Cultivated northern wild rice (NWR; Zizania palustris L.) has been bred and studied since the 1950s. One challenge facing researchers is the lack of storage options, due to the seed's unorthodox behaviour. This study evaluated varying storage temperature and moisture conditions for the maintenance of seed viability and dormancy breaking in Minnesota-grown NWR. First, seeds were placed in non-submerged, freezing storage (NSFS) for 12–26 weeks, then in submerged, cold storage (SCS) for 2 weeks. The addition of SCS increased germination (%G) relative to NSFS alone (<0.1% NSFS, 15% NSFS and SCS), indicating that NSFS does not kill seeds but also does not break seed dormancy. Next, the required length of SCS was evaluated by placing seeds in NSFS for 12 weeks and then in SCS for 2–14 weeks. A longer SCS period increased %G from 3 to 79%, at 2 and 14 weeks of SCS, respectively. Lastly, seeds were placed in NSFS, followed by SCS, at varying intervals over a 29-week period. Across lines, germination increased from 20 to 76% between 4 and 7 weeks of SCS, respectively, then plateaued. The results of this study indicate that NSFS could be used to store NWR seeds, but at least 7 weeks in SCS is required to overcome dormancy. Additionally, while NSFS did not break seed dormancy, physiological changes related to stratification processes were occurring in non-submerged, freezing conditions. Results also suggest that the genotypic variation in NWR could be utilized for selection to improve germination and storage viability.

Outdoor experiments were conducted at two locations in Minnesota to characterize the growth, development, and vegetative reproduction potential of giant burreed grown with and without wild rice. Giant burreed growth was influenced by environment more than the presence of wild rice. Shoots emerged from corms 2 to 3 wk after planting (WAP), and continued throughout the growing season. Giant burreed attained a maximum height of 135 cm with an average 36 shoots/plant. Rhizome production started 4 to 6 WAP, and continued throughout the growing season. Corm formation at the base of shoots started 8 WAP and continued throughout the growing season. Rhizomes grew to a maximum cumulative length of 2500 cm/plant spreading in all directions and produced up to 250 buds/plant. Corm and rhizome bud viability was 15 and 10%, respectively. These data suggest that giant burreed grown in wild rice should be controlled by 2 to 3 wk after emergence to prevent vegetative reproduction.

Field experiments were conducted to evaluate the effect of application time on common waterplantain control in wild rice with MCPA and 2,4-D. Common waterplantain control was greatest when MCPA or 2,4-D were applied at 1.1 or 1.7 kg ai/ha at the two-aerial leaf stage. The best late-season control was MCPA applied at the scape elongation growth stage. Common waterplantain was controlled adequately when 0.6 to 0.8 kg/ha of MCPA were applied at the scape elongation or early flowering stage. However, because of common water plantain interference and sensitivity of wild rice to late herbicide applications, the best treatment stage for wild rice yield was when MCPA was applied at 0.6 kg/ha to common waterplantain at the two-aerial leaf stage. Wild rice at this time is at the more tolerant one-aerial leaf growth stage.

The desiccation tolerance of Zizania palustris seeds has been debatable, but recently it has emerged that survival to low moisture contents is a function of the temperature during dehydration. Survival of dehydration is greatest at 25–30°C and viability declines as the dehydration temperature is reduced. On the other hand, extended hydrated chilling (stratification) is required to break dormancy. The present contribution examines the ultrastructural condition of embryonic axes of Zizania palustris after dehydration at various temperatures, and following reimbibition and stratification. Axis cells sustained least damage when dehydration was carried out at 25°C and ultrastructural deterioration was more severe with lower temperatures during water loss. Damage sustained as a result of unfavourably low dehydration temperatures was visible when seeds were fixed from the dry state and was generally exacerbated during fully imbibed stratification. However, 25°C represented the optimum dehydration temperature; seeds that had been dried at 30°C also showed considerable ultrastructural disturbance when fixed from the dry state. This was largely reversed during fully imbibed stratification, although signs of the damage that had been sustained still persisted. These observations are in keeping with the germination behaviour of Z. palustris seeds dehydrated at temperatures above and below 25°C. The results are discussed in terms of the predominance of one of two mechanisms of membrane deterioration, depending on the dehydration temperature, which are probably not mutually exclusive. It is hypothesized that, at temperatures above 25°C, damage by free-radical-mediated events may predominate, whereas, at temperatures below the optimum, irreversible lipid-phase transitions may be the major factor resulting in membrane damage.

Seeds of wild rice (Zizania palustris var. interior) have been reported to show maximum survival when dehydrated at 25°C. It has also been reported that axis cells sustain least damage at this drying temperature. In the present study, a linear relationship between drying rate and dehydration temperature was established. Whereas the highest positive tetrazolium staining and lowest leakage were recorded for seeds dehydrated at 25°C, maximum germination was recorded for seeds dried at 20°C. A proportion of seeds showed glass formation irrespective of the dehydration temperatures used. Parameters of the glass to liquid transition, however, correlated with neither water content nor sugar profiles. The ratio of raffinose to sucrose was similar in all the treatments. A hydroperoxide test revealed a linear relationship between peroxide levels and drying temperature, although fatty acid amounts were not correlated with hydroperoxide amounts. Butanal amounts and total aldehydes evolved, on the other hand, showed a high negative correlation with peroxide amounts. Electron microscopy showed that the variability and relative abundance of peripheral membrane complexes (PMCs) was highest for embryonic axes dehydrated at 25°C and lowest for cells of embryonic axes of seeds dried at 10°C. Furthermore, intramembrane particles (IMPs) were evenly distributed in cells of axes dried at 25 or 37°C. In contrast, membranes of cells of axes dehydrated at 10°C showed large IMP-free areas. The relative abundance of IMPs was highest in cells of embryonic axes dried at 25°C and lowest in cells of axes dehydrated at 10°C. From these observations, it is suggested that membrane phase transitions, with the concomitant elimination of proteins, accompany dehydration of Z. palustris seeds at 10°C, whereas at 37°C peroxidation may predominate.

Partial drying of non-dormant seeds had little effect on germination behaviour compared with undried controls. In contrast, partial drying resulted in a marked increase in the germination response of freshly harvested (dormant) seeds of Z. palustris. Partial drying also resulted in a 100-fold reduction in the concentration of gibberellins (GA4+7) required for maximum germination. Although the concentration range of applied abscisic acid (ABA) that permitted germination was unaltered, partial drying increased the final germination percentage at all concentrations tested. The concentration of ABA above which germination was reduced in freshly harvested (dormant) seeds of Z. palustris was 3.16 × 10−7m compared with 10−4m in fresh (non-dormant) seeds of P. coarctata. Changes in the germination response of Z. palustris seeds to applied growth regulators, following partial drying or cold stratification might be explained by similar changes in hormonal status.