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Địa sinh vật học của hai loài tảo sống trong thủy triều, Gelidium lingulatum và G. rex (Rhodophyta: Gelidiales), dọc theo Tây Nam Thái Bình Dương: các mô hình được giải thích bởi sự phân tán bằng cách trôi nổi?
Tóm tắt
Sự trôi nổi trên các loài tảo biển giúp phân bố các sinh vật liên quan, nhưng vẫn còn ít thông tin về cách thức trôi nổi ảnh hưởng đến cấu trúc di truyền của các loài tảo bám. Các nghiên cứu trước đây cho thấy sự hiện diện cao của tảo thuộc chi Gelidium gắn với tảo bull kelp Durvillaea antarctica (Chamisso) Hariot. Trong nghiên cứu này, chúng tôi đã phân tích các mẫu hình địa sinh vật học của Gelidium lingulatum (Kützing 1868) và G. rex (Santelices và Abbott 1985), các loài có phân bố một phần dọc theo bờ biển Chile (28°S–42°S). Tổng cộng có 319 cá thể từ G. lingulatum và 179 từ G. rex (tương ứng 20 và 11 địa điểm đáy biển) đã được phân tích bằng dấu hiệu ti thể (COI) và, đối với một tập hợp con, bằng dấu hiệu lục lạp (rbcL). Gelidium lingulatum cho thấy sự đa dạng di truyền cao hơn, nhưng cấu trúc di truyền của nó không theo một mô hình địa lý rõ ràng, trong khi G. rex có sự đa dạng di truyền thấp hơn với một cấu trúc di truyền nông và một ranh giới địa sinh học trùng với sự gián đoạn địa sinh vật học được mô tả cho khu vực này (29°S–33°S). Đối với G. lingulatum, không có sự cô lập theo khoảng cách được quan sát, trái ngược với G. rex. Mô hình địa sinh vật học của G. lingulatum có thể được giải thích chính bằng sự phân tán bằng cách trôi nổi như là một loài ký sinh của D. antarctica, mặc dù các cơ chế khác không thể bị loại trừ hoàn toàn (ví dụ: sự phân tán do tác động của con người). Mô hình tương phản quan sát thấy ở G. rex có thể được quy cho các yếu tố khác như phân bố thủy triều (tức là G. rex xuất hiện ở khu vực thấp hơn so với G. lingulatum) hoặc hiệu quả khác nhau của việc tuyển sinh sau khi phân tán xa. Nghiên cứu này cho thấy rằng sự phân tán bằng cách trôi nổi, kết hợp với phân bố thủy triều, có thể điều chỉnh các mẫu hình địa sinh vật học của các loài tảo.
Từ khóa
#trôi nổi #tảo biển #Gelidium #cấu trúc di truyền #phân bố thủy triều #phân tánTài liệu tham khảo
Alberto F, Santos R, Leitão JM (1999) Assessing patterns of geographic dispersal of Gelidium sesquipedale (Rhodophyta) through RAPD differentiation of populations. Mar Ecol Prog Ser 191:101–108. doi:10.3354/Meps191101
Alberto F, Raimondi PT, Reed DC, Coelho NC, Leblois R, Whitmer A, Serrão EA (2010) Habitat continuity and geographic distance predict population genetic differentiation in giant kelp. Ecology 91:49–56. doi:10.1890/09-0050.1
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215:403–410. doi:10.1016/S0022-2836(05)80360-2
Aravena G, Broitman B, Stenseth NC (2014) Twelve years of change in coastal upwelling along the central-northern coast of Chile: spatially heterogeneous responses to climatic variability. PLoS One 9:e90276. doi:10.1371/journal.pone.0090276
Astudillo JC, Bravo M, Dumont CP, Thiel M (2009) Detached aquaculture buoys in the SE Pacific: potential dispersal vehicles for associated organisms. Aquat Biol 5:219–231. doi:10.3354/ab00151
Ballard JW, Whitlock MC (2004) The incomplete natural history of mitochondria. Mol Ecol 13:729–744. doi:10.1046/j.1365-294X.2003.02063.x
Bandelt HJ, Forster P, Rohl A (1999) Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol 16:37–48
Banks NC, Paini DR, Bayliss KL, Hodda M (2015) The role of global trade and transport network topology in the human-mediated dispersal of alien species. Ecol Lett 18:188–199. doi:10.1111/ele.12397
Billard E, Daguin C, Pearson G, Serrão E, Engel C, Valero M (2005) Genetic isolation between three closely related taxa: Fucus vesiculosus, F. spiralis, and F. ceranoides (Phaeophyceae). J Phycol 41:900–905. doi:10.1111/j.0022-3646.2005.04221.x
Bobadilla M, Santelices B (2005) Variations in the dispersal curves of macroalgal propagules from a source. J Exp Mar Biol Ecol 327:47–57. doi:10.1016/j.jembe.2005.06.006
Boo GH, Park JK, Boo SM (2013) Gelidiophycus (Rhodophyta: Gelidiales): a new genus of marine algae from East Asia. Taxon 62:1105–1116. doi:10.12705/626.7
Boo GH, Mansilla A, Nelson W, Bellgrove A, Boo SM (2014a) Genetic connectivity between trans-oceanic populations of Capreolia implexa (Gelidiales, Rhodophyta) in cool temperate waters of Australasia and Chile. Aquat Bot 119:73–79. doi:10.1016/j.aquabot.2014.08.004
Boo GH, Kim KM, Nelson WA, Riosmena-Rodríguez R, Yoon KJ, Boo SM (2014b) Taxonomy and distribution of selected species of the agarophyte genus Gelidium (Gelidiales, Rhodophyta). J Appl Phycol 26:1243–1251. doi:10.1007/s10811-013-0111-7
Boo GH, Le Gall L, Miller KA, Freshwater DW, Wernberg T, Terada R, Yoon KJ, Boo SM (2016) A novel phylogeny of the Gelidiales (Rhodophyta) based on five genes including the nuclear CesA, with descriptions of Orthogonacladia gen. nov and Orthogonacladiaceae fam. nov. Mol Phylogenet Evol 101:359–372. doi:10.1016/j.ympev.2016.05.018
Bouza N, Caujape-Castells J, González-Pérez MA, Sosa PA (2006) Genetic structure of natural populations in the red algae Gelidium canariense (Gelidiales, Rhodophyta) investigated by random amplified polymorphic DNA (RAPD) markers. J Phycol 42:304–311. doi:10.1111/j.1529-8817.2006.00201.x
Broitman BR, Navarrete SA, Smith F, Gaines SD (2001) Geographic variation of southeastern Pacific intertidal communities. Mar Ecol Prog Ser 224:21–34. doi:10.3354/Meps224021
Camus PA (2001) Biogeografía marina de Chile continental. Rev Chil Hist Nat 74:587–617
Castilla JC, Manríquez PH, Camaño A (2010) Effects of rocky shore coseismic uplift and the 2010 Chilean mega-earthquake on intertidal biomarker species. Mar Ecol Prog Ser 418:17–23. doi:10.3354/meps08830
Coyer JA, Hoarau G, Costa JF, Hogerdijk B, Serrão EA, Billard E, Valero M, Pearson GA, Olsen JL (2011a) Evolution and diversification within the intertidal brown macroalgae Fucus spiralis/F. vesiculosus species complex in the North Atlantic. Mol Phylogenet Evol 58:283–296. doi:10.1016/j.ympev.2010.11.015
Coyer JA, Hoarau G, Van Schaik J, Luijckx P, Olsen JL (2011b) Trans-Pacific and trans-Arctic pathways of the intertidal macroalga Fucus distichus L. reveal multiple glacial refugia and colonizations from the North Pacific to the North Atlantic. J Biogeogr 38:756–771. doi:10.1111/j.1365-2699.2010.02437.x
Cumming RA, Nikula R, Spencer HG, Waters JM (2014) Transoceanic genetic similarities of kelp-associated sea slug populations: long-distance dispersal via rafting? J Biogeogr 41:2357–2370. doi:10.1111/jbi.12376
Dawson MN, Hays CG, Grosberg RK, Raimondi PT (2014) Dispersal potential and population genetic structure in the marine intertidal of the eastern North Pacific. Ecol Monogr 84:435–456. doi:10.1890/13-0871.1
Destombe C, Godin J, Lefebvre C, Dehorter O, Vernet P (1992) Differences in dispersal abilities of haploid and diploid spores of Gracilaria verrucosa (Gracilariales, Rhodophyta). Bot Mar 35:93–98. doi:10.1515/botm.1992.35.2.93
Dixon PS, Irvine LM (1977) Seaweeds of the British Isles. Volume 1. Rhodophyta. Part 1. Introduction, Nemaliales, Gigartinales. The Natural History Museum, London, p 252
Dupanloup I, Schneider S, Excoffier L (2002) A simulated annealing approach to define the genetic structure of populations. Mol Ecol 11:2571–2581. doi:10.1046/j.1365-294X.2002.01650.x
Engel CR, Destombe C, Valero M (2004) Mating system and gene flow in the red seaweed Gracilaria gracilis: effect of haploid-diploid life history and intertidal rocky shore landscape on fine-scale genetic structure. Heredity 92:289–298. doi:10.1038/sj.hdy.6800407
Engel CR, Billard E, Voisin M, Viard F (2008) Conservation and polymorphism of mitochondrial intergenic sequences in brown algae (Phaeophyceae). Eur J Phycol 43:195–205. doi:10.1080/09670260701823437
Ewers-Saucedo C, Pringle JM, Sepúlveda HH, Byers JE, Navarrete SA, Wares JP (2016) The oceanic concordance of phylogeography and biogeography: a case study in Notochthamalus. Ecol Evol 6:4403–4420. doi:10.1002/ece3.2205
Excoffier L (2004) Patterns of DNA sequence diversity and genetic structure after a range expansion: lessons from the infinite-island model. Mol Ecol 13:853–864. doi:10.1046/j.1365-294X.2003.02004.x
Excoffier L, Lischer HEL (2010) Arlequin (version 3.5): arlequin suite ver 3.5: A new series of programs to perform population genetics analyses under Linux and Windows. Mol Ecol Resour 10:564–567. doi:10.1111/j.1755-0998.2010.02847.x
Försterra G (2009) Ecological and biogeographical aspects of the Chilean Fjord region. In: Häussermann V, Försterra G (eds) Marine benthic fauna of chilean patagonia. Nature in Focus, Puerto Montt, pp 61–76
Fraser CI, Nikula R, Spencer HG, Waters JM (2009a) Kelp genes reveal effects of subantarctic sea ice during the Last Glacial Maximum. Proc Natl Acad Sci USA 106:3249–3253. doi:10.1073/pnas.0810635106
Fraser CI, Hay CH, Spencer HG, Waters JM (2009b) Genetic and morphological analyses of the southern bull kelp Durvillaea antarctica (Phaeophyceae: Durvillaeales) in New Zealand reveal cryptic species. J Phycol 45:436–443. doi:10.1111/j.1529-8817.2009.00658.x
Fraser CI, Thiel M, Spencer HG, Waters JM (2010) Contemporary habitat discontinuity and historic glacial ice drive genetic divergence in Chilean kelp. BMC Evol Biol 10:203. doi:10.1186/1471-2148-10-203
Freshwater DW, Rueness J (1994) Phylogenetic relationships of some European Gelidium (Gelidiales, Rhodophyta) species, based on rbcL nucleotide sequence analysis. Phycologia 33:187–194. doi:10.2216/i0031-8884-33-3-187.1
Fu YX (1997) Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics 147:915–925
Gavio B, Fredericq S (2002) Grateloupia turuturu (Halymeniaceae, Rhodophyta) is the correct name of the non-native species in the Atlantic known as Grateloupia doryphora. Eur J Phycol 37:349–359. doi:10.1017/s0967026202003839
Gómez IM, Westermeier RC (1991) Frond regrowth from basal disc in Iridaea laminarioides (Rhodophyta, Gigartinales) at Mehuín, southern Chile. Mar Ecol Prog Ser 73:83–91. doi:10.3354/meps073083
González S, Stotz W, Toledo P, Jorquera M, Romero M (1991) Utilización de diferentes microambientes del intermareal como lugares de asentamiento por Fissurella spp (Gastropoda: Prosobranchia) (Palo Colorado, Los Vilos, Chile). Rev Biol Mar Oceanogr 26: 325–338. http://www.revbiolmar.cl/escaneados/262-325.pdf. Accessed 29 Aug 2016
González A, Beltrán J, Hiriart-Bertrand L, Flores V, de Reviers B, Correa JA, Santelices B (2012) Identification of cryptic species in the Lessonia nigrescens complex (Phaeophyceae, Laminariales). J Phycol 48:1153–1165. doi:10.1111/j.1529-8817.2012.01200.x
Grant SW (2016) Paradigm shifts in the phylogeographic analysis of seaweeds. In: Hu ZM, Fraser CI (eds) Seaweed phylogeography. Springer, Dordrecht, pp 23–62. doi:10.1007/978-94-017-7534-2_2
Guillemin ML, Valero M, Faugeron S, Nelson W, Destombe C (2014) Tracing the trans-pacific evolutionary history of a domesticated seaweed (Gracilaria chilensis) with archaeological and genetic data. PLoS One 9:e114039. doi:10.1371/journal.pone.0114039
Guillemin ML, Valero M, Tellier F, Macaya EC, Destombe C, Faugeron S (2016a) Phylogeography of seaweeds in the South East Pacific: complex evolutionary processes along a latitudinal gradient In: Hu ZM, Fraser CI (eds) Seaweed Phylogeography. Springer, Dordrecht, pp 251–278. doi:10.1007/978-94-017-7534-2_10
Guillemin ML, Contreras-Porcia L, Ramírez ME, Macaya EC, Bulboa-Contador C, Woods H, Wyatt C, Brodie J (2016b) The bladed Bangiales (Rhodophyta) of the South Eastern Pacific: molecular species delimitation reveals extensive diversity. Mol Phylogenet Evol 94:814–826. doi:10.1016/j.ympev.2015.09.027
Guo B, Wares JP (2017) Large-scale gene flow in the barnacle Jehlius cirratus and contrasts with other broadly-distributed taxa along the Chilean coast. PeerJ 5:e2971. doi:10.7717/peerj.2971
Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acids Symp Ser 41:95–98
Haye PA, Varela AI, Thiel M (2012) Genetic signatures of rafting dispersal in algal-dwelling brooders Limnoria spp. (Isopoda) along the SE Pacific (Chile). Mar Ecol Prog Ser 455:111–122. doi:10.3354/meps09673
Haye PA, Segovia NI, Muñoz-Herrera NC, Gálvez FE, Martínez A, Meynard A, Pardo-Gandarillas MC, Poulin E, Faugeron S (2014) Phylogeographic structure in benthic marine invertebrates of the southeast Pacific coast of Chile with differing dispersal potential. PLoS One 9:e88613. doi:10.1371/journal.pone.0088613
Hernández CJ (1997) Análisis de la variación estacional e interanual de la cosecha de Gelidium robustum en Baja California Sur, México. Master thesis, Centro Interdisciplinario de Ciencias Marinas, La Paz, Baja California Sur, México
Hinojosa IA, Pizarro M, Ramos M, Thiel M (2010) Spatial and temporal distribution of floating kelp in the channels and fjords of southern Chile. Estuar Coast Shelf Sci 87:367–377. doi:10.1016/j.ecss.2009.12.010
Hinojosa IA, Rivadeneira MM, Thiel M (2011) Temporal and spatial distribution of floating objects in coastal waters of central-southern Chile and Patagonian fjords. Cont Shelf Res 31:172–186. doi:10.1016/j.csr.2010.04.013
Hoffmann A, Santelices B (1997) Flora marina de Chile Central. Ediciones Universidad Católica de Chile, Santiago de Chile
Hu ZM, De-Lin D, López-Baptista J (2016) Seaweed phylogeography from 1994 to 2014: an overview. In: Hu ZM, Fraser CI (eds) Seaweed Phylogeography. Springer, Dordrecht, pp 3–22. doi:10.1007/978-94-017-7534-2_1
Jaramillo E, Dugan JE, Hubbard DM, Melnick D, Manzano M, Duarte C, Campos C, Sánchez R (2012) Ecological implications of extreme events: footprints of the 2010 earthquake along the Chilean coast. PLoS One 7:8. doi:10.1371/journal.pone.0035348
John D, Paterson G, Evans N, Ramírez M, Spencer J, Báez P, Ferrero T, Valentine C, Reid D (2003) Manual de biotopos marinos de la región de Aysén, Sur de Chile (A manual of marine biotopes of Region Aysén, Southern Chile. The Laguna San Raphael National Park, Estero Elefantes, Chonos Archipelago and Katalalixar). The Natural History Museum, London
Kelly RP, Palumbi SR (2010) Genetic structure among 50 species of the Northeastern Pacific rocky intertidal community. PLoS One 5:13. doi:10.1371/journal.pone.0008594
Kiessling T, Gutow L, Thiel M (2015) Marine litter as habitat and dispersal vector. In: Bergmann M, Gutow L, Klages K (eds) Marine anthropogenic litter, Springer, Berlin, pp 141–184. doi:10.1007/978-3-319-16510-3_6
Kim KM, Boo SM (2012) Phylogenetic relationships and distribution of Gelidium crinale and G. pusillum (Gelidiales, Rhodophyta) using cox1 and rbcL sequences. Algae 27:83–94. doi:10.4490/algae.2012.27.2.083
Kim KM, Hwang IK, Park JK, Boo SM (2011) A new agarophyte species, Gelidium eucorneum sp. nov. (Gelidiales, Rhodophyta), based on molecular and morphological data. J Phycol 47:904–910. doi:10.1111/j.1529-8817.2011.01005.x
Kim KM, Hoarau GG, Boo SM (2012) Genetic structure and distribution of Gelidium elegans (Gelidiales, Rhodophyta) in Korea based on mitochondrial cox1 sequence data. Aquat Bot 98:27–33. doi:10.1016/j.aquabot.2011.12.005
Krueger-Hadfield SA, Hoban SM (2016) The importance of effective sampling for exploring the population dynamics of haploid–diploid seaweeds. J Phycol 52:1–9. doi:10.1111/jpy.12366
Krueger-Hadfield SA, Roze D, Mauger S, Valero M (2013) Intergametophytic selfing and microgeographic genetic structure shape populations of the intertidal red seaweed Chondrus crispus. Mol Ecol 22:3242–3260. doi:10.1111/mec.12191
Kützing FT (1868) Tabulae phycologicae; oder, Abbildungen der Tange. Vol. XVIII pp. [i–iii], 1–35, 100 pls. Nordhausen: Gedruckt auf kosten des Verfassers (in commission bei W. Köhne)
Lachkar Z, Gruber N (2012) A comparative study of biological production in eastern boundary upwelling systems using an artificial neural network. Biogeosciences 9:293–308. doi:10.5194/bg-9-293-2012
Lin SM, Fredericq S, Hommersand MH (2001) Systematics of the Delesserlaceae (Ceramiales, Rhodophyta) based on large subunit rDNA and rbcL sequences, including the Phycodryoideae, subfam. nov. J Phycol 37:881–899. doi:10.1046/j.1529-8817.2001.01012.x
Lindstrom SC, Gabrielson PW, Hughey JR, Macaya EC, Nelson WA (2015) Sequencing of historic and modern specimens reveals cryptic diversity in Nothogenia (Scinaiaceae, Rhodophyta). Phycologia 54:97–108. doi:10.2216/14-077.1
López B, Macaya EC, Tellier F, Tala F, Thiel M (2017) The variable routes of rafting: stranding dynamics of floating bull-kelp Durvillaea antarctica (Fucales, Phaeophyceae) on beaches in the SE Pacific. J Phycol 54:70–84. doi:10.1111/jpy.12479
Macaya EC, Zuccarello GC (2010a) Genetic structure of the giant kelp Macrocystis pyrifera along the southeastern Pacific. Mar Ecol Prog Ser 420:103–112. doi:10.3354/meps08893
Macaya EC, Zuccarello GC (2010b) DNA barcoding and genetic divergence in the giant kelp Macrocystis (Laminariales). J Phycol 46:736–742. doi:10.1111/j.1529-8817.2010.00845.x
Macaya EC, López B, Tala F, Tellier F, Thiel M (2016) Float and raft: role of buoyant seaweeds in the phylogeography and genetic structure of non-buoyant associated flora. In: Hu ZM, Fraser CI (eds) Seaweed phylogeography, Springer, Dordrecht, pp 97–130. doi:10.1007/978-94-017-7534-2_4
Matsuhiro B, Urzúa CC (1990) Agars from Gelidium rex (Gelidiales, Rhodophyta). Hydrobiologia 204:545–549. doi:10.1007/bf00040284
Matsuhiro B, Urzúa CC (1991) Agars from Chilean Gelidiaceae. Hydrobiologia 221:149–156. doi:10.1007/bf00028371
Melo RA (1998) Gelidium commercial exploitation: natural resources and cultivation. J Appl Phycol 10:303–314. doi:10.1023/A:1008070419158
Montecinos A, Broitman BR, Faugeron S, Haye PA, Tellier F, Guillemin ML (2012) Species replacement along a linear coastal habitat: phylogeography and speciation in the red alga Mazzaella laminarioides along the south east Pacific. BMC Evol Biol 12:97. doi:10.1186/1471-2148-12-97
Muhlin JF, Engel CR, Stessel R, Weatherbee RA, Brawley SH (2008) The influence of coastal topography, circulation patterns, and rafting in structuring populations of an intertidal alga. Mol Ecol 17:1198–1210. doi:10.1111/j.1365-294X.2007.03624.x
Neiva J, Assis J, Fernandes F, Pearson GA, Serrão EA, Maggs C (2014) Species distribution models and mitochondrial DNA phylogeography suggest an extensive biogeographical shift in the high-intertidal seaweed Pelvetia canaliculata. J Biogeogr 41:1137–1148. doi:10.1111/jbi.12278
Nelson WA, Farr TJ, Broom JES (2006) Phylogenetic diversity of New Zealand gelidiales as revealed by rbcL sequence data. J Appl Phycol 18:653–661. doi:10.1007/s10811-006-9068-0
Nikula R, Fraser CI, Spencer HG, Waters JM (2010) Circumpolar dispersal by rafting in two subantarctic kelp-dwelling crustaceans. Mar Ecol Prog Ser 405:221–230. doi:10.3354/meps08523
Nikula R, Spencer HG, Waters JM (2011a) Evolutionary consequences of microhabitat: population-genetic structuring in kelp- vs. rock-associated chitons. Mol Ecol 20:4915–4924. doi:10.1111/j.1365-294X.2011.05332.x
Nikula R, Spencer HG, Waters JM (2011b) Comparison of population-genetic structuring in congeneric kelp- versus rock-associated snails: a test of a dispersal-by-rafting hypothesis. Ecol Evol 1:169–180. doi:10.1002/ece3.16
Nikula R, Spencer HG, Waters JM (2013) Passive rafting is a powerful driver of transoceanic gene flow. Biol Lett 9:20120821. doi:10.1098/rsbl.2012.0821
Oliger P, Santelices B (1981) Physiological ecology studies on Chilean Gelidiales. J Exp Mar Biol Ecol 53:65–75. doi:10.1016/0022-0981(81)90084-8
Ortega M, Godínez-Ortega J, Garduño G (2001) Catálogo de algas bénticas de las costas mexicanas del Golfo de México y Mar Caribe. Instituto de Biología, Universidad Nacional Autónoma de México, México
Palumbi SR (1994) Genetic divergence, reproductive isolation, and marine speciation. Annu Rev Ecol Syst 25:547–572. doi:10.1146/annurev.ecolsys.25.1.547
Perrone C, Felicini GP, Bottalico A (2006) The prostrate system of the Gelidiales: diagnostic and taxonomic importance. Bot Mar 49:23–33. doi:10.1515/Bot2006.003
Petit RJ, El Mousadik A, Pons O (1998) Identifying populations for conservation on the basis of genetic markers. Conserv Biol 12:844–855. doi:10.1046/j.1523-1739.1998.96489.x
Piazzi L, Balata D, Bulleri F, Gennaro P, Ceccherelli G (2016) The invasion of Caulerpa cylindracea in the Mediterranean: the known, the unknown and the knowable. Mar Biol 163:161–174. doi:10.1007/S00227-016-2937-4
Polzin T, Daneshmand SV (2003) On Steiner trees and minimum spanning trees in hypergraphs. Oper Res Lett 31:12–20. doi:10.1016/s0167-6377(02)00185-2
Ramírez M, Santelices B (1981) Análisis biogeográfico de la flora algológica de Antofagasta (norte de Chile). Bol Mus Nac Hist Nat Santiago de Chile 38:5–20
Ramírez ME, Santelices B (1991) Catálogo de las algas marinas bentónicas de la costa temperada del Pacífico de Sudamérica. Monografías Biológicas 5, Ediciones Universidad Católica de Chile, Santiago de Chile
Robuchon M, Le Gall L, Mauger S, Valero M (2014) Contrasting genetic diversity patterns in two sister kelp species co-distributed along the coast of Brittany, France. Mol Ecol 23:2669–2685. doi:10.1111/mec.12774
Rogers AR, Harpending H (1992) Population growth makes waves in the distribution of pairwise genetic differences. Mol Biol Evol 9:552–569
Rojas R, León N, Rojas R (1996) Practical and descriptive techniques for Gelidium rex (Gelidiales, Rhodophyta) culture. Hydrobiologia 327:367–370
Sánchez R, Sepúlveda RD, Brante A, Cárdenas L (2011) Spatial pattern of genetic and morphological diversity in the direct developer Acanthina monodon (Gastropoda: Mollusca). Mar Ecol Prog Ser 434:121–131. doi:10.3354/meps09184
Santelices B (1980) Phytogeographic characterization of the temperate coast of Pacific South-America. Phycologia 19:1–12. doi:10.2216/i0031-8884-19-1-1.1
Santelices B (1986) The wild harvest and culture of the economically important species of Gelidium in Chile. In: Doty MS, Caddy JS, Santelices B (eds) Case of studies of seven commercial seaweed resources. FAO Fisheries Technical Paper, vol 281, FAO, Rome, pp 165–192
Santelices B (1990) New and old problems in the taxonomy of the Gelidiales (Rhodophyta). Hydrobiologia 204:125–135. doi:10.1007/bf00040224
Santelices B, Abbott IA (1985) Gelidium rex sp. nov. (Gelidiales. Rhodophyta) from central Chile. In: Abbott IA, Norris JN (eds) Taxonomy of economic seaweeds with reference to some Pacific and Caribbean species. California Sea Grant College Program, La Jolla, pp 33–36
Santelices B, Montalva S (1983) Taxonomic studies on Gelidiaceae (Rhodophyta) from central Chile. Phycologia 22:185–196. doi:10.2216/i0031-8884-22-2-185.1
Santelices B, Stewart JG (1985) Pacific species of Gelidium Lamouroux and other Gelidiales (Rhodophyta), with keys and descriptions to the common or economically important species. In: Abbott IA, Norris JN (eds) Taxonomy of economic seaweeds with reference to some Pacific and Caribbean species. California Sea Grant College Program, California, La Jolla, pp 17–31
Santelices B, Varela D (1994) Abiotic control of reattachment in Gelidium chilense (Montagne) Santelices and Montalva (Gelidiales, Rhodophyta). J Exp Mar Biol Ecol 177:145–155. doi:10.1016/0022-0981(94)90233-x
Santelices B, Aedo D, Hoffmann A (2002) Banks of microscopic forms and survival to darkness of propagules and microscopic stages of macroalgae. Rev Chil Hist Nat 75:547–555. doi:10.4067/S0716-078X2002000300006
Saunders GW (2005) Applying DNA barcoding to red macroalgae: a preliminary appraisal holds promise for future applications. Philos Trans R Soc Lond B Biol Sci 360:1879–1888. doi:10.1098/rstb.2005.1719
Selkoe KA, Toonen RJ (2011) Marine connectivity: a new look at pelagic larval duration and genetic metrics of dispersal. Mar Ecol Prog Ser 436:291–305. doi:10.3354/meps09238
Slatkin M (1993) Isolation by distance in equilibrium and nonequilibrium populations. Evolution 47:264–279. doi:10.2307/2410134
Sosa P, García-Reina G (1992) Genetic variability and differentiation of sporophytes and gametophytes in populations of Gelidium arbuscula (Gelidiaceae: Rhodophyta) determined by isozyme electrophoresis. Mar Biol 113:679–688
Sosa PA, Valero M, Batista F, González-Pérez MA (1998) Genetic structure of natural populations of Gelidium species: a re-evaluation of results. J Appl Phycol 10:279–284. doi:10.1023/A:1008092023549
Soto EH, Báez P, Ramírez ME, Letelier S, Naretto J, Rebolledo A (2012) Biotopos marinos intermareales entre Canal Trinidad y Canal Smyth, Sur de Chile. Rev Biol Mar Oceanogr 47:177–191
Tajima F (1989) Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123:585–595
Tapia FJ, Largier JL, Castillo M, Wieters EA, Navarrete SA (2014) Latitudinal discontinuity in thermal conditions along the nearshore of central-northern Chile. PLoS One 9:e110841. doi:10.1371/journal.pone.0110841
Technelysium Pty Ltd (2016) CHROMAS LITE. Available at: http://www.technelysium.com.au/chromas_lite.html. Accessed 12 April 2016
Tellier F, Meynard AP, Correa JA, Faugeron S, Valero M (2009) Phylogeographic analyses of the 30°S south-east Pacific biogeographic transition zone establish the occurrence of a sharp genetic discontinuity in the kelp Lessonia nigrescens: vicariance or parapatry? Mol Phylogenet Evol 53:679–693. doi:10.1016/j.ympev.2009.07.030
Tellier F, Vega JMA, Broitman BR, Vásquez JA, Valero M, Faugeron S (2011) The importance of having two species instead of one in kelp management: the Lessonia nigrescens species complex. Cah Biol Mar 52:455–465
Thiel M, Gutow L (2005a) The ecology of rafting in the marine environment. I. The floating substrata. Oceanogr Mar Biol Ann Rev 42:181–263. doi:10.1201/9780203507810
Thiel M, Gutow L (2005b) The ecology of rafting in the marine environment. II. The rafting organisms and community. Oceanogr Mar Biol Ann Rev 43:279–418. doi:10.1201/9781420037449
Thiel M, Haye PA (2006) The ecology of rafting in the marine environment. III. Biogeographical and evolutionary consequences. Oceanogr Mar Biol Ann Rev 44:323–429. doi:10.1201/9781420006391.ch7
Thiel M, Macaya EC, Acuña E, Arntz WE, Bastias H, Brokordt K, Camus PA, Castilla JC, Castro LR, Cortés M, Dumont CP, Escribano R, Fernández M, Gajardo JA, Gaymer CF, Gómez I, González AE, González HE, Haye PA, Illanes JE, Iriarte JL, Lancellotti DA, Luna-Jorquera G, Luxoroi C, Manríquez PH, Marín V, Muñoz P, Navarrete SA, Pérez E, Poulin E, Sellanes J, Sepúlveda HH, Stotz W, Tala F, Thomas A, Vargas CA, Vásquez JA, Vega JMA (2007) The Humboldt Current system of northern and central Chile. Oceanogr Mar Biol Ann Rev 45:195–344. doi:10.1201/9781420050943
Thomas DT, Freshwater DW (2001) Studies of Costa Rican Gelidiales (Rhodophyta): four Caribbean taxa including Pterocladiella beachii sp nov. Phycologia 40:340–350. doi:10.2216/i0031-8884-40-4-340.1
Valero M, Destombe C, Mauger S, Ribout C, Engel CR, Daguin-Thiebaut C, Tellier F (2011) Using genetic tools for sustainable management of kelps: a literature review and the example of Laminaria digitata. Cah Biol Mar 52:467–483
Vargas DR, Collado-Vides L (1996) Architectural models for apical patterns in Gelidium (Gelidiales, Rhodophyta): hypothesis of growth. Phycol Res 44:95–100
Vásquez JA, Vega JMA (2004) Ecosistemas marinos costeros del Parque Nacional Bosque Fray Jorge. In: Squeo F, Gutiérrez J, Hernández I (eds) Historia Natural del Parque Nacional Bosque Fray Jorge. Ediciones Universidad de La Serena, La Serena, pp 235–252
Voisin M, Engel CR, Viard F (2005) Differential shuffling of native genetic diversity across introduced regions in a brown alga: aquaculture vs. maritime traffic effects. Proc Natl Acad Sci USA 102:5432–5437. doi:10.1073/pnas.0501754102
Waters JM, Fraser CI, Hewitt GM (2013) Founder takes all: density-dependent processes structure biodiversity. Trends Ecol Evol 28:78–85. doi:10.1016/j.tree.2012.08.024
Weersing K, Toonen RJ (2009) Population genetics, larval dispersal, and connectivity in marine systems. Mar Ecol Prog Ser 393:1–12. doi:10.3354/meps08287
Wichmann CS, Hinojosa IA, Thiel M (2012) Floating kelps in Patagonian Fjords: an important vehicle for rafting invertebrates and its relevance for biogeography. Mar Biol 159:2035–2049. doi:10.1007/s00227-012-1990-x
Yoon KJ, Kim KM, Boo GH, Miller KA, Boo SM (2014) Mitochondrial cox1 and cob sequence diversities in Gelidium vagum (Gelidiales, Rhodophyta) in Korea. Algae 29:15–25. doi:10.4490/algae.2014.29.1.015
Zakas C, Binford J, Navarrete SA, Wares JP (2009) Restricted gene flow in Chilean barnacles reflects an oceanographic and biogeographic transition zone. Mar Ecol Prog Ser 394:165–177. doi:10.3354/meps08265