Academic literature on the topic 'Primers, Mohawk'

<em>Abstract</em>.—The striped bass <em>Morone saxatilis </em>was introduced into the lower Colorado River in the late 1950s and into Lake Mead, Nevada and Arizona, in the late 1960s. The unintended immigration of striped bass into Lake Mohave, Nevada and Arizona, on the main stem, and Lake Pleasant, a tributary reservoir in central Arizona, has resulted in changing management practices. Striped bass entered Lake Mohave via downstream emigration from Lake Mead through Hoover Dam at various life stages, and the newly established population quickly became the primary sport fish in the reservoir. Predation from the striped bass population in Lake Mohave coincided with elimination of threadfin shad <em>Dorosoma petenense </em>and a rapid decline in the survival of stocked rainbow trout <em>Oncorhynchus mykiss</em>. Striped bass are also believed to be hindering ongoing efforts to reestablish the native endangered species razorback sucker <em>Xyrauchen texanus </em>and bonytail chub <em>Gila elegans</em>. Striped bass gained access to Lake Pleasant via Lake Havasu, California and Arizona, by way of the Central Arizona Project (CAP) Canal. Operation of the CAP Canal began in 1985 and the canal was fully connected to Lake Pleasant in 1992. In 1986 and 1989, striped bass population densities in the CAP Canal were estimated at 70 ± 37 fish/ha and 3 ± 1 fish/ha, respectively. Striped bass were first captured in Lake Pleasant in 1998 during a gill-netting survey. Catch per unit effort increased almost yearly from 0.13 fish/net-night in 1998 to 6.74 fish/net-night in 2005. Since their unintended introduction into both reservoirs, striped bass have established viable reproducing populations. Management efforts have emphasized promoting harvest and minimizing the impacts of striped bass on existing fisheries. These experiences provide guidance for evaluating unintended dispersion of striped bass elsewhere.

After tracing the early Christian presence in India and discussing the nature of the caste system, this chapter profiles individuals—well-known upper-caste nineteenth-century converts from Hinduism. As in China, the missionary presence in India was a necessary but not sufficient factor in Christianity’s spread. Missionaries initiated the first conversions, but within a generation or two, Indian Christians became the primary instruments for the spread of the gospel. Communication never flowed in one direction, from missionary to Indians. Increasingly, Indians converted on their own terms and adapted Christianity to meet their own particular concerns and to indigenize their faith by separating Christ from the trappings of Western, colonial Christianity. Converts discussed include Krishna Mohan Banerjea, Baba Padmanjee, Krishna Pillai, Narayan Vaman Tilak, Pandita Ramabai, and Brahmabandhab Upadhyay.

The chapter considers the scope of film to act as what is described as a ‘docu-drama-ment’ for conveying affective engagements with political history. It does so with a focus on unique incidents in the history of Indian popular cinema with the example of the film, Aman (Mohan Kumar, 1967). The discussion centers on the cameo appearance of a British philosopher, Bertrand Russell, in the film along with phantasmal invocations of Indian anti-nuclear weapons protagonists such as India’s first prime minister, Jawaharlal Nehru, and reproductions of the 1945 atomic attack in Hiroshima and subsequent nuclear tests in the Pacific. The chapter considers how the film may be viewed in terms of a ‘corporeal compound lens’ on the political vicissitudes of the 1960s. With such an approach – on the one hand to do with the assemblage of a historical film, and on the other, to do with the way this intersects with compound lines of reflexive reception – the author shows how the ‘docu-drama-ment’ moves away from linear equations of the filmic signifier with the signified - or the film and the represented - to one that revels in affective residues and resonances that are a constitutive force in socio-political realities of the Cold War era.

Bekington Myrboh of North-Eastern Hill University reported (Tetrahedron Lett. 2010, 51, 2862) a convenient procedure for the oxidative removal of a 1,3-oxathiolane 1 or a 1,3-dithiolane. Sang-Gyeong Lee and Yong-Jin Yoon of Gyeongsang National University developed (J. Org. Chem. 2010, 75, 484) the pyridazin-3(2H )-one 4 for the microwave-mediated deprotection of an oxime 3. Dario M. Bassani of Université Bordeaux 1 and John S. Snaith of the University of Birmingham devised (J. Org. Chem. 2010, 75, 4648) a procedure for the facile preparation of esters such as 6. Brief photolysis (350 nm) returned the parent carboxylic acid 7. Craig M. Williams of the University of Queensland prepared (Tetrahedron Lett. 2010, 51, 1158) the trithioorthoester 8 by iterative opening of epichlorohydrin. He found that the keto ester 9 could be efficiently released by Hg-mediated hydrolysis. Masatoshi Mihara of the Osaka Municipal Technical Research Institute established (Synlett 2010, 253) that even very congested alcohols such as 10 could be acetylated by acetic anhydride containing a trace of FeCl3. Colleen N. Scott, now at Southern Illinois University, developed (J. Org. Chem. 2010, 75, 253) a convenient procedure for the preparation of the hydridosilane 13, which on Mn catalysis added the alcohol 12 to make the unsymmetrical bisalkoxysilane 14. Sabine Berteina-Raboin of the Université d’Orléans found (Tetrahedron Lett. 2010, 51, 2115) that NaBH4 in EtOH cleanly removed the chloroacetates from 15. Both other esters and silyl ethers were stable under these conditions. Ram S. Mohan of Illinois Wesleyan University established (Tetrahedron Lett. 2010, 51, 1056) that Fe(III) tosylate in methanol selectively removed the alkyl silyl ether from 17 without affecting the aryl silyl ether. Alakananda Hajra and Adinath Majee of Visva-Bharati University effected (Tetrahedron Lett. 2010, 51, 2896) formylation of an amine 19 by heating with commercial 85% formic acid as the solvent in a sealed tube at 80°C. Although both primary and secondary amines could be effi ciently formylated, the primary amines were much more reactive. Doo Ok Jang of Yonsei University found (Tetrahedron Lett. 2010, 51, 683) that the conveniently handled CF3CCO2H (the acid chloride is a gas) could be activated in situ to selectively convert 22 into 24.