CHROMOSOME NUMBERS OF THE FAMILY CRUCIFERAE. I

1964 ◽  
Vol 42 (11) ◽  
pp. 1509-1520 ◽  
Author(s):  
Gerald A. Mulligan

Chromosome numbers are given for 69 collections of 24 species of Cruciferae in the genera Alyssum, Arabidopsis, Arabis, Barbarea, Cakile, Eutrema, Hali-molobos, Nasturtium, Rorippa, Thellungiella, and Turritis. The following chromosome numbers are reported for the first time: Alyssum desertorum, n = 16; Arabis canadensis, 2n = 14; A. divaricarpa, 2n = 13 + 2B, 14, 20 + 2B, 21, 28; A. drummondii, 2n = 20; A. holboellii, 2n = 13 + 2B, 20 + 2B; A. lemmonii, 2n = 14; A. lyallii, 2n = 21; A. lyrata, 2n = 32; A. pendulocarpa, 2n = 14; Barbarea orthoceras, 2n = 16; Cakile edentula, 2n = 18; Rorippa curvisiliqua, 2n = 16; Thellungiella salsuginea, 2n = 14. It is concluded that species of Arabis native to North America and western Greenland have the base number x = 7 and many of them are apomictic whereas Eurasiatic species of this genus have an x = 8 base number and are sexual.


1965 ◽  
Vol 43 (6) ◽  
pp. 657-668 ◽  
Author(s):  
Gerald A. Mulligan

Chromosome numbers and taxonomic discussions are given for North American material of species in the genera Braya and Cardamine. The following chromosome numbers are reported for the first time: Braya humilis s.l., n = 14 and 2n = 28; Cardamine angulata, n = 20, and 2n = 40; C. cordifolia, 2n = 24; C. microphylla, 2n = 32; C. occidentalis, n = 32 and 2n = 64; C. oligosperma, 2n = 16; C. pensylvanica, 2n = 64; C. umbellata, n = 24 and 2n = 48. It is concluded that the base number of Braya is x = 7 not x = 8 and that North American species of Cardamine have the base numbers x = 6, 8, and 10.



Zootaxa ◽  
2007 ◽  
Vol 1423 (1) ◽  
pp. 27-38 ◽  
Author(s):  
CHRISTOPHER G. MAJKA ◽  
MIKAEL SÖRENSSON

The Ptiliidae of the Maritime Provinces of Canada is surveyed. Twenty-nine new provincial records from the Maritime Provinces of Canada are reported including the first records of the family from Prince Edward Island. Fourteen species are recorded for the first time for the Maritime Provinces as a whole. Acrotrichis josephi (Matthews) is recorded for the first time in eastern North America and Acrotrichis haldemani (LeConte) is recorded for the first time in Canada. The genus Pteryx is reported for the first time in Canada. At least 29 species of Ptiliidae are now known to occur in the region. The fauna is briefly discussed in terms of its overall composition, introduced species, and species associated with particular habitats. Saproxylic species found in mature forests are discussed and attention is drawn to their possible relationship to undisturbed forest conditions and the scarcity of old-growth habitats in the region.



Author(s):  
Nana Bakhtadze ◽  
Nino Gabroshvili ◽  
Levan Mumladze ◽  
Nino Gabroshvili

Chromosome number data on the Hygromiidae (Gastropoda: Stylommatophora) are summarized and reviewed briefly in the context of the phylogeny of the family. In hygromiids, the haploid chromosome numbers range from 21 to 26. It is supposed that n = 21 is the ancestral chromosome number in the family. The modal haploid number for Hygromiidae is 23. Description of karyotype in terms of chromosome number and morphology of hygromiid land snail Circassina frutis is provided for the first time. The diploid chromosome number of this species is 2n = 46. The karyotype is symmetric and consists of 21 pairs of metacentric and 2 pairs of submetacentric chromosomes. The karyotype formula is as follows: 2n = 42m + 4sm (n = 21m + 2sm). The fundamental number (FN) is 92. Chromosomes range in length from 2.53 μm for the smallest pair to 6.00 μm for the largest pair. The total length of chromosomes in diploid complement (TCL) is 170.40 ± 3.22 μm.



1999 ◽  
Vol 12 (6) ◽  
pp. 781 ◽  
Author(s):  
K. Watanabe ◽  
P. S. Short ◽  
T. Denda ◽  
N. Konishi ◽  
M. Ito ◽  
...  

Chromosome number determinations from 152 collections representing 42 genera and 106 species of the Australian Gnaphalieae and Plucheeae are reported. The chromosome numbers of 75 of these species have not been previously counted or differ from those previously reported for species. Chromosome numbers have been documented for the first time for 14 genera: Argyroglottis (n = 12), Cephalosorus (2n = 24), Decazesia (n = 14), Dielitzia (2n = 26), Eriochlamys (n = 14), Erymophyllum (n = 11 and 14), Gilruthia (n = 13), Leucochrysum (n = 9), Myriocephalus s. str. (n = 14, 2n = 24), Polycalymma s. str. (n = 14), Pterocaulon (n = 10), Pterochaeta (n = 12), Quinetia (2n – 24) and Sondottia (2n = 6). Remaining counts augment and agree with previously reported determinations. Some problems with generic delimitation and interpretation of chromosome data are outlined. There is an array of karyotypes within the Australian Gnaphalieae and dysploidy is widespread. Polyploidy has also played an important role in the evolution of some taxa. Evidence suggests that the base number for Australian Gnaphalieae is x = 14. This may be the base number for the entire tribe.



<em>Abstract</em>.—The systematics of lampreys was investigated using complete mitochondrial cytochrome <em>b</em> sequences from all genera and nearly all recognized species. The families Geotriidae and Petromyzontidae are monophyletic, but the family Mordaciidae was resolved as two divergent lineages at the base of the tree. Within Petromyzontidae, the nonparasitic <em>Lethenteron</em> sp. S and <em>Okkelbergia aepyptera</em> were recognized as distinct lineages, <em>Lethenteron morii</em> and <em>Lampetra zanandreai</em> were moved to new genera, a sister species relationship was recovered between <em>Caspiomyzon wagneri </em>and <em>Eudontomyzon hellenicus</em>, and a clade was recovered inclusive of <em>Entosphenus hubbsi</em> and western North American <em>Lampetra </em>(<em>L. ayresii </em>and <em>L. richardsoni</em>). The placement of <em>E. hellenicus</em> as the sister species to <em>C. wagneri </em>reduces the number of genera comprised entirely of parasitic species to two, <em>Geotria</em> and <em>Petromyzon</em>. The recognition of distinct lineages for <em>O. aepyptera</em> and <em>Lethenteron</em> sp. S recognizes, for the first time, lineages comprised entirely of nonparasitic species. Apart from the results mentioned above, monophyly was supported for the multispecific genera <em>Entosphenus</em>, <em>Eudontomyzon</em>, <em>Ichthyomyzon</em>, <em>Lampetra</em> (restricted to European species), and <em>Lethenteron</em>. Intergeneric relationships within Petromyzontidae were poorly resolved, but separate clades inclusive of <em>Entosphenus</em> and <em>Tetrapleurodon</em> (subfamily Entospheninae) and one comprised of <em>Eudontomyzon</em>, <em>Lampetra</em>, and <em>Okkelbergia</em> were recovered.



Taxonomy ◽  
2021 ◽  
Vol 1 (4) ◽  
pp. 290-301
Author(s):  
John C. Semple ◽  
Jie Zhang ◽  
Rachel E. Cook ◽  
Bambang Agus Suripto

Chromosome numbers are reported here for the first time from 117 individuals of Solidago rugosa and S. fistulosa. Including 178 previously published reports for the two species plus S. latissimifolia, chromosome numbers have been determined from 295 individuals from 269 locations. Only diploids (2n = 18) were found throughout the range of S. fistulosa on the coastal plain in the eastern U.S.A. (44 counts). Diploids (2n = 18) were found in the northern portion of the range of S. latissimifolia, and tetraploids (2n = 36) and hexaploids (2n = 54) were found in the central and southern portions of the range (nine counts in total). Diploids (2n = 18) were found throughout the range of S. rugosa in much of eastern North America in four of the five varieties (northern var. rugosa, var. sphagnophila; southern var. aspera and var. celtidifolia). Tetraploids (2n = 36) were found in all four of these varieties and exclusively in var. cronquistiana in the southern high Appalachian Mountains. Hexaploids (2n = 54) were found in var. sphagnophila at scattered locations. One possible hexaploid in var. rugosa was found in the Allegheny Mountains. The diversity in ploidy levels was independent of the size of the range and the diversity of growing conditions among the three species of S. subsect. Venosae.



2013 ◽  
Vol 87 (1) ◽  
pp. 123-146 ◽  
Author(s):  
Vladimir N. Makarkin ◽  
S. Bruce Archibald

The early Eocene green lacewings (Neuroptera, Chrysopidae) of the Okanagan Highlands deposits of McAbee, and Driftwood Canyon, British Columbia (Canada) and Republic, Washington (U.S.A.) are treated in detail for the first time. At least six genera are present, one unnamed, three new, with at least 10 new species, six named:Protochrysa fuscobasalisn. sp. (McAbee) (Limaiinae, the youngest known record of the subfamily),Okanaganochrysa coltsunaen. gen. n. sp. (McAbee),Adamsochrysa asperan. gen. n. sp. (McAbee),A. wilsonin. gen. n. sp. (Republic),Archaeochrysa profractan. sp. (McAbee), andPseudochrysopa harveyin. gen. n. sp. (Driftwood Canyon) (all Nothochrysinae, the latter provisionally). The four unnamed species include one assigned toPseudochrysopa, two likely belonging toAdamsochrysa, and one of an unknown nothochrysine genus. Microtholi are detected on the abdominal sclerites ofAdamsochrysa wilsoni, and the spermatheca and spermathecal duct in the abdomen ofPseudochrysopa harveyi, the first reported occurrences of these preserved in fossil Chrysopidae. Structures were detected on the apical wing margins of some species that appear similar to trichosors, which are unknown in Chrysopidae, but are present in some other neuropteran families. This is the richest described assemblage of the family anywhere in the fossil record. Okanagan chrysopids were also morphologically and presumably ecologically diverse, including large species with rich venation and well as those with simplified venation and the smallest known fossil species. This is the oldest reported occurrence of the family in North America.



2003 ◽  
Vol 51 (2) ◽  
pp. 211 ◽  
Author(s):  
P. J. de Lange ◽  
B. G. Murray

Documented chromosome numbers are reported for the first time for 11 (encompassing 11 genera and families) of the 49 endemic vascular plants from Norfolk Island. Confirmatory counts are provided for the endemic Achyranthes arborescens and Rhopalostylis baueri var. baueri. At least 11 of the taxa counted are probable polyploids, supporting the common cytological feature of oceanic island floras. In addition to these new counts, we also infer a base number of x = 5 for the recently reinstated monogeneric Pennantiaceae and query the generic placement of the two arborescent species of Achyranthes, A. arborescens and A. margaretarum.



2020 ◽  
Vol 52 (1) ◽  
pp. 3-15
Author(s):  
Nicolas Magain ◽  
Toby Spribille ◽  
Joseph DiMeglio ◽  
Peter R. Nelson ◽  
Jolanta Miadlikowska ◽  
...  

AbstractSince the advent of molecular taxonomy, numerous lichen-forming fungi with homoiomerous thalli initially classified in the family Collemataceae Zenker have been transferred to other families, highlighting the extent of morphological convergence within Lecanoromycetes O. E. Erikss. & Winka. While the higher level classification of these fungi might be clarified by such transfers, numerous specific and generic classifications remain to be addressed. We examined the relationships within the broadly circumscribed genus Arctomia Th. Fr., which has been the recipient of several transfers from Collemataceae. We demonstrated that Arctomia insignis (P. M. Jørg. & Tønsberg) Ertz does not belong to Arctomia s. str. but forms a strong monophyletic group with Gabura fascicularis (L.) P. M. Jørg. We also confirmed that Arctomia borbonica Magain & Sérus. and the closely related Arctomia insignis represent two species. We formally transferred A. insignis and A. borbonica to the genus Gabura Adans. and introduced two new combinations: Gabura insignis and Gabura borbonica. We reported Gabura insignis from Europe (Scotland and Ireland) for the first time. While material from Europe and North America is genetically almost identical, specimens from Madagascar, South Africa and Reunion Island belong to three distinct phylogenetic lineages, all of which are present in the latter area and may represent distinct species. In its current circumscription, the genus Gabura may contain up to six species, whereas Arctomia s. str. includes only two species (A. delicatula Th. Fr. and A. teretiuscula P. M. Jørg.). The Gabura insignis group is shown to have an unexpectedly large, subcosmopolitan distribution. With the extended sampling from Arctomiaceae Th. Fr., the placement of Steinera sorediata P. James & Henssen in the genus Steinera Zahlbr. is confirmed and the presence of a new Steinera species from Chile is highlighted.



2010 ◽  
Vol 5 (6) ◽  
pp. 777-784 ◽  
Author(s):  
Tereza Kořínková ◽  
Alena Morávková

AbstractSome representatives of the bivalve family Sphaeriidae are assumed to be polyploid. In this study, 11 sphaeriid species (nine of the genus Pisidium, one of Musculium, and one of Sphaerium) inhabiting central Europe were studied karyologically, 10 of them for the first time. Analysis revealed high chromosome numbers (from 140 to 240). To elucidate the origin of high chromosome numbers, DNA contents were measured by flow cytometry in 5 of the studied species and, for comparison, in S. corneum and S. nucleus, which are known to be diploid (2n=30). Species with high chromosome counts yielded very similar DNA contents that are not higher than in the related species with low diploid numbers. This finding contradicts a possible origin of these species by recent polyploidization or hybridization of related species. Chromosome complements of the investigated species with high chromosome numbers differ from those with low 2n in their small chromosome size and the high proportion of subtelo- or acrocentric chromosomes. This indicates their possible origin either by an ancient polyplodization event followed by chromosomal rearrangements or by multiple chromosome fissions.



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