Ictalurus Furcatus) Ecological Risk Screening Summary
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WDFW Washington State Status Report for the Bald Eagle
STATE OF WASHINGTON October 2001 WashingtonWashington StateState StatusStatus ReportReport forfor thethe BaldBald EagleEagle by Derek W. Stinson, James W. Watson and Kelly R. McAllister Washington Department of FISH AND WILDLIFE Wildlife Program WDFW 759 The Washington Department of Fish and Wildlife maintains a list of endangered, threatened and sensitive species (Washington Administrative Codes 232-12-014 and 232-12-011, Appendix I). In 1990, the Washington Fish and Wildlife Commission adopted listing procedures developed by a group of citizens, interest groups, and state and federal agencies (Washington Administrative Code 232-12-297, Appendix I). The procedures include how species listing will be initiated, criteria for listing and delisting, public review and recovery and management of listed species. The first step in the process is to develop a preliminary species status report. The report includes a review of information relevant to the species’ status in Washington and addresses factors affecting its status including, but not limited to: historic, current, and future species population trends, natural history including ecological relationships, historic and current habitat trends, population demographics and their relationship to long term sustainability, and historic and current species management activities. The procedures then provide for a 90-day public review opportunity for interested parties to submit new scientific data relevant to the draft status report and classification recommendation. During the 90-day review period, the Department held three public meetings to take comments and answer questions. The Department has now completed the final status report, listing recommendation and State Environmental Policy Act findings for presentation to the Washington Fish and Wildlife Commission. -
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.................................................................................................. -
Electrophorus Electricus ERSS
Electric Eel (Electrophorus electricus) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, August 2011 Revised, July 2018 Web Version, 8/21/2018 Photo: Brian Gratwicke. Licensed under CC BY-NC 3.0. Available: http://eol.org/pages/206595/overview. (July 2018). 1 Native Range and Status in the United States Native Range From Eschmeyer et al. (2018): “Distribution: Amazon and Orinoco River basins and other areas in northern Brazil: Brazil, Ecuador, Colombia, Bolivia, French Guiana, Guyana, Peru, Suriname and Venezuela.” Status in the United States This species has not been reported as introduced or established in the United States. This species is in trade in the United States. From AquaScapeOnline (2018): “Electric Eel 24” (2 feet) (Electrophorus electricus) […] Our Price: $300.00” 1 The State of Arizona has listed Electrophorus electricus as restricted live wildlife. Restricted live wildlife “means wildlife that cannot be imported, exported, or possessed without a special license or lawful exemption” (Arizona Secretary of State 2006a,b). The Florida Fish and Wildlife Conservation Commission has listed the electric eel Electrophorus electricus as a prohibited species. Prohibited nonnative species, "are considered to be dangerous to the ecology and/or the health and welfare of the people of Florida. These species are not allowed to be personally possessed or used for commercial activities” (FFWCC 2018). The State of Hawaii Plant Industry Division (2006) includes Electrophorus electricus on its list of prohibited animals. From -
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. -
Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi
Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 (http://www.accessscience.com/) Article by: Boschung, Herbert Department of Biological Sciences, University of Alabama, Tuscaloosa, Alabama. Gardiner, Brian Linnean Society of London, Burlington House, Piccadilly, London, United Kingdom. Publication year: 2014 DOI: http://dx.doi.org/10.1036/1097-8542.680400 (http://dx.doi.org/10.1036/1097-8542.680400) Content Morphology Euteleostei Bibliography Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi The most recent group of actinopterygians (rayfin fishes), first appearing in the Upper Triassic (Fig. 1). About 26,840 species are contained within the Teleostei, accounting for more than half of all living vertebrates and over 96% of all living fishes. Teleosts comprise 517 families, of which 69 are extinct, leaving 448 extant families; of these, about 43% have no fossil record. See also: Actinopterygii (/content/actinopterygii/009100); Osteichthyes (/content/osteichthyes/478500) Fig. 1 Cladogram showing the relationships of the extant teleosts with the other extant actinopterygians. (J. S. Nelson, Fishes of the World, 4th ed., Wiley, New York, 2006) 1 of 9 10/7/2015 1:07 PM Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 Morphology Much of the evidence for teleost monophyly (evolving from a common ancestral form) and relationships comes from the caudal skeleton and concomitant acquisition of a homocercal tail (upper and lower lobes of the caudal fin are symmetrical). This type of tail primitively results from an ontogenetic fusion of centra (bodies of vertebrae) and the possession of paired bracing bones located bilaterally along the dorsal region of the caudal skeleton, derived ontogenetically from the neural arches (uroneurals) of the ural (tail) centra. -
Sandies, Hybrids Hot Bites
Hunting Texas Special section inside * August 8, 2008 Texas’ Premier Outdoor Newspaper Volume 4, Issue 24 * Hunting Annual 2008 www.lonestaroutdoornews.com INSIDE HUNTING Sandies, hybrids hot bites Schools keep anglers in class The Texas Animal Health Commission approved new BY CRAIG NYHUS rules permitting the transport of male hogs to Summer means hot white bass and hybrid striped authorized game ranches bass action at many Texas lakes, and North Texas without requiring blood lakes like Lake Ray Hubbard, Ray Roberts, Lewisville tests for swine disease. and Richland Chambers lead the way for many. Page 6 Gary Goldsmith, a retired principal, fished Lewisville Lake with Art Kenney and Michael The U.S. Fish and Wildlife Anderson. “We caught and released more than 100 Service approved liberal sand bass reaching the 2-pound mark,” Goldsmith waterfowl limits for the said. “With 30 minutes of daylight left we went to an 2008-2009 season. area called Queen’s Point for hybrids. As soon as we Page 7 started the bite was on — we caught 20 more fish at that spot.” FISHING The group was fishing Lead Babies Slabs in 18 feet of water. “It’s best to keep them as close to the bottom as possible when fishing for hybrids,” Goldsmith said. East Texas lakes find crappie fishermen switching gears to chase sandies when the crappie bite slows. West Texas reservoirs see the whites hitting on top. And in the Hill Country, the Highland Lakes often get hot. “All of the fish are on the main lakes,” said Joe Bray, who guides on several Hill Country lakes. -
The Koi Herpesvirus (Khv): an Alloherpesviru
Aquacu nd ltu a r e s e J Bergmann et al., Fish Aquac J 2016, 7:2 i o r u e r h n http://dx.doi.org/10.4172/2150-3508.1000169 s a i l F Fisheries and Aquaculture Journal ISSN: 2150-3508 ResearchResearch Artilce Article OpenOpen Access Access Is There Any Species Specificity in Infections with Aquatic Animal Herpesviruses?–The Koi Herpesvirus (KHV): An Alloherpesvirus Model Sven M Bergmann1*, Michael Cieslak1, Dieter Fichtner1, Juliane Dabels2, Sean J Monaghan3, Qing Wang4, Weiwei Zeng4 and Jolanta Kempter5 1FLI Insel Riems, Südufer 10, 17493 Greifswald-Insel Riems, Germany 2University of Rostock, Aquaculture and Sea Ranching, Justus-von-Liebig-Weg 6, Rostock 18059, Germany 3Aquatic Vaccine Unit, Institute of Aquaculture, School of Natural Sciences, University of Stirling, Stirling, FK9 4LA, UK 4Pearl-River Fisheries Research Institute, Xo. 1 Xingyu Reoad, Liwan District, Guangzhou 510380, P. R. of China 5West Pomeranian Technical University, Aquaculture, K. Królewicza 4, 71-550, Szczecin, Poland Abstract Most diseases induced by herpesviruses are host-specific; however, exceptions exist within the family Alloherpesviridae. Most members of the Alloherpesviridae are detected in at least two different species, with and without clinical signs of a disease. In the current study the Koi herpesvirus (KHV) was used as a model member of the Alloherpesviridae and rainbow trout as a model salmonid host, which were infected with KHV by immersion. KHV was detected using direct methods (qPCR and semi-nested PCR) and indirect (enzyme-linked immunosorbant assay; ELISA, serum neutralization test; SNT). The non-koi herpesvirus disease (KHVD)-susceptible salmonid fish were demonstrated to transfer KHV to naïve carp at two different temperatures including a temperature most suitable for the salmonid (15°C) and cyprinid (20°C). -
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. -
Invasive Catfish Management Strategy August 2020
Invasive Catfish Management Strategy August 2020 A team from the Virginia Department of Game and Inland Fisheries uses electrofishing to monitor invasive blue catfish in the James River in 2011. (Photo by Matt Rath/Chesapeake Bay Program) I. Introduction This management strategy portrays the outcomes of an interactive workshop (2020 Invasive Catfish Workshop) held by the Invasive Catfish Workgroup at the Virginia Commonwealth University (VCU) Rice Rivers Center in Charles City, Virginia on January 29-30, 2020. The workshop convened a diverse group of stakeholders to share the current scientific understanding and priority issues associated with invasive catfishes in Chesapeake Bay. The perspectives shared and insights gained from the workshop were used to develop practical, synergistic recommendations that will improve management and mitigate impacts of these species across jurisdictions within the watershed. Blue catfish (Ictalurus furcatus) and flathead catfish (Pylodictis olivaris) are native to the Ohio, Missouri, Mississippi, and Rio Grande river basins, and were introduced into the Virginia tributaries of Chesapeake Bay in the 1960s and 1970s to establish a recreational fishery. These non-native species have since spread, inhabiting nearly all major tributaries of the Bay watershed. Rapid range expansion and population growth, particularly of blue catfish, have led to increasing concerns about impacts on the ecology of the Chesapeake Bay ecosystem. 1 Chesapeake Bay Management Strategy Invasive Catfish Blue and flathead catfishes are long-lived species that can negatively impact native species in Chesapeake Bay through predation and resource competition. Blue catfish are generalist feeders that prey on a wide variety of species that are locally abundant, including those of economic importance and conservation concern, such as blue crabs, alosines, Atlantic menhaden, American eels, and bay anchovy. -
Third International Symposium on Mangroves As Fish Habitat Abstracts*
Bull Mar Sci. 96(3):539–560. 2020 abstracts https://doi.org/10.5343/bms.2019.0047 Third International Symposium on Mangroves as Fish Habitat Abstracts* COMMUNITY COMPOSITION AND DIVERSITY OF PHYTOPLANKTON IN RELATION TO ENVIRONMENTAL VARIABLES AND SEASONALITY IN A TROPICAL MANGROVE ESTUARY, MALAYSIA by ABU HENA MK, Saifullah ASM, Idris MH, Rajaee AH, Rahman MM.—Phytoplankton are the base of the aquatic food chain from which energy is transferred to higher organisms. The community and abundance of phytoplankton in a tropical mangrove estuary were examined in Sarawak, Malaysia. Monthly-collected data from January 2013 to December 2013 was pooled into seasons to examine the influence of seasonality. The estuary was relatively species-rich and a total of 102 species under 43 genera were recorded, comprising 6 species of Cyanophyceae, 4 species of Chlorophyceae, 63 species of Bacillariophyceae, and 29 species of Dinophyceae. The mean abundance (cells L−1) of phytoplankton was found in the following order: Bacillariophyceae > Dinophyceae > Cyanophyceae > Chlorophyceae. Mean abundance of phytoplankton ranged from 5694 to 88,890 cells L−1 over the study period, with a higher value in the dry season. Species recorded from the estuary were dominated by Pleurosigma normanii, Coscinodiscus sp., Coscinodiscus centralis, Coscinodiscus granii, Dinophysis caudata, Ceratium carriense, Ceratium fusus, and Ceratium lineatum. Abundance of phytoplankton was positively influenced by chlorophyll a (R = 0.69), ammonium (R = 0.64), and silica (R = 0.64). Significant differences (ANOSIM and NMDS) were observed in the species community structure between the intermediate and wet season. The species assemblages were positively correlated with surface water temperature, salinity, pH, ammonium, and nitrate in the intermediate and dry season toward larger species composition in the respective seasons, whereas silica influenced species assemblage in the wet season. -
Endangered Species
FEATURE: ENDANGERED SPECIES Conservation Status of Imperiled North American Freshwater and Diadromous Fishes ABSTRACT: This is the third compilation of imperiled (i.e., endangered, threatened, vulnerable) plus extinct freshwater and diadromous fishes of North America prepared by the American Fisheries Society’s Endangered Species Committee. Since the last revision in 1989, imperilment of inland fishes has increased substantially. This list includes 700 extant taxa representing 133 genera and 36 families, a 92% increase over the 364 listed in 1989. The increase reflects the addition of distinct populations, previously non-imperiled fishes, and recently described or discovered taxa. Approximately 39% of described fish species of the continent are imperiled. There are 230 vulnerable, 190 threatened, and 280 endangered extant taxa, and 61 taxa presumed extinct or extirpated from nature. Of those that were imperiled in 1989, most (89%) are the same or worse in conservation status; only 6% have improved in status, and 5% were delisted for various reasons. Habitat degradation and nonindigenous species are the main threats to at-risk fishes, many of which are restricted to small ranges. Documenting the diversity and status of rare fishes is a critical step in identifying and implementing appropriate actions necessary for their protection and management. Howard L. Jelks, Frank McCormick, Stephen J. Walsh, Joseph S. Nelson, Noel M. Burkhead, Steven P. Platania, Salvador Contreras-Balderas, Brady A. Porter, Edmundo Díaz-Pardo, Claude B. Renaud, Dean A. Hendrickson, Juan Jacobo Schmitter-Soto, John Lyons, Eric B. Taylor, and Nicholas E. Mandrak, Melvin L. Warren, Jr. Jelks, Walsh, and Burkhead are research McCormick is a biologist with the biologists with the U.S. -
MEXICO Las Moras Seco Creek K Er LAVACA MEDINA US HWY 77 Springs Uvalde LEGEND Medina River
Cedar Creek Reservoir NAVARRO HENDERSON HILL BOSQUE BROWN ERATH 281 RUNNELS COLEMAN Y ANDERSON S HW COMANCHE U MIDLAND GLASSCOCK STERLING COKE Colorado River 3 7 7 HAMILTON LIMESTONE 2 Y 16 Y W FREESTONE US HW W THE HIDDEN HEART OF TEXAS H H S S U Y 87 U Waco Lake Waco McLENNAN San Angelo San Angelo Lake Concho River MILLS O.H. Ivie Reservoir UPTON Colorado River Horseshoe Park at San Felipe Springs. Popular swimming hole providing relief from hot Texas summers. REAGAN CONCHO U S HW Photo courtesy of Gregg Eckhardt. Y 183 Twin Buttes McCULLOCH CORYELL L IRION Reservoir 190 am US HWY LAMPASAS US HWY 87 pasas R FALLS US HWY 377 Belton U S HW TOM GREEN Lake B Y 67 Brady iver razos R iver LEON Temple ROBERTSON Lampasas Stillhouse BELL SAN SABA Hollow Lake Salado MILAM MADISON San Saba River Nava BURNET US HWY 183 US HWY 190 Salado sota River Lake TX HWY 71 TX HWY 29 MASON Buchanan N. San G Springs abriel Couple enjoying the historic mill at Barton Springs in 1902. R Mason Burnet iver Photo courtesy of Center for American History, University of Texas. SCHLEICHER MENARD Y 29 TX HW WILLIAMSON BRAZOS US HWY 83 377 Llano S. S an PECOS Gabriel R US HWY iver Georgetown US HWY 163 Llano River Longhorn Cavern Y 79 Sonora LLANO Inner Space Caverns US HW Eckert James River Bat Cave US HWY 95 Lake Lyndon Lake Caverns B. Johnson Junction Travis CROCKETT of Sonora BURLESON 281 GILLESPIE BLANCO Y KIMBLE W TRAVIS SUTTON H GRIMES TERRELL S U US HWY 290 US HWY 16 US HWY P Austin edernales R Fredericksburg Barton Springs 21 LEE Somerville Lake AUSTIN Pecos