Decomposing Multi‐Level Ethnic Segregation in Auckland, New Zealand, 2001–2013: Segregation Intensity for Multiple Groups at Multiple Scales

There has been a growing appreciation that the processes generating urban residential segregation operate at multiple scales, stimulating innovations into the measurement of their outcomes. This paper applies a multi‐level modelling approach to that issue to the situation in Auckland, where multiple migration streams from both Pacific Island and Asian origins have created a complex multi‐ethnic city. We identify two distinct trends. For the larger ethnic groups segregation remained static despite rapid growth over a recent twelve‐year period. For the smaller groups growth has been combined with considerable change; they initially clustered in a few localities and areas within them but then experienced considerable reduction in the intensity of that segregation. By spatially decomposing the segregation levels, this paper extends our appreciation of its underpinning processes when they apply to migration streams that differ in their nature from those on which traditional residential location‐decision theory has been based.OLD Urban Renewal and Housin

The genomic organization of retrotransposons in Brassica oleracea

We have investigated the copy numbers and genomic organization of five representative reverse transcriptase domains from retrotransposons in Brassica oleracea. Two non-homologous Pseudoviridae (Ty1/copia-like) elements, two Metaviridae (Ty3/gypsy-like) elements (one related to the Athila family) and one Retroposinae (LINE) element were hybridized to a gridded BAC library, “BoB”. The results indicated that the individual LTR retrotransposons (copia and gypsy-like) were represented by between 90 and 320 copies in the haploid genome, with only evidence of a single location for the LINE. Sequence analysis of the same elements against genome survey sequence gave estimates of between 60 and 570, but no LINE was found. There was minimal evidence for clustering between any of these retroelements: only half the randomly expected number of BACs hybridized to both LTR-retrotransposon families. Fluorescent in situ hybridization showed that each of the retroelements had a characteristic genomic distribution. Our results suggest there are preferential sites and perhaps control mechanisms for the insertion or excision of different retrotransposon groups