Microendolithic Structures from the Fort Payne Formation (Lower
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Tennessee Reservoir Fisheries Management Report 2001
TENNESSEE RESERVOIR FISHERIES 18-03 STATEWIDE MANAGEMENT REPORT 2016 Tim Broadbent, Michael Clark, John Hammonds, Mike Jolley, Lyle Mason , Jim Pipas, and Wm. Patrick Black Tennessee Wildlife Resources Agency Fisheries Management Division P.O. Box 40747 Nashville, Tennessee 37204 TENNESSEE RESERVOIR FISHERIES MANAGEMENT REPORT 2016 TWRA Fisheries Report No. 18-03 By Tim Broadbent, Michael Clark John Hammonds, Mike Jolley, Lyle Mason, Jim Pipas, and Wm. Patrick Black Development of this report was financed in part by funds from Federal Aid in Fish and Wildlife Restoration (Public Law 91-503) as documented in Federal Aid Project FW-6 ( TWRA Projects 1311, 1312, 1313, 2310, 2311, 3310, 3311, 3312, 3313, 3341, 4310, 4311, 4312, 4313, 7305, 7311, 7315, and 7397). This program receives Federal Aid in Fish and Wildlife Restoration. Under Title VII of the Civil Rights Act of 1964 and Section 504 of the Rehabilitation Act of 1973, the U. S. Department of the Interior prohibits discrimination on the basis of race, color, national origin, or disability. If you believe you have been discriminated against in any program, activity, or facility as described above, or if you desire further information, please write to: Office of Equal Opportunity U. S. Department of the Interior Washington, D.C. 20240 Table of Contents Page Regional Biologists…………………………………………………………………….……………….. 2 Introduction……………………………………………………………………………….………………. 3 Table of Reservoir Acreage……………………………………………………….…………………… 5 Methods…………………………………………………………………………………………………… 6 Region 1 Barkley…….……………………………………………………………………………………… -
The Distributions Of, and Relationship Between, 3He and Nitrate in Eddies
ARTICLE IN PRESS Deep-Sea Research II 55 (2008) 1389– 1397 Contents lists available at ScienceDirect Deep-Sea Research II journal homepage: www.elsevier.com/locate/dsr2 The distributions of, and relationship between, 3He and nitrate in eddies W.J. Jenkins Ã, D.J. McGillicuddy Jr., D.E. Lott III Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA article info abstract Article history: We present and discuss the distribution of 3He and its relationship to nutrients in two eddies (cyclone Accepted 4 February 2008 C1 and anticyclone A4) with a view towards examining eddy-related mechanisms whereby nutrients Available online 9 May 2008 are transported from the upper 200–300 m into the euphotic zone of the Sargasso Sea. The different Keywords: behavior of these tracers in the euphotic zone results in changes in their distributions and relationships Biogeochemical tracers that may provide important clues as to the nature of physical and biological processes involved. Tracer techniques The cyclonic eddy (C1) is characterized by substantial 3He excesses within the euphotic zone. The 3 He distribution of this excess 3He is strongly suggestive of both past and recent ongoing deep-water Eddies injection into the euphotic zone. Crude mass balance calculations suggest that an average of Atlantic Ocean approximately 1.470.7 mol mÀ2 of nitrate has been introduced into the euphotic zone of eddy C1, Sargasso Sea consistent with the integrated apparent oxygen utilization anomaly in the aphotic zone below. The 3 He–NO3 relationship within the eddy deviates substantially from the linear thermocline trend, suggestive of incomplete drawdown of nutrients and/or substantial mixing between euphotic and aphotic zone waters. -
Grade 3 Unit 2 Overview Open Ocean Habitats Introduction
G3 U2 OVR GRADE 3 UNIT 2 OVERVIEW Open Ocean Habitats Introduction The open ocean has always played a vital role in the culture, subsistence, and economic well-being of Hawai‘i’s inhabitants. The Hawaiian Islands lie in the Pacifi c Ocean, a body of water covering more than one-third of the Earth’s surface. In the following four lessons, students learn about open ocean habitats, from the ocean’s lighter surface to the darker bottom fl oor thousands of feet below the surface. Although organisms are scarce in the deep sea, there is a large diversity of organisms in addition to bottom fi sh such as polycheate worms, crustaceans, and bivalve mollusks. They come to realize that few things in the open ocean have adapted to cope with the increased pressure from the weight of the water column at that depth, in complete darkness and frigid temperatures. Students fi nd out, through instruction, presentations, and website research, that the vast open ocean is divided into zones. The pelagic zone consists of the open ocean habitat that begins at the edge of the continental shelf and extends from the surface to the ocean bottom. This zone is further sub-divided into the photic (sunlight) and disphotic (twilight) zones where most ocean organisms live. Below these two sub-zones is the aphotic (darkness) zone. In this unit, students learn about each of the ocean zones, and identify and note animals living in each zone. They also research and keep records of the evolutionary physical features and functions that animals they study have acquired to survive in harsh open ocean habitats. -
Respiration in the Mesopelagic and Bathypelagic Zones of the Oceans
CHAPTER 10 Respiration in the mesopelagic and bathypelagic zones of the oceans Javier Arístegui1, Susana Agustí2, Jack J. Middelburg3, and Carlos M. Duarte2 1 Facultad de Ciencias del Mar, Universidad de las Palmas de Gran Canaria, Spain 2 IMEDEA (CSIC–UIB), Spain 3 Netherlands Institute of Ecology, The Netherlands Outline In this chapter the mechanisms of transport and remineralization of organic matter in the dark water-column and sediments of the oceans are reviewed. We compare the different approaches to estimate respiration rates, and discuss the discrepancies obtained by the different methodologies. Finally, a respiratory carbon budget is produced for the dark ocean, which includes vertical and lateral fluxes of organic matter. In spite of the uncertainties inherent in the different approaches to estimate carbon fluxes and oxygen consumption in the dark ocean, estimates vary only by a factor of 1.5. Overall, direct measurements of respiration, as well as − indirect approaches, converge to suggest a total dark ocean respiration of 1.5–1.7 Pmol C a 1. Carbon mass − balances in the dark ocean suggest that the dark ocean receives 1.5–1.6 Pmol C a 1, similar to the estimated respiration, of which >70% is in the form of sinking particles. Almost all the organic matter (∼92%) is remineralized in the water column, the burial in sediments accounts for <1%. Mesopelagic (150–1000 m) − − respiration accounts for ∼70% of dark ocean respiration, with average integrated rates of 3–4 mol C m 2 a 1, − − 6–8 times greater than in the bathypelagic zone (∼0.5 mol C m 2 a 1). -
Read Book // Articles on Reservoirs in Tennessee, Including: List Of
RCWFANOBAC > Articles On Reservoirs In Tennessee, including: List Of Dams And Reservoirs Of... \ Book A rticles On Reservoirs In Tennessee, including: List Of Dams A nd Reservoirs Of Th e Tennessee River, Lake Barkley, W atts Bar Lake, Dale Hollow Reservoir, Center Hill Lake, Old Hickory Lake, Percy Pries By Books, Hephaestus To get Articles On Reservoirs In Tennessee, including: List Of Dams And Reservoirs Of The Tennessee River, Lake Barkley, Watts Bar Lake, Dale Hollow Reservoir, Center Hill Lake, Old Hickory Lake, Percy Pries PDF, remember to refer to the hyperlink below and download the document or have accessibility to additional information which are highly relevant to ARTICLES ON RESERVOIRS IN TENNESSEE, INCLUDING: LIST OF DAMS AND RESERVOIRS OF THE TENNESSEE RIVER, LAKE BARKLEY, WATTS BAR LAKE, DALE HOLLOW RESERVOIR, CENTER HILL LAKE, OLD HICKORY LAKE, PERCY PRIES book. Our solutions was released having a wish to function as a full on the web digital local library that provides usage of large number of PDF file document collection. You will probably find many dierent types of e-book and also other literatures from the papers data bank. Particular well- known subject areas that distribute on our catalog are trending books, answer key, assessment test question and solution, guide paper, skill information, test trial, consumer handbook, consumer guidance, support instruction, restoration manual, etc. READ ONLINE [ 3.02 MB ] Reviews This book is worth getting. Yes, it really is enjoy, continue to an amazing and interesting literature. You can expect to like how the author publish this book. -- Prof. Cindy Paucek I It is fantastic and great. -
Skeletonized Microfossils from the Lower–Middle Cambrian Transition of the Cantabrian Mountains, Northern Spain
Skeletonized microfossils from the Lower–Middle Cambrian transition of the Cantabrian Mountains, northern Spain SÉBASTIEN CLAUSEN and J. JAVIER ÁLVARO Clausen, S. and Álvaro, J.J. 2006. Skeletonized microfossils from the Lower–Middle Cambrian transition of the Cantabrian Mountains, northern Spain. Acta Palaeontologica Polonica 51 (2): 223–238. Two different assemblages of skeletonized microfossils are recorded in bioclastic shoals that cross the Lower–Middle Cambrian boundary in the Esla nappe, Cantabrian Mountains. The uppermost Lower Cambrian sedimentary rocks repre− sent a ramp with ooid−bioclastic shoals that allowed development of protected archaeocyathan−microbial reefs. The shoals yield abundant debris of tube−shelled microfossils, such as hyoliths and hyolithelminths (Torellella), and trilobites. The overlying erosive unconformity marks the disappearance of archaeocyaths and the Iberian Lower–Middle Cambrian boundary. A different assemblage occurs in the overlying glauconitic limestone associated with development of widespread low−relief bioclastic shoals. Their lowermost part is rich in hyoliths, hexactinellid, and heteractinid sponge spicules (Eiffelia), chancelloriid sclerites (at least six form species of Allonnia, Archiasterella, and Chancelloria), cambroclaves (Parazhijinites), probable eoconchariids (Cantabria labyrinthica gen. et sp. nov.), sclerites of uncertain af− finity (Holoplicatella margarita gen. et sp. nov.), echinoderm ossicles and trilobites. Although both bioclastic shoal com− plexes represent similar high−energy conditions, the unconformity at the Lower–Middle Cambrian boundary marks a drastic replacement of microfossil assemblages. This change may represent a real community replacement from hyolithelminth−phosphatic tubular shells to CES (chancelloriid−echinoderm−sponge) meadows. This replacement coin− cides with the immigration event based on trilobites previously reported across the boundary, although the partial infor− mation available from originally carbonate skeletons is also affected by taphonomic bias. -
MICROFILMED 1990 INFORMATION to USERS the Most Advanced Technology Has Been Used to Photo Graph and Reproduce This Manuscript from the Microfilm Master
■ V . • r MICROFILMED 1990 INFORMATION TO USERS The most advanced technology has been used to photo graph and reproduce this manuscript from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are re produced by sectioning the original, beginning at the upper left-hand corner and continuing from left to right in equal sections with small overlaps. Each original is also photographed in one exposure and is included in reduced form at the back of the book. These are also available as one exposure on a standard 35mm slide or as a 17" x 23" black and white photographic print for an additional charge. Photographs included in the original manuscript have been reproduced xerographically in this copy. Higher quality 6" x 9" black and white photographic prints are available for any photographs or illustrations appearing in this copy for an additional charge. Contact UMI directly to order. University Microtilms International A Bell & Howell Information Company 300 North Z eeb Road. -
Ocean Depths: the Mesopelagic and Implications for Global Warming
Current Biology Dispatches Ocean Depths: The Mesopelagic and Implications for Global Warming Mark J. Costello1,* and Sean Breyer2 1Institute of Marine Science, University of Auckland, Auckland, 1142, New Zealand 2ESRI, Redlands, CA 92373, USA *Correspondence: [email protected] http://dx.doi.org/10.1016/j.cub.2016.11.042 The mesopelagic or ‘twilight zone’ of the oceans occurs too deep for photosynthesis, but is a major part of the world’s carbon cycle. Depth boundaries for the mesopelagic have now been shown on a global scale using the distribution of pelagic animals detected by compiling echo-soundings from ships around the world, and been used to predict the effect of global warming on regional fish production. Depth Zonation Analyses were at 5 m depth intervals to However, it remains to be clearly shown The classical concepts for depth zonation 1,000 m deep, and a spatial resolution of whether the abyssal zone is ecologically [1] in the ocean begin at the seashore 300 km2. distinct from the bathyal. (Table 1). Distinct communities are visible The environment changes less as we The data shown in Figure 1 are global on the rocky seashore, and reflect the go deeper (Figure 1), so we expect the averages, and local exceptions will occur, adaptations of their animals and plants vertical extent of ecological zones to particularly in more enclosed waters such to exposure to air and wave action, increase with depth. While the rocky as the Mediterranean and Black Seas [6]. as well as the effects of grazing and seashore may have distinct habitats only The seabed-resident fauna (benthos) will predation [2]. -
Biological Oceanography - Legendre, Louis and Rassoulzadegan, Fereidoun
OCEANOGRAPHY – Vol.II - Biological Oceanography - Legendre, Louis and Rassoulzadegan, Fereidoun BIOLOGICAL OCEANOGRAPHY Legendre, Louis and Rassoulzadegan, Fereidoun Laboratoire d'Océanographie de Villefranche, France. Keywords: Algae, allochthonous nutrient, aphotic zone, autochthonous nutrient, Auxotrophs, bacteria, bacterioplankton, benthos, carbon dioxide, carnivory, chelator, chemoautotrophs, ciliates, coastal eutrophication, coccolithophores, convection, crustaceans, cyanobacteria, detritus, diatoms, dinoflagellates, disphotic zone, dissolved organic carbon (DOC), dissolved organic matter (DOM), ecosystem, eukaryotes, euphotic zone, eutrophic, excretion, exoenzymes, exudation, fecal pellet, femtoplankton, fish, fish lavae, flagellates, food web, foraminifers, fungi, harmful algal blooms (HABs), herbivorous food web, herbivory, heterotrophs, holoplankton, ichthyoplankton, irradiance, labile, large planktonic microphages, lysis, macroplankton, marine snow, megaplankton, meroplankton, mesoplankton, metazoan, metazooplankton, microbial food web, microbial loop, microheterotrophs, microplankton, mixotrophs, mollusks, multivorous food web, mutualism, mycoplankton, nanoplankton, nekton, net community production (NCP), neuston, new production, nutrient limitation, nutrient (macro-, micro-, inorganic, organic), oligotrophic, omnivory, osmotrophs, particulate organic carbon (POC), particulate organic matter (POM), pelagic, phagocytosis, phagotrophs, photoautotorphs, photosynthesis, phytoplankton, phytoplankton bloom, picoplankton, plankton, -
Articles on Reservoirs in Kentucky, Including: List of Dams and Reservoirs Of
APM7V91KSUTO » Doc » Articles On Reservoirs In Kentucky, including: List Of Dams And Reservoirs Of... Read eBook ARTICLES ON RESERVOIRS IN KENTUCKY, INCLUDING: LIST OF DAMS AND RESERVOIRS OF THE TENNESSEE RIVER, LAKE CUMBERLAND, LAKE BARKLEY, NOLIN RIVER LAKE, DALE HOLLOW RESERVOIR, BARREN RIVER LAKE, BOLTZ LAKE To read Articles On Reservoirs In Kentucky, including: List Of Dams And Reservoirs Of The Tennessee River, Lake Cumberland, Lake Barkley, Nolin River Lake, Dale Hollow Reservoir, Barren River Lake, Boltz Lake eBook, you should access the link under and download the document or have accessibility to other information which might be in conjuction with ARTICLES ON RESERVOIRS IN KENTUCKY, INCLUDING: LIST OF DAMS AND RESERVOIRS OF THE TENNESSEE RIVER, LAKE CUMBERLAND, LAKE BARKLEY, NOLIN RIVER LAKE, DALE HOLLOW RESERVOIR, BARREN RIVER LAKE, BOLTZ LAKE ebook. Read PDF Articles On Reservoirs In Kentucky, including: List Of Dams And Reservoirs Of The Tennessee River, Lake Cumberland, Lake Barkley, Nolin River Lake, Dale Hollow Reservoir, Barren River Lake, Boltz Lake Authored by Books, Hephaestus Released at 2016 Filesize: 9.56 MB Reviews The publication is easy in read better to understand. It is writter in basic words and phrases rather than hard to understand. You wont truly feel monotony at anytime of your respective time (that's what catalogues are for about if you question me). -- Kaya Rippin Absolutely among the nest publication I actually have actually go through. It really is rally fascinating throgh reading time. I am easily could possibly get a pleasure of looking at a composed ebook. -- Prof. Rick Romaguera Extensive manual for publication fans. -
Communities of Baltic Lower Circalittoral Soft Sediments (Mud and Sand)
European Red List of Habitats - Marine: Baltic Sea Habitat Group Communities of Baltic lower circalittoral soft sediments (mud and sand) Summary This is a Baltic Sea benthic habitat in the aphotic zone, comprising areas of soft sediment, predominantly mud, below the halocline, typically at depths below 70-100m. The strong permanent halocline and seasonal thermocline in summer limits vertical mixing of the water column leading to the formation of oxygen-depleted zones in the deep areas of the central Baltic. The environmental conditions of the deep zone of the Baltic are not uniform but vary widely in terms of salinity (14-21 ppt) and oxygenation (3-80% saturation). During periods of stagnation, this separation by the halocline gives rise to an oxygen deficit and periodically to complete oxygen depletion and formation of hydrogen sulphide (H2S). In places there is a continuously oxygen poor zone which is virtually devoid of macrofauna and has an extremely impoverished meiofauna generally consisting of a few thousand nematodes per square meter only. Although this habitat is naturally periodically affected by oxygen depletion, eutrophication is believed to be responsible for increasing the affected area and the duration of these episodes. Bottom trawling which, even on a single year of data, has been reported to potentially impact more than 30% of the area of this habitat, can also affect benthic communities directly and influence the recovery time. Climate change effects, such as modification of hydrographic conditions is likely to be another pressure. Measures to reduce eutrophication can reduce the impact and longevity of naturally occuring anoxic periods which affect this habitat and limiting bottom trawling can contribute to allowing recovery of this habitat . -
Photosynthetically-Competent Phytoplankton from the Aphotic Zone of the Deep Ocean
MARINE ECOLOGY - PROGRESS SERIES Published January 3 Mar. Ecol. Prog. Ser. 1 I Photosynthetically-Competent Phytoplankton from the Aphotic Zone of the Deep Ocean T. Platt, D. V. Subba Rao, J. C. Smith, W. K. Li., B. Irwin, E. P. W. Horne and D. D. Sameoto Marine Ecology Laboratory, Bedford Institute of Oceanography. Dartmouth, Nova Scotia B2Y 4A2, Canada ABSTRACT: Comparison of 2 water samples, one collected from 10 m, the other from the aphotic zone (1000 m) on the Costa Rica Dome in the eastern tropical Pacific Ocean, revealed the presence in both samples of pigmented cells of several diatoms, dinoflagellates and coccoid organisms. Measurements of carbon assimilation rates in temperature-controlled incubators across a light gradlent demonstrated that the assimilation number (mg C [mg Chl a]-' h-') of the 1000 m sample was about 0.8, slmilar to that of the 10 m sample. The ratios of RuBP carboxylase to other carboxylating enzymes were also similar between 10 m and the aphotic zone. However, the initial slope a and the inhlbltion parameter P were considerably higher for the deep sample than for the 10 m sample. Possible mechanisms by which these viable algae reached the aphotic zone are discussed. INTRODUCTION depth 3200 m. Samples were taken on 27 March from 10 m uslng a submersible pumping system (Herman, The existence of chlorophyll-containing microorgan- unpubl.) and from 1000 m using a 30-1 Niskin bottle. isms has been reported at various times in samples The possibility that the deep sample bottle had closed from the aphotic zone of the oceans (Wood, 1956; prematurely in the surface layer could be discounted Kimball et.