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1

Spencer, Hamish G., Jonathan M. Waters, and Thomas E. Eichhorst. "Taxonomy and nomenclature of black nerites (Gastropoda:Neritimorpha:Nerita) from the South Pacific." Invertebrate Systematics 21, no. 3 (2007): 229. http://dx.doi.org/10.1071/is06038.

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Members of the genus Nerita are abundant components of the intertidal fauna in many parts of the world and yet Nerita taxonomy remains unsettled. Here, the relationships among black-shelled Nerita populations from Australia, New Zealand, Norfolk Island, Lord Howe Island, the Kermadec Islands and Easter Island are discussed. Four species are recognised: N. atramentosa Reeve, 1855 from the southern half of Australia; N. melanotragus E.A. Smith, 1884 from eastern Australia, northern New Zealand, Lord Howe Island, Norfolk Island and the Kermadec Islands; N. morio (G. B. Sowerby I, 1833) from Easter Island and the Austral Islands; and N. lirellata Rehder, 1980 from Easter Island alone. These species are of great importance in studies of intertidal community structure and yet two of them have been consistently confused in the ecological and taxonomic literature. Moreover, the relationships among the species are not at all as implied by recent subgeneric classifications; it is argued that all four species should be placed in the subgenus Lisanerita Krijnen, 2002. The superficially similar N. picea Récluz, 1841 is not closely related. An accurate taxonomy of the genus will almost certainly require considerable genetic analysis. The nomenclature for each species is herein established by complete synonymies, and lectotypes for both N. atramentosa and N. melanotragus are selected.
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2

Foot, David K. "Easter Island." Greener Management International 2004, no. 48 (December 1, 2004): 11–20. http://dx.doi.org/10.9774/gleaf.3062.2004.wi.00004.

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3

González-García, A. César. "Easter Island." Journal for the History of Astronomy 45, no. 4 (November 2014): 487–88. http://dx.doi.org/10.1177/0021828614538383.

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4

Ayres, Williams S. "Easter Island Subsistence." Journal de la Société des océanistes 41, no. 80 (1985): 103–24. http://dx.doi.org/10.3406/jso.1985.2805.

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5

Keenan, Michael. "Rhode Island Easter." Colorado Review 43, no. 1 (2016): 121. http://dx.doi.org/10.1353/col.2016.0045.

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6

MCCALL, GRANT. "Exploring Easter Island." Journal of the Royal Anthropological Institute 17, no. 2 (May 3, 2011): 394–96. http://dx.doi.org/10.1111/j.1467-9655.2011.01697.x.

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7

Bogomolov, Fedor, Ivan Cheltsov, Adrien Dubouloz, and Alvaro Liendo. "Easter Island volume." European Journal of Mathematics 5, no. 3 (August 9, 2019): 611–21. http://dx.doi.org/10.1007/s40879-019-00364-1.

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8

Savill, J. "Academic paediatrics: Easter Island or Easter Sunday?" Archives of Disease in Childhood 90, no. 5 (May 1, 2005): 441. http://dx.doi.org/10.1136/adc.2004.063057.

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9

Diamond, J. "ARCHAEOLOGY: Easter Island Revisited." Science 317, no. 5845 (September 21, 2007): 1692–94. http://dx.doi.org/10.1126/science.1138442.

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10

Nagarajan, Palanisamy. "Collapse of Easter Island." Journal of Developing Societies 22, no. 3 (September 2006): 287–301. http://dx.doi.org/10.1177/0169796x06068032.

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11

Pollock, Nancy J. "Recent Easter Island Studies." Current Anthropology 26, no. 3 (June 1985): 379. http://dx.doi.org/10.1086/203281.

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12

Álvarez-Varas, Rocío, Carol Medrano, Hugo A. Benítez, Felipe Guerrero, Fabiola León Miranda, Juliana A. Vianna, Camila González, and David Véliz. "Genetics, Morphometrics and Health Characterization of Green Turtle Foraging Grounds in Mainland and Insular Chile." Animals 12, no. 12 (June 7, 2022): 1473. http://dx.doi.org/10.3390/ani12121473.

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Two divergent genetic lineages have been described for the endangered green turtle in the Pacific Ocean, occurring sympatrically in some foraging grounds. Chile has seven known green turtle foraging grounds, hosting mainly juveniles of different lineages. Unfortunately, anthropic factors have led to the decline or disappearance of most foraging aggregations. We investigated age-class/sex structure, morphological variation, genetic diversity and structure, and health status of turtles from two mainland (Bahia Salado and Playa Chinchorro) and one insular (Easter Island) Chilean foraging grounds. Bahia Salado is composed of juveniles, and with Playa Chinchorro, exclusively harbors individuals of the north-central/eastern Pacific lineage, with Galapagos as the major genetic contributor. Conversely, Easter Island hosts juveniles and adults from both the eastern Pacific and French Polynesia. Morphological variation was found between lineages and foraging grounds, suggesting an underlying genetic component but also an environmental influence. Turtles from Easter Island, unlike Bahia Salado, exhibited injuries/alterations probably related to anthropic threats. Our findings point to establishing legal protection for mainland Chile’s foraging grounds, and to ensure that the administrative plan for Easter Island’s marine protected area maintains ecosystem health, turtle population viability, and related cultural and touristic activities.
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13

Junk, C., and M. Claussen. "Simulated climate variability in the region of Rapa Nui during the last millennium." Climate of the Past Discussions 7, no. 1 (January 26, 2011): 381–95. http://dx.doi.org/10.5194/cpd-7-381-2011.

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Abstract. Easter Island, an isolated island in the Southeast Pacific, was settled by the Polynesians probably between 600 and 1200 AD and discovered by the Europeans in 1722 AD. While the Polynesians presumably found a profuse palm woodland on Easter Island, the Europeans faced a landscape dominated by grassland. Scientists have examined potential anthropogenic, biological and climatic induced vegetation changes on Easter Island. Here, we analyze observational climate data for the last decades and climate model results for the period 800–1750 AD to explore potential causes for a climatic-induced vegetation change. A direct influence of the ENSO phenomenon on the climatic parameters of Easter Island could not be found in the model simulations. Furthermore, strong climatic trends from a warm Medieval Period to a Little Ice Age or rapid climatic fluctuations due to large volcanic eruptions were not verifiable for the Easter Island region, although they are detectable in the simulations for many regions world wide. Hence we tentatively conclude that large-scale climate changes in the oceanic region around Easter Island might be too small to explain strong vegetation changes on the island over the last millennium.
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14

Hunt, T. L. "Late Colonization of Easter Island." Science 311, no. 5767 (March 17, 2006): 1603–6. http://dx.doi.org/10.1126/science.1121879.

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15

Rull, Valentí. "The deforestation of Easter Island." Biological Reviews 95, no. 1 (October 10, 2019): 124–41. http://dx.doi.org/10.1111/brv.12556.

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16

Markov, Vladimir, and Jeremy Howard. "The Art of Easter Island." Art in Translation 6, no. 1 (March 2014): 29–58. http://dx.doi.org/10.2752/175613114x13972161909607.

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17

Sanger, Kay Kenady. "Easter Island: The Essential Guide." Rapa Nui Journal 29, no. 2 (2015): 73. http://dx.doi.org/10.1353/rnj.2015.0025.

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18

Baker, P. E. "Archaeological stone of Easter Island." Geoarchaeology 8, no. 2 (April 1993): 127–39. http://dx.doi.org/10.1002/gea.3340080205.

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19

Lynn, Michael R. ":Inventing "Easter Island."." Sixteenth Century Journal 41, no. 3 (September 1, 2010): 961–62. http://dx.doi.org/10.1086/scj40997460.

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20

Flores, Marcelo A., Roberto P. Schlatter, and Rodrigo Hucke Gaete. "Seabirds of Easter Island, Salas y Gomez Island and Desventuradas Islands, southeastern Pacific Ocean." Latin American Journal of Aquatic Research 42, no. 4 (October 10, 2014): 752–59. http://dx.doi.org/10.3856/vol42-issue4-fulltext-6.

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21

Hedlin, Michael A. H., and John A. Orcutt. "A comparative study of island, seafloor, and subseafloor ambient noise levels." Bulletin of the Seismological Society of America 79, no. 1 (February 1, 1989): 172–79. http://dx.doi.org/10.1785/bssa0790010172.

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Abstract A study of seafloor and island stations shows that for the frequency band 0.1 to 10 Hz the seismic noise levels on islands are comparable to the levels on the seafloor. The microseism peak at the seafloor appears to be comparable to the highest levels observed on small islands. For this band, seafloor stations are realistic alternatives when island sites are not available. Seven year averages of the ambient noise levels recorded by Seismic Research Observatory (SRO) stations on three islands (Guam [GUMO], Taiwan [TATO], and New Zealand's north island [SNZO]) are compared with those recorded by the International Deployment of Accelerometers (IDA) station on Easter Island and on and beneath the ocean floor by Ocean Bottom Seismometers (OBSs) and the Marine Seismic System (MSS) deployed in a south Pacific DSDP drill hole at 23.8°S., 165.5°W (Adair et al., 1986). From 0.3 to 2 Hz the SRO displacement power levels fall in the range historically observed by the Scripps' OBSs (decreasing at 70 dB/decade from 1 by 106 nm2/Hz at 0.3 Hz to 1 nm2/Hz at 2 Hz) and are 10 to 15 dB above MSS levels. Above 2 Hz it appears that the same ratios hold (the SRO power levels decrease at 70 dB/decade to 1 by 10−3 nm2/Hz at a frequency of 10 Hz), although this correlation is based on very limited, high gain, short-period data. At frequencies below 0.3 Hz the SRO noise levels peak and decrease to approximately 2 by 103 nm2/Hz at 40 mHz. The noise levels recorded at Easter Island are somewhat higher (decreasing at 70 dB/decade from 1 by 107 nm2/Hz at 0.2 Hz to 1 nm2/Hz at 10 Hz and to 1 by 105 nm2/Hz at 50 mHz). At the microseism peak near 0.2 Hz the MSS levels are from 15 to 20 dB higher than observed by the SRO stations and equivalent to those recorded at Easter Island. There appears to be little dependence of the variance in noise level estimates on frequency. The upper 95 per cent confidence limit generally lies 10 dB above the average noise levels for all island stations. All island noise level curves are dominated by the broad double-frequency microseism peak centered between 0.15 to 0.2 Hz. The single-frequency peak ranges from absent (Easter Island) to discernable (Guam and New Zealand) to obvious (at Taiwan). The center frequency of this peak ranges from 0.07 Hz at Guam and New Zealand to 0.1 Hz at Taiwan. We speculate that the increased amplitude and frequency of the single-frequency microseism peak is due to the interaction between the shallow continental shelf and surface gravity waves and/or the presence of Taiwan in a region of limited fetch.
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22

Hunt, Terry L., and Carl P. Lipo. "Revisiting Rapa Nui (Easter Island) “Ecocide”." Pacific Science 63, no. 4 (October 2009): 601–16. http://dx.doi.org/10.2984/049.063.0407.

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23

Rjabchikov, Sergei V. "The rongorongo Schools on Easter Island." Anthropos 107, no. 2 (2012): 564–70. http://dx.doi.org/10.5771/0257-9774-2012-2-564.

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24

Taylor, David, P. Bahn, and J. Flenley. "Easter Island: Portent for the World?" Journal of Biogeography 20, no. 2 (March 1993): 246. http://dx.doi.org/10.2307/2845680.

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25

De los Ríos-Escalante, Patricio, and Eliana Ibáñez. "Inland water crustaceans of Easter Island." Crustaceana 88, no. 9 (2015): 1061–64. http://dx.doi.org/10.1163/15685403-00003465.

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26

RØSVIK ANDREASSEN, OLAUG IRENE. "Inventing ‘Easter Island’- By Beverley Haun." Journal of the Royal Anthropological Institute 17, no. 2 (May 3, 2011): 413. http://dx.doi.org/10.1111/j.1467-9655.2011.01698_15.x.

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27

Wagner, Jennifer. "Easter Island, Myths and Popular Culture." Journal of New Zealand & Pacific Studies 3, no. 1 (May 1, 2015): 89–92. http://dx.doi.org/10.1386/nzps.3.1.89_7.

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28

Torrence, R. "Ecocide or Utopia on Easter Island?" Science 335, no. 6067 (January 26, 2012): 403–4. http://dx.doi.org/10.1126/science.1216863.

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29

Gibbons, A. "ARCHAEOLOGY: Dates Revise Easter Island History." Science 311, no. 5766 (March 10, 2006): 1360. http://dx.doi.org/10.1126/science.311.5766.1360.

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30

Hunt, Terry. "Rethinking the Fall of Easter Island." American Scientist 94, no. 5 (2006): 412. http://dx.doi.org/10.1511/2006.61.1002.

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31

Butler, Kevin, Christine A. Prior, and John R. Flenley. "Anomalous Radiocarbon Dates from Easter Island." Radiocarbon 46, no. 1 (2004): 395–405. http://dx.doi.org/10.1017/s0033822200039709.

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The largest volcanic crater on Easter Island in the South Pacific contains a lake 1 km in diameter with large floating mats of vegetation, mainly Scirpus californicus. A core taken through a mat near the center produced anomalous dates, with older dates above younger ones. The possibility that the mat had become inverted was considered, but palynological evidence refutes this idea because it shows a progressive upward decline of forest pollen, which is well known from other swamp cores on the island. A new series of radiocarbon dates made directly on pollen concentrates was obtained. These dates also produced inconsistencies, particularly when pollen concentrate ages were compared with 14C ages on plant fragments from the same depth. This series of 14C ages seems to indicate that both old and young organic components in the sediment are deposited contiguously and that the depositional history of these cores is more complex than previously known. Previous age determinations on bulk sediments from Easter Island, which also show anomalous dates, may be too simplistic. This paper provides a warning to other researchers dating sediments from Easter Island. We suggest that sample selection and dating procedures be carefully considered for these sediments.
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32

Moraga, Julio, Arnoldo Valle-Levinson, and Jorge Olivares. "Hydrography and geostrophy around Easter Island." Deep Sea Research Part I: Oceanographic Research Papers 46, no. 4 (April 1999): 715–31. http://dx.doi.org/10.1016/s0967-0637(98)00083-1.

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33

Dalton, Thomas R., R. Morris Coats, and R. Andrew Luccasen. "Exploring Easter Island economics with Excel." International Review of Economics Education 18 (January 2015): 1–10. http://dx.doi.org/10.1016/j.iree.2014.10.001.

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34

Kensley, Brian Frederick. "Marine Isopod Crustaceans from Easter Island." Pacific Science 57, no. 3 (2003): 287–317. http://dx.doi.org/10.1353/psc.2003.0023.

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35

Hughes, J. Donald. "Easter Island: Model for Environmental History?" Capitalism Nature Socialism 14, no. 2 (June 2003): 77–83. http://dx.doi.org/10.1080/10455750308565524.

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36

Bahn, Paul G., Catherine Orliac, and Michel Orliac. "Picasso and the Easter Island "palm"." Rapa Nui Journal 29, no. 1 (2015): 45–48. http://dx.doi.org/10.1353/rnj.2015.0002.

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37

Dumont, Henri J., and Koen Martens. "The freshwater microcrustacea of Easter Island." Hydrobiologia 325, no. 2 (June 1996): 83–99. http://dx.doi.org/10.1007/bf00028269.

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38

Rose, David L. "Note from the Easter Island Foundation." Rapa Nui Journal 31, no. 1&2 (2018): 61. http://dx.doi.org/10.1353/rnj.2018.a716988.

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39

Parmentier, Richard J. "Rongorongo, The Easter Island Script: History, Traditions, Texts.:Rongorongo, The Easter Island Script: History, Traditions, Texts." Journal of Linguistic Anthropology 8, no. 2 (December 1998): 253–55. http://dx.doi.org/10.1525/jlin.1998.8.2.253.

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40

Finney, Ben. "Voyage to Polynesia's land's end." Antiquity 75, no. 287 (March 2001): 172–81. http://dx.doi.org/10.1017/s0003598x0005287x.

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Evidence that the earliest settlers on Rapa Nui (Easter Island) may have come from Mangareva and its outlying islands in Central East Polynesia is supported by the journey of the experimental voyaging canoe Hōkūle'a from Mangareva to Rapa Nui.
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41

HOESE, DOUGLASS F., and HELEN K. LARSON. "Description of two new species of Hetereleotris (Gobiidae) from the south Pacific, with a revised key to species and synonymization of the genus Pascua with Hetereleotris." Zootaxa 1096, no. 1 (December 16, 2005): 1. http://dx.doi.org/10.11646/zootaxa.1096.1.1.

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Two new species of the genus Hetereleotris are described from the south Pacific. One species is known only from reefs off southeastern Australia and the second from Rapa and Pitcairn islands. Both species are close to a species recently described from Easter Island in the genus Pascua. The Easter Island species is redescribed herein. Previously only one species of the genus was reported from the Pacific. All of the species described here share a number of characteristics suggesting that they form a monophyletic group, including: the flattened and elongate urogenital papilla of the males, modified basicaudal scales, posterior nostril a simple pore or with only a slightly elevated margin anteriorly, two papillae just behind the mental frenum and the reduced transverse papilla pattern.
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42

Irwin, Geoffrey, Simon Bickler, and Philip Quirke. "Voyaging by canoe and computer: experiments in the settlement of the Pacific Ocean." Antiquity 64, no. 242 (March 1990): 34–50. http://dx.doi.org/10.1017/s0003598x00077280.

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There is no expansion of human settlement to match the colonization of the Pacific islands, from Island Southeast Asia right across to Hawaii, Easter Island and down to New Zealand. The expansion is given an extra interest by the new finding that it began as early as the Pleistocene. The settlement of the remote Pacific began after 3500 BP and computer modelling and analysis of inter-island transits explains not just how settlement was possible-but how it must have followed from the controlled navigation of directed voyages and strategies for survival.
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43

Ireland, Robert R., and Gilda Bellolio. "The Mosses of Easter Island." Bryophyte Diversity and Evolution 21, no. 1 (August 24, 2002): 11–19. http://dx.doi.org/10.11646/bde.21.1.3.

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The bryophyte flora of Easter Island has been poorly known primarily because few botanists have collected there. In order to increase the knowledge of the flora the two authors collected bryophytes from 12 localities on the island from April 28-May 3, 2000. The small island, which is south of the Tropic of Capricorn, is of volcanic origin and the volcanic soil as well as the destruction of most of the native flora have undoubtedly contributed to the paucity of bryophytes. The present study revealed that the bryophyte flora consists of only a few species, including one unidentifiable member of the Anthocerotaceae, 11 hepatics and 30 mosses. Eighteen mosses are new to the island. Three mosses, Chenia leptophylla (Müll. Hal.) R. H. Zander, Dicranella hawaiica (Müll. Hal.) Broth. and Tortella humilis (Hedw.) Jennings, are new for Chile, while three, Fissidens pascuanus Broth. in Skottsb., Ptychomitrium subcylindricum Thér. and Trematodon pascuanus Thér., are presently known to be endemic to Easter Island. Two of the three endemics, Fissidens pascuanus and Ptychomitrium subcylindricum, were rediscovered on the island. Fissidens pascuanus was found with sporophytes for the first time and a revised description of the species is provided.
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44

Matthew, Richard A., and Ted Gaulin. "Conflict or Cooperation? The Social and Political Impacts of Resource Scarcity on Small Island States." Global Environmental Politics 1, no. 2 (May 1, 2001): 48–70. http://dx.doi.org/10.1162/152638001750336596.

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This paper examines the social and political consequences of natural resource scarcity on three Pacific island territories: Easter Island, Nauru and Solomon Islands. In contrast to prominent theories in the environmental security literature, the case studies in this paper indicate that resource scarcity does not perforce lead to violent conflict. The authors explain differential outcomes on the basis of four variables: extent of scarcity; level of democracy; degree of economic openness; and involvement in regional regimes.
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45

McCOSKER, JOHN E., and JOHN E. RANDALL. "Notes on the snake eels of the genera Apterichtus and Ichthyapus (Anguilliformes: Ophichthidae) of the Central and South Pacific, with the description of a new species." Zootaxa 800, no. 1 (January 7, 2005): 1. http://dx.doi.org/10.11646/zootaxa.800.1.1.

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Apterichtus australis, new species, collected by dredge and rotenone in 12–100 m is described from Rapa, Pitcairn, Easter and Kermadec islands. It is closely related to A. flavicaudus (Snyder) but differs from it and all congeners in its high vertebral number, cephalic pore condition, and dentition. Ichthyapus from Easter Island and Pitcairn are recognized as I. acutirostris Brisout de Barneville. Caecula (Sphagebranchus) platyrhyncha Gosline from Hawaii is resurrected from the synonymy of I. vulturis (Weber & de Beaufort). First records of I. vulturis and Apterichtus klazingai (Weber) from Hawaii are reported.
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46

Edwards, Edmundo. "Astronomically aligned religious structures on Raiatea and Raivavae and the Matariki festival of 1770 on Easter Island." Proceedings of the International Astronomical Union 7, S278 (January 2011): 275–81. http://dx.doi.org/10.1017/s1743921311012701.

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AbstractEastern Polynesian astronomy was practiced by navigators and astronomer-priests who were in charge of adjusting the lunar calendar and their annual ritual cycle of activities known as ‘The Work of the Gods’. The festivity known in Polynesia as Matariki, Matali'i or Matari'i was related to the heliacal and acronical rising and setting of the Pleiades. A study of 75 marae on the island of Raivavae, Austral Islands and of 7 marae in the island of Raiatea, Society Islands shows that there are alignments towards important star positions associated with this ritual cycle. Their use as observatories has not been documented and therefore these alignments could have served solely ritual purposes. On Easter Island all information regarding the Matariki festival coincides with the arrival of a Spanish expedition in 1770.
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47

Grolle, Riclef. "The Hepaticae of the Easter Island (Chile)." Bryologist 105, no. 1 (March 2002): 126–27. http://dx.doi.org/10.1639/0007-2745(2002)105[0126:thotei]2.0.co;2.

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48

Arana, Patricio M. "Ancient fishing activities developed in Easter Island." Latin American Journal of Aquatic Research 42, no. 4 (October 10, 2014): 673–89. http://dx.doi.org/10.3856/vol42-issue4-fulltext-2.

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49

Edwards, Edmundo R., and Juan Antonio Belmonte. "Megalithic Astronomy of Easter Island: A Reassessment." Journal for the History of Astronomy 35, no. 4 (November 2004): 421–33. http://dx.doi.org/10.1177/002182860403500403.

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50

Rjabchikov, Sergei V. "Rongorongo Glyphs Clarify Easter Island Rock Drawings." Journal de la société des océanistes, no. 113 (December 1, 2001): 215–20. http://dx.doi.org/10.4000/jso.1625.

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