Factors Influencing the Initiation of Blooms of the Raphidophyte Heterosigma akashiwo and the Diatom Skeletonema costatum in a Port in Japan
We investigated how environmental factors initiate Heterosigma akashiwo and Skeletonema costatum blooms from resting stages in bottom sediments in a shallow port over 2 yr. Using field-collected sediments, we also conducted laboratory experiments on how light intensity affects germination of resting...
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description | We investigated how environmental factors initiate Heterosigma akashiwo and Skeletonema costatum blooms from resting stages in bottom sediments in a shallow port over 2 yr. Using field-collected sediments, we also conducted laboratory experiments on how light intensity affects germination of resting stages and growth of the germinated cells. Both phytoplankton species bloomed only in summer, when water temperature and solar radiation were high enough for growth. All three blooms of H. akashiwo and the earliest bloom of S. costatum in a year occurred right after transmission of strong light (>200 micromol quanta m⁻² s⁻¹) to the bottom layer and a peak occurred in dissolved inorganic phosphorus (DIP). In the laboratory, resting stages of H. akashiwo and S. costatum germinated even in dim light (20 and 65 micromol quanta m⁻² s⁻¹, respectively), but germinated cells required stronger light of >130 and 280 micromol quanta m⁻² s⁻¹, respectively, for rapid growth. This value is much higher than the threshold for survival, and is higher than the half-saturating light intensity for growth of vegetative cells. Abundance of the resting stages of both species in the sediments rapidly increased during blooms and logarithmically decreased during nonbloom periods, suggesting that resting stages are continuously consumed. For both species, our results suggest that blooms initiate when transmission of sufficient light permits: first, germination of cells from the sediment; second, rapid growth of these germinated cells. Temperature and DIP must also exceed a facilitating threshold. |
doi_str_mv | 10.4319/lo.2008.53.6.2503 |
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Using field-collected sediments, we also conducted laboratory experiments on how light intensity affects germination of resting stages and growth of the germinated cells. Both phytoplankton species bloomed only in summer, when water temperature and solar radiation were high enough for growth. All three blooms of H. akashiwo and the earliest bloom of S. costatum in a year occurred right after transmission of strong light (>200 micromol quanta m⁻² s⁻¹) to the bottom layer and a peak occurred in dissolved inorganic phosphorus (DIP). In the laboratory, resting stages of H. akashiwo and S. costatum germinated even in dim light (20 and 65 micromol quanta m⁻² s⁻¹, respectively), but germinated cells required stronger light of >130 and 280 micromol quanta m⁻² s⁻¹, respectively, for rapid growth. This value is much higher than the threshold for survival, and is higher than the half-saturating light intensity for growth of vegetative cells. Abundance of the resting stages of both species in the sediments rapidly increased during blooms and logarithmically decreased during nonbloom periods, suggesting that resting stages are continuously consumed. For both species, our results suggest that blooms initiate when transmission of sufficient light permits: first, germination of cells from the sediment; second, rapid growth of these germinated cells. Temperature and DIP must also exceed a facilitating threshold.</description><identifier>ISSN: 0024-3590</identifier><identifier>EISSN: 1939-5590</identifier><identifier>DOI: 10.4319/lo.2008.53.6.2503</identifier><identifier>CODEN: LIOCAH</identifier><language>eng</language><publisher>Waco, TX: American Society of Limnology and Oceanography</publisher><subject>Akashiwo ; Animal and plant ecology ; Animal, plant and microbial ecology ; Bacillariophyceae ; Biological and medical sciences ; Cell growth ; Diatoms ; Flux density ; Fundamental and applied biological sciences. Psychology ; Germination ; Heterosigma akashiwo ; Marine ; Photons ; Phytoplankton ; Ports ; Sea water ecosystems ; Sediments ; Skeletonema costatum ; Somatic cells ; Synecology ; Water temperature</subject><ispartof>Limnology and oceanography, 2008-11, Vol.53 (6), p.2503-2518</ispartof><rights>Copyright 2008 American Society of Limnology and Oceanography, Inc.</rights><rights>2008, by the Association for the Sciences of Limnology and Oceanography, Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4913-f3eae60a768521f16d2bca03e4167d366d2a31636a034945b33a38dc08a783dc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/40058340$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/40058340$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,1411,1427,27901,27902,45550,45551,46384,46808,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20897729$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Shikata, Tomoyuki</creatorcontrib><creatorcontrib>Nagasoe, Sou</creatorcontrib><creatorcontrib>Matsubara, Tadashi</creatorcontrib><creatorcontrib>Yoshikawa, Souta</creatorcontrib><creatorcontrib>Yamasaki, Yasuhiro</creatorcontrib><creatorcontrib>Shimasaki, Yohei</creatorcontrib><creatorcontrib>Oshima, Yuji</creatorcontrib><creatorcontrib>Jenkinson, Ian R.</creatorcontrib><creatorcontrib>Honjo, Tsuneo</creatorcontrib><title>Factors Influencing the Initiation of Blooms of the Raphidophyte Heterosigma akashiwo and the Diatom Skeletonema costatum in a Port in Japan</title><title>Limnology and oceanography</title><description>We investigated how environmental factors initiate Heterosigma akashiwo and Skeletonema costatum blooms from resting stages in bottom sediments in a shallow port over 2 yr. Using field-collected sediments, we also conducted laboratory experiments on how light intensity affects germination of resting stages and growth of the germinated cells. Both phytoplankton species bloomed only in summer, when water temperature and solar radiation were high enough for growth. All three blooms of H. akashiwo and the earliest bloom of S. costatum in a year occurred right after transmission of strong light (>200 micromol quanta m⁻² s⁻¹) to the bottom layer and a peak occurred in dissolved inorganic phosphorus (DIP). In the laboratory, resting stages of H. akashiwo and S. costatum germinated even in dim light (20 and 65 micromol quanta m⁻² s⁻¹, respectively), but germinated cells required stronger light of >130 and 280 micromol quanta m⁻² s⁻¹, respectively, for rapid growth. This value is much higher than the threshold for survival, and is higher than the half-saturating light intensity for growth of vegetative cells. Abundance of the resting stages of both species in the sediments rapidly increased during blooms and logarithmically decreased during nonbloom periods, suggesting that resting stages are continuously consumed. For both species, our results suggest that blooms initiate when transmission of sufficient light permits: first, germination of cells from the sediment; second, rapid growth of these germinated cells. Temperature and DIP must also exceed a facilitating threshold.</description><subject>Akashiwo</subject><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Bacillariophyceae</subject><subject>Biological and medical sciences</subject><subject>Cell growth</subject><subject>Diatoms</subject><subject>Flux density</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Germination</subject><subject>Heterosigma akashiwo</subject><subject>Marine</subject><subject>Photons</subject><subject>Phytoplankton</subject><subject>Ports</subject><subject>Sea water ecosystems</subject><subject>Sediments</subject><subject>Skeletonema costatum</subject><subject>Somatic cells</subject><subject>Synecology</subject><subject>Water temperature</subject><issn>0024-3590</issn><issn>1939-5590</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkc9u1DAQxiMEEkvhATgg-QK3pONM7CQHDlAoLVpRxJ-zNXWcrlsnDrFX1b4DD43TrHrl5Jnx7_tG_pxlrzkUFfL21PmiBGgKgYUsSgH4JNvwFttciBaeZhuAssox1c-zFyHcAkArhNhkf89JRz8Hdjn2bm9GbccbFncm9TZaitaPzPfso_N-CEu13P2gaWc7P-0O0bALE83sg70ZiNEdhZ2994zG7oH8lCz8wH7eGWeiH01itA-R4n5gdmTEvvs5LtVXmmh8mT3ryQXz6nieZL_PP_86u8i3V18uzz5sc121HPMeDRkJVMtGlLznsiuvNQGaisu6Q5l6Qi5RplnVVuIakbDpNDRUN9hpPMnerb7T7P_sTYhqsEEb52g0fh9UCZhkgAnkK6jTC8NsejXNdqD5oDioJXflvFpyVwKVVOWqeXs0p6DJ9TOlUMOjsISmreuyTdz7lbu3zhz-b6y2366WiUB53PNm1d-G9IGP-gpANFgB_gOjEKAp</recordid><startdate>200811</startdate><enddate>200811</enddate><creator>Shikata, Tomoyuki</creator><creator>Nagasoe, Sou</creator><creator>Matsubara, Tadashi</creator><creator>Yoshikawa, Souta</creator><creator>Yamasaki, Yasuhiro</creator><creator>Shimasaki, Yohei</creator><creator>Oshima, Yuji</creator><creator>Jenkinson, Ian R.</creator><creator>Honjo, Tsuneo</creator><general>American Society of Limnology and Oceanography</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7TN</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope></search><sort><creationdate>200811</creationdate><title>Factors Influencing the Initiation of Blooms of the Raphidophyte Heterosigma akashiwo and the Diatom Skeletonema costatum in a Port in Japan</title><author>Shikata, Tomoyuki ; Nagasoe, Sou ; Matsubara, Tadashi ; Yoshikawa, Souta ; Yamasaki, Yasuhiro ; Shimasaki, Yohei ; Oshima, Yuji ; Jenkinson, Ian R. ; Honjo, Tsuneo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4913-f3eae60a768521f16d2bca03e4167d366d2a31636a034945b33a38dc08a783dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Akashiwo</topic><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Bacillariophyceae</topic><topic>Biological and medical sciences</topic><topic>Cell growth</topic><topic>Diatoms</topic><topic>Flux density</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Germination</topic><topic>Heterosigma akashiwo</topic><topic>Marine</topic><topic>Photons</topic><topic>Phytoplankton</topic><topic>Ports</topic><topic>Sea water ecosystems</topic><topic>Sediments</topic><topic>Skeletonema costatum</topic><topic>Somatic cells</topic><topic>Synecology</topic><topic>Water temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shikata, Tomoyuki</creatorcontrib><creatorcontrib>Nagasoe, Sou</creatorcontrib><creatorcontrib>Matsubara, Tadashi</creatorcontrib><creatorcontrib>Yoshikawa, Souta</creatorcontrib><creatorcontrib>Yamasaki, Yasuhiro</creatorcontrib><creatorcontrib>Shimasaki, Yohei</creatorcontrib><creatorcontrib>Oshima, Yuji</creatorcontrib><creatorcontrib>Jenkinson, Ian R.</creatorcontrib><creatorcontrib>Honjo, Tsuneo</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Limnology and oceanography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shikata, Tomoyuki</au><au>Nagasoe, Sou</au><au>Matsubara, Tadashi</au><au>Yoshikawa, Souta</au><au>Yamasaki, Yasuhiro</au><au>Shimasaki, Yohei</au><au>Oshima, Yuji</au><au>Jenkinson, Ian R.</au><au>Honjo, Tsuneo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factors Influencing the Initiation of Blooms of the Raphidophyte Heterosigma akashiwo and the Diatom Skeletonema costatum in a Port in Japan</atitle><jtitle>Limnology and oceanography</jtitle><date>2008-11</date><risdate>2008</risdate><volume>53</volume><issue>6</issue><spage>2503</spage><epage>2518</epage><pages>2503-2518</pages><issn>0024-3590</issn><eissn>1939-5590</eissn><coden>LIOCAH</coden><abstract>We investigated how environmental factors initiate Heterosigma akashiwo and Skeletonema costatum blooms from resting stages in bottom sediments in a shallow port over 2 yr. Using field-collected sediments, we also conducted laboratory experiments on how light intensity affects germination of resting stages and growth of the germinated cells. Both phytoplankton species bloomed only in summer, when water temperature and solar radiation were high enough for growth. All three blooms of H. akashiwo and the earliest bloom of S. costatum in a year occurred right after transmission of strong light (>200 micromol quanta m⁻² s⁻¹) to the bottom layer and a peak occurred in dissolved inorganic phosphorus (DIP). In the laboratory, resting stages of H. akashiwo and S. costatum germinated even in dim light (20 and 65 micromol quanta m⁻² s⁻¹, respectively), but germinated cells required stronger light of >130 and 280 micromol quanta m⁻² s⁻¹, respectively, for rapid growth. This value is much higher than the threshold for survival, and is higher than the half-saturating light intensity for growth of vegetative cells. Abundance of the resting stages of both species in the sediments rapidly increased during blooms and logarithmically decreased during nonbloom periods, suggesting that resting stages are continuously consumed. For both species, our results suggest that blooms initiate when transmission of sufficient light permits: first, germination of cells from the sediment; second, rapid growth of these germinated cells. Temperature and DIP must also exceed a facilitating threshold.</abstract><cop>Waco, TX</cop><pub>American Society of Limnology and Oceanography</pub><doi>10.4319/lo.2008.53.6.2503</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Akashiwo Animal and plant ecology Animal, plant and microbial ecology Bacillariophyceae Biological and medical sciences Cell growth Diatoms Flux density Fundamental and applied biological sciences. Psychology Germination Heterosigma akashiwo Marine Photons Phytoplankton Ports Sea water ecosystems Sediments Skeletonema costatum Somatic cells Synecology Water temperature |
title | Factors Influencing the Initiation of Blooms of the Raphidophyte Heterosigma akashiwo and the Diatom Skeletonema costatum in a Port in Japan |
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