Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera

Las variaciones en el tamaño corporal representan un motor para la colonización de nuevos nichos representado en patrones ecogeográficos. La ley de Bergmann describe un patrón ecogeográfico donde las especies con mayor tamaño corporal se distribuyen a mayor latitud. No obstante, la ley de Bergmann s...

Full description

Autores:

Tipo de recurso:

Fecha de publicación:: 2020

Institución:: Universidad del Rosario

Repositorio:: Repositorio EdocUR - U. Rosario

Idioma:: spa

id	EDOCUR2_94b21748d38d9d872bc9454978f40fff
oai_identifier_str	oai:repository.urosario.edu.co:10336/28206
network_acronym_str	EDOCUR2
network_name_str	Repositorio EdocUR - U. Rosario
repository_id_str
dc.title.spa.fl_str_mv	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera
dc.title.TranslatedTitle.eng.fl_str_mv	Effects of elevation on sensory allometry in the honey bee, Apis mellifera
title	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera
spellingShingle	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera Morfometría Ecología sensorial Sensilas placodeas Ley de Bergmann Altitud Tamaño Invertebrados Morphometry Sensory ecology Sensilla placodea Bergmann's law Altitude Size
title_short	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera
title_full	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera
title_fullStr	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera
title_full_unstemmed	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera
title_sort	Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera
dc.contributor.advisor.none.fl_str_mv	Riveros Rivera, Andre Josafat
dc.contributor.none.fl_str_mv	Herrera Gutiérrez, Laura Maria Orjuela, Rafael
dc.subject.spa.fl_str_mv	Morfometría Ecología sensorial Sensilas placodeas Ley de Bergmann Altitud Tamaño
topic	Morfometría Ecología sensorial Sensilas placodeas Ley de Bergmann Altitud Tamaño Invertebrados Morphometry Sensory ecology Sensilla placodea Bergmann's law Altitude Size
dc.subject.ddc.spa.fl_str_mv	Invertebrados
dc.subject.keyword.spa.fl_str_mv	Morphometry Sensory ecology Sensilla placodea Bergmann's law Altitude Size
description	Las variaciones en el tamaño corporal representan un motor para la colonización de nuevos nichos representado en patrones ecogeográficos. La ley de Bergmann describe un patrón ecogeográfico donde las especies con mayor tamaño corporal se distribuyen a mayor latitud. No obstante, la ley de Bergmann sensu lato incluye factores abióticos como temperatura y altitud. En consecuencia, la ley de Bergmann sensu lato extiende el patrón modificado a distintos grupos que antes no se habían incluido, como en el caso de la Clase Insecta. Se sabe que las variaciones en el tamaño corporal de los insectos influyen en las dinámicas de forrajeo. Por lo tanto, la información ambiental que perciben y procesan los insectos varía con cambios en el tamaño corporal absoluto y relativo. En este estudio se evaluó la ley de Bergmann sensu lato aplicada en A. mellifera con respecto a una clina altitudinal en dos zonas de la cordillera oriental colombiana; evaluando variaciones de rasgos morfométricos y sensoriales, además de su relación con la percepción de la información olfativa y sus consecuencias en las actividades de forrajeo. Se encontró que las abejas de menor elevación presentaron menor magnitud para rasgos sensoriales y morfométricos a diferencia de las abejas que se distribuyen en la localidad con mayor elevación. Este patrón responde al principio de la ley de Bergmann sensu lato en función de una clina altitudinal. Las variaciones alométricas a nivel morfométrico registradas en el estudio tienen efecto en los rasgos sensoriales de A. mellifera. En consecuencia, se puede sugerir como la temperatura asociada a la altitud moldea las comunidades de A. mellifera, específicamente en tareas de polinización.
publishDate	2020
dc.date.accessioned.none.fl_str_mv	2020-08-20T21:39:02Z
dc.date.available.none.fl_str_mv	2020-08-20T21:39:02Z
dc.date.created.none.fl_str_mv	2020-08-12
dc.type.eng.fl_str_mv	bachelorThesis
dc.type.coar.fl_str_mv	http://purl.org/coar/resource_type/c_7a1f
dc.type.document.spa.fl_str_mv	Artículo
dc.type.spa.spa.fl_str_mv	Trabajo de grado
dc.identifier.doi.none.fl_str_mv	https://doi.org/10.48713/10336_28206
dc.identifier.uri.none.fl_str_mv	https://repository.urosario.edu.co/handle/10336/28206
url	https://doi.org/10.48713/10336_28206 https://repository.urosario.edu.co/handle/10336/28206
dc.language.iso.spa.fl_str_mv	spa
language	spa
dc.rights.coar.fl_str_mv	http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv	Abierto (Texto Completo)
rights_invalid_str_mv	Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv	application/pdf
dc.publisher.spa.fl_str_mv	Universidad del Rosario
dc.publisher.department.spa.fl_str_mv	Facultad de Ciencias Naturales y Matemáticas
dc.publisher.program.spa.fl_str_mv	Biología
institution	Universidad del Rosario
dc.source.bibliographicCitation.spa.fl_str_mv	Abel, R., Rybak, J., & Menzel, R. (2001). Structure and response patterns of olfactory interneurons in the honeybee, Apis mellifera. Journal of Comparative Neurology, 437(3), 363-383 Alloway TM. 1972. Learning and memory in insects. Annu. Rev. Entomol. 17:43–56 Apfelbach R, Russ D, Slotnick BM (1991) Ontogenetic changes in odor sensitivity, olfactory receptor area and olfactory receptor density in the rat. Chem Sens 16:209–218 Ashman, T. L., & Stanton, M. (1991). Seasonal variation in pollination dynamics of sexually dimorphic Sidalcea oregana ssp. spicata (Malvaceae). Ecology, 72(3), 993-1003 Bidau, C. J., & Martí, D. A. (2007). Clinal variation of body size in Dichroplus pratensis (Orthoptera: Acrididae): inversion of Bergmann's and Rensch's rules. Annals of the Entomological Society of America, 100(6), 850-860 Blackburn, T. M. et al. 1999. Geographic gradients in body size: a clarification of Bergmann's rule. Div. Distr. 5: 165–174. Blanckenhorn, W. U., & Demont, M. (2004). Bergmann and converse Bergmann latitudinal clines in arthropods: two ends of a continuum?. Integrative and Comparative Biology, 44(6), 413-424. Buchmann CM, Schurr FM, Nathan R, Jeltsch F. Habitat loss and fragmentation affecting mammal and bird communities—The role of interspecific competition and individual space use. Ecological Informatics. 2013; 14:90–8 Chittka, L., Thomson, J. D., & Waser, N. M. (1999). Flower constancy, insect psychology, and plant evolution. Naturwissenschaften, 86(8), 361-377. Cohen, J. M., Lajeunesse, M. J., & Rohr, J. R. (2018). A global synthesis of animal phenological responses to climate change. Nature Climate Change, 8(3), 224-228. Domic, A. I., & Capriles, J. M. (2009). Allometry and effects of extreme elevation on growth velocity of the Andean tree Polylepis tarapacana Philippi (Rosaceae). Plant ecology, 205(2), 223-234. Dudley R (2001) The biomechanics and functional diversity of flight. In: Woiwod IP, Reynolds DR, Thomas CD (eds) Insect movement: mechanisms and consequences. CABI, Cambridge Elekonich, M. M., & Roberts, S. P. (2005). Honey bees as a model for understanding mechanisms of life history transitions. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 141(4), 362-371. Faber T, Menzel R. (2001). Visualizing mushroom body response to a conditioned odor in honeybees. Naturwissenschaften 88:472–76. Farris, S. M., Robinson, G. E., Davis, R. L., & Fahrbach, S. E. (1999). Larval and pupal development of the mushroom bodies in the honey bee, Apis mellifera. Journal of Comparative Neurology, 414(1), 97-113. Frasnelli, E., Anfora, G., Trona, F., Tessarolo, F., & Vallortigara, G. (2010). Morpho-functional asymmetry of the olfactory receptors of the honeybee (Apis mellifera). Behavioural brain research, 209(2), 221-225. Galizia CG, Menzel R. (2000). Odour perception in honeybees: Coding information in glomerular patterns. Curr Op Neurobiol 10:504–510. Greenfield M (2002) Signalers and receivers. Oxford University Press. Oxford Hegland, S. J., Nielsen, A., Lázaro, A., Bjerknes, A. L., & Totland, Ø. (2009). How does climate warming affect plant‐pollinator interactions?. Ecology letters, 12(2), 184-195. Heinrich, B. (1993). The Hot Blooded Insects. Harvard University Press, Cambridge. Homberg, U. (1984). Processing of antennal information in extrinsic mushroom body neurons of the bee brain. Journal of Comparative Physiology A, 154(6), 825-836. Jander U, Jander R (2002) Allometry and resolution of bee eyes (Apoidea). Arthropod Structure and Development. 30: 179-193 Jeanson, R., Clark, R. M., Holbrook, C. T., Bertram, S. M., Fewell, J. H., & Kukuk, P. F. (2008). Division of labour and socially induced changes in response thresholds in associations of solitary halictine bees. Animal Behaviour, 76(3), 593-602. Jin, Y. et al. 2007. Elevational variation in body size of Phrynocephalus vlangalii in the North Qinghai‐Xizang (Tibetan) Plateau. Belg. J. Zool. 137: 197–202. Kaissling, K. E., & Renner, M. (1968). Specialized chemoreceptors in the pore plates of. Apis. Z. Vergl. Physiol, 59, 357-361. Kelber C, Rössler W, Kleineidam CJ. (2006). Multiple olfactory receptor neurons and their axonal projections in the antennal lobe of the honeybee Apis mellifera. J Comp Neurol 496:395–405 Ken, T., Fuchs, S., Koeniger, N., & Ruiguang, Z. (2003). Morphological characterization of Apis cerana in the Yunnan Province of China. Apidologie, 34(6), 553-561. Klingenberg, C. P., Badyaev, A. V., Sowry, S. M., & Beckwith, N. J. (2001). Inferring developmental modularity from morphological integration: analysis of individual variation and asymmetry in bumblebee wings. The American Naturalist, 157(1), 11-23). Levinton, J.1988. Genetics, paleontology and macroevolution. Cambridge University Press, Cambridge Liu X, Cheng Z, Yan L, Yin Z-Y (2009) Elevation dependency of recent and future minimum surface air temperature trends in the Tibetan Plateau and its surroundings. Glob Planet Chang 68:164–174 Malo, J. y Baonza, J. 2002. Are there predictable clines in plant–pollinator interactions along altitudinal gradients? The example of Cytisus scoparius (L.) Link in the Sierra de Guadarrama (Central Spain). Diversity and Distributions 8, 365–371 Mattu, V. K., & Verma, L. R. (1983). Comparative morphometric studies on the Indian honeybee of the north-west Himalayas 1. Tongue and antenna. Journal of Apicultural Research, 22(2), 79-85. Mayr, E. 1956. Geographical character gradients and climatic adaptation. Evolution 10: 105–108. McNab, B. K. 1971. On the ecological significance of Bergmann's rule. Ecology 52: 845–854. Meiri, S. et al. 2007. What determines conformity to Bergmann's rule?. Global Ecol. Biogeogr. 16: 788–794 Menzel R. 1990. Learning, memory and “cognition” in honey bees. In: Kesner RP, Olten DS, editors. Neurobiology of comparative cognition. Hillsdale, NJ: Erlbaum Inc. p 237–292 Nijhout, H. F. (2003). The control of body size in insects. Developmental biology, 261(1), 1-9. Olalla-Tarraga, M.A. (2011). ‘Nullius in Bergmann’ or the pluralistic approach to ecogeographical rules: a reply to Watt et al. (2010). Oikos, 120, 1441–1444 Osorio‐Canadas, S., Arnan, X., Rodrigo, A., Torné‐Noguera, A., Molowny, R., & Bosch, J. (2016). Body size phenology in a regional bee fauna: a temporal extension of Bergmann's rule. Ecology Letters, 19(12), 1395-1402. Page R.E. Jr., Erber J., Fondrk M.K. (1998) The effect of genotype on response thresholds to sucrose and foraging behavior of honey bees ( Apis mellifera L.), J. Comp. Physiol. A 182, 489–500. Peters, M.K., Peisker, J., Steffan-Dewenter, I. & Hoiss, B. (2016). Morphological traits are linked to the cold performance and distribution of bees along elevational gradients. J. Biogeogr., doi:10.1111/jbi.12768. Reinhard, J., & Srinivasan, M. V. (2009). The role of scents in honey bee foraging and recruitment. Food exploitation by social insects: ecological, behavioral, and theoretical approaches, 1, 165-182. Riveros, A. J., & Gronenberg, W. (2010). Sensory allometry, foraging task specialization and resource exploitation in honeybees. Behavioral ecology and sociobiology, 64(6), 955-966. Robertson, F.W., 1959. Studies in quantitative inheritance. XII. Cell size and number in relation to genetic and environmental variation of body size in Drosophila. Genetics 44, 869–896 Schlichting, C. D. and Piggliucci, M. (1998). Phenotypic Evolution: A Reaction Norm Perspective. Sunderland, Mass: Sinauer Associates. Schwarz, S., Albert, L., Wystrach, A., & Cheng, K. (2011). Ocelli contribute to the encoding of celestial compass information in the Australian desert ant Melophorus bagoti. Journal of Experimental Biology, 214(6), 901-906. Searcy, W. A. 1980. Optimum body sizes at different ambient temperatures: an energetics explanation of Bergmann's rule. J. Theor. Biol. 83: 579–593. Shelomi, M. (2012). Where are we now? Bergmann’s rule sensu lato in insects. The American Naturalist, 180(4), 511-519. Shingleton, A. W., Frankino, W. A., Flatt, T., Nijhout, H. F., & Emlen, D. J. (2007). Size and shape: the developmental regulation of static allometry in insects. BioEssays, 29(6), 536-548. Spaethe J, Brockmann A, Halbig C, Tautz J (2007) Size determines antennal sensitivity and behavioral threshold to odors in bumblebee workers. Naturwissenschaften 94:733- 739 Steudel, K. et al. 1994. The biophysics of Bergmann's rule: a comparison of the effects of pelage and body size variation on metabolic rate. Can. J. Zool. 72: 70–77. Stevenson, R.D. (1985). The relative importance of behavioral and physiological adjustments controlling body temperature in terrestrial ectotherms. Am. Nat., 126, 362–386. T'ai, H. R., & Cane, J. H. (2002). The effect of pollen protein concentration on body size in the sweat bee Lasioglossum zephyrum (Hymenoptera: Apiformes). Evolutionary Ecology, 16(1), 49-65. Tilman D. Resource competition and community structure. New Jersey, UK: Princeton University Press; 1982. Vareschi E (1971) Duftunterscheidung bei der Honigbiene— Einzelzellableitungen und Verhaltensreaktionen. Zeitschrift fur Vergleichende Physiologie 75:143–173 Wenner AM, Meade DE, Friesen LJ. (1991). Recruitment, search behavior, and flight ranges of honey bees. Am Zool 31:768–82 Williams, R.J. & Martinez, N.D. (2000) Simple rules yield complex food webs. Nature, 404, 180–183. Woodward, G., & Hildrew, A. G. (2002). Body‐size determinants of niche overlap and intraguild predation within a complex food web. Journal of Animal Ecology, 71(6), 1063-1074. Yodzis P. Competition for space and the structure of ecological communities. Berlin, Germany: Springer Science & Business Media; 2013
dc.source.instname.spa.fl_str_mv	instname:Universidad del Rosario
dc.source.reponame.spa.fl_str_mv	reponame:Repositorio Institucional EdocUR
bitstream.url.fl_str_mv	https://repository.urosario.edu.co/bitstreams/61ffefe1-86e8-4aea-a085-3f078f8e4acc/download https://repository.urosario.edu.co/bitstreams/3be63c2b-4948-4c85-a5e2-a08efaa5d03e/download https://repository.urosario.edu.co/bitstreams/73766a5f-249c-4d04-a911-f8728d05b628/download https://repository.urosario.edu.co/bitstreams/3a4f0070-7594-44c5-8402-5f12f1afee1d/download
bitstream.checksum.fl_str_mv	957c3add710e7eadfcda90aa5e0866b3 fab9d9ed61d64f6ac005dee3306ae77e cafad6e5920c26559db80f27847f813c b9f4f33e34dd12e4cc1c57fa05c61283
bitstream.checksumAlgorithm.fl_str_mv	MD5 MD5 MD5 MD5
repository.name.fl_str_mv	Repositorio institucional EdocUR
repository.mail.fl_str_mv	edocur@urosario.edu.co
_version_	1818107001611223040
spelling	Herrera Gutiérrez, Laura MariaOrjuela, RafaelRiveros Rivera, Andre Josafat79974449600Barragán Barrera, Heidy NataliaBiólogoFull time7502bcc2-9aad-4548-a9d3-a4aa1e03eef46002020-08-20T21:39:02Z2020-08-20T21:39:02Z2020-08-12Las variaciones en el tamaño corporal representan un motor para la colonización de nuevos nichos representado en patrones ecogeográficos. La ley de Bergmann describe un patrón ecogeográfico donde las especies con mayor tamaño corporal se distribuyen a mayor latitud. No obstante, la ley de Bergmann sensu lato incluye factores abióticos como temperatura y altitud. En consecuencia, la ley de Bergmann sensu lato extiende el patrón modificado a distintos grupos que antes no se habían incluido, como en el caso de la Clase Insecta. Se sabe que las variaciones en el tamaño corporal de los insectos influyen en las dinámicas de forrajeo. Por lo tanto, la información ambiental que perciben y procesan los insectos varía con cambios en el tamaño corporal absoluto y relativo. En este estudio se evaluó la ley de Bergmann sensu lato aplicada en A. mellifera con respecto a una clina altitudinal en dos zonas de la cordillera oriental colombiana; evaluando variaciones de rasgos morfométricos y sensoriales, además de su relación con la percepción de la información olfativa y sus consecuencias en las actividades de forrajeo. Se encontró que las abejas de menor elevación presentaron menor magnitud para rasgos sensoriales y morfométricos a diferencia de las abejas que se distribuyen en la localidad con mayor elevación. Este patrón responde al principio de la ley de Bergmann sensu lato en función de una clina altitudinal. Las variaciones alométricas a nivel morfométrico registradas en el estudio tienen efecto en los rasgos sensoriales de A. mellifera. En consecuencia, se puede sugerir como la temperatura asociada a la altitud moldea las comunidades de A. mellifera, específicamente en tareas de polinización.Variations in body size represent an important driver in colonization of new niches, indicated by ecogeographic patterns. Bergmann's Law describes an ecogeographic pattern where species with larger body size are distributed at higher latitudes. However, Bergmann's law sensu lato includes abiotic factors such as temperature and altitude to complement the explanation of this pattern. Consequently, Bergmann's law sensu lato extends the modified pattern within groups that had not previously been included before, specifically, the Class Insecta. Variations in insect body size are known to influence foraging dynamics. Therefore, the environmental information that insects perceive and process varies with changes in absolute and relative body size. In this study, the Bergmann sensu lato law applied in A. mellifera was evaluated within an altitudinal cline in two areas of the Colombian eastern mountain range. We include the variations in morphometric and sensory traits, and their relationship with the perception of olfactory information and its consequences on foraging activities. We found that bees of lower elevation exhibited lower magnitude for sensory and morphometric traits, unlike bees that are distributed in the locality with higher elevation. This pattern follows the principle of Bergmann sensu lato based on an altitudinal cline. The allometric variations at the morphometric level evaluated in the study have an effect on the sensory features of A. mellifera. Consequently, we suggested how the temperature associated with the altitude shapes the A. mellifera communities, specifically in pollination tasks.Dirección de Investigación e Innovación de la Universidad del Rosario (Beca de fondos concursables para semilleros)application/pdfhttps://doi.org/10.48713/10336_28206 https://repository.urosario.edu.co/handle/10336/28206spaUniversidad del RosarioFacultad de Ciencias Naturales y MatemáticasBiologíaAbierto (Texto Completo)EL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma.http://purl.org/coar/access_right/c_abf2Abel, R., Rybak, J., & Menzel, R. (2001). Structure and response patterns of olfactory interneurons in the honeybee, Apis mellifera. Journal of Comparative Neurology, 437(3), 363-383Alloway TM. 1972. Learning and memory in insects. Annu. Rev. Entomol. 17:43–56Apfelbach R, Russ D, Slotnick BM (1991) Ontogenetic changes in odor sensitivity, olfactory receptor area and olfactory receptor density in the rat. Chem Sens 16:209–218Ashman, T. L., & Stanton, M. (1991). Seasonal variation in pollination dynamics of sexually dimorphic Sidalcea oregana ssp. spicata (Malvaceae). Ecology, 72(3), 993-1003Bidau, C. J., & Martí, D. A. (2007). Clinal variation of body size in Dichroplus pratensis (Orthoptera: Acrididae): inversion of Bergmann's and Rensch's rules. Annals of the Entomological Society of America, 100(6), 850-860Blackburn, T. M. et al. 1999. Geographic gradients in body size: a clarification of Bergmann's rule. Div. Distr. 5: 165–174.Blanckenhorn, W. U., & Demont, M. (2004). Bergmann and converse Bergmann latitudinal clines in arthropods: two ends of a continuum?. Integrative and Comparative Biology, 44(6), 413-424.Buchmann CM, Schurr FM, Nathan R, Jeltsch F. Habitat loss and fragmentation affecting mammal and bird communities—The role of interspecific competition and individual space use. Ecological Informatics. 2013; 14:90–8Chittka, L., Thomson, J. D., & Waser, N. M. (1999). Flower constancy, insect psychology, and plant evolution. Naturwissenschaften, 86(8), 361-377.Cohen, J. M., Lajeunesse, M. J., & Rohr, J. R. (2018). A global synthesis of animal phenological responses to climate change. Nature Climate Change, 8(3), 224-228.Domic, A. I., & Capriles, J. M. (2009). Allometry and effects of extreme elevation on growth velocity of the Andean tree Polylepis tarapacana Philippi (Rosaceae). Plant ecology, 205(2), 223-234.Dudley R (2001) The biomechanics and functional diversity of flight. In: Woiwod IP, Reynolds DR, Thomas CD (eds) Insect movement: mechanisms and consequences. CABI, CambridgeElekonich, M. M., & Roberts, S. P. (2005). Honey bees as a model for understanding mechanisms of life history transitions. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 141(4), 362-371.Faber T, Menzel R. (2001). Visualizing mushroom body response to a conditioned odor in honeybees. Naturwissenschaften 88:472–76.Farris, S. M., Robinson, G. E., Davis, R. L., & Fahrbach, S. E. (1999). Larval and pupal development of the mushroom bodies in the honey bee, Apis mellifera. Journal of Comparative Neurology, 414(1), 97-113.Frasnelli, E., Anfora, G., Trona, F., Tessarolo, F., & Vallortigara, G. (2010). Morpho-functional asymmetry of the olfactory receptors of the honeybee (Apis mellifera). Behavioural brain research, 209(2), 221-225.Galizia CG, Menzel R. (2000). Odour perception in honeybees: Coding information in glomerular patterns. Curr Op Neurobiol 10:504–510.Greenfield M (2002) Signalers and receivers. Oxford University Press. OxfordHegland, S. J., Nielsen, A., Lázaro, A., Bjerknes, A. L., & Totland, Ø. (2009). How does climate warming affect plant‐pollinator interactions?. Ecology letters, 12(2), 184-195.Heinrich, B. (1993). The Hot Blooded Insects. Harvard University Press, Cambridge.Homberg, U. (1984). Processing of antennal information in extrinsic mushroom body neurons of the bee brain. Journal of Comparative Physiology A, 154(6), 825-836.Jander U, Jander R (2002) Allometry and resolution of bee eyes (Apoidea). Arthropod Structure and Development. 30: 179-193Jeanson, R., Clark, R. M., Holbrook, C. T., Bertram, S. M., Fewell, J. H., & Kukuk, P. F. (2008). Division of labour and socially induced changes in response thresholds in associations of solitary halictine bees. Animal Behaviour, 76(3), 593-602.Jin, Y. et al. 2007. Elevational variation in body size of Phrynocephalus vlangalii in the North Qinghai‐Xizang (Tibetan) Plateau. Belg. J. Zool. 137: 197–202.Kaissling, K. E., & Renner, M. (1968). Specialized chemoreceptors in the pore plates of. Apis. Z. Vergl. Physiol, 59, 357-361.Kelber C, Rössler W, Kleineidam CJ. (2006). Multiple olfactory receptor neurons and their axonal projections in the antennal lobe of the honeybee Apis mellifera. J Comp Neurol 496:395–405Ken, T., Fuchs, S., Koeniger, N., & Ruiguang, Z. (2003). Morphological characterization of Apis cerana in the Yunnan Province of China. Apidologie, 34(6), 553-561.Klingenberg, C. P., Badyaev, A. V., Sowry, S. M., & Beckwith, N. J. (2001). Inferring developmental modularity from morphological integration: analysis of individual variation and asymmetry in bumblebee wings. The American Naturalist, 157(1), 11-23).Levinton, J.1988. Genetics, paleontology and macroevolution. Cambridge University Press, CambridgeLiu X, Cheng Z, Yan L, Yin Z-Y (2009) Elevation dependency of recent and future minimum surface air temperature trends in the Tibetan Plateau and its surroundings. Glob Planet Chang 68:164–174Malo, J. y Baonza, J. 2002. Are there predictable clines in plant–pollinator interactions along altitudinal gradients? The example of Cytisus scoparius (L.) Link in the Sierra de Guadarrama (Central Spain). Diversity and Distributions 8, 365–371Mattu, V. K., & Verma, L. R. (1983). Comparative morphometric studies on the Indian honeybee of the north-west Himalayas 1. Tongue and antenna. Journal of Apicultural Research, 22(2), 79-85.Mayr, E. 1956. Geographical character gradients and climatic adaptation. Evolution 10: 105–108.McNab, B. K. 1971. On the ecological significance of Bergmann's rule. Ecology 52: 845–854.Meiri, S. et al. 2007. What determines conformity to Bergmann's rule?. Global Ecol. Biogeogr. 16: 788–794Menzel R. 1990. Learning, memory and “cognition” in honey bees. In: Kesner RP, Olten DS, editors. Neurobiology of comparative cognition. Hillsdale, NJ: Erlbaum Inc. p 237–292Nijhout, H. F. (2003). The control of body size in insects. Developmental biology, 261(1), 1-9.Olalla-Tarraga, M.A. (2011). ‘Nullius in Bergmann’ or the pluralistic approach to ecogeographical rules: a reply to Watt et al. (2010). Oikos, 120, 1441–1444Osorio‐Canadas, S., Arnan, X., Rodrigo, A., Torné‐Noguera, A., Molowny, R., & Bosch, J. (2016). Body size phenology in a regional bee fauna: a temporal extension of Bergmann's rule. Ecology Letters, 19(12), 1395-1402.Page R.E. Jr., Erber J., Fondrk M.K. (1998) The effect of genotype on response thresholds to sucrose and foraging behavior of honey bees ( Apis mellifera L.), J. Comp. Physiol. A 182, 489–500.Peters, M.K., Peisker, J., Steffan-Dewenter, I. & Hoiss, B. (2016). Morphological traits are linked to the cold performance and distribution of bees along elevational gradients. J. Biogeogr., doi:10.1111/jbi.12768.Reinhard, J., & Srinivasan, M. V. (2009). The role of scents in honey bee foraging and recruitment. Food exploitation by social insects: ecological, behavioral, and theoretical approaches, 1, 165-182.Riveros, A. J., & Gronenberg, W. (2010). Sensory allometry, foraging task specialization and resource exploitation in honeybees. Behavioral ecology and sociobiology, 64(6), 955-966.Robertson, F.W., 1959. Studies in quantitative inheritance. XII. Cell size and number in relation to genetic and environmental variation of body size in Drosophila. Genetics 44, 869–896Schlichting, C. D. and Piggliucci, M. (1998). Phenotypic Evolution: A Reaction Norm Perspective. Sunderland, Mass: Sinauer Associates.Schwarz, S., Albert, L., Wystrach, A., & Cheng, K. (2011). Ocelli contribute to the encoding of celestial compass information in the Australian desert ant Melophorus bagoti. Journal of Experimental Biology, 214(6), 901-906.Searcy, W. A. 1980. Optimum body sizes at different ambient temperatures: an energetics explanation of Bergmann's rule. J. Theor. Biol. 83: 579–593.Shelomi, M. (2012). Where are we now? Bergmann’s rule sensu lato in insects. The American Naturalist, 180(4), 511-519.Shingleton, A. W., Frankino, W. A., Flatt, T., Nijhout, H. F., & Emlen, D. J. (2007). Size and shape: the developmental regulation of static allometry in insects. BioEssays, 29(6), 536-548.Spaethe J, Brockmann A, Halbig C, Tautz J (2007) Size determines antennal sensitivity and behavioral threshold to odors in bumblebee workers. Naturwissenschaften 94:733- 739Steudel, K. et al. 1994. The biophysics of Bergmann's rule: a comparison of the effects of pelage and body size variation on metabolic rate. Can. J. Zool. 72: 70–77.Stevenson, R.D. (1985). The relative importance of behavioral and physiological adjustments controlling body temperature in terrestrial ectotherms. Am. Nat., 126, 362–386.T'ai, H. R., & Cane, J. H. (2002). The effect of pollen protein concentration on body size in the sweat bee Lasioglossum zephyrum (Hymenoptera: Apiformes). Evolutionary Ecology, 16(1), 49-65.Tilman D. Resource competition and community structure. New Jersey, UK: Princeton University Press; 1982.Vareschi E (1971) Duftunterscheidung bei der Honigbiene— Einzelzellableitungen und Verhaltensreaktionen. Zeitschrift fur Vergleichende Physiologie 75:143–173Wenner AM, Meade DE, Friesen LJ. (1991). Recruitment, search behavior, and flight ranges of honey bees. Am Zool 31:768–82Williams, R.J. & Martinez, N.D. (2000) Simple rules yield complex food webs. Nature, 404, 180–183.Woodward, G., & Hildrew, A. G. (2002). Body‐size determinants of niche overlap and intraguild predation within a complex food web. Journal of Animal Ecology, 71(6), 1063-1074.Yodzis P. Competition for space and the structure of ecological communities. Berlin, Germany: Springer Science & Business Media; 2013instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURMorfometríaEcología sensorialSensilas placodeasLey de BergmannAltitudTamañoInvertebrados592600MorphometrySensory ecologySensilla placodeaBergmann's lawAltitudeSizeEfectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis melliferaEffects of elevation on sensory allometry in the honey bee, Apis melliferabachelorThesisArtículoTrabajo de gradohttp://purl.org/coar/resource_type/c_7a1fORIGINALEfectos-de-la-elevacion-sobre-la-alometria-sensorial-en-la-abeja-de-la-miel,-Apis-mellifera.pdfEfectos-de-la-elevacion-sobre-la-alometria-sensorial-en-la-abeja-de-la-miel,-Apis-mellifera.pdfapplication/pdf403407https://repository.urosario.edu.co/bitstreams/61ffefe1-86e8-4aea-a085-3f078f8e4acc/download957c3add710e7eadfcda90aa5e0866b3MD51LICENSElicense.txtlicense.txttext/plain1475https://repository.urosario.edu.co/bitstreams/3be63c2b-4948-4c85-a5e2-a08efaa5d03e/downloadfab9d9ed61d64f6ac005dee3306ae77eMD52TEXTEfectos-de-la-elevacion-sobre-la-alometria-sensorial-en-la-abeja-de-la-miel,-Apis-mellifera.pdf.txtEfectos-de-la-elevacion-sobre-la-alometria-sensorial-en-la-abeja-de-la-miel,-Apis-mellifera.pdf.txtExtracted texttext/plain40654https://repository.urosario.edu.co/bitstreams/73766a5f-249c-4d04-a911-f8728d05b628/downloadcafad6e5920c26559db80f27847f813cMD53THUMBNAILEfectos-de-la-elevacion-sobre-la-alometria-sensorial-en-la-abeja-de-la-miel,-Apis-mellifera.pdf.jpgEfectos-de-la-elevacion-sobre-la-alometria-sensorial-en-la-abeja-de-la-miel,-Apis-mellifera.pdf.jpgGenerated Thumbnailimage/jpeg2393https://repository.urosario.edu.co/bitstreams/3a4f0070-7594-44c5-8402-5f12f1afee1d/downloadb9f4f33e34dd12e4cc1c57fa05c61283MD5410336/28206oai:repository.urosario.edu.co:10336/282062020-11-21 18:38:38.468https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.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

Efectos de la elevación sobre la alometría sensorial en la abeja de la miel, Apis mellifera

Publicaciones similares