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*graduate and postgraduate students
** undergraduate students
*Appiah-Madson, H.J., E.B. Knox, C.M. Caruso, A.L. Case. 2022. Do gene flow and genetic drift affect the geographic distribution of female plants in gynodioecious Lobelia siphilitica? Plants 11, 825 https://doi.org/10.3390/plants11060825
*Adhikari, B., C.M. Caruso, A.L. Case. 2019. Beyond balancing selection: frequent mitochondrial recombination contributes to high female frequencies in gynodioecious Lobelia siphilitica L (Campanulaceae). New Phytologist 244: 1381-1393 doi.org/10.1111/nph.16136.
Case, A.L. & L.K. Jesson. 2018. Phylogeny, ecology, and evolution of sexual systems across the land plants. In The Evolution of Sexual Systems. J. Leonard, ed. Springer-Verlag, New York. https://link.springer.com/chapter/10.1007/978-3-319-94139-4_2
Heenan, P.B., T.D. Macfarlane, A.L. Case, S.W. Graham, A. Vinnersten & C. Mitchell. 2017. Morphological and phylogenetic relationships of threatened geophyte Wurmbea novaezelandiae (Colchicaceae) from New Zealand, with notes on typification. Phytotaxa 307: 123-132. doi.org/10.11646/phytotaxa.307.2.3
Bailey, M.F., A.L. Case & C.M. Caruso. 2017. Physiological effects of temperature do not explain prevalence of females in populations of gynodioecious Lobelia siphilitica growing in warmer climates. American Journal of Botany 104: 411-418. doi.org/10.3732/ajb.1600380
*Eisen, K., A.L. Case & C.M. Caruso. 2017. Variation in pollen dispensing schedules of Lobelia siphilitica. International Journal of Plant Sciences 178: 79-84. doi/full/10.1086/688961
Case, A.L., F.R. Finseth, C.M. Barr, & L. Fishman. 2016. Selfish evolution of cytonuclear hybrid incompatibility in Mimulus. Proceedings of the Royal Society B: Biological Sciences 283: 2016.1493 [Shared first-authorship] doi/full/10.1098/rspb.2016.1493 Publicity: Phys.org
**Rivkin, L.R., A.L. Case & C.M. Caruso. 2016. Why is gynodioecy a rare but widely distributed sexual system? Lessons from the Lamiaceae. New Phytologist 211:688-696. doi: 10.1111/nph.13926.
Caruso, C.M., *K. Eisen & A.L. Case. 2016. An angiosperm-wide analysis of the correlates of gynodioecy. International Journal of Plant Sciences 177:115-121. doi/full/10.1086/684260
**Rivkin, L.R., A.L. Case & C.M. Caruso. 2015. Frequency-dependent fitness in gynodioecious Lobelia siphilitica. Evolution 69: 1232-1243. https://onlinelibrary.wiley.com/doi/abs/10.1111/evo.12654
Caruso, C.M., **A. Benscoter, *N. Gale, *E. Seifert, **E. Mills, & A.L. Case. 2015. The effect of crossing distance on fitness of the native wildflower Lobelia siphilitica: implications for ecological restoration. Journal of the Torrey Botanical Society 142:140-151. https://doi.org/10.3159/TORREY-D-13-00055.1
*Hovatter, S.R., C.B. Blackwood, & A.L. Case. 2013. Conspecific plant–soil feedback scales with population size in Lobelia siphilitica (Lobeliaceae). Oecologia 173: 1295-1307. https://link.springer.com/article/10.1007/s00442-013-2710-z
Caruso, C.M. & A.L. Case. 2013. Testing models of sex-ratio evolution in a gynodioecious plant: female frequency co-varies with the cost of male fertility restoration. Evolution 67: 561-566. https://doi.org/10.1111/j.1558-5646.2012.01798.x
Caruso, C.M., A.L. Case, & M.F. Bailey. 2012. The evolutionary ecology of cytonuclear interactions in angiosperms. Trends in Plant Science 17: 638-643. https://doi.org/10.1016/j.tplants.2012.06.006
Mower, J.P., A.L. Case, *E.R. Floro, & J.H. Willis. 2012. Evidence against equimolarity of large repeat arrangements and a predominant master circle structure of the mitochondrial genome from a monkeyflower (Mimulus guttatus) lineage with cryptic CMS. Genome Biology & Evolution 4: 670-686. https://doi.org/10.1093/gbe/evs042
Karron, J.D., C.T. Ivey, R.J. Mitchell, M. Whitehead, R. Peakall, & A.L. Case. 2012. New perspectives on the evolution of plant mating systems. Annals of Botany 109(3): 493-503. Special issue co-editors doi.org/10.1093/aob/mcr319
*Hovatter, S.R., **C. Dejelo, A.L. Case, & C.B. Blackwood. 2011. Metacommunity organization of soil microorganisms depends on habitat type defined by presence of Lobelia siphilitica plants. Ecology 92: 57-65. https://doi.org/10.1890/10-0332.1
Macfarlane, T.D. & A.L. Case. 2011. Wurmbea fluviatilis (Colchicaceae), a new riverine species from the Gascoyne region of Western Australia. Nuytsia 21:25-30. https://library.dbca.wa.gov.au/static/Journals/080057/080057-21.002.pdf
Case, A.L. & C.M. Caruso. 2010. A novel approach to estimating the cost of male fertility restoration in gynodioecious plants. New Phytologist 186:549-557. https://doi.org/10.1111/j.1469-8137.2010.03199.x
Case, A.L. & T-L. Ashman. 2009. Resources and pollinators contribute to population sex-ratio bias and pollen limitation in Fragaria virginiana (Rosaceae). Oikos 118: 1250-1260. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1600-0706.2009.17520.x
Case, A.L. & J.H. Willis. 2008. Hybrid male sterility in Mimulus (Phrymaceae) is associated with a geographically restricted mitochondrial rearrangement. Evolution 65: 1026-1039. https://doi.org/10.1111/j.1558-5646.2008.00360.x
Case, A.L., S.W. Graham, T.D. Macfarlane, & S.C.H. Barrett. 2008. A phylogenetic study of evolutionary transitions in sexual systems in Australasian Wurmbea (Colchicaceae). International Journal of Plant Sciences 169:141-156. Shared first authorship
https://www.journals.uchicago.edu/doi/abs/10.1086/523368
Macfarlane, T.D. & A.L. Case. 2007. Wurmbea inflata (Colchicaceae), a new species from the Gascoyne region of Western Australia. Nuytsia 17: 223-228.
Case, A.L. & T-L. Ashman. 2007. An experimental test of the effects of resources and sex ratio on maternal fitness and phenotypic selection in gynodioecious Fragaria virginiana. Evolution 61: 1900-1911. https://doi.org/10.1111/j.1558-5646.2007.00148.x
Caruso, C.M. & A.L. Case. 2007. Sex-ratio variation in gynodioecious Lobelia siphilitica: effects of population size and geographic location. Journal of Evolutionary Biology 20:1396-1405. https://doi.org/10.1111/j.1420-9101.2007.01361.x
Barrett, S.C.H. & A.L. Case. 2006. The ecology and evolution of gender strategies in plants: The example of Australian Wurmbea (Colchicaceae). Australian Journal of Botany 54:417-433. https://doi.org/10.1071/BT05151
Case, A.L. & T-L. Ashman. 2005. Sex-specific physiology and its implications for reproductive cost. In The Allocation of Resources to Reproduction in Plants. E. Reekie and F. Bazzaz, eds. Springer-Verlag, New York. https://doi.org/10.1016/B978-012088386-8/50005-3
Case, A.L. & S.C.H. Barrett. 2004. Floral biology of gender monomorphism and dimorphism in Wurmbea dioica (Colchicaceae) in Western Australia. International Journal of Plant Sciences 165(2): 289-301. https://doi.org/10.1086/382796
Case, A.L. & S.C.H. Barrett. 2004. Environmental stress and the evolution of dioecy: Wurmbea dioica (Colchicaceae) in Western Australia. Evolutionary Ecology 18(2): 145-164. https://link.springer.com/article/10.1023/B:EVEC.0000021152.34483.77
Case, A.L. & S.C.H. Barrett. 2001. Ecological differentiation of combined and separate sexes of Wurmbea dioica (Colchicaceae) in sympatry. Ecology 82 (9): 2601-2616. https://doi.org/10.1890/0012-9658(2001)082[2601:EDOCAS]2.0.CO;2
Barrett, S.C.H., M.E. Dorken, & A.L. Case. 2000. A geographical context for the evolution of plant reproductive systems. In Integrating Ecological and Evolutionary Processes in a Spatial Context. (Eds. J. Silvertown & J. Antonovics). Blackwell, Oxford, UK.
Barrett, S.C.H., A. L. Case, & G.B. Peters. 1999. Gender modification and resource allocation in subdioecious Wurmbea dioica (Colchicaceae). Journal of Ecology 87 (1): 123-137. https://doi.org/10.1046/j.1365-2745.1999.00336.x
Case, A.L., P.S. Curtis, & A.A. Snow. 1998. Heritable variation in stomatal and growth response to elevated CO2 in wild radish, Raphanus raphanistrum (Brassicaceae). American Journal of Botany 85(2): 253-258. https://doi.org/10.2307/2446313
Lacey, E.P., S. Smith, & A.L. Case. 1997. Parental effects on seed mass: seed coat but not embryo/endosperm effects. American Journal of Botany 84(11): 1617-1620. https://bsapubs.onlinelibrary.wiley.com/doi/abs/10.2307/2446624
Case, A.L., E.P. Lacey, & R.G. Hopkins. 1996. Parental effects in Plantago lanceolata L. II.: Manipulation of grandparental temperature and parental flowering time. Heredity 76(3): 287-295. https://www.nature.com/articles/hdy199642
** undergraduate students
*Appiah-Madson, H.J., E.B. Knox, C.M. Caruso, A.L. Case. 2022. Do gene flow and genetic drift affect the geographic distribution of female plants in gynodioecious Lobelia siphilitica? Plants 11, 825 https://doi.org/10.3390/plants11060825
*Adhikari, B., C.M. Caruso, A.L. Case. 2019. Beyond balancing selection: frequent mitochondrial recombination contributes to high female frequencies in gynodioecious Lobelia siphilitica L (Campanulaceae). New Phytologist 244: 1381-1393 doi.org/10.1111/nph.16136.
Case, A.L. & L.K. Jesson. 2018. Phylogeny, ecology, and evolution of sexual systems across the land plants. In The Evolution of Sexual Systems. J. Leonard, ed. Springer-Verlag, New York. https://link.springer.com/chapter/10.1007/978-3-319-94139-4_2
Heenan, P.B., T.D. Macfarlane, A.L. Case, S.W. Graham, A. Vinnersten & C. Mitchell. 2017. Morphological and phylogenetic relationships of threatened geophyte Wurmbea novaezelandiae (Colchicaceae) from New Zealand, with notes on typification. Phytotaxa 307: 123-132. doi.org/10.11646/phytotaxa.307.2.3
Bailey, M.F., A.L. Case & C.M. Caruso. 2017. Physiological effects of temperature do not explain prevalence of females in populations of gynodioecious Lobelia siphilitica growing in warmer climates. American Journal of Botany 104: 411-418. doi.org/10.3732/ajb.1600380
*Eisen, K., A.L. Case & C.M. Caruso. 2017. Variation in pollen dispensing schedules of Lobelia siphilitica. International Journal of Plant Sciences 178: 79-84. doi/full/10.1086/688961
Case, A.L., F.R. Finseth, C.M. Barr, & L. Fishman. 2016. Selfish evolution of cytonuclear hybrid incompatibility in Mimulus. Proceedings of the Royal Society B: Biological Sciences 283: 2016.1493 [Shared first-authorship] doi/full/10.1098/rspb.2016.1493 Publicity: Phys.org
**Rivkin, L.R., A.L. Case & C.M. Caruso. 2016. Why is gynodioecy a rare but widely distributed sexual system? Lessons from the Lamiaceae. New Phytologist 211:688-696. doi: 10.1111/nph.13926.
Caruso, C.M., *K. Eisen & A.L. Case. 2016. An angiosperm-wide analysis of the correlates of gynodioecy. International Journal of Plant Sciences 177:115-121. doi/full/10.1086/684260
**Rivkin, L.R., A.L. Case & C.M. Caruso. 2015. Frequency-dependent fitness in gynodioecious Lobelia siphilitica. Evolution 69: 1232-1243. https://onlinelibrary.wiley.com/doi/abs/10.1111/evo.12654
Caruso, C.M., **A. Benscoter, *N. Gale, *E. Seifert, **E. Mills, & A.L. Case. 2015. The effect of crossing distance on fitness of the native wildflower Lobelia siphilitica: implications for ecological restoration. Journal of the Torrey Botanical Society 142:140-151. https://doi.org/10.3159/TORREY-D-13-00055.1
*Hovatter, S.R., C.B. Blackwood, & A.L. Case. 2013. Conspecific plant–soil feedback scales with population size in Lobelia siphilitica (Lobeliaceae). Oecologia 173: 1295-1307. https://link.springer.com/article/10.1007/s00442-013-2710-z
Caruso, C.M. & A.L. Case. 2013. Testing models of sex-ratio evolution in a gynodioecious plant: female frequency co-varies with the cost of male fertility restoration. Evolution 67: 561-566. https://doi.org/10.1111/j.1558-5646.2012.01798.x
Caruso, C.M., A.L. Case, & M.F. Bailey. 2012. The evolutionary ecology of cytonuclear interactions in angiosperms. Trends in Plant Science 17: 638-643. https://doi.org/10.1016/j.tplants.2012.06.006
Mower, J.P., A.L. Case, *E.R. Floro, & J.H. Willis. 2012. Evidence against equimolarity of large repeat arrangements and a predominant master circle structure of the mitochondrial genome from a monkeyflower (Mimulus guttatus) lineage with cryptic CMS. Genome Biology & Evolution 4: 670-686. https://doi.org/10.1093/gbe/evs042
Karron, J.D., C.T. Ivey, R.J. Mitchell, M. Whitehead, R. Peakall, & A.L. Case. 2012. New perspectives on the evolution of plant mating systems. Annals of Botany 109(3): 493-503. Special issue co-editors doi.org/10.1093/aob/mcr319
*Hovatter, S.R., **C. Dejelo, A.L. Case, & C.B. Blackwood. 2011. Metacommunity organization of soil microorganisms depends on habitat type defined by presence of Lobelia siphilitica plants. Ecology 92: 57-65. https://doi.org/10.1890/10-0332.1
Macfarlane, T.D. & A.L. Case. 2011. Wurmbea fluviatilis (Colchicaceae), a new riverine species from the Gascoyne region of Western Australia. Nuytsia 21:25-30. https://library.dbca.wa.gov.au/static/Journals/080057/080057-21.002.pdf
Case, A.L. & C.M. Caruso. 2010. A novel approach to estimating the cost of male fertility restoration in gynodioecious plants. New Phytologist 186:549-557. https://doi.org/10.1111/j.1469-8137.2010.03199.x
Case, A.L. & T-L. Ashman. 2009. Resources and pollinators contribute to population sex-ratio bias and pollen limitation in Fragaria virginiana (Rosaceae). Oikos 118: 1250-1260. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1600-0706.2009.17520.x
Case, A.L. & J.H. Willis. 2008. Hybrid male sterility in Mimulus (Phrymaceae) is associated with a geographically restricted mitochondrial rearrangement. Evolution 65: 1026-1039. https://doi.org/10.1111/j.1558-5646.2008.00360.x
Case, A.L., S.W. Graham, T.D. Macfarlane, & S.C.H. Barrett. 2008. A phylogenetic study of evolutionary transitions in sexual systems in Australasian Wurmbea (Colchicaceae). International Journal of Plant Sciences 169:141-156. Shared first authorship
https://www.journals.uchicago.edu/doi/abs/10.1086/523368
Macfarlane, T.D. & A.L. Case. 2007. Wurmbea inflata (Colchicaceae), a new species from the Gascoyne region of Western Australia. Nuytsia 17: 223-228.
Case, A.L. & T-L. Ashman. 2007. An experimental test of the effects of resources and sex ratio on maternal fitness and phenotypic selection in gynodioecious Fragaria virginiana. Evolution 61: 1900-1911. https://doi.org/10.1111/j.1558-5646.2007.00148.x
Caruso, C.M. & A.L. Case. 2007. Sex-ratio variation in gynodioecious Lobelia siphilitica: effects of population size and geographic location. Journal of Evolutionary Biology 20:1396-1405. https://doi.org/10.1111/j.1420-9101.2007.01361.x
Barrett, S.C.H. & A.L. Case. 2006. The ecology and evolution of gender strategies in plants: The example of Australian Wurmbea (Colchicaceae). Australian Journal of Botany 54:417-433. https://doi.org/10.1071/BT05151
Case, A.L. & T-L. Ashman. 2005. Sex-specific physiology and its implications for reproductive cost. In The Allocation of Resources to Reproduction in Plants. E. Reekie and F. Bazzaz, eds. Springer-Verlag, New York. https://doi.org/10.1016/B978-012088386-8/50005-3
Case, A.L. & S.C.H. Barrett. 2004. Floral biology of gender monomorphism and dimorphism in Wurmbea dioica (Colchicaceae) in Western Australia. International Journal of Plant Sciences 165(2): 289-301. https://doi.org/10.1086/382796
Case, A.L. & S.C.H. Barrett. 2004. Environmental stress and the evolution of dioecy: Wurmbea dioica (Colchicaceae) in Western Australia. Evolutionary Ecology 18(2): 145-164. https://link.springer.com/article/10.1023/B:EVEC.0000021152.34483.77
Case, A.L. & S.C.H. Barrett. 2001. Ecological differentiation of combined and separate sexes of Wurmbea dioica (Colchicaceae) in sympatry. Ecology 82 (9): 2601-2616. https://doi.org/10.1890/0012-9658(2001)082[2601:EDOCAS]2.0.CO;2
Barrett, S.C.H., M.E. Dorken, & A.L. Case. 2000. A geographical context for the evolution of plant reproductive systems. In Integrating Ecological and Evolutionary Processes in a Spatial Context. (Eds. J. Silvertown & J. Antonovics). Blackwell, Oxford, UK.
Barrett, S.C.H., A. L. Case, & G.B. Peters. 1999. Gender modification and resource allocation in subdioecious Wurmbea dioica (Colchicaceae). Journal of Ecology 87 (1): 123-137. https://doi.org/10.1046/j.1365-2745.1999.00336.x
Case, A.L., P.S. Curtis, & A.A. Snow. 1998. Heritable variation in stomatal and growth response to elevated CO2 in wild radish, Raphanus raphanistrum (Brassicaceae). American Journal of Botany 85(2): 253-258. https://doi.org/10.2307/2446313
Lacey, E.P., S. Smith, & A.L. Case. 1997. Parental effects on seed mass: seed coat but not embryo/endosperm effects. American Journal of Botany 84(11): 1617-1620. https://bsapubs.onlinelibrary.wiley.com/doi/abs/10.2307/2446624
Case, A.L., E.P. Lacey, & R.G. Hopkins. 1996. Parental effects in Plantago lanceolata L. II.: Manipulation of grandparental temperature and parental flowering time. Heredity 76(3): 287-295. https://www.nature.com/articles/hdy199642