Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae)
Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especia...
Ausführliche Beschreibung
Autor*in: |
Fukuda, Katsuto [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2016 |
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Schlagwörter: |
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Anmerkung: |
© The Japanese Society of Applied Entomology and Zoology 2016 |
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Übergeordnetes Werk: |
Enthalten in: Applied entomology and zoology - Tokyo : Springer, 1966, 51(2016), 4 vom: 20. Aug., Seite 641-651 |
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Übergeordnetes Werk: |
volume:51 ; year:2016 ; number:4 ; day:20 ; month:08 ; pages:641-651 |
Links: |
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DOI / URN: |
10.1007/s13355-016-0441-4 |
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Katalog-ID: |
SPR031442978 |
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520 | |a Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. | ||
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650 | 4 | |a Sensilla per area density |7 (dpeaa)DE-He213 | |
650 | 4 | |a Sensory hair thickness |7 (dpeaa)DE-He213 | |
700 | 1 | |a Yanagawa, Aya |4 aut | |
700 | 1 | |a Tuda, Midori |4 aut | |
700 | 1 | |a Sakurai, Gen |4 aut | |
700 | 1 | |a Kamitani, Satoshi |4 aut | |
700 | 1 | |a Furuya, Naruto |4 aut | |
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10.1007/s13355-016-0441-4 doi (DE-627)SPR031442978 (SPR)s13355-016-0441-4-e DE-627 ger DE-627 rakwb eng Fukuda, Katsuto verfasserin aut Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Japanese Society of Applied Entomology and Zoology 2016 Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. Antennal sensilla (dpeaa)DE-He213 Bean beetle (dpeaa)DE-He213 Bruchidae (dpeaa)DE-He213 Sensilla per area density (dpeaa)DE-He213 Sensory hair thickness (dpeaa)DE-He213 Yanagawa, Aya aut Tuda, Midori aut Sakurai, Gen aut Kamitani, Satoshi aut Furuya, Naruto aut Enthalten in Applied entomology and zoology Tokyo : Springer, 1966 51(2016), 4 vom: 20. Aug., Seite 641-651 (DE-627)377757136 (DE-600)2133001-3 1347-605X nnns volume:51 year:2016 number:4 day:20 month:08 pages:641-651 https://dx.doi.org/10.1007/s13355-016-0441-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 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_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 AR 51 2016 4 20 08 641-651 |
spelling |
10.1007/s13355-016-0441-4 doi (DE-627)SPR031442978 (SPR)s13355-016-0441-4-e DE-627 ger DE-627 rakwb eng Fukuda, Katsuto verfasserin aut Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Japanese Society of Applied Entomology and Zoology 2016 Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. Antennal sensilla (dpeaa)DE-He213 Bean beetle (dpeaa)DE-He213 Bruchidae (dpeaa)DE-He213 Sensilla per area density (dpeaa)DE-He213 Sensory hair thickness (dpeaa)DE-He213 Yanagawa, Aya aut Tuda, Midori aut Sakurai, Gen aut Kamitani, Satoshi aut Furuya, Naruto aut Enthalten in Applied entomology and zoology Tokyo : Springer, 1966 51(2016), 4 vom: 20. Aug., Seite 641-651 (DE-627)377757136 (DE-600)2133001-3 1347-605X nnns volume:51 year:2016 number:4 day:20 month:08 pages:641-651 https://dx.doi.org/10.1007/s13355-016-0441-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 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_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 AR 51 2016 4 20 08 641-651 |
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10.1007/s13355-016-0441-4 doi (DE-627)SPR031442978 (SPR)s13355-016-0441-4-e DE-627 ger DE-627 rakwb eng Fukuda, Katsuto verfasserin aut Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Japanese Society of Applied Entomology and Zoology 2016 Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. Antennal sensilla (dpeaa)DE-He213 Bean beetle (dpeaa)DE-He213 Bruchidae (dpeaa)DE-He213 Sensilla per area density (dpeaa)DE-He213 Sensory hair thickness (dpeaa)DE-He213 Yanagawa, Aya aut Tuda, Midori aut Sakurai, Gen aut Kamitani, Satoshi aut Furuya, Naruto aut Enthalten in Applied entomology and zoology Tokyo : Springer, 1966 51(2016), 4 vom: 20. Aug., Seite 641-651 (DE-627)377757136 (DE-600)2133001-3 1347-605X nnns volume:51 year:2016 number:4 day:20 month:08 pages:641-651 https://dx.doi.org/10.1007/s13355-016-0441-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 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_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 AR 51 2016 4 20 08 641-651 |
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10.1007/s13355-016-0441-4 doi (DE-627)SPR031442978 (SPR)s13355-016-0441-4-e DE-627 ger DE-627 rakwb eng Fukuda, Katsuto verfasserin aut Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Japanese Society of Applied Entomology and Zoology 2016 Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. Antennal sensilla (dpeaa)DE-He213 Bean beetle (dpeaa)DE-He213 Bruchidae (dpeaa)DE-He213 Sensilla per area density (dpeaa)DE-He213 Sensory hair thickness (dpeaa)DE-He213 Yanagawa, Aya aut Tuda, Midori aut Sakurai, Gen aut Kamitani, Satoshi aut Furuya, Naruto aut Enthalten in Applied entomology and zoology Tokyo : Springer, 1966 51(2016), 4 vom: 20. Aug., Seite 641-651 (DE-627)377757136 (DE-600)2133001-3 1347-605X nnns volume:51 year:2016 number:4 day:20 month:08 pages:641-651 https://dx.doi.org/10.1007/s13355-016-0441-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 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_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 AR 51 2016 4 20 08 641-651 |
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10.1007/s13355-016-0441-4 doi (DE-627)SPR031442978 (SPR)s13355-016-0441-4-e DE-627 ger DE-627 rakwb eng Fukuda, Katsuto verfasserin aut Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Japanese Society of Applied Entomology and Zoology 2016 Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. Antennal sensilla (dpeaa)DE-He213 Bean beetle (dpeaa)DE-He213 Bruchidae (dpeaa)DE-He213 Sensilla per area density (dpeaa)DE-He213 Sensory hair thickness (dpeaa)DE-He213 Yanagawa, Aya aut Tuda, Midori aut Sakurai, Gen aut Kamitani, Satoshi aut Furuya, Naruto aut Enthalten in Applied entomology and zoology Tokyo : Springer, 1966 51(2016), 4 vom: 20. Aug., Seite 641-651 (DE-627)377757136 (DE-600)2133001-3 1347-605X nnns volume:51 year:2016 number:4 day:20 month:08 pages:641-651 https://dx.doi.org/10.1007/s13355-016-0441-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 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_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 AR 51 2016 4 20 08 641-651 |
language |
English |
source |
Enthalten in Applied entomology and zoology 51(2016), 4 vom: 20. Aug., Seite 641-651 volume:51 year:2016 number:4 day:20 month:08 pages:641-651 |
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Enthalten in Applied entomology and zoology 51(2016), 4 vom: 20. Aug., Seite 641-651 volume:51 year:2016 number:4 day:20 month:08 pages:641-651 |
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Antennal sensilla Bean beetle Bruchidae Sensilla per area density Sensory hair thickness |
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Applied entomology and zoology |
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Fukuda, Katsuto @@aut@@ Yanagawa, Aya @@aut@@ Tuda, Midori @@aut@@ Sakurai, Gen @@aut@@ Kamitani, Satoshi @@aut@@ Furuya, Naruto @@aut@@ |
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2016-08-20T00:00:00Z |
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The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Antennal sensilla</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Bean beetle</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Bruchidae</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Sensilla per area density</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Sensory hair thickness</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yanagawa, Aya</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Tuda, Midori</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Sakurai, Gen</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kamitani, Satoshi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Furuya, Naruto</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Applied entomology and zoology</subfield><subfield code="d">Tokyo : Springer, 1966</subfield><subfield code="g">51(2016), 4 vom: 20. 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|
author |
Fukuda, Katsuto |
spellingShingle |
Fukuda, Katsuto misc Antennal sensilla misc Bean beetle misc Bruchidae misc Sensilla per area density misc Sensory hair thickness Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) |
authorStr |
Fukuda, Katsuto |
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Not Illustrated |
issn |
1347-605X |
topic_title |
Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) Antennal sensilla (dpeaa)DE-He213 Bean beetle (dpeaa)DE-He213 Bruchidae (dpeaa)DE-He213 Sensilla per area density (dpeaa)DE-He213 Sensory hair thickness (dpeaa)DE-He213 |
topic |
misc Antennal sensilla misc Bean beetle misc Bruchidae misc Sensilla per area density misc Sensory hair thickness |
topic_unstemmed |
misc Antennal sensilla misc Bean beetle misc Bruchidae misc Sensilla per area density misc Sensory hair thickness |
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misc Antennal sensilla misc Bean beetle misc Bruchidae misc Sensilla per area density misc Sensory hair thickness |
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Elektronische Aufsätze Aufsätze Elektronische Ressource |
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Applied entomology and zoology |
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title |
Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) |
ctrlnum |
(DE-627)SPR031442978 (SPR)s13355-016-0441-4-e |
title_full |
Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) |
author_sort |
Fukuda, Katsuto |
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Applied entomology and zoology |
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Applied entomology and zoology |
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2016 |
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641 |
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Fukuda, Katsuto Yanagawa, Aya Tuda, Midori Sakurai, Gen Kamitani, Satoshi Furuya, Naruto |
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51 |
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Elektronische Aufsätze |
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Fukuda, Katsuto |
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10.1007/s13355-016-0441-4 |
title_sort |
sexual difference in antennal sensilla abundance, density and size in callosobruchus rhodesianus (coleoptera: chrysomelidae: bruchinae) |
title_auth |
Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) |
abstract |
Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. © The Japanese Society of Applied Entomology and Zoology 2016 |
abstractGer |
Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. © The Japanese Society of Applied Entomology and Zoology 2016 |
abstract_unstemmed |
Abstract Sexual difference in antennal sensilla size and per area density has rarely been studied in insects. The bruchine seed beetle Callosobruchus rhodesianus (Pic) (Coleoptera: Chrysomelidae: Bruchinae) is distributed over Central and Southern Africa and is a pest of stored legume seeds, especially cowpeas Vigna unguiculata. Here, we study the type, abundance, morphology and per area density of antennal sensilla on each antennal segment and their sexual differences in C. rhodesianus. The antennae of normal individuals consist of the scape, pedicel and nine flagellomeres as in other congeneric species. Sizes of most antennomeres are larger in males than in females. We observed the following eight different types of antennal sensilla: sensilla trichodea types 1 and 2 (ST1, ST2), sensillacavitae (SCa), sensilla chaetica (SC), sensilla basiconica types 1, 2 and 3 (SB1, SB2, SB3) and Böhm bristles (BB). The SCa is found on all antennomeres unlike in congeners (C. chinensis and C. maculatus). The ST1, the most numerous and longest antennal sensilla type, is denser and thinner in females than in males but more abundant in males than in females. Since the ST1 is considered to serve as a chemoreceptor, the sexual difference in the ST1 may benefit males in searching for mates. © The Japanese Society of Applied Entomology and Zoology 2016 |
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container_issue |
4 |
title_short |
Sexual difference in antennal sensilla abundance, density and size in Callosobruchus rhodesianus (Coleoptera: Chrysomelidae: Bruchinae) |
url |
https://dx.doi.org/10.1007/s13355-016-0441-4 |
remote_bool |
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author2 |
Yanagawa, Aya Tuda, Midori Sakurai, Gen Kamitani, Satoshi Furuya, Naruto |
author2Str |
Yanagawa, Aya Tuda, Midori Sakurai, Gen Kamitani, Satoshi Furuya, Naruto |
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hochschulschrift_bool |
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doi_str |
10.1007/s13355-016-0441-4 |
up_date |
2024-07-03T23:44:47.364Z |
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score |
7.401272 |