Bud dormancy pattern, chilling requirement, and cold hardiness in Vitis vinifera L. cv. ‘Chardonnay’ and ‘Riesling’

In recent years, new vineyards have been established in southwestern Ontario. The open water of Lake Erie provides some winter protection for Vitis hybrids and winter-hardy Vitis vinifera L. cultivars in this area. However, winter damage is possible when vines are grown distant from the open water or when lakes are frozen. To better understand the risks to winter survival, the dormancy and chilling phenology were studied over three winters from 2013-2016. Ten dormant canes of two V. vinifera cultivars, ‘Chardonnay’ and ‘Riesling’, were collected weekly from September 1 until March 30 from the mature vines in a commercial vineyard located at St. Williams (Ontario). The canes defoliated in early October, and the endodormancy was completed by the end of December. The cumulative chilling hours (0-7.2 °C) from defoliation until the completion of endodormancy were averaged 606 hours for ‘Chardonnay’ and 665 hours for ‘Riesling’. ‘Chardonnay’ buds were slightly less hardy than ‘Riesling’ to cold temperatures, with a threshold of about -24 °C for ‘Chardonnay’ and -25 °C for ‘Riesling’. Most primary buds of both cultivars died after February 16, 2015, and more than half died after February 12, 2014, due to severe low temperatures of -33.1 and -26 °C, respectively.

The seasonal dormancy pattern and germination of Matricaria maritima subsp. inodora (L.) Dostal seeds in hydrotime model terms

Changes in hydrotime model parameters were determined in <em>Matricaria maritima</em> L. subsp. inodora seeds during burial in a field in order to describe the seasonal dormancy pattern. Seeds were exhumed at regular intervals over a year and incubated at different water potentials at 19°C. Germination time courses were analyzed to determine hydrotime population parameters. Values of ѱb(50), ѲH and σѱb varied each month. Mean base water potential values in seeds exhumed each month were related to precipitation over 20 days before their exhumation. Soil temperature could be a trend-controlling factor of this relationship. The seeds were in deep dormancy after remaining 80-90 days in soil below or above limit temperature 15°C. The application of the hydrotime model to describe and predict seasonal dormancy patterns of weed seed is promising, especially for species with a considerable diversification of life strategies and ecophysiological flexibility of diaspores. It could also suggest mechanisms of seasonal dormancy changes of seeds in natural conditions and provide a basis for their examination. One of advantages of the dormancy pattern description of weed seeds remaining in a soil bank by means of threshold models is its simplicity.

Germination in seed species ingested by opossums: implications for seed dispersal and forest conservation

Seed germination in plant species consumed by opossums, genus Didelphis, was investigated in southern Brazil, in order to improve knowledge of the strategies of zoochorous plants in the Neotropics. Seeds were obtained from opossum feces. Thirteen of the most frequent species in the diet of local opossums were tested for germination rates and germination responses under different qualities (red/far red ratio) and different intensities of light. Most seeds from feces germinated similarly to the control groups, except for seeds of Rubus rosifolius, which appeared to depend on gut passage. Other experiments revealed that most seeds in the opossums' diet were of pioneer species, with most germination occurring during favorable humid conditions in the rainy season. A few species showed negative photoblastism, or no dormancy pattern. Small mammals are suggested as possible tools for area recuperation programs, through seed dispersal of many pioneer and some shade-tolerant plants, under suitable management.

Ecotypic variation for seed dormancy contributes to the success of capeweed (Arctotheca calendula) in Western Australia

The seed dormancy characteristics of 2 capeweed [Arctotheca calendula (L.) Levyns] ecotypes from Western Australia were studied to determine aspects of seed dormancy that contribute to the success of this species in southern Australia. Short- and long-term dormancy pattern of buried and soil surface seed, effect of summer temperatures on afterripening, and effect of temperature on seed germination were investigated using seed produced in a common environment. There were large differences in the seed dormancy pattern of the 2 ecotypes studied. On the soil surface, >95% of seed of the Mt Barker ecotype became non-dormant and germinated in the first year, the remainder germinating the following season. In contrast, only 5% of Mullewa seed germinated in the first year, with 75% germinating in the second year and 20% of seed remaining dormant after 2 years. Cycling of dormancy was observed for buried seed of both ecotypes, with periods of non-dormancy corresponding with the likely timing of the break of the season. Dormancy cycling was also apparent in seed stored under constant conditions in the laboratory. Burial prevented germination of both ecotypes; however, the ability to resist germination while buried was lost in 30% of the Mt Barker seed in the second season. Differences in the duration of dormancy of soil surface and buried capeweed seed have evolved as an adaptation to the different environments likely to be experienced by plants at their site of collection. All seeds possessed primary dormancy at maturity, with any afterripening during the first year occurring by the end of summer. Afterripening was enhanced by exposure to typical soil surface temperatures, providing some protection against germination during early summer rainfall. Protection from late summer rains is insured by the inability of seed to germinate at temperatures >30°C and a relatively slow rate of germination. These features of capeweed seed dormancy, combined with the ability to evolve genetically distinct populations suited to particular environments, help explain why capeweed is so widespread and abundant across southern Australia.

The effect of environmental conditions on the annual dormancy pattern of seeds of Spergula arvensis

The effect of environmental factors on the germination of exhumed seeds of Spergula arvensis L. after variable periods of burial in soil was investigated. Seeds were buried in the field and exhumed at regular intervals after which germination was tested over a range of conditions. These tests showed clear seasonal changes in dormancy during 3 successive years. Dormancy was broken in spring and reinduced in autumn at rising and falling temperatures, respectively. In experiments in incubators, greater loss of dormancy occurred at 10 and 15 °C than at 2 and 6 °C. As in the field, induction of dormancy occurred when the preincubation temperature was lowered. The expression of the dormancy pattern was strongly influenced by the germination tests conditions. At 15 °C, seeds germinated during a longer period of the year than at 2 or 30 °C. Irradiation with red light, addition of nitrate, and desiccation of the seeds prior to the germination test strongly stimulated germination. All three factors enabled germination of exhumed seeds during a longer period of the year. When light, nitrate, and desiccation were combined, exhumed seeds could germinate in all seasons. The seasonal germination pattern was modelled with a descriptive model based on the dual effect of temperature, which regulates dormancy and also affects germination. This model closely simulated germination at field temperatures. Germination of exhumed seeds in the field was restricted to the period of overlap between the germination temperature range computed with the model and field temperature. The features of the model supported the hypothesis that dormancy of S. arvensis is regulated by the actual changes in temperature rather than the combined effects of a cold and heat sum. Key words: Spergula arvensis, dormancy pattern, germination, regression model, weed seeds.

Seasonal Variation in Intensity of Bud Dormancy in Apple Cultivars and Related Malus Species

Dormancy patterns throughout the season were studied in more than 90 apple (Malus ×domestica Borkh.) cultivars and related Malus spp. The seasonal apple bud dormancy pattern resembles a normal curve: it starts to intensify soon after bud formation and reaches maximum intensity by the time of leaf fall/senescence. Genotypes were grouped into three general classes based on maximum dormancy intensity. Maximum intensity of bud dormancy measured in cold winters is inversely related to adaptation to the subtropics. Low-chilling requirement (CR) cultivars have a shallow depth of dormancy with very little alteration throughout the year. High-CR cultivars have intense bud dormancy, the first stage of which can be induced by growing these cultivars at temperatures above 20C. Genotypes differed in their rates of dormancy dissipation. The efficiency of chilling unit (CU) accumulation to break dormancy was negatively correlated with CR, which indicates the importance of factors other than CU accumulation in terminating bud dormancy in low-CR cultivars. The inherent length of bud dormancy plays a major role in determining the time of budbreak in the spring. Deviations may be related to the genotypic efficiency in which chilling modifies dormancy and possibly the basal temperatures to which buds respond. Chill unit requirement and heat unit requirement are dependent factors. Heat requirement comparisons may be meaningless if the dormancy intensities of the genotypes are not taken into consideration.