OrangerV1, PascalFrancis, Curation, bibRecord, 000189

Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine

Identifieur interne : 000189 ( PascalFrancis/Curation ); précédent : 000188; suivant : 000190

Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine

Auteurs : Jin-Hu Wu [Nouvelle-Zélande] ; Pauline Mooney [Nouvelle-Zélande]

Source :

Plant cell, tissue and organ culture [ 0167-6857 ] ; 2002.

RBID : Pascal:02-0459190

Descripteurs français

Pascal (Inist)
- Tétraploïdie, Régénération, Haploïde doublé, Modalité traitement, Callogenèse, Effet concentration, Multiplication végétative in vitro, Nombre chromosomique, Cytométrie flux, Citrus reticulata, Citrus paradisi, Colchicine, Embryon somatique, Cytogénétique, Citrus reticulata Citrus sinensis, Oryzalin, Autoploïdie.

English descriptors

KwdEn :
- Application method, Autoploidy, Callogenesis, Chromosomic number, Citrus paradisi, Citrus reticulata, Colchicine, Concentration effect, Cytogenetics, Doubled haploid, Flow cytometry, Micropropagation, Regeneration, Somatic embryo, Tetraploidy.

Abstract

In vitro chromosome doubling of embryogenic callus lines of the Citrus cultivars 'Umatilla' and 'Dweet' tangors (Citrus reticulata Blanco×C. sinensis [L.] Osb.), 'Caffin' clementine (C. clementina Hort. ex Tan.) and 'Wheeny' grapefruit (C. paradisi Macf) was carried out in the presence of either 0.05 or 0.1% colchicine, or 0.01, 0.05 or 0.1% oryzalin. Embryogenic callus development was partly suppressed in the presence of colchicine, and completely suppressed by oryzalin at all concentrations tested. No plants were regenerated from any of the oryzalin treatments. Ploidy level of plants regenerated from the colchicine treatments was determined using flow cytometry and chromosome squashes. Three desirable non-chimeric, autotetraploid plants of the mono-embryonic cultivar 'Umatilla' were produced using 0.05% colchicine and one from 0.1% colchicine. One mixoploid 'Dweet' plant was produced using 0.1% colchicine.

A01	`01`	`1`		`@0 0167-6857`
A02	`01`			`@0 PTCEDJ`
A03		`1`		`@0 Plant cell tissue organ cult.`
A05				`@2 70`
A06				`@2 1`
A08	`01`	`1`	`ENG`	`@1 Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine`
A09	`01`	`1`	`ENG`	`@1 Special issue on the New Zealand Regional IAPTC & B Conference 2001`
A11	`01`	`1`		`@1 WU (Jin-Hu)`
A11	`02`	`1`		`@1 MOONEY (Pauline)`
A12	`01`	`1`		`@1 SEELYE (John F.) @9 ed.`
A12	`02`	`1`		`@1 BURGE (Garry K.) @9 ed.`
A12	`03`	`1`		`@1 MORGAN (Ed R.) @9 ed.`
A12	`04`	`1`		`@1 DE KLERK (Geert-Jan M.) @9 ed.`
A14	`01`			`@1 The Horticulture and Food Research Institute of New Zealand, Kerikeri Research Centre, P.O. Box 23 @2 Kerikeri @3 NZL @Z 1 aut. @Z 2 aut.`
A15	`01`			`@1 New Zealand Institute for Crop & Food Research Limited, Private Bag 11 600 @2 Palmerston North @3 NZL @Z 1 aut.`
A18	`01`	`1`		`@1 International Association for Plant Tissue Culture and Biotechnology. New Zealand Branch @3 NZL @9 patr.`
A20				`@1 99-104`
A21				`@1 2002`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 19374 @5 354000104408250120`
A44				`@0 0000 @1 © 2002 INIST-CNRS. All rights reserved.`
A45				`@0 27 ref.`
A47	`01`	`1`		`@0 02-0459190`
A60				`@1 P @2 C`
A61				`@0 A`
A64	`01`	`1`		`@0 Plant cell, tissue and organ culture`
A66	`01`			`@0 NLD`
C01	`01`		`ENG`	@0 In vitro chromosome doubling of embryogenic callus lines of the Citrus cultivars 'Umatilla' and 'Dweet' tangors (Citrus reticulata Blanco×C. sinensis [L.] Osb.), 'Caffin' clementine (C. clementina Hort. ex Tan.) and 'Wheeny' grapefruit (C. paradisi Macf) was carried out in the presence of either 0.05 or 0.1% colchicine, or 0.01, 0.05 or 0.1% oryzalin. Embryogenic callus development was partly suppressed in the presence of colchicine, and completely suppressed by oryzalin at all concentrations tested. No plants were regenerated from any of the oryzalin treatments. Ploidy level of plants regenerated from the colchicine treatments was determined using flow cytometry and chromosome squashes. Three desirable non-chimeric, autotetraploid plants of the mono-embryonic cultivar 'Umatilla' were produced using 0.05% colchicine and one from 0.1% colchicine. One mixoploid 'Dweet' plant was produced using 0.1% colchicine.
C02	`01`	`X`		`@0 002A32D01C`
C02	`02`	`X`		`@0 002A31C07C6`
C02	`03`	`X`		`@0 215`
C03	`01`	`X`	`FRE`	`@0 Tétraploïdie @5 01`
C03	`01`	`X`	`ENG`	`@0 Tetraploidy @5 01`
C03	`01`	`X`	`SPA`	`@0 Tetraploidía @5 01`
C03	`02`	`X`	`FRE`	`@0 Régénération @5 02`
C03	`02`	`X`	`ENG`	`@0 Regeneration @5 02`
C03	`02`	`X`	`SPA`	`@0 Regeneración @5 02`
C03	`03`	`X`	`FRE`	`@0 Haploïde doublé @5 03`
C03	`03`	`X`	`ENG`	`@0 Doubled haploid @5 03`
C03	`03`	`X`	`SPA`	`@0 Doble haploide @5 03`
C03	`04`	`X`	`FRE`	`@0 Modalité traitement @5 04`
C03	`04`	`X`	`ENG`	`@0 Application method @5 04`
C03	`04`	`X`	`SPA`	`@0 Modalidad tratamiento @5 04`
C03	`05`	`X`	`FRE`	`@0 Callogenèse @5 05`
C03	`05`	`X`	`ENG`	`@0 Callogenesis @5 05`
C03	`05`	`X`	`SPA`	`@0 Callogénesis @5 05`
C03	`06`	`X`	`FRE`	`@0 Effet concentration @5 06`
C03	`06`	`X`	`ENG`	`@0 Concentration effect @5 06`
C03	`06`	`X`	`SPA`	`@0 Efecto concentración @5 06`
C03	`07`	`X`	`FRE`	`@0 Multiplication végétative in vitro @5 07`
C03	`07`	`X`	`ENG`	`@0 Micropropagation @5 07`
C03	`07`	`X`	`SPA`	`@0 Multiplicación vegetativa in vitro @5 07`
C03	`08`	`X`	`FRE`	`@0 Nombre chromosomique @5 08`
C03	`08`	`X`	`ENG`	`@0 Chromosomic number @5 08`
C03	`08`	`X`	`SPA`	`@0 Número cromosómico @5 08`
C03	`09`	`X`	`FRE`	`@0 Cytométrie flux @5 09`
C03	`09`	`X`	`ENG`	`@0 Flow cytometry @5 09`
C03	`09`	`X`	`SPA`	`@0 Citometría flujo @5 09`
C03	`10`	`X`	`FRE`	`@0 Citrus reticulata @2 NS @5 11`
C03	`10`	`X`	`ENG`	`@0 Citrus reticulata @2 NS @5 11`
C03	`10`	`X`	`SPA`	`@0 Citrus reticulata @2 NS @5 11`
C03	`11`	`X`	`FRE`	`@0 Citrus paradisi @2 NS @5 12`
C03	`11`	`X`	`ENG`	`@0 Citrus paradisi @2 NS @5 12`
C03	`11`	`X`	`SPA`	`@0 Citrus paradisi @2 NS @5 12`
C03	`12`	`X`	`FRE`	`@0 Colchicine @2 NK @2 FR @5 15`
C03	`12`	`X`	`ENG`	`@0 Colchicine @2 NK @2 FR @5 15`
C03	`12`	`X`	`SPA`	`@0 Colchicina @2 NK @2 FR @5 15`
C03	`13`	`X`	`FRE`	`@0 Embryon somatique @5 34`
C03	`13`	`X`	`ENG`	`@0 Somatic embryo @5 34`
C03	`13`	`X`	`SPA`	`@0 Embrión somático @5 34`
C03	`14`	`X`	`FRE`	`@0 Cytogénétique @5 35`
C03	`14`	`X`	`ENG`	`@0 Cytogenetics @5 35`
C03	`14`	`X`	`SPA`	`@0 Citogenética @5 35`
C03	`15`	`X`	`FRE`	`@0 Citrus reticulata Citrus sinensis @2 NS @4 INC @5 77`
C03	`16`	`X`	`FRE`	`@0 Oryzalin @2 FF @4 INC @5 82`
C03	`17`	`X`	`FRE`	`@0 Autoploïdie @4 CD @5 96`
C03	`17`	`X`	`ENG`	`@0 Autoploidy @4 CD @5 96`
C03	`17`	`X`	`SPA`	`@0 Autoploidía @4 CD @5 96`
C07	`01`	`X`	`FRE`	`@0 Rutaceae @2 NS`
C07	`01`	`X`	`ENG`	`@0 Rutaceae @2 NS`
C07	`01`	`X`	`SPA`	`@0 Rutaceae @2 NS`
C07	`02`	`X`	`FRE`	`@0 Dicotyledones @2 NS`
C07	`02`	`X`	`ENG`	`@0 Dicotyledones @2 NS`
C07	`02`	`X`	`SPA`	`@0 Dicotyledones @2 NS`
C07	`03`	`X`	`FRE`	`@0 Angiospermae @2 NS`
C07	`03`	`X`	`ENG`	`@0 Angiospermae @2 NS`
C07	`03`	`X`	`SPA`	`@0 Angiospermae @2 NS`
C07	`04`	`X`	`FRE`	`@0 Spermatophyta @2 NS`
C07	`04`	`X`	`ENG`	`@0 Spermatophyta @2 NS`
C07	`04`	`X`	`SPA`	`@0 Spermatophyta @2 NS`
C07	`05`	`X`	`FRE`	`@0 Ploïdie @5 33`
C07	`05`	`X`	`ENG`	`@0 Ploidy @5 33`
C07	`05`	`X`	`SPA`	`@0 Ploidía @5 33`
C07	`06`	`X`	`FRE`	`@0 Agrume @5 39`
C07	`06`	`X`	`ENG`	`@0 Citrus fruit @5 39`
C07	`06`	`X`	`SPA`	`@0 Agrios @5 39`
C07	`07`	`X`	`FRE`	`@0 Alcaloïde @5 50`
C07	`07`	`X`	`ENG`	`@0 Alkaloid @5 50`
C07	`07`	`X`	`SPA`	`@0 Alcaloide @5 50`
C07	`08`	`X`	`FRE`	`@0 Mutagène @5 51`
C07	`08`	`X`	`ENG`	`@0 Mutagen @5 51`
C07	`08`	`X`	`SPA`	`@0 Mutágeno @5 51`
C07	`09`	`X`	`FRE`	`@0 Composé nitro @2 FX @5 52`
C07	`09`	`X`	`ENG`	`@0 Nitro compound @2 FX @5 52`
C07	`09`	`X`	`SPA`	`@0 Compuesto nitro @2 FX @5 52`
C07	`10`	`X`	`FRE`	`@0 Aniline dérivé @5 66`
C07	`10`	`X`	`ENG`	`@0 Aniline derivatives @5 66`
C07	`10`	`X`	`SPA`	`@0 Anilina derivado @5 66`
C07	`11`	`X`	`FRE`	`@0 Aniline(dinitro) @4 CD @5 98`
C07	`11`	`X`	`ENG`	`@0 Aniline(dinitro) @4 CD @5 98`
N21				`@1 266`
N82				`@1 PSI`

A30	`01`	`1`	`ENG`	`@1 New Zealand Regional IAPTC & B. Biennial Conference @2 14 @3 Grand Chateau, Mount Ruapehu NZL @4 2001-02-21`

Links toward previous steps (curation, corpus...)

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Pascal:02-0459190

Le document en format XML

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<author><name sortKey="Wu, Jin Hu" sort="Wu, Jin Hu" uniqKey="Wu J" first="Jin-Hu" last="Wu">Jin-Hu Wu</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>The Horticulture and Food Research Institute of New Zealand, Kerikeri Research Centre, P.O. Box 23</s1>
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<author><name sortKey="Mooney, Pauline" sort="Mooney, Pauline" uniqKey="Mooney P" first="Pauline" last="Mooney">Pauline Mooney</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>The Horticulture and Food Research Institute of New Zealand, Kerikeri Research Centre, P.O. Box 23</s1>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine</title>
<author><name sortKey="Wu, Jin Hu" sort="Wu, Jin Hu" uniqKey="Wu J" first="Jin-Hu" last="Wu">Jin-Hu Wu</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>The Horticulture and Food Research Institute of New Zealand, Kerikeri Research Centre, P.O. Box 23</s1>
<s2>Kerikeri</s2>
<s3>NZL</s3>
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<author><name sortKey="Mooney, Pauline" sort="Mooney, Pauline" uniqKey="Mooney P" first="Pauline" last="Mooney">Pauline Mooney</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>The Horticulture and Food Research Institute of New Zealand, Kerikeri Research Centre, P.O. Box 23</s1>
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<series><title level="j" type="main">Plant cell, tissue and organ culture</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Application method</term>
<term>Autoploidy</term>
<term>Callogenesis</term>
<term>Chromosomic number</term>
<term>Citrus paradisi</term>
<term>Citrus reticulata</term>
<term>Colchicine</term>
<term>Concentration effect</term>
<term>Cytogenetics</term>
<term>Doubled haploid</term>
<term>Flow cytometry</term>
<term>Micropropagation</term>
<term>Regeneration</term>
<term>Somatic embryo</term>
<term>Tetraploidy</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Tétraploïdie</term>
<term>Régénération</term>
<term>Haploïde doublé</term>
<term>Modalité traitement</term>
<term>Callogenèse</term>
<term>Effet concentration</term>
<term>Multiplication végétative in vitro</term>
<term>Nombre chromosomique</term>
<term>Cytométrie flux</term>
<term>Citrus reticulata</term>
<term>Citrus paradisi</term>
<term>Colchicine</term>
<term>Embryon somatique</term>
<term>Cytogénétique</term>
<term>Citrus reticulata  Citrus sinensis</term>
<term>Oryzalin</term>
<term>Autoploïdie</term>
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<front><div type="abstract" xml:lang="en">In vitro chromosome doubling of embryogenic callus lines of the Citrus cultivars 'Umatilla' and 'Dweet' tangors (Citrus reticulata Blanco×C. sinensis [L.] Osb.), 'Caffin' clementine (C. clementina Hort. ex Tan.) and 'Wheeny' grapefruit (C. paradisi Macf) was carried out in the presence of either 0.05 or 0.1% colchicine, or 0.01, 0.05 or 0.1% oryzalin. Embryogenic callus development was partly suppressed in the presence of colchicine, and completely suppressed by oryzalin at all concentrations tested. No plants were regenerated from any of the oryzalin treatments. Ploidy level of plants regenerated from the colchicine treatments was determined using flow cytometry and chromosome squashes. Three desirable non-chimeric, autotetraploid plants of the mono-embryonic cultivar 'Umatilla' were produced using 0.05% colchicine and one from 0.1% colchicine. One mixoploid 'Dweet' plant was produced using 0.1% colchicine.</div>
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<fA08 i1="01" i2="1" l="ENG"><s1>Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine</s1>
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<fA09 i1="01" i2="1" l="ENG"><s1>Special issue on the New Zealand Regional IAPTC & B Conference 2001</s1>
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<s9>ed.</s9>
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<fA12 i1="04" i2="1"><s1>DE KLERK (Geert-Jan M.)</s1>
<s9>ed.</s9>
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<fA14 i1="01"><s1>The Horticulture and Food Research Institute of New Zealand, Kerikeri Research Centre, P.O. Box 23</s1>
<s2>Kerikeri</s2>
<s3>NZL</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
</fA14>
<fA15 i1="01"><s1>New Zealand Institute for Crop & Food Research Limited, Private Bag 11 600</s1>
<s2>Palmerston North</s2>
<s3>NZL</s3>
<sZ>1 aut.</sZ>
</fA15>
<fA18 i1="01" i2="1"><s1>International Association for Plant Tissue Culture and Biotechnology. New Zealand Branch</s1>
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<fC01 i1="01" l="ENG"><s0>In vitro chromosome doubling of embryogenic callus lines of the Citrus cultivars 'Umatilla' and 'Dweet' tangors (Citrus reticulata Blanco×C. sinensis [L.] Osb.), 'Caffin' clementine (C. clementina Hort. ex Tan.) and 'Wheeny' grapefruit (C. paradisi Macf) was carried out in the presence of either 0.05 or 0.1% colchicine, or 0.01, 0.05 or 0.1% oryzalin. Embryogenic callus development was partly suppressed in the presence of colchicine, and completely suppressed by oryzalin at all concentrations tested. No plants were regenerated from any of the oryzalin treatments. Ploidy level of plants regenerated from the colchicine treatments was determined using flow cytometry and chromosome squashes. Three desirable non-chimeric, autotetraploid plants of the mono-embryonic cultivar 'Umatilla' were produced using 0.05% colchicine and one from 0.1% colchicine. One mixoploid 'Dweet' plant was produced using 0.1% colchicine.</s0>
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<s5>02</s5>
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<s5>02</s5>
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<fC03 i1="03" i2="X" l="FRE"><s0>Haploïde doublé</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Doubled haploid</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Doble haploide</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Modalité traitement</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Application method</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Modalidad tratamiento</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Callogenèse</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Callogenesis</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Callogénesis</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Effet concentration</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Concentration effect</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Efecto concentración</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Multiplication végétative in vitro</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Micropropagation</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Multiplicación vegetativa in vitro</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Nombre chromosomique</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Chromosomic number</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Número cromosómico</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Cytométrie flux</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Flow cytometry</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Citometría flujo</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Citrus reticulata</s0>
<s2>NS</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Citrus reticulata</s0>
<s2>NS</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Citrus reticulata</s0>
<s2>NS</s2>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE"><s0>Citrus paradisi</s0>
<s2>NS</s2>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>Citrus paradisi</s0>
<s2>NS</s2>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA"><s0>Citrus paradisi</s0>
<s2>NS</s2>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE"><s0>Colchicine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>15</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG"><s0>Colchicine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>15</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA"><s0>Colchicina</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>15</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>Embryon somatique</s0>
<s5>34</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG"><s0>Somatic embryo</s0>
<s5>34</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA"><s0>Embrión somático</s0>
<s5>34</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE"><s0>Cytogénétique</s0>
<s5>35</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG"><s0>Cytogenetics</s0>
<s5>35</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA"><s0>Citogenética</s0>
<s5>35</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Citrus reticulata  Citrus sinensis</s0>
<s2>NS</s2>
<s4>INC</s4>
<s5>77</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE"><s0>Oryzalin</s0>
<s2>FF</s2>
<s4>INC</s4>
<s5>82</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE"><s0>Autoploïdie</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="17" i2="X" l="ENG"><s0>Autoploidy</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="17" i2="X" l="SPA"><s0>Autoploidía</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Ploïdie</s0>
<s5>33</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Ploidy</s0>
<s5>33</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Ploidía</s0>
<s5>33</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Agrume</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Citrus fruit</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Agrios</s0>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Alcaloïde</s0>
<s5>50</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Alkaloid</s0>
<s5>50</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Alcaloide</s0>
<s5>50</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Mutagène</s0>
<s5>51</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Mutagen</s0>
<s5>51</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Mutágeno</s0>
<s5>51</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Composé nitro</s0>
<s2>FX</s2>
<s5>52</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Nitro compound</s0>
<s2>FX</s2>
<s5>52</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Compuesto nitro</s0>
<s2>FX</s2>
<s5>52</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Aniline dérivé</s0>
<s5>66</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Aniline derivatives</s0>
<s5>66</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Anilina derivado</s0>
<s5>66</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE"><s0>Aniline(dinitro)</s0>
<s4>CD</s4>
<s5>98</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG"><s0>Aniline(dinitro)</s0>
<s4>CD</s4>
<s5>98</s5>
</fC07>
<fN21><s1>266</s1>
</fN21>
<fN82><s1>PSI</s1>
</fN82>
</pA>
<pR><fA30 i1="01" i2="1" l="ENG"><s1>New Zealand Regional IAPTC & B. Biennial Conference</s1>
<s2>14</s2>
<s3>Grand Chateau, Mount Ruapehu NZL</s3>
<s4>2001-02-21</s4>
</fA30>
</pR>
</standard>
</inist>
</record>

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   |texte=   Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine
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Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine

Autotetraploid tangor plant regeneration from in vitro Citrus somatic embryogenic callus treated with colchicine

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