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Volume III, Chapter 9 Channel Catfish
Volume III, Chapter 9 Channel Catfish TABLE OF CONTENTS 9.0 Channel Catfish (Ictalurus punctatus) ........................................................................ 9-1 9.1 Introduction................................................................................................................. 9-1 9.2 Life History & Requirements...................................................................................... 9-2 9.2.1 Spawn Timing & Conditions................................................................................ 9-2 9.2.2 Incubation ............................................................................................................ 9-3 9.2.3 Larvae & Juveniles .............................................................................................. 9-3 9.2.4 Adult..................................................................................................................... 9-4 9.2.5 Movements ........................................................................................................... 9-5 9.3 Status & Abundance.................................................................................................... 9-5 9.3.1 Abundance............................................................................................................ 9-5 9.3.2 Productivity.......................................................................................................... 9-5 9.3.3 Supplementation.................................................................................................. -
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. -
Channel Catfish Life History and Biology
SRAC Publication No. 180 Southern Regional Aquaculture Center December, 1988 . Channel Catfish Life History and Biology Thomas L. Wellborn* Channel cattish, Ictalurus punctatus Rocky Mountains. Since then chan- is located on the back between the (Rafinesque), is the most important nel catfish have been widely intro- dorsal and caudal fins (Fig. 1). One species of aquatic animal commer- duced throughout the United States conspicuous characteristic of all cially cultured in the United States. and the world. catfish is the presence of barbels It belongs to the family Ictaluridae, around the mouth. The barbels are order Siluriformes. Members of the Physical characteristics arranged in a definite pattern with order Siluriformes are found in fresh Like all native North American cat- four under the jaw and one on each and salt water worldwide. There are fishes, a channel catfish has a body tip of the maxilla (upper jaw). at least 39 species of catfish in North that is cylindrical in cross-section, America, but only six have been cul- and lacks scales. Fins are soft-rayed The channel catfish is the only tured or have potential for commer- except for the dorsal and pectoral spotted North American catfish with cial production. They are the blue fins which have sharp, hard spines a deeply forked tail. There are 24-29 catfish, Ictalurus furcatus (LeSueur); that can inflict a nasty, painful rays in the anal fin. They are general- the white catfish, Ictalurus catus wound if a catfish is handled care- ly olivaceous to blue on the back, (Linnaeus); the black bullhead, Ic- lessly. -
A Draft Genome of the Striped Catfish, Pangasianodon Hypophthalmus, for Comparative Analysis of Genes Relevant to Development An
Kim et al. BMC Genomics (2018) 19:733 https://doi.org/10.1186/s12864-018-5079-x RESEARCHARTICLE Open Access A draft genome of the striped catfish, Pangasianodon hypophthalmus, for comparative analysis of genes relevant to development and a resource for aquaculture improvement Oanh T. P. Kim1*† , Phuong T. Nguyen1†, Eiichi Shoguchi2†, Kanako Hisata2, Thuy T. B. Vo1, Jun Inoue2, Chuya Shinzato2,4, Binh T. N. Le1, Koki Nishitsuji2, Miyuki Kanda3, Vu H. Nguyen1, Hai V. Nong1 and Noriyuki Satoh2* Abstract Background: The striped catfish, Pangasianodon hypophthalmus, is a freshwater and benthopelagic fish common in the Mekong River delta. Catfish constitute a valuable source of dietary protein. Therefore, they are cultured worldwide, and P. hypophthalmus is a food staple in the Mekong area. However, genetic information about the culture stock, is unavailable for breeding improvement, although genetics of the channel catfish, Ictalurus punctatus, has been reported. Toacquiregenomesequencedataasausefulresourcefor marker-assisted breeding, we decoded a draft genome of P. hypophthalmus and performed comparative analyses. Results: Using the Illumina platform, we obtained both nuclear and mitochondrial DNA sequences. Molecular phylogeny using the mitochondrial genome confirmed that P. hypophthalmus is a member of the family Pangasiidae and is nested within a clade including the families Cranoglanididae and Ictaluridae. The nuclear genome was estimated at approximately 700 Mb, assembled into 568 scaffolds with an N50 of 14.29 Mbp, and was estimated to contain ~ 28,600 protein-coding genes, comparable to those of channel catfish and zebrafish. Interestingly, zebrafish produce gadusol, but genes for biosynthesis of this sunscreen compound have been lost from catfish genomes. -
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. -
Butterfly Splitfin (Ameca Splendens) Ecological Risk Screening Summary
Butterfly Splitfin (Ameca splendens) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, January 2013 Revised, January 2018 Web Version, 8/27/2018 Photo: Ameca splendens. Source: Getty Images. Available: https://rmpbs.pbslearningmedia.org/resource/128605480-endangered-species/butterfly-goodeid- ameca-splendens/#.Wld1X7enGUk. (January 2018). 1 1 Native Range and Status in the United States Native Range From Fuller (2018): “This species is confined to a very small area, the Río Ameca basin, on the Pacific Slope of western Mexico (Miller and Fitzsimons 1971).” From Goodeid Working Group (2018): “This species comes from the Pacific Slope and inhabits the Río Ameca and its tributary, the Río Teuchitlán in Jalisco. More habitats in the ichthyological [sic] closely connected Sayula valley have been detected quite recently.” Status in the United States From Fuller (2018): “Reported from Nevada. Records are more than 25 years old and the current status is not known to us. One individual was taken in November 1981 (museum specimen) and another in August 1983 from Rodgers Spring, Nevada (Courtenay and Deacon 1983, Deacon and Williams 1984). Others were seen and not collected (Courtenay, personal communication).” From Goodeid Working Group (2018): “Miller reported, that on 6 May 1982, this species was collected in Roger's Spring, Clark County, Nevada, (pers. comm. to Miller by P.J. Unmack) where it is now extirpated. It had been exposed there with several other exotic species (Deacon [and Williams] 1984).” From FAO (2018): “Status of the introduced species in the wild: Probably not established.” From Froese and Pauly (2018): “Raised commercially in Florida, U.S.A.” Means of Introductions in the United States From Fuller (2018): “Probably an aquarium release.” Remarks From Fuller (2018): “Synonyms and Other Names: butterfly goodeid.” 2 From Goodeid Working Group (2018): “Some hybridisation attempts have been undertaken with the Butterfly Splitfin to solve its relationship. -
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. -
Monoculture of Channel Catfish in Farm Ponds
AQUAGUIDE MISSOURI DEPARTMENT OF CONSERVATION Monoculture of Channel Catfish in Farm Ponds Channel catfish, one of Missouri’s most popular to spawn as the water temperature reaches 75 to 80 sport and food fish, have been stocked in ponds degrees. When this happens, the male will seek out throughout the state. Many small ponds are managed and prepare a nest site in a secluded, semi-dark area. exclusively for channel catfish. The female spawns only once per year, though she will A small, well-managed pond can produce 300 to 500 sometimes pair before she is ready to spawn. After pounds of catfish per surface acre each year, providing spawing, the eggs usually take eight days to hatch and many hours of recreation and an abundance of high another eight days for the fry to prepare to leave the nest. quality food for the table. During this time, the male will first protect the eggs, then Channel catfish have scaleless, cylindrical bodies the fry until they leave the nest. with soft fins, except for the dorsal and pectoral fins, which have hard, sharp spines that can inflict a painful wound. A catfish’s color varies, depending on water Ponds for Catfish clarity. In clear water, catfish may appear dark blue or Ponds suitable for exclusive channel catfish black, while in muddy water they may be a light yellow production should be at least eight feet deep with pond or gray. Young channel catfish are typically spotted. edges sloping quickly to three feet deep to reduce Channel catfish eat a variety of both plant and aquatic vegetation problems. -
2021 Fish Suppliers
2021 Fish Suppliers A.B. Jones Fish Hatchery Largemouth bass, hybrid bluegill, bluegill, black crappie, triploid grass carp, Nancy Jones gambusia – mosquito fish, channel catfish, bullfrog tadpoles, shiners 1057 Hwy 26 Williamsburg, KY 40769 (606) 549-2669 ATAC, LLC Pond Management Specialist Fathead minnows, golden shiner, goldfish, largemouth bass, smallmouth bass, Rick Rogers hybrid bluegill, bluegill, redear sunfish, walleye, channel catfish, rainbow trout, PO Box 1223 black crappie, triploid grass carp, common carp, hybrid striped bass, koi, Lebanon, OH 45036 shubunkin goldfish, bullfrog tadpoles, and paddlefish (513) 932-6529 Anglers Bait-n-Tackle LLC Fathead minnows, rosey red minnows, bluegill, hybrid bluegill, goldfish and Kaleb Rodebaugh golden shiners 747 North Arnold Ave Prestonsburg, KY 606-886-1335 Andry’s Fish Farm Bluegill, hybrid bluegill, largemouth bass, koi, channel catfish, white catfish, Lyle Andry redear sunfish, black crappie, tilapia – human consumption only, triploid grass 10923 E. Conservation Club Road carp, fathead minnows and golden shiners Birdseye, IN 47513 (812) 389-2448 Arkansas Pondstockers, Inc Channel catfish, bluegill, hybrid bluegill, redear sunfish, largemouth bass, Michael Denton black crappie, fathead minnows, and triploid grass carp PO Box 357 Harrisbug, AR 75432 (870) 578-9773 Aquatic Control, Inc. Largemouth bass, bluegill, channel catfish, triploid grass carp, fathead Clinton Charlton minnows, redear sunfish, golden shiner, rainbow trout, and hybrid striped bass 505 Assembly Drive, STE 108 -
A Brief Diet Analysis of Common Carp and Channel Catfish by Brent Campos
A Brief Diet Analysis of Common Carp and Channel Catfish By Brent Campos Four mainstem nonnative fish, two channel catfish (Ictalurus punctatus) and two common carp (Cyprinus carpio), were captured using hook-and-line during our research expedition down the Grand Canyon in March, 2005. The stomachs of the fish were removed and their contents analyzed. The two species of fish appeared to exhibit divergent methods of feeding, despite having very similar organisms in their stomachs. Catfish displayed a selective, possibly mid-water picking strategy, while carp appeared to be consuming benthic substrates with their prey. Figure 1. The 405 mm common carp with its abdominal cavity cut open. Note the large ovaries, which are yellow and grainy in appearance (photo: Chris Hammersmark). One common carp was caught near sunset in a small eddy near Bass Camp at river mile 108 on March 21. It was male, measured 370 mm standard length (SL) and exhibited spawning colors. Identifiable stomach contents included aquatic Coeloptra (beetles), one oligochete, many pebbles, and detritus, among other benthic inverts. The presence of numerous pebbles indicates this fish was probing substrates for food, as would be expected for this species. The second common carp was caught near the mouth of the backwater at river mile 137, which was at the separation point of the eddy that created the site’s sandbar. The carp was female, 405 mm in length (standard length), and displayed spawning colors. Her ovaries made up approximately 50% of her abdominal cavity by volume. Gut contents were comprised of 95% algae and 5% a mix of detritus and aquatic invertebrates. -
Goodea Atripinnis; a Fish) Ecological Risk Screening Summary
Blackfin Goodeid (Goodea atripinnis; a fish) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, July 2017 Revised, February 2018 Web Version, 8/16/2018 1 Native Range and Status in the United States Native Range From Froese and Pauly (2017): “Central America: Lerma River basin and Ayuquila River, Guanajuato, Mexico.” Status in the United States This species has not been reported as introduced or established in the United States. From Imperial Tropicals (2015): “Black-Finned Goodeid (Goodea atripinnis) IMPERIAL TROPICALS […] Out of stock Up for sale are Black Finned Goodeids. They can grow upwards of 6" making them much larger than other livebearers. Goodeids are a unique livebearer from Mexico. $ 15.99 $ 10.99” 1 Means of Introductions in the United States Goodea atripinnis has not been reported as introduced or established in the United States. Remarks From Goodeid Working Group (2017): “Common Name: Blackfin Goodea” “Mexican Name: Tiro” 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing From ITIS (2018): “Kingdom Animalia Subkingdom Bilateria Infrakingdom Deuterostomia Phylum Chordata Subphylum Vertebrata Infraphylum Gnathostomata Superclass Actinopterygii Class Teleostei Superorder Acanthopterygii Order Cyprinodontiformes Suborder Cyprinodontoidei Family Goodeidae Subfamily Goodeinae Genus Goodea Species Goodea atripinnis (Jordan, 1880)” “Current Standing: Valid” Size, Weight, and Age Range From Froese and Pauly (2017): “Max length : 13.0 cm TL male/unsexed [Miranda et al. 2009]” Environment From Froese and Pauly (2017): “Freshwater; demersal; pH range: 7.5 - 8.0; […].” 2 “[…] 18°C - 24°C [Baensch et al. 1991; assumed to represent recommended aquarium water temperatures]” From Goodeid Working Group (2017): “In contrast to all other Goodeids, Goodea atripinnis is high tolerant of highly degraded environments […]” “The habitats are very versatile, including lakes, ponds, streams, springs and outflows.