Jointed goatgrass (Aegilops cylindrica Host. ♯3 AEGCY) has a quantitative requirement for vernalization in order to flower. In greenhouse and field studies, increasing periods of vernalization progressively reduced the number of days needed for plants to mature following transfer from the cold treatment to favorable growing conditions. Plants that had been vernalized at 3 ± 2 C for 8 weeks as imbibed seed took 120 days to flower following transfer to the greenhouse. Unvernalized controls flowered 197 to 222 days after planting in the greenhouse. Lengthening periods of vernalization from 2 to 8 weeks increased the number of seedheads per plant and dry weight per seedhead. Vernalized plants partitioned more dry matter into seedheads than unvernalized controls. The ratio of seedhead dry weight to vegetative shoot dry weight increased with duration of vernalization, even though vernalization did not alter total shoot dry-matter production. In field studies, plants that were established in the fall flowered sooner and more synchronously after resumption of growth in the spring than those that were planted in the spring and flowered in the summer. Plants seeded after May failed to flower in the same summer.

Ripgut brome has a quantitative response to vernalization in relation to flowering. In greenhouse studies, cold treatment (5 ± 2 C) of 2, 4, or 6 wk shortened the vegetative period, but longer exposure did not further decrease the time required to flower. Plants vernalized as imbibed seeds for 8 wk took 17 d to flower following transfer from cold treatment to the greenhouse. Unvernalized controls flowered 53 d after planting in the greenhouse. Greatest total seed dry weight and vegetative shoot dry weight were produced by unvernalized plants, whereas lengthening periods of vernalization from 2 to 8 wk decreased both parameters. The percent of total seed dry weight to total shoot dry weight was significantly greater for vernalized plants than unvernalized controls. In field studies, ripgut brome plants established in the fall flowered sooner after resumption of growth in the spring than those planted in the spring. Plants seeded after April failed to flower until the following spring.

Key metabolic enzymes and germination were studied in developing and mature, dormant and nondormant prickly sida (Sida spinosa L.) seeds. Isocitrate dehydrogenase, glucose-6-phosphate dehydrogenase, fructose-1,6-diphosphatase, and phosphofructokinase activities were determined in developing and mature prickly sida seeds. Developing seeds less than 7 days after anthesis and at 17 days or greater after anthesis were unable to germinate. The 7-day-old seeds lacked all but fructose-1,6-diphosphatase activity. The 17-day-old seeds demonstrated all enzyme activities but failed to germinate because dehydration had occurred and seeds were unable to imbibe sufficient water without an afterripening period. Comparison of enzyme activities of dormant and nondormant seeds on incubation showed that only glucose-6-phosphate dehydrogenase was considerably different within the first 8 h of incubation. Nondormant seeds had considerable glucose-6-phosphate dehydrogenase activity before germination (radical protrusion at 8 h), suggesting an active pentose phosphate pathway.

Five common cocklebur biotypes from southern Minnesota, central Iowa, southern Iowa, and Ohio were grown at the Iowa State University Curtiss Research Farm in 1995 and 1996 to examine intraspecific variations. Maximum plant heights were measured, and anthesis dates and day of bur set were recorded. At the end of the growing season, all plants were excised at the soil surface and weighed. Common cocklebur biotypes did not differ significantly in height. Flowering date was associated strongly with photoperiod and varied little between years within a biotype. But flowering date and bur set date differed among biotypes. The highest dry matter yields occurred in later flowering biotypes.

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.

Information on jointed goatgrass caryopsis development is currently lacking in published literature. It is hoped that through a better understanding of jointed goatgrass caryopsis ontogeny more effective weed-management strategies will be developed. Greenhouse experiments were initiated in fall 2002 and 2003 and completed the following spring seasons. Jointed goatgrass plants were started from spikelets, vernalized for 8 wk at 4 C, and grown in a greenhouse. Treatments were the number of days after anthesis (DAA) that a spike was allowed to remain on the plant before harvesting and ranged from 2 to 34 DAA, in increments of 1 (2002) or 2 (2003) d. Individual spikes were divided at harvest into three sections: top, middle, and bottom, disarticulated from the rachis, placed into a germinator, and germination recorded each day. Goatgrass spikelets germinated as early as 2 DAA, although spikelets harvested <7 DAA had <3% germination for all spike sections and were extremely variable, especially for the middle and bottom sections. Time to germination was similar for all sections of the spike. Maximum average germination of the top section was 72% compared with 86% for the bottom and middle sections. Our data suggest that factors other than developmental rate (i.e., dormancy) may affect germination in sections of the spike. A second year of the experiment was conducted for validation. Model validation suggested that although trends were similar in both years, variation in germination response might be too great for accurate, predictive model construction. The early germination shown in this research demonstrates that control measures must be implemented earlier than previously prescribed to prevent jointed goatgrass reproduction.

Integrated weed management (IWM) for agronomic and vegetable production systems utilizes all available options to effectively manage weeds. Late-season weed control measures are often needed to improve crop harvest and stop additions to the weed seed bank. Eliminating the production of viable weed seeds is one of the key IWM practices. The objective of this research was to determine how termination method and timing influence viable weed seed production of late-season weed infestations. Research was conducted in Delaware, Michigan, and New York over a 2-yr period. The weeds studied included: common lambsquarters, common ragweed, giant foxtail, jimsonweed, and velvetleaf. Three termination methods were imposed: cutting at the plant base (simulating hand hoeing), chopping (simulating mowing), and applying glyphosate. The three termination timings were flowering, immature seeds present, and mature seeds present. Following termination, plants were stored in the field in mesh bags until mid-Fall when seeds were counted and tested for viability. Termination timing influenced viable seed development; however, termination method did not. Common ragweed and giant foxtail produced viable seeds when terminated at the time of flowering. All species produced some viable seed when immature seeds were present at the time of termination. The time of viable seed formation varied based on species and site-year, ranging from plants terminated the day of flowering to 1,337 growing degree d after flowering (base 10, 0 to 57 calendar d). Viable seed production was reduced by 64 to 100% when common lambsquarters, giant foxtail, jimsonweed, and velvetleaf were terminated with immature seeds present, compared to when plants were terminated with some mature seeds present. Our results suggest that terminating common lambsquarters, common ragweed, and giant foxtail prior to flowering, and velvetleaf and jimsonweed less than 2 and 3 wk after flowering, respectively, greatly reduces weed seed bank inputs.

The dioecious character (sex ratios and stand structures, conspecific neighbour relationships, inflorescence numbers and structure) and reproductive process (phenology, anthesis, flower visitors and fruit production) of a miombo woodland species, Uapaca kirkiana were investigated in natural populations in Malawi. The sex ratio of reproductive individuals ≥ 10 cm diameter at breast height was about 1:1 and departures from this ratio mostly resulted from a higher proportion of the males. Spatially, the sexes were randomly distributed but generally within 10 m of each other with no obvious gender differences in size. Throughout Malawi, male and female reproductive individuals flower synchronously between October–April (with a peak period in February–March). A 6 : 1 male to female inflorescence sex ratio was common. Anthesis in female inflorescences lasts almost twice as long as in male inflorescences and only the latter have any odour. On male trees, inflorescences are in fascicles, whereas on female trees, they are solitary. In both cases, the inflorescences are generally similar in size except for the peduncles of the male inflorescences which are longer than the female's. A range of insects visits U. kirkiana flowers but the most likely pollinators are bees (Apis mellifera), and beetles (Dothera bennigseni, Chelomenes lunata, Alcidodes denticulatus and Mitracamenta sp.). Apart from pollen from the male inflorescences, female flowers do not offer any obvious reward for flower visitors. Pollination studies revealed that assisted pollination did not significantly improve fruit production or seed quality over unpollinated or naturally pollinated inflorescences. Facultative agamospermy (apomixis) is suspected as a phenomenon requiring further attention in U. kirkiana.