identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
7D2487ECFFB91B7BFF3EFB44FAEFFE2C.text	7D2487ECFFB91B7BFF3EFB44FAEFFE2C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Acanthodrilidae Claus 1880	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Acanthodrilidae Claus, 1880</p>
            <p> The  Acanthodrilidae is the second most speciose earthworm family – 746 species and 48 subspecies in 68 genera. Csuzdi (1996) divided it into three subfamilies:  Acanthodrilinae , Octochaetinae and Benhamiinae, but the molecular work of James and Davidson (2012) provided evidence that suggested raising the Behamiinae to family level (  Benhamiidae ). Hence, we consider  Benhamiidae as a separate family here. Diplocardinae Michaelsen 1899 has been proposed, but differently defined. The African, Central and South American, and Austral-Asian octochaetine worms surely belong to  Acanthodrilinae (Buckley et al. 2011; James &amp; Davidson 2012). Various other subfamilies were proposed by Blakemore (2013), but to date there has been limited acceptance of these subfamilies due to unresolved taxonomic issues and disagreement, and pending further molecular work within the  Acanthodrilidae (see Fragoso &amp; Rojas 2016, 2019). </p>
            <p> The endemic taxa of  Acanthodrilinae can be found throughout the southern continents (South America, South Africa, Madagascar, Australia, New Zealand, New Caledonia and the Antarctic Islands), as well as in the USA, Mexico and the Caribbean Islands (Fragoso &amp; Rojas 2016, 2019; Buckley et al. 2011). However, they are completely missing from Europe and the Northern part of Asia (the Palearctic Region). This widely distributed Gondwanan subfamily includes 41 genera and ca. 580 species (updated from Fragoso &amp; Rojas 2016). From continental Central America and the Caribbean Islands and Mexico, we know 14 genera (  Balanteodrilus ,  Borgesia ,  Diplocardia ,  Diplotrema ,  Exxus ,  Kaxdrilus ,  Larsonidrilus ,  Lavellodrilus ,  Mayadrilus ,  Protozapotecia ,  Neotrigaster, Trigaster ,  Zapatadrilus ,  Zapotecia ) and around 120 species (Fragoso &amp; Rojas 2016, 2018, 2019; Cervantes et al. 2016). Further endemic genera are found in Eastern African countries and in Madagascar (  Howascolex and Vazimbascolex, with four and one species, respectively; Csuzdi et al. 2016; Hong et al. 2019). </p>
            <p> In USA and Mexico there are over 50 species of  Diplocardia , and in Mexico, the following additional native genera can be found:  Balanteodrilus (3 species),  Diplotrema (6 species),  Kaxdrilus (3 species),  Larsonidrilus (2 species),  Lavellodrilus (3 species),  Mayadrilus (1 species),  Microscolex (3 species),  Protozapotecia (4 species), and  Zapotecia (2 species) (Reynolds 2020; Fragoso &amp; Rojas 2016, updated with new species). In Central America and the Caribbean, there are the following native genera:  Balanteodrilus (1 sp.),  Diplotrema (4 species),  Kaxdrilus (4 species),  Parachilota (2 species),  Protozapotecia (3 species) and  Zapotecia (1 sp.), while in South America, we find mostly  Chilota (26 species),  Diplotrema (9 species),  Microscolex (10 species) and  Yagansia (21 species) in the Andean and Pampean regions of Chile and Argentina (Fragoso &amp; Rojas 2016, 2018; Cervantes &amp; Fragoso 2018).  Exxus is of unknown provenance, but suspected to be Caribbean or Central American. </p>
            <p> In Africa, the  Acanthodrilinae are distributed mainly in South Africa comprising 5 genera (  Chilota, Eodriloides ,  Microscolex ,  Parachilota and  Udeina ) and ca. 110 species (Plisko &amp; Nxele 2015). In Australia, native acanthodrilinae include six native genera (  Diplotrema, Kayarmacia ,  Microscolex, Neodiplotrema, Rhododrilu s and  Torresiella ) and approximately 120 species (expanded from Fragoso &amp; Rojas 2016). However, the genus  Diplotrema is in need of further work (particularly molecular) within the  Acanthodrilinae , which will probably end up splitting off the Neotropical species present in Mexico from those in Oceania (Fragoso &amp; Rojas 2019). </p>
            <p> At least two  Acanthodrilinae species –  Microscolex dubius (Fletcher) , and  M. phosphoreus (Dugés) , probably originally from Southern South America (Argentina) – are cosmopolitan, although they tend to be more common in subtropical and temperate climate regions (Rota et al. 2018b). These species were described from specimens collected outside their native range, and have been widely reported from North American and European countries (e.g., Portugal, Spain, France, Italy, Hungary, Serbia, Bulgaria, Albania and Greece), Australia, New Zealand and South Africa. The species  M. phosphoreus is a well-known widespread bioluminescent worm, but recent work has shown the need for more detailed analysis of its taxonomy (both morphology and genetics) and questioned the identity of samples deposited throughout the world, due to the presence of cryptic morphs that may be different species (Rota et al. 2018b). However, this high morphological plasticity and deep genetic differentiation can also be due to its well-known parthenogenetic reproduction mode (as in many peregrine species) (Gates 1972). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB91B7BFF3EFB44FAEFFE2C	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBF1B7BFF3EFE6CFF13FAA8.text	7D2487ECFFBF1B7BFF3EFE6CFF13FAA8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Almidae Duboscq 1902	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Almidae Duboscq, 1902</p>
            <p> Together with  Acanthodrilidae this is the most widely distributed family of earthworms (excluding exotic species), being found in tropical Africa, South-East Asia, South America and the Caribbean. It includes 64 species and four subspecies in seven genera. The genera  Alma (16 spp.) and  Callidrilus (3 spp.) are exclusively African, while the monospecific genus  Progizzardus is unique to its type locality in India (Nair et al. 2010). The genus  Glyphidrilus (36 spp.) is found mainly in Southeast Asia (Myanmar, Laos, Cambodia, Thailand, Indonesia, China, Singapore, India, Sri Lanka), with one species  G. stuhlmanni Michaelsen , present in Africa (Tanzania). In South America and the Caribbean there are three genera present:  Drilocrius , with seven species spread from Costa Rica to Southeastern Brazil,  Glyphidrilocrius (1 sp.) in Amazonia, and  Guarani (1 sp.; see below) in southernmost Brazil and probably Uruguay (Grosso &amp; Brown 2007). </p>
            <p> Omodeo (2000) suggested restricting  Almidae to  Alma , moving African  Callidrilus and Asian  Glyphidrilus to the Glyphidrilidae, which also included the South American  Drilocrius ,  Glyphidrilocrius and  Areco , but  Guarani does not fit into either of his family definitions (Lima &amp; Rodríguez 2007).  Areco also does not fit with the Glyphidrilidae as defined by Omodeo (2000). Furthermore, Omodeo placed  Criodrilus ,  Lutodrilus ,  Sparganophilus ,  Biwadrilus , and  Komarekiona in an expanded  Criodrilidae , but all of those latter are phylogenetically well-separated from  Criodrilus (James &amp; Davidson 2012) and each is the sole genus in their respective monogeneric families. At present we cannot clarify phylogenetic relationships among the genera either now or historically assigned to  Almidae and/or Glyphidrilidae, because no single phylogenetic analysis includes adequate representation. For now,  Almidae are placed between  Glossoscolecidae s.s. and  Rhinodrilidae in molecular phylogenies; where  Alma and  Guarani are present in the same analysis, they are sister taxa (James &amp; Davidson 2012; Anderson et al. 2017). Will additional genera from South America (Steffen et al. 2018; Ferreira et al. 2023) change the picture? Preliminary indications say no. </p>
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	https://treatment.plazi.org/id/7D2487ECFFBF1B7BFF3EFE6CFF13FAA8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBF1B7AFF3EF8FAFD75FCF8.text	7D2487ECFFBF1B7AFF3EF8FAFD75FCF8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Arecoidae James, Csuzdi & Brown 2023	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Arecoidae James, Csuzdi &amp; Brown, 2023 Fam. nov.</p>
            <p> Type genus:  Areco Righi, Ayres &amp; Bittencourt, 1978</p>
            <p> Diagnosis:  Crassiclitellata with quadrangular body, and dorsal post-clitellar groove. Four pairs of closelypaired, regularly distributed hook-shaped setae. Dorsal pores present. Genital pores microscopic. Long muscular esophagus, but no gizzard. No calciferous glands, no prostates or copulatory pouches. Intestine begins in XXXVII, typhlosole present. Pretesticular spermathecae, ovaries in XIII. Moniliform hearts in segments VIII to XI. No subneural vessel. Nephridia holoic, without bladders. Metandric, with one pair of testicles and seminal funnels in segment XI. Seminal vesicles in XII to XV. </p>
            <p> Etymology: This new family name derives from the genus name  Areco which with the species name  reco is derived from “arecoreco”, originally in the Tupi indigenous language, meaning to confuse or to mix something up (Drumond 1952). </p>
            <p> Considerations: The intriguing aqua-megadrile (sensu Jamieson 1988) species  Areco reco was described by Righi et al. (1978) from four specimens collected at the Reserva Ducke near Manaus, Amazonas (Brazil) in 1975. Type specimens are deposited in the Instituto Nacional de Pesquisas da Amazonia (INPA) collection in Manaus. The authors placed the species tentatively in  Sparganophilidae , but emphasized that the exact position of  Areco was uncertain. They claimed similarity with Glyphydrilocrius by shape of body and organization of digestive system, and with  Sparganophilus by presence of pretesticular spermathecae, though this is a feature shared with several other South American families (e.g.,  Glossoscolecidae ,  Rhinodrilidae ). Furthermore,  Sparganophilus and Glyphydrilocrius are holandric, while  Areco is metandric. Additional  Areco specimens were collected at the type locality by S. James and S. Tapia-Coral in 2012 (Erséus et al. 2020), and molecular phylogenomic analyses revealed it to be sister to  Rhinodrilidae , and far from  Sparganophilidae and other semi-aquatic families (Erséus et al. 2020). Nonetheless, Arecoidae shows important genetic divergence and major morphological differences with  Rhinodrilidae , lacking gizzard and calciferous glands, so we propose here the erection of this new monotypic family to accommodate its only species and genus. </p>
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	https://treatment.plazi.org/id/7D2487ECFFBF1B7AFF3EF8FAFD75FCF8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBE1B79FF3EFC18FDF2FEC0.text	7D2487ECFFBE1B79FF3EFC18FDF2FEC0.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Benhamiidae Michaelsen 1897	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Benhamiidae Michaelsen, 1897</p>
            <p> Native species of the  Benhamiidae (351 species and 6 subspecies in 20 genera) are mainly restricted to subSaharan Africa, Oceania, Central America and northern South America (Csuzdi 2010). However, a few  Dichogaster (including the type species of the genus) are also known from the Pacific islands of Fiji and Samoa (Easton 1984; James &amp; Davidson 2012). In Africa, the native  Benhamiidae are present mainly in the tropical region with 16 genera (  Afrogaster ,  Agastrodrilus ,  Benhamia ,  Benhamiona ,  Dichogaster ,  Dudichiodrilus ,  Guineoscolex ,  Loksaia ,  Millsonia ,  Monogaster ,  Monothecodrilus ,  Omodeona ,  Pickfordia ,  Pickfordiella ,  Reginaldia and  Wegeneriella ) and ca. 250 species. From the Neotropics, i.e., the Caribbean islands, Central America, Mexico, and Northern South America we know five genera (  Dichogaster ,  Eutrigaster ,  Neogaster ,  Omodeoscolex , and  Wegeneriona ) and around 100 species, mainly of  Dichogaster and  Eutrigaster , many of which show high endemism rates, particularly on the Caribbean islands. The diversity of the minute South-American species is certainly underestimated due to a lack of sampling, especially in Amazonia, where recent work (in French Guyana), revealed several new species, that are presently being described. </p>
            <p> Several species in the family  Benhamiidae , particularly in the genus  Dichogaster , are widespread anthropochores in the tropics, as their native ranges were probably originally in Central and Eastern Africa (Gates 1972; Csuzdi 2010). These species were probably widely dispersed during the centuries of commercial product exchanges between Africa and other continents, where ships could have transported soil in planted pots containing these generally parthenogenetic species. More recent transport with manure piles or agricultural equipment may also have led to the abundance of  Dichogaster gracilis (Michaelsen) ,  Dichogaster bolaui (Michaelsen) ,  Dichogaster saliens (Beddard) , and  Dichogaster affinis (Michaelsen) in many no-tillage sites in Southern and Central Brazil, where they may reach abundances well over 100 individuals m-2 (Bartz et al. 2009; Bartz et al. 2014; Santos et al. 2018). Although  Dichogaster spp. are generally restricted to warm and humid tropical regions, several species have been reported from greenhouses in temperate climates and at least one species (  D. bolaui ) was considered a domicole (adapted to human homes) species, as it was found in bathtubs, showers and sewage pipes in Hungary, Ireland, Finland, Sweden and Israel (Terhivuo 1991; Erséus et al. 1994; Rota &amp; Schmidt 2006; Csuzdi et al. 2008). In fact, the type locality of  D. bolaui is Hamburg, where it was found in fermenting bark at a factory (Michaelsen 1891).  Dichogaster annae (Horst) is an epigeic species, common in vermicomposting ventures in tropical countries such as Brazil (James &amp; Guimar„es 2010), but its distribution is probably much wider than presently known or reported, due to the lack of recognition by worm composters, and the little knowledge of its life-cycle and biology.  Dichogaster modiglianii (Rosa) is an epi-endogeic species also with wide distribution (Africa, Southeast Asia, Australia, Oceania, Central America, Caribbean, Southern North America (Blakemore 2010), and was recently found in several Amazonian sites, associated with Pre-Columbian human activities (Conrado 2018). Specimens of  D. bolaui were also recently reported from a remote and human-free Amazonian rainforest area in Southern French Guyana, highlighting the potential of these cosmopolitan species to establish stable populations that persist centuries after original introduction by humans (Maggia et al. 2021). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBE1B79FF3EFC18FDF2FEC0	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBD1B79FF3EFE1AFF14FD67.text	7D2487ECFFBD1B79FF3EFE1AFF14FD67.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Biwadrilidae Jamieson 1971	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Biwadrilidae Jamieson, 1971</p>
            <p> This monogeneric family includes only one species,  Biwadrilus bathybates (Stephenson) , known only from the Lake Biwa region in Japan. It was originally described as a  Criodrilus species , and Blakemore (2008b) transferred it back to  Criodrilidae based on new material and re-analysis of previously observed material. However, molecular analysis shows this family solidly placed as the sister family to  Kynotidae , and therefore quite distant phylogenetically from the  Criodrilidae (James &amp; Davidson 2012) , hence we maintain it within  Biwadrilidae , following Jamieson (1971, 1988). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBD1B79FF3EFE1AFF14FD67	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBD1B79FF3EFCBFFB0AFBC2.text	7D2487ECFFBD1B79FF3EFCBFFB0AFBC2.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Criodrilidae Vejdovsky 1884	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Criodrilidae Vejdovský, 1884</p>
            <p> The Palearctic family  Criodrilidae includes mainly aquatic species in a single genus,  Criodrilus with two valid species,  C. lacuum from Europe, and  C. ghianae Qiu &amp; Bouché , from Mediterranean Algeria. The former species, may be among the longest living of earthworms, known to achieve 46 years of age when kept in aquaria (Timm 2020). The species is widely distributed in Europe and common all around the Mediterranean, with its northernmost distribution in Latvia (Smiljkov et al. 2005; Blakemore 2008b; Atanacković et al. 2013; Valchovski 2013; Mısırlıoğlu 2017; Timm 2020). Outside its native range,  C. lacuum has only been reported from potted plants in Baltimore (USA) (McKey-Fender &amp; MacNab 1953). Previous reports of this species from Brazil (Knäpper 1976; Knäpper &amp; Porto 1979) actually refer to  G. camaqua , a species of  Almidae (see above, and Ferreira et al. 2023). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBD1B79FF3EFCBFFB0AFBC2	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBD1B79FF3EFB0FFD30FA0E.text	7D2487ECFFBD1B79FF3EFB0FFD30FA0E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Diporodrilidae Bouche 1970	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Diporodrilidae Bouché, 1970</p>
            <p> This monogeneric family with three species and two subspecies was erected by Bouché (1970) for specimens collected in the Mediterranean islands of Corsica and Sardinia, from where they are endemic. Recent sampling in Corsica revealed several new lineages and species that must still be described (Marchán et al., 2022b). The validity of this family was also re-affirmed with recent molecular (Anchor-Hybrid Enrichment) analyses, which placed it as sister to the  Lumbricidae (Marchán et al., 2022c) . </p>
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	https://treatment.plazi.org/id/7D2487ECFFBD1B79FF3EFB0FFD30FA0E	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBD1B79FF3EFA4BFA99F84E.text	7D2487ECFFBD1B79FF3EFA4BFA99F84E.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Eudrilidae Claus 1880	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Eudrilidae Claus, 1880</p>
            <p> The  Eudrilidae is a peculiar earthworm family with internal fertilisation (Clausen 1965; Sims 1969). It consists of 45 genera and 305 species (plus 21 subspecies) distributed in tropical Africa from south of the Sahara to the Kalahari Desert and northern South Africa (Sims 1987). There are only two species in the family regarded as widely introduced peregrines:  Eudrilus eugeniae (Kinberg) and  Hyperiodrilus africanus Beddard. The first species, commonly called the "African Nightcrawler" is widespread, found mainly in vermiculture outside its native range (West Africa) throughout the tropics and sub-tropics in Latin America, the Caribbean, Madagascar, Sri Lanka, India, Philippines, Malaysia, Indonesia, Vietnam and Australia (Blakemore 2015). Rarely has this species been found inhabiting soils (Blakemore 2015) and not compost beds, and its survival under these conditions probably requires high moisture and the presence of abundant litter, or organic resources, which are its major food source. The second species,  H. africanus can also be found frequently in compost-beds and high organic content soils, but its distribution is more restricted, being known from Western (Ivory Coast, Nigeria, Gabon) and Central Africa (Congo, Democratic Republic of Congo, Angola) (Tondoh &amp; Lavelle 2005) and Brazil (Righi 1972; Sousa et al. 2020). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBD1B79FF3EFA4BFA99F84E	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBC1B78FF3EFF21FEF0FD68.text	7D2487ECFFBC1B78FF3EFF21FEF0FD68.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Glossoscolecidae Michaelsen 1900	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Glossoscolecidae Michaelsen, 1900</p>
            <p> In its more restricted sense, after the splitting up of the  Rhinodrilidae by James (2012), the  Glossoscolecidae family is distributed mainly in continental Central and South America from Panama to Northern Argentina and Uruguay. The first species described from Latin America belongs to this family,  Glossoscolex giganteus Leuckart , a large earthworm from Southeastern Brazil. In fact, the genus contains a relatively large proportion of large-bodied (&gt; 30 cm long) species (18 out of 58 known species; Feijoo &amp; Brown 2023). So far, native species are known in the Caribbean Islands only from Guadeloupe (James &amp; Gamiette 2016), but they may likely occur on other islands. The family includes six genera (  Enantiodrilus, Fimoscolex, Glossodrilus ,  Glossoscolex, Holoscolex , and  Righiodrilus ) and 156 species (plus 9 subspecies). One widespread species,  Enantiodrilus borellii Cognetti (with which both  Diaguita species ,  D. vivianae Righi and  D. michaelseni Cordero were synonymized by Moreno et al. 2005) may constitute a potentially invasive species in the tropics, considering its distribution from Argentina to Venezuela (Fragoso &amp; Brown 2007). As the family occurs in a region with high endemicity (Lavelle &amp; Lapied 2003), there is a large potential to find many new species and possibly genera, with further sampling efforts, particularly in the Andean region and Northern South America, but also in the Atlantic Forest region of Southeastern Brazil (Silva et al. 2017). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBC1B78FF3EFF21FEF0FD68	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBC1B78FF3EFCA9FB5EFB60.text	7D2487ECFFBC1B78FF3EFCA9FB5EFB60.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Hormogastridae Michaelsen 1900	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Hormogastridae Michaelsen, 1900</p>
            <p> The family  Hormogastridae was recently revised by Marchán et al. (2018) using an integrative approach including ecological, morphological and molecular data, and was shown to include nine genera (  Ailoscolex ,  Boucheona ,  Carpetania ,  Diazcosinia ,  Hemigastrodrilus ,  Hormogaster, Norana ,  Vignysa, Xanina ) and 37 species (plus three subspecies). The genus  Ailoscolex , with its single known species  Ailoscolex lacteospumosus Bouché , formerly in the family  Ailoscolecidae was basal to all  Hormogastridae but kept within the family. The genera show rather restricted distribution and little geographic overlap, with the exception of Norana with  Hormogaster and  Boucheona (Marchán et al. 2018) . Overall, the family is restricted to Europe and Northern Africa, being found in Southern France, the Spanish Iberian Peninsula, Corsica, Sardinia, the Tuscan Archipelago, mainland Italy, Sicily, Algeria and Tunisia. So far, no  Hormogastridae have been found in Portugal. Given the restricted range of most known species, the future discovery of new taxa in this family is highly probable (see Marchán et al. 2023b). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBC1B78FF3EFCA9FB5EFB60	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBC1B78FF3EFAA1FEDCF9AC.text	7D2487ECFFBC1B78FF3EFAA1FEDCF9AC.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Kazimierzidae Nxele & Plisko 2016	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Kazimierzidae Nxele &amp; Plisko, 2016</p>
            <p> This recently erected family of earthworms, which includes 25 nominal species all in the single genus  Kazimierzus , is restricted to the Western Cape and Northern Cape provinces, including the Namaqualand areas, along the Atlantic region of South Africa. This is a hotspot of biodiversity (Myers et al. 2000), with considerable topographical and botanic diversity, which will probably still lead to the discovery of new earthworm species, as observed by Nxele et al. (2017). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBC1B78FF3EFAA1FEDCF9AC	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBC1B78FF3EF9EDFA9CF8A0.text	7D2487ECFFBC1B78FF3EF9EDFA9CF8A0.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Komarekionidae Gates 1974	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Komarekionidae Gates, 1974</p>
            <p> There is only one species in this monogeneric Nearctic family:  Komarekiona eatoni Gates. It is found only in the mid-Atlantic states west to southern Illinois, USA (Gates 1974; Reynolds 2020). Interestingly, the specimens east of the Smoky Mountains are amphimictic while those west of the Smokies are parthenogenetic (Reynolds 2020). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBC1B78FF3EF9EDFA9CF8A0	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFBC1B77FF3EF8E1FF14FF5C.text	7D2487ECFFBC1B77FF3EF8E1FF14FF5C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Kynotidae Jamieson 1971	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Kynotidae Jamieson, 1971</p>
            <p> This endemic family appears to be restricted to Madagascar (Razafindrakoto et al. 2017) and includes a single genus (  Kynotus ) and 22 species. The description of  K. verticillatus Perrier , was not adequate and it cannot be assigned to any other named species or any other genus or species. It was described as  Acanthodrilus “ pas du tout développé et paraissant réduit aux quatre pénis formés de soies courbes caractéristiques jusqu'ici des vers de ce genre ” (Perrier 1872). </p>
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	https://treatment.plazi.org/id/7D2487ECFFBC1B77FF3EF8E1FF14FF5C	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB31B76FF3EFEFCFEE1FEB8.text	7D2487ECFFB31B76FF3EFEFCFEE1FEB8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Lumbricidae Rafinesque-Schmaltz 1815	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Lumbricidae Rafinesque-Schmaltz, 1815</p>
            <p> The  Lumbricidae is the phylogenetically youngest family in the subclass of  Oligochaeta . The family perhaps originated in the Palearctic but there is a well-supported clade native to Eastern North America. Overall, the  Lumbricidae family comprises some 615 species and 74 subspecies belonging to 47 genera (Brown et al. 2023), although the lumbricid taxonomy is still controversial and not yet settled (Bouché 1972; Mršić 1991; Qiu &amp; Bouché 1998; Csuzdi &amp; Zicsi 2003; Domínguez et al. 2015; de Sosa et al. 2019; Marchán et al. 2022a; Marchán et al. 2022c). Around 33 cosmopolitan species of the family are widespread and often invasive in numerous regions (Blakemore 2009), such as North America, Australia, New Zealand, South Africa, Southern South America, and even in equatorial countries at higher elevation (e.g., Zicsi 2007). </p>
            <p> In North America there are both native and non-native species and genera. The native genera are  Bimastos and  Eisenoides with 15 and two species, respectively. There are 11 genera of non-native invasive lumbricids in North America (Fragoso &amp; Rojas 2014; Reynolds 2020, 2022), and 10 genera of invasives in South America (Fragoso &amp; Brown 2007). In Europe, centers of diversity of lumbricids are situated in the Pyrenees and the Balkan Peninsula, as well as in the Carpathians and the Caucasus (Kvavadze 1985, 1999; Rota &amp; de Jong 2015). The biodiversity of the Balkans is the largest in Europe (Griffiths et al. 2004), due to the complex geological history and the specific geographical position with several biogeographical regions, each characterized by specific ecological, climatic and geomorphological conditions, as well as a great variety of habitats (Trakić et al. 2016). </p>
            <p>For the last 2 million years, repeated glaciations have destroyed the biotas of much of northern and alpine Europe, and on the major mountain ranges such as the Carpathians, Caucasus, and Pyrenees. The present European earthworm fauna consists of the survivors in unglaciated, non-permafrosted areas, and their descendants who colonized the rest of the continent after the end of the last (W̧rm or Wisconsinan) glaciation. There is no way to know how many species were driven to local or global extinction. Repeated cycles could have contributed to inrefuge speciation by changing vegetation zonation. However, the pre-Pleistocene conditions were probably adequate to support earthworm populations throughout Europe and even into the Arctic, including the North American Arctic, as subtropical vegetation fossils from the Eocene occur on Ellesmere Island (Eberle &amp; Greenwood 2012; Francis 1991).</p>
            <p>Today, most earthworm scientists agree that the original lumbricid fauna was significantly destroyed during the glacial period in much of Europe. Today's lumbricid fauna come from various elements, differing both in their historical age and in their origins. Namely, the present faunal elements are fragments of modified fauna from the Tertiary Period, that are thought to have originated in the Paleocene or Eocene. These are species that, due to their adaptability to specific conditions, have survived to this day. Such relic species are now present in the Balkans, the Pyrenees and the Apennine peninsula, the northwestern part of Africa (Maghreb), the southern part of France, Sardinia, Corsica, the southern parts of Switzerland and the Czech Republic, Turkey and the central parts of Asia (Omodeo 1952, 1956, 1961, 1988; Bouché 1972, 1983; Mısırlıoğlu 2017; Mršić &amp; Šapkarev 1988; Mršić 1991; Marchán et al. 2020; Marchán et al. 2022b). In addition to relic species, there are also "modern" species that are thought to have appeared in the Miocene and later. A greater expansion of new "modern" species occurred during interglacial and postglacial periods, mainly in the Holocene (Mršić 1991).</p>
            <p> On the Balkan Peninsula there are 90 endemic species with the largest share in  Dendrobaena (25) and  Allolobophora (20) (Trakić et al. 2016; Popovic et al. 2022), while 39 have been discovered in the basin of the Carpathians, mostly Dacian endemics. Of these, 12 species are of the genus  Octodrilus whose distribution center is located in the Apuseni Mountains in the southern part of the Carpathians (Csuzdi et al. 2011). Other genera appear to be endemic from southern France to the northern Iberian Peninsula. The most speciose is presently  Scherotheca with 42 species/subspecies recognized to date, though many other species are still expected to be found (e.g., eight new species were recently described from Corsica; Marchán et al. 2023a). </p>
            <p> The ecologically important  Lumbricidae have been explored using various tools by numerous researchers. Despite significant molecular research, there are still many species that do not have a stable taxonomic status, most of which relate to archaic species with unique taxonomic characteristics and disjunctive distributions (Marchán et al. 2022c). Answers to some of these questions are expected in the near future, and will certainly lead to a better understanding of many concerns regarding the origin and dynamics of the development of the  Lumbricidae family as a whole. </p>
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	https://treatment.plazi.org/id/7D2487ECFFB31B76FF3EFEFCFEE1FEB8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB21B76FF3EFED8FAC5FDC4.text	7D2487ECFFB21B76FF3EFED8FAC5FDC4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Lutodrilidae McMahan 1976	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Lutodrilidae McMahan, 1976</p>
            <p> There is only one species in this semi-aquatic family,  Lutodrilus multivesiculatus McMahan , with a distribution restricted to four parishes/counties in eastern Louisiana, USA (McMahan 1976; Anderson et al. 2017). It has developed caudal respiration similar to that observed in  Alma and  Drilocrius (both in the family  Almidae ), a special respiratory adaptation to survive in its mostly anaerobic habitat, consisting of areas with large accumulations of fine-textured mud and organic debris along the margins of slow-moving water courses (McMahan 1998). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB21B76FF3EFED8FAC5FDC4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB21B76FF3EFD1EFC3EF92B.text	7D2487ECFFB21B76FF3EFD1EFC3EF92B.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Megascolecidae Rosa 1891	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Megascolecidae Rosa, 1891</p>
            <p> The  Megascolecidae is the most speciose family of earthworms (2,208 spp. and 127 subspecies) and includes 85 genera. The most speciose genera are  Amynthas (713 spp./ssp.),  Metaphire (242 spp./sspp.),  Pheretima (171 spp./ sspp.), and  Megascolex (104 sp. /sspp.). The available molecular studies all support its monophyly and show just slight differentiation inside the family. Therefore, given the contradictory taxonomic divisions (e.g., Jamieson et al. 2002; Blakemore 2013) here we do not distinguish subordinate family rank taxa. </p>
            <p> The  Megascolecidae show a predominantly Australasian distribution being most speciose in Australia (ca. 45 genera and 400 species), New Zealand (8 genera and 50 spp.), Eastern and Southeastern Asia (over 1,500 spp.) (Sims 1980; Jamieson 2000). But interestingly, the North American megascolecids seem to be basal to several modern megascolecid groups such as the Asian  Amynthas and Australian  Perionychella ,  Megascolides , and  Diporochaeta (Buckley et al. 2011) . These include  Arctiostrotus (7 species),  Argilophilus (9 species),  Chetcodrilus (3 species),  Kincaidodrilus (1 species),  Macnabodrilus (2 species),  Nephrallaxis (2 species) and  Toutellus (4 species), present mostly in the Pacific Northwestern States of the United States and Southern Canada (near Vancouver), but also in California (Reynolds, 2020, 2022). </p>
            <p> At least 27 species in the genera  Amynthas and  Metaphire , as well as  Perionyx excavatus Perrier ,  Pithemera bicincta (Perrier) ,  Polypheretima elongata (Perrier) ,  Polypheretima taprobanae (Beddard) and  Pontodrilus litoralis (Grube) are probably some of the most widely distributed earthworms in the world (Blakemore, 2009). In fact, many of these species were described from specimens collected outside their native ranges in Asia: for instance,  Metaphire californica (Kinberg) from San Francisco,  Amynthas gracilis (Kinberg) from Rio de Janeiro,  Amynthas corticis (Kinberg) from Hawaii, and  P. elongata from Peru. Therefore, they had been already extensively transported by humans from Asia to other continents even before they were recorded from their home ranges. The presence of parthenogenetic morphs, and wide plasticity in terms of soil and habitat preferences in several of these species means that they are excellent invaders, particularly in subtropical, tropical and even temperate regions (Brown et al. 2006; Chang et al. 2017). Some species, such as  Pi. bicincta may have been extensively transported with Polynesians that sailed throughout the Pacific Ocean, as well as in flotsam or sailing ship ballast (Blakemore 2007; James 2011). Several  Amynthas and  Metaphire species have invaded cold-temperate regions, including the continental USA, causing extreme alterations in the native ecosystems (Chang et al. 2021). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB21B76FF3EFD1EFC3EF92B	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB11B75FF3EFF21FCC7FDC4.text	7D2487ECFFB11B75FF3EFF21FCC7FDC4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Microchaetidae Michaelsen 1900	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Microchaetidae Michaelsen, 1900</p>
            <p> The family  Microchaetidae is closely related to the two other Microchaetoidea families  Tritogeniidae and  Kazimierzidae (Plisko 2013; Nxele et al. 2016), and consists of three genera (  Geogenia ,  Microchaetus and  Proandricus ) and 81 species (plus six subspecies) distributed exclusively in temperate and Mediterranean Southern Africa. They are known from Northern South Africa near the vicinity of the Limpopo River down to the southern limit of the continent, in all provinces as well as in Lesotho and Swaziland (Plisko 2013). The three genera appear to have a rather geographically separate distribution, with little overlap. None of the known species have been reported outside of this rather restricted range, although Plisko (2013) predicted that  Microchaetidae would also be found in Zimbabwe, Botswana and Mozambique. Interestingly, some of the longest known earthworm species in the world, including  Microchaetus vernoni Plisko (measuring up to 2.6 m when alive) belong to this family, which contains a reasonably large number of giant (very large or long) earthworm species, some with over 1,000 segments, particularly in the genus  Microchaetus (Plisko 1992, 2013). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB11B75FF3EFF21FCC7FDC4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB11B75FF3EFD05FD2FFBD8.text	7D2487ECFFB11B75FF3EFD05FD2FFBD8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Moniligastridae Claus 1880	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Moniligastridae Claus, 1880</p>
            <p> Although moniligastrids are not considered part of the  Crassiclitellata since their clitella have only a single layer like the  Enchytraeidae , they tend to have much larger individual body size and mass than enchytraeids and are phylogenetically sister to the  Crassiclitellata (James &amp; Davidson 2012; Schmelz et al. 2021). The family is mainly distributed in the Oriental region from south India east to the Philippines and north to southern Siberia and Japan (Gates 1972; Perel 1997). It includes 185 species (and 19 subspecies), distributed among five genera (  Desmogaster ,  Drawida ,  Eupolygaster ,  Hastirogaster ,  Moniligaster ), of which  Drawida is the most widely distributed and speciose (162 spp./sspp.). Three species,  Drawida barwelli (Beddard) ,  Drawida japonica (Michaelsen) , and  Drawida nepalensis Michaelsen , are cosmopolitan, but of these,  D. barwelli is the most widely distributed. It is also sometimes mentioned under its synonymous names  D. bahamensis (Beddard) , or  D. beddardi (Rosa) , being reported from Africa (Csuzdi 2005), Australia, South-East Asia, Mexico, Central America, the Caribbean, and several Pacific Islands (Blakemore et al. 2014; Csuzdi et al. 2017). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB11B75FF3EFD05FD2FFBD8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB11B74FF3EFB79FC05FE2C.text	7D2487ECFFB11B74FF3EFB79FC05FE2C.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Ocnerodrilidae Beddard 1891	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Ocnerodrilidae Beddard, 1891</p>
            <p> The widespread  Ocnerodrilidae family, with 37 genera and 172 species (plus four subspecies), sister taxon to the  Megascolecidae +  Acanthodrilidae s.l. clade (James &amp; Davidson 2012), was last reviewed by Fragoso &amp; Rojas (2009) and Hernández-García et al. (2018), who provided keys to the genera known until then.Two sub-families (Ocnerodrilinae and Malabariinae) were proposed by Gates (1966) and their definitions expanded by Gates (1972) and Fragoso and Rojas (2009). Ocnerodrilinae is more speciose and wider spread, while Malabariinae includes species only from India, China and Myanmar (Fragoso &amp; Rojas 2009), without extramural glands and internal calciferous lamellae. With the exception of several peregrine species with worldwide distribution, all endemic genera and species of Ocnerodrilinae are confined to South and Central America, sub-Saharan Africa, India (  Curgiona ), and the Seychelles (  Maheina ). A large number of new species and several new genera were recently found in Brazil (James et al. 2023; HernándezGarcía et al. 2018), and it is likely that further sampling particularly in Northern South America, and in Brazil’s Northeastern region will reveal many more. The majority (27) of the known genera occur in Latin America, while nine genera are known from Africa and five from Asia (India, China and Myanmar). In Latin America, many of the smaller and pigmented ocnerodriles, particularly in the genera  Kerriona and  Eukerria inhabit wetlands or bromeliads, and some of them are quite resistant to disturbance, being present in intensively plowed rice or no-tillage row-crop fields in Southern Brazil (Bartz et al. 2013; Bartz et al. 2014; Ferreira et al. 2023; Lima &amp; Rodríguez 2007). </p>
            <p> There are nine widespread anthropochorous ocnerodriles:  Eukerria eiseniana (Rosa) ,  Eukerria kuekenthali (Michaelsen) ,  Eukerria saltensis (Beddard) ,  Eukerria stagnalis (Kinberg) ,  Gordiodrilus elegans Beddard ,  Gordiodrilus habessinus Michaelsen ,  Gordiodrilus paski Stephenson ,  Nematogenia lacuum Beddard , and  Ocnerodrilus occidentalis Eisen , that typically live in wet or saturated soils, generally close to water sources. Some of these are of uncertain origin, being possibly of South America or Africa but, in any case, are of Gondwanan or Central Pangean origin (Fragoso &amp; Rojas 2009). The presence of many parthenogenetic morphs in some species (e.g.,  O. occidentalis ), has resulted in extensive synonymies which must be checked (James et al. 2023), although the use of molecular methods may help unravel some of these. The species  Nematogenia panamaensis Eisen was synonymized with  N. lacuum by Righi (1984a), because variations between the two species were included in a group of specimens collected at the same location in Mato Grosso do Sul, Brazil. Similar to  O. occidentalis further work is warranted on these poorly known ocnerodriles, particularly using more detailed genetic methods, in order to confirm the presence of potential cryptic species (Fragoso &amp; Rojas 2009). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB11B74FF3EFB79FC05FE2C	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB01B74FF3EFE66FDE4FAA7.text	7D2487ECFFB01B74FF3EFE66FDE4FAA7.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Rhinodrilidae Benham 1890	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Rhinodrilidae Benham, 1890</p>
            <p> Recent changes in classification (James &amp; Davidson 2012) moved many genera from  Glossoscolecidae to  Rhinodrilidae (James 2012) . This family now includes 38 genera and some 376 species (plus seven subspecies) including one widespread invasive species,  Pontoscolex corethrurus (M̧ller), probably the most widely distributed earthworm in the world (James 2011; Taheri et al. 2018b). Native species of this family occur from Argentina (Mischis 2007) up to Mexico (Fragoso &amp; Rojas 2014), including several on Caribbean Islands (Rodríguez et al. 2007), although none are known from Chile (Zicsi &amp; Csuzdi 2007). Studies on the genetic diversity of several  Pontoscolex species highlighted the importance of proper identification of  P. corethrurus , requiring at least barcoding, to certify species status (Taheri et al. 2018a). Species belonging to  P. corethrurus must conform to the genetic lineage L1, as identified in Taheri et al. (2018a) and James et al. (2019). The genus  Martiodrilus with 88 known species and subspecies is the most speciose, occurring from Panama in the north to Peru in the south, and to French Guyana in the east (Fragoso &amp; Brown 2007), with a large number of species still to be found with additional sampling efforts in Amazonia and the Andes region. The following other speciose  Rhinodrilidae genera by decreasing order of species richness are:  Rhinodrilus (52 spp./sspp.),  Andiorrhinus (48 spp./sspp.) and  Andiodrilus (40 spp./sspp.). Together with  Rhinodrilus ,  Martiodrilus is also remarkable for the presence of several very large-bodied earthworm species (Brown &amp; James 2007; Zicsi 2007). One other widespread species of  Rhinodrilidae is worth mentioning here:  Urobenus brasiliensis Benham , found in Paraguay (Brown &amp; Fragoso, 2007) and in Brazil from Manaus in the Amazon (R̂mbke et al. 1999; Zicsi et al. 2001) to Pelotas in the Pampa biome (Santos et al. 2019). This cryptic species requires further morphological and molecular work in order to separate the many genetic lineages that have little morphological differentiation (da Silva et al. 2017). Furthermore, the genus  Alexidrilus Righi , was recently synonymized with  Urobenus Benham , and its two species,  A. lourdesae Righi and  A. littoralis Ljungstr ̂m, with  U. brasiliensis (Ferreira et al. 2023) . </p>
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	https://treatment.plazi.org/id/7D2487ECFFB01B74FF3EFE66FDE4FAA7	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB01B74FF3EF907FE29F862.text	7D2487ECFFB01B74FF3EF907FE29F862.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Sparganophilidae Michaelsen 1918	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Sparganophilidae Michaelsen, 1918</p>
            <p> This family native to North America has only one genus (  Sparganophilus ), with 12 species and 2 subspecies (Reynolds 1980, 2008). At least one species,  Sparganophilus tamesis Benham (  Sparganophilus eiseni Smith , is a junior synonym of  S. tamesis ; see Rota et al. 2016), is cosmopolitan, and found mainly in limicole habitats, throughout the USA (within and outside of its native range), Mexico (Ikeda et al. 2020), Canada (Reynolds 2022) and in several European countries including Germany, France, England, Switzerland, Italy and Spain (Rota et al. 2018a; Bouché &amp; Qiu 1998). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB01B74FF3EF907FE29F862	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB71B73FF3EFF21FB08FEE4.text	7D2487ECFFB71B73FF3EFF21FB08FEE4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Tritogeniidae Plisko 2013	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Tritogeniidae Plisko, 2013</p>
            <p> The family  Tritogeniidae was erected by Plisko(2013) as part of important housekeeping duties within the  Microchaetidae , and includes two genera,  Michalakus with a single species and the others all belonging to  Tritogenia . All 39 species are endemic to Southern Africa, with only one species newly described from Botswana (Nxele et al. 2018). </p>
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	https://treatment.plazi.org/id/7D2487ECFFB71B73FF3EFF21FB08FEE4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
7D2487ECFFB71B73FF3EFE3EFE04FD66.text	7D2487ECFFB71B73FF3EFE3EFE04FD66.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Tumakidae Righi 1995	<html xmlns:mods="http://www.loc.gov/mods/v3">
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            <p> Tumakidae Righi, 1995</p>
            <p> The monogeneric  Tumakidae family has only three known species,  Tumak hammeni Righi ,  Tumak amari Celis &amp; Rangel-Ch., and  Tumak congorum Celis &amp; Rangel-Ch., found in relatively drier, lower-elevation forests in Central Colombia and the Caribbean region, along the Magdalena River valley (Righi 1995; Celis &amp; Rangel-Ch. 2015). Given the relatively small amount of remaining forest fragments of its native habitat in Colombia, due primarily to agricultural expansion and pastures for cattle, further efforts are needed to ensure adequate conservation of the few species known. Additional sampling efforts are also needed to discover if there are any other species present along its potential distribution range. </p>
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	https://treatment.plazi.org/id/7D2487ECFFB71B73FF3EFE3EFE04FD66	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Misirlioğlu, Mete;Reynolds, John Warren;Stojanović, Mirjana;Trakić, Tanja;Sekulić, Jovana;James, Samuel W.;Csuzdi, Csaba;Decaëns, Thibaud;Lapied, Emmanuel;Phillips, Helen R. P.;Cameron, Erin K.;Brown, George G.	Misirlioğlu, Mete, Reynolds, John Warren, Stojanović, Mirjana, Trakić, Tanja, Sekulić, Jovana, James, Samuel W., Csuzdi, Csaba, Decaëns, Thibaud, Lapied, Emmanuel, Phillips, Helen R. P., Cameron, Erin K., Brown, George G. (2023): Earthworms (Clitellata, Megadrili) of the world: an updated checklist of valid species and families, with notes on their distribution. Zootaxa 5255 (1): 417-438, DOI: 10.11646/zootaxa.5255.1.33, URL: http://dx.doi.org/10.11646/zootaxa.5255.1.33
