Technically Speaking, What Is Sturgeon Caviar?1 Frank A
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Cytogenetic Analysis of Global Populations of Mugil Cephalus (Striped Mullet) by Different Staining Techniques and Fluorescent in Situ Hybridization
Heredity 76 (1996) 77—82 Received 30 May 1995 Cytogenetic analysis of global populations of Mugil cephalus (striped mullet) by different staining techniques and fluorescent in situ hybridization ANNA RITA ROSSI, DONATELLA CROSETTIt, EKATERINA GORNUNG & LUCIANA SOLA* Department of Animal and Human Biology, University of Rome 7, Via A. Bore/li 50, 00161 Rome and tICRAM, Central Institute for Marine Research, Via L. Respighi 5, 00197 Rome, Italy Thepresent paper reports the results of cytogenetic analysis carried out on several scattered populations of the striped mullet, Mugil cephalus, the most widespead among mugilid species. The karyotype was investigated through Ag-staining, C-banding, fluorochrome-staining (chro- momycin A3/DAPI) and fluorescent in situ hybridization with rDNA genes. All populations showed the same chromosome number and morphology and no changes were detected in heterochromatin and NORs. Therefore, neither population- nor sex-specific marker chromo- somes were identified. In some of the specimens, NOR size heteromorphism was detected. Results are discussed with respect to karyotype and ribosomal cistrons organization and to cytotaxonomic implications. Keywords:cytotaxonomy,FISH, heterochromatin, karyotype, NOR. Although the karyotype of M cephalus is already Introduction known (Table 1), there are no data from differential Thestriped mullet, Mugil cephalus, is the most wide- staining techniques, except for observations on spread among mugilid species, and inhabits the trop- nucleolar organizer regions (NOR5) by Amemiya & ical and subtropical seas of the world. Both the Gold (1986). Moreover, previous studies cover only worldwide distribution, the range discontinuity few localities from the wide species range and speci- (Thomson, 1963) and the coastally-dependent life mens from more than one collecting site have never history have raised questions on the conspecificity of been observed in the same laboratory. -
Fish Species and for Eggs and Larvae of Larger Fish
BATIQUITOS LAGOON FOUNDATION F I S H Fishes of the Lagoon There were only a few species of fish in Batiquitos Lagoon (just five!) BATIQUITOS LAGOON FOUNDATION before it was opened to the ocean and tides at the end of 1996. High temperatures in the summer, low oxygen levels, and wide ranges of ANCHOVY salinity did not allow the ecosystem to flourish. Since the restoration of tidal action to the lagoon, the fish populations have significantly increased in numbers and diversity and more than sixty-five species have been found. Lagoons serve as breeding and nursery areas for a wide array of coastal fish, provide habitat and food for resident species TOPSMELT and serve as feeding areas for seasonal species. Different areas of the lagoon environment provide specific habitat needs. These include tidal creeks, sandy bottoms, emergent vegetation, submergent vegetation, nearshore shallows, open water, saline pools and brackish/freshwater areas. These habitats are defined by water YELLOWFIN GOBY characteristics including salinity, water temperature, water velocity and water depth. The lagoon bottom varies with the type of substrate such as rock, cobble, gravel, sand, clay, mud and silt. Tidal creeks and channels provide refuges for small fish species and for eggs and larvae of larger fish. Species in tidal creeks include ROUND STINGRAY gobies and topsmelt. Sandy bottoms provide important habitat for bottom-dwelling fish species such as rays, sharks and flatfish. The sandy areas provide important refuges for crustaceans, which are prey to many fish species within the lagoon. The burrows of ghost shrimp are utilized by the arrow goby. -
Clean &Unclean Meats
Clean & Unclean Meats God expects all who desire to have a relationship with Him to live holy lives (Exodus 19:6; 1 Peter 1:15). The Bible says following God’s instructions regarding the meat we eat is one aspect of living a holy life (Leviticus 11:44-47). Modern research indicates that there are health benets to eating only the meat of animals approved by God and avoiding those He labels as unclean. Here is a summation of the clean (acceptable to eat) and unclean (not acceptable to eat) animals found in Leviticus 11 and Deuteronomy 14. For further explanation, see the LifeHopeandTruth.com article “Clean and Unclean Animals.” BIRDS CLEAN (Eggs of these birds are also clean) Chicken Prairie chicken Dove Ptarmigan Duck Quail Goose Sage grouse (sagehen) Grouse Sparrow (and all other Guinea fowl songbirds; but not those of Partridge the corvid family) Peafowl (peacock) Swan (the KJV translation of “swan” is a mistranslation) Pheasant Teal Pigeon Turkey BIRDS UNCLEAN Leviticus 11:13-19 (Eggs of these birds are also unclean) All birds of prey Cormorant (raptors) including: Crane Buzzard Crow (and all Condor other corvids) Eagle Cuckoo Ostrich Falcon Egret Parrot Kite Flamingo Pelican Hawk Glede Penguin Osprey Grosbeak Plover Owl Gull Raven Vulture Heron Roadrunner Lapwing Stork Other birds including: Loon Swallow Albatross Magpie Swi Bat Martin Water hen Bittern Ossifrage Woodpecker ANIMALS CLEAN Leviticus 11:3; Deuteronomy 14:4-6 (Milk from these animals is also clean) Addax Hart Antelope Hartebeest Beef (meat of domestic cattle) Hirola chews -
Amphibious Fishes: Terrestrial Locomotion, Performance, Orientation, and Behaviors from an Applied Perspective by Noah R
AMPHIBIOUS FISHES: TERRESTRIAL LOCOMOTION, PERFORMANCE, ORIENTATION, AND BEHAVIORS FROM AN APPLIED PERSPECTIVE BY NOAH R. BRESSMAN A Dissertation Submitted to the Graduate Faculty of WAKE FOREST UNIVESITY GRADUATE SCHOOL OF ARTS AND SCIENCES in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY Biology May 2020 Winston-Salem, North Carolina Approved By: Miriam A. Ashley-Ross, Ph.D., Advisor Alice C. Gibb, Ph.D., Chair T. Michael Anderson, Ph.D. Bill Conner, Ph.D. Glen Mars, Ph.D. ACKNOWLEDGEMENTS I would like to thank my adviser Dr. Miriam Ashley-Ross for mentoring me and providing all of her support throughout my doctoral program. I would also like to thank the rest of my committee – Drs. T. Michael Anderson, Glen Marrs, Alice Gibb, and Bill Conner – for teaching me new skills and supporting me along the way. My dissertation research would not have been possible without the help of my collaborators, Drs. Jeff Hill, Joe Love, and Ben Perlman. Additionally, I am very appreciative of the many undergraduate and high school students who helped me collect and analyze data – Mark Simms, Tyler King, Caroline Horne, John Crumpler, John S. Gallen, Emily Lovern, Samir Lalani, Rob Sheppard, Cal Morrison, Imoh Udoh, Harrison McCamy, Laura Miron, and Amaya Pitts. I would like to thank my fellow graduate student labmates – Francesca Giammona, Dan O’Donnell, MC Regan, and Christine Vega – for their support and helping me flesh out ideas. I am appreciative of Dr. Ryan Earley, Dr. Bruce Turner, Allison Durland Donahou, Mary Groves, Tim Groves, Maryland Department of Natural Resources, UF Tropical Aquaculture Lab for providing fish, animal care, and lab space throughout my doctoral research. -
ADVENTURES in ICHTHYOLOGY Pacific Northwest Fish of the Lewis and Clark Expedition by Dennis D
WashingtonHistory.org ADVENTURES IN ICHTHYOLOGY Pacific Northwest Fish of the Lewis anD Clark ExpeDition By Dennis D. Dauble COLUMBIA The Magazine of Northwest History, Fall 2005: Vol. 19, No. 3 Captains Meriwether Lewis and William Clark and other members of their expedition collecteD anD iDentified nearly 400 species of plants anD animals During their voyage of Discovery. Of this total, 31 species of fish were incluDeD in Burroughs' summary of the natural history of the expedition, incluDing 12 fish consiDered unknown to science at that time. While there is little doubt of the identity of fish for which Lewis and Clark provided detailed descriptions in their daily logs, other species designations were largely conjecture based on later scholars' interpretations of Lewis anD Clark's accounts. Unlike other biological specimens encountered during the expedition, no fish were brought back for study. As a result, the identity of some was never resolveD. Many other fish were reclassified during the past century based on updated scientific methoDs. As Lewis and Clark's party crossed the Continental Divide in August 1805 in search of a water route to the Pacific Ocean, they reacheD the upper Columbia River watersheD anD crosseD the thresholD toward a whole new assemblage of freshwater fish. Their encounters with Native American fishermen and fish were well-documented in some instances. Other accounts were sketchy at best. In aDDition to their Daily log, Lewis anD Clark wrote long passages summarizing life history anD taxonomic features of several fish species while within the rainy confines of Fort Clatsop in March 1806. Many reconstructed notes were of fish encountered several months earlier when the expedition crossed the Rockies. -
Mullet River Watersheds Watershed
Wisconsin Mullet River Watersheds Watershed 2010 Water Quality Management Plan Update Sheboygan River Basin, Wisconsin August, 2010 Executive Summary The intent of this plan is to provide updated information about current water quality conditions known for the major waterways contained within the Mullet River Watershed. In addition, the plan identifi es current watershed issues. It lists opportunities and recommenda- tions for improving waterway and watershed conditions. Five sub- Contents watershed planning areas were Executive Summary . 1 identifi ed in the plan to aff ord an Introduction . 2 increased focus on local conditions Watershed Description . 2 and an improved planning scale. Water Resources . 3 Ecological Landscapes . 4 This plan is an update to information contained in the October, 2001 “State of the She- Rare Species, Natural Communities . 5 boygan River Basin” report, specifi c to the Mullet River watershed. This plan is intended Watershed Issues . 6 to satisfy federal and state watershed planning laws contained in State Administrative Watershed Recommendations . 10 Code NR121 and Section 208 of the Federal Clean Water Act. Comments on the plan Mullet Creek Subwatershed . 11 were solicited from key stakeholders and partners in the watershed area and from the Kettle Moraine Subwatershed . 14 general public. It provides a framework for improving Mullet River watershed conditions La Budde Creek Subwatershed . 18 in the coming years, by addressing the following issues which impact the river: Municipal Plymouth Subwatershed . 20 Lower Mullet Subwatershed . 24 • Lack of water quality inventory, monitoring, and biological assessment data Conclusions . 25 • Polluted runoff from agricultural areas References and Resources . 25 • Polluted runoff from developed areas Contributors: . -
Flying Fish! by Guy Belleranti
Name: __________________________________ It's Not a Bird... Not a Plane... It's a Flying Fish! by Guy Belleranti Did you know there is group of fish known as flying fish? Flying fish are found in all the major oceans. There are over 40 known species. They are most common in warmer tropical and sub-tropical areas. Of course, a flying fish doesn't actually fly like a birds does. But it can jump out of the water and glide through the air. How does it do this? First, the flying fish swims near the water's surface. Holding its side (pectoral) fins close to its body, the fish's tail (called the caudal fin) propels the Night fishermen use lights to help them catch torpedo-shaped fish at speeds of 35 to 40 miles flying fish. The fishermen know that flying fish are per hour. The tail is forked, with the lower lobe attracted to the lights so this is a great way to lure longer than the upper lobe. This lower lobe acts the fish to their boats and canoes. like an outboard motor. Angling upward, the fish bursts above the water's surface and into the air. Near Catalina Island, off the coast of California, Then the fish spreads its extra large pectoral fins night tour boats also use lights. But this time the and glides for hundreds of feet. What a great lights are used to attract flying fish for tourists to way to escape predators like mackerel, marlin, see not for fishermen to catch. One type of flying tuna and swordfish! fish that might be seen on these tours is the California flying fish. -
Capture-Based Aquaculture of Mullets in Egypt
109 Capture-based aquaculture of mullets in Egypt Magdy Saleh General Authority for Fish Resources Development Cairo, Egypt E-mail: [email protected] Saleh, M. 2008. Capture-based aquaculture of mullets in Egypt. In A. Lovatelli and P.F. Holthus (eds). Capture-based aquaculture. Global overview. FAO Fisheries Technical Paper. No. 508. Rome, FAO. pp. 109–126. SUMMARY The use of wild-caught mullet seed for the annual restocking of inland lakes has been known in Egypt for more than eight decades. The importance of wild seed collection increased with recent aquaculture developments. The positive experience with wild seed collection and high seed production costs has prevented the development of commercial mullet hatcheries. Mullet are considered very important aquaculture fish in Egypt with 156 400 tonnes produced in 2005 representing 29 percent of the national aquaculture production. Current legislation prohibits wild seed fisheries except under the direct supervision of the relevant authorities. In 2005, 69.4 million mullet fry were caught for both aquaculture and culture-based fisheries. A parallel illegal fishery exists, undermining proper management of the resources. The effect of wild seed fisheries on the wild stocks of mullet is not well studied. The negative effect of the activity is a matter of debate between fish farming and capture fisheries communities. Data on the capture of wild mullet fisheries shows no observable effect of fry collection on the catch during the last 25 years. DESCRIPTION OF THE SPECIES AND USE IN AQUACULTURE Species presentation Mullets are members of the Order Mugiliformes, Family Mugilidae. Mullets are ray- finned fish found worldwide in coastal temperate and tropical waters and, for some species, also in freshwater. -
Status of Lake Sturgeon (Acipenser Fulvescens Rafinesque 1817)
Journal of Applied Ichthyology J. Appl. Ichthyol. 32 (Suppl. 1) (2016), 162–190 Received: August 12, 2016 © 2016 Blackwell Verlag GmbH Accepted: October 19, 2016 ISSN 0175–8659 doi: 10.1111/jai.13240 Status of Lake Sturgeon (Acipenser fulvescens Rafinesque 1817) in North America By R. M. Bruch1, T. J. Haxton2, R. Koenigs1, A. Welsh3 and S. J. Kerr2 1Wisconsin Department of Natural Resources, Oshkosh, WI, USA; 2Ontario Ministry of Natural Resources and Forestry, Peterborough, ON, Canada; 3School of Natural Resources, West Virginia University, Morgantown, WV, USA Summary The species Lake Sturgeon (LS) had been assigned at least Lake Sturgeon is a potamodromous, fluvial-dependent spe- 17 different scientific names during the 19th and 20th cen- cies from the family Acipenseridae, and one of the largest turies due to the variation in color and shape displayed by freshwater fishes within its North American range extending the different life stages and populations (Scott and Cross- to the Great lakes, Mississippi River, and Hudson Bay drai- man, 1973). Eventually LS was recognized as one species nages. Like almost all other sturgeon species, Lake Stur- with the scientific designation Acipenser fulvescens (ful- = geon populations throughout its range suffered mass vescens yellowish or tawny) originally proposed by Con- – declines or extirpation in the late 1800s into the early stantine Samuel Rafinesque (1783 1840). The common name 1900s, due to extensive overexploitation and habitat loss Lake Sturgeon was given due to the abundance of the species and -
Roe-Guide.Pdf
WILD | NATURA L | SUSTAINABLE SUJIKO The cold, clean waters of Alaska provide a healthy, natural habitat for the five species of wild Alaska salmon. Each year, this e e raditional Japanese sujiko features salted and cured Alaska salmon roe within L e v e T the natural membrane or film (in-sac). Sujiko is a Japanese word composed t rich environment yields millions of high quality fish, famous S of “suji,” which means “line,” and “ko,” which means “child.” The name refers to the way in which the eggs are lined up in the ovary. The raw egg sacs are washed for their delicious flavor and superior texture. These same wild in a saturated brine solution, drained, packed with salt and then allowed to cure. All Alaska seafood is wild and sustainable and is managed Grading Information salmon produce some of the world’s finest roe, bursting with all Typically, there are three standard grades of sujiko: No.1, No.2 and No.3, plus for protection against overfishing, habitat damage and pollution. “off-grade” which includes roe that is cut, broken, soft, or off-color. In general, that is best about Alaska salmon. In Alaska, the fish come first! high-grade sujiko usually follow these guidelines: • Eggs are large in size for the species Alaska salmon roe is a wild, natural product high in lean Unlike fish stocks in other parts of the world, no Alaska • Color is bright and uniform throughout salmon stocks are threatened or endangered. For this reason, the sac protein and omega-3 fatty acids. -
Predator-Driven Macroevolution in Flyingfishes Inferred from Behavioural Studies 59
Predator-driven macroevolution in flyingfishes inferred from behavioural studies 59 Predator-driven macroevolution in flyingfishes inferred from behavioural studies: historical controversies and a hypothesis U. Kutschera Abstract Flyingfishes (Exocoetidae) are unique oceanic animals that use their tail and their large, wing-like pectoral fins to launch themselves out of the water and glide through the air. Independent observations document that flyingfishes use their gliding ability to escape from aquatic predators such as dolphins (marine mammals). The fossil record of flyingfishes is very poor. Nevertheless, the evolution of gliding among flyingfishes and their allies (Beloniformes) was analysed and reconstructed by the ethologist Konrad Lorenz (1903 – 1989) and other zoologists. In this article I review the comparative method in evolutionary biology, describe historical controversies concerning the biology and systematics of flyingfishes and present a hypothesis on the phylogenetic development of gliding among these marine vertebrates. This integrative model is based on behavioural studies and has been corroborated by molecular data (evolutionary trees derived from DNA sequences). Introduction Since the publication of Darwin´s classical book (1872, 1st ed. 1859), evolutionary biology has relied primarily upon comparative studies of extant organisms (animals, plants), supplemented whenever possible by information obtained from the fossil record. This interaction between neontological and palaeontological research has greatly enriched our knowledge of the evolutionary history (phylogeny) of a variety of macro- organisms, notably hard-shelled marine invertebrates (molluscs etc.) and vertebrates, for which thousands of well-preserved fossils have been described. Such comparative studies have become considerably more significant with the development of molecular methods for reconstructing DNA-sequence-based phylogenies and with the increased rigour with which the comparative method has been applied. -
Indiana Division of Fish & Wildlife's Animal Information Series: Paddlefish
Indiana Division of Fish & Wildlife’s Animal Information Series Paddlefish (Polyodon spathula) Do they have any other names? Paddlefish are also called spoonbill, spoonbill cat, shovelnose cat, and boneless cat. Why are they called paddlefish? They are called paddlefish because of their paddle-like nose. Polyodon is Greek for “many tooth” in reference to the numerous long gill rakers and spathula is Latin for “spatula” or “blade.” What do they look like? Paddlefish are shark-like fish with long, paddle-shaped snouts. They have large mouths, without teeth, that are located far back on the underside of the head. Paddlefish have many gill rakers (filaments used to filter food from the water) that are long and slender. The eyes are small and just above the front edge of the mouth. The rear margin of the gill cover is long and pointed into a fleshy flap. The tail is deeply lobed with the upper lobe longer than the lower lobe. The skin is without scales and the skeleton is made of cartilage. Paddlefish are bluish-gray to black on the upper parts and light gray to white on the belly. Photo Credit: Duane Raver, USFWS Where do they live in Indiana? Paddlefish are rare to occasional in Indiana and they live in large rivers. What kind of habitat do they need? A paddlefish needs very specific habitat conditions to meet its needs. During most of its life it lives in quiet or slow-flowing waters rich in the microscopic life (zooplankton) on which it feeds. However, it must have access to a large, free-flowing river with gravel bars that flood frequently during its spawning season.