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Redescription of Ancistrus greeni (Siluriformes: Loricariidae), and description of a new species from the río Madre de Dios basin, Peru

ABSTRACT

A new species of Ancistrus is described from minor tributaries of the río Madre de Dios basin (Cusco - Madre de Dios - Puno), in Peru. The new species shares with A. greeni an uncommon unicusp dentition; but it is distinguished from A. greeni by a larger orbital diameter, deeper caudal peduncle, and larger adipose-fin spine. The redescription of A. greeni is provided, and its recognition along with the discovery of this new species increases to five the officially number of Ancistrus species from the río Madre de Dios basin. The lectotype and paralectotype of A. greeni are provided.

Keywords:
Amazon basin; Ancistrini; Armored catfish; Río Inambari basin; Taxonomy

RESUMO

Uma nova espécie de Ancistrus é descrita de pequenos tributários da bacia do rio Madre de Dios (Cusco - Madre de Dios - Puno), no Peru. A nova espécie compartilha com A. greeni uma dentição unicuspidada pouco comum e é diagnosticada de A. greeni pelo maior diâmetro orbital, maior altura do pedúnculo caudal e maior espinho da nadadeira adiposa. A redescrição de A. greeni é fornecida, e seu reconhecimento juntamente com a descoberta dessa nova espécie incrementam para cinco o número oficial de Ancistrus registradas para a bacia do rio Madre de Dios. O lectótipo e paralectótipo de A. greeni são fornecidos.

Palavras-chave:
Ancistrini; Bacia amazônica; Bacia do rio Inambari; Cascudo; Taxonomia

INTRODUCTION

Loricariidae is the largest family of the Siluriformes in the Neotropics. Loricariidae is widespread in Central and South America, ranging from Costa Rica in the north to Argentina in the south (Weber, 2003Weber C. Subfamily Hypostominae (Armored catfishes). In: Reis RE, Kullander SO, Ferraris CJ Jr., organizers. Check list of the freshwater fishes of South and Central America . Porto Alegre: Edipucrs ; 2003. p.351-72.). Ancistrus is one of the most species-rich loricariid genera, and diagnosed by having well-developed cheek spines, snout border naked and ornamented with fleshy tentacles. The general taxonomic knowledge of the genus is limited to incomplete descriptions and type material are often either lacking or poorly preserved.

Currently, three valid species are recognized from the río Madre de Dios basin: Ancistrus marcapatae (Regan, 1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350.), A. megalostomus Pearson, 1924, and A. montanus (Regan, 1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350.) (Bifi et al., 2019Bifi AG, de Oliveira RR, Py-Daniel LR. A new species of Ancistrus Kner, 1854 (Siluriformes: Loricariidae) from rio Madeira basin, Amazonas State, Brazil. Neotrop Ichthyol. 2019; 17(2):e180135. http://dx.doi.org/10.1590/1982-0224-20180135
http://dx.doi.org/10.1590/1982-0224-2018...
). Regan (1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350.) also described Chaetostomus maculatus from Rozmaiu, Upper Peru, but this type locality has never been found under that name. According to Fish-Muller (2003Fish-Muller S. Subfamily Ancistrinae (Armored catfishes). In: Reis RE, Kullander SO, Ferraris CJ Jr., organizers. Check list of the freshwater fishes of South and Central America. Porto Alegre: Edipucrs; 2003. p.373-400.) “Rozmaiu“ means Roz River in Quechua idiom, a language spoken by indigenous people living in Peru, Ecuador, Bolivia, Chile, Colombia and Argentina. However, Roz River was also not located. Therefore, Chaetostomus maculatus is only known from syntypes and its geographical distribution remains unknown, solely mentioned as río Roz basin (Fish-Muller, 2003Fish-Muller S. Subfamily Ancistrinae (Armored catfishes). In: Reis RE, Kullander SO, Ferraris CJ Jr., organizers. Check list of the freshwater fishes of South and Central America. Porto Alegre: Edipucrs; 2003. p.373-400.).

Posteriorly, Isbrücker (2001Isbrücker IJH, Seidel I, Michels JP, Schraml E, Werner A. Diagnose vierzehn neuer Gattungen der Familie Loricariidae Rafinesque, 1815 (Teleostei, Ostariophysi). DATZ-Sonderheft Harnischwelse. 2001; 2:17-24.) replaced the name Chaetostomus maculatus by Chaetostoma greeni, because the epithet was preoccupied by Chaetostomus (Ancistrus) cirrhosus var. maculata Steindachner, 1881. In a review of Chaetostoma, Lujan et al. (2015Lujan NK, Armbruster JW, Lovejoy N, Lopez-Fernandez H. Multilocus molecular phylogeny of the suckermouth armored catfishes (Siluriformes: Loridariidae) with a focus on subfamily Hypostominae. Mol Phylogenet Evol. 2015; 82:269-88. https://doi.org/10.1016/j.ympev.2014.08.020
https://doi.org/10.1016/j.ympev.2014.08....
) transferred C. greeni to Ancistrus greeni (Isbrücker, 2001) justified by the presence of seven branched dorsal-fin rays, three plate rows at the thinnest portion of the caudal peduncle, and the unplated snout.

During the expeditions to río Madre de Dios basin in Peru, a new species of Ancistrus was collected and the material deposited in Museo de Historia Natural de la Universidad Nacional Mayor de San Marcos (Lima, Peru), and is described herein. The new species possesses an uncommon tooth shape among congeners, only shared with A. greeni for which we provide a redescription.

MATERIAL AND METHODS

Measurements were taken using digital calipers to the nearest 0.1 mm, and are presented as percents of standard length (SL) or head length (HL). Counts were made under a stereomicroscope. Measurements and plate counts follow Fisch-Muller et al. (2001Fisch-Muller S, Mazzoni R, Weber C. Genetic and morphological evidences for two new sibling species of Ancistrus (Siluriformes: Loricariidae) in upper rio Tocantins drainage, Brazil. Ichthyol Explor Freshw. 2001; 12(4):289-304.) and Bifi et al. (2009Bifi AG, Pavanelli CS, Zawadzki CH. Three new species of Ancistrus Kner, 1854 (Siluriformes: Loricariidae) from the rio Iguaçu basin, Paraná State, Brazil. Zootaxa. 2009; 2275(1):41-59.), with addition of occipital-orbital distance (from tip of occipital process to posterior border of orbit). Body plate nomenclature was based on Schaefer (1997Schaefer SA. The Neotropical cascudinhos: systematics and biogeography of the Otocinclus catfishes (Siluriformes: Loricariidae). P Acad Nat Sci Phila. 1997; 148:1-120.), with modifications of Oyakawa et al. (2005Oyakawa OT, Akama A, Zanata AM. Review of the genus Hypostomus Lacépède, 1803 from rio Ribeira de Iguape basin, with description of a new species (Pisces, Siluriformes, Loricariidae). Zootaxa . 2005; 921(1):1-27. http://dx.doi.org/10.11646/zootaxa.921.1.1
http://dx.doi.org/10.11646/zootaxa.921.1...
). The map (Fig. 3) was prepared using both Google Earth v.7.3.2 and Quantum GIS v. 3.6.0, available at http://qgis.org. Image of teeth detail using a Leica M205A stereomicroscope coupled with a Leica DMC4500 and a Leica Application Suite V4.10.0 Interactive Measurement, Montage. Institutional acronyms: BMNH, Natural History Museum, London; ZMB, Zoological Museum, Berlin; CAS, California Academy of Sciences, San Francisco; INPA, Instituto Nacional de Pesquisas da Amazônia, Manaus; MCP, Museu de Ciências e Tecnologia, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre; MNRJ, Museu Nacional, Rio de Janeiro; MPUJ, Museo Javeriano de Historia Natural, Bogotá; MUSM, Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Lima; NMW, Naturhistorisches Museum, Wien; NUP, Coleção Ictiológica do Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura (Nupélia), Universidade Estadual de Maringá, Maringá.

RESULTS

Ancistrus greeni ( Isbrücker, 2001Isbrücker IJH, Seidel I, Michels JP, Schraml E, Werner A. Diagnose vierzehn neuer Gattungen der Familie Loricariidae Rafinesque, 1815 (Teleostei, Ostariophysi). DATZ-Sonderheft Harnischwelse. 2001; 2:17-24. )

(Figs. 1-2, Tab. 1)

Chaetostomus maculatusRegan, 1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350.:246, pl.14 (Fig. 4) [original description; type locality: Rozmaiu, Upper Peru].

Chaetostoma maculatum. -Isbrücker, 1980Isbrücker IJH. Classification and catalogue of the mailed Loricariidae (Pisces, Siluriformes). Amsterdam: Instituut voor Taxonomische Zoöogie, Universiteit van Amsterdam; 1980.:62 [check list]. -Ortega, Vari, 1986Ortega H, Vari RP. Annotated checklist of the freshwater fishes of Peru. Washington (DC): Smithsonian Institution Press; 1986.:17 [check list]. -Burgess, 1989Burgess WE. An atlas of freshwater and marine catfishes. A preliminary survey of the Siluriformes. New Jersey: T.F.H. Publications; 1989.:436 [check list]. -Isbrücker, 2001:26 [check list].

Chaetostoma greeniIsbrücker in Isbrücker et al., 2001Isbrücker IJH, Seidel I, Michels JP, Schraml E, Werner A. Diagnose vierzehn neuer Gattungen der Familie Loricariidae Rafinesque, 1815 (Teleostei, Ostariophysi). DATZ-Sonderheft Harnischwelse. 2001; 2:17-24.:24 [replacement name for Chaetostomus maculatusRegan 1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350., preoccupied by Chaetostomus (Ancistrus) cirrhosus var. maculata Steindachner 1881]. -Isbrücker 2001:26 [check list]. -Fish-Muller, 2003Fish-Muller S. Subfamily Ancistrinae (Armored catfishes). In: Reis RE, Kullander SO, Ferraris CJ Jr., organizers. Check list of the freshwater fishes of South and Central America. Porto Alegre: Edipucrs; 2003. p.373-400.:380 [check list]. -Ferraris, 2007Ferraris CJ. Checklist of catfishes, recent and fossil (Osteichthyes: Siluriformes), and catalogue of siluriform primary types. Zootaxa . 2007; 1418(1):1-628. http://dx.doi.org/10.11646/zootaxa.1418.1.1
http://dx.doi.org/10.11646/zootaxa.1418....
:228 [check list].

Ancistrus greeni. -Lujan et al., 2015Lujan NK, Armbruster JW, Lovejoy N, Lopez-Fernandez H. Multilocus molecular phylogeny of the suckermouth armored catfishes (Siluriformes: Loridariidae) with a focus on subfamily Hypostominae. Mol Phylogenet Evol. 2015; 82:269-88. https://doi.org/10.1016/j.ympev.2014.08.020
https://doi.org/10.1016/j.ympev.2014.08....
:673 [comments; new combination].

FIGURE 1
| Dorsal, lateral and ventral views (left to right) of Ancistrus greeni: BNHM 1903.10.12.3, female, 51.4 mm SL, lectotype; BNHM 1903.10.12.4, female, 44.8 mm SL, paralectotype.

FIGURE 2
| Ancistrus greeni, MUSM 57798, 74.8 mm SL, male, río Tono; MUSM 56232, 67.6 mm SL, female, quebrada San Isidro.

FIGURE 3
| Details of the teeth showing lack of lateral cusp in a. Ancistrus greeni and b. Ancistrus maldonadoi. Bars = 0.1mm.

Diagnosis. Ancistrus greeni is diagnosed from all congeners, except A. maldonadoi, by having unicuspid teeth (vs. bicuspid). Ancistrus greeni is diagnosed from A. maldonadoi by smaller eye (orbital diameter 8.8-13.0% of HL, vs. 13.8-20.6%); a slender caudal peduncle (depth of caudal peduncle 8.4-10.6% of SL, vs. 12.2-14.0%); smaller adipose-fin spine (adipose spine length 3.7-6.3% of SL, vs. 7.2-9.5%). Furthermore, A. greeni can be distinguished from the species described from río Madre de Dios basin by having 4-8 preadipose plates (vs. 2-3 in A. montanus); and smaller orbital diameter (8.8-13.0% of HL vs. 14.0-16.7% in A. marcapatae; and 16.9-20.1% in A. megalostomus).

Description. Morphometric data and counts in Tab. 1. Head and trunk moderately depressed with greatest body depth at supraoccipital. Dorsal profile of body convexly raising from tip of snout to dorsal-fin origin, then straight or slightly convex to adipose fin, and concave from that point to caudal fin. Ventral profile of body straight, slightly convex on caudal peduncle. Caudal peduncle compressed; slightly flattened ventrally.

TABLE 1
| Morphometric and meristic data of Ancistrus greeni. SD= standard deviation, N= number (including types)

Head moderately large and wide; snout large and rounded in dorsal view, with large naked margin bordered by dermal platelets on lateral portion in males. Adult males with middle- to large-sized tentacles, sometimes branched on dorsal region of snout. Females usually with two small tentacles on each side of snout border. Evertible cheek plates supporting (8-19) hypertrophied odontodes (cheek spines).

Eye small-sized, 8.6-11.9% of HL, dorsal orbit not raised; dorsolaterally positioned. Interorbital region slightly concave. Exposed portion of opercle roughly triangular, supporting odontodes; supra-opercular region with few platelets near compound pterotic.

Oral disk circular covered with small papillae; lower lip large almost reaching pectoral girdle, with papillae reducing in size toward its margin; maxillary barbel short, attached to lip by membrane and with reduced free tip. Branchial opening small. Premaxillary and dentary tooth rows from moderate to large width; teeth short, thin, numerous, unicuspid (Fig. 3A), curved inward. Only one small central buccal papilla positioned between premaxillae.

Head covered by dermal bones; dorsum covered by dermal plates, except at dorsal-fin base. Supraoccipital process limited posteriorly by first pair of predorsal plates and posterolaterally by the first plate of the mid-dorsal series. Trunk with five series of lateral plates, three lateral series on the narrowest portion of caudal peduncle. Mid-dorsal and mid-ventral series not surpassing adipose fin. Median series supporting lateral line. Short odontodes on fin rays and body plates. Ventral surface devoid of plates from snout tip to anal-fin insertion. Base of first anal-fin pterygiophore covered by skin.

Dorsal-fin origin situated slightly anterior to vertical through pelvic-fin origin; dorsal fin usually reaching preadipose plate when adpressed; dorsal-fin spine flexible, shorter than head length. Adipose-fin spine short, with small membrane. Pectoral-fin spine inflexible and slightly curved inward, with hypertrophied odontodes and tentacles on distal portion; pectoral fin reaching or slightly surpassing pelvic-fin origin when adpressed. Pelvic fin flexible and curved inward, depressed pelvic-fin unbranched ray surpassing origin of anal fin. Anal fin short. Caudal-fin margin obliquely truncate with ventral unbranched ray longer than dorsal one. Fin-ray formula: dorsal II,7; pectoral I,6; pelvic i,5; anal i,3-4; caudal i,14,i.

Color in alcohol. Body background color yellowish-brown to dark brown. Dorsal surface of head and trunk with rounded light small spots. Ventral surface of head and abdomen yellowish to light brown, brown on ventral surface of caudal peduncle. All fins with alternating dark and light spots on the rays, sometimes organized into transverse bands.

Sexual dimorphism. Largest male and female with 85.2 mm and 74.5 mm SL, respectively. Mature males have small- to middle-sized tentacles on dorsal region and border of snout. Females sometimes with fewer and shorter tentacles than males limited to one series on lateral border of snout, usually two to four on each side of snout. Males have smaller dentary length 21.8-27.1% of HL (mean = 25.0%) than females 26.1-31.4 % of HL (mean= 27.9%).

Geographical distribution. Ancistrus greeni is only known from the río Madre de Dios and río Inambari basins (Fig. 5).

Conservation status. Ancistrus greeni occurs along a well-conserved region, with good water quality and little or no human pressure. Thus, considering the good environmental conditions of the known area of occurrence for the species, we suggest that A. greeni be classified as LC (Least Concern) in the International Union for Conservation of Nature (IUCN) categories and criteria (IUCN, 2019International Union for Conservation of Nature (IUCN). Standards and petitions subcommittee. Guidelines for using the IUCN Red List categories and criteria. Version 14 [Internet]. Gland; 2019. Available from: http://cmsdocs.s3.amazonaws.com/RedListGuidelines.pdf
http://cmsdocs.s3.amazonaws.com/RedListG...
) of extinction risk.

Material examined. All from Peru: Lectotype [designated here]: BMNH 1903.10.12.3, female, 51.4 mm SL, syntype of Chaetostomus maculatusRegan, 1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350., “Rozmaiu, Upper Peru”, Kalinowski. Paralectotype [designated here]: BMNH 1903.10.12.4, female, 44.8 mm SL, syntype of Chaetostomus maculatus Regan, 1904, “Rozmaiu, Upper Peru”, Kalinowski. Non-type specimens: río Madre de Dios basin: INPA 58909, 8, 30.1-61.9 mm SL (4, 55.1-61.9 mm SL), Cuzco, río Inambari basin, tributary of río Araza, main road crossing vicinity of Quincemil, 13º18’52”S 70º49’13”W, 25 Jul 2004, M. Sabaj, N. Salcedo, B. Rengifo, M. Arce; MUSM 25426, 12, 31.2-55.6 mm SL (1, 55.6 mm SL), Tambopata, río Inambari basin, quebrada Miraflores, 13º21’41”S 70º53’40”W, 25 Jul 2004, M. Hidalgo; MUSM 26312, 2, 31.9-85.2 mm SL (1, 85.2 mm SL); Quispicanchi, Camanti, río Araza basin, quebrada Sirihua, 13º23’46”S 70º53’59”W, 17 Out 2005, M. Hidalgo; MUSM 56232, 7, 34.0-74.5 mm SL (5, 51.6-74.5 mm SL), Carabaya, Ollachea, San Gaban, río Inambari basin, quebrada San Isidro, 13º37’45”S 70º26’46”W, 12 Out 2006, M. Hidalgo; MUSM 56233, 1, 82.8 mm SL, Carabaya, Ollachea, San Gaban, río Inambari basin, quebrada San Isidro, 13º37’45”S 70º26’46”W, 12 Out 2006, M. Hidalgo; MUSM 57367, 1, 73.6 mm SL, Carabaya, San Gaban, río Inambari basin, quebrada Yuri Yuri, 13º33’09”S 70º26’15”W, 13 Out 2006, M. Hidalgo; MUSM 57771, 8, 39.0-62.4 mm SL (4, 51.9-62.4 mm SL), Paucartambo, Kosñipata, río Quita Calzon, 13º02’01”S 71º31’32”W, 11 May 2006, M. Hidalgo; MUSM 57776, 1, 53.6 mm SL, Paucartambo, Kosñipata, quebrada Euaraya, 13º02’05”S 71º31’01”W, 11 May 2006, M. Hidalgo; MUSM 57794, 15, 27.5-64.8 mm SL (4, 54.6-64.8 mm SL), Paucartambo, Pillcopata, río Tono, 12º57’31”S 71º31’45”W, 13 May 2006, M. Hidalgo; MUSM 57798, 74.8 mm SL, Cusco Department, Paucartambo Province and District of Pillcopata, río Tono, 12º57’31”S 71º31’45”W, 13 May 2006, M. Hidalgo. Non-measured material: río Madre de Dios basin: MUSM 25428, 36, 24.7-55.6 mm SL, Tambopata, río Inambari basin, tributary of río Araza, 13º18’52”S 70º49’13”W, 25 Jul 2004, M. Hidalgo; MUSM 57372, 24, 24.5-40.0 mm SL, Carabaya, San Gaban, río Inambari basin, quebrada Prodocarpa, 13º25’50”S 70º19’45”W, 17 Out 2006, M. Hidalgo; MUSM 57750, 1, 37.5 mm SL, Paucartambo, Kosñipata, río San Pedro, 13º03’18”S 71º32’49”W, 10 May 2006, M. Hidalgo; MUSM 57758, 1, 42.4 mm SL, Paucartambo, Kosñipata, río Kosñipata, 13º03’23”S 71º32’40”W, 10 May 2006, M. Hidalgo; MUSM 58517, 11, 30.7-48.4 mm SL, Paucartambo, Kosñipata, quebrada km 160 AMD 16, 13º02’03”S 71º30’55”W, 12 May 2006, M. Hidalgo.

Ancistrus maldonadoi, new species

urn:lsid:zoobank.org:act:ED1397C7-5087-4EB8-94D8-326A42AEEE2D

(Fig. 4, Tab. 2)

Holotype. MUSM 57733, 114.7 mm SL, male, Peru, Manu District, Manu Province, río Madre de Dios basin, río Salvación, 12º55’05”S 71º27’36”W, 21 May 2006, M. Hidalgo.

Paratypes. Peru: río Madre de Dios basin: INPA 58921, 10, 40.6-101.9 mm SL (2, 68.6-101.9 mm SL), Manu, Parque Nacional del Manu, quebrada Culli, ca. 12º10’S 71º00’W, 5 Sep 1988, H. Ortega et al.; MPUJ 14358, 2, 68.9-72.7 mm SL, same data from holotype; MUSM 3763, 1, 87.0 mm SL, Manu, Salvación, quebrada Culli, 12º51’S 71º23’W, 5 Sep 1988, H. Ortega; MUSM 11620, 1, 77.5 mm SL, Sandia, Zona Reservada Tambopata Candamo, río Ebehua-baeji basin, río Beshuajali, 13º14’45”S 70º00’02”W, 25 Jul 1997, F. Chang; MUSM 11665, 2, 68.3-81.1 mm SL, Sandia, Zona Reservada Tambopata Candamo, río Ebehua-baeji basin, río Explorada, 13º14’34”S 70º00’01”W, 28 Jul 1997, F. Chang; MUSM 57732, 4, 58.0-64.2 mm SL (2, 61.6-64.2 mm SL), same data from holotype; MUSM 57832, 5, 61.5-147.2 mm SL (4, 74.5-147.2 mm SL), Paucartambo, Pillcopata, Tono, rio Huacarya, 12º55’05”S 71º27’36”W, 13 May 2006, M. Hidalgo; MUSM 58079, 2, 47.6-74.4 mm SL (1, 74.4 mm SL), Paucartambo, Pillcopata, río Queros, 12º56’41”S 71º21’22”W, 17 May 2006, M. Hidalgo; MUSM 58521, 6, 49.5-76.3 mm SL (2, 65.6-67.6 mm SL), Paucartambo, Pillcopata, Queros, río Sabaluyoc, 12º56’38”S 71º21’09”W, 17 May 2006, M. Hidalgo; MUSM 58671, 4, 40.9-83.0 mm SL (1, 83.0 mm SL), Quispicanchis, Camanti, río Inambari basin, stream without name, 13º11’29”S 70º33’16”W, 7 Aug 2010, M. Hidalgo; MZUSP 125014, 2, 85.1-85.4 mm SL, Paucartambo, Pillcopata, Queros, río Sabaluyoc, 12º56’38”S 71º21’09”W, 17 May 2006, M. Hidalgo; NUP 21719, 2, 70.4-75.6 mm SL, Paucartambo, Pillcopata, Queros, río Sabaluyoc, 12º56’38”S 71º21’09”W, 17 May 2006, M. Hidalgo.

FIGURE 4
| Ancistrus maldonadoi, MUSM 57733, holotype, 114.7 mm SL, male, Peru, Manu, río Madre de Dios basin, río Salvación.

FIGURE 5
| Partial map of Peru, showing the collecting sites of Ancistrus greeni (yellow) and Ancistrus maldonadoi (white). Star indicates type locality. Both symbols can represent more than one lot and/or locality.

Diagnosis. Ancistrus maldonadoi is diagnosed from congeners, except A. greeni, by having unicuspid teeth (vs. bicuspid). Ancistrus maldonadoi is diagnosed from A. greeni by larger orbital diameter 13.8-20.6% of HL (vs. 8.8-13.0%); and longer adipose-fin spine (adipose spine length 7.2-9.5% of SL vs. 3.7-6.3%). Furthermore, A. maldonadoi is distinguished from the species described from rio Madre de Dios basin by larger dentary width 25.9-31.4 % of HL (vs. 18.0-21.3% in A. montanus); deeper caudal peduncle (12.2-14.0% of SL; vs. 9.4-11.2% in A. marcapatae, 9.6-10.5% in A. megalostomus, and 10.1-10.7% in A. montanus).

Description. Morphometric data and counts in Tab. 2. Head and trunk moderately depressed with body depth greatest at supraoccipital. Dorsal profile of body convexly raising from tip of snout to dorsal-fin origin, then straight or slightly convex to adipose fin, and concave from that point to caudal fin. Ventral profile of body straight, slightly convex on caudal peduncle. Caudal peduncle compressed; slightly flattened ventrally.

TABLE 2
| Morphometric and meristic data of Ancistrus maldonadoi. SD= standard deviation, N= number (including holotype).

Head moderately large and wide; snout large and rounded in dorsal view, with large naked margin bordered by dermal platelets on lateral portion in males. Adult males with middle- to large-sized tentacles, sometimes branched on dorsal region of snout. Females usually with two small tentacles on each side of snout border. Evertible cheek plates supporting (14-26) hypertrophied odontodes (cheek spines).

Eye mid-sized, 13.8-20.6% of HL, dorsal orbit not raised; dorsolaterally positioned. Interorbital region slightly concave. Exposed portion of opercle roughly triangular, supporting odontodes; supra-opercular region with few platelets near compound pterotic.

Oral disk circular covered with small papillae; lower lip not reaching pectoral girdle, with papillae reducing in size toward margin; maxillary barbel short, attached to lip. Branchial opening small. Premaxillary and dentary tooth rows mid- to large; teeth short, thin, numerous, unicuspid (Fig. 3b), curved inward. Three specimens having tiniest lateral cusp, almost imperceptible (MUSM 11665, 2, 68.3-81.1 mm SL; MUSM 57732, 1, 59.6 mm SL). Only one small buccal papilla positioned between premaxillae.

Head covered by dermal bones; dorsum covered by dermal plates, except at dorsal-fin base. Supraoccipital process limited posteriorly by first pair of predorsal plates and posterolaterally by the first plate of the mid-dorsal series. Trunk with five series of lateral plates, three lateral series on the narrowest portion of caudal peduncle. Mid-dorsal and mid-ventral series not surpassing adipose fin. Median series supporting lateral line. Short odontodes on fin rays and body plates. Ventral surface devoid of plates from snout tip to anal-fin insertion. Base of first anal-fin pterygiophore covered by skin.

Dorsal-fin origin situated slightly anterior to vertical through pelvic-fin origin; dorsal fin usually reaching preadipose plate when adpressed; dorsal-fin spine flexible, shorter than head length. Adipose-fin spine short. Pectoral-fin spine inflexible and slightly curved inward, with hypertrophied odontodes and tentacles on its distal portion; pectoral fin surpassing pelvic-fin origin when adpressed. Pelvic fin flexible and curved inward, depressed pelvic-fin unbranched ray surpassing origin of anal fin. Anal fin short. Caudal-fin margin obliquely truncate with ventral unbranched ray longer than dorsal one. Fin-ray formula: dorsal II,7; pectoral I,6; pelvic i,5; anal i,4; caudal i,14,i.

Color in alcohol. Body background color yellowish-brown to greenish. Dorsal surface of head and trunk with rounded mid size spots, diameter similar or larger than pupil. Ventral surface of head and abdomen yellowish to light brown, brown on ventral surface of caudal peduncle. All fins with alternating dark and light spots on the rays, sometimes organized into transverse bands.

Sexual dimorphism. Largest male and female with 114.7 mm and 147.2 mm SL, respectively. Mature males have small- to middle-sized tentacles on dorsal region and border of snout. Females sometimes with fewer and shorter tentacles than males limited to one series on lateral border of snout, usually two to four on each side of snout.

Geographical distribution. Ancistrus maldonadoi is only known from the río Madre de Dios and río Inambari basins (Fig. 5).

Etymology. The specific name maldonadoi is a special dedication in memoriam to professor Dr. Javier Maldonado-Ocampo, Pontificia Universidad Javeriana in Bogotá, Colombia for his great contribution to the Neotropical Ichthyology.

Conservation status. Ancistrus maldonadoi occurs along a well-conserved region, with good water quality and little or no human pressure. Thus, considering the good environmental conditions of the known area of occurrence for the species, we suggest that A. maldonadoi be classified as LC (Least Concern) under the International Union for Conservation of Nature (IUCN) categories and criteria (IUCN Standards and Petitions Subcommittee, 2019) of extinction risk.

DISCUSSION

Regan (1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350.) described Chaetostomus maculatus (= A. greeni) using interorbital width 36.4-37.5% of HL and orbital diameter 11.1% of HL as diagnostic characters. Another character mentioned by Regan was the presence of 3 to 4 preadipose plates, a state not common in Ancistrus. However, an analysis of the syntypes revealed a presence of unicuspid tooth, a rare characteristic in members of the genus. We were not able to determine the type locality, because in the original description of A. greeni it was mentioned as “Upper Peru”, making it difficult to establish the true original sampling site of the types.

Eight valid species of Ancistrus were recorded from the rio Madeira basin (Fish-Muller, 2003Fish-Muller S. Subfamily Ancistrinae (Armored catfishes). In: Reis RE, Kullander SO, Ferraris CJ Jr., organizers. Check list of the freshwater fishes of South and Central America. Porto Alegre: Edipucrs; 2003. p.373-400.; Ferraris, 2007Ferraris CJ. Checklist of catfishes, recent and fossil (Osteichthyes: Siluriformes), and catalogue of siluriform primary types. Zootaxa . 2007; 1418(1):1-628. http://dx.doi.org/10.11646/zootaxa.1418.1.1
http://dx.doi.org/10.11646/zootaxa.1418....
; Bifi et al., 2019Bifi AG, de Oliveira RR, Py-Daniel LR. A new species of Ancistrus Kner, 1854 (Siluriformes: Loricariidae) from rio Madeira basin, Amazonas State, Brazil. Neotrop Ichthyol. 2019; 17(2):e180135. http://dx.doi.org/10.1590/1982-0224-20180135
http://dx.doi.org/10.1590/1982-0224-2018...
): A. dubius Eigenmann, Eigenmann, 1889; A. hoplogenys (Günther, 1864); A. dolichopterus Kner, 1854; A. marcapatae; A. megalostomus; A. miracollis Bifi, de Oliveira, Rapp Py-Daniel, 2019; A. montanus, and A. verecundus Fisch-Muller, Cardoso, Silva, Bertaco, 2005; and three additional species probably new to science: Ancistrus sp. “sideral”; Ancistrus sp.1 “baixinho” and Ancistrus sp.2 “sotério” (Zawadzki, Chamon, 2013Zawadzki CH, Chamon CC. Hypostominae. In: Queiroz LJ, Torrente-Vilara G, Ohara WM, Pires THS, Zuanon J, Doria CRC, organizers. Peixes do rio Madeira. São Paulo: Dialeto Latin American Documentary; 2013. p.302-37.). We added other two records to this river basin: A. greeni and A. maldonadoi, which share a unique feature among mentioned congeners: the uniscupid teeth.

In addition, Ancistrus greeni shares the presence of a keel formed by four or more preadipose plates with A. bufonius, A. marcapatae, A. tolima, and A. vericaucanus, but as already mentioned can be diagnosed from them by tooth shape (unicuspid vs. bicuspid). Furthermore, A. greeni can be distinguished from the most similar looking congener, A. maldonadoi, by having a colour pattern of small pale dots on a dark background (vs. large); dorsal-fin spine length 19.3-25.4% of SL, mean= 22.5% (vs. 24.1-27.6%, mean= 26.0%); and pectoral-fin spine length 21.5-26.6% of SL, mean= 23.9% (vs. 25.2-30.5%, mean= 26.6%). The sharing of unicuspid teeth suggests a close relationship between A. greeni and A. maldonadoi, as do the presence of three to eight preadipose plates, which is a state present in many species from the Andes, suggesting a close relationship among the Ancistrus species of the region.

The genus has many unsolved taxonomic problems and a complete study is necessary for fully understand this taxon. Similarly, there are few published studies that advance the taxonomic understanding of the loricariids from Peru. Moreover, we suggest that redescription of species poorly known, with improvement of diagnostic characters should be developed for the better comprehension of the taxonomy of Ancistrus, and the phylogenetic relationship within it.

Comparative material examined. Ancistrus abilhoai. Brazil: MZUSP 104116, 99.3 mm SL, holotype of A. abilhoaiBifi, Pavanelli, Zawadzki, 2009Bifi AG, Pavanelli CS, Zawadzki CH. Three new species of Ancistrus Kner, 1854 (Siluriformes: Loricariidae) from the rio Iguaçu basin, Paraná State, Brazil. Zootaxa. 2009; 2275(1):41-59.. Ancistrus agostinhoi. Brazil: MZUSP 104118, 96.1 mm SL, holotype of A. agostinhoi Bifi, Pavanelli, Zawadzki, 2009. Ancistrus aguaboensis. Brazil: INPA 377612, 1, 61.9 mm SL. Ancistrus alga. Peru: ANSP 8298, 1, 115.6 mm SL, syntype of Chaetostomus tectirostris Cope, 1872; ANSP 8300, 1, 110.0 mm SL, syntype of Chaetostomus tectirostris Cope, 1872; ANSP 16461-62, 2, 93.0-125.6 mm SL, syntypes of Chaetostomus alga Cope, 1872. Ancistrus amaris. Colombia: MPUJ 9369, 7, 52.2-77.1 mm SL. Ancistrus brevipinnis. Brazil: BMNH 1891.3.16.76, 78.8 mm SL, holotype of Xenocara brevipinnisRegan, 1904Regan CT. A monograph of the fishes of the family Loricariidae. Trans Zool Soc London. 1904; 17(3):191-350.. Ancistrus bufonius. Peru: MNHN 2227, 2, 109.9-112.5 mm SL, syntypes of Hypostomus calamita, 1840; MNHN 2228, 2, 103.1-104.3 mm SL, syntypes of Hypostomus bufonius Valenciennes, 1840. Ancistrus centrolepis. Colombia: ANSP 71709, 180.0 mm SL, holotype of A. baudensis Fowler, 1945; ANSP 71710, 179.9 mm SL, holotype of Pristiancistrus eustictus Fowler, 1945; BMNH 1910.7.11.122, 150.2 mm SL, syntype of A. centrolepis Regan 1913; BMNH 1913.10.1.58, 113.7 mm SL, syntype of A. centrolepis Regan, 1913; Panama: FMNH 9842, 165.6 mm SL, holotype of A. spinosus Meek, Hildebrand, 1916. Ancistrus cirrhosus. Argentina: MNHN B.0603, 82.6 mm SL, lectotype of Hypostomus cirrhosus Valenciennes, 1836, subsequent designation by Isbrücker (1980Isbrücker IJH. Classification and catalogue of the mailed Loricariidae (Pisces, Siluriformes). Amsterdam: Instituut voor Taxonomische Zoöogie, Universiteit van Amsterdam; 1980.); MNHN A.9565, 2, 66.2-79.5 mm SL, paralectotypes of H. cirrhosus Valenciennes, 1836, subsequent designation by Isbrücker (1980); MNHN 4845, 4, 46.2-51.9 mm SL, paralectotypes of H. cirrhosus Valenciennes, 1836, subsequent designation by Isbrücker (1980). Ancistrus claro. Brazil: MCP 28667, 67.8 mm SL, holotype of A. claro Knaack, 1999. Ancistrus cryptophthalmus. Brazil: MCP 10523, 1, 49.2 mm SL, paratype of A. cryptophthalmus Reis, 1987. Ancistrus cuiabae. Brazil: MCP 28671, 112.8 mm SL, holotype of A. cuiabae Knaack, 1999; NUP 933, 7 of 74, 64.4-92.2 mm SL; NUP 3441, 8 of 14, 66.0-81.1 mm SL. Ancistrus cf. dubius. Brazil: INPA 19071, 1, 91.1 mm SL. Ancistrus galani. Venezuela: MCP 15634, 1, 55.9 mm SL, paratype of A. galani Peres, Vilória, 1994. Ancistrus damasceni. Brazil: NMW 43489, 4, 29.3-41.4 mm SL, syntypes of Xenocara damasceni Steindachner, 1907; NMW 43490, 7, 25.6-35.8 mm SL, syntypes of Xenocara damasceni Steindachner, 1907. Ancistrus dolichopterus. Brazil: NMW 46276, 2, 80.9-90.7 mm SL, syntypes of A. dolichopterus Kner, 1854; NMW 47164, 2, 86.2-101.0 mm SL, syntypes of A. dolichopterus Kner, 1854. Ancistrus erinaceus. Chile?: MNHN A.9568, 74.9 mm SL, holotype of H. erinaceus Valenciennes, 1840. Ancistrus falconensis. Venezuela: ANSP 189316, 2, 95.5-121.7 mm SL, paratypes of A. falconensis Taphorn et al., 2010. Ancistrus fulvus. Brazil. NMW 57203, 87.5 mm SL, holotype of Xenocara fulva Holly, 1929. Ancistrus gymnorhynchus. Venezuela: BMNH 1904.11.9.27-31, 5, 83.8-134.0 mm SL, syntypes of Xenocara rothschildi Regan, 1905; NMW 43495, 111.3 mm SL, holotype of A. gymnorhynchus Kner, 1854. Ancistrus hoplogenys. Brazil: BMNH 1849.11.8.89-91, 3, 74.3-99.7 mm SL, syntypes of Chaetostomus hoplogenys Günther, 1864. Ancistrus jataiensis. Brazil: MCP 35244, 54.0 mm SL, holotype of A. jataiensis Fisch-Muller, Cardoso, da Silva, Bertaco, 2005. Ancistrus karajas. Brazil: INPA 57583, 39.0 mm SL, holotype of A. karajas de Oliveira et al., 2016. Ancistrus krenakarore. Brazil: INPA 34155, 46.7 mm SL, holotype of A. krenakarore de Oliveira et al., 2016. Ancistrus latifrons. Peru: BMNH 1869.5.21.4, 122.6 mm SL, holotype of Chaetostomus latifrons Günther, 1869. Ancistrus leoni. Brazil: INPA 49622, 3, 46.8-105.6 mm SL. Ancistrus leucostictus. Guyana: BMNH 1864.1.21.85, 49.3 mm SL, holotype of Chaetostomus leucostictus Günther. Ancistrus lithurgicus. British Guiana: BMNH 1911.10.31.107-108, 1, 35.6 mm SL (plus one specimen of Ancistrus sp. with 58.3 mm SL), paratype of A. lithurgicus Eigenmann, 1912; FMNH, 53091, 69.3 mm SL, holotype of A. lithurgicus Eigenmann, 1912; FMNH, 64613, 4, 35.0-63.7 mm SL, paratype of A. lithurgicus Eigenmann, 1912. Ancistrus macrophthalmus. Venezuela: MNHN 1887-0650, 1, 76.7 mm SL, holotype of Xenocara macrophthalma Pellegrin, 1912. Ancistrus maculatus. Brazil: NMW 47290, 1, 106.1 mm SL, syntype of Chaetostomus (Ancistrus) cirrhosus var. maculatus Steindachner, 1881. Ancistrus malacops. Colombia: ANSP 70517, 90.8 mm SL, holotype of A. lineolatus Fowler, 1943; Peru: ANSP 8299, 2, 72.0 mm SL (one specimen broken), syntype of Chaetostomus malacops Cope, 1872; MUSM 38968, 1, 81.2 mm SL; Ecuador: BMNH 1880.12.8.69-74, 6, 60.2-85.4 mm SL, syntypes of Xenocara occidentalis Regan, 1904; Brazil: INPA 2393, 2, 55.0-69.1 mm SL; INPA 49272, 7, 29.3-110.8 mm SL. Ancistrus marcapatae. Peru: BMNH 1902.5.29.211, 79.1 mm SL, holotype of Chaetostomus marcapatae Regan, 1904; BMNH 1911.12.20.35-36, 2, 45.7-63.2 mm SL, syntypes of Xenocara heterorhynchus Regan, 1912; MUSM 10087, 1, 88.5 mm SL; MUSM 57498, 1, 66.6 mm SL; MUSM 58097, 2, 57.9-59.9 mm SL. Bolivia: NMW 43475, 2, 40.8-58.0 mm SL, syntypes of Xenocara boliviana Steindachner, 1915; NMW 43476, 27, 31.2-65.6 mm SL, syntypes of Xenocara boliviana Steindachner, 1915. Ancistrus martini. Venezuela: USNM 121064, 82.3 mm SL, holotype of A. triradiatus martini Schultz, 1944; USNM 121065, 1, 51.4 mm SL, paratype of A. triradiatus martini Schultz, 1944; USNM 121066, 61.4 mm SL, holotype Ancistrus brevifilis bodenhameri Schultz, 1944; USNM 121069, 2, 27.3-52.1 mm SL, paratypes A. brevifilis bodenhameri Schultz, 1944. Ancistrus maximus. Brazil: INPA 35952, 4, 91.4-147.6 mm SL, paratypes of A. maximus de Oliveira et al., 2015. Ancistrus megalostomus. Bolivia: CAS 64614, 2, 81.7-83.5 mm SL, syntypes of A. megalostomus Pearson, 1924; Peru: MUSM 10366, 1, 64.9 mm SL; MUSM 11606, 2, 70.5-85.5 mm SL. Ancistrus miracollis. Brazil: INPA 57624, 66.7 mm SL, holotype of A. miracollis Bifi, de Oliveira, Rapp Py-Daniel, 2019. Ancistrus montanus. Bolivia: BMNH 1902.12.18.4, 81.3 mm SL, holotype of Xenocara montana Regan, 1904; Peru: MUSM 57817, 1, 82.0 mm SL; MUSM 57830, 1, 48.5 mm SL. Ancistrus mullerae. Brazil: MZUSP 104121, 119.1 mm SL, holotype of A. mullerae Bifi, Pavanelli, Zawadzki, 2009. Ancistrus multispinis. Brazil: BMNH 1910.7.26.31, 74.6 mm SL, lectotype of Xenocara multispinis Regan, 1912, subsequent designation by Muller (1989Muller S. Description de deux nouvelles espèces paraguayennes du genre Ancistrus Kner, 1854 (Pisces, Siluriformes, Loricariidae). Rev Suisse Zool. 1989; 96: 885-904.); BMNH 1910.7.26.32-33, 2, 86.7-98.5 mm SL, paraleclotypes of Xenocara multispinis Regan, 1912; MNRJ 1078, 15 of 70, 61.1-89.9 mm SL. Ancistrus nudiceps. Brazil: INPA 58328, 1, 141.6 mm SL. Ancistrus occloi. Peru: CAS 66847, 89.3 mm SL, holotype of A. occloi Eigenmann, 1928; MUSM 41133, 1, 119.9 mm SL. Ancistrus parecis. Brazil: MCP 35570, 59.5 mm SL, holotype of A. parecis Fisch-Muller, Cardoso, da Silva, Bertaco, 2005. Ancistrus pirareta. Paraguay: NUP 3425, 7 of 14, 72.0-104.9 mm SL. Ancistrus piriformis. Paraguay: MCP 13703, 2, 63.4-65.0 mm SL, paratype of A. piriformis Muller, 1989; USNM 307766, 1, 64.9 mm SL, paratype of A. piriformis Muller, 1989. Ancistrus ranunculus. Brazil: INPA 9509, 93.5 mm SL, holotype of A. ranunculus Muller, Rapp Py-Daniel, Zuanon, 1994. Ancistrus cf. shuar. Peru: MUSM 21930, 8, 41.5-86.6mm SL. Ancistrus tamboensis. Peru: ANSP 71643, 79.2 mm SL, holotype of A. tamboensis Fowler, 1945; MUSM 13602, 7 of 10, 57.1-83.7 mm SL. Ancistrus taunay. Brazil: MCP 18783, 11, 56.2-98.0 mm SL. Ancistrus trinitatis. Trinidad: ANSP 71723, 81.8 mm SL, holotype of A. maracasae Fowler, 1946, neotype of A. trinitatis by subsequent designation by Souza et al. (2019: 48). Ancistrus triradiatus. Colombia: CAS 60164, 88.3 mm SL, holotype of A. triradiatus Eigenmann, 1918. Ancistrus verecundus. Brazil: MCP 35572, 53.7 mm SL, holotype of A. verecundus Fisch-Muller, Cardoso, da Silva, Bertaco, 2005. Ancistrus variolus. Peru: ANSP 21284-21285, 2, 46.8 mm SL (one specimen broken), syntypes of Chaetostomus variolus Cope, 1872. Ancistrus tombador. Brazil: MCP 33001, 10, 24.9-57.6 mm SL, paratypes of A. tombador Fisch-Muller, Cardoso, da Silva, Bertaco, 2005.

ACKNOWLEDGMENTS

The Instituto Nacional de Pesquisas da Amazônia (INPA) and Museo de Historia Natural, Universidad Nacional Mayor de San Marcos provided logistical and technical support. We are grateful to Adrian Barnett for reviewing the English. AGB is grateful to Anja Palandacic and Ernst Mikschi (NMW), Carlos Lucena and Margarete Lucena (MCP), Guy Duhamel and Aurelie Laurent (MNHN), James Maclaine and Oliver Crimmen (BMNH), Carla Pavanelli and Cláudio Zawadzki (NUP), Richard Vari (in memoriam), David Santana and Jeffrey Willian (USNM), Saul Prada, Javier Maldonado-Ocampo (in memoriam) and Alexander Bonilla (MPUJ), Max Hidalgo (MUSM), and Mark Sabaj and Mariangeles Arce (ANSP) for hospitality during museum visits. We also thank John Lundberg (ANSP), Luiz Rocha and Dave Catania (CAS) Vinícius Abilhoa (MHNCI) and Paulo Buckup (MNRJ) for loaning of material. Carlison de Oliveira for support and Invertebrate Collection of INPA for allowing the use of photographic equipment used in this work. Financial support: AGB benefited from a DCR/AM fellowship from Fundação de Amparo à Pesquisa do Estado do Amazonas - FAPEAM and Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq (process 062.01066/2015) and grants to analyze the type material in BMNH, MNHN, MUSM and NMW. Visit to The Academy of Natural Sciences of Philadelphia (ANSP) supported in part by Böhlke Award to AGB.

REFERENCES

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  • Bifi AG, de Oliveira RR, Py-Daniel LR. A new species of Ancistrus Kner, 1854 (Siluriformes: Loricariidae) from rio Madeira basin, Amazonas State, Brazil. Neotrop Ichthyol. 2019; 17(2):e180135. http://dx.doi.org/10.1590/1982-0224-20180135
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    » http://dx.doi.org/10.11646/zootaxa.1418.1.1
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  • Weber C. Subfamily Hypostominae (Armored catfishes). In: Reis RE, Kullander SO, Ferraris CJ Jr., organizers. Check list of the freshwater fishes of South and Central America . Porto Alegre: Edipucrs ; 2003. p.351-72.
  • Zawadzki CH, Chamon CC. Hypostominae. In: Queiroz LJ, Torrente-Vilara G, Ohara WM, Pires THS, Zuanon J, Doria CRC, organizers. Peixes do rio Madeira. São Paulo: Dialeto Latin American Documentary; 2013. p.302-37.

ADDITIONAL NOTES

  • HOW TO CITE THIS ARTICLE

    Bifi AG, Ortega H. Redescription of Ancistrus greeni (Siluriformes: Loricariidae), and description of a new species from the río Madre de Dios basin, Peru. Neotrop Ichthyol. 2020; 18(1):e190070. https://doi.org/10.1590/1982-0224-20190070
  • ZOOBANK REGISTER

    urn:lsid:zoobank.org:pub:B0B62C38-2D9A-4F59-8310-FE9ABFED0075

Edited by

Marcelo Britto

Publication Dates

  • Publication in this collection
    17 Apr 2020
  • Date of issue
    2020

History

  • Received
    03 July 2019
  • Accepted
    02 Dec 2019
Sociedade Brasileira de Ictiologia Neotropical Ichthyology, Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura, Universidade Estadual de Maringá., Av. Colombo, 5790, 87020-900, Phone number: +55 44-3011-4632 - Maringá - PR - Brazil
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