Effects of mycorrhizae, established from an existing intact hyphal network, on the growth response of capsicum ( L.) and tomato ( Mill.) to five rates of applied phosphorus
The growth response of 2 vegetable crops to 5 rates of applied phosphorus (P)in the presence or absence of an existing network of extraradical mycorrhizalmycelium was determined in 2 greenhouse pot experiments (Expt 1, autumnwinter; Expt 2, summer autumn) using a low-P growth medium (6 or 5 mgNaHCO...
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description | The growth response of 2 vegetable crops to 5 rates of applied phosphorus (P)in the presence or absence of an existing network of extraradical mycorrhizalmycelium was determined in 2 greenhouse pot experiments (Expt 1, autumnwinter; Expt 2, summer autumn) using a low-P growth medium (6 or 5 mgNaHCO 3 -extractable P/kg for Expt 1 or 2,respectively). In both experiments, capsicum( Capsicum annuum L.) and tomato( Lycopersicon esculentum Mill.) plants were grown at 0(P 1 ), 9.2 (P 2 ), 27.5(P 3 ), 82.5 (P 4 ), or 248(P 5 ) mg P/kg oven-dry soil (spot-placed at sowing)within a nylon mesh (pore size 44 µm). The mesh excluded roots from theoriginal sunflower ( Helianthus annuus L.) host plants,to which either live (VAM+) or killed (VAM–) mycorrhizal[ Glomus etunicatum Becker & Gerdemann and Glomus mosseae (Nicol. & Gerd.) Gerdemann & Trappe] inoculum was added at sowing. The mesh did allow fungal hyphae togrow into the growth medium contained by the mesh. Whereas VAM+ plants generally had higher P concentrations in indextissues than VAM– plants at low P rates, a concomitant increase in drymatter yield was restricted to the P 1 rate. AtP 1 in Expt 2, the increase in the dry weight of wholeplants as a result of VAM colonisation was as large as 91.7-fold and 17.9-foldfor capsicum and tomato, respectively. Root starch analysis indicated that thelower dry matter yields of VAM+ plants than of VAM– plants at≥P 2 could be attributed to insufficient photosynthateproduction by VAM+ plants to meet the carbon (C) demand of both host andendophytes within the relatively low-light environment of the greenhouse(average daily solar irradiance of 8.4 MJ/m 2 forExpt 1 and 13.4 MJ/m 2 for Expt 2). The growth response of vegetable crops grown within the greenhouse fromcolonisation by an established mycorrhizal mycelium appears to depend on acritical balance of P and C supply; i.e. at P 1 , P wasmore limiting than C, and the increased uptake of P as a result ofcolonisation of plant roots by VAM resulted in a growth response. At higher Prates, C was more limiting than P due to low light in the greenhouse, and theadditional demand for photosynthate imposed by the endophytes on the hostresulted in a growth depression relative to non-mycorrhizal plants. Australian Journal of Agricultural Research 50(2) 223 - 238 Full text doi:10.1071/A97167 © CSIRO 1999 |
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In both experiments, capsicum( Capsicum annuum L.) and tomato( Lycopersicon esculentum Mill.) plants were grown at 0(P 1 ), 9.2 (P 2 ), 27.5(P 3 ), 82.5 (P 4 ), or 248(P 5 ) mg P/kg oven-dry soil (spot-placed at sowing)within a nylon mesh (pore size 44 µm). The mesh excluded roots from theoriginal sunflower ( Helianthus annuus L.) host plants,to which either live (VAM+) or killed (VAM–) mycorrhizal[ Glomus etunicatum Becker & Gerdemann and Glomus mosseae (Nicol. & Gerd.) Gerdemann & Trappe] inoculum was added at sowing. The mesh did allow fungal hyphae togrow into the growth medium contained by the mesh. Whereas VAM+ plants generally had higher P concentrations in indextissues than VAM– plants at low P rates, a concomitant increase in drymatter yield was restricted to the P 1 rate. AtP 1 in Expt 2, the increase in the dry weight of wholeplants as a result of VAM colonisation was as large as 91.7-fold and 17.9-foldfor capsicum and tomato, respectively. Root starch analysis indicated that thelower dry matter yields of VAM+ plants than of VAM– plants at≥P 2 could be attributed to insufficient photosynthateproduction by VAM+ plants to meet the carbon (C) demand of both host andendophytes within the relatively low-light environment of the greenhouse(average daily solar irradiance of 8.4 MJ/m 2 forExpt 1 and 13.4 MJ/m 2 for Expt 2). The growth response of vegetable crops grown within the greenhouse fromcolonisation by an established mycorrhizal mycelium appears to depend on acritical balance of P and C supply; i.e. at P 1 , P wasmore limiting than C, and the increased uptake of P as a result ofcolonisation of plant roots by VAM resulted in a growth response. At higher Prates, C was more limiting than P due to low light in the greenhouse, and theadditional demand for photosynthate imposed by the endophytes on the hostresulted in a growth depression relative to non-mycorrhizal plants. Australian Journal of Agricultural Research 50(2) 223 - 238 Full text doi:10.1071/A97167 © CSIRO 1999</description><identifier>ISSN: 0004-9409</identifier><identifier>EISSN: 1836-5795</identifier><identifier>DOI: 10.1071/A97167</identifier><identifier>CODEN: AJAEA9</identifier><language>eng</language><publisher>Collingwood: Commonwealth Scientific and Industrial Research Organization</publisher><subject>Agronomy. Soil science and plant productions ; application rate ; Biological and medical sciences ; Capsicum annuum ; colonization ; Economic plant physiology ; Fundamental and applied biological sciences. Psychology ; General agronomy. Plant production ; Glomus etunicatum ; Glomus mosseae ; growth ; Nitrogen, phosphorus, potassium fertilizations ; nutrient uptake ; Phosphorus fertilization ; phosphorus fertilizers ; plant nutrition ; roots ; Soil-plant relationships. Soil fertility. Fertilization. Amendments ; Solanum lycopersicum var. lycopersicum ; Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...) ; vesicular arbuscular mycorrhizae</subject><ispartof>Australian journal of agricultural research, 1999, Vol.50 (2), p.223-238</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-4da1da578f40bae69ec74849d3ae7cf6dc23fc85666195e751308234de2fb53c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3336,3337,4009,27848,27902,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1745290$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Olsen, J.K</creatorcontrib><creatorcontrib>Schaefer, J.T</creatorcontrib><creatorcontrib>Edwards, D.G</creatorcontrib><creatorcontrib>Hunter, M.N</creatorcontrib><creatorcontrib>Galea, V.J</creatorcontrib><creatorcontrib>Muller, L.M</creatorcontrib><title>Effects of mycorrhizae, established from an existing intact hyphal network, on the growth response of capsicum ( L.) and tomato ( Mill.) to five rates of applied phosphorus</title><title>Australian journal of agricultural research</title><description>The growth response of 2 vegetable crops to 5 rates of applied phosphorus (P)in the presence or absence of an existing network of extraradical mycorrhizalmycelium was determined in 2 greenhouse pot experiments (Expt 1, autumnwinter; Expt 2, summer autumn) using a low-P growth medium (6 or 5 mgNaHCO 3 -extractable P/kg for Expt 1 or 2,respectively). In both experiments, capsicum( Capsicum annuum L.) and tomato( Lycopersicon esculentum Mill.) plants were grown at 0(P 1 ), 9.2 (P 2 ), 27.5(P 3 ), 82.5 (P 4 ), or 248(P 5 ) mg P/kg oven-dry soil (spot-placed at sowing)within a nylon mesh (pore size 44 µm). The mesh excluded roots from theoriginal sunflower ( Helianthus annuus L.) host plants,to which either live (VAM+) or killed (VAM–) mycorrhizal[ Glomus etunicatum Becker & Gerdemann and Glomus mosseae (Nicol. & Gerd.) Gerdemann & Trappe] inoculum was added at sowing. The mesh did allow fungal hyphae togrow into the growth medium contained by the mesh. Whereas VAM+ plants generally had higher P concentrations in indextissues than VAM– plants at low P rates, a concomitant increase in drymatter yield was restricted to the P 1 rate. AtP 1 in Expt 2, the increase in the dry weight of wholeplants as a result of VAM colonisation was as large as 91.7-fold and 17.9-foldfor capsicum and tomato, respectively. Root starch analysis indicated that thelower dry matter yields of VAM+ plants than of VAM– plants at≥P 2 could be attributed to insufficient photosynthateproduction by VAM+ plants to meet the carbon (C) demand of both host andendophytes within the relatively low-light environment of the greenhouse(average daily solar irradiance of 8.4 MJ/m 2 forExpt 1 and 13.4 MJ/m 2 for Expt 2). The growth response of vegetable crops grown within the greenhouse fromcolonisation by an established mycorrhizal mycelium appears to depend on acritical balance of P and C supply; i.e. at P 1 , P wasmore limiting than C, and the increased uptake of P as a result ofcolonisation of plant roots by VAM resulted in a growth response. At higher Prates, C was more limiting than P due to low light in the greenhouse, and theadditional demand for photosynthate imposed by the endophytes on the hostresulted in a growth depression relative to non-mycorrhizal plants. Australian Journal of Agricultural Research 50(2) 223 - 238 Full text doi:10.1071/A97167 © CSIRO 1999</description><subject>Agronomy. Soil science and plant productions</subject><subject>application rate</subject><subject>Biological and medical sciences</subject><subject>Capsicum annuum</subject><subject>colonization</subject><subject>Economic plant physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General agronomy. Plant production</subject><subject>Glomus etunicatum</subject><subject>Glomus mosseae</subject><subject>growth</subject><subject>Nitrogen, phosphorus, potassium fertilizations</subject><subject>nutrient uptake</subject><subject>Phosphorus fertilization</subject><subject>phosphorus fertilizers</subject><subject>plant nutrition</subject><subject>roots</subject><subject>Soil-plant relationships. Soil fertility. Fertilization. Amendments</subject><subject>Solanum lycopersicum var. lycopersicum</subject><subject>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</subject><subject>vesicular arbuscular mycorrhizae</subject><issn>0004-9409</issn><issn>1836-5795</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>K30</sourceid><recordid>eNpFkcFu1DAQhi0EEkuBV8ASqCpSU-w4tuNjVbWAtIgD9BzNOuONSxIH20tZnomHxO1W9GDZGn_6_tEMIa85O-NM8w_nRnOln5AVb4WqpDbyKVkxxprKNMw8Jy9SumFMNZKrFfl76RzanGhwdNrbEOPg_wCeUkwZNqNPA_bUxTBRmCn-9in7eUv9nMFmOuyXAUY6Y74N8ccpDTPNA9JtDLd5oBHTEuaEd2oLS_J2N9ETuj57X1w9zWGCHErhix_HUitv538hjZDxvh1YltGX9GUIqZy4Sy_JMwdjwlcP9xG5vrr8fvGpWn_9-PnifF1ZIdtcNT3wHqRuXcM2gMqg1U3bmF4AautUb2vhbCuVUtxI1JIL1tai6bF2GymsOCJvD94lhp-7MonuJuziXCK7MlPTMmmEKdTxgbIxpBTRdUv0E8R9x1l3t4nusIkCvnvQQbIwugiz9emR1o2sDSvYmwPmIHSwjQW5_laz0lz5raWSj4RNPob_AriP6YY8iX-vrJzO</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>Olsen, J.K</creator><creator>Schaefer, J.T</creator><creator>Edwards, D.G</creator><creator>Hunter, M.N</creator><creator>Galea, V.J</creator><creator>Muller, L.M</creator><general>Commonwealth Scientific and Industrial Research Organization</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>HFXKP</scope><scope>IBDFT</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope></search><sort><creationdate>1999</creationdate><title>Effects of mycorrhizae, established from an existing intact hyphal network, on the growth response of capsicum ( L.) and tomato ( Mill.) to five rates of applied phosphorus</title><author>Olsen, J.K ; Schaefer, J.T ; Edwards, D.G ; Hunter, M.N ; Galea, V.J ; Muller, L.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-4da1da578f40bae69ec74849d3ae7cf6dc23fc85666195e751308234de2fb53c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Agronomy. Soil science and plant productions</topic><topic>application rate</topic><topic>Biological and medical sciences</topic><topic>Capsicum annuum</topic><topic>colonization</topic><topic>Economic plant physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General agronomy. Plant production</topic><topic>Glomus etunicatum</topic><topic>Glomus mosseae</topic><topic>growth</topic><topic>Nitrogen, phosphorus, potassium fertilizations</topic><topic>nutrient uptake</topic><topic>Phosphorus fertilization</topic><topic>phosphorus fertilizers</topic><topic>plant nutrition</topic><topic>roots</topic><topic>Soil-plant relationships. Soil fertility. Fertilization. Amendments</topic><topic>Solanum lycopersicum var. lycopersicum</topic><topic>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</topic><topic>vesicular arbuscular mycorrhizae</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Olsen, J.K</creatorcontrib><creatorcontrib>Schaefer, J.T</creatorcontrib><creatorcontrib>Edwards, D.G</creatorcontrib><creatorcontrib>Hunter, M.N</creatorcontrib><creatorcontrib>Galea, V.J</creatorcontrib><creatorcontrib>Muller, L.M</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Periodicals Index Online Segment 17</collection><collection>Periodicals Index Online Segment 27</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</collection><jtitle>Australian journal of agricultural research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Olsen, J.K</au><au>Schaefer, J.T</au><au>Edwards, D.G</au><au>Hunter, M.N</au><au>Galea, V.J</au><au>Muller, L.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of mycorrhizae, established from an existing intact hyphal network, on the growth response of capsicum ( L.) and tomato ( Mill.) to five rates of applied phosphorus</atitle><jtitle>Australian journal of agricultural research</jtitle><date>1999</date><risdate>1999</risdate><volume>50</volume><issue>2</issue><spage>223</spage><epage>238</epage><pages>223-238</pages><issn>0004-9409</issn><eissn>1836-5795</eissn><coden>AJAEA9</coden><abstract>The growth response of 2 vegetable crops to 5 rates of applied phosphorus (P)in the presence or absence of an existing network of extraradical mycorrhizalmycelium was determined in 2 greenhouse pot experiments (Expt 1, autumnwinter; Expt 2, summer autumn) using a low-P growth medium (6 or 5 mgNaHCO 3 -extractable P/kg for Expt 1 or 2,respectively). In both experiments, capsicum( Capsicum annuum L.) and tomato( Lycopersicon esculentum Mill.) plants were grown at 0(P 1 ), 9.2 (P 2 ), 27.5(P 3 ), 82.5 (P 4 ), or 248(P 5 ) mg P/kg oven-dry soil (spot-placed at sowing)within a nylon mesh (pore size 44 µm). The mesh excluded roots from theoriginal sunflower ( Helianthus annuus L.) host plants,to which either live (VAM+) or killed (VAM–) mycorrhizal[ Glomus etunicatum Becker & Gerdemann and Glomus mosseae (Nicol. & Gerd.) Gerdemann & Trappe] inoculum was added at sowing. The mesh did allow fungal hyphae togrow into the growth medium contained by the mesh. Whereas VAM+ plants generally had higher P concentrations in indextissues than VAM– plants at low P rates, a concomitant increase in drymatter yield was restricted to the P 1 rate. AtP 1 in Expt 2, the increase in the dry weight of wholeplants as a result of VAM colonisation was as large as 91.7-fold and 17.9-foldfor capsicum and tomato, respectively. Root starch analysis indicated that thelower dry matter yields of VAM+ plants than of VAM– plants at≥P 2 could be attributed to insufficient photosynthateproduction by VAM+ plants to meet the carbon (C) demand of both host andendophytes within the relatively low-light environment of the greenhouse(average daily solar irradiance of 8.4 MJ/m 2 forExpt 1 and 13.4 MJ/m 2 for Expt 2). The growth response of vegetable crops grown within the greenhouse fromcolonisation by an established mycorrhizal mycelium appears to depend on acritical balance of P and C supply; i.e. at P 1 , P wasmore limiting than C, and the increased uptake of P as a result ofcolonisation of plant roots by VAM resulted in a growth response. At higher Prates, C was more limiting than P due to low light in the greenhouse, and theadditional demand for photosynthate imposed by the endophytes on the hostresulted in a growth depression relative to non-mycorrhizal plants. Australian Journal of Agricultural Research 50(2) 223 - 238 Full text doi:10.1071/A97167 © CSIRO 1999</abstract><cop>Collingwood</cop><pub>Commonwealth Scientific and Industrial Research Organization</pub><doi>10.1071/A97167</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agronomy. Soil science and plant productions application rate Biological and medical sciences Capsicum annuum colonization Economic plant physiology Fundamental and applied biological sciences. Psychology General agronomy. Plant production Glomus etunicatum Glomus mosseae growth Nitrogen, phosphorus, potassium fertilizations nutrient uptake Phosphorus fertilization phosphorus fertilizers plant nutrition roots Soil-plant relationships. Soil fertility. Fertilization. Amendments Solanum lycopersicum var. lycopersicum Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...) vesicular arbuscular mycorrhizae |
title | Effects of mycorrhizae, established from an existing intact hyphal network, on the growth response of capsicum ( L.) and tomato ( Mill.) to five rates of applied phosphorus |
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