J. H. A. Barker
University of Bristol
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Featured researches published by J. H. A. Barker.
Molecular Ecology | 1997
H. Beismann; J. H. A. Barker; A. Karp; T. Speck
Amplified fragment length polymorphism (AFLP) analysis of 26 trees of three Salix taxa: Salix alba L. (White Willow), S. fragilis L. (Crack Willow) and their hybrid S. x rubens Schrank, across an example of their habitat range in south‐west Germany, supported the distribution previously determined using morphological characterization. UPGMA and principal coordinates analysis of the AFLP data revealed three distinct clusters corresponding to the three taxa. In addition, AFLP analysis on individuals which were difficult to identify morphologically revealed that they were either the hybrid S. x rubens or S. fragilis. Four specimens of S. fragilis were indistinguishable with three primer combinations suggesting they are members of one clone.
Molecular Ecology | 2001
J. M. Green; J. H. A. Barker; E. J. P. Marshall; R. J. Froud-Williams; N. C. B. Peters; G M Arnold; Kevin J. Dawson; A. Karp
Nine microsatellites were used to screen 131 samples of Barren Brome (Anisantha sterilis: synonym Bromus sterilis) collected from within the fields of three English farms [from Oxfordshire (Oxon), Leicestershire (Leics) and Wiltshire (Wilts)] and eight seeds taken from samples of each of 10 farms across England, UK. Most individuals (~97%) were homozygous. Polymorphism occurred at all nine loci in all three farms sampled at the field scale, and at most loci for nine of the other 10 farm samples. Between three and 11 alleles were found per locus. Gene diversity (D = 1 − ∑pi2) ranged from 0.088 to 0.760. Polymorphism occurred among individuals within and among fields, and farms. Some alleles were found in only one farm. On the basis of the alleles at all nine loci in the 211 sampled plants, a total of 92 (44%) different genotypes was identified. Clustering analysis using the unweighted pair group method with arithmetic averages (upgma) for the combined Oxon, Wilts and Leics samples did not cluster them into their respective farms. Similarly, a phenogram of samples from all 10 farms showed considerable mixing of individuals with respect to farm origins. Identification of genotypes on field plans showed evidence of both spatial localization and mixing. Previous reports have suggested that A. sterilis is strictly inbreeding with little intrapopulation variation at the genetic level. Our data reveal that A. sterilis exists as numerous separate and genetically different lines, which are maintained by inbreeding but which very occasionally outcross. Possible explanations for this pattern of high genetic diversity are discussed.
Theoretical and Applied Genetics | 2002
Kg Gilbert; S Garton; Ma Karam; G M Arnold; A. Karp; Keith J. Edwards; Dt Cooke; J. H. A. Barker
Abstract.Genetic diversity in 38 genotypes, representing 28 individual genotypes from five landraces of Isatis tinctoria (three German: Tubingen, Potsdam and Erfurt, one Swiss and one English), five genotypes of Isatis indigotica (Chinese woad) and five genotypes of Isatis glauca, were investigated using AFLP analysis. Five primer combinations detected a total of 502 fragments of which 436 (86.9%) were polymorphic. The level of polymorphism recorded within each species was 29.8, 86.9 and 35.8% for I. indigotica, I. tinctoria and I. glauca, respectively. Clearly, genetic diversity within I. tinctoria was greater than that observed in I. indigotica or I. glauca. Cluster analyses of the AFLP data using UPGMA and PCO revealed the complete separation of the genotypes of each species into distinct groups. I. indigotica separated as an entirely independent group, whereas I. glauca formed a separate cluster within the I. tinctoria group. Indeed, I. tinctoria and I. glauca are more closely related to each other than either is to I. indigotica. In addition, the genotypes of each landrace, apart from one from the English group, were clearly discriminated. However, the anomalous genotype did associate with the rest of its group when it was linked with the Erfurt group. These results provide new and useful information about the make-up of the Isatis genome, which has not previously been evaluated. They will be useful in the selection of plant material for variety development and conservation of the gene-pool.
Insect Molecular Biology | 2004
Jacqueline Batley; Keith J. Edwards; J. H. A. Barker; Kevin J. Dawson; Cw Wiltshire; Dm Glen; A. Karp
Phyllodecta (=Phratora) vulgatissima and P. vitellinae (Coleoptera: Chrysomelidae) are important pests of willows and poplars. Their differences in host species preference may provide a non‐chemical control strategy for pest control. However, little is known about population structure with respect to hosts, regions or seasons. Using five microsatellites, 850 P. vulgatissima and 1100 P. vitellinae individuals, comprising 17 and 22 UK samples, respectively, were genotyped. High diversity was observed at all loci. Migrant numbers exchanged per generation (Nm) were high (2.1–12.6 for P. vulgatissima and 0.9–12.2 for P. vitellinae), suggesting high genetic exchange between samples. Estimates of population differentiation (FST) and analyses of the data using Bayesian methods (Partition and Structure) showed little evidence of subdivision in relation to geography, sampling time or host.
BioTechniques | 1996
Keith J. Edwards; J. H. A. Barker; A. Daly; C.J. Jones; A. Karp
Theoretical and Applied Genetics | 2002
Steven J. Hanley; J. H. A. Barker; J. W. van Ooijen; C. Aldam; Sarah L. Harris; I. Åhman; S. Larsson; A. Karp
Genome | 1999
R.L. Rivera; Keith J. Edwards; J. H. A. Barker; G M Arnold; G. Ayad; T. Hodgkin; A. Karp
Molecular Ecology Notes | 2002
J. H. A. Barker; A Pahlich; S Trybush; Keith J. Edwards; A. Karp
Molecular Ecology | 2000
J. M. Green; Keith J. Edwards; Sarah Usher; J. H. A. Barker; E. J. P. Marshall; R. J. Froud-Williams; A. Karp
Molecular Ecology Notes | 2001
R. C. Brookes; J. H. A. Barker; David A. Bohan; Dm Glen; A. Karp