Literature DB >> 25709528

Two new species of Pseudancistrus (Siluriformes, Loricariidae) from the Amazon basin, northern Brazil.

Gabriel S C Silva1, Fábio F Roxo1, Claudio Oliveira1.   

Abstract

Two new species of Pseudancistrus, a genus diagnosed by non-evertible cheek plates and hypertrophied odontodes along the snout margin, are described from two drainages of the Brazilian Shield: Pseudancistruskayabi from the rio Teles Pires (rio Tapajós basin) and Pseudancistrusasurini from the rio Xingu. The new species are distinguished from congeners (Pseudancistrusbarbatus, Pseudancistruscorantijniensis, Pseudancistrusdepressus, Pseudancistrusnigrescens, Pseudancistrusreus, and Pseudancistruszawadzkii) by the coloration pattern. Pseudancistruskayabi has dark bars on the dorsal and caudal fins which are similar to that of Pseudancistrusreus from the Caroní River, Venezuela. Pseudancistrusasurini is unique among Pseudancistrus in having whitish tips of the dorsal and caudal fins in juveniles to medium-sized adults.

Entities:  

Keywords:  Ancistrini; Brazilian Shield; Neotropical fish; freshwater; taxonomy

Year:  2015        PMID: 25709528      PMCID: PMC4337218          DOI: 10.3897/zookeys.482.6909

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.546


Introduction

With 892 species, the suckermouth armoured catfish family is the fifth most species-rich family of vertebrates and one of the most species-rich groups among Neotropical fishes (Eschmeyer and Fong 2014). The loricariids are easily distinguished by having a ventral oral disk, the body covered with ossified dermal plates, and the presence of small external teeth known as odontodes. Within this family, all species that have highly evertible clusters of cheek odontodes are placed within the subfamily PageBreak, the tribe (Armbruster 2004a, 2008). Morphology-based studies by Armbruster (2004a, 2008) showed as a monophyletic group; however, recent molecular studies supported the conclusion that the tribe was polyphyletic (e.g. Covain and Fish-Muller 2012; Lujan et al. 2015). was redefined by Lujan et al. (2015) and currently includes only ten valid genera but stays the second most genus-rich of the nine tribe-level clades of . Bleeker, 1862 was known to contain 15 valid species (Eschmeyer and Fong 2014) but recent publications (e.g. Chambrier and Montoya-Burgos 2008; Covain and Fisch-Muller 2012; Silva et al. 2014; Lujan et al. 2015) revealed that the genus is not monophyletic and that the type species, (Valenciennes, 1840), is closely related only with four species known as the species group: de Chambrier & Montoya-Burgos, 2008, (Günther, 1868), Eigenmann, 1912, and Silva, Roxo, Britzke & Oliveira, 2014, the latter being the only species described to date from rivers flowing from the Brazilian Shield into the Amazon. Other species not included in these works were considered to possibly belong to : (Regan, 1904) Willink, Mol & Chernoff, 2010 (Covain and Fisch-Muller 2012), and Armbruster & Taphorn, 2008 (Lujan et al. 2015). This last work retained as the only species belonging to this group from the eastern Orinoco basin. The genus is diagnosed by a combination of characters state as follows: a depressed body, hypertrophied odontodes along the lateral margin of the snout (regardless of either sex or season), and hypertrophied cheek odontodes which are evertible to less than 45° from the body (Lujan et al. 2015). Recently, an examination of the fish collections at the LBP (Laboratório de Biologia e Genética de Peixes de Botucatu) and MZUSP (Museu de Zoologia da Universidade de São Paulo) revealed the existence of two undescribed species of from the rio Xingu (the first species of for this basin) and the rio Teles Pires (the second species of for rio Tapajós basin), both of which are tributaries of the Amazon basin draining the Brazilian Shield. In the present paper these two new species are described.

Material and methods

After capture, fishes were anesthetized using 1% benzocaine in water, fixed in 10% formaldehyde, and preserved in 70% ethanol. Vouchers and tissues were deposited in the collection of AUM (Auburn University Natural History Museum, Auburn, USA), LBP (Laboratório de Biologia e Genética de Peixes, Botucatu, Brazil), and MZUSP (Museu de Zoologia da Universidade de São Paulo, São Paulo, Brazil). Measurements and counts were taken from the left side. Body plate follows Schaefer (1997) and measurements were taken point to point to the nearest 0.1 mm using digital calipers on left side of specimens following Armbruster (2003). Morphometrics are given as percentages of , except for subunits of the head region that are expressed as percentages of . Dorsal-fin ray counts include PageBreakthe spinelet as the first unbranched ray. Zoological nomenclature follows the International Code of Zoological Nomenclature (International Commission on Zoological Nomenclature 1999). standard length head length

Results

sp. n.

http://zoobank.org/F8B055A4-C576-4FC5-B0CF-8021F0B7DD93 Figure 1 , Table 1
Figure 1.

, holotype, MZUSP 116322, male 88.4 mm SL, from rio Teles Pires (Amazon basin), municipality of Itaúba, Mato Grosso State, Brazil.

Table 1.

Morphometric data for and . SD = standard deviation.

Pseudancistrus kayabi n = 21Pseudancistrus asurini n = 21
HolotypeRangeMeanSDHolotypeRangeMeanSD
SL88.461.5−87.778.57.2195.8195.8−45.985.937.9
Percentage of SL
Predorsal length42.739.4−48.543.81.939.539.1−42.740.91.2
Head length34.630.2−40.234.91.933.631.9−35.833.90.9
Head-dorsal length8.07.1−11.09.31.07.55.3−8.26.90.7
Cleithral width33.431.2−38.633.51.735.830.9−35.832.81.4
Head-pectoral length29.124.5−33.629.62.031.721.9−31.728.31.8
Thorax length22.819.6−25.622.21.620.120.1−25.522.71.5
Pectoral spine length30.022.3−29.727.71.736.227.8−36.731.62.5
Abdominal length24.220.3−30.424.32.220.520.5−26.023.91.4
Pelvic spine length25.920.3−29.823.72.027.023.8−27.425.91.0
Postanal length32.325.9−35.931.32.529.229.2−35.332.81.6
Anal-fin spine length9.65.4−12.910.11.716.67.8−16.610.11.9
Dorsal-pectoral depth26.420.2−29.425.91.924.023.3−26.524.80.9
Dorsal spine length24.317.7−29.223.02.122.522.5−32.720.02.2
Dorsal-pelvic depth22.415.2−26.721.22.319.317.2−26.520.12.0
Dorsal-fin base length28.120.4−28.126.01.729.924.9−30.627.41.6
Dorsal-adipose distance14.39.0−14.312.01.913.313.1−17.415.41.2
Adipose-spine length10.16.3−16.99.12.48.67.7−10.38.60.6
Dorsal adipose-caudal distance16.013.4−22.016.32.312.112.1−16.515.01.0
Caudal peduncle depth11.310.0−16.711.01.510.69.1−11.010.20.5
Ventral adipose-caudal distance22.620.3−25.622.21.219.519.5−22.921.31.0
Adipose-anal distance18.916.9−24.819.61.918.816.9−19.918.80.8
Dorsal-anal distance33.129.3−35.432.81.412.612.1−19.113.31.5
Pelvic-dorsal distance27.617.4−27.621.11.828.218.3−29.425.72.7
Percentage of HL
Head-eye length26.425.8−31.428.81.527.725.9−33.129.21.8
Orbital diameter13.812.7−20.315.51.713.113.1−19.916.81.7
Snout length67.462.3−69.365.41.669.556.6−72.462.24.5
Internares width14.813.2−18.715.81.315.511.9−16.314.51.2
Minimal interorbital distance30.627.4−35.729.11.931.924.0−32.628.22.4
Mouth length48.848.8−62.357.52.549.739.8−51.945.93.5
Barbel length10.94.2−10.98.01.65.54.6−8.77.21.3
Dentary tooth cup length20.815.4−24.620.52.620.116.1−22.419.81.7
Premaxillary tooth cup length19.516.5−25.619.52.218.117.8−24.320.51.9
Head depth64.259.7−65.762.41.864.356.6−66.262.62.4

Holotype.

MZUSP 116322, male, 88.4 mm SL. Brazil: Mato Grosso State: municipality of Itaúba: rio Teles Pires (Tapajós River basin), 10°58'30"S, 55°44'03"W, 01 October 2007, JLO Birindelli, P Hollanda-Carvalho.

Paratypes.

All from Brazil: Mato Grosso State: rio Teles Pires (Tapajós River basin): Amazon basin. AUM 65641 2, 74.5−80.3 mm SL, municipality of Itaúba, 11°03'44"S, 55°19'08"W, 26 September 2007, JLO Birindelli, P Hollanda-Carvalho. LBP 19552, 2, 79.1−87.1 mm SL, municipality of Itaúba, 11°03'44"S, 55°19'08"W, 26 September 2007, JLO Birindelli, P Hollanda-Carvalho. MZUSP 95851, 1, 60.9 mm SL, collected with holotype. MZUSP 95912, 54, 27.1−86.5 mm SL, municipality of Itaúba, 11°03'44"S, 55°19'08"W, 26 September 2007, JLO Birindelli, P Hollanda-Carvalho. MZUSP 96157, 34, 29.5−85.8 mm SL, municipality of Paranaíta, 09°26'58"S, 56°29'19"W, 28 September 2007, LMS Souza, AL Netto-Ferreira.

Diagnosis.

differs from all congeners except by having caudal and dorsal fins with dark bars (vs. with white spots in caudal and dorsal fins). Also, the new species differs from all except by having a dark brown body with whitish spots that fade along the posterior portion of the dorsal fin and forming mottled pattern (vs. either dark brown with conspicuous rounded spots not covering more than one plate in , , , , and or with dark brown bars in ). It further differs from and by having the snout with yellowish hypertrophied odontodes (vs. reddish-brown odontodes) (see Fig. 3 in De Chambrier and Montoya-Burgos 2008 for comparison). In addition, is distinguished by having a shorter pectoral spine, 22−30% SL (vs. 29−34% in , 31−33% in , and 30−34% in ); a shorter dorsal-fin base, 20−28% SL (vs. 28−29% in , 29−31% in , and 28−31% in ); a greater internares width, 13−19% HL (vs. 10.5−12.9% in ); head depth, 60−66% HL, greater than in (56−57%) and in (41−53%) but smaller than in (67−73%); and a greater adipose-anal distance (17−25% SL vs. 15−17% in and 12−15% in ).
Figure 3.

, holotype, MZUSP 116323, male 195.8 mm SL, from rio Xingu (Amazon basin), municipality of Altamira, Pará State, Brazil.

, holotype, MZUSP 116322, male 88.4 mm SL, from rio Teles Pires (Amazon basin), municipality of Itaúba, Mato Grosso State, Brazil.

Description.

Morphometric data is presented in Table 1. In lateral view, dorsal profile convex from snout tip to dorsal-fin origin; straight, gradually descending from dorsal-fin origin to posterior insertion of adipose fin; straight, steeply ascending to insertion of caudal-fin; ventral profile flat from snout tip to anal-fin origin; shallowly concave from anal-fin insertion to lower caudal-fin spine; greatest body depth at dorsal-fin origin. In dorsal view, greatest body width across cleithral region; snout broadly elliptical; body progressively narrow from opercular region to caudal fin. Cross-section of body between pectoral and pelvic fins rounded dorsally and flattened ventrally; cross-section of caudal peduncle ellipsoid. Body almost entirely covered with plates except on ventral portions of head, abdomen, and dorsal-fin base. Five lateral rows of dermal plates, dorsal plates 21−22, lateral mid-dorsal plates 21−22, lateral median plates 22−23, lateral mid-ventral plates 21−22, lateral ventral plates 19−20. Three predorsal plates; eight plates below dorsal-fin base; four plates between dorsal fin and adipose fin; five rows of plates on caudal peduncle. Dorsal spinelet present. Morphometric data for and . SD = standard deviation. Body plates and cleithrum with minute odontodes. Odontodes slightly hypertrophied on pectoral-fin spines, gradually larger towards tips. Numerous yellowish hypertrophied odontodes along lateral margins of head including snout; odontodes small on tip of snout increasing gradually in length from anterolateral margin of snout to PageBreakcheeks; longest odontodes on posteriormost portion of non-evertible cheek plates. Eye small (orbital diameter 13−20% HL), dorsolaterally positioned. Oral disk transversely ellipsoid. Lower lip not reaching transverse line between gill openings. Lower lip covered with numerous small papillae. Maxillary barbel developed. Mouth relatively large. Premaxillary teeth 33−70 per ramus; dentary teeth 39−74 per ramus. Teeth bifid, medial cusp large and rounded, lateral cusp minute and rounded. Jaws wide, dentaries forming oblique angle, premaxillaries almost co-linear. Dorsal fin I,7, origin approximately at midpoint between pectoral- and pelvic-fin origins, last dorsal-fin ray reaching adipose fin when depressed. Pectoral fin I,6, spine tip slightly curved inward, covered with enlarged odontodes distally; depressed tip reaching one-third length of pelvic-fin spine. Pelvic fin I,5, spine tip curved inward, almost reaching anal-fin origin when depressed. Anal fin I,5, spine tip straight, reaching sixth plate posterior to its origin. Caudal fin I,7-7I, distal margin concave, inferior lobe longer than superior. Adipose fin with straight spine, preceded by single median preadipose plate.

Color in alcohol.

Ground color dark brown on back and sides of body, and lighter brown ventrally. Anterior portion of head to posterior margin of orbits with many small, crowded, white spots; spots getting abruptly larger on posterior portion of head, continuing on body, fading along posterior portion of dorsal fin and forming mottled pattern. Dorsal-fin spine rays and membranes with 6−7 dark bars. Pectoral, pelvic, anal with 4−5 dark bars and caudal-fin with four dark bars. Hypertrophied odontodes along head margin yellowish.

Sexual dimorphism.

Males possess a papilla posterior to urogenital opening, an attribute absent in females. Both sexes in exhibit highly hypertrophied odontodes along snout margin, as well as in other species of (Armbruster 2004b).

Etymology.

The specific name “kayabi” is a reference to the Kayabi indigenous people that inhabited the region of the rivers Arinos, dos Peixes and Teles Pires, in Mato Grosso State, Brazil. A noun in apposition.

Distribution.

is known from the rio Teles Pires, rio Tapajós basin, municipality of Itaúba and Paranaíta, Mato Grosso State, Brazil (Fig. 2a).
Figure 2.

Distribution maps. a . Star shows holotype locality, rio Teles Pires, 10°58'30"S, 55°44'03"W. Circle shows paratype locality b . Star shows holotype locality, rio Xingu, 03°39'05"S, 52°22'42"W. Circles show paratypes localities.

Distribution maps. a . Star shows holotype locality, rio Teles Pires, 10°58'30"S, 55°44'03"W. Circle shows paratype locality b . Star shows holotype locality, rio Xingu, 03°39'05"S, 52°22'42"W. Circles show paratypes localities. http://zoobank.org/02D58958-6DD0-441A-8755-96F8387F2C33 Figures 3 , 4 , Table 1
Figure 4.

, paratype, LBP 16551, female 100.5 mm SL, from rio Xingu (Amazon basin), showing the dorsal and caudal fins tips whitish.

sp. L17: sp. L67: MZUSP 116323, male, 195.8 mm SL. Brazil: Pará State: municipality of Altamira: rio Xingu (Amazon basin), Cachoeira do Espelho, 03°39'05"S, 52°22'42"W, 18 November 2011, OT Oyakawa, JLO Birindelli, C Moreira, A Akama, LMS Souza. All from Brazil: Pará State: municipality of Altamira: Amazon basin. AUM 65640, 2, 79.1−82.9 mm SL, rio Xingu, Cachoeira da Mucucura, 03°24'31"S, 51°44'40"W, 09 November 2011, OT Oyakawa, JLO Birindelli, C Moreira, LMS PageBreakSouza. LBP 16551, 2, 75.6−101.4 mm SL, rio Xingu, 03°15'24"S, 52°05'47"W, 28 September 2012, C Oliveira, R Britzke, LMS Sousa. MZUSP 107174, 4, 45.9−123.4 mm SL, rio Xingu, Cachoeira de Mucura, 03°24'51"S, 51°44'23"W, ECIX team. MZUSP 107179, 2, 62.3−68.7 mm SL, rio Xingu, Cachoeira do Mucura, 03°24'51"S, 51°44'23"W, 07 July 2010, ECIX team. MZUSP 107435, 3, 74.6−105 mm SL, rio Xingu, 03°10'40"S, 51°36'58"W, 26 September 2007, FCT Lima, AK Zeinad. MZUSP 111285, 2, 84.4−106.6 mm SL, rio Iriri (trib. rio Xingu) Cachoeira Grande, 03°50'37"S, 52°44'02"W, OT Oyakawa, JLO Birindelli, C Moreira, A Akama, LMS Souza. MZUSP 111441, 6, 49.5−152.3 mm SL, rio Xingu, Cachoeira da Mucucura, 03°24'31"S, 51°44'40"W, 09 November 2011, OT Oyakawa, JLO Birindelli, C Moreira, LMS Souza. MZUSP 111558, 1, 91.4 mm SL, collected with holotype. The new species differs from all congeners by having the dorsal-and caudal-fin tips whitish (Fig. 4) (vs. entirely dark). It further differs from and by having conspicuous whitish spots on the body (vs. body mottled or with bars in and with whitish spots that fade along the body and can cover more than one plate in ). It is also distinguishable from and by having the snout with yellowish odontodes (vs. reddish-brown) (see Fig. 3 in De Chambrier and Montoya-Burgos 2008 for comparison) and from , , and by having smaller whitish spots covering the body which increase gradually in size on the head (diameter 0.3−0.8 mm) and further on the body (diameter 0.7−1.3) (vs. spots abruptly increasing size between the head (diameter 1.1−1.3) and the body (diameter 2.6−2.3 mm). In addition, the new species is distinguished by a shorter predorsal length, 39−43% SL (vs. 43−46% in and 43−45% in ), a smaller dorsal pectoral depth, 23−27% SL (vs. 27−31% in ); a smaller caudal peduncle depth, 9−11% SL (vs. 13−14% in and 13% in ), a shorter barbel, 5−9% HL (vs. 10−11 in ), and head depth, 57−66% SL, which is smaller than in (67−73%) but greater than in (41−53%). , holotype, MZUSP 116323, male 195.8 mm SL, from rio Xingu (Amazon basin), municipality of Altamira, Pará State, Brazil. , paratype, LBP 16551, female 100.5 mm SL, from rio Xingu (Amazon basin), showing the dorsal and caudal fins tips whitish. Morphometric data is presented in Table 1. In lateral view, dorsal profile convex from snout tip to dorsal-fin origin; straight, gradually descending from dorsal-fin origin to posterior insertion of adipose fin; straight, steeply ascending to insertion of caudal fin; ventral profile flat from snout tip to anal-fin origin; shallowly concave from anal-fin insertion to lower caudal-fin spine; greatest body depth at dorPageBreaksal-fin origin. In dorsal view, greatest body width across cleithral region; snout broadly elliptical; body decreasing in width from opercular region to caudal fin. Cross-section of body between pectoral and pelvic fins rounded dorsally and flattened ventrally; cross-section of caudal peduncle ellipsoid. Body almost entirely covered with plates, except on ventral portions of head, abdomen, and dorsal-fin base. Five lateral rows of dermal plates, dorsal plates 21−22, lateral mid-dorsal plates 18−22, lateral median plates 22−23, lateral mid-ventral plates 23−24, lateral ventral plates 18−19. Three predorsal plates; seven plates below dorsal-fin base; four plates between dorsal fin and adipose fin; five rows of plates on caudal peduncle. Dorsal spinelet present. Body plates and cleithrum with minute odontodes. Odontodes gradually getting larger towards tips on pectoral-fin spines. Numerous whitish hypertrophied odontodes along lateral margins of head including snout; homogenous in length excepting in anterior portion of snout where odontodes are smaller; longest odontodes on posteriormost portion of non-evertible cheek plates. Eye small (orbital diameter 13−10% HL), dorsolaterally positioned. Oral disk transversely ellipsoid. Lower lip not reaching transverse line between gill openings. Lower lip covered with numerous small papillae. Maxillary barbel poorly developed. Mouth relatively large. Premaxillary teeth 38−77 per ramus; dentary teeth 39−86 per ramus. Teeth bifid, medial cusp large and rounded, lateral cusp minute and rounded. Jaws wide, dentaries forming oblique angle, premaxillaries almost co-linear. Dorsal fin II,7, origin approximately at midpoint between pectoral- and pelvic-fin origins, last dorsal-fin ray not reaching adipose-fin when depressed. Pectoral fin I,6, spine tip not curved inward; depressed tip reaching one-third length of pelvic-fin spine. Pelvic fin I,5, spine tip curved inward, almost reaching anal-fin origin when depressed. Anal-fin I,5, spine tip straight, reaching fifth plate posterior to its origin. Caudal fin I,7-7I, distal margin concave, inferior lobe longer than superior. Adipose fin with almost straight spine, preceded by single median preadipose plate. Ground color dark brown on back and sides of body, and lighter brown ventrally. Anterior portion of head to posterior margin of orbits with many small, crowded, white spots; spots increasing slightly and gradually in size between snout to body. Dorsal plate series usually with two or three spots per plate in anterior portion of body and one spot on posterior portion of body. Mid-dorsal plates usually with two or three spots per plate. Lateral median plates with one or two spot per plate. Mid-ventral plates and ventral plates with two or three spots per plate. Dorsal-fin spine, rays and membranes with small round spots. Adipose fin with three small spots on spine and membrane. Pectoral, pelvic, anal and caudal fins with numerous and white spots of equal size. Dorsal and caudal fin tips whitish. Hypertrophied odontodes along head margin yellowish.

Color in life.

Similar to pattern described for alcohol individuals, but with ground color dark greenish-brown, and with yellow spots on body and on tips of dorsal and caudal fins. Males possess a papilla posterior to urogenital opening, an attribute absent in females. Both sexes in PageBreak exhibit highly hypertrophied odontodes along snout margin, as well as in others species of (Armbruster 2004b). The specific name “asurini” is a reference to the Asurini indigenous peoples who inhabit the right margin and median portions of rio Xingu, close to the municipality of Altamira in Pará State, Brazil. A noun in apposition. is known from the rio Xingu, municipality of Altamira, from the Xingu river basin, Pará State, Brazil (Fig. 2b).

Discussion

The two new species, and , are typical (sensu Chambrier and Montoya-Burgos 2008), recognized by non-evertible cheek plates and the presence of hypertrophied odontodes along the snout margin. This last character is shared with species of and . However, in , the odontodes along the snout are quite well developed, especially in . Additionally, (Armbruster and Provenzano 2000) can be distinguished from by the presence of three rows of plates on the caudal peduncle (vs. five), and can be distinguished from by the presence of three buccal papillae (vs. one; Isbrücker et al. 1988). The most conspicuous character used to distinguish the two new species from all other described is the coloration pattern. has a pattern of dark bars on dorsal and caudal fins (Fig. 1) as in from the Caroní River, Venezuela. However, possesses dark brown bars also on the body. This character is absent in , which has a dark brown base color with whitish spots fading posterior to the dorsal fin and are large enough to cover more than one lateral body plate, a pattern that is similar to that found in . has whitish tabs on the dorsal- and caudal-fin tips (Fig. 4) in juveniles and medium-sized adults (to approximately 100 mm SL), a pattern unique among . This character is similar to that found in (Py Daniel et al. 2011) and (Py Daniel et al. 2011), both of which are also from the rio Xingu basin and live sympatrically with . Additionally, the new species has a color pattern consisting of spots that increase in size from the head (diameter 0.3−0.8 mm) to posterior part of body (diameter 0.7−1.3). The species , , and present a similar coloration pattern; however, the size of the spots increase abruptly from the head (diameter 1.1−1.3) to posterior part of body (diameter 2.6−2.3 mm).

Comparative material examined

(Heitmans, Nijssen & Isbrücker, 1983): LBP 5253, 2, 58.5–83.8 mm SL, MZUSP 103488, 23, 102.3–55.1 mm SL, Jari river, Brazil; ANSP 189128, 3, 56.8−125.7 mm SL, Marowini river, Sipalawini, Suriname. Silva, Roxo, Britzke & Oliveira, 2014: Holotype, MZUSP 115056, 116.4 mm SL, Tapajós river, Brazil; Paratypes, LBP 15045, 2, 97.9−128.7 mm SL, LBP 17724, 1, 87.5 mm SL, LBP 16195, 1, 116.4 mm SL. (Valenciennes, 1840): ANSP 177366, 2, 76.5−103.7 mm SL, Burro Burro river, Water Dog Falls, Essequibo river basin, Guyana; ANSP 189119, 3, 75.1−151.5 mm SL, Lawa river, Sipalawini, Suriname. Eigenmann, 1912: ANSP 177379, 5, 96.4−133.5 mm SL, Burro Burro river, Water Dog Falls, Essequibo river basin, Guyana. (Isbrücker, Nijssen & Cala, 1988): ANSP 160600, 6, 68.0−78.5 mm SL, Orinoco river, Venezuela. Lujan, Armbruster & Sabaj, 2007: ANSP 190755, 1, 206.2 mm SL, Ventuari river, Orinoco river basin, Venezuela. Armbruster, 2004b: ANSP 185321, 4, 148.6−154.1 mm SL, Casiquiari river, Venezuela.
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1.  Multilocus molecular phylogeny of the suckermouth armored catfishes (Siluriformes: Loricariidae) with a focus on subfamily Hypostominae.

Authors:  Nathan K Lujan; Jonathan W Armbruster; Nathan R Lovejoy; Hernán López-Fernández
Journal:  Mol Phylogenet Evol       Date:  2014-09-02       Impact factor: 4.286

2.  New species of the Pseudancistrus barbatus group (Siluriformes, Loricariidae) with comments on its biogeography and dispersal routes.

Authors:  Gabriel de Souza da Costa E Silva; Fábio Fernandes Roxo; Ricardo Britzke; Claudio Oliveira
Journal:  Zookeys       Date:  2014-04-29       Impact factor: 1.546

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1.  An integrative framework to reevaluate the Neotropical catfish genus Guyanancistrus (Siluriformes: Loricariidae) with particular emphasis on the Guyanancistrus brevispinis complex.

Authors:  Sonia Fisch-Muller; Jan H A Mol; Raphaël Covain
Journal:  PLoS One       Date:  2018-01-03       Impact factor: 3.240

  1 in total

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