Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus

Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic com...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Polukonova, N. V. [verfasserIn] Shaternikov, A. N. [verfasserIn] Karmokov, M. Kh. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2015

Schlagwörter:	Polytene Chromosome Chromosomal Polymorphism Somatic Mosaicism Banding Sequence Inversion Polymorphism

Übergeordnetes Werk:	Enthalten in: Russian journal of genetics - Moscow : MAIK Nauka/Interperiodica Publ., 1996, 51(2015), 1 vom: Jan., Seite 22-32
Übergeordnetes Werk:	volume:51 ; year:2015 ; number:1 ; month:01 ; pages:22-32

Links:	Volltext

DOI / URN:	10.1134/S1022795415010111

Katalog-ID:	SPR017468256

Internformat


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100	1		\|a Polukonova, N. V. \|e verfasserin \|4 aut
245	1	0	\|a Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus
264		1	\|c 2015
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520			\|a Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct.
650		4	\|a Polytene Chromosome \|7 (dpeaa)DE-He213
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700	1		\|a Karmokov, M. Kh. \|e verfasserin \|4 aut
773	0	8	\|i Enthalten in \|t Russian journal of genetics \|d Moscow : MAIK Nauka/Interperiodica Publ., 1996 \|g 51(2015), 1 vom: Jan., Seite 22-32 \|w (DE-627)324825641 \|w (DE-600)2031145-X \|x 1608-3369 \|7 nnns
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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_101
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_120
912			\|a GBV_ILN_138
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_171
912			\|a GBV_ILN_187
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_250
912			\|a GBV_ILN_281
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_636
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_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
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_2031
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2037
912			\|a GBV_ILN_2038
912			\|a GBV_ILN_2039
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_2057
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_2070
912			\|a GBV_ILN_2086
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2093
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2107
912			\|a GBV_ILN_2108
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2113
912			\|a GBV_ILN_2116
912			\|a GBV_ILN_2118
912			\|a GBV_ILN_2119
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2144
912			\|a GBV_ILN_2147
912			\|a GBV_ILN_2148
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
912			\|a GBV_ILN_2188
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2232
912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2446
912			\|a GBV_ILN_2470
912			\|a GBV_ILN_2472
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_2522
912			\|a GBV_ILN_2548
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_4246
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_4336
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
936	b	k	\|a 42.20 \|q ASE
951			\|a AR
952			\|d 51 \|j 2015 \|e 1 \|c 01 \|h 22-32

Indexfelder

author_variant	n v p nv nvp a n s an ans m k k mk mkk
matchkey_str	article:16083369:2015----::nesoplmrhsonniigigsapohrnmsetnfbiis85itrciooiafoppltos
hierarchy_sort_str	2015
bklnumber	42.20
publishDate	2015
allfields	10.1134/S1022795415010111 doi (DE-627)SPR017468256 (SPR)S1022795415010111-e DE-627 ger DE-627 rakwb eng 570 ASE 42.20 bkl Polukonova, N. V. verfasserin aut Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct. Polytene Chromosome (dpeaa)DE-He213 Chromosomal Polymorphism (dpeaa)DE-He213 Somatic Mosaicism (dpeaa)DE-He213 Banding Sequence (dpeaa)DE-He213 Inversion Polymorphism (dpeaa)DE-He213 Shaternikov, A. N. verfasserin aut Karmokov, M. Kh. verfasserin aut Enthalten in Russian journal of genetics Moscow : MAIK Nauka/Interperiodica Publ., 1996 51(2015), 1 vom: Jan., Seite 22-32 (DE-627)324825641 (DE-600)2031145-X 1608-3369 nnns volume:51 year:2015 number:1 month:01 pages:22-32 https://dx.doi.org/10.1134/S1022795415010111 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 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_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 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_4246 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_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.20 ASE AR 51 2015 1 01 22-32
spelling	10.1134/S1022795415010111 doi (DE-627)SPR017468256 (SPR)S1022795415010111-e DE-627 ger DE-627 rakwb eng 570 ASE 42.20 bkl Polukonova, N. V. verfasserin aut Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct. Polytene Chromosome (dpeaa)DE-He213 Chromosomal Polymorphism (dpeaa)DE-He213 Somatic Mosaicism (dpeaa)DE-He213 Banding Sequence (dpeaa)DE-He213 Inversion Polymorphism (dpeaa)DE-He213 Shaternikov, A. N. verfasserin aut Karmokov, M. Kh. verfasserin aut Enthalten in Russian journal of genetics Moscow : MAIK Nauka/Interperiodica Publ., 1996 51(2015), 1 vom: Jan., Seite 22-32 (DE-627)324825641 (DE-600)2031145-X 1608-3369 nnns volume:51 year:2015 number:1 month:01 pages:22-32 https://dx.doi.org/10.1134/S1022795415010111 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 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_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 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_4246 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_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.20 ASE AR 51 2015 1 01 22-32
allfields_unstemmed	10.1134/S1022795415010111 doi (DE-627)SPR017468256 (SPR)S1022795415010111-e DE-627 ger DE-627 rakwb eng 570 ASE 42.20 bkl Polukonova, N. V. verfasserin aut Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct. Polytene Chromosome (dpeaa)DE-He213 Chromosomal Polymorphism (dpeaa)DE-He213 Somatic Mosaicism (dpeaa)DE-He213 Banding Sequence (dpeaa)DE-He213 Inversion Polymorphism (dpeaa)DE-He213 Shaternikov, A. N. verfasserin aut Karmokov, M. Kh. verfasserin aut Enthalten in Russian journal of genetics Moscow : MAIK Nauka/Interperiodica Publ., 1996 51(2015), 1 vom: Jan., Seite 22-32 (DE-627)324825641 (DE-600)2031145-X 1608-3369 nnns volume:51 year:2015 number:1 month:01 pages:22-32 https://dx.doi.org/10.1134/S1022795415010111 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 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_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 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_4246 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_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.20 ASE AR 51 2015 1 01 22-32
allfieldsGer	10.1134/S1022795415010111 doi (DE-627)SPR017468256 (SPR)S1022795415010111-e DE-627 ger DE-627 rakwb eng 570 ASE 42.20 bkl Polukonova, N. V. verfasserin aut Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct. Polytene Chromosome (dpeaa)DE-He213 Chromosomal Polymorphism (dpeaa)DE-He213 Somatic Mosaicism (dpeaa)DE-He213 Banding Sequence (dpeaa)DE-He213 Inversion Polymorphism (dpeaa)DE-He213 Shaternikov, A. N. verfasserin aut Karmokov, M. Kh. verfasserin aut Enthalten in Russian journal of genetics Moscow : MAIK Nauka/Interperiodica Publ., 1996 51(2015), 1 vom: Jan., Seite 22-32 (DE-627)324825641 (DE-600)2031145-X 1608-3369 nnns volume:51 year:2015 number:1 month:01 pages:22-32 https://dx.doi.org/10.1134/S1022795415010111 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 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_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 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_4246 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_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.20 ASE AR 51 2015 1 01 22-32
allfieldsSound	10.1134/S1022795415010111 doi (DE-627)SPR017468256 (SPR)S1022795415010111-e DE-627 ger DE-627 rakwb eng 570 ASE 42.20 bkl Polukonova, N. V. verfasserin aut Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct. Polytene Chromosome (dpeaa)DE-He213 Chromosomal Polymorphism (dpeaa)DE-He213 Somatic Mosaicism (dpeaa)DE-He213 Banding Sequence (dpeaa)DE-He213 Inversion Polymorphism (dpeaa)DE-He213 Shaternikov, A. N. verfasserin aut Karmokov, M. Kh. verfasserin aut Enthalten in Russian journal of genetics Moscow : MAIK Nauka/Interperiodica Publ., 1996 51(2015), 1 vom: Jan., Seite 22-32 (DE-627)324825641 (DE-600)2031145-X 1608-3369 nnns volume:51 year:2015 number:1 month:01 pages:22-32 https://dx.doi.org/10.1134/S1022795415010111 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 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_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 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_4246 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_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.20 ASE AR 51 2015 1 01 22-32
language	English
source	Enthalten in Russian journal of genetics 51(2015), 1 vom: Jan., Seite 22-32 volume:51 year:2015 number:1 month:01 pages:22-32
sourceStr	Enthalten in Russian journal of genetics 51(2015), 1 vom: Jan., Seite 22-32 volume:51 year:2015 number:1 month:01 pages:22-32
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Polytene Chromosome Chromosomal Polymorphism Somatic Mosaicism Banding Sequence Inversion Polymorphism
dewey-raw	570
isfreeaccess_bool	false
container_title	Russian journal of genetics
authorswithroles_txt_mv	Polukonova, N. V. @@aut@@ Shaternikov, A. N. @@aut@@ Karmokov, M. Kh. @@aut@@
publishDateDaySort_date	2015-01-01T00:00:00Z
hierarchy_top_id	324825641
dewey-sort	3570
id	SPR017468256
language_de	englisch
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author	Polukonova, N. V.
spellingShingle	Polukonova, N. V. ddc 570 bkl 42.20 misc Polytene Chromosome misc Chromosomal Polymorphism misc Somatic Mosaicism misc Banding Sequence misc Inversion Polymorphism Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus
authorStr	Polukonova, N. V.
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topic_title	570 ASE 42.20 bkl Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus Polytene Chromosome (dpeaa)DE-He213 Chromosomal Polymorphism (dpeaa)DE-He213 Somatic Mosaicism (dpeaa)DE-He213 Banding Sequence (dpeaa)DE-He213 Inversion Polymorphism (dpeaa)DE-He213
topic	ddc 570 bkl 42.20 misc Polytene Chromosome misc Chromosomal Polymorphism misc Somatic Mosaicism misc Banding Sequence misc Inversion Polymorphism
topic_unstemmed	ddc 570 bkl 42.20 misc Polytene Chromosome misc Chromosomal Polymorphism misc Somatic Mosaicism misc Banding Sequence misc Inversion Polymorphism
topic_browse	ddc 570 bkl 42.20 misc Polytene Chromosome misc Chromosomal Polymorphism misc Somatic Mosaicism misc Banding Sequence misc Inversion Polymorphism
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title	Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus
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title_full	Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus
author_sort	Polukonova, N. V.
journal	Russian journal of genetics
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author_browse	Polukonova, N. V. Shaternikov, A. N. Karmokov, M. Kh.
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class	570 ASE 42.20 bkl
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author-letter	Polukonova, N. V.
doi_str_mv	10.1134/S1022795415010111
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title_sort	inversion polymorphism of non-biting midges camptochironomus tentans (fabricius) 1805 (diptera, chironomidae) from populations of the lower volga region and central caucasus
title_auth	Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus
abstract	Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct.
abstractGer	Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct.
abstract_unstemmed	Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. The zygotic combinations in all the studied populations were distinct.
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title_short	Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus
url	https://dx.doi.org/10.1134/S1022795415010111
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author2	Shaternikov, A. N. Karmokov, M. Kh
author2Str	Shaternikov, A. N. Karmokov, M. Kh
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doi_str	10.1134/S1022795415010111
up_date	2024-07-04T03:28:06.665Z
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V.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2015</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</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">Abstract The karyotype of Camptochironomus tentans (Fabricius), 1805 (Diptera, Chironomidae) from the populations of the Lower Volga region and Central Caucasus (the northern macroslope) has been studied. In the karyotype of C. tentans from Saratov oblast, 14 banding sequences (BS), 13 genotypic combinations, and 14 zygotic combinations were identified. Four new BSs were described: ten B12, ten F4, ten F5, and ten G4, which are distinguished by simple paracentric inversions from those already known for the species. The chromosomal polymorphism belongs to the inversion type; its level in the Saratov population is generally the same as in populations of other parts of the area. The number of heterozygous inversions per specimen was 1.3; the number of heterozygous inversions per arm was 0.86; the percentage of heterozygous larvae was 84.5. The polymorphic arms in C. tentans were A, B, C, and F. Nine previously known BSs were revealed in the karyotype of C. tentans from Central Caucasus, and no new sequences were found. Arm B in C. tentans was polymorphic. 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Inversion polymorphism of non-biting midges Camptochironomus tentans (Fabricius) 1805 (Diptera, Chironomidae) from populations of the Lower Volga region and Central Caucasus

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