請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/50419
完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 何傳愷 | |
dc.contributor.author | Chinh Lun Lin | en |
dc.contributor.author | 林靖倫 | zh_TW |
dc.date.accessioned | 2021-06-15T12:39:59Z | - |
dc.date.available | 2026-12-31 | |
dc.date.copyright | 2016-08-02 | |
dc.date.issued | 2016 | |
dc.date.submitted | 2016-07-28 | |
dc.identifier.citation | Literature Cited
Anstett, D. N., Ahern, J. R., Glinos, J., Nawar, N., Salminen, J.-P. and Johnson, M. T. J. (2015). Can genetically based clines in plant defence explain greater herbivory at higher latitudes?. Ecology Letters, 18, 1376-1386. Arribas, P., Velasco, J., Abellán, P., Sánchez-Fernández, D., Andújar, C., Calosi, P., Millán, A., Ribera, I. and Bilton, D. T. (2012). Dispersal ability rather than ecological tolerance drives differences in range size between lentic and lotic water beetles (Coleoptera: Hydrophilidae). Journal of Biogeography, 39, 984-994. Athey, L. A., & Connor, E. F. (1989). The relationship between foliar nitrogen content and feeding by Odontota dorsalis Thun. on Robinia pseudoacacia L. Oecologia, 79(3), 390-394. Awmack, C. S., & Leather, S. R. (2002). Host plant quality and fecundity in herbivorous insects. Annual review of entomology, 47(1), 817-844. Baker, E. J., Clauss, M., & Clements, K. D. (2016). Selection and intake of algal species in butterfish (Odax pullus; Labridae). Marine Biology, 163(6), 1-12. Bale, J. S., Masters, G. J., Hodkinson, I. D., Awmack, C., Bezemer, T. M., Brown, V. K., Butterfield, J., Buse, A., Coulson, J. C., Farrar, J., Good, J. E. G., Harrington, R., Hartley, S., Jones, T. H., Lindroth, R. L., Press, M. C., Symrnioudis, I., Watt, A. D. and Whittaker, J. B. (2002). Herbivory in global climate change research: direct effects of rising temperature on insect herbivores. Global Change Biology, 8, 1-16. Bell, T. M., & Sotka, E. E. (2012). Local adaptation in adult feeding preference and juvenile performance in the generalist herbivore Idotea lthica. Oecologia, 170(2), 383-393. Berenbaum, M. R. (1990). Coevolution between herbivorous insects and plants: tempo and orchestration. In F. Gilbert (Ed.), Insect Life Cycles (pp. 87-99). London, UK: Springer-Verlag London. Bergmann, C. (1847). Über die Verhältnisse der Wärmeökonomie der Thiere zu ihrer Grösse. Göttinger Studien, 3, 595-708. Bernays, E. A., & Chapman, R. E. (1994). Host-plant selection by phytophagous insects, New York, NY: Springer US. Bolser, R. C., & Hay, M. E. (1996). Are tropical plants better defended? Palatability and defenses of temperate vs. tropical seaweeds. Ecology, 77(8), 2269-2286. Caldwell, E., Read, J., & Sanson, G. D. (2015). Which leaf mechanical traits correlate with insect herbivory among feeding guilds? Annals of Botany, 117, 349-361. Clayton, D. (1991). Assortative mating in the dune beetle Erodius sauditus (Tenebrionidae: Erodiini) in Kuwait. Journal of Arid Environments, 21, 81-89. Clissold, F. J. (2007). The biomechanics of chewing and plant fracture: mechanisms and implications. Advances in Insect Physiology, 34, 317-372. Clissold, F., Sanson, G., & Read, J. (2006). The paradoxical effects of nutrient ratios and supply rates on an outbreaking insect herbivore, the Australian plague locust. Journal of Animal Ecology, 75, 1000-1013. Clissold, F. J., Sanson, G. D., Read, J., & Simpson, S. J. (2009). Gross vs. net income: how plant toughness affects performance of an insect herbivore. Ecology, 90(12), 3393-3405. Coley, P. D., & Aide, T. M. (1991). Comparison of herbivory and plant defenses in temperate and tropical broad-leaved forests. In P. W. Price, T. M. Lewinsohn, G. W. Fernandes, W. W. Benson (Eds.), Plant-Animal Interactions: Evolutionary Ecology in Tropical and Temperate Regions (pp. 25-49). New York, NY: John Wiley & Sons, Inc. Deutsch, C. A., Tewksbury, J. J., Huey, R. B., Sheldon, K. S., Ghalambor, C. K., Haak, D. C., & Martin, P. R. (2008). Impacts of climate warming on terrestrial ectotherms across latitude. Proceedings of the National Academy of Sciences, 105(18), 6668-6672. Dillon, M. E., Frazier, M. R., & Dudley, R. (2006). Into thin air: physiology and evolution of alpine insects. Integrative and Comparative Biology, 46(1), 49-61. Dillon, M. E., Wang, G., & Huey, R. B. (2010). Global metabolic impacts of recent climate warming. Nature, 467(7316), 704-706. Edmunds, G. F., & Alstad, D. N. (1978). Coevolution in insect herbivores and conifers. Science, 199(4332), 941-945. Forister, M. L., & Wilson, J. S. (2013). The population ecology of novel plant–herbivore interactions. Oikos, 122(5), 657-666. Funk, D. J., Filchak, K. E., & Feder, J. L. (2002). Herbivorous insects: model systems for the comparative study of speciation ecology. In W. J. Etges & M. A. F. Noor (Eds.), Genetics of Mate Choice: From Sexual Selection to Sexual Isolation (pp. 251-267). Springer Netherlands. Garrido, E., Andraca‐Gómez, G., & Fornoni, J. (2012). Local adaptation: simultaneously considering herbivores and their host plants. New Phytologist, 193(2), 445-453. Gaston, K. J., & Chown, S. L. (1999). Elevation and climatic tolerance: a test using dung beetles. Oikos, 584-590. Goecker, M. E., Heck Jr, K. L., & Valentine, J. F. (2005). Effects of nitrogen concentrations in turtlegrass Thalassia testudinum on consumption by the bucktooth parrotfish Sparisoma radians. Marine Ecology Progress Series, 286, 239-248. Gripenberg, S., Mayhew, P. J., Parnell, M., & Roslin, T. (2010). A meta‐analysis of preference–performance relationships in phytophagous insects. Ecology Letters, 13(3), 383-393. Hayata, B. (1908). Flora montana Formosae. An enumeration of the plants found on Mt. Morrison, the central chain, and other mountainous regions of Formosa at altitudes of 3,000-13,000 ft. Journal of the College of Science, 25, 1-260. Ho, C. K., & Pennings, S. C. (2013). Preference and performance in plant–herbivore interactions across latitude—a study in us Atlantic salt marshes. PloS one, 8(3), e59829. Ho, C. K., Pennings, S. C., & Carefoot, T. H. (2010). Is diet quality an overlooked mechanism for Bergmann’s rule? The American Naturalist, 175(2), 269-276. Hothorn, T., Bretz F., Westfall, P., Heiberger, R. M., Schuetzenmeister, A., & Scheibe, S. (2016). multcomp: Simultaneous Inference in General Parametric Models. R package version 1.4-5. Houston, W. W. K. (1981). The life cycles and age of Carabus glabratus Paykull and C. problematicus Herbst (Col.: Carabidae) on moorland in northern England. Ecological Entomology, 6(3), 263-271. Huang, T. C. (1996). Flora of Taiwan, 2nd, Vol. 2. Editorial Committee of the Flora of Taiwan, Taiwan. Huey, R. B., Deutsch, C. A., Tewksbury, J. J., Vitt, L. J., Hertz, P. E., Pérez, H. J. Á., & Garland, T. (2009). Why tropical forest lizards are vulnerable to climate warming. Proceedings of the Royal Society of London B: Biological Sciences, rspb-2008. Janzen, D. H. (1967). Why mountain passes are higher in the tropics. The American Naturalist, 101(919), 233-249. Jefferies, R. L. (2000). Allochthonous inputs: integrating population changes and food-web dynamics. Trends in Ecology & Evolution, 15(1), 19-22. Jump, A. S., Mátyás, C., & Peñuelas, J. (2009). The altitude-for-latitude disparity in the range retractions of woody species. Trends in Ecology & Evolution, 24(12), 694-701. Kempel, A., Razanajatovo, M., Stein, C., Unsicker, S. B., Auge, H., Weisser, W. W., Fischer, M. and Prati, D. (2015). Herbivore preference drives plant community composition. Ecology, 96(11), 2923-2934. Kingsolver, J. G., & Huey, R. B. (2008). Size, temperature, and fitness: three rules. Evolutionary Ecology Research, 10(2), 251-268. Körner, C. (2003). Alpine plant life: functional plant ecology of high mountain ecosystems; with 47 tables. Springer Science & Business Media. Körner, C., & Diemer, M. (1987). In situ photosynthetic responses to light, temperature and carbon dioxide in herbaceous plants from low and high altitude. Functional Ecology, 1, 179-194. Lee, C.-F., & Cheng, H.-T. (2007). The Chrysomelidae of Taiwan I. Taipei: Sishou-Hills Insect Observation Network Press. [In Chinese] Lee, C.-F., & Bezdek, J. (2016). Revision of the wingless Sikkimia Duvivier (Coleoptera, Chrysomelidae, Galerucinae) from Taiwan, including a new generic synonymy and four new species descriptions. ZooKeys, 553, 79-106. Li, J., Yang, J., Li, D., Fei, P., Guo, T., Ge, C., & Chen, W. Chlorophyll meter’s estimate of weight-based nitrogen concentration in rice leaf is influenced by leaf thickness, Plant Production Science, 14(2), 177-183. Marenco, R. A., Antezana-Vera, S. A., & Nascimento, H. C. S. (2009). Relationship between specific leaf area, leaf thickness, leaf water content and SPAD-502 readings in six Amazonian tree species. Photosynthetica, 47(2), 184-190. Martinez, G., Soler, R., & Dicke, M. (2013). Behavioral ecology of oviposition-site selection in herbivorous true bugs. In Advances in the Study of Behavior (No. 45, pp. 175-207). Elsevier. Matsubayashi, K. W., Ohshima, I., & Nosil, P. (2010). Ecological speciation in phytophagous insects. Entomologia Experimentalis et Applicata, 134(1), 1-27. Mattson, W. J. (1980). Herbivory in relation to plant nitrogen content. Annual Review of Ecology and Systematics, 11, 119-161. Mayhew, P. J. (2001). Herbivore host choice and optimal bad motherhood. Trends in Ecology & Evolution, 16(4), 165-167. Mayr, E. (1956). Geographical character gradients and climatic adaptation. Evolution, 10(1), 105-108. Minkenberg, O. P., & Ottenheim, J. J. (1990). Effect of leaf nitrogen content of tomato plants on preference and performance of a leafmining fly. Oecologia, 83(3), 291-298. Moles, A. T., Bonser, S. P., Poore, A. G., Wallis, I. R., & Foley, W. J. (2011). Assessing the evidence for latitudinal gradients in plant defence and herbivory. Functional Ecology, 25(2), 380-388. Oksanen, J., Blanchet, F. G., Friendly, M., Kindt, R., Legendre, P., McGlinn, D., Minchin, P. R., O'Hara, R. B., Simpson, G. L., Solymos, P., Stevens, M. H. H., Szoecs, E., & Wagner, H. (2016). vegan: Community Ecology Package. R package version 2.4-0. Peacock, A. J. (1998). Oxygen at high altitude. Bmj, 317(7165), 1063-1066. Pearse, I. S., & Altermatt, F. (2013). Predicting novel trophic interactions in a non‐native world. Ecology Letters, 16(8), 1088-1094. Pellissier, L., Roger, A., Bilat, J., & Rasmann, S. (2014). High elevation Plantago lanceolata plants are less resistant to herbivory than their low elevation conspecifics: is it just temperature? Ecography, 37(10), 950-959. Pennings, S. C., Siska, E. L., & Bertness, M. D. (2001). Latitudinal differences in plant palatability in Atlantic coast salt marshes. Ecology, 82(5), 1344-1359. Pennings, S. C., Ho, C. K., Salgado, C. S., Więski, K., Davé, N., Kunza, A. E., & Wason, E. L. (2009). Latitudinal variation in herbivore pressure in Atlantic Coast salt marshes. Ecology, 90(1), 183-195. Pinheiro J, Bates D, DebRoy S, Sarkar D and R Core Team (2016). nlme: Linear and Nonlinear Mixed Effects Models. R package version 3.1-127. R Development Core Team (2011). R: A Language and Environment for Statistical Computing. Vienna, Austria: the R Foundation for Statistical Computing. Raupp, M. J. (1985). Effects of leaf toughness on mandibular wear of the leaf beetle, Plagiodera versicolora. Ecological Entomology, 10, 73-79. Reid, C. A. M., & Beatson, M. (2015). Disentangling a taxonomic nightmare: a revision of the Australian, Indomalayan and Pacific species of Altica Geoffroy, 1762 (Coleoptera: Chrysomelidae: Galerucinae). Zootaxa, 3918(4), 503-551. Salgado, C. S., & Pennings, S. C. (2005). Latitudinal variation in palatability of salt-marsh plants: Are differences constitutive? Ecology, 86(6), 1571-1579. Siska, E. L., Pennings, S. C., Buck, T. L., & Hanisak, M. D. (2002). Latitudinal variation in palatability of salt-marsh plants: which traits are responsible? Ecology, 83(12), 3369-3381. Sternberg, E. D., & Thomas, M. B. (2014). Local adaptation to temperature and the implications for vector-borne diseases. Trends in Parasitology, 30(3), 115-122. Stiling, P., & Rossi, A. M. (1996). Complex effects of genotype and environment on insect herbivores and their enemies. Ecology, 77(7), 2212-2218. Sunday, J. M., Bates, A. E., & Dulvy, N. K. (2011). Global analysis of thermal tolerance and latitude in ectotherms. Proceedings of the Royal Society of London B: Biological Sciences, 278(1713), 1823-1830. Taiwan Typhoon and Flood Research Institute, National Applied Research Laboratories. (2014). Data Bank for Atmospheric and Hydrologic Research [Hourly weather data 2005 - 2014]. Retrieved from https://dbahr.narlabs.org.tw. Theis, N., & Lerdau, M. (2003). The evolution of function in plant secondary metabolites. International Journal of Plant Sciences, 164(S3), S93-S102. Thompson, J.N. (1988). Evolutionary ecology of the relationship between oviposition preference and performance of offspring in phytophagous insects. Entomologia Experimentalis et Applicata, 47, 3-14. Thompson, J. N. (2005). The geographic mosaic of coevolution. Chicago, IL: University of Chicago Press. Tomas, F., Abbott, J. M., Steinberg, C., Balk, M., Williams, S. L., & Stachowicz, J. J. (2011). Plant genotype and nitrogen loading influence seagrass productivity, biochemistry, and plant–herbivore interactions. Ecology, 92(9), 1807-1817. Turlure, C., Radchuk, V., Baguette, M., Meijrink, M., den Burg, A., Vries, M. W., & Duinen, G. J. (2013). Plant quality and local adaptation undermine relocation in a bog specialist butterfly. Ecology and Evolution, 3(2), 244-254. Utsumi, S. (2015). Feeding evolution of a herbivore influences an arthropod community through plants: implications for plant‐mediated eco‐evolutionary feedback loop. Journal of Ecology, 103(4), 829-839. Valladares F, Matesanz S, Guilhaumon F et al. (2014). The effects of phenotypic plasticity and local adaptation on forecasts of species range shifts under climate change. Ecology Letters, 17, 1351-1364. Van Hook Jr, R. I. (1971). Energy and nutrient dynamics of spider and orthopteran populations in a grassland ecosystem. Ecological Monographs, 1-26. Ward, D. & Seely, M.K. (1996). Adaptation and constraint in the evolution of the physiology and behaviour of the Namib desert tenebrionid beetle genus Onymacris. Evolution, 50, 1231-1240. Yu, S.-H. (2016). Experimental warming impact on a native butterfly (Pieris canidia), an invasive butterfly (P. rapae), and their nectar plant (Bidens pilosa var. radiata) across altitude? Unpublished master’s thesis, National Taiwan University. Zvereva, E. L., Kozlov, M. V., & Hilker, M. (2010). Evolutionary variations on a theme: host plant specialization in five geographical populations of the leaf beetle Chrysomela lapponica. Population ecology, 52(3), 389-396. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/50419 | - |
dc.description.abstract | The relationship between herbivore feeding preference for host plants and herbivore performance is central to the study of plant–herbivore interactions. While the correlation and causation between herbivore preference and performance have been documented in latitudinal systems, little is known in altitudinal systems. To help fill up this knowledge gap, this altitudinal study tested four hypotheses: 1) Field herbivores, regardless of altitudinal origin, will show a feeding preference for higher-altitude plants. In other words, higher-altitude plants have a higher palatability. 2) Field plant traits will suggest a higher plant quality for herbivores at higher altitude, helping explain the altitudinal variation in plant palatability. 3) Accordingly, field herbivore performance (body size) increases with altitude, implying a link between field preference and performance. 4) A laboratory factorial experiment will support the causative link between preference and performance. Herbivores will perform better on plants collected from higher altitude (biotic factor), regardless of herbivore growth temperature (abiotic factor) or adaptation, if exists. Focusing on a specialist herbivore (Altica birmanensis) and its host plant (Polygonum chinense L.) at low vs. medium altitude (100 vs. 1000 m) in Taiwan, this study found a correlation between field herbivore preference and performance across altitude, consistently with latitudinal systems. In specific, field herbivores preferred higher-altitude plants. This higher preference (or plant palatability) was associated with the variation in field plant traits across altitude. Furthermore, the variation in field plant traits also correlated with field herbivore performance across altitude (larger body size at higher altitude). However, the correlation between field herbivore preference and performance across altitude was not supported by the laboratory experiment, in contrast to latitudinal systems. In specific, the laboratory results showed that an abiotic factor (temperature) was the most important factor affecting herbivore performance, compared to a biotic factor (plants with different palatability across altitude) or herbivores’ adaptation to abiotic or biotic factors. This suggests that while latitudinal and altitudinal systems share similar temperature gradients, the patterns of plant–herbivore interactions in each system could be driven by different factors. | en |
dc.description.provenance | Made available in DSpace on 2021-06-15T12:39:59Z (GMT). No. of bitstreams: 1 ntu-105-R01b44014-1.pdf: 2394494 bytes, checksum: 55b8c8e50b92efb57ff38fba5f602fe1 (MD5) Previous issue date: 2016 | en |
dc.description.tableofcontents | Table of Contents
口試委員會審定書 Acknowledgements …………………………………………………………… I 中文摘要 ………………………………………………………………………… II Abstract …………………………………………………………………………. III Introduction ……………………………………………………………………… 1 Materials and Methods ……………………………………………………………… 6 Study system ………………………………………………………………… 6 Study sites ……………………………………………………………………… 7 Herbivore feeding preference …...…………………………………………… 7 Field plant traits across altitude …...…………………………………………… 8 Field herbivore performance (body size) across altitude……………………… 10 A laboratory factorial experiment...…………………………………………… 11 Statistical analysis ...………………………………………………………… 13 Results ……………………………………………………………………………… 15 Herbivore feeding preference …...…………………………………………… 15 Field plant traits across altitude …...………………………………………… 15 Field herbivore performance (body size) across altitude……………………… 17 Herbivore performance in the laboratory factorial experiment …………… 17 Discussion …………………………………………………………………………… 19 Herbivores prefer more palatable plants at higher altitude …………………… 20 Some field plant traits help explain herbivore feeding preference for higher-altitude plants ………………………………………………………… 20 Field herbivore performance correlates with plant leaf toughness ……… 22 The laboratory experiment suggests that field herbivore performance is mainly driven by temperature …………………………………………………… 23 Herbivore preference and performance across latitude vs. altitude ……… 24 Conclusions ………………………………………………………………………… 25 Literature cited ……………………………………………………………………… 43 | |
dc.language.iso | en | |
dc.title | 動植物關係的取食偏好與個體表現——以跨海拔分佈的專食性植食動物與寄主植物為例 | zh_TW |
dc.title | Preference and Performance in Plant–Herbivore Interactions across Altitude — A Study on a Specialist Herbivore and its Host Plant | en |
dc.type | Thesis | |
dc.date.schoolyear | 104-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 黃紹毅,李佩珍,莊汶博 | |
dc.subject.keyword | 海拔,動植物關係,取食偏好,植食動物表現,適應, | zh_TW |
dc.subject.keyword | altitude,plant–herbivore interaction,preference,performance,adaptation, | en |
dc.relation.page | 56 | |
dc.identifier.doi | 10.6342/NTU201601111 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2016-07-28 | |
dc.contributor.author-college | 生命科學院 | zh_TW |
dc.contributor.author-dept | 生態學與演化生物學研究所 | zh_TW |
顯示於系所單位: | 生態學與演化生物學研究所 |
文件中的檔案:
檔案 | 大小 | 格式 | |
---|---|---|---|
ntu-105-1.pdf 目前未授權公開取用 | 2.34 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。