Low level of resistance to major diseases such as ascochyta blight (AB), botrytis grey mould (BGM) and dry root rot (DRR) in the cultivated chickpea genepool necessitates harnessing wild Cicer species. Sixty-eight accessions belonging to eight annual wild Cicer species and seven chickpea cultivars were screened for AB, BGM and DRR under controlled environmental conditions over the years. Intra-accession variability was observed among wild Cicer accessions for each disease. Hence, progenies of single resistant plants were selected for further evaluations and the trait-specific genetic stocks (TGS) were developed for each disease after re-screening following the single seed descent method. For AB, a high level of resistance was identified in four accessions belonging to tertiary genepool species, ICC 17334 (Cicer judaicum), ICC 17302, ICC 17308 and ICC 20177 (C. bijugum). Nine accessions, ICC 17160, ICC 17264, ICC 17270, ICC 20170, ICC 20186, ICC 20225, ICC 20247, ICC 20251 and IG 72941 of primary (C. reticulatum) and one accession, ICC 20190 of secondary (C. echinospermum) genepool species were resistant to BGM whereas, four accessions, ICC 20187 (C. reticulatum) and ICC 20218, ICC 20244 and ICC 20257 (C. echinospermum) were resistant to DRR. Development and utilization of these TGS in chickpea pre-breeding will assist in developing disease-resistant chickpea cultivars with broad genetic base.

Verbascum blattaria L., commonly known as moth mullein, naturalized in the USA that produces white or yellow flowers could be considered as a potential ornamental plant. However, genetic characterization using molecular markers and leaf morphology, colourimetric analysis and flowering of V. blattaria influenced by low temperature treatments was not investigated to evaluate as a potential horticultural and landscape plant use. The basal leaves developed during the rosette-growth stage were oblanceolate with an obtuse leaf apex and incisions at the margin. Leaves produced on the stem during the reproductive development were ovate or lanceolate with an obtuse or acute leaf apex. Regardless of the colour of the petiole and leaf blade during the rosette-growth stage, there were no differences in the sequences of nuclear ribosomal ITS and chloroplast interspacer. All plants produced creamy white flowers with a purplish base corolla. All leaves formed during the vegetative and reproductive development were glabrous. Numerous stalked glandular trichomes were observed in the sepal, pedicel and bracts. Seeds started to germinate in 10 days at 25°C and reached the plateau in 30 days after sowing. The earliest flowering occurred in 131 days when the plants received 20 days of low temperature treatment (CD) (20 CD), producing 76 flowers, the highest number compared to the number of flowers produced by plants that received 0, 40 and 60 CD. Plants that received 20 CD exhibited early flowering, probably because of the early transition from vegetative growth to reproductive development, as judged by the short stem to the first flower.

In Morocco, sugar-beet seed production represents a new challenge to meet the main breeding programme goals. The identification of a suitable zone for plant vernalization represents a bottleneck for seed production. This study aimed chiefly at evaluating the vernalization aptitude of 18 sugar beet half-sib progenies. Trials were conducted during three selection cycles in a specifically chosen environment. The experimental site of Merchouch is 40 km south-east of Rabat city. Field trials design is according to an open-pollinated experimental block. Yield components and five phenological traits were recorded during the growing cycle and at the plant maturation. The variance analysis showed a significant effect of the selection cycle on the phenological traits and grain yield. The plant cycle duration increased by 10.7 days between the first and the third selection cycles. According to the principal component analysis and the hierarchical clustering, F2, F5, F6, F9, F10, F11, F14 and F15 half-sib progenies are described as long cycle and high grain yield families. Grain yield reached 257.3 g per plant, the duration to maturity 350.6 days and the germination rate 93%. The three selection cycles and the suitability of the site vernalization conditions are potentially effective for seed production progress. Our results are relevant as they established an adequate site for the sugar beet seed production. The half-sib selection is a valuable method for sugar beet germplasm enhancement.

Cereal rye (Secale cereale L.) control in wheat (Triticum aestivum L.) can be difficult with existing selective herbicides. High phenotypic diversity within populations coupled with suboptimal herbicide application conditions leads to varying degrees of control with herbicide treatments. The following research focused on the consequence of low temperature on imazamox fate in S. cereale. A greenhouse study was conducted to determine the number of warm-temperature days required for imazamox to control S. cereale. Absorption, translocation, and metabolism of imazamox was evaluated under warm (22/18C) and cold (4/4C) temperatures to identify changes to the fate of imazamox under different environmental conditions. In greenhouse conditions, more than 5 d of warm temperature following herbicide application was required to achieve 80% S. cereale mortality. Absorption of imazamox was reduced 20% when S. cereale was subjected to cold compared with warm temperatures. Only 10% of applied imazamox was moved from the treated leaf in continuous cool temperatures compared with greater than 60% in warm conditions. In cold conditions, imazamox content increased in all tested plant parts evaluated for the duration of the study, whereas in warm conditions, imazamox concentrations decreased in root and crown tissues after 3 d. Imazamox behavior was affected more by temperature than S. cereale growth stage. Secale cereale metabolism of imazamox was reduced, but not stopped in cold temperatures. After 6 d, only a 10% difference in intact imazamox remained between temperature treatments. In cold temperatures, reduced absorption and translocation, coupled with continued metabolism, allow plants to recover from an otherwise lethal imazamox treatment.

Seedling vernalization was more effective than seed vernalization in promoting flowering of downy brome (Bromus tectorum L. # BROTE). Vernalizing imbibed downy brome caryopses at 3 C for 0 to 30 days did not induce rapid flowering when the caryopses were planted. Downy brome seedlings were exposed for 30 days to six photoperiod/temperature treatments. After subsequent transfer to long days, plants from the short-day/3 C treatment flowered within 30 days. Flowering was delayed or was absent in treatments with higher temperatures or long days. The shoot apex increased in volume during the short-day/3 C vernalization period. Two days following vernalization, floral initiation had occurred. By day 5, lateral organs had proliferated. Rudimentary glumes and lemmas were visible by day 8.

Exotic annual weeds on western U.S. rangelands owe at least part of their invasion success to prolific seed production. Reproductive output is determined largely by timing of flowering in relation to soil moisture, light, and competing vegetation. This study investigated the influence of temperature (including vernalization), photoperiod, and intraspecific competition on reproductive phenology in three populations (two varieties, typica and bracbypappa) of common crupina. Monthly plantings at four densities were grown in field plots through two consecutive cycles, and the date each plant reached bud and flowering stage was recorded. Development of greenhouse-grown plants from the same populations was compared with those grown outside for 4, 6, 8, and 10 wk of cold induction. Reproductive development in common crupina was influenced by all factors investigated: temperature, photoperiod, density, and vernalization. Conditions fostering the shortest thermal time from emergence to floral induction were a period of cold temperatures/short photoperiod as seedlings followed by warming temperatures and lengthening photoperiod. Both varieties of common crupina responded quantitatively to vernalization, but lack of vernalization caused a greater delay of flowering in var. brachypappa than in var. typica. Vernalization contributed to convergence of spring flowering among the August to December plantings, but earlier emergence and lower plant density greatly increased final plant size and fecundity. Lack of vernalization, high temperatures, and shortening day length delayed flowering of spring/summer emergents, increasing the probability of succumbing to drought before producing seed.

Morphological and physiological variation among annual bluegrass populations from the green, fairway, and rough were measured to determine the role annual bluegrass infestations outside the green play in maintaining the population in the green. Annual bluegrass populations from the fairway and the rough were similar to each other but differed from that of the green in habit, dry mass production, flowering, seed size, and germination. Seeds from each population established best in the type of turf from which they originated. It is concluded that, since few genotypes were common to the green and its surroundings, the populations in the fairway and rough played little or no role in maintaining the population of the green. The same is likely to be true wherever the management of greens and their surroundings differs sufficiently for marked population differentiation to occur. This finding does not preclude the possibility that some genotypes adapted to the green persist in the surroundings, and that these genotypes serve as sources of seeds for the colonization or reinfestation of annual bluegrass-free greens.

The growth and development of leafy spurge (Euphorbia esula L. #3 EPHES) collected during postsenescent dormancy and grown in the greenhouse was increasingly stimulated by chilling treatments longer than 14 days duration at 0 to 6 C. Production of stems with flower buds, primary flowers, and secondary flowers was greater in plants chilled for 42 days or more. The effects of chilling on total number of stems, number of strictly vegetative stems, or number of stems with vegetative branching were not significant. The height of the tallest stem per pot was influenced by chilling longer than 42 days. Growth rate also increased as a function of chilling duration. Based on our findings, we believe that there is little possibility that any significant growth can occur in the postsenescent period because of the prevailing climatic conditions found in areas of leafy spurge distribution in North America.

To assess the risk of gene movement between winter wheat and jointed goatgrass, information about the reproductive development of jointed goatgrass, winter wheat, and related hybrid plants is required. Seedlings from five jointed goatgrass populations, winter wheat, spring wheat, and jointed goatgrass by wheat reciprocal hybrid plants were exposed to 4, 7, or 10 C temperatures for 0, 2, 4, 5, 6, 6.5, 7, or 8 wk. Vernalized seedlings were transferred to a greenhouse set to 30/18 C day/night temperatures and 16-h photoperiod. Growth stages on all plants were recorded twice a week. All spring wheat and spring wheat related hybrid plants reproduced (as measured by the first reproductive node) in the absence of vernalization. Plants of jointed goatgrass population A-R, winter wheat, and winter wheat related hybrids were unlikely to reproduce in the absence of vernalization. Plants of jointed goatgrass populations B-W, G-S, E-S, and F-W reproduced in the absence of vernalization, and the likelihood that these plants would reproduce was different from all other plants. Plants that entered their reproductive phases together were not in synchronous development at anthesis. Plants in these studies differentially passed through the reproductive phases between the first reproductive node and anthesis. Our results demonstrate that variation in vernalization response exists among several jointed goatgrass populations, and reveal that the reproductive behavior of vernalized jointed goatgrass plants at anthesis is delayed compared to vernalized winter wheat and related hybrid plants. Hybrid plants produced between spring wheat and jointed goatgrass were vernalization insensitive. We hypothesize that hybridization between wheat and jointed goatgrass occurs as a result of cross-pollination between the younger reproductive tillers of jointed goatgrass and older reproductive tillers of wheat. The use of an early maturing wheat cultivar may exploit the difference in reproductive development and reduce the risk of hybrid production.

Control of rattail fescue, a winter annual grass, can be difficult in spring or winter wheat. Although rattail fescue is not a new weed species in the Pacific Northwest, occurrences have been increasing in circumstances where soil disturbances are minimized, such as in direct-seed cropping systems. To develop integrated management strategies for rattail fescue, information is needed on the longevity of seed viability in the soil, the presence of seed dormancy, vernalization requirements, and optimal environmental conditions for seed germination and establishment under field conditions. Controlled experiments on the biology of rattail fescue indicated that newly mature seed required an afterripening period of 1 to 12 mo to obtain high levels of seed germination, depending on germination temperature. Maximum seed germination was observed at constant day/night temperatures of approximately 20 C from thermogradient plate studies. Germination tests from seed burial studies indicated that a majority of buried seed was not viable after 2 to 3 yr. Field-grown rattail fescue plants required vernalization to produce panicles and germinable seed. A short afterripening period, cool germination temperature, and vernalization requirements support the classification of rattail fescue as a winter annual. This information will facilitate development of rattail fescue management systems, including crop rotations and various control tactics such as tillage or herbicide application timing during fallow periods.

Feral rye is an agricultural and ruderal weed of the western United States. We investigated how it has phenotypically diverged from its cultivated ancestor, domesticated cereal rye, and across its range since the introduction of its progenitor. Vegetative growth, flowering phenology, and reproductive characters of feral populations from across a 13° range in latitude in the northwestern United States were compared to that of rye cultivars under both vernalized (cold-treated) and nonvernalized conditions. Feral populations as a whole had smaller seeds, thinner culms, and a delay in flowering relative to cultivars, regardless of cold treatment. Vernalized feral populations from northern latitudes (northern California and eastern Washington) produced more, but smaller leaves and more tillers than both vernalized rye cultivars and southern California feral populations. Northern feral populations also flowered significantly later, irrespective of vernalization treatment. We conclude that feral rye is phenotypically distinct from domesticated cereal rye and that feral populations have diverged regionally from one another. Reproductive isolation from domesticated rye, due both to the loss in popularity of the crop and to phenological shifts in feral rye relative to cultivars, may be contributing to the rapid evolution of this weed away from its domesticated ancestor in less than 120 yr since its introduction.

The most common strategy recommended for management of jointed goatgrass infestations is to rotate from winter wheat to a spring crop for several years. A field study was conducted at three locations in 1998 and 1999 to determine the effects of spring seeding date on the ability of jointed goatgrass to flower and produce viable seed in the presence or absence of spring wheat and to determine the effect of jointed goatgrass competition and crop seeding date on spring wheat grain yield. Spring wheat was seeded on four dates at each location in both hand-sown and natural jointed goatgrass infestations. Jointed goatgrass plants from hand-sown spikelets flowered and developed spikelets on all seeding dates except the last; viable seed was produced on the two earliest seeding dates. Jointed goatgrass plant densities from natural infestations were from 1 to 12 plants m−2, and spikelet production ranged from 0 to 480 spikelets m−2. Natural jointed goatgrass infestations produced spikelets containing viable seed on all seeding dates at one location in 1998, the driest location. Spring wheat yield was not affected by jointed goatgrass competition; however, jointed goatgrass spikelet production was reduced by spring wheat competition compared with that of monoculture jointed goatgrass. The last seeding date of spring wheat was associated with 51% less crop yield compared with the recommended seeding date. The decision to manage jointed goatgrass infestations with a spring crop rotation should consider delayed seeding dates to minimize viable spikelet production by spring-germinating jointed goatgrass; however, the cost of this decision may include grain yield reduction.

Black henbane can be either annual or biennial. We investigated which life cycle is found in four introduced western North American populations. Plants were grown in a greenhouse common garden until half were vernalized by exposure to natural winter temperatures, while the other half remained in the greenhouse above 20 C, with 16 h of light and 8 h of dark. In total the plants were monitored 313 d after germination. We measured whether plants bolted, the time it took for bolting to commence, and the size at bolting. All vernalized plants bolted after 117 d of active growth (within 26 d of the end of the vernalization treatment), whereas only 26% of the nonvernalized plants bolted after an average of 278 d of active growth. Vernalized plants bolted at a smaller size than the nonvernalized plants that bolted (28 vs. 41 leaves on average). In the nonvernalized plants, the relationship between time to bolting and size was strong, but not so with the vernalized plants. Our results indicate that introduced black henbane plants are biennial, and that vernalization is more critical to bolting and flowering than reaching a certain size. Nonetheless, the fact that nonvernalized plants were capable of bolting if grown long enough suggests that vernalization is not the only cue that can trigger reproduction in introduced populations.

The worldwide spread of barley cultivation required adaptation to agricultural environments far distant from those found in its centre of domestication. An important component of this adaptation is the timing of flowering, achieved predominantly in response to day length and temperature. Here, we use a collection of cultivars, landraces and wild barley accessions to investigate the origins and distribution of allelic diversity at four major flowering time loci, mutations at which have been under selection during the spread of barley cultivation into Europe. Our findings suggest that while mutant alleles at the PPD-H1 and PPD-H2 photoperiod loci occurred pre-domestication, the mutant vernalization non-responsive alleles utilized in landraces and cultivars at the VRN-H1 and VRN-H2 loci occurred post-domestication. The transition from wild to cultivated barley is associated with a doubling in the number of observed multi-locus flowering-time haplotypes, suggesting that the resulting phenotypic variation has aided adaptation to cultivation in the diverse ecogeographic locations encountered. Despite the importance of early-flowering alleles during the domestication of barley in Europe, we show that novel VRN alleles associated with early flowering in wild barley have been lost in domesticates, highlighting the potential of wild germplasm as a source of novel allelic variation for agronomic traits.

The potential non-target effects of genetically modified crops are some of the more debated topics within applied biotechnologies in agriculture and environmental risk assessment. The objective of the present research was to study the potential Bt-toxin uptake by the non-target herbivore Myzus persicae Sulzer (Hemiptera: Aphididae) feeding on transgenic oilseed rape plants (Brassica napus cv. ‘Westar’ lines GT 2–4) expressing the Cry1Ac endotoxin. A specific aim was to replicate our previous experiment in controlled laboratory conditions to avoid or minimize the risk of contamination leading to potential false positive results. The toxin levels in vernalized (V) and not-vernalized (not-V) transgenic oilseed rape plants was also monitored to better clarify the role of physiological processes on Bt-toxin expression. Cry1Ac expression in not-V plants (mean concentration±SE=167.8±5.7 μg kg−1 FW) showed a pattern of large variability, in comparison with V plants whose expression (mean concentration±SE=227.7±1.9 μg kg−1 FW) was significantly more stable. Cry1Ac toxin was detected in three aphid samples reared on V plants with a mean toxin concentration±SE of 4.8±0.6 μg Kg−1 FW and in three out of six samples of aphids reared on not-V plants (mean toxin concentration±SE=7.1±1.2 μg kg−1 FW). The mean Bt-toxin concentration of all the positive aphid samples was 5.9±1.0 μg kg−1 FW. Our results confirmed the findings of our previous experiment and highlighted the potential for Cry1Ac toxin uptake by aphids feeding on transgenic oilseed rape plants.

In the monocarpic perennial Cynoglossum officinale L. the probability of flowering is related to the size of the plant. In previous work it was observed that this relation varies between years. We hypothesized that variable conditions during the winter, the period of vernalization, explain this variation.

We collected plants from the field in autumn and placed these under different simulated winter conditions in a climate room. In contrast to our hypothesis, the probability of initiating flowering at a given size was not affected by: (a) the temperature during the cold period, (b) the duration of the cold period, or (c) the application of a plant hormone (GA3) or an inhibitor of gibberellin synthesis (paclobutazol) during the cold period. Winter cold is not necessary for floral initiation, and is only required for elongation of the inflorescence. It is unlikely that winter temperature affects the fraction of plants flowering.

Subsequent morphological investigation of flower development in material collected in the field showed that large plants had primordial inflorescences well before vernalization, sometimes as early as August. In plants grown from seeds under constant conditions in a climate room, the probability of initiating the inflorescence differed for plants grown at various temperatures (34·1% at 15°C, 100% at 20°C, and 95% at 25°C). Our results suggest that environmental conditions in August and September, up to 10 months before actual flowering, could affect the fraction of flowering plants.