Non-Metallic Minerals of Tasmania
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Updated Checklist of Marine Fishes (Chordata: Craniata) from Portugal and the Proposed Extension of the Portuguese Continental Shelf
European Journal of Taxonomy 73: 1-73 ISSN 2118-9773 http://dx.doi.org/10.5852/ejt.2014.73 www.europeanjournaloftaxonomy.eu 2014 · Carneiro M. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:9A5F217D-8E7B-448A-9CAB-2CCC9CC6F857 Updated checklist of marine fishes (Chordata: Craniata) from Portugal and the proposed extension of the Portuguese continental shelf Miguel CARNEIRO1,5, Rogélia MARTINS2,6, Monica LANDI*,3,7 & Filipe O. COSTA4,8 1,2 DIV-RP (Modelling and Management Fishery Resources Division), Instituto Português do Mar e da Atmosfera, Av. Brasilia 1449-006 Lisboa, Portugal. E-mail: [email protected], [email protected] 3,4 CBMA (Centre of Molecular and Environmental Biology), Department of Biology, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal. E-mail: [email protected], [email protected] * corresponding author: [email protected] 5 urn:lsid:zoobank.org:author:90A98A50-327E-4648-9DCE-75709C7A2472 6 urn:lsid:zoobank.org:author:1EB6DE00-9E91-407C-B7C4-34F31F29FD88 7 urn:lsid:zoobank.org:author:6D3AC760-77F2-4CFA-B5C7-665CB07F4CEB 8 urn:lsid:zoobank.org:author:48E53CF3-71C8-403C-BECD-10B20B3C15B4 Abstract. The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. -
Order MYCTOPHIFORMES NEOSCOPELIDAE Horizontal Rows
click for previous page 942 Bony Fishes Order MYCTOPHIFORMES NEOSCOPELIDAE Neoscopelids By K.E. Hartel, Harvard University, Massachusetts, USA and J.E. Craddock, Woods Hole Oceanographic Institution, Massachusetts, USA iagnostic characters: Small fishes, usually 15 to 30 cm as adults. Body elongate with no photophores D(Scopelengys) or with 3 rows of large photophores when viewed from below (Neoscopelus).Eyes variable, small to large. Mouth large, extending to or beyond vertical from posterior margin of eye; tongue with photophores around margin in Neoscopelus. Gill rakers 9 to 16. Dorsal fin single, its origin above or slightly in front of pelvic fin, well in front of anal fins; 11 to 13 soft rays. Dorsal adipose fin over end of anal fin. Anal-fin origin well behind dorsal-fin base, anal fin with 10 to 14 soft rays. Pectoral fins long, reaching to about anus, anal fin with 15 to 19 rays.Pelvic fins large, usually reaching to anus.Scales large, cycloid, and de- ciduous. Colour: reddish silvery in Neoscopelus; blackish in Scopelengys. dorsal adipose fin anal-fin origin well behind dorsal-fin base Habitat, biology, and fisheries: Large adults of Neoscopelus usually benthopelagic below 1 000 m, but subadults mostly in midwater between 500 and 1 000 m in tropical and subtropical areas. Scopelengys meso- to bathypelagic. No known fisheries. Remarks: Three genera and 5 species with Solivomer not known from the Atlantic. All Atlantic species probably circumglobal . Similar families in occurring in area Myctophidae: photophores arranged in groups not in straight horizontal rows (except Taaningichthys paurolychnus which lacks photophores). Anal-fin origin under posterior dorsal-fin anal-fin base. -
A Review of Lanternfishes (Families: Myctophidae and Neoscopelidae)
Zoological Studies 40(2): 103-126 (2001) A Review of Lanternfishes (Families: Myctophidae and Neoscopelidae) and Their Distributions around Taiwan and the Tungsha Islands with Notes on Seventeen New Records John Ta-Ming Wang* and Che-Tsung Chen Graduate School of Fisheries Science, National Taiwan Ocean University, Keelung, Taiwan 202, R.O.C. Fax: 886-2-28106688. E-mail: [email protected] (Accepted December 20, 2000) John Ta-Ming Wang and Che-Tsung Chen (2001) A review of lanternfishes (Families: Myctophidae and Neoscopelidae) and their distributions around Taiwan and the Tungsha Islands with notes on seventeen new records. Zoological Studies 40(2): 103-126. Lanternfishes collected during 9 cruises from 1991 to 1997 were studied. The area sampled lies between 19°N and 25°N and 114°E and 123°E. The specimens collected in this area comprise 40 species belong to 16 genera, among which 17 species are first records. These first record species include Benthosema fibulatum, Bolinichthys supralateralis, Electrona risso, Hygophum proximum, H. reinhardtii, Lampadena anomala, Lobianchia gemellarii, Lampanyctus niger, L. turneri, L. tenuiformis, Myctophum asperum, M. aurolaternatum, M. nitidulum, M. spinosum, Notolychnus valdiviae, Notoscopelus caudispinosus, and N. resplendens. Among these, six species, Bolinichthys supralateralis, Electrona risso, Lampanyctus turneri, Lampadena anomala, Notolychnus valdiviae, and Notoscopelus caudispinosus, are first records for the South China Sea, and the species, Lampadena anomala is a new record for Asian oceans (Table 1). Four species (Triphoturus microchir, Diaphus diadematus, D. latus, and D. taaningi) were controversial in previous reports, so they are discussed in this study. Geographic distributions and localities of catches of all lanternfish species are shown on the maps (Figs. -
Marine Ecology Progress Series 370:239
Vol. 370: 239–247, 2008 MARINE ECOLOGY PROGRESS SERIES Published October 28 doi: 10.3354/meps07673 Mar Ecol Prog Ser Stable isotopes reveal the trophic position and mesopelagic fish diet of female southern elephant seals breeding on the Kerguelen Islands Y. Cherel1,*, S. Ducatez1, C. Fontaine1, P. Richard2, C. Guinet1 1Centre d’Etudes Biologiques de Chizé, UPR 1934 du CNRS, BP 14, 79360 Villiers-en-Bois, France 2Centre de Recherche sur les Ecosystèmes Littoraux Anthropisés, UMR 6217 du CNRS-IFREMER-ULR, Place du Séminaire, BP 5, 17137 L’Houmeau, France ABSTRACT: Trophic interactions between organisms are the main drivers of ecosystem dynamics, but scant dietary information is available for wide-ranging predators during migration. We investi- gated feeding habits of a key consumer of the Southern Ocean, the southern elephant seal Miroun- gia leonina, by comparing its blood δ13C and δ15N values with those of various marine organisms, including crustaceans, squid, fishes, seabirds and fur seals. At the end of winter, δ13C values (–23.1 to –20.1‰) indicate that female elephant seals forage mainly in the vicinity of the Polar Front and in the Polar Frontal Zone. Trophic levels derived from δ15N values (trophic level = 4.6) show that the southern elephant seal is a top consumer in the pelagic ecosystem that is dominated by colossal squid. The mean δ15N value of seals (10.1 ± 0.3‰) indicates that they are not crustacean eaters, but instead feed on crustacean-eating prey. Surprisingly, most of the previously identified prey species have isotope δ13C and δ15N values that do not fit with those of potential food items. -
Downloaded Tri-Axial Acceleration Data and GPS Files, Analyses
Masello et al. Movement Ecology (2021) 9:24 https://doi.org/10.1186/s40462-021-00255-9 RESEARCH Open Access How animals distribute themselves in space: energy landscapes of Antarctic avian predators Juan F. Masello1* , Andres Barbosa2, Akiko Kato3, Thomas Mattern1,4, Renata Medeiros5,6, Jennifer E. Stockdale5, Marc N. Kümmel7, Paco Bustamante8,9, Josabel Belliure10, Jesús Benzal11, Roger Colominas-Ciuró2, Javier Menéndez-Blázquez2, Sven Griep7, Alexander Goesmann7, William O. C. Symondson5 and Petra Quillfeldt1 Abstract Background: Energy landscapes provide an approach to the mechanistic basis of spatial ecology and decision- making in animals. This is based on the quantification of the variation in the energy costs of movements through a given environment, as well as how these costs vary in time and for different animal populations. Organisms as diverse as fish, mammals, and birds will move in areas of the energy landscape that result in minimised costs and maximised energy gain. Recently, energy landscapes have been used to link energy gain and variable energy costs of foraging to breeding success, revealing their potential use for understanding demographic changes. Methods: Using GPS-temperature-depth and tri-axial accelerometer loggers, stable isotope and molecular analyses of the diet, and leucocyte counts, we studied the response of gentoo (Pygoscelis papua) and chinstrap (Pygoscelis antarcticus) penguins to different energy landscapes and resources. We compared species and gentoo penguin populations with contrasting population trends. Results: Between populations, gentoo penguins from Livingston Island (Antarctica), a site with positive population trends, foraged in energy landscape sectors that implied lower foraging costs per energy gained compared with those around New Island (Falkland/Malvinas Islands; sub-Antarctic), a breeding site with fluctuating energy costs of foraging, breeding success and populations. -
Age and Growth of Electrona Antarctica (Pisces: Myctophidae), the Dominant Mesopelagic ®Sh of the Southern Ocean
Marine Biology (1999) 133: 145±158 Ó Springer-Verlag 1999 T. M. Greely á J. V. Gartner Jr á J. J. Torres Age and growth of Electrona antarctica (Pisces: Myctophidae), the dominant mesopelagic ®sh of the Southern Ocean Received: 12 September 1997 / Accepted: 25 July 1998 Abstract Numerically and in biomass, the lantern®sh simple energy budget using the best information avail- Electrona antarctica is the dominant ®sh in the vast pe- able suggests that a surplus of energy is available to lagic region of the Southern Ocean bounded on the support the observed growth rates (0.05 to 0.07 mm north by the Antarctic Convergence and in the south by d)1). The results of the present study contrast markedly the Antarctic continental shelf. It is an important krill with previous estimates of an 8 to 11 yr maximum age predator, and in turn is important in the diets of ¯ighted for E. antarctica. These results provide important data and swimming seabirds. Further, it is the southernmost addressing the ecology and population dynamics of the and coldest-dwelling representative of the globally dis- pelagic Antarctic ecosystem. E. antarctica is the end- tributed ®sh family Myctophidae. The present study was member species in the continuum of vertically migrating undertaken to estimate the species' growth rate and myctophids that extend from the equator to the polar average life span, to incorporate the information in a circle. Its growth rate is consonant with that of all other basic energy budget, and to compare the growth of myctophid species examined using primary growth in- E. -
Electrona Carlsbergi (Taning, 1932), the Principal Component of a Deep Scattering Layer in the Pacific Sector of the Antarctic Ocean
POLISH POLAR RESEARCH (POL. POLAR RES.) 4 1 ~4 71 -78 1983 POLSKIE BADANIA POLARNE Tomasz В. LINKOWSKI Department of Ichthyology, Sea Fisheries Institute, al. Zjednocze- nia 1, 81-345 Gdynia, Poland Electrona carlsbergi (Taning, 1932), the principal component of a deep scattering layer in the Pacific sector of the Antarctic Ocean ABSTRACT: During a cruise of the fishing vessel m/t "Sagitta" around the Antarctic, the occurrence of DSL was noted in a small area of the Pacific sector of the Antarctic waters. The layers were found at depths of 50—150 m. Their main component was E. carlsbergi (family Myctophidae), whose maximum density was within the range of 219—437 x 10" fish/m3. Key words: Antarctic, Myctophidae, DSL 1. Introduction The occurrence of water layers with sound-scattering properties (the so-called deep scattering layers, DSL) is typical for most areas of the open ocean (Marshall 1951). The absence of DSL in the Antarctic waters south of the Antarctic Convergence was noted by Dietz (1948) and Batzler and Vent (1967). Deep scattering layers were first observed in Antarctic waters by Nunez and Novarini (1976) who investgated the Drake Passage area by means of a 12 kHz echosounder. It was noted that myctophids are often the main component of deep scattering layers (Pearcy and Laurs 1966, Barham 1966, Backus et al. 1968, Backus et al. 1970, Baird et al. 1974, Taylor 1968, Gjosaeter 1981, and others). 2. Material and methods Materials for the present paper were collected during a research cruise of a commercial trawler m/t "Sagitta", taking part in the 3rd Polish Marine 72 Tomasz В. -
Prey Composition and Daily Rations of Myctophid Fishes in the Southern Ocean
MARINE ECOLOGY PROGRESS SERIES Vol. 134: 1-14, 1996 Published April 25 Mar Ecol Prog Ser I I Prey composition and daily rations of myctophid fishes in the Southern Ocean E. A. Pakhomov*, R. Perissinotto, C. D. McQuaid Southern Ocean Group. Department of Zoology and Entomology, Rhodes University. PO Box 94, Grahamstown. 6140, South Africa ABSTRACT. The feeding ecology of myctophids was studied using data collected during 5 South African scientific cruises to the Southern Ocean from 1985 to 1995, A total of 362 specimens, compris- ing 36 species, were analyzed for gut contents. Myctophid biomass levels, estimated from Bongo net tows, are among the lowest yet recorded for the Southern Ocean. Peak biomass levels were associated with the main frontal zones and with a permanent polynya region in the Lazarev Sea. Results show that all myctophid species are opportunistic mesozooplankton feeders exhibiting a high degree of overlap in their food spectrum and consuming primanly the most abundant species of copepods, euphauslids, hyperiids and pteropods. Daily rations were estimated using 3 different approaches and ranged from 0.2 to 4.4% of dry body weights. Generally, the daily food intake was equivalent to 0.5 (lower mean] to 2.9 (upper mean) of dry body weight for Antarctic and subantarctic species, and between 1.2 and 3.8% for temperate and s~~btrop~calspecies. Antarctic krill, Euphausia superba, was usually poorly repre- sented in the stomachs of all but 1 myctophid specles. The I-esultsof this study therefore do not support the hypothesis that krill plays a major role in the feeding ecology and budget of myctophids. -
MYCTOPHIDAE Lanternfishes Head and Trunk Compresse
click for previous page MYCT 1982 FAO SPECIES IDENTIFICATION SHEETS FISHING AREA 51 (W. Indian Ocean) MYCTOPHIDAE Lanternfishes Head and trunk compressed. Eyes large. Mouth usually terminal (inferior in Loweina, Gonichthys and Centrobranchus); jaws extending to or far beyond vertical through posterior margin of eye. Jaws (premaxillaries in upper, and dentaries in lower jaws) with bands of closely-set teeth, the inner ones of which may be enlarged; posterior teeth on jaws broad-based and strongly hooked forward in some species of Diaphus. Teeth also present on roof of mouth (palatines with a long, narrow band of closely-set small teeth or with one or two rows of enlarged, widely-spaced ones; mesopterygoids with a patch of closely-set and small or widely-spaced and enlarged teeth; most species with a cluster of minute teeth on each side of vomer). Branchiostegal rays 7 to 11, but there may be as few as 6 and as many as 12. Well developed gill rakers present in all genera except Centrobranchus. All fins lacking spines; adipose fin present; origin of anal fin under or close behind base of dorsal fin. Pelvic fins with 8 rays, except in Notolychnus (6) and Gonichthys (sometimes 7); caudal fin with 10 dorsal and 9 ventral principal rays. Discrete, round or kidney-shaped photophores in distinct groups on trunk and head of all species except Taaningichthys paurolychnus. Much smaller, secondary photophores on trunk and head in some species. Additional luminous organs of various shapes and sizes present on head, caudal peduncle, or on both. Scales usually cycloid or smooth to touch (ctenoid or comb-like in a few species of Myctophum), firm in forms found in relatively shallow depths, loose and easily lost in deeper-dwelling species. -
The Industrial Mineral Deposits of Tasmania
THE INDUSTRIAL MINERAL DEPOSITS OF TASMANIA Mineral Resources Tasmania Department of Infrastructure, Energy and Resources Mineral Resources Tasmania Department of Infrastructure, Energy and Resources Mineral Resources of Tasmania 13 THE INDUSTRIAL MINERAL DEPOSITS OF TASMANIA by C A Bacon, C R Calver, J Pemberton June 2008 ISBN 0 7246 4020 7 ISSN 0313-1998 While every care has been taken in the preparation of this report, no warranty is given as to the correctness of the information and no liability is accepted for any statement or opinion or for any error or omission. No reader should act or fail to act on the basis of any material contained herein. Readers should consult professional advisers. As a result the Crown in Right of the State of Tasmania and its employees, contractors and agents expressly disclaim all and any liability (including all liability from or attributable to any negligent or wrongful act or omission) to any persons whatsoever in respect of anything done or omitted to be done by any such person in reliance whether in whole or in part upon any of the material in this report. Contents Overview ............................................................................................................................................................4 Industrial Mineral Summaries ..................................................................................................................5 Construction materials Hard rock (dolerite, basalt, quartzite) ....................................................................................... -
Lanternfish Otoliths (Teleostei, Myctophidae) from the Pliocene and Pleistocene of Japan
Rivista Italiana di Paleontologia e Stratigrafia (Research in Paleontology and Stratigraphy) vol. 125(2): 355-400. July 2019 LANTERNFISH OTOLITHS (TELEOSTEI, MYCTOPHIDAE) FROM THE PLIOCENE AND PLEISTOCENE OF JAPAN WERNER SCHWARZHANS1 & FUMIO OHE2 1Ahrensburger Weg 103, D-22359 Hamburg; Natural History Museum of Denmark, Zoological Museum, Universitetsparken 15, DK-2100 Copenhagen. E-mail: [email protected] 2Nara National Research Institute for Cultural Properties, Nara 630-8577, Japan. E-mail: [email protected] To cite this article: Schwarzhans W. & Ohe F. (2019) - Lanternfish otoliths (Teleostei, Myctophidae) from the Pliocene and Pleistocene of Japan. Riv. It. Paleontol. Strat., 125(2): 355-400. Keywords: Japan; late Neogene; Myctophidae; otoliths; Kakegawa; Okinawa; Shikoku; Fiji. Abstract. Myctophid otoliths are the most common fossil otoliths to be found in Neogene deep water se- diments below approximately 200 m depositional depth. The southeastern part of Japan is particularly rich in such locations. Here we describe myctophid otoliths from late Pliocene to early Pleistocene locations on Okinawa, Shikoku and central Honshu and review previous publications. These faunas represent the tropical to subtropical faunal zone, which was established as the “Kakegawa Fauna” based on molluscs. A total of 37 species are recognized by means of otoliths in the family Myctophidae and one in the family Neoscopelidae. Two species are recorded in open nomencla- ture, 23 as persistent extant species and 12 extinct species, thereof 7 new. The new species are: Diaphus caurus, Diaphus endoi, Diaphus kakegawaensis, Diaphus nafpaktitisi, Diaphus noboriensis, Symbolophorus moriguchii and Notoscopelus praejaponicus. Two very large myctophid otoliths (>8 mm length) from the putative Piacenzian of Fiji are also described, one being a new species - Diaphus grebneffi - representing the largest by far otolith associated with the So-group of species in the genus so far known. -
Order Myctophiformes Family Neoscopelidae Two Benthopelagic Species in the Genus Neoscopelus Have Been Reported from the Western North Atlantic Ocean North of 35°N
442 Order Myctophiformes Family Neoscopelidae Two benthopelagic species in the genus Neoscopelus have been reported from the western North Atlantic Ocean north of 35°N. Both species are primarily tropical in their distributions, and have been collected in the study area only as isolated occur- rences, or only as young stages (Moore et al., 2003). Adults of these two species have ventrolateral rows of photophores on the body and also have light organs on the sides of the tongue. Eggs are undescribed. Larvae are deep-bodied with large guts, large heads and well developed teeth. Spines occur along the edge of the preopercle in Neoscopelus larvae. See Moser and Watson (2001) for more detail on ontogenetic development in this tropical family. Family Myctophidae Eighty-two species in 20 genera occur in the North Atlantic Ocean. Seventy species have been reported from the study area, north of 35°N and west of 40°W. Larvae have been described for 48 of these but eggs are undescribed in all myctophids except for those of Lampanyctodes hectoris collected off New Zealand (Robertson, 1977). Characters of those eggs are: Shell: Weakly oval, fragile Yolk: Strongly segmented Diameter (long): 0.74–0.83 mm Oil globule: Single, 0.21–0.23 mm Diameter (short): 0.65–0.72 mm Perivitelline space: Narrow Myctophid eggs in general (none identified to species), have been described as being about 0.70–0.90 mm in diameter, with a segmented yolk, moderately wide perivitelline space, single oil globule (0.1–0.3 mm in diameter), and a fragile chorion (Moser and Watson, 2001).