Cryptic speciation in Pelobates fuscus (Anura, Pelobatidae): evidence from DNA flow cytometry

2001 ◽  
Vol 22 (4) ◽  
pp. 387-396 ◽  
Author(s):  
◽  
◽  
◽  
Keyword(s):  
Flow Cytometry ◽  
Eastern Europe ◽  
Genome Size ◽  
Nuclear Dna ◽  
Size Variation ◽  
Dna Flow Cytometry ◽  
Cryptic Speciation ◽  
Genome Size Variation ◽  
The West ◽  
Pelobates Fuscus

AbstractThe amount of nuclear DNA in 173 specimens of Pelobates f. fuscus from 34 localities in Russia, Ukraine, Moldavia and Latvia was determined by DNA flow cytometry. Two distinct groups with different genome sizes were identified. The ranges of the genome size variation in the two groups did not overlap. Geographically, these groups with smaller or larger genome size are distributed in the west and in the east of eastern Europe, respectively.

The genome sizes of Hordeum species show considerable variation

Genome ◽  
1996 ◽  
Vol 39 (4) ◽  
pp. 730-735 ◽  
Author(s):  
Juha Kankanpää ◽  
Alan H. Schulman ◽  
Leena Mannonen
Keyword(s):  
Flow Cytometry ◽  
Hordeum Vulgare ◽  
Genome Size ◽  
Nuclear Dna ◽  
Size Variation ◽  
Nuclear Dna Content ◽  
Meiotic Pairing ◽  
Genome Size Variation ◽  
Dapi Staining ◽  
Hordeum Vulgare Ssp

Hordeum, distributed worldwide in temperate zones, is the second largest genus in the tribe Triticeae and includes diploid, tetraploid, and hexaploid species. We determined, by DAPI staining and flow cytometry, the nuclear DNA content for 35 accessions of the genus Hordeum, from a total of 19 species, including specimens of 2 cultivars and 2 landraces of Hordeum vulgare ssp. vulgare as well as samples of 12 Hordeum vulgare ssp. spontaneum populations. Genome sizes ranged from 5.69 to 9.41 pg for the G1 nuclei of the diploids, and from 13.13 to 18.36 pg for those of the tetraploids. This constitutes a 1.7-fold variation for the diploids, contrasting with a 4% variation previously reported. For H. vulgare ssp. vulgare (barley), the accessions examined differed by 18%. These variations in genome size cannot be correlated with meiotic pairing groups (I, H, X, Y) or with proposed phylogenetic relationships within the genus. Genome size variation between barley accessions cannot be related to status as cultivated or wild, or to climatic or geological gradients. We suggest these data may indicate rapid but sporadic changes in genome size within the genus. Key words : barley, Hordeum, Triticeae, genome size, flow cytometry.

scholarly journals Genome size variation in the Artemisia arborescens complex (Asteraceae, Anthemideae) and its cultivars

Genome ◽  
2006 ◽  
Vol 49 (3) ◽  
pp. 244-253 ◽  
Author(s):  
Sònia Garcia ◽  
Teresa Garnatje ◽  
John D Twibell ◽  
Joan Vallès
Keyword(s):  
Flow Cytometry ◽  
Genome Size ◽  
Nuclear Dna ◽  
Size Variation ◽  
Interspecific Variation ◽  
Dna Amount ◽  
Genome Size Variation ◽  
Artemisia Absinthium ◽  
Mediterranean Populations ◽  
C Value

Different wild Mediterranean populations of Artemisia arborescens from diverse locations representing its geographical distribution, as well as some of its well-known cultivars and some specimens cultivated as ornamentals in gardens, streets, roads and nurseries, were analysed for genome size. Other closely related species endemic to Macaronesia, Artemisia canariensis, Artemisia argentea, and Artemisia gorgonum, were also analysed, and their nuclear DNA amount has been related to the biogeography of this group of species. Additionally, 5 populations of the closely related Artemisia absinthium were analysed to establish comparisons. Measurements acquired by flow cytometry ranged from 8.29 to 11.61 pg for 2C values. Statistically significant differences of 2C nuclear DNA amounts with respect to factors such as insularity or domestication have been detected. However, quite a low intraspecific genome size variation has been found in these species. Furthermore, the study also addressed the possible hybrid origins and possible misidentifications of some of the supposed cultivars of A. arborescens.Key words: Artemisia arborescens, Artemisia absinthium, Artemisia argentea, Artemisia canariensis, Artemisia gorgonum, C value, Compositae, cultivar, domestication, flow cytometry, genome size, hybridization, interspecific variation, intraspecific variation, speciation.

scholarly journals Miscanthus: Inter- and Intraspecific Genome Size Variation Among M. × Giganteus, M. Sinensis, M. Sacchariflorus Accessions

2015 ◽  
Vol 57 (1) ◽  
pp. 104-113
Author(s):  
Sandra Cichorz ◽  
Maria Gośka ◽  
Monika Rewers
Keyword(s):  
Genome Size ◽  
Dna Content ◽  
Nuclear Dna ◽  
Size Variation ◽  
Nuclear Dna Content ◽  
Interspecific Variation ◽  
Genome Size Variation ◽  
2C Dna Content ◽  
Cytological Characteristics ◽  
Stomatal Length

AbstractSinceM. sinensisAnderss.,M. sacchariflorus(Maxim.) Hack. andM. ×giganteusJ.M.Greef & Deuter ex Hodk. and Renvoize have considerably the highest potential for biomass production amongMiscanthusAnderss. species, there is an urgent need to broaden the knowledge about cytological characteristics required for their improvement. In this study our objectives were to assess the genome size variation among eighteenMiscanthusaccessions, as well as estimation of the monoploid genome size (2C and Cx) of theM. sinensiscultivars, which have not been analyzed yet. The characterization of threeMiscanthusspecies was performed with the use of flow cytometry and analysis of the stomatal length. The triploid (2n = 3x = 57)M. sinensis‘Goliath’ andM. ×giganteusclones possessed the highest 2C DNA content (8.34 pg and 7.43 pg, respectively). The intermediate 2C-values were found in the nuclei of the diploid (2n = 2x = 38)M. sinensisaccessions (5.52–5.72 pg), whereas they were the lowest in the diploid (2n = 2x = 38)M. sacchariflorusecotypes (4.58–4.59 pg). The presented study revealed interspecific variation of nuclear DNA content (P<0.01) and therefore allowed for recognition of particular taxa, inter- and intraspecific hybrids and prediction of potential parental components. Moreover, intraspecific genome size variation (P<0.01) was observed inM. sinensiscultivars at 3.62%. The values of the stomatal size obtained for the triploidM. ×giganteus‘Great Britain’ (mean 30.70 μm) or ‘Canada’ (mean 29.67 μm) and diploidM. sinensis‘Graziella’ (mean 29.96 μm) did not differ significantly, therefore this parameter is not recommended for ploidy estimation.

Genome-size variation in bivalve molluscs determined by flow cytometry

1996 ◽  
Vol 126 (3) ◽  
pp. 489-497 ◽  
Author(s):  
A. M. Rodr�guez-Ju�z ◽  
M. Torrado ◽  
J. M�ndez
Keyword(s):  
Flow Cytometry ◽  
Genome Size ◽  
Size Variation ◽  
Bivalve Molluscs ◽  
Genome Size Variation

scholarly journals Genome size variation and karyotype diversity in eight taxa of Sorbus sensu stricto (Rosaceae) from China

2021 ◽  
Vol 15 (2) ◽  
pp. 137-148
Author(s):  
Jiabao Li ◽  
Kailin Zhu ◽  
Qin Wang ◽  
Xin Chen
Keyword(s):  
Flow Cytometry ◽  
Genome Size ◽  
Size Variation ◽  
Sensu Stricto ◽  
Chromosome Size ◽  
Chromosome Counting ◽  
Genome Size Variation ◽  
Ploidy Levels ◽  
First Time ◽  
Karyotype Symmetry

Eight taxa of Sorbus Linnaeus, 1753 sensu stricto (Rosaceae) from China have been studied karyologically through chromosome counting, chromosomal measurement and karyotype symmetry. Genome size was also estimated by flow cytometry. Six taxa, S. amabilis Cheng ex T.T.Yu et K.C.Kuan, 1963, S. hupehensis var. paucijuga (D.K. Zang et P.C. Huang, 1992) L.T. Lu, 2000, S. koehneana C.K. Schneider, 1906, S. pohuashanensis (Hance, 1875) Hedlund, 1901, S. scalaris Koehne, 1913 and S. wilsoniana C.K. Schneider, 1906 are diploids with 2n = 34, whereas two taxa, S. filipes Handel-Mazzetti,1933 and S. ovalis McAllister, 2005 are tetraploid with 2n = 68. In general, the chromosome size is mainly small, and karyotypes are symmetrical with predominance of metacentric chromosomes. Genome size variation of diploids and tetraploids is 1.401 pg –1.676 pg and 2.674 pg –2.684 pg, respectively. Chromosome numbers of S. amabilis and S. hupehensis var. paucijuga, and karyotype and genome size of eight taxa studied are reported for the first time. This study emphasised the reliability of flow cytometry in genome size determination to infer ploidy levels in Chinese native Sorbus species.

Nuclear DNA content in Sinningia (Gesneriaceae); intraspecific genome size variation and genome characterization in S. speciosa

Genome ◽  
2010 ◽  
Vol 53 (12) ◽  
pp. 1066-1082 ◽  
Author(s):  
David Zaitlin ◽  
Andrew J. Pierce
Keyword(s):  
Genome Size ◽  
Nuclear Dna ◽  
Size Variation ◽  
Nuclear Genome ◽  
Nuclear Dna Content ◽  
Size Estimation ◽  
Cell Nuclei ◽  
Genome Size Variation ◽  
Genome Survey ◽  
Size Estimates

The Gesneriaceae (Lamiales) is a family of flowering plants comprising >3000 species of mainly tropical origin, the most familiar of which is the cultivated African violet ( Saintpaulia spp.). Species of Gesneriaceae are poorly represented in the lists of taxa sampled for genome size estimation; measurements are available for three species of Ramonda and one each of Haberlea , Saintpaulia, and Streptocarpus , all species of Old World origin. We report here nuclear genome size estimates for 10 species of Sinningia , a neotropical genus largely restricted to Brazil. Flow cytometry of leaf cell nuclei showed that holoploid genome size in Sinningia is very small (approximately two times the size of the Arabidopsis genome), and is small compared to the other six species of Gesneriaceae with genome size estimates. We also documented intraspecific genome size variation of 21%–26% within a group of wild Sinningia speciosa (Lodd.) Hiern collections. In addition, we analyzed 1210 genome survey sequences from S. speciosa to characterize basic features of the nuclear genome such as guanine–cytosine content, types of repetitive elements, numbers of protein-coding sequences, and sequences unique to S. speciosa. We included several other angiosperm species as genome size standards, one of which was the snapdragon ( Antirrhinum majus L.; Veronicaceae, Lamiales). Multiple measurements on three accessions indicated that the genome size of A. majus is ∼633 × 106 base pairs, which is approximately 40% of the previously published estimate.

scholarly journals Genome size variation in the pine fusiform rust pathogenCronartium quercuumf.sp.fusiformeas determined by flow cytometry

Mycologia ◽  
2010 ◽  
Vol 102 (6) ◽  
pp. 1295-1302 ◽  
Author(s):  
Claire L. Anderson ◽  
Thomas L. Kubisiak ◽  
C. Dana Nelson ◽  
Jason A. Smith ◽  
John M. Davis
Keyword(s):  
Flow Cytometry ◽  
Genome Size ◽  
Size Variation ◽  
Genome Size Variation ◽  
Fusiform Rust

scholarly journals Substantial intraspecific genome size variation in golden-brown algae and its phenotypic consequences

2020 ◽  
Vol 126 (6) ◽  
pp. 1077-1087
Author(s):  
Dora Čertnerová ◽  
Pavel Škaloud
Keyword(s):  
Growth Rate ◽  
Genome Size ◽  
Cell Size ◽  
Nuclear Dna ◽  
Gc Content ◽  
Size Variation ◽  
Nuclear Dna Content ◽  
Genome Size Variation ◽  
Adaptive Consequences ◽  
Genomic Gc Content

Abstract Background and Aims While nuclear DNA content variation and its phenotypic consequences have been well described for animals, vascular plants and macroalgae, much less about this topic is known regarding unicellular algae and protists in general. The dearth of data is especially pronounced when it comes to intraspecific genome size variation. This study attempts to investigate the extent of intraspecific variability in genome size and its adaptive consequences in a microalgal species. Methods Propidium iodide flow cytometry was used to estimate the absolute genome size of 131 strains (isolates) of the golden-brown alga Synura petersenii (Chrysophyceae, Stramenopiles), identified by identical internal transcribed spacer (ITS) rDNA barcodes. Cell size, growth rate and genomic GC content were further assessed on a sub-set of strains. Geographic location of 67 sampling sites across the Northern hemisphere was used to extract climatic database data and to evaluate the ecogeographical distribution of genome size diversity. Key Results Genome size ranged continuously from 0.97 to 2.02 pg of DNA across the investigated strains. The genome size was positively associated with cell size and negatively associated with growth rate. Bioclim variables were not correlated with genome size variation. No clear trends in the geographical distribution of strains of a particular genome size were detected, and strains of different genome size occasionally coexisted at the same locality. Genomic GC content was significantly associated only with genome size via a quadratic relationship. Conclusions Genome size variability in S. petersenii was probably triggered by an evolutionary mechanism operating via gradual changes in genome size accompanied by changes in genomic GC content, such as, for example, proliferation of transposable elements. The variation was reflected in cell size and relative growth rate, possibly with adaptive consequences.

Sign in / Sign up

Export Citation Format

Share Document