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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Veröffentlicht in:Limnology and oceanography 2008-11, Vol.53 (6), p.2503-2518
Hauptverfasser: Shikata, Tomoyuki, Nagasoe, Sou, Matsubara, Tadashi, Yoshikawa, Souta, Yamasaki, Yasuhiro, Shimasaki, Yohei, Oshima, Yuji, Jenkinson, Ian R., Honjo, Tsuneo
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container_end_page 2518
container_issue 6
container_start_page 2503
container_title Limnology and oceanography
container_volume 53
creator Shikata, Tomoyuki
Nagasoe, Sou
Matsubara, Tadashi
Yoshikawa, Souta
Yamasaki, Yasuhiro
Shimasaki, Yohei
Oshima, Yuji
Jenkinson, Ian R.
Honjo, Tsuneo
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.
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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 &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Aquatic Science &amp; 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 (&gt;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 &gt;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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source Jstor Complete Legacy; Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
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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