Tag Archives: fleas

Should we save or should we get rid of parasites?

by Piter Kehoma Boll

Parasites are special types of organisms that live on or inside other lifeforms, slowly feeding on them but usually not killing them, just reducing their fitness to some degree. This is a much more discrete way to survive than killing or biting entire parts off, as predators (both carnivores and herbivores) do. However, different from these creatures, parasites are often regarded as unpleasant and disgusting. Yet parasitism is the most common way to get food in nature.

When I introduced the rhinoceros tick in a recent Friday Fellow, I mentioned the dilemma caused by it. Since the rhinoceros tick is a parasite of rhinoceroses, and rhinoceroses are threatened with extinction, a common practice to improve the reproductive fitness of rhinos is removing their ticks, but this may end up leading the rhinoceros tick to extinction.

This actually happened already with other parasites, such as the louse Coleocephalum californici, which was an exclusive parasite of the California condor Gymnogyps californianus. In order to save the condor, a common practice among veterinarians working with conservationists was to delouse the birds and, as a result, this louse is now extinct. The harm that the louse caused to the condor was so little, though, that its extinction was not at all necessary, being nothing more than a case of negligence and lack of empathy for a small and non-charismatic species.

The California condor louse Coleocephalum californici was extinct during a poorly managed campaign to save the California condor Gymnogyps californianus. Image extracted from https://www.hcn.org/blogs/goat/the-power-and-plight-of-the-parasite

The louse Rallicola (Aptericola) pilgrimi has also vanished forever during the conservation campaigns to save its host, the little spotted kiwi, Apteryx owenii, in another failed work.

The efforts to save the little spotted kiwi, Apteryx owenii, from extinction led to the extinction of its louse. Photo by Judi Lapsley Miller.*
The now extinct Rallicola (Aptericola) pilgrimi. Credits to the Museum of New Zealand.***

Another group of parasites that is facing extinction are fleas. The species Xenopsylla nesiotes was endemic to the Christmas Island together with its host, the Christmas Island rat, Rattus macleari. The introduction of the black rat, Rattus rattus, in the island led to a quick decline in the population of the Christmas Island rat, which went extinct at the beginning of the 20th century and, of course, the flea went extinct with it. The flea Acanthopsylla saphes has likely become extinct as well. It was a parasite of the eastern quoll, Dasyurus viverrinus, in mainland Australia. The eastern quoll today is only found in Tasmania, as the mainland Australia’s population went extinct in the mid-20th century. However, the flea was never found in the Tasmanian populations, so it is likely that it died away in mainland Australia together with the local population of its host.

The Manx shearwater flea Ceratophyllus (Emmareus) fionnus. Photo by Olha Schedrina, Natural History Museum.*

But things have been changing lately and fortunately the view on parasites is improving. A recent assessment was made on the population of another flea, the Manx shearwater flea, Ceratophyllus (Emmareus) fionnus. This flea is host-specific, being found only on the Manx shearwater Puffinus puffinus. Although the Manx shearwater is not at all a threatened species and has many colonies along the North Atlantic coast, the flea is endemic to the Isle of Rùm, a small island off the west coast of Scotland. Due to the small population of its host in this island, the flea has ben evaluated as vulnerable. If the Manx shearwater population in the Island were stable, things would be fine but, as you may have guessed already, things are not fine. Just like it happened in Christmas Island, the black rat was also introduced in the Isle of Rúm and has become a predator of the Manx shearwater, attacking its nests.

The Manx shearwater, Puffinus puffinus, is the sole host of the Manx shearwater flea. Photo by Martin Reith.**

Some ideas have been suggested to protect the flea from extinction. One of them is to eradicate the black rat from the Isle or at least manage its population near the Manx shearwater colonies. Another proposal is to translocate some fleas to another island to create additional populations in other Manx shearwater colonies.

But why bother protecting parasites? Well, there are plenty of reasons. First, they comprise a huge part of the planet’s biodiversity and their loss would have a strong impact on any ecosystem. Second, they are an essential part of their host’s evolutionary history and are, therefore, promoters of diversity by natural selection. Removing the parasites from a host would eventually decrease its genetic variability and let it more vulnerable to other new parasites. Due to their coevolution with the host, parasites are also a valuable source of knowledge about the host’s ecology and evolutionary history, helping us know their population dynamics. We can even find ways to deal with our own parasites by studying the parasites of other species, and parasites are certainly something that humans managed to collect in large numbers while spreading across the globe.

Parasites may be annoying but they are necessary. They may seem to weaken their host at first but, in the long run, what doesn’t kill you makes you stronger.

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References:

Kirst ML (2012) The power and plight of the parasite. High Country News. Available at < https://www.hcn.org/blogs/goat/the-power-and-plight-of-the-parasite >. Access on 3 November 2019.

Kwak ML (2018) Australia’s vanishing fleas (Insecta: Siphonaptera): a case study in methods for the assessment and conservation of threatened flea species. Journal of Insect Conservation 22(3–4): 545–550. doi: 10.1007/s10841-018-0083-7

Kwak ML, Heath ACG, Palma RL (2019) Saving the Manx Shearwater Flea Ceratophyllus (Emmareus) fionnus (Insecta: Siphonaptera): The Road to Developing a Recovery Plan for a Threatened Ectoparasite. Acta Parasitologica. doi: 10.2478/s11686-019-00119-8

Rózsa L, Vas Z (2015) Co-extinct and critically co-endangered species of parasitic lice, and conservation-induced extinction: should lice be reintroduced to their hosts? Oryx 49(1): 107–110. doi: 10.1017/S0030605313000628

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

**Creative Commons License This work is licensed under a Creative Commons Attribution-ShareAlike 3.0 Unported License.

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

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Filed under Conservation, Ecology, Evolution, Extinction, Parasites

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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Filed under Systematics, Zoology