The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae)
Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organ...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Packer, Laurence [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1986 |
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| Schlagwörter: |
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| Anmerkung: |
© Springer-Verlag 1986 |
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| Übergeordnetes Werk: |
Enthalten in: Behavioral ecology and sociobiology - Berlin : Springer, 1976, 18(1986), 5 vom: 01. Apr., Seite 363-375 |
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| Übergeordnetes Werk: |
volume:18 ; year:1986 ; number:5 ; day:01 ; month:04 ; pages:363-375 |
| Links: |
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| DOI / URN: |
10.1007/BF00299667 |
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| Katalog-ID: |
SPR003293467 |
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| 100 | 1 | |a Packer, Laurence |e verfasserin |4 aut | |
| 245 | 1 | 4 | |a The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) |
| 264 | 1 | |c 1986 | |
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| 520 | |a Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. | ||
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| 650 | 4 | |a Colony Development |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Knerer, Gerd |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Behavioral ecology and sociobiology |d Berlin : Springer, 1976 |g 18(1986), 5 vom: 01. Apr., Seite 363-375 |w (DE-627)25339032X |w (DE-600)1458476-1 |x 1432-0762 |7 nnns |
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1986 |
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1986 |
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10.1007/BF00299667 doi (DE-627)SPR003293467 (SPR)BF00299667-e DE-627 ger DE-627 rakwb eng Packer, Laurence verfasserin aut The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) 1986 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 1986 Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. Ovarian Development (dpeaa)DE-He213 Head Width (dpeaa)DE-He213 Natal Nest (dpeaa)DE-He213 Female Pupa (dpeaa)DE-He213 Colony Development (dpeaa)DE-He213 Knerer, Gerd aut Enthalten in Behavioral ecology and sociobiology Berlin : Springer, 1976 18(1986), 5 vom: 01. Apr., Seite 363-375 (DE-627)25339032X (DE-600)1458476-1 1432-0762 nnns volume:18 year:1986 number:5 day:01 month:04 pages:363-375 https://dx.doi.org/10.1007/BF00299667 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_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_121 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_206 GBV_ILN_224 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 GBV_ILN_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4277 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 AR 18 1986 5 01 04 363-375 |
| spelling |
10.1007/BF00299667 doi (DE-627)SPR003293467 (SPR)BF00299667-e DE-627 ger DE-627 rakwb eng Packer, Laurence verfasserin aut The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) 1986 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 1986 Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. Ovarian Development (dpeaa)DE-He213 Head Width (dpeaa)DE-He213 Natal Nest (dpeaa)DE-He213 Female Pupa (dpeaa)DE-He213 Colony Development (dpeaa)DE-He213 Knerer, Gerd aut Enthalten in Behavioral ecology and sociobiology Berlin : Springer, 1976 18(1986), 5 vom: 01. Apr., Seite 363-375 (DE-627)25339032X (DE-600)1458476-1 1432-0762 nnns volume:18 year:1986 number:5 day:01 month:04 pages:363-375 https://dx.doi.org/10.1007/BF00299667 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_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_121 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_206 GBV_ILN_224 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 GBV_ILN_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4277 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 AR 18 1986 5 01 04 363-375 |
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10.1007/BF00299667 doi (DE-627)SPR003293467 (SPR)BF00299667-e DE-627 ger DE-627 rakwb eng Packer, Laurence verfasserin aut The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) 1986 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 1986 Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. Ovarian Development (dpeaa)DE-He213 Head Width (dpeaa)DE-He213 Natal Nest (dpeaa)DE-He213 Female Pupa (dpeaa)DE-He213 Colony Development (dpeaa)DE-He213 Knerer, Gerd aut Enthalten in Behavioral ecology and sociobiology Berlin : Springer, 1976 18(1986), 5 vom: 01. Apr., Seite 363-375 (DE-627)25339032X (DE-600)1458476-1 1432-0762 nnns volume:18 year:1986 number:5 day:01 month:04 pages:363-375 https://dx.doi.org/10.1007/BF00299667 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_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_121 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_206 GBV_ILN_224 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 GBV_ILN_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4277 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 AR 18 1986 5 01 04 363-375 |
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10.1007/BF00299667 doi (DE-627)SPR003293467 (SPR)BF00299667-e DE-627 ger DE-627 rakwb eng Packer, Laurence verfasserin aut The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) 1986 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 1986 Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. Ovarian Development (dpeaa)DE-He213 Head Width (dpeaa)DE-He213 Natal Nest (dpeaa)DE-He213 Female Pupa (dpeaa)DE-He213 Colony Development (dpeaa)DE-He213 Knerer, Gerd aut Enthalten in Behavioral ecology and sociobiology Berlin : Springer, 1976 18(1986), 5 vom: 01. Apr., Seite 363-375 (DE-627)25339032X (DE-600)1458476-1 1432-0762 nnns volume:18 year:1986 number:5 day:01 month:04 pages:363-375 https://dx.doi.org/10.1007/BF00299667 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_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_121 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_206 GBV_ILN_224 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 GBV_ILN_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4277 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 AR 18 1986 5 01 04 363-375 |
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10.1007/BF00299667 doi (DE-627)SPR003293467 (SPR)BF00299667-e DE-627 ger DE-627 rakwb eng Packer, Laurence verfasserin aut The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) 1986 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 1986 Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. Ovarian Development (dpeaa)DE-He213 Head Width (dpeaa)DE-He213 Natal Nest (dpeaa)DE-He213 Female Pupa (dpeaa)DE-He213 Colony Development (dpeaa)DE-He213 Knerer, Gerd aut Enthalten in Behavioral ecology and sociobiology Berlin : Springer, 1976 18(1986), 5 vom: 01. Apr., Seite 363-375 (DE-627)25339032X (DE-600)1458476-1 1432-0762 nnns volume:18 year:1986 number:5 day:01 month:04 pages:363-375 https://dx.doi.org/10.1007/BF00299667 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_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_121 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_206 GBV_ILN_224 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 GBV_ILN_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4277 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 AR 18 1986 5 01 04 363-375 |
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Enthalten in Behavioral ecology and sociobiology 18(1986), 5 vom: 01. Apr., Seite 363-375 volume:18 year:1986 number:5 day:01 month:04 pages:363-375 |
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Enthalten in Behavioral ecology and sociobiology 18(1986), 5 vom: 01. Apr., Seite 363-375 volume:18 year:1986 number:5 day:01 month:04 pages:363-375 |
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The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Ovarian Development</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Head Width</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Natal Nest</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Female Pupa</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Colony Development</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Knerer, Gerd</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Behavioral ecology and sociobiology</subfield><subfield code="d">Berlin : Springer, 1976</subfield><subfield code="g">18(1986), 5 vom: 01. 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Packer, Laurence |
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Packer, Laurence misc Ovarian Development misc Head Width misc Natal Nest misc Female Pupa misc Colony Development The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) |
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The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) Ovarian Development (dpeaa)DE-He213 Head Width (dpeaa)DE-He213 Natal Nest (dpeaa)DE-He213 Female Pupa (dpeaa)DE-He213 Colony Development (dpeaa)DE-He213 |
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The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) |
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Behavioral ecology and sociobiology |
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Packer, Laurence |
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biology of a subtropical population of halictus ligatus say (hymenoptera: halictidae) |
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The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) |
| abstract |
Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. © Springer-Verlag 1986 |
| abstractGer |
Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. © Springer-Verlag 1986 |
| abstract_unstemmed |
Summary A large population of Halictus ligatus was studied in the subtropical climate of Knights Key, Monroe County, Florida. The dissection of 858 female bees caught on flowers and 420 bees from completely excavated nests gives the following picture of phenology, colony development and social organisation. In the Florida keys, H. ligatus is continuously brooded and multivoltine. However, towards the coldest time of year young gynes may rest in their natal nests rather than found a new colony. This may result in a partial synchronisation of nest initiation when warm weather returns after a particularly cold spell. Most nests are started by a single foundress that usually survives until near the end of the production of reproductives. The first brood is very variable in size and males average 11% of the bees produced at this stage. This figure increases to 56% when the first brood workers begin provisioning. Queens are produced some time after the rise in male production and colony longevity is extended by the presence of some worker brood during this phase. Queens average 16% larger than their workers but appear to exert little inhibition of worker reproductivity: 57% of worker bees mate and 68% show ovarian development. This population is unique amongst social halictines in being continuously brooded, multivoltine and in having such weak physiological caste differentiation. It seems to represent an intermediate stage between the primitively eusocial colonies of H. ligatus found in temperate regions and the communal-like ones of the tropics. © Springer-Verlag 1986 |
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| title_short |
The biology of a subtropical population of Halictus ligatus Say (Hymenoptera: Halictidae) |
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https://dx.doi.org/10.1007/BF00299667 |
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Knerer, Gerd |
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| score |
7.4012938 |