Content uploaded by Hudson Pinheiro
Author content
All content in this area was uploaded by Hudson Pinheiro on Dec 06, 2014
Content may be subject to copyright.
Accepted by W. Holleman: 21 Aug. 2013; published: 3 Sept. 2013
ZOOTAXA
ISSN 1175-5326 (print edition)
ISSN 1175-5334 (online edition)
Copyright © 2013 Magnolia Press
Zootaxa 3709 (1): 095–100
www.mapress.com
/
zootaxa
/
Article
95
http://dx.doi.org/10.11646/zootaxa.3709.1.5
http://zoobank.org/urn:lsid:zoobank.org:pub:655EF550-2290-41D3-993A-282C1C7D2A80
A new species of the genus Hypleurochilus (Teleostei: Blenniidae) from Trindade
Island and Martin Vaz Archipelago, Brazil
HUDSON T. PINHEIRO1,3, JOÃO LUIZ GASPARINI1 & CARLOS A. RANGEL2
¹ Departamento de Oceanografia e Ecologia, Universidade Federal do Espírito Santo. Av Fernando Ferrari, 514, CEP 29041-970,
Vitória, Espírito Santo, Brasil. E-mail: htpinheiro@gmail.com; gaspa.vix@terra.com.br
² Pós-Graduação em Biologia Marinha, Universidade Federal Fluminense (UFF), Outeiro São João Batista, s/nº, CP: 100.644 -
CEP: 24001-970, Niterói, Rio de Janeiro, Brasil. E-mail: carangel@vm.uff.br
3 Corresponding author
Abstract
A new species of the genus Hypleurochilus, endemic to Trindade Island and Martin Vaz Archipelago, off Brazil, is described.
Hypleurochilus brasil sp. n. differs from its congeners in color pattern and anal-ray counts. A recent study shows a close
relationship between H. brasil sp. n. and H. fissicornis. This new species is recorded from 3 to 15 m depth, solitary or in small
groups (up to 10 individuals), always in small holes or associated with sea-urchins and sponges on the rocky reefs.
Hypleurochilus brasil sp. n. is the eleventh recognized species of Hypleurochilus and the third species of this genus reported
from the Brazilian Province.
Key words: combtooth blenny, endemism, oceanic islands, reef fish, South Atlantic
Introduction
Ten species of the genus Hypleurochilus Gill, 1861 are currently recognized as valid. All are restricted to the
Atlantic Ocean and the Mediterranean Sea. In the most recent review of the genus, Bath (1994) reports seven
species from the western Atlantic: H. bermudensis Beebe & Tee-Van, 1933, H. caudovittatus Bath, 1994, H.
fissicornis (Quoy & Gaimard, 1824), H. geminatus (Wood, 1825), H. multifilis (Girard, 1858), H.
pseudoaequipinnis Bath, 1994 and H. springeri Randall, 1966. Three other species occur in the eastern Atlantic: H.
aequipinnis (Günther, 1861), H. bananensis and H. langi (Fowler, 1923). Two species (H. fissicornis and H.
pseudoaequipinnis) are known from Brazil (Bath 1994; Floeter et al. 2008; Rangel & Guimarães 2010).
Hypleurochilus bananensis (Poll, 1959) is the only species of the genus that occurs in the Mediterranean Sea.
Trindade Island and the Martin Vaz Archipelago lie about 1 160 km off the Brazilian coast, making them the
most remote islands of Brazil (Figure 1). Fringing reefs of encrusting coralline algae and rocky boulders compose
the main shallow habitats of the islands, sheltering a high richness and biomass of reef fishes (Pinheiro et al. 2011).
There are four species of Blenniidae known to occur at these islands (Gasparini & Floeter 2001; Pinheiro et al.
2009): Ophioblennius trinitatis Miranda Ribeiro, 1919; Scartella poiti Rangel, Gasparini & Guimarães, 2004,
Entomacrodus sp. and Hypleurochilus sp.; the latter three being endemic to these islands. Herein, we describe the
species of Hypleurochilus as new, it being the 11th (eleventh) recognized species of Hypleurochilus known from the
Atlantic Ocean and the third from Brazilian waters.
Material and methods
All specimens were collected using hand nets. Methods of counting and measuring follow Bath (1994).
Morphometric and meristic data for the type series are presented in Table 1 and counts of dorsal- and anal-fin rays
for Brazilian species of Hypleurochilus are given in Table 2. In the description, meristic values for the holotype are
PINHEIRO ET AL.
96 · Zootaxa 3709 (1) © 2013 Magnolia Press
provided first, followed by the range of counts for all type specimens (holotype plus paratypes) in parentheses.
Clearing and staining — diafanization — follow Dingerkus & Uhler (1977). Type specimens were deposited in the
fish collections of Universidade Federal do Espírito Santo (CIUFES), Universidade Estadual de Campinas
(ZUEC), Laboratório de Biologia do Nécton e Ecologia Pesqueira, Universidade Federal Fluminense (LNEP-UFF)
and California Academy of Sciences (CAS).
FIGURE 1. Map of the Brazilian Coast, Western South Atlantic. Square indicates Trindade Island and Martin Vaz
Archipelago, volcanic formations lying about 1160–1207 km, respectively, off Brazil. Type-locality of Hypleurochilus brasil.
TABLE 1. Occurrence percents of number of dorsal- and anal-fin rays of Hypleurochilus brasil sp. nov. (9 individuals
analyzed), H. pseudoaequipinnis (91) and H. fissicornis (22) (data for H. pseudoaequipinnis and H. fissicornis are from Bath
1994).
Taxonomy
Hypleurochilus brasil sp. n.
Brazil blenny (Figures 2–4, Tables 1 and 2)
Hypleurochilus fissicornis (non Quoy & Gaimard, 1824): Gasparini & Floeter 2001 (misidentification).
Holotype. CIUFES 1901, male, 30.85 mm SL, Ponta da Calheta, Ilha da Trindade, Espírito Santo, Brasil, 20°30’S,
29°20’W, depth 8 m, collected by T. Simon and R. Macieira, 19 Nov 2009.
Paratypes. ZUEC 6353, female, 26.9 mm SL, Ponta da Calheta, Ilha da Trindade, Espírito Santo, Brazil,
20°30’S, 29°20’W, depth 10 m, collected by H.T. Pinheiro, 03 May 2009; LNEP-UFF 300, male, 18.5 mm SL,
Species Segmented dorsal rays Segmented anal rays
11 13 14 15 14 15 16 17
H. brasil 55.5 44.4 33.3 66.6
H. pseudoaequipinnis 1.1 63.4 34.4 1.1 3.23 59.14 37.63
H. fissicornis 13.6 86.4 9.1 90.9
Zootaxa 3709 (1) © 2013 Magnolia Press · 97
NEW HYPLEUROCHILUS FROM TRINIDADE ISLAND
Ponta da Calheta, Ilha da Trindade, Espírito Santo, Brazil, 20°30’S, 29°20’W, depth 8 m, collected by H.T.
Pinheiro, 10 May 2009; CIUFES 1945, male, 21.45 mm SL, Ponta da Calheta, Ilha da Trindade, Espírito Santo,
Brazil, 20°30’S, 29°20’W, depth 8 m, collected by H.T. Pinheiro, 10 May 2009; CIUFES 1925, male, 17.6 mm SL,
Ponta da Calheta, Ilha da Trindade, Espírito Santo, Brazil, 20°30’S, 29°20’W, depth 8 m, collected by H.T.
Pinheiro, 10 May 2009; CIUFES 1946, male, 19.5 mm SL, Ponta da Calheta, Ilha da Trindade, Espírito Santo,
Brazil, 20°30’S, 29°20’W, depth 8 m, collected by H.T. Pinheiro, 10 May 2009; CIUFES 1938, female, 15.4 mm
SL, Ponta da Calheta, Ilha da Trindade, Espírito Santo, Brazil, 20°30’S, 29°20’W, depth 8 m, collected by H.T.
Pinheiro, 10 May 2009; CAS 235154, 21.45 mm SL, Ponta da Calheta, Ilha da Trindade, Espírito Santo, Brazil,
20°30’S, 29°20’W, depth 8 m, collected by H.T. Pinheiro, 10 May 2009; CAS 235155, 19.65 mm SL, Ponta da
Calheta, Ilha da Trindade, Espírito Santo, Brazil, 20°30’S, 29°20’W, depth 8 m, collected by H.T. Pinheiro, 10 May
2009.
Comparative material. Hypleurochilus fissicornis: CIUFES 1055, 1086, MNRJ 20822; Hypleurochilus
pseudoaequipinnis: CIUFES 783, MNRJ 20498, LNEP-UFF 087, 099.
Diagnosis. Hypleurochilus brasil differs from its congeners by the following combination of characters:
pelvic-fin rays I, 3, dorsal fin predominantly XII,13, anal fin II, 15 or 16 (usually 16), absence of blackened stripes,
nape green or white and presence of numerous tiny red spots along body, diminishing in size posteriorly (Figures 3
and 4).
FIGURE 2. Hypleurochilus brasil, Preserved holotype CIUFES 1901. Photo by R. Macieira.
FIGURE 3. Hypleurochilus brasil, Paratype (ZUEC 6353).Photographed shortly after death (up to 2 hours). Photo by H.
Pinheiro.
PINHEIRO ET AL.
98 · Zootaxa 3709 (1) © 2013 Magnolia Press
Description. Dorsal-fin rays XII, 13 or 14, 13 in 5 specimens and 14 in 4 specimens; anal-fin rays II, 15 or 16,
15 in 3 specimens and 16 in 6 specimens; branched caudal-fin rays 8, total segmented caudal-fin 12; pectoral-fin
rays 14; pelvic-fin rays I, 3; precaudal vertebrae 11, caudal vertebrae 25. Gill opening ending at or slightly above
dorsal end of the pectoral fin base. Lateral line straight and short, with 24 distinct tubes, never extending beyond
the first segmented dorsal ray. One to four cirri present on anterior nasal opening and one or two on top of eyes.
Body moderately elongate, without scales. Head length 3.18 (2.98–4.14) in SL, orbit diameter 4.09 (2.84–4.64)
in head length, pectoral-fin length 3.74 (2.73–3.9) in SL and pelvic-fin length 6.11 (4.61–7.69) in SL (Table 2).
Horizontal mouth situated low on the head; maxilla reaching posteriorly to a vertical through the centre of eye.
Incisiform teeth 25 in the upper jaw and 24 or 25 in the lower jaw. Two large curved canine teeth posteriorly on
each side of dentary, at end of incisiform series, and in upper and lower jaws. Cephalic sensory pores arranged in
two rows inferior and posterior of eye, one row above superior lip, two rows below lower lip; two arrow-shaped
rows on nape, one right posterior to eyes and one slightly anterior to dorsal fin.
FIGURE 4. Hypleurochilus brasil in its natural habitat on the rocky reef of Trindade Island. Photo by R. Macieira.
Colour in life. Individuals shortly after death (approx 2 h) and alive are shown in Figures 3 and 4 to illustrate
the colour pattern of the new species. The body is translucent with pale brown tint in juveniles and strongly orange
in adults, both with many red spots along sides of body. Adults with transverse pale and dark bars on head and
posterior part of body. Nape variable in coloration, green or whitish in juveniles, black in adults. Black pupil
surrounded by red iris with black stripes giving the appearance of spokes in a wheel. Snout pale yellow with
whitish or bluish streaks. Operculum and pre-operculum bordered with series of white dots. Pectoral, pelvic and
anal fins, and basal part of caudal fin yellow, without dots or spots. Dorsal and caudal fins hyaline.
Colour in alcohol. Body pale brown, red spots in live specimens turn brown (Figure 2). Top of head dark
brown. Snout with brownish streaks. Fins pale. Series of white dots on the operculum and pre-operculum
disappear.
Etymology. The name of the new species refers to the vivid red spots that are like incandescent pieces of a
brazing. Brazil’s country name (Brasil in Portuguese), where the species is endemic, originally has a similar
Zootaxa 3709 (1) © 2013 Magnolia Press · 99
NEW HYPLEUROCHILUS FROM TRINIDADE ISLAND
derivation. The name of the country was given in recognition of the reddish colour of the wood of a large Brazilian
native tree (Caesalpinia echinata – “Pau-Brasil” in Portuguese), very abundant in the past. The name is treated as a
noun in apposition.
TABLE 2. Sex and measurements (in mm) of the holotype and paratypes of Hypleurochilus brasil sp. nov.
FIGURE 5. Type-locality of Hypleurochilus brasil, rocky shore at Trindade Island. Photo by R. Francini-Filho.
Distribution and habitat. Hypleurochilus brasil sp. n. is known only from the type locality (Figure 5), and is
considered to be endemic to Trindade Island and the Martin Vaz Archipelago. This species was recorded from 3 to
15 m depth, it was found either solitary or in small groups (up to 10 individuals), always in small holes or
associated with sea-urchins and sponges on the rocky reefs (Figure 4).
Sex Standard length Head length Eye diameter Pectoral fin length Pelvic fin length
Holotype Male 30.85 9.4 2.3 8.25 5.05
Paratype Female 26.9 6.5 1.4 6.9 3.5
Paratype Male 18.5 4.55 1.6 4.8 3
Paratype Male 21.45 6.15 1.95 6.5 3.5
Paratype Male 17.6 6 2.05 5.1 3
Paratype Male 19.5 6.55 1.8 5.8 3.9
Paratype Female 15.4 5.1 1.5 4 2.2
Paratype Juvenile 21.45 7.1 2 7.85 4.65
Paratype Juvenile 19.65 5.65 1.75 5.9 4.15
PINHEIRO ET AL.
100 · Zootaxa 3709 (1) © 2013 Magnolia Press
Remarks: Hypleurochilus brasil is distinguished from H. langi, H. bananensis, H. springeri, H. bermudensis,
H. aequipinnis and H. pseudoaequipinnis by having pelvic-fin rays I, 3 (versus I, 4). It differs from H.
caudovittatus, H. fissicornis, H. germinatus and H. multifilis by dorsal fin predominantly XII,13, anal fin II, 15 or
16 (usually 16), absence of black stripes and presence of numerous tiny red spots along body (Figures 3 and 4),
diminishing in size posteriorly. Its peculiar coloration (vivid orange spots, nape green or white) is different from all
congeners except H. springeri and some H. aequipinnis. A recent phylogenetic analysis shows a low level of
divergence between Hypleurochilus brasil sp. n. and H. fissicornis (0.6–0.8%; Levy et al. 2013). These two species
differ in number of dorsal and anal-fin rays (Table 1).
Hypleurochilus brasil was misidentified as H. fissicornis by Gasparini & Floeter (2001) and is considered as
Hypleurochilus n. sp. by Levy et al. (2013).
Acknowledgements
We thank the Brazilian Navy (Marinha do Brasil – 1° Distrito Naval) and TAMAR/ICMBio Project for logistical
support; Flamar, Windive, Voz da Natureza and Fauna for diving support; R. Santos, T. Simon, R. Macieira for
collaboration on dives and collecting specimens; L. B. Stocco for the diafanization of specimens; R. Macieira, S.
Floeter, J.C. Joyeux and M. Gaither for revision and assistance; I. Sazima for ZUEC and L. Rocha and D. Catania
for CAS holdings; A.S. Martins, J.C. Joyeux and C. Pimentel for assistance at research labs and CIUFES. We are
especially grateful to A. Levy for sharing with us his preliminary DNA analysis, to R. Macieira and R. Francini-
Filho for the excellent photographs and V. Uhlig for the map elaboration. Coordenação de Aperfeiçoamento de
Pessoal de Nível Superior (CAPES) provided a postdoctoral fellowship for one of the authors (CAR). This paper is
part of the project “Cadeia Vitória-Trindade: testando a teoria de conectividade por “stepping stones” em peixes
recifais” (grant CNPq 470725/2009-5 to J.C. Joyeux).
References
Almada, F., Almada, V.C., Guillemaud, T. & Wirtz, P. (2005) Phylogenetic relationships of the north-eastern Atlantic and
Mediterranean blenniids. Biological Journal of the Linnean Society, 86, 283–295.
http://dx.doi.org/10.1111/j.1095-8312.2005.00519.x
Bath, H. (1994) Untersuchung der Arten Hypleurochilus geminatus (Wood 1825), H. fissicornis (Quoy & Gaimard 1824) und
H. aequipinnis (Günther 1861), mit Revalidation von Hypleurochilus multifilis (Girard 1858) und Beschreibung von zwei
neuen Arten. Senckenbergiana Biologica, 74, 59–85.
Dingerkus, G. & Uhler, L.D. (1977) Enzyme clearing of alcian blue stained whole small vertebrates for demonstration of
cartilage. Stain Technology, 52 (4), 229–232.
http://dx.doi.org/10.3109/10520297709116780
Floeter, S.R., Rocha, L., Robertson, D.R., Joyeux, J.-C., Smith-Vaniz, W.F., Wirtz, P., Edwards, A.J., Barreiros, J.P., Ferreira,
C.E.L., Gasparini, J.L., Brito, A., Falcòn, J.M., Bowen, B.W. & Bernardi, G. (2008) Atlantic reef fish biogeography and
evolution. Journal of Biogeography, 35, 22–47.
Gasparini, J.L. & Floeter, S.R. (2001) The shore fishes of Trindade Island, western South Atlantic. Journal of Natural History,
35 (11), 1639–1656.
http://dx.doi.org/10.1080/002229301317092379
Levy, A., von der Heyden, S., Floeter, S.R., Bernardi, G. & Almada, V.C. (2013) Phylogeny of Parablennius Miranda Ribeiro,
1915 reveals a paraphyletic genus and recent Indo- Pacific diversification from an Atlantic ancestor. Molecular
Phylogenetics and Evolution, 67, 1–8.
http://dx.doi.org/10.1016/j.ympev.2012.12.010
Rangel, C.A. & Guimarães, R.Z.P. (2010) Taxonomia e distribuição da família Blenniidae (Teleostei: Blennioidei) na costa
leste do Brasil. Revista Brasileira de Zoociências, 12 (1), 17–41.
Pinheiro, H.T., Camilato, V., Gasparini, J.L. & Joyeux, J.-C. (2009) New records of fishes for Trindade-Martin Vaz oceanic
insular complex, Brazil. Zootaxa, 2298, 45–54.
Pinheiro, H.T., Ferreira, C.E.L., Joyeux, J.-C., Santos, R.G. & Horta, P.A. (2011) Reef fish structure and distribution in a south-
western Atlantic Ocean tropical island. Journal of Fish Biology, 79, 1984–2006.
http://dx.doi.org/10.1111/j.1095-8649.2011.03138.x
Tamura, K., Dudley, J., Nei, M. & Kumar, S. (2007) MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software
version 4.0. Molecular Biology and Evolution, 24, 1596–1599.
http://dx.doi.org/10.1093/molbev/msm092