Isozyme diversity in large and isolated populations of Luma apiculata (Myrtaceae) in north-western Patagonia, Argentina
Mayra S. Caldiz A B and Andrea C. Premoli A CA Laboratorio Ecotono, Centro Regional Universitario Bariloche, Universidad Nacional del Comahue, Quintral 1250, 8400 Bariloche, Argentina.
B Present address: Southern Swedish Forest Research Centre, PO Box 49, S 230 53-Alnarp, Sweden.
C Corresponding author. Email: apremoli@crub.uncoma.edu.ar
Australian Journal of Botany 53(8) 781-787 https://doi.org/10.1071/BT05037
Submitted: 23 February 2003 Accepted: 1 August 2005 Published: 14 December 2005
Abstract
We evaluated the amount and distribution of genetic variation in large and small isolated populations of Luma apiculata (DC.) Burret (Myrtaceae) in north-western Patagonia. The hypothesis tested was that isolated smaller populations were more affected by drift and isolation than large stands. Higher genetic diversity was predicted in the latter. Fresh leaf material for isozyme electrophoresis was collected from 30 individuals in four isolated and two large and continuous stands (Quetrihue Peninsula and Punta Norte, Isla Victoria). Five subpopulations were sampled in both large stands, and in addition, three regeneration gaps in Punta Norte. Eleven loci were resolved; 91% were polymorphic in at least one population. Isolated and large populations had similar levels of genetic variation. Reduced observed heterozygosity and elevated inbreeding were measured in subpopulations and regeneration gaps within dense stands. Although small populations consist of a reduced number of individuals they are mostly coastal populations nearby rivers and lakes that may maintain considerable gene flow with other faraway populations counteracting the effects of drift. In addition to potential selfing, increased inbreeding within large populations and regeneration gaps may be due to an intra-population Wahlund effect from local seedling establishment and vegetative spread, resulting in clustered cohorts of similar genotypes.
Acknowledgments
We thank Delegación Técnica Regional Patagonia, National Park Service, especially A. Pérez, M. Mermoz and C. Chehébar for advice on location of L. apiculata natural populations and authorisation to work in protected areas. We are also grateful to park rangers D. Núñez and D. Mujica for field assistance. This research was supported by the European Commission funded project SUCRE, IC18-CT97-0146 and by Universidad Nacional del Comahue Project 04-B081. ACP is a member of CONICET (Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina).
Amico GC, Aizen MA
(2005
) Dispersión de semillas por aves en un bosque templado de Sudamérica austral: ¿quién dispersa a quién? Ecología Austral 15, 89–100.
Barrett SCH, Kohn JR
(1991) Genetic and evolutionary consequences of small population size in plants: implications for conservation. In ‘Genetics and conservation of rare plants’. (Eds DA Falk, KE Holsinger)
pp. 3–30. (Oxford University Press: New York)
Brion, C ,
Puntieri, J ,
Grigera, D ,
and
Calvelo, S (1988).
Bush MM, Smouse PE
(1992
) Evidence for the adaptive significance of allozymes in forest trees. New Forests 6, 179–196.
| Crossref | GoogleScholarGoogle Scholar |
Caldiz MS
(1999) Estructura genética del arrayán, Luma apiculata (DC.) Burret (Myrtaceae), una especie endémica del noroeste patagónico: su relación con el sistema reproductivo y modo de regeneración. Licenciatura in Biology Thesis.
(Centro Regional Universitario Bariloche, Universidad Nacional del Comahue:
Bariloche, Argentina)
Correa, MN (1998).
Ennos RA, Clegg MT
(1982) Effect of population substructuring on estimates of outcrossing rate in plant populations. Heredity 48, 283–292.
Epperson, BK (1989). Spatial patterns of genetic variation within plant populations. In ‘Plant population genetics, breeding and genetic resources’. pp. 229–253. (Sinauer Associates: Sunderland, MA)
Figueroa JA, Castro SA
(2002) Effects of bird ingestion on seed germination of four woody species of the temperate rainforest of Chiloé Island, Chile. Plant Ecology 160, 17–23.
| Crossref | GoogleScholarGoogle Scholar |
Goudet J
(1995) FSTAT version 1.2: a computer program to calculate F-statistics. Journal of Heredity 86, 485–486.
Hamrick JL, Godt MJ
(1989) Allozyme diversity in plant species. In ‘Plant population genetics, breeding and genetic resources’. (Eds AHD Brown, MT Clegg, AL Kahler, BS Weir)
pp. 43–63. (Sinauer Associates: Sunderland, MA)
Hamrick JL,
Godt MJ, Sherman-Broyles S
(1992) Factors influencing levels of genetic diversity in woody plant species. New Forests 6, 95–124.
| Crossref | GoogleScholarGoogle Scholar |
Huenneke LF
(1985) Spatial distribution of genetic individuals of thickets of Alnus icana ssp. rugosa, a clonal shrub. American Journal of Botany 72, 152–158.
King NJ, Dancik BP
(1983) Inheritance and linkage of isozymes in white spruce (Picea glauca). Canadian Journal of Genetics and Cytology 25, 430–436.
Landrum LR
(1988) The myrtle family (Myrtaceae) in Chile. Proceedings of the California Academy of Sciences 45, 277–317.
Legendre P, Fortin MJ
(1989) Spatial pattern and ecological analysis. Vegetatio 80, 107–138.
| Crossref | GoogleScholarGoogle Scholar |
Linhart YB, Grant MC
(1996) Evolutionary significance of local genetic differentiation in plants. Annual Review of Ecology and Systematics 27, 237–277.
| Crossref | GoogleScholarGoogle Scholar |
Linhart YB,
Mitton JB,
Sturgeon KB, Davis ML
(1981) Genetic variation in space and time in population of ponderosa pine. Heredity 46, 407–426.
McDonald MW,
Rawlings M,
Butcher PA, Bell JC
(2003) Regional divergence and inbreeding in Eucalyptus cladocalyx (Myrtaceae). Australian Journal of Botany 51, 393–403.
| Crossref | GoogleScholarGoogle Scholar |
Mitton JB
(1989) Physiological and demographic variation associated with allozyme variation. In ‘Isozymes in plant biology’. (Eds D Soltis, P Soltis)
pp. 127–145. (Dioscorides Press: Portland, OR)
Mitton JB,
Linhart YB,
Sturgeon KB, Hamrick JL
(1979) Allozyme polymorphisms detected in mature needle tissue of ponderosa pine. Journal of Heredity 70, 86–89.
Moran GF
(1992) Patterns of genetic diversity in Australian tree species. New Forests 6, 49–66.
| Crossref | GoogleScholarGoogle Scholar |
Moran GF, Bell C
(1993) Eucalyptus. In ‘Isozymes in plant genetics and breeding’. (Eds SD Tanksley, TJ Orton)
pp. 423–441. (Elsevier: Amsterdam)
Nei M
(1978) Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics 89, 583–590.
Oden NL
(1984) Assessing the significance of a spatial correlogram. Geographical Analysis 16, 1–16.
Perry DJ, Knowles P
(1991) Spatial genetic structure within three sugar maple (Acer saccharum Marsh.) stands. Heredity 66, 137–142.
Premoli AC, Kitzberger T
(2005) Regeneration mode affects spatial genetic structure of Nothofagus dombeyi forests. Molecular Ecology 14, 2319–2329.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Premoli AC,
Kitzberger T,
Caldiz M,
Souto C,
Arana S,
García F, Palópoli C
(2000) Cultivemos nuestras plantas nativas: técnicas de germinación. Patagonia Silvestre 7, 3–7.
Ranker TA,
Haufler CH,
Soltis PS, Soltis DE
(1989) Genetic evidence for allopolyploidy in the neotropical fern Hemionitis (Adiantaceae) and the reconstruction of an ancestral genome. Systematic Botany 14, 439–447.
Rivero MC
(1991) Biología reproductiva en especies vegetales de dos comunidades de la zona templada del sur de Chile, 40°S. Doctoral Thesis.
(Universidad de Chile:
Santiago, Chile)
Schanbel A,
Laushman RH, Hamrick JL
(1991) Comparative genetic structure of two co-occurring tree species, Maclura pomifera (Moreceae) and Gleditsia triacanthos (Leguminoseae). Heredity 67, 357–364.
Shapcott A
(1995) The spatial genetic structure in natural populations of the Australian temperate rainforest tree Atherosperma moschatum Labill. (Monimiaceae). Heredity 74, 28–38.
Shea KL, Furnier GR
(2002) Genetic variation and population structure in central and isolated populations of balsam fir Abies balsamea (Pinaceae). American Journal of Botany 89, 783–791.
| Crossref |
Smith-Ramirez C, Armesto JJ
(1994) Flowering and fruiting patterns in the temperate rainforest of Chiloé, Chile—ecologies and climatic constraints. Journal of Ecology 82, 353–365.
Smith-Ramirez C,
Armesto JJ, Figueroa J
(1998) Flowering, fruiting and seed germination in Chilean rain forest Myrtaceae: ecological and phylogenetic constraints. Plant Ecology 136, 119–131.
| Crossref | GoogleScholarGoogle Scholar |
Smith-Ramirez C,
Martinez P,
Nuñez M,
González C, Armesto JJ
(2005) Diversity, flower visitation frequency and generalism of pollinators in temperate rain forests of Chiloé Island, Chile. Botanical Journal of the Linnean Society 147, 399–416.
| Crossref | GoogleScholarGoogle Scholar |
Sokal RR, Oden NL
(1978) Spatial autocorrelation in biology. 1. Methodology. Biological Journal of the Linnean Society 10, 199–228.
Soltis, DE ,
and
Soltis, PS (1989).
Souto CP,
Aizen MA, Premoli AC
(2002) Effects of crossing distance and genetic relatedness on pollen performance in Alstroemeria aurea (Alstroemeriaceae). American Journal of Botany 89, 427–432.
| Crossref |
Turner ME,
Stephens JC, Anderson WW
(1982) Homozygosity and patch structure in plant populations as a result of nearest-neighbor pollination. Proceedings of the National Academy of Sciences, USA 79, 203–207.
Weinberger P
(1978) Estudios sobre adaptación climática y las asociaciones de mirtáceas Arauco-Patagonicas. Anales de Parques Nacionales 14, 133–160.
Wright S
(1951) The genetic structure of populations. Annals of Eugenics 5, 323–354.