Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species
Elops smithi , new species Figure 1; Table 1 Elops saurus non Linnaeus 1766: Regan, 1909 (in part), Hildebrand, 1943 (in part); Bertin, 1944 (in part); Fowler, 1931; Gehringer, 1959 (in part); Whitehead, 1962 (in part); Hildebrand, 1963 (in part); Eldred and Lyons, 1966 (in part); Carles, 1967; Mill...
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Online Access: | https://dx.doi.org/10.5281/zenodo.5658998 https://zenodo.org/record/5658998 |
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Biodiversity Taxonomy Animalia Chordata Actinopterygii Elopiformes Elopidae Elops Elops smithi |
spellingShingle |
Biodiversity Taxonomy Animalia Chordata Actinopterygii Elopiformes Elopidae Elops Elops smithi Mcbride, Richard S. Rocha, Claudia R. Ruiz-Carus, Ramon Bowen, Brian W. Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species |
topic_facet |
Biodiversity Taxonomy Animalia Chordata Actinopterygii Elopiformes Elopidae Elops Elops smithi |
description |
Elops smithi , new species Figure 1; Table 1 Elops saurus non Linnaeus 1766: Regan, 1909 (in part), Hildebrand, 1943 (in part); Bertin, 1944 (in part); Fowler, 1931; Gehringer, 1959 (in part); Whitehead, 1962 (in part); Hildebrand, 1963 (in part); Eldred and Lyons, 1966 (in part); Carles, 1967; Miller and Jorgenson, 1973 (in part), Santos-Martίnez and Arboleda (1993). These studies examined what we recognize here as E. smithi , either in whole or in part, based on their reports of meristic values, sample locality, or both. Elops sp.: Smith, 1989; Smith-Vaniz et al. , 1999; Obermiller and Pfeiler, 2003 Holotype. UF 45683, 303 mm SL, marine waters of Guyana, by trawl, 16 July 1967. Paratypes. UF 45682, marine waters of Trinidad, 13 December 1967; GCRL 11950, 4, Commewijne River, Suriname, 14 October 1973; GCRL 12733, Gatun Locks, Canal Zone, Panama, 4 March 1974; UF 11269, 2, Tortuguero Lagoon, Costa Rica, August 1963. Other museum material examined. Elops saurus : FSBC 0 0 258, Florida, Pinellas County, 13 December 1957; FSBC 10270, Florida, Pinellas County, 15 December 1977; FSBC 12589, 3, Florida, Hillsborough County, 3 June 1983; GCRL 0 345, Louisiana, 8 September 1959; GCRL 1938, Mississippi, 8 August 1966; UF 47036, Honduras, 26 April 1967; UF 105715, 2, Florida, Volusia County, 17 November 1972. Diagnosis. Elops smithi is distinguished from E. saurus in the number of vertebrae (73–80, usually 75–78 versus 79–87, usually 81–85, respectively). According to McBride and Horodysky (2004), vertebrae counts in the overlap range (79–80) occurred in only 94 of 3,255 (2.9 %) specimens examined from the coasts of the Americas, the Bahamas, and the Caribbean islands. As reported by Whitehead (1962) counts of gill rakers and total vertebrae can be used to separate all species of Elops . Western Atlantic Elops , now recognized as E . smithi and E . saurus , have lower gill raker counts (10–15 on the lower part of the first arch) than E . affinis (16–20) and E . lacerta (17–19). Elops smithi and E . saurus have higher vertebrae counts (> 72; see above for ranges) than E . senegalensis (67), E . machnata (63–64), and E . hawaiensis (68–70). Description. Body elongate (head length 25–29 % of SL) and slender (width 7.5–9.4 % of SL). Mouth large (maxilla 56–60 % of head length) and nearly terminal. Caudal fin deeply forked, with lobes equal. Principal dorsal-fin rays 19–20 (24–27 total); anal rays 12–13 (16–19 total); pectoral rays 17–18; pelvic rays 13–16; branchiostegal rays 30–34; gill rakers on lower arch 13–15 (total 21–23 excluding rudiments); lateralline scales (102–118, but may be higher if specimen is found north of the Caribbean Sea [see below]); and 73– 80 vertebrae (usually 75–78). Data for above description are from Table 1, Figure 2, and McBride and Horodysky (2004). Meristic characters continued. The larvae are of leptocephalus form, and the total myomere number of the leptocephalus equals that of total vertebrae (McBride & Horodysky 2004). Predorsal (61–66) and preanal (68–72) myomeres are also reliable characters for identifying premetamorphic leptocephali (Smith 1989). Others examining Elops from the Caribbean Sea have noted minor variations in these meristic characters (Carles 1967; Santos-Martίnez and Arboleda 1993), indicating differences in counting methods or geographic variation. Coloration. Living adults bright silver, particularly on sides; may be bluish-gray on back with yellowish hue on fins. Not as silvery in preservative. Comparisons. We found no character other than counts of vertebrae that separates adult E . smithi from E . saurus (Table 1). Although lateral-line scale counts appeared to be a diagnostic character, the scales are formed late in larval development so this character is indicative of latitude where larval transformation occurs instead of where spawning occurred. To demonstrate this, it can be shown that lateral-line scale counts are distinct among E. smith and E. saurus that had not been dispersed outside their typical range (Table 1, Fig. 2 A), but the lateral-line scale counts are not distinct among a test collection from the southern Indian River Lagoon, Florida, which included E. smithi that had presumably been dispersed from their spawning grounds (Fig. 2 B). This disconnect can be explained because vertebral number is set during embryogenesis but scales are not developed until about 50 mm in the late metamorphic period (Gehringer 1959). Thus, lateral-line scale counts will be a misleading diagnostic character when measured from specimens collected within areas of sympatry. The leptocephalus larva, common to this genus, is associated with long-distance dispersal (McBride & Horodysky 2004), so scale counts may be problematic as a taxonomic character in other species of Elops as well. In addition, the scales of these species are small and easily displaced, further confounding their use as a taxonomic character. Mitochondrial DNA sequence data provide an independent character for recognizing two species of Elops in the western North Atlantic. We observed 14 haplotypes in two primary lineages corresponding to E. saurus and E. smithi (Table 2). These sequences have been deposited in GenBank under accession numbers GQ 183881 – GQ 183882 ( E. saurus , haplotypes A, B) and GQ 183883 – GQ 183894 ( E. smithi , haplotypes C – N). The genetic difference ( d ) between the E. saurus haplotypes and the E. smithi haplotypes ranged from 0.023 to 0.029 (Fig. 3). Obermiller and Pfeiler (2003) reported a similar level of divergence between what we recognized as E . smithi and E . saurus ( d = 0.021 with 12 S and 16 S rRNA mtDNA sequences). In addition, Obermiller and Pfeiler (2003) observed a similar level of divergence between E . saurus and E . hawaiiensis ( d = 0.024), two recognized species that occupy different ocean basins. TABLE 2. Data associated with fish used in the genetic analysis. Collection date and locale are listed, along with standard length (SL), and total number of vertebrae (Vert.). Fish are sorted as vertebrae morph (high vs. low-count) and haplotype. *Mismatches between phenotype and genotype are indicated with an asterisk. Locality codes are: IR = Indian River Lagoon (northern or southern regions of the lagoon), southeast Florida, CK = Cedar Key, west coast Florida, and FW = Fort Walton, panhandle Florida. continued next page Although the mtDNA data presented here and data presented previously by Obermiller and Pfeiler (2003) indicate two evolutionary lineages, the mtDNA character was not absolutely diagnostic. In seven of 56 specimens (12.5 %), there was a mismatch between classification based on genetics and that on morphology (Table 2). Five of these individuals had morphology similar to E . smithi but haplotypes in the E . saurus lineage, and two had the reverse. These mismatches may indicate ecophenotype plasticity within species, hybridization, or retention of ancestral polymorphisms. All three phenomena have been documented in fishes (see Rocha et al. 2007). The sympatric sturgeons Scaphirhynchus albus and S. platorynchus share mtDNA haplotypes because of their recent speciation and hybridization (Campton et al. 2000). The marine angelfishes Centropyge argi and C. aurantonotus are sister species that share haplotypes despite diagnostic differences in coloration (Bowen et al. 2006). And the Atlantic bluefin tuna ( Thunnus thynnus ) has haplotypes derived from both Pacific bluefin ( Thunnus orientalis ) and albacore ( Thunnus alalunga Alvarado Bremer et al. 2005). Surveys of multiple nuclear loci have resolved these phenomena in other species and could profitably be applied to Elops . Nonetheless, given these genetic results, it is unlikely that we are observing an intraspecific, or population-level, genetic phenomenon, so we reject the hypothesis that E . smithi and E . saurus are ecophenotypes. Distribution. Elops smithi occurs along the northern coast of South America, in the Caribbean Sea, and throughout the Bahamas; it also occurs sympatrically with E. saurus in the Gulf of Mexico and along the eastern seaboard of North America (Smith 1989; see McBride & Horodysky [2004] for distribution maps of larvae, juveniles and adults). In addition, there are two records of Elops from Bermuda (Linton 1907) although no resident population has been found there (Smith-Vaniz et al. 1999). Only one specimen is available, a 181 mm SL fish (BAMZ 1990 -083-037) with 73 vertebrae; this apparently represents a waif from the population inhabiting the Caribbean (Smith-Vaniz et al. 1999). Elops smithi is found in a wide range of salinities. Mature adults and early-life-history stages are found in offshore, marine habitats, where spawning presumably occurs (Gehringer 1959; Santos-Martínez & Arboleda 1993; McBride & Horodysky 2004). Transforming larvae and subadults are found throughout estuaries, as far up as the oligohaline zone, as well as in hypersaline lagoons (Carles 1967; McBride et al. 2001; McBride & Horodysky 2004). Etymology. The specific epithet honors David G. Smith, of the Smithsonian Institution, for his thoroughness in examining leptocephali of Elops to reveal that two morphs were present. We recommend the vernacular name Malacho, which is already used for Elops in several countries bordering the Caribbean basin. : Published as part of Mcbride, Richard S., Rocha, Claudia R., Ruiz-Carus, Ramon & Bowen, Brian W., 2010, A new species of ladyfish, of the genus Elops (Elopiformes: Elopidae), from the western Atlantic Ocean, pp. 29-41 in Zootaxa 2346 on pages 31-38, DOI: 10.5281/zenodo.193392 : {"references": ["Linnaeus, C. (1766) Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I, [Regnum animale]. [Pars I]. Holmiae: Impensis Direct. Laurentii Salvii. Available from http: // gallica. bnf. fr / ark: / 12148 / bpt 6 k 99004 c. r = Systema + naturae. langEN (accessed 30 April 2009)", "Regan, C. T. (1909) A revision of the fishes of the genus Elops. Annals and Magazine of Natural History Series 8 3, 37 - 40.", "Hildebrand, S. F. (1943) Notes on the affinity, anatomy, and development of Elops saurus Linnaeus. Journal of the Washington Academy of Sciences, 33, 90 - 94.", "Bertin, L. (1944) La distribution mesogeenne des Elops. Compte Rendu Sommaire des Seances. Societe de Biogeographie, Paris, 21, 17 - 23.", "Fowler, H. W. (1931) Fishes obtained by the Barber Asphalt Company in Trinidad and Venezuela in 1930. Proceedings of the Academy of Natural Sciences of Philadelphia, 83, 391 - 410.", "Gehringer, J. W. (1959) Early development and metamorphosis of the ten-pounder Elops saurus Linnaeus. Fishery Bulletin, U. S., 59, 618 - 647.", "Whitehead, P. J. P. (1962) The species of Elops (Pisces: Elopidae). Annals and Magazine of Natural History Series 13, 5, 321 - 329.", "Hildebrand, S. F. (1963) Family Elopidae. Memoir Sears Foundation for Marine Research Number I. Fishes of the Western North Atlantic. Part Three. Sears Foundation for Marine Research, Yale Univ., New Haven, pp. 111 - 131.", "Eldred, B. & Lyons, W. G. (1966) Larval ladyfish, Elops saurus Linnaeus 1766, (Elopidae) in Florida and adjacent waters. Florida Department of Natural Resources, Marine Research Laboratory, Leaflet Series, IV, Part 1, No. 2, unpaginated.", "Carles, C. A. (1967) Datos sobre la biologia del banano Elops saurus Linnaeus (Teleostomi: Elopidae). Instituto Nacional De La Pesca Cuba, Contribucion No. 27, 1 - 53.", "Miller, G. L. & Jorgenson, S. C. (1973) Meristic characters of some marine fishes of the Western Atlantic Ocean. Fishery Bulletin, U. S., 71, 301 - 312.", "Santos-Martinez, A. & Arboleda, S. (1993) Aspectos biologicos y ecologicos del macabi Elops saurus Linnaeus (Pisces: Elopidae) en la Cienaga Grande de Santa Marta y costa adyacente, Caribe Colombiano. Anales del Instituto de Investigaciones Marinas de Punta de Betin, 22, 77 - 96.", "Smith, D. G. (1989) Order Elopiformes; Families Elopidae, Megalopidae, and Albulidae: Leptocephali. Memoir Sears Foundation for Marine Research. Number I. Fishes of the Western North Atlantic. Part Nine. Volume Two. Sears Foundation for Marine Research, Yale Univ., New Haven, pp. 961 - 972.", "Smith-Vaniz, W. F., Collette, B. B. & Luckhurst, B. E. (1999) Fishes of Bermuda: History, Zoogeography, Annotated checklist, and Identification Keys. American Society of Ichthyologists and Herpetologists Special Publication No. 4. American Society of Ichthyologists and Herpetologists, 424 pp.", "Obermiller, L. E. & Pfeiler, E. (2003) Phylogenetic relationships of elopomorph fishes inferred from mitochondrial ribosomal DNA sequences. Molecular Phylogenetics and Evolution 26, 202 - 214.", "McBride, R. S. & Horodysky, A. Z. (2004) Mechanisms maintaining sympatric distributions of two ladyfish (Elopidae: Elops) morphs in the Gulf of Mexico and western North Atlantic Ocean. Limnology and Oceanography, 49, 1173 - 1181.", "Rocha, L. A., Craig, M. T. & Bowen, B. W. (2007) Phylogeography and the conservation of coral reef fishes. Coral Reefs, 26, 501 - 512.", "Campton, D. E., Bass, A. L., Chapman, F. A. & Bowen, B. W. (2000) Genetic distinction of pallid, shovelnose, and Alabama sturgeon: emerging species and the US endangered species act. Conservation Genetics, 1, 17 - 32.", "Bowen, B. W., Muss, A., Rocha, L. A. & Grant, W. S. (2006) Shallow mtDNA coalescence in Atlantic pygmy angelfishes (genus Centropyge) indicates a recent invasion from the Indian Ocean. Journal of Heredity, 97, 1 - 12.", "Alvarado Bremer, J. R., Vinas, J., Mejuto, J., Ely, B. & Pla, C. (2005) Comparative phylogeography of bluefin tuna and swordfish: the combined effects of vicariance, secondary contact, introgression, and population expansion on the regional phylogenies of two highly migratory pelagic fishes. Molecular Phylogenetics and Evolution, 36, 169 - 187.", "Linton, E. (1907) Notes on parasites of Bermuda fishes. Proceedings of the United States National Museum, 33, 85 - 126.", "McBride, R. S., MacDonald, T. C., Matheson, R. E., Rydene, D. A. & Hood, P. B. (2001) Nursery habitats for ladyfish, Elops saurus, along salinity gradients in two Florida estuaries. Fishery Bulletin, U. S., 99, 443 - 458."]} |
format |
Text |
author |
Mcbride, Richard S. Rocha, Claudia R. Ruiz-Carus, Ramon Bowen, Brian W. |
author_facet |
Mcbride, Richard S. Rocha, Claudia R. Ruiz-Carus, Ramon Bowen, Brian W. |
author_sort |
Mcbride, Richard S. |
title |
Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species |
title_short |
Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species |
title_full |
Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species |
title_fullStr |
Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species |
title_full_unstemmed |
Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species |
title_sort |
elops smithi mcbride, rocha, ruiz-carus & bowen, 2010, new species |
publisher |
Zenodo |
publishDate |
2010 |
url |
https://dx.doi.org/10.5281/zenodo.5658998 https://zenodo.org/record/5658998 |
long_lat |
ENVELOPE(-60.734,-60.734,-63.816,-63.816) ENVELOPE(-62.183,-62.183,-64.650,-64.650) ENVELOPE(-67.059,-67.059,-67.449,-67.449) ENVELOPE(11.650,11.650,-70.750,-70.750) ENVELOPE(-72.167,-72.167,-75.088,-75.088) ENVELOPE(-60.800,-60.800,-62.450,-62.450) |
geographic |
Pacific Indian Alabama Trinidad Martínez Rendu Langen Matheson Alvarado |
geographic_facet |
Pacific Indian Alabama Trinidad Martínez Rendu Langen Matheson Alvarado |
genre |
North Atlantic |
genre_facet |
North Atlantic |
op_relation |
http://publication.plazi.org/id/2376E46A7076CC27F37AF01FFFA0FFB0 http://table.plazi.org/id/03997D8C7075CC24F3EDF2DBFD18FC2C http://zoobank.org/65B72EBA-3A1D-48B0-A03D-B50690751AAF https://zenodo.org/communities/biosyslit https://dx.doi.org/10.5281/zenodo.193392 http://publication.plazi.org/id/2376E46A7076CC27F37AF01FFFA0FFB0 https://dx.doi.org/10.5281/zenodo.193393 https://dx.doi.org/10.5281/zenodo.193394 https://dx.doi.org/10.5281/zenodo.193395 http://table.plazi.org/id/03997D8C7075CC24F3EDF2DBFD18FC2C http://zoobank.org/65B72EBA-3A1D-48B0-A03D-B50690751AAF https://dx.doi.org/10.5281/zenodo.5658997 https://zenodo.org/communities/biosyslit |
op_rights |
Open Access info:eu-repo/semantics/openAccess |
op_doi |
https://doi.org/10.5281/zenodo.5658998 https://doi.org/10.5281/zenodo.193392 https://doi.org/10.5281/zenodo.193393 https://doi.org/10.5281/zenodo.193394 https://doi.org/10.5281/zenodo.193395 https://doi.org/10.5281/zenodo.5658997 |
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ftdatacite:10.5281/zenodo.5658998 2023-05-15T17:37:21+02:00 Elops smithi Mcbride, Rocha, Ruiz-Carus & Bowen, 2010, new species Mcbride, Richard S. Rocha, Claudia R. Ruiz-Carus, Ramon Bowen, Brian W. 2010 https://dx.doi.org/10.5281/zenodo.5658998 https://zenodo.org/record/5658998 unknown Zenodo http://publication.plazi.org/id/2376E46A7076CC27F37AF01FFFA0FFB0 http://table.plazi.org/id/03997D8C7075CC24F3EDF2DBFD18FC2C http://zoobank.org/65B72EBA-3A1D-48B0-A03D-B50690751AAF https://zenodo.org/communities/biosyslit https://dx.doi.org/10.5281/zenodo.193392 http://publication.plazi.org/id/2376E46A7076CC27F37AF01FFFA0FFB0 https://dx.doi.org/10.5281/zenodo.193393 https://dx.doi.org/10.5281/zenodo.193394 https://dx.doi.org/10.5281/zenodo.193395 http://table.plazi.org/id/03997D8C7075CC24F3EDF2DBFD18FC2C http://zoobank.org/65B72EBA-3A1D-48B0-A03D-B50690751AAF https://dx.doi.org/10.5281/zenodo.5658997 https://zenodo.org/communities/biosyslit Open Access info:eu-repo/semantics/openAccess Biodiversity Taxonomy Animalia Chordata Actinopterygii Elopiformes Elopidae Elops Elops smithi Taxonomic treatment article-journal Text ScholarlyArticle 2010 ftdatacite https://doi.org/10.5281/zenodo.5658998 https://doi.org/10.5281/zenodo.193392 https://doi.org/10.5281/zenodo.193393 https://doi.org/10.5281/zenodo.193394 https://doi.org/10.5281/zenodo.193395 https://doi.org/10.5281/zenodo.5658997 2022-02-08T13:14:21Z Elops smithi , new species Figure 1; Table 1 Elops saurus non Linnaeus 1766: Regan, 1909 (in part), Hildebrand, 1943 (in part); Bertin, 1944 (in part); Fowler, 1931; Gehringer, 1959 (in part); Whitehead, 1962 (in part); Hildebrand, 1963 (in part); Eldred and Lyons, 1966 (in part); Carles, 1967; Miller and Jorgenson, 1973 (in part), Santos-Martίnez and Arboleda (1993). These studies examined what we recognize here as E. smithi , either in whole or in part, based on their reports of meristic values, sample locality, or both. Elops sp.: Smith, 1989; Smith-Vaniz et al. , 1999; Obermiller and Pfeiler, 2003 Holotype. UF 45683, 303 mm SL, marine waters of Guyana, by trawl, 16 July 1967. Paratypes. UF 45682, marine waters of Trinidad, 13 December 1967; GCRL 11950, 4, Commewijne River, Suriname, 14 October 1973; GCRL 12733, Gatun Locks, Canal Zone, Panama, 4 March 1974; UF 11269, 2, Tortuguero Lagoon, Costa Rica, August 1963. Other museum material examined. Elops saurus : FSBC 0 0 258, Florida, Pinellas County, 13 December 1957; FSBC 10270, Florida, Pinellas County, 15 December 1977; FSBC 12589, 3, Florida, Hillsborough County, 3 June 1983; GCRL 0 345, Louisiana, 8 September 1959; GCRL 1938, Mississippi, 8 August 1966; UF 47036, Honduras, 26 April 1967; UF 105715, 2, Florida, Volusia County, 17 November 1972. Diagnosis. Elops smithi is distinguished from E. saurus in the number of vertebrae (73–80, usually 75–78 versus 79–87, usually 81–85, respectively). According to McBride and Horodysky (2004), vertebrae counts in the overlap range (79–80) occurred in only 94 of 3,255 (2.9 %) specimens examined from the coasts of the Americas, the Bahamas, and the Caribbean islands. As reported by Whitehead (1962) counts of gill rakers and total vertebrae can be used to separate all species of Elops . Western Atlantic Elops , now recognized as E . smithi and E . saurus , have lower gill raker counts (10–15 on the lower part of the first arch) than E . affinis (16–20) and E . lacerta (17–19). Elops smithi and E . saurus have higher vertebrae counts (> 72; see above for ranges) than E . senegalensis (67), E . machnata (63–64), and E . hawaiensis (68–70). Description. Body elongate (head length 25–29 % of SL) and slender (width 7.5–9.4 % of SL). Mouth large (maxilla 56–60 % of head length) and nearly terminal. Caudal fin deeply forked, with lobes equal. Principal dorsal-fin rays 19–20 (24–27 total); anal rays 12–13 (16–19 total); pectoral rays 17–18; pelvic rays 13–16; branchiostegal rays 30–34; gill rakers on lower arch 13–15 (total 21–23 excluding rudiments); lateralline scales (102–118, but may be higher if specimen is found north of the Caribbean Sea [see below]); and 73– 80 vertebrae (usually 75–78). Data for above description are from Table 1, Figure 2, and McBride and Horodysky (2004). Meristic characters continued. The larvae are of leptocephalus form, and the total myomere number of the leptocephalus equals that of total vertebrae (McBride & Horodysky 2004). Predorsal (61–66) and preanal (68–72) myomeres are also reliable characters for identifying premetamorphic leptocephali (Smith 1989). Others examining Elops from the Caribbean Sea have noted minor variations in these meristic characters (Carles 1967; Santos-Martίnez and Arboleda 1993), indicating differences in counting methods or geographic variation. Coloration. Living adults bright silver, particularly on sides; may be bluish-gray on back with yellowish hue on fins. Not as silvery in preservative. Comparisons. We found no character other than counts of vertebrae that separates adult E . smithi from E . saurus (Table 1). Although lateral-line scale counts appeared to be a diagnostic character, the scales are formed late in larval development so this character is indicative of latitude where larval transformation occurs instead of where spawning occurred. To demonstrate this, it can be shown that lateral-line scale counts are distinct among E. smith and E. saurus that had not been dispersed outside their typical range (Table 1, Fig. 2 A), but the lateral-line scale counts are not distinct among a test collection from the southern Indian River Lagoon, Florida, which included E. smithi that had presumably been dispersed from their spawning grounds (Fig. 2 B). This disconnect can be explained because vertebral number is set during embryogenesis but scales are not developed until about 50 mm in the late metamorphic period (Gehringer 1959). Thus, lateral-line scale counts will be a misleading diagnostic character when measured from specimens collected within areas of sympatry. The leptocephalus larva, common to this genus, is associated with long-distance dispersal (McBride & Horodysky 2004), so scale counts may be problematic as a taxonomic character in other species of Elops as well. In addition, the scales of these species are small and easily displaced, further confounding their use as a taxonomic character. Mitochondrial DNA sequence data provide an independent character for recognizing two species of Elops in the western North Atlantic. We observed 14 haplotypes in two primary lineages corresponding to E. saurus and E. smithi (Table 2). These sequences have been deposited in GenBank under accession numbers GQ 183881 – GQ 183882 ( E. saurus , haplotypes A, B) and GQ 183883 – GQ 183894 ( E. smithi , haplotypes C – N). The genetic difference ( d ) between the E. saurus haplotypes and the E. smithi haplotypes ranged from 0.023 to 0.029 (Fig. 3). Obermiller and Pfeiler (2003) reported a similar level of divergence between what we recognized as E . smithi and E . saurus ( d = 0.021 with 12 S and 16 S rRNA mtDNA sequences). In addition, Obermiller and Pfeiler (2003) observed a similar level of divergence between E . saurus and E . hawaiiensis ( d = 0.024), two recognized species that occupy different ocean basins. TABLE 2. Data associated with fish used in the genetic analysis. Collection date and locale are listed, along with standard length (SL), and total number of vertebrae (Vert.). Fish are sorted as vertebrae morph (high vs. low-count) and haplotype. *Mismatches between phenotype and genotype are indicated with an asterisk. Locality codes are: IR = Indian River Lagoon (northern or southern regions of the lagoon), southeast Florida, CK = Cedar Key, west coast Florida, and FW = Fort Walton, panhandle Florida. continued next page Although the mtDNA data presented here and data presented previously by Obermiller and Pfeiler (2003) indicate two evolutionary lineages, the mtDNA character was not absolutely diagnostic. In seven of 56 specimens (12.5 %), there was a mismatch between classification based on genetics and that on morphology (Table 2). Five of these individuals had morphology similar to E . smithi but haplotypes in the E . saurus lineage, and two had the reverse. These mismatches may indicate ecophenotype plasticity within species, hybridization, or retention of ancestral polymorphisms. All three phenomena have been documented in fishes (see Rocha et al. 2007). The sympatric sturgeons Scaphirhynchus albus and S. platorynchus share mtDNA haplotypes because of their recent speciation and hybridization (Campton et al. 2000). The marine angelfishes Centropyge argi and C. aurantonotus are sister species that share haplotypes despite diagnostic differences in coloration (Bowen et al. 2006). And the Atlantic bluefin tuna ( Thunnus thynnus ) has haplotypes derived from both Pacific bluefin ( Thunnus orientalis ) and albacore ( Thunnus alalunga Alvarado Bremer et al. 2005). Surveys of multiple nuclear loci have resolved these phenomena in other species and could profitably be applied to Elops . Nonetheless, given these genetic results, it is unlikely that we are observing an intraspecific, or population-level, genetic phenomenon, so we reject the hypothesis that E . smithi and E . saurus are ecophenotypes. Distribution. Elops smithi occurs along the northern coast of South America, in the Caribbean Sea, and throughout the Bahamas; it also occurs sympatrically with E. saurus in the Gulf of Mexico and along the eastern seaboard of North America (Smith 1989; see McBride & Horodysky [2004] for distribution maps of larvae, juveniles and adults). In addition, there are two records of Elops from Bermuda (Linton 1907) although no resident population has been found there (Smith-Vaniz et al. 1999). Only one specimen is available, a 181 mm SL fish (BAMZ 1990 -083-037) with 73 vertebrae; this apparently represents a waif from the population inhabiting the Caribbean (Smith-Vaniz et al. 1999). Elops smithi is found in a wide range of salinities. Mature adults and early-life-history stages are found in offshore, marine habitats, where spawning presumably occurs (Gehringer 1959; Santos-Martínez & Arboleda 1993; McBride & Horodysky 2004). Transforming larvae and subadults are found throughout estuaries, as far up as the oligohaline zone, as well as in hypersaline lagoons (Carles 1967; McBride et al. 2001; McBride & Horodysky 2004). Etymology. The specific epithet honors David G. Smith, of the Smithsonian Institution, for his thoroughness in examining leptocephali of Elops to reveal that two morphs were present. We recommend the vernacular name Malacho, which is already used for Elops in several countries bordering the Caribbean basin. : Published as part of Mcbride, Richard S., Rocha, Claudia R., Ruiz-Carus, Ramon & Bowen, Brian W., 2010, A new species of ladyfish, of the genus Elops (Elopiformes: Elopidae), from the western Atlantic Ocean, pp. 29-41 in Zootaxa 2346 on pages 31-38, DOI: 10.5281/zenodo.193392 : {"references": ["Linnaeus, C. (1766) Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I, [Regnum animale]. [Pars I]. Holmiae: Impensis Direct. Laurentii Salvii. Available from http: // gallica. bnf. fr / ark: / 12148 / bpt 6 k 99004 c. r = Systema + naturae. langEN (accessed 30 April 2009)", "Regan, C. T. (1909) A revision of the fishes of the genus Elops. Annals and Magazine of Natural History Series 8 3, 37 - 40.", "Hildebrand, S. F. (1943) Notes on the affinity, anatomy, and development of Elops saurus Linnaeus. Journal of the Washington Academy of Sciences, 33, 90 - 94.", "Bertin, L. (1944) La distribution mesogeenne des Elops. Compte Rendu Sommaire des Seances. Societe de Biogeographie, Paris, 21, 17 - 23.", "Fowler, H. W. (1931) Fishes obtained by the Barber Asphalt Company in Trinidad and Venezuela in 1930. Proceedings of the Academy of Natural Sciences of Philadelphia, 83, 391 - 410.", "Gehringer, J. W. (1959) Early development and metamorphosis of the ten-pounder Elops saurus Linnaeus. Fishery Bulletin, U. S., 59, 618 - 647.", "Whitehead, P. J. P. (1962) The species of Elops (Pisces: Elopidae). Annals and Magazine of Natural History Series 13, 5, 321 - 329.", "Hildebrand, S. F. (1963) Family Elopidae. Memoir Sears Foundation for Marine Research Number I. Fishes of the Western North Atlantic. Part Three. Sears Foundation for Marine Research, Yale Univ., New Haven, pp. 111 - 131.", "Eldred, B. & Lyons, W. G. (1966) Larval ladyfish, Elops saurus Linnaeus 1766, (Elopidae) in Florida and adjacent waters. Florida Department of Natural Resources, Marine Research Laboratory, Leaflet Series, IV, Part 1, No. 2, unpaginated.", "Carles, C. A. (1967) Datos sobre la biologia del banano Elops saurus Linnaeus (Teleostomi: Elopidae). Instituto Nacional De La Pesca Cuba, Contribucion No. 27, 1 - 53.", "Miller, G. L. & Jorgenson, S. C. (1973) Meristic characters of some marine fishes of the Western Atlantic Ocean. Fishery Bulletin, U. S., 71, 301 - 312.", "Santos-Martinez, A. & Arboleda, S. (1993) Aspectos biologicos y ecologicos del macabi Elops saurus Linnaeus (Pisces: Elopidae) en la Cienaga Grande de Santa Marta y costa adyacente, Caribe Colombiano. Anales del Instituto de Investigaciones Marinas de Punta de Betin, 22, 77 - 96.", "Smith, D. G. (1989) Order Elopiformes; Families Elopidae, Megalopidae, and Albulidae: Leptocephali. Memoir Sears Foundation for Marine Research. Number I. 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Coral Reefs, 26, 501 - 512.", "Campton, D. E., Bass, A. L., Chapman, F. A. & Bowen, B. W. (2000) Genetic distinction of pallid, shovelnose, and Alabama sturgeon: emerging species and the US endangered species act. Conservation Genetics, 1, 17 - 32.", "Bowen, B. W., Muss, A., Rocha, L. A. & Grant, W. S. (2006) Shallow mtDNA coalescence in Atlantic pygmy angelfishes (genus Centropyge) indicates a recent invasion from the Indian Ocean. Journal of Heredity, 97, 1 - 12.", "Alvarado Bremer, J. R., Vinas, J., Mejuto, J., Ely, B. & Pla, C. (2005) Comparative phylogeography of bluefin tuna and swordfish: the combined effects of vicariance, secondary contact, introgression, and population expansion on the regional phylogenies of two highly migratory pelagic fishes. Molecular Phylogenetics and Evolution, 36, 169 - 187.", "Linton, E. (1907) Notes on parasites of Bermuda fishes. Proceedings of the United States National Museum, 33, 85 - 126.", "McBride, R. S., MacDonald, T. C., Matheson, R. E., Rydene, D. A. & Hood, P. B. (2001) Nursery habitats for ladyfish, Elops saurus, along salinity gradients in two Florida estuaries. Fishery Bulletin, U. S., 99, 443 - 458."]} Text North Atlantic DataCite Metadata Store (German National Library of Science and Technology) Pacific Indian Alabama Trinidad ENVELOPE(-60.734,-60.734,-63.816,-63.816) Martínez ENVELOPE(-62.183,-62.183,-64.650,-64.650) Rendu ENVELOPE(-67.059,-67.059,-67.449,-67.449) Langen ENVELOPE(11.650,11.650,-70.750,-70.750) Matheson ENVELOPE(-72.167,-72.167,-75.088,-75.088) Alvarado ENVELOPE(-60.800,-60.800,-62.450,-62.450) |