One of 18 Chorthippus vagans males from a natural population was heterozygous for an interchange between the L1 and M4 chromosomes when examined cytologically. Chiasma distribution within multiple chromosome configurations and the relation between chiasma formation in the interstitial segments and centromere orientation were investigated. Our results confirm previous observations that adjacent-2 is the most common orientation in absence of chiasmata on the interstitial segments.Key words: Chorthippus, interchange, interstitial segments, chiasma distribution, orientation.
{"title":"Chiasma distribution and centromere orientation in a spontaneous interchange in the grasshopper Chorthippus vagans","authors":"J. Cabrero, J. Camacho","doi":"10.1139/G86-127","DOIUrl":"https://doi.org/10.1139/G86-127","url":null,"abstract":"One of 18 Chorthippus vagans males from a natural population was heterozygous for an interchange between the L1 and M4 chromosomes when examined cytologically. Chiasma distribution within multiple chromosome configurations and the relation between chiasma formation in the interstitial segments and centromere orientation were investigated. Our results confirm previous observations that adjacent-2 is the most common orientation in absence of chiasmata on the interstitial segments.Key words: Chorthippus, interchange, interstitial segments, chiasma distribution, orientation.","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"59 1","pages":"913-920"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79921028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Two nonallelic Four-spore mutants are known in which ascospore walls enclose the four immediate products of meiosis rather than the normal eight products of a postmeiotic mitosis. Expression depends on temperature. The Four-spore phenotype is expressed when the developing asci are subjected either to high temperatures (25-30 degrees C) for Fsp-1 or to low temperatures (15-20 degrees C) for Fsp-2. Heterozygous Fsp-1 X Fsp-1+ crosses make eight-spored asci at 15-20 degrees C but produce many four-spored asci at 25 degrees C and mostly four-spored asci at 30 degrees C. Homozygous Fsp-1 X Fsp-1 crosses respond similarly to increasing temperature but make 40-50% four-spored asci even at 20 degrees C. Heterozygous Fsp-2 X Fsp-2+ crosses produce almost exclusively four-spored asci at 15 degrees C but a mixture of four- and eight-spored asci at 20, 25, and 30 degrees C. Homozygous Fsp-2 X Fsp-2 crosses make all four-spored asci at 15 and 20 degrees C and a mixture of four- and eight-spored asci at 25 and 30 degrees C. When both Fsp-1 and Fsp-2 are present in a cross, either homozygous or heterozygous, no asci contain more than four ascospores at any temperature. Limited temperature-shift experiments with Fsp-1 and Fsp-2 show that the sensitive period for Four-spore expression is sometime after meiotic prophase, possibly at interphase II.
已知有两种非等位基因的四孢子突变体,其中子囊孢子壁包围着减数分裂后的四个直接产物,而不是减数分裂后有丝分裂的正常八个产物。表情取决于温度。当发育中的asci经受高温(25-30℃)(Fsp-1)或低温(15-20℃)(Fsp-2)时,表达四孢子表型。杂合子Fsp-1 X Fsp-1+杂交在15-20℃时产生8孢子子囊,但在25℃时产生许多4孢子子囊,在30℃时产生大部分4孢子子囊。纯合子Fsp-1 X Fsp-1杂交对温度升高的反应相似,但即使在20℃时也产生40-50%的4孢子子囊。Fsp-2与Fsp-2的纯合子杂交在15℃和20℃时产生所有四孢子子囊,在25℃和30℃时产生四孢子和八孢子子囊的混合物。当Fsp-1和Fsp-2同时存在于一个杂交中,无论是纯合子还是杂合子,在任何温度下,子囊都不含有超过四个子囊孢子。Fsp-1和Fsp-2的有限温度变换实验表明,四孢子表达的敏感期在减数分裂前期后的某个时间,可能在II间期。
{"title":"Ascus development in two temperature-sensitive four-spore mutants of Neurospora crassa.","authors":"N B Raju","doi":"10.1139/g86-136","DOIUrl":"https://doi.org/10.1139/g86-136","url":null,"abstract":"<p><p>Two nonallelic Four-spore mutants are known in which ascospore walls enclose the four immediate products of meiosis rather than the normal eight products of a postmeiotic mitosis. Expression depends on temperature. The Four-spore phenotype is expressed when the developing asci are subjected either to high temperatures (25-30 degrees C) for Fsp-1 or to low temperatures (15-20 degrees C) for Fsp-2. Heterozygous Fsp-1 X Fsp-1+ crosses make eight-spored asci at 15-20 degrees C but produce many four-spored asci at 25 degrees C and mostly four-spored asci at 30 degrees C. Homozygous Fsp-1 X Fsp-1 crosses respond similarly to increasing temperature but make 40-50% four-spored asci even at 20 degrees C. Heterozygous Fsp-2 X Fsp-2+ crosses produce almost exclusively four-spored asci at 15 degrees C but a mixture of four- and eight-spored asci at 20, 25, and 30 degrees C. Homozygous Fsp-2 X Fsp-2 crosses make all four-spored asci at 15 and 20 degrees C and a mixture of four- and eight-spored asci at 25 and 30 degrees C. When both Fsp-1 and Fsp-2 are present in a cross, either homozygous or heterozygous, no asci contain more than four ascospores at any temperature. Limited temperature-shift experiments with Fsp-1 and Fsp-2 show that the sensitive period for Four-spore expression is sometime after meiotic prophase, possibly at interphase II.</p>","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"28 6","pages":"982-90"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1139/g86-136","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"14085911","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The effects of single wild-type immigrants on populations of Tribolium castaneum initially homozygous for the antennapedia (ap) allele were examined in reference to gene frequencies and age structu...
{"title":"Genetic and demographic effects of single wild-type immigrants on a mutant population of Tribolium castaneum","authors":"Michael A. Delgado, D. C. Englert","doi":"10.1139/G86-139","DOIUrl":"https://doi.org/10.1139/G86-139","url":null,"abstract":"The effects of single wild-type immigrants on populations of Tribolium castaneum initially homozygous for the antennapedia (ap) allele were examined in reference to gene frequencies and age structu...","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"115 1","pages":"1003-1008"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75465768","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cytomorphology of solanum nigrum L. (2n = 6x = 72) and S. americanum Mill. (2n = 2x = 24) was studied. Crosses were made between these two species, but crosses were successful only when the higher ploidy form was used as the maternal parent. The F1 hybrid was a tetraploid (2n = 4x = 48) and showed highly irregular meiosis. It did not set fruit either on selfing or on open pollination. A fertile octoploid branch spontaneously grew from the sterile hybrid. The octoploid had regular meiosis and produced several fruits with viable seeds. Pollen stainability was 82%. From cytological studies of the tetraploid and its amphiploid, it is concluded that hybridization and polyploidy have played a significant role in the origin and evolution of higher chromosomal forms of Solanum section Solanum (Maurella).Key words: Solanum, polyploid, sterility.
{"title":"Nature of sterility and mechanism of the evolution of higher ploidy in Solanum section Solanum (Maurella)","authors":"A. Ganapathi, G. R. Rao","doi":"10.1139/G86-146","DOIUrl":"https://doi.org/10.1139/G86-146","url":null,"abstract":"Cytomorphology of solanum nigrum L. (2n = 6x = 72) and S. americanum Mill. (2n = 2x = 24) was studied. Crosses were made between these two species, but crosses were successful only when the higher ploidy form was used as the maternal parent. The F1 hybrid was a tetraploid (2n = 4x = 48) and showed highly irregular meiosis. It did not set fruit either on selfing or on open pollination. A fertile octoploid branch spontaneously grew from the sterile hybrid. The octoploid had regular meiosis and produced several fruits with viable seeds. Pollen stainability was 82%. From cytological studies of the tetraploid and its amphiploid, it is concluded that hybridization and polyploidy have played a significant role in the origin and evolution of higher chromosomal forms of Solanum section Solanum (Maurella).Key words: Solanum, polyploid, sterility.","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"50 1","pages":"1044-1048"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74945494","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Adult Glossina morsitans morsitans Westwood emerging from puparia collected at Rekometjie, Zimbabwe, were compared at 13 loci with G. m. morsitans from a closed colony at the Tsetse Research Labortory (TRL), University of Bristol, by polyacrylamide gel electrophoresis. The populations were not significantly different with respect to mean heterozygosity per locus, average effective number of alleles per locus, number of polymorphic loci, or allele frequencies at 12 loci. (The exception was Alkph.) Rare alleles at To, Est-t, and Alkph were found only in Rekometjie flies while rare alleles at G6pd and Est-2 were found only in TRL flies. No significant level of sterility was found in F1 flies produced in reciprocal crosses of Rekometjie flies with G. m. morsitans from the University of Alberta colony.Key words: Glossina, tsetse fly, isozymes, heterozygosity.
采用聚丙烯酰胺凝胶电泳方法,对津巴布韦Rekometjie采集的蝇蛹中出现的morsitans Westwood成虫与布里斯托尔大学采采研究实验室(TRL)封闭菌落中的morsitans进行了13个位点的比较。每个位点的平均杂合度、每个位点的平均有效等位基因数、多态性位点数和12个位点的等位基因频率均无显著差异。(阿尔克夫是个例外。)To、Est-t和Alkph位点罕见等位基因仅在Rekometjie蝇中发现,G6pd和Est-2位点罕见等位基因仅在TRL蝇中发现。Rekometjie蝇与来自阿尔伯塔大学群体的G. m. morsitans反向杂交产生的F1蝇未发现显著的不育水平。关键词:舌蝇,采采蝇,同工酶,杂合性
{"title":"Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). XII: Comparison of field-collected and laboratory-reared flies","authors":"R. Gooding, A. Jordan","doi":"10.1139/G86-141","DOIUrl":"https://doi.org/10.1139/G86-141","url":null,"abstract":"Adult Glossina morsitans morsitans Westwood emerging from puparia collected at Rekometjie, Zimbabwe, were compared at 13 loci with G. m. morsitans from a closed colony at the Tsetse Research Labortory (TRL), University of Bristol, by polyacrylamide gel electrophoresis. The populations were not significantly different with respect to mean heterozygosity per locus, average effective number of alleles per locus, number of polymorphic loci, or allele frequencies at 12 loci. (The exception was Alkph.) Rare alleles at To, Est-t, and Alkph were found only in Rekometjie flies while rare alleles at G6pd and Est-2 were found only in TRL flies. No significant level of sterility was found in F1 flies produced in reciprocal crosses of Rekometjie flies with G. m. morsitans from the University of Alberta colony.Key words: Glossina, tsetse fly, isozymes, heterozygosity.","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"471 1","pages":"1016-1021"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85576502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
An acrotrisomic plant was identified in the progeny of a telotrisomic for 1S. The acrocentric chromosome had a complete short arm (5S) and 40% of the proximal segment of the long arm (5L). Morphology of the acrotrisomic 5S5L was similar to the primary trisomic (triplo 5) and triplo 5L. At meiosis the acrocentric 5S5L either paired with its normal homologues forming a trivalent or remained as a univalent. Seed fertility was high. Transmission of the acrocentric was 37.6% through the female and 9% through the male. Genetic tests showed that fs2 and g were located in this 40% proximal segment of the 5L. Gene f3 showed a trisomic ratio with acrotrisomic 5S5L, but its arm location is not known. Two genes, f7 and trd, were located on the 60% distal segment of the 5L. The segregation ratio with gene int-a1 was also disomic but it could not be assigned to the 60% distal segment because its location on chromosome 5 is questionable at this time. This experiment demonstrates the usefulness of acrotrisomics in physic...
{"title":"Cytogenetics of the acrotrisomic 5S5L in barley","authors":"A. Shahla, T. Tsuchiya","doi":"10.1139/G86-143","DOIUrl":"https://doi.org/10.1139/G86-143","url":null,"abstract":"An acrotrisomic plant was identified in the progeny of a telotrisomic for 1S. The acrocentric chromosome had a complete short arm (5S) and 40% of the proximal segment of the long arm (5L). Morphology of the acrotrisomic 5S5L was similar to the primary trisomic (triplo 5) and triplo 5L. At meiosis the acrocentric 5S5L either paired with its normal homologues forming a trivalent or remained as a univalent. Seed fertility was high. Transmission of the acrocentric was 37.6% through the female and 9% through the male. Genetic tests showed that fs2 and g were located in this 40% proximal segment of the 5L. Gene f3 showed a trisomic ratio with acrotrisomic 5S5L, but its arm location is not known. Two genes, f7 and trd, were located on the 60% distal segment of the 5L. The segregation ratio with gene int-a1 was also disomic but it could not be assigned to the 60% distal segment because its location on chromosome 5 is questionable at this time. This experiment demonstrates the usefulness of acrotrisomics in physic...","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"42 1","pages":"1026-1033"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77262851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
'Rescue', 'Cadet', and the 42 reciprocal chromosome substitution lines derived from these two spring wheat cultivars were tested for vernalization response and cold hardiness. Cold hardiness was tested after hardening under a 16-h day for 8 weeks with 6 °C day and 4 °C night temperatures or in the dark for 7 weeks at 0.8 °C followed by 8 weeks at −5 °C. Chromosomes 5A, 5B, 7B, and possibly 2A carried loci for vernalization response. Chromosomes 2A, 5A, and 5B carried loci affecting cold hardiness measured after 8 weeks in the light at 6 °C during the day and 4 °C at night, whereas chromosomes 6A, 3B, 5B, and 5D were involved in cold hardiness after hardening in the dark at 0.8 °C followed by −5 °C. The results suggest that the rank order of cultivars for cold hardiness depends on the hardening technique used since the two different techniques tested had different genetic and presumably somewhat different biochemical bases.Key words: Triticum aestivum L., cold hardiness, vernalization.
{"title":"Chromosomes in 'Cadet' and 'Rescue' wheats carrying loci for cold hardiness and vernalization response","authors":"D. Roberts","doi":"10.1139/G86-137","DOIUrl":"https://doi.org/10.1139/G86-137","url":null,"abstract":"'Rescue', 'Cadet', and the 42 reciprocal chromosome substitution lines derived from these two spring wheat cultivars were tested for vernalization response and cold hardiness. Cold hardiness was tested after hardening under a 16-h day for 8 weeks with 6 °C day and 4 °C night temperatures or in the dark for 7 weeks at 0.8 °C followed by 8 weeks at −5 °C. Chromosomes 5A, 5B, 7B, and possibly 2A carried loci for vernalization response. Chromosomes 2A, 5A, and 5B carried loci affecting cold hardiness measured after 8 weeks in the light at 6 °C during the day and 4 °C at night, whereas chromosomes 6A, 3B, 5B, and 5D were involved in cold hardiness after hardening in the dark at 0.8 °C followed by −5 °C. The results suggest that the rank order of cultivars for cold hardiness depends on the hardening technique used since the two different techniques tested had different genetic and presumably somewhat different biochemical bases.Key words: Triticum aestivum L., cold hardiness, vernalization.","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"41 1","pages":"991-997"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90186672","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chromosome pairing in hybrids between diploid species of Festuca is described. The chromosome complements of the species from different taxonomic sections vary in chromosome size and DNA content. In interspecific hybrids involving species of the section Montanae there was a relationship between the difference in DNA content of the parental species and chromosome pairing in the F1 hybrids. The larger the difference between the DNA content of the parental species, the more pronounced the failure of chromosome pairing in the F1 hybrids. Factors other than divergence in genome size were also shown to have an effect on chromosome pairing in other hybrid combinations.Key words: chromosome pairing, DNA content, Festuca, hybrids (interspecific).
{"title":"Cytogenetic studies of interspecific hybrids between diploid species of Festuca","authors":"W. Morgan, H. Thomas, M. Evans, M. Borrill","doi":"10.1139/G86-128","DOIUrl":"https://doi.org/10.1139/G86-128","url":null,"abstract":"Chromosome pairing in hybrids between diploid species of Festuca is described. The chromosome complements of the species from different taxonomic sections vary in chromosome size and DNA content. In interspecific hybrids involving species of the section Montanae there was a relationship between the difference in DNA content of the parental species and chromosome pairing in the F1 hybrids. The larger the difference between the DNA content of the parental species, the more pronounced the failure of chromosome pairing in the F1 hybrids. Factors other than divergence in genome size were also shown to have an effect on chromosome pairing in other hybrid combinations.Key words: chromosome pairing, DNA content, Festuca, hybrids (interspecific).","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"54 1","pages":"921-925"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89054140","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A dwarf early Brassica napus line (D-001), derived from crosses with Diplotaxis muralis, was crossed to two B. napus cultivars, 'Regent' and 'Pivot' to study the inheritance of earliness (days to bud, days to first flower, and days to maturity), height, and leaf number. Spaced plants of P1, P2, F1, F2, BC1, and BC2 generations for both crosses were grown in a completely randomized design at two locations in Manitoba in 1984. Results of means analyses indicated that additive gene action predominated for all traits for both crosses and both locations. In addition, dominance gene action was found to influence days to first flower, days to maturity, and leaf number for the D-001 × 'Regent' cross and all traits for the D-001 × 'Pivot' cross. Nonallelic interactions were nonsignificant in all cases. Genotype × environment interactions were not significant for all traits except height. Variance analyses indicated a predominance of additive gene action. Broad sense heritabilities for phenological traits ranged fr...
{"title":"Inheritance of earliness, height, and leaf number in crosses of early maturing rapeseed","authors":"E. A. Ringdahl, P. McVetty, J. L. Sernyk","doi":"10.1139/G86-140","DOIUrl":"https://doi.org/10.1139/G86-140","url":null,"abstract":"A dwarf early Brassica napus line (D-001), derived from crosses with Diplotaxis muralis, was crossed to two B. napus cultivars, 'Regent' and 'Pivot' to study the inheritance of earliness (days to bud, days to first flower, and days to maturity), height, and leaf number. Spaced plants of P1, P2, F1, F2, BC1, and BC2 generations for both crosses were grown in a completely randomized design at two locations in Manitoba in 1984. Results of means analyses indicated that additive gene action predominated for all traits for both crosses and both locations. In addition, dominance gene action was found to influence days to first flower, days to maturity, and leaf number for the D-001 × 'Regent' cross and all traits for the D-001 × 'Pivot' cross. Nonallelic interactions were nonsignificant in all cases. Genotype × environment interactions were not significant for all traits except height. Variance analyses indicated a predominance of additive gene action. Broad sense heritabilities for phenological traits ranged fr...","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"1 1","pages":"1009-1015"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77201247","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lethal genetic load might be caused by a few lethal genes or by large numbers of mildly deleterious polygenes. The extent of this lethal load can be quantified as the number of "lethal equivalents"...
{"title":"Genetic load and heterozygosity in the Pinaceae","authors":"T. Mitchell-Olds, R. Guries","doi":"10.1139/G86-131","DOIUrl":"https://doi.org/10.1139/G86-131","url":null,"abstract":"Lethal genetic load might be caused by a few lethal genes or by large numbers of mildly deleterious polygenes. The extent of this lethal load can be quantified as the number of \"lethal equivalents\"...","PeriodicalId":9589,"journal":{"name":"Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie","volume":"1 1","pages":"942-946"},"PeriodicalIF":0.0,"publicationDate":"1986-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87435174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}