Go to: content | top | bottom | search
You are hereUNIL > Department of Ecology and Evolution > Research > Pannell Group

Pannell Group - Ecology and Evolution of Plant Sexual Systems.

Pannell lab overview

Current projects in the group are addressing a number of questions concerning evolutionary transitions between sexual systems and their implications for mating and resource allocation. Some of these are summarised under the project descriptions below. For further details, follow the links to the corresponding webpages of the postdocs or students concerned.


The lab benefits from interactions fostered by the Swiss Plants Sciences Web

Transitions between combined and separate sexes in Mercurialis annua

Several projects aim to explain and understand transitions between combined and separate sexes in the European annual plant Mercurialis annua, which displays dioecy (fully separate sexes), monoecy (self-fertile functional hermaphroditism) and androdioecy (the coexistence of males and hermaphrodites) and occasional male sterility.


Male (A), female (B) and monoecious (C) individuals of Mercurialis annua. Photos: J. Baker.

Using whole genome sequencing and transcriptomics analysis postdoc Katie Ridout (in collaboration with Dr. Dmitry Filatov at the University of Oxford) is assembling and annotating the sex chromosomes of Mercurialis annua in order to investigate the evolution of sex chromosomes and dioecy in Mercurialis. Using a combination of these tools, analysis of interspecific crosses, and natural selection experiments, PhD student Guillaume Cossard is attempting to further unravel the ecological and genetic factors responsible for sexual-system variation in the group. Postdoc Dr. Camille Roux is using Approximate Bayesian Computation to understand the order of key events that have been involved in the diversification of the group, notably sexual-system and ploidy transitions.


Diagrams depicting four of the many possible scenarios underlying genome duplication via autotetraploidy and subsequent diploidisation of the genome (the cessation of gene flow between homoleogous genomes). Tube width reflects population size. Approximate Bayesian Computation is being used to discriminate among these and other scenarios.

Evolutionary ecology of flower and inflorescence strategies under wind pollination

We are also using phenotypic variation in Mercurialis annua to test hypothesis concerning the evolution of inflorescence architecture and how it affects the population mating system. One study, conducted by postdoc Dr. Anne-Marie Labouche, considers the effects of pollen limitation and pollen competition on offspring number and quality as a function of plant density. Another, conducted by postdoc Dr. Luis Santos del Blanco, attempts to tease apart the effects of density and plant size on plant mating (selfing and outcrossing rates) under wind pollination. Luis is also using field and manipulative array experiments to understand the costs and benefits of different inflorescence architecture found across the species’ range.


Experimental arrays of wind-pollinated Mercurialis annua, in which distance from a pollen source regulates the intensity of pollen competition. Photo: A-M. Labouche

Transitions between nocturnal and diurnal pollination

Postdoc Dr. Anne-Marie Labouche is studying the characters that have diverged between the nocturnally pollinated Silene latifolia and diurnally pollinated Silene dioica. Nocturnal pollination would appear to be costly for S. latifolia, because the pollinator (Hadena bicruris) lays eggs in the flowers that hatch seed-eating caterpillars. By assessing the fitness costs and benefits in experimental hybrid populations, Marie is attempting to understand why an apparently maladaptive pollination syndrome is maintained.


Female flower of Silene latifolia being visited by Hadena bicruris. Photo : A-M. Labouche

Breakdown of self-incompatibility in Linaria cavanillesii

Self-incompatibility has been lost on numerous occasions in flowering plants. To contribute to our understanding of how and why this transition occurs, PhD student Marie Voillemot is using self-compatible and self-incompatible (SI) populations of the Spanish toadflax Linaria cavanillesii as a model. Commonly, when SI breaks down, plants evolved smaller, less rewarding flowers. Interestingly, this ‘selfing syndrome’ does not appear to have evolved in L. cavanillesii. The project aims to determine what might have caused this loss of SI, to ascertain its effect on the mating system and pollination biology, and to characterize the population genetic consequences at the locus causing SI and other loci across the genome.


Habitat of Linaria cavanillesii in southeastern Spain. Photo: J.R. Pannell

Maintenance of males with hermaphrodites in Fraxinus ornus

Over the last decade or so, my lab has contributed much that is known about how males can be maintained with hermaphrodites (the androdioecious sexual system), with substantial effort invested into understanding androdioecy in Mercurialis annua. We are currently also working on this sexual system in the Mediterranean tree Fraxinus ornus. In collaboration with Miguel Verdu at CSIC in Valencia, Spain, and PhD student Marie Voillemot, postdoc Dr. Alok Gupta is testing the hypothesis that differences in the fitness of male-sired and hermaphrodite-sired progeny in the Mediterranean tree Fraxinus ornus can be attributed to differences in paternally transmitted patterns of gene expression. Alok is also studying the evolution of sexual dimorphism in this species using gas chromatography-mass spectrometry (GC-MS) to analyze the scent volatiles from males and hermaphrodites in natural populations of F. ornus, followed by the use of next-generation sequencing to identify scent-related floral transcripts.



The lab group at a recent research and fondue away day on the top of Moléson.

2016 |  2015 |  2014 |  2013 |  2012 |  2011 |  2010 |  2009 |  2008 |  2007 |  2006 |  2005 |  2004 |  2003 |  2002 |  2001 |  2000 |  1999 |  1997 |  1993 | 

Cossard G., Sannier J., Sauquet H., Damerval C., de Craene R.L., Jabbour F., Nadot S., 2016. Subfamilial and tribal relationships of Ranunculaceae: evidence from eight molecular markers. Plant Systematics and Evolution 302(4) pp. 419-431. [DOI] [Web of Science]
Labouche A.M., Pannell J.R., 2016. A test of the size-constraint hypothesis for a limit to sexual dimorphism in plants. Oecologia 181(3) pp. 873-884. [DOI] [Web of Science] [Pubmed]
Ma W.J., Pannell J.R., 2016. Sex Determination: Separate Sexes Are a Double Turnoff in Melons. Current Biology : Cb 26(4) pp. R171-R174. [DOI] [Web of Science] [Pubmed]
Olivieri I., Tonnabel J., Ronce O., Mignot A., 2016. Why evolution matters for species conservation: perspectives from three case studies of plant metapopulations. Evolutionary Applications 9(1) pp. 196-211. [DOI] [Web of Science]
Pannell J.R., Cossard G., 2016. Long story short. Elife 5 pp. e20314. [Document] [DOI] [Web of Science] [Pubmed]
Pannell J.R., Farmer E.E., 2016. Mimicry in plants. Current Biology 26(17) pp. R784-R785. [DOI] [Web of Science] [Pubmed]
Pellissier Loic, Oppliger Anne, Hirzel Alexandre H., Savova-Bianchi Dessislava, Mbayo Guilain, Mascher Fabio, Kellenberger Stefan, Niculita-Hirzel Hélène, 04-2016. The composition of airborne and grain-dust fungal communities is shaped at regional scale by plant genotypes and farming practices. Applied and Environmental Microbiology 82(7) pp. 2121-2131. [DOI] [Pubmed]
Camille Roux, John R. Pannell, 01-2015. Inferring the mode of origin of polyploid species from next-generation sequence data. Molecular Ecology . [DOI]
Jaramillo-Correa J.P., Rodríguez-Quilón I., Grivet D., Lepoittevin C., Sebastiani F., Heuertz M., Garnier-Géré P.H., Alía R., Plomion C., Vendramin G.G. et al., 2015. Molecular Proxies for Climate Maladaptation in a Long-Lived Tree (Pinus pinaster Aiton, Pinaceae). Genetics 199(3) pp. 793-807. [DOI] [Web of Science] [Pubmed]
Pannell J.R., 2015. Evolution of the mating system in colonizing plants. Molecular Ecology 24(9) pp. 2018-2037. [DOI] [Web of Science] [Pubmed]
Pannell J.R., Auld J.R., Brandvain Y., Burd M., Busch J.W., Cheptou P.O., Conner J.K., Goldberg E.E., Grant A.G., Grossenbacher D.L. et al., 2015. The scope of Baker's law. New Phytologist 208(3) pp. 656-667. [DOI] [Web of Science] [Pubmed]
Pannell J.R., Voillemot M., 2015. Plant Mating Systems: Female Sterility in the Driver's Seat. Current Biology 25(12) pp. R511-R514. [DOI] [Web of Science] [Pubmed]
Roux C., Pannell J.R., 2015. Inferring the mode of origin of polyploid species from next-generation sequence data. Molecular Ecology 24(5) pp. 1047-1059. [DOI] [Web of Science] [Pubmed]
Santos-Del-Blanco L., Alía R., González-Martínez S.C., Sampedro L., Lario F., Climent J., 2015. Correlated genetic effects on reproduction define a domestication syndrome in a forest tree. Evolutionary Applications 8(4) pp. 403-410. [DOI] [Web of Science] [Pubmed]
Tedder A., Helling M., Pannell J.R., Shimizu-Inatsugi R., Kawagoe T., van Campen J., Sese J., Shimizu K.K., 2015. Female sterility associated with increased clonal propagation suggests a unique combination of androdioecy and asexual reproduction in populations of Cardamine amara (Brassicaceae). Annals of Botany 115(5) pp. 763-776. [DOI] [Web of Science] [Pubmed]
Toups M., Veltsos P., Pannell J.R., 2015. Plant sex chromosomes: lost genes with little compensation. Current Biology 25(10) pp. R427-R430. [DOI] [Web of Science] [Pubmed]
Alía R., Chambel R., Notivol E., Climent J., González-Martínez S.C., 2014. Environment-dependent microevolution in a Mediterranean pine (Pinus pinaster Aiton). BMC Evolutionary Biology 14 p. 200. [Document] [DOI] [Web of Science] [Pubmed]
Fraïsse C., Roux C., Welch J.J., Bierne N., 2014. Gene-flow in a mosaic hybrid zone: is local introgression adaptive? Genetics 197(3) pp. 939-951. [DOI] [Web of Science] [Pubmed]
Hernández-Serrano A., Verdú M., Santos-Del-Blanco L., Climent J., González-Martínez S.C., Pausas J.G., 2014. Heritability and quantitative genetic divergence of serotiny, a fire-persistence plant trait. Annals of Botany 114(3) pp. 571-577. [DOI] [Web of Science] [Pubmed]
Jabbour F., Cossard G., Le Guilloux M., Sannier J., Nadot S., Damerval C., 2014. Specific duplication and dorsoventrally asymmetric expression patterns of Cycloidea-like genes in zygomorphic species of Ranunculaceae. PLoS One 9(4) pp. e95727. [Document] [DOI] [Web of Science] [Pubmed]
Pannell J.R., 2014. Leaf Mimicry: Chameleon-like Leaves in a Patagonian Vine. Current Biology 24(9) pp. R357-R359. [DOI] [Web of Science] [Pubmed]
Pannell J.R., Eppley S.M., Dorken M.E., Berjano R., 2014. Regional variation in sex ratios and sex allocation in androdioecious Mercurialis annua. Journal of Evolutionary Biology 27(7) pp. 1467-1477. [DOI] [Web of Science] [Pubmed]
Pinosio S., González-Martínez S.C., Bagnoli F., Cattonaro F., Grivet D., Marroni F., Lorenzo Z., Pausas J.G., Verdú M., Vendramin G.G., 2014. First insights into the transcriptome and development of new genomic tools of a widespread circum-Mediterranean tree species, Pinus halepensis Mill. Molecular Ecology Resources 14(4) pp. 846-856. [DOI] [Web of Science] [Pubmed]
Pujol B., Marrot P., Pannell J.R., 2014. A quantitative genetic signature of senescence in a short-lived perennial plant. Current Biology 24(7) pp. 744-747. [DOI] [Web of Science] [Pubmed]
Romiguier J., Gayral P., Ballenghien M., Bernard A., Cahais V., Chenuil A., Chiari Y., Dernat R., Duret L., Faivre N. et al., 2014. Comparative population genomics in animals uncovers the determinants of genetic diversity. Nature 515(7526) pp. 261-263. [DOI] [Web of Science] [Pubmed]
Roux C., Fraïsse C., Castric V., Vekemans X., Pogson G.H., Bierne N., 2014. Can we continue to neglect genomic variation in introgression rates when inferring the history of speciation? A case study in a Mytilus hybrid zone. Journal of Evolutionary Biology 27(8) pp. 1662-1675. [DOI] [Web of Science] [Pubmed]
Santos del Blanco L., Climent J., 2014. Costs of female reproduction in a conifer tree: a whole-tree level assessment. Journal of Ecology 102(5) pp. 1310-1317. [DOI] [Web of Science]
Vizcaíno-Palomar N., Revuelta-Eugercios B., Zavala M.A., Alía R., González-Martínez S.C., 2014. The role of population origin and microenvironment in seedling emergence and early survival in Mediterranean maritime pine (Pinus pinaster Aiton). PLoS One 9(10) pp. e109132. [Document] [DOI] [Web of Science] [Pubmed]
Labouche A.M., Bernasconi G., 2013. Cost limitation through constrained oviposition site in a plant-pollinator/seed predator mutualism. Functional Ecology 27(2) pp. 509-521. [DOI] [Web of Science]
Pannell J.R., Fields P.D., 2013. Evolution in subdivided plant populations: concepts, recent advances and future directions. New Phytologist 201(2) pp. 417-432. [DOI] [Web of Science] [Pubmed]
Pannell J.R., Labouche A.M., 2013. The incidence and selection of multiple mating in plants. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 368(1613) p. 20120051. [DOI] [Web of Science] [Pubmed]
Ruch N., McCoy T., Grace O.M., 2013. The genus Aloe L. (Xanthorrhoeaceae) in Djibouti. Bradleya 31 pp. 15-24. [Web of Science]
Pannell J.R., 2012. Speciation genetics: reinforcement by shades and hues. Current Biology 22(9) pp. R299-R302. [DOI] [Web of Science] [Pubmed]
Pannell J.R., 2012. The ecology of plant populations: their dynamics, interactions and evolution. Annals of Botany 110(7) pp. 1351-1355. [DOI] [Web of Science]
Sanchez Vilas J., Pannell J.R., 2012. Do plants adjust their sex allocation and secondary sexual morphology in response to their neighbours? Annals of Botany 110(7) pp. 1471-1478. [DOI] [Web of Science] [Pubmed]
Santos-del-Blanco L., Climent J., González-Martínez S.C., Pannell J.R., 2012. Genetic differentiation for size at first reproduction through male versus female functions in the widespread Mediterranean tree Pinus pinaster. Annals of Botany 110(7) pp. 1449-1460. [DOI] [Web of Science] [Pubmed]
Hesse E, Pannell J.R., 2011. Sexual dimorphism in androdioecious Mercurialis annua, a wind-pollinated herb. International Journal of Plant Sciences 172(1) pp. 49-59. [DOI] [Web of Science]
Magalhaes I.S., Gleiser G., Labouche A.M., Bernasconi G., 2011. Comparative population genetic structure in a plant-pollinator/seed predator system. Molecular Ecology 20(22) pp. 4618-4630. [DOI] [Web of Science] [Pubmed]
Moore J.C., Pannell J.R., 2011. Sexual selection in plants. Current Biology 21(5) pp. R176-R182. [DOI] [Web of Science] [Pubmed]
Pfeiffer T., Roschanski A.M., Pannell J.R., Korbecka G., Schnittler M., 2011. Characterization of microsatellite loci and reliable genotyping in a polyploid plant, Mercurialis perennis (Euphorbiaceae). Journal of Heredity 102(4) pp. 479-488. [DOI] [Web of Science] [Pubmed]
Sánchez Vilas J., Pannell J.R., 2011. Sex-differential herbivory in androdioecious Mercurialis annua. PLoS One 6(7) pp. e22083. [DOI] [Web of Science] [Pubmed]
Sánchez Vilas J., Pannell J.R., 2011. Sexual dimorphism in resource acquisition and deployment: both size and timing matter. Annals of Botany 107(1) pp. 119-126. [DOI] [Web of Science] [Pubmed]
Harris M.S., Pannell J.R., 2010. Canopy seed storage is associated with sexual dimorphism in the woody dioecious genus Leucadendron. Journal of Ecology 98(2) pp. 509-515. [DOI] [Web of Science]
Pannell J.R., Korbecka G., 2010. Mating-system evolution: rise of the irresistible males. Current Biology 20(11) pp. R482-R484. [DOI] [Web of Science] [Pubmed]
Pujol B, Obbard D.J, Pannell J.R., 2010. Symptoms of population range expansion: lessons from phenotypic and genetic differentiation in hexaploid Mercurialis annua. Plant Ecology and Diversity 3(2) pp. 103-108. [DOI] [Web of Science]
Sánchez-Vilas J., Pannell J.R., 2010. Differential niche modification by males and females of a dioecious herb: extending the Jack Sprat effect. Journal of Evolutionary Biology 23(10) pp. 2262-2266. [DOI] [Web of Science] [Pubmed]
Zhou S., Zhou C., Pannell J.R., 2010. Genetic load, inbreeding depression and heterosis in an age-structured metapopulation. Journal of Evolutionary Biology 23(11) pp. 2324-2332. [DOI] [Web of Science] [Pubmed]
Zhou S.R., Pannell J.R., 2010. Inbreeding depression and genetic load at partially linked loci in a metapopulation. Genetics Research 92(2) pp. 127-140. [DOI] [Web of Science] [Pubmed]
Bernasconi G., Antonovics J., Biere A., Charlesworth D., Delph L.F., Filatov D., Giraud T., Hood M.E., Marais G.A., McCauley D. et al., 2009. Silene as a model system in ecology and evolution. Heredity 103(1) pp. 5-14. [DOI] [Web of Science] [Pubmed]
Dorken M.E., Pannell J.R., 2009. Hermaphroditic sex allocation evolves when mating opportunities change. Current Biology 19(6) pp. 514-517. [DOI] [Web of Science] [Pubmed]
Harris S.R., Henbest K.B., Maeda K., Pannell J.R., Timmel C.R., Hore P.J., Okamoto H., 2009. Effect of magnetic fields on cryptochrome-dependent responses in Arabidopsis thaliana. Journal of the Royal Society, Interface 6(41) pp. 1193-1205. [DOI] [Web of Science] [Pubmed]
Pannell J.R, Pujol B., 2009. The paradoxical spread of a new Y chromosome - a novel explanation. Trends in Ecology and Evolution 24(2) pp. 59-63. [DOI] [Web of Science]
Pannell J.R., 2009. Mating-system evolution: genies from a bottleneck. Current Biology 19(9) pp. R369-R370. [DOI] [Web of Science] [Pubmed]
Pannell J.R., 2009. Mating-system evolution: succeeding by celibacy. Current Biology 19(21) pp. R983-R985. [DOI] [Web of Science] [Pubmed]
Pannell J.R., 2009. On the problems of a closed marriage: celebrating Darwin 200. Biology Letters 5(3) pp. 332-335. [DOI] [Web of Science] [Pubmed]
Pujol B., Zhou S.R., Sanchez Vilas J., Pannell J.R., 2009. Reduced inbreeding depression after species range expansion. Proceedings of the National Academy of Sciences of the United States of America 106(36) pp. 15379-15383. [DOI] [Web of Science] [Pubmed]
Dorken M.E., Pannell J.R., 2008. Density-dependent regulation of the sex ratio in an annual plant. American Naturalist 171(6) pp. 824-830. [DOI] [Web of Science] [Pubmed]
Gleiser G., Segarra-Moragues J.G., Pannell J.R., Verdú M., 2008. Siring success and paternal effects in heterodichogamous Acer opalus. Annals of Botany 101(7) pp. 1017-1026. [DOI] [Web of Science] [Pubmed]
Gleiser G., Verdú M., Segarra-Moragues J.G., González-Martínez S.C., Pannell J.R., 2008. Disassortative mating, sexual specialization, and the evolution of gender dimorphism in heterodichogamous Acer opalus. Evolution 62(7) pp. 1676-1688. [DOI] [Web of Science] [Pubmed]
Harris M.S., Pannell J.R., 2008. Roots, shoots and reproduction: sexual dimorphism in size and costs of reproductive allocation in an annual herb. Proceedings of the Royal Society B Biological Sciences 275(1651) pp. 2595-2602. [DOI] [Web of Science] [Pubmed]
Pannell J.R., Dorken M.E., Pujol B., Berjano R., 2008. Gender variation and transitions between sexual systems in Mercurialis annua (Euphorbiaceae). International Journal of Plant Sciences 169(1) pp. 129-139. [DOI] [Web of Science]
Pujol B., Pannell J.R., 2008. Reduced responses to selection after species range expansion. Science 321(5885) p. 96. [DOI] [Web of Science] [Pubmed]
Pujol B., Wilson A.J., Ross R.I., Pannell J.R., 2008. Are Q(ST)-F(ST) comparisons for natural populations meaningful? Molecular Ecology 17(22) pp. 4782-4785. [DOI] [Web of Science] [Pubmed]
Dorken M.E., Pannell J.R., 2007. The maintenance of hybrid zones across a disturbance gradient. Heredity 99(1) pp. 89-101. [DOI] [Web of Science] [Pubmed]
Pannell J.R., 2007. Dispersal ecology: where have all the seeds gone? Current Biology 17(10) pp. R360-R362. [DOI] [Web of Science] [Pubmed]
Obbard D.J, Pannell J.R, Harris S.A., 2006. Mercurialis canariensis (Euphorbiaceae), a new endemic to the Canary Islands. Kew Bulletin 61(1) pp. 99-106. [url editor site]
Obbard D.J., Harris S.A., Buggs R.J., Pannell J.R., 2006. Hybridization, polyploidy, and the evolution of sexual systems in Mercurialis (Euphorbiaceae). Evolution 60(9) pp. 1801-1815. [DOI] [Web of Science] [Pubmed]
Obbard D.J., Harris S.A., Pannell J.R., 2006. Sexual systems and population genetic structure in an annual plant: testing the metapopulation model. American Naturalist 167(3) pp. 354-366. [DOI] [Web of Science] [Pubmed]
Obbard D.J., Harris S.A., Pannell J.R., 2006. Simple allelic-phenotype diversity and differentiation statistics for allopolyploids. Heredity 97(4) pp. 296-303. [DOI] [Web of Science] [Pubmed]
Verdú M., González-Martínez S.C., Montilla A.I., Mateu I., Pannell J.R., 2006. Ovule discounting in an outcrossing, cryptically dioecious tree. Evolution 60(10) pp. 2056-2063. [DOI] [Web of Science] [Pubmed]
Pannell J.R., Dorken M.E., Eppley S.M., 2005. 'Haldane's Sieve' in a metapopulation: sifting through plant reproductive polymorphisms. Trends in Ecology and Evolution 20(7) pp. 374-379. [DOI] [Web of Science] [Pubmed]
Pannell J.R, Obbard D.J, Buggs R.J.A., 2004. Polyploidy and the sexual system: what can we learn from Mercurialis annua? Biological Journal of the Linnean Society 82(4) pp. 547-560. [DOI] [Web of Science]
Pannell J.R., Eppley S.M., 2004. Intraorganismal genetic heterogeneity: is it a useful concept? Journal of Evolutionary Biology 17(6) pp. 1180-1; discussion 1192-4. [DOI] [Web of Science] [Pubmed]
Verdú M., Montilla A.I., Pannell J.R., 2004. Paternal effects on functional gender account for cryptic dioecy in a perennial plant. Proceedings of the Royal Society of London B Biological Sciences 271(1552) pp. 2017-2023. [DOI] [Web of Science] [Pubmed]
López-Almansa J.C., Pannell J.R., Gil L., 2003. Female sterility in Ulmus minor (Ulmaceae): a hypothesis invoking the cost of sex in a clonal plant. American Journal of Botany 90(4) pp. 603-609. [DOI] [Web of Science] [Pubmed]
Pannell J.R, Obbard D.J., 2003. Probing the primacy of the patch: what makes a metapopulation? Journal of Ecology 91(3) pp. 485-488. [DOI] [Web of Science]
Pannell J.R., 2002. The evolution and maintenance of androdioecy. Annual Review of Ecology and Systematics 33 pp. 397-425. [DOI] [Web of Science]
Pannell J.R., 2002. What is functional androdioecy? Functional Ecology 16(6) pp. 862-865. [DOI] [Web of Science]
Pannell J.R., Barrett S.C., 2001. Effects of population size and metapopulation dynamics on a mating-system polymorphism. Theoretical Population Biology 59(2) pp. 145-155. [DOI] [Web of Science] [Pubmed]
Pannell J.R., 2000. Evolution in subdivided populations. Trends in Ecology and Evolution 15(3) pp. 90-92. [DOI] [Web of Science]
Pannell J.R., Charlesworth B., 2000. Effects of metapopulation processes on measures of genetic diversity. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 355(1404) pp. 1851-1864. [DOI] [Web of Science] [Pubmed]
Pannell J., 1997. Widespread functional androdioecy in Mercurialis annua L. (Euphorbiaceae). Biological Journal of the Linnean Society 61(1) pp. 95-116. [DOI] [Web of Science]
Pannell J.R, Myerscough P.J., 1993. Canopy-stored seed banks of Allocasuarina distyla and A. nana in relation to time since fire Australian. Australian Journal of Botany 41(1) pp. 1-9. [DOI] [Web of Science]

Group leader

Former Group Members



John Pannell
Office room: 4320.1
Phone: +4121 692 41 70
Fax: +4121 692 42 65

Administrative assistant
Office room: 3106
Phone: +4121 692 4200
Fax: +4121 692 4265

Biophore - CH-1015 Lausanne  - Switzerland  -  Tel. +41 21 692 41 60  -  Fax +41 21 692 41 65
Swiss University