Zeitschriften und Ausgaben

Volumen 68 (2022): Heft 1 (December 2022)

Volumen 67 (2022): Heft 1 (October 2022)

Volumen 66 (2022): Heft 1 (June 2022)

Volumen 65 (2022): Heft 1 (March 2022)

Volumen 64 (2021): Heft 1 (December 2021)

Volumen 63 (2021): Heft 1 (September 2021)

Volumen 62 (2021): Heft 1 (June 2021)

Volumen 61 (2021): Heft 2 (March 2021)

Volumen 60 (2020): Heft 1 (December 2020)

Volumen 59 (2020): Heft 1 (September 2020)

Volumen 58 (2020): Heft 1 (June 2020)

Volumen 57 (2020): Heft 1 (March 2020)

Volumen 56 (2019): Heft 1 (December 2019)

Volumen 55 (2019): Heft 1 (September 2019)

Volumen 54 (2019): Heft 1 (June 2019)

Volumen 53 (2019): Heft 1 (March 2019)

Volumen 52 (2018): Heft 1 (December 2018)

Volumen 51 (2018): Heft 1 (September 2018)

Volumen 50 (2018): Heft 1 (June 2018)

Volumen 49 (2018): Heft 1 (March 2018)

Volumen 48 (2017): Heft 1 (December 2017)

Volumen 47 (2017): Heft 1 (September 2017)

Volumen 46 (2017): Heft 1 (June 2017)

Volumen 45 (2017): Heft 1 (January 2017)

Volumen 44 (2016): Heft 1 (December 2016)

Volumen 43 (2016): Heft 1 (September 2016)

Volumen 41 (2016): Heft 1 (March 2016)

Volumen 40 (2015): Heft 1 (December 2015)

Volumen 39 (2015): Heft 1 (September 2015)

Volumen 38 (2015): Heft 1 (June 2015)

Volumen 37 (2015): Heft 1 (March 2015)

Volumen 36 (2014): Heft 1 (December 2014)

Volumen 35 (2014): Heft 1 (September 2014)

Volumen 34 (2014): Heft 1 (June 2014)

Volumen 33 (2014): Heft 1 (March 2014)

Volumen 32 (2013): Heft 1 (December 2013)

Volumen 30 (2013): Heft 2013 (June 2013)

Volumen 29 (2013): Heft 2013 (March 2013)

Volumen 28 (2012): Heft 2012 (December 2012)

Volumen 27 (2013): Heft 2012 (February 2013)

Volumen 26 (2012): Heft 2012 (November 2012)

Volumen 25 (2012): Heft 2012 (November 2012)

Volumen 24 (2012): Heft 2011 (September 2012)

Volumen 23 (2011): Heft 2011 (January 2011)

Volumen 22 (2011): Heft 2011 (January 2011)

Volumen 21 (2011): Heft 2011 (January 2011)

Volumen 20 (2010): Heft 2010 (January 2010)

Volumen 19 (2010): Heft 2010 (January 2010)

Volumen 18 (2010): Heft 2010 (January 2010)

Volumen 17 (2010): Heft 2010 (January 2010)

Volumen 16 (2009): Heft 2009 (January 2009)

Volumen 15 (2009): Heft 2009 (January 2009)

Volumen 14 (2009): Heft 2009 (January 2009)

Volumen 13 (2009): Heft 2009 (January 2009)

Zeitschriftendaten
Format
Zeitschrift
eISSN
2080-945X
ISSN
1897-2810
Erstveröffentlichung
17 May 2010
Erscheinungsweise
4 Hefte pro Jahr
Sprachen
Englisch

Suche

Volumen 27 (2013): Heft 2012 (February 2013)

Zeitschriftendaten
Format
Zeitschrift
eISSN
2080-945X
ISSN
1897-2810
Erstveröffentlichung
17 May 2010
Erscheinungsweise
4 Hefte pro Jahr
Sprachen
Englisch

Suche

0 Artikel
Uneingeschränkter Zugang

Genetic Diversity of Leafy Liverwort Species (Jungermanniidae, Marchantiophyta) in Poland: Diversity of Leafy Liverwort Species with Various Reproductive Modes

Online veröffentlicht: 13 Feb 2013
Seitenbereich: 3 - 54

Zusammenfassung

Abstract

This monograph presents results of research on genetic diversity of 8 leafy liverwort species differing in reproductive mode. The frst 4 species in Poland are regarded as sterile and reproduce only vegetatively: Bazzania trilobata, Trichoc-olea tomentella, Lophozia hatcheri, and Mylia anomala. The next 4 are fertile, including the monoecious Lepidozia reptans and Calypogeia integristipula as well as the dioecious Mylia taylorii and Tritomaria quinquedentata. For each species, 9-10 populations were sampled. In total, 4744 gametophytes from 73 populations were examined by isozyme analysis. The level of their genetic diversity (total, HT, and within populations, HS) was high, higher than in thallose liverworts, but comparable to the genetic diversity of mosses or even some species of vascular plants. Thus the traditional opinion that the entire group of liverworts has a much lower level of genetic diversity than mosses is erroneous, as it holds true only for thallose liverworts (Metzgeriidae and Marchantiopsida). My results indicate that the effect of reproductive mode on genetic diversity in leafy liverworts is lower than in vascular plants. Sterile and fertile species of liverworts exhibited similar levels of genetic diversity. Moreover, both groups included species that had both high and low levels of HT and HS. In fertile species, monoecious and dioecious species also did not differ signifcantly in genetic diversity, but dioecious liverworts had slightly higher total diversity (HT) than monoecious species. In most of the studied leafy liverworts, the share of genetic diversity within populations in the total genetic diversity of species is greater than between populations. The percentage share of variation among populations (ΦPT) in the total genetic variation was correlated with the total genetic diversity of the species (HT). In species with high HT, differences between populations tended to be rather small. By contrast, in species with lower HT, the percentage share of differentiation among populations in the total diversity of species was much higher. My results confrm theory, based on studies by Kimura, that the main causes of genetic diversity of bryophytes are neutral somatic mutations developing in various vegetative parts of plants. The separation of branches or other plant sections with somatic mutations, followed by the growth of new shoots, can increase the level of genetic diversity. The high level of genetic diversity in sterile liverworts indicates that vegetative reproduction has a greater infuence on the level of genetic diversity than recombination. My results suggest also that mutation rates are similar in closely related species, but species with a wider ecological range exhibit higher genetic diversity because the variability of habitats can infuence the rate and type of somatic mutations. Accordingly, species inhabiting more diverse environments may be more genetically diverse. Patches of the studied species generally consisted of several genotypes (MLGs). Two types of distribution of genotypes in patches were noticed. Patches of species with low total diversity (HT), were often dominated by 1-2 genotypes, which constituted the major part of a patch. In patches of species with higher HT, there was no tendency to form patches with predomination of a single genotype. Different genotypes constituted similar proportions of a patch. In all the studied leafy liverwort species there was a high degree of repeatability of the same genotypes (MLGs) in plants from various patches within the same population or in various populations. Probably the main cause of this is the independent repeatability of the same mutations in different specimens.

Keywords

  • Bryophyta
  • Bazzania trilobata
  • Trichocolea tomentella
  • Lophozia hatcheri
  • Mylia anomala
  • Lepidozia reptans
  • Calypogeia integristipula
  • Mylia taylorii
  • Tritomaria quinquedentata
  • genetic variation
  • population genetics
  • sterile and fertile species
  • population differentiation
  • breeding system
  • monoecious
  • dioecious
Uneingeschränkter Zugang

Genetic Diversity of Leafy Liverwort Species (Jungermanniidae, Marchantiophyta) in Poland: Regional Genetic Differentiation of Leafy Liverworts

Online veröffentlicht: 13 Feb 2013
Seitenbereich: 55 - 76

Zusammenfassung

Abstract

For each of 8 species of leafy liverworts, 9-10 populations were sampled in 2-3 regions of Poland. In total, 5 regions were taken into account: the Tatra National Park, Bieszczady Mts., Białowieża Forest, Pomeranian Lake District, and Suwałki Lake District. Populations of most of the studied species did not show any correlation between genetic differentiation and geographic distances. Clear differences between regional groups of populations were found in only 2 species. The other species showed a complete or partial lack of genetic differentiation between groups of populations from various geographic regions. Generally, however, mountain populations had greater genetic diversity (HT, HS) and coefficient of genetic differentiation (GST) than lowland populations. In the Tatra National Park all the studied liverworts turned out to be more diverse than in the Bieszczady Mts. Białowieża Forest created a uniform group, standing out markedly from mountainous populations but population in this region had slightly smaller genetic diversity, then in the mountains. In the Pomeranian and Suwałki Lake Districts, genetic diversity of liverworts was significantly lower than in mountains. The decrease in diversity in these regions is a likely consequence of habitat fragmentation (causing population depletion) combined with negative effects of urban development. Habitat fragmentation results in genetic drift and inbreeding depression, which cause a decrease in genetic diversity. In the Pomeranian Lake District the level of total diversity (HT) and intra-population diversity (HS) was markedly higher than in the Suwałki Lake District. It may be linked to differences in climate, in the Suwałki Lake District climate is stronger.

Keywords

  • Bazzania trilobata
  • Trichocolea tomentella
  • Lophozia hatcheri
  • Mylia anomala
  • Lepidozia reptans
  • Calypogeiaintegristipula
  • Mylia taylorii
  • Tritomaria quinquedentata
  • genetic variation
  • regional variability
  • habitat fragmentation
0 Artikel
Uneingeschränkter Zugang

Genetic Diversity of Leafy Liverwort Species (Jungermanniidae, Marchantiophyta) in Poland: Diversity of Leafy Liverwort Species with Various Reproductive Modes

Online veröffentlicht: 13 Feb 2013
Seitenbereich: 3 - 54

Zusammenfassung

Abstract

This monograph presents results of research on genetic diversity of 8 leafy liverwort species differing in reproductive mode. The frst 4 species in Poland are regarded as sterile and reproduce only vegetatively: Bazzania trilobata, Trichoc-olea tomentella, Lophozia hatcheri, and Mylia anomala. The next 4 are fertile, including the monoecious Lepidozia reptans and Calypogeia integristipula as well as the dioecious Mylia taylorii and Tritomaria quinquedentata. For each species, 9-10 populations were sampled. In total, 4744 gametophytes from 73 populations were examined by isozyme analysis. The level of their genetic diversity (total, HT, and within populations, HS) was high, higher than in thallose liverworts, but comparable to the genetic diversity of mosses or even some species of vascular plants. Thus the traditional opinion that the entire group of liverworts has a much lower level of genetic diversity than mosses is erroneous, as it holds true only for thallose liverworts (Metzgeriidae and Marchantiopsida). My results indicate that the effect of reproductive mode on genetic diversity in leafy liverworts is lower than in vascular plants. Sterile and fertile species of liverworts exhibited similar levels of genetic diversity. Moreover, both groups included species that had both high and low levels of HT and HS. In fertile species, monoecious and dioecious species also did not differ signifcantly in genetic diversity, but dioecious liverworts had slightly higher total diversity (HT) than monoecious species. In most of the studied leafy liverworts, the share of genetic diversity within populations in the total genetic diversity of species is greater than between populations. The percentage share of variation among populations (ΦPT) in the total genetic variation was correlated with the total genetic diversity of the species (HT). In species with high HT, differences between populations tended to be rather small. By contrast, in species with lower HT, the percentage share of differentiation among populations in the total diversity of species was much higher. My results confrm theory, based on studies by Kimura, that the main causes of genetic diversity of bryophytes are neutral somatic mutations developing in various vegetative parts of plants. The separation of branches or other plant sections with somatic mutations, followed by the growth of new shoots, can increase the level of genetic diversity. The high level of genetic diversity in sterile liverworts indicates that vegetative reproduction has a greater infuence on the level of genetic diversity than recombination. My results suggest also that mutation rates are similar in closely related species, but species with a wider ecological range exhibit higher genetic diversity because the variability of habitats can infuence the rate and type of somatic mutations. Accordingly, species inhabiting more diverse environments may be more genetically diverse. Patches of the studied species generally consisted of several genotypes (MLGs). Two types of distribution of genotypes in patches were noticed. Patches of species with low total diversity (HT), were often dominated by 1-2 genotypes, which constituted the major part of a patch. In patches of species with higher HT, there was no tendency to form patches with predomination of a single genotype. Different genotypes constituted similar proportions of a patch. In all the studied leafy liverwort species there was a high degree of repeatability of the same genotypes (MLGs) in plants from various patches within the same population or in various populations. Probably the main cause of this is the independent repeatability of the same mutations in different specimens.

Keywords

  • Bryophyta
  • Bazzania trilobata
  • Trichocolea tomentella
  • Lophozia hatcheri
  • Mylia anomala
  • Lepidozia reptans
  • Calypogeia integristipula
  • Mylia taylorii
  • Tritomaria quinquedentata
  • genetic variation
  • population genetics
  • sterile and fertile species
  • population differentiation
  • breeding system
  • monoecious
  • dioecious
Uneingeschränkter Zugang

Genetic Diversity of Leafy Liverwort Species (Jungermanniidae, Marchantiophyta) in Poland: Regional Genetic Differentiation of Leafy Liverworts

Online veröffentlicht: 13 Feb 2013
Seitenbereich: 55 - 76

Zusammenfassung

Abstract

For each of 8 species of leafy liverworts, 9-10 populations were sampled in 2-3 regions of Poland. In total, 5 regions were taken into account: the Tatra National Park, Bieszczady Mts., Białowieża Forest, Pomeranian Lake District, and Suwałki Lake District. Populations of most of the studied species did not show any correlation between genetic differentiation and geographic distances. Clear differences between regional groups of populations were found in only 2 species. The other species showed a complete or partial lack of genetic differentiation between groups of populations from various geographic regions. Generally, however, mountain populations had greater genetic diversity (HT, HS) and coefficient of genetic differentiation (GST) than lowland populations. In the Tatra National Park all the studied liverworts turned out to be more diverse than in the Bieszczady Mts. Białowieża Forest created a uniform group, standing out markedly from mountainous populations but population in this region had slightly smaller genetic diversity, then in the mountains. In the Pomeranian and Suwałki Lake Districts, genetic diversity of liverworts was significantly lower than in mountains. The decrease in diversity in these regions is a likely consequence of habitat fragmentation (causing population depletion) combined with negative effects of urban development. Habitat fragmentation results in genetic drift and inbreeding depression, which cause a decrease in genetic diversity. In the Pomeranian Lake District the level of total diversity (HT) and intra-population diversity (HS) was markedly higher than in the Suwałki Lake District. It may be linked to differences in climate, in the Suwałki Lake District climate is stronger.

Keywords

  • Bazzania trilobata
  • Trichocolea tomentella
  • Lophozia hatcheri
  • Mylia anomala
  • Lepidozia reptans
  • Calypogeiaintegristipula
  • Mylia taylorii
  • Tritomaria quinquedentata
  • genetic variation
  • regional variability
  • habitat fragmentation