Nematode

The nematodes (UK: /ˈnɛmətoʊdz/ NEM-ə-tohdz, US: /ˈniːm-/ NEEM- Greek: Νηματώδη; Latin: Nematoda) or roundworms constitute the phylum Nematoda (also called Nemathelminthes),[2][3] with plant-parasitic nematodes being known as eelworms. They are a diverse animal phylum inhabiting a broad range of environments. Taxonomically, they are classified along with insects and other moulting animals in the clade Ecdysozoa, and unlike flatworms, have tubular digestive systems with openings at both ends. Like tardigrades they have a reduced number of Hox genes, but as their sister phylum Nematomorpha has kept the ancestral protostome Hox genotype, it shows that the reduction has occurred within the nematode phylum.[4]

This article is about the organism. For the infection, see Helminthiasis.

Nematode
Temporal range: Precambrian–Recent[1]
Caenorhabditis elegans,
a model species of roundworm
Scientific classification
Kingdom: Animalia
Subkingdom: Eumetazoa
Clade: ParaHoxozoa
Clade: Bilateria
Clade: Nephrozoa
(unranked): Protostomia
Superphylum: Ecdysozoa
Clade: Nematoida
Phylum: Nematoda
Diesing, 1861
Classes

(see text)

Synonyms
  • Nematodes Burmeister, 1837
  • Nematoidea sensu stricto Cobb, 1919
  • Nemates Cobb, 1919
  • Nemata Cobb, 1919 emend.

Nematode species can be difficult to distinguish from one another. Consequently, estimates of the number of nematode species described to date vary by author and may change rapidly over time. A 2013 survey of animal biodiversity published in the mega journal Zootaxa puts this figure at over 25,000.[5][6] Estimates of the total number of extant species are subject to even greater variation. A widely referenced[7] article published in 1993 estimated there may be over 1 million species of nematode,[8] a claim which has since been repeated in numerous publications. Many other publications have since vigorously refuted this claim on the grounds that it is unsupported by fact. More recent, fact-based estimates have placed the true figure closer to 40,000 species worldwide.[9]

Nematodes have successfully adapted to nearly every ecosystem: from marine (salt) to fresh water, soils, from the polar regions to the tropics, as well as the highest to the lowest of elevations (including mountains). They are ubiquitous in freshwater, marine, and terrestrial environments, where they often outnumber other animals in both individual and species counts, and are found in locations as diverse as mountains, deserts, and oceanic trenches. They are found in every part of the earth's lithosphere,[10] even at great depths, 0.9–3.6 km (3,000–12,000 ft) below the surface of the Earth in gold mines in South Africa.[11][12][13][14][15] They represent 90% of all animals on the ocean floor.[16] In total, 4.4 × 1020 nematodes inhabit the Earth's topsoil, or approximately 60 billion for each human, with the highest densities observed in tundra and boreal forests.[17] Their numerical dominance, often exceeding a million individuals per square meter and accounting for about 80% of all individual animals on earth, their diversity of lifecycles, and their presence at various trophic levels point to an important role in many ecosystems.[17][18] They have been shown to play crucial roles in polar ecosystems.[19][20] The roughly 2,271 genera are placed in 256 families.[21] The many parasitic forms include pathogens in most plants and animals. A third of the genera occur as parasites of vertebrates; about 35 nematode species occur in humans.[21]

Nathan Cobb, a nematologist, described the ubiquity of nematodes on Earth as thus:

In short, if all the matter in the universe except the nematodes were swept away, our world would still be dimly recognizable, and if, as disembodied spirits, we could then investigate it, we should find its mountains, hills, vales, rivers, lakes, and oceans represented by a film of nematodes. The location of towns would be decipherable since, for every massing of human beings, there would be a corresponding massing of certain nematodes. Trees would still stand in ghostly rows representing our streets and highways. The location of the various plants and animals would still be decipherable, and, had we sufficient knowledge, in many cases even their species could be determined by an examination of their erstwhile nematode parasites.[22]

The term is from Greek νηματώδης (plural νηματώδεις), ntr. νηματῶδες (plural νηματώδη);[23] Latin: Nematoda.

Etymology

The word nematode comes from the Modern Latin compound of nemat- "thread" (from Greek nema, genitive nematos "thread," from stem of nein "to spin"; see needle) + -odes "like, of the nature of" (see -oid).

Taxonomy and systematics
See also: List of nematode families
Eophasma jurasicum, a fossilized nematode
Caenorhabditis elegans
Rhabditia
Nippostrongylus brasiliensis
Unidentified Anisakidae (Ascaridina: Ascaridoidea)
Oxyuridae Threadworm
Spiruridae Dirofilaria immitis

History

In 1758, Linnaeus described some nematode genera (e.g., Ascaris), then included in the Vermes.

The name of the group Nematoda, informally called "nematodes", came from Nematoidea, originally defined by Karl Rudolphi (1808),[24] from Ancient Greek νῆμα (nêma, nêmatos, 'thread') and -eiδἠς (-eidēs, 'species'). It was treated as family Nematodes by Burmeister (1837).[24]

At its origin, the "Nematoidea" erroneously included Nematodes and Nematomorpha, attributed by von Siebold (1843). Along with Acanthocephala, Trematoda, and Cestoidea, it formed the obsolete group Entozoa,[25] created by Rudolphi (1808).[26] They were also classed along with Acanthocephala in the obsolete phylum Nemathelminthes by Gegenbaur (1859).

In 1861, K. M. Diesing treated the group as order Nematoda.[24] In 1877, the taxon Nematoidea, including the family Gordiidae (horsehair worms), was promoted to the rank of phylum by Ray Lankester. The first clear distinction between the nemas and gordiids was realized by Vejdovsky when he named a group to contain the horsehair worms the order Nematomorpha. In 1919, Nathan Cobb proposed that nematodes should be recognized alone as a phylum.[27] He argued they should be called "nema" in English rather than "nematodes" and defined the taxon Nemates (later emended as Nemata, Latin plural of nema), listing Nematoidea sensu restricto as a synonym.

However, in 1910, Grobben proposed the phylum Aschelminthes and the nematodes were included in as class Nematoda along with class Rotifera, class Gastrotricha, class Kinorhyncha, class Priapulida, and class Nematomorpha (The phylum was later revived and modified by Libbie Henrietta Hyman in 1951 as Pseudoceolomata, but remained similar). In 1932, Potts elevated the class Nematoda to the level of phylum, leaving the name the same. Despite Potts' classification being equivalent to Cobbs', both names have been used (and are still used today) and Nematode became a popular term in zoological science.[28]

Since Cobb was the first to include nematodes in a particular phylum separated from Nematomorpha, some researchers consider the valid taxon name to be Nemates or Nemata, rather than Nematoda,[29] because of the zoological rule that gives priority to the first used term in case of synonyms.

Phylogeny

The phylogenetic relationships of the nematodes and their close relatives among the protostomian Metazoa are unresolved. Traditionally, they were held to be a lineage of their own, but in the 1990s, they were proposed to form the group Ecdysozoa together with moulting animals, such as arthropods. The identity of the closest living relatives of the Nematoda has always been considered to be well resolved. Morphological characters and molecular phylogenies agree with placement of the roundworms as a sister taxon to the parasitic Nematomorpha; together, they make up the Nematoida. Along with the Scalidophora (formerly Cephalorhyncha), the Nematoida form the clade Cycloneuralia, but much disagreement occurs both between and among the available morphological and molecular data. The Cycloneuralia or the Introverta—depending on the validity of the former—are often ranked as a superphylum.[30]

Nematode systematics

Due to the lack of knowledge regarding many nematodes, their systematics is contentious. An earliest and influential classification was proposed by Chitwood and Chitwood[31]—later revised by Chitwood[32]—who divided the phylum into two—the Aphasmidia and the Phasmidia. These were later renamed Adenophorea (gland bearers) and Secernentea (secretors), respectively.[33] The Secernentea share several characteristics, including the presence of phasmids, a pair of sensory organs located in the lateral posterior region, and this was used as the basis for this division. This scheme was adhered to in many later classifications, though the Adenophorea were not in a uniform group.

Initial studies of incomplete DNA sequences[34] suggested the existence of five clades:[35]

As it seems, the Secernentea are indeed a natural group of closest relatives, but the "Adenophorea" appear to be a paraphyletic assemblage of roundworms simply retaining a good number of ancestral traits. The old Enoplia do not seem to be monophyletic, either, but to contain two distinct lineages. The old group "Chromadoria" seems to be another paraphyletic assemblage, with the Monhysterida representing a very ancient minor group of nematodes. Among the Secernentea, the Diplogasteria may need to be united with the Rhabditia, while the Tylenchia might be paraphyletic with the Rhabditia.[36]

The understanding of roundworm systematics and phylogeny as of 2002 is summarised below:

Phylum Nematoda

Later work has suggested the presence of 12 clades.[37] The Secernentea—a group that includes virtually all major animal and plant 'nematode' parasites—apparently arose from within the Adenophorea.

A major effort to improve the systematics of this phylum is in progress and being organised by the 959 Nematode Genomes.[38]

A complete checklist of the world's nematode species can be found in the World Species Index: Nematoda.[39]

An analysis of the mitochondrial DNA suggests that the following groupings are valid[40]

The Ascaridomorpha, Rhabditomorpha, and Diplogasteromorpha appear to be related.

The suborders Spirurina and Tylenchina and the infraorders Rhabditomorpha, Panagrolaimomorpha, and Tylenchomorpha are paraphytic.

The monophyly of the Ascaridomorph is uncertain.

Anatomy
Internal anatomy of a male C. elegans nematode

Nematodes are very small, slender worms: typically about 5 to 100 µm thick, and 0.1 to 2.5 mm long.[41] The smallest nematodes are microscopic, while free-living species can reach as much as 5 cm (2 in), and some parasitic species are larger still, reaching over 1 m (3 ft) in length.[42]:271 The body is often ornamented with ridges, rings, bristles, or other distinctive structures.[43]

The head of a nematode is relatively distinct. Whereas the rest of the body is bilaterally symmetrical, the head is radially symmetrical, with sensory bristles and, in many cases, solid 'head-shields' radiating outwards around the mouth. The mouth has either three or six lips, which often bear a series of teeth on their inner edges. An adhesive 'caudal gland' is often found at the tip of the tail.[44]

The epidermis is either a syncytium or a single layer of cells, and is covered by a thick collagenous cuticle. The cuticle is often of a complex structure and may have two or three distinct layers. Underneath the epidermis lies a layer of longitudinal muscle cells. The relatively rigid cuticle works with the muscles to create a hydroskeleton, as nematodes lack circumferential muscles. Projections run from the inner surface of muscle cells towards the nerve cords; this is a unique arrangement in the animal kingdom, in which nerve cells normally extend fibers into the muscles rather than vice versa.[44]

Digestive system

The oral cavity is lined with cuticle, which is often strengthened with structures, such as ridges, especially in carnivorous species, which may bear a number of teeth. The mouth often includes a sharp stylet, which the animal can thrust into its prey. In some species, the stylet is hollow and can be used to suck liquids from plants or animals.[44]

The oral cavity opens into a muscular, sucking pharynx, also lined with cuticle. Digestive glands are found in this region of the gut, producing enzymes that start to break down the food. In stylet-bearing species, these may even be injected into the prey.[44]

No stomach is present, with the pharynx connecting directly to a muscleless intestine that forms the main length of the gut. This produces further enzymes, and also absorbs nutrients through its single-cell-thick lining. The last portion of the intestine is lined by cuticle, forming a rectum, which expels waste through the anus just below and in front of the tip of the tail. The movement of food through the digestive system is the result of the body movements of the worm. The intestine has valves or sphincters at either end to help control the movement of food through the body.[44]

Excretory system

Nitrogenous waste is excreted in the form of ammonia through the body wall, and is not associated with any specific organs. However, the structures for excreting salt to maintain osmoregulation are typically more complex.[44]

In many marine nematodes, one or two unicellular 'renette glands' excrete salt through a pore on the underside of the animal, close to the pharynx. In most other nematodes, these specialized cells have been replaced by an organ consisting of two parallel ducts connected by a single transverse duct. This transverse duct opens into a common canal that runs to the excretory pore.[44]

Nervous system
See also: Muscle arms

Four peripheral nerves run along the length of the body on the dorsal, ventral, and lateral surfaces. Each nerve lies within a cord of connective tissue lying beneath the cuticle and between the muscle cells. The ventral nerve is the largest, and has a double structure forward of the excretory pore. The dorsal nerve is responsible for motor control, while the lateral nerves are sensory, and the ventral combines both functions.[44]

The nervous system is also the only place in the nematode body that contains cilia, which are all nonmotile and with a sensory function.[45][46]

At the anterior end of the animal, the nerves branch from a dense, circular nerve (nerve ring) round surrounding the pharynx, and serving as the brain. Smaller nerves run forward from the ring to supply the sensory organs of the head.[44]

The bodies of nematodes are covered in numerous sensory bristles and papillae that together provide a sense of touch. Behind the sensory bristles on the head lie two small pits, or 'amphids'. These are well supplied with nerve cells and are probably chemoreception organs. A few aquatic nematodes possess what appear to be pigmented eye-spots, but whether or not these are actually sensory in nature is unclear.[44]

Reproduction
Extremity of a male nematode showing the spicule, used for copulation, bar = 100 µm [47]

Most nematode species are dioecious, with separate male and female individuals, though some, such as Caenorhabditis elegans, are androdioecious, consisting of hermaphrodites and rare males. Both sexes possess one or two tubular gonads. In males, the sperm are produced at the end of the gonad and migrate along its length as they mature. The testis opens into a relatively wide seminal vesicle and then during intercourse into a glandular and muscular ejaculatory duct associated with the vas deferens and cloaca. In females, the ovaries each open into an oviduct (in hermaphrodites, the eggs enter a spermatheca first) and then a glandular uterus. The uteri both open into a common vulva/vagina, usually located in the middle of the morphologically ventral surface.[44]

Reproduction is usually sexual, though hermaphrodites are capable of self-fertilization. Males are usually smaller than females or hermaphrodites (often much smaller) and often have a characteristically bent or fan-shaped tail. During copulation, one or more chitinized spicules move out of the cloaca and are inserted into the genital pore of the female. Amoeboid sperm crawl along the spicule into the female worm. Nematode sperm is thought to be the only eukaryotic cell without the globular protein G-actin.

Eggs may be embryonated or unembryonated when passed by the female, meaning their fertilized eggs may not yet be developed. A few species are known to be ovoviviparous. The eggs are protected by an outer shell, secreted by the uterus. In free-living roundworms, the eggs hatch into larvae, which appear essentially identical to the adults, except for an underdeveloped reproductive system; in parasitic roundworms, the lifecycle is often much more complicated.[44]

Nematodes as a whole possess a wide range of modes of reproduction.[48] Some nematodes, such as Heterorhabditis spp., undergo a process called endotokia matricida: intrauterine birth causing maternal death.[49] Some nematodes are hermaphroditic, and keep their self-fertilized eggs inside the uterus until they hatch. The juvenile nematodes then ingest the parent nematode. This process is significantly promoted in environments with a low food supply.[49]

The nematode model species C. elegans and C. briggsae exhibit androdioecy, which is very rare among animals. The single genus Meloidogyne (root-knot nematodes) exhibits a range of reproductive modes, including sexual reproduction, facultative sexuality (in which most, but not all, generations reproduce asexually), and both meiotic and mitotic parthenogenesis.

The genus Mesorhabditis exhibits an unusual form of parthenogenesis, in which sperm-producing males copulate with females, but the sperm do not fuse with the ovum. Contact with the sperm is essential for the ovum to begin dividing, but because no fusion of the cells occurs, the male contributes no genetic material to the offspring, which are essentially clones of the female.[44]

Free-living species

Different free-living species feed on materials as varied as algae, fungi, small animals, fecal matter, dead organisms, and living tissues. Free-living marine nematodes are important and abundant members of the meiobenthos. They play an important role in the decomposition process, aid in recycling of nutrients in marine environments, and are sensitive to changes in the environment caused by pollution. One roundworm of note, C. elegans, lives in the soil and has found much use as a model organism. C. elegans has had its entire genome sequenced, the developmental fate of every cell determined, and every neuron mapped.

Parasitic species
Eggs (mostly nematodes) from stools of wild primates

Nematodes that commonly parasitise humans include ascarids (Ascaris), filarias, hookworms, pinworms (Enterobius), and whipworms (Trichuris trichiura). The species Trichinella spiralis, commonly known as the 'trichina worm', occurs in rats, pigs, bears, and humans, and is responsible for the disease trichinosis. Baylisascaris usually infests wild animals, but can be deadly to humans, as well. Dirofilaria immitis is known for causing heartworm disease by inhabiting the hearts, arteries, and lungs of dogs and some cats. Haemonchus contortus is one of the most abundant infectious agents in sheep around the world, causing great economic damage to sheep. In contrast, entomopathogenic nematodes parasitize insects and are mostly considered beneficial by humans, but some attack beneficial insects.

One form of nematode is entirely dependent upon fig wasps, which are the sole source of fig fertilization. They prey upon the wasps, riding them from the ripe fig of the wasp's birth to the fig flower of its death, where they kill the wasp, and their offspring await the birth of the next generation of wasps as the fig ripens.

Colorized electron micrograph of soybean cyst nematode (Heterodera sp.) and egg

A newly discovered parasitic tetradonematid nematode, Myrmeconema neotropicum, apparently induces fruit mimicry in the tropical ant Cephalotes atratus. Infected ants develop bright red gasters (abdomens), tend to be more sluggish, and walk with their gasters in a conspicuous elevated position. These changes likely cause frugivorous birds to confuse the infected ants for berries, and eat them. Parasite eggs passed in the bird's feces are subsequently collected by foraging C. atratus and are fed to their larvae, thus completing the lifecycle of M. neotropicum.[50]

Similarly, multiple varieties of nematodes have been found in the abdominal cavities of the primitively social sweat bee, Lasioglossum zephyrus. Inside the female body, the nematode hinders ovarian development and renders the bee less active, thus less effective in pollen collection.[51]

Plant-parasitic nematodes include several groups causing severe crop losses. The most common genera are Aphelenchoides (foliar nematodes), Ditylenchus, Globodera (potato cyst nematodes), Heterodera (soybean cyst nematodes), Longidorus, Meloidogyne (root-knot nematodes), Nacobbus, Pratylenchus (lesion nematodes), Trichodorus, and Xiphinema (dagger nematodes). Several phytoparasitic nematode species cause histological damages to roots, including the formation of visible galls (e.g. by root-knot nematodes), which are useful characters for their diagnostic in the field. Some nematode species transmit plant viruses through their feeding activity on roots. One of them is Xiphinema index, vector of grapevine fanleaf virus, an important disease of grapes, another one is Xiphinema diversicaudatum, vector of arabis mosaic virus.

Other nematodes attack bark and forest trees. The most important representative of this group is Bursaphelenchus xylophilus, the pine wood nematode, present in Asia and America and recently discovered in Europe.

Agriculture and horticulture

Depending on the species, a nematode may be beneficial or detrimental to plant health. From agricultural and horticulture perspectives, the two categories of nematodes are the predatory ones, which kill garden pests such as cutworms and corn earworm moths, and the pest nematodes, such as the root-knot nematode, which attack plants, and those that act as vectors spreading plant viruses between crop plants.[52] Plant-parasitic nematodes are often known as eelworms and attack leaves and buds. Predatory nematodes can be bred by soaking a specific recipe of leaves and other detritus in water, in a dark, cool place, and can even be purchased as an organic form of pest control.

Rotations of plants with nematode-resistant species or varieties is one means of managing parasitic nematode infestations. For example, marigolds, grown over one or more seasons (the effect is cumulative), can be used to control nematodes.[53] Another is treatment with natural antagonists such as the fungus Gliocladium roseum. Chitosan, a natural biocontrol, elicits plant defense responses to destroy parasitic cyst nematodes on roots of soybean, corn, sugar beet, potato, and tomato crops without harming beneficial nematodes in the soil.[54] Soil steaming is an efficient method to kill nematodes before planting a crop, but indiscriminately eliminates both harmful and beneficial soil fauna.

The golden nematode Globodera rostochiensis is a particularly harmful variety of nematode pest that has resulted in quarantines and crop failures worldwide. CSIRO has found a 13- to 14-fold reduction of nematode population densities in plots having Indian mustard Brassica juncea green manure or seed meal in the soil.[55]

Epidemiology
Disability-adjusted life year for intestinal nematode infections per 100,000 in 2002.
    <  25
  25–50
  50–75
  75–100
  100–120
  120–140
  140–160
  160–180
  180–200
  200–220
  220–240
    >  240
  no data

A number of intestinal nematodes cause diseases affecting human beings, including ascariasis, trichuriasis, and hookworm disease. Filarial nematodes cause filariasis.

Soil ecosystems

About 90% of nematodes reside in the top 15 cm of soil. Nematodes do not decompose organic matter, but, instead, are parasitic and free-living organisms that feed on living material. Nematodes can effectively regulate bacterial population and community composition—they may eat up to 5,000 bacteria per minute. Also, nematodes can play an important role in the nitrogen cycle by way of nitrogen mineralization.[41]

One group of carnivorous fungi, the nematophagous fungi, are predators of soil nematodes. They set enticements for the nematodes in the form of lassos or adhesive structures.[56][57][58]

Society and culture

Nematode worms (C. elegans), part of an ongoing research project conducted on the 2003 Space Shuttle Columbia mission STS-107, survived the re-entry breakup. It is believed to be the first known life form to survive a virtually unprotected atmospheric descent to Earth's surface.[59][60]

gollark: Three if you count mine.
gollark: Chorus City now has *two* houses! That's two more than zero!
gollark: Ah.
gollark: No, but I mean, first it says "Success!" then gives an error.
gollark: It should probably not say "success" until it's actually linked without an error.

See also

References
  1. "Nematode Fossils—Nematoda". The Virtual Fossil Museum.
  2. Classification of Animal Parasites
  3. Garcia, Lynne (29 October 1999). "Classification of Human Parasites, Vectors, and Similar Organisms" (PDF). Los Angeles, California: Department of Pathology and Laboratory Medicine, UCLA Medical Center. Retrieved 21 July 2017.
  4. "How Weird is The Worm? Evolution of the Developmental Gene Toolkit in Caenorhabditis elegans - MDPI". Archived from the original on 2019-11-12. Retrieved 2019-11-12.
  5. Hodda, M (2011). "Phylum Nematoda Cobb, 1932. In: Zhang, Z.-Q. (Ed.) Animal biodiversity: An outline of higher-level classification and survey of taxonomic richness". Zootaxa. 3148: 63–95. doi:10.11646/zootaxa.3148.1.11.
  6. Zhang, Z (2013). "Animal biodiversity: An update of classification and diversity in 2013. In: Zhang, Z.-Q. (Ed.) Animal Biodiversity: An Outline of Higher-level Classification and Survey of Taxonomic Richness (Addenda 2013)". Zootaxa. 3703 (1): 5–11. doi:10.11646/zootaxa.3703.1.3.
  7. "Recent developments in marine benthic biodiversity research". ResearchGate. Retrieved 5 November 2018.
  8. Lambshead, PJD (1993). "Recent developments in marine benthic biodiversity research". Oceanis. 19 (6): 5–24.
  9. Anderson, Roy C. (8 February 2000). Nematode Parasites of Vertebrates: Their Development and Transmission. CABI. pp. 1–2. ISBN 9780851994215. Estimates of 500,000 to a million species have no basis in fact.
  10. Borgonie G, García-Moyano A, Litthauer D, Bert W, Bester A, van Heerden E, Möller C, Erasmus M, Onstott TC (June 2011). "Nematoda from the terrestrial deep subsurface of South Africa". Nature. 474 (7349): 79–82. Bibcode:2011Natur.474...79B. doi:10.1038/nature09974. hdl:1854/LU-1269676. PMID 21637257.
  11. Lemonick MD (8 June 2011). "Could 'worms from Hell' mean there's life in space?". Time. ISSN 0040-781X. Retrieved 8 June 2011.
  12. Bhanoo SN (1 June 2011). "Nematode found in mine is first subsurface multicellular organism". The New York Times. ISSN 0362-4331. Retrieved 13 June 2011.
  13. "Gold mine". Nature. 474 (7349): 6. June 2011. doi:10.1038/474006b. PMID 21637213.
  14. Drake N (1 June 2011). "Subterranean worms from hell: Nature News". Nature News. doi:10.1038/news.2011.342. Retrieved 13 June 2011.
  15. Borgonie G, García-Moyano A, Litthauer D, Bert W, Bester A, van Heerden E, Möller C, Erasmus M, Onstott TC (2 June 2011). "Nematoda from the terrestrial deep subsurface of South Africa". Nature. 474 (7349): 79–82. Bibcode:2011Natur.474...79B. doi:10.1038/nature09974. hdl:1854/LU-1269676. ISSN 0028-0836. PMID 21637257.
  16. Danovaro R, Gambi C, Dell'Anno A, Corinaldesi C, Fraschetti S, Vanreusel A, Vincx M, Gooday AJ (January 2008). "Exponential decline of deep-sea ecosystem functioning linked to benthic biodiversity loss". Curr. Biol. 18 (1): 1–8. doi:10.1016/j.cub.2007.11.056. PMID 18164201. Lay summary – EurekAlert!.
  17. van den Hoogen, Johan; Geisen, Stefan; Routh, Devin; Ferris, Howard; Traunspurger, Walter; Wardle, David A.; de Goede, Ron G. M.; Adams, Byron J.; Ahmad, Wasim (2019-07-24). "Soil nematode abundance and functional group composition at a global scale". Nature. 572 (7768): 194–198. Bibcode:2019Natur.572..194V. doi:10.1038/s41586-019-1418-6. ISSN 0028-0836. PMID 31341281. Archived from the original on 2020-03-02. Retrieved 2019-12-10.
  18. Platt HM (1994). "foreword". In Lorenzen S, Lorenzen SA (eds.). The phylogenetic systematics of freeliving nematodes. London, UK: The Ray Society. ISBN 978-0-903874-22-9.
  19. Cary, S. Craig; Green, T. G. Allan; Storey, Bryan C.; Sparrow, Ashley D.; Hogg, Ian D.; Katurji, Marwan; Zawar-Reza, Peyman; Jones, Irfon; Stichbury, Glen A. (2019-02-15). "Biotic interactions are an unexpected yet critical control on the complexity of an abiotically driven polar ecosystem". Communications Biology. 2 (1): 62. doi:10.1038/s42003-018-0274-5. ISSN 2399-3642. PMC 6377621. PMID 30793041.
  20. Adams, Byron J.; Wall, Diana H.; Storey, Bryan C.; Green, T. G. Allan; Barrett, John E.; S. Craig Cary; Hopkins, David W.; Lee, Charles K.; Bottos, Eric M. (2019-02-15). "Nematodes in a polar desert reveal the relative role of biotic interactions in the coexistence of soil animals". Communications Biology. 2 (1): 63. doi:10.1038/s42003-018-0260-y. ISSN 2399-3642. PMC 6377602. PMID 30793042.
  21. Roy C. Anderson (8 February 2000). Nematode Parasites of Vertebrates: Their development and transmission. CABI. p. 1. ISBN 978-0-85199-786-5.
  22. Cobb, Nathan (1914). "Nematodes and their relationships". Yearbook. United States Department of Agriculture. pp. 472, 457–490. Archived from the original on 9 June 2016. Retrieved 25 September 2012. Quote on p. 472.
  23. νηματώδης, νηματῶδες. Liddell, Henry George; Scott, Robert; A Greek–English Lexicon at the Perseus Project.
  24. Chitwood BG (1957). "The English word "Nema" revised". Systematic Biology. 4 (45): 1619. doi:10.2307/sysbio/6.4.184.
  25. Siddiqi MR (2000). Tylenchida: parasites of plants and insects. Wallingford, Oxon, UK: CABI Pub. ISBN 978-0-85199-202-0.
  26. Schmidt-Rhaesa A (2014). "Gastrotricha, Cycloneuralia and Gnathifera: General History and Phylogeny". In Schmidt-Rhaesa A (ed.). Handbook of Zoology (founded by W. Kükenthal). 1, Nematomorpha, Priapulida, Kinorhyncha, Loricifera. Berlin, Boston: de Gruyter.
  27. Cobb NA (1919). "The orders and classes of nemas". Contrib. Sci. Nematol. 8: 213–216.
  28. Wilson, E. O. "Phylum Nemata". Plant and insect parasitic nematodes. Archived from the original on 30 April 2018. Retrieved 29 April 2018.
  29. "ITIS report: Nematoda". Itis.gov. Retrieved 12 June 2012.
  30. "Bilateria". Tree of Life Web Project. Tree of Life Web Project. 2002. Retrieved 2 November 2008.
  31. Chitwood BG, Chitwood MB (1933). "The characters of a protonematode". J Parasitol. 20: 130.
  32. Chitwood BG (1937). "A revised classification of the Nematoda". Papers on Helminthology published in commemoration of the 30 year Jubileum of ... K.J. Skrjabin ... Moscow: All-Union Lenin Academy of Agricultural Sciences. pp. 67–79.
  33. Chitwood BG (1958). "The designation of official names for higher taxa of invertebrates". Bull Zool Nomencl. 15: 860–895. doi:10.5962/bhl.part.19410.
  34. Coghlan, A. (7 Sep 2005). "Nematode genome evolution" (PDF). WormBook: 1–15. doi:10.1895/wormbook.1.15.1. PMC 4781476. PMID 18050393. Archived from the original (PDF) on 5 March 2016. Retrieved 13 January 2016.
  35. Blaxter ML, De Ley P, Garey JR, Liu LX, Scheldeman P, Vierstraete A, Vanfleteren JR, Mackey LY, Dorris M, Frisse LM, Vida JT, Thomas WK (March 1998). "A molecular evolutionary framework for the phylum Nematoda". Nature. 392 (6671): 71–75. Bibcode:1998Natur.392...71B. doi:10.1038/32160. PMID 9510248.
  36. "Nematoda". Tree of Life Web Project. Tree of Life Web Project. 2002. Retrieved 2 November 2008.
  37. Holterman M, van der Wurff A, van den Elsen S, van Megen H, Bongers T, Holovachov O, Bakker J, Helder J (2006). "Phylum-wide analysis of SSU rDNA reveals deep phylogenetic relationships among nematodes and accelerated evolution toward crown Clades". Mol Biol Evol. 23 (9): 1792–1800. doi:10.1093/molbev/msl044. PMID 16790472.
  38. "959 Nematode Genomes – NematodeGenomes". Nematodes.org. 11 November 2011. Archived from the original on 5 August 2015. Retrieved 12 June 2012.
  39. World Species Index: Nematoda. 2012.
  40. Liu GH, Shao R, Li JY, Zhou DH, Li H, Zhu XQ (2013). "The complete mitochondrial genomes of three parasitic nematodes of birds: a unique gene order and insights into nematode phylogeny". BMC Genomics. 14 (1): 414. doi:10.1186/1471-2164-14-414. PMC 3693896. PMID 23800363.
  41. Nyle C. Brady & Ray R. Weil (2009). Elements of the Nature and Properties of Soils (3rd ed.). Prentice Hall. ISBN 9780135014332.
  42. Ruppert EE, Fox RS, Barnes RD (2004). Invertebrate Zoology: A Functional Evolutionary Approach (7th ed.). Belmont, California: Brooks/Cole. ISBN 978-0-03-025982-1.
  43. Weischer B, Brown DJ (2000). An Introduction to Nematodes: General Nematology. Sofia, Bulgaria: Pensoft. pp. 75–76. ISBN 978-954-642-087-9.
  44. Barnes RG (1980). Invertebrate zoology. Philadelphia: Sanders College. ISBN 978-0-03-056747-6.
  45. "The sensory cilia of Caenorhabditis elegans". www.wormbook.org.
  46. Kavlie, RG; Kernan, MJ; Eberl, DF (May 2010). "Hearing in Drosophila requires TilB, a conserved protein associated with ciliary motility". Genetics. 185 (1): 177–88. doi:10.1534/genetics.110.114009. PMC 2870953. PMID 20215474.
  47. Lalošević, V.; Lalošević, D.; Capo, I.; Simin, V.; Galfi, A.; Traversa, D. (2013). "High infection rate of zoonotic Eucoleus aerophilus infection in foxes from Serbia". Parasite. 20: 3. doi:10.1051/parasite/2012003. PMC 3718516. PMID 23340229.
  48. Bell G (1982). The masterpiece of nature: the evolution and genetics of sexuality. Berkeley: University of California Press. ISBN 978-0-520-04583-5.
  49. Johnigk SA, Ehlers RU (1999). "Endotokia matricida in hermaphrodites of Heterorhabditis spp. and the effect of the food supply". Nematology. 1 (7–8): 717–726. doi:10.1163/156854199508748. ISSN 1388-5545.
  50. Yanoviak SP, Kaspari M, Dudley R, Poinar G (April 2008). "Parasite-induced fruit mimicry in a tropical canopy ant". Am. Nat. 171 (4): 536–44. doi:10.1086/528968. PMID 18279076.
  51. Batra, Suzanne W. T. (1965-10-01). "Organisms associated with Lasioglossum zephyrum (Hymenoptera: Halictidae)". Journal of the Kansas Entomological Society. 38 (4): 367–389. JSTOR 25083474.
  52. Purcell M, Johnson MW, Lebeck LM, Hara AH (1992). "Biological Control of Helicoverpa zea (Lepidoptera: Noctuidae) with Steinernema carpocapsae (Rhabditida: Steinernematidae) in Corn Used as a Trap Crop". Environmental Entomology. 21 (6): 1441–1447. doi:10.1093/ee/21.6.1441.
  53. Riotte L (1975). Secrets of companion planting for successful gardening. p. 7.
  54. US application 2008072494, Stoner RJ, Linden JC, "Micronutrient elicitor for treating nematodes in field crops", published 2008-03-27
  55. Loothfar R, Tony S (22 March 2005). "Suppression of root knot nematode (Meloidogyne javanica) after incorporation of Indian mustard cv. Nemfix as green manure and seed meal in vineyards". Australasian Plant Pathology. 34 (1): 77–83. doi:10.1071/AP04081. Retrieved 14 June 2010.
  56. Pramer C (1964). "Nematode-trapping fungi". Science. 144 (3617): 382–388. Bibcode:1964Sci...144..382P. doi:10.1126/science.144.3617.382. PMID 14169325.
  57. Hauser JT (December 1985). "Nematode-trapping fungi" (PDF). Carnivorous Plant Newsletter. 14 (1): 8–11.
  58. Ahrén D, Ursing BM, Tunlid A (1998). "Phylogeny of nematode-trapping fungi based on 18S rDNA sequences". FEMS Microbiology Letters. 158 (2): 179–184. doi:10.1016/s0378-1097(97)00519-3. PMID 9465391.
  59. "Columbia Survivors". Astrobiology Magazine. Jan 1, 2006. Archived from the original on March 4, 2016. Retrieved January 12, 2016.
  60. Szewczyk, Nathaniel J.; Mancinelli, Rocco L.; McLamb, William; Reed, David; Blumberg, Baruch S.; Conley, Catharine A. (December 2005). "Caenorhabditis elegans Survives Atmospheric Breakup of STS–107, Space Shuttle Columbia". Astrobiology. 5 (6): 690–705. Bibcode:2005AsBio...5..690S. doi:10.1089/ast.2005.5.690. PMID 16379525.

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