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Thematische Bibliographien / Indians of South America—Guyana / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Indians of South America—Guyana“

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Veröffentlicht am 4. Juni 2021

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1

Schnepel, Ellen M. „East Indians in the Caribbean“. New West Indian Guide / Nieuwe West-Indische Gids 73, Nr. 3-4 (01.01.1999): 83–91. http://dx.doi.org/10.1163/13822373-90002579.

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[First paragraph]Transients to Settlers: The Experience of Indians in Jamaica 1845-J950. VERENE SHEPHERD. Leeds, U.K.: Peepal Tree Books, 1993. 281 pp. (Paper £12.95)Survivors of Another Crossing: A History of East Indians in Trinidad, 1880-1946. MARIANNE D. SOARES RAMESAR. St. Augustine, Trinidad and Tobago: U.W.I. School of Continuing Education, 1994. xiii + 190 pp. (Paper n.p.)Les Indes Antillaises: Presence et situation des communautes indiennes en milieu caribeen. ROGER TOUMSON (ed.). Paris: L'Harmattan, 1994. 264 pp. (Paper 140.00 FF)Nation and Migration: The Politics of Space in the South Asian Diaspora. PETER VAN DER VEER (ed.). Philadelphia: University of Pennsylvania Press, 1995. vi + 256 pp. (Cloth US$ 39.95, Paper US$ 17.95)In the decade since 1988, Caribbean nations with Indian communities have commemorated the 150th anniversary of the arrival of East Indians to the West Indies. These celebrations are part of local revitalization movements of Indian culture and identity stretching from the French departement of Guadeloupe in the Windward Islands to Trinidad and Guyana in the south. Political changes have mirrored the cultural revival in the region. While the debate so often in the past centered on the legitimacy of East Indian claims to local nationality in these societies where African or Creole cultures dominate, in the 1990s leaders of Indian descent were elected heads of government in the two Caribbean nations with the most populous East Indian communities: Cheddi Jagan as President of Guyana in October 1992 (after a 28-year hiatus) and Basdeo Panday as Prime Minister of Trinidad in November 1995. Both men have long been associated with their respective countries' struggles for economic, political, and social equality. Outside the region during the summer of 1997, fiftieth-anniversary celebrations marking the independence of India and Pakistan from Britain confirmed that Indo chic — or "Indofrenzy" as anthropologist Arjun Appadurai calls it (Sengupta 1997:13) - has captured the American imagination with the new popularity of literature, art, and film emanating from India and its diaspora.

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KITLV, Redactie. „Book Reviews“. New West Indian Guide / Nieuwe West-Indische Gids 62, Nr. 1-2 (01.01.1988): 51–101. http://dx.doi.org/10.1163/13822373-90002046.

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-Brenda Plummer, Carol S. Holzberg, Minorities and power in a black society: the Jewish community of Jamaica. Maryland: The North-South Publishing Company, Inc., 1987. xxx + 259 pp.-Scott Guggenheim, Nina S. de Friedemann ,De sol a sol: genesis, transformacion, y presencia de los negros en Colombia. Bogota: Planeta Columbiana Editorial, 1986. 47 1pp., Jaime Arocha (eds)-Brian L. Moore, Mary Noel Menezes, Scenes from the history of the Portuguese in Guyana. London: Sister M.N. Menezes, RSM, 1986. vii + 175 PP.-Charles Rutheiser, Brian L. Moore, Race, power, and social segmentation in colonial society: Guyana after slavery 1838-1891. New York; Gordon and Breach, 1987. 310 pp.-Thomas Fiehrer, Virginia R. Dominguez, White by definition: social classification in Creole Louisiana. Rutgers, New Jersey: Rutgers University Press, 1986. xviii + 325 pp.-Kenneth Lunn, Brian D. Jacobs, Black politics and urban crisis in Britain. Cambridge, London, New Rochelle, Melbourne and Sydney: Cambridge University Press, 1986. vii + 227 pp.-Brian D. Jacobs, Kenneth Lunn, Race and labour in twentieth-cenruty Britain, London: Frank Cass and Co. Ltd., 1985. 186 pp.-Kenneth M. Bilby, Dick Hebdige, Cut 'n' mix: culture, identity and Caribbean Music. New York: Metheun and Co. Ltd, 1987. 177 pp.-Riva Berleant-Schiller, Robert Dirks, The black saturnalia: conflict and its ritual expression on British West Indian slave plantations. Gainesville, Fl.: University of Florida Press, Monographs in Social Sciences No. 72. xvii + 228.-Marilyn Silverman, James Howe, The Kuna gathering: contemporary village politics in Panama. Austin, Texas: University of Texas Press, 1986. xvi + 326 pp.-Paget Henry, Evelyne Huber Stephens ,Democratic socialism in Jamaica: the political movement and social transformation in dependent capitalism. Princeton, N.J.: Princeton University Press, 1985. xx + 423 pp., John D. Stephens (eds)-Bridget Brereton, Scott B. Macdonald, Trinidad and Tobago: democracy and development in the Caribbean. New York, Connecticut, London: Praeger Publishers, 1986. ix + 213 pp.-Brian L. Moore, Kempe Ronald Hope, Guyana: politics and development in an emergent socialist state. Oakville, New York, London: Mosaic Press, 1985, 136 pp.-Roland I. Perusse, Richard J. Bloomfield, Puerto Rico: the search for a national policy. Boulder and London: Westview Press, Westview Special Studies on Latin America and the Caribbean, 1985. x + 192 pp.-Charles Gilman, Manfred Gorlach ,Focus on the Caribbean. 1986. Amsterdam/Philadelphia, John Benjamins., John A. Holm (eds)-Viranjini Munasinghe, EPICA, The Caribbean: survival, struggle and sovereignty. Washington, EPICA (Ecumenical Program for Interamerican Communication and Action), 1985.-B.W. Higman, Sidney W. Mintz, Sweetness and power: the place of sugar in modern history. New York: Elisabeth Sifton Books, Viking Penguin Inc., 1985. xxx + 274 pp.

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C. Rawlins, T. Tiwari, D. D. Chadee, S. „American cutaneous leishmaniasis in Guyana, South America“. Annals of Tropical Medicine And Parasitology 95, Nr. 3 (01.04.2001): 245–51. http://dx.doi.org/10.1080/00034980120053357.

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Rawlins, S. C., T. Tiwari, D. D. Chadee, L. Validum, H. Alexander, R. Nazeer und S. R. S. Rawlins. „American cutaneous leishmaniasis in Guyana, South America“. Annals of Tropical Medicine & Parasitology 95, Nr. 3 (April 2001): 245–51. http://dx.doi.org/10.1080/00034983.2001.11813636.

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Barrett, Janice P., und Ronald H. Behrens. „Prophylaxis Failure AgainstVivaxMalaria in Guyana, South America“. Journal of Travel Medicine 3, Nr. 1 (01.03.1996): 60–61. http://dx.doi.org/10.1111/j.1708-8305.1996.tb00699.x.

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6

Best Plummer, Wallis S., Premini Persaud und Penelope J. Layne. „Ethnicity and cancer in Guyana, South America“. Infectious Agents and Cancer 4, Suppl 1 (2009): S7. http://dx.doi.org/10.1186/1750-9378-4-s1-s7.

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7

Nadeau, Serge, Wei Chen, Jimmy Reece, Deokumar Lachhman, Randy Ault, Maria Telma Lins Faraco, Lêda Maria Fraga, Nelson Joaquim Reis und Léandro Menezes Betiollo. „Guyana: the Lost Hadean crust of South America?“ Brazilian Journal of Geology 43, Nr. 4 (01.12.2013): 601–6. http://dx.doi.org/10.5327/z2317-48892013000400002.

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Kelloff, Carol L., und Gregory S. McKee. „A New Species of Hecistopteris from Guyana, South America“. American Fern Journal 88, Nr. 4 (Oktober 1998): 155. http://dx.doi.org/10.2307/1547767.

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Mistry, Jayalaxshmi, Andrea Berardi, Céline Tschirhart, Elisa Bignante, Lakeram Haynes, Ryan Benjamin, Grace Albert, Rebecca Xavier, Deirdre Jafferally und Géraud de Ville. „Indigenous identity and environmental governance in Guyana, South America“. cultural geographies 22, Nr. 4 (05.12.2014): 689–712. http://dx.doi.org/10.1177/1474474014560998.

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Watson, L. Cynthia, Jorge L. Hurtado-Gonzales, Christopher J. Chin und Juliana Persaud. „Survey of Methylmercury Exposures and Risk Factors Among Indigenous Communities in Guyana, South America“. Journal of Health and Pollution 10, Nr. 26 (Juni 2020): 200604. http://dx.doi.org/10.5696/2156-9614-10.26.200604.

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Background. Gold mining activities in forested areas across Guyana have been a common practice for more than a century. The intensification of artisanal and small-scale gold mining (ASGM) in recent decades caused by global market demand is contributing to the mobilization of mercury into aquatic systems. Indigenous populations who consume high levels of locally sourced fish are greater at risk for methylmercury poisoning from ingestion of contaminated fish. Objectives. The aim of the present study was to investigate the levels of mercury contamination and identify the risk factors associated with hair mercury levels in four indigenous communities in Guyana. Methods. Concentrations of total mercury were measured in hair samples from 99 participants from four indigenous communities in the south Rupununi region in Guyana. The findings of this study were compared with those of previous studies to assess the prevalence of mercury contamination in indigenous communities across Guyana. Results. Hair mercury levels were found to be above the World Health Organization (WHO) reference value for residents who live close to ASGM activities and who consume high quantities of locally sourced fish. Our results are not only consistent with those obtained in previous studies, but also evidence that mercury poisoning has become a generalized problem for indigenous communities in Guyana. Conclusions. Fish is the main source of protein for many riverine communities and consumption of mercury-contaminated fish poses a serious health hazard for these vulnerable populations. The situation is especially dire for community members of Parabara with 100% of participants showing elevated (>15 μg*g−1) hair mercury levels. It is therefore crucial that Parabara residents be evaluated by relevant health agencies for clinical symptoms related to mercury toxicity. Participant Consent. Obtained Ethics Approval. The study protocol was approved by the Institutional Review Board of the Ministry of Public Health, Guyana. Competing Interests. The authors declare no competing financial interests.

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Sedgley, M., und J. A. Gardner. „SOUTH AMERICA (COLOMBIA, VENEZUELA, GUYANA, SURINAME, PERU, BRAZIL, CHILE, ARGENTINA)“. Acta Horticulturae, Nr. 250 (September 1989): 63–92. http://dx.doi.org/10.17660/actahortic.1989.250.4.

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Craw, LA, NR Saunders, E. Koelink, J. Roth, L. Aronson, MS Silverman, S. Roth, B. Ortuoste und D. Scolnik. „Anthropometric Measurement of School-Aged Children in Guyana, South America“. Paediatrics & Child Health 15, suppl_A (01.05.2010): 56A. http://dx.doi.org/10.1093/pch/15.suppl_a.56ab.

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Sozzo, Maximo. „Postneoliberalism and Penality in South America: By Way of Introduction“. International Journal for Crime, Justice and Social Democracy 6, Nr. 1 (01.03.2017): 133–45. http://dx.doi.org/10.5204/ijcjsd.v6i1.391.

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In the last two decades, there has been an extraordinary growth in incarceration rates in South America, with some variations across national contexts but generally in line with the same trend. Twenty years ago, incarceration rates were relatively low in most countries in the region; despite that knowledge, it has proved difficult to reconstruct the official data for that period. In 1992, with the exclusion of the small countries with less than one million inhabitants in the Northern region of South America such as Guyana, French Guyana and Surinam, only three countries had 100 prisoners or more per 100,000 inhabitants: Uruguay (100), Venezuela (133) and Chile (154) (see Figure 1). Several other national contexts reflected ‘Scandinavian’ rates, such as Argentina (62), Peru (69), Ecuador (75) and Brazil (74). Download the PDF file to continue with this introduction to the articles in the dossier within this issue of the journal.

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Altieri, Maria, Tarun R. Jindal, Mayur Patel, David K. Oliver, Edward M. Falta, Eric A. Elster, Alden Doyle, Stephen R. Guy, Arthur L. Womble und Rahul M. Jindal. „Report of the First Peritoneal Dialysis Program in Guyana, South America“. Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis 33, Nr. 2 (März 2013): 116–23. http://dx.doi.org/10.3747/pdi.2012.00001.

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Introduction In 2008, we initiated the first Guyanese comprehensive kidney replacement program, comprising hemodialysis (HD), peritoneal dialysis (PD), vascular access procedures, and living-donor kidney transplantation. The government of Guyana, US-based philanthropists, US-based physicians, and Guyanese caregivers teamed up to form a public–private partnership. This pilot program was free of cost to the patients. Methods From July 2010 to the time of writing, we placed 17 patients with end-stage kidney disease on PD, which was used as a bridge to living-donor kidney transplantation. During the same period, we placed 12 primary arteriovenous fistulae. Results The 17 patients who received a PD catheter had a mean age of 43.6 years and a mean follow-up of 5.3 months. In that group, 2 deaths occurred (from multi-organ failure) within 2 weeks of catheter placement, and 2 patients were switched to HD because of inadequate clearance. Technical issues were noted in 2 patients, and 3 patients developed peritonitis (treated with intravenous antibiotics). An exit- site abscess in 1 patient was drained under local anesthesia. The peritonitis rate was 0.36 episodes per patient–year. Of the 17 patients who received PD, 4 underwent living-donor kidney transplantation. Conclusions In Guyana, PD is a safe and cost-effective option; it may be equally suitable for similar developing countries. In Guyana, PD was used as a bridge to living-donor kidney transplantation. We have been able to sustain this program since 2008 by making incremental gains and nurturing the ongoing public– private partnership.

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Girón, Jennifer C., und Andrew Edward Z. Short. „Three new genera of acidocerine water scavenger beetles from tropical South America (Coleoptera, Hydrophilidae, Acidocerinae)“. ZooKeys 768 (19.06.2018): 113–58. http://dx.doi.org/10.3897/zookeys.768.24423.

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Recent collecting efforts in the Neotropics have led to the discovery of numerous new species and lineages of aquatic beetles. Here, three new genera are described to accommodate fifteen new species of water scavenger beetles of the subfamily Acidocerinae from northern South America:Crucisternumgen. n.forC.escalerasp. n.(Venezuela),C.ouboterisp. n.(Guyana, French Guiana, Suriname, Venezuela),C.queneyisp. n.(French Guiana),C.sinuatussp. n.(Brazil),C.toboganensissp. n.(Venezuela),C.vanessaesp. n.(Suriname), andC.xingusp. n.(Brazil);Katasophistesgen. n. forK.charynaesp. n.(Peru),K.cuzcosp. n.(Peru),K.meridasp. n.(Venezuela) andK.superficialissp. n.(Ecuador); andNanosaphesgen. n.forN.castaneussp. n.(Brazil),N.hesperussp. n.(Suriname),N.punctatussp. n.(Guyana), andN.tricolorsp. n.(Guyana, Suriname). It was also found that the monotypic Neotropical endemic genusDieroxenusSpangler, 1979,syn. n.is congeneric withChasmogenusSharp, 1882 resulting in the single new combinationChasmogenuscremnobates(Spangler, 1979),comb. n..Katasophistesmeridasp. n.is known exclusively from seepage habitats, while the remaining taxa described herein are primarily associated with the margins of densely forested streams. Diagnoses, illustrations, distribution maps, and habitat summaries are provided for all new genera and species. A key to the genera of Acidocerinae of the New World is provided.

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MacCulloch, Ross D., Amy Lathrop, Philippe J. R. Kok, Raffael Ernst und Michelle Kalamandeen. „The genus Oxyrhopus (Serpentes: Dipsadidae: Xenodontinae) in Guyana: morphology, distributions and comments on taxonomy“. Papéis Avulsos de Zoologia 49, Nr. 36 (2009): 487–95. http://dx.doi.org/10.1590/s0031-10492009003600001.

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Considerable confusion exists regarding taxonomy and distributions of Oxyrhopus in northern South America. Specimens and records of Oxyrhopus from Guyana were examined. Oxyrhopus melanogenys, O. occipitalis and O. petola occur in Guyana. Data on morphology and colouration of these species are presented. Species distributions and characters to distinguish among the species are discussed.

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Bacchus, Nazreen S. „Belonging and boundaries in Little Guyana: Conflict, culture, and identity in Richmond Hill, New York“. Ethnicities 20, Nr. 5 (04.10.2019): 896–914. http://dx.doi.org/10.1177/1468796819878885.

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Research on the assimilation of contemporary second-generation Americans has shown that ethnic enclaves are saturated with several cultural, religious, and transnational amenities that facilitate the process of immigrant integration in the United States. Missing from this research is a discussion of how middle-class, second-generation Americans use urban enclaves as a means of remaining attached to their ethnic identities. One such group with members who has achieved middle-class status and remained culturally attached to their enclave is Indo-Guyanese Americans of Indian Caribbean descent. This ethnographic study examines the ways in which second-generation Indo-Guyanese Americans use familial, cultural, and religious interactions in Little Guyana to create a sense of belonging and community. As the descendants of re-migrants, their multiethnic identities are complicating their assimilation in American society. Their experiences with racialization and social exclusion from white, South Asian American, and non-co-ethnic circles have pushed them toward developing their multiethnic identity. I use the term ethnic restoration to discuss how second-generation Indo-Guyanese Americans are using transnational ethnic consumption, religious institutions, and co-ethnic interactions to validate their ethnic identities and resist racialization. Their engagement in ethno-religious institutions in Richmond Hill is central to this analysis, as they embrace their Indian Caribbean identities more intensely after experiencing racialization. The findings of this research point to the need to understand why middle-class second-generation Americans are ethnically attached to urban enclaves.

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Eapen, V., und M. M. Robertson. „Gilles de la Tourette Syndrome—A Case Report from Guyana in South America“. Behavioural Neurology 5, Nr. 1 (1992): 39–41. http://dx.doi.org/10.1155/1992/929671.

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A case of the Gilles de la Tourette syndrome from Guyana in South America is presented. The patient had a positive family history as well as coprolalia, echolalia, and attention deficit disorder with hyperactivity. The family history and cross-cultural similarity emphasise the biological factors in the aetiology of the syndrome.

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Strong, Mark T. „Three New Cyperaceae from the Cuyuni-Mazaruni Region of Guyana (South America)“. Novon: A Journal for Botanical Nomenclature 24, Nr. 4 (24.05.2016): 401–7. http://dx.doi.org/10.3417/2015032.

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Saisongkorh, W., L. Barrassi, B. Davoust, C. A. de Broucker, D. Raoult und J. M. Rolain. „First isolation of Bartonella bovis from animals in French Guyana, South America“. Clinical Microbiology and Infection 15 (Dezember 2009): 124–26. http://dx.doi.org/10.1111/j.1469-0691.2008.02198.x.

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COLE, CHARLES J., und PHILIPPE J. R. KOK. „A New Species of Gekkonid Lizard (Sphaerodactylinae: Gonatodes) from Guyana, South America“. American Museum Novitates 3524, Nr. 1 (2006): 1. http://dx.doi.org/10.1206/0003-0082(2006)3524[1:ansogl]2.0.co;2.

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Lowe-McConnell, Rosemary H. „BIOLOGY OF THE IMMIGRANT CATTLE EGRET ARDEOLA IBIS IN GUYANA, SOUTH AMERICA“. Ibis 109, Nr. 2 (03.04.2008): 168–79. http://dx.doi.org/10.1111/j.1474-919x.1967.tb00416.x.

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Oyedotun, Temitope D. Timothy, und Linda Johnson Bhola. „Shoreline change identification and analysis along the coast of Guyana, South America“. Interdisciplinary Environmental Review 20, Nr. 1 (2019): 7. http://dx.doi.org/10.1504/ier.2019.098348.

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Johnson Bhola, Linda, und Temitope D. Timothy Oyedotun. „Shoreline change identification and analysis along the coast of Guyana, South America“. Interdisciplinary Environmental Review 20, Nr. 1 (2019): 7. http://dx.doi.org/10.1504/ier.2019.10019703.

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Redden, Karen M. „A new species of Paloue (Leguminosae: Caesalpinioideae: Detarieae) from Guyana, South America“. Brittonia 60, Nr. 3 (September 2008): 257–60. http://dx.doi.org/10.1007/s12228-008-9037-9.

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Smith, Rachel R., und Andrew Edward Z. Short. „Review of the genus Chasmogenus Sharp, 1882 of northeastern South America with an emphasis on Venezuela, Suriname, and Guyana (Coleoptera, Hydrophilidae, Acidocerinae)“. ZooKeys 934 (19.05.2020): 25–79. http://dx.doi.org/10.3897/zookeys.934.49359.

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The water scavenger beetle genus Chasmogenus Sharp, 1882 is reviewed in northeastern South America using an integrative approach that combines adult morphology and molecular data from the gene cytochrome c oxidase I (COI). Eighteen new species are described: Chasmogenus acuminatussp. nov. (Brazil, French Guiana, Guyana, Suriname), C. ampliussp. nov. (Venezuela), C. berbicensissp. nov. (Guyana), C. brownsbergensissp. nov. (Suriname), C. castaneussp. nov. (Venezuela), C. clavijoisp. nov. (Venezuela), C. cuspifersp. nov. (Venezuela), C. flavomarginatussp. nov. (Venezuela), C. gatosp. nov. (Venezuela), C. guianensissp. nov. (Suriname, Guyana), C. ignotussp. nov. (Brazil), C. ligulatussp. nov. (Suriname), C. lineatussp. nov. (Venezuela), C. pandussp. nov. (Brazil, French Guiana, Suriname), C. schmitssp. nov. (Suriname), C. sinnamarensissp. nov. (French Guiana), C. tafelbergensissp. nov. (Suriname), and C. undulatussp. nov. (Guyana). We found genetic support for an additional new species in Guyana which is currently only known from females that we refer to as Chasmogenus sp. C. We examined the holotypes of the four species previously known from the region, and found that C. occidentalis García syn. nov. and C. yukparum García syn. nov. are conspecific with C. bariorum García, 2000 and are synonymized with that species, which is here redescribed. We redescribe C. australis García and expand the range of this species to include northern Brazil, Guyana, and French Guiana. All species are aquatic, with most being associated with forested streams and forest pools. Of the 21 species, more than half (11) are only known from a single locality indicating the genus may have many more micro-endemic species yet to be discovered in the region. Characters of the male genitalia are essential for confirming the identity of some species, consequently it is not always possible to make positive identifications of unassociated female specimens based on morphology alone. Habitus images are provided as well as a revised key to the genus for northeastern South America.

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Schultz, M., B. Büdel und S. Porembski. „Thyrea Porphyrella, a new Species of the Lichinaceae from inselbergs in tropical South America“. Lichenologist 33, Nr. 3 (Mai 2001): 211–14. http://dx.doi.org/10.1006/lich.2000.0317.

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AbstractThe new species Thyrea porphyrella Schultz, Büdel & Porembski, in the Lichinaceae, is described from tropical South America. It grows on granite inselbergs in SE Brazil and in southern Guyana. Diagnostic characters are the very thin, superficially smooth but conspicuously uneven to folded thallus lobes of reddish-brown to crimson colour.

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CUMBERLIDGE, NEIL. „A new species of freshwater crab of the genus Microthelphusa (Brachyura: Pseudothelphusidae) from a remote isolated cloud forest on a tabletop mountain in western Guyana, South America“. Zootaxa 1447, Nr. 1 (12.04.2007): 57–62. http://dx.doi.org/10.11646/zootaxa.1447.1.4.

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A new species of freshwater crab of the genus Microthelphusa Pretzmann, 1968, from Guyana, South America is described. Microthelphusa meansi, new species, was collected from a remote isolated cloud forest in the Wokomung Massif, a tabletop mountain (tepui) in western Guyana at over 1,000 m above sea level. The conspicuous horseshoe-like marginal lobe and the dome-like auxiliar cephalic lobe of the first gonopod clearly distinguish this species from all 12 congeners.

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Hinchliff, C. E., S. Petersen und E. H. Roalson. „Eleocharis endounifascis: A new species of Eleocharis subgenus Limnochloa (Cyperaceae) from northern South America“. Phytotaxa 7, Nr. 1 (29.05.2013): 19–24. http://dx.doi.org/10.11646/phytotaxa.7.1.2.

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A new species, Eleocharis endounifascis, is described and illustrated. This species inhabits standing water in disturbed, open habitats, occurring among a mosaic of wet forest, and probably also flourishes in sunny, seasonally inundated wetlands from Belize to southeastern Venezuela and Guyana to Brazil. It was previously confused with Eleocharis interstincta in herbarium collections and floristic works.

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Callegari-Jacques, S. M., F. M. Salzano, T. A. Weimer, M. H. L. P. Franco, M. A. Mestriner, M. H. Hutz und L. Schüler. „The Wai Wai Indians of South America: history and genetics“. Annals of Human Biology 23, Nr. 3 (Januar 1996): 189–201. http://dx.doi.org/10.1080/03014469600004422.

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Heath, Dwight B., und James S. Olson. „The Indians of Central and South America: An Ethnohistorical Dictionary“. Ethnohistory 40, Nr. 1 (1993): 151. http://dx.doi.org/10.2307/482187.

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Tedeschi, Michael, Steffen G. Hagemann, Malcolm P. Roberts und Noreen J. Evans. „The Karouni Gold Deposit, Guyana, South America: Part II. Hydrothermal Alteration and Mineralization“. Economic Geology 113, Nr. 8 (01.12.2018): 1705–32. http://dx.doi.org/10.5382/econgeo.2018.4610.

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Jindal, RM, R. Soni, K. Mehta und TG Patel. „Incidence of diabetes and hypertension in indigenous Amerindian village in Guyana, South America“. Indian Journal of Nephrology 26, Nr. 5 (2016): 389. http://dx.doi.org/10.4103/0971-4065.181471.

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BONILLA, J. ALFREDO, LLOYD VALIDUM, RUDOLPH CUMMINGS und CAROL J. PALMER. „GENETIC DIVERSITY OF PLASMODIUM VIVAX PVCSP AND PVMSP 1 IN GUYANA, SOUTH AMERICA“. American Journal of Tropical Medicine and Hygiene 75, Nr. 5 (01.11.2006): 830–35. http://dx.doi.org/10.4269/ajtmh.2006.75.830.

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35

Chale, Francis M. M. „Litter production in an Avicennia Gerrninans (L.) stearn forest in Guyana, South America“. Hydrobiologia 330, Nr. 1 (August 1996): 47–53. http://dx.doi.org/10.1007/bf00020822.

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KOK, PHILIPPE J. R. „A new snake of the genus Atractus Wagler, 1828 (Reptilia: Squamata: Colubridae) from Kaieteur National Park, Guyana, northeastern South America“. Zootaxa 1378, Nr. 1 (11.12.2006): 19. http://dx.doi.org/10.11646/zootaxa.1378.1.2.

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A new colubrid snake of the genus Atractus Wagler 1828 is described from Kaieteur National Park, west-central Guyana. The new species differs from all other congeners by the combination of two postoculars, 15 dorsal scale rows, eight supralabials, seven to eight infralabials, loreal much longer than high, six maxillary teeth, and a color pattern consisting of irregular red or pale red markings, sometimes forming an incomplete broken dorsolateral stripe, on a medium brown to brownish black ground color, and heavy brownish black mottling on a yellowish cream venter. A key to the species of the genus Atractus from Guyana is provided.

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CONSTANTINO, REGINALDO. „A revised and geo-referenced list of type localities for termites in South America“. Zootaxa 4638, Nr. 3 (17.07.2019): 389–409. http://dx.doi.org/10.11646/zootaxa.4638.3.5.

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A revised, geo-referenced, and cross-referenced list of 270 termite type localities in South America is presented. A total of 543 nominal species-group extant taxa are listed, 442 of them valid and 97 synonyms. The type-locality comprising the greatest number of nominal taxa in South America is Kartabo, Guyana (A.E. Emerson study site), with 59 taxa, followed by Cuiabá, Brazil (F. Sivestri), with 34, and Ribeirão Cascalheira, Brazil (Xavantina-Cachimbo Expedition, A.G.A. Mathews) with 26.

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Stauffer Viveros, Raquel, und Alexandre Salino. „Two new species of Ctenitis (Dryopteridaceae) from South America and taxonomic notes on similar species“. Phytotaxa 239, Nr. 1 (18.12.2015): 1. http://dx.doi.org/10.11646/phytotaxa.239.1.1.

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Two new species of Ctenitis (Dryopteridaceae) from South America are described and illustrated: Ctenitis christensenii is endemic to southeastern Brazil and C. glandulosa occurs from southeastern to northeastern Brazil and in Guyana. An identification key and notes about the distribution, habitat and taxonomy of the new species, C. falciculata and allies are provided. Moreover, seven lectotypifications and two new synonyms are proposed.

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Panelli, Luis Fernando. „Is Guyana a new oil El Dorado?“ Journal of World Energy Law & Business 12, Nr. 5 (01.10.2019): 365–68. http://dx.doi.org/10.1093/jwelb/jwz022.

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Abstract The Co-operative Republic of Guyana has become one of the most interesting and dynamic oil producing countries in the world at the start of the 21st century. The country already holds 5 billion barrels of proved reserves, which will certainly grow with new discoveries. Exxon leads a consortium of four companies that have the concession of the Stabroek Block (Liza Field), where nine discoveries have been made so far. Five FPSOs will be operating in the future, one of which is due to arrive in Guyana before the end of 2019 and another is due for 2020. By then, the country will be producing 340,000 barrels a day. This production will double and then reach 1 million barrels a day before the end of the next decade. The challenges and opportunities regarding the Guyanese people are dire. The lack of proper infrastructure is certainly one of the biggest challenges. But it is important to stress that the oil proceeds will transform Guyana into the highest GDP per capita of South America. The political stage is also analysed, since political instability might raise concerns for long-term investors. The Venezuela–Guyana differences regarding the sovereignty of the Essequibo Region are again a cause for concern. Brazil is a key player in supporting the geopolitical stability of South America. Presidential elections will be held in 2019/2020: the dispute will probably be between the current President Granger and the Opposition candidate Irfaan Ali. Guyana has a lot to profit from the wealth brought by oil exploitation, but its people fear the risk of growing corruption.

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Girón, Jennifer C., und Andrew Edward Z. Short. „Three additional new genera of acidocerine water scavenger beetles from the Guiana and Brazilian Shield regions of South America (Coleoptera, Hydrophilidae, Acidocerinae)“. ZooKeys 855 (13.06.2019): 109–54. http://dx.doi.org/10.3897/zookeys.855.33013.

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Recent study of the water scavenger beetle subfamily Acidocerinae in the Neotropical region has uncovered numerous undescribed species that are not able to be placed in existing genera. Here, we describe three new genera to accommodate 17 of these new species from South America: Aulonocharesgen. nov. for Aulonochareslingulatussp. nov. (French Guiana, Suriname), Aulonocharesnovoairensissp. nov. (Brazil), and Aulonocharestubulussp. nov. (Brazil, Guyana, Suriname, Venezuela); Ephydrolithusgen. nov. for Ephydrolithushamadaesp. nov. (Brazil), Ephydrolithusminorsp. nov. (Brazil), Ephydrolithusogmossp. nov. (Brazil), Ephydrolithusspiculatussp. nov. (Brazil), and Ephydrolithustelisp. nov. (Brazil); and Primocerusgen. nov. for Primoceruscuspidissp. nov. (Venezuela), Primocerusgigassp. nov. (Venezuela), Primocerusneutrumsp. nov. (Guyana, Suriname, Venezuela), Primocerusocellatussp. nov. (Venezuela), Primoceruspetilussp. nov. (Brazil), Primoceruspijiguaensesp. nov. (Venezuela), Primocerusmaipuresp. nov. (Venezuela), Primocerussemipubescenssp. nov. (Guyana), and Primocerusstriatolatussp. nov. (Suriname). The genus Ephydrolithusgen. nov. is currently known to be restricted to seepages in the mountainous regions of the Brazilian Shield. Aulonocharesgen. nov. and Primocerusgen. nov. are both currently only known from the Guiana Shield, though widespread in that region where they are associated with streams and seeps. We present differential diagnoses, maps, habitat details, and illustrations of all new genera and species here described.

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„Cerataphis lataniae. [Distribution map].“ Distribution Maps of Plant Pests, No.December (01.07.2007). http://dx.doi.org/10.1079/dmpp/20073255771.

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Abstract A new distribution map is provided for Cerataphis lataniae (Boisduval) Hemiptera: Aphididae. Hosts: mainly coconut (Cocos nucifera) and Latania spp. Information is given on the geographical distribution in Europe (Germany, Italy, Spain, Canary Islands, UK), Asia (China, Hainan, Hong Kong, India, Maharashtra, Indonesia, Java, Malaysia, Philippines, Taiwan), Africa (Burundi), North America (USA, California, Colorado, Florida, Hawaii, Indiana, New York, Ohio, South Dakota), Central America and Caribbean (Bermuda, Cuba, Dominican Republic, Jamaica, Montserrat, Puerto Rico, St Lucia, Trinidad and Tobago), South America (Brazil, Ceara, Sao Paulo, Colombia, French Guiana, Guyana), Oceania (Australia, New South Wales, Queensland, Federal States of Micronesia, Guam, Northern Mariana Islands, Solomon Islands).

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„Anastrepha obliqua. [Distribution map].“ Distribution Maps of Plant Pests, June (Revised) (01.08.1988). http://dx.doi.org/10.1079/dmpp/20046600090.

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Abstract A new distribution map is provided for Anastrepha obliqua (Macquart). Diptera: Tephritidae (West Indian fruit fly). Attacks many fruits, notably Spondias spp., mango, Eugenia spp., guava, passionfruit, rarely Citrus. Information is given on the geographical distribution in North America, USA, Florida, Texas, Central America and Caribbean, Belize, Bermuda, Costa Rica, Cuba, Dominica, Dominican Republic, Guadeloupe, Haiti, Jamaica, Marinique, Mexico, Montserrat, Nevis, Panama, Puerto Rico, St. Kitts, St. Lucia, Trinidad and Tobago, South America, Argentina, Brazil, Guyana, Colombia, Ecuador, Venezuela.

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„Pantoea stewartii. [Distribution map].“ Distribution Maps of Plant Diseases, No.April (01.08.2018). http://dx.doi.org/10.1079/dmpd/20183138507.

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Abstract A new distribution map is provided for Pantoea stewartii (Smith) Mergaert et al. Gammaproteobacteria: Enterobacteriales: Enterobacteriaceae. Hosts: sweetcorn and maize (Zea mays), recent reports on jackfruit (Artocarpus heterophyllus). Information is given on the geographical distribution in Europe (Italy, Poland), Asia (Indonesia, Java, Korea Republic, Malaysia, Peninsular Malaysia, Philippines, Thailand), Africa (Benin, Togo), North America (Canada, Ontario, Quebec, Mexico, Alabama, USA, Arkansas, California, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Mississippi, Missouri, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Vermont, Virginia, West Virginia, Wisconsin, Wyoming), Central America & Caribbean (Costa Rica, Puerto Rico), South America (Argentina, Bolivia, Guyana, Peru).

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„Pantoea stewartii. [Distribution map].“ Distribution Maps of Plant Diseases, No.April (01.08.2009). http://dx.doi.org/10.1079/dmpd/20093074276.

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Abstract A new distribution map is provided for Pantoea stewartii (Smith) Mergaert et al. Bacteria. Major hosts: maize (Zea mays), sweetcorn (Z. mays subsp. mays), teosinte (Z. mexicana). Information is given on the geographical distribution in Europe (Austria, Greece (Mainland Greece), Italy (Mainland Italy), Poland, Romania, Russia (European Russia)), Asia (China (Taiwan), India, Malaysia (Peninsular Malaysia), Thailand, Vietnam), North America (Canada (Alberta, British Columbia, Ontario, Quebec), Mexico, USA (Alabama, Arkansas, California, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Mississippi, Missouri, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Dakota, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Vermont, Virginia, Washington, West Virginia, Wisconsin)), Central America and Caribbean (Costa Rica, Puerto Rico, Trinidad and Tobago), South America (Bolivia, Guyana, Peru).

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„Colletotrichum dematium. [Distribution map].“ Distribution Maps of Plant Diseases, No.October (01.08.2006). http://dx.doi.org/10.1079/dmpd/20063191815.

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Abstract A new distribution map is provided for C. dematium (Pers.) Grove. Ascomycota: Sordariomycetidae. Hosts: Plurivorous. Information is given on the geographical distribution in Europe (Austria, Denmark, France, Germany, Greece, Malta, Poland, Romania, Spain, Sweden, Switzerland, UK), Asia (Bangladesh, China, Guangdong, Guangxi, Hong Kong, Shaanxi, India, Andhra Pradesh, Assam, Gujarat, Haryana, Himachal Pradesh, Jammu and Kashmir, Karnataka, Kerala, Madhya Pradesh, Maharashtra, Rajasthan, Tamil Nadu, Uttar Pradesh, West Bengal, Japan, Korea Republic, Laos, Malaysia, Sabah, Nepal, Pakistan, Singapore, Sri Lanka, Taiwan), Africa (Burkina Faso, Ethiopia, Kenya, Malawi, Mozambique, Niger, Nigeria, Senegal, Sierra Leone, South Africa, Tanzania, Zambia, Zimbabwe), North America (Canada, Alberta, British Columbia, Manitoba, Nova Scotia, Ontario, Quebec, Saskatchewan, USA, California, Colorado, Florida, Idaho, Illinois, Indiana, Iowa, Maryland, Massachusetts, Minnesota, Mississippi, Missouri, Nebraska, New York, North Carolina, Pennsylvania, South Carolina, Texas, Vermont, Virginia, Washington), Central America and Caribbean (Barbados, Cuba, El Salvador, Guatemala, Jamaica, Nicaragua, Panama, Puerto Rico, Trinidad and Tobago, United States, Virgin Islands), South America (Argentina, Brazil, Maranhao, Chile, Guyana, Peru, Venezuela), Oceania (American Samoa, Australia, New South Wales, Northern Territory, Tasmania, Victoria, Western Australia, Fiji, French Polynesia, Guam, Kiribati, New Caledonia, New Zealand, Niue, Papua New Guinea, Samoa, Solomon Islands, Vanuatu).

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Andrianova, T. V. „Cercospora carotae. [Descriptions of Fungi and Bacteria].“ IMI Descriptions of Fungi and Bacteria, Nr. 202 (01.07.2014). http://dx.doi.org/10.1079/dfb/20153006338.

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Abstract A description is provided for Cercospora carotae, a colonizer of leaves, and less frequently, other overground parts of cultivated carrot and other species of Daucus. Some information on its habitat, dispersal and transmission, and conservation status is given, along with details of its geographical distribution (Africa (Ghana, Kenya, Libya, Morocco, Somalia, South Africa, Zambia and Zimbabwe), North America (Canada (British Columbia, Nova Scotia, Quebec), Mexico and USA (California, Colorado, Connecticut, Florida, Iowa, Minnesota, Mississippi, Missouri, Nebraska, Oregon, South Dakota, Washington, West Virginia, Wisconsin)), Central America (El Salvador, Guatemala and Panama), South America (Argentina, Brazil (Distrito Federal, Rio Grande do Sul), Chile, Guyana and Venezuela), Asia (Afghanistan, Azerbaijan, China, Georgia, India (Jammu and Kashmir), Japan, Jordan, Nepal, Pakistan, South Korea and Taiwan), Australasia (Australia (New South Wales, Queensland, South Australia, Tasmania, Victoria, Western Australia) and New Zealand), Caribbean (American Virgin Islands, Antigua and Barbuda, Barbados, Cuba, Dominican Republic, Guadeloupe, Jamaica, Martinique, Puerto Rico, St Vincent and the Grenadines, and Trinidad and Tobago), Europe (Austria, Bulgaria, Denmark, Estonia, Germany, Hungary, Ireland, Italy, Latvia, Lithuania, Norway, Poland, Romania, Russia (Kabardino-Balkaria Republic, Stavropol krai, Republic of Tatarstan), Serbia, Slovakia, Spain, Sweden and UK) and Ukraine), Indian Ocean (Mauritius) and Pacific Ocean (Fiji, French Polynesia, New Caledonia, Tonga and USA (Hawaii)) and hosts.

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„Liriomyza trifolii. [Distribution map].“ Distribution Maps of Plant Pests, Nr. 2nd revision) (01.07.1997). http://dx.doi.org/10.1079/dmpp/20066600450.

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Abstract A new distribution map is provided for Liriomyza trifolii (Burgess) Diptera: Agromyzidae Highly polyphagous, attacking many ornamental and vegetable crops. Information is given on the geographical distribution in EUROPE, Austria, Belgium, Bulgaria, Croatia, Czech Republic, Denmark, Finland, France, Mainland France, Germany, Hungary, Ireland, Italy, Mainland Italy, Sardinia, Sicily, Malta, Netherlands, Norway, Poland, Portugal, Mainland Portugal, Romania, Russia, Central Russia, Southern Russia, Slovakia, Slovenia, Spain, Canary Islands, Mainland Spain, Sweden, Switzerland, UK, England and Wales, Yugoslavia (Fed. Rep), ASIA, China, Fujian, Cyprus, India, Andhra Pradesh, Delhi, Gujarat, Karnataka, Madhya Pradesh, Maharashtra, Orissa, Punjab, Tamil Nadu, Israel, Japan, Honshu, Kyushu, Korea Republic, Lebanon, Philippines, Taiwan, Turkey, Yemen, AFRICA, Benin, Cote d'Ivoire, Egypt, Ethiopia, Guinea, Kenya, Madagascar, Mauritius, Mayotte, Nigeria, Reunion, Senegal, South Africa, Sudan, Tanzania, Tunisia, Zambia, Zimbabwe, NORTH AMERICA, Canada, Alberta, Nova Scotia, Ontario, Quebec, USA, Arizona, California, Delaware, District of Columbia, Florida, Hawaii, Indiana, Iowa, Maryland, Massachusetts, Michigan, New Jersey, New Mexico, Ohio, Pennsylvania, South Carolina, Texas, Washington, Wisconsin, CENTRAL AMERICA & CARIBBEAN, Bahamas, Barbados, Bermuda, Costa Rica, Cuba, Dominican Republic, Guadeloupe, Guatemala, Martinique, Trinidad and Tobago, SOUTH AMERICA, Brazil, Minas Gerais, Pernambuco, Sao Paulo, Colombia, French Guiana, Guyana, Peru, Venezuela, OCEANIA, American Samoa, Australia, New South Wales, Victoria, Fed States of Micronesia, Guam, Northern Mariana Islands, Samoa, Tonga.

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„Nemorimyza maculosa. [Distribution map].“ Distribution Maps of Plant Pests, June (01.08.2021). http://dx.doi.org/10.1079/dmpp/20210280695.

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Abstract A new distribution map is provided for Nemorimyza maculosa (Malloch). Diptera: Agromyzidae. Hosts: Chrysanthemum, lettuce (Lactuca sativa) and other Asteraceae. Information is given on the geographical distribution in Europe (Portugal, Madeira, Spain, Canary islands), North America (Antigua and Barbuda, Bahamas, Barbados, Bermuda, Canada, Ontario, Cayman Islands, Costa Rica, Martinique, Mexico, Saint Kitts and Nevis, Trinidad and Tobago, United States, California, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Indiana, Kentucky, Massachusetts, Mississippi, New York, North Carolina, Ohio, Oklahoma, Wisconsin), South America (Argentina, Bolivia, Brazil, Para, Pernambuco, Sao Paulo, Chile, Easter Island, Colombia, French Guiana, Guyana, Peru, Uruguay, Venezuela).

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„Maconellicoccus hirsutus. [Distribution map].“ Distribution Maps of Plant Pests, No.June (01.07.2015). http://dx.doi.org/10.1079/dmpp/20153229063.

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Abstract A new distribution map is provided for Maconellicoccus hirsutus (Green). Hemiptera: Pseudococcidae. Hosts: Polyphagous. Information is given on the geographical distribution in Europe (Cyprus), Asia (Bangladesh, Brunei Darussalam, Cambodia, China, Guangdong, Hong Kong, Macau, Shanxi, Tibet, Yunnan, India, Andaman and Nicobar Islands, Andhra Pradesh, Assam, Bihar, Delhi, Gujarat, Karnataka, Kerala, Madhya Pradesh, Maharashtra, Odisha, Indian Punjab, Tamil Nadu, Tripura, Uttar Pradesh, West Bengal, Indonesia, Irian Jaya, Java, Nusa Tenggara, Sulawesi, Sumatra, Iran, Japan, Ryukyu Archipelago, Jordan, Laos, Lebanon, Malaysia, Peninsular Malaysia, Maldives, Myanmar, Nepal, Oman, Pakistan, Philippines, Saudi Arabia, Singapore, Sri Lanka, Taiwan, Thailand, United Arab Emirates, Vietnam and Yemen), Africa (Benin, Burkina Faso, Cameroon, Central African Republic, Chad, Congo, Congo Democratic Republic, Cote d'Ivore, Egypt, Gabon, Gambia, Kenya, Liberia, Niger, Nigeria, Reunion, Senegal, Seychelles, Somalia, Sudan, Tanzania and Tunisia), North America (Mexico, USA, California, Florida and Hawaii), Central America and Caribbean (Antigua and Barbuda, Bahamas, Barbados, Belize, British Virgin Islands, Cayman Islands, Costa Rica, Dominica, Grenada, Guadeloupe, Haiti, Jamaica, Martinique, Montserrat, Netherlands Antilles, Puerto Rico, Saint Kitts and Nevis, Saint Lucia, Saint Vincent and the Grenadines, Trinidad and Tobago and United States Virgin Islands), South America (Brazil, Alagoas, Bahia, Espirito Santo, Roraima, Colombia, French Guyana, Guyana, Suriname and Venezuela) and Oceania (Australia, Northern Territory, Queensland, South Australia, Western Australia, Federated States of Micronesia, Fiji, Guam, Northern Mariana Islands, Palau, Papua New Guinea, Samoa, Solomon Islands, Tonga, Tuvalu and Vanuatu).

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„Pestalotiopsis palmarum. [Distribution map].“ Distribution Maps of Plant Diseases, No.April (01.08.2017). http://dx.doi.org/10.1079/dmpd/20173134798.

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Annotation:

Abstract A new distribution map is provided for Pestalotiopsis palmarum (Cooke) Steyaert. Sordariomycetes: Amphisphaeriales: Pestalotiopsidaceae. Hosts: Palmae, especially coconut (Cocos nucifera) and oilpalm (Elaeis guineensis). Information is given on the geographical distribution in Europe (Cyprus, Italy, Sicily and Ukraine), Asia (Bangladesh, Brunei Darussalam, Cambodia, British Indian Ocean Territory, China, Guangdong, Hainan, Hong Kong, India, Andaman and Nicobar Islands, Andhra Pradesh, Assam, Bihar, Gujarat, Karnataka, Kerala, Madhya Pradesh, Maharashtra, Odisha, Rajasthan, Tamil Nadu, Uttar Pradesh, West Bengal, Indonesia, Japan, Korea Republic, Laos, Malaysia, Sabah, Sarawak, Maldives, Myanmar, Pakistan, Philippines, Sri Lanka, Taiwan, Thailand and Vietnam), Africa (Benin, Congo, Cote d'Ivoire, Egypt, Ghana, Guinea, Kenya, Madagascar, Malawi, Mauritius, Morocco, Mozambique, Nigeria, Senegal, Seychelles, Sierra Leone, South Africa, Tanzania, Togo, Uganda and Zambia), North America (Mexico, USA, California, Florida and South Carolina), Central America and Caribbean (Barbados, Bermuda, Cayman Islands, Cuba, Dominica, Dominican Republic, El Salvador, Haiti, Honduras, Jamaica, Panama, Puerto Rico, Trinidad and Tobago and United States Virgin Islands), South America (Argentina, Brazil, Bahia, Ceara, Paraiba, Pernambuco, Sergipe, Colombia, Guyana, Suriname and Venezuela) and Oceania (American Samoa, Australia, Northern Territory, Queensland, Victoria, Western Australia, Fiji, French Polynesia, Kiribati, Marshall Islands, New Caledonia, New Zealand, Niue, Papua New Guinea, Samoa, Solomon Islands, Tonga, Tuvalu, Vanuatu and Wallis and Futuna).

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