Butterfly Splitfin (Ameca Splendens) Ecological Risk Screening Summary
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Histochemical Characteristics of Macrophages of Butterfly Splitfin Ameca Splendens
e-ISSN 1734-9168 Folia Biologica (Kraków), vol. 67 (2019), No 1 http://www.isez.pan.krakow.pl/en/folia-biologica.html https://doi.org/10.3409/fb_67-1.05 Histochemical Characteristics of Macrophages of Butterfly Splitfin Ameca splendens Ewelina LATOSZEK, Maciej KAMASZEWSKI , Konrad MILCZAREK, Kamila PUPPEL, Hubert SZUDROWICZ, Antoni ADAMSKI, Pawe³ BURY-BURZYMSKI, and Teresa OSTASZEWSKA Accepted March 18, 2019 Published online March 29, 2019 Issue online March 29, 2019 Original article LATOSZEK E., KAMASZEWSKI M., MILCZAREK K., PUPPEL K., SZUDROWICZ H., ADAMSKI A., BURY-BURZYMSKI P., OSTASZEWSKA T. 2019. Histochemical characteristics of macrophages of butterfly splitfin Ameca splendens. Folia Biologica (Kraków) 67: 53-60. The butterfly splitfin (Ameca splendens) is a fish species that belongs to the Goodeidae family. The biology of this species, which is today at risk of extinction in its natural habitats, has not been fully explored. The objective of the present study was to characterize melanomacrophages (MMs) and the melanomacrophage centers (MMCs) that they form, associated with the immunological system of butterfly splitfin. Butterfly splitfin is a potential new model species with a placenta for scientific research. In addition, knowledge about the location and characteristics of MMCs will allow the effective development of a conservation strategy for this species and monitoring of the natural environment. The results of histological analyses show that the immune system of fish aged 1 dph was completely developed. Single MMs were observed in hepatic sinusoids and in head kidney and their agglomerations were noticed in the exocrine pancreas and in the spleen. Hemosiderin was detected in single MMs in the head kidney of fish aged 1 dph, and in the spleen, exocrine pancreas and liver of older fish. -
2017 JMIH Program Book Web Version 6-26-17.Pub
Organizing Societies American Elasmobranch Society 33rd Annual Meeting President: Dean Grubbs Treasurer: Cathy Walsh Secretary: Jennifer Wyffels Editor and Webmaster: David Shiffman Immediate Past President: Chris Lowe American Society of Ichthyologists and Herpetologists 97th Annual Meeting President: Carole Baldwin President Elect: Brian Crother Past President: Maureen A. Donnelly Prior Past President: Larry G. Allen Treasurer: F. Douglas Martin Secretary: Prosanta Chakrabarty Editor: Christopher Beachy Herpetologists’ League 75th Annual Meeting President: David M. Green Immediate Past President: James Spotila Vice-President: David Sever Treasurer: Laurie Mauger Secretary: Renata Platenburg Publications Secretary: Ken Cabarle Communications Secretary: Wendy Palin Herpetologica Editor: Stephen Mullin Herpetological Monographs Editor: Michael Harvey Society for the Study of Amphibians and Reptiles 60th Annual Meeting President: Richard Shine President-Elect: Marty Crump Immediate Past-President: Aaron Bauer Secretary: Marion R. Preest Treasurer: Kim Lovich Publications Secretary: Cari-Ann Hickerson Thank you to our generous sponsor We would like to thank the following: Local Hosts David Hillis, University of Texas at Austin, LHC Chair Dean Hendrickson, University of Texas at Austin Becca Tarvin, University of Texas at Austin Anne Chambers, University of Texas at Austin Christopher Peterson, University of Texas at Austin Volunteers We wish to thank the following volunteers who have helped make the Joint Meeting of Ichthyologists and Herpetologists -
Morphological and Genetic Comparative
Revista Mexicana de Biodiversidad 79: 373- 383, 2008 Morphological and genetic comparative analyses of populations of Zoogoneticus quitzeoensis (Cyprinodontiformes:Goodeidae) from Central Mexico, with description of a new species Análisis comparativo morfológico y genético de diferentes poblaciones de Zoogoneticus quitzeoensis (Cyprinodontiformes:Goodeidae) del Centro de México, con la descripción de una especie nueva Domínguez-Domínguez Omar1*, Pérez-Rodríguez Rodolfo1 and Doadrio Ignacio2 1Laboratorio de Biología Acuática, Facultad de Biología, Universidad Michoacana de San Nicolás de Hidalgo, Fuente de las Rosas 65, Fraccionamiento Fuentes de Morelia, 58088 Morelia, Michoacán, México 2Departamento de Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales, José Gutiérrez Abascal 2, 28006 Madrid, España. *Correspondent: [email protected] Abstract. A genetic and morphometric study of populations of Zoogoneticus quitzeoensis (Bean, 1898) from the Lerma and Ameca basins and Cuitzeo, Zacapu and Chapala Lakes in Central Mexico was conducted. For the genetic analysis, 7 populations were sampled and 2 monophyletic groups were identifi ed with a genetic difference of DHKY= 3.4% (3-3.8%), one being the populations from the lower Lerma basin, Ameca and Chapala Lake, and the other populations from Zacapu and Cuitzeo Lakes. For the morphometric analysis, 4 populations were sampled and 2 morphotypes identifi ed, 1 from La Luz Spring in the lower Lerma basin and the other from Zacapu and Cuitzeo Lakes drainages. Using these 2 sources of evidence, the population from La Luz is regarded as a new species Zoogoneticus purhepechus sp. nov. _The new species differs from its sister species Zoogoneticus quitzeoensis_ in having a shorter preorbital distance (Prol/SL x = 0.056, SD = 0.01), longer dorsal fi n base length (DFL/SL x = 0.18, SD = 0.03) and 13-14 rays in the dorsal fi n. -
The Evolution of the Placenta Drives a Shift in Sexual Selection in Livebearing Fish
LETTER doi:10.1038/nature13451 The evolution of the placenta drives a shift in sexual selection in livebearing fish B. J. A. Pollux1,2, R. W. Meredith1,3, M. S. Springer1, T. Garland1 & D. N. Reznick1 The evolution of the placenta from a non-placental ancestor causes a species produce large, ‘costly’ (that is, fully provisioned) eggs5,6, gaining shift of maternal investment from pre- to post-fertilization, creating most reproductive benefits by carefully selecting suitable mates based a venue for parent–offspring conflicts during pregnancy1–4. Theory on phenotype or behaviour2. These females, however, run the risk of mat- predicts that the rise of these conflicts should drive a shift from a ing with genetically inferior (for example, closely related or dishonestly reliance on pre-copulatory female mate choice to polyandry in conjunc- signalling) males, because genetically incompatible males are generally tion with post-zygotic mechanisms of sexual selection2. This hypoth- not discernable at the phenotypic level10. Placental females may reduce esis has not yet been empirically tested. Here we apply comparative these risks by producing tiny, inexpensive eggs and creating large mixed- methods to test a key prediction of this hypothesis, which is that the paternity litters by mating with multiple males. They may then rely on evolution of placentation is associated with reduced pre-copulatory the expression of the paternal genomes to induce differential patterns of female mate choice. We exploit a unique quality of the livebearing fish post-zygotic maternal investment among the embryos and, in extreme family Poeciliidae: placentas have repeatedly evolved or been lost, cases, divert resources from genetically defective (incompatible) to viable creating diversity among closely related lineages in the presence or embryos1–4,6,11. -
AC Summer 2008
9 American Currents Vol. 34, No. 3 The Mummichog: Master of Survival Robert Bock 1602 Tilton Dr., Silver Spring, MD 20902, [email protected] Photographs by David Snell ew aquarium hobbyists have even heard of the filled an old laundry sink with a few inches of water, straight Mummichog. Others know it only as a bait fish. from the tap, and dropped them in. Chlorine didn’t appear to Yet this determined survivor is not only easy to care bother them too much. They lived for months. F for, but an interesting and attractive species worthy Back then, New Jersey’s Hackensack meadowlands were of aquarium study. shamefully polluted, both from massive garbage dumps that The Mummichog, Fundulus heteroclitus, occurs in the filled the marshes and the many factories that sprang up along tidal waters of North America, from the Gulf of Saint the river. I can remember taking a few steps along the river Lawrence southward to northeastern Florida. The name bank, then looking back and seeing heavy black oil oozing “Mummichog” comes from an American Indian word that from my footprints. means “they go in great numbers.” Reaching a maximum Yet Mummichog were abundant. Frequently, I saw shoals length of about five inches, Mummichog are a shoaling fish of at least a thousand in the shallows. Similarly, shoals of that prefer the quieter waters of estuaries and salt marshes. Mummichog covered the surface of the toxin-laden ponds Like many coastal species, they can tolerate a wide range of that formed at the base of the landfills. salinities, ranging from fresh water to sea water. -
Copyrighted Material
Index INDEX Note: page numbers in italics refer to fi gures, those in bold refer to tables and boxes. abducens nerve 55 activity cycles 499–522 inhibition 485 absorption effi ciency 72 annual patterns 515, 516, 517–22 interactions 485–6 abyssal zone 393 circadian rhythms 505 prey 445 Acanthaster planci (Crown-of-Thorns Starfi sh) diel patterns 499, 500, 501–2, 503–4, reduction 484 579 504–7 aggressive mimicry 428, 432–3 Acanthocybium (Wahoo) 15 light-induced 499, 500, 501–2, 503–4, aggressive resemblance 425–6 Acanthodii 178, 179 505 aglomerular 52 Acanthomorpha 284–8, 289 lunar patterns 507–9 agnathans Acanthopterygii 291–325 seasonal 509–15 gills 59, 60 Atherinomorpha 293–6 semilunar patterns 507–9 osmoregulation 101, 102 characteristics 291–2 supra-annual patterns 515, 516, 517–22 phylogeny 202 distribution 349, 350 tidal patterns 506–7 ventilation 59, 60 jaws 291 see also migration see also hagfi shes; lampreys Mugilomorpha 292–3, 294 adaptive response 106 agnathous fi shes see jawless fi shes pelagic 405 adaptive zones 534 agonistic interactions 83–4, 485–8 Percomorpha 296–325 adenohypophysis 91, 92 chemically mediated 484 pharyngeal jaws 291 adenosine triphosphate (ATP) 57 sound production 461–2 phylogeny 292, 293, 294 adipose fi n 35 visual 479 spines 449, 450 adrenocorticotropic hormone (ACTH) 92 agricultural chemicals 605 Acanthothoraciformes 177 adrianichthyids 295 air breathing 60, 61–2, 62–4 acanthurids 318–19 adult fi shes 153, 154, 155–7 ammonia production 64, 100–1 Acanthuroidei 12, 318–19 death 156–7 amphibious 60 Acanthurus bahianus -
The Etyfish Project © Christopher Scharpf and Kenneth J
CYPRINODONTIFORMES (part 3) · 1 The ETYFish Project © Christopher Scharpf and Kenneth J. Lazara COMMENTS: v. 3.0 - 13 Nov. 2020 Order CYPRINODONTIFORMES (part 3 of 4) Suborder CYPRINODONTOIDEI Family PANTANODONTIDAE Spine Killifishes Pantanodon Myers 1955 pan(tos), all; ano-, without; odon, tooth, referring to lack of teeth in P. podoxys (=stuhlmanni) Pantanodon madagascariensis (Arnoult 1963) -ensis, suffix denoting place: Madagascar, where it is endemic [extinct due to habitat loss] Pantanodon stuhlmanni (Ahl 1924) in honor of Franz Ludwig Stuhlmann (1863-1928), German Colonial Service, who, with Emin Pascha, led the German East Africa Expedition (1889-1892), during which type was collected Family CYPRINODONTIDAE Pupfishes 10 genera · 112 species/subspecies Subfamily Cubanichthyinae Island Pupfishes Cubanichthys Hubbs 1926 Cuba, where genus was thought to be endemic until generic placement of C. pengelleyi; ichthys, fish Cubanichthys cubensis (Eigenmann 1903) -ensis, suffix denoting place: Cuba, where it is endemic (including mainland and Isla de la Juventud, or Isle of Pines) Cubanichthys pengelleyi (Fowler 1939) in honor of Jamaican physician and medical officer Charles Edward Pengelley (1888-1966), who “obtained” type specimens and “sent interesting details of his experience with them as aquarium fishes” Yssolebias Huber 2012 yssos, javelin, referring to elongate and narrow dorsal and anal fins with sharp borders; lebias, Greek name for a kind of small fish, first applied to killifishes (“Les Lebias”) by Cuvier (1816) and now a -
Characterization and Phylogenetic Analysis of Complete Mitochondrial MARK Genomes for Two Desert Cyprinodontoid fishes, Empetrichthys Latos and Crenichthys Baileyi
Gene 626 (2017) 163–172 Contents lists available at ScienceDirect Gene journal homepage: www.elsevier.com/locate/gene Research paper Characterization and phylogenetic analysis of complete mitochondrial MARK genomes for two desert cyprinodontoid fishes, Empetrichthys latos and Crenichthys baileyi ⁎ Miguel Jimeneza,b, Shawn C. Goodchildc,d, Craig A. Stockwellc, Sean C. Lemab, a Alan Hancock College, Santa Maria, CA, USA b Biological Sciences Department, Center for Coastal Marine Sciences, California Polytechnic State University, San Luis Obispo, CA, USA c Department of Biological Sciences, North Dakota State University, Fargo, ND, USA d Environmental & Conservation Sciences Graduate Program, North Dakota State University, Fargo, ND, USA ARTICLE INFO ABSTRACT Keywords: The Pahrump poolfish (Empetrichthys latos) and White River springfish (Crenichthys baileyi) are small-bodied Cyprinodontiformes teleost fishes (order Cyprinodontiformes) endemic to the arid Great Basin and Mojave Desert regions of western Goodeidae North America. These taxa survive as small, isolated populations in remote streams and springs and evolved to mtDNA tolerate extreme conditions of high temperature and low dissolved oxygen. Both species have experienced severe Conservation population declines over the last 50–60 years that led to some subspecies being categorized with protected status Pahrump poolfish under the U.S. Endangered Species Act. Here we report the first sequencing of the complete mitochondrial DNA White River springfish Endangered species genomes for both E. l. latos and the moapae subspecies of C. baileyi. Complete mitogenomes of 16,546 bp Fish nucleotides were obtained from two E. l. latos individuals collected from introduced populations at Spring Desert Mountain Ranch State Park and Shoshone Ponds Natural Area, Nevada, USA, while a single mitogenome of 16,537 bp was sequenced for C. -
5 Year Review of the Springfish of the Pahranagat Valley
Hiko White River Springfish (Crenichthys baileyii grandis) and White River Springfish (Crenichthys baileyi baileyi) 5-Year Review: Summary and Evaluation Illustration of Hiko White River springfish by Joseph R. Tomelleri U.S. Fish and Wildliffee Service Nevada Fish and Wilddlife Office Reno, Nevada December 14, 2012 5-YEAR REVIEW Hiko White River Springfish (Crenichthys baileyi grandis) and White River Springfish (Crenichthys baileyi baileyi) I. GENERAL INFORMATION Purpose of 5-Year Reviews: The U.S. Fish and Wildlife Service (USFWS) is required by section 4(c)(2) of the Endangered Species Act (Act) to conduct a status review of each listed species at least once every 5 years. The purpose of a 5-year review is to evaluate whether or not the species’ status has changed since it was listed (or since the most recent 5-year review). Based on the 5-year review, we recommend whether the species should be removed from the list of endangered and threatened species, be changed in status from endangered to threatened, or be changed in status from threatened to endangered. Our original listing of a species as endangered or threatened is based on the existence of threats attributable to one or more of the five threat factors described in section 4(a)(1) of the Act, and we must consider these same five factors in any subsequent consideration of reclassification or delisting of a species. In the 5-year review, we consider the best available scientific and commercial data on the species, and focus on new information available since the species was listed or last reviewed. -
Conserving Endangered Mexican Goodeid Livebearers: the Critical Role of the Aquarium Hobbyist
Conserving Endangered Mexican Goodeid Livebearers: The Critical Role of the Aquarium Hobbyist Ameca splendens Dr. John Lyons University of Wisconsin Zoological Museum Outline 1) Who are the Goodeids? - Taxonomic definitions - Evolutionary relationships 2) Mexican Goodeid biology - Life history - Habitats 3) Mexican Goodeid status and conservation - Impacts and threats - Some dire statistics 4) How YOU, the hobbyist, can help - Captive maintenance - Involvement in ALA and GWG Lago Zirahuén, Michoacán, Mexico 1) Who are the Goodeids? A family of fishes (Goodeidae; aka “Splitfins”) in the order Cyprinodontiformes, with two subfamilies: Goodeinae Empetrichthyinae ~ 40 species (~ 87 ESU’s) 4 species (8 ESU’s) Central Mexico Southwestern USA Livebearers Egg Layers Skiffia lermae Crenichthys baileyi Current Goodeid Distribution Family ~ 16.5 million years old; subfamilies split 5-10 million years ago Durango Puerto Vallarta Mexico City In Mexico, a generalized Goodeid ancestor Fossilized Tapatia occidentalis, Barranca de Santa Rosa, Jalisco; from Pliocene Epoch, at least 2.6 million years ago gave rise to a rich modern fauna Goodeid Evolutionary Relationships Cyprinodontiformes Goodeidae (Tooth Carps): Profundulidae Family Tree Cyprinodontidae1 Fundulidae Poeciliidae Valenciidae Cyprinodontidae2 Are Goodeids and Rivulidae Poeciliids merely Nothobranchidae livebearing killies? Aplocheilidae (or vice versa)? 2) Mexican Goodeid Biology - Small (maximum size 1.5” to 7”; most ~ 2.5”) - Short-lived (mature in 1 year, max age 3-5 years) - Livebearers -
Two New Species of the Genus Xenotoca Hubbs and Turner, 1939 (Teleostei, Goodeidae) from Central-Western Mexico
Zootaxa 4189 (1): 081–098 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4189.1.3 http://zoobank.org/urn:lsid:zoobank.org:pub:9BF8660A-4817-4EEA-853F-5856D1B8F6FA Two new species of the genus Xenotoca Hubbs and Turner, 1939 (Teleostei, Goodeidae) from central-western Mexico OMAR DOMÍNGUEZ-DOMÍNGUEZ1,3, DULCE MARÍA BERNAL-ZUÑIGA1 & KYLE R. PILLER2 1Laboratorio de Biología Acuática, Facultad de Biología, Universidad Michoacana de San Nicolás de Hidalgo, Edificio “R” planta baja, Ciudad Universitaria, Morelia, Michoacán, México 2Department of Biological Sciences, Southeastern Louisiana University, Hammond, LA, 70402, USA 3Corresponding author. E-mail: [email protected] Abstract The subfamily Goodeinae (Goodeidae) is one of the most representative and well-studied group of fishes from central Mexico, with around 18 genera and 40 species. Recent phylogenetic studies have documented a high degree of genetic diversity and divergences among populations, suggesting that the diversity of the group may be underestimated. The spe- cies Xenotoca eiseni has had several taxonomic changes since its description. Xenotoca eiseni is considered a widespread species along the Central Pacific Coastal drainages of Mexico, inhabiting six independent drainages. Recent molecular phylogenetic studies suggest that X. eiseni is a species complex, represented by at least three independent evolutionary lineages. We carried out a meristic and morphometric study in order to evaluate the morphological differences among these genetically divergent populations and describe two new species. The new species of goodeines, Xenotoca doadrioi and X. lyonsi, are described from the Etzatlan endorheic drainage and upper Coahuayana basin respectively. -
Phylogeny and Taxonomy of the Genus Ilyodon Eigenmann, 1907 (Teleostei: Goodeidae), Based on Mitochondrial and Nuclear DNA Sequences
Accepted: 19 March 2017 DOI: 10.1111/jzs.12175 ORIGINAL ARTICLE Phylogeny and taxonomy of the genus Ilyodon Eigenmann, 1907 (Teleostei: Goodeidae), based on mitochondrial and nuclear DNA sequences Rosa Gabriela Beltran-L opez 1,2 | Omar Domınguez-Domınguez3 | Jose Antonio Guerrero4 | Diushi Keri Corona-Santiago5 | Humberto Mejıa-Mojica2 | Ignacio Doadrio5 1Programa Institucional de Doctorado en Ciencias Biologicas, Facultad de Biologıa, Abstract Universidad Michoacana de San Nicolas de Taxonomy of the live-bearing fish of the genus Ilyodon Eigenmann, 1907 (Goodei- Hidalgo, Morelia, Michoacan, Mexico dae), in Mexico, is controversial, with morphology and mitochondrial genetic analy- 2Laboratorio de Ictiologıa, Centro de Investigaciones Biologicas, Universidad ses in disagreement about the number of valid species. The present study Autonoma del Estado de Morelos, accumulated a comprehensive DNA sequences dataset of 98 individuals of all Ilyo- Cuernavaca, Morelos, Mexico 3Laboratorio de Biologıa Acuatica, Facultad don species and mitochondrial and nuclear loci to reconstruct the evolutionary his- de Biologıa, Universidad Michoacana de San tory of the genus. Phylogenetic inference produced five clades, one with two sub- Nicolas de Hidalgo, Morelia, Michoacan, Mexico clades, and one clade including three recognized species. Genetic distances in mito- 4Facultad de Ciencias Biologicas, chondrial genes (cytb: 0.5%–2.1%; coxI: 0.5%–1.1% and d-loop: 2.3%–10.2%) were Universidad Autonoma del Estado de relatively high among main clades, while, as expected, nuclear genes showed low Morelos, Cuernavaca, Morelos, Mexico – 5Departamento de Biodiversidad y Biologıa variation (0.0% 0.2%), with geographic concordance and few shared haplotypes Evolutiva, Museo Nacional de Ciencias among river basins.