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Population dynamics of Arctica islandica at Georges Bank (USA): an analysis of sex-based demographics
- Kathleen M. Hemeon, Eric N. Powell, Sara M. Pace, Theresa E. Redmond, Roger Mann
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- Journal:
- Journal of the Marine Biological Association of the United Kingdom / Volume 101 / Issue 7 / November 2021
- Published online by Cambridge University Press:
- 18 March 2022, pp. 1003-1018
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The ocean quahog, Arctica islandica, is a commercially important bivalve in the eastern USA but very little is known about the recruitment frequency and rebuilding capacity of this species. As the longest-living bivalve on Earth, A. islandica can achieve lifespans in excess of 200 y; however, age determinations are difficult to estimate and age variability at size is extreme. Objectives for this study included the creation of an extremely large age-composition dataset to constrain age at length variability, development of reliable age-length keys (ALK), and descriptions of sex-based population dynamics for the quasi-virgin A. islandica population at Georges Bank (GB) within the greater US Mid-Atlantic stock. Sexually dimorphic characteristics are clearly present, as females are larger than males within age classes and males tend to dominate the oldest age classes. A male represented the maximum age of 261 years and is older than the maximum age previously documented for this region. Sex-specific ALKs were robust and reliable but not interchangeable. This population had higher estimated natural mortality rates than presumed for other regions in the Mid-Atlantic, and females have the highest mortality rate. However, recruitment expansion was also occurring which would affect the age-frequency data used to derive mortality estimates and result in higher mortality. Age frequencies at GB suggest effective recruitment to the population each year since 1867 CE. Reduced recruitment periods are documented and likely attributed to fluctuating environmental conditions. Sex-based demographics are clearly divergent in regard to growth rate, maximum size, longevity and mortality rates.
Sex Differences in Endovascular Treatment for Stroke: A Population-based Analysis
- Charlotte Zerna, Edwin Rogers, Doreen M. Rabi, Andrew M. Demchuk, Noreen Kamal, Balraj Mann, Tom Jeerakathil, Brian Buck, Ashfaq Shuaib, Jeremy Rempel, Bijoy K. Menon, Mayank Goyal, Michael D. Hill
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- Journal:
- Canadian Journal of Neurological Sciences / Volume 48 / Issue 4 / July 2021
- Published online by Cambridge University Press:
- 21 October 2020, pp. 479-486
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Background:
Acute ischemic stroke may affect women and men differently. We aimed to evaluate sex differences in outcomes of endovascular treatment (EVT) for ischemic stroke due to large vessel occlusion in a population-based study in Alberta, Canada.
Methods and Results:Over a 3-year period (April 2015–March 2018), 576 patients fit the inclusion criteria of our study and constituted the EVT group of our analysis. The medical treatment group of the ESCAPE trial had 150 patients. Thus, our total sample size was 726. We captured outcomes in clinical routine using administrative data and a linked database methodology. The primary outcome of our study was home-time. Home-time refers to the number of days that the patient was back at their premorbid living situation without an increase in the level of care within 90 days of the index stroke event. In adjusted analysis, EVT was associated with an increase of 90-day home-time by an average of 6.08 (95% CI −2.74–14.89, p-value 0.177) days in women compared to an average of 11.20 (95% CI 1.94–20.46, p-value 0.018) days in men. Further analysis revealed that the association between EVT and 90-day home-time in women was confounded by age and onset-to-treatment time.
Conclusions:We found a nonsignificant nominal reduction of 90-day home-time gain for women compared to men in this province-wide population-based study of EVT for large vessel occlusion, which was only partially explained by confounding.
Growth and longevity of the Antarctic scallop Adamussium colbecki under annual and multiannual sea ice
- Kelly E. Cronin, Sally E. Walker, Roger Mann, Antonie S. Chute, M. Chase Long, Samuel S. Bowser
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- Journal:
- Antarctic Science / Volume 32 / Issue 6 / December 2020
- Published online by Cambridge University Press:
- 18 June 2020, pp. 466-475
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Ecosystem engineers such as the Antarctic scallop (Adamussium colbecki) shape marine communities. Thus, changes to their lifespan and growth could have far-reaching effects on other organisms. Sea ice is critical to polar marine ecosystem function, attenuating light and thereby affecting nutrient availability. Sea ice could therefore impact longevity and growth in polar bivalves unless temperature is the overriding factor. Here, we compare the longevity and growth of A. colbecki from two Antarctic sites: Explorers Cove and Bay of Sails, which differ by sea-ice cover, but share similar seawater temperatures, the coldest on Earth (-1.97°C). We hypothesize that scallops from the multiannual sea-ice site will have slower growth and greater longevity. We found maximum ages to be similar at both sites (18–19 years). Growth was slower, with higher inter-individual variability, under multiannual sea ice than under annual sea ice, which we attribute to patchier nutrient availability under multiannual sea ice. Contrary to expectations, A. colbecki growth, but not longevity, is affected by sea-ice duration when temperatures are comparable. Recent dramatic reductions in Antarctic sea ice and predicted temperature increases may irrevocably alter the life histories of this ecosystem engineer and other polar organisms.
Sex and site-specific trends in veined rapa whelk (Rapana venosa) tributyltin bioaccumulation: considerations for biomonitoring
- Juliana M. Harding, Michael A. Unger, E. Alex Jestel, Roger Mann
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- Journal:
- Journal of the Marine Biological Association of the United Kingdom / Volume 97 / Issue 7 / November 2017
- Published online by Cambridge University Press:
- 09 June 2016, pp. 1495-1504
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The imposition of male sexual characteristics onto the female (imposex) is present in wild populations of the non-native veined rapa whelk (Rapana venosa) in Chesapeake Bay, USA but does not appear to compromise reproductive function. Cultured whelks were used to test two hypotheses: (1) Observed imposex metrics will be similar to tributyltin (TBT) water concentrations at each of three sites; (2) Male and imposex/female whelks from the same site will have similar TBT body burdens. Cultured 2-year-old whelks were transplanted to three field sites in the York River, USA at the onset of their second reproductive season. Transplant site mean TBT water concentrations ranged from 1.4 ± 0.77 to 64.2 ± 57.8 ng l−1. Imposex incidence was 100% after 28 weeks with an observed M:F:IF ratio of 81:0:92 across all sites. Imposex stages (median vas deferens scale index = 4) and reproductive output were similar across sites. The imposex severity (IS = penis length/shell length) increased with increasing TBT concentrations. The relative penis length (RPLI) and relative penis size (RPSI) indices were positively related to site-specific TBT levels. Male whelks accumulated significantly higher TBT concentrations than female whelks at the site with the highest TBT concentration. Mean TBT concentrations in whelk egg capsules were significantly higher than concentrations in male or female whelk tissue. Egg capsule deposition provides a depuration mechanism for female whelks to reduce body burden of lipophilic TBT. Sex, season and reproductive status should be considered when using gastropod bioaccumulation to monitor TBT effects.
The allometry of oysters: spatial and temporal variation in the length–biomass relationships for Crassostrea virginica
- Eric N. Powell, Roger Mann, Kathryn A. Ashton-Alcox, Yungkul Kim, David Bushek
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- Journal:
- Journal of the Marine Biological Association of the United Kingdom / Volume 96 / Issue 5 / August 2016
- Published online by Cambridge University Press:
- 05 June 2015, pp. 1127-1144
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We examine the relationship of biomass B and length L in the eastern oyster Crassostrea virginica by focusing on the scaling exponent b in the allometric equation B = aLb using four datasets: Delaware Bay, Chesapeake Bay, Galveston Bay and a regionally extensive compilation from the NOAA Mussel Watch Program. The average value of the scaling exponent in Delaware Bay and Chesapeake Bay is about 2. For Galveston Bay, the value is distinctly higher, near 2.6. Over all Mussel Watch sites, the value is again near 2. Within Delaware Bay, the salinity gradient exerts an important effect. Shells are longer for their meat weight at lower salinities. The range of scaling exponents revealed by Mussel Watch data is exceedingly large (b < 1 to >3). Scaling exponents below 2.5 are unusual in bivalves. Among bivalves, only other oyster taxa have comparably low scaling exponents averaging near 2. We propose that oyster biomass routinely scales nearer the square of the length rather than the cube and that this is a constraint imposed by the exigency of carbonate production for reef maintenance and accretion in the face of high rates of taphonomic degradation. The adaptation as a reef builder requires the formation of carbonate that rapidly breaks down, thus requiring that carbonate produced be maximized. A biomass-to-length scaling exponent of 2 provides a mechanism to maximize shell production relative to biomass, while at the same time providing maximum surface area for the all-important settling of oyster spat to maintain the population.
Contributors
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- By Mitchell Aboulafia, Frederick Adams, Marilyn McCord Adams, Robert M. Adams, Laird Addis, James W. Allard, David Allison, William P. Alston, Karl Ameriks, C. Anthony Anderson, David Leech Anderson, Lanier Anderson, Roger Ariew, David Armstrong, Denis G. Arnold, E. J. Ashworth, Margaret Atherton, Robin Attfield, Bruce Aune, Edward Wilson Averill, Jody Azzouni, Kent Bach, Andrew Bailey, Lynne Rudder Baker, Thomas R. Baldwin, Jon Barwise, George Bealer, William Bechtel, Lawrence C. Becker, Mark A. Bedau, Ernst Behler, José A. Benardete, Ermanno Bencivenga, Jan Berg, Michael Bergmann, Robert L. Bernasconi, Sven Bernecker, Bernard Berofsky, Rod Bertolet, Charles J. Beyer, Christian Beyer, Joseph Bien, Joseph Bien, Peg Birmingham, Ivan Boh, James Bohman, Daniel Bonevac, Laurence BonJour, William J. Bouwsma, Raymond D. Bradley, Myles Brand, Richard B. Brandt, Michael E. Bratman, Stephen E. Braude, Daniel Breazeale, Angela Breitenbach, Jason Bridges, David O. Brink, Gordon G. Brittan, Justin Broackes, Dan W. Brock, Aaron Bronfman, Jeffrey E. Brower, Bartosz Brozek, Anthony Brueckner, Jeffrey Bub, Lara Buchak, Otavio Bueno, Ann E. Bumpus, Robert W. Burch, John Burgess, Arthur W. Burks, Panayot Butchvarov, Robert E. Butts, Marina Bykova, Patrick Byrne, David Carr, Noël Carroll, Edward S. Casey, Victor Caston, Victor Caston, Albert Casullo, Robert L. Causey, Alan K. L. Chan, Ruth Chang, Deen K. Chatterjee, Andrew Chignell, Roderick M. Chisholm, Kelly J. Clark, E. J. Coffman, Robin Collins, Brian P. Copenhaver, John Corcoran, John Cottingham, Roger Crisp, Frederick J. Crosson, Antonio S. Cua, Phillip D. Cummins, Martin Curd, Adam Cureton, Andrew Cutrofello, Stephen Darwall, Paul Sheldon Davies, Wayne A. Davis, Timothy Joseph Day, Claudio de Almeida, Mario De Caro, Mario De Caro, John Deigh, C. F. Delaney, Daniel C. Dennett, Michael R. DePaul, Michael Detlefsen, Daniel Trent Devereux, Philip E. Devine, John M. Dillon, Martin C. Dillon, Robert DiSalle, Mary Domski, Alan Donagan, Paul Draper, Fred Dretske, Mircea Dumitru, Wilhelm Dupré, Gerald Dworkin, John Earman, Ellery Eells, Catherine Z. Elgin, Berent Enç, Ronald P. Endicott, Edward Erwin, John Etchemendy, C. Stephen Evans, Susan L. Feagin, Solomon Feferman, Richard Feldman, Arthur Fine, Maurice A. Finocchiaro, William FitzPatrick, Richard E. Flathman, Gvozden Flego, Richard Foley, Graeme Forbes, Rainer Forst, Malcolm R. Forster, Daniel Fouke, Patrick Francken, Samuel Freeman, Elizabeth Fricker, Miranda Fricker, Michael Friedman, Michael Fuerstein, Richard A. Fumerton, Alan Gabbey, Pieranna Garavaso, Daniel Garber, Jorge L. A. Garcia, Robert K. Garcia, Don Garrett, Philip Gasper, Gerald Gaus, Berys Gaut, Bernard Gert, Roger F. Gibson, Cody Gilmore, Carl Ginet, Alan H. Goldman, Alvin I. Goldman, Alfonso Gömez-Lobo, Lenn E. Goodman, Robert M. Gordon, Stefan Gosepath, Jorge J. E. Gracia, Daniel W. Graham, George A. Graham, Peter J. Graham, Richard E. Grandy, I. Grattan-Guinness, John Greco, Philip T. Grier, Nicholas Griffin, Nicholas Griffin, David A. Griffiths, Paul J. Griffiths, Stephen R. Grimm, Charles L. Griswold, Charles B. Guignon, Pete A. Y. Gunter, Dimitri Gutas, Gary Gutting, Paul Guyer, Kwame Gyekye, Oscar A. Haac, Raul Hakli, Raul Hakli, Michael Hallett, Edward C. Halper, Jean Hampton, R. James Hankinson, K. R. Hanley, Russell Hardin, Robert M. Harnish, William Harper, David Harrah, Kevin Hart, Ali Hasan, William Hasker, John Haugeland, Roger Hausheer, William Heald, Peter Heath, Richard Heck, John F. Heil, Vincent F. Hendricks, Stephen Hetherington, Francis Heylighen, Kathleen Marie Higgins, Risto Hilpinen, Harold T. Hodes, Joshua Hoffman, Alan Holland, Robert L. Holmes, Richard Holton, Brad W. Hooker, Terence E. Horgan, Tamara Horowitz, Paul Horwich, Vittorio Hösle, Paul Hoβfeld, Daniel Howard-Snyder, Frances Howard-Snyder, Anne Hudson, Deal W. Hudson, Carl A. Huffman, David L. Hull, Patricia Huntington, Thomas Hurka, Paul Hurley, Rosalind Hursthouse, Guillermo Hurtado, Ronald E. Hustwit, Sarah Hutton, Jonathan Jenkins Ichikawa, Harry A. Ide, David Ingram, Philip J. Ivanhoe, Alfred L. Ivry, Frank Jackson, Dale Jacquette, Joseph Jedwab, Richard Jeffrey, David Alan Johnson, Edward Johnson, Mark D. Jordan, Richard Joyce, Hwa Yol Jung, Robert Hillary Kane, Tomis Kapitan, Jacquelyn Ann K. Kegley, James A. Keller, Ralph Kennedy, Sergei Khoruzhii, Jaegwon Kim, Yersu Kim, Nathan L. King, Patricia Kitcher, Peter D. Klein, E. D. Klemke, Virginia Klenk, George L. Kline, Christian Klotz, Simo Knuuttila, Joseph J. Kockelmans, Konstantin Kolenda, Sebastian Tomasz Kołodziejczyk, Isaac Kramnick, Richard Kraut, Fred Kroon, Manfred Kuehn, Steven T. Kuhn, Henry E. Kyburg, John Lachs, Jennifer Lackey, Stephen E. Lahey, Andrea Lavazza, Thomas H. Leahey, Joo Heung Lee, Keith Lehrer, Dorothy Leland, Noah M. Lemos, Ernest LePore, Sarah-Jane Leslie, Isaac Levi, Andrew Levine, Alan E. Lewis, Daniel E. Little, Shu-hsien Liu, Shu-hsien Liu, Alan K. L. Chan, Brian Loar, Lawrence B. Lombard, John Longeway, Dominic McIver Lopes, Michael J. Loux, E. J. Lowe, Steven Luper, Eugene C. Luschei, William G. Lycan, David Lyons, David Macarthur, Danielle Macbeth, Scott MacDonald, Jacob L. Mackey, Louis H. Mackey, Penelope Mackie, Edward H. Madden, Penelope Maddy, G. B. Madison, Bernd Magnus, Pekka Mäkelä, Rudolf A. Makkreel, David Manley, William E. Mann (W.E.M.), Vladimir Marchenkov, Peter Markie, Jean-Pierre Marquis, Ausonio Marras, Mike W. Martin, A. P. Martinich, William L. McBride, David McCabe, Storrs McCall, Hugh J. McCann, Robert N. McCauley, John J. McDermott, Sarah McGrath, Ralph McInerny, Daniel J. McKaughan, Thomas McKay, Michael McKinsey, Brian P. McLaughlin, Ernan McMullin, Anthonie Meijers, Jack W. Meiland, William Jason Melanson, Alfred R. Mele, Joseph R. Mendola, Christopher Menzel, Michael J. Meyer, Christian B. Miller, David W. Miller, Peter Millican, Robert N. Minor, Phillip Mitsis, James A. Montmarquet, Michael S. Moore, Tim Moore, Benjamin Morison, Donald R. Morrison, Stephen J. Morse, Paul K. Moser, Alexander P. D. Mourelatos, Ian Mueller, James Bernard Murphy, Mark C. Murphy, Steven Nadler, Jan Narveson, Alan Nelson, Jerome Neu, Samuel Newlands, Kai Nielsen, Ilkka Niiniluoto, Carlos G. Noreña, Calvin G. Normore, David Fate Norton, Nikolaj Nottelmann, Donald Nute, David S. Oderberg, Steve Odin, Michael O’Rourke, Willard G. Oxtoby, Heinz Paetzold, George S. Pappas, Anthony J. Parel, Lydia Patton, R. P. Peerenboom, Francis Jeffry Pelletier, Adriaan T. Peperzak, Derk Pereboom, Jaroslav Peregrin, Glen Pettigrove, Philip Pettit, Edmund L. Pincoffs, Andrew Pinsent, Robert B. Pippin, Alvin Plantinga, Louis P. Pojman, Richard H. Popkin, John F. Post, Carl J. Posy, William J. Prior, Richard Purtill, Michael Quante, Philip L. Quinn, Philip L. Quinn, Elizabeth S. Radcliffe, Diana Raffman, Gerard Raulet, Stephen L. Read, Andrews Reath, Andrew Reisner, Nicholas Rescher, Henry S. Richardson, Robert C. Richardson, Thomas Ricketts, Wayne D. Riggs, Mark Roberts, Robert C. Roberts, Luke Robinson, Alexander Rosenberg, Gary Rosenkranz, Bernice Glatzer Rosenthal, Adina L. Roskies, William L. Rowe, T. M. Rudavsky, Michael Ruse, Bruce Russell, Lilly-Marlene Russow, Dan Ryder, R. M. Sainsbury, Joseph Salerno, Nathan Salmon, Wesley C. Salmon, Constantine Sandis, David H. Sanford, Marco Santambrogio, David Sapire, Ruth A. Saunders, Geoffrey Sayre-McCord, Charles Sayward, James P. Scanlan, Richard Schacht, Tamar Schapiro, Frederick F. Schmitt, Jerome B. Schneewind, Calvin O. Schrag, Alan D. Schrift, George F. Schumm, Jean-Loup Seban, David N. Sedley, Kenneth Seeskin, Krister Segerberg, Charlene Haddock Seigfried, Dennis M. Senchuk, James F. Sennett, William Lad Sessions, Stewart Shapiro, Tommie Shelby, Donald W. Sherburne, Christopher Shields, Roger A. Shiner, Sydney Shoemaker, Robert K. Shope, Kwong-loi Shun, Wilfried Sieg, A. John Simmons, Robert L. Simon, Marcus G. Singer, Georgette Sinkler, Walter Sinnott-Armstrong, Matti T. Sintonen, Lawrence Sklar, Brian Skyrms, Robert C. Sleigh, Michael Anthony Slote, Hans Sluga, Barry Smith, Michael Smith, Robin Smith, Robert Sokolowski, Robert C. Solomon, Marta Soniewicka, Philip Soper, Ernest Sosa, Nicholas Southwood, Paul Vincent Spade, T. L. S. Sprigge, Eric O. Springsted, George J. Stack, Rebecca Stangl, Jason Stanley, Florian Steinberger, Sören Stenlund, Christopher Stephens, James P. Sterba, Josef Stern, Matthias Steup, M. A. Stewart, Leopold Stubenberg, Edith Dudley Sulla, Frederick Suppe, Jere Paul Surber, David George Sussman, Sigrún Svavarsdóttir, Zeno G. Swijtink, Richard Swinburne, Charles C. Taliaferro, Robert B. Talisse, John Tasioulas, Paul Teller, Larry S. Temkin, Mark Textor, H. S. Thayer, Peter Thielke, Alan Thomas, Amie L. Thomasson, Katherine Thomson-Jones, Joshua C. Thurow, Vzalerie Tiberius, Terrence N. Tice, Paul Tidman, Mark C. Timmons, William Tolhurst, James E. Tomberlin, Rosemarie Tong, Lawrence Torcello, Kelly Trogdon, J. D. Trout, Robert E. Tully, Raimo Tuomela, John Turri, Martin M. Tweedale, Thomas Uebel, Jennifer Uleman, James Van Cleve, Harry van der Linden, Peter van Inwagen, Bryan W. Van Norden, René van Woudenberg, Donald Phillip Verene, Samantha Vice, Thomas Vinci, Donald Wayne Viney, Barbara Von Eckardt, Peter B. M. Vranas, Steven J. Wagner, William J. Wainwright, Paul E. Walker, Robert E. Wall, Craig Walton, Douglas Walton, Eric Watkins, Richard A. Watson, Michael V. Wedin, Rudolph H. Weingartner, Paul Weirich, Paul J. Weithman, Carl Wellman, Howard Wettstein, Samuel C. Wheeler, Stephen A. White, Jennifer Whiting, Edward R. Wierenga, Michael Williams, Fred Wilson, W. Kent Wilson, Kenneth P. Winkler, John F. Wippel, Jan Woleński, Allan B. Wolter, Nicholas P. Wolterstorff, Rega Wood, W. Jay Wood, Paul Woodruff, Alison Wylie, Gideon Yaffe, Takashi Yagisawa, Yutaka Yamamoto, Keith E. Yandell, Xiaomei Yang, Dean Zimmerman, Günter Zoller, Catherine Zuckert, Michael Zuckert, Jack A. Zupko (J.A.Z.)
- Edited by Robert Audi, University of Notre Dame, Indiana
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- The Cambridge Dictionary of Philosophy
- Published online:
- 05 August 2015
- Print publication:
- 27 April 2015, pp ix-xxx
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Variations in eastern oyster (Crassostrea virginica) sex-ratios from three Virginia estuaries: protandry, growth and demographics
- Juliana M. Harding, Eric N. Powell, Roger Mann, Melissa J. Southworth
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- Journal of the Marine Biological Association of the United Kingdom / Volume 93 / Issue 2 / March 2013
- Published online by Cambridge University Press:
- 01 May 2012, pp. 519-531
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Oyster population reproductive capacity and dynamics are controlled at the most basic level by the observed sex-ratios. Since oysters are sequential, protandric hermaphrodites the population sex-ratio is related to the demographics (shell length, age, and biomass). Oysters were collected from June through to August 2008 at twelve bars in the James, Rappahannock and Great Wicomico Rivers, Virginia, USA. Bars were aggregated into five groups on the basis of similar age–length relationships. Sex-ratios (fraction female), age–length, and biomass–length relationships were determined for each group. The fraction female increased within increasing shell length, age, and biomass at all sites. Simultaneous hermaphrodites were rarely observed. Group specific differences in shell length (SL, mm) and age (yr) for the timing of the protandric shift were observed with the earliest shift from male to female occurring at ~60 mm SL and ~1.6 yr. The proportion of females observed in the larger or older individuals was at least 70–80%. Sex-ratios from summer 2008 were used to develop sex–length, sex–age, and sex–biomass keys that were applied to autumn-survey data from 2006, 2007, 2008 and 2009. In these years, sex-ratios by shell length and age were strongly biased towards males while the sex-ratio by biomass was strongly biased towards females. Disease mortality compounds natural and fishing mortality resulting in age/size specific cropping yielding truncated population demographics and an earlier protandric shift in populations on the extremes of the range examined. Regardless of location, market (>76 mm SL) oysters are predominantly female.
Demonstration of a right circumflex aortic arch with aberrant left subclavian artery and a hypoplastic arch by multi-detector computer tomography
- Wesley Mann, Roger Shifrin, Arun Chandran
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- Cardiology in the Young / Volume 21 / Issue 3 / June 2011
- Published online by Cambridge University Press:
- 28 January 2011, pp. 341-342
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Some biochemical and physiological aspects of growth and gametogenesis in Crassostrea gigas and Ostrea edulis grown at sustained elevated temperatures*
- Roger Mann
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- Journal of the Marine Biological Association of the United Kingdom / Volume 59 / Issue 1 / February 1979
- Published online by Cambridge University Press:
- 11 May 2009, pp. 95-110
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Crassostrea gigas (Thunberg) and Ostrea edulis L. were grown at sustained temperatures of 12°, 15°, 18° and 21°C for a period of 19 weeks. Regular assays of weight specific ammonia excretion rate were made, following which animals were sacrificed for estimation of dry meat weight, dry shell weight, biochemical composition (percentage carbon, nitrogen, carbohydrate, ash) and gonadal development (histological assessment). Crassostrea gigas grew from an intial live weight of 5·2 g to values of 23·5, 28·2, 34·6 and 38·7 g at 120, 150, 180 and 21 °C respectively.