A Database for Triticeae and Avena
THE RUSSIAN ACADEMY OF AGRICULTURAL SCIENCES
Far Eastern Branch, Cereal Crops Department, 107 Karl Marx str.,
Khabarovsk, 680009 Russia.
Achievements and problems of spring wheat selection in the
Russian far east.
Ivan Shindin.
Which spring wheats to use for gene pyramiding to
create wheat cultivars for far-eastern Russia are determined best
by considering the agronomic characteristics of the parental lines
and climate of the region. The climate of this area of Russia
is characterized by conditions of drought during tillering and
an excess of moisture during anthesis, grain ripening, and harvest.
The high humidity during flowering and preharvest (95-100
%) causes disease epidemics and lodging of the crop.
From our evaluation of wheat germplasm, we have established
a list of cultivars that are best used for wheat breeding in far-eastern
Russia. Cultivars with a high number of grains/spike, 1,000-kernel
weight, yield/spike, and yield/plant include Lutescens 50, Lutescens
51, Primorskaya 1737, and Primorskaya 1748 from Russia; Siete
Cerros 66, Sonora 64, and Nadadores from Mexico; Bailly, Mida,
and Bledso from the U.S. Cultivars best for breeding semidwarf
plants resistant to lodging include Nainari 60, Sonora 64, and
Indus 66. Acadia, Manitou, and IAC-4 are disease- and lodging-resistant
high-yielding cultivars that also are drought tolerant. Cultivars
resistant to F. culmorum and leaf and stem rust
are Noroeste 66, Nainari 60, and Weibulls.
We have developed criteria for selecting and discarding
breeding materials based on our evaluation of cultivars. When
breeding for high yield, heterozygote combinations where one parent
has high combining capacity are preferable. Reduced vegetation
period, shorter height, and higher yields per spike and per plant
are found in `winter
x spring'
crosses over in `spring
x spring'
crosses. Thus, `winter
x spring'
crosses can be used for breeding high-yielding spring cultivars.
Accounting for the climate of far-eastern Russia,
quality-traits, and level of agriculture expected between the
present and 2010, we developed a model of the ideal wheat cultivar.
We identified 30 traits in this cultivar that are important for
wheat improvement.
Forty-five cultivars of spring wheat have resulted
from the work of far-east breeders. Six of the 45 . Dalnevostochnaya
10, Khabarovchanka, Amurskaya 75, Amurskaya 90, Primorskaya 14,
and Primorskaya 41, are planted on 100 % of wheat hectarage in
far-eastern Russia. In 1996, a state commission evaluated the
new high-yielding cultivar Zaryamka that was created by breeders
in Khabarov (I. Shindin, E. Meshkova, and I. Lomakina). This
cultivar is moderately resistant to Fusarium spp., highly
resistant to U. tritici, and resistant to shattering
and sprouting in the spike. Zaryamka also has high-quality grain
and flour.
In spite of these successes in spring wheat breeding, there are still unresolved problems, mainly in breeding activity. Hopefully, we can increase the potential yield by increasing its resistance to climactic factors, drought high humidity, and waterlogging. The productivity of a cultivar can be evaluated by assessing the areas where it is growing. For developing resistant cultivars, we need to focus on 1) using germplasm from diverse areas; 2) using forms with opposite characteristics for environmental traits, which will increase variability for high adaptability; and 3) evaluating the parental cultivars and hybrids in a variety of growing conditions.
Fusarium is a very serious problem in far-eastern
Russia. Cultivars from our institute are not resistant in years
of high humidity. No resistant cultivars are known. Thus, we
concentrated our breeding efforts on developing moderately resistant
cultivars using the spring wheats Monakenka, Zaryanka, and Nainari
60 (Russia), and Dunun 120 (China); and the winter wheats Odesskaya
16 and Odesskaya 51 (Ukraine) and Scout, Parker, and Redcoat (U.S.).
We continue to try and identify cultivars highly resistant to
Fusarium.
Our breeding efforts on viral pathogens of wheat
are just beginning. Enzymatic degradation (ED) of grain by fungi,
high precipitation, and dew in periods of grain-filling of wheat
cause losses of yield of 15-30
%. Losses can be even greater during years when lodging and untimely
harvests occur in addition. This problem has not yet been addressed
by breeders. We have not identified any cultivars resistant to
ED, necessitating the development of programs to find sources
of resistance to ED and viruses. There also have been no releases
of high-gluten quality cultivars in far-eastern Russia. However,
we have promising lines with high glutenin that may be released
for state cultivar evaluation soon. Co-operation
among scientists of far-eastern Russia will help to resolve these
problems in the future.
(Text translated from Russian by E.V. Boiko)
THE RUSSIAN ACADEMY OF AGRICULTURAL SCIENCES
Information and Computation Centre, P.O. Emmaus, 171330, Tver,
Russia.
S.P. Martynov and T.V. Dobrotvorskaya.
The most common parents of Russian spring wheat released from 1980 to 1996.
The pedigrees of spring wheat released from 1980
to 1996 in the former U.S.S.R. and post-Soviet Russia were studied
with the aid of the Genetic Resources Information System (GRIS2).
With the exception of three cultivars having questionable pedigrees,
115 cultivars were analyzed including 89 from Russia, 17 from
Kazakhstan, 6 from the Ukraine, and 3 from Belarus.
Our objective was to determine which improved cultivars
contributed directly to the parentage of the current spring wheats.
The pedigree of each spring wheat was traced to a named cultivar.
Breeding lines used as parents of cultivars were traced through
their pedigrees to named cultivars. A value for the direct coefficient
of parentage between a parental cultivar and a progeny cultivar
was calculated. This value excluded collateral relationships
that may have existed between parents and progeny, because of
common parents earlier in the pedigree. The coefficient of parentage
for each parent was summed across all 115 progeny cultivars and
divided by 115 to estimate the percent ancestral contribution.
The coefficients of parentage values were pooled within some
cultivar groups in some cases.
Saratovskaya-29 and Bezostaya-1 were the most common
parents of spring wheats released in the former U.S.S.R between
1980 and 1996. (Table 1). The HRSW Saratovskaya-29 (Albidum-24/Lutescens-55-11)
was bred in the early 1950s at the Research Institute of South-East,
Saratov. Because of its drought resistance and good baking quality,
Saratovskaya-29 reached a peak of nearly 21.2 million ha in the
former U.S.S.R in 1996. Bezostaya-1 (Lutescens-17/Skorospelka-2)
is a well-known, HRWW cultivar widely used in Russia and abroad,
because of its high yield and good bread making qualities.
Winter wheats accounted for 10.6 % of the total contribution in pedigrees of new spring cultivars. Crossing of winter and spring wheats was done commonly in breeding programs to increase of yield potential. These crosses are most common in central Russia (18.8 %) and the Middle Volga (20.8 %) regions, but rare in the Lower Volga (1.9 %) and Kazakhstan (7.4 %) areas. Winter by spring wheat crosses are common in Ural and west and east Siberia (Table 2).
Table 1. The percent of ancestral contribution of the five most common parents of Russian spring wheats released between 1980 and 1996.
Parent | Contribution1 |
---|---|
Saratovskaya-29 | 10.6 (15.2) |
Bezostaya-1 | 5.3 (8.6) |
Skala | 3.6 (4.6) |
Saratovskaya-46 | 3.3 |
Novosibirskaya-67 | 2.8 |
Total | 25.6 |
1 Complete contribution
shown in parentheses.
Table 2. Percent ancestral contribution of the most common parents of spring wheat cultivars released in different regions of the former U.S.S.R.
Parent | Central Russia | Volga region | Ural | Kazakhstan | West Siberia | East Siberia |
---|---|---|---|---|---|---|
Saratovskaya-29 | 4.2 (5.2)1 | 11.9 (21.4) | 6.8 (8.0) | 20.6 (26.5) | 14.9 (20.2) | 3.6 (7.1) |
Bexostaya-1 | 4.2 (20.0) | 3.9 (5.5) | 9.1 (11.4) | 1.4 (3.7) | 4.2 (8.6) | 7.11 (11.6) |
Skala | - | - | 2.3 | 2.89 | 7.8 (10.1) | 14.3 (17.0) |
Saratovskaya-46 | - | 12.2 | 4.5 | - | - | - |
Novosibirskaya-67 | - | - | 8.8 | 5.9 | 6.0 | - |
Moskovskaya-35 | 12.5 | - | - | - | - | - |
Saratovskaya-55 | - | 5.3 | - | - | - | - |
Strela | - | - | 6.8 | - | - | 3.6 |
Kometa | - | - | 6.8 | - | - | - |
Tselinnaya-21 | - | - | - | 7.4 | - | - |
Shortandindskaya-25 | - | - | - | 5.9 | - | - |
Skorospelka-uluchshennaya | - | - | - | - | - | 7.1 |
Scandinavian wheats | - | - | 11.4 | - | 15.5 | - |
Winter wheats | 18.8 | 7.9 | 13.6 | 7.4 | 13.4 | 14.3 |
1 Complete contribution shown in parentheses.
The considerable variation of the most common parent of each region (Table 2) can be explained by quite diverse climatic conditions (temperature and rainfall). Moskovskaya-35 (Minskaya/Bexostaya-1) was the most common parent in central Russia. Saratovskaya-46 (C-1616/Selkirk//C-1615/Saratovskaya-38), Saratovskaya-29, and Saratovskaya-55 (Saratovskaya-29/Saratovskaya-51), red and white hard spring cultivars from the Saratov Research Institute, are used widely as parents for cultivars from the Volga region. Within the Ural cultivars, the most common parents were Bezostaya-1, the cold-tolerant Scandinavian wheats Svenno and Vendel, Novosibirskaya-67 (a mutant of Novosibirskaya-7), and local breeding material Strela (Diamant/open pollination) and Kometa (Garnet/open pollination). The most common parent in Kazakhstan is Saratovskaya-29. Tselinnaya-21 (Lastochka/Saratovskaya-29), Shortandinskaya-25 (Saratovskaya-36//(Lutescens-38) Akmolinka-1/Akmolinka-6), and Novosibirskaya-67 are also common parents in Kazakhstan. In western Siberia, Saratovskaya-29 and Scandinavian wheats are the most common parents. However, Skala (Udarnitsa/Garnet//selection from an east Siberian local variety) and Novosibirskaya-67 were widely used. Skala is the most common and Skorospelka-uluchshennaya the second most common parent in eastern Siberia. Thus, Russian wheat breeding programs have specific parents depending on the breeding region.
SARATOV STATE VAVILOV AGRICULTURAL ACADEMY
Department of Biotechnology, Selection, and Genetics, 1. Theatre
sq., Saratov 410710, Russia.
The interaction of 1-anilinonaphthalene-8-sulfonic
acid with membranes and proteins of wheat callus.
S.V. Tuchin.
Fluorescent probes, such as 1-anilinonaphthalene-8-sulfonic
acid (ANS), fluoresce more in hydrophobic than in hydrophilic
environments. Therefore, they are useful for the study of the
structure and interaction among proteins and membranes. Because
ANS has a negative charge, it can be used as a probe to study
charged surfaces. Callus cultures of spring bread wheat were
grown on Linsmaer and Skoog's media with two levels of water chemical
potential: -9
J/mol (control calli) and -36
J/mol (adapted calli). Crude extracts of the callus tissues were
obtained and different amounts of KCl were added after 30 days.
Ten different KCl solutions (from 0.1 to 1.0 mol/l) were used.
Fluorescence of ANS was excited at wavelength 360 nm and registered
at 480 nm. The addition of ANS to extracts resulted in an increase
in fluorescence, indicating that ANS interacts with the hydrophobic
core of membranes and proteins. The fluorescence of ANS in pure
solutions of KCl was several times less than that in the calli
extracts. The effect of KCl may be attributed to an increase
in ANS binding, facilitated by cation suppression of electrostatic
repulsion between the anionic ANS and negative groups of proteins
and lipids. As a result, the intensity of fluorescence can be
increased gradually via salt concentration in the extracts of
both types of calli. However, the slow increase of the fluorescence
was disrupted at several points. Three peaks of ANS fluorescence
were found, corresponding to 0.3, 0.6, and 0.9 mol/l of KCl concentrations
for extracts of control calli. A cation effect due to neutralization
of negative charges on the surface of proteins and membranes cannot
explain this. Sharp changes in fluorescence intensity probably
cause changes in the interaction between bound dye molecules and
their hydrophobic microenvironment induced by the addition of
salt. Only two peaks (0.6 and 0.9 mol/l of KCl concentrations)
of ANS intensity fluorescence were observed for extracts of adapted
calli. The absence of a peak at 0.3 mol/l indicates that the
structure of the hydrophobic microenvironment was less labile
for ANS molecules than for the control calli.
Saratovskaya 64, a new spring wheat variety created by combining
conventional and haploid breeding.
A.I. Kusmenko and T.I. Djatchouk.
Saratovskaya 64 originated from the cross made in
1986 using the local advanced line S-1976 as female and the
local variety Saratovskaya 60 as male. In spring of 1987, 100
grains of an F2 generation were used to obtain homozygous
lines using anther culture. The DH variety Saratovskaya 64 (S-2045
var. erythrospermum) was selected from among 39 DH lines.
The grain yield of Saratovskaya 64 is given in Table 1.
Saratovskaya 64 had the highest yields compared with the control groups Saratovskaya 42 and Saratvskaya 58, in test plots from 1990-96. The yield was 118.9-156.4 % greater than that of Saratovskaya 42 and 106.5-120.9 % greater than that of Saratovskaya 58. The highest yield of this variety was 3.97 T/h in 1990, an increase of 135.5 % over the check Saratovskaya 42. In the dry year of 1995, the increase in yield over the best check Saratovskaya 58 was 0.22 T/ha. Ecological testing at three locations showed yield increases from 0.17 to 0.36 T/ha. The 1,000-kernel weight (average from 1994-96) was 36.4 g compared to 34.8 g in Saratovskaya 58. The baking quality data of Saratovskaya 64 are given in the Table 2.
Morphologically, Saratovskaya 64 has higher tillering
and plant density compared with check varieties. Saratovskaya
64 is more tolerant to virus diseases, and may serve as source
of resistance for wheat breeding programs. Thus, the anther culture
method can produce breeding material adapted to extreme climatic
conditions.
Table 1. Yield performance (T/ha)of the doubled-haploid
variety Saratovskaya 64.
Year | Check varieties | ||
---|---|---|---|
Saratovskaya 58 | Saratovskaya 42 | ||
1994 | 1.98 | 1.78 | 1.62 |
1995 | 1.25 | 1.05 | 0.94 |
1996 | 2.52 | 2.35 | 2.22 |
Average | 1.92 | 1.72 | 1.62 |
Table 2. A summary of the baking quality data of the new wheat variety Saratovskaya 64, compared to a control.
Protein content degree | Gluten % content (cu. sm.) | Volume % texture value (u.a.) | Loaf volume | Alveo- graph | |
---|---|---|---|---|---|
Saratovskaya 64 | 12.9 | 30.1 | 4.7 | 740 | 166 |
Control | 13.7 | 32.6 | 4.7 | 702 | 171 |
The leaf rust-resistant somaclone of spring bread wheat.
Yu.V. Italianskaya and S.V. Tuchin.
The leaf rust-resistant somaclonal variant L
184 from the spring bread wheat rust-susceptible cultivar
Ershovskaya 32 was obtained through cell selection for osmotic
stress resistance followed by plant regeneration. After infection
with rust, this line appeared to have the metabolic changes typically
correlated with disease resistance, i.e., the formation of lignin-like
polymers in damaged cells and sharp increases (as compared with
the parental cultivar) in the activity of enzymes that have been
proposed to play an important role in the metabolism of phenolics;
peroxidase and phenylalanine ammonia-lyase (Table 3).
Table 3. Peroxidase and phenylalanine ammonia-lyase activity (%) in rust-infected wheat leaves in the somaclonal variant L 184, derived from the rust-susceptible cultivar Epshovskaya 32.
Line | Peroxidase | Phenylalanine ammonia lyase |
---|---|---|
Epshovskaya 32 (rust susceptible) L 184 (resistant somaclone) | 230 | 1,950 |
1991 | 380 | 3,960 |
1994 | 350 | 3,750 |
Eight-day-old seedling leaves were inoculated
with urediospores of a local wheat leaf rust population, and enzyme
activities were determined 48 h later and expressed as a percentage
of the untreated controls. Although peroxidase and phenylalanine
ammonia-lyase activities increased after pathogen invasion
in both wheat samples, resistant plants of L 184 were significantly
more sensitive than the susceptible parental plants. The selected
somaclonal variant L 184 has retained its leaf rust-resistance
for several years.
Effects of eleven Rht-genes in spring bread wheats
of the Volga Region.
Yu.V. Lobachev.
The Volga Region is one of the main grain-producing
regions in Russia. However, wheat yields have remained low for
a number of reasons, including the lack of semidwarf varieties.
We created NIL and backcross lines of the variety Saratovskaya
29, differing in 11 identified and unidentified genes, to study
the influence of dwarfing genes on the major characters of spring
bread wheat. The taller variety Saratovskaya 29 and its near
isogenic and backcross lines were studied from 1994-96
in nonirrigated fields at the Saratov Agricultural Research Institute
for South-East Regions.
The height of the taller variety Saratovskaya 29
averaged 81.5 cm during the last 3 years. The majority of the
genes studied (Rht1, Rht4, Rht5, Rht14,
RhtML, RhtPK, RhtR, and Q) resulted
in significant decreases of plant height of 16-25
%; the Rht8 and s1 genes reduced height from 31-33
%, and the Rht3 gene by 52 %. Ear length increased significantly
from 8-12
% under the influence of the Rht3 and RhtPK genes
and decreased significantly (22 %) with the s1 and Q
genes. The other Rht genes have had no significant influence
on ear length. The variety Saratovskaya 29 had an average yield
of 1.85 T/ha over the last 3 years.
The genes can be subdivided into three groups based
on their influence on grain yield. The first group of genes (Rht1,
Rht5, Rht14, and RhtML) had no significant
influence on grain yields in the standard varieties. The second
group of genes (Rht8, RhtR, and Q) significantly
decreased grain yields, 19 % on the average. Lines with the Rht3,
Rht4, RhtPK, and s1 genes had the greatest
decrease in grain yield, 47 % on the average. There were no significant
differences between the varieties studied for the number of spikelets/ear,
ear weight, mean grains/ear, and 1,000-kernel weight. The
number of grains/ear significantly increased by an average 41
%, but only under the influence of the RhtPK gene. The
other Rht genes did not influence this component.
Thus, the genes Rht1 and Rht14, transferred from T. durum, and RhtML, are the most important genes for breeding short varieties for the nonirrigated fields of the Volga Region.
N.I. VAVILOV INSTITUTE OF GENERAL GENETICS
Gubkin st.3, 117809 Moscow, Russia.
Analysis of necrotic genotypes in Triticum aestivum L. cultivars
produced in the former USSR republics.
V.A. Pukhalskiy.
Intensive breeding in different regions of the former
U.S.S.R. led to production of numerous cultivars of common winter
and spring wheat. Many of these cultivars were registered as
commercial varieties by the State Seed Testing Commission, and
presently are cultivated by individual or cooperative farmers.
Other nonregistered varieties are widely used in different breeding
centers for creating new varieties. We have identified necrotic
genotypes in these varieties (Table 1).
Samples from the State Crop Seed Testing Commission
and breeding centers were used in our experiments. The following
cultivars were used as testers for winter wheat: Felix (genotype
Ne1Ne1ne2ne2), Co 725082 (Ne1Ne1ne2ne2), Berthold
(Ne1Ne1ne2ne2), Mironovskaya 808 (ne1ne1Ne2Ne2),
Nemchinovskaya 52 (ne1ne1Ne2Ne2). Spring wheat tester-varieties
included: Marquillo (Ne1Ne1ne2ne2), Opal (Ne1Ne1ne2ne2),
Balaganka (ne1ne1Ne2Ne2), and Barletta 10 (ne1ne1Ne2Ne2).
Crosses were made on isolated spikes. The F1 and
F2 hybrids were grown in the field and the greenhouse.
In analyzing our results, we considered that breeders
do not conduct directional selection against hybrid necrosis genes.
Breeders do not select for particular necrotic genotypes either,
although there is linkage between Ne2 and Lr13 (Singh
and Gupta 1991). The frequency of necrotic genotypes in breeding
populations most likely depends on their linkage with unknown
traits that increase plant fitness. As seen from the data, modern
varieties of winter wheat do not have the Ne1 gene. The
frequency of the ne1ne1Ne2Ne2 genotype is 32.2 %, whereas
the frequency of the ne1ne1ne2ne2 genotype is 67.8 %.
In contrast to winter types, the frequency of the Ne1Ne1ne2ne2
and ne1ne1Ne2Ne2 genotypes in spring varieties is similar
(19.8 %). However, the genotype ne1ne1ne2ne2 (60.4 %)
is higher. A comparison of our data with that from different
regions of the former U.S.S.R. (Pukhalskiy 1996) shows the important
role of modern selection on the frequency of hybrid necrosis genes
in T. aestivum cultivars. (This work was partly supported
by the Russian State Program "Frontiers in Genetics".)
References.
Pukhalskiy VA. 1996. Data on hybrid necrosis genes
in the genus Triticum L. Russ J Genet 32:469-473.
Singh RP and Gupta AK. 1991. Genes for leaf rust
resistance in Indian and Pakistan wheats tested with Mexican
pathotypes of Puccinia recondita f. sp. tritici.
Euphytica 57:27-36.
Table 1. Identification of necrotic genotypes in wheats from the State Crop Seed Testing Commission and breeding centers in the former U.S.S.R.
Necrotic genotype of winter wheat cultivars: | ||
---|---|---|
Ne2-carriers. | ||
Berezina | Khar'kovskaya 20 | Polukarlik 3 |
Deda | Khar'kovskaya 75 | Severodonskaya Severodonskaya 2 |
Dneprovskaya 775 | Krasnodarskaya 39 | Stende |
Donskaya b/o | Lastochka | Tarasovskaya 61 |
Donskaya polukarlikovaya | Mironovskaya Nizkoroslaya | Tarasovskaya Intensivnaya |
Erytrospermum 10 | Mytnitskaya 201 | Verkhnyachskaya 20 |
Erytrospermum 103 | Nadzeya | Veselopodolyanskaya 78 |
Faleshskaya 2 | Polesskaya 70 | Veselopodolyanskaya 81 |
Faleshskaya 3 | Polesskaya 80 | Poltavskaya b/o |
Noncarriers. | ||
Albidum 12 | Komsomol'skaya | Podol'skaya 501 |
Albidum 114 | Kotovchanka | Polesskaya |
Armyanka 60 | Krasnogvardeyskaya | Polukarlikovaya 49 |
Brigantina | Kuryanka | Progress |
Chaika | Lan | Prometei |
Chernozyomka 153 | Luna | Rosinka |
Dneprovskaya 37 | Lutescens 46 | Sevana 4 |
Dneprovskaya 846 | Lutescens 118 | Slavyanka |
Donetskaya 5 | Mechta 1 | Spektr |
Donetskaya 58 | Mechta 2 | Start |
Erytrospermum 80 | Nakhodka | Stepnyak |
Erytrospermum 604 | Nemcinovskaya 110 | Trofimovskaya |
Graecum 439 | Nemcinovskaya 846 | Urozhaynaya |
Izumrudnaya | Nerl (Era) | Yantarnaya 50 |
Khar'kovskaya 11 | Obriy | Yuzhnaya Zarya |
Khar'kovskaya 81 | Odesskaya 66 | Zarya |
Khar'kovskaya 82 | Olimpiya | Zernogradka |
Khersonskaya 94 | Oniks 1 | Znamenya |
Kishinyovskaya | Peresvet | Zolotaya Niva |
Kiyanka | Pitikul | |
Necrotic genotypes of spring wheat cultivars: | ||
Ne1-carriers. | ||
Araks | Lutescens 12 | Vesna |
Belarus | Lutescens 180 | Volzhskaya 2 |
Buryatskaya 34 | Mana | Zarechnaya |
Kazakhstanskaya 3 | Mechta | Ziryanovskaya |
Khar'kovskaya 3 | Otrada | Zazerchanka |
Leningradskaya 176 | Soanovskaya
| |
Ne2-carriers. | ||
Buryatskaya 79 | Kurganskaya | Olimp |
Diana | Mironovskaya 808 lin 6 | Omskaya 6 |
Ershovskaya 32 | Mironovskaya yarovaya | Rena |
Gorskaya | Molodyozhnaya | Sibiryachka 8 |
Komsomol'skaya 3 | Nabat | Skorospelka 14 |
Kuibyshevskaya 1 | Navruz | |
Non-carriers. | ||
Adamant | Komsomolka | Primorskaya 18 |
Akademicheskaya | Kuibyshevskaya 2 | Rodina |
Aktyubinskaya | Kurganskaya 1 | Saratovskaya 29 |
Albidum 28 | Luganskaya | Saratovskaya 54 |
Altaiskaya 80 | Luganskaya 3 | Saratovskaya 55 |
AN 6 | Luganskaya 4 | Sayanskaya 55 |
AS 13 | Luganskaya 5 | Selenga |
AS 29 | Luninskaya | |
Bashkirskaya 20 | Lutescens 28 | Shadrinskaya |
Bezenchukskaya 128 | Lutescens 29/34 | Sibakovskaya 3 |
Botanicheskaya 2 | Lutescens 34 | Sigma |
Botanicheskaya 3 | Lutescens 53 | Simbirka |
Botanicheskaya 4 | Lutescens 80 | Sviyaga |
Chakinskaya | Lutescens 32 H 60/1 | Tarasovskaya 5 |
Dal'nevostochnaya 23 | Lyubov | Tselinnaya 26 |
Diana 3 | Michurinskaya Rannyaya | Tul'skaya Nepolegaycshaya |
Druzhba | Mironovskaya 808 lin 8 | Tyumen'skaya 2 |
Druzhina | Mironovskaya 3 | Tyumen'skaya 80 |
Egisar 29 | Moskovskaya 21 | Ul'binka 78 |
Ershovskaya 30 | Moskovskaya 35 | Ul'yanovskaya 75 |
Erytrospermum 23 | Nevskaya Volna | Velutinum 377/76-39 |
Erytrospermum 74 | Novosibirskaya 22 | Venets |
Estafeta | Omskaya 9 | Vera |
Intensivnaya 50 | Omskaya 16 | Voronezhskaya 6 |
Kazanchulovskaya | Omskaya 17 | Voronezhskaya 8 |
Khar'kovskaya 8 | Penzenskaya | Zaural'skaya |
Kinel'skaya 40 | Plamya | Zhigulovskaya |
Kinel'skaya 89 | Povolzhskaya | Zhnitsa |
Kommunar | Pred'ural'skaya | Zhuravka |