19 research outputs found

    Nest Success and Duckling Survival of Greater Scaup, Aythya marila, at Grassy Island, New Brunswick

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    Nesting biology and duckling survival of Greater Scaup (Aythya marila) at Grassy Island on the Saint John River in southern New Brunswick were compared between 1995 and 1996. Grassy Island in New Brunswick is an area that is notably removed from other scaup breeding areas, being located farther south from main breeding areas in North America. The Mayfield estimates of nest success were 61% and 21% in 1995 and 1996, respectively. Mean daily survival rates were 0.99 in 1995 and 0.96 in 1996 and were significantly different (t = 4.86, P < 0.001). Duckling survival was estimated to range from 38 to 54% in 1995, and was 8% in 1996. The lower breeding success in 1996 may have been due to factors associated with decreased temperatures and increased precipitation, but the fact that the breeding location is atypical to other Greater Scaup breeding areas should not be overlooked

    The decarbonization of coal tar via microwave-initiated catalytic deep dehydrogenation

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    Coal tar, a major by-product of the coal industry, presents considerable difficulties in its refining and conversion into fuels due to its complex chemical composition and physical properties, such as high viscosity, corrosiveness, thermal instability, etc. Here we report a new route for producing hydrogen-rich gases together with carbonaceous materials, including carbon nanotubes, through the microwave-initiated catalytic deep dehydrogenation of coal tar using inexpensive iron catalysts. The resulting carbonaceous materials generated over the catalyst were investigated using a variety of techniques including scanning electron microscopy (SEM), transmission electron microscopy (TEM), temperature programmed oxidation (TPO) and Raman spectroscopy. Importantly, we have found that an aqueous emulsion feed of the coal tar enables considerably easier handling and an enhanced hydrogen production whilst also significantly reducing the extent of catalyst deactivation. This behaviour is shown to be assisted by the phenomenon of micro-explosion that enhances mass and heat transfer during the catalytic reactions

    C~48~H~51~CoN~3~P~3~S~3~

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    Greater Scaup, Aythya marila, Nest Site Characteristics on Grassy Island, New Brunswick

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    We studied Greater Scaup (Aythya marilla) nest site selection on Grassy Island, New Brunswick, during 1995 and 1996 by describing site selection in relation to habitat characteristics and association with larids using univariate comparisons. We pooled nesting data from both years and found that nesting sites were significantly closer to larid colonies and the edge of the patch of vegetation in which the nests were situated, had less forb canopy cover, more sedge cover, greater overhead concealment and lateral cover at 0–0.25 m, and less ground moisture than random sites. We evaluated Greater Scaup nests delimited as close to or far from larid colonies at 30 m and documented that nests closer to larid colonies were found in shorter vegetation that was closer to the edge of the patch of vegetation with less lateral cover at 0.25–0.5 m, but had greater overhead concealment than nests farther away. Advancements in the ecological understanding of the species, including habitat use patterns and species associations, will increase the likelihood of conservation successes

    SYNTHESES AND STRUCTURES OF [RE(SC(6)H(3)ME(2)-2,6)(3)(PPH(3))], [RE(SC(6)H(3)ME(2)-2,6)(3)(BU(T)NC)(2)], [RE(SC6H2PR3I-2,4,6)(3)L(PPH(3))] (L=N-2 OR CO) AND [REH4(PPH(3))(4)] [REO(SC6H2PR3I-2,4,6)(4)]

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    The hydride [ReH7(PPh(3))(2)] reacted with 2,6-dimethylbenzenethiol in toluene to give a complex of stoichiometry [Re(SC(6)H(3)Me(2)-2,6)(3)(PPh(3))] 1. A crystal structure showed a trigonal-bipyramidal geometry about the Re with Bn agostic interaction to a thiolate methyl occupying an apical site. trans to the PPh(3) ligand. Complex 1 reacts rapidly with MeCN to give the known [Re(SC(6)H(3)Me(2)-2,6)(3)(MeCN)(PPh(3))] 2 and with Bu(dagger)NC to form [Re(SC(6)H(3)Me(2)-2,6)(3)(Bu(t)NC)(2)]. 3 The crystal structure of 3 showed trigonal-pyramidal geometry about the Re with asymmetric co-ordination of the isocyanide ligands and an unusual configuration for the thiolate aromatic groups; The reactions of the hydrides [ReH7(PPh(3))(2)] and [ReH5(PPh(3))(3)] with 2,4,6-triisopropyl-. 2.6-dimethdxy-benzenethiol and tris(2-sulfanylphenyl)phosphine were also studied. With HSC6H2Pr3i-2,4,6 the dinitrogen complex [Re(SC6H2Pr3i-2,4,6)(3)(N-2)(PPh(3))] 4 was formed and its structure determined. The preparations and structures of the complexes [ReH4(PPh(3))(4)][ReO(SC6H2Pr3i-2,4,6)(4)], [Re{SC6H3(OMe)(2)-2,6}(3)(PPh(3))] and [Re{P(C6H4S-2)(3)}(PPh(3))] are also discussed. An alternative convenient route to [ReH4(PPh(3))(4)](+) from [ReH5(PPh(3))(3)] is presented
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