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Removal of Prymnesium parvum (Haptophyceae) cells under different nutrient conditions by clay
In this study, we have shown that the ichthyotoxic Prymnesium parvum (haptophyte) can be successfully removed by spraying the surface with a phosphatic clay/polyaluminium chloride (PAC) mix (final concentration, 4 g l −1 and 5 ppm, respectively). The alga was grown in non-axenic batch cultures with...
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Published in: | Harmful algae 2005-02, Vol.4 (2), p.249-260 |
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description | In this study, we have shown that the ichthyotoxic
Prymnesium parvum (haptophyte) can be successfully removed by spraying the surface with a phosphatic clay/polyaluminium chloride (PAC) mix (final concentration, 4
g
l
−1 and 5
ppm, respectively). The alga was grown in non-axenic batch cultures with nitrogen deficient, phosphorus deficient and nutrient sufficient media. Sub-samples of the nutrient sufficient culture were diluted to obtain cell abundances equal to those in the nutrient deficient cultures. Clay/PAC removed up to 100% of the cells in the low cell nutrient sufficient treatment after 72
h, but removal in the other treatments was lower (up to 84%). The nitrogen deficient cells were found to be the most toxic, measured as haemolytic activity of the cells (HE
50), just prior to the start of the experiment. However, the toxicity of the cells in all treatments was found to fluctuate during the incubation time with a general increase in toxicity towards the end, suggesting that the cells became stressed during sedimentation and/or when trapped in the clay. But the amount of released toxins was always below the detection limit of the haemolytic assay, and the abundance of free-living bacteria, derived from flow cytometer counts, increased throughout the experiment. This suggests that released toxins were either trapped by the clay particles or effectively degraded by the bacterial community. The study shows that the clay method can be efficient in mitigation of
P. parvum blooms, but further studies have to be conducted where optimum clay concentrations are determined to ensure that the efficiency is high against nutrient deficient cells and at high cell abundances, i.e. conditions found during blooms in eutrophic coastal waters, and to determine the fate of the cells and their toxins during and after sedimentation. |
doi_str_mv | 10.1016/j.hal.2004.03.004 |
format | article |
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Prymnesium parvum (haptophyte) can be successfully removed by spraying the surface with a phosphatic clay/polyaluminium chloride (PAC) mix (final concentration, 4
g
l
−1 and 5
ppm, respectively). The alga was grown in non-axenic batch cultures with nitrogen deficient, phosphorus deficient and nutrient sufficient media. Sub-samples of the nutrient sufficient culture were diluted to obtain cell abundances equal to those in the nutrient deficient cultures. Clay/PAC removed up to 100% of the cells in the low cell nutrient sufficient treatment after 72
h, but removal in the other treatments was lower (up to 84%). The nitrogen deficient cells were found to be the most toxic, measured as haemolytic activity of the cells (HE
50), just prior to the start of the experiment. However, the toxicity of the cells in all treatments was found to fluctuate during the incubation time with a general increase in toxicity towards the end, suggesting that the cells became stressed during sedimentation and/or when trapped in the clay. But the amount of released toxins was always below the detection limit of the haemolytic assay, and the abundance of free-living bacteria, derived from flow cytometer counts, increased throughout the experiment. This suggests that released toxins were either trapped by the clay particles or effectively degraded by the bacterial community. The study shows that the clay method can be efficient in mitigation of
P. parvum blooms, but further studies have to be conducted where optimum clay concentrations are determined to ensure that the efficiency is high against nutrient deficient cells and at high cell abundances, i.e. conditions found during blooms in eutrophic coastal waters, and to determine the fate of the cells and their toxins during and after sedimentation.</description><identifier>ISSN: 1568-9883</identifier><identifier>EISSN: 1878-1470</identifier><identifier>DOI: 10.1016/j.hal.2004.03.004</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Algae ; Animal and plant ecology ; Animal, plant and microbial ecology ; Autoecology ; Biological and medical sciences ; Cell abundance ; Fundamental and applied biological sciences. Psychology ; HAB ; Haptophyta ; Intracellular nutrient conditions ; Marine ; Mitigation ; Plant cytology, morphology, systematics, chorology and evolution ; Plants and fungi ; Prymnesium parvum ; Thallophyta ; Toxicity</subject><ispartof>Harmful algae, 2005-02, Vol.4 (2), p.249-260</ispartof><rights>2004 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-c160750d6376f3225b44789c772a5d4dc6cc3b50bd7e64e3bfc422cccba648a53</citedby><cites>FETCH-LOGICAL-c358t-c160750d6376f3225b44789c772a5d4dc6cc3b50bd7e64e3bfc422cccba648a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16516188$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Hagstroem, JA</creatorcontrib><creatorcontrib>Graneli, E</creatorcontrib><title>Removal of Prymnesium parvum (Haptophyceae) cells under different nutrient conditions by clay</title><title>Harmful algae</title><description>In this study, we have shown that the ichthyotoxic
Prymnesium parvum (haptophyte) can be successfully removed by spraying the surface with a phosphatic clay/polyaluminium chloride (PAC) mix (final concentration, 4
g
l
−1 and 5
ppm, respectively). The alga was grown in non-axenic batch cultures with nitrogen deficient, phosphorus deficient and nutrient sufficient media. Sub-samples of the nutrient sufficient culture were diluted to obtain cell abundances equal to those in the nutrient deficient cultures. Clay/PAC removed up to 100% of the cells in the low cell nutrient sufficient treatment after 72
h, but removal in the other treatments was lower (up to 84%). The nitrogen deficient cells were found to be the most toxic, measured as haemolytic activity of the cells (HE
50), just prior to the start of the experiment. However, the toxicity of the cells in all treatments was found to fluctuate during the incubation time with a general increase in toxicity towards the end, suggesting that the cells became stressed during sedimentation and/or when trapped in the clay. But the amount of released toxins was always below the detection limit of the haemolytic assay, and the abundance of free-living bacteria, derived from flow cytometer counts, increased throughout the experiment. This suggests that released toxins were either trapped by the clay particles or effectively degraded by the bacterial community. The study shows that the clay method can be efficient in mitigation of
P. parvum blooms, but further studies have to be conducted where optimum clay concentrations are determined to ensure that the efficiency is high against nutrient deficient cells and at high cell abundances, i.e. conditions found during blooms in eutrophic coastal waters, and to determine the fate of the cells and their toxins during and after sedimentation.</description><subject>Algae</subject><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Autoecology</subject><subject>Biological and medical sciences</subject><subject>Cell abundance</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HAB</subject><subject>Haptophyta</subject><subject>Intracellular nutrient conditions</subject><subject>Marine</subject><subject>Mitigation</subject><subject>Plant cytology, morphology, systematics, chorology and evolution</subject><subject>Plants and fungi</subject><subject>Prymnesium parvum</subject><subject>Thallophyta</subject><subject>Toxicity</subject><issn>1568-9883</issn><issn>1878-1470</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp9kEFL5TAUhYM4oL7xB7jLRtFFO0nTJhVXIjoKDxyGcSkhvbnl5dE2NWkf9N-bxxPczeqcxbnn3vsRcsFZzhmXv7b5xnR5wViZM5EnOSKnvFZ1xkvFjpOvZJ3d1rU4IWcxbhkrOGPslLz_xd7vTEd9S_-EpR8wurmnowm7JNfPZpz8uFkADd5QwK6LdB4sBmpd22LAYaLDPAW3N-AH6ybnh0ibhUJnlp_kR2u6iOdfuiJvT4__Hp6z9evvl4f7dQaiqqcMuGSqYlYKJVtRFFVTlqq-BaUKU9nSggQQTcUaq1CWKJoWyqIAgMbIsjaVWJGrQ-8Y_MeMcdK9i_trzYB-jporJQsuRAryQxCCjzFgq8fgehMWzZneg9RbnUDqPUjNhE6SZi6_yk0E07XBDODi96CsuOSJ7IrcHXKYPt05DDpC4gJoXUCYtPXuP1s-Ae81iW0</recordid><startdate>20050201</startdate><enddate>20050201</enddate><creator>Hagstroem, JA</creator><creator>Graneli, E</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TN</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope></search><sort><creationdate>20050201</creationdate><title>Removal of Prymnesium parvum (Haptophyceae) cells under different nutrient conditions by clay</title><author>Hagstroem, JA ; Graneli, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-c160750d6376f3225b44789c772a5d4dc6cc3b50bd7e64e3bfc422cccba648a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Algae</topic><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Autoecology</topic><topic>Biological and medical sciences</topic><topic>Cell abundance</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HAB</topic><topic>Haptophyta</topic><topic>Intracellular nutrient conditions</topic><topic>Marine</topic><topic>Mitigation</topic><topic>Plant cytology, morphology, systematics, chorology and evolution</topic><topic>Plants and fungi</topic><topic>Prymnesium parvum</topic><topic>Thallophyta</topic><topic>Toxicity</topic><toplevel>online_resources</toplevel><creatorcontrib>Hagstroem, JA</creatorcontrib><creatorcontrib>Graneli, E</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</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) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Harmful algae</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hagstroem, JA</au><au>Graneli, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Removal of Prymnesium parvum (Haptophyceae) cells under different nutrient conditions by clay</atitle><jtitle>Harmful algae</jtitle><date>2005-02-01</date><risdate>2005</risdate><volume>4</volume><issue>2</issue><spage>249</spage><epage>260</epage><pages>249-260</pages><issn>1568-9883</issn><eissn>1878-1470</eissn><abstract>In this study, we have shown that the ichthyotoxic
Prymnesium parvum (haptophyte) can be successfully removed by spraying the surface with a phosphatic clay/polyaluminium chloride (PAC) mix (final concentration, 4
g
l
−1 and 5
ppm, respectively). The alga was grown in non-axenic batch cultures with nitrogen deficient, phosphorus deficient and nutrient sufficient media. Sub-samples of the nutrient sufficient culture were diluted to obtain cell abundances equal to those in the nutrient deficient cultures. Clay/PAC removed up to 100% of the cells in the low cell nutrient sufficient treatment after 72
h, but removal in the other treatments was lower (up to 84%). The nitrogen deficient cells were found to be the most toxic, measured as haemolytic activity of the cells (HE
50), just prior to the start of the experiment. However, the toxicity of the cells in all treatments was found to fluctuate during the incubation time with a general increase in toxicity towards the end, suggesting that the cells became stressed during sedimentation and/or when trapped in the clay. But the amount of released toxins was always below the detection limit of the haemolytic assay, and the abundance of free-living bacteria, derived from flow cytometer counts, increased throughout the experiment. This suggests that released toxins were either trapped by the clay particles or effectively degraded by the bacterial community. The study shows that the clay method can be efficient in mitigation of
P. parvum blooms, but further studies have to be conducted where optimum clay concentrations are determined to ensure that the efficiency is high against nutrient deficient cells and at high cell abundances, i.e. conditions found during blooms in eutrophic coastal waters, and to determine the fate of the cells and their toxins during and after sedimentation.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.hal.2004.03.004</doi><tpages>12</tpages></addata></record> |
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subjects | Algae Animal and plant ecology Animal, plant and microbial ecology Autoecology Biological and medical sciences Cell abundance Fundamental and applied biological sciences. Psychology HAB Haptophyta Intracellular nutrient conditions Marine Mitigation Plant cytology, morphology, systematics, chorology and evolution Plants and fungi Prymnesium parvum Thallophyta Toxicity |
title | Removal of Prymnesium parvum (Haptophyceae) cells under different nutrient conditions by clay |
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