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Annotated checklist of the freshwater fishes of continental and insular Honduras

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The freshwater fishes of Honduras were surveyed for a period of four years (2005-2008). Surveys were supplemented with both literature and museum collection reviews. Our results show that there are at least 172 species of fishes inhabiting Honduran mainland and insular freshwater systems, 166 native and six exotic. Primary freshwater fish diversity was low, with only eigth species (4.8%). The remaining species were either secondary freshwater (47 species, 28.3%) or peripheral (111 species, 66.9%). This checklist includes 36 new records for Honduras, and 12 range expansions. Nine species were found to be endemic; however, just two of them (Amphilophus hogaboomorum and Theraps wesseli) are already described. The depauperate primary freshwater fishes fauna of Honduras (8) is congruent with low primary freshwater fishes diversity found in the region between the Usumacinta River and the Nicaraguan great lakes. Although many previously unsampled regions of Honduras were visited as part of this project, there are a variety of remote areas that remain unstudied. While this paper contributes much to the understanding of the distribution and diversity of Honduran freshwater fishes, it is likely that much diversity there remains undocumented.
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Accepted by L. Page: 9 Nov. 2009; published: 9 Dec. 2009
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Copyright © 2009 · Magnolia Press
Zootaxa 2307: 138 (2009)
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Article
Annotated checklist of the freshwater fishes of continental and insular Honduras
WILFREDO A. MATAMOROS
1
, JACOB F. SCHAEFER
2
& BRIAN R. KREISER
2
1
Department of Biological Sciences, The University of Southern Mississippi, 118 College Dr. Box 5018, Hattiesburg, MS 39406,
U.S.A., Instituto Regional para la Biodiversidad. Escuela Agrícola Panamericana El Zamorano, El Zamorano, Francisco Morazán,
Honduras. E-mail: wilfredo.matamoros@usm.edu
2
Department of Biological Sciences, The University of Southern Mississippi, 118 College Dr. Box 5018, Hattiesburg, MS 39406, U.S.A.
E-mail: jake.schaefer@usm.edu, brian.kreiser@usm.edu
Table of contents
Abstract............................................................................................................................................................................... 2
Resumen ..............................................................................................................................................................................2
Introduction .........................................................................................................................................................................3
Materials and methods .......................................................................................................................................................5
Annotated Checklist ............................................................................................................................................................7
CARCHARHINIFORMES .................................................................................................................................................7
PRISTIFORMES .................................................................................................................................................................7
ELOPIFORMES ................................................................................................................................................................. 7
ANGUILLIFORMES.......................................................................................................................................................... 7
CLUPEIFORMES ...............................................................................................................................................................8
CYPRINIFORMES .............................................................................................................................................................8
CHARACIFORMES........................................................................................................................................................... 9
SILURIFORMES ................................................................................................................................................................9
GYMNOTIFORMES........................................................................................................................................................ 11
BATRACHOIDIFORMES................................................................................................................................................ 11
GOBIESOCIFORMES .....................................................................................................................................................11
ATHERINIFORMES ........................................................................................................................................................ 12
CYPRINODONTIFORMES............................................................................................................................................. 12
BELONIFORMES............................................................................................................................................................ 15
SYNGNATHIFORMES ....................................................................................................................................................16
SYNBRANCHIFORMES................................................................................................................................................. 16
PERCIFORMES ............................................................................................................................................................... 17
PLEURONECTIFORMES ...............................................................................................................................................26
TETRAODONTIFORMES ...............................................................................................................................................27
Results and discussion .......................................................................................................................................................27
Acknowledgements ...........................................................................................................................................................28
References .........................................................................................................................................................................29
Appendix ..........................................................................................................................................................................32
MATAMOROS ET AL. 2 · Zootaxa 2307 © 2009 Magnolia Press
Abstract
The freshwater fishes of Honduras were surveyed for a period of four years (2005–2008). Surveys were supplemented
with both literature and museum collection reviews. Our results show that there are at least 172 species of fishes
inhabiting Honduran mainland and insular freshwater systems, 166 native and six exotic. Primary freshwater fish
diversity was low, with only eigth species (4.8%). The remaining species were either secondary freshwater (47 species,
28.3%) or peripheral (111 species, 66.9%). This checklist includes 36 new records for Honduras, and 12 range
expansions. Nine species were found to be endemic; however, just two of them (Amphilophus hogaboomorum and
Theraps wesseli
) are already described. The depauperate primary freshwater fishes fauna of Honduras (8) is congruent
with low primary freshwater fishes diversity found in the region between the Usumacinta River and the Nicaraguan great
lakes. Although many previously unsampled regions of Honduras were visited as part of this project, there are a variety
of remote areas that remain unstudied. While this paper contributes much to the understanding of the distribution and
diversity of Honduran freshwater fishes, it is likely that much diversity there remains undocumented.
Key words: Central America, Nuclear Middle America, Obligate freshwater fishes, Primary freshwater fishes,
Distribution, Ichthyofauna, Fish fauna, Biodiversity
Resumen
Los peces de agua dulce de Honduras fueron estudiados por un periodo de cuatro años (2005 a 2008). Los muestreos de
campo fueron complementados con revisiones tanto de colecciones de museos como de la literatura disponible. Nuestros
resultados muestran la presencia de 172 especies de peces que habitan los sistemas de aguas continentales del país y de
sus islas, de ellas 166 son nativas y seis exóticas. La diversidad de peces primarios de ambientes dulceacuícolas fue baja,
con tan solo ocho especies (4.8%) presentes. El resto fueron secundarias (47 especies, 28.3%) o periféricas (111 especies,
66.9%). Esta lista incluye 36 registros nuevos para Honduras y 12 expansiones de rango geográfico. Nueve especies
fueron reportadas como endémicas; sin embargo solamente dos (Amphilophus hogaboomorum y Theraps wesseli) son
consideradas especies válidas. La descripción de las ocho especies restantes está aún pendiente. El bajo número de
especies primarias dulceacuícolas (8) en Honduras coincide con el bajo número de especies primarias reportadas
anteriormente en la región entre el río Usumacinta y los grandes lagos de Nicaragua. Aunque muchas regiones de
Honduras que no habían sido previamente muestreadas fueron visitadas como parte de este proyecto, todavía hay áreas
remotas del país que precisan ser estudiadas. Este trabajo contribuirá extensamente al entendimiento de la distribución y
diversidad de los peces de agua dulce de Honduras; sin embargo, mucha de la diversidad ictiológica del país requiere aún
ser investigada con mayor profundidad.
Zootaxa 2307 © 2009 Magnolia Press · 3
FRESHWATER FISHES OF HONDURAS
Introduction
The diversity and distributional patterns of Honduran freshwater fishes are the product of recent geological
events (Myers, 1966). All primary and secondary freshwater species that inhabit Honduras are of South
American origin (Miller, 1966, Myers, 1966), moving to the region during or after the raising and closure of
the Isthmus of Panama during the Pliocene (Marshall et al., 1979, Stehli & Webb, 1985). The proposed timing
of the enclosure of the Panamanian isthmus varies from between 3.1 to 3.5 million years ago (Coates et al.,
1992, Coates & Obando, 1996) to as early as 1.8 million years ago (Keller et al., 1989). While the formation
of this land bridge is often cited as the major event structuring Honduran freshwater fish diversity, local
geologic, climatic and other factors have also certainly played a role (Savage, 1982). Unfortunately, few
attempts have been made at studying Honduran freshwater fish biodiversity on a scale adequate to assess the
role of local vs. regional processes in structuring biogeographic patterns in the country. As a result, Honduras
(Fig. 1) has long represented a large gap in biogeographical knowledge of Central America fishes (Carr and
Giovannoli, 1950, Miller, 1966, Lyons, 2005).
Accordingly, as a baseline for future biogeographical studies, we present an updated checklist of the
freshwater fishes of Honduras that has been compiled from: 1) field sampling of all major drainages, 2) data
from published literature and 3) review of museum holdings from Honduras. Checklists like this are an
important tool for researchers, governmental and non-governmental agencies with interest in documenting
and conserving biodiversity. It will serve as a foundation for future research aimed at understanding the origin
and status of Honduran fish diversity as well as effective management and conservation programs (McNeely
et al., 1990).
Review of freshwater ichthyographical research in Honduras
Most of what is known about Honduran ichthyology is based on work done at a larger regional scale.
Distributional ranges of freshwater fishes that included the territory of Honduras were mentioned in the works
of Jordan & Evermann (1896–1900), Regan (1906–1908), and Jordan et al. (1930). These publications
analyzed the freshwater ichthyofauna of Central America in general. However, sampling in Honduras was
almost non-existent at the time. In his work with cyprinodonts, Hubbs (1924, 1926 and 1931) mentioned a
number of Honduran collections containing Phallichthys amates, Belonesox belizanus, and Alfaro huberi.
Fowler (1932) reported collections in the Lancetilla and Choluteca Rivers. Rehn (1932) reported some
collections in the Honduran Mosquitia region. Strong (1934) reported a bull shark (Carcharhinus leucas) in
the Patuca River in La Mosquitia. Miller (1955) reported specimens of Profundulus guatemalensis collected
in 1934 by A. Greenberg in western Honduras. Fowler (1943) reported collections made by G. Orr in Islas de
la Bahía, and described Poecilia orri with specimens collected in the island of Bonnaca. The first detailed
sampling of rivers in the country was carried out by A. Carr in the late 1940’s. Carr focused on rivers of the
Honduran Pacific slope, culminating with an analysis of the fishes of the Choluteca River and the description
of Amphilophus hogaboomorum (Carr & Giovannoli, 1950). Carr also published a second paper on the
distribution and systematic relationships of some freshwater fishes of the Honduran and Nicaraguan
Mosquitia region (Miller & Carr, 1974).
The overall structure of Central American ichthyographical provinces was first proposed by Miller
(1966). He proposed that Honduras was part of the Chiapas-Nicaraguan Province that extends from southern
México to southern Nicaragua. Miller (1966) did not suggest separate provinces for the Honduran and
Nicaraguan Atlantic slope, arguing there was not enough information available for that part of Central
America. Ten years later, however, Bussing (1976), proposed a second additional ichthyographical province
for Honduras: the Usumacinta province on the Honduran Atlantic slope. This province extends from the
Usumacinta River in southern México to northern Nicaragua. From 1968 to 1970, Martin (1972) intensively
sampled parts of Honduras as part of an unpublished thesis. For the next two decades, there were no major
collections conducted on Honduran freshwaters fishes. In 1996, Theraps wesseli was described from
MATAMOROS ET AL. 4 · Zootaxa 2307 © 2009 Magnolia Press
individuals collected in the Bellaire River, close to the city of Jutiapa in the Department of Atlántida (Miller,
1996).
Geological history
The region of Nuclear Central America that corresponds to Honduras has a complex geological history
characterized by intensive faulting, orogeny, sea level change, sedimentation, and volcanism. The land
connection between North and South America was lost in the early Jurassic as Pangaea broke apart (Dietz &
Holden, 1970). It is widely accepted that no land connection existed between North and South America from
the early Cretaceous to the Pliocene (Holden & Dietz, 1972; Malfait & Dinkelman, 1972; Ladd, 1976;
Duellman, 1979; Savage, 1982). However, parts of Nuclear Central America, including the majority of
Honduras, may have been above water since the Cretaceous (Savage, 1982). A faunal exchange between
México and Nuclear Central America through the Isthmus of Tehuantepec happened during the Tertiary
(Olson & McGrew, 1941). This faunal exchange was facilitated by a climatic filter barrier and a probable
partial sea barrier across the Isthmus (Savage, 1982). The Miocene was characterized by intensive faulting in
the area, which produced several graben valleys, including the Honduras depression that is a corridor from the
Caribbean to the Pacific slope (Roberts & Irving, 1957). During the Miocene – Pliocene intense volcanism
occurred in the area (Roberts & Irving, 1957). Intense orogeny during late Pliocene or early Pleistocene
formed the terrace systems of interior Honduras. Much of the Caribbean lowlands emerged during the
Pleistocene as a result of extensive erosion and deposition in alluvial lowland depressions. There were also
hypothesized fluctuations in sea level and climate during the Pleistocene glaciations (Roberts & Irving, 1957).
The uplifting of the Isthmus of Panama during the mid-Pliocene created the land bridge connecting North and
South America (Beu, 2001). This facilitated a massive faunal migration from both continents, referred to as
the Great American Biotic Interchange (Marshall et al., 1979; Stehli & Webb, 1985).
Although there are no currently active volcanoes in Honduras, volcanism has shaped the physiographic
features of the country. Volcanic activity in Nuclear Central America was widespread during the Miocene and
Pliocene, which resulted in the deposition of andesitic and rhyolitic ejecta over the majority of the southern
half of Honduras (Roberts & Irving, 1957). The rough terrain in this region was largely created during the
Oligocene (the Sierras Madre in México), Miocene (highlands of Nuclear Central America) and Pliocene
(highlands of Lower Central America including the Comayagua Graben) (Roberts & Irving, 1957;
Maldonado-Koerdell, 1964; Savage, 1982). The Gulf of Fonseca was formed by downfaulting at the
Comayagua Graben and the Nicaraguan Graben (West, 1964). Finally, Islas de la Bahía on the Honduran
Caribbean coast (Fig. 1) appear to be a northward extension of the Sierra de Omoa and were apparently
connected to the mainland throughout most of the middle and late Tertiary (Vinson & Brineman, 1963).
Physiography
A physiographical region is defined as a geographic area with similar geologic, topographic, and edaphic
features (West, 1964). Subdivisions of these physiographic regions are called sub-regions, in which there is a
general uniformity of surface features (Martin, 1972). There are three major physiographic regions proposed
for Honduras (Bengston, 1926; Carr, 1950; Martin, 1972): the Pacific Lowlands, the Caribbean Lowlands, and
the Interior Serranía Region. The Pacific Lowlands region does not contain any sub-regions, but includes the
river basins that drain into the Gulf of Fonseca (Bengston, 1926; Carr 1950). This includes the Goascorán,
Nacaome, Choluteca, and Negro rivers (Fig. 2). The Caribbean Lowlands extend from the delta of the
Motagua River in western Honduras to the Coco River bordering Nicaragua. The Caribbean lowlands are
divided into five sub-regions (Bengston 1926; Carr 1950); the Motagua River Delta, the Ulúa-Chamelecón
River Valley, the Nombre de Dios Plain, the Aguán-Negro River Plain, and the Mosquitia Coast (Fig. 2). The
Interior Serrania Region is formed by the Northern Cordillera and the Southern Cordillera sub-regions.
Detailed description of Honduran physiographic regions and sub-regions are found in Bengston (1926), Carr
(1950), Martin (1972), Wilson & Meyer (1985) and McCraine & Wilson (1985).
Zootaxa 2307 © 2009 Magnolia Press · 5
FRESHWATER FISHES OF HONDURAS
FIGURE 1. Map of Honduras showing the political divisions (Departments). Dots represent localities sampled during
2005–2008.
Materials and methods
Institutional abbreviations are as follows: CAS = California Academy of Sciences; FLMNH = Florida
Museum of Natural History; FMNH = Field Museum of Natural History; GCRL = Gulf Coast Research
Laboratory; LACM = Los Angeles County Museum; UMMZ = University of Michigan Museum of Zoology;
USM = University of Southern Mississippi Museum of Ichthyology; USNM = United States National
Museum.
Field sampling at 278 localities in Honduras was performed in July 2005, November 2005, May–July
2006, May–August 2007, January–March 2008, and June–August 2008 (Fig. 1). Sampling gear included
seines (various sizes) with a mesh of 3.1 mm, cast nets, spear fishing, and backpack electrofishers. Captured
fishes were fixed in 10% buffered formalin solution before being rinsed in water and preserved in 75%
ethanol. Specimens were deposited at USM. To complement distribution and diversity data collected in our
field surveys, we reviewed both the scientific and “grey” literature. We also queried the inter-institutional
database NEODAT (http://www.neodat.org) and the online data bases of FLMNH, FMNH, GCRL, LACM,
and UMMZ. The first author personally reviewed the Honduran freshwater fish holdings at the collections of
the following museums: FLMNH, FMNH, GCRL, and parts of the Honduran holdings at UMMZ.
The annotated checklist is arranged by order and family following Eschmeyer & Fong (2008). Genera and
species within a family are arranged in alphabetical order. The family tolerance to salinity is listed according
MATAMOROS ET AL. 6 · Zootaxa 2307 © 2009 Magnolia Press
to the classification by Myers (1949). Species valid name, authority, and year of description follow
Eschmeyer & Fricke (2009), with the exception of Rhamdia quelen from which we follow Perdices et al.
(2002) in considering all Honduran R. quelen as belonging to the species R. guatemalensis. Honduran taxa
included in the genus Cichlasoma is referred to here as Cichlasoma’ following Kullander (2003).
After the authority name, the common English name was provided followed by the common Spanish
name. After the common name, we specify its origin as native, endemic or exotic. The exotic species included
in the checklist are only those for which there is evidence of reproductive populations in Honduras.
The distribution of each species is given in two ways and is based on our own collections, literature
reviews, online databases and museum specimens. First, we list the Honduran departments (alphabetical
order) for which there are records for the species. Second, we list the major river drainage basins (Atlantic
slope before Pacific slope drainages, all listed in west to east order) for which there are records for the species.
A considerable number of records on the checklist represent expansions of the known range or new
reports of the species for Honduras. For range expansions and new country records (or both), we list the
museum specimens that are associated with the individual specimens of interest. In the event that the museum
specimen is not available, the field collection number is given. Finally, we considered a species new to
Honduras as one that is not listed for Honduras either in FishBase (Froese & Pauly, 2009) or Reis et al.
(2003).
FIGURE 2. Map of Honduras showing 19 major Honduran river drainage basins. Shaded areas depict drainages located
on the Pacific slope; unshaded areas are on the Atlantic Slope.
Zootaxa 2307 © 2009 Magnolia Press · 7
FRESHWATER FISHES OF HONDURAS
Annotated Checklist
CARCHARHINIFORMES
Carcharhinidae. Peripheral.
Carcharhinus leucas (Müller & Henle, 1839). Bull shark, tiburón toro. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Remarks: Martin (1972) listed C. leucas in Honduras based on a photograph taken by Strong (1934) in
the Patuca River. This is the only documented report of C. leucas in Honduran freshwaters. Greenfield &
Thomerson (1997) referred to a C. leucas in the “Patula River”, which we assume is an error and they were in
fact referring to the Patuca River.
Rhizoprionodon porosus (Poey, 1861). Caribbean sharpnose shark, cazón antillano. Native.
Department: Gracias a Dios. Drainages: Atlantic slope: Patuca and Coco.
PRISTIFORMES
Pristidae. Peripheral.
Pristis pectinata Latham, 1794. Smalltooth sawfish, pez sierra. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
ELOPIFORMES
Megalopidae. Peripheral.
Megalops atlanticus Valenciennes, 1847. Tarpon, sábalo. Native.
Departments: Atlántida, Colón and Gracias a Dios. Drainages: Atlantic slope: Cangrejal, Aguán, Plátano
and Patuca.
ANGUILLIFORMES
Anguillidae. Peripheral.
Anguilla rostrata (Lesueur, 1817). American eel, anguila americana. Native.
Departments: Atlántida, Colón, Cortés, Islas de la Bahía and Yoro. Drainages: Atlantic slope: Motagua,
Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Roatán and Guanaja.
Ophichthidae. Peripheral.
Myrophis punctatus Lütken, 1852. Speckled worm eel, tieso gusano. Native.
Departments: Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón,
Patuca, Roatán and Guanaja..
MATAMOROS ET AL. 8 · Zootaxa 2307 © 2009 Magnolia Press
CLUPEIFORMES
Clupeidae. Peripheral.
Harengula clupeola (Cuvier, 1829). False pilchard, sardinita carapachona. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Harengula humeralis (Cuvier, 1829). Redear sardine, sardinita de ley. Native.
Department: Islas de la Bahía. Drainage: Atlantic slope: Roatán.
Jenkinsia lamprotaenia (Gosse, 1851). Dwarf herring, sardinita flaca. Native.
Department: Islas de la Bahía. Drainage: Atlantic slope: Roatán.
Opisthonema oglinum (Lesueur, 1818). Atlantic thread herring, sardinita vivita de hebra. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Engraulidae. Peripheral.
Anchoa colonensis Hildebrand, 1943. Narrowstriped anchovy, anchoa rayita. Native.
Departments: Cortés and Gracias a Dios. Drainages: Atlantic slope: Chamelecón and Patuca.
Anchoa filifera (Fowler, 1915). Longfinger anchovy, anchoa dedolarga. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Anchoa parva (Meek & Hildebrand, 1923). Little anchovy, anchoa parva. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Anchovia clupeoides (Swainson, 1839). Zabaleta anchovy, anchoveta sardina. Native.
Department: Gracias a Dios. Drainage: Patuca.
Anchoviella elongata (Meek & Hildebrand, 1923). Elongate anchovy, anchoveta alargada. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
CYPRINIFORMES
Cyprinidae. Primary.
Ctenopharyngodon idella (Valenciennes, 1844). Grass carp, carpa herbívora. Exotic.
Departments: Cortés and Santa Bárbara. Drainages: Atlantic slope: Chamelecón and Ulúa.
Remarks: Introduced by government agencies in an attempt to strengthen aquaculture activities and
provide animal protein to rural communities (D. Meyer, pers. comm.).
Hypophthalmichthys molitrix (Valenciennes, 1844). Silver carp, carpa plateada. Exotic.
Departments: Cortés and Santa Bárbara. Drainages: Atlantic slope: Chamelecón and Ulúa.
Remarks: Introduced by government agencies in an attempt to strengthen aquaculture activities and
provide animal protein to rural communities (D. Meyer, pers. comm.).
Zootaxa 2307 © 2009 Magnolia Press · 9
FRESHWATER FISHES OF HONDURAS
CHARACIFORMES
Characidae. Primary.
Astyanax aeneus (Günther, 1860). Banded tetra, sardina. Native.
Departments: Atlántida, Choluteca, Colón, Comayagua, Copán, Cortés, El Paraíso, Francisco Morazán,
Gracias a Dios, Intibucá, La Paz, Olancho, Santa Bárbara, Valle and Yoro. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Pacific slope: Lempa, Goascorán, Nacaome, Choluteca and Negro.
Brycon guatemalensis Regan, 1908. Macabi tetra, machaca. Native.
Departments: Choluteca, Comayagua, Copán, Cortés, El Paraíso, Francisco Morazán, La Paz, Lempira,
Santa Bárbara and Yoro. Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa, Leán and Choluteca.
Hyphessobrycon tortuguerae Böhlke, 1958. Tortuguero tetra, sardinita de Tortuguero. Native.
Departments: El Paraíso, Gracias a Dios and Olancho. Drainages: Atlantic slope: Patuca, Warunta and
Coco. Pacific slope: Choluteca.
Roeboides bouchellei Fowler, 1923. Crystal tetra, sardinita plateada. Native.
Departments: Choluteca, El Paraíso, Francisco Morazán, Gracias a Dios, Olancho and Valle. Drainages:
Atlantic slope: Sico-Tinto, Plátano, Patuca, Warunta and Coco. Pacific slope: Lempa, Goascorán, Nacaome,
Choluteca and Negro.
Remarks: Bussing (2002) describes the distributional range for R. bouchellei as across the Atlantic slope
of Central America from the Patuca River in Honduras to the Matina River in Costa Rica. Martin (1972)
reported R. bouchellei (field numbers MMH 1969-14, MMH 1969-19, material deposited at LACM) in the
Sico-Tinto o Negro River, which is located west of the Patuca River. We consider the distributional range of R.
bouchellei to extend from the Sico-Tinto o Negro River in Honduras to the Matina River in Costa Rica, in the
Atlantic slope of Central America.
SILURIFORMES
Ariidae. Peripheral.
Cathorops higuchii Marceniuk & Betancur-R., 2008. Higuchi’s Sea Catfish, bagre de Higuchi. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Coco.
Remarks: Details about the distribution of this species in Honduras and Mesoamerica are given by
Marceniuk & Betancur-R. (2008).
Cathorops melanopus (Günther, 1864). Dark sea catfish, bagre prieto. Native.
Departments: Cortés and Santa Bárbara. Drainages: Atlantic slope: Motagua and Ulúa.
Remarks: C. melanopus was thought to be endemic to the Motagua river basin in Guatemala and possibly
occurring in Honduras (Marceniuk & Betancur-R., 2008). Vouchers LACM 32355-1 collected in the Río Ulúa
in the department of Santa Bárbara, and LACM 32405-1 collected in the Río Blanco (tributary of the Ulúa
River) represent the first records of C. melanopus in Honduras as well as a significant range extension.
Furthermore, Vaux (1985) collected C. melanopus at the Yure River (at the confluence with the Quebrada de
Chamo), which is a tributary of the Humuya River, Río Ulúa system.
Cathorops sp. Raredon’s sea catfish, bagre de Raredon. Native.
MATAMOROS ET AL. 10 · Zootaxa 2307 © 2009 Magnolia Press
Remarks: The distributional range of the Raredon’s sea catfish as reported by Marceniuk et al. (in press),
extends from Sinaloa México to the department of La Libertad to La Unión in El Salvador. In the description
of the species, Marceniuk et al. (in press) included material collected in La Unión Bay. La Unión Bay is a
small body of water located in the Gulf of Fonseca bordering Honduras and El Salvador. Based on the
geographical location of the La Unión Bay, it is most likely that the Raredon’s sea catfish also occurs in
Honduras (R. Betancur-R., pers. comm.).
Cathorops steindachneri (Gilbert & Starks, 1904). Steindachner’s sea catfish, bagre de Steindachner. Native.
Remarks: The distributional range of C. steindachneri extends from El Salvador to Panama (Marceniuk
et al., in press). This species has been reported from the Gulf of Fonseca in El Salvador, but is also potentially
present on the Honduran side of the Gulf of Fonseca (R. Betancur-R., pers. comm.; Marceniuk et al., in press),
since the Gulf of Fonseca is a shared body of water between these two countries.
Cathorops taylori (Hildebrand, 1925). Taylors sea catfish, bagre de Taylor. Native.
Remarks: While no specimens of this species have been collected in Honduras, its occurrence in the
country is very likely (R. Betancur-R., pers. comm.). Marceniuk et al. (in press) listed specimens collected in
La Unión Bay, which is a small shared body of water at the Honduras – El Salvador border.
Sciades assimilis (Günther, 1864). Maya sea catfish, bagre maya. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Sciades guatemalensis (Günther, 1864). Widehead sea catfish, bagre guatemalense. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Nacaome and Choluteca.
Sciades seemanni (Günther, 1864). Tete sea catfish, bagre tete. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Lempa, Goascorán, Nacaome and Negro.
Ictaluridae. Primary.
Ictalurus punctatus (Rafinesque, 1818). Channel catfish, bagre de canal. Exotic.
Departments: Comayagua, Cortés and Santa Bárbara. Drainages: Atlantic slope: Chamelecón and Ulúa.
Remarks: I. punctatus was introduced in Honduras in the early 1960s for aquaculture purposes by
technicians of the United Fruit Company. During Hurricane Fifi in 1975, many fish escaped into the Ulúa and
Chamelecón Rivers. In the environmental impact study prior to building the El Cajón reservoir, Vaux (1985)
reported I. punctatus. There is also evidence of at least one fish farmer in Comayagua that has been capable of
reproducing catfish locally (D. Meyer, pers. comm.).
Heptapteridae. Primary.
Rhamdia guatemalensis (Günther, 1864). Guatemalan chulin, barbudo de Guatemala. Native.
Departments: Atlántida, Choluteca, Colón, Comayagua, Copán, Cortés, El Paraíso, Francisco Morazán,
Gracias a Dios, Intibucá, La Paz, Olancho, Santa Bárbara, Valle and Yoro. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Pacific slope: Lempa, Goascorán, Nacaome, Choluteca and Negro.
Remarks: Silfvergrip’s (1996) revision of the genus Rhamdia synonymized R. guatemalensis with R.
quelen. Perdices et al. (2002) analyzed the evolutionary history of the genus in Central America and
concluded that South American R. quelen are evolutionarily distinct from R. guatemalensis from Central
America. Here we treat R. guatemalensis as a distinct species.
Zootaxa 2307 © 2009 Magnolia Press · 11
FRESHWATER FISHES OF HONDURAS
Rhamdia laticauda (Kner, 1858). Filespine Chulin, chulín. Native.
Departments: Atlántida, Comayagua, Copán, Cortés, El Paraíso, Francisco Morazán, Intibucá, Lempira,
Olancho and Santa Bárbara. Drainages: Atlantic slope: Motagua, Ulúa, Chamelecón, Leán, Cangrejal, Lislis,
Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco. Pacific slope: Lempa and Choluteca.
GYMNOTIFORMES
Gymnotidae. Primary.
Gymnotus cylindricus La Monte, 1935. Knifefish, pez cuchillo. Native.
Departments: Atlántida, Choluteca, Colón, Comayagua, Cortés, Gracias a Dios, Santa Bárbara and Yoro.
Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano,
Patuca, Warunta and Coco. Pacific slope: Choluteca.
Remarks: Albert & Miller et al. (1995) stated that G. cylindricus occurs only in drainages on the Atlantic
slope of Central America. However, some of the material they examined in their paper came from localities in
the Honduran Pacific slope, wrongly identified as Atlantic slope localities. This material includes: UMMZ
155831, UMMZ 188296, UMMZ 188297 (see Albert & Miller, 1995; Albert et al., 1999; Albert, 2001).
Further, Bussing (2002) reported G. cylindricus from the Yeguare River, a tributary of the Choluteca River,
which drains to the Gulf of Fonseca on the Honduran Pacific slope.
Gymnotus maculosus Albert & Miller, 1995. Spotted knifefish, cuchillo manchado. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Lempa, Goascorán, Nacaome, Choluteca,
and Negro.
Remarks: Albert & Miller (1995) did not include material from Honduras in the description of the
species. However, Bussing (2002) and Miller et al. (2005) report a continuous distribution extending from
southern México to Costa Rica, including the Honduran Pacific slope.
BATRACHOIDIFORMES
Batrachoididae. Peripheral.
Batrachoides gilberti Meek & Hildebrand, 1928. Large-eye toadfish, sapo ojón. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca
Remarks: The following five vouchers collected in Brus Laguna represent the first report of B. gilberti in
Honduras: FMNH 84545-84549.
GOBIESOCIFORMES
Gobiesocidae. Peripheral.
Gobiesox strumosus Cope, 1870. Skilletfish, cazoleta. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: The following two vouchers collected in the Cieneguita River (GCRL 4446) and the Tulián
River (GCRL 4459) represents the first report of G. strumosus in Honduras.
MATAMOROS ET AL. 12 · Zootaxa 2307 © 2009 Magnolia Press
ATHERINIFORMES
Atherinopsidae. Peripheral.
Atherinella argentea Chernoff, 1986. Moon silverside, plateadita de la luna. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Lempa, Goascorán, Nacaome, Choluteca
and Negro.
Atherinella blackburni (Schultz, 1949). Beach silverside, plateadita playera. Native.
Departments: Colón and Islas de la Bahía. Drainages: Atlantic slope: Lislis and Roatán.
Remarks: The following two vouchers collected in a stream in the island of Roatán; FMNH 84961, and
UMMZ 199672 collected 5 km west of the city of Trujillo represent the first report of A. blackburni
in Honduras.
Atherinella guija (Hildebrand, 1925). Guija silverside, plateadita del Guija. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Lempa, Goascorán, Nacaome and
Choluteca.
Atherinella meeki (Miller, 1907). Meek’s silverside, plateadita de Meek. Native.
Department: Cortés. Drainages: Atlantic slope: Motagua and Chamelecón.
Remarks: A. meeki was described by Miller (1907) from material collected in the Motagua River. A.
meeki has been considered endemic to the Motagua River in Guatemala since its description. Voucher GCRL
6004 identified as A. meeki, collected in the Chivana River which is a tributary of the Chamelecón River in
Honduras, represents the first report of A. meeki in Honduras as well as an extension of its distributional
range.
Atherinella milleri (Bussing, 1979). Miller’s silverside, plateadita de Miller. Native.
Departments: Atlántida, Colón and Gracias a Dios. Drainages: Atlantic slope: Cangrejal, Lislis, Aguán,
Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Atherinella pachylepis (Günther, 1864). Thickscale silverside, plateadita de escama gruesa. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Lempa, Goascorán, Nacaome, Choluteca
and Negro.
CYPRINODONTIFORMES
Rivulidae. Secondary.
Kryptolebias marmoratus (Poey, 1880). Mangrove rivulus, almirante de manglar. Native.
Departments: Atlántida and Islas de la Bahía. Drainages: Atlantic slope: Cangrejal, Roatán and Guanaja.
Remarks: Voucher FLMNH 116518 from the island of Guanaja and USM 31675 collected in the Río
Cangrejal represent the first report of K. marmoratus in Honduras.
Rivulus tenuis (Meek, 1904). Maya rivulus, almirante maya. Native.
Departments: Atlántida and Cortés. Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa, Leán and
Cangrejal.
Zootaxa 2307 © 2009 Magnolia Press · 13
FRESHWATER FISHES OF HONDURAS
Profundulidae. Secondary.
Profundulus guatemalensis (Günther, 1866). Guatemalan killifish, escamudo de Guatemala. Native.
Departments: Copán, Intibucá and Lempira. Drainages: Atlantic slope: Motagua and Ulúa. Pacific slope:
Lempa.
Profundulus sp. 1. Ulúan killifish, escamudo del Ulúa. Endemic.
Departments: Comayagua and Francisco Morazán. Drainages: Atlantic slope: Ulúa. Pacific slope:
Nacaome.
Remarks: This species is pending description (Matamoros & Schaefer, in review).
Profundulus sp. 2. Santa Barbara killifish, escamudo de Santa Barbara. Endemic.
Department: Santa Bárbara. Drainage: Atlantic slope: Ulúa.
Remarks: This species is pending description.
Poeciliidae. Secondary.
Alfaro cultratus (Regan, 1908). Alfaro’s livebearer, olomina de Alfaro. Native.
Departments: Gracias a Dios. Drainage: Atlantic slope: Coco.
Remarks: The known distributional range of A. cultratus extends from the Prinzapolka River in the
Nicaraguan Mosquitia to the Cricamola River in Panama, in the Atlantic slope of Central America (Bussing,
2002). USM collection field number WAM08-06 collected in the Rus Rus River which is a tributary of the
Coco River in the Honduran Mosquitia, department of Gracias a Dios, represents the first report of A.
cultratus in Honduras, as well as a range extension.
Alfaro huberi (Fowler, 1923). Hubers livebearer, olomina de Huber. Native.
Departments: Atlántida, Cortés, Comayagua, Copán, El Paraíso, Francisco Morazán, Gracias a Dios,
Intibucá, La Paz, Lempira, Olancho, Santa Bárbara and Yoro. Drainages: Atlantic slope: Motagua,
Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco. Pacific
slope: Lempa and Choluteca.
Belonesox belizanus Kner, 1860. Pike killifish, picudito. Native.
Departments: Atlántida, Cortés, Colón, Gracias a Dios and Yoro. Drainages: Atlantic slope: Motagua,
Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Gambusia nicaraguensis Günther, 1866. Nicaraguan mosquitofish, bubuchita de Nicaragua. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios, Islas de la Bahía and Yoro. Drainages: Atlantic
slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta,
Coco, Roatán and Guanaja.
Heterandria anzuetoi Rosen & Bailey, 1979. Anzueto’s killifish, olomina de Anzueto. Native.
Departments: Atlántida , Colón, Comayagua, Copán, Cortés, Francisco Morazán, Gracias a Dios,
Olancho, Santa Bárbara and Yoro. Drainages: Atlantic slope: Motagua, Ulúa, Chamelecón, Leán, Cangrejal,
Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco. Pacific slope: Lempa and Choluteca.
Heterandria bimaculata (Heckel, 1848). Spottail killifish, olomina de dos manchas. Native.
Departments: Atlántida and Cortés. Drainages: Atlantic slope: Motagua and Cangrejal.
MATAMOROS ET AL. 14 · Zootaxa 2307 © 2009 Magnolia Press
Phallichthys amates (Miller, 1907). Merry widow, bubuchita de amates. Native.
Departments: Atlántida, Cortés, Colón, Gracias a Dios, Olancho and Yoro. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Poecilia gilli (Kner, 1863). Gill’s Molly, olomina de Gill. Native.
Departments: Atlántida, Choluteca, Colón, Comayagua, Copán, Cortés, El Paraíso, Francisco Morazán,
Gracias a Dios, Intibucá, La Paz, Lempira, Ocotepeque, Olancho and Santa Bárbara. Drainages: Atlantic
slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta,
Coco and Lempa. Pacific slope: Goascorán, Nacaome, Choluteca and Negro.
Remarks: The distribution of P. gillii presented here is based on Bussing (2002).
Poecilia marcellinoi Poeser, 1995. Marcellino’s Molly, olomina de Marcellino. Native.
Departments: Choluteca, Comayagua, Copán, Cortés, El Paraíso and Santa Bárbara. Drainages: Atlantic
slope: Motagua and Ulúa. Pacific slope: Lempa and Choluteca.
Remarks: Miller (1907) found P. marcellinoi in the Motagua River basin. In redescribing the species,
Poeser (1995) listed a number of localities from the Lempa River in El Salvador. Because Salvadorian
drainages all have headwaters in Honduras, it would not be surprising to find this species on the Honduran
side of the Lempa River. Furthermore, Villa (1982) listed a Poecilia sp. from the Ulúa River in Honduras.
This species is considered by Poeser (unpubl. data) to be P. marcellinoi. Finally, we collected P. marcellinoi in
the Choluteca River drainage, meaning the Honduran distribution of P. marcellinoi may be broader than
presented here.
Poecilia sp. 1. Miller’s Molly, olomina de Miller. Endemic.
Departments: Atlántida, Cortés, Gracias a Dios and Olancho. Drainages: Atlantic slope: Chamelecón,
Ulúa, Leán, Cangrejal, Lislis, Aguán and Sico-Tinto.
Poecilia sp. 2. Cangrejal Molly, olomina del Cangrejal. Endemic.
Department: Atlántida. Drainage: Atlantic slope: Cangrejal.
Poecilia sp. 3. Pacific Molly, olomina del Pacifico. Endemic.
Departments: Choluteca and Francisco Morazán. Drainage: Pacific slope: Choluteca.
Poecilia orri Fowler, 1943. Mangrove Molly, olomina de manglar. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios, Islas de la Bahía and Yoro. Drainages: Atlantic
slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Roatán and
Guanaja.
Poeciliopsis pleurospilus (Günther, 1866). Largespot livebearer, bubucha punteada. Native.
Departments: Choluteca, Comayagua, Copán, Cortés, Francisco Morazán, Intibucá, Lempira, Santa
Bárbara and Valle. Drainages: Atlantic slope: Motagua, Chamelecón and Ulúa. Pacific slope: Lempa,
Goascorán, Nacaome and Choluteca.
Remarks: P. gracilis and P. pleurospilus were placed in synonymy by Rosen & Bailey (1963). Miller et
al. (2005) recognized P. gracilis as a distinct species with a range restricted to eastern México and P.
pleurospilus as a second species occurring in México and Honduras.
Poeciliopsis turrubarensis (Meek, 1912). Barred livebearer, bubucha rayada. Native.
Departments: Choluteca, Francisco Morazán, and Valle. Drainages: Pacific slope: Lempa, Goascorán,
Nacaome, Choluteca and Negro.
Zootaxa 2307 © 2009 Magnolia Press · 15
FRESHWATER FISHES OF HONDURAS
Xiphophorus helleri Heckel, 1848. Green swordtail, cola de espada. Native.
Departments: Copán and Santa Bárbara. Drainages: Atlantic slope: Motagua and Chamelecón.
Remarks: Miller et al., (2005) restricts the distributional range of X. helleri to the Nautla River in
Mexico, south to the Usumacinta River in Guatemala, and also to the Sarstún River in Belize. In this research,
we have collected X. helleri in the Motagua River drainage (vouchers USM 34171 from the Copan River and
USM 31500 from the Blanco River, which is a tributary of the Copan River) and in the Chamelecón River
(USM field number WAM09-31). Accordingly, the distributional range of X. helleri is larger than that
proposed by Miller et al. (2005).
Xiphophorus mayae Meyer & Schartl, 2002. Mayan swordtail, cola de espada maya. Native.
Departments: Atlántida, Cortés and Santa Bárbara. Drainages: Atlantic slope: Chamelecón, Ulúa, Leán
and Cangrejal.
Remarks: Meyer and Schartl (2002) suggest that X. mayae may occur in the Chamelecón and Lancetilla
Rivers in Honduras. Voucher USM 31836 confirm the ocurrance of X. mayae in Lancetilla River. Vouchers
USM 34338 collected in the Blanco River at Pulapanzack in the Ulúa River Drainage, USM 31076 from the
Cuero River, USM 31144 from Las Camelias River, USM 31121 from Santiago River and USM 33993 from
the Danto River represent a range expansion for X. mayae.
Anablepidae. Secondary.
Anableps dowei Gill, 1861. Northern four-eyed, cuatrojos. Native.
Departments: Choluteca, El Paraíso and Valle. Drainages: Pacific slope: Lempa, Goascorán, Nacaome,
Choluteca and Negro.
BELONIFORMES
Belonidae. Peripheral.
Strongylura marina (Walbaum, 1792). Atlantic needlefish, agujón verde. Native.
Departments: Atlántida, Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope:
Chamelecón, Cangrejal, Patuca, Roatán and Guanaja.
Strongylura notata (Poey, 1860). Redfin needlefish, agujón negro. Native.
Department: Islas de la Bahía. Drainage: Atlantic slope: Roatán.
Remarks: USM field number WAM08-105 from a freshwater stream in the island of Roatán represents
the first report of S. notata in Honduras.
Strongylura timucu (Walbaum, 1792). Timucu, agujón timucú. Native.
Departments: Cortés, Gracias a Dios and the Bay Island. Drainages: Atlantic slope: Chamelecón, Patuca
and Roatán.
Hemiramphidae. Peripheral.
Hyporhamphus roberti hildebrandi Jordan & Evermann, 1927. Central American halfbeak, agujeta. Native.
Departments: Comayagua, Cortés, Gracias a Dios, Islas de la Bahía, Santa Bárbara and Yoro. Drainages:
Atlantic slope: Ulúa, Patuca, Roatán and Guanaja.
MATAMOROS ET AL. 16 · Zootaxa 2307 © 2009 Magnolia Press
Remarks: Matamoros et al. (2007) reported USM 31216 and USM 33917 as the first records of this
species in Honduras. H. roberti hildebrandi was found to be common in Lake Yojoá and El Cajon reservoir.
Hyporhamphus unifasciatus (Ranzani, 1841). Atlantic silverstripe halfbeak, agujeta del Atlántico. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
SYNGNATHIFORMES
Syngnathidae. Peripheral.
Microphis brachyurus lineatus (Kaup, 1856). Opossum pipefish, pez pipa culebra. Native.
Departments: Atlántida and Cortés. Drainages: Atlantic slope: Chamelecón, Leán, Cangrejal and Lislis.
Remarks: The following vouchers represent the first report of M. brachiurus lineatus in Honduras:
Chamelecón River drainage - USM 31922 from Chivana River, USM 31902 from the Tulián River; Leán
River drainage - USM 31804 and USM 31843 from Lancentilla River; Cangrejal River drainage - USM
31685 from the Cangrejal River, USM 31751, and USM 31764 from Salado River; Lislis River drainage -
USM 31465, USM 31723, USM 31734 from the Papaloteca River, and USM 34042 from the Mármol River
west of the city of Trujillo.
Pseudophallus mindii (Meek & Hildebrand, 1923). Freshwater pipefish, pez pipa de agua dulce. Native.
Department: Atlántida. Drainages: Atlantic slope: Leán and Lislis.
Remarks: Voucher USM 31806 collected in Lancetilla River represents the first report of P. mindii in
Honduras. P. mindii has also been collected in the Papaloteca River east of La Ceiba (C. Small, pers. comm.).
Pseudophallus starksii (Jordan & Culver, 1895). Yellowbelly pipefish, pez pipa de río. Native.
Department: Valle. Drainage: Pacific slope: Nacaome.
Syngnathus pelagicus Linnaeus, 1758. Sargassum pipefish, pez pipa oceánico. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Remarks: Voucher FMNH 84369 collected in Brus Laguna represents the first report of S. pelagicus in
Honduras.
Syngnathus scovelli (Evermann & Kendall, 1896). Gulf pipefish, pez pipa del Golfo. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
SYNBRANCHIFORMES
Synbranchidae. Secondary.
Ophisternon aenigmaticum Rosen & Greenwood, 1976. Obscure swamp eel, anguila falsa. Native.
Departments: Atlántida, Copán and Cortés. Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa,
Leán and Cangrejal.
Synbranchus marmoratus Bloch, 1795. Marbled swamp eel, anguila de lodo. Native.
Departments: Atlántida, Choluteca, Colón, Comayagua, Copán, Cortés, El Paraíso, Francisco Morazán,
Intibucá, La Paz, Olancho, Santa Bárbara, Gracias a Dios, Valle and Yoro. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Pacific slope: Lempa, Goascorán, Nacaome, Choluteca and Negro.
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FRESHWATER FISHES OF HONDURAS
PERCIFORMES
Centropomidae. Peripheral.
Centropomus ensiferus Poey, 1860. Swordspine snook, robalo de espolón. Native.
Departments: Cortés and Gracias a Dios. Drainage: Atlantic slope: Chamelecón, Patuca and Coco.
Centropomus nigrescens Günther, 1864. Black snook, robalo negro. Native.
Department: Choluteca. Drainage: Pacific slope: Choluteca.
Centropomus parallelus Poey, 1860. Smallscale fat snook, robalo escama pequeña. Native.
Departments: Cortés, Gracias a Dios and Santa Bárbara. Drainages: Atlantic slope: Chamelecón, Ulúa
and Patuca.
Centropomus pectinatus Poey, 1860. Tarpon snook, robalo grande. Native.
Departments: Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope: Plátano, Patuca and
Roatán.
Centropomus undecimalis (Bloch, 1792). Common snook, robalo blanco. Native.
Departments: Atlántida, Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Patuca and Roatán.
Centropomus unionensis Bocourt, 1868. Humpback snook, robalo serrano. Native.
Department: Choluteca. Drainage: Pacific slope: Choluteca.
Centrarchidae. Primary.
Micropterus salmoides (Lacepède, 1802). Largemouth bass, lobina negra. Exotic.
Remarks: Micropterus salmoides was introduced into Lake of Yojoá as a sport fish (Ostmark, 1964;
Cruz, 1985). The literature suggests an introduction in the early 1950s (Ostmark, 1964; Cruz, 1985).
However, an earlier arrival in Honduras is possible. Cruz (1985) studied the biology of M. salmoides in the
Lake of Yojoá and provided a synopsis of the introduction. Vaux (1985) collected M. salmoides in the Laguna
de Yure which is adjacent to the Lake of Yojoá. We have not collected M. salmoides outside of the previously
mentioned localities.
Carangidae. Peripheral.
Caranx bartholomaei (Cuvier, 1833). Yellow jack, cojinuda amarilla. Native.
Department: Islas de la Bahía. Drainage: Atlantic slope: Roatán.
Remarks: USM field number WAM08-105 collected in freshwater streams in the island of Roatán
represent the first report of C. bartholomaei in Honduras.
Caranx latus Agassiz,1831. Horse-eye jack, jurel blanco. Native.
Departments: Atlántida and Cortés. Drainages: Atlantic slope: Chamelecón, Leán and Cangrejal.
Oligoplites saurus (Bloch & Schneider, 1801). Leather jack, piña sietecueros. Native
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
MATAMOROS ET AL. 18 · Zootaxa 2307 © 2009 Magnolia Press
Remarks: Voucher USM 34351 collected in the Tulián River, a tributary of the Chamelecón River,
represents the first report of O. saurus in Honduras.
Trachinotus goodei Jordan & Evermann, 1896. Palometa, pámpano listado. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Lutjanidae. Peripheral.
Lutjanus apodus (Walbaum, 1792). Schoolmaster, pargo amarillo. Native.
Departments: Atlántida, Cortés and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón, Cangrejal
and Roatán.
Lutjanus jocu (Bloch & Schneider, 1801). Dog snapper, pargo jocu. Native.
Departments: Cortés and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón and Roatán.
Gerreidae. Peripheral.
Diapterus auratus Ranzani, 1842. Irish pompano, mojarra guacha. Native.
Departments: Cortés and Islas de la Bahía. Drainages. Atlantic slope: Chamelecón and Roatán.
Eucinostomus argenteus Baird & Girard, 1855. Spotfin mojarra, mojarra plateada. Native.
Departments: Colón, Cortés and Gracias a Dios. Drainages: Atlantic slope: Chamelecón, Lislis and
Patuca.
Eucinostomus harengulus Goode & Bean, 1879. Tidewater mojarra, mojarra costera. Native.
Department: Islas de la Bahía. Drainage: Atlantic slope: Roatán.
Remarks: Vouchers collected in freshwater streams in the island of Roatán (USM field number WAM08-
105) represent the first report E. harengulus in Honduras.
Eucinostomus jonesii (Günther, 1879). Slender mojarra, mojarra flaca. Native.
Department: Islas de la Bahía. Drainage: Atlantic slope: Roatán.
Remarks: Vouchers collected in freshwater streams in the island of Roatán (USM field number WAM08-
106 and WAM08-114) represent the first report of E. jonesii in Honduras.
Eucinostomus melanopterus (Bleeker, 1863). Flagfin mojarra, mojarrita de ley. Native.
Departments: Colón, Cortés and Islas de la Bahía. Drainages: Chamelecón, Lislis and Guanaja.
Eugerres plumieri (Cuvier, 1830). Striped mojarra, mojarra rayada. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Coco.
Gerres cinereus (Walbaum, 1792). Yellow fin mojarra, mojarra plateada. Native.
Departments: Cortés and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón, Roatán and Guanaja.
Haemulidae. Peripheral.
Pomadasys crocro (Cuvier, 1830). Burro grunt, corocoro crocro. Native.
Departments: Atlántida, Colón, Cortés, Islas de la Bahía and Santa Bárbara. Drainages: Atlantic slope:
Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Roatán and Guanaja.
Zootaxa 2307 © 2009 Magnolia Press · 19
FRESHWATER FISHES OF HONDURAS
Sciaenidae. Peripheral.
Bairdiella ronchus (Cuvier, 1830). Ground croaker, ronco rayado. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Cynoscion praedatorius (Jordan & Gilbert, 1889). Boccone weakfish, corvina bocona. Native.
Department: Choluteca. Drainage: Pacific slope: Choluteca.
Remarks: The vouchers CAS 3206 and CAS 3207 collected in the Pedregal River, a tributary of the
Choluteca River drainage, represent the first records of C. praedatorius in Honduras.
Menticirrhus americanus (Linnaeus, 1758). Southern kingfish, berrugato zorro. Native.
Department: Cortés. Drainage: Pacific slope: Chamelecón.
Paralonchurus dumerilii (Bocourt, 1869). Suco croaker, suco rayado. Native.
Department: Choluteca. Drainage: Pacific slope: Choluteca.
Umbrina broussonnetii Cuvier, 1830. Striped drum, corvina rayada. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: Voucher GCRL 21697 collected in the Omoa River, which is part of the Chamelecón River
system, represents the first record of U. broussonnetii in Honduras.
Polynemidae. Peripheral.
Polydactylus virginicus (Linnaeus, 1758). Barbu, barbudo barbú. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Mugilidae. Peripheral.
Agonostomus monticola (Bancroft, 1834). Mountain mullet, tepemechín. Native.
Departments: Atlántida, Colón, Cortés, El Paraíso, Gracias a Dios, Islas de la Bahía, Santa Bárbara and
Yoro. Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto,
Plátano, Patuca, Coco, Warunta, Guanaja and Roatán. Pacific slope: Choluteca.
Joturus pichardi Poey, 1860. Bobo mullet, cuyamel. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios. Drainages: Atlantic slope: Motagua,
Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico, Plátano, Patuca, Warunta and Coco.
Mugil curema Valenciennes, 1836. White mullet, lisa blanca. Native.
Departments: Cortés, Gracias a Dios, Islas de la Bahía and Choluteca. Drainages: Atlantic slope:
Chamelecón, Patuca, Roatán and Guanaja. Pacific slope: Choluteca.
Mugil liza Valenciennes, 1836. Liza, lisa. Native.
Departments: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: voucher UMMZ 173259 (originally identified as M. brasiliensis) collected in the Omoa River,
which is part of the Chamelecón River system, represents the first record of M. liza in Honduras.
MATAMOROS ET AL. 20 · Zootaxa 2307 © 2009 Magnolia Press
Cichlidae. Secondary.
Amatitlania nigrofasciata (Günther, 1867). Convict cichlid, conguito convicto. Native.
Departments: Choluteca, El Paraíso, Francisco Morazán, Gracias a Dios, Intibucá, Olancho, Valle and
Yoro. Drainages: Atlantic slope: Lislis, Aguán, Sico-Tinto, Patuca, Warunta and Coco. Pacific slope: Lempa,
Goascorán, Nacaome, Choluteca and Negro.
Amatitlania siquia Schmitter-Soto, 2007. Siquia cichlid, conguito del Siquia. Native.
Departments: El Paraíso, Francisco Morazán, and Gracias a Dios. Drainages: Atlantic slope: Coco.
Pacific slope: Choluteca.
Remarks: The locality from the Yeguare River listed in Schmitter-Soto (2007) as an Atlantic locality is
an error. The Yeguare River is a tributary of the Choluteca River which drains into the Gulf of Fonseca. Thus,
in Honduras, A. siquia is found in both the Pacific and Atlantic slopes.
Amphilophus alfari (Meek, 1907). Pastel Cichlid, mojarra pastel. Native.
Departments: Gracias a Dios and Olancho. Drainages: Atlantic slope: Plátano, Patuca, Warunta and
Coco.
Amphilophus hogaboomorum (Carr & Giovannoli, 1950). Cholutecan Mojarra, Mojarra de Choluteca.
Endemic.
Departments: Choluteca. Drainages: Pacific slope: Choluteca and Negro.
Remarks: The distribution of this fish was limited to the lower reaches of the Choluteca River. We
collected this species in the Negro River (USM field number WAM08-18) near the community El Ojo de
Agua, and in a second locality in the lower reaches of the Choluteca River (USM 31935) near the community
of El Mal Paso on the road to Orocuina. These two reports represent a range extension for A. hogaboomorum.
Amphilophus longimanus (Günther, 1867). Redbreast cichlid, mojarra pecho rojo. Native.
Departments: Choluteca, El Paraíso, Francisco Morazán, Gracias a Dios, Olancho, Valle and Yoro,
Drainages: Atlantic slope: Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco. Pacific slope: Nacaome,
Choluteca and Negro.
Amphilophus robertsoni (Regan, 1905). Honduran cichlid, mojarra hondureña. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios, Santa Bárbara and Yoro. Drainages: Atlantic
slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano and Patuca.
Remarks: Greenfield & Thomerson (1997) limited the southernmost range of this species to the
department of Atlántida. However, Miller et al. (2005) listed UMMZ 188235 as A. robertsoni collected in the
upper Patuca River in eastern Honduras.
Archocentrus centrarchus (Gill, 1877). Flier cichlid, mojarrita rayada. Native.
Department: Choluteca. Drainages: Pacific slope: Choluteca and Negro.
Remarks: Schmitter-Soto (2007) states that A. centrarchus is found in drainages of the Gulf of Fonseca.
A. centrarchus has been reported in Honduras only in two Gulf of Fonseca drainages, the Negro and
Choluteca Rivers (Cruz & Espinal, 1989), but there is no evidence of its occurrence in the Nacaome and
Goascorán Rivers.
Archocentrus multispinosus (Günther, 1867). Rainbow cichlid, mojarrita arcoiris. Native.
Departments: Choluteca and Gracias a Dios. Drainages: Atlantic slope: Patuca, Warunta and Coco.
Pacific slope: Choluteca and Negro.
Zootaxa 2307 © 2009 Magnolia Press · 21
FRESHWATER FISHES OF HONDURAS
Remarks: Schmitter-Soto (2007) found the northernmost limit of this species on the Pacific slope of
Central America in the Guasaule River in Nicaragua. We collected this species in the Negro River (USM field
number WAM08-20) and the Choluteca River (USM 31494). In addition, Cruz and Espinal (1989) also
reported A. multispinosus in the Negro and Choluteca Rivers.
‘Cichlasoma’ trimaculatum (Günther, 1867). Threespot cichlid, mojarra prieta. Native.
Department: Valle. Drainages: Pacific slope: Lempa and Goascorán.
‘Cichlasoma’ urophthalmus (Günther, 1862). Mayan cichlid, mojarra maya. Native.
Departments: Atlántida and Cortés. Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa, Leán and
Lislis.
Cryptoheros cutteri (Fowler, 1932). Honduran congo, congo hondureño. Native.
Departments: Atlántida, Colón, Comayagua, Copán, Cortés, Francisco Morazán, Santa Bárbara and
Yoro. Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto and
Patuca. Pacific slope: Choluteca.
Remarks: Schmitter-Soto (2007) restricts the distribution of this species to the Atlantic slope drainages of
Honduras and Guatemala with its easternmost boundary at the Aguán River in Honduras. We collected C.
cutteri in the Honduran Pacific slope (USM field number WAM08-43; Choluteca River basin, Valle de
Zamorano). This collection represents a range extension for C. cutteri.
Hypsophrys nicaraguensis (Günther, 1864). Butterfly cichlid, moga amarilla. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Coco.
Remarks: The northern most reported boundary of H. nicaraguensis is a locality in the Nicaraguan side
of the Coco River bordering Honduras (Schmitter-Soto, 2007). During this project H. nicaraguensis was
colleted in the Rus Rus River on the Honduran side of the Coco River (USM field numbers WAM08-05 and
WAM08-08). These records represent a range expansion for the species and a new species report for
Honduras.
Oreochromis mossambicus (Peters, 1852). Mozambique tilapia, tilapia mozambiqueña. Exotic.
Departments: Intibucá, La Paz. Drainage: Pacific slope: Lempa.
Remarks: O. mossambicus was introduced to Honduras by a group of Taiwanese scientists on a mission
to bring common carp and tilapia aquaculture to Central America (D. Meyer, pers. comm.).
Oreochromis niloticus (Linnaeus, 1758). Nile tilapia, tilapia del Nilo. Exotic.
Departments: Atlántida, Choluteca, Colón, Comayagua, Copán, Cortés, El Paraíso, Francisco Morazán,
Gracias a Dios, Intibucá, La Paz, Lempira, Ocotepeque, Olancho and Santa Bárbara. Drainages: Atlantic
slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and
Coco. Pacific slope: Lempa, Goascorán, Nacaome, Choluteca and Negro.
Remarks: O. niloticus was brought to Honduras by governmental agencies in 1979 for stocking in the
new ponds and facilities of the El Carao station (D. Meyer, pers. comm.).
Parachromis dovii (Günther, 1864). Guapote, guapote blanco. Native.
Departments: Colón, El Paraíso, Gracias a Dios, Olancho and Yoro. Drainages: Atlantic slope: Aguán,
Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Parachromis friedrichsthalii (Heckel, 1840). Yellowjacket, guapote hondureño. Native.
Departments: Atlántida, Copán, Cortés and Yoro. Drainages: Atlantic slope: Motagua, Chamelecón,
Ulúa, Leán, Cangrejal and Lislis.
MATAMOROS ET AL. 22 · Zootaxa 2307 © 2009 Magnolia Press
Parachromis loisellei (Bussing, 1989). Yellow guapote, guapote amarillo. Native.
Departments: Atlántida, Cortés, Choluteca, Colón, Copán and Gracias a Dios. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Remarks: Bussing (2002) states that the range of P. loisellei extends from the Ulúa River in the Honduran
Atlantic slope through the Cricamola River basin in Panama. Vouchers FMNH 50014 from the Chamelecón
River and USM 31501 from the Blanco River (Motagua River drainage) represent a range expansion for the
species. USM field number WAM08-138 from the upper reaches of the Coco River Close to San Marcos de
Colón in theDepartment of Choluteca represents a new locality for Honduras.
Parachromis managuensis (Günther, 1867). Jaguar guapote, guapote jaguar. Native.
Departments: Comayagua, Cortés, El Paraíso, Gracias a Dios, Olancho, Santa Bárbara and Yoro.
Drainages: Atlantic slope: Chamelecón, Ulúa, Sico-Tinto, Plátano, Patuca, Warunta and Coco.
Remarks: The natural distribution of P. managuensis includes most of the Atlantic slope of Honduras,
from the Ulúa River (Martin, 1972) to the drainage of the Matina River in Costa Rica (Bussing, 2002). In
Honduras, P. managuensis has been introduced in all Pacific slope drainages.
Parachromis motaguensis (Günther, 1867). Motagua cichlid, guapote del Motagua. Native.
Departments: Choluteca, Copán, Cortés, Francisco Morazán and Intibucá. Drainages: Atlantic slope:
Motagua, Chamelecón and Ulúa. Pacific slope: Lempa, Goascorán, Nacaome and Choluteca.
Remarks: The distribution of P. motaguensis in Honduras was already recorded by Martin (1972). Carr
and Giovannoli (1950) gave distributional details of the species in the drainage of the Choluteca River.
Rocio octofasciata (Regan, 1903). Jack Dempsey, mojarra castarrica. Native.
Departments: Cortés and Yoro. Drainages: Atlantic slope: Motagua, Chamelecón and Ulúa.
Theraps wesseli Miller, 1996. Cangrejal guapotillo, guapotillo del Cangrejal. Endemic.
Department: Atlántida. Drainages: Atlantic slope: Cangrejal and Lislis.
Remarks: T. wesseli was previously known only by the type locality in the drainage of the Papaloteca
River. We collected T. wesseli in the Cangrejal River (USM 31003, USM 31009, USM 31017, USM 31022,
USM 31552, USM 31561, USM 31574, USM 31582, USM 31774, USM 31780) and the Danto River (USM
31050) in La Ceiba, Department of Atlántida. Reports from the above mentioned rivers respresent a range
extension for T. wesseli.
Thorichthys aureus (Günther, 1862). Blue flash, mojarrita dorada. Native.
Department: Copán. Drainage: Atlantic slope: Motagua.
Vieja maculicauda (Regan, 1905). Blackbelt cichlid, machaca. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios, Santa Bárbara and Yoro. Drainages: Atlantic
slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta and
Coco.
Vieja microphthalma (Günther, 1862). Motagua machaca, machaca del Motagua. Native.
Department: Copán. Drainage: Atlantic slope: Motagua.
Labrisomidae. Peripheral.
Labrisomus nuchipinnis (Quoy & Gaimard, 1824). Hairy blenny, trambollo peludo. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Zootaxa 2307 © 2009 Magnolia Press · 23
FRESHWATER FISHES OF HONDURAS
Dactyloscopidae. Peripheral.
Dactyloscopus tridigitatus Gill, 1859. Sand stargazer, miraestrellas ojilargo. Native.
Departments: Colón and Cortés. Drainages: Atlantic slope: Chamelecón and Aguán.
Blenniidae. Peripheral.
Lupinoblennius vinctus (Poey, 1867). Herre, 1942. Mangrove blenny, blenio de mangle. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: Specimen GCRL 4439 collected in the Cieneguita River, which is a tributary of the
Chamelecón drainage, represents the first report of the species in the country.
Eleotridae. Peripheral.
Dormitator latifrons (Richardson, 1844). Pacific fat sleeper, dormilón del Pacifico. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Lempa, Goascorán, Nacaome, Choluteca
and Negro.
Dormitator maculatus (Bloch, 1792). Fat sleeper, dormilón del Atlantico. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Lislis, Cangrejal, Aguán, Sico-Tinto, Plátano, Patuca, Warunta, Coco and
Roatán.
Eleotris amblyopsis (Cope, 1871). Largescaled spinycheek sleeper, Dormilon oscuro. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Warunta, Coco, Roatán and
Guanaja.
Eleotris perniger (Cope, 1871). Smallscaled spinycheek sleeper, Guavina espinosa. Native.
Departments: Atlántida, Colón, Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope:
Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca, Warunta, Coco,
Roatán and Guanaja.
Remarks: Earlier collections in Honduras identified as E. pisonis actually refer to E. perniger (see Pezold
& Cage, 2002). The distribution of E. pisonis extends from the delta of the Orinoco River in Venezuela to
Brazil (Pezold & Cage, 2002).
Eleotris picta Kner,1863. Spotted sleeper, guavina manchada. Native.
Department: Choluteca and Valle Drainages: Pacific slope: Lempa, Goascorán, Nacaome, Choluteca and
Negro.
Erotelis smaragdus (Valenciennes, 1837). Emerald sleeper, guavina de concha. Native.
Department: Islas de la Bahía. Drainage: Atlantic slope: Roatán
Remarks: Vouchers FMNH 84942, FMNH 95589 and UMMZ 199452 collected in creeks of Roatán
represent the first record of E. smaragdus for Honduras.
MATAMOROS ET AL. 24 · Zootaxa 2307 © 2009 Magnolia Press
Gobiomorus dormitor Lacepède, 1800. Bigmouth sleeper, guavina del Atlantico. Native.
Departments: Atlántida, Colón, Comayagua, Cortés, Gracias a Dios and Islas de la Bahía, Drainages:
Atlantic slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lislis, Aguán, Sico-Tinto, Plátano, Patuca,
Warunta, Coco, Roatán and Guanaja.
Gobiomorus maculatus (Günther, 1859). Pacific sleeper, guavina del Pacifico. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Goascoran, Nacaome, Choluteca and
Negro.
Leptophilypnus fluviatilis (Meek & Hildebrand, 1916). Dwarf guavina, guavina enana. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Remarks: Thacker et al. (2006) redescribed the genus Leptophilypnus and included several specimens
from the Patuca River (GCRL 7850, UMMZ 199575, UMMZ 199594, and UMMZ 199611).
Gobiidae. Peripheral.
Awaous banana (Valenciennes, 1837). River goby, gobio de río. Native.
Departments: Atlántida, Choluteca, Colón, Copán, Cortés, Francisco Morazán, Gracias a Dios, Islas de
la Bahía and Valle. Drainages: Atlantic slope: Motagua, Chamelecón, Ulúa, Leán, Cangrejal, Lis-Lis, Aguán,
Sico-Tinto, Plátano, Patuca, Warunta, Coco, Roatán and Guanaja. Pacific slope: Lempa, Goascorán,
Nacaome, Choluteca and Negro.
Bathygobius soporator (Valenciennes, 1837). Frillfin goby, mapo aguado. Native.
Department: Cortés and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón and Roatán.
Remarks: Vouchers USM 31766 and USM 31743 collected in the lower reaches of Salado River near La
Ceiba, and USM field collection numbers WAM08-103 and WAM08-109 collected in creeks of the island of
Roatán represent the first record of B. soporator in Honduras.
Ctenogobius boleosoma (Jordan & Gilbert, 1882). Darter goby, madrejuile. Native.
Departments: Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón,
Patuca, and Roatán.
Ctenogobius fasciatus Gill, 1858. Blotchcheek goby, gobio caramarcada. Native.
Departments: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: Voucher USM 34352 collected in the Tulián River, a tributary of the Chamelecón River,
represents the first record of the species in Honduran freshwaters.
Ctenogobius sagittula (Günther, 1861). Longtail goby, gobio aguzado. Native.
Departments: Choluteca and Valle. Drainages: Pacific slope: Negro and Nacaome.
Ctenogobius stigmaticus (Poey, 1860). Marked goby, gobio marcado. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Evorthodus lyricus (Girard, 1858). Lyre goby, gobio lyra. Native.
Department: Atlántida, Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope:
Chamelecón, Cangrejal, Patuca and Roatán.
Zootaxa 2307 © 2009 Magnolia Press · 25
FRESHWATER FISHES OF HONDURAS
Remarks: Vouchers UMMZ 17385, UMMZ 17314, UMMZ 17302, UMMZ 173286, FMNH 98044,
FMNH 84978, USM 31687, USM 31878, and USM 31912, as well as USM field collection numbers
WAM08-103 and WAM08-109 represent the first reports of E. lyricus in Honduras.
Gobionellus oceanicus (Pallas, 1770). Highfin goby, madrejuile flecha. Native.
Departments: Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón,
Patuca and Roatán.
Remarks: Vouchers FMNH 86679, FMNH 84944, and UMMZ 199456 collected in creeks of the island
of Roatán, and FMNH 86861collected in Brus Laguna, represent the first formal report of G. oceanicus in
Honduras.
Lophogobius cyprinoides (Pallas, 1770). Crested goby, gobio crestado. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: Voucher USM 31896 represents the first report of L. cyprinoides in Honduras.
Sicydium gymnogaster Ogilvie-Grant, 1884. Smoothbelly goby, chupa-piedras desnudo. Native.
Departments: Atlántida and Colón. Drainages: Atlantic slope: Leán, Cangrejal and Lislis.
Sicydium multipunctatum Regan, 1906. Multispotted goby, chupa-piedras pecoso. Native.
Department: El Paraíso. Drainage: Pacific slope: Choluteca.
Sicydium plumieri (Bloch, 1786). Sirajo. chupa-piedras de plumer. Native.
Departments: Atlántida, Colón and Islas de la Bahía. Drainages: Atlantic slope: Leán, Cangrejal, Lislis,
Roatán and Guanaja.
Remarks: Vouchers FLMNH 16334 collected in a creek in the island of Rotan, USM 31858, USM 31866
from the Lancetilla River, USM 31540, USM31545, USM 31556, USM 31563 from the Cangrejal River,
USM 31792 from the Coloradito River and USM 33996 from the Danto River represent the first report of S.
plumieri in Honduras.
Sicydium punctatum Perugia, 1896. Spotted algae-eating goby, chupa-piedras punteado. Native.
Departments: Atlántida, Colón and Islas de la Bahía. Drainages: Atlantic slope: Leán, Cangrejal, Lislis
and Guanaja.
Remarks: Vouchers USM 31860, USM 31868 and USM 31891 from the Lancetilla River, USM 31606,
USM 31788 from the Coloradito River, USM 31544, USM 31555, USM 31562, USM 31580, USM31776
from the Cangrejal River, and USM 34047 from the Marmol River west of Trujillo on the Honduran
Caribbean Coast, represet the first report of S. punctatum in Honduras as well as a expansion of its known
distributional range.
Sicydium sp. 1. Native.
Departments: Atlántida, Colón and Islas de la Bahía. Drainages: Atlantic slope: Leán, Cangrejal, Lislis
and Guanaja.
Sicydium sp. 2. Native.
Departments: Atlántida and Colón. Drainages: Atlantic slope: Leán, Cangrejal and Lislis.
MATAMOROS ET AL. 26 · Zootaxa 2307 © 2009 Magnolia Press
Microdesmidae. Peripheral.
Microdesmus carri Gilbert, 1966. Stippled wormfish, pez lombriz punteado. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: Voucher GCRL 3704 collected in the Omoa River, which is part of the Chamelecón river system,
represents the first record M. carri in Honduras.
Acanthuridae. Peripheral.
Acanthurus bahianus Castelnau, 1855. Ocean surgeon, cirujano pardo. Native.
Department: Gracias a Dios. Drainage: Atlantic slope: Patuca.
Sphyraenidae. Peripheral.
Sphyraena barracuda (Edwards, 1771). Great barracuda, barracuda. Native.
Department: Islas de la Bahía. Drainages: Atlantic slope: Roatán and Guanaja.
Sphyraena guachancho Cuvier, 1829. Guaguanche, tolete. Native.
Departments: Cortés and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón, Roatán and Guanaja.
PLEURONECTIFORMES
Paralichthyidae. Peripheral.
Citharichthys abbotti Dawson, 1969. Veracruz whiff, lenguado veracruzano. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: Voucher GCRL 4470 collected in the Omoa River, which is part of the Chamelecón River
system, represents the first record of C. abbotti in Honduras.
Citharichthys arenaceus Evermann & Marsh, 1900. Sand whiff, lenguado de arena. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: Vouchers GCRL 21631 and GCRL 21698 collected at the Omoa River, which is part of the
Chamelecón River system, represent the first record of C. arenaceus in Honduras.
Citharichthys gilberti Jenkins & Evermann, 1889. Bigmouth sanddab, lenguado escondido. Native.
Department: Choluteca. Drainage: Pacific slope: Choluteca.
Citharichthys macrops Dresel, 1885. Spotted whiff, lenguado manchado. Native.
Departments: Cortés and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón and Roatán.
Citharichthys spilopterus Günther, 1862. Bay whiff, lenguado pardo. Native.
Department: Cortés. Drainage: Atlantic slope: Chamelecón.
Remarks: the following two vouchers, GCRL 4487 and GCRL 4471, collected in the Omoa River, which
is part of the Chamelecón River system, represents the first record of C. spilopterus in Honduras.
Zootaxa 2307 © 2009 Magnolia Press · 27
FRESHWATER FISHES OF HONDURAS
Achiridae. Peripheral.
Achirus lineatus (Linnaeus, 1758). Lined sole, suela listada. Native.
Departments: Cortés and Islas de la Bahía. Drainages: Atlantic slope: Chamelecón and Roatán.
Remarks: Vouchers GCRL 4478, GCRL 21693 from the Omoa River part of the Chamelecón River
system, GCRL 4492, GCRL 6002, USM 31914 from the Chibana River, a tributary of the Chamelecón River,
USM 31690 from the Cangrejal River, USM 31756 from the Salado River, USM 31805 from Lancetilla River
USM 33991 from the Danto River, and FMNH 84968 from a small stream of the island of Roatán represent
the first records of the A. lineatus in Honduras.
Trinectes fonsecensis (Günther, 1862). Spottedfin sole, suela rayada. Native.
Department: Valle. Drainage: Pacific slope: Goascorán.
Remarks: Voucher USM 33950 collected in the Goascorán River near the community of Caridad
represents the first record T. fonsecensis in Honduras.
Trinectes maculatus (Bloch & Schneider, 1801). Hogchoker, suela tortilla. Native.
Department: Islas de la Bahía. Drainages: Atlantic slope: Roatán and Guanaja.
Remarks: USM field collection numbers WAM08-103 collected in creeks of the island of Roatán and
WAM08-118 collected in creeks of the island of Guanaja represent the first records of T. maculatus in
Honduras.
TETRAODONTIFORMES
Tetraodontidae. Peripheral.
Sphoeroides testudineus (Linnaeus, 1758). Checkered puffer, botete sapo. Native.
Departments: Atlántida, Cortés, Gracias a Dios and Islas de la Bahía. Drainages: Atlantic slope:
Chamelecón, Cangrejal, Ulúa, Patuca and Roatán.
Results and discussion
The native freshwater fish fauna of Honduras is composed of 166 species in 96 genera, 41 families, and 18
orders (Appendix). In addition to the native species, six exotic species were found in the country. The most
speciose families are Cichlidae (22 species), Poeciliidae (17 species), and Gobiidae (15 species). Based on
published salinity tolerances (Myers, 1949), just 4.8% (8 species) of the total freshwater native fish species
are primary or obligate freshwater. These eight species are represented in just three families: Characidae (A.
aeneus, B. guatemalensis, H. tortuguerae and R. bouchellei), Heptapteridae (R. guatemalensis and R.
laticauda.) and Gymnotidae (G. cylindricus and G. maculosus). The secondary and peripheral freshwater
species represent 28.3% and 66.9% of the freshwater fish fauna, respectively. The paucity of Honduran
primary or obligate freshwater fishes found in this study is not surprising, given Myers’ (1966) suggested
history and composition of the Central American freshwater fish fauna.
A total of 36 species were new records for Honduras, and there were 12 species found to have expanded
ranges. Nine species appear to be endemic to Honduras, of which only two have been formally described: the
cichlids A. hogaboomorun and T. wesseli. Of the remaining six endemic species, descriptions of Profundulus
sp.1 and Poecilia sp.1 are either in review or in preparation and four other species listed herein are awaiting
description.
MATAMOROS ET AL. 28 · Zootaxa 2307 © 2009 Magnolia Press
With the exception of El Salvador, most Central American countries now have fairly recent formal species
lists. These lists include: México (Miller et al., 2005), Belize (Greenfield & Thomerson, 1997), Guatemala
(Kihn-Pineda et al. 2006), Nicaragua (Villa, 1982), Costa Rica (Bussing, 2002), Panama (Loftin, 1965) and
Honduras (this publication). The only formal list for El Salvador dates back to 1925 (Hildebrand, 1925). In
addition, large areas of some countries, such as the Mosquitia region of both Honduras and Nicaragua, are
logistically difficult to sample and require more exploratory work which would likely yield additional
diversity. Compared to other Central American countries, Honduras appears to have the smallest primary or
obligate freshwater fish diversity (8 species). Given the geologic history and drainage patterns for the region,
it is likely that El Salvador is similarly depauperate in these groups.
The primary freshwater fish composition of Nicaragua is very similar to that of Honduras and differs only
for a few species in the family Characidae which are absent in Honduras. A number of species in the families
Heptapteridae (See Villa, 1982; Bussing, 2002) and Gymnotidae are found in both countries (see Albert &
Miller, 1995, Albert et al., 1999, Albert, 2001). Moving north of Honduras, major differences in fish
assemblages appear to start in northern Guatemala near the Mexican border (see Kihn-Pineda et al. 2006;
Valdez-Moreno et al., 2005), Belize (see Greenfield and Thomerson 1997) and Southern México (see Miller
et al., 2005, Lozano-Vilano et al., 2007 and González-Díaz et al., 2008). A number of species of primary or
obligate North American freshwater fishes families Ictaluridae and Catostomidae extend their ranges this far
south. However, the central and southern portions of Guatemala bordering Honduras appears to have primary
or obligate freshwater species assemblages very similar to that of Honduras.
Martin (1972) was struck by the apparent lack of endemism seen in Honduras. His surveys found just one
endemic freshwater fish for the country (A. hogaboomorum). It was not until 1996 that T. wesseli was
described (Miller, 1996). Our samples appear to contain a number of putatively undescribed species
(Appendix), which are endemic to Honduras. We suspect that the perceived lack of endemism in Honduras is
due to insufficient ichthyological research in the country. Further, of all putative new species reported here,
none are primary freshwater fishes, and most are in the families Poeciliidae, Profundulidae, and Gobiidae.
As with most aspects of Honduran freshwater fish biogeography, the ecology and conservation impacts of
exotic species are largely unknown. Most freshwater exotics were introduced for aquaculture purposes, with
the notable exception of largemouth bass (M. salmoides) introduced in the early 1950’s as a sport fish (Cruz,
1985). All indications are that M. salmoides has not spread beyond the original site of introduction. Of the
remaining five exotic species, the Nile and Mozambique tilapias (O. niloticus and O. mossambicus,
respectively) have spread the most widely and potentially pose the greatest threat to native species. Three
other species have been introduced to Honduras since the early 1980’s for the purpose of aquaculture
(Colossoma macropomum, Oncorhynchus mykiss and Oreochromis urolepis hornorum; D. Meyer, pers.
comm.), but there is no evidence that these species are reproducing in the wild.
One of the main goals of this project was to compile data from as much of Honduras as possible. Our
broad approach was intended to be thorough, including museum material, published literature, and extensive
direct sampling throughout the country. While our four-year sampling effort increased the number of
Honduran freshwater fish on this checklist, substantial areas of the country remain unexplored. In particular,
remote areas of the departments of Gracias a Dios and Olancho in the east, and Lempira, Intibucá and
Ocotepeque in the west require further sampling (Fig. 1). Given these gaps, this study is not the definitive
work on Honduran freshwater fishes, but it is our hope that the data presented here will serve as the
foundation for further study and conservation action.
Acknowledgements
Funds for this study were provided by Critical Ecosystem Partnership Fund (CEPF), the United States Agency
for International Development / Project MIRA Honduras (USAID/MIRA Honduras), and the World Wildlife
Foundation (WWF). WAM was partially supported by NEIU Foundation Dr. Bernard J. Brommel Doctoral
Zootaxa 2307 © 2009 Magnolia Press · 29
FRESHWATER FISHES OF HONDURAS
Scholarship and the USM Alliance for Graduate Education in Mississippi. The authors are grateful to Jorge
Iván Restrepo of IRBIO and Juan Carlos Carrasco of REHDES for their assistance with logistics while
performing field work in Honduras. We thank Luigi Lodo for all the help he provided while sampling in the
Coco River. Thanks to Luis Morales of DIGEPESCA and Claudia Cárcamo, Ivonne Oviedo and Andrés
Alegría from the Instituto de Conservacion Forestal for their assistance in obtaining collection permits. We
would like to thank Bob Jordan of USAID/ Project MIRA Honduras for his initial support in 2005 and Pepe
Herrero of USAID/Project MIRA Honduras for arranging logistics while working in the Cangrejal River and
Pico Bonito. Since the beginning of this project many people have volunteered with long hours of field work.
We are very grateful to everyone who has contributed to this project with their hard work including: Julio
Mérida, Maritza Montoya, Merci Barahona, Carlos O’Reilly, Juan Carlos Funes, Oqueli Banegas, Julio
Ancheta, Marcela Matamoros, Alejandra Sánchez, Edis López, Héctor Portillo, Fausto Elvir, Jonathan
Hernández, Hermes Vega, Tomás Manzanares, Bryant Bowen, James Kerfoot, Matthew Wittenrich, Joshua
Ennen, Michi Tobler, Chris Jones, Gregg Thompson, Kevin Merwing and Hsin-Hsin Hsia. We thank Leonel
Marineros and Mario Espinal for providing samples from Copán and Santa Bárbara. Daniel Meyer of El
Zamorano, Ricardo Betancur-R., and Sheri L. Glowinski provided helpful comments during the preparation of
the manuscript. Liliana Hernández helped translate and edit the Spanish version of the abstract. Many thanks
to Phil Willinks, Rocio Rodilez-Hernandez and an anonymous reviewer for their critical comments on earlier
versions of the manuscript.
References
Albert, J.S. (2001) Species diversity and phylogenetic systematics of American knifefishes (Gymnotiformes, Teleostei).
Miscellaneous Publications of the Museum of Zoology, University of Michigan, 190, 1–127.
Albert, J.S., de Campos Fernandes-Matioli, F.M. & de Almeida-Toledo, L.F. (1999) New species of Gymnotus
(Gymnotiformes, Teleostei) from Southeastern Brazil: toward the deconstruction of Gymnotus carapo. Copeia,
1999, 410–421.
Albert, J.S. & Miller, R.R. (1995) Gymnotus maculosus, a new species of electric fish (Chordata: Teleostei:
Gymnotoidei) from Middle America, with a key to species of Gymnotus. Proceedings of the Biological Society of
Washington, 108, 662–678.
Bengtson, N.A. (1926) Notes on the physiography of Honduras. Geographical Review, 16, 403–413.
Beu, A.G. (2001) Gradual Miocene to Pleistocene uplift of the Central American Isthmus: evidence from tropical
American tonnoidean gastropods. Journal of Paleontology, 75, 706–720.
Bussing, W. (1976) Geographic distribution of the San Juan ichthyofauna of Central America with remarks on its origin
and ecology. In: Thorson, T.B. (Ed.) Investigations of the Ichthyofauna of Nicaraguan Lakes. University of
Nebraska, Lincoln, Nebraska, pp. 157–175.
Bussing, W.A. (2002) Peces de las aguas continentales de Costa Rica/Freshwater fishes of Costa Rica. Universidad de
Costa Rica, San Jose, Costa Rica, 468 pp.
Carr, A.F. (1950) Outline for a classification of animal habitats in Honduras. Bulletin of the American Museum of Natural
History, 94, 563–594.
Carr, A.F. & Giovannoli, L. (1950) The fishes of the Choluteca drainage of southern Honduras. Occasional Papers of the
Museum Zoology, University of Michigan, 523, 1–38.
Coates, A.G., Jackson, J.B.C., Collins, L.S., Cronin, T.M., Dowsett, H.J., Bybell, L.M., Jung, P. & Obando, J.A. (1992)
Closure of the Isthmus of Panama; the near-shore marine record of Costa Rica and western Panama. Geological
Society of America Bulletin, 104, 814–828.
Coates, A.G. & Obando, J.A. (1996) The geologic evolution of the Central American Isthmus. In: Jackson, J.B.C., Budd,
A.F. & Coates, A.G. (Eds.) Evolution and Environment in Tropical America. University of Chicago Press, Chicago,
pp. 21–57.
Cruz, G.A. (1985) Biology of the black bass (Micropterus salmoides) in Yojoá Lake, Honduras. Revista Latinoamericana
de Acuicultura, 23, 12–25.
Cruz, G.A. & Espinal, M. (1989) Six new records of freshwater fishes from the Pacific versant of Honduras. Revista de
Biología Tropical, 37, 229–230.
Dietz, R.Z. & Holden, J.C. (1970) Reconstruction of Pangea: breakup and dispersion of continents, Permian to present.
Journal of Geophysical Research, 75, 4939–4956.
MATAMOROS ET AL. 30 · Zootaxa 2307 © 2009 Magnolia Press
Duellman, W.E. (1979) The South American herpetofauna: a panoramic view. In: Duellman, W.E. (Ed.) The South
American Herpetofauna: its Origin, Evolution, and Dispersal. Monograph of the Museum of Natural History of the
University of Kansas, Kansas, pp. 1–28.
Eschmeyer, W.N. & Fong, J.D. (2008) Species of Fishes by family/subfamily On-line version up dated 23/April/2008.
California Academy of Sciences. Available from http://research.calacademy.org/research/ichthyology/catalog/
SpeciesByFamily.html (acessed 22 August 2008)
Eschmeyer, W.N. & Fricke, R. (2009) Catalog of Fishes electronic version (updated 13 Mar. 2009). Eschmeyer, W.N.
and Fricke, R. (eds.) Catalog of Fishes electronic version (updated 13 Mar. 2009). http://research.calacademy.org/
ichthyology/catalog/fishcatsearch.html (accessed 20 April 2008)
Fowler, H.W. (1932) Notes on freshwater fishes from Central America. Proceedings of the Academy of Natural Sciences
of Philadelphia, 84, 379–85.
Fowler, H.W. (1943) A new poeciliid fish from Honduras. Notulae Naturae, 117, 1–3.
Froese, R. & Pauly, D. (2009) FishBase. Available from http://www.fishbase.org (accesed 13 May 2009)
González-Díaz, A.A., Quiñones, R.M., Velásquez-Martínez, J. & Rodiles-Hernández, R. (2008) Fishes of La Venta River
in Chiapas, México. Zootaxa, 1685, 47–54.
Greenfield, D.W. & Thomerson, J.E. (1997) Fishes of the Continental Waters of Belize. University Press of Florida,
Gainesville, FL, 311 pp.
Hildebrand, S.F. (1925) Fishes of the Republic of El Salvador, Central America. Bulletin of the Bureau of Fisheries, 41,
237–287.
Holden, J.C. & Dietz, R.S. (1972) Galapagos Gore, NazCoPac triple junction and Carnegie/Cocos ridges. Nature, 235,
266–269.
Hubbs, C.L. (1924) Studies of the fishes of the order Cyprinodontes. I–IV. Miscellaneous Publications of the Museum of
Zoology, University of Michigan, 13, 1–31.
Hubbs, C.L. (1926) Studies of the fishes of the order Cyprinodontes VI. Material for the revision of the American genera
and species. Miscellaneous Publications of the Museum of Zoology, University of Michigan, 16, 1–87.
Hubbs, C.L. (1931) Studies of the fishes of the order Cyprinodontes, IX: A new and primitive genus of Poeciliidae from
Central America. Occasional Papers of the Museum Zoology, University of Michigan, 230, 1–3.
Jordan, D.S. & Everman, B.W. (1896–1900) The fishes of North and Middle America: a descriptive catalogue of the
species of fish-like vertebrates found in the waters of North America, north of the isthmus of Panama. Part I (1896),
II (1898), III (1898) & IV (1900). Bulletin of the United States National Museum, 47, 1–3313.
Jordan, D.S., Evermann, B.W. & Clark, H.W. (1930) Check list of the fishes and fishlike vertebrates of North and Middle
America north of the northern boundary of Venezuela and Colombia. Report 2 (for 1928). United States
Commission of Fish and Fisheries, 670 pp.
Keller, G., Zenker, C.E. & Stone, S.M. (1989) Late Neogene history of the Pacific-Caribbean gateway. Journal of South
American Earth Science, 2, 73–108.
Kihn-Pineda, P.H., Cano, E.B. & Morales, A. (2006) Peces de las aguas interiores de Guatemala. In: Cano, E.B. (Ed.)
Biodiversidad de Guatemala. Universidad del Valle de Guatemala, Guatemala, pp. 457–486.
Kullander, S.O. (2003) Family Cichlidae. In: Reis, R.E., Kullander, S.O. & Ferraris Jr.., C.J. (Eds.) Checklist of the
Freshwater Fishes of South and Central America. Edipucrs, Porto Alegre, pp. 605–654.
Ladd, J.W. (1976) Relative motion of South America with respect to North America and Caribbean tectonics. Bulletin of
the Geological Society of America, 87, 967–976.
Loftin, H.G. (1965) The Geographical Distribution of Freshwater Fishes in Panama. Florida State University,
Tallahassee, FL., 528 pp.
Lozano-Vilano, M.L., García-Ramírez, M.E., Contreras-Balderas, S. & Ramírez-Martínez, Y.C. (2007) Diversity and
conservation status of the ichthyofauna of the Río Lacantún basin in the Biosphere Reserve Monte Azules, Chiapas,
México. Zootaxa, 1410, 43–53.
Lyons, J. (2005) Distribution of Sicydium Valenciennes 1837 (Pisces: Gobiidae) in Mexico and Central America.
Hidrobiológica, 15, 239–243.
Maldonado-Koerdell, M. (1964) Geohistory and paleogeography of Middle America. In: West, C. (Ed.) Handbook of
Middle American Indians. The University of Texas Press, Austin, pp. 3–32.
Malfait, B.T. & Dinkelman, M.G. (1972) Circum-Caribbean tectonic and igneous activity and the evolution of the
Caribbean Plate. Bulletin of the Geological Society of America, 83, 251–271.
Marceniuk, A.P. & Betancur-R, R. (2008) Revision of the species of the genus Cathorops (Siluriformes: Ariidae) from
Mesoamerica and the Central American Caribbean, with description of three new species. Neotropical Ichthyology,
6, 25–44.
Marceniuk, A.P., Betancur-R., R. & Acero P., A. (in press.) A new species of Cathorops (Siluriformes; Ariidae) from
Mesoamerica, with redescription of four species from the eastern Pacific. Bulletin of Marine Science.
Marshall, L., Buttler, R.F., Drake, R.E., Curtis, G.A. & Tedforth, R.H. (1979) Calibration of the Great American
Interchange. Science, 204, 272–279.
Zootaxa 2307 © 2009 Magnolia Press · 31
FRESHWATER FISHES OF HONDURAS
Martin, M. (1972) A biogeographic analysis of the freshwater fishes of Honduras. Unpubl. Ph.D. Dissertation.
University of Southern California. Los Angeles, 588. pp.
Matamoros, W.A., Palmer, J. & Mérida, J. (2007) First record in Honduras of the Halfbeak Hyporhamphus roberti
hildebrandi Jordan and Evermann 1927, (Hemiramphidae) collected in an inland reservoir. Gulf and Caribbean
Research, 19, 1–3.
McCranie, J.R. & Wilson, L.D. (2002) The Amphibians of Honduras. Society for the Study of Amphibians and Reptiles,
Contributions to Herpetology, 19, 1–625.
McNeely, J.A., Miller, K.R., Reid, W.V. & Mittermeier, R. (1990) Conserving the world's biological diversity.
International Union for Conservation of Nature and Natural Resources, World Resources Institute, Conservation
International, World Wildlife Fund, US. World Bank, Gland, Switzerland. 174 pp.
Meyer, M.K. & Schartl, M. (2002) Xiphophorus mayae, a new species of swordtail from Guatemala (Teleostei:
Poeciliidae). Ichthyological Explorations of Freshwaters, 13, 59–66.
Miller, N. (1907) Fishes of the Motagua River, Guatemala. Bulletin of the American Museum of Natural History, 23, 95–
123.
Miller, R.R. (1955) A systematic review of the Middle American fishes of the genus Profundulus. Miscellaneous
Publications of the Museum of Zoology, University of Michigan, 92, 1–64.
Miller, R.R. (1966) Geographical distribution of Central American freshwater fishes. Copeia, 1966, 773–802.
Miller, R.R. (1996) Theraps wesseli, a new species of cichlid fish from the Caribbean slope of northern Honduras.
Tropical Fish Hobbyist, 44, 179–183.
Miller, R.R. & Carr, A.F. (1974) Systematics and distribution of some freshwater fishes from Honduras and Nicaragua.
Copeia, 1974, 120–125.
Miller, R.R., Minckley, W.L. & Norris, S.M. (2005) Freshwater Fishes of México. The University of Chicago Press,
Chicago, 490 pp.
Myers, G.S. (1949) Salt-tolerance of fresh-water fish groups in relation to zoogeographical problems. Bijdragen tot de
Dierkunde, 28, 315–322.
Myers, G.S. (1966) Derivation of the freshwater fish fauna of Central America. Copeia, 1966, 766–733.
Olson, E.C. & McGrew, P.O. (1941) Mammalian fauna from the Pliocene of Honduras. Bulletin of the Geological
Society of America, 52, 1219–1244.
Ostmark, H.E. (1964) La introduccion reciente de la lobina boca ancha a los tropicos. Apuntes Agricolas, 6, 10–15.
Perdices, A., Bermingham, E., Montilla, A. & Doadrio, I. (2002) Evolutionary history of the genus Rhamdia (Teleostei:
Pimelodidae) in Central America. Molecular Phylogenetics and Evolution, 25, 172–189.
Pezold, F. & Cage, B. (2002) A review of the spinycheek sleepers, genus Eleotris (Teleostei: Eleotridae), of the western
hemisphere, with comparison to the West African species. Tulane Studies in Zoology and Botany, 31, 19–63.
Poeser, F.N. (1995) Nonrandon variation on Poecilia marcellinoi n. sp. and P. salvatoris Regan, 1907 in El Salvador
(Pisces, Poeciliidae). Bijdragen tot de Dierkunde, 64, 239–252.
Regan, C.T. (1906–08) Pisces. In: Goldman, F.D. & Salvin, O. (Eds.) Biologia Centrali-Americana. Porter, R.H.,
London, pp. 1–203.
Rehn, J.A.G. (1932) A naturalist in Honduras. Bulletin of the Panamerican Union, 66, 390–400.
Reis, R.E., Kullander, S.O. & Ferraris Jr., C.J. (2003) Check List of the Freshwater Fishes of South and Central America.
EDIPUCRS, Porto Alegre, Brazil, 742 pp.
Roberts, R.J. & Irving, E.M. (1957) Mineral Deposits of Central America. United States Goverment Printing Office,
Washington, D.C., 205 pp.
Rosen, D.E. & Bailey, R.M. (1963) The poeciliid fishes (Cyprinidontiformes), their structure, zoogeography, and
systematics. Bulletin of the American Museum of Natural History, 126, 1–176.
Savage, J.M. (1982) The enigma of the Central American herpetofauna: dispersal or vicariance? Annals of the Missouri
Botanical Garden, 69, 464–547.
Schmitter-Soto, J.J. (2007) A systematic revision of the genus Archocentrus (Perciformes: Cichlidae), with the
description of two new genera and six new species. Zootaxa, 1603, 1–78.
Silfvergrip, A.M.C. (1996) A systematic revision of the neotropical catfish genus Rhamdia (Teleostei, Pimelodidae).
Department of Zoology, Stockholm University and Department of Vertebrate Zoology, Swedish Museum of Natural
History, Stockholm, 156 pp.
Stehli, F.G. & Webb, S.D. (1985) The Great American Biotic Interchange. Plenun Press, New York, 532 pp.
Strong, W.D. (1934) An archaeological cruise among the Islas de la Bahía of Honduras. Smithsonian Institution
Explorations and Fieldwork, 1933–1934, 1–59.
Thacker, C.E., Pezold, F., Suttkus, R.D. & Buth, D. (2006) Redescription of the dwarf Neotropical eleotrid genus
Leptophilypnus (Teleostei: Gobioidei), including a new species and comments on Microphilypnus. Copeia, 2006,
489–499.
Valdez-Moreno, M.E., Pool-Canul, J. & Contreras-Balderas, S. (2005) A checklist of the freshwater ichthyofauna from
El Petén and Alta Verapaz, Guatemala, with notes for its conservation and management. Zootaxa, 1072, 43–70.
MATAMOROS ET AL. 32 · Zootaxa 2307 © 2009 Magnolia Press
Vaux, P.D. (1985) The ecology of the freshwater fishes of central Honduras. Unpubl. Ph.D. Dissertation. University of
California, Davis. 258 pp.
Villa, J. (1982) Peces nicaragüenses de agua dulce. Banco de America, Managua, Nicaragua, 253 pp.
Vinson, G.L. & Brineman, J.H. (1963) Nuclear Central America, hub of the Antillean transverse belt. In: Childs, O.E. &
Beebe, B.W. (Eds.) Backbone of the Americas: Tectonic History from Pole to Pole. American Association of
Petroleum Geologist, Tulsa, Oklahoma, pp. 101–112.
West, R.C. (1964) Surface configuration and associated geology of Middle America. In: Wauchope, R. & West, R.C.
(Eds.) Handbook of the Middle American Indians. University of Texas Press, Austin, Texas, pp. 33–83.
Wilson, L.D. & Meyer, J.R. (1985) The Snakes of Honduras. Second edition. Milwaukee Public Museum, Milwaukee,
150 pp.
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Appendix
Honduran freshwater fish species by political department (Fig. 1). Sal. refers to tolerance to salinity based on Meyers
(1949); primary = Pri; secondary = Se; and peripheral = Pe. Con. Sta. Stands for conservation status, and species were
classified as native, endemic and exotic. NR stands for New Records. These are fishes that are reported for the first time
in Honduras. RE stands for Range Extension. These are fishes whose natural range has been expanded based on the
findings of this study.
FAMILY / species
Atlántida
Choluteca
Colón
Comayagua
Copán
Cortés
El Paraíso
Francisco
Gracias a
Intibucá
Isl. Bahía
La Paz
Lempira
Ocotepeque
Olancho
Santa
Valle
Yoro
Sa l.
Con. Sta.
N
R
R
E
CARCHARHINIDAE
Carcharhinus leucas 00000000 1 0000000 00PENat
Rhizoprionodon porosus 00000000 1 0000000 00PENat
PRISTIDAE
Pristis pectinata 00000000 1 0000000 00PENat
MEGALOPIDAE
Megalops atlanticus 10100000 1 0000000 00PENat
ANGUILLIDAE
Anguilla rostrata 10100100 0 0100000 01PENat
OPHICTHIDAE
Myrophis punctatus 00000100 1 0100000 00PENat
CLUPEIDAE
Harengula clupeola 00000100 0 0000000 00PENat
Harengula humeralis 00000000 0 0100000 00PENat
Jenkinsia lamprotaenia 00000000 0 0100000 00PENat
Ophistonema oglinum 00000000 1 0000000 00PENat
ENGRAULIDAE
Anchoa colonensis 00000100 1 0000000 00PENat
Anchoa filifera 00000000 1 0000000 00PENat
Anchoa parva 00000000 1 0000000 00PENat
Anchovia clupeoides 00000000 1 0000000 00PENat
Anchoviella elongata 00000000 1 0000000 00PENat
CYPRINIDAE
Ctenopharyngodon idella 00000100 0 0000001 00PRExo
Hypophthalmichthys
molitrix 00000100 1 0000000 00PRExo
CHARACIDAE
Astyanax aeneus 11111111 1 1011111 11PRNat
Brycon guatemalensis 01011111 0 0011001 01PRNat
Hyphessobrycon
tortuguerae 00000010 1 0000010 00PRNat
Roeboides bouchellei 01000011 1 0000010 10PRNat X
ARIIDAE
Cathorops higuchii 00000000 1 0000000 00PENat
Cathorops melanopus 00000100 0 0000001 00PENatXX
MATAMOROS ET AL. 34 · Zootaxa 2307 © 2009 Magnolia Press
Cathorops sp 00000000 0 0000000 10PENat
Cathorops steindachneri 00000000 0 0000000 10PENat
Cathorops taylori 00000000 0 0000000 10PENat
Sciades assimilis 00000100 0 0000000 00PENat
Sciades guatemalensis 01000000 0 0000000 10PENat
sciades seemanni 01000000 0 0000000 10PENat
ICTALURIDAE
Ictalurus punctatus 00010100 0 0000001 00PRExo
HEPTAPTERIDAE
Rhamdia guatemalensis 11111111 1 1011111 11PRNat
Rhamdia laticauda 10011111 0 1001011 00PRNat
GYMNOTIDAE
Gymnotus cylindricus 11110100 1 0000001 01PRNat
Gymnotus maculosus 01000000 0 0000000 10PRNat
BATRACHOIDIDAE
Batrachoides gilberti 00000000 1 0000000 00PENatX
GOBIESOCIDAE
Gobiesox strumosus 00000100 0 0000000 00PENatX
ATHERINOPSIDAE
Atherinella argentea 01000000 0 0000000 10PENat
Atherinella blackburni 00100000 0 0100000 00PENatX
Atherinella guija 01000000 0 0100000 00PENat
Atherinella meeki 00000100 0 0000000 00PENatXX
Atherinella milleri 10100000 1 0000000 00PENat
Atherinella pachylepis 01000000 0 0000000 10PENat
RIVULIDAE
Kryptolebias marmoratus 10000000 0 0100000 00SENatX
Rivulus tenius 10000100 0 0000000 00SENat
PROFUNDULIDAE
Profundulus
guatemalensis 00001000 0 1001000 00SENat
Profundulus sp.1 00010001 0 0000000 00SEEnd
Profundulus sp.2 00000000 0 0000001 00SEEnd
POECILIIDAE
Alfaro cultratus 00000000 1 0000000 00SENatXX
Alfaro huberi 10011111 1 1011011 01SENat
Belonesox belizanus 10100100 1 0000000 01SENat
Gambusia nicaraguensis 10100100 1 0100000 01SENat
Heterandria anzuetoi 10111101 1 0000011 01SENat
Heterandria bimaculata 10000100 0 0000000 00SENat
Phallichthys amates 10100100 1 0000010 01SENat
Poecilia gillii 11111111 1 1111111 00SENat
Poecilia marcellinoi 01011110 0 0000001 00SENat
Poecilia sp.1 10000100 1 0000010 00SEEnd
Zootaxa 2307 © 2009 Magnolia Press · 35
FRESHWATER FISHES OF HONDURAS
Poecilia sp.2 10000000 0 0000000 00SEEnd
Poecilia sp.3 01000001 0 0000000 00SEEnd
Poecilia orri 10100100 1 0100000 01SENat
Poeciliopsis pleurospilus 01011101 0 1001001 10SENat
Poeciliopsis turrubarensis 01000001 0 0000000 10SENat
Xiphophorus helleri 00001000 0 0000001 00SENat
Xiphophorus mayae 10000100 0 0000001 00SENatXX
ANABLEPIDAE
Anableps dowei 01000010 0 0000000 10SENat
BELONIDAE
Strongylura marina 10000100 1 0100000 00PENat
Strongylura notata 00000000 0 0100000 00PENatX
Strongylura timucu 00000100 1 0100000 00PENat
HEMYRHAMPHIDAE
Hyporhamphus roberti
hildebrandi 00010100 1 0100001 01PENat
Hyporhamphus
unifasciatus 00000100 0 0000000 00PENat
SYNGNATHIDAE
Microphis brachyurus
lineatus 10000100 0 0000000 00PENatX
Pseudophallus mindii 10000000 0 0000000 00PENatX
Pseudophallus starksi 00000000 0 0000000 10PENat
Syngnathus pelagicus 00000000 1 0000000 00PENatX
Syngnathus scovelli 00000000 1 0000000 00PENat
SYNBRANCHIDAE
Ophisternon
aenigmaticum 10001100 0 0000000 00SENat
Synbranchus marmoratus 11111111 1 1010011 11SENat
CENTROPOMIDAE
Centropomus ensiferus 00000100 1 0000000 00PENat
Centropomus nigrescens 01000000 0 0000000 00PENat
Centropomus parallelus 00000100 1 0000000 00PENat
Centropomus pectinatus 00000000 1 0100000 00PENat
Centropomus undecimalis 10000100 1 0100000 00PENat
Centropomus unionensis 01000000 0 0000000 00PENat
CENTRARCHIDAE
Micropterus salmoides 00010100 0 0000001 00PRExo
CARANGIDAE
Caranx bartholomaei 00000000 0 0100000 00PENatX
Caranx latus 10000100 0 0000000 00PENat
Olygoplites saurus 00000100 0 0000000 00PENatX
Trachinotus goodei 00000100 0 0000000 00PENat
LUTJANIDAE
Lutjanus apodus 10000100 0 0100000 00PENat
MATAMOROS ET AL. 36 · Zootaxa 2307 © 2009 Magnolia Press
Lutjanus jocu 00000100 0 0100000 00PENat
GERREIDAE
Diapterus auratus 00000100 0 0100000 00PENat
Eucinostomus argenteus 00100100 1 0000000 00PENat
Eucinostomus harengulus 00000000 0 0100000 00PENatX
Eucinostomus jonesi 00000000 0 0100000 00PENatX
Eucinostomus
melanopterus 00100100 0 0100000 00PENat
Eugerres plumieri 00000000 1 0000000 00PENat
Gerres cinereus 00000100 0 0100000 00PENat
HAEMULIDAE
Pomadasys crocro 10100100 0 0100001 00PENat
SCIAENIDAE
Bairdiella ronchus 00000100 0 0000000 00PENatX
Cynoscion praedatorius 01000000 0 0000000 00PENatX
Menticirrhus americanus 00000100 0 0000000 00PENat
Paralonchurus dumerilii 01000000 0 0000000 00PENat
Umbrina broussonnetii 00000100 0 0000000 00PENatX
POLYNEMIDAE
Polydactylus virginicus 00000000 1 0000000 00PENat
MUGILIDAE
Agonostomus monticola 10100110 1 0100001 01PENat
Joturus pichardi 10100100 1 0000000 00PENat
Mugil curema 01000100 1 0100000 00PENat
Mugil liza 00000100 0 0000000 00PENatX
CICHLIDAE
Amatitlania nigrofasciata 01000011 1 1000010 11SENat
Amatitlania siquia 00000011 1 0000000 00SENat
Amphilophus alfari 00000000 1 0000010 00SENat
Amphilophus
hogaboomorum 01000000 0 0000000 00SEEnd X
Amphilophus longimanus 01000011 1 0000010 11SENat
Amphilophus robertsoni 10100100 1 0000001 01SENat
Archocentrus centrarchus 01000000 0 0000000 00SENat
Archocentrus
multispinosus 01000000 1 0000000 00SENat
‘Cichlasoma’
trimaculatum 00000000 0 0000000 10SENat
‘Cichlasoma’
urophthalmus 10000100 0 0000000 00SENat
Criptoheros cutteri 10111101 0 0000001 01SENat X
Hypsophrys nicaraguensis 00000000 1 0000000 00SENatXX
Oreochromis
mossambicus 00000000 0 1010000 00SEExo
Oreochromis niloticu 11111111 1 1011111 11SEExo
Zootaxa 2307 © 2009 Magnolia Press · 37
FRESHWATER FISHES OF HONDURAS
Parachromis dovii 00100010 1 0000010 01SENat
Parachromis
friedrichsthalii 10001100 0 0000000 01SENat
Parachromis loisellei 11101100 1 0000000 00SENat X
Parachromis managuensis 00010110 1 0000011 01SENat
Parachromis motaguensis 01001101 0 1000000 00SENat
Rocio octofasciata 00000100 0 0000000 01SENat
Theraps wesseli 10000000 0 0000000 00SEEnd X
Thorichthys aureus 00001000 0 0000000 00SENat
Vieja maculicauda 10100100 1 0000001 01SENat
Vieja microphthalma 00001000 0 0000000 00SENat
LABRISOMIDAE
Labrisomus nuchipinnis 00000100 0 0000000 00PENat
DACTYLOSCOPIDAE
Dactyloscopus tridigitatus 00100100 0 0000000 00PENat
BLENNIIDAE
Lupinoblennius vinctus 00000100 0 0000000 00PENatX
ELEOTRIDAE
Dormitator latifrons 01000000 0 0000000 10PENat
Dormitator maculatus 10100100 1 0100000 00PENat
Eleotris amblyopsis 10100100 1 0100000 00PENat
Eleotris perniger 10100100 1 0100000 00PENat
Eleotris picta 01000000 0 0000000 10PENat
Erotelis smaragdus 00000000 0 0100000 00PENatX
Gobiomorus dormitor 10110100 1 0100000 00PENat
Gobiomorus maculatus 01000000 0 0000000 10PENat
Leptophilypnus fluviatilis 00000000 1 0000000 00PENat
GOBIIDAE
Awous banana 11101101 1 0100000 10PENat
Bathygobius soporator 00000100 0 0100000 00PENatX
Ctenogobius boleosoma 00000100 1 0100000 00PENat
Ctenogobius fasciatus 00000100 0 0000000 00PENatX
Ctenogobius sagitulla 01000000 0 0000000 10PENat
Ctenogobius stigmaticus 00000000 1 0000000 00PENat
Evorthodus lyricus 10000100 1 0100000 00PENatX
Gobionellus oceanicus 00000100 1 0100000 00PENatX
Lophogobius cyprinoides 00000100 0 0000000 00PENatX
Sicydium gymnogaster 10100000 0 0000000 00PENat
Sicydium multipunctatum 01000000 0 0000000 00PENat
Sicydium plumieri 10100000 0 0100000 00PENatXX
Sicydium punctatum 10100000 0 0100000 00PENatXX
Sicydium sp1 10100000 0 0100000 00PENat
Sicydium sp2 10100000 0 0100000 00PENat
MICRODESMIDAE
MATAMOROS ET AL. 38 · Zootaxa 2307 © 2009 Magnolia Press
Microdesmus carri 00000100 0 0000000 00PENatX
ACANTHURIDAE
Acanthurus bahianus
castelnau 00000000 1 0000000 00PENat
SPHYRAENIDAE
Sphyraena barracuda 00000000 0 0100000 00PENat
Sphyraena guachancho 00000100 0 0100000 00PENat
PARALICHTHYIDAE
Citharichthys abbotti 00000100 0 0000000 00PENatX
Citharichthys arenaceus 00000100 0 0000000 00PENatX
Citharichthys gilberti 01000000 0 0000000 00PENat
Citharichthys macrops 00000100 0 0100000 00PENat
Citharichthys spilopterus 00000100 0 0000000 00PENatX
ACHIRIDAE
Achirus lineatus 00000100 0 0100000 00PENatX
Trinectes fonsecensis 00000000 0 0000000 10PENatX
Trinectes maculatus 00000000 0 0100000 00PENatX
TETRAODONTIDAE
Sphoeroides testudineus 10000100 1 0100000 00PENat
... Sin embargo, pocos estudios se han centrado en especies endémicas (Aksu, 2021;Hopkins & Burr, 2009;Sifundza et al., 2021;Yousefi et al., 2020), especialmente en el Neotrópico; región donde las especies más susceptibles al cambio climático muestran patrones geográficos claros (Foden et al., 2008), como el hemisferio sur donde las mayores proporciones de riqueza de especies fluviales representa una proporción importante a escala continental en relación con otras zonas como África y Centroamérica (Oberdorff et al., 2011). Chortiheros wesseli (Miller, 1996) y Amphilophus hogaboomorum (Carr y Giovannoli, 1950) son las únicas dos especies de cíclidos endémicos de Honduras descritas formalmente (Matamoros et al., 2009) y se encuentran incluidas en la lista de especies de preocupación especial de Honduras (Secretaría de Recursos Naturales y Ambiente, SERNA, 2008). Actualmente, C. wesseli ha sido la especie más estudiada (McMahan et al., 2020;Miller, 1996;Říčan et al., 2016), clasificada anteriormente como Theraps pero la investigación genética mostró que no había parentesco con ese género (Říčan et al., 2016). ...
... Sin embargo, se encuentra como especie vulnerable en la Lista Roja de la UICN (Carrasco & Lyons, 2020). Por otro lado, las únicas fuentes de información para A. hogaboomorum solo incluyen aportes en investigación genética y diversificación (Hulsey et al., 2010;Matamoros et al., 2009;Říčan et al., 2016). Se distribuye en la cuenca del río Choluteca y río Negro (Matamoros et al., 2009), asociada a hábitats con sustrato descubierto, suelos generalmente de arena, guijarros, roca y limo (Allgayer, 2013). ...
... Por otro lado, las únicas fuentes de información para A. hogaboomorum solo incluyen aportes en investigación genética y diversificación (Hulsey et al., 2010;Matamoros et al., 2009;Říčan et al., 2016). Se distribuye en la cuenca del río Choluteca y río Negro (Matamoros et al., 2009), asociada a hábitats con sustrato descubierto, suelos generalmente de arena, guijarros, roca y limo (Allgayer, 2013). Las predicciones del cambio climático futuro sugieren cambios en los patrones de precipitación y sequía en Centro América (Imbach et al., 2018) ...
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The consequences of climate change on freshwater ecosystems and fish are evident, as their phenology and distribution have been altered. The objective of this study was to assess future climate change models as predictors of range reduction of two endemic cichlid species (Chortiheros wesseli and Amphilophus hogaboomorum) in Honduras. Bioclimatic and hydroclimatic variables and four modeling techniques were used: Maximum Entropy, Random Forest, MaxNet and Boosted Regression Trees. The best model was validated using the Area Under the Curve (AUC) and True Skill Statistics (TSS). The general circulation model HADGEM2_ES was used under the scenarios of Representative Concentration Pathways RCP4.5 and RCP8.5 at the 2050 and 2080 horizons. The projections show Random Forest as the best model and under the climate change scenarios the distribution of both species decreased from 17.94% to 57.02% for RCP4.5 and 19.19% to 69.48 for RCP8.5. Suitable protected areas will not maintain favorable conditions for C. wesseli and potential areas for A. hogaboomorum are not included in the Honduran protected areas system. These results have important implications for the conservation of two endemic freshwater cichlid species in Honduras.
... Es importante resaltar que en este estudio no se detectó la presencia de especies exóticas, sin embargo, la Cuenca Baja del río se conecta con las lagunas de Brus, Ibans y Rapa y los ríos Sico y Patuca, donde se manifiesta la presencia de Oreochromis niloticus (Matamoros et al., 2009), siendo una especie de conocido éxito como invasora (Trewavas, 1983;Ehrlich, 1988) y efectos negativos sobre la biodiversidad (Canonico et al., 2005). La misma es considerada una amenaza para las comunidades de peces en el Río Plátano, por lo que se recomienda a los gestores del área protegida iniciar un proceso de monitoreo de esta especie, sobre todo considerando la importancia en términos de conservación de este río y de la Reserva del Hombre y de la Biosfera de Río Plátano para Honduras y la región del Corredor Biológico Mesoamericano. ...
... To obtain data on invasive fishes documented in the region, the Global Invasive Species Database (GISD) was utilized to generate a report on the occurrence of invasive freshwater fishes in the seven Central American countries, producing 50 records for 14 species [140]. Results from GISD were collated with occurrences of an additional 15 invasive species reported throughout the primary literature [108,121,[141][142][143][144][145][146][147][148], resulting in a total of 29 invasive fish species reported in the region (Supplementary Materials Table S3). ...
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Central America contains a rich diversity of freshwater habitats that support more than 600 species of freshwater fishes. However, despite several perceived threats to the integrity of the freshwater habitats throughout the region, a formal analysis of extinction risk for the region’s ichthyofauna is lacking. In this manuscript, we report an updated checklist of species and a novel comprehensive assessment of the conservation status of Central American freshwater fishes by applying the IUCN Red List Categories and Criteria to species at the global level. We also analyze the distribution of freshwater fishes across Central America and generate baseline geospatial data that can be used in multi-species conservation planning processes, which is available through the Red List Website. Our results indicate that between 15 and 28% of freshwater fishes in the region are threatened with extinction, with considerable uncertainty resulting from elevated data deficiency. We identify major and widespread threats in the region, including pollution, agriculture, aquaculture, biological resource use, natural system modifications, invasive species, and land development. This analysis represents an important first step in formulating effective conservation planning and action initiatives for a taxonomic group that historically has received few protections and can be used to inform conservation priorities of freshwater ecosystems at both national and regional scales.
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20 In biogeography, vicariance and long-distance dispersal are often characterized as 21 competing scenarios. However, they are related concepts, both relying on 22 reciprocal illumination from geological, ecological, and phylogenetic evidence. This 23 can be illustrated for freshwater fishes, which may immigrate to islands when 24 freshwater connections are temporarily present (vicariance), or by unusual means 25 when oceanic gaps are crossed (long-distance dispersal). Marine barriers have a 26 strong filtering effect, limiting immigrants to those most capable of oceanic 27 dispersal. The roles of landspans and oceanic dispersal are being debated for 28 freshwater fishes of the Greater Antilles. We review three active hypotheses 29 (Cretaceous vicariance, GAARlandia, long-distance dispersal) and propose long-30
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El área contiene una muestra representativa de la comunidad de murciélagos del suroeste de Perú y norte de Chile. Incluye 18 de las 20 especies registradas para esta región. IUCN: En Peligro (Tomopeas ravus y Myotis atacamensis), Vulnerable (Amorphochilus schnablii), Casi Amenazada (Platalina genovensium) y Datos Deficientes (Promops davisoni), las cuatro primeras Amenazadas o Casi Amenazadas en Perú. Asimismo, Eumops chiribaya y Lasiurus arequipae cumplirían con IUCN para ser consideradas como amenazadas. Tres de las especies reportadas son endémicas de Perú (T. ravus, E. chiribaya y L. arequipae) y ocho son endémicas del Desierto Pacífico de Perú y norte Chile (las enlistadas anteriormente y Mormopterus kalinowskii). Existen colonias reproductivas de especies amenazadas, refugios permanentes. El área sufre de vandalismo y disminución de la calidad del hábitat.
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El área posee una alta diversidad de murciélagos (cinco especies) en relación a la riqueza de la provincia de San Juan, donde solo se registraron seis especies. Se reportan dos especies migratorias: Tadarida brasiliensis (Molossidae), Lasiurus blossevillii (Vespertilionidae), además de colonias maternales de Myotis dinellii y Tadarida brasiliensis. En el interior del área existen comunidades humanas con intensas actividades productivas como la ganadería, agricultura y turismo. Los murciélagos registrados en el área son insectívoros por lo que ejercen una importante actividad reguladora de las poblaciones de insectos perjudiciales para los bosques nativos, la agricultura y vectores de enfermedades.
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This datasheet on Ictalurus punctatus covers Identity, Overview, Associated Diseases, Pests or Pathogens, Distribution, Dispersal, Diagnosis, Biology & Ecology, Environmental Requirements, Natural Enemies, Impacts, Uses, Prevention/Control, Management, Genetics and Breeding, Economics, Further Information.
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Region description
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Este libro es el corolario de muchos años de trabajo y dedicación de los miembros de la RELCOM (Red Latinoamericana y del Caribe para la Conservación de los Murciélagos), cuyo objetivo es poner a disposición de la comunidad los resultados de una actividad de carácter regional, que se viene realizando de manera ininterrumpida desde 2011, cuando el primer AICOM fue reconocido. En 2009, la RELCOM elaboró una “Estrategia para la conservación de los murciélagos en Latinoamérica y el Caribe”, donde se identificaron las amenazas que sufren los murciélagos de la región. Esto despertó la necesidad de crear una figura como grupo para proteger a los murciélagos a través de una propuesta regional. Y es así que surgen las Áreas y Sitios de Importancia para la Conservación de los Murciélagos (AICOMs-SICOMs), inspiradas en las AICAs (Áreas de Importancia para la Conservación de las Aves). El reconocimiento de AICOMs y SICOMs surge como una herramienta para que, de algún modo, pueda ser utilizada por los diferentes países que conforman la red, para orientar los planes de conservación en localidades donde especies y poblaciones de murciélagos se encuentren amenazadas. Si bien no es un instrumento legal, sienta bases para el desarrollo de políticas nacionales y regionales que avancen en ese sentido.
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Silfvergrip, A.M.C. 1996. A systematic revision of the Neotropical catfish genus Rhamdia (Teleostei, Pimelodidae). Department of Zoology, Stockholm University and Department of Vertebrate Zoology, Swedish Museum of Natural History, Stockholm. 156 pp. + 8 pls. This monograph is a revison of the species of the genus Rhamdia, a genus of pimelodid catfishes with about 100 described species. The results, based on an evaluation of characters previously used in literature, show that morphological variation is great and that only few of the nominal species remain diagnosable. The valid species are: Rhamdia foina (Müller & Troschel), R. humilis (Günther), R. itacaiunas n.sp., R. jequitinhonha n.sp., R. laticauda (Kner), R. laukidi Bleeker, R. muelleri (Günther), R. nicaraguensis (Günther), R. poeyi Eigenmann & Eigenmann, R. quelen (Quoy & Gaimard), and R. xetequepeque n.sp.; the work includes several lecto- and neotype designations. The internal morphology of Rhamdia quelen, the type species of Rhamdia, is described to provide a basis for comparative work. The two main reasons for variation in body proportions are size allometry and a phenomenon here called the 'Segmental effect'. The Segmental effect represents an elongation of body proportions posterior to the head, in fish with many vertebrae, which puts constraints on the use of body proportions in phylogenetic analyses. Previous opinions on relationships of Rhamdia are reviewed and in part considered inconclusive because of their use of data which included body proportions with unsatisfactory reference distances.
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The Biosphere Reserve Montes Azules (RBMA), located in the Mexican southeastern state of Chiapas, is the most important floral and faunal reserve in México and Mesoamerica, The reserve contains the largest and best preserved forests in the region, as well as the few remaining pristine rivers. The primary objective of this paper is to update the fish diversity along the southern part of this important reserve, based on material collected during eight expeditions carried out from 2004 to 2006. Fish samples were obtained from 20 localities, of which seven were inside the protected natural area. A total of 8, 977 specimens were collected, representing 55 species (including one unidentified and three aliens) in 41 genera and 23 families. This paper adds 9 more species to the regional fish fauna, one of them are exotic. According to their zoogeographic origin, three are Nearctic, 32 are Neotropical, and 17 are in other groups; ecologically, nine species are of primary derivation, 26 are Secondary, and 17 are Peripheral or Vicarious, according to Myers' (1938) classification based on historical salinity tolerance. The most diverse fish families were the Cichlidae and Poeciliidae, with 15 and eight species, respectively. Compared to other Mexican hydrological regions, the study area contains a fish fauna that is still well preserved in terms of diversity, but ecological damage is due to humans living adjacent to the reserve. If this situation continues unchecked, it could threaten the survival of some species.
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Gobies of the genus Sicydium Valenciennes are widespread in Mexico and Central America, but have a different distribution pattern on the Atlantic and Pacific slopes of the region. On the Pacific slope, where mountain ranges are found near the coast and the coastal plain is narrow, Sicydium is continuously distributed in rivers from Mazatlán, Sinaloa, Mexico, to central Panama. On the Atlantic slope, Sicydium is known from to three disjunct areas where coastal mountain ranges are present, central Mexico, northern Honduras, and northeastern Costa Rica and northern Panama, and has not been recorded from intervening areas with broad coastal plains. The amphidromous life history of Sicydium gobies may prevent them from occupying rivers flowing through broad coastal plains. Sicydium gobies spawn in rocky mountainous river reaches and their larvae drift downstream to the ocean where they begin feeding. In rivers crossing broad coastal plains the distance to the ocean is relatively long, and I hypothesize that newly hatched larvae might starve before they reached their marine feeding habitat or that post-larvae might starve on their return migration up river to adult habitat.
Article
Guatemala is characterized by high diversity of its freshwater fishes. Among the most important regions of biodiversity are the Departments of El Petén and Alta Verapaz, located in the northern part of the country south of the Mexican border. Several authors consider the ichthyofauna of this country to be relatively well studied, but the majority of available information is dispersed and sporadic. We present an updated systematic list, comprising all species collected by us, and which includes an exhaustive check of literature records. A total of 55 collecting localities are included in this study. The total species number is 88, distributed in 47 genera, 24 families, and 14 orders. The two departments together include 35.2% of the total estimated number of fish species for the entire country. The Cichlidae and Poeciliidae are the most speciose families. Of the total of 88 species, 11 are primary fishes, 54 are secondary, and 23 peripheral, according to Myers (1938) classification. One endemic species is known from El Petén and 12 from Alta Verapaz. Three species are considered to be exotics: Ctenopharyngodon idella, Carassius auratus, and Oreochromis aureus. Several of our collections confirm the presence of species not reported for more than 30 years (e.g., Bramocharax species), but others require more study (i.e. Heterandria species). Only 18 species from Guatemala are recognized as threatened or endangered by different organizations, but included are some of the more common and widespread species, such as Astyanax aeneus. Several endemics are excluded from such listings, possibly due to lack of knowledge. The actual condition of the Guatemalan populations for the majority of the fish species, including the endemics, is not known.