Photosynthesis and growth of water hyacinth under CO2 enrichment

Water hyacinth (Eichhornia crassipes [Mart.] Solms) plants were grown in environmental chambers at ambient and enriched CO2 levels (330 and 600 microliters CO2 per liter). Daughter plants (ramets) produced in the enriched CO2 gained 39% greater dry weight than those at ambient CO2, but the original...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Plant physiology (Bethesda) 1986-10, Vol.82 (2), p.528-533
Hauptverfasser: Spencer, W, Bowes, G
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 533
container_issue 2
container_start_page 528
container_title Plant physiology (Bethesda)
container_volume 82
creator Spencer, W
Bowes, G
description Water hyacinth (Eichhornia crassipes [Mart.] Solms) plants were grown in environmental chambers at ambient and enriched CO2 levels (330 and 600 microliters CO2 per liter). Daughter plants (ramets) produced in the enriched CO2 gained 39% greater dry weight than those at ambient CO2, but the original mother plants did not. The CO2 enrichment increased the number of leaves per ramet and leaf area index, but did not significantly increase leaf size or the number of ramets formed. Flower production was increased 147%. The elevated CO2 increased the net photosynthetic rate of the mother plants by 40%, but this was not maintained as the plants acclimated to the higher CO2 level. After 14 days at the elevated CO2, leaf resistance increased and transpiration decreased, especially from the adaxial leaf surface. After 4 weeks in elevated as compared to ambient CO2, ribulose bisphosphate carboxylase activity was 40% less, soluble protein content 49% less, and chlorophyll content 26% less; whereas starch content was 40% greater. Although at a given CO2 level the enriched CO2 plants had only half the net photosynthetic rate of their counterparts grown at ambient CO2 they showed similar internal CO2 concentrations. This suggested that the decreased supply of CO2 to the mesophyll, as a result of the increased stomatal resistance, was counterbalanced by a decreased utilization of CO2. Photorespiration and dark respiration were lower, such that the CO2 compensation point was not altered. The photosynthetic light and CO2 saturation points were not greatly changed, nor was the O2 inhibition of photosynthesis (measured at 330 microliters CO2 per liter). It appears that with CO2 enrichment the temporary increase in net photosynthesis produced larger ramets. After acclimation, the greater total ramet leaf area more than compensated for the lower net photosynthetic rate on a unit leaf area basis, and resulted in a sustained improvement in dry weight gain.
doi_str_mv 10.1104/pp.82.2.528
format Article
fullrecord <record><control><sourceid>jstor_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1056153</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>4270220</jstor_id><sourcerecordid>4270220</sourcerecordid><originalsourceid>FETCH-LOGICAL-f376t-3469e88c508fb9da25bdce11b00cdf3c0dcf9428cb9006bd6597d9155a32e23d3</originalsourceid><addsrcrecordid>eNqFkE1Lw0AQhhdRbK2evImHHLwmzn5mcxGl-AWFCtpz2OxumpR2E3ZTS_-9Cy2CJ08zw_vMc3gRusaQYQzsvu8zSTKScSJP0BhzSlLCmTxFY4C4g5TFCF2EsAIATDE7RyMshOAg6Bg9fjTd0IW9Gxob2pAoZ5Kl73ZDk3R1slOD9UmzV7qNQLJ1Jp7TOUms861uNtYNl-isVutgr45zghYvz1_Tt3Q2f32fPs3SmuZiSCkThZVSc5B1VRhFeGW0xbgC0KamGoyuC0akrgoAURnBi9wUmHNFiSXU0Al6OHj7bbWx8dcNXq3L3rcb5fdlp9ryb-Laplx23yUGLmIpUXB3FKig1br2yuk2_Aok5ZzEfv7DiKQALGK3B2wVhs7_xozkQAjE-OYQ16or1dJHw-JT5oQxRukPaBSCbA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Photosynthesis and growth of water hyacinth under CO2 enrichment</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>JSTOR Archive Collection A-Z Listing</source><source>Alma/SFX Local Collection</source><creator>Spencer, W ; Bowes, G</creator><creatorcontrib>Spencer, W ; Bowes, G</creatorcontrib><description>Water hyacinth (Eichhornia crassipes [Mart.] Solms) plants were grown in environmental chambers at ambient and enriched CO2 levels (330 and 600 microliters CO2 per liter). Daughter plants (ramets) produced in the enriched CO2 gained 39% greater dry weight than those at ambient CO2, but the original mother plants did not. The CO2 enrichment increased the number of leaves per ramet and leaf area index, but did not significantly increase leaf size or the number of ramets formed. Flower production was increased 147%. The elevated CO2 increased the net photosynthetic rate of the mother plants by 40%, but this was not maintained as the plants acclimated to the higher CO2 level. After 14 days at the elevated CO2, leaf resistance increased and transpiration decreased, especially from the adaxial leaf surface. After 4 weeks in elevated as compared to ambient CO2, ribulose bisphosphate carboxylase activity was 40% less, soluble protein content 49% less, and chlorophyll content 26% less; whereas starch content was 40% greater. Although at a given CO2 level the enriched CO2 plants had only half the net photosynthetic rate of their counterparts grown at ambient CO2 they showed similar internal CO2 concentrations. This suggested that the decreased supply of CO2 to the mesophyll, as a result of the increased stomatal resistance, was counterbalanced by a decreased utilization of CO2. Photorespiration and dark respiration were lower, such that the CO2 compensation point was not altered. The photosynthetic light and CO2 saturation points were not greatly changed, nor was the O2 inhibition of photosynthesis (measured at 330 microliters CO2 per liter). It appears that with CO2 enrichment the temporary increase in net photosynthesis produced larger ramets. After acclimation, the greater total ramet leaf area more than compensated for the lower net photosynthetic rate on a unit leaf area basis, and resulted in a sustained improvement in dry weight gain.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.82.2.528</identifier><identifier>PMID: 16665063</identifier><identifier>CODEN: PPHYA5</identifier><language>eng</language><publisher>Rockville, MD: American Society of Plant Physiologists</publisher><subject>Acclimatization ; ADAPTACION FISIOLOGICA ; ADAPTATION ; Agronomy. Soil science and plant productions ; ANALISIS ; ANALYSE ; ANALYSIS ; Applied sciences ; Biological and medical sciences ; BIOMASA ; BIOMASS ; Biomass production ; BIOMASSE ; CARBON DIOXIDE ; CRECIMIENTO ; CROISSANCE ; DIOXIDO DE CARBONO ; DIOXYDE DE CARBONE ; Economic plant physiology ; EICHHORNIA ; EICHHORNIA CRASSIPES ; Exact sciences and technology ; FONCTION PHYSIOLOGIQUE ; FOTOSINTESIS ; FUNCION FISIOLOGICA ; Fundamental and applied biological sciences. Psychology ; GROWTH ; LEAF AREA ; Leaves ; Metabolism ; Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia) ; Nutrition. Photosynthesis. Respiration. Metabolism ; Other techniques and industries ; PHOTOSYNTHESE ; PHOTOSYNTHESIS ; Photosynthesis, respiration. Anabolism, catabolism ; PHYSIOLOGICAL FUNCTIONS ; Plant growth ; Plant physiology and development ; Plants ; Starches ; SUPERFICIE FOLIAR ; SURFACE FOLIAIRE ; Transpiration</subject><ispartof>Plant physiology (Bethesda), 1986-10, Vol.82 (2), p.528-533</ispartof><rights>Copyright 1986 American Society of Plant Physiologists</rights><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4270220$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4270220$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,780,784,803,885,27923,27924,58016,58249</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8283004$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8355201$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Spencer, W</creatorcontrib><creatorcontrib>Bowes, G</creatorcontrib><title>Photosynthesis and growth of water hyacinth under CO2 enrichment</title><title>Plant physiology (Bethesda)</title><description>Water hyacinth (Eichhornia crassipes [Mart.] Solms) plants were grown in environmental chambers at ambient and enriched CO2 levels (330 and 600 microliters CO2 per liter). Daughter plants (ramets) produced in the enriched CO2 gained 39% greater dry weight than those at ambient CO2, but the original mother plants did not. The CO2 enrichment increased the number of leaves per ramet and leaf area index, but did not significantly increase leaf size or the number of ramets formed. Flower production was increased 147%. The elevated CO2 increased the net photosynthetic rate of the mother plants by 40%, but this was not maintained as the plants acclimated to the higher CO2 level. After 14 days at the elevated CO2, leaf resistance increased and transpiration decreased, especially from the adaxial leaf surface. After 4 weeks in elevated as compared to ambient CO2, ribulose bisphosphate carboxylase activity was 40% less, soluble protein content 49% less, and chlorophyll content 26% less; whereas starch content was 40% greater. Although at a given CO2 level the enriched CO2 plants had only half the net photosynthetic rate of their counterparts grown at ambient CO2 they showed similar internal CO2 concentrations. This suggested that the decreased supply of CO2 to the mesophyll, as a result of the increased stomatal resistance, was counterbalanced by a decreased utilization of CO2. Photorespiration and dark respiration were lower, such that the CO2 compensation point was not altered. The photosynthetic light and CO2 saturation points were not greatly changed, nor was the O2 inhibition of photosynthesis (measured at 330 microliters CO2 per liter). It appears that with CO2 enrichment the temporary increase in net photosynthesis produced larger ramets. After acclimation, the greater total ramet leaf area more than compensated for the lower net photosynthetic rate on a unit leaf area basis, and resulted in a sustained improvement in dry weight gain.</description><subject>Acclimatization</subject><subject>ADAPTACION FISIOLOGICA</subject><subject>ADAPTATION</subject><subject>Agronomy. Soil science and plant productions</subject><subject>ANALISIS</subject><subject>ANALYSE</subject><subject>ANALYSIS</subject><subject>Applied sciences</subject><subject>Biological and medical sciences</subject><subject>BIOMASA</subject><subject>BIOMASS</subject><subject>Biomass production</subject><subject>BIOMASSE</subject><subject>CARBON DIOXIDE</subject><subject>CRECIMIENTO</subject><subject>CROISSANCE</subject><subject>DIOXIDO DE CARBONO</subject><subject>DIOXYDE DE CARBONE</subject><subject>Economic plant physiology</subject><subject>EICHHORNIA</subject><subject>EICHHORNIA CRASSIPES</subject><subject>Exact sciences and technology</subject><subject>FONCTION PHYSIOLOGIQUE</subject><subject>FOTOSINTESIS</subject><subject>FUNCION FISIOLOGICA</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GROWTH</subject><subject>LEAF AREA</subject><subject>Leaves</subject><subject>Metabolism</subject><subject>Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia)</subject><subject>Nutrition. Photosynthesis. Respiration. Metabolism</subject><subject>Other techniques and industries</subject><subject>PHOTOSYNTHESE</subject><subject>PHOTOSYNTHESIS</subject><subject>Photosynthesis, respiration. Anabolism, catabolism</subject><subject>PHYSIOLOGICAL FUNCTIONS</subject><subject>Plant growth</subject><subject>Plant physiology and development</subject><subject>Plants</subject><subject>Starches</subject><subject>SUPERFICIE FOLIAR</subject><subject>SURFACE FOLIAIRE</subject><subject>Transpiration</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><recordid>eNqFkE1Lw0AQhhdRbK2evImHHLwmzn5mcxGl-AWFCtpz2OxumpR2E3ZTS_-9Cy2CJ08zw_vMc3gRusaQYQzsvu8zSTKScSJP0BhzSlLCmTxFY4C4g5TFCF2EsAIATDE7RyMshOAg6Bg9fjTd0IW9Gxob2pAoZ5Kl73ZDk3R1slOD9UmzV7qNQLJ1Jp7TOUms861uNtYNl-isVutgr45zghYvz1_Tt3Q2f32fPs3SmuZiSCkThZVSc5B1VRhFeGW0xbgC0KamGoyuC0akrgoAURnBi9wUmHNFiSXU0Al6OHj7bbWx8dcNXq3L3rcb5fdlp9ryb-Laplx23yUGLmIpUXB3FKig1br2yuk2_Aok5ZzEfv7DiKQALGK3B2wVhs7_xozkQAjE-OYQ16or1dJHw-JT5oQxRukPaBSCbA</recordid><startdate>19861001</startdate><enddate>19861001</enddate><creator>Spencer, W</creator><creator>Bowes, G</creator><general>American Society of Plant Physiologists</general><scope>FBQ</scope><scope>IQODW</scope><scope>5PM</scope></search><sort><creationdate>19861001</creationdate><title>Photosynthesis and growth of water hyacinth under CO2 enrichment</title><author>Spencer, W ; Bowes, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f376t-3469e88c508fb9da25bdce11b00cdf3c0dcf9428cb9006bd6597d9155a32e23d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Acclimatization</topic><topic>ADAPTACION FISIOLOGICA</topic><topic>ADAPTATION</topic><topic>Agronomy. Soil science and plant productions</topic><topic>ANALISIS</topic><topic>ANALYSE</topic><topic>ANALYSIS</topic><topic>Applied sciences</topic><topic>Biological and medical sciences</topic><topic>BIOMASA</topic><topic>BIOMASS</topic><topic>Biomass production</topic><topic>BIOMASSE</topic><topic>CARBON DIOXIDE</topic><topic>CRECIMIENTO</topic><topic>CROISSANCE</topic><topic>DIOXIDO DE CARBONO</topic><topic>DIOXYDE DE CARBONE</topic><topic>Economic plant physiology</topic><topic>EICHHORNIA</topic><topic>EICHHORNIA CRASSIPES</topic><topic>Exact sciences and technology</topic><topic>FONCTION PHYSIOLOGIQUE</topic><topic>FOTOSINTESIS</topic><topic>FUNCION FISIOLOGICA</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GROWTH</topic><topic>LEAF AREA</topic><topic>Leaves</topic><topic>Metabolism</topic><topic>Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia)</topic><topic>Nutrition. Photosynthesis. Respiration. Metabolism</topic><topic>Other techniques and industries</topic><topic>PHOTOSYNTHESE</topic><topic>PHOTOSYNTHESIS</topic><topic>Photosynthesis, respiration. Anabolism, catabolism</topic><topic>PHYSIOLOGICAL FUNCTIONS</topic><topic>Plant growth</topic><topic>Plant physiology and development</topic><topic>Plants</topic><topic>Starches</topic><topic>SUPERFICIE FOLIAR</topic><topic>SURFACE FOLIAIRE</topic><topic>Transpiration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spencer, W</creatorcontrib><creatorcontrib>Bowes, G</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spencer, W</au><au>Bowes, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photosynthesis and growth of water hyacinth under CO2 enrichment</atitle><jtitle>Plant physiology (Bethesda)</jtitle><date>1986-10-01</date><risdate>1986</risdate><volume>82</volume><issue>2</issue><spage>528</spage><epage>533</epage><pages>528-533</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>Water hyacinth (Eichhornia crassipes [Mart.] Solms) plants were grown in environmental chambers at ambient and enriched CO2 levels (330 and 600 microliters CO2 per liter). Daughter plants (ramets) produced in the enriched CO2 gained 39% greater dry weight than those at ambient CO2, but the original mother plants did not. The CO2 enrichment increased the number of leaves per ramet and leaf area index, but did not significantly increase leaf size or the number of ramets formed. Flower production was increased 147%. The elevated CO2 increased the net photosynthetic rate of the mother plants by 40%, but this was not maintained as the plants acclimated to the higher CO2 level. After 14 days at the elevated CO2, leaf resistance increased and transpiration decreased, especially from the adaxial leaf surface. After 4 weeks in elevated as compared to ambient CO2, ribulose bisphosphate carboxylase activity was 40% less, soluble protein content 49% less, and chlorophyll content 26% less; whereas starch content was 40% greater. Although at a given CO2 level the enriched CO2 plants had only half the net photosynthetic rate of their counterparts grown at ambient CO2 they showed similar internal CO2 concentrations. This suggested that the decreased supply of CO2 to the mesophyll, as a result of the increased stomatal resistance, was counterbalanced by a decreased utilization of CO2. Photorespiration and dark respiration were lower, such that the CO2 compensation point was not altered. The photosynthetic light and CO2 saturation points were not greatly changed, nor was the O2 inhibition of photosynthesis (measured at 330 microliters CO2 per liter). It appears that with CO2 enrichment the temporary increase in net photosynthesis produced larger ramets. After acclimation, the greater total ramet leaf area more than compensated for the lower net photosynthetic rate on a unit leaf area basis, and resulted in a sustained improvement in dry weight gain.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Physiologists</pub><pmid>16665063</pmid><doi>10.1104/pp.82.2.528</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0032-0889
ispartof Plant physiology (Bethesda), 1986-10, Vol.82 (2), p.528-533
issn 0032-0889
1532-2548
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1056153
source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; JSTOR Archive Collection A-Z Listing; Alma/SFX Local Collection
subjects Acclimatization
ADAPTACION FISIOLOGICA
ADAPTATION
Agronomy. Soil science and plant productions
ANALISIS
ANALYSE
ANALYSIS
Applied sciences
Biological and medical sciences
BIOMASA
BIOMASS
Biomass production
BIOMASSE
CARBON DIOXIDE
CRECIMIENTO
CROISSANCE
DIOXIDO DE CARBONO
DIOXYDE DE CARBONE
Economic plant physiology
EICHHORNIA
EICHHORNIA CRASSIPES
Exact sciences and technology
FONCTION PHYSIOLOGIQUE
FOTOSINTESIS
FUNCION FISIOLOGICA
Fundamental and applied biological sciences. Psychology
GROWTH
LEAF AREA
Leaves
Metabolism
Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia)
Nutrition. Photosynthesis. Respiration. Metabolism
Other techniques and industries
PHOTOSYNTHESE
PHOTOSYNTHESIS
Photosynthesis, respiration. Anabolism, catabolism
PHYSIOLOGICAL FUNCTIONS
Plant growth
Plant physiology and development
Plants
Starches
SUPERFICIE FOLIAR
SURFACE FOLIAIRE
Transpiration
title Photosynthesis and growth of water hyacinth under CO2 enrichment
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T19%3A33%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Photosynthesis%20and%20growth%20of%20water%20hyacinth%20under%20CO2%20enrichment&rft.jtitle=Plant%20physiology%20(Bethesda)&rft.au=Spencer,%20W&rft.date=1986-10-01&rft.volume=82&rft.issue=2&rft.spage=528&rft.epage=533&rft.pages=528-533&rft.issn=0032-0889&rft.eissn=1532-2548&rft.coden=PPHYA5&rft_id=info:doi/10.1104/pp.82.2.528&rft_dat=%3Cjstor_pubme%3E4270220%3C/jstor_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/16665063&rft_jstor_id=4270220&rfr_iscdi=true