Fish Species Associated with Shipwreck and Natural Hard-Bottom
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Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011
August 2012 Indo-Pacific Division Indonesia Report No 6/12 Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011 Report Compiled By: Purwanto, Muhajir, Joanne Wilson, Rizya Ardiwijaya, and Sangeeta Mangubhai August 2012 Indo-Pacific Division Indonesia Report No 6/12 Coral Reef Monitoring in Kofiau and Boo Islands Marine Protected Area, Raja Ampat, West Papua. 2009—2011 Report Compiled By: Purwanto, Muhajir, Joanne Wilson, Rizya Ardiwijaya, and Sangeeta Mangubhai Published by: TheNatureConservancy,Indo-PacificDivision Purwanto:TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia.Email: [email protected] Muhajir: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia.Email: [email protected] JoanneWilson: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur,Bali, Indonesia. RizyaArdiwijaya:TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2,Sanur, Bali,Indonesia.Email: [email protected] SangeetaMangubhai: TheNatureConservancy,IndonesiaMarineProgram,Jl.Pengembak2, Sanur,Bali,Indonesia.Email: [email protected] Suggested Citation: Purwanto,Muhajir,Wilson,J.,Ardiwijaya,R.,Mangubhai,S.2012.CoralReefMonitoringinKofiau andBooIslandsMarineProtectedArea,RajaAmpat,WestPapua.2009-2011.TheNature Conservancy,Indo-PacificDivision,Indonesia.ReportN,6/12.50pp. © 2012012012201 222 The Nature Conservancy AllRightsReserved.Reproductionforanypurposeisprohibitedwithoutpriorpermission. AllmapsdesignedandcreatedbyMuhajir. CoverPhoto: -
Checklist of Serranid and Epinephelid Fishes (Perciformes: Serranidae & Epinephelidae) of India
Journal of the Ocean Science Foundation 2021, Volume 38 Checklist of serranid and epinephelid fishes (Perciformes: Serranidae & Epinephelidae) of India AKHILESH, K.V. 1, RAJAN, P.T. 2, VINEESH, N. 3, IDREESBABU, K.K. 4, BINEESH, K.K. 5, MUKTHA, M. 6, ANULEKSHMI, C. 1, MANJEBRAYAKATH, H. 7, GLADSTON, Y. 8 & NASHAD M. 9 1 ICAR-Central Marine Fisheries Research Institute, Mumbai Regional Station, Maharashtra, India. Corresponding author: [email protected]; Email: [email protected] 2 Andaman & Nicobar Regional Centre, Zoological Survey of India, Port Blair, India. Email: [email protected] 3 Department of Health & Family Welfare, Government of West Bengal, India. Email: [email protected] 4 Department of Science and Technology, U.T. of Lakshadweep, Kavaratti, India. Email: [email protected] 5 Southern Regional Centre, Zoological Survey of India, Chennai, Tamil Nadu, India. Email: [email protected] 6 ICAR-Central Marine Fisheries Research Institute, Visakhapatnam Regional Centre, Andhra Pradesh, India. Email: [email protected] 7 Centre for Marine Living Resources and Ecology, Kochi, Kerala, India. Email: [email protected] 8 ICAR-Central Island Agricultural Research Institute, Port Blair, Andaman and Nicobar Islands, India. Email: [email protected] 9 Fishery Survey of India, Port Blair, Andaman and Nicobar Islands, 744101, India. Email: [email protected] Abstract We provide an updated checklist of fishes of the families Serranidae and Epinephelidae reported or listed from India, along with photographs. A total of 120 fishes in this group are listed as occurring in India based on published literature, of which 25 require further confirmation and validation. We confirm here the presence of at least 95 species in 22 genera occurring in Indian marine waters. -
Fish Populations and Habitat Assessment on the Oculina Bank
195 Abstract—A portion of the Oculina Assessment of fish populations and habitat Bank located off eastern Florida is a marine protected area (MPA) pre- on Oculina Bank, a deep-sea coral marine served for its dense populations of the ivory tree coral (Oculina varicosa), protected area off eastern Florida which provides important habitat for fish. Surveys of fish assemblages Stacey L. Harter (contact author)1 and benthic habitat were conducted 1 inside and outside the MPA in 2003 Marta M. Ribera and 2005 by using remotely operated Andrew N. Shepard2 vehicle video transects and digital 3 still imagery. Fish species composi- John K. Reed tion, biodiversity, and grouper densi- Email address for contact author: [email protected] ties were used to determine whether 1 National Marine Fisheries Service O. varicosa forms an essential habitat Southeast Fisheries Science Center compared to other structure-forming 3500 Delwood Beach Rd. habitats and to examine the effective- Panama City, Florida 32408 ness of the MPA. Multivariate analy- 2 NOAA Undersea Research Center ses indicated no differences in fish University of North Carolina at Wilmington assemblages or biodiversity among 5600 Marvin Moss Lane hardbottom habitat types and grou- Wilmington, North Carolina 28409 per densities were highest among the most complex habitats; however the 3 Harbor Branch Oceanographic Institute higher densities were not exclusive to Florida Atlantic University coral habitat. Therefore, we conclude 5600 U.S. 1 North that O. varicosa was functionally Ft. Pierce, Florida 34946 equivalent to other hardbottom habi- tats. Even though fish assemblages were not different among manage- ment areas, biodiversity and grouper densities were higher inside the MPA compared to outside. -
Deep-Water Sinkholes and Bioherms of South Florida and the Pourtalès Terrace — Habitat and Fauna
BULLETIN OF MARINE SCIENCE, 77(2): 267–296, 2005 CORAL REEF PAPER DEEP-WATER SINKHOLES AND BIOHERMS OF SOUTH FLORIDA AND THE POURTALÈS TERRACE — HABITAT AND FAUNA John K. Reed, Shirley A. Pomponi, Doug Weaver, Charles K. Paull, and Amy E. Wright ABSTRACT Only a small percentage of deep-water reefs have had their benthic and fish re- sources characterized. This study surveyed eight deep-water, high-relief, hard-bot- tom sites off south Florida using human occupied submersibles to characterize habitat and describe the fish and macrobenthic communities: the Naples deep-water sink- hole on the southwest Florida shelf, Jordan and Marathon deep-water sinkholes on the Pourtalès Terrace, and five high-relief bioherms on the Pourtalès Terrace. These submersible dives were the first to enter and explore any of these features. The up- per sinkhole rims ranged from 175 to 461 m in depth and had a maximum relief of 180 m. The Jordan sinkhole may be one of the deepest and largest sinkholes known. The high-relief bioherms occurred at depths of 198–319 m, with a maximum height of 120 m. A total of 26 and 16 fish taxa were identified from the sinkhole and bio- herm sites, respectively. Species of potentially commercial importance included tilefish, sharks, speckled hind, yellowedge grouper, warsaw grouper, snowy grouper, blackbelly rosefish, red porgy, drum, scorpionfish, amberjack, and phycid hakes. In total, 66 Porifera taxa were identified and four are possible new species. Twenty- one species of Cnidaria included Antipatharia (three spp.), stylasterid hydrocorals (five spp.), octocorals (11 spp.), and one scleractinian. -
Constraints on the Timescale of Animal Evolutionary History
Palaeontologia Electronica palaeo-electronica.org Constraints on the timescale of animal evolutionary history Michael J. Benton, Philip C.J. Donoghue, Robert J. Asher, Matt Friedman, Thomas J. Near, and Jakob Vinther ABSTRACT Dating the tree of life is a core endeavor in evolutionary biology. Rates of evolution are fundamental to nearly every evolutionary model and process. Rates need dates. There is much debate on the most appropriate and reasonable ways in which to date the tree of life, and recent work has highlighted some confusions and complexities that can be avoided. Whether phylogenetic trees are dated after they have been estab- lished, or as part of the process of tree finding, practitioners need to know which cali- brations to use. We emphasize the importance of identifying crown (not stem) fossils, levels of confidence in their attribution to the crown, current chronostratigraphic preci- sion, the primacy of the host geological formation and asymmetric confidence intervals. Here we present calibrations for 88 key nodes across the phylogeny of animals, rang- ing from the root of Metazoa to the last common ancestor of Homo sapiens. Close attention to detail is constantly required: for example, the classic bird-mammal date (base of crown Amniota) has often been given as 310-315 Ma; the 2014 international time scale indicates a minimum age of 318 Ma. Michael J. Benton. School of Earth Sciences, University of Bristol, Bristol, BS8 1RJ, U.K. [email protected] Philip C.J. Donoghue. School of Earth Sciences, University of Bristol, Bristol, BS8 1RJ, U.K. [email protected] Robert J. -
Phylogeny of the Epinephelinae (Teleostei: Serranidae)
BULLETIN OF MARINE SCIENCE, 52(1): 240-283, 1993 PHYLOGENY OF THE EPINEPHELINAE (TELEOSTEI: SERRANIDAE) Carole C. Baldwin and G. David Johnson ABSTRACT Relationships among epinepheline genera are investigated based on cladistic analysis of larval and adult morphology. Five monophyletic tribes are delineated, and relationships among tribes and among genera of the tribe Grammistini are hypothesized. Generic com- position of tribes differs from Johnson's (1983) classification only in the allocation of Je- boehlkia to the tribe Grammistini rather than the Liopropomini. Despite the presence of the skin toxin grammistin in the Diploprionini and Grammistini, we consider the latter to be the sister group of the Liopropomini. This hypothesis is based, in part, on previously un- recognized larval features. Larval morphology also provides evidence of monophyly of the subfamily Epinephelinae, the clade comprising all epinepheline tribes except Niphonini, and the tribe Grammistini. Larval features provide the only evidence of a monophyletic Epine- phelini and a monophyletic clade comprising the Diploprionini, Liopropomini and Gram- mistini; identification of larvae of more epinephelines is needed to test those hypotheses. Within the tribe Grammistini, we propose that Jeboehlkia gladifer is the sister group of a natural assemblage comprising the former pseudogrammid genera (Aporops, Pseudogramma and Suttonia). The "soapfishes" (Grammistes, Grammistops, Pogonoperca and Rypticus) are not monophyletic, but form a series of sequential sister groups to Jeboehlkia, Aporops, Pseu- dogramma and Suttonia (the closest of these being Grammistops, followed by Rypticus, then Grammistes plus Pogonoperca). The absence in adult Jeboehlkia of several derived features shared by Grammistops, Aporops, Pseudogramma and Suttonia is incongruous with our hypothesis but may be attributable to paedomorphosis. -
A New Species of Serranid Fish of the Genus Anthias from the Hawaiian Islands and Johnston Island1
Pacific Science (1984), vol. 38, no. 3 © 1984 by the University of Hawaii Press. All rights reserved A New Species of Serranid Fish of the Genus Anthias from the Hawaiian Islands and Johnston Island1 JOHN E. RANDALL 2 AND STEPHEN RALSTON 3 ABSTRACT: The serranid fish Anthiasfucinus is described from 15 specimens collected from steep rocky slopes atdepths of168-198 m in the Hawaiian Islands and 214-237 m atJohnston Island. It is unique among the known species of the genus in lacking vomerine teeth. Other diagnostic characters are 9 soft anal rays (ofthe Indo-Pacific species ofAnthias only A. ventralis has this count); 16 dorsal soft rays; 15 or 16 pectoral rays (all unbranched); lateral line with a distinct angle at anterior end of straight peduncular part, the pored scales 34-36 (only A. boulengeri from the GulfofOman has this number ofpored scales); membranes ofdorsal fin not incised; no prolonged dorsal spine (fourth or fifth spines barely longest); and a distinctive head color pattern ofalternating stripes ofviolet and yellow. THE FISHES OF THE GENUS Anthias (family Ser Randall (1979) reviewed the three Hawai ranidae, subfamily Anthiinae) are small color ian species of Anthias known to him at that ful species generally found on coral reefs or time, the endemic A. thompsoni (Fowler) and rocky bottoms in tropical and subtropical two widespread new species, A. bicolor and A. seas. They feed on zooplankton, usually in ventralis. The latter is subspecifically different small aggregations a meter or more above the in the Hawaiian region, hence was named A. substratum, retiring to the shelter of the reef ventralis hawaiiensis. -
FAU Institutional Repository
FAU Institutional Repository http://purl.fcla.edu/fau/fauir This paper was submitted by the faculty of FAU’s Harbor Branch Oceanographic Institute. Notice: ©1992 Rosenstiel School of Marine and Atmospheric Science, University of Miami. This manuscript is available at http://www.rsmas.miami.edu/bms and may be cited as: Gilmore, R.G. & Jones, R. S. (1992). Color variation and associated behavior in the epinepheline groupers, Mycteroperca microlepis (Goode and Bean) and M. phenax Jordan and Swain. Bulletin of Marine Science, 51(1), 83-103. BULLETIN OF MARINE SCIENCE, 51(1): 83-103,1992 CORAL REEF PAPER COLOR VARIATION AND ASSOCIATED BEHAVIOR IN THE EPINEPHELINE GROUPERS, MYCTEROPERCA MICROLEPIS (GOODE AND BEAN) AND M. PHENAX JORDAN AND SWAIN R. Grant Gilmore and Robert S. Jones ABSTRACT Color variants and behavior of scamp, Mycteroperca phenax. and gag, M, microlepis, are described from 64 submersible dives made on reef structures at depths between 20 and 100 m off the east coast of Florida from February 1977 to September 1982. These dives yielded 146 h of observations augmented with video and 35 mm photography. Both species display a variety of color phases associated with social behavior. They are expressed in each case by an aggressive, dominant territorial individual which displays to a group of smaller subor- dinates. Social hierarchy is evident in both species, with the alpha individual being a male in the gag and of undetermined sex in the scamp. Although actual spawning was not docu- mented, hierarchical behavior and displays are interpreted as courtship associated with spawn- ing activity. Courtship is further implied based on the similarity of these behaviors to those recorded for a variety of other fishes including serranids. -
Gadiformes: Moridae), with Description of a New Species from Saint Peter and Saint Paul Archipelago, Equatorial Atlantic
Zootaxa 4671 (1): 067–080 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2019 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4671.1.5 http://zoobank.org/urn:lsid:zoobank.org:pub:2DAC5AD3-6DAA-4D57-9FF0-C024174BAC0C Review of the Brazilian species of Physiculus (Gadiformes: Moridae), with description of a new species from Saint Peter and Saint Paul Archipelago, equatorial Atlantic ALESSANDRA M. A. PIRES1, ALFREDO CARVALHO-FILHO2,4, RÔMULO C. P. FERREIRA1, DANIELLE VIANA1, DIOGO NUNES3 & FABIO H. V. HAZIN1. ¹Universidade Federal Rural de Pernambuco, Rua Dom Manuel de Medeiros, s/n, Dois Irmãos, 52171-900, Recife, PE, Brasil E-mail: [email protected] ²Fish Bizz Ltda. Rua Moncorvo Filho 51, 05424-070, São Paulo, SP, Brasil. E-mail: [email protected] 3Unidade Acadêmica de Serra Talhada, Universidade Federal Rural de Pernambuco Fazenda Saco, Serra Talhada-PE, Brasil. 4Corresponding author Abstract Three valid species of the genus Physiculus are known from the Brazilian marine waters. A fourth, new species, Physiculus cirm n. sp.., is described based on seventeen specimens collected in the surroundings of Saint Peter and Saint Paul Archipelago, equatorial Atlantic. A review of the Brazilian species of Physiculus is provided, as well as a key to the species of the genus reported from the Atlantic Ocean. The new species is distinguished from all its congeners, except P. cynodon and P. karrerae, by the large number of longitudinal series of scales (156–189 vs. 70–150). P. cynodon from the Northern Pacific has about 200 longitudinal series of scales, and it differs from the new species by the number of rays of the first dorsal fin (6–8 vs. -
Zoogeography of Digenetic Trematodes from West African Marine Fishes1
192 PROCEEDINGS OF THE HELMINTHOLOGICAL SOCIETY Zoogeography of Digenetic Trematodes from West African Marine Fishes1 JACOB H. FISCHTHAL Department of Biological Sciences, State University of New York at Binghamton, Binghamton, New York 13901. ABSTRACT: Of the 107 species of trematodes found in West African (Mauritania to Gabon) marine fishes, 100 are allocated to 64 genera in 24 families while seven are immature didymozoids. Many of these genera are located in most of the world's seas with the exception of the polar seas; only five are en- demic to West Africa. The data for the 41 species known from West Africa and elsewhere, and those morphologically closest to the 55 endemic species, indicate that they are very widely distributed, particularly in the Western and North Atlantic, and Mediterranean. Historical and present- day events concerning physical and biological environmental factors and their effects on actual and po- tential hosts as well as on life cycle stages of the trematodes have resulted in the geographical distribution reported. The distribution of marine fishes has been emphasized to explain in part the trematode distribu- tion. Studies on the geographical distribution of (Gulf of Guinea from 5° S to 15° N) and digenetic trematodes of marine fishes in various warm temperate Mauritania have been pre- seas have been presented by Manter (1955, sented by Ekman (1953), Buchanan (1958), 1963, 1967), Szidat (1961), and Lebedev Longhurst (1962), and Ingham (1970). (1969), but West African waters were not included as sufficient data were not available Zoogeographical Distribution until more recently. The digenetic trematodes Of the 107 species of trematodes found in of West African marine fishes (mainly shore West African fishes, 100 are allocated to 64 and shelf inhabitants) have been reported by genera in 24 families while seven are immature Dollfus (1929, 1937a, b, 1946, 1951, 1960), didymozoids of unknown generic status (Ap- Dollfus and Capron (1958), Thomas (1959, pendix I). -
Order ZEIFORMES PARAZENIDAE Parazens P.C
click for previous page Zeiformes: Parazenidae 1203 Order ZEIFORMES PARAZENIDAE Parazens P.C. Heemstra, South African Institute for Aquatic Biodiversity, South Africa iagnostic characters: Small to moderate-sized (to 30 cm) oblong fishes, the head and body com- Dpressed; body depth slightly less than head length, contained 2.6 to 2.9 times in standard length; head naked, the bones thin and soft; opercular bones weakly serrate; mouth large, terminal, the upper jaw extremely protrusile; maxilla widely expanded posteriorly, and mostly exposed when mouth is closed; no supramaxilla; jaws with 1 or 2 rows of small, slender, conical teeth; vomer with a few short stout teeth;gill rakers (including rudiments) 2 on upper limb, 8 on lower limb.Eye diameter about 1/3 head length and slightly less than snout length.Branchiostegal rays 7.Dorsal fin divided, with 8 slender spines and 26 to 30 soft rays; anal fin with 1 minute spine and 30 to 32 soft rays; dorsal-, anal-, and pectoral-fin rays un- branched; caudal fin forked, with 11 principal rays and 9 branched rays; pectoral fin with 15 or 16 rays, shorter than eye diameter; pelvic fins with 1 unbranched and 5 or 6 branched soft rays, but no spine, fin origin posterior to a vertical at pectoral-fin base. Scales moderate in size, weakly ctenoid, and deciduous; 2 lateral lines originating on body at upper end of operculum and running posteriorly about 4 scale rows apart, gradually converging to form a single line on caudal peduncle. Caudal peduncle stout, the least depth about equal to its length and slightly less than eye diameter.Vertebrae 34.Colour: body reddish or silvery; large black blotch on anterior margin of dorsal fin. -
South Carolina Department of Natural Resources
FOREWORD Abundant fish and wildlife, unbroken coastal vistas, miles of scenic rivers, swamps and mountains open to exploration, and well-tended forests and fields…these resources enhance the quality of life that makes South Carolina a place people want to call home. We know our state’s natural resources are a primary reason that individuals and businesses choose to locate here. They are drawn to the high quality natural resources that South Carolinians love and appreciate. The quality of our state’s natural resources is no accident. It is the result of hard work and sound stewardship on the part of many citizens and agencies. The 20th century brought many changes to South Carolina; some of these changes had devastating results to the land. However, people rose to the challenge of restoring our resources. Over the past several decades, deer, wood duck and wild turkey populations have been restored, striped bass populations have recovered, the bald eagle has returned and more than half a million acres of wildlife habitat has been conserved. We in South Carolina are particularly proud of our accomplishments as we prepare to celebrate, in 2006, the 100th anniversary of game and fish law enforcement and management by the state of South Carolina. Since its inception, the South Carolina Department of Natural Resources (SCDNR) has undergone several reorganizations and name changes; however, more has changed in this state than the department’s name. According to the US Census Bureau, the South Carolina’s population has almost doubled since 1950 and the majority of our citizens now live in urban areas.