Nematoda

Life-forms

Superregnum: Eukaryota
Cladus: Unikonta
Cladus: Opisthokonta
Cladus: Holozoa
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Cladus: Protostomia
Cladus: Ecdysozoa
Cladus: Cycloneuralia
Cladus: Nematoida
Phylum: Nematoda
Classes (2): Chromadorea - Enoplea
Taxa incertae sedis: Metastrongyloidea - Sphaeronematidae
Overview of orders (12)

Araeolaimida - Benthimermithida - Chromadorida - Desmodorida - Desmoscolecida - Dorylaimia - Enoplia - Monhysterida - Oxyurida - Plectida - Rhabditida - Rhaptothyreida - Teratocephalida
References

Abolafia, J., Ruiz-Cuenca, A.N., Fernandes, B.M.M., Cohen, S.C. & Cárdenas, M.Q. 2015: Description of free-living marine nematodes found in the intestine of fishes from the Brazilian coast. Zootaxa 3948(3): 549–572. DOI: 10.11646/zootaxa.3948.3.8. Preview (PDF) Reference page.
Acosta-Virgen, K., López-Caballero, J., García-Prieto, L. & Mata-López, R. 2015: Helminths of three species of opossums (Mammalia, Didelphidae) from Mexico. Zookeys, 511: 131–152. DOI: 10.3897/zookeys.511.9571 Full article view Reference page.
Adams, B.J. et al. 2014: Ecological biogeography of the terrestrial nematodes of Victoria Land, Antarctica. ZooKeys, 419: 29–71. DOI: 10.3897/zookeys.419.7180 Reference page.
Anderson, R.C. 2000: Nematode parasites of vertebrates: their development and transmission. 2nd edition. CABI Publishing. ISBN 0-85199-421-0 Google books
Boufahja, F.; Vitiello, P.; Aissa, P. 2014: More than 35 years of studies on marine nematodes from Tunisia: a checklist of species and their distribution. Zootaxa 3786(3): 269–300. DOI: 10.11646/zootaxa.3786.3.3 Reference page.
De Ley, P.; Blaxter, M.L. 2004: A new system for Nematoda: combining morphological characters with molecular trees, and translating clades into ranks and taxa. Pp. 633-653 in: Cook, R.; Hunt, D.J. (eds) Proceedings of the Fourth International Congress of Nematology, 8-13 June 2002, Tenerife, Spain. Nematology monographs and perspectives, (2). Leiden: E.J. Brill.
Fugassa, M.H. 2015. Checklist of helminths found in Patagonian wild mammals. Zootaxa 4012(2): 271–328. DOI: 10.11646/zootaxa.4012.2.3. Preview (PDF) Reference page.
Dewi, K.; Purwaningsih, E. 2013: A checklist of nematode parasites from Indonesian murids. Zootaxa 3608(7): 531–546. DOI: 10.11646/zootaxa.3608.7.1 Reference page.
Gagarin, V.G. 2018. An annotated checklist of the free-living nematodes from mangrove thickets of Vietnam. Zootaxa 4403(2): 261–288. DOI: 10.11646/zootaxa.4403.2.3 Reference page.
González, C.E. & Inés, H.M. 2015: Checklist of nematode parasites of amphibians from Argentina. Zootaxa 3980(4): 451–476. DOI: 10.11646/zootaxa.3980.4.1. Preview (PDF) Reference page.
Hernández-Orts, J.S., Viola, M.N.P., Garcia, N.A., Crespo, E.A., González, R., García-Varela, M. & Kuchta, R. 2015: A checklist of the helminth parasites of marine mammals from Argentina. Zootaxa 3936(3): 301–334. DOI: 10.11646/zootaxa.3936.3.1. Reference page.
Hodda, M. 2007: Phylum Nematoda. Pp. 265-293 In: Zhang, Z.-Q. & Shear, W.A. (eds) Linnaeus tercentenary: progress in invertebrate taxonomy. Zootaxa, 1668: 1–766. Abstract & excerpt
Hodda, M. 2011: Phylum Nematoda Cobb 1932. Pp 63–95 In
Zhang, Z.-Q. (ed.) 2011. Animal biodiversity: an outline of higher-level classification and survey of taxonomic richness. Zootaxa 3148: 1–237. Open access. Reference page . Zootaxa 3148: 63–95. PDF Reference page.
Malysheva, S.V., Mohagan, A.B. & Spiridonov, S. 2015. Heth impalutiensis n. sp. (Nematoda: Ransomnematoidea: Hethidae) a millipede parasite from Central Mindanao, Philippines. Zootaxa 3926(1): 100–110. DOI: 10.11646/zootaxa.3926.1.4 Reference page.
Meldal, B.H.M.; Debenham, N.J.; De Ley, P.; De Ley, I.T.; Vanfleteren, J.R.; Vierstraete, A.R.; Bert, W.; Borgonie, G.; Moens, T.; Tyler, P.A.; Austen, M.C.; Blaxter, M.L.; Rogers, A.D.; Lambshead, P.J.D. 2007: An improved molecular phylogeny of the Nematoda with special emphasis on marine taxa. Molecular phylogenetics and evolution, 42: 622–636. DOI: 10.1016/j.ympev.2006.08.025
Moleón, M.S., Kinsella, J.M., Moreno, P.G., Ferreyra, H.D.V., Pereira, J., Pía, M. & Beldomenico, P.M. 2015. New hosts and localities for helminths of carnivores in Argentina. Zootaxa 4057(1): 106–114. DOI: 10.11646/zootaxa.4057.1.6. Preview (PDF) Reference page.
Nermuť, J., Půža, V., Mráček, Z. & Lewis, E. 2016. Alloionema californicum n. sp. (Nematoda: Alloionematidae): a new alloionematid from USA. Zootaxa 4184(3): 505–516. DOI: 10.11646/zootaxa.4184.3.5. Reference page.
Pinacho-Pinacho, C.D., Garcia-Varela, M., Hernandez-Orts, J.S., Mendoza-Palmero, C.A., Sereno-Uribe, A.L., Martinez-Ramirez, E., Andrade-Gomez, L., Hernandez-Cruz, E. & Pérez-Ponce de León, G. 2015. Checklist of the helminth parasites of the genus Profundulus Hubbs, 1924 (Cyprinodontiformes, Profundulidae), an endemic family of freshwater fishes in Middle-America. Zookeys 523: 1–30. DOI: 10.3897/zookeys.523.6088 Preview (PDF) Reference page.
Porazinska, D.L. et al. 2010: Linking operational clustered taxonomic units (OCTUs) from parallel ultra sequencing (PUS) to nematode species. Zootaxa, 2427: 55–63. Preview
Santos, C.P. & Gibson, D.I. 2015: Checklist of the Helminth Parasites of South American Bats. Zootaxa 3937(3): 471–499. DOI: 10.11646/zootaxa.3937.3.3. Reference page.
Venekey, V.; Fonseca-Genevois, V.G.; Santos, P.J.P. 2010: Biodiversity of free-living marine nematodes on the coast of Brazil: a review. Zootaxa, 2568: 39–66. Preview
2011: Zootaxa, 3103: 57–68. Preview
2011: Zootaxa, 3107: 1–37. Preview
Xu, Y.M.; Zhao, Z.Q.; Wang, J.M. 2013: An index to new genera and species of Nematoda in Zootaxa from 2007 to 2012. Zootaxa 3646(2): 160–170. DOI: 10.11646/zootaxa.3646.2.4 Reference page.
Zeng, Y. et al. 2012: Taxonomy and morphology of plant-parasitic nematodes associated with turfgrasses in North and South Carolina, USA. Zootaxa 3452: 1–46. Preview PDF Reference page.
Zullini, A. 2012: What is a nematode? Zootaxa 3363: 63–64. Preview Reference page.

Additional references

Ansari, K.G.M.T. & Bhadury, P. 2017. An updated species checklist for free-living marine nematodes from the world’s largest mangrove ecosystem, Sundarbans. Zootaxa 4290(1): 177–191. DOI: 10.11646/zootaxa.4290.1.11. Reference page.
Arai, H.P. & Smith, J.W. 2016. Guide to the Parasites of Fishes of Canada Part V: Nematoda. Zootaxa 4185(1): 1–274. DOI: 10.11646/zootaxa.4185.1.1. Full article (PDF) ISBN 978-1-77670-004-2 (paperback); ISBN 978-1-77670-005-9 (Online edition). Reference page.
Besteiro, C. & Ayora, M. 2017. Checklist of the Free-Living Marine Nematodes of the Iberian Peninsula (north east Atlantic). Zootaxa 4347(2): 228–254. DOI: 10.11646/zootaxa.4347.2.2. Reference page.
Doweld, A.B. 2016. Dogielophis, a replacement name for Dogielina Sobolev 1950 (Nematoda) non Bogdanowicz & Woloszynova 1949 (Foraminifera). Zootaxa 4114(1): 81–82. DOI: 10.11646/zootaxa.4114.1.5. Reference page.
Ghaderi, R. & Karegar, A. 2016. One new and three known species of Geocenamus Thorne & Malek, 1968 (Nematoda: Merliniidae) from Iran. Zootaxa 4079(2): 151–178. DOI: 10.11646/zootaxa.4079.2.1.Reference page.
Gusakov, V.A. & Gagarin, V.G. 2017. An annotated checklist of the main representatives of meiobenthos from inland water bodies of Central and Southern Vietnam. I. Roundworms (Nematoda). Zootaxa 4300(1): 1–43. DOI: 10.11646/zootaxa.4300.1.1. Reference page.
Lopes, D.A., Corrêa-Gomes, D. & Knoff, M. 2017. Type material of Acanthocephala, Nematoda and other non-helminths phyla (Cnidaria, Annelida, and Arthropoda) housed in the Helminthological Collection of the Oswaldo Cruz Institute/ FIOCRUZ (CHIOC), Rio de Janeiro, Brazil, from 1979 to 2016. ZooKeys 711: 1—52. DOI: 10.3897/zookeys.711.14753. Reference page.
Panti-May, J.A., Digiani, M.C., Palomo-Arjona, E.E., Gurubel-González, Y.M., Navone, G.T., Machain-Williams, C., Hernández-Betancourt, S.F & Robles, M.D.R. 2018. A checklist of the helminth parasites of sympatric rodents from two Mayan villages in Yucatán, México. Zootaxa 4403(3): 495–512. DOI: 10.11646/zootaxa.4403.3.4 Reference page.
Pieterse, A., Malan, A.P., Kruitbos, L.M., Sirgel, W. & Ross, J.L. 2017. Nematodes associated with terrestrial slugs from canola fields and ornamental nurseries in South Africa. Zootaxa 4312(1): 194–200. DOI: 10.11646/zootaxa.4312.1.12. Reference page.
Spratt, D.M. & Beveridge, I. 2016. Helminth parasites of Australasian monotremes and marsupials. Zootaxa 4123(1): 1–198. DOI: 10.11646/zootaxa.4123.1.1 Reference page.
Venekey, V. 2017. Updates on information about free-living marine nematodes in Brazil: new records and comments on problems in taxonomic studies. Zootaxa 4337(1): 38–72. DOI: 10.11646/zootaxa.4337.1.2. Reference page.
Villares, G., Russo, V.L., de Ward, C.P., Milano, V., Mayashiro, L. & Mazzanti, R. 2016. Free-living marine nematodes from San Antonio Bay (Río Negro, Argentina). ZooKeys 574: 43-55. DOI: 10.3897/zookeys.574.7222.Reference page.

Links

Catalogue of Life: 2012 Annual Checklist
WoRMS (2010). Nematoda. In: Deprez, T. et al. (2005). NeMys. World Wide Web electronic publication. Accessed through: World Register of Marine Species on 2010-10-16

Vernacular names
Afrikaans: Rondewurm
Alemannisch: Fadewirmer, Faadewürmli
aragonés: Nematodo
asturianu: Nematodo
azərbaycanca: Yumru qurd, Nematod
Boarisch: Foonwyrmer
башҡортса: Йомро селәү
беларуская: Круглыя чэрві
български: Живи влакна
বাংলা: নেমাটোডা
bosanski: valjkasti crvi, obli crvi
буряад: Хилгааһан хорхой
català: Nematode
Cebuano: Ulod nga lingin
čeština: Hlístice
Cymraeg: Llyngyren gron
dansk: Rundorm
Deutsch: Fadenwürmer, Nematoden
Ελληνικά: Νηματόδεις
English: Nematodes, roundworm
español: Nematodo, gusano redondo
eesti: Ümarussid, Nematoodid
suomi: sukkulamado
Nordfriisk: Triadwirmer
français: Nématodes, Vers ronds
हिन्दी: सूत्रकृमि
hrvatski: Oblići
magyar: Fonálférgek
հայերեն: Կլոր որդեր
italiano: Nematoda
日本語: 線形動物
lietuvių: Apvaliosios kirmėlės, nematodai
latviešu: velteniskie tārpi, nematodes
македонски: Цевчести (кружни) црви
Bahasa Melayu: Cacing Gelang
Nederlands: Rondwormen
norsk: Rundorm
Diné bizaad: Táyiʼ naatʼiʼítsʼósí
polski: Nicienie
português: Nematelmintos, Nematelmintes, Nematódeos, Nemátodes, Nemátodos, Nematoides, Nematódios
română: Nematode, limbric
русский: Нематоды, Круглые черви
srpskohrvatski / српскохрватски: Valjkasti crvi, nematode
slovenčina: Hlístovce
slovenščina: Gliste
Kiswahili: mnyoo
தமிழ்: உருளைப்புழுக்கள்
тоҷикӣ: bilulod
Türkçe: Nematot
українська: Круглі черви
中文: 线形动物

The nematodes (/ˈnɛmətoʊdz/ NEM-ə-tohdz or /ˈniːm-/ NEEM- Greek: Νηματώδη; Latin: Nematoda) or roundworms constitute the phylum Nematoda (also called Nemathelminthes),[2][3] with plant-parasitic nematodes also known as eelworms.[4] 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 their sister phylum Nematomorpha has kept the ancestral protostome Hox genotype, which shows that the reduction has occurred within the nematode phylum.[5]

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.[6][7] Estimates of the total number of extant species are subject to even greater variation. A widely referenced[8] article published in 1993 estimated there may be over 1 million species of nematode.[9] A subsequent publication challenged this claim, estimating the figure to be at least 40,000 species.[10] Although the highest estimates (up to 100 million species) have since been deprecated, estimates supported by rarefaction curves,[11][12] together with the use of DNA barcoding[13] and the increasing acknowledgment of widespread cryptic species among nematodes,[14] have placed the figure closer to 1 million species.[15]

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,[16] 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.[17][18][19][20][21] They represent 90% of all animals on the ocean floor.[22] 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.[23] 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.[23][24] They have been shown to play crucial roles in polar ecosystems.[25][26] The roughly 2,271 genera are placed in 256 families.[27] 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.[27]

Nathan Cobb, a nematologist, described the ubiquity of nematodes on Earth 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.[28]

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),[29] from Ancient Greek νῆμα (nêma, nêmatos, 'thread') and -eiδἠς (-eidēs, 'species'). It was treated as family Nematodes by Burmeister (1837).[29]

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,[30] created by Rudolphi (1808).[31] 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.[29] 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.[32] 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.[33]

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,[34] 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.[35]
Nematode systematics

Due to the lack of knowledge regarding many nematodes, their systematics is contentious. An early and influential classification was proposed by Chitwood and Chitwood[36]—later revised by Chitwood[37]—who divided the phylum into two classes—Aphasmidia and Phasmidia. These were later renamed Adenophorea (gland bearers) and Secernentea (secretors), respectively.[38] 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[39] suggested the existence of five clades:[40]

Dorylaimida
Enoplia
Spirurina
Tylenchina
Rhabditina

The Secernentea seem to be a natural group of close relatives, while the "Adenophorea" appear to be a paraphyletic assemblage of roundworms that retain a good number of ancestral traits. The old Enoplia do not seem to be monophyletic, either, but do 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.[41]

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

Phylum Nematoda

Basal order Monhysterida
Class Dorylaimida
Class Enoplea
Class Secernentea
Subclass Diplogasteria (disputed)
Subclass Rhabditia (paraphyletic?)
Subclass Spiruria
Subclass Tylenchia (disputed)
"Chromadorea" assemblage

Later work has suggested the presence of 12 clades.[42] The Secernentea—a group that includes virtually all major animal and plant 'nematode' parasites—apparently arose from within the Adenophorea.

In 2019, a study identified one conserved signature indel (CSI) found exclusively in members of the phylum Nematoda through comparative genetic analyses.[43] The CSI consists of a single amino acid insertion within a conserved region of a Na(+)/H(+) exchange regulatory factor protein NRFL-1 and is a molecular marker that distinguishes the phylum from other species.[43]

A major effort by a collaborative wiki called 959 Nematode Genomes is underway to improve the systematics of this phylum.[44]

An analysis of the mitochondrial DNA suggests that the following groupings are valid[45]

subclass Dorylaimia
orders Rhabditida, Trichinellida and Mermithida
suborder Rhabditina
infraorders Spiruromorpha and Oxyuridomorpha

In 2022 a new classification of the entire phylum Nematoda was presented by M. Hodda. It was based on current molecular, developmental and morphological evidence.[46]
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.[47] 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.[48]: 271 The body is often ornamented with ridges, rings, bristles, or other distinctive structures.[49]

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.[50]

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.[50]
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.[50]

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.[50]

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.[50]
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.[50]

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.[50]
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.[50]

The nervous system is also the only place in the nematode body that contains cilia, which are all nonmotile and with a sensory function.[51][52]

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.[50]

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.[50]
Reproduction
Extremity of a male nematode showing the spicule, used for copulation, bar = 100 µm[53]

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.[50]

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.[50]

Nematodes as a whole possess a wide range of modes of reproduction.[54] Some nematodes, such as Heterorhabditis spp., undergo a process called endotokia matricida: intrauterine birth causing maternal death.[55] 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.[55]

The nematode model species C. elegans, C. briggsae, and Pristionchus pacificus, among other species, exhibit androdioecy,[56] which is otherwise 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.[50]
Free-living species

Different free-living species feed on materials as varied as bacteria, 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.[57]

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.[58]

Plant-parasitic nematodes include several groups causing severe crop losses, taking 10% of crops worldwide every year.[59] 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 its 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.[60] 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.[citation needed]

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.[61] 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.[62] 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.[63]
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
File:Anthelmintic effect of papain on Heligmosomoides bakeri.ogvPlay media
Anthelmintic effect of papain on Heligmosomoides bakeri

A number of intestinal nematodes cause diseases affecting human beings, including ascariasis, trichuriasis, and hookworm disease. Filarial nematodes cause filariases. Furthermore, studies have shown that parasitic nematodes infect American eels causing damage to the eel's swim bladder,[64] dairy animals like cattle and buffalo,[65] and all species of sheep.[66]
Soil ecosystems
Further information: Soil ecology

About 90% of nematodes reside in the top 15 cm (6") 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.[47]

One group of carnivorous fungi, the nematophagous fungi, are predators of soil nematodes.[67] They set enticements for the nematodes in the form of lassos or adhesive structures.[68][69][70]
Survivability

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.[71][72] In a research project published in 2012, it was found that the Antarctic Nematodes (P. davidi) was able to withstand intracellular freezing depending on how well it was fed. When compared between fed and starved nematodes, the survival rate increased in the fed group and decreased in the starved group.[73]
See also

Biological pest control – Controlling pests using other organisms
Capillaria – Genus of roundworms
List of organic gardening and farming topics
List of parasites of humans
Toxocariasis – Illness of humans caused by larvae of the dog, the cat or the fox roundworm: A helminth infection of humans caused by the dog or cat roundworm, Toxocara canis or Toxocara cati
Worm bagging – Process where nematode eggs hatch within the parent and the larvae proceed to consume and emerge from the parent

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