Effects of nematicides on cotton root mycobiota
Baseline information on the diversity and population densities of fungi collected from soil debris and cotton (Gossypium hirsutum L.) roots was determined. Samples were collected from Tifton, GA, and Starkville, MS containing cotton field soil treated with the nematicides 1,3-dichloroproprene (fumig...
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description | Baseline information on the diversity and population densities of fungi collected from soil debris and cotton (Gossypium hirsutum L.) roots was determined. Samples were collected from Tifton, GA, and Starkville, MS containing cotton field soil treated with the nematicides 1,3-dichloroproprene (fumigant) and aldicarb (granules). A total of 10,550 and 13,450 fungal isolates were collected from these two study sites, respectively. Of this total, 34 genera of plant pathogenic or saprophytic species were identified. Pathogenic root fungi included Fusarium spp. (40% of all isolations), Macrophomina, Pythium, Rhizoctonia, and Sclerotium. Fusarium and Rhizoctonia were the most common fungal species identified and included F. oxysporum, F. verticillioides and F. solani, the three Fusarium species pathogenic on cotton plants. Population densities of Fusarium were not significantly different among locations or tissue types sampled. Macrophomina was isolated at greater numbers near the end of the growing seasons. Anastomosis groups of R. solani isolated from roots and soil debris included AG-3, -4, -7, 2-2, and -13 and anastomosis groups of binucleate Rhizoctonia included CAG-2, -3, and -5. Occurrences and frequency of isolations among sampling dates were not consistent. Fluctuations in the frequency of isolation of Rhizoctonia did not correspond with changes in frequency of isolation of the biological control fungus, Trichoderma. When individual or pooled frequencies of the mycobiota were compared to nematicide treatments, no specific trends occurred between treatments, application methods or rates. Results from this study show that use of 1,3-D and aldicarb in cotton fields does not significantly impact plant pathogenic fungi or saprophytic fungal populations. Thus cotton producers need not adjust seedling disease control measures when these two nematicides are used. |
doi_str_mv | 10.1023/B:MYCO.0000020589.82402.81 |
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Samples were collected from Tifton, GA, and Starkville, MS containing cotton field soil treated with the nematicides 1,3-dichloroproprene (fumigant) and aldicarb (granules). A total of 10,550 and 13,450 fungal isolates were collected from these two study sites, respectively. Of this total, 34 genera of plant pathogenic or saprophytic species were identified. Pathogenic root fungi included Fusarium spp. (40% of all isolations), Macrophomina, Pythium, Rhizoctonia, and Sclerotium. Fusarium and Rhizoctonia were the most common fungal species identified and included F. oxysporum, F. verticillioides and F. solani, the three Fusarium species pathogenic on cotton plants. Population densities of Fusarium were not significantly different among locations or tissue types sampled. Macrophomina was isolated at greater numbers near the end of the growing seasons. Anastomosis groups of R. solani isolated from roots and soil debris included AG-3, -4, -7, 2-2, and -13 and anastomosis groups of binucleate Rhizoctonia included CAG-2, -3, and -5. Occurrences and frequency of isolations among sampling dates were not consistent. Fluctuations in the frequency of isolation of Rhizoctonia did not correspond with changes in frequency of isolation of the biological control fungus, Trichoderma. When individual or pooled frequencies of the mycobiota were compared to nematicide treatments, no specific trends occurred between treatments, application methods or rates. Results from this study show that use of 1,3-D and aldicarb in cotton fields does not significantly impact plant pathogenic fungi or saprophytic fungal populations. Thus cotton producers need not adjust seedling disease control measures when these two nematicides are used.</description><identifier>ISSN: 0301-486X</identifier><identifier>EISSN: 1573-0832</identifier><identifier>DOI: 10.1023/B:MYCO.0000020589.82402.81</identifier><identifier>PMID: 15119856</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Aldicarb - pharmacology ; Allyl Compounds - pharmacology ; Animals ; Antinematodal Agents - pharmacology ; Cotton ; Fungi ; Fungi - drug effects ; Fungi - growth & development ; Fungi - isolation & purification ; Gossypium - microbiology ; Herbicides ; Hydrocarbons, Chlorinated ; Loam soils ; Microorganisms ; Nematodes ; Plant Diseases - microbiology ; Plant Diseases - parasitology ; Plant Roots - microbiology ; Soil Microbiology</subject><ispartof>Mycopathologia (1975), 2004-02, Vol.157 (2), p.191-199</ispartof><rights>Copyright (c) 2004 Kluwer Academic Publishers</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-296dd4c5187f867e840d6ded219be6d5affb785f05511ffbf65291c9249993813</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15119856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baird, R E</creatorcontrib><creatorcontrib>Carling, D E</creatorcontrib><creatorcontrib>Watson, C E</creatorcontrib><creatorcontrib>Scruggs, M L</creatorcontrib><creatorcontrib>Hightower, P</creatorcontrib><title>Effects of nematicides on cotton root mycobiota</title><title>Mycopathologia (1975)</title><addtitle>Mycopathologia</addtitle><description>Baseline information on the diversity and population densities of fungi collected from soil debris and cotton (Gossypium hirsutum L.) roots was determined. Samples were collected from Tifton, GA, and Starkville, MS containing cotton field soil treated with the nematicides 1,3-dichloroproprene (fumigant) and aldicarb (granules). A total of 10,550 and 13,450 fungal isolates were collected from these two study sites, respectively. Of this total, 34 genera of plant pathogenic or saprophytic species were identified. Pathogenic root fungi included Fusarium spp. (40% of all isolations), Macrophomina, Pythium, Rhizoctonia, and Sclerotium. Fusarium and Rhizoctonia were the most common fungal species identified and included F. oxysporum, F. verticillioides and F. solani, the three Fusarium species pathogenic on cotton plants. Population densities of Fusarium were not significantly different among locations or tissue types sampled. Macrophomina was isolated at greater numbers near the end of the growing seasons. Anastomosis groups of R. solani isolated from roots and soil debris included AG-3, -4, -7, 2-2, and -13 and anastomosis groups of binucleate Rhizoctonia included CAG-2, -3, and -5. Occurrences and frequency of isolations among sampling dates were not consistent. Fluctuations in the frequency of isolation of Rhizoctonia did not correspond with changes in frequency of isolation of the biological control fungus, Trichoderma. When individual or pooled frequencies of the mycobiota were compared to nematicide treatments, no specific trends occurred between treatments, application methods or rates. Results from this study show that use of 1,3-D and aldicarb in cotton fields does not significantly impact plant pathogenic fungi or saprophytic fungal populations. Thus cotton producers need not adjust seedling disease control measures when these two nematicides are used.</description><subject>Aldicarb - pharmacology</subject><subject>Allyl Compounds - pharmacology</subject><subject>Animals</subject><subject>Antinematodal Agents - pharmacology</subject><subject>Cotton</subject><subject>Fungi</subject><subject>Fungi - drug effects</subject><subject>Fungi - growth & development</subject><subject>Fungi - isolation & purification</subject><subject>Gossypium - microbiology</subject><subject>Herbicides</subject><subject>Hydrocarbons, Chlorinated</subject><subject>Loam soils</subject><subject>Microorganisms</subject><subject>Nematodes</subject><subject>Plant Diseases - microbiology</subject><subject>Plant Diseases - parasitology</subject><subject>Plant Roots - microbiology</subject><subject>Soil Microbiology</subject><issn>0301-486X</issn><issn>1573-0832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkE1rwzAMhs3YWLtuf2GEHnZLatlxYve2lu4DOnrZYDuZxB-Q0sRd7Bz675e0hcKEQBK8kl4ehKaAE8CEzhbzj5_lJsFDEMy4SDhJMUk4XKExsJzGmFNyjcaYYohTnn2P0J33W4yhz_wWjYABCM6yMZqtrDUq-MjZqDF1ESpVadOPTaRcCH1pnQtRfVCurFwo7tGNLXbePJzrBH29rD6Xb_F68_q-fF7HiqYkxERkWqeKAc8tz3LDU6wzbTQBUZpMs8LaMufMYtY76XubMSJACZIKISgHOkFPp7v71v12xgdZV16Z3a5ojOu8zIGLlOWDcPpPuHVd2_TeJCFAIBMk70Xzk0i1zvvWWLlvq7poDxKwHJjKhRyYygtTeWQqj1Yezx-6sjb6snqGSP8AuUdxKA</recordid><startdate>200402</startdate><enddate>200402</enddate><creator>Baird, R E</creator><creator>Carling, D E</creator><creator>Watson, C E</creator><creator>Scruggs, M L</creator><creator>Hightower, P</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200402</creationdate><title>Effects of nematicides on cotton root mycobiota</title><author>Baird, R E ; 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Samples were collected from Tifton, GA, and Starkville, MS containing cotton field soil treated with the nematicides 1,3-dichloroproprene (fumigant) and aldicarb (granules). A total of 10,550 and 13,450 fungal isolates were collected from these two study sites, respectively. Of this total, 34 genera of plant pathogenic or saprophytic species were identified. Pathogenic root fungi included Fusarium spp. (40% of all isolations), Macrophomina, Pythium, Rhizoctonia, and Sclerotium. Fusarium and Rhizoctonia were the most common fungal species identified and included F. oxysporum, F. verticillioides and F. solani, the three Fusarium species pathogenic on cotton plants. Population densities of Fusarium were not significantly different among locations or tissue types sampled. Macrophomina was isolated at greater numbers near the end of the growing seasons. Anastomosis groups of R. solani isolated from roots and soil debris included AG-3, -4, -7, 2-2, and -13 and anastomosis groups of binucleate Rhizoctonia included CAG-2, -3, and -5. Occurrences and frequency of isolations among sampling dates were not consistent. Fluctuations in the frequency of isolation of Rhizoctonia did not correspond with changes in frequency of isolation of the biological control fungus, Trichoderma. When individual or pooled frequencies of the mycobiota were compared to nematicide treatments, no specific trends occurred between treatments, application methods or rates. Results from this study show that use of 1,3-D and aldicarb in cotton fields does not significantly impact plant pathogenic fungi or saprophytic fungal populations. Thus cotton producers need not adjust seedling disease control measures when these two nematicides are used.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>15119856</pmid><doi>10.1023/B:MYCO.0000020589.82402.81</doi><tpages>9</tpages></addata></record> |
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subjects | Aldicarb - pharmacology Allyl Compounds - pharmacology Animals Antinematodal Agents - pharmacology Cotton Fungi Fungi - drug effects Fungi - growth & development Fungi - isolation & purification Gossypium - microbiology Herbicides Hydrocarbons, Chlorinated Loam soils Microorganisms Nematodes Plant Diseases - microbiology Plant Diseases - parasitology Plant Roots - microbiology Soil Microbiology |
title | Effects of nematicides on cotton root mycobiota |
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