Genetic diversity of wild grape hyacinth (
Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Khaleghi, Alireza [verfasserIn] Khadivi, Ali [verfasserIn] |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2022 |
|---|
| Schlagwörter: |
|---|
| Übergeordnetes Werk: |
Enthalten in: South African journal of botany - Amsterdam : Elsevier, 1982, 148, Seite 307-314 |
|---|---|
| Übergeordnetes Werk: |
volume:148 ; pages:307-314 |
| DOI / URN: |
10.1016/j.sajb.2022.05.001 |
|---|
| Katalog-ID: |
ELV008265410 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | ELV008265410 | ||
| 003 | DE-627 | ||
| 005 | 20230524125917.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 230508s2022 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1016/j.sajb.2022.05.001 |2 doi | |
| 035 | |a (DE-627)ELV008265410 | ||
| 035 | |a (ELSEVIER)S0254-6299(22)00218-6 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rda | ||
| 041 | |a eng | ||
| 082 | 0 | 4 | |a 580 |q DE-600 |
| 084 | |a AFRIKA |q DE-30 |2 fid | ||
| 084 | |a BIODIV |q DE-30 |2 fid | ||
| 084 | |a 42.38 |2 bkl | ||
| 100 | 1 | |a Khaleghi, Alireza |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Genetic diversity of wild grape hyacinth ( |
| 264 | 1 | |c 2022 | |
| 336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
| 338 | |a Online-Ressource |b cr |2 rdacarrier | ||
| 520 | |a Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. | ||
| 650 | 4 | |a Accession | |
| 650 | 4 | |a Breeding | |
| 650 | 4 | |a Conservation | |
| 650 | 4 | |a Morphological diversity | |
| 650 | 4 | |a Wild grape hyacinth | |
| 700 | 1 | |a Khadivi, Ali |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t South African journal of botany |d Amsterdam : Elsevier, 1982 |g 148, Seite 307-314 |h Online-Ressource |w (DE-627)373504608 |w (DE-600)2126918-X |w (DE-576)259486205 |7 nnns |
| 773 | 1 | 8 | |g volume:148 |g pages:307-314 |
| 912 | |a GBV_USEFLAG_U | ||
| 912 | |a SYSFLAG_U | ||
| 912 | |a GBV_ELV | ||
| 912 | |a FID-AFRIKA | ||
| 912 | |a FID-BIODIV | ||
| 912 | |a GBV_ILN_20 | ||
| 912 | |a GBV_ILN_22 | ||
| 912 | |a GBV_ILN_23 | ||
| 912 | |a GBV_ILN_24 | ||
| 912 | |a GBV_ILN_31 | ||
| 912 | |a GBV_ILN_32 | ||
| 912 | |a GBV_ILN_39 | ||
| 912 | |a GBV_ILN_40 | ||
| 912 | |a GBV_ILN_60 | ||
| 912 | |a GBV_ILN_62 | ||
| 912 | |a GBV_ILN_63 | ||
| 912 | |a GBV_ILN_65 | ||
| 912 | |a GBV_ILN_69 | ||
| 912 | |a GBV_ILN_70 | ||
| 912 | |a GBV_ILN_73 | ||
| 912 | |a GBV_ILN_74 | ||
| 912 | |a GBV_ILN_90 | ||
| 912 | |a GBV_ILN_95 | ||
| 912 | |a GBV_ILN_100 | ||
| 912 | |a GBV_ILN_105 | ||
| 912 | |a GBV_ILN_110 | ||
| 912 | |a GBV_ILN_151 | ||
| 912 | |a GBV_ILN_161 | ||
| 912 | |a GBV_ILN_213 | ||
| 912 | |a GBV_ILN_224 | ||
| 912 | |a GBV_ILN_230 | ||
| 912 | |a GBV_ILN_285 | ||
| 912 | |a GBV_ILN_293 | ||
| 912 | |a GBV_ILN_370 | ||
| 912 | |a GBV_ILN_602 | ||
| 912 | |a GBV_ILN_702 | ||
| 912 | |a GBV_ILN_2001 | ||
| 912 | |a GBV_ILN_2003 | ||
| 912 | |a GBV_ILN_2004 | ||
| 912 | |a GBV_ILN_2005 | ||
| 912 | |a GBV_ILN_2006 | ||
| 912 | |a GBV_ILN_2008 | ||
| 912 | |a GBV_ILN_2011 | ||
| 912 | |a GBV_ILN_2014 | ||
| 912 | |a GBV_ILN_2015 | ||
| 912 | |a GBV_ILN_2020 | ||
| 912 | |a GBV_ILN_2021 | ||
| 912 | |a GBV_ILN_2025 | ||
| 912 | |a GBV_ILN_2026 | ||
| 912 | |a GBV_ILN_2027 | ||
| 912 | |a GBV_ILN_2034 | ||
| 912 | |a GBV_ILN_2038 | ||
| 912 | |a GBV_ILN_2044 | ||
| 912 | |a GBV_ILN_2048 | ||
| 912 | |a GBV_ILN_2049 | ||
| 912 | |a GBV_ILN_2050 | ||
| 912 | |a GBV_ILN_2055 | ||
| 912 | |a GBV_ILN_2056 | ||
| 912 | |a GBV_ILN_2059 | ||
| 912 | |a GBV_ILN_2061 | ||
| 912 | |a GBV_ILN_2064 | ||
| 912 | |a GBV_ILN_2065 | ||
| 912 | |a GBV_ILN_2068 | ||
| 912 | |a GBV_ILN_2088 | ||
| 912 | |a GBV_ILN_2111 | ||
| 912 | |a GBV_ILN_2112 | ||
| 912 | |a GBV_ILN_2113 | ||
| 912 | |a GBV_ILN_2118 | ||
| 912 | |a GBV_ILN_2122 | ||
| 912 | |a GBV_ILN_2129 | ||
| 912 | |a GBV_ILN_2143 | ||
| 912 | |a GBV_ILN_2147 | ||
| 912 | |a GBV_ILN_2148 | ||
| 912 | |a GBV_ILN_2152 | ||
| 912 | |a GBV_ILN_2153 | ||
| 912 | |a GBV_ILN_2190 | ||
| 912 | |a GBV_ILN_2232 | ||
| 912 | |a GBV_ILN_2336 | ||
| 912 | |a GBV_ILN_2470 | ||
| 912 | |a GBV_ILN_2507 | ||
| 912 | |a GBV_ILN_2522 | ||
| 912 | |a GBV_ILN_4012 | ||
| 912 | |a GBV_ILN_4035 | ||
| 912 | |a GBV_ILN_4037 | ||
| 912 | |a GBV_ILN_4046 | ||
| 912 | |a GBV_ILN_4112 | ||
| 912 | |a GBV_ILN_4125 | ||
| 912 | |a GBV_ILN_4126 | ||
| 912 | |a GBV_ILN_4242 | ||
| 912 | |a GBV_ILN_4249 | ||
| 912 | |a GBV_ILN_4251 | ||
| 912 | |a GBV_ILN_4305 | ||
| 912 | |a GBV_ILN_4306 | ||
| 912 | |a GBV_ILN_4307 | ||
| 912 | |a GBV_ILN_4313 | ||
| 912 | |a GBV_ILN_4322 | ||
| 912 | |a GBV_ILN_4323 | ||
| 912 | |a GBV_ILN_4324 | ||
| 912 | |a GBV_ILN_4325 | ||
| 912 | |a GBV_ILN_4326 | ||
| 912 | |a GBV_ILN_4333 | ||
| 912 | |a GBV_ILN_4334 | ||
| 912 | |a GBV_ILN_4335 | ||
| 912 | |a GBV_ILN_4338 | ||
| 912 | |a GBV_ILN_4367 | ||
| 912 | |a GBV_ILN_4393 | ||
| 912 | |a GBV_ILN_4700 | ||
| 936 | b | k | |a 42.38 |j Botanik: Allgemeines |
| 951 | |a AR | ||
| 952 | |d 148 |h 307-314 | ||
| author_variant |
a k ak a k ak |
|---|---|
| matchkey_str |
khaleghialirezakhadiviali:2022----:eeidvriyfidr |
| hierarchy_sort_str |
2022 |
| bklnumber |
42.38 |
| publishDate |
2022 |
| allfields |
10.1016/j.sajb.2022.05.001 doi (DE-627)ELV008265410 (ELSEVIER)S0254-6299(22)00218-6 DE-627 ger DE-627 rda eng 580 DE-600 AFRIKA DE-30 fid BIODIV DE-30 fid 42.38 bkl Khaleghi, Alireza verfasserin aut Genetic diversity of wild grape hyacinth ( 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. Accession Breeding Conservation Morphological diversity Wild grape hyacinth Khadivi, Ali verfasserin aut Enthalten in South African journal of botany Amsterdam : Elsevier, 1982 148, Seite 307-314 Online-Ressource (DE-627)373504608 (DE-600)2126918-X (DE-576)259486205 nnns volume:148 pages:307-314 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-AFRIKA FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.38 Botanik: Allgemeines AR 148 307-314 |
| spelling |
10.1016/j.sajb.2022.05.001 doi (DE-627)ELV008265410 (ELSEVIER)S0254-6299(22)00218-6 DE-627 ger DE-627 rda eng 580 DE-600 AFRIKA DE-30 fid BIODIV DE-30 fid 42.38 bkl Khaleghi, Alireza verfasserin aut Genetic diversity of wild grape hyacinth ( 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. Accession Breeding Conservation Morphological diversity Wild grape hyacinth Khadivi, Ali verfasserin aut Enthalten in South African journal of botany Amsterdam : Elsevier, 1982 148, Seite 307-314 Online-Ressource (DE-627)373504608 (DE-600)2126918-X (DE-576)259486205 nnns volume:148 pages:307-314 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-AFRIKA FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.38 Botanik: Allgemeines AR 148 307-314 |
| allfields_unstemmed |
10.1016/j.sajb.2022.05.001 doi (DE-627)ELV008265410 (ELSEVIER)S0254-6299(22)00218-6 DE-627 ger DE-627 rda eng 580 DE-600 AFRIKA DE-30 fid BIODIV DE-30 fid 42.38 bkl Khaleghi, Alireza verfasserin aut Genetic diversity of wild grape hyacinth ( 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. Accession Breeding Conservation Morphological diversity Wild grape hyacinth Khadivi, Ali verfasserin aut Enthalten in South African journal of botany Amsterdam : Elsevier, 1982 148, Seite 307-314 Online-Ressource (DE-627)373504608 (DE-600)2126918-X (DE-576)259486205 nnns volume:148 pages:307-314 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-AFRIKA FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.38 Botanik: Allgemeines AR 148 307-314 |
| allfieldsGer |
10.1016/j.sajb.2022.05.001 doi (DE-627)ELV008265410 (ELSEVIER)S0254-6299(22)00218-6 DE-627 ger DE-627 rda eng 580 DE-600 AFRIKA DE-30 fid BIODIV DE-30 fid 42.38 bkl Khaleghi, Alireza verfasserin aut Genetic diversity of wild grape hyacinth ( 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. Accession Breeding Conservation Morphological diversity Wild grape hyacinth Khadivi, Ali verfasserin aut Enthalten in South African journal of botany Amsterdam : Elsevier, 1982 148, Seite 307-314 Online-Ressource (DE-627)373504608 (DE-600)2126918-X (DE-576)259486205 nnns volume:148 pages:307-314 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-AFRIKA FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.38 Botanik: Allgemeines AR 148 307-314 |
| allfieldsSound |
10.1016/j.sajb.2022.05.001 doi (DE-627)ELV008265410 (ELSEVIER)S0254-6299(22)00218-6 DE-627 ger DE-627 rda eng 580 DE-600 AFRIKA DE-30 fid BIODIV DE-30 fid 42.38 bkl Khaleghi, Alireza verfasserin aut Genetic diversity of wild grape hyacinth ( 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. Accession Breeding Conservation Morphological diversity Wild grape hyacinth Khadivi, Ali verfasserin aut Enthalten in South African journal of botany Amsterdam : Elsevier, 1982 148, Seite 307-314 Online-Ressource (DE-627)373504608 (DE-600)2126918-X (DE-576)259486205 nnns volume:148 pages:307-314 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-AFRIKA FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 42.38 Botanik: Allgemeines AR 148 307-314 |
| language |
English |
| source |
Enthalten in South African journal of botany 148, Seite 307-314 volume:148 pages:307-314 |
| sourceStr |
Enthalten in South African journal of botany 148, Seite 307-314 volume:148 pages:307-314 |
| format_phy_str_mv |
Article |
| bklname |
Botanik: Allgemeines |
| institution |
findex.gbv.de |
| topic_facet |
Accession Breeding Conservation Morphological diversity Wild grape hyacinth |
| dewey-raw |
580 |
| isfreeaccess_bool |
false |
| container_title |
South African journal of botany |
| authorswithroles_txt_mv |
Khaleghi, Alireza @@aut@@ Khadivi, Ali @@aut@@ |
| publishDateDaySort_date |
2022-01-01T00:00:00Z |
| hierarchy_top_id |
373504608 |
| dewey-sort |
3580 |
| id |
ELV008265410 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV008265410</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230524125917.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230508s2022 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.sajb.2022.05.001</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV008265410</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0254-6299(22)00218-6</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">580</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">AFRIKA</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">BIODIV</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">42.38</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Khaleghi, Alireza</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Genetic diversity of wild grape hyacinth (</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2022</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Accession</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Breeding</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Conservation</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Morphological diversity</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Wild grape hyacinth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Khadivi, Ali</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">South African journal of botany</subfield><subfield code="d">Amsterdam : Elsevier, 1982</subfield><subfield code="g">148, Seite 307-314</subfield><subfield code="h">Online-Ressource</subfield><subfield code="w">(DE-627)373504608</subfield><subfield code="w">(DE-600)2126918-X</subfield><subfield code="w">(DE-576)259486205</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:148</subfield><subfield code="g">pages:307-314</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-AFRIKA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-BIODIV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_31</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_32</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_90</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_100</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_224</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_370</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_702</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2001</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2003</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2004</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2005</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2006</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2008</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2011</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2015</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2020</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2025</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2026</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2027</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2034</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2038</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2044</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2048</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2049</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2050</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2055</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2056</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2059</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2061</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2064</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2065</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2068</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2088</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2111</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2113</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2118</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2122</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2129</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2143</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2147</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2148</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2152</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2153</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2190</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2232</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2336</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2470</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2507</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2522</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4035</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4046</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4242</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4251</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4326</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4333</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4334</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4335</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4393</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">42.38</subfield><subfield code="j">Botanik: Allgemeines</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">148</subfield><subfield code="h">307-314</subfield></datafield></record></collection>
|
| author |
Khaleghi, Alireza |
| spellingShingle |
Khaleghi, Alireza ddc 580 fid AFRIKA fid BIODIV bkl 42.38 misc Accession misc Breeding misc Conservation misc Morphological diversity misc Wild grape hyacinth Genetic diversity of wild grape hyacinth ( |
| authorStr |
Khaleghi, Alireza |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)373504608 |
| format |
electronic Article |
| dewey-ones |
580 - Plants (Botany) |
| delete_txt_mv |
keep |
| author_role |
aut aut |
| collection |
elsevier |
| remote_str |
true |
| illustrated |
Not Illustrated |
| topic_title |
580 DE-600 AFRIKA DE-30 fid BIODIV DE-30 fid 42.38 bkl Genetic diversity of wild grape hyacinth ( Accession Breeding Conservation Morphological diversity Wild grape hyacinth |
| topic |
ddc 580 fid AFRIKA fid BIODIV bkl 42.38 misc Accession misc Breeding misc Conservation misc Morphological diversity misc Wild grape hyacinth |
| topic_unstemmed |
ddc 580 fid AFRIKA fid BIODIV bkl 42.38 misc Accession misc Breeding misc Conservation misc Morphological diversity misc Wild grape hyacinth |
| topic_browse |
ddc 580 fid AFRIKA fid BIODIV bkl 42.38 misc Accession misc Breeding misc Conservation misc Morphological diversity misc Wild grape hyacinth |
| format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
cr |
| hierarchy_parent_title |
South African journal of botany |
| hierarchy_parent_id |
373504608 |
| dewey-tens |
580 - Plants (Botany) |
| hierarchy_top_title |
South African journal of botany |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)373504608 (DE-600)2126918-X (DE-576)259486205 |
| title |
Genetic diversity of wild grape hyacinth ( |
| ctrlnum |
(DE-627)ELV008265410 (ELSEVIER)S0254-6299(22)00218-6 |
| title_full |
Genetic diversity of wild grape hyacinth ( |
| author_sort |
Khaleghi, Alireza |
| journal |
South African journal of botany |
| journalStr |
South African journal of botany |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
500 - Science |
| recordtype |
marc |
| publishDateSort |
2022 |
| contenttype_str_mv |
zzz |
| container_start_page |
307 |
| author_browse |
Khaleghi, Alireza Khadivi, Ali |
| container_volume |
148 |
| class |
580 DE-600 AFRIKA DE-30 fid BIODIV DE-30 fid 42.38 bkl |
| format_se |
Elektronische Aufsätze |
| author-letter |
Khaleghi, Alireza |
| doi_str_mv |
10.1016/j.sajb.2022.05.001 |
| dewey-full |
580 |
| author2-role |
verfasserin |
| title_sort |
genetic diversity of wild grape hyacinth ( |
| title_auth |
Genetic diversity of wild grape hyacinth ( |
| abstract |
Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. |
| abstractGer |
Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. |
| abstract_unstemmed |
Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs. |
| collection_details |
GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-AFRIKA FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 |
| title_short |
Genetic diversity of wild grape hyacinth ( |
| remote_bool |
true |
| author2 |
Khadivi, Ali |
| author2Str |
Khadivi, Ali |
| ppnlink |
373504608 |
| mediatype_str_mv |
c |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| doi_str |
10.1016/j.sajb.2022.05.001 |
| up_date |
2024-07-06T19:06:30.169Z |
| _version_ |
1803857732745297920 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV008265410</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230524125917.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230508s2022 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.sajb.2022.05.001</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV008265410</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0254-6299(22)00218-6</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">580</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">AFRIKA</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">BIODIV</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">42.38</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Khaleghi, Alireza</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Genetic diversity of wild grape hyacinth (</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2022</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Grape hyacinth (Muscari neglectum Guss ex Ten.) is one of the economically important species that can be cultivated as an ornamental crop as well as in pharmaceutical, food, and dyeing industries. In the present study, a total of 140 wild accessions of this species from central regions of Iran were evaluated using 29 morphological characteristics. Significant phenotypic variations were observed among the accessions; especially desirable variations were detected for commercial traits such as peduncle length, peduncle diameter, length and width of leaf, inflorescence length, inflorescence density, floral scent, and bulblet number. The highest variability corresponded to floral scent, bulblet number, inflorescence shape, peduncle color, and inflorescence color. Coefficient of variation (CV) was the lowest for bulb length /bulb diameter, floret length, bulb diameter, and bulb length. Peduncle length, the most important feature of cut flower, varied from 7.5 to 25.2 cm with an average of 14.7. Bottommost leaf length ranged from 5.8 to 30 cm, while bottommost leaf width varied from 1 to 6 mm. Inflorescence length varied from 6 to 37 mm with an average of 19, while inflorescence diameter ranged from 1 to 16 mm. Senjegan-8 accession with the highest values for inflorescence length, inflorescence density, and rate for the length of peduncle was one of the superior accessions. According to principal component analysis (PCA), the first seven components of data accounted for 70.92% of the total variance. Scatter plot showed high level of phenotypic diversity among the studied accessions. Some of the superior accessions such as Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 were separated from others in scatter plot and characterized by the highest values for inflorescence density, bulblet number, bulb length, and bulb diameter. According to ornamental potential, five accessions, including Senjegan-8, Rudbaran-8, Rudbaran-20, Rudbaran-45, and Rudbaran-56 can be utilized in breeding programs.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Accession</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Breeding</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Conservation</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Morphological diversity</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Wild grape hyacinth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Khadivi, Ali</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">South African journal of botany</subfield><subfield code="d">Amsterdam : Elsevier, 1982</subfield><subfield code="g">148, Seite 307-314</subfield><subfield code="h">Online-Ressource</subfield><subfield code="w">(DE-627)373504608</subfield><subfield code="w">(DE-600)2126918-X</subfield><subfield code="w">(DE-576)259486205</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:148</subfield><subfield code="g">pages:307-314</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-AFRIKA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-BIODIV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_31</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_32</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_90</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_100</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_224</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_370</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_702</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2001</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2003</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2004</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2005</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2006</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2008</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2011</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2015</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2020</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2025</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2026</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2027</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2034</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2038</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2044</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2048</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2049</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2050</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2055</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2056</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2059</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2061</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2064</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2065</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2068</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2088</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2111</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2113</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2118</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2122</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2129</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2143</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2147</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2148</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2152</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2153</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2190</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2232</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2336</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2470</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2507</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2522</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4035</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4046</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4242</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4251</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4326</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4333</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4334</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4335</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4393</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">42.38</subfield><subfield code="j">Botanik: Allgemeines</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">148</subfield><subfield code="h">307-314</subfield></datafield></record></collection>
|
| score |
7.4016075 |