Natural history, life history, and diet of Priapella chamulae Schartl, Meyer & Wilde 2006 (Teleostei: Poeciliidae).
Life-history evolution has been an integral part of evolutionary research over the past few decades, and livebearing fishes (Poeciliidae) have proven to be excellent models for studying life history adaptations (e.g., Reznick & Miles 1989; Magurran 2005). Originally, the more than 200 species and 22-29 genera of poeciliids were endemic to the Americas, but due to human introductions they are now found worldwide (Lucinda 2003). Within the Poeciliidae, at least three characters evolved to give rise to the present diversity within the family: (1) internal fertilization using a transformed anal fin in males, the gonopodium, for sperm transfer, (2) livebearing, and (3) different degrees of maternal provisioning for the developing young (Constantz 1989; Reznick & Miles 1989). With the sole exception of Tomeurus gracilis Eigenmann, which is characterized by oviparous egg retention, internal fertilization and viviparity are found in all species of poeciliids (Rosen 1964). Furthermore, some poeciliids are able to accommodate several clutches simultaneously, so-called superfetation (e.g., Turner 1937; Thibault & Schulz 1978; Reznick & Miles 1989).
Priapella chamulae Schartl, Meyer & Wilde (2006), is a medium-sized livebearing fish inhabiting the waters of the Rio Grijalva basin in Tabasco, Mexico (Schartl et al. 2006). The genus Priapella comprises at least six species (e.g., Miller 2005; Schartl et al. 2006; Meyer et al. 2011) and is considered the least derived (i.e., most basal) group within the tribe Gambusiini (Hrbek et al. 2007). The other genera in this tribe are Scolichthys, Carlhubbsia, Xiphophorus, Heterandria, Belonesox, Heterophallus, and Gambusia (Miller 2005; Hrbek et al. 2007). The natural history of the members of the genus Priapella and several other genera in this tribe remains largely unknown (see Miller 2005; Schartl et al. 2006; Meyer et al. 2011; Riesch et al. 2011a). However, to fully understand the evolution of reproductive strategies in livebearing fishes (e.g., Reznick & Miles 1989; Pires et al. 2011), it is of utmost importance to also collect data on smaller and lesser-known clades.
We report on basic natural history of P. chamulae as observed over the last five years while conducting fieldwork in Tabasco, southern Mexico. We also report on life history and diet data derived from specimens collected in January 2010. Furthermore, we describe the fish species communities in the lotic environments they inhabit.
MATERIAL AND METHODS
Study population and sampling procedure: We conducted life-history dissections on a total of 55 P. chamulae (6 males and 49 females). All fish were collected in January 2010 in the Arroyo Tres (17[degrees]29'1.24"N, 92[degrees]46'34.57"W; Fig. 1), a small creek and tributary to the Rio Oxolotan (part of the Rio Grijalva drainage) near the village of Tapijulapa in Tabasco (Fig. 1). Collections were made using seine nets, and fish were field-preserved in 10% formaldehyde.
Life-history analysis: Following the protocol of Reznick & Endler (1982), all preserved fish were weighed and measured for standard length. Males were classified as mature based on the morphology of their modified anal fin (i.e. gonopodium; Fig. 2C). The anal fin in poeciliids undergoes a complex metamorphosis as fish attain maturity, and the endpoint of this metamorphosis provides a reliable index of sexual maturity, allowing us to determine the state of complete maturation based on external cues alone (e.g. Constantz 1989; Greven 2011; Langerhans 2011). We therefore consulted the illustration of the fully developed gonopodium of P. chamulae presented by Schartl et al. (2006). Unfortunately, almost all males that we collected turned out to be sexually immature (5 out of 6), and so their data had to be discarded for most life history analyses. However, male poeciliids are characterized by determinate growth and therefore almost completely cease growth after reaching sexual maturity (Snelson 1989). Since all immature males were within days of reaching sexual maturity (i.e., only the terminal structures of the gonopodium were not yet fully developed; Turner 1941) we did use their standard length (SL) data for statistical comparisons with females, and included them in our gut length analysis (see below).
The reproductive tissue (i.e., testes for males and ovaries for females) and, if present, all developing offspring were removed. Offspring were counted and their stage of development determined (Haynes 1995; Reznick 1981). Somatic tissues, reproductive tissues, and embryos were then dried for 10 days at 40 [degrees]C and weighed again. To assess male, female, and embryo condition, somatic tissues and embryos were rinsed six times for at least six hours in petroleum ether to extract soluble non-structural fats (Heulett et al. 1995; Riesch et al. 2010a, b, 2011b) and were then dried again and reweighed.
We thus measured standard length [mm], dry mass [mg], lean mass [mg] (i.e., weight after fat extraction), and fat content [%] for males and females, gonadosomatic index [GSI, %] for males only, and fecundity [number of developing embryo], reproductive allocation [RA, %], embryo dry mass [mg], offspring lean weight [mg], and embryo fat content [%] for females only. GSI is calculated as testis dry mass [g] divided by the sum of testis dry mass [mg] and somatic dry mass [mg]. RA, on the other hand, was calculated as the total dry mass of all developing embryos [mg] divided by the sum of the total dry mass of all developing embryos [mg] and somatic dry mass [mg].
Finally, we calculated the matrotrophy index [MI] as a measure to indirectly evaluate post-fertilization maternal provisioning (Marsh-Matthews 2011). The MI equals the estimated dry mass of the embryo at birth divided by the estimated dry mass of the oocyte at fertilization and is derived from a linear regression of log-transformed embryo dry mass against stage of development (Marsh-Matthews 2011). Thus, if the eggs were fully provisioned by yolk prior to fertilization (lecithotrophy), we would expect the embryos to lose 30-40% of their dry mass during development (MI [less than or equal to]0.75; Marsh-Matthews 2011; Pires et al. 2011). On the other hand, in the case of continuous maternal provisioning even after fertilization (matrotrophy), one would expect the embryos to lose less mass (MI between 0.75 and 1.00) or even to gain mass during development (MI [greater than or equal to]1.00; Marsh-Matthews 2011; Pires et al. 2011).
Gut content analysis: We inferred the diet of P. chamulae by dissecting the guts of all preserved fish and identifying the contents. We identified gut contents to Order in most cases. If this was not possible, we identified items to the lowest possible taxonomic level. We counted the number of gut contents within each diet category - except for woody plant material - and calculated the percentage of guts containing each diet category, and the proportion of each diet category relative to the total diet, and in total for all individuals.
Additionally, before dissecting out gut contents we measured gut length [mm] with digital calipers. We used these gut length measures to calculate relative gut length (gut length/standard length) and tested for sexual dimorphism in relative gut length with a Mann-Whitney U-test.
General natural history: Over the last five years and while sampling other poeciliid fishes, we found P. chamulae at a variety of habitats in Tabasco, ranging from small creeks [Arroyo Tres, Arroyo Bonita (17[degrees]25'37.42"N, 92[degrees]45'6.98"W), Arroyo Cristal (17 [degrees] 27'2.13" N, 92 [degrees] 45'49.40" W), and Arroyo Tacubaya (17 [degrees] 27'12.78 " N, 92 [degrees] 47'4.16" W)] to large rivers [Rio Amat a n (17 [degrees] 27'33.26" N, 92 [degrees] 46'42.53" W)] all near the village of Tapijulapa (Fig. 1). Surprisingly, we have so far never caught P. chamulae in the Rio Oxolotan, but this is probably an artifact of our sampling efforts, as all other positive locations suggest that P. chamulae also inhabits that river (Fig. 1). Teleost species communities at these habitats are quite complex (Tobler et al . 2006; Riesch et al . 2009) and at Arroyo Tres P. chamulae share the habitat with Poecilia mexicana Steindachner, Xiphophorus hellerii Heckel, Heterophallus milleri Radda, Heterandria bimaculata Heckel (all Poeciliidae), Astyanax aeneus G u nther (Characidae), Thorichthys helleri Steindachner, and Vieja bifasciata Steindachner (both Cichlidae) (see also Tobler et al . 2006). In some of the other habitats, species communities are even more complex (e. g., Riesch et al . 2011a). More generally, P. chamulae appears to prefer the slightly faster flowing parts (e. g., riffles) of these habitats, as we rarely catch significant numbers in the stagnant pools that are usually dominated by P. mexicana and A. aeneus.
Life-history analysis: General life history data are compiled in Table I. Priapella chamulae at Arroyo Tres was characterized by sexual size dimorphism, with males being smaller than females (female SL = 30.30[+ or -]4.21 mm; male SL = 26.02[+ or -]2.93 mm; t-test: [t.sub.38] = 2.379, P = 0.022; Fig. 2A). The tertiary (adult) sex ratio was female-biased and approximately 1:8.2 (males: females; Table I). The majority of dissected females (69.3%) were reproductively active, but only one out of the six collected males was sexually mature (16.7%). Embryo weight decreased with developmental stage ([R .sup.2] = 0.292, P > 0.001) in a fashion corresponding to a predomi-nantly lecithotrophic provisioning strategy (MI = 0.71; Fig. 2B, Fig. 3). We did not find any evidence for superfetation in P. chamulae, as all developing embryos of the same clutch were always of approximately the same developmental stage.
Table I. Raw values for male and mean[+ or -]SD of female lif history traits for reproductively active Prlapella chamulae caught in Arroyo Tres (Tabasco, Mexico) in January 2010. Values in parentheses provide minimum-maximum. GSI: gonadosomatic index; RA: reproductive allocation; MI: matrotrophy index. males females Sample size (a) 1/6 34/49 SL [mm] 28.4 30.30[+ or -]4.20 (24-40) Somatic dry mass [mg] 138 162.12[+ or -]76.76 (72-386) Fat content [%] 1.45 5.64[+ or -]3.75 (0-14) Fecundity - 6.38[+ or -]3.75 (2-16) Estimated embryo dry mass at - 2.31 birth (b) [mg] Embryo fat content [%] - 16.92[+ or -]3.91 (3-23) GSI [%] 1.27 - RA [%] - 10.31[+ or -]3.42 (4-23) MI - 0.71 (a.) the numerator corresponds to reproductively active males and females & the denominator equals the total number of collected and dissected males and females (b.) estimated dry mass at birth is calculated using the slope and intercept from the regression between log-transformed embryonic dry mass and stage of development.
Gut content analysis: Only one individual had an empty gut (except for some incidental woody plant material). Priapella chamulae at Arroyo Tres are almost exclusively carnivorous (Table II); on average, individual P. chamulae had 4.6[+ or -]2.5 (mean[+ or -]SD, range: 0-10) diet items in their guts, and the vast majority of their diet was made up by terrestrial arthropods (~98 %), with ants being the single most common identifiable diet item (Table II). Males and females did not differ in their relative gut length (females: median = 21.08%, IQR = 9.22%; males: median = 23.75%, IQR = 11.55%; Mann-Whitney U-test: U = 166.00, P = 0.545).
Table II. Diet of Prlapella chamulae as inferred by gut-content analysis. Diet Number of Individuals Total categories diet with diet item diet items [%]* [%] Arachnida 4 7 2 Blattaria 1 1 > 1 Chironomidae larvae 5 7 2 Coleoptera adults 14 18 6 larvae 7 10 3 Diptera adults 27 21 11 Gastropoda 1 1 > 1 Hemiptera 1 1 > 1 Hymenoptera adult ants 59 54 25 adult 12 16 5 wasps Lepidoptera larvae 2 3 > 1 Oligochaeta 1 1 > 1 Orthoptera 6 10 1 Unidentified insects adults 88 65 37 larvae 6 10 3 Plant material seeds 2 3 > 1 rootlets -- 18 -- * percentages may not sum to 100 due to rounding
Our observations confirm previous accounts that described P. chamulae to prefer the medium to fast flowing parts of small creeks (Miller 2005; Schartl et al. 2006). Like many other life history traits, off-spring size and fecundity are usually related to female body size (Reznick & Miles 1989). It is therefore slightly surprising that this medium-sized poeciliid produces only relatively few, average-sized off-spring, which translates into low values for RA. For example, similar sized Poecilia mexicana from comparable creeks around Tapijulapa produce two to three times more offspring, which are also larger (Riesch et al. 2010b). However, RA-values of P. chamulae are surprisingly similar to those of P. mexicana (given the pronounced differences in fecundity and offspring size), while more closely related poeciliids like H. milleri or Gambusia sexradiata Hubbs (that are also considerably smaller in body size) from nearby habitats invest almost twice as much per clutch (i.e., RA around 20 %; Riesch et al. 2010a, 2011a). Nonetheless, several life history traits of P. chamulae are similar to those of other members of the tribe Gambusiini (e.g., no superfetation and lecithotrophy; but see Pires et al. 2011 for citations on rare occurrences of superfetation in Gambusiini). Likewise, offspring fat content matches that found in other Gambusiini from the same drainage (i.e., G. sexradiata and G. eurystoma Miller, Riesch et al. 2010a; H. milleri, Riesch et al. 2011a).
Furthermore, the sexual size dimorphism we report on here is typical for most poeciliids (Pires et al. 2011). Most natural populations of poeciliids are characterized by a female-skewed sex ratio (Snelson 1989; Magurran 2005) and P. chamulae from Arroyo Tres were no exception. Since secondary sex ratios (i.e., sex ratio at birth) are typically 1:1 in poeciliids, higher male mortality is usually thought to be the reason for a female-biased sex ratio at maturity (Snelson 1989).
Our results clearly demonstrate that P. chamulae at Arroyo Tres are carnivorous. While there is at least one other purely carnivorous species in the tribe Gambusiini (i.e., Belonesox belizanus Kner; Miller 2005), the diet of P. chamulae more closely resembles that described for Heterandria bimaculata, Gambusia affinis (Baird & Girard), G. holbrooki Girard, G. sexradiata, and other Gambusia spp. that are known to prey heavily on insects and other invertebrates (Miller 2005; Trujillo-Jimenez & Beto 2007). Other close relatives, swordtails and platyfish of the genus Xiphophorus, however, are known to be mostly omnivorous with an emphasis on herbivory (e.g., Maddern et al. 2011). In agreement with this apparent carnivorous dietary specialization, P. chamulae had relatively small gut-to-SL ratios. This clearly sets them apart from other more herbivorous/omnivorous species like Poecilia latipinna (Lesueur) and all-female Poecilia formosa (Girard) that have considerably longer gut-to-SL ratios (Scharnweber et al. 2011a, b). However, based on the predominance of terrestrial arthropods in the diet it is likely that P. chamulae is an opportunistic feeder that, rather than actively hunting for its prey, mainly waits for arthropods to fall or land on the water surface.
This study represents the first diet and life history characterization of a poeciliid fish from the little investigated genus Priapella. While the present study already provides us with relevant insights into their general biology, it is important to keep in mind that the diet data and life history data we report on here were derived from specimens collected from a single point in space and time. Previous studies have clearly shown that diet and life histories vary considerably between habitats and seasons in livebearing fishes (e. g., Reznick & Endler 1982; Meffe & Snelson 1989; Reznick & Miles 1989; Johnson & Bagley 2011; Riesch et al . 2010 a-c, 2011; Scharnweber et al . 2011b). However, water chemistry and the teleost community at Arroyo Tres are representative for a range of similar environments in this part of southern M e xico (Tobler et al . 2006, 2008; Riesch et al . 2009). We are therefore fairly confident that the life history data presented in the current study are largely representative of P. chamulae life-history strategies in the other creek environments inhabited by this species (i .e., Arroyos Bonita, Cristal, and Tacubaya). Nonetheless, P. chamulae from larger rivers, such as the R i os Amatan and Oxolot a n, may differ in life histories (and potentially also diets) from those reported here, and more extensive studies (i .e., comparisons of P. chamulae from different sample sites, or of laboratory-reared specimens with field-caught fish) are clearly warranted to help characterize the full dietary niche width and breadth of life-history strategies exhibited by this species.
We thank two anonymous reviewers for improving a previous version of this manuscript and the Deutsche Forschungsgemeinschaft (DFG) for financial support (PL 470/2-1). This research was conducted under the Mexican authorization from the Municipio de Tacotalpa in Tabasco and SEMARNAT.
Received: 22 October 2011 - Accepted: 05 January 2012
CONSTANTZ, G. D. 1989. Reproductive biology of poeciliid fishes. In: Ecology and Evolution of Livebearing Fishes (Pociliidae) (Eds. G. K. Meffe & F.F. Snelson Jr.): 33-50. Prentice Hall, Englewood Cliffs.
GREVEN, H. 2011. Gonads, genitals, and reproductive biology. In: Ecology and Evolution of Poeciliid Fishes (Eds. J. P. Evans, A. Pilastro & I. Schlupp): 3-17. University of Chicago Press, Chicago.
HAYNES, J. L. 1995. Standardized classification of poeciliid development for life-history studies. Copeia 1995: 147-154.
HEULETT, S. T., WEEKS, S. C. & MEFFE, G. K. 1995. Lipid dynamics and growth relative to resource level in juvenile eastern moquitofish (Gambusia holbrooki: Poeciliidae). Copeia 1995: 97-104.
HRBEK, T., SECKINGER, J. & MEYER, A. 2007. A phylogenetic and biogeographic perspective on the evolution of poeciliid fishes. Molecular Phylogenetics and Evolution 43: 986-998.
JOHNSON, J. B. & BAGLEY J. C. 2011. Ecological drivers of life-history divergence. In: Ecology & Evolution of Poeciliid Fishes (Eds. J. P. Evans, A. Pilastro & I. Schlupp): 38-49. University of Chicago Press, Chicago.
LANGERHANS, R. B. 2011. Genital evolution. In: Ecology & Evolution of Poeciliid Fishes (Eds. J. P. Evans, A. Pilastro & I. Schlupp): 228-240. University of Chicago Press, Chicago.
LUCINDA, P. H. F. 2003. Family Poeciliidae. In: Checklist of the Fresh Water Fishes of South and Central America (Eds. R. E. Reis, S. O. Kullander & C. J. Ferraris): 555-581. EDIPUCRS, Porte Alegro.
MADDERN, M. G., GILL, H. S., & MORGAN, D. L. 2011. Biology and invasive potential of the introduced swordtail Xiphophorus hellerii Heckel (Poeciliidae) in Western Australia. Aquatic Conservation: Marine and Freshwater Ecosystems 21: 282-291.
MAGURRAN, A. E. 2005. Evolutionary Ecology: the Trinidadian Guppy. Oxford University Press, Oxford, 224 pp.
MARSH-MATTHEWS, E. 2011. Matrotrophy. In: Ecology and Evolution of Poeciliid Fishes (Eds. J. P. Evans, A. Pilastro & I. Schlupp): 18-27. University of Chicago Press, Chicago.
MEFFE, G. K. & SNELSON, F. F. JR. 1989. An ecological overview of poeciliid fishes. In: Ecology & Evolution of Live-bearing Fishes (Poeciliidae) (Eds. G. K. Meffe & F. F. SNELSON, Jr.): 13-31. Prentice Hall, Englewood Cliffs.
MEYER, M. K., SCHORIES, S. & SCHARTL, M. 2011. Description of Priapella lacandonae sp. n. - a new poeciliid fish from the rio Tulija basin, Grijalva system, Chiapas, Mexico (Teleostei: Cyprinodontiformes: Poeciliidae). Vertebrate Zoology 61: 91-97.
MILLER, R. R. 2005. Freshwater Fishes of Mexico. University of Chicago Press, Chicago, 419 pp.
PIRES, M. N., BANET, A., POLLUX, B. L. A. & REZNICK, D. N. 2011. Variation and evolution of reproductive strategies in poeciliid fishes. In: Ecology & Evolution of Poeciliid Fishes (Eds. J. P. Evans, A. Pilastro & I. Schlupp): 28-37. University of Chicago Press, Chicago.
REZNICK, D. 1981. "Grandfather effects": The genetics of interpopulation differences in offspring size in the mosquitofish. Evolution 35: 941-953.
REZNICK, D. N. & ENDLER, J. A. 1982. The impact of predation on life history evolution in Trinidadian guppies (Poecilia reticulata). Evolution 36: 160-177.
REZNICK, D. N. & MILES, D. B. 1989. A review of life history patterns in poeciliids fishes. In: Ecology and Evolution of Livebearing Fishes (Poeciliidae) (Eds. G. K. Meffe & F.F. Snelson Jr.): 125-148. Prentice Hall, Englewood Cliffs.
RIESCH, R., COLSTON, T. J., JOACHIM, B. L. & SCHLUPP, I. 2011a. Natural history and life history of the Grijalva Gambusia Heterophallus milleri Radda, 1987 (Teleostei: Poeciliidae). Aqua, International Journal of Ichthyology 17: 95-102.
RIESCH, R., DUWE, V., HERRMANN, N., PADUR, L., RAMM, A., SCHARNWEBER, K., SCHULTE, M., SCHULZ-MIRBACH, T., ZIEGE, M. & PLATH, M. 2009. Variation along the shybold continuum in extremophile fishes (Poecilia mexicana, Poecilia sulphuraria). Behavioral Ecology and Sociobiology 63: 1515-1526.
RIESCH, R., PLATH, M., GARC?A DE LE?N, F. J. & SCHLUPP, I. 2010a. Convergent life-history shifts: toxic environments result in big babies in two clades of poeciliids. Naturwissenschaften 97: 133-141.
RIESCH, R., PLATH, M. & SCHLUPP, I. 2010b. Toxic hydrogen sulfide and dark caves: life-history adaptations in a livebearing fish (Poecilia mexicana, Poeciliidae). Ecology 91: 1494-1505.
RIESCH, R., PLATH, M. & SCHLUPP, I. 2011b. Toxic hydrogen sulphide and dark caves: pronounced male life-history divergence among locally adapted Poecilia mexicana (Poeciliidae). Journal of Evolutionary Biology 24: 596-606.
RIESCH, R., SCHLUPP, I., LANGERHANS, R. B. & PLATH, M. 2011c. Shared and unique patterns of embryo development in extremophile Poecilia. PLoS ONE 6: e27377.
ROSEN, D. E. 1964. The relationships and taxonomic position of the halfbeaks, killifishes, silversides, and their relatives. Bulletin of the American Museum of Natural History 127: 217-268.
SCHARNWEBER, K., PLATH, M. & TOBLER, M. 2011a. Trophic niche segregation between the sexes in two species of livebearing fishes (Poeciliidae). Bulletin of Fish Biology, in press.
SCHARNWEBER, K., PLATH, M., WINEMILLER, K. O. & TOBLER, M. 2011b. Dietary niche overlap in sympatric asexual and sexual livebearing fishes Poecilia spp. Journal of Fish Biology 79: 1760-1773.
SCHARTL, M., MEYER, M. K. & WILDE, B. 2006. Description of Priapella chamulae sp. n. - a new poeciliid fish from the upper rio Grijalva system, Tabasco, Mexico (Teleostei: Cyprinodontiformes: Poeciliidae). Zoologische Abhandlungen (Dresden) 55: 59-67.
SNELSON, JR., F. F. 1989. Social and environmental control of life history traits in poeciliid fishes. In: Ecology and Evolution of Livebearing Fishes (Poeciliidae) (Eds. G. K. Meffe & F. F. Snelson Jr.): 149-161. Prentice Hall, Englewood Cliffs.
THIBAULT, R. E. & SCHULTZ R. J. 1978. Reproductive adaptations among viviparous fishes (Cyprinodontiformes: Poeciliidae). Evolution 32: 320-333.
TOBLER, M., DEWITT, T. J., SCHLUPP, I., GARC?A DE LE?N, F. J., HERRMANN, R., FEULNER, P. G. D., TIEDEMANN, R. & PLATH, M. 2008. Toxic hydrogen sulfide and dark caves: Phenotypic and genetic divergence across two abiotic environmental gradients in Poecilia mexicana. Evolution 62: 2643-2659.
TOBLER, M., SCHLUPP, I., HEUBEL, K. U., RIESCH, R., GARCIA DE LEON, F. J., GIERE, O. & PLATH, M. 2006. Life on the edge: hydrogen sulfide and the fish communities of a Mexican cave and surrounding waters. Extremophiles 10: 577-585.
TRUJILLO-JIMENEZ, P. & BETO, H. T. 2007. Diet of the tropical freshwater fish Heterandria bimaculata (Haeckel) and Poecilia sphenops Valenciennes (Cyprinodontiformes: Poeciliidae). Revista de Biologia Tropical 55: 603-615.
TURNER, C. L. 1937. Reproductive cycles and superfetation in poeciliid fishes. Biological Bulletin 72: 145-163.
TURNER, C. L. 1941. Morphogenesis of the gonopodium in Gambusia affinis affinis. Journal of Morphology 69: 161-185.
Rudiger Riesch (1)*, Ryan A. Martin (1), David Bierbach (2), Martin Plath (2), R. Brian Langerhans (1) and Lenin Arias-Rodriguez (3)
(1.) North Carolina State University, Department of Biology & W. M. Keck Center for Behavioral Biology, 127 David Clark Labs, Raleigh, NC 27695-7617, USA: Email: firstname.lastname@example.org; email@example.com
(2.) J. W. Goethe-University of Frankfurt, Department of Evolutionary Ecology, Max-von-Laue Strasse 13, D-60438 Frankfurt am Main, Germany. Email: David.Bierbach@gmx.de; firstname.lastname@example.org
(3.) Division Academica de Ciencias Biologicas, Universidad Juarez Autonoma de Tabasco (UJAT), C.P. 86150 Villahermosa, Tabasco, Mexico: Email: email@example.com
* Corresponding author's address: North Carolina State University, Department of Biology, 127 David Clark Labs, Raleigh, NC 27695-7617, USA - Tel: +1-9195137552 - Fax: +1-9195135327. Email: firstname.lastname@example.org
|Printer friendly Cite/link Email Feedback|
|Author:||Riesch, Rudiger; Martin, Ryan A.; Bierbach, David; Plath, Martin; Langerhans, R. Brian; Arias-Rodrig|
|Publication:||aqua: International Journal of Ichthyology|
|Date:||Apr 15, 2012|
|Previous Article:||Review of the western Atlantic species of Bollmannia (Teleostei: Gobiidae: Gobiosomatini) with the description of a new allied genus and species.|
|Next Article:||Aspects of the life history of Acipenser stellatus (Acipenseriformes, Acipenseridae), the starry sturgeon, in Iranian waters of the Caspian Sea.|