Showing posts with label Poeciliidae. Show all posts
Showing posts with label Poeciliidae. Show all posts

Tuesday, December 9, 2025

[Ichthyology • 2025] Gambusia nobilis, G. pyrros & G. echelleorum • A Total Evidence Approach justifies Taxonomic Splitting of the Endangered Pecos gambusia (Cyprinodontiformes: Poeciliidae: Gambusia) into Three Species


 Gambusia nobilis (Baird & Girard 1853)

Gambusia pyrros 
Gambusia echelleorum 

 Portnoy, Bretzing-Tungate, Fields, Bean, Smith, Dolan, Blanchard & Conway, 2025 

Abstract
Gambusia nobilis is a federally endangered species found across a fragmented distribution within the Pecos River Drainage of Texas and New Mexico, USA. Drought, human water usage, and potential hybridization and competition with introduced congeners threaten species persistence. Therefore, a population genomics study was conducted to provide critical information for conservation planning. Unsupervised clustering suggested hierarchical structure, with a primary K = 3, and deep divergences were detected among samples grouped into the Leon Creek watershed, the Toyah Creek watershed, and water bodies within the Bitter Lake National Wildlife Refuge (F’ST = 0.55–0.76 for putatively neutral data). Phylogenetic analyses showed three distinct clades corresponding to these groups, with divergence times estimated to be in the last 50 000 years. Complimentary morphological analyses detected differences among the three groups, including features of male colour pattern, and the number of caudal-fin rays in both sexes. Taken as a whole, the results indicate that the endangered G. nobilis comprises three species (two of which are named herein as G. pyrros n. sp. and G. echelleorum n. sp.), rather than one, and the study highlights the daunting yet critical task of documenting species diversity during a period of unprecedented diversity loss.

Keywords: Chihuahua desert, genetic drift, taxonomy, Poeciliidae, species delimitation
Subjects:biology, evolution, genomics, taxonomy and systematics

Distribution and relationships of the Gambusia nobilis species complex.
  
(a) Map showing distribution of G. nobilis, G. pyrros n. sp. and G. echelleorum n.sp. within Chihuahuan desert ecoregion of western Texas and southeastern New Mexico. (b) Closer view of area surrounded by dashed rectangle (b) in (a), showing location of G. echelleorum samples from Bitter Lake watershed in New Mexio, type locality indicated by black asterisk (*). (c) Closer view of area surrounded by dashed rectangle (c) in (a), showing location of G. nobilis samples from Leon Creek watershed and G. pyrros samples from Toyah Creek watershed in Texas, type localities indicated by black asterisk (*).
(d) Clade equivalent to the Gambusia nobilis species complex from the Maximum Likelihood phylogram based on 5989 loci showing relationships of G. nobilis, G. pyrros and G. echelleorum, numbers above branches represent bootstrap values (full topology available in electronic supplementary material, figure S7). (e) Discriminant analysis of principal components using the unsupervised clustering algorithm, K-means (= 3), using 3502 single nucleotide polymorphism-containing loci and 212 individuals (G. nobilis, n = 63; G. pyrros, n = 79; G. echelleorum, n = 70). Basemap in (a) created with SimpleMappr. Satellite images in (b) and (c) obtained from Google Earth.



Male individuals of the three members of the Gambusia nobilis species complex photographed in life against different background and in different views (lateral and dorsal) to document variation in colour pattern.
(a) Left side, lateral view, against light grey background: (i) G. nobilis (TCWC 21102.01); (ii, iii) G. pyrros (TCWC 21103.02, paratypes); (iv) G. echelleorum (TCWC 21104.01, holotype); (v-vii) G. echelleorum (TCWC 21105.01, paratypes). (b) Left side, lateral view, against dark grey background: (i, ii) G. nobilis (TCWC 21102.01); (iii) G. pyrros (TCWC 21103.02, paratype); (iv) G. echelleorum (TCWC 21104.01, holotype); (v) G. echelleorum (TCWC 21105.01, paratype). (c) Dorsal view (background variable): (i, ii) G. nobilis (TCWC 21102.01); (iii, iv) G. pyrros (TCWC 21103.02, paratypes); (v) G. echelleorum (TCWC 21104.01, holotype); (vi) G. echelleorum (TCWC 21105.01, paratype

 Gambusia nobilis (Baird & Girard 1853)

  Gambusia pyrros new species

Diagnosis: A member of the Gambusia nobilis species group (sensu Rauchenberger [1989]) most similar to G. nobilis and G. echelleorum. The characters distinguishing G. pyrros from G. nobilis are listed in the diagnosis of the latter. Gambusia pyrros is distinguished from G. echelleorum by the same characters that distinguish G. nobilis from G. echelleorum, plus: body colour of males orange-red or yellow-orange (figures 1d and 2b(ii); electronic supplementary material, figure S8) (versus yellow-grey to light cream; figures 1d and 2b(iii); electronic supplementary material, figure S8), anal fin of male orange-red at base in life (figure 2d(ii)) (versus orange; figure 2d(iii)), a higher modal number of total caudal-fin rays (29–32, mode 31 versus 25–29, mode 27; figure 2e), a higher modal number of branched caudal-fin rays (12–15, mode 14 versus 9–14, mode 12).

Etymology: From the Greek pyrros, meaning flame-coloured, a reference to the bright yellow, orange and red colours of the median fins of males in life. A noun in apposition. Proposed common name: flame gambusia.


  Gambusia echelleorum new species

Diagnosis: A member of the Gambusia nobilis species group (sensu Rauchenberger [1989]) most similar to G. nobilis and G. pyrros. The characters distinguishing G. echelleorum from G. nobilis and G. pyrros are listed in the diagnoses provided for the latter two.

Etymology: Named for Alice and Anthony Echelle in honour of their work on Gambusia nobilis. A noun in the genitive. Proposed common name: New Mexico Gambusia.


David S. Portnoy; Robert J. Bretzing-Tungate; Andrew T. Fields; Megan G. Bean; Ryan K. Smith; Elizabeth P. Dolan; Rose Blanchard and Kevin W. Conway. 2025. A Total Evidence Approach justifies Taxonomic Splitting of the Endangered Pecos gambusia into Three Species. R Soc Open Sci. (2025) 12 (11): 251025. DOI: doi.org/10.1098/rsos.251025 [26 Nov 2025]
 

Thursday, April 17, 2025

[Ichthyology • 2025] Phalloceros mimbi • A New Species of the Phalloceros harpagos species complex (Cyprinodontiformes: Poeciliidae) from the middle and lower Uruguay River Floodplains

 

Phalloceros mimbi
 Serra, Scarabino, Gobel & Laufer, 2025


Abstract
Phalloceros mimbi sp. nov. is described from specimens collected in the floodplains of the middle and lower Uruguay River in Uruguay (Río Negro and Salto Departments) and Argentina (Entre Ríos Province). This species belongs to the P. harpagos species complex and is diagnosed by the following unique combination of characters: 1) presence of a symmetric hood-like structure located immediately anterior to the urogenital papilla in females, 2) absence of large papillae at the mandibular symphysis of large adult females, 3) possession of well-developed hooks positioned in distal portion of gonopodial appendices of males and 4) lateral spot usually present in both sexes. To date, P. mimbi has not been found coexisting in sympatry with other Phalloceros species. The geographically closest species is P. caudimaculatus, who differs from P. mimbi by the absence of hooks in gonopodial appendix in males. Two of the three known populations of P. mimbi are relatively protected from the main threats to the species. However, conservation initiatives should consider its presence and ensure that it receives the necessary attention; considering that its global distribution occupies less than 200.000 km2 and its occurrence area represents less than 10% of the national territory it must be considered a priority for conservation and an Threatened Species for the species list of Sistema Nacional de Áreas Protegidas (SNAP) of Uruguay.

Keywords: Poeciliinae, freshwater fishes, conservation, Argentina, Uruguay



Phalloceros mimbi sp. nov. 


 
Wilson Serra, Fabrizio Scarabino, Noelia Gobel and Gabriel Laufer. 2025. A New Species of the Phalloceros harpagos species complex (Cyprinodontiformes: Poeciliidae) from the middle and lower Uruguay River floodplains. Acta Zoológica Lilloana. 309–326. DOI: doi.org/10.30550/j.azl/2096 


Monday, May 4, 2020

[Ichthyology • 2020] Limia mandibularis • A New Livebearing Fish (Cyprinodontiformes: Poeciliidae) from Lake Miragoane, Haiti


Limia mandibularis 
 Rodriguez-Silva, Torres-Pineda & Josaphat, 2020


Abstract
Limia mandibularis, a new livebearing fish of the family Poeciliidae is described from Lake Miragoane in southwestern Haiti on Hispaniola. The new species differs from all other species in the genus Limia by the presence of a well-developed lower jaw, the absence of preorbital and preopercular pores, and preorbital and preopercular canals forming an open groove each. The description of this new Limia species from Lake Miragoane confirms this lake as an important center of endemism for the genus with a total of nine described species so far.

Keywords: Pisces, Caribbean, jaw, morphology, endemism, preopercular canal

FIGURE 6. Female of Limia mandibularis sp. nov. (48.5 mm SL) showing coloration in a live specimen.

Limia mandibularis, sp. nov.  

Diagnosis. Limia mandibularis sp. nov. is uniquely diagnosed by the presence of a well-developed lower jaw due to the presence of an elongate anguloarticular bone (Fig. 3). The new species can also be identified by the lack of preorbital and preopercular pores and by the presence of single preorbital and preopercular canals forming open grooves (Fig. 4). Limia mandibularis sp. nov. can be further distinguished by the combination of the following characters: dorsal fin with 8 rays and its origin is slightly behind of the origin of the anal fin in females; 13 predorsal scales; caudal fin symmetrical and truncate or slightly convex; no crossbars, spots or blotches on body in both sexes. ...

FIGURE 7. Habitat where Limia mandibularis sp. nov. was collected. 

Distribution and ecological notes. Limia mandibularis sp. nov. is only known from the north bight of Lake Miragoane in Haiti. The lake seems very isolated in terms of connectivity with other water bodies as we did not see any tributary river or stream, but only mountain springs that lead to the lake. Our observations agree with the classification of Curtis & Hodell (1993) of the lake as an endorheic drainage. The species herein described was collected in a clear water path with slow current exiting the lake. Water temperature was 29.9 °C and water conductivity was 321 microS/cm on the collecting date (June 5th, 2019). The area is characterized by the presence of muddy bottoms and some semi-submerged and submerged vegetation growing near the banks (Fig. 7). Limia mandibularis was sympatric with Gambusia beebei, five other Limia species (L. miragoanensis, L. immaculata, L. nigrofasciata, L. garnieri and L. islai), Nandopsis haitiensis and two species of African cichlids introduced in the lake (Oreochromis aureus and Tilapia sp.). 

Etymology. The specific epithet mandibularis, from the Latin mandibula (jaw), is in reference to the well-developed lower jaw, a character that distinguishes the species.
 The vernacular name “Jawed Limia” is proposed for this species, due to the distinct protuberance that can be seen in the lower jaw.


Rodet Rodriguez-Silva, Patricia Torres-Pineda and James Josaphat. 2020. Limia mandibularis, A New Livebearing Fish (Cyprinodontiformes: Poeciliidae) from Lake Miragoane, Haiti. Zootaxa. 4768(3); 395–404. DOI: 10.11646/zootaxa.4768.3.6

     

Friday, July 28, 2017

[Ichthyology • 2017] Sex-specific Evolution during the Diversification of Live-bearing Fishes


Samples of fish species from the Poeciliidae family show the diversity in color, fin size and body shape. Kansas State University researchers studied 112 species of these live-bearing fishes and found that males and females evolve differently.


Abstract
Natural selection is often assumed to drive parallel functional diversification of the sexes. But males and females exhibit fundamental differences in their biology, and it remains largely unknown how sex differences affect macroevolutionary patterns. On microevolutionary scales, we understand how natural and sexual selection interact to give rise to sex-specific evolution during phenotypic diversification and speciation. Here we show that ignoring sex-specific patterns of functional trait evolution misrepresents the macroevolutionary adaptive landscape and evolutionary rates for 112 species of live-bearing fishes (Poeciliidae). Males and females of the same species evolve in different adaptive landscapes. Major axes of female morphology were correlated with environmental variables but not reproductive investment, while male morphological variation was primarily associated with sexual selection. Despite the importance of both natural and sexual selection in shaping sex-specific phenotypic diversification, species diversification was overwhelmingly associated with ecological divergence. Hence, the inter-predictability of mechanisms of phenotypic and species diversification may be limited in many systems. These results underscore the importance of explicitly addressing sex-specific diversification in empirical and theoretical frameworks of evolutionary radiations to elucidate the roles of different sources of selection and constraint.


Samples of fish species from the Poeciliidae family show the diversity in color, fin size and body shape. Kansas State University researchers studied 112 species of these live-bearing fishes and found that males and females evolve differently.

  

 Conclusions 
Some of our most basic tenets and enduring theories of evolution have come from systems in which phenotypes or species have diversified in response to putatively clear and strong sources of selection. However, even in those systems, evolutionary dynamics are more complex than previously assumed. Compartmentalizing our understanding of diversification into male or female (or, worse yet, sex averages), natural or sexual selection, phenotypic or species patterns, and micro- or macroevolution provides an incomplete assessment of evolutionary patterns and processes. Only integrative analysis of evolutionary dynamics across these areas will allow us to develop robust understanding of the origins of biodiversity.


Zachary W. Culumber and Michael Tobler. 2017. Sex-specific Evolution during the Diversification of Live-bearing Fishes.
 Nature Ecology & Evolution. DOI: 10.1038/s41559-017-0233-4

A tale of two fishes: Biologists find male, female live-bearing fish evolve differently
 phy.so/419594245 via @physorg_com