Role of the Gut as a Nutrient-Storage Organ in the Purple Sea Urchin (Strongylocentrotus purpuratus)
1966; University of Chicago Press; Volume: 39; Issue: 4 Linguagem: Inglês
10.1086/physzool.39.4.30152352
ISSN1937-4267
AutoresJean M. Lawrence, A. L. Lawrence, Arthur C. Giese,
Tópico(s)Marine and coastal plant biology
ResumoPrevious articleNext article No AccessRole of the Gut as a Nutrient-Storage Organ in the Purple Sea Urchin (Strongylocentrotus purpuratus)J. M. Lawrence, A. L. Lawrence, and A. C. GieseJ. M. Lawrence Search for more articles by this author , A. L. Lawrence Search for more articles by this author , and A. C. Giese Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by Volume 39, Number 4Oct., 1966 Article DOIhttps://doi.org/10.1086/physzool.39.4.30152352 Views: 5Total views on this site Citations: 55Citations are reported from Crossref Journal History This article was published in Physiological Zoology (1928-1998), which is continued by Physiological and Biochemical Zoology (1999-present). Copyright 1966 University of ChicagoPDF download Crossref reports the following articles citing this article:Fletcher Warren-Myers, Stephen E. Swearer, David S. Francis, Giovanni M. Turchini, Kathy Overton, Tim Dempster Algal supplements in formulated feeds: Effects on sea urchin gonad quality, Aquaculture 548 (Feb 2022): 737673.https://doi.org/10.1016/j.aquaculture.2021.737673Roberto Anedda, Silvia Siliani, Riccardo Melis, Barbara Loi, Maura Baroli Lipid metabolism of sea urchin Paracentrotus lividus in two contrasting natural habitats, Scientific Reports 11, no.11 (Jul 2021).https://doi.org/10.1038/s41598-021-93669-9Wenping Feng, Nobuyasu Nakabayashi, Eri Inomata, Masakazu N. Aoki, Yukio Agatsuma Sexually unbalanced gonad development and nutrition of the newly range-extended sea urchin Heliocidaris crassispina in the northeastern Honshu, Japan, Estuarine, Coastal and Shelf Science 249 (Feb 2021): 107120.https://doi.org/10.1016/j.ecss.2020.107120Margot Arnould-Pétré, Charlène Guillaumot, Bruno Danis, Jean-Pierre Féral, Thomas Saucède Individual-based model of population dynamics in a sea urchin of the Kerguelen Plateau (Southern Ocean), Abatus cordatus, under changing environmental conditions, Ecological Modelling 440 (Jan 2021): 109352.https://doi.org/10.1016/j.ecolmodel.2020.109352E. Yeruham, M. Shpigel, A. Abelson, G. Rilov Ocean warming and tropical invaders erode the performance of a key herbivore, Ecology 101, no.22 (Dec 2019).https://doi.org/10.1002/ecy.2925Mark D. Cyrus, John J. Bolton, Brett M. Macey The use of stable isotope ratios δ 13 C and δ 15 N to track the incorporation of Ulva and other important dietary ingredients into the gonads of the sea urchin Tripneustes gratilla, Aquaculture Nutrition 26, no.11 (Sep 2019): 174–185.https://doi.org/10.1111/anu.12979Mickie L. Powell, Adam G. Marsh, Stephen A. Watts Biochemical and energy requirements of gonad development in regular sea urchins, (Jan 2020): 51–64.https://doi.org/10.1016/B978-0-12-819570-3.00004-4Stephen A. Watts, Addison L. Lawrence, John M. Lawrence Nutrition, (Jan 2020): 191–208.https://doi.org/10.1016/B978-0-12-819570-3.00010-XAngela Stevenson, Fraser J.G. Mitchell Evidence of nutrient partitioning in coexisting deep-sea echinoids, and seasonal dietary shifts in seasonal breeders: Perspectives from stable isotope analyses, Progress in Oceanography 141 (Feb 2016): 44–59.https://doi.org/10.1016/j.pocean.2015.12.004Victoria K. Gibbs, Laura E. Heflin, Warren T. Jones, Mickie L. Powell, Addison L. Lawrence, Robert Makowsky, Stephen A. Watts Optimizing dietary levels of menhaden and soybean oils and soybean lecithin for pre-gonadal somatic growth in juveniles of the sea urchin Lytechinus variegatus, Aquaculture 446 (Sep 2015): 198–205.https://doi.org/10.1016/j.aquaculture.2015.05.013Roberta C. Challener, Stephen A. Watts, James B. McClintock Effects of hypercapnia on aspects of feeding, nutrition, and growth in the edible sea urchin Lytechinus variegatus held in culture, Marine and Freshwater Behaviour and Physiology 47, no.11 (Feb 2014): 41–62.https://doi.org/10.1080/10236244.2013.875273Victoria K. Gibbs, Mickie L. Powell, Hugh S. Hammer, Warren T. Jones, Stephen A. Watts, Addison L. Lawrence, John M. Lawrence Evaluation of the Effects of Menhaden Oil and Soybean Oil Levels in Purified Diets on Growth and Gonad Production in Adult Sea Urchin Lytechinus variegatus, North American Journal of Aquaculture 75, no.22 (Apr 2013): 277–284.https://doi.org/10.1080/15222055.2012.741559Adam G. Marsh, Mickie L. Powell, Stephen A. Watts Biochemical and Energy Requirements of Gonad Development, (Jan 2013): 45–57.https://doi.org/10.1016/B978-0-12-396491-5.00004-6Stephen A. Watts, Addison L. Lawrence, John M. Lawrence Nutrition, (Jan 2013): 155–169.https://doi.org/10.1016/B978-0-12-396491-5.00010-1Carissa M. Graydon, Shawn M.C. Robinson, Robert E Scheibling, J. Andrew Cooper Canthaxanthin as a potential tracer of salmon feed in mussels (Mytilus spp.) and sea urchins (Strongylocentrotus droebachiensis), Aquaculture 366-367 (Nov 2012): 90–97.https://doi.org/10.1016/j.aquaculture.2012.08.043Victoria K. Gibbs, Stephen A. Watts, Addison L. Lawrence, John M. Lawrence Dietary phospholipids affect growth and production of juvenile sea urchin Lytechinus variegatus, Aquaculture 292, no.1-21-2 (Jul 2009): 95–103.https://doi.org/10.1016/j.aquaculture.2009.03.046Analía F. Pérez, Elba Morriconi, Claudia Boy, Jorge Calvo Seasonal changes in energy allocation to somatic and reproductive body components of the common cold temperature sea urchin Loxechinus albus in a Sub-Antarctic environment, Polar Biology 31, no.44 (Oct 2007): 443–449.https://doi.org/10.1007/s00300-007-0370-3Hugh Hammer, Brenda Hammer, Stephen Watts, Addison Lawrence, John Lawrence The effect of dietary protein and carbohydrate concentration on the biochemical composition and gametogenic condition of the sea urchin Lytechinus variegatus, Journal of Experimental Marine Biology and Ecology 334, no.11 (Jun 2006): 109–121.https://doi.org/10.1016/j.jembe.2006.01.015T. Unuma, T. Yamamoto, T. Akiyama, M. Shiraishi, H. Ohta Quantitative changes in yolk protein and other components in the ovary and testis of the sea urchin Pseudocentrotus depressus, Journal of Experimental Biology 206, no.22 (Jan 2003): 365–372.https://doi.org/10.1242/jeb.00102John M Lawrence, Larry R Plank, Addison L Lawrence The effect of feeding frequency on consumption of food, absorption efficiency, and gonad production in the sea urchin Lytechinus variegatus, Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 134, no.11 (Jan 2003): 69–75.https://doi.org/10.1016/S1095-6433(02)00222-2S.M.C Robinson, J.D Castell, E.J Kennedy Developing suitable colour in the gonads of cultured green sea urchins (Strongylocentrotus droebachiensis), Aquaculture 206, no.3-43-4 (Apr 2002): 289–303.https://doi.org/10.1016/S0044-8486(01)00723-2Susan C. McBride, John M. Lawrence, Addison L. Lawrence, Timothy J. Mulligan Ingestion, Absorption, and Gonad Production of Adult Strongylocentrotus franciscanus Fed Different Rations of a Prepared Diet, Journal of the World Aquaculture Society 30, no.33 (Sep 1999): 364–370.https://doi.org/10.1111/j.1749-7345.1999.tb00687.xM.T Lares, C.M Pomory Use of body components during starvation in Lytechinus variegatus (Lamarck) (Echinodermata: Echinoidea), Journal of Experimental Marine Biology and Ecology 225, no.11 (Jul 1998): 99–106.https://doi.org/10.1016/S0022-0981(97)00216-5C. Fernandez Seasonal Changes in the Biochemical Composition of the Edible Sea Urchin Paracentrotus lividus Echinodermata: Echinoidea in a Lagoonal Environment, Marine Ecology 19, no.11 (Mar 1998): 1–11.https://doi.org/10.1111/j.1439-0485.1998.tb00449.xKarin Hollertz, Mattias Sköld, Rutger Rosenberg Interactions between two deposit feeding echinoderms: the spatangoid Brissopsis lyrifera (Forbes) and the ophiuroid Amphiura chiajei Forbes, (Jan 1998): 287–295.https://doi.org/10.1007/978-94-017-2864-5_23Catherine Fernandez Effect of diet on the biochemical composition of Paracentrotus lividus (Echinodermata: Echinoidea) under natural and rearing conditions (effect of diet on biochemical composition of urchins), Comparative Biochemistry and Physiology Part A: Physiology 118, no.44 (Dec 1997): 1377–1384.https://doi.org/10.1016/S0300-9629(97)00221-1C. D. Bishop, S. A. Watts Biochemical and morphometric study of growth in the stomach and intestine of the echinoid Lytechinus variegatus (Echinodermata), Marine Biology 114, no.33 (Nov 1992): 459–467.https://doi.org/10.1007/BF00350038C.A. Comely, A.D. Ansell The reproductive cycle of Echinus esculentus L. on the Scottish west coast, Estuarine, Coastal and Shelf Science 29, no.44 (Oct 1989): 385–407.https://doi.org/10.1016/0272-7714(89)90035-8JOHN M. LAWRENCE Echinodermata, (Jan 1987): 229–321.https://doi.org/10.1016/B978-0-12-544792-8.50009-7Y. Boivin, D. Larrivée, J. H. Himmelman Reproductive cycle of the subarctic brooding asteroid Leptasterias polaris, Marine Biology 92, no.33 (Aug 1986): 329–337.https://doi.org/10.1007/BF00392673D. Nichols, G. M. Bishop, A. A. T. Sime Reproductive and Nutritional Periodicities in Populations of the European Sea-Urchin, Echinus Esculentus (Echinodermata: Echinoidea) from the English Channel, Journal of the Marine Biological Association of the United Kingdom 65, no.11 (May 2009): 203–220.https://doi.org/10.1017/S0025315400060914J.-P. F�ral Effect of short-term starvation on the biochemical composition of the apodous holothurian Leptosynapta galliennei (Echinodermata): possible role of dissolved organic material as an energy source, Marine Biology 86, no.33 (Jan 1985): 297–306.https://doi.org/10.1007/BF00397516A. Grant, P. A. Tyler The analysis of data in studies of invertebrate reproduction. I. Introduction and statistical analysis of gonad indices and maturity indices, International Journal of Invertebrate Reproduction 6, no.5-65-6 (Dec 1983): 259–269.https://doi.org/10.1080/01651269.1983.10510052P. Magniez Reproductive cycle of the brooding echinoid Abatus cordatus (Echinodermata) in Kerguelen (Antarctic Ocean): changes in the organ indices, biochemical composition and caloric content of the gonads, Marine Biology 74, no.11 (Jan 1983): 55–64.https://doi.org/10.1007/BF00394275John M. Lawrence, Alain Guille Organic composition of tropical, polar and temperate-water echinoderms, Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 72, no.22 (Jan 1982): 283–287.https://doi.org/10.1016/0305-0491(82)90047-5Robert D. Burke Structure of the digestive tract of the pluteus larva of Dendraster excentricus (Echinodermata: Echinoida), Zoomorphology 98, no.33 (Nov 1981): 209–225.https://doi.org/10.1007/BF00312050Jacqueline M. Lane, John M. Lawrence Seasonal changes in caloric composition of gonad and whole animal of the sand dollar, Mellita quinquiesperforata (Leske), Comparative Biochemistry and Physiology Part A: Physiology 70, no.44 (Jan 1981): 607–609.https://doi.org/10.1016/0300-9629(81)92585-8L. Fenaux, G. Malara, C. Cellario, R. Charra, I. Palazzoli Évolution des constituants biochimiques des principaux compartiments de l'oursin Arbacia lixula (L.) au cours d'un cycle sexuel et effets d'un jeûne de courte durée au cours de la maturation sexuelle, Journal of Experimental Marine Biology and Ecology 28, no.11 (Jun 1977): 17–30.https://doi.org/10.1016/0022-0981(77)90059-4Joan Rattenbury Marsden Classes of lipid in two polychaetes, an echiuroid and a sipunculid from the coast of Kenya, East Africa, Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 53, no.22 (Jan 1976): 225–229.https://doi.org/10.1016/0305-0491(76)90040-7Mary Griffiths, Pamela Perrott Seasonal changes in the carotenoids of the sea urchin Strongylocentrotus dröbachiensis, Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 55, no.33 (Jan 1976): 435–441.https://doi.org/10.1016/0305-0491(76)90317-5L. Fenaux, G. Malara, R. Charra Effets d'un je�ne de courte dur�e sur les principaux constituants biochimiques de l'oursin Arbacia lixula. I. Stade de repos sexuel, Marine Biology 30, no.33 (Jan 1975): 239–244.https://doi.org/10.1007/BF00390746W. Ross Ellington, J.M. Lawrence Seasonal temperature characteristics of supernatant malic dehydrogenase of adult and juvenile Mellita quinquiesperforata (Echinodermata: Echinoidea), Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 48, no.11 (May 1974): 107–115.https://doi.org/10.1016/0305-0491(74)90046-7William V Allen Interorgan transport of lipids in the purple sea urchin, Strongylocentrotus purpuratus, Comparative Biochemistry and Physiology Part A: Physiology 47, no.44 (Apr 1974): 1297–1311.https://doi.org/10.1016/0300-9629(74)90104-2Arthur C. Giese, John S. Pearse INTRODUCTION: GENERAL PRINCIPLES, (Jan 1974): 1–49.https://doi.org/10.1016/B978-0-12-282501-9.50006-5W.Ross Ellington, J.M. Lawrence Malic and lactic dehydrogenase activities and ratios in regular and irregular echinoids (Echinodermata), Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 45, no.44 (Aug 1973): 727–730.https://doi.org/10.1016/0305-0491(73)90133-8John M. Lawrence Level, content, and caloric equivalents of the lipid, carbohydrate, and protein in the body components of Luidia clathrata (echinodermata: asteroidea: platyasterida) in Tampa bay, Journal of Experimental Marine Biology and Ecology 11, no.33 (May 1973): 263–274.https://doi.org/10.1016/0022-0981(73)90026-9Prudence Talbot, Wallis H. Clark, Addison L. Lawrence Fine structure of the midgut epithelium in the developing brown shrimp,Penaeus aztecus, Journal of Morphology 138, no.44 (Dec 1972): 467–485.https://doi.org/10.1002/jmor.1051380407Jacqueline E. Moss, John M. Lawrence Changes in carbohydrate, lipid, and protein levels with age and season in the sand dollar Mellita Quinquiesperforata, Journal of Experimental Marine Biology and Ecology 8, no.33 (May 1972): 225–239.https://doi.org/10.1016/0022-0981(72)90062-7 REFERENCES, (Jan 1972): 200–240.https://doi.org/10.1016/B978-0-08-016991-0.50019-2William B. Stickle The metabolic effects of starving Thais lamellosa immediately after spawning, Comparative Biochemistry and Physiology Part A: Physiology 40, no.33 (Nov 1971): 627–634.https://doi.org/10.1016/0300-9629(71)90247-7D. M. Holdich Changes in physiology, structure and histochemistry occurring during the life-history of the sexually dimorphic isopod Dynamene bidentata (Crustacea: Peracarida), Marine Biology 8, no.11 (Jan 1971): 35–47.https://doi.org/10.1007/BF00349343Philip Doezema, John H Phillips Glycogen storage and synthesis in the gut of the purple sea urchin, Strongylocentrotus purpuratus, Comparative Biochemistry and Physiology 34, no.33 (Jun 1970): 691–697.https://doi.org/10.1016/0010-406X(70)90294-XPhilip Doezema Carbohydrates and Carbohydrate Metabolism of Echinoderms, (Jan 1969): 101–122.https://doi.org/10.1016/B978-0-12-395536-4.50011-6U.H.M. Fagerlund Lipid Metabolism, (Jan 1969): 123–134.https://doi.org/10.1016/B978-0-12-395536-4.50012-8S. Krishnan Histochemical studies on reproductive and nutritional cycles of the holothurian, Holothuria scabra, Marine Biology 2, no.11 (Oct 1968): 54–65.https://doi.org/10.1007/BF00351639
Referência(s)