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    <title>UC Research Repository Collection:</title>
    <link>http://hdl.handle.net/10092/24</link>
    <description />
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        <rdf:li rdf:resource="http://hdl.handle.net/10092/7741" />
        <rdf:li rdf:resource="http://hdl.handle.net/10092/7715" />
        <rdf:li rdf:resource="http://hdl.handle.net/10092/7379" />
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    <dc:date>2013-05-22T04:07:22Z</dc:date>
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  <item rdf:about="http://hdl.handle.net/10092/7741">
    <title>Changing epidemiological trends of legionellosis in New  Zealand, 1979-2009</title>
    <link>http://hdl.handle.net/10092/7741</link>
    <description>Title: Changing epidemiological trends of legionellosis in New  Zealand, 1979-2009
Authors: Graham, F.F.; White, P.S.; Harte, D.J.G.; Kingham, S.P.
Abstract: This study evaluated the spatio-temporal variation of Legionella spp. in New Zealand using&#xD;
notification and laboratory surveillance data from 1979 to 2009 and analysed the epidemiological&#xD;
trends. To achieve this we focused on changing incidence rates and occurrence of different species&#xD;
over this time. We also examined whether demographic characteristics such as ethnicity may be&#xD;
related to incidence. The annual incidence rate for laboratory-proven cases was 2.5/100 000 and&#xD;
1.4/100 000 for notified cases. Incidence was highest in the European population and showed&#xD;
large geographical variations between 21 District Health Boards. An important finding of this&#xD;
study is that the predominant Legionella species causing disease in New Zealand differs from that&#xD;
found in other developed countries, with about 30–50% of cases due to L. longbeachae and a&#xD;
similar percentage due to L. pneumophila for any given year. The environmental risk exposure&#xD;
was identified in 420 (52%) cases, of which 58% were attributed to contact with compost; travel&#xD;
was much less significant as a risk factor (6.5%). This suggests that legionellosis has a distinctive&#xD;
epidemiological pattern in New Zealand.</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10092/7715">
    <title>Adaptive evolution by recombination is not associated with increased mutation rates in Maize streak virus</title>
    <link>http://hdl.handle.net/10092/7715</link>
    <description>Title: Adaptive evolution by recombination is not associated with increased mutation rates in Maize streak virus
Authors: Monjane, A.L.; Pande, D.; Lakay, F.; Shepherd, D.N.; van der Walt, E.; Lefeurve, P.; Lett, J-M.; Varsani, A.; Rybicki, E.P.; Martin, D.P.
Abstract: Background&#xD;
Single-stranded (ss) DNA viruses in the family Geminiviridae are proving to be very useful&#xD;
in real-time evolution studies. The high mutation rate of geminiviruses and other ssDNA&#xD;
viruses is somewhat mysterious in that their DNA genomes are replicated in host nuclei by&#xD;
high fidelity host polymerases. Although strand specific mutation biases observed in virus&#xD;
species from the geminivirus genus Mastrevirus indicate that the high mutation rates in&#xD;
viruses in this genus may be due to mutational processes that operate specifically on ssDNA,&#xD;
it is currently unknown whether viruses from other genera display similar strand specific&#xD;
mutation biases. Also, geminivirus genomes frequently recombine with one another and an&#xD;
alternative cause of their high mutation rates could be that the recombination process is either&#xD;
directly mutagenic or produces a selective environment in which the survival of mutants is&#xD;
favoured. To investigate whether there is an association between recombination and increased&#xD;
basal mutation rates or increased degrees of selection favoring the survival of mutations, we&#xD;
compared the mutation dynamics of the MSV-MatA and MSV-VW field isolates of Maize&#xD;
streak virus (MSV; Mastrevirus), with both a laboratory constructed MSV recombinant, and&#xD;
MSV recombinants closely resembling MSV-MatA. To determine whether strand specific&#xD;
mutation biases are a general characteristic of geminivirus evolution we compared mutation&#xD;
spectra arising during these MSV experiments with those arising during similar experiments&#xD;
involving the geminivirus Tomato yellow leaf curl virus (Begomovirus genus).&#xD;
Results&#xD;
Although both the genomic distribution of mutations and the occurrence of various&#xD;
convergent mutations at specific genomic sites indicated that either mutation hotspots or&#xD;
selection for adaptive mutations might elevate observed mutation rates in MSV, we found no&#xD;
association between recombination and mutation rates. Importantly, when comparing the&#xD;
mutation spectra of MSV and TYLCV we observed similar strand specific mutation biases&#xD;
arising predominantly from imbalances in the complementary mutations G → T: C → A. Conclusions&#xD;
While our results suggest that recombination does not strongly influence mutation rates in&#xD;
MSV, they indicate that high geminivirus mutation rates are at least partially attributable to&#xD;
increased susceptibility of all geminivirus genomes to oxidative damage while in a single&#xD;
stranded state.</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10092/7379">
    <title>Single-Pulse Pulsed Laser Polymerization–Electron Paramagnetic Resonance Investigations into the Termination Kinetics of n-Butyl Acrylate Macromonomers</title>
    <link>http://hdl.handle.net/10092/7379</link>
    <description>Title: Single-Pulse Pulsed Laser Polymerization–Electron Paramagnetic Resonance Investigations into the Termination Kinetics of n-Butyl Acrylate Macromonomers
Authors: Barth, J.; Buback, M.; Barner-Kowollik, C.; Junkers, T.; Russell, G.T.
Abstract: The termination of model mid-chain radicals (MCRs), which mimic radicals that occur in&#xD;
acrylate polymerization over a broad range of reaction conditions, has been studied by singlepulse&#xD;
pulsed-laser polymerization (SP PLP) in conjunction with electron paramagnetic&#xD;
resonance (EPR) spectroscopy. The model radicals were generated by initiator-fragment&#xD;
addition to acrylic macromonomers that were preformed prior to the kinetic experiments, thus&#xD;
enabling separation of termination from the propagation reaction, for these model radicals&#xD;
propagate sparingly, if at all, on the timescale of SP-PLP experiments. Termination rate&#xD;
coefficients of the MCRs were determined in the temperature range 0–60 °C in acetonitrile&#xD;
and butyl propionate solution as well as in bulk macromonomer over 0–100 °C. Termination&#xD;
rate coefficients slightly below those of the corresponding secondary radicals were deduced,&#xD;
demonstrating the relatively high termination activity of this species, even when undergoing MCR-MCR termination. For chain length 10, a reduction by a factor of 6 is observed.&#xD;
Unusually high activation energies were found for the termination rate coefficient in these&#xD;
systems, with 35 kJ mol⁻¹ being determined for bulk macromonomer.
Description: The definitive version is available at www3.interscience.wiley.com</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10092/7350">
    <title>Determining the order of a molecular point group</title>
    <link>http://hdl.handle.net/10092/7350</link>
    <description>Title: Determining the order of a molecular point group
Authors: Williamson, B.E.
Abstract: Conventional methods of identifying the point group of a molecule require skills in finding symmetry elements and&#xD;
operations. A useful aid to error checking is an ability to determine the order of a group purely from its label. To this&#xD;
end, Curnow has promulgated a set of simple empirical rules. In this article, Curnow’s rules are substantiated using&#xD;
simple geometric considerations from the basis of point group generators. The proof is provided in a form that will be&#xD;
accessible to undergraduate chemistry students and their teachers</description>
    <dc:date>2011-01-01T00:00:00Z</dc:date>
  </item>
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