scholarly journals Length of vegetation period as parameter of common oak (Quercus robur L.) phenological variability

Genetika ◽  
2012 ◽  
Vol 44 (1) ◽  
pp. 139-152 ◽  
Author(s):  
Branislava Batos ◽  
Danijela Miljkovic ◽  
Jelena Ninic-Todorovic
Keyword(s):  
Genetic Structure ◽  
Quercus Robur ◽  
Average Length ◽  
Vegetation Period ◽  
Genetic Structure Of Population ◽  
Structure Of Population ◽  
Common Oak

Paper presents results for length of vegetation period as factor in common oak?s (Quercus robur L.) phenological variability. Trees in two common oaks populations on two locations in area of Belgrade were researched. Average length of vegetation period on site Ada Ciganlija is 166 days, while in location Bojcinska suma is 179 days. Regarding that populations are in similar environmental and habitual conditions, differences in results should be treated as consequence of common oaks intra-specific variability and genetic structure of population. Significant differences in three consecutive years of observation are confirmed.

Genetic epidemiological study of Bashkortostan Republic: The effect of genetic structure of population on the load of monogenic hereditary diseases

2009 ◽  
Vol 45 (4) ◽  
pp. 478-485 ◽  
Author(s):  
S. Sh. Murzabaeva ◽  
R. A. Zinchenko ◽  
Ya. I. Greenberg ◽  
V. A. Galkina ◽  
O. V. Khlebnikova ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Epidemiological Study ◽  
Hereditary Diseases ◽  
Genetic Structure Of Population ◽  
Structure Of Population

scholarly journals An algorithmic model for constructing a linkage and linkage disequilibrium map in outcrossing plant populations

2009 ◽  
Vol 91 (1) ◽  
pp. 9-21 ◽  
Author(s):  
JIAHAN LI ◽  
QIN LI ◽  
WEI HOU ◽  
KUN HAN ◽  
YAO LI ◽  
...  
Keyword(s):  
Linkage Disequilibrium ◽  
Genetic Structure ◽  
Complex Traits ◽  
Molecular Genetic ◽  
Simultaneous Estimation ◽  
Genetic Studies ◽  
Genetic Structure Of Population ◽  
Structure Of Population ◽  
Algorithmic Model ◽  
Linkage Disequilibrium Map

SummaryA linkage–linkage disequilibrium map that describes the pattern and extent of linkage dis-equilibrium (LD) decay with genomic distance has now emerged as a viable tool to unravel the genetic structure of population differentiation and fine-map genes for complex traits. The prerequisite for constructing such a map is the simultaneous estimation of the linkage and LD between different loci. Here, we develop a computational algorithm for simultaneously estimating the recombination fraction and LD in a natural outcrossing population with multilocus marker data, which are often estimated separately in most molecular genetic studies. The algorithm is founded on a commonly used progeny test with open-pollinated offspring sampled from a natural population. The information about LD is reflected in the co-segregation of alleles at different loci among parents in the population. Open mating of parents will reveal the genetic linkage of alleles during meiosis. The algorithm was constructed within the polynomial-based mixture framework and implemented with the Expectation–Maximization (EM) algorithm. The by-product of the derivation of this algorithm is the estimation of outcrossing rate, a parameter useful to explore the genetic diversity of the population. We performed computer simulation to investigate the influences of different sampling strategies and different values of parameters on parameter estimation. By providing a number of testable hypotheses about population genetic parameters, this algorithmic model will open a broad gateway to understand the genetic structure and dynamics of an outcrossing population under natural selection.

Analysis of the matrilineal genetic structure of population in the early Iron Age from Tarim Basin, Xinjiang, China

2009 ◽  
Vol 54 (21) ◽  
pp. 3916-3923 ◽  
Author(s):  
YinQiu Cui ◽  
ShiZhu Gao ◽  
ChengZhi Xie ◽  
QuanChao Zhang ◽  
HaiJing Wang ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Iron Age ◽  
Tarim Basin ◽  
Early Iron Age ◽  
Genetic Structure Of Population ◽  
Structure Of Population

scholarly journals Phenotypic variability of spike characteristics and genetic structure of population in the collection of spring barley

2018 ◽  
Vol 24 (2) ◽  
pp. 49-58
Author(s):  
Aleksandra Miletić ◽  
Dejana Panković ◽  
Miroslav Zorić ◽  
Novo Pržulj ◽  
Gordana Šurlan-Momirović ◽  
...  
Keyword(s):  
Genetic Structure ◽  
Phenotypic Variability ◽  
Spring Barley ◽  
Genetic Structure Of Population ◽  
Structure Of Population

Potenzielle Eichenwuchsgebiete und aktuelle Eichenmischwälder der Schweiz | Potential oak sites and actual mixed oak forests in Switzerland

2008 ◽  
Vol 159 (5) ◽  
pp. 103-111
Author(s):  
Urs Mühlethaler ◽  
Yvonne Reisner ◽  
Nele Rogiers
Keyword(s):  
Information System ◽  
Quercus Robur ◽  
Geographical Information ◽  
Oak Forests ◽  
Natural Growth ◽  
Growth Area ◽  
Entire Country ◽  
Middle Spotted Woodpecker ◽  
Evaluation Matrix ◽  
Common Oak

On behalf of the Federal Office for the Environment (FOEN), the Swiss College for Agriculture established the basis to foster oak species in Switzerland. For this, the growth areas of three oak species, common oak (Quercus robur), sessile oak (Q. petraea) and pubescent oak (Q. pubescens) were assessed throughout the entire country. The assessment was based on their physiological potential, their natural growth area and on the appearance of the middle spotted woodpecker. In addition, the older mixed oak stands were surveyed. These fundamental data were collected with a geographical information system and analyzed for each canton. Altogether, approximately one-fourth of the Swiss forest area is suitable for oak. The natural oak growth area covers however 38 500 ha only. About 19 000 ha of forest are populated by the middle spotted woodpecker and extended older mixed oak forests are found on approximately 24 500 ha. According to the applied evaluation matrix, the greatest potential for fostering oak species lies in eight cantons: Aargau, Zürich, Solothurn, Thurgau, Vaud, BaselLandschaft, Ticino and Schaffhausen.

The resistance of the phenological forms of the common oak (Quercus robur L.) to unfavorable external factors

2017 ◽  
Author(s):  
И.А. Уткина ◽  
В.В. Рубцов
Keyword(s):  
Quercus Robur ◽  
Insect Pests ◽  
Weather Conditions ◽  
External Factors ◽  
Individual Species ◽  
Early Form ◽  
The Common ◽  
Spring Frosts ◽  
Common Oak ◽  
Late Form

Ранняя (Quercus robur var. praecox Czern.) и поздняя (Q. robur var. tardiflora Czern.) фенологические формы дуба черешчатого, выделенные в самостоятельные таксоны в середине XIX в., неоднократно становились объектами исследований для специалистов разного профиля. Собрано немало данных о различиях в их росте, требованиях к условиям местообитания, устойчивости к неблагоприятным внешним факторам. Иногда кроме ранней и поздней феноформ выделяют еще и промежуточные между ними. Наиболее отчетливо различия между феноформами, обусловленные разными сроками листораспускания, проявляются в реакции на поздние весенние заморозки и повреждение листвы насекомыми-филлофагами. Так как на деревьях поздней формы листовые и цветочные почки раскрываются намного позже, чем на ранней, поздняя форма избегает повреждения весенними заморозками. Кроме того, обладая меньшей способностью к формированию летних побегов, она меньше повреждается и ранними осенними заморозками, а также зимними морозами, что способствует образованию у нее более прямых и полнодревесных стволов, по сравнению с ранней формой. Ранняя форма чаще и сильнее повреждается филлофагами ранневесеннего комплекса, у которых отрождение гусениц из яиц синхронизировано с раскрытием почек и распусканием листьев. Есть данные, что видовой состав вредителей листвы на деревьях ранней и поздней форм дуба при их совместном произрастании примерно одинаков, зато численность отдельных видов филлофагов и их соотношение различны. На деревьях ранней формы их больше в несколько раз, что объясняется совпадением фаз развития большинства ранневесенних видов филлофагов и листвы этой формы дуба. Согласно результатам проведенных исследований, поздняя форма предпочтительнее для создания лесных культур дуба как более устойчивая к неблагоприятным погодным условиям и насекомым-вредителям. Early (Quercus robur var. praecox Czern.) and late (Q. robur var. tardiflora Czern.) phenological forms of the common oak, recognized as independent taxa in the mid-nineteenth century, have been subjects of multiple studies by specialists of different fields. Abundant data on the differences in their growth requirements, habitat conditions, and resistance to unfavorable external factors have been collected. Some specialists in addition to early and late phenoforms distinguish intermediate forms. Most clearly the differences between these forms appear in response to late spring frosts and damage of leaves by phyllophagous insects due to different timing of the forms' leafing. As leaf and flower buds in late oaks are revealed much later than in early oaks, late form avoids damage by spring frosts. In addition, due to lower ability to form summer shoots, late oaks are less damaged by early autumn frosts and winter freeze, which contributes to the formation of more straight and full trunks comparing to early oaks. Early oaks are damaged more severely by phyllophagous insects of spring complex, in which hatching of caterpillars from eggs is synchronized with opening buds and unfolding of leaves. There is evidence that species composition of foliage pests on co-occurant early and late forms of oak is nearly the same, but the number of individual species of phyllophagous insects and their ratio are different. In the early form the number of phyllophagous insects is greater by several fold due to concurrence of developmental phases in most early spring phyllophagous species and foliage of this oak form. The obtained results show that the late form of common oak is preferable for forest plantations as more resistant to unfavorable weather conditions and insect pests.

scholarly journals Sucrose synthase expression pattern in the rhythmically growing shoot of common oak (Quercus robur L.)

2005 ◽  
Vol 62 (6) ◽  
pp. 585-591 ◽  
Author(s):  
Rozenn Le Hir ◽  
Sandrine Pelleschi-Travier ◽  
Jean-Daniel Viémont ◽  
Nathalie Leduc
Keyword(s):  
Expression Pattern ◽  
Sucrose Synthase ◽  
Quercus Robur ◽  
Common Oak ◽  
Growing Shoot

scholarly journals Ampelographic description of cluster, berry and seed of merlot cultivar (Vitis vinifera L.) and its selected clones

2016 ◽  
Vol 61 (1) ◽  
pp. 45-55
Author(s):  
Dragan Vujovic ◽  
Dragoljub Zunic ◽  
Boris Pejin ◽  
Jelena Popovic-Djordjevic
Keyword(s):  
Clonal Selection ◽  
Average Length ◽  
Research Work ◽  
Principal Component ◽  
Vegetation Period ◽  
Vitis Vinifera L ◽  
Cluster Number ◽  
The Third ◽  
Third Phase ◽  
Shoot Number

During a four-year period, ampelographic experiments focusing on the berry cluster (average length of grape cluster, number of grape clusters per shoot, number of berries per grape cluster and length of peduncle), berry (length of berry and berry juice yield), length of pedicel and seed (length of berry seed) of Merlot cultivar (used as a relevant standard) and 11 clones (Nos. 022, 023, 025, 026, 027, 028, 029, 030, 031, 033 and 034) were performed in order to establish the differences among them. These experiments were actually conducted in the third phase of individual clonal selection of Merlot cultivar carried out in Serbia. The lengths of grape cluster and pedicel as well as berry must yields differed significantly among the examined clones. The cluster and principal component analyses classified 12 samples into three divergent clusters/groups, respectively. The clones belonging to the cluster II /the second group/ had significantly higher values of numbers of grape clusters per shoot and berries per grape cluster; lengths of peduncle and berry; berry must yield and length of pedicel, compared both to standard Merlot /the cluster I, the first group/ and the clones of the cluster III /the third group/. The phenological observations showed no significant differences in the beginnings and durations of phenological stages and vegetation period of the examined clones. The obtained results indicate the real need for further research work focused both on the agrobiological and technological properties of the grapes and wines aiming to better describe the selected clones.

scholarly journals Population genetic structure of pedunculate oak (Quercus robur L.) in Belarus according to the analysis of chloroplast DNA

2021 ◽  
pp. 59-70
Author(s):  
Vladimir E. Padutov
Keyword(s):  
Genetic Structure ◽  
Chloroplast Dna ◽  
Population Genetic Structure ◽  
Population Genetic ◽  
Quercus Robur ◽  
Phylogenetic Trees ◽  
Rflp Analysis ◽  
Pedunculate Oak ◽  
Maximum Likelihood Methods ◽  
The Republic

Pedunculate oak (Quercus robur L.) is one of the main forest forming species in the Republic of Belarus. Its population genetic structure was formed under the influence of various migration processes. Six chloroplast DNA loci (µdt1, µdt3, µdt4, µcd4, µcd5 and µkk4) were used for the genogeographic study. The material for the analysis was collected in 100 oak forest stands (2325 samples); 18 allelic variants were identified, which are grouped into 17 different combinations (haplotypes). Five of them are widespread (the proportion of occurrence varies from 7 to 48 %, totalling 85 %). The remaining 12 are rare (the proportion of occurrence varies from 1 to 3 %, totalling 15 %). Phylogenetic trees constructed using the nearest neighbour and maximum likelihood methods show the presence of two groups (branches) of haplotypes. One of it comprises 8 variants including 2 dominant haplotypes and the other comprises 9 variants including 3 dominant haplotypes. PCR-RFLP analysis of chloroplast DNA showed that the pedunculate oak in Belarus originates from the Balkan refugium. Haplotype No. 1 (µdt189, µdt3123, µdt4142, µcd494, µcd574, µkk4109) is found almost everywhere in Belarus with the exception of the southwest and northeast, while haplotype No. 8 (µdt189, µdt3121, µdt4142, µcd494, µcd574, µkk4109) is mainly localised in the southwest and northeast. Haplotypes No. 3 (µdt189, µdt3120, µdt4141, µcd494, µcd575, µkk4109) and No. 7 (µdt189, µdt3122, µdt4142, µcd494, µcd574, µkk4109) predominantly found in the west of the country. Haplotype No. 2 (µdt190, µdt3120, µdt4141, µcd495, µcd574, µkk4109) is typical for the southeast.

Sign in / Sign up

Export Citation Format

Share Document