestrus ovis), garden cranefly (Tipula hortorum), common housefly (Musca domestica), pale giant horse-fly (Tabanus bovinus), common house mosquito (Culex pipiens), northern dance fly (Empis borealis), yellow thick-headed fly (Conops flavipes), hornet robberfly (Asilus crabroniformis), large beefly (Bombylius major), and forest fly (Hippobosca equina). Credits to picotverd user from diptera.info (botfly), James K. Lindsey (cranefly, horse-fly, dance fly), Kamran Iftikhar (housefly), David Barillet-Portal (mosquito), Martin Harvey (robberfly), Richard Bartz (beefly), Wikimedia user Janswart (forest fly).

5.7 Aptera (no wings), without wings: Lepisma (silverfishes), Podura (springtails), Termes (termites and barklice), Pediculus (lice), Pulex (fleas), Acarus (mites and ticks), Phalangium (harvestmen, whip spider and whip scorpions), Aranea (spiders), Scorpio (scorpions), Cancer (crabs, lobsters, shrimp), Monoculus (tadpole shrimps, water fleas, horseshoe crabs), Oniscus (woodlice), Scolopendra (centipedes), Julus (milipedes).

The messy order Aptera included (from left to right, top to bottom) the silverfish (Lepisma saccharina), the water sprintail (Podura aquatic), the larger pale trogiid (Termes pulsatorium, now Trogium pulsatorium), the head louse (Pediculus humanus), the human flea (Pulex irritans), the flour mite (Acarus siro), the common harvestman (Phalangium opilio), the angular garden spider (Aranea angulata, now Araneus angulatus), the large clawed scorpion (Scorpio maurus), the brown crab (Cancer pagurus), the common tadpole shrimp (Monoculus apus, now Lepidurus apus), the common woodlouse (Oniscus asellus), the Amazonian giant centipede (Scolopendra gigantea), common millipede (Julus terrestris). Credits to Christian Fischer (silverfish, springtail), Josef Reischig (louse), Michael Wunderli (flea), Joel Mills (mite), Didier Descouens (harvestman), Thomas Kraft (spider), Guy Haimovitch (scorpion), Hans Hillewaert (crab), Christian Fischer (tadpole shrimp), Fritz Geller-Grimm (woodlouse), Katka Nemčoková (centipede), Carmen Juaréz/Pedro do Rego (millipede).

The messy order Aptera included (from left to right, top to bottom) the silverfish (Lepisma saccharina), the water springtail (Podura aquatica), the larger pale trogiid (Termes pulsatorium, now Trogium pulsatorium), the head louse (Pediculus humanus), the human flea (Pulex irritans), the flour mite (Acarus siro), the common harvestman (Phalangium opilio), the angular garden spider (Aranea angulata, now Araneus angulatus), the large clawed scorpion (Scorpio maurus), the brown crab (Cancer pagurus), the common tadpole shrimp (Monoculus apus, now Lepidurus apus), the common woodlouse (Oniscus asellus), the Amazonian giant centipede (Scolopendra gigantea), and the common millipede (Julus terrestris). Credits to Christian Fischer (silverfish, springtail), Josef Reischig (louse), Michael Wunderli (flea), Joel Mills (mite), Didier Descouens (harvestman), Thomas Kraft (spider), Guy Haimovitch (scorpion), Hans Hillewaert (crab), Christian Fischer (tadpole shrimp), Fritz Geller-Grimm (woodlouse), Katka Nemčoková (centipede), Carmen Juaréz/Pedro do Rego (millipede).

As one can notice, Linnaeus was pretty good at classifying hymenopterans, dipterans and lepidopterans. His orders Coleoptera and Hemiptera were not that bad too. Neuroptera was a little messy, but nothing compares to Aptera, where he put everything without wings, from silverfish to spiders, crabs and millipedes! It’s amazing how accurate he was with certain groups, but a complete disaster with others.

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References:

Linnaeus, C. 1758. Systema Naturae per regna tria naturae…

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