31 research outputs found

    Revisiting strategies for breeding anthracnose resistance in lentil: the case with wild species

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    Non-Peer ReviewedBreeders at the Crop Development Centre (CDC) have up to now only used germplasm resources available in the cultivated lentil to develop new varieties with resistance to diseases. Based on recent studies, the available cultivated germplasm does not offer sufficient genetic variation for resistance to anthracnose and ascochyta diseases. Lentil crop is attacked by two major diseases (anthracnose and ascochyta) that can cause 100% loss in the worst scenarios. Since anthracnose is only a major lentil disease in North America, no work has been done to improve resistance to this disease elsewhere. Wild species of many crops are known to carry many disease resistance genes lacking in the cultivated crop. We began the search for anthracnose resistance in the six wild species of lentil (world collection), of which two can be easily crossed with the cultivated type. Two strains of anthracnose (race 1 and race 2) with varying degrees of virulence were reported. The 2002 field data suggested that some of the Lens ervoides and Lens lamottei accessions exhibited no lesions at all when exposed to the combination of the two anthracnose strains. The cultivated types that show resistance to the less virulent strain were severely affected by anthracnose. In the greenhouse study the wild species were inoculated with the two strains separately and results indicate that no accession is immune to the more virulent type. However, some of the L. ervoides and L. lamottei accessions had good resistance compared to their cultivated counterparts. As a long term strategy, the lentil breeding program at CDC, University of Saskatchewan has a goal of fully utilizing the available resistance sources. However, these two species cannot be easily crossed with the cultivated types using the conventional/manual crossing techniques. A tissue culture procedure involving embryo rescue is used to facilitate crossing. We have been able to successfully rescue some embryos from crosses with Lens ervoides. The hybrid plants produce some fertile seeds which will be evaluated for resistance to both anthracnose and ascochyta. The selected resistant lines will then be backcrossed to the adopted backgrounds in order to deploy resistance genes

    Provenance and tectonic significance of the Palaeoproterozoic metasedimentary successions of central and northern Madagascar

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    New detrital zircon U-Pb age data obtained from various quartzite units of three spatially separated supracrustal packages in central and northern Madagascar, show that these units were deposited between 1.8 and 0.8 Ga and have similar aged provenances. The distribution of detrital zircon ages indicates an overwhelming contribution of sources with ages between 2.5 and 1.8 Ga. Possible source rocks with an age of 2.5 Ga are present in abundance in the crustal segments (Antananarivo, Antongil and Masora Domains) either side of a purported Neoproterozoic suture ("Betsimisaraka Suture Zone"). Recently, possible source rocks for the 1.8 Ga age peak have been recognised in southern Madagascar. All three supracrustal successions, as well as the Archaean blocks onto which they were emplaced, are intruded by mid-Neoproterozoic magmatic suites placing a minimum age on their deposition. The similarities in detrital pattern, maximum and minimum age of deposition in the three successions, lend some support to a model in which all of Madagascar's Archaean blocks form a coherent crustal entity (the Greater Dharwar Craton), rather than an amalgamate of disparate crustal blocks brought together only during Neoproterozoic convergence. However, potential source terranes exist outside Madagascar and on either side of the Neoproterozoic sutures, so that a model including a Neoproterozoic suture in Madagascar cannot be dispelled outright

    The Kaiparowits Formation: a remarkable record of late Cretaceous terrestrial environments, ecosystems, and evolution in western North America

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    [Extract] Updated Sedimentological and paleontological data support earlier assertions that the Kaiparowits Formation was deposited in a wet alluvial to coastal plain setting with an abundance of large river channels and perennial ponds, lakes, and wetlands. A synthesis of available geochronological data from contemporaneous Upper Cretaceous continental sedimentary units was compiled, and many ages were recalibrated on the basis of new standards to provide\ud the most up-to-date correlations of coeval strata and associated faunas across the Western Interior Basin. Recalibration of Kaiparowits Formation ash beds demonstrates that the\ud formation is approximately half a million years older than previously suggested, deposited ~76.6-74.5 Ma. In addition, a new ash bed (bentonite) from the Horse Mountain area, collected in the lower portion of the middle unit of the Kaiparowits Formation (~19o-m level), was radiometrically dated by both 40Ar/39Ar and U-Pb techniques, resulting in similar ages of 75.97 ± 0.18 Ma and 76.26 ± 0.05 Ma. Importantly, both ages are consistent with dated ash beds sitting above and below this level. Measured sections from throughout the outcrop expanse of the Kaiparowits Formation are correlated by an updated tephrostratigraphy, and key vertebrate\ud fossil sites from throughout the formation are precisely tied into this stratigraphy. Updated geochronology and stratigraphy reveals that many of the most richly fossiliferous intervals\ud across the Western Interior Basin are constrained to extremely narrow temporal intervals. The term taphozone was coined to describe broad geographic zones of exceptional and elevated continental fossil preservation within narrow temporal windows. Taphozones imply the existence\ud of regional or basin-scale controls on fossil preservation. The Kaiparowits-Dinosaur Park-upper Two Medicine taphozone is assigned to the widespread interval of middle to late Campanian strata in the Western Interior Basin defined by the Kaiparowits, Dinosaur Park, and upper Two Medicine formations. Preliminary analysis of this phenomenon suggests that synchronous deposition of large volumes of volcanic ash across the basin during this time may be the primary driver of elevated fossil preservation in the Kaiparowits-Dinosaur Park-upper Two Medicine taphozone

    Selective sweeps in populations of the broad host range plant pathogenic fungus Sclerotinia sclerotiorum

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    The pathogenic fungus Sclerotinia sclerotiorum infects over 600 species of plant. It is present in numerous environments throughout the world and causes significant damage to many agricultural crops. Fragmentation and lack of gene flow between populations may lead to population sub-structure. Within discrete recombining populations, positive selection may lead to a "selective sweep". This is characterised by an increase in frequency of a favourable allele leading to reduction in genotypic diversity in a localised genomic region due to the phenomenon of genetic hitchhiking. We aimed to assess whether isolates of S. sclerotiorum from around the world formed genotypic clusters associated with geographical origin and to determine whether signatures of population-specific positive selection could be detected. To do this, we sequenced the genomes of 25 isolates of S. sclerotiorum collected from four different continents, Australia, Africa (north and south), Europe and North America (Canada and the northen United States) and conducted SNP based analyses of population structure and selective sweeps. Among the 25 isolates, there was evidence for four population clusters. One of these consisted of 11 isolates from Canada, the USA and France (population 1), another consisted of five isolates from Australia and one from Morocco (population 2). A further cluster was made up of Australian isolates, and the single South African isolate appeared to be from a separate population. We found that there was evidence of distinct selective sweeps between population 1 and population 2. Many of these sweeps overlapped genes involved in transcriptional regulation, such as transcription factors. It is possible that distinct populations of S. sclerotiorum from differing global environments have undergone selective sweeps at different genomic loci. This study lays the foundation for further work into investigation of the differing selective pressures that S. sclerotiorum populations are subjected to on a global scale

    Post-collisional magmatism in the central East African Orogen: the Maevarano Suite of north Madagascar

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    Late tectonic, post-collisional granite suites are a feature of many parts of the Late Neoproterozoic to Cambrian East African Orogen (EAO), where they are generally attributed to late extensional collapse of the orogen, accompanied by high heat flow and asthenospheric uprise. The Maevarano Suite comprises voluminous plutons which were emplaced in some of the tectonostratigraphic terranes of northern Madagascar, in the central part of the EAO, following collision and assembly during a major orogeny at ca. 550 Ma. The suite comprises three main magmatic phases: a minor early phase of foliated gabbros, quartz diorites, and granodiorites; a main phase of large batholiths of porphyritic granitoids and charnockites; and a late phase of small-scale plutons and sheets of monzonite, syenite, leucogranite and microgranite. The main phase intrusions tend to be massive, but with variably foliated margins. New U–Pb SHRIMP zircon data show that the whole suite was emplaced between ca. 537 and 522 Ma. Geochemically, all the rocks of the suite are enriched in the LILE, especially K, and the LREE, but are relatively depleted in Nb, Ta and the HREE. These characteristics are typical of post-collisional granitoids in the EAO and many other orogenic belts. It is proposed that the Maevarano Suite magmas were derived by melting of sub-continental lithospheric mantle that had been enriched in the LILE during earlier subduction events. The melting occurred during lithospheric delamination, which was associated with extensional collapse of the East African Orogen

    Surface expression of eastern Mediterranean slab dynamics: Neogene topographic and structural evolution of the southwest margin of the Central Anatolian Plateau, Turkey

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    he southwest margin of the Central Anatolian Plateau has experienced multiple phases of topographic growth, including the formation of localized highs prior to the Late Miocene that were later affected by wholesale uplift of the plateau margin. Our new biostratigraphic data limit the age of uplifted marine sediments at the southwest plateau margin at 1.5 km elevation to <7.17 Ma, and regional lithostratigraphic correlations imply that the age is <6.7 Ma. Single-grain CA-TIMS U-Pb zircon analyses from a reworked ash within the marine sediments yield dates as young as 10.6 Ma, indicating a maximum age that is consistent with the biostratigraphy. Our structural measurements within the uplifted region and fault inversion modeling agree with previous findings in surrounding regions, with early contraction followed by strike-slip and extensional deformation during uplift. Focal mechanisms from shallow earthquakes show that the extensional phase has continued to the present. Broad similarities in the change in the tectonic stress regime (after 8 Ma) and the onset of surface uplift (after 7 Ma) imply that deep-seated process(es) caused post-7 Ma uplift. The geometry of lithospheric slabs beneath the plateau margin, Pliocene to recent alkaline volcanism, and the uplift pattern with accompanying normal faulting point toward slab tearing and localized heating at the base of the lithosphere as a probable mechanism for post-7 Ma uplift of the southwest margin. Considering previous work in the region, there appears to be an important link between slab dynamics and surface uplift throughout the Anatolian Plateau's southern margin.TOPO-EUROPE Initiative (Vertical Anatolian Movements Project (VAMP))Institute of Environmental Geology and Geoengineering (com. TA.P05.009)Institute of Environmental Geology and Geoengineering (mod. TA.P05.009.003)German Science Foundation (DFG: STR373/25–1)German Science Foundation (EC 138/5–1
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