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Institution

Agriculture and Agri-Food Canada

FacilityOttawa, Ontario, Canada
About: Agriculture and Agri-Food Canada is a facility organization based out in Ottawa, Ontario, Canada. It is known for research contribution in the topics: Population & Soil water. The organization has 10921 authors who have published 21332 publications receiving 748193 citations. The organization is also known as: Department of Agriculture and Agri-Food.
Topics: Population, Soil water, Manure, Tillage, Loam


Papers
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Journal ArticleDOI
TL;DR: These markers will provide a solid basis for future efforts in genomic discovery, comparative mapping, and the generation of an oat consensus map, and provide new opportunities for directed breeding of superior oat varieties, and guidance in the maintenance of oat genetic diversity.
Abstract: Genomic discovery in oat and its application to oat improvement have been hindered by a lack of genetic markers common to different genetic maps, and by the difficulty of conducting whole-genome analysis using high-throughput markers. This study was intended to develop, characterize, and apply a large set of oat genetic markers based on Diversity Array Technology (DArT). Approximately 19,000 genomic clones were isolated from complexity-reduced genomic representations of pooled DNA samples from 60 oat varieties of global origin. These were screened on three discovery arrays, with more than 2000 polymorphic markers being identified for use in this study, and approximately 2700 potentially polymorphic markers being identified for use in future studies. DNA sequence was obtained for 2573 clones and assembled into a non-redundant set of 1770 contigs and singletons. Of these, 705 showed highly significant (Expectation < 10E-10) BLAST similarity to gene sequences in public databases. Based on marker scores in 80 recombinant inbred lines, 1010 new DArT markers were used to saturate and improve the 'Kanota' × 'Ogle' genetic map. DArT markers provided map coverage approximately equivalent to existing markers. After binning markers from similar clones, as well as those with 99% scoring similarity, a set of 1295 non-redundant markers was used to analyze genetic diversity in 182 accessions of cultivated oat of worldwide origin. Results of this analysis confirmed that major clusters of oat diversity are related to spring vs. winter type, and to the presence of major breeding programs within geographical regions. Secondary clusters revealed groups that were often related to known pedigree structure. These markers will provide a solid basis for future efforts in genomic discovery, comparative mapping, and the generation of an oat consensus map. They will also provide new opportunities for directed breeding of superior oat varieties, and guidance in the maintenance of oat genetic diversity.

155 citations

Journal ArticleDOI
TL;DR: The EST-SSRs developed herein represent the first large-scale development of SSR markers in flax and have potential to be used for the development of genetic and physical maps, quantitative trait loci mapping, genetic diversity studies, association mapping and fingerprinting cultivars for example.
Abstract: A set of 146,611 expressed sequence tags (ESTs) were generated from 10 flax cDNA libraries. After assembly, a total of 11,166 contigs and 11,896 singletons were mined for the presence of putative simple sequence repeats (SSRs) and yielded 806 (3.5%) non-redundant sequences which contained 851 putative SSRs. This is equivalent to one EST-SSR per 16.5 kb of sequence. Trinucleotide motifs were the most abundant (76.9%), followed by dinucleotides (13.9%). Tetra-, penta- and hexanucleotide motifs represented <10% of the SSRs identified. A total of 83 SSR motifs were identified. Motif (TTC/GAA)n was the most abundant (10.2%) followed by (CTT/AAG)n (8.7%), (TCT/AGA)n (8.6%), (CT/AG)n (6.7%) and (TC/GA)n (5.3%). A total of 662 primer pairs were designed, of which 610 primer pairs yielded amplicons in a set of 23 flax accessions. Polymorphism between the accessions was found for 248 primer pairs which detected a total of 275 EST-SSR loci. Two to seven alleles were detected per marker. The polymorphism information content value for these markers ranged from 0.08 to 0.82 and averaged 0.35. The 635 alleles detected by the 275 polymorphic EST-SSRs were used to study the genetic relationship of 23 flax accessions. Four major clusters and two singletons were observed. Sub-clusters within the main clusters correlated with the pedigree relationships amongst accessions. The EST-SSRs developed herein represent the first large-scale development of SSR markers in flax. They have potential to be used for the development of genetic and physical maps, quantitative trait loci mapping, genetic diversity studies, association mapping and fingerprinting cultivars for example.

155 citations

Journal ArticleDOI
TL;DR: Applying enzymes onto feeds before feeding was more effective than dosing directly into the artificial rumen for increasing ruminal fibrolytic activity.
Abstract: The effects of an exogenous enzyme preparation, the application method and feed type on ruminal fermentation and microbial protein synthesis were investigated using the rumen simulation technique (Rusitec). Steam-rolled barley grain and chopped alfalfa hay were sprayed with water (control, C), an enzyme preparation with a predominant xylanase activity (EF), or autoclaved enzyme (AEF) 24 h prior to feeding, or the enzyme was supplied in the buffer infused into the Rusitec (EI). Microbial N incorporation was measured using (15NH4)2SO4 in the buffer. Spent feed bags were pummelled mechanically in buffer to segregate the feed particle-associated (FPA) and feed particle-bound (FPB) bacterial fractions. Enzymes applied to feed reduced neutral-detergent fibre content, and increased the concentration of reducing sugars in barley grain, but not alfalfa hay. Ruminal cellulolytic bacteria were more numerous with EF than with C. Disappearance of DM from barley grain was higher with EF than with C, but alfalfa was unaffected by EF. Treatment EF increased incorporation of 15N into FPA and FPB fractions at 24 and 48 h. In contrast, AEF reduced the 24 h values, relative to C; AEF and C were similar at 48 h. Infused enzyme (EI) did not affect 15N incorporation. Xylanase activity in effluent was increased by EF and EI, compared to C, but not by AEF. Xylanase activity in FPA was higher at 48 h than at 24 h with all treatments; it was higher with EF than C at 24 and 48 h, but was not altered by AEF or EI. Applying enzymes onto feeds before feeding was more effective than dosing directly into the artificial rumen for increasing ruminal fibrolytic activity.

155 citations

Journal ArticleDOI
TL;DR: In this article, the proportions of recently deposited organic matter in water-stable macroaggregates were determined and the estimated half-life of the Cj-derived C of stable aggregates > 2 mm was 13 yr.
Abstract: Some suggest that young labile soil organic matter accumulates preferentially in water-stable macroaggregates (>250 um) where it acts as a transient binding agent We determined the proportions of recently deposited C ( 2 mm) than for smaller ones Assuming first-order kinetics, the estimated half-life of the Cj-derived C of stable aggregates >2 mm was 13 yr, which corresponds to that reported for macro organic matter in similar systems Analysis of water-stable macroaggregates under corn showed that they were enriched in recently deposited C relative to microaggregat es and to the whole soil, which partly compensated for their loss in Cj-C On average, 20% of the C in water-stable aggregates >1 mm was derived from corn whereas this value was down to 9% in the whole soil and 1% in the microaggregates The results of this study provide further quantitative evidence that slaking-resistant macroaggregates are enriched in, and probably stabilized by, recently deposited organic matter

155 citations

Journal ArticleDOI
TL;DR: Methods used for RNA extraction, DNA microarrays, real-time PCR, competitive RT-PCR, stable isotope probing and the use of reporter genes provide methods for detecting and quantifying gene expression.

155 citations


Authors

Showing all 10964 results

NameH-indexPapersCitations
Fereidoon Shahidi11995157796
Miao Liu11199359811
Xiang Li97147242301
Eviatar Nevo9584840066
Tim A. McAllister8586232409
Hubert Kolb8442025451
Daniel M. Weary8343722349
Karen A. Beauchemin8342322351
Nanthi Bolan8355031030
Oene Oenema8036123810
Santosh Kumar80119629391
Yueming Jiang7945220563
Denis A. Angers7625619321
Tong Zhu7247218205
Christophe Lacroix6935315860
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202314
202282
20211,078
20201,035
2019992
2018988