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11.
David M. Spooner Andrés Contreras M. John B. Bamberg 《American Journal of Potato Research》1991,68(10):681-690
A joint Chilean, United States potato (Solanum sect.Petota) germplasm collecting expedition was conducted in Chile between January 21–March 30, 1989. The trip resulted in collections ofSolanum brevidens (50 accessions),S. etuberosum (28 accessions),S. maglia (3 accessions) and indigenous primitive landraces ofS. tuberosum (24 accessions). Comments are presented on the habitats, distribution, and potential and realized breeding value of these species. 相似文献
12.
David M. Spooner Roel Hoekstra Ronald G. Van den Berg Vincente Martínez 《American Journal of Potato Research》1998,75(1):3-17
There are five wild potato species in Guatemala:Solanum agrimonifolium,S. bulbocastanum,S. clarum,S. demissum, andS. morelliforme. We conducted a collecting expedition there from September 11 to November 5, 1995. The goals of the expedition were to gather field data for taxonomic studies of the five species of Guatemalan wild potatoes and to collect potato germplasm. Our 43 true seed collections nearly quadruple the available wild potato germplasm for Guatemala, provide germplasm from most previously known localities, and add new ones. We provide a systematic treatment of Guatemalan wild potatoes, geographic and logistical data for collecting wild potatoes in Guatemala, statistics on human population growth and deforestation to help explain decline of wild potato populations, recommend areas for future collecting, and suggest two areas as in-situ reserves for wild potatoes 相似文献
13.
Alberto R. Salas David M. Spooner Zósimo Huamán Rafael Vinci Torres Maita Roel Hoekstra Konrad Schüler Robert J. Hijmans 《American Journal of Potato Research》2001,78(3):197-207
Peru contains about half of the described wild potato taxa, and many of these are not yet preserved in genebanks. This paper reports results of the second of a series of five planned collecting expeditions to Peru. Collections were made in the central Peruvian departments of Ancash, Huancavelica, La Libertad, and Lima, from March 8 to April 25,1999. They follow collections in 1998 in the southern Peruvian departments of Apurimac, Arequipa, Cusco, Moquegua, Puno, and Tacna. We collected 101 germplasm accessions, including first germplasm collections of the following 22Solanum taxa:Solanum amayanum, S. anamatophilum, S. arahuayum (lost in germplasm increase),S. augustii, S. bill- hookeri, S. cantense, S. chavinense, S. chomatophilum var. subnivale, S. chrysoflorum, S. gracilifrons, S. hapalos um, S. huarochiriense, S. hypacrarthrum, S.jalcae, S. moniliforme, S. multiinterruptum f. longipilosum, S. multiinterruptum var. machaytambinum, S. peloquinianum, S. rhombilanceolatum, S. simplicissimum, S. taulisense (lost in germplasm increase), andS. wittmackii. In addition, new collections were made of the under-collected speciesS. hastiforme (three collections). The above taxonomy is that used in planning our expedition, that we compare to a new treatment of Peruvian wild potatoes published by C. Ochoa in 1999. This paper reports the collection and new species identifications of the 1999 collections, and germplasm conservation and survival of the 1998 and 1999 collections. In addition, chromosome counts are provided for 134 accessions from the 1998 and 1999 expeditions, including first reports forS. chomatophilum var. subnivale (2n = 2x = 24),S. megistacrolobum subsp.purpureum (2n = 2x = 24), andS. multiinterruptum var.multiinterruptum f.albiflorum (2n = 2x = 24); we also report the first triploid count of an accession ofS. immite. 相似文献
14.
Summary We conducted a joint Ecuador/Colombia/United States wild potato (Solanum sect. Petota) germplasm collecting expedition in Ecuador from April 13–July 1, 1991. The goals of the expedition were to collect germplasm and study the species boundaries of all of the 25 Ecuadorian taxa accepted by current taxonomists. We made 126 collections of 24 of these 25 taxa, 113 as germplasm samples, 13 only as herbarium collections. We synonymize six of these 25 names (S. baezense Ochoa, S. cyanophyllum Correll, S. pichinchense Bitter & Sodiro, S. serratoris Ochoa, S. suffrutescens Correll as synonyms of S. andreanum Baker; S. correllii Ochoa as a synonym of S. regularifolium Correll). Four other names (S. chomatophilum f. angustifoliolum Correll, S. moscopanum Hawkes, S. solisii Hawkes, S. tundalomense Ochoa) could not be consistently distinguished from S. colombianum Dunal in the field. We are currently investigating them to determine their species status. 相似文献
15.
David M. Spooner Alberto Salas López Zósimo Huamán Robert J. Hijmans 《American Journal of Potato Research》1999,76(3):103-119
Peru has 103 taxa of wild potatoes (species, subspecies, varieties, and forms) according to Hawkes (1990; modified by us by a reduction of species in theSolanum brevicaule complex) and including taxa described by C. Ochoa since 1989. Sixty-nine of these 103 taxa (67% ) were unavailable from any of the world’s genebanks and 85 of them (83%) had less than three germplasm accessions. We conducted a collaborative Peru (INIA), United States (NRSP-6), and International Potato Center (CIP) wild potato (Solanum sect.Petota) collecting expedition in Peru to collect germplasm and gather taxonomic data. This is the first of a series of planned expeditions from 1998–2002. We collected from February 18 to April 18, 1998, in the southern departments of Apurímac, Arequipa, Cusco, Moquegua, Puno, and Tacna. We made 57 germplasm collections, including 14 taxa that are the first available as germplasm for any country (Solanum aymaraesense, S. chillonanum, S. incasicum, S. megistacrolobum subsp.megistacrolobum f. purpureum, S. longiusculus, S. multiflorum,S. pillahuatense, S. sawyeri, S. sandemanii, S. tacnaense, S. tarapatanum, S. urubambae, S. velardei, S. villuspetalum), and two additional taxa that are the first available for Peru but with germplasm from Bolivia (S. megistacrolobum subsp.toralapanum, S. yungasense). Collections also were made for the rare taxaS. acroscopicum, S. buesii, S. limbaniense, andS. santolallae. Our collections suggest the following minimum synonymy may be needed for Peruvian potatoes:S. sawyeri as a synonym ofS. tuberosum;S. hawkesii andS. incasicum as synonyms ofS. raphanifolium;S. multiflorum andS. villuspetalum as synonyms ofS. urubambae. 相似文献
16.
17.
Lymphocyte antigens controlled by alleles at the BoLA-A locus were used to indicate which of two bulls could be eliminated as the sire in 18 cases of disputed parentage. The use of bovine lymphocyte antigens (BoLA) significantly increased the exclusion probability over that of the standard red cell and electrophoretic techniques. 相似文献
18.
Requirement for MHC class II positive accessory cells in an antigen specific bovine T cell response 总被引:1,自引:0,他引:1
Purified populations of bovine antigen presenting cells (APCs) and T cells have been isolated from peripheral blood and characterised using various monoclonal antibodies (mAbs) for cell surface markers. Bovine APCs were found in an adherent cell fraction and were non-specific esterase positive, phagocytic and expressed bovine major histocompatibility complex (MHC) class II determinants, all of which are typical macrophage characteristics. T cells were rigorously depleted of accessory cell function before being used in an antigen presenting cell assay. The generation of T helper cells in response to the soluble antigen, ovalbumin, was entirely dependent upon a critical number of APCs. Further the proliferative response was inhibited by several mAbs to bovine MHC class II molecules. Thus the interaction between bovine APCs and helper/inducer T lymphocytes (TH/I) appears to be similar to that in other species. 相似文献
19.
China is the world’s leading producer of potatoes, growing 22% of all potatoes. Production continues to rise, owing to increases
in both land devoted to potato production and yield per hectare. Most potato production occurs in the northern and southwest
regions of the country. The processing of coarse starch is the most important component of the potato processing industry
in China, but other processing industries, such as crisps and French fries, are expanding. Major production constraints include
inadequate germplasm resources for cultivar development, the lack of high quality seed potatoes, and limited access to equipment
for mechanized cultivation, planting, fertilizing, spraying, and harvesting. Additional weaknesses in storage and transportation
technologies must be addressed, as they are the major constraints for the healthy development of the potato industry. The
introduction and improvement of these technologies will ensure the sustainable development of the potato industry in China. 相似文献
20.
Bishop R Geysen D Spooner P Skilton R Nene V Dolan T Morzaria S 《Veterinary parasitology》2001,94(4):227-237
The 'Muguga cocktail' which is composed of three Theileria parva stocks Muguga, Kiambu 5 and Serengeti-transformed has been used extensively for live vaccination against East Coast fever in cattle in eastern, central and southern Africa. Herein we describe the molecular characterisation of the T. parva vaccine stocks using three techniques, an indirect fluorescent antibody test with a panel of anti-schizont monoclonal antibodies (MAb), Southern blotting with four T. parva repetitive DNA probes and polymerase chain reaction (PCR)-based assays detecting polymorphism within four single copy loci encoding antigen genes. The Muguga and Serengeti-transformed stocks exhibited no obvious differences in their reactivity with the panel of MAbs, whereas Kiambu 5 differed with several MAbs. Kiambu 5 DNA was very distinct from the Muguga and Serengeti-transformed isolates in the hybridisation pattern with all four nucleic acid probes, whereas Muguga and Serengeti-transformed isolates exhibited minor differences and could not be discriminated with one of the probes. PCR amplification in combination with restriction fragment length polymorphism analysis indicated that Kiambu 5 was also markedly divergent from the Muguga and Serengeti-transformed stocks within two of the four antigen coding genes. The T. parva Serengeti-transformed stock did not contain a 130 base pair insert within the p67 sporozoite antigen gene, which has been observed previously in most T. parva parasites isolated from buffalo, and could not be discriminated from T. parva Muguga at any of the four single copy loci. Collectively the data indicate that two of the cocktail components T. parva Serengeti-transformed and Muguga are genetically closely related, while the third component Kiambu 5 is quite distinct. Based on the findings, there may be a need to include only one of the T. parva Muguga and Serengeti-transformed components in the immunising cocktail. The study demonstrates the value of molecular characterisation data for monitoring of live vaccines. 相似文献