Hypoxylon serpens: cytology and taxonomic considerations

1975 ◽  
Vol 53 (1) ◽  
pp. 52-55 ◽  
Author(s):  
Jack D. Rogers
Keyword(s):  
Chromosome Number ◽  
Haploid Chromosome Number ◽  
Taxonomic Implications

The haploid chromosome number of Hypoxylon serpens is seven. Ascospores are initially uninucleate, becoming binucleate after a mitosis. One nucleus is cut off in a cellular appendage which degenerates before ascospores become colored. Mature ascospores are uninucleate and devoid of appendages. Taxonomic implications of these data are discussed.

scholarly journals A long reads-based de-novo assembly of the genome of the Arlee homozygous line reveals chromosomal rearrangements in rainbow trout

2021 ◽  
Author(s):  
Guangtu Gao ◽  
Susana Magadan ◽  
Geoffrey C Waldbieser ◽  
Ramey C Youngblood ◽  
Paul A Wheeler ◽  
...  
Keyword(s):  
Rainbow Trout ◽  
Chromosome Number ◽  
Genome Assembly ◽  
De Novo Assembly ◽  
De Novo ◽  
Sequence Data ◽  
Structural Variations ◽  
High Coverage ◽  
Haploid Chromosome Number ◽  
Long Reads

Abstract Currently, there is still a need to improve the contiguity of the rainbow trout reference genome and to use multiple genetic backgrounds that will represent the genetic diversity of this species. The Arlee doubled haploid line was originated from a domesticated hatchery strain that was originally collected from the northern California coast. The Canu pipeline was used to generate the Arlee line genome de-novo assembly from high coverage PacBio long-reads sequence data. The assembly was further improved with Bionano optical maps and Hi-C proximity ligation sequence data to generate 32 major scaffolds corresponding to the karyotype of the Arlee line (2 N = 64). It is composed of 938 scaffolds with N50 of 39.16 Mb and a total length of 2.33 Gb, of which ∼95% was in 32 chromosome sequences with only 438 gaps between contigs and scaffolds. In rainbow trout the haploid chromosome number can vary from 29 to 32. In the Arlee karyotype the haploid chromosome number is 32 because chromosomes Omy04, 14 and 25 are divided into six acrocentric chromosomes. Additional structural variations that were identified in the Arlee genome included the major inversions on chromosomes Omy05 and Omy20 and additional 15 smaller inversions that will require further validation. This is also the first rainbow trout genome assembly that includes a scaffold with the sex-determination gene (sdY) in the chromosome Y sequence. The utility of this genome assembly is demonstrated through the improved annotation of the duplicated genome loci that harbor the IGH genes on chromosomes Omy12 and Omy13.

scholarly journals Chromosomal and DNA barcode analysis of the Melitaea ala Staudinger, 1881 species complex (Lepidoptera, Nymphalidae)

2021 ◽  
Vol 15 (2) ◽  
pp. 199-216
Author(s):  
Vladimir A. Lukhtanov ◽  
Anastasia V. Gagarina ◽  
Elena A. Pazhenkova
Keyword(s):  
Chromosome Number ◽  
Central Asia ◽  
Species Complex ◽  
Dna Barcode ◽  
Monophyletic Group ◽  
Geographic Proximity ◽  
Haploid Chromosome Number ◽  
East Central ◽  
North East ◽  
Peter The Great

The species of the Melitaea ala Staudinger, 1881 complex are distributed in Central Asia. Here we show that this complex is a monophyletic group including the species, M. ala, M. kotshubeji Sheljuzhko, 1929 and M. enarea Fruhstorfer, 1917. The haploid chromosome number n=29 is found in M. ala and M. kotshubeji and is, most likely, a symplesiomorphy of the M. ala complex. We show that M. ala consists of four subspecies: M. ala zaisana Lukhtanov, 1999 (=M. ala irtyshica Lukhtanov, 1999, syn. nov.) (South Altai, Zaisan Lake valley), M. ala ala (Dzhungarian Alatau), M. ala bicolor Seitz, 1908 (North, East, Central and West Tian-Shan) and M. ala determinata Bryk, 1940 (described from “Fu-Shu-Shi”, China). We demonstrate that M. kotshubeji kotshubeji (Peter the Great Mts in Tajikistan) and M. kotshubeji bundeli Kolesnichenko, 1999 (Alai Mts in Tajikistan and Kyrgyzstan) are distinct taxa despite their geographic proximity in East Tajikistan. Melitaea enarea is widely distributed in the southern part of Central Asia and is sympatric with M. kotshubeji.

scholarly journals Unprecedented reorganization of holocentric chromosomes provides insights into the enigma of lepidopteran chromosome evolution

2019 ◽  
Vol 5 (6) ◽  
pp. eaau3648 ◽  
Author(s):  
Jason Hill ◽  
Pasi Rastas ◽  
Emily A. Hornett ◽  
Ramprasad Neethiraj ◽  
Nathan Clark ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Chromosome Evolution ◽  
Chromosome Structure ◽  
Holocentric Chromosomes ◽  
Chromosome Counts ◽  
Pieris Napi ◽  
Haploid Chromosome Number ◽  
Genome Wide ◽  
The Face ◽  
Chromosome Level

Chromosome evolution presents an enigma in the mega-diverse Lepidoptera. Most species exhibit constrained chromosome evolution with nearly identical haploid chromosome counts and chromosome-level gene collinearity among species more than 140 million years divergent. However, a few species possess radically inflated chromosomal counts due to extensive fission and fusion events. To address this enigma of constraint in the face of an exceptional ability to change, we investigated an unprecedented reorganization of the standard lepidopteran chromosome structure in the green-veined white butterfly (Pieris napi). We find that gene content in P. napi has been extensively rearranged in large collinear blocks, which until now have been masked by a haploid chromosome number close to the lepidopteran average. We observe that ancient chromosome ends have been maintained and collinear blocks are enriched for functionally related genes suggesting both a mechanism and a possible role for selection in determining the boundaries of these genome-wide rearrangements.

A contribution towards elucidating the life history of Palmaria palmate (=Rhodymenia palmata)

1976 ◽  
Vol 54 (24) ◽  
pp. 2903-2906 ◽  
Author(s):  
J. P. van der Meer
Keyword(s):  
Life History ◽  
Chromosome Number ◽  
Atlantic Coast ◽  
Palmaria Palmata ◽  
Haploid Chromosome Number ◽  
History Of

Palmaria palmata from a region of the Atlantic coast of Canada has been examined cytologically. Plants bearing tetrasporangia were found to be diploid with meiosis occurring in the tetrasporangia. Spermatangial plants and sporelings growing from tetraspores were haploid. The haploid chromosome number appears to be 22–23.

Karyotypic analysis of Polymyxa betae (Plasmodiophoromycetes) based on serial thin sections of pachytene nuclei

1983 ◽  
Vol 61 (12) ◽  
pp. 3202-3206 ◽  
Author(s):  
James P. Braselton
Keyword(s):  
Chromosome Number ◽  
Plasmodiophora Brassicae ◽  
Polymyxa Betae ◽  
Karyotypic Analysis ◽  
Thin Sections ◽  
Haploid Chromosome Number ◽  
Synaptonemal Complexes

Three pachytene nuclei of Polymyxa betae Keskin were reconstructed from serial thin sections. Thirty synaptonemal complexes (SCs) were counted, indicating a haploid chromosome number of 30. SCs of Polymyxa were similar to those of Sorosphaera veronicae Schroeter and Membranosorus heterantherae Ostenfeld and Peterson but differed from SCs of Plasmodiophora brassicae Woron. and Woronina pythii Goldie-Smith.

Recherches sur les Alaria (Phaeophyceae) de l'est canadien. I. Nombres chromosomiques et identité des Alaria de l'estuaire du St-Laurent

1974 ◽  
Vol 52 (4) ◽  
pp. 691-694 ◽  
Author(s):  
M.-J. Feller-Demalsy ◽  
P. Demalsy
Keyword(s):  
Chromosome Number ◽  
Single Species ◽  
Chromosome Counts ◽  
Eastern Canada ◽  
Lawrence Estuary ◽  
Haploid Chromosome Number ◽  
Biosystematic Study ◽  
Alaria Esculenta ◽  
St Lawrence Estuary

Chromosome counts in gametophytes and sporophylls of Alaria collected in the St. Lawrence Estuary show that all the specimens of this genus in eastern Canada may not belong to the single species A. esculenta Greville. Indeed, the haploid chromosome number (n) found in these algae is equal to half of the number attributed in the literature to Alaria esculenta from the British coasts. Three hypotheses for the interpretation of these observations are considered. The solution of the problem of the identity of Alaria can only be hoped for from their global, morphological, and biosystematic study.

scholarly journals GENETIC MAPPING IN SACCHAROMYCES IV. MAPPING OF TEMPERATURE-SENSITIVE GENES AND USE OF DISOMIC STRAINS IN LOCALIZING GENES

Genetics ◽  
1973 ◽  
Vol 74 (1) ◽  
pp. 33-54
Author(s):  
R K Mortimer ◽  
D C Hawthorne
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Chromosome Number ◽  
Genetic Mapping ◽  
Genetic Markers ◽  
Genetic Maps ◽  
Temperature Sensitive ◽  
Yeast Saccharomyces Cerevisiae ◽  
Haploid Chromosome Number ◽  
Number Of Genes

ABSTRACT Through use of tetrad, random spore, trisomic, and mitotic analysis procedures a large number of genes, including 48 new genetic markers, were studied for their locations on the genetic maps of the yeast Saccharomyces cerevisiae. Eighteen new centromere linked genes were discovered and all but one was located on various ones of the 16 previously-established chromosomes. Five fragments of linked genes were also assigned to chromosomes; four were located on known chromosomes while the fifth determined one arm of a new chromosome. The experiments indicate that seventeen is likely to be the haploid chromosome number in this yeast. Most chromosomes have been established by genetic means to be metacentric and their genetic lengths vary from 5 cM to approximately 400 cM. Functionally-related sets of genes generally were found to be dispersed over the genome.

Chromosome Number Variation in the Myrtaceae and Its Taxonomic Implications

1979 ◽  
Vol 27 (5) ◽  
pp. 547 ◽  
Author(s):  
BL Rye
Keyword(s):  
Chromosome Number ◽  
Chromosome Numbers ◽  
Evolutionary Potential ◽  
The Family ◽  
Number Variation ◽  
Taxonomic Implications ◽  
Chromosome Number Variation ◽  
Australian Flora ◽  
Base Chromosome Number ◽  
Western Australian

New chromosome number determinations are reported for some 150 Western Australian species of the Myrtaceae. These include the lowest number (n = 5) so far recorded in the family and several newly recorded descending dysploid series. Dysploid chromosome numbers are far less common than the base chromosome number of n = 11 but parallel dysploid series have occurred in many groups and some have played a role in the origin of genera. Polyploidy has been successful at the intraspecific and interspecific levels but is of limited evolutionary potential. The cytoevolutionary trends in the Myrtaceae are examined in relation to taxonomic problems within the family and in relation to cytoevolution in the woody Australian flora as a whole. Smith- White's suggestion that a more natural generic classification in the Chamelauciinae could be obtained by grouping species with the same base chromosome numbers is found to be untenable.

Obligatory amphimixis and variation in chromosome number within and among South American populations of Nacobbus aberrans (Thorne, 1935) Thorne & Allen, 1944 (Nematoda: Pratylenchidae)

Nematology ◽  
2005 ◽  
Vol 7 (5) ◽  
pp. 783-787 ◽  
Author(s):  
Géraldine Anthoine ◽  
Didier Mugniéry
Keyword(s):  
Chromosome Number ◽  
Chromosome Numbers ◽  
Experimental Approach ◽  
Taxonomic Status ◽  
Reproductive Mode ◽  
South American ◽  
Complementary Information ◽  
Haploid Chromosome Number ◽  
Nacobbus Aberrans

AbstractThere are conflicting opinions concerning the reproductive mode and the taxonomic status of Nacobbus aberrans, so we have addressed these issues by an experimental approach based on the inoculation of immature and vermiform females in in vitro conditions. Complementary information on chromosome number was provided. Five South American populations of Nacobbus aberrans were tested. No population was observed to be able to reproduce by parthenogenesis in in vitro conditions. The basic haploid chromosome number seems to be seven, at least for four of the five populations studied. However, all populations had individuals with haploid chromosome numbers ranging from five to eight, six to eight being the most frequent number, regardless of the 'race' group or the native country. The variation in the chromosome number suggests that N. aberrans may be considered as a set of different karyological genetic entities.

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