versão impressa ISSN 1870-3453
Rev. Mex. Biodiv. v.79 n.1 México jun. 2008
Taxonomía y Sistemática
A new rhabdiasid species from Craugastor occidentalis (Anura: Brachycephalidae) from Sierra de Manantlan, Jalisco, Mexico
Una especie nueva de rhabdiásido de Craugastor occidentalis (Anura: Brachycephalidae) de la sierra de Manantlán, Jalisco, México
Elizabeth A. MartínezSalazar
Laboratorio de Helmintología Dr. Eduardo Caballero y Caballero, Instituto de Biología, Universidad Nacional Autónoma de México. Apartado postal 70153, 04510 México, D. F., México.
Recibido: 16 abril 2007
Aceptado: 12 junio 2007
Rhabdias manantlanensis n. sp., parasite of the lungs of Craugastor occidentalis is illustrated and described. Rhabdias manantlanensis differs from related species in the genus by the combination of the following characters: elongated body, cuticle slightly swollen (thin and smooth), 6 weakly developed lips (4 submedian + 2 lateral), localization of nerve ring at 193244 (220) µm from anterior end, muscular corpus slightly inflated, esophagus length/ body length ratio 5.116.57 (5.79%), tail relatively small, conical and with sharp terminal point, tail length/ body length ratio 1.483.27 (2.48) %, slightly preequatorial vulva (vulva length / body length ratio 41.6651.59 [47.74] %), and cupshape buccal capsule (1119  x 1927 ). This is the seventeenth species of the genus Rhabdias described in the Neotropical realm and the third described in the Sierra Madre del Sur, Mexico.
Key words: Anura, Craugastor occidentalis, taxonomy, lung worm, Rhabdias manantlanensis n. sp., Sierra Madre del Sur, México.
Se describe e ilustra Rhabdias manantlanensis n. sp., parásito pulmonar de Craugastor occidentalis. Rhabdias manantlanensis difiere de las otras especies relacionadas del género por la combinación de los siguientes caracteres: cuerpo alargado, cutícula ligeramente ensanchada (delgada y lisa), 6 labios débilmente desarrollados (4 submediales y 2 laterales), localización del anillo nervioso a 193244 (220) µm de la región anterior, corpus esofágico ligeramente ensanchado; relación longitud del esófago/ longitud corporal 5.116.57 (5.79) %, cola relativamente pequeña, cónica y con una terminación en punta, relación longitud de la cola/ longitud corporal 1.483.27 (2.48) %, vulva ligeramente preecuatorial (relación longitud de la vulva/ longitud corporal 41.6651.59 [47.74] %), y una cápsula bucal en forma de copa (1119  x 1927 ). Con ésta son 17 especies del género Rhabdias descritas de la región neotropical y la tercera en la Sierra Madre del Sur, México.
Palabras clave: Anura, Craugastor occidentalis, taxonomía, parásito pulmonar, Rhabdias manantlanensis n. sp., Sierra Madre del Sur, México.
Fifteen of about 60 species of the cosmopolitan genus Rhabdias Stiles and Hassall, 1905 are parasites of the lungs of anurans in the Americas. There are 4 Nearctic species, R. americanus Baker, 1987, R. joaquinensis Ingles, 1935, R. ranae Walton, 1929, and R. bakeri Tkach, Kuzmin and Pulis, 2006 and 11 Neotropical species, R. alabialis Kuzmin, Tkach and Brooks, 2007, R. androgyna Kloss, 1971, R. elegans Gutierrez, 1945, R. füelleborni Travassos, 1926, R. hermaphrodita Kloss, 1971, R. mucronata Schuurmans Stekhoven, 1952 (species inquirenda, adults unknown), R. tobagoensis Moravec and Kaiser, 1995; R. truncata Schuurmans Stekhoven, 1952 (species inquirenda, adults unknown), R. savagei Bursey and Goldberg, 2005, R. pseudospherocephala Kuzmin, Tkach and Brooks, 2007 (=R. sphaerocephala of BravoHollis and Caballero, 1940, Brenes and BravoHollis, 1959, and Kloss, 1971, 1974), and finally R. kuzmini MartínezSalazar and LeónRègagnon, 2007.
According to MartínezSalazar and LeónRègagnon (2007), 8 species of this general group have been recorded in México: Rhabdias americanus, R. elegans, R. füelleborni, R. ranae, R. savagei, R. cf. sphaerocephala (=R. seudospherocephala records of BravoHollis and Caballero, 1940), R. tobagoensis, and R. kuzmini.
The Sierra de Manantlán Biosphere Reserve is located in the transition of the Nearctic and Neotropical realms and encompasses parts of the Sierra Madre del Sur (SPP, 1985). Studies of the parasite fauna of wild vertebrates in the Sierra de Manantlán, Jalisco, Mexico are practically nonexistent. There is only one study in the region, examining helminths of freshwater fish (SalgadoMaldonado et al., 2004).
The aim of this paper is to describe a new species of Rhabdias parasitizing an endemic anuran of the Sierra de Manantlán, Jalisco State, Mexico, as part of a biodiversity inventory of parasites of amphibians and reptiles in México.
Materials and methods
On June 15, 2003, 2 specimens of Craugastor occidentalis Taylor, 1921 were collected in Puerto los Mazos, Rancho los Mojos, in the Sierra de Manantlán, Jalisco State (19°41'18" N, 104°23'43" W; 1687 m). Anurans were collected by hand, and then deposited in herpetological bags for their transportation. Hosts were killed by intraperitoneal overdoses of sodium pentobarbital. Each host was subsequently necropsied, and the organs were examined for helminths using a stereomicroscope. Lung worms were initially placed in saline (0.65%), and afterwards killed by immersion in hot 4% formalin and stored in 70 % ethanol. Nematodes were cleared with glycerin in temporary preparations. Drawings were made with the aid of a drawing tube. Measurements are given in micrometers ((jm) unless otherwise stated. Minimum and maximum values are given followed by mean and SD in parentheses. Taxonomic determinations at specific level were made comparing with original descriptions and specialized literature. For the scanning electron microscopy (SEM), specimens were stored in 4% formalin, dehydrated in a series of gradual alcohol, and critical point dried with carbon dioxide. Specimens were coated with a goldpalladium mixture and examined in a Hitachi S2460N scanning electron microscope at 15kV.
Voucher specimens of hosts were deposited in the Herpetological Collection, University of Texas in Arlington, Texas (UTA). Holotype and paratypes are deposited in the Colección Nacional de Helmintos (CNHE), Instituto de Biología, Universidad Nacional Autónoma de México, Mexico City, México.
The following specimens were also examined during this study: Rhabdias agkistrodontis Sharpilo,1976 (USPNC 092278.02), R. ambystomae Kuzmin, Tkach and Snyder, 2001 (USPNC 082125.02), R. alabialis Kuzmin, Tkach and Brooks, 2007 (USPNC 098144.00), R. americanus Baker, 1987 (USPNC 081011.00, 089802.00), R. bakeri Tkach, Kuzmin and Pulis, 2006 (USPNC 096379.00, 096381.00), R. bufonis (Schrank, 1788) Stiles and Hassall, 1905 (USPNC 027065.00), R. chamaeleonis (USPNC 059095.00), R. elegans Gutiérrez, 1945 (USPNC 084920.00, 087516.00), R. eustreptos MaCallum, 1921 (USPNC 042118.00), R. füelleborni Travassos, 1926 (USPNC 032536.00, 083796.00; CNHE 001975, 3771, 3776), R. cf. fuscovenosa (CNHE 3631),R. hermaphrodita Kloss, 1971 (USPNC 08525.00), R. hylae Johnston and Simpson, 1942 (USPNC 091190.00), R. joaquinensis Ingles, 1935 (USPNC 088047.02), R. kuzmini MartínezSalazar and LeónRègagnon, 2007 (CNHE 05807, 5808, 5809, 5810, 5811; USPNC 99550.00), R. lamothei MartínezSalazar and LeónRègagnon, 2006 (CNHE 5375; 53765378, 5380), R. leonae MartínezSalazar, 2006 (CNHE 5543, 5444, 5445, 54465449), R. nipponica Yamaguti, 1935 (USPNC 091354.00), R. ranae Walton, 1929 (USPNC 088586.00, 089190.00), R. savagei Bursey and Goldberg, 2005 (USPNC 094848.00; CNHE 5034), R. pseudospherocephala Kuzmin, Tkach and Brooks, 2007 (USPNC 098146.00), material originally assigned to R. cf. sphaerocephala Goodey, 1924 (CNHE 001986, 002057, 002227, 002284), and R. vellardi Pereira, 1928 (CNHE, 1425).
Description based on 11 gravid individuals (measurements on 8). Body cylindrical. Body length 6.489.64 (7.85±1.13) mm, maximum width 175239 (203±26). Anterior end truncated, posterior end tapered with terminal point. Body cuticle typically not swollen or only slightly swollen, thin and smooth. Oral opening oval, surrounded with 6 weakly developed lips: 4 submedian situated close to the edge of oral opening, and 2 lateral, all with small cephalic papillae. Two small lateral amphids present near to lateral papillae. Buccal capsule well developed, cupshape in lateral view, circular in apical view, 1119 (13±2) depth, with 1927 (21±2) width. Esophagus clubshaped. With a muscular corpus slightly inflated. Esophagus length 387515 (451±38), representing 5.116.57 (5.79) % of the body length. Esophagus width 3446 (39±4) at anterior region, 3854 (47±4) at muscular region, 5065 (55±5) at the glandular region. Posterior bulb 5477 (67±9) wide. Inconspicuous cuticular nerve ring at 193244 (220±17) from the anterior region of the body. Inconspicuous excretory duct, located near posterior margin of nerve ring. Intestine straight, with dark brown contents. Rectum thickwalled. Vulva near to middle body (slightly preequatorial), lips indistinct, distance from the anterior region of the body to vulva 2.864.57 (3.74±0.52) mm, representing 41.6651.59 (47.74) % of body length. Genital system amphidelphic. Ovaries straight, lying along intestine. Tail comparatively short, conical, 143232 (190±31) long, representing 1.483.27 (2.48) % of body length, with sharp terminal point.
Uteri relatively large. Eggs numerous, oval, thinwalled containing fully developed larvae. Egg size 88102 (94±4) long x 4355 (50±3) wide (n=54).
Type specimens: Holotype, CNHE 5804; and paratypes CNHE 5805, 5806.
Type host: Craugastor occidentalis Taylor, 1941 (Brachycephalidae). Symbiotype UTA A57872.
Synonymized with Eleutherodactylus occidentalis Taylor, 1941 (Eleutherodactylidae) (see Crawford and Smith, 2005; Frost et al., 2006).
Type locality: Puerto los Mazos, Rancho los Mojos, Sierra de Manantlán, Jalisco, México (19°41'18"N; 104°23'43"W, 1687m).
Site of infection: Lungs.
Prevalence and intensity of infection: 1 of 2 host infected (50%), 13.
Etymology: The new species is named after the type locality, in the Sierra de Manantlán, Jalisco, Mexico.
Rhabdias manantlanensis differs from the related species by the following characteristics: body elongated, truncated anterior end, cuticle slightly swollen (thin and smooth), 6 weakly development lips (4 submedian + 2 lateral), localization of nerve ring at 193244 (220) from anterior end, muscular corpus slightly inflated, esophagus length / body length ratio 5.116.57 (5.79) %, tail relatively small, conical and with sharp terminal point, tail length/body length ratio 1.483.27 (2.48) %, slightly preequatorial vulva (vulva length / body length ratio 41.6651.59 [47.74] %), and the typical cupshape of the buccal capsule [1119 (13) x 1927 (21)].
There are 15 Rhabdias species recorded in the Americas considered to be typical of anurans (see Bursey et al., 2003; Bursey and Goldberg, 2005; Kuzmin et al., 2007; MartínezSalazar and LeónRègagnon, 2007): R. alabialis, R. americanus, R. androgyna, R. bakeri, R. elegans, R. füelleborni, R. hermaphrodita, R. joaquinensis, R. kuzmini, R. mucronata, R. ranae, R. savagei, R. pseudospherocephala, R. tobagoensis and R. truncata. Comparison of R. manantlanensis with R. mucronata and R. truncata is not possible because adults of these species are unknown.
Rhabdias alabialis, R. americanus, R. androgyna, R. elegans, R. füelleborni, R. hermaphrodita, R. kuzmini, and R. pseudospherocephala differs from R. manantlanensis n. sp. in host preference because all of them are typical parasites of Bufonidae.
Rhabdias alabialis differs from R. manantlanensis principally by the absence of lips, buccal capsule shape (triangular vs. cup in R. manantlanensis), and the dimensions of the body, is larger and wider in R. alabialis (7.679.27 (7.97) mm x 260328 (315) in R. alabialis) (Kuzmin et al., 2007).
Rhabdias americanus can be distinguished from R. manantlanensis in the dimensions of the body, being larger and wider in R. americanus (10.7414.14 (12.46) mm x 210310 in R. americanus), the evident cuticular swelling along the body (outer layers of cuticle inflated in R. americanus), the presence of a evident corpus inflated in R. americanus (vs. slightly inflated in R. manantlanensis), the dimensions of the buccal capsule is smaller in R. americanus (10 x 1215 (13) in R. americanus), the tail length / body length ratio is larger in R. americanus (3.34.5 (4.0) in R. americanus) (data based on Kuzmin et al., 2003).
Rhabdias androgyna is slightly larger than R. manantlanensis (9.413.4 mm in R. androgyna), and is also distinguished by the presence of evident corpus inflation in R. androgyna (vs. slightly inflated in R. manantlanensis), the esophagus length is larger in R. androgyna (577618 in R. androgyna), the evident cuticular swelling along the body (outer layers of cuticle inflated in R. androgyna) (data based on Kloss, 1971).
Rhabdias manantlanensis differs from R. elegans principally in the dimensions of the body, being larger and wider in R. elegans (8.0710.25 (9.59) mm x 270357 in R. elegans). In addition, the buccal capsule is smaller in R. elegans (7 x 7 in R. elegans), the swelling of the cuticle is completely inflated in R. elegans, the length tail / body length ratio is larger in R. elegans (3.254.59 (4.98) % in R. elegans), and the lips structure was not described in R. elegans (data based on Kloss, 1971; Gutiérrez, 1945).
The new species differs from Rhabdias füelleborni in body size (10 20 mm vs. 6.48 9.64 (7.85) mm in R. manantlanensis), the presence of an evident inflated corpus in R. füelleborni (vs. slightly inflated in R. manantlanensis), and the swelling of the cuticle (cuticle swollen with irregular folds vs. cuticle slightly, thin and smooth in R. manantlanensis) (data based on Travassos, 1926).
Rhabdias hermaphrodita differs from R. manantlanensis in its evident cuticular swelling along the body in R. hermaphrodita (vs. slightly swollen, thin and smooth in R. manantlanensis), the esophagus is longer in R. hermaphrodita (4.339.17 (6.08) in R. hermaphrodita), and the length tail / body length ratio is greater in R. hermaphrodita (2.546.57 (4.26) in R. hermaphrodita) (data based on Kloss, 1971).
Rhabdias manantlanensis differs from R. kuzmini by the dimensions of the body, being larger and wider in R. kuzmini (15.1519.19 mm x 351542 in R. kuzmini). In addition, the buccal capsule is larger and wider in R. kuzmini (3170 (58) x 3547 (40) in R. kuzmini)), the shape of the buccal capsule differs (barrelshaped vs. cupshaped in R. manantlanensis), as does the cuticle swelling (cuticle slightly swollen in anterior and terminal ends with irregular folds vs. cuticle slightly swollen, thin and smooth in R. manantlanensis), data based on MartínezSalazar and LeónRégagnon, 2007).
The new species differs from Rhabdias pseudospherocephala (=R. spherocephala in Central and South America from Chaunus marinus, according to Kuzmin et al., 2007) in the dimensions of the body, being wider in R. pseudospherocephala (6.179.60 (7.90) mm x 290380 (330) in R. pseudospherocephala). The buccal capsule is of a different shape (funnelshaped vs. cupshaped in R. manantlanensis), the length tail / body length ratio is larger in R. pseudospherocephala (3.75.0 (4.4)% in R. pseudospherocephala), and the swelling of the cuticle also differs (cuticle swollen principally on anterior end with irregular folds vs. cuticle slightly swollen, thin and smooth in R. manantlanensis) (Kuzmin et al., 2007).
Rhabdias bakeri, R. joaquinensis, R. ranae, and R. savagei differ from R. manantlanensis n. sp. by the host specificity and the presence of the postequatorial vulvae, all of them are typical parasites of Ranidae.
Rhabdias manantlanensis differs from R. ranae and R. bakeri in body size. The new taxon is thinner than R. ranae and R. bakeri [4.998.24 (6.61) mm x 250350 (299) in R. ranae; 6.2210.69 (9.27) mm x 225406 (319) in R. bakeri vs. 6.489.64 (7.85) mm x 175239 (203) in R. manantlanensis]; the cuticle is inflated in R. ranae, and R. bakeri, the esophagus length / body length ratio is slightly smaller in R. manantlanensis [5.116.57 (5.79) vs. 7.311.2 (8.7) % in R. ranae, and 5.48.8 (6.1) % in R. bakeri]. Rhabdias ranae and R. bakeri also differ from the new species in the presence of a evident postequatorial vulvae in (data based on Kuzmin et al., 2003; Tkach et al., 2006).
Rhabdias manantlanensis differs from R. joaquinensis in that the body is smaller and wider in R. joaquinensis, the cuticle swelling in posterior twothirds comparatively thin in the anterior third of the body with a fine cuticle with fine longitudinal striations in the anterior portion of the body, covered with irregular longitudinal and oblique folds in the posterior portion, transverse folds present in the posterior quarter of the body cuticle in R. joaquinensis (vs. cuticle not swollen or slightly swollen, thin and smooth in the new taxon); the buccal capsule is smaller and 6 prominent inner circle papillae are present, 10 small papillae in the outer circle, and 2 porelike amphids present in R. joaquinensis (vs. lips weakly developed, 4 submedian and 2 lateral, all with small cephalic papillae and 2 amphids)(data based on Kuzmin et al., 2003; Table 1).
The body of Rhabdias manantlanensis is larger and thinner than that of R. savagei, the buccal capsule is smaller in R. savagei, the length tail / body length ratio is larger in R. savagei, the cuticle is inflated in R. savagei (vs. cuticle slightly swollen, thin and smooth in R. manantlanensis), and the esophagus length / body length ratio is smaller in R. manantlanensis (data based on Bursey and Goldberg, 2005; Table I).
Finally, Rhabdias tobagoensis is a neotropical species resembling R. manantlanensis in general morphology (both species present a relatively large buccal capsule), and are typical for Brachycephalidae. This species was described from Eleutherodactylus charlottevillensis Kaiser, Dwyer, Feichtinger, and Schmid, 1995, which is distributed exclusively in Tobago, West Indies (previously confused withE. cf. terraebolivaris Rivero, 1961 [Moravec and Kaiser, 1995]). However, Rhabdias manantlanensis differs from R. tobagoensis principally in the body width, being wider in R. tobagoensis. The outer body layers are inflated in R. tobagoensis (vs. cuticle slightly swollen, thin and smooth in R. manantlanensis), the buccal capsule is slightly larger in R. manantlanensis [1119 (13) x 1927 (21) vs. 69 (6) x 1821 (18) in R. tobagoensis], the lips structure also differs (4 submedian lips and 2 lateral lips vs. circumoral lips in R. tobagoensis), the localization of the nerve ring is more proximal to the anterior end in R. tobagoensis, the shape of the vulvar lips (lips indistinct vs. slightly elevated in R. tobagoensis), the esophagus length / body length ratio is slightly smaller in R. manantlanensis, and the length tail / body length ratio is slightly smaller in R. manantlanensis (data based on Moravec and Kaiser, 1995; Table I).
With respect to other species distributed in the Americas, only Rhabdias eustreptos (MacCallum, 1921) Chitwood and Chitwood, 1934, the American form of R. fuscovenosa (Railliet, 1899) Goodey, 1924) (its original distribution is in the Palaearctic Realm, and presents a preequatorial vulva, see Bursey et al. (2003); however, the American specimens present an equatorial vulva, see MartínezSalazar and LeónRègagnon, 2006), R. lamothei MartínezSalazar and LeónRègagnon, 2006, and R. vellerdi Pereira, 1928 belong to the general group of species that present 6 lips and equatorial vulvae as is the condition in R. manantlanensis. However, based on host preference, R. manantlanensis differs from all 4 species, which are parasites of snakes, whereas R. manantlanensis parasitizes anurans (Brachycephalidae). It has been observed that species of Rhabdias parasites of snakes never parasitize hosts of different orders (Kuzmin et al., 2003; MartínezSalazar, 2006; Tkach et al., 2006).
There are other species that share with Rhabdias manantlanensis the condition of having 6 lips and equatorial vulva, but are distributed in other geographic realms, namely R. hylae Johnston and Simpson, 1942, distributed in the Australian Realm, R. japalurae, Kuzmin, 2003 in the Oriental Realm, finally R. bufonis (Schrank, 1788) Stiles and Hassall, 1905, R. bermani Rausch and Atrashkevich, 1984, and R. vibakari Kuzmin, 1996 in the Palaearctic Realm. All the species listed also differ from R. manantlanensis by the host preference (hylids in R. hylae, lizards R. japalurae, toads in R. bufonis, salamanders in R. bermani, and snakes in R. vibakari).
A single species of Rhabdias is rarely found in representatives of more than one host group. The host preference can be quite narrow, even at the family level (Bursey et al., 2003; Kuzmin et al., 2003, MartínezSalazar and LeónRègagnon, 2006; MartínezSalazar, 2006; Tkach et al., 2006). For example, Rhabdias bakeri is typical of ranids, Rana sylvatica LeConte, 1825 (syn. Lithobates sylvaticus (LeConte, 1825), see Frost et al., 2006), and Ra. pipiens Schreber, 1782 (syn. L. pipiens (Schreber, 1782 ), see Frost et al., 2006) (Tkach et al., 2006). Furthermore, more than 1 species of Rhabdias are typical of 1 bufonid species i.e., R. füelleborni, R. alabialis and R. pseudospherocephala are typical from Bufo marinus Linnaeus, 1758 (syn. Chaunus marinus (Linnaeus ,1758), see Frost et al., 2006) (Travassos, 1926; Kuzmin et al., 2007).
Rhabdias tobagoensis resembles the new species, with both of them parasitizing Brachycephalidae, but R. tobagoensis is distributed in Tobago, West Indies. There is 1 single record of Rhabdias cf. tobagoensis in Mexico; however, it was found parasitizing a different host group, i.e., Dendropsaphus microcephalus Cope, 1886 (Hylidae) (syn. Hyla microcephala (Cope, 1886), see Frost et al., 2006) in Veracruz State (Goldberg et al., 2002). Due to the conservative morphology of Rhabdias, some species can be misidentified (see redeterminations on Kuzmin et al., 2003, Tkach et al., 2006; Kuzmin et al., 2007). The specimens reported as Rhabdias cf. tobagoenesis by Goldberg et al. (2002) could correspond to other species of the genus; however, the Mexican specimens are not available for reexamination. It is necessary to recollect this lung worm of the same host species in the Tuxtlas region, Veracruz State, to clarify the identity of this record, using other sources of characters such as SEM or using molecular data.
In the only study regarding the helminth fauna of Brachycephalidae in Mexico, the records from Craugastor rhodopis (Cope, 1867) (syn. Eleutherodactylus rhodopis Stejneger, 1904), in Veracruz State, Mexico are described (Goldberg et al., 2002). These authors reported the infection of 1 digenean, Gorgoderina attenuata Stafford, 1902, 5 nematodes, Aplectana incerta Caballero, 1949, Cosmocerca podicipinus Baker and Vaucher, 1934, Oswaldocruzia sp., Porrocaecum sp. (larva), and Strongyluris sp.; and 1 acanthocephalan, Centrorhynchus sp.; they did not find lung worms in this host species.
This host group present a geographic distribution that is strongly infl uenced by humidity, reasons why microendemic species are commonly restricted to small highland habitats of the mountain ranges of Middle American (Campbell, 1999). For this reason, and considering the host specificity observed in species of Rhabdias, it is possible that the geographical distribution of Rhabdias manantlanensis is restricted to Western Mexico (where this endemic anuran is located).
According to Crawford and Smith (2005), Craugastor dispersed into northern Central America from South America in the early Paleocene; based on this hypothesis and considering the host preference of species of Rhabdias, it possible that the origin of this new rhabdiasid could be Neotropical, although this hypothesis needs to be corroborated with a molecular phylogenetic analysis of the species of the Rhabdias.
Rhabdias manantlanensis is the first species described from an endemic Mexican Brachycephalidae and the third Rhabdias species recorded in the Sierra Madre del Sur (MartínezSalazar, 2006; MartínezSalazar and LeónRègagnon, 2007). The Sierra Madre del Sur is home to many endemic organisms, and represents the highest biodiversity of amphibians and reptiles in Mexico (FloresVillela, 1998). Richness of these vertebrates in this zone of the country suggests the existence of Rhabdiasidae still waiting to be discovered. Additional studies on the parasite fauna of the Sierra de Manantlán, and vertebrates, need to be conducted.
To Ma. Antonieta Arizmendi, Florencia Bertoni, Luis Canseco, Tom Devitt, John Malone, Rosario Mata, Jesse Meik, Alejandro Oceguera, Ricardo Paredes, Paulino Ponce, and Eric N. Smith for their assistance in fieldwork; Berenit MendozaGarfias for assisting in processing samples for SEM, and Jorge FalcónOrdaz for his advice in the handling of specimens for optical microscopy. Rogelio Rosas for his help in microphotography. I thank Dr. Eric P. Hoberg, USNPC, Beltsville, Maryland, and Luis GarcíaPrieto, CNHE, Instituto de Biología, UNAM, for the loan of specimens. Eric N. Smith for host identification (UTA). I also thank V. LeónRègagnon for her valuable comments on an early draft of the manuscript. The specimens were collected under the Scientific Collecting License FAUT0056, issued to V. León Règagnon. Funding for this study was provided by National Science Foundation DEB0102383 to V. LeónRègagnon (Universidad Nacional Autónoma de México), and J. A. Campbell (University of Texas at Arlington); and CONACyT and DGEPUNAM in form of scholarships to EAMS.
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