The genetic diversity and reproductive dynamics of sandalwood in Gunung Sewu (Java, Indonesia) in 2012-2019: designing conservation strategies in a continuous versus fragmented landrace
##plugins.themes.bootstrap3.article.main##
Abstract
Abstract. Ratnaningrum YWN, Indrioko S, Karrin A, Kurniawan A, Putri ADC. 2021. The genetic diversity and reproductive dynamics of sandalwood in Gunung Sewu (Java, Indonesia) in 2012-2019: designing conservation strategies in a continuous versus fragmented landrace. Biodiversitas 22: 3219-3229. This research aimed to compare the dynamics of the genetic diversity, mating systems, and reproductive outputs of the most fragmented (Bejiharjo) and continuous (Bleberan) sandalwood landraces in Gunung Sewu in the flowering periods of 2012-2019. Among the different sandalwood landraces found in Gunung Sewu, Bejiharjo has the highest levels of santalol; unfortunately, this landrace also requires the most attention because of heavy habitat fragmentation resulting from overexploitation, urbanization, and cave-tourism activities. Compared with Bejiharjo, Bleberan demonstrated a wider genetic base and greater outcrossing. Mature and flowering individuals in Bejiharjo decreased from 2012 to 2019 as fragmentation increased, particularly in 2019, during which extreme individual reduction due to illegal logging and land conversion was noted. Recent years consisted of more-clonalized stands, as indicated by the finding of fewer distinct genotypes and higher clonality rates. Increases in clonality and narrowing of the genetic base over time increased selfing rates and reduced offspring heterozygosity and seedling recruitment. The dynamics of genetic diversity in Bleberan, which was relatively undisturbed, appeared to be highly affected by fluctuations in the number of parental genetic bases (i.e., flowering parents) in each flowering season. Some parents bore flowers in one flowering season but remained in a vegetative state in the following season. This irregularity of flowering individuals caused fluctuations in actual population size, resulting in a different genetic base, mating system, and reproductive outputs in every season. All six loci (i.e., Dia-1, Dia-2, Est-1, Est-2, Est-3, and Skd-1) examined in Bleberan are polymorphic sites, and no missing alleles were noted in any of the observation years. Est-2 was monomorphic in Bejiharjo, where rare and missing alleles were more apparent, particularly at the seedling level. Genetic differentiation over time was observed between Bejiharjo and Bleberan, and increased fragmentation was noted in Bejiharjo. The migration rate between these two landraces also decreased over time. Focusing on maintaining the reproductive and genetic processes of each population by implementing different strategies based on the genetic base, mating systems, and degree of fragmentation and clonality of the landrace is recommended.
##plugins.themes.bootstrap3.article.details##
Bottin L, Tassin J, Nasi R, Bouvet J. 2007. Molecular, quantitative and abiotic variables for the delineation of evolutionary significant units: case of sandalwood (Santalum austrocaledonicum Vieillard) in New Caledonia. Conserv Genet. 8: 99-109.
Bradbury D, Grayling PM, MacDonald B, Hankinson M, Byrne M. 2015. Clonality, interspecific hybridisation and inbreeding in a rare mallee eucalypt, Eucalyptus absita (Myrtaceae), and implications for conservation. Conserv Genet. September 2015, 17 (1): 193–205
Brand JE. 1994. Genotypic variation in Santalum album. Sandalwood Research Newsletter. Issue 2-1994.
Byrne M, MacDonald B, Broadhurst L, Brand J. 2003. Regional genetic differentiation in Western Australian sandalwood (Santalum spicatum) as revealed by nuclear RFLP analysis. Theor Appl Genet 107: 1208-1214.
da Silva JAT, Kher MM, Soner D, Nataraj M, Dobranszki J, Millar MA. 2017. Santalum molecular biology: molecular markers for genetic diversity, phylogenetics and taxonomy, and genetic transformation. Agroforest Syst DOI 10.1007/s10457-017-0075-8
da Silva JAT, Page T, Zhang X, Kher MM, Nataraj M, Soner D, Ma G. 2016. Sandalwood: basic biology, tissue culture, and genetic transformation. Planta 243: 847-887.
Dani KGS, Ravikumar P, Kumar RP, Kush A. 2011. Genetic variation within and among small isolated populations of Santalum album. Biologia Plantarum 55 (2): 323-326.
Fathin AN, Ratnaningrum YWN. 2018. The differences in floral structure of three sandalwood variants in one of Gunung Sewu (Indonesia) population, and their consequences on visitor diversity and visitation rate. Biodiversitas 19(3): 1097-1101.
Frankham R, Ballou JD, Briscoe DA. 2002. Introduction to Forest Genetics. Cambridge University Press. Cambridge, UK.
Garfì G, Mercati F, Fontana I, Collesano G, Pasta S, Vendramin GG, Michele R, Carimi F. 2013. Habitat features and genetic integrity of wild grapevine Vitis vinifera L. subsp. sylvestris (C.C. Gmel.) Hegi populations: A case study from Sicily. Flora 208: 538–548.
Harbaugh DT, Baldwin BG. 2007. Phylogeny and biogeography of the Sandalwoods (Santalum, Santalaceae): repeated dispersals throughout Pacific. Am J Bot 94(6): 1028–1040.
Haryjanto L, Widowati TB, Sumardi. 2017. Variation of chemical compounds of sandalwood oil from various provenances in Indonesia. FORDA Journal 11(1): 2017. DOI: 10.20886/jpth.2017.11.1.77-86.
Hmeljevski KV, Freitas L, Domingues R, Pereira AR, Cancio AS, Andrade AC, Machado MA, Viccini LF, Forzza RC. 2014. Conservation assessment of an extremely restricted bromeliad highlights the need for population-based conservation on granitic inselbergs of the Brazilian Atlantic Forest. Flora 209: 250–259.
Indrioko S, Ratnaningrum YWN. 2015. Habitat loss caused clonality, genetic diversity reduction and reproductive failure in Santalum album, an endangered endemic species of Indonesia. Proc Env Sci V: 613-620.
IUCN. 1994. IUCN Red List Categories And Criteria: Version 1.2. IUCN Species Survival Commission. International Union for Conservation of Nature and Natural Resources. Glad, Switzerland, and Cambridge, UK.
IUCN. 2009. IUCN Red List Categories And Criteria: Version 3.1. IUCN Species Survival Commission. International Union for Conservation of Nature and Natural Resources. Glad, Switzerland, and Cambridge, UK.
Jones CE and Little RJ. 1983. Handbook of experimental pollination biology. Van Nostrand Reinhold Co. Inc. New York.
Klank C, Ghazoul J, Pluess AR. 2012. Genetic variation and plant performance in fragmented populations of globeflowers (Trollius europaeus) within agricultural landscapes. Conserv Genet 2012, 13 (2) :873–884
Lhuillier E, Butaud JF, Bouvet JM. 2006. Extensive clonality and strong differentiation in the Insular Pacific tree Santalum insulare: implications for its conservation. Ann Bot 98: 1061-1072.
Moreira PA, Brandao MM, Araujo NH, Oliveira DA, Fernandes GW. 2015. Genetic diversity and structure of the tree Enterolobium contortisiliquum (Fabaceae) associated with remnants of a seasonally dry tropical forest. Flora 210: 40–46.
Pautasso M. 2009. Geographical genetics and the conservation of forest trees. Persp in Plant Ecol, Evol and Syst 11: 157-189.
Rao MN, Ganeshaiah KN, Shaanker RU. 2007. Assessing threats and mapping sandal resources to identify genetic ‘hot-spot’ for in-situ conservation in peninsular India. Conserv Genet 8: 925-935.
Ratnaningrum YWN, Kurniawan A. 2019. Floral structure and genetical differences of sandalwood variants in Gunung Sewu (Java, Indonesia), and its effects on breeding systems and reproductive ability. Biodiversitas 20 (2): 393-404
Ratnaningrum YWN, Indrioko S, Faridah E, Syahbudin A. 2018. Population structures and seasons affected flowering, pollination and reproductive outputs of sandalwood in Gunung Sewu, Java, Indonesia. Nusantara Bioscience 10 (1): 2087-3948
Ratnaningrum YWN, Indrioko S, Faridah E, Syahbudin A. 2017. Gene flow and selection evidence of sandalwood under various population structures in Gunung Sewu (Java, Indonesia), and its effect on genetic differentiation. Biodiversitas 18 (4): 1493-1505.
Ratnaningrum YWN, Indrioko S, Faridah E, Syahbudin A. 2015. The effects of population size on genetic parameters and mating system of sandalwood in Gunung Sewu, Indonesia. Indo J Biotech 20(2): 182-201.
Sampson JF, Byrne M, Gibson N, Yates C. 2016. Limiting inbreeding in disjunct and isolated populations of a woody shrub. Ecol and Evol 6(16): 5867–5880.
Sandeep KA, Rodrigues V, Viswanath S, Shukla AK, Sundaresan V. 2019. Morpho?genetic divergence and population structure in Indian Santalum album L. Trees. https://doi.org/10.1007/s00468-020-01963-2
Seido K. 1993. Manual of isozyme analysis. Japan International Cooperation Agency (JICA) and Dirjen RLPS, Departemen Kehutanan Republik Indonesia.
Sindhu-Veerendra HCS, Anantha-Padmanabha HSA. 1996. The breeding system in Sandal (Santalum album L.). Silvae Genetica 45 (4): 188-190.
Suma TB, Balasundaran M. 2003. Isozyme variation in five provenances of Santalum album in India. Aust J Bot 51(3): 243 – 249.
Tamla HT, Cornelius JP, Page T. 2012. Reproductive biology of three commercially valuable Santalum species: development of flowers and inflorescences, breeding systems, and interspecific crossability. Euphytica 184: 323-333.
Torres E, Iriondo JM, and Perez C. 2003. Genetic structure of an endangered plant, Antirrhinum microphyllum (Scrophulariaceae): allozyme and RAPD analysis. Am J Bot 90(1): 85–92.
Warburton CL, James EA, Fripp YJ, Trueman SJ, Wallace HM. 2000. Clonality and sexual reproductive failure in remnant populations of Santalum lanceolatum (Santalaceae). Biol Conserv 96(1).
Young A, Boshier D, Boyle T. 2000. Forest Conservation Genetics: principles and practices. CSIRO Publishing, Collingwood, Australia.
Most read articles by the same author(s)
- YENI W.N. RATNANINGRUM, SAPTO INDRIOKO, ENY FARIDAH, ATUS SYAHBUDIN, Gene flow and selection evidence of sandalwood (Santalum album) under various population structures in Gunung Sewu (Java, Indonesia), and its effects on genetic differentiation , Biodiversitas Journal of Biological Diversity: Vol. 18 No. 4 (2017)
- NESTY PRATIWI ROMADINI, SAPTO INDRIOKO, WIDIYATNO, ENY FARIDAH, YENI W.N. RATNANINGRUM, Genetic diversity in seedling populations of Dipterocarpus gracilis in Kecubung Ulolanang Nature Conservation Reserve, Indonesia , Biodiversitas Journal of Biological Diversity: Vol. 22 No. 3 (2021)
- GUNAWAN NUGRAHANTO, MOHAMMAD NA’IEM, SAPTO INDRIOKO, ENY FARIDAH, WIDIYATNO, ERLANGGA ABDILLAH, Genetic parameters for resin production of Pinus merkusii progeny test collected from three landraces in Banyumas Barat Forest District, Indonesia , Biodiversitas Journal of Biological Diversity: Vol. 23 No. 4 (2022)
- SITI MAIMUNAH, PAUL J.A. KESSLER, SAPTO INDRIOKO, MUHAMMAD NAIEM, Natural distribution of the genus Dacrydium Lamb. (Podocarpaceae) in Central Kalimantan, Indonesia , Biodiversitas Journal of Biological Diversity: Vol. 23 No. 6 (2022)
- NESTY PRATIWI ROMADINI, SAPTO INDRIOKO, WIDIYATNO, ENY FARIDAH, Regeneration failure and seedling growth of Dipterocarpus gracilis, a vulnerable dipterocarp in a tropical monsoon forest in Central Java, Indonesia , Biodiversitas Journal of Biological Diversity: Vol. 23 No. 9 (2022)