Production and use of maize seed for sowing in Bolívar,Ecuador

In the province of Bolívar in the Andean region 212 farmers, six salesmen and 14 technicians, involved in maize production, were interviewed. The majority of the farmers interviewed were small-holders; 64% of the farmers had a farm size of less than 4.5 ha. Maize is the most important crop and is often grown in association with beans. Most maize, 96%, is soft maize meant for human consumption. The cultivars grown are open pollinated ones. One cultivar, ‘Guagal’, was grown extensively. A few others, among which an improved version of Guagal were of some importance. In the production of maize the farmers consider damage due to insects, wind (lodging), diseases, drought and hail, the low prices for their surplus maize and the high costs of fertilizers, chemicals, sowing seed and labour as the most important constraints. The seed for sowing the next crop mainly came from seed kept from the last harvest. Farmers indicated that they select from the harvested ears the healthy looking larger ones. Kernel type also was a selection criterion. Selection for plant type in the field was rarely done. Of the farmers 71% stored the maize as kernels while 29% stored the seed kept on the ears. The storage was predominantly done somewhere in the house in plastic (56%) or cloth bags (14%), in a pile (13%), just on the floor (4%) or in cans (4%). Some farmers still had seed left from the last sowing and were willing to give a sample for testing. From 32 such samples the quality was assessed by INIAP, the Ecuadorean governmental research and breeding organisation. The samples were consistently of a low quality. Especially the vigour of the seedlings was poor and most of the seeds were infected or contaminated by fungi. In the region a few salesmen offer maize seed for sale of cultivar Guagal at prices affordable by the farmer. Of improved cultivars the prices were higher than most farmers are willing to pay. The technicians considered good seed quality and good maintenance of the cultivars effective methods in obtaining better yields. Many farmers do not have access to seed of INIAP and are not familiar with the improved cultivars.     

Variation for resistance to Puccinia hordei in Ethiopian barley landraces

Summary Up to 100 single plant derived lines of 18 Ethiopian barley landraces were evaluated for infection type in the seedling and adult plant stage, and for latent period in the adult plant stage only. A low infection type indicates the presence of race-specific resistance genes of the hypersensitive type, while the latent period is the major component of the polygenic, partial resistance.In the seedling stage 1721 of these single plant derived landrace lines were assessed for infection type against two barley leaf rust races. In the adult plant stage 1227 from these 1721 lines were evaluated for infection type against one race. In the seedling stage 2 (against race 1-2-1) and 29 against race A) out of the 1721 lines showed an infection type lower than 6–7 on the 0 to 9 scale. In the adult plant stage none of the 1227 lines had an infection type lower than 6–7 against race 1-2-1.The variation between and within the landraces for latent period in the adult plant stage was large. Some landraces such as landrace 212845 showed a highly significant and longer mean latent period than most other landraces. Virtually all plants in all landraces carry at least some partial resistance.The near-absence of race-specific, major, resistance genes and the high frequency of moderate levels of partial resistance indicates that the durability of leaf rust resistance in Ethiopian barley landraces is due to the latter type of resistance, and that the multiline principle does not operate.     

Genetic analysis of,and selection for,factors affecting quantitative resistance to Xanthomonas campestris pv. oryzae in rice

Summary This study assessed 46 potato cultivars, breeding lines and Solanum spp. for heat-tolerance using short-term growth rates and carbon assimilation measurements of young in-vitro-derived plants. Plants of the 46 clones and species were transferred from greenhouse conditions to controlled conditions set at 33/25°C day/night with 12 h photosynthetic photon flux density (PPFD) at 430–450 mol m^-2s^-1 and an 8 h daylength extension (6 mol m^-2s^-1), to inhibit tuberization. Twenty eight accessions were also grown in a 20/10°C controlled environment. Plants were harvested after 10 and 20 days and dry weights of the plant components were measured for plant growth analysis. Gas exchange (leaf net photosynthesis and maintenance dark respiration) and leaf chlorophyll fluorescence parameters (O, P, and T) were measured at 30°C. Amongst the 30 accessions grown at both hot and cool temperatures, only two accessions (Yungay and AVRDC 1287.19) produced more dry weight in the hot chamber than the cool chamber. Hot/cool ratioss for net assimilation rate (NAR) and relative growth rate (RGR) exceoded unity in five and six accessions, respectively. For the 46 accessions grown under hot conditions, none had significantly greater values than those of the control clones for RGR and NAR. Differences between clones in maintenance respiration and net photosynthesis were more closely related to RGR, NAR, and total dry weight (TDWT) in clones which invested more dry weight in leaves and less in stems. Attributes of the chlorophyll fluorescence curve did not explain more of the clonal variation in RGR, NAR, and TDWT than did gas exchange parameters. No single gas exchange or fluorescence character explained more than 50% of the variability among clones for NAR, RGR, or TDWT, but combination of favourable attributes could improve potato heat tolerance in the future.     

Residual effects of the Xa-4 resistance gene in three rice cultivars when exposed to a virulent isolate of Xanthomonas campestris pv. oryzae

Summary F₂ plants of five, and F₃ plants of three, crosses between genotypes carrying the race-specific resistance gene Xa-4 and genotypes not carrying this gene were inoculated with two isolates of Xanthomonas campestris pv. oryzae. Half the tillers of each plant received isolate PX061, avirulent on the Xa-4 gene, the other half of the tillers received isolate PX099, virulent for the Xa-4 gene. The F₂ and F₃ populations segregated for a single dominant resistance gene, Xa-4.The parental, F₂ and F₃ genotypes not carrying Xa-4 had mean lesion lengths between 28 and 29 cm for both isolates. The Xa-4 carrying parents showed a mean lesion length of 2.7 cm with the avirulent isolate and of 12.4 cm with the virulent isolate. The Xa-4 carrying F₂ and F₃ genotypes had mean lesion lengths of 5.2 and 20.1 cm for the two isolates, respectively. These observations strongly indicate that the Xa-4 gene, carried by the rice genotypes studied (IR28, Cisadane and BR51-282-8), had a considerable residual effect when exposed to virulent isolate PXO99.     

Characterization of the durable resistance to yellow rust in old winter wheat cultivars in the Netherlands

Summary Winter wheat cultivars released in the Netherlands before 1930 carried durable resistance to yellow rust. Cultivars released in the period between 1930 and 1950 often were durably resistant while recent cultivars infrequently showed durable resistance. This durable resistance was not difficult to transfer to new cultivars. Twenty nine older cultivars with durable resistance and eight recent non-durably resistant cultivars were tested in the seedling stage and in the adult plant stage against 12 West-European yellow rust races and against some non-European races in the seedling stage only. The adult plant tests were carried out in race nursery tests in the Flevopolder. Per race nursery all 37 cultivars, planted in hills of about 20 plants on both sides of the highly susceptible cv. Michigan Amber, were exposed to one race.The infection type of each cultivar-race combination was scored on 0 to 9 scale once in the seedling stage and twice in the adult plant stage. In the race nurseries the percentage leaf area affected was evaluated three times to be used to calculate the area under the disease progress curve (AUDPC). This AUDPC multiplied with the mean infection type in the field gave the susceptibility index (SI).The infection types were classified into resistant (R), intermediate (I) or susceptible (S) when the infection types were 0 to 3, 4 to 6 or 7 to 9, respectively. Four categories of resistance were discerned on the basis of the three infection type scores: 1) RRR, overall resistance; complete or near-complete resistant at all stages. 2) SRR, adult plant resistance, complete- or near-complete resistant at the adult plant stage only. 3) SRS and SSR, temperature sensitive resistance, the resistance changed from the one evaluation data to the other. 4) SSS and an SI lower than that of Michigan Amber, partial resistance.The frequencies of overall, adult plant and temperature sensitive resistance were 1.4, 52 and 54% in the older cultivars and 40, 62 and 22% in the recent ones, respectively. Among the older cultivars all had a fair to high level of partial resistance, the SI being on average only 20% of that of Michigan Amber, while most cultivars also seemed to carry temperature sensitive resistance. The partial resistance of the recent cultivars was of a much lower level with a mean SI compared to that of Michigan Amber of 61%. Partial resistance was highly correlated (r = –0.94) with the mean resistance scores from the Dutch Recommended Cultivars Lists. It was concluded that partial resistance and temperature sensitive resistance were the major components of the durable resistance in the older cultivars.     

Race-specific effects in major genic and polygenic resistance of barley to barley leaf rust in the field: identification and distinction

Summary Six partially resistant spring barley cultivars were exposed to four barley leaf rust (Puccinia hordei) races in the field and in the greenhouse. The 24 cultivar-race combinations were tested in field plots of 1.5×1.5 m² in two replications over two years. To reduce the interplot exchange of urediospores each plot was surrounded by winter rye.The level of barley leaf rust varied among cultivars, races and years. In both years the variance for cultivar-race interactions was highly significant and originating largely from the cultivar-race combinations Berac-22. Armelle-22, Armelle-A and Tyra-A. The Berac-22 interaction was towards higher, the other three interactions towards a lower level of barley leaf rust. The reduced rust levels of these three combinations were not due to interactions between the partial resistance of these cultivars and the aggressiveness of the races but to major genes for hypersensitivity not effective to the races 1-2-1 and F, common in Western Europe, but effective against the rare races 22 and A. This was revealed in the greenhouse experiments where all combinations had a susceptible infection type except Armelle-22, Armelle-A and Tyra-A, which showed low infection types in both the seedling and adult plant stages. The urediosori present in the field plots of these three combinations apparently arose from spores derived from other plots; this interplot interchange suggesting partial resistance.The interaction of Berac with race 22 truly was a small race-specific effect within the polygenic, partial resistance of barley to barley leaf rust like the one reported before between Julia and race 18.     

Mature plant and tissue resistance in the groundnut-peanut bud necrosis virus system

Summary Leaves and plants of different ages of a susceptible and two resistant groundnut genotypes were mechanically inoculated with peanut bud necrosis virus, and the percentage of plants with systemic symptoms (incidence) and the incubation period were determined. The incidence decreased sharply in all three genotypes with the age of the inoculated leaves and plants. The incubation period increased with the age of leaves and plants. Apparently, only young tissue of young plants is susceptible, while mature tissue and plants are highly resistant. This mature tissue and plant resistance occurs irrespective of the susceptibility level of the genotype to peanut bud necrosis virus, however, it develops earlier in the resistant than in the susceptible genotypes.Abbreviations IP₅₀ incubation period - PBNV peanut bud necrosis virus - TSWV tomato spotted wilt virus     

Interplot interference and the assessment of barley cultivars for partial resistance to leaf rust,Puccinia hordei

Summary The barley cultivars Akka, highly susceptible, and Vada, partially resistant to barley leaf rust, Puccinia hordei, were evaluated for the amount of leaf rust in five experimental field plot situations over three successive years. The field plot situations were: A) plots well isolated from each other by distance and non-leaf rust contributing host plants; B) adjacent plots of 4×41/2 m (18 rows); C) adjacent plots of 4×11/2 m (6 rows); D) adjacent plots of 4×1/4 m (1 row); E) adjacent plots of only one plant (cultivar mixtures).The sporulating leaf area of each plot was measured from samples of 20 tillers taken at random from each plot. In each year the difference in sporulating area between Akka and Vada was large to very large in the absence of interplot interference in the isolated plots, ranging from 150 to 2100 times. In the adjacent plots the partial resistance of Vada was greatly underestimated, 5 to 16 times in the situation B, 14 to 30 times in C, and 75 to 130 times in D and E.Testing lines or cultivars in adjacent plots is the standard procedure in use in breeding programs and in tests of cultivars for their agricultural value. To avoid such under estimation the following procedure is suggested. A few cultivars representing the known range of partial resistance and whose level of partial resistance is well known are evaluated together with the lines and cultivars whose partial resistance has to be assessed. This is demonstrated with a number of cultivars of which resistance values are know from the recommended variety lists for England and Wales. Cultivars have been assessed in Wageningen over four years together with the check cultivars Akka, Sultan, Julia and Vada representing the range of partial resistance with values (on a 1 to 10 scale) of 1, 3–4, 7 and 8 respectively, based on isolated plots experiments.     

Further evidence of polygenic inheritance of partial resistance in barley to leaf rust,Puccinia hordei

Summary The latent period (LP) is a crucial component of partial resistance. Five cultivars, L94, Sultan (Su), Volla (Vl), Julia (Ju) and Vada (Va), representing the known range in partial resistance and LP were crossed in a diallel, and the F₁, F₂ and F₃ tested. The LP effectuated by the five cultivars is about 9, 10^1/2, 10^1/2, 13 and 15^1/2 days, respectively. The crosses Su×L94, Vl×L94 and Ju×L94 had an F₂ positively skewed. Their F₂ means were similar or only slightly larger than the F₁ means. The F₂ frequency distributions in the crosses Vl×Su, Ju×Su and Ju×Vl were normal or nearly so with F₁ and F₂ means similar to each other and to the mid-parent value. The crosses involving Va as a parent again showed a positive skewness but with F₂ means considerably larger than the F₁ moans.Most F₂'s ranged from the low parent to the high parent values without transgression. In the crosses Va×L94 (reported earlier) and Ju×L94 the parental values were not recovered among 216 and 154 F₂ plants, respectively. The cross Ju×Va showed transgression beyond the low parent, Ju.From these data it is concluded, assuming no linkage, that seven loci are involved. The + alleles (governing a longer LP) are thought to be distributed over the parents as follows: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGceaqabeaacaqGmb% GaaeyoaiaabsdacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaab2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGTaGaaeylaiaabccacaqGGaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeylaiaab2caca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaa% b2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae% iiaiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGaGaaeiiaiaabc% cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGTaGaaeyl% aiaabccaaeaacaqGtbGaaeyDaiaabccacaqGGaGaaeiiaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaa% bccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae% 4kaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqG% RaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2% cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeii% aiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccacaqGGa% GaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGTaGaaeylaa% qaaiaabAfacaqGSbGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGaaeiiaiaabc% cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGaaeii% aiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGa% GaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUca% caqGRaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiai% aab2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGa% aeiiaiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2cacaqGTaaabaGaaeOs% aiaabwhacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGa% GaaeiiaiaabccacaqGGaGaae4kaiaabUcacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaabccacaqGGaGaae4kaiaabUcacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaabccacaqGGaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaa% bccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2cacaqGTaGaae% iiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeylaiaab2caaeaacaqGwbGaaeyyaiaabccacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcaca% qGRaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae4kaiaa% bUcacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae% 4kaiaabUcacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeylaiaab2cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabc% cacaqGGaGaae4kaiaabUcacaqGGaGaaeiiaiaabccacaqGGaGaaeii% aiaabccacaqGGaGaaeiiaiaabUcacaqGRaaaaaa!1BBA!\[\begin{gathered} {\text{L94 - - - - - - - - - - - - - - }} \hfill \\ {\text{Su + + + + + + - - - - - - - - }} \hfill \\ {\text{Vl + + + + - - + + - - - - - - }} \hfill \\ {\text{Ju + + + + + + + + + + - - - - }} \hfill \\ {\text{Va + + + + + + + + - - + + + + }} \hfill \\ \end{gathered} \]The genes are supposed to act additively (intermediate inheritance) with the exception of one locus (the 6th or 7th locus) which shows dominance for the shorter LP (for the-alleles). The effect of this locus on LP seems considerably larger than that of the other loci. There are indications of physiological barriers, which means that LP's shorter than the one of L94 or much longer than that of Va are not possible.The effect of + genes in genotypes governing LP's close to these barriers (with very few or very many + alleles respectively) is smaller than in genotypes governing intermediate LP's.     

Spontaneous formation of macroscopic chiral domains in a fluid smectic phase of achiral molecules

A smectic liquid-crystal phase made from achiral molecules with bent cores was found to have fluid layers that exhibit two spontaneous symmetry-breaking instabilities: polar molecular orientational ordering about the layer normal and molecular tilt. These instabilities combine to form a chiral layer structure with a handedness that depends on the sign of the tilt. The bulk states are either antiferroelectric-racemic, with the layer polar direction and handedness alternating in sign from layer to layer, or antiferroelectric-chiral, which is of uniform layer handedness. Both states exhibit an electric field-induced transition from antiferroelectric to ferroelectric.