INTERNATIONAL WINTER WHEAT IMPROVEMENT PROGRAM
P.K. 39 Emek, 06511 Ankara, Turkey.
H.-J. Braun1, A.I. Morgounov1, H. Ketata2, S.P.S. Beniwal2, L. Cetin3, H. Ekiz3, V. Eser3, M. Keser3, M. Kanbertay3, and N. Zencirci3.
1 CIMMYT, 2
ICARDA, and 3 Cereals Improvement Program, Turkey.
Current activities.
The International Winter Wheat Improvement Program
(IWWIP) was established in Turkey in 1985 to enhance winter and
facultative wheat germplasm for West Asia and North Africa (WANA),
and other regions of the developing world where this crop is important.
The program is a joint venture between the Ministry of Agriculture
and Rural Affairs (Republic of Turkey), CIMMYT, and ICARDA. The
IWWIP annually distributes the Facultative and Winter Wheat Observation
Nursery (FAWWON) to cooperators worldwide. The nursery includes
elite germplasm from the IWWIP, CIMMYT-Mexico;
Oregon State University (USA); and other national breeding programs
for international testing.
Breeding work in 1996 was structured in the following
manner. The bulk of crosses was made in Izmir (Turkey), supplemented
by crosses at ICARDA-Syria
and CIMMYT-Mexico.
Segregating populations (F2-F4)
were planted in Eskisehir and Cumra. Yield tests were conducted
in Cumra (irrigated and rainfed), Eskisehir (rainfed), and ICARDA-Syria
(rainfed and irrigated). Efficient screening for yellow rust
resistance was done at ICARDA-Syria,
and in Ankara, by pathologists of the Central Field Crop Research
Institute. Natural epithytotics of Septoria in Adana, Turkey,
and powdery mildew in Fundulea, Romania, proved useful to screen
the advanced germplasm for these pathogens.
A line derived from CIMMYT-Mexico
and distributed from Turkey in the IWWSN was released in Argentina
under the name Buck Oportuno.
The following crosses with high yields under diverse
environments were identified in 1996:
PTZ NISKA / UT1556-170
PJ / HN4 // GLL /3/ SERI
SN64 // SKE / 2*ANE /3/ SX /4/ BEZ /5/ SERI
LOV26 // LFN / SDY(ES84-24) /3/ SERI /4/ SERI
VORONA / HD2402
ATAY / GALVEZ87
338-K1-1 // ANB / BUC
OK82282 // BOW / NKT
MANNING / SDV1 // DOGU88
GRK / CTY // MESA
88ZHONG257 // CNO79 / PRL
BEZ // BEZ / TVR /3/ KREMENA / LOV29 /4/ KATYA1
CA8055 / GRK
FAWWON (Facultative and Winter Wheat Observation Nursery)
and germplasm distribution.
The results of the 4th FAWWON were analyzed and compiled
into a report that was printed and distributed to cooperators
in March, 1996. The highlights of the results are the following:
germplasm from the joint Turkey/CIMMYT/ICARDA program continues
to perform well in a facultative type of environment, i.e., in
the immediate target area in west Asia and north Africa. However,
it lacks winter hardiness, and powdery mildew and Septoria resistance,
thus limiting its usage in true winter and/or high rainfall areas.
The inclusion of introduced germplasm into the FAWWON is useful
because it provides access to broader genetic variation. A number
of superior lines were identified (i.e., 1D13.1/MLT, KNR/TRAKIA,
AGRI/NAC, and KS822114/GALVEZ87), which combine broad adaptability
with resistance to diseases.
The 5th FAWWON was distributed for planting in the
1995-96
cycle and consisted of 210 entries. The seeds were sent to 170
cooperators worldwide. Preliminary observations and results indicate
that a number of selections have been made by cooperators in the
region.
The 6th FAWWON was distributed in July 1996 for the
1996-97
crop season and consisted of 200 entries. Excellent collaboration
with Oregon State University, USA, which multiplies the candidates
of the FAWWON and distributes the sets to cooperators in the North
and South America, allows efficient dispatch of FAWWON in the
western hemisphere.
Facultative and Winter Wheat Elite Yield Trial (F &
W EYT).
The F & W EYT is a regional trial designed to
serve two purposes: i) to give cooperators access to superior
germplasm and ii) to identify lines with broad adaptability.
Two sets of the 1st EYT (one targeted for irrigated and another
for rainfed conditions) were prepared and distributed to 20 cooperators
in the WANA region, Central Asia, Russia, and the Ukraine for
the 1995-96
crop season. The yield data collected from 16 locations demonstrated
that the region has very heterogeneous environment with very high `G x E'
interaction. Several lines were identified combining high yield
across locations with other useful traits. The results of the
EYTs are compiled in a report, which is available from the program
on request. Now the two yield trials are regularly distributed
regional nurseries.
The importance of `spring x winter' crosses for winter wheat improvement.
The program utilizes different types of crosses for
winter/facultative wheat enhancement. The performance of two
major groups of crosses, namely `spring
x winter'
and `winter
x winter'=
was compared based on grain yield in preliminary yield trials
conducted during 3 years (1994-96).
Each year the number of lines in each group was comparable'
varying from 200 to 400. Lines originating from `spring
x winter'
crosses were higher yielding compared to those of `winter
x winter'
crosses in 1994. The frequency of lines advanced to the text
stage of testing was almost three times higher among the first
group. In 1995 and 1996, both groups demonstrated almost similar
grain yields and equal frequencies of the selected lines. The
yield evaluation was done in a typical facultative environment
of the Central Anatolian Plateau of Turkey, which is characterized
by mild winters. The data suggest that `spring
x winter'
crosses are at least as useful for winter wheat improvement as
`winter
x winter'
crosses. Prescreening of spring parents in a winter environment
prior to making crosses appears to be very useful. The importance
of `spring
x winter'
crosses for the environments similar to winter wheat areas of
Turkey is further justified by the fact that the majority of varieties
released in the region have spring wheat as an immediate parent.
Personnel.
In September, 1996 Dr. Hasan Ekiz, head of international
program at Bahri Dagdas International Cereals Improvement Center,
Konya, was appointed as the director of the Center.
Publications.
Morgounov A, Alboran M, and Rajaram S. 1996. The
possibility of selecting winter/facultative genotypes from spring
x spring crosses using segregation for vrn genes. In:
Book of Abstracts, 5th Inter Wheat Conf, Ankara, Turkey, 10-14
June.
Sigh G, Rajaram S, Morgounov A, and Fuentes Davila
G. 1996. Genetic basis of Karnal bunt resistance in wheat.
In: Book of Abstracts, 5th International Wheat Conference,
Ankara, Turkey, 10-14
June. pp.151-152.
Ketata H, Morgounov A, Braun H, and Larrah M. 1996.
Effect of yellow rust and drought and heat stress on the performance
of facultative and winter bread wheat germplasm. In:
Book of Abstracts, 5th Inter Wheat Conf, Ankara, Turkey, 10-14
June. pp. 189-190.
Pena R, Braun H, Morgounov A, Ketata H, and Payne
TS. 1996. The frequencies of Glu-1 alleles in germplasm
from the International Winter Wheat Improvement program (Turkey-CIMMYT-ICARDA).
In: Book of Abstracts, 5th Inter Wheat Conf, Ankara,
Turkey, 10-14
June. pp. 385-386.
Braun H, Morgounov EH, Kesr M, Zencirci N, Eser V,
Ketata H, and Marcucci G. 1996. Breeding priorities of winter
wheat programs. In: Book of Abstracts, 5th International
Wheat Conference, Ankara, Turkey, 10-14
June. pp. 457.
Rajaram S and Morgounov A. 1996. Wheat germplasm
improvement at CIMMYT Mexico. In: Wheat Breeding Objectives,
Methodology and Progress: Proc of the Ukraine-CIMMYT Workshop.
Wheat Special Report No. 37. Mexico D.F.:CIMMYT.
Braun HJ, Morgounov A, Ketata H, Ekiz H, Kambertay
M, Keser M, and Zencirci N. 1996. The International Wheat Improvement
Program: objectives and achievements. In: Wheat Breeding
Objectives, Methodology and Progress: Proc of the Ukraine-CIMMYT
Workshop. Wheat Special report No. 37. Mexico D.F.:CIMMYT.
Braun HJ, Rajaram S, and van Ginkel M. 1996. CIMMYT's
approach to breeding for wide adaptation. Euphytica 92:147-153.
Cakmak I, Yilmaz A, Kalayci M, Ekiz H, Torun B, Erenoglu
B, and Braun HJ. 1996. Zinc deficiency as a critical problem
in wheat production in Central Anatolia. Plant and Soil 180:165-172.
Cakmak I, Sari N, Marschner H, Ekiz H, Kalayci M,
Yilmaz A, and Braun HJ. 1996. Phytosiderophore release in bread
and durum wheat genotypes differing in zinc efficiency. Plant
and Soil 180:183-189.
Rajaram S, Braun HJ, and van Ginkel M. 1996. CIMMYT's
approach to breed for drought tolerance. Euphytica 92:175-183.
Schlegel R, Cakmak I, Torun B, Eker S, Tolay I, Ekiz
H, Kalayci M, and Braun HJ. 1996. Screening for zinc efficiency
among wheat relatives and their utilisation for an alien gene
transfer. In: Book of Abstracts, 5th Inter Wheat Conf,
Ankara, Turkey, 10-14
June.
KHARKOV STATE UNIVERSITY
Department of Plant Physiology and Biochemistry, Svobody sq.,
4, Kharkov, 310077, Ukraine.
Monitoring the mode of gene interaction of the photoperiodic
response in winter wheat.
Vasily V. Zhmurko.
In previous experiments with more than 30 varieties
of winter wheat, heading occurred at different times. One group
headed quickly under 24- and 16-hour day lengths. Time-to-heading
under 8-hour day length increased in the second group. The
third group remained unchanged in their development under different
light conditions. Thus, among the winter wheats, there are the
cultivars with long, short, and neutral photoperiods. Short-day
cultivars normally are more winter hardy compared to long-day
and day-neutral plants (Cybulko, Zhmurko, Gridin 1986). Therefore,
photoperiodic response in winter wheat is correlated with winter
hardiness.
Developing cultivars with good winter hardiness and
high productivity is one of the most important objectives of breeders
in the Ukraine. A study of the genetic control of the photoperiodic
response may help to solve problems associated with the development
of highly winter hardy cultivars.
We used the long-day Bezostaya 1, the short-day
Mironovskaya 808, and the day-neutral Obriy cultivars in our experiments.
The following crosses were made: 'Mironovskaya 808 x Bezostaya
1', 'Mironovskaya 808 x Obriy', and 'Bezostaya 1 x Obriy'. The
parental lines and hybrids were grown in the autumn in continuous
light and natural and short-day lengths. One group of plants
was placed in a phytotron at the end of vegetative growth and
grown under 16-hour day length. A second group remained
in the field during the winter and was grown under continuous
light or natural or short-day lengths in the spring. The degree
of dominance in the F1 was determined according to
Griffing (1956), and the mode of gene interaction and differences
between the parental lines for the number of genes producing the
photoperiodic response in the F2 according to A.F.
Merezhko (1984). A `germination-to-heading'
period (days) served as the measure of photoperiodic response
under different day lengths. At least 100 seeds per plant were
analyzed for response to light.
The results from the F1 hybrids indicate
that in all photoperiodic conditions, a short photoperiodic response
is dominant in crosses between short- and long-day cultivars.
The neutral photoperiodic response is dominant in crosses between
short-day and day-neutral plants. A long photoperiodic response
dominates in crosses between long-day and day-neutral cultivars.
Thus, the nature of photoperiodic dominance in the F1
does not depend on day length (Table 1).
Table 1. Photoperiodic response in parental lines and F1 hybrids from crosses between short-day, long-day, and day-neutral cultivars.
Parental lines and hybrids | Photoperiodic response of parental lines | Day length in autumn (hours) | Day length in spring (hours) | ||||
---|---|---|---|---|---|---|---|
24 | 11-9* | 7 | 24 | 15-16* | 7 | ||
P1 Mironovskaya 808 | short day | 131 | 132 | 111 | 235 | 238 | 255 |
F1 (P1 x P2) | 129 | 122 | 109 | 230 | 237 | 255 | |
P2 Bezostaya 1 | long day | 108 | 111 | 116 | 232 | 235 | 245 |
Degree of dominance | 0.8 | 0.05 | -1.8 | -2.3 | 0.3 | 0.0 | |
P1 Mironovskaya 808 | short day | 131 | 132 | 111 | 235 | 238 | 255 |
F1 (P1 x P2) | 112 | 112 | 112 | 230 | 236 | 247 | |
P2 Obriy | day neutral | 95 | 96 | 95 | 230 | 235 | 243 |
Degree of dominance | -0.06 | -0.1 | 1.1 | -1.0 | -0.3 | -0.3 | |
P1 Bezostaya 1 | long day | 103 | 111 | 116 | 232 | 235 | 245 |
F1 (P1 x P2) | 105 | 106 | 110 | 231 | 236 | 247 | |
P2 Obriy | day neutral | 95 | 96 | 95 | 230 | 235 | 243 |
Degree of dominance | 1.5 | 0.3 | 0.4 | 0.0 | 1.0 | 3.0 |
* natural day length.
Analysis of F2 hybrids indicated that
the mode of gene interaction monitoring photoperiodic responses
in the parental lines was dependent on day length. The mode of
cumulative polymery was evident in all the cross combinations
under continuous light and short days, whereas recessive epistasis
occurred in natural day length. The results also showed that
the short-day cultivar Mironovskaya 808 differs from the day-neutral
Obriy and the long-day Bezostaya 1 by dominant, nonallelic genes
monitoring a photoperiodic response (Table 2).
Table 2. Mode of gene interaction monitoring a photoperiodic response in winter wheat hybrids under different day lengths.
Cross combination | Day length (hours) | XMF1 | XMF2 | Mode of gene interaction |
---|---|---|---|---|
`Mironovskaya 808 x Bezostaya 1' | 24 | 0.8 | -0.8 | cumulative polymery |
16 | 0.05 | -1.3 | recessive epistasis | |
8 | 1.8 | -1.2 | cumulative polymery | |
`Mironovskaya 808 x Obriy' | 24 | -0.05 | 0.01 | cumulative polimery |
16 | -0.05 | -0.2 | recessive epistasis | |
8 | 0.8 | 1.3 | cumulative polimery | |
`Bezostaya 1 x Obriy' | 24 | 0.25 | 0.62 | cumulative polimery |
16 | 0.33 | -0.12 | recessive epistasis | |
8 | 0.87 | 1.16 | cumulative polimery |
Thus, photoperiodic domination is determined by the
genotype of the parental lines, but not the day length when F1
hybrids are grown. At the same time, the mode of gene interaction
monitoring a day length response is modified by photoperiodic
conditions. Obviously, the highest mode of gene interaction could
be investigated in contrast to photoperiodic conditions. Because
winter wheat photoperiodic response is correlated with its winter
hardiness, the most complete expression of genes monitoring winter
hardiness could reveal photoperiodic conditions.
References.
Merezhko AF. 1984. The system of the genetic studies
of original material for plant selection. VIR, Leningrad.
Cybulko V, Zmurko V, Gridin N. 1987. Response
of to winter wheat (Triticum aestivum L.) to temperature
- light conditions. Selection and genetic seeds culture,
Vol. 3. Praha. pp. 203-209.
Griffing B. 1956. Concept of general and specific
combining ability in relation to diallel crossing systems. Austr
J Biol Sci 9:463
V.Ya. YUR'EV INSTITUTE FOR PLANT PRODUCTION
National Centre for Plant Genetic Resources of Ukraine, Moskovsky
prospekt, 142, 310060 Kharkov, Ukraine.
Pedigree analysis of T. durum cultivars grown in the Ukraine
and the Russian Federation in 1996 and their relationships in
cultivars.
S.V. Rabinovich and N.K. Il'chenko.
The pedigrees of 32 T. durum cultivars grown
in 1996, four grown previously, and four unreleased germplasms
are the basis of publications by Rabinovich 1972; Dorofeev et
al. 1976; Catalogue 1983, 1992; Martynov et al. 1990; Register
1995, 1996; Golik 1996; State register 1996; and some others.
The titles of the majority of these works (except Golik 1996)
are listed in the publications of Rabinovich, Panchenko, Parchomenko,
and Usova on p. 249.
A pedigree analysis of 32 contemporary of T. durum
cultivars indicates that the most are derivatives of wide
spread wheats (Table 1). Among these cultivars are some Russian
cultivars Melanopus (MEL) 69 (released in 1929, selected from
the landrace Sivouska) and MEL 26 (1956) that have been grown
for 45 and 30 years, respectively. The Ukrainian cultivars Narodnaya
(NAR, 1947; a selection from a landrace) has been grown for more
than 30 years, and Khar'kovskaya 46 (KHR, 1957; a trispecific
Triticum hybrid) is still widely cultivated after 40 years.
P.V. Kuchumov and E.E. Vatulya are breeders of KHR 46. The largest
areas of cultivation for these lines ranged from 2.7 million ha
for MEL 69 in 1940, to 4.9 million ha for KHR 46 in 1969. Russian
cultivars Hordeiforme (HRD) 10 (a selection from a mixture of
the T. aestivum cultivar Noe from a farmer's
field) from western Siberia, HRD 432 (a selection from the landrace
Beloturka) from the Volga region, and the Azerbaidzhanian intermediate
wheat Shark (in the pedigree of the Palestinian cultivar Horanka)
were grown widely for many years (HRD 10 from 1930-60,
HRD 432 from 1930-70,
and Shark from 1940-90).
Unreleased cultivars also occur in pedigrees of wheats KHR 51,
KHR 5, Saratovskaya (SAR) 47, HRD 5866 (also a selection from
the landrace Beloturka), and others.
A `T.
turgidum/T. dicoccum'
cross was in a majority of pedigrees of the cultivars grown (30
of 32), either directly or through the pedigrees of the wheats
KHR 46 and KHR 51 or the old Khar'kov line 34-5129 (a selection
made in 1934). The contribution of the Khar'kov
line in pedigrees fluctuated between 25-50
% in most cultivars to only 6-12
% in some Russian wheats (Novodonskaya (NVD), Ljudmila (LDM),
Bezenchukskiy yantar' (BZN YNT)), and Damsinskaya (DMS) 90 from
Kazakhstan. The Khar'kov
line 34-5129 is absent in pedigrees of only two Russian wheats
from the Volga region, the older Krasnokutka (KRK) 6 and the newer
SAR 59. The index of the Ukrainian wheat NAR in the pedigrees
of 12 modern cultivars is 3-25
%, that of KHR 46 in 25 cultivars is 12-100
%, that of KHR 51 in six cultivars is 6-50
%, and that of KHR 5 in four cultivars is 25-50
%.
The contribution of five old Russian wheats from
the Volga Region HRD 432, HRD 5866 (Saratov), MEL 69, MEL 1932,
and MEL 26 (Krasnyj Kut) in the pedigrees of seven Russian and
one Kazakhstanian wheats grown in this study were between 6 and
25 %. The index of HRD 5866 in SAR 57, SAR Zolotistaya (SAR ZOL),
and Ludmila was between 12-25
%; that of HRD 432 and MEL 1932 in VRN 7 and SID 88 was 12-25
%; that of MEL 1932 in KRK 6 was 12 %; and that of MEL 69, MEL
1932, and their derivative MEL 26 in SAR 59 and SAR ZOL was 6-25
%. Table 1 lists a summary of the participation quotas for the
five above-mentioned cultivars from the Volga Region.
Russian cultivars occur rarely in the pedigrees of
Ukrainian wheats. We noted only Raketa improved in KHR 37 and
KHR 23 and SAR 29 in KHR 15. At the same time, Ukrainian cultivars
were used in a majority of Russian wheats, and their contributions
may be higher than those of Russian wheats. Ukrainian wheats
KHR 46, KHR 3, KHR 17, KHR 21, and KHR 23 also were grown in 1996
in five regions of the Russian Federation from the central region
of Black-Earth to the Ural Region.
Foreign cultivars also are found in the pedigrees
of the wheats in this study. The Italian cultivar Russelo is
in BEZ 182, BEZ YNT, Orenburgskaya (ORB) 2, and ORB 10. The old
Palestinian wheat K 12950 is in KHR 37, KHR 17, and KHR 23; SID
88 is in KHR 1 (from KHR 5), KHR 21 (from 61-29), and KHR
29 (from KHR 5 and Kharkovchanka 1); and Horanka (from Shark)
is in SAR 59 and SAR ZOL. MEL from Pakistan is in LDM. The Canadian
cultivar Hercules and Leeds from the U.S.A. are found in NVD.
Another wheat from the U.S., WS MP 13, is in the pedigree of
SAR 59. The CIMMYT releases Oviachik 65 and Pabellon 67 are found
in Persianovskaya 115 and Kollektivnaya 2, respectively. Triticum
dicoccum has been used often as a parent of modern cultivars;
34-5129, KHR 46, KHR 51, KHR 5, Raketa, Raketa improved,
and Almaz are all derivatives of T. dicoccum.
Ukrainian and Russian cultivars are tested constantly
in our experiments, including the 1996 survey. Most cultivars
are highly adaptable to different growing conditions, tall, and
not resistant to lodging, with the exception of Persianovskaya
115. In tests from 1992-95,
cultivars with long stems (115-130
cm) KHR 23, SAR 59, LDM, BZN 182, BZN YNT, and DMS 90 met or exceeded
the national standard of the Ukraine (KHR 37 at 450 g/m2).
BZN 182 is noted for its high number of kernels/spike (30-40
kernels), and KHR 37, KHR 23, SAR 59, LDM, Zarnitsa Altaya, and
DMS 90 for large kernel size (1,000-kernel weight = 45-55
g). The cultivars SAR ZOL and BSN YNT had indices of 38 and 42
kernels/spike and a 1,000-kernel weight of 45 and 49 g, respectively.
The cultivar KHR 46 grows slowly as a seedling.
The slow development of a stem may promote plant vigor during
the spring cold spells and early frosts that occur in Siberia
and north Kazakhstan. However, KHR 37 grows quickly in the spring.
We have not found any wheat that heads earlier than KHR 37.
KHR 21, KHR 23, and KRK 10 headed simultaneously with KHR 37,
BZN 182, or BZN YNT; and DMS 90 was 5-7
days later.
The high yields of spring wheats in many regions
of the Ukraine and the Russian Federation result from resistance
to fruit fly injury. Cultivars KHR 37, KHR 23, Novodonskaya,
KRK 10, BZN 182, and DMS 90 have the best resistance to this pest
(Dolgova et al. 1996). All of these cultivars have resistance
from descendants of KHR 46 (with line 34-5129 in the pedigree).
The wheats LDM, KRK 10, and BZN YNT had high levels
of resistance to the loose smut fungus when artificially inoculated.
Intermediate levels of resistance (rating 1.3-4.5
%) were found in KHR 21, SAR 59, SAR ZOL, and BZN 182. Seventy
percent of the cultivars were susceptible.
In 1970, the Department of Grain Quality (Melnikov
et al. 1972; Kuchu-mova at al. 1972; Golik at al. 1980) selected
several lines (59-131, 59-158, 59-204, 51-29,
61-29, 62-36, and others) that had been selected in
our Institute in the 1950s and early 1960s. The grain of these
lines has a dual purpose, combining both high pasta-cooking and
breadmaking qualities. Khar'kov's line 34-5129 and Melanopus
falcatum (K 12950) from Palestine were both used in pedigrees
of these cultivars. Line HRD 13-236, bred from the landrace
Khar'kov in 1913, also is present in pedigrees of lines 59-158
and 59-204. These lines and some cultivars bred in Khar'kov
were used in the pedigrees of dual-purpose cultivars (see Table
1). These lines are KHR 5, KHR 17, and the new cultivar KHR 29
(Pedigree: 34-5129/NAR//KHR 46 (62-36)/3/KHR 5/4/Sas
449).
Bushuk (1997), Damidaux and Feillet (1978), and Zillman
(1978) have shown that the presence of g-gliadin
45 (instead of g-gliadin
42) is closely linked with good cooking quality of pasta. A statistical
analysis of a large sample of durum wheats from many countries
confirmed the close linkage of g-gliadin
45 and strong gluten (good cooking quality), and of g-gliadin
42 and poor cooking quality. Gliadin spectra data from the Department
of Quality at our Institute (Golik et al. 1992; Golik 1996) indicate
that in KHR 46, KHR 3, KHR 37, KHR 21, and ORB 10 only g-gliadin
42 is present; KHR 5 has g-gliadin
42 and traces of g-gliadin
45; whereas the older cultivars NAR, KHR 51, contemporary KHR
15 (in the pedigree of SAR 29), KHR 17, and the new cultivar KHR
29 have g-gliadin
45 and a trace of g-gliadin
42. These data confirm that the cultivars KHR 5, KHR 15, KHR
17, and KHR 29 belong to the group of wheats with dual uses for
pasta and bread.
Table 1. Pedigrees and contributions of parents and their ancestors in modern cultivars of Triticum durum.
Year of release | Cultivar | Pedigree | Year in pedigree1 | |||||
---|---|---|---|---|---|---|---|---|
1 | 2 | 3 | 4 | 5 | 6 | |||
The Ukraine | ||||||||
V.Ja. Yur'jev Institute for Plant Production. | ||||||||
- | 34-5129 | T.turgidum/T.dicoccum | - | - | - | - | - | - |
1947 2 | NARODNAYA 3 | sel. from local wheat of the Kharkov region | - | - | - | - | - | - |
1957 | KHAR'KOVSKAYA 46 3 | 34-5129/the best cultivar from the Volga region | 50 | - | - | - | - | - |
1957 | KHAR'KOVSRAYA | NAR/34-5129 51 | 50 | 50 | - | - | - | - |
1983 | KHAR'KOVSKAYA | KHR 46//KHR 46/NAR 3 | 38 | 25 | 75 | - | - | - |
1983 | KHAR'KOVSKAYA 5 | sel from 59-204, K 12950, Palestine/34-5129(51-29)//(50-150)13-236/34-5129 | 50 | - | - | - | - | - |
1988 | KHAR'KOVSKAYA 37 | Raketa improved, RUS/KHR 5 | 25 | - | - | 50 | - | 50 |
1993 | KHAR'KOVSKAYA 15 | SAR 29, T. aestivum RUS/KHR 51 | 25 | 25 | - | 50 | - | - |
1990 | KHAR'KOVSKAYA 17 | 34-5129/NAR(50-62)//KHR 46{62-36}/3/KHR 5 | 38 | 12 | 25 | 50 | - | - |
1993 | KHAR'KOVSKAYA 21 | natural hybrid of 61-29- K 12950/34-5129 (50-165) //NAR/3/KHR 46 | 38 | 25 | 50 | 50 | - | - |
1995 | KHAR'KOVSKAYA 23 3 | Raketa improved, RUS/KHR 5//KHR 46 | 38 | - | 50 | - | - | 25 |
Lugansk State Regional Experimental Agricultural Station. | ||||||||
1985 | LUGANSKAYA 7 | Vinnitskaya 6/KHR 46 | 25 | - | 50 | - | - | - |
The Russian Federation | ||||||||
V.V. Dokuchaev Agricultural Institute for Central Regions of Black Earth. | ||||||||
1987 | SVETLANA 3 | Raketa/KHR 46, UKR | 25 | - | 50 | - | - | 50 |
1993 | VORONEZHSKAYA 7 | Bezostaya 54 (in pedigree of HRD 432, MEL 1932)/KHR 3, UKR | 19 | 12 | 38 | - | 50 | - |
Don Institute of Agriculture. | ||||||||
1990 | PERSIANOVSKAYA 115 | KHR 46, UKR/Oviachik 65, MEX | 25 | - | 50 | - | - | - |
1993 | NOVODONSKAYA | Leeds, USA//Hercules, CAN/M2 Lazorevaya (in pedigree of KHR 46, UKR) F1 | 6 | - | 12 | - | - | - |
Agricultural Research Institute for South-East Region. | ||||||||
1984 2 | SARATOVSKAYA (SAR) | MEL 26/KHR 46 47 | 25 | - | 50 | - | 100 | - |
1987 | SARATOVSKAYA 57 | Shark, AZB/HRD 5866 (LCR 1699)//KHR 51, UKR | 25 | 25 | - | 50 | 25 | - |
1992 | SARATOVSKAYA 59 | WS MP13, USA/(MEL 1700) MEL 26 /MEL 1576 (in pedigree of MEL 69) | - | - | - | - | 62 | - |
1993 | SARATOVSKAYA ZOLOTISTAYA | KHR 51, UKR/SAR 47 (LCR 1858)//(LCR 1830)Raketa improved/MEL 1755-Shark, AZB/HRD 5866//MEL, PAK/HRD 5866 | 19 | 12 | 12 | 25 | 38 | 25 |
1995 | LJUDMILA | MEL, PAK/HRD5866//KHR 46(LKR 1803)/3/D 2629, KAZ) | 12 | - | 25 | - | 12 | - |
Krasnyj Kut Plant Breeding Station of Agricultural Research Institute for South-East Region. | ||||||||
1956 2 | MELANOPUS (MEL) 26 | MEL 69 (sel. from landrace)/MEL 1932 (a hybrid from two Saratov lines) | - | - | - | - | 100 | - |
1974 | KRASNOKUTKA 6 | LKR 2677(in pedigree of MEL 1932)/MEL | - | - | - | - | 12 | - |
Krasnyj Kut Plant Breeding Station and the V.Ja. Yur'jev Institute for Plant Production. | ||||||||
1993 | KRASNOKUTKA 10 3 | sel. from 75-113, UKR natural hybrid from KHR 46, UKR | 25 | - | 50 | - | - | - |
N.M. Tulajkov Samara Agricultural Research Institute. | ||||||||
1980 | BEZENCHUKSKAYA (BZN) 139 3 | BZN 121 (in pedigree of HRD 10)/KHR 46, UKR | 25 | - | 50 | - | - | - |
1993 | BEZENCHUKSKAYA 182 3 | KHR 46, UKR/BZN 105-Russelo, ITA/LCR BG 40 (interspecific hybrid)//KHR 46, UKR/BZN 105 | 25 | - | 50 | - | - | - |
1995 | BEZENCHUKSKIY YANTAR' | HOD 93-75/Jugo-Vostochnaya 144 (in pedigree of HRD 432)//KHR 46, UKR/BZN 105 | 12 | - | 25 | - | 12 | - |
Orenburg Agricultural Research Institute. | ||||||||
1982 | ORENBURGSKAYA 2 | KHR 46, UKR/BZN 105 | 25 | - | 50 | - | - | - |
1989 | ORENBURGSKAYA 10 3 | sel. from Orenburgskaya 2 | 25 | - | 50 | - | - | - |
Kurgan Research Institute of Grain and the V.Ja. Yur'jev Institute for Plant Production. | ||||||||
1991 | KOLLEKTIVNAYA 2 | 34-5129/NAR, UKR(50-62)//KHR 46, UKR (62-36} /3/KHR 46, UKR/4/Pabellon 67, MEX | 25 | 6 | 38 | - | - | - |
Siberian Agricultural Research Institute. | ||||||||
1979 | ALMAZ | Raketa/Kokchetavskaya polba, T. dicoccum//Coerul. 95/3/LCR 18 (sel. from KHR 46, UKR) | 25 | - | 50 | - | - | 12 |
1991 | OMSKIY RUBIN 3 | Almaz/KHR 46, UKR//KHR 46, UKR/HORD 10/3/ Wells,USA | 19 | - | 38 | - | - | 3 |
Altay Agriculture and Agricultural Crops Breeding Research Institute. | ||||||||
1980 | ALTAJKA 3 | sel. from KHR 46, UKR | 50 | - | 100 | - | - | - |
1990 | HORDEIFORME (HRD) 53 | KHR 51, UKR/P 274//P 274/3/KHR 46, UKR | 31 | 6 | 50 | 12 | - | - |
1991 | ALTAJSKAYA NIVA | KHR 51, UKR/P 274//P 274/3/KHR 46, UKR | 31 | 6 | 50 | 12 | - | - |
1996 | ZARNITSA ALTAJA | Altajskaya niva/LKR 42 | 16 | 3 | 25 | 6 | - | - |
Krasnojarsk Agricultural Research Institute. | ||||||||
1962* | Raketa | HRD 27(sel. from Landrace)//HRD 27/Zabajkal'skaya polba, T. dicoccum | - | - | - | - | - | - |
- | Raketa improved | Raketa/B 2537(sib of Raketa) | - | - | - | - | - | - |
Kazakstan | ||||||||
Kustanay Agricultural Research Institute. | ||||||||
1993 | SID 88 | Bezostaya 54 (in pedigree of Hord 432, MEL 1232)/KHR 46, UKR//KHR 5, UKR | 38 | - | 25 | 50 | 25 | - |
V.R. Wil'jams Kazakhstan Institute of Land Use. | ||||||||
1995 | DAMSINSKAYA 90 | Hybrid 491/Almaz | 12 | - | 25 | - | - | 6 |
1 Considered participation quotas (%) from parents and ancestors in pedigree of wheat cultivar: 1. 34-5129; 2. Narodnaya; 3. Khar'kovaya 46; 4. Khar'kovskaya 51 or Khar'kovskaya 5; 5. Cultivars from the Volga Region: Hordeiforme 432, Hordeiforme 5866 (Saratov), Melanopus 69, Melanopus 1932, and Melanopus 26 (Krasnyj Kut); and 6. Raketa or Raketa improved.
2 Cultivars grown in the past.
3 Widespread cultivars in different years.
References.
Bushuk W. 1997. Wheat breeding for end-product use. Proc 5th Inter Wheat Conf. In press.
Dolgova EM, Il'chenko NK, and Markova TU. 1996.
Spring durum wheat resistance to common bunt and fruit fly injury
in the northeastern Forrest-Steppe region of the Ukraine.
Ann Wheat Newslet 42:212.
Golik VS. 1996. Triticum durum Desf. breeding.
Khar'kov. 387 pp (in Russian).
Golik VS and Kuchumova LP. 1980. Breeding of wheats
with dual functionality. Scientific-technical bulletin of
Siberian department of VASKHNIL. N.5-6:72-74 (in Russian).
Golik VS, Panshenko IA, Parchomenko RG, Alad'in VS,
Skljarevskiy KM, and Kuz'mina NV. 1992. The utilization of electrophoretic
gliadin spektra and phenol test as the factors of estimation of
cooking and breadmaking qualities of durum and bread wheat. Breed
Seed Prod 73:27-36 (in Ukrainian).
Il'chenko NK. 1996. Initial material for breeding
of spring durum wheat for productivity. In: Breeding,
seed growing and technologies of field cultures growing. Materials
of International Scientific-Practical Conference. "Bucovina".
Chernivtsi pp. 42-43 (in Russian).
Kuchumova LP, Melnikov NI, and Golik VS. 1972.
Biochemical peculiarities of durum wheat of dual functionality.
Theses of reports of All-Union seminar. Edition of Kazan'
University. Kazan' (in Russian).
Melnikov NI, Golik VS, and Kuchumova LP. 1972.
Triticum durum bred lines with good macaroni and excellent
baking qualities. Report of VASKHNIL. N.9:9-11 (in Russian).
Zillman RR. 1978. Wheat cultivar identification
by gliadin electrophoregramms. M.Sc. Thesis, University of Manitoba,
Winnipeg, Canada (cited in Bushuk 1997).
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