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Hydrothermal Vents. Teacher's Notes
Hydrothermal Vents Hydrothermal Vents. Teacher’s notes. A hydrothermal vent is a fissure in a planet's surface from which geothermally heated water issues. They are usually volcanically active. Seawater penetrates into fissures of the volcanic bed and interacts with the hot, newly formed rock in the volcanic crust. This heated seawater (350-450°) dissolves large amounts of minerals. The resulting acidic solution, containing metals (Fe, Mn, Zn, Cu) and large amounts of reduced sulfur and compounds such as sulfides and H2S, percolates up through the sea floor where it mixes with the cold surrounding ocean water (2-4°) forming mineral deposits and different types of vents. In the resulting temperature gradient, these minerals provide a source of energy and nutrients to chemoautotrophic organisms that are, thus, able to live in these extreme conditions. This is an extreme environment with high pressure, steep temperature gradients, and high concentrations of toxic elements such as sulfides and heavy metals. Black and white smokers Some hydrothermal vents form a chimney like structure that can be as 60m tall. They are formed when the minerals that are dissolved in the fluid precipitates out when the super-heated water comes into contact with the freezing seawater. The minerals become particles with high sulphur content that form the stack. Black smokers are very acidic typically with a ph. of 2 (around that of vinegar). A black smoker is a type of vent found at depths typically below 3000m that emit a cloud or black material high in sulphates. White smokers are formed in a similar way but they emit lighter-hued minerals, for example barium, calcium and silicon. -
Introduction to Co2 Chemistry in Sea Water
INTRODUCTION TO CO2 CHEMISTRY IN SEA WATER Andrew G. Dickson Scripps Institution of Oceanography, UC San Diego Mauna Loa Observatory, Hawaii Monthly Average Carbon Dioxide Concentration Data from Scripps CO Program Last updated August 2016 2 ? 410 400 390 380 370 2008; ~385 ppm 360 350 Concentration (ppm) 2 340 CO 330 1974; ~330 ppm 320 310 1960 1965 1970 1975 1980 1985 1990 1995 2000 2005 2010 2015 Year EFFECT OF ADDING CO2 TO SEA WATER 2− − CO2 + CO3 +H2O ! 2HCO3 O C O CO2 1. Dissolves in the ocean increase in decreases increases dissolved CO2 carbonate bicarbonate − HCO3 H O O also hydrogen ion concentration increases C H H 2. Reacts with water O O + H2O to form bicarbonate ion i.e., pH = –lg [H ] decreases H+ and hydrogen ion − HCO3 and saturation state of calcium carbonate decreases H+ 2− O O CO + 2− 3 3. Nearly all of that hydrogen [Ca ][CO ] C C H saturation Ω = 3 O O ion reacts with carbonate O O state K ion to form more bicarbonate sp (a measure of how “easy” it is to form a shell) M u l t i p l e o b s e r v e d indicators of a changing global carbon cycle: (a) atmospheric concentrations of carbon dioxide (CO2) from Mauna Loa (19°32´N, 155°34´W – red) and South Pole (89°59´S, 24°48´W – black) since 1958; (b) partial pressure of dissolved CO2 at the ocean surface (blue curves) and in situ pH (green curves), a measure of the acidity of ocean water. -
MIMOC: a Global Monthly Isopycnal Upper-Ocean Climatology with Mixed Layers*
1 * 1 MIMOC: A Global Monthly Isopycnal Upper-Ocean Climatology with Mixed Layers 2 3 Sunke Schmidtko1,2, Gregory C. Johnson1, and John M. Lyman1,3 4 5 1National Oceanic and Atmospheric Administration, Pacific Marine Environmental 6 Laboratory, Seattle, Washington 7 2University of East Anglia, School of Environmental Sciences, Norwich, United 8 Kingdom 9 3Joint Institute for Marine and Atmospheric Research, University of Hawaii at Manoa, 10 Honolulu, Hawaii 11 12 Accepted for publication in 13 Journal of Geophysical Research - Oceans. 14 Copyright 2013 American Geophysical Union. Further reproduction or electronic 15 distribution is not permitted. 16 17 8 February 2013 18 19 ______________________________________ 20 *Pacific Marine Environmental Laboratory Contribution Number 3805 21 22 Corresponding Author: Sunke Schmidtko, School of Environmental Sciences, University 23 of East Anglia, Norwich, NR4 7TJ, UK. Email: [email protected] 2 24 Abstract 25 26 A Monthly, Isopycnal/Mixed-layer Ocean Climatology (MIMOC), global from 0–1950 27 dbar, is compared with other monthly ocean climatologies. All available quality- 28 controlled profiles of temperature (T) and salinity (S) versus pressure (P) collected by 29 conductivity-temperature-depth (CTD) instruments from the Argo Program, Ice-Tethered 30 Profilers, and archived in the World Ocean Database are used. MIMOC provides maps 31 of mixed layer properties (conservative temperature, Θ, Absolute Salinity, SA, and 32 maximum P) as well as maps of interior ocean properties (Θ, SA, and P) to 1950 dbar on 33 isopycnal surfaces. A third product merges the two onto a pressure grid spanning the 34 upper 1950 dbar, adding more familiar potential temperature (θ) and practical salinity (S) 35 maps. -
Major Ions, Carbonate System, Alkalinity, Ph (Kalff Chapters 13 and 14) A. Major Ions 1. Common Ions There Are 7 Common Ions I
Major Ions, Carbonate System, Alkalinity, pH (Kalff Chapters 13 and 14) A. Major ions 1. Common Ions There are 7 common ions in freshwater: (e.g. Table 13-3, p207) +2 +2 +1 +1 cations: Ca , Mg , Na , K -1 -2 -1 anions: Cl , SO4 , HCO3 +1 -1 In some surface waters, other ionic species are sometimes important (e.g. NH4 , F , organic acids, etc.), but in most cases the 7 ions listed above are the only ions present in significant concentration. In addition to the common ions, OH-1 and H+1 are important species because of the dissociation of water itself. In freshwater, the total concentration of ions and the relative abundance of each are highly variable, reflecting the influence of precipitation (rain), weathering and evaporation. In contrast to freshwater, the world ocean is very uniform (Table 13-6, p214). The total concentration of ions varies only slightly, depending on local advection of freshwater from major rivers and regions of surplus rainfall or evaporation. For “standard” seawater, with “chlorinity” = 19.000 parts per thousand, the following concentrations are observed for the common ions. (Similar ratios are available for nearly the entire periodic table, although at lower concentrations.) These fixed ratios in the sea are the result of the “constancy of composition” of seawater. Ion parts per thousand (g/kg) - - - Cl 18.980 (the definition of "clorinity" includes Br , I , etc.) + Na 10.556 -2 SO4 2.649 +2 Mg 1.272 +2 Ca 0.400 + K 0.380 - HCO3 0.140 Br- 0.065 2. Sources of ions in freshwater a. -
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). -
Causes of Sea Level Rise
FACT SHEET Causes of Sea OUR COASTAL COMMUNITIES AT RISK Level Rise What the Science Tells Us HIGHLIGHTS From the rocky shoreline of Maine to the busy trading port of New Orleans, from Roughly a third of the nation’s population historic Golden Gate Park in San Francisco to the golden sands of Miami Beach, lives in coastal counties. Several million our coasts are an integral part of American life. Where the sea meets land sit some of our most densely populated cities, most popular tourist destinations, bountiful of those live at elevations that could be fisheries, unique natural landscapes, strategic military bases, financial centers, and flooded by rising seas this century, scientific beaches and boardwalks where memories are created. Yet many of these iconic projections show. These cities and towns— places face a growing risk from sea level rise. home to tourist destinations, fisheries, Global sea level is rising—and at an accelerating rate—largely in response to natural landscapes, military bases, financial global warming. The global average rise has been about eight inches since the centers, and beaches and boardwalks— Industrial Revolution. However, many U.S. cities have seen much higher increases in sea level (NOAA 2012a; NOAA 2012b). Portions of the East and Gulf coasts face a growing risk from sea level rise. have faced some of the world’s fastest rates of sea level rise (NOAA 2012b). These trends have contributed to loss of life, billions of dollars in damage to coastal The choices we make today are critical property and infrastructure, massive taxpayer funding for recovery and rebuild- to protecting coastal communities. -
Ocean Storage
277 6 Ocean storage Coordinating Lead Authors Ken Caldeira (United States), Makoto Akai (Japan) Lead Authors Peter Brewer (United States), Baixin Chen (China), Peter Haugan (Norway), Toru Iwama (Japan), Paul Johnston (United Kingdom), Haroon Kheshgi (United States), Qingquan Li (China), Takashi Ohsumi (Japan), Hans Pörtner (Germany), Chris Sabine (United States), Yoshihisa Shirayama (Japan), Jolyon Thomson (United Kingdom) Contributing Authors Jim Barry (United States), Lara Hansen (United States) Review Editors Brad De Young (Canada), Fortunat Joos (Switzerland) 278 IPCC Special Report on Carbon dioxide Capture and Storage Contents EXECUTIVE SUMMARY 279 6.7 Environmental impacts, risks, and risk management 298 6.1 Introduction and background 279 6.7.1 Introduction to biological impacts and risk 298 6.1.1 Intentional storage of CO2 in the ocean 279 6.7.2 Physiological effects of CO2 301 6.1.2 Relevant background in physical and chemical 6.7.3 From physiological mechanisms to ecosystems 305 oceanography 281 6.7.4 Biological consequences for water column release scenarios 306 6.2 Approaches to release CO2 into the ocean 282 6.7.5 Biological consequences associated with CO2 6.2.1 Approaches to releasing CO2 that has been captured, lakes 307 compressed, and transported into the ocean 282 6.7.6 Contaminants in CO2 streams 307 6.2.2 CO2 storage by dissolution of carbonate minerals 290 6.7.7 Risk management 307 6.2.3 Other ocean storage approaches 291 6.7.8 Social aspects; public and stakeholder perception 307 6.3 Capacity and fractions retained -
Trophic Diversity of Plankton in the Epipelagic and Mesopelagic Layers of the Tropical and Equatorial Atlantic Determined with Stable Isotopes
diversity Article Trophic Diversity of Plankton in the Epipelagic and Mesopelagic Layers of the Tropical and Equatorial Atlantic Determined with Stable Isotopes Antonio Bode 1,* ID and Santiago Hernández-León 2 1 Instituto Español de Oceanografía, Centro Oceanográfico de A Coruña, Apdo 130, 15080 A Coruña, Spain 2 Instituto de Oceanografía y Cambio Global (IOCAG), Universidad de las Palmas de Gran Canaria, Campus de Taliarte, Telde, Gran Canaria, 35214 Islas Canarias, Spain; [email protected] * Correspondence: [email protected]; Tel.: +34-981205362 Received: 30 April 2018; Accepted: 12 June 2018; Published: 13 June 2018 Abstract: Plankton living in the deep ocean either migrate to the surface to feed or feed in situ on other organisms and detritus. Planktonic communities in the upper 800 m of the tropical and equatorial Atlantic were studied using the natural abundance of stable carbon and nitrogen isotopes to identify their food sources and trophic diversity. Seston and zooplankton (>200 µm) samples were collected with Niskin bottles and MOCNESS nets, respectively, in the epipelagic (0–200 m), upper mesopelagic (200–500 m), and lower mesopelagic layers (500–800 m) at 11 stations. Food sources for plankton in the productive zone influenced by the NW African upwelling and the Canary Current were different from those in the oligotrophic tropical and equatorial zones. In the latter, zooplankton collected during the night in the mesopelagic layers was enriched in heavy nitrogen isotopes relative to day samples, supporting the active migration of organisms from deep layers. Isotopic niches showed also zonal differences in size (largest in the north), mean trophic diversity (largest in the tropical zone), food sources, and the number of trophic levels (largest in the equatorial zone). -
Impact of the Pycnocline Layer on Bacterioplankton
MARINE ECOLOGY - PROGRESS SERIES Vol. 38: 295403, 1987 Published July 13 Mar. Ecol. Prog. Ser. l Impact of the pycnocline layer on bacterioplankton: diel and spatial variations in microbial parameters in the stratified water column of the Gulf of Trieste (Northern Adriatic Sea) Gerhard J. ~erndl'& Vlado ~alaCiC~ ' Institute for Zoology. University of Vienna. Althanstr. 14, A-1090 Vienna, Austria Marine Biology Station Piran, Cesta JLA 65, YU-66330 Piran. Yugoslavia ABSTRACT: Die1 variations in bacterial density, frequency of bvidlng cells (FDC) and bssolved organic carbon (DOC) in the stratified water column of the Gulf of Trieste were investigated at various depths. In the surface layers morning and afternoon DOC peaks (up to 10 mg I-') were observed in 3 out of 4 diel cycles. Bacterial abundance remained fairly constant over the diel cycles; however, bacterial activity as measured by FDC showed pronounced peaks in late afternoon and dawn coinciding with the DOC maximum concentrations. The pycnocline layer exhibited DOC concentrations similar to those of the overlying waters. The frequency of dividing cells (FDC), however, remained high throughout the entire diel cycle. The observed pronounced diel variations in bacterial production were therefore largely restricted to the layers well above the pycnocline; bacterial production contributed less than 20 % to the overall diel production (500 to 1000 pg C 1-' d-') in the uppermost 5 m water body. Highest diel production was found in the pycnocline layer at the end of the phytoplankton bloom (June and July) probably reflecting the formation of nutrient-enriched microzones around decaying phytoplankton cells due to reduced sinking velocities in the pycnocline layer. -
Dispersion in the Open Ocean Seasonal Pycnocline at Scales of 1–10Km and 1–6 Days
FEBRUARY 2020 S U N D E R M E Y E R E T A L . 415 Dispersion in the Open Ocean Seasonal Pycnocline at Scales of 1–10km and 1–6 days a MILES A. SUNDERMEYER AND DANIEL A. BIRCH University of Massachusetts Dartmouth, North Dartmouth, Massachusetts JAMES R. LEDWELL Woods Hole Oceanographic Institution, Woods Hole, Massachusetts b MURRAY D. LEVINE, STEPHEN D. PIERCE, AND BRANDY T. KUEBEL CERVANTES Oregon State University, Corvallis, Oregon (Manuscript received 23 January 2019, in final form 14 November 2019) ABSTRACT Results are presented from two dye release experiments conducted in the seasonal thermocline of the 2 2 Sargasso Sea, one in a region of low horizontal strain rate (;10 6 s 1), the second in a region of intermediate 2 2 horizontal strain rate (;10 5 s 1). Both experiments lasted ;6 days, covering spatial scales of 1–10 and 1–50 km for the low and intermediate strain rate regimes, respectively. Diapycnal diffusivities estimated from 26 2 21 2 21 the two experiments were kz 5 (2–5) 3 10 m s , while isopycnal diffusivities were kH 5 (0.2–3) m s , with the range in kH being less a reflection of site-to-site variability, and more due to uncertainties in the background strain rate acting on the patch combined with uncertain time dependence. The Site I (low strain) experiment exhibited minimal stretching, elongating to approximately 10 km over 6 days while maintaining a width of ;5 km, and with a notable vertical tilt in the meridional direction. By contrast, the Site II (inter- mediate strain) experiment exhibited significant stretching, elongating to more than 50 km in length and advecting more than 150 km while still maintaining a width of order 3–5 km. -
Article Is Available Gen Availability
Hydrol. Earth Syst. Sci., 23, 1763–1777, 2019 https://doi.org/10.5194/hess-23-1763-2019 © Author(s) 2019. This work is distributed under the Creative Commons Attribution 4.0 License. Oxycline oscillations induced by internal waves in deep Lake Iseo Giulia Valerio1, Marco Pilotti1,4, Maximilian Peter Lau2,3, and Michael Hupfer2 1DICATAM, Università degli Studi di Brescia, via Branze 43, 25123 Brescia, Italy 2Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Müggelseedamm 310, 12587 Berlin, Germany 3Université du Quebec à Montréal (UQAM), Department of Biological Sciences, Montréal, QC H2X 3Y7, Canada 4Civil & Environmental Engineering Department, Tufts University, Medford, MA 02155, USA Correspondence: Giulia Valerio ([email protected]) Received: 22 October 2018 – Discussion started: 23 October 2018 Revised: 20 February 2019 – Accepted: 12 March 2019 – Published: 2 April 2019 Abstract. Lake Iseo is undergoing a dramatic deoxygena- 1 Introduction tion of the hypolimnion, representing an emblematic exam- ple among the deep lakes of the pre-alpine area that are, to a different extent, undergoing reduced deep-water mixing. In Physical processes occurring at the sediment–water inter- the anoxic deep waters, the release and accumulation of re- face of lakes crucially control the fluxes of chemical com- duced substances and phosphorus from the sediments are a pounds across this boundary (Imboden and Wuest, 1995) major concern. Because the hydrodynamics of this lake was with severe implications for water quality. In stratified shown to be dominated by internal waves, in this study we in- lakes, the boundary-layer turbulence is primarily caused by vestigated, for the first time, the role of these oscillatory mo- wind-driven internal wave motions (Imberger, 1998). -
Microbiology of Seamounts Is Still in Its Infancy
or collective redistirbution of any portion of this article by photocopy machine, reposting, or other means is permitted only with the approval of The approval portionthe ofwith any articlepermitted only photocopy by is of machine, reposting, this means or collective or other redistirbution This article has This been published in MOUNTAINS IN THE SEA Oceanography MICROBIOLOGY journal of The 23, Number 1, a quarterly , Volume OF SEAMOUNTS Common Patterns Observed in Community Structure O ceanography ceanography S BY DAVID EmERSON AND CRAIG L. MOYER ociety. © 2010 by The 2010 by O ceanography ceanography O ceanography ceanography ABSTRACT. Much interest has been generated by the discoveries of biodiversity InTRODUCTION S ociety. ociety. associated with seamounts. The volcanically active portion of these undersea Microbial life is remarkable for its resil- A mountains hosts a remarkably diverse range of unusual microbial habitats, from ience to extremes of temperature, pH, article for use and research. this copy in teaching to granted ll rights reserved. is Permission S ociety. ociety. black smokers rich in sulfur to cooler, diffuse, iron-rich hydrothermal vents. As and pressure, as well its ability to persist S such, seamounts potentially represent hotspots of microbial diversity, yet our and thrive using an amazing number or Th e [email protected] to: correspondence all end understanding of the microbiology of seamounts is still in its infancy. Here, we of organic or inorganic food sources. discuss recent work on the detection of seamount microbial communities and the Nowhere are these traits more evident observation that specific community groups may be indicative of specific geochemical than in the deep ocean.