Soil Moisture Rather than Soil Nutrient Regulates the Belowground Bud Bank of Rhizomatous Species <i>Psammochloa villosa</i> in Arid Sand Dunes

In arid and semi-arid sand dune ecosystems, belowground bud bank plays an important role in population regeneration and vegetation restoration. However, the responses of belowground bud bank size and composition to sand burial and its induced changes in soil environmental factors have been rarely studied. In arid sand dunes of Northwestern China, we investigated belowground bud bank size and composition of the typical rhizomatous psammophyte Psammochloa villosa as well as three key soil environmental factors (soil moisture, total carbon and total nitrogen) under different depths of sand burial. Total buds and rhizome buds increased significantly with increasing burial depth, whereas tiller buds first increased and then decreased, with a peak value at the depth of 20–30 cm. Soil moisture increased significantly with sand burial depth, and was positively correlated with the number of all buds and rhizome buds. Soil total carbon concentration first increased and then decreased with sand burial depth, and total nitrogen concentration was significantly lower under deep sand burial than those at shallow depths, and only the number of tiller buds was positively correlated with soil total nitrogen concentration. These results indicate that soil moisture rather than soil nutrient might regulate the belowground bud bank of P. villosa, and that clonal psammophytes could regulate their belowground bud bank in response to sand burial and the most important environmental stress (i.e., soil moisture). These responses, as the key adaptive strategy, may ensure clonal plant population regeneration and vegetation restoration in arid sand dunes.     

东北草地异质生境芦苇种群根茎芽年龄结构及输出规律

为明确异质生境条件下芦苇种群根茎芽年龄结构及输出规律,揭示芦苇种群的营养繁殖特性,采用单位土体挖掘取样,分别计数各龄级根茎芽的调查与统计方法,对东北草甸草原草甸土和盐碱土两个生境单优群落芦苇种群根茎芽动态进行比较分析。结果表明,两个生境芦苇种群根茎芽库主要均由6个龄级组成;草甸土生境在6—10月均为增长型年龄结构;盐碱土生境6—7月份为衰退型年龄结构,8月份为稳定型年龄结构,9—10月份为增长型年龄结构。根茎芽数量1—4a普遍以草甸土生境高于盐碱土生境,5—6a普遍以盐碱土生境高于草甸土生境,各龄级根茎芽数量与月份之间均符合y=a+bx直线关系(P0.05)。随着龄级的增加,休眠芽比率呈逐渐下降趋势,而萌发芽比率则呈逐渐上升趋势,5个生育期的休眠芽比率和萌发芽比率与龄级之间均符合y=a+bx直线关系(P0.01)。各龄级根茎的休眠芽具有一个相对稳定的萌发输出过程,草甸土生境根茎休眠芽按每年11%的比率萌发输出,而盐碱土生境根茎休眠芽按每年7%的比率萌发输出。虽然芦苇种群根茎芽年龄结构及年龄谱在异质生境中存在显著差异,但却有着相同的季节变化规律,均以不断形成新根茎的芽来维持着种群的营养繁殖更新。     

Dispersal by rodent caching increases seed survival in multiple ways in canopy‐fire ecosystems

Seed‐caching rodents have long been seen as important actors in dispersal ecology. Here, we focus on the interactions with plants in a fire‐disturbance community, specifically Arctostaphylos species (Ericaceae) in California chaparral. Although mutualistic relationships between caching rodents and plants are well studied, little is known how this type of relationship functions in a disturbance‐driven system, and more specifically to systems shaped by fire disturbance. By burying seeds in the soil, rodents inadvertently improve the probability of seed surviving high temperatures produced by fire. We test two aspects of vertical dispersal, depth of seed and multiple seeds in caches as two important dimensions of rodent‐caching behavior. We used a laboratory experimental approach to test seed survival under different heating conditions and seed bank structures. Creating a synthetic soil seed bank and synthetic fire/heating in the laboratory allowed us to have control over surface heating, depth of seed in the soil, and seed cache size. We compared the viability of Arctostaphylos viscida seeds from different treatment groups determined by these factors and found that, as expected, seeds slightly deeper in the soil had substantial increased chances of survival during a heating event. A key result was that some seeds within a cache in shallow soil could survive fire even at a depth with a killing heat pulse compared to isolated seeds; temperature measurements indicated lower temperatures immediately below caches compared to the same depth in adjacent soil. These results suggest seed caching by rodents increases seed survival during fire events in two ways, that caches disrupt heat flow or that caches are buried below the heat pulse kill zone. The context of natural disturbance drives the significance of this mutualism and further expands theory regarding mutualisms into the domain of disturbance‐driven systems.     

Bud damage from controlled heat treatments in Quercus garryana

Quercus garryana habitats are increasingly being managed with prescribed fire, but acorn dependent wildlife might be adversely affected if fires damage acorn crops. We examined one way that fire might affect subsequent acorn crops: through direct heating and damage of buds containing the following year’s floral organs. We measured internal bud temperatures during controlled time and temperature treatments, described damage to heated buds at the tissue and cellular levels and quantified spring flowering to assess the consequences of the treatments. We found that internal bud temperature was logarithmically related to exposure time and linearly related to treatment temperature. Tissue damage was more common in bud scales, staminate and bud scale scar primordia than in leaf, pistillate, leaf axillary primordia and apical meristems. Damaged tissues were sequestered by cells with thickened cell walls. A 133°C treatment applied for 60 s produced minimal damage or mortality, but damage increased rapidly in hotter or longer treatments, culminating in 100% mortality at 273°C for 60 s. Our experiments account only for radiative, not convective heating, but suggest that fires might produce sublethal effects that affect flowering and acorn crops. Q. garryana’s large buds possess an internal organ arrangement well suited to minimizing heat damage. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Belowground bud banks and meristem limitation in tallgrass prairieplant populations

Rhizome meristem populations were sampled in tallgrass prairie to quantify the size, grass?:?forb composition, and temporal and spatial variability of the soil bud bank and to compare fire effects on bud bank and seed bank composition. Soil cores (10.5 cm diameter, 15 cm deep) were collected from replicate annually and infrequently burned tallgrass prairie sites, and intact rhizomes and rhizome buds were censused. Bud bank densities ranged from approximately 600 to 1800 meristems/m(2) among sites and had high spatial and seasonal variability. In annually burned prairie, the total bud bank density was two-fold greater and the grass?:?forb meristem ratio was more than 30-fold greater than that of infrequently burned prairie. These patterns are opposite those observed in soil seed banks at this site. The rhizome population in annually burned prairie was 34% larger than the established aboveground tiller population. By contrast, the bud bank density in unburned prairie was significantly lower than aboveground stem densities, indicating possible belowground meristem limitation of stem density and net primary production on infrequently burned prairie. The patterns observed in this study suggest that the densities and dynamics of tallgrass prairie plant populations, as well as their response to disturbance (e.g., fire and grazing) and climatic variability, may be mediated principally through effects on the demography of belowground bud populations. Patterns of seed reproduction and seed bank populations have little influence on short-term aboveground population dynamics of tallgrass prairie perennials.     

Shoot regeneration after fire or freezing temperatures and its relation to plant life-form for some heathland species

Shoot regeneration after prescribed burning or following the freezing temperatures of winter was monitored for nineteen heathland species present in an Arctostaphyleto-Callunetum community in northeast Scotland. Species whose renewal buds were near the surface of the ground started to grow earlier in the spring than species with renewal buds above the surface, but grouping species according to the position of their renewal bud (i.e. their life-form) did not account for all of the interspecific variation apparent. In the case of shoot regeneration after fire, species whose renewal buds were destroyed by fire because they were above-ground started to regenerate about the same time as species with belowground buds, protected from fire, but reached their maximum frequency of occurrence later. Grouping species by life-form was of limited value as a means of interpreting this interspecific variation in the timing of shoot regeneration after fire. It would be unwise to use plant life-form as the sole basis for interpreting or predicting a species' response to temperature stress when extreme temperatures occur regularly, as they do in heathland. The possible use of other plant traits to interpret and predict interspecific variation in the regeneration rate of heathland plants is discussed.Nomenclature follows Tutin et al. (1964–1980) for vascular plants. Acknowledgements. The Nature Conservancy Council and Mr J. J. Humphries kindly allowed Dinnet Moor to be used for the work presented here. One of us (RJR) received financial support for field work from the Natural Sciences and Engineering Research Council of Canada.     

中国东北地区流动沙丘生态系统丘间低地地下芽库的时空变化

中国东北地区流动沙丘生态系统丘间低地地下芽库的时空变化 地下芽库在半干旱区沙丘生态系统植被恢复中起着重要作用。然而,目前针对流动沙丘丘间低地地下芽库时空变化的研究却很少。本研究通过调查一个生长季内5个不同面积流动沙丘丘间低地地下芽库的大小和组成,确定流动沙丘丘间低地地下芽库的时空变化。研究结果显示,中等面积丘间低地的总芽库密度与分蘖芽密度最高,茎基部芽密度呈相反趋势,而根茎芽密度不随丘间低地的面积变化而变化。地下芽库大小具有明显的季节变化特征。总芽密度在8月份达到高峰,10月份最低,根茎芽密度变化趋势与总芽密度相似,而茎基芽密度变化趋势与总芽密度相反,分蘖芽密度的变化不明显。以上结果表明,地下芽库密度随丘间低地的面积和季节变化而变化。这一结果有助于认识流动沙丘生态系统中植物生长的适应策略,并可为半干旱区沙丘植被恢复和保护提供理论指导。     

Anatomical inferences on aerial bud protection of three Eugenia shrub species from the Cerrado

• Location and degree of protection of aerial buds are important functional traits in disturbance- or stress-prone environments since aerial buds ensure the development of new organs under favourable growing conditions. This study was carried out in a Brazilian Cerrado area under regeneration after long-term Pinus cultivation, where the trees were clear-cut in 2012 and the remaining material was burned in 2014.
• After the fire treatment, several species resprouted from belowground organs and their aboveground organs were directly exposed to full sunlight. We collected 15 terminal branches with fully expanded leaves from three individuals of each of three Eugenia species to investigate if those with well-developed belowground organs invest in bark for aboveground bud protection. The samples were analysed using light and electron microscopy.
• In addition to terminal and axillary buds, all species presented accessory buds, and the number varied according to the node analysed. None of the aerial buds were protected by bark, but all were well protected by cataphylls and densely pubescent leaf primordia. There were also inter- and intra-petiolar colleters that released a mucilaginous protein exudate. The distance between the shoot apical meristem and the outer surface was longer in the terminal bud than in axillary buds. The bud leaf primordia covering the shoot apical meristem had a thick cuticle, unicellular non-glandular trichomes that accumulate phenolic and lipophilic compounds, and secretory cavities.
• Our study shows that all three Eugenia species studied here had highly protected aerial buds allocated from belowground organs. These morphological traits may improve the chances of the species' persistence in areas subjected to frost events, low relative humidity, high irradiance and harmful UV levels.

     

EVOLUTIONARY MODIFICATION IN CLARKIA. II. ROLE OF FLOWER BUD PUBESCENCE IN SECTION PHAEOSTOMA

Observations of the habitats and relative flowering of a Clarkia species with hairy flower buds and several with hairless flower buds led to the hypothesis that long hairs on flower buds regulate bud temperature. This hypothesis predicts that hairless buds would be warmer and develop faster than hairy buds, which would be cooler, develop more slowly, and avoid high temperature stress. The hypothesis was tested by comparing flower bud growth rates and temperatures in three genetically similar biotypes of Clarkia unguiculata and in all six species of section Phaeostoma. Flower buds of the three biotypes included hairy (HY) and hairless (HN) from the same coastal population and densely hairy (HD) from an interior locality. The six species included C. unguiculata with densely hairy buds (HD) and five related species with hairless buds. Contrary to expectations, HY buds grew more rapidly than HN buds. HD buds grew more rapidly than either and also more rapidly than the hairless buds of five related species. Again contrary to expectations, the three biotypes of C. unguiculata had equivalent temperature relations, with bud temperatures mostly somewhat below air temperatures. In a comparative experiment, bud temperatures in C. unguiculata approximated air temperatures while bud temperatures in five related species mostly fell well below air temperatures. Thus, predictions of the hypothesis were not borne out. Long bud hairs apparently have minimal effect on bud growth rates and temperatures, and we conclude that physiological adaptations are more important. Bud cooling mechanisms are discussed.     

Bud banks of perennial savanna grasses in Botswana

Three semi‐arid savanna grasses in Botswana (Stipagrostis uniplumis, Eragrostis lehmanniana, and Aristida stipitata) were sampled to quantify their belowground bud banks during the dormant season and to estimate their relative allocation to vegetative and sexual reproduction. Bud banks of these African perennial caespitose grasses were also compared with four perennial caespitose grasses of semi‐arid North American grasslands. The three African grasses each maintained approximately two buds per tiller and showed a high percentage (88–99%) of tillers producing seed. Only E. lehmanniana produced new aerial tillers from axillary buds at elevated nodes on the stem as well as from the belowground bud bank. Compared with species of North American grasslands, these African grasses produced fewer belowground buds but showed a much higher percentage of tillers producing seed. These patterns indicate relatively greater belowground meristem limitation, lower allocation to vegetative reproduction (tillering) and higher allocation to seed reproduction in these African grasses, although studies of more species are needed to assess the generality of this pattern. The management of savannas in ways that favour the maintenance of a reserve population of belowground buds may increase the ability of grasses to respond to pulses of resource availability, increase their compensatory growth capacity following grazing or drought, and decrease the invasibility of these plant communities by exotic species, whereas maintaining allocation to sexual reproduction may be important for conserving genetic variation and enhancing their capacity to adapt to environmental change.     

Heat effects on seeds and rhizomes of a selection of boreal forest plants and potential reaction to fire

To analyse the potential reaction to firegenerated heat pulses, seeds of 12 species of plants and rhizomes of three species were exposed to elevated temperatures for 10 min. The tested material split into three groups with respect to heat tolerance: (1) the rhizomes, for which the lethal temperatures were in the range 55–59° C; (2) the seeds of most of the species tested, for which the lethal temperatures were in the range 65–75° C; (3) The seeds of two species of Leguminosae and three species of Geranium for which the lethal temperatures were around 100° C. For all three Geranium species and for one of the legume species, Anthyllis vulneraria, exposure temperatures above ca. 45° C resulted in dormancy release, and maximum germination occurred above 60–65° C. Speed of germination was little affected for most species, except after exposure to nearlethal temperatures, where it slowed down dramatically, although the seedlings emerging were healthy. We conclude that due to sharp temperature gradients in the soil during fire, differences in heat tolerance between species in most cases are not large enough to be a decisive factor in their post-fire colonising success. There are exceptions: the seeds of certain taxa that are impermeable to water in the dormant state, some of which have heat triggered germination.     

Fire temperatures and postfire plant community dynamics in Ecuadorian grass páramo

Three aspects of the páramo vegetation's response to fires were investigated: the measurement of fire temperatures, general observations of changes in plant communities following fires, and monitoring the fate of individual plants after burning.Fire temperatures were strongly influenced by the physiognomy of the vegetation, dominated by tussocks of Calamagrostis spp. Temperatures were highest amongst the upper leaves of the tussock (sometimes >500°C). The middle levels of the tussock experienced temperatures in excess of 400°C, but in the dense leaf bases temperatures were often below 65°C. On the ground between tussocks, temperatures were variable, whereas 2 cm below ground temperatures failed to reach 65°C.Plant survival depended on the intensity of the fire and the plant's position within the tussock structure. Survival was often the result of high temperature avoidance (with buds shielded by other plant parts or buried beneath the soil surface).Post-fire Calamagrostis tiller mortality rates were high and tussock regrowth was slow. Some other species appear to maintain their populations by exploiting this recovery phase for seedling establishment on tussocks.Between tussocks, changes of occupancy at the level of the individual plants were greater after fire than in control vegetation. Most transitions were random. Those which departed from random often involved gaps and were related to post-fire mortality, regrowth from below-ground parts, colonisation or, in the case of a clonal mat-forming species, to spatial rearrangement of rosettes. Recovery was slower at higher altitude. Recovery was much slower in burned plots when the upper 2 cm of soil was removed (along with buried plant parts) compared with burned plots.Qualitative observations suggest that recovery may consist of a cyclical process, mediated by the serial dominance of several species that are physiognomically important.The frequency of fires determines the amount of fuel accumulated within grass tussocks and some plants may be unable to survive repeated burning. Chance survival of species in unburned patches of vegetation and random colonisation of gaps may be important determinants of subsequent community structure.     

Plasticity in bud demography of a rhizomatous clonal plantLeymus chinensis L. in response to soil water status

We surveyed the bud demography ofLeymus chinensis L plants along a soil-moisture gradient that was caused by a flood in 1998 on the Song-nen Plain in northeastern China. The number of vegetative buds per ramet was influenced by soil water content, with regression curves being quadratic and the opening of the parabola pointing downward. In addition, the optimum regression models for the numbers of rhizomatous buds and tiller buds relative to soil water resulted in a quadratic parabola and exponential curve, respectively. Vegetative buds flourished between August and October, with plants producing more of those buds on flooded plots than on control sites. The number of rhizomatous buds per ramet was much higher than for tiller buds throughout most of the growing season, and production of the former was more apt to be affected by soil water status. This observed superiority of rhizomatous bud production was thought to be a consequence of the whole-plant adjustment that was stimulated by an abnormally high moisture content. It could also be interpreted as a strategy for “escape” from disadvantageous overly wet conditions. Moreover, the position-based preference for bud emergence along the ramets could be an underlying mechanism for selective ramet placement.     

Initiation, Orientation and Early Development of Primary Rhizomes in Sorghum halepense (L.) Pers.

Axillary buds on the most basal portion of the seedling shootof Sorghum halepense differentiate directly into rhizome buds.The initial orientation of these buds is upwards, but this orientationstarts to be reversed almost immediately. The reversal is causedby the combined effect of differential radial expansion of thebasal internodes immediately above and below the bud, and differencesin the extent of mitotic activity on the abaxial and adaxialsides of the bud. Reorientation is a geotropic and is progressivelyless with acropetal nodal position of the bud. Further growthof the rhizomes proceeds in the same orientation as that ofthe bud from which they had developed, until they change theirorientation again by exhibiting diageotropic, or negativelygeotropic responses. The second reorientation coincides moreor less with the onset of flowering and it exhibits a positionalgradient, such that the change is more extensive the higherthe nodal position of the rhizome. Sorghum halepense, rhizome, geotropism, morphogenesis, perennial weeds     

Drivers of post-fire resprouting success in restored Banksia woodlands

Disturbances can alter persistence trajectories of restored ecosystems. Resprouting is a common response of plants to disturbances such as fire or herbivory. Therefore, understanding a plant's resprouting response can inform successful restoration. We investigated patterns and drivers of resprouting following fire in fire-prone Banksia woodlands restored after sand mining in the Mediterranean-climate region of Western Australia. We applied experimental fire to samples of nine species with different resprouting types (rhizome, root crown, root sucker and lignotuber) across a 4- to 27-year-old restoration chronosequence. We investigated the influence of pre-fire plant size, restoration age and soil conditions on resprouting success, defined by: (i) the probability of resprouting (measured ~5 months after fire), (ii) the probability of surviving the first summer and, (iii) vigour (both measured ~12 months post-fire). We found that the probability of initial resprouting was high across most species, but summer survival was lower but comparable to that in other post-mining restored ecosystems following fire. Generally, pre-fire plant size did not influence probability of resprouting, while size and soil conditions were important for two species survival. Pre-fire plant size was a significant predictor of vigour for all species with soil conditions influencing four species. Restoration age significantly influenced survival of three species. However, as our models explained low amounts of variation in probabilities of resprouting and survival (R² = <0.11), other factors influencing resprouting success remain unidentified. Resprouting response to fire disturbance in restored Banksia woodlands are species and resprouter type specific, with plant size and soil conditions potentially more informative for understanding responses to disturbances than restoration age alone.     

Pseudomonas syringae pv. syringae as One of the Factors Affecting the Ice Nucleation of Grapevine Buds in Controlled Conditions

Ice nucleation in grapevine buds (cv. Pinot noir) was studied in freezing chamber in container grown plants. The ice nucleation of individual 278 buds at different stages of their development (between stage B and stage E according to Baggiolini scale) was measured by differential thermal analysis. Treatments were applied to plants to modify the Pseudomonas syringae pv. syringae content of buds and alter their water potential. Based on the results it was pointed out that (i) the ice nucleation temperatures of buds were generally normally distributed, (ii) the probability of bud nucleation at a given temperature was, to a certain extent, dependent on the amount of Pseudomonas present, (iii) the modification of water potential following an artificial rain led to a signification increase of the probability of bud nucleation and (iv) the nucleation probability did not increase significantly with the bud development between stage B and stage E.     

Acclimation and adaptive responses of woody plants to environmental stresses

The predominant emphasis on harmful effects of environmental stresses on growth of woody plants has obscured some very beneficial effects of such stresses. Slowly increasing stresses may induce physiological adjustment that protects plants from the growth inhibition and/or injury that follow when environmental stresses are abruptly imposed. In addition, short exposures of woody plants to extreme environmental conditions at critical times in their development often improve growth. Furthermore, maintaining harvested seedlings and plant products at very low temperatures extends their longevity. Drought tolerance: Seedlings previously exposed to water stress often undergo less inhibition of growth and other processes following transplanting than do seedlings not previously exposed to such stress. Controlled wetting and drying cycles often promote early budset, dormancy, and drought tolerance. In many species increased drought tolerance following such cycles is associated with osmotic adjustment that involves accumulation of osmotically active substances. Maintenance of leaf turgor often is linked to osmotic adjustment. A reduction in osmotic volume at full turgor also results in reduced osmotic potential, even in the absence of solute accumulation. Changes in tissue elasticity may be important for turgor maintenance and drought tolerance of plants that do not adjust osmotically. Water deficits and nutrient deficiencies promote greater relative allocation of photosynthate to root growth, ultimately resulting in plants that have higher root:shoot ratios and greater capacity to absorb water and minerals relative to the shoots that must be supported. At the molecular level, plants respond to water stress by synthesis of certain new proteins and increased levels of synthesis of some proteins produced under well-watered conditions. Evidence has been obtained for enhanced synthesis under water stress of water-channel proteins and other proteins that may protect membranes and other important macromolecules from damage and denaturation as cells dehydrate. Flood tolerance: Both artificial and natural flooding sometimes benefit woody plants. Flooding of orchard soils has been an essential management practice for centuries to increase fruit yields and improve fruit quality. Also, annual advances and recessions of floods are crucial for maintaining valuable riparian forests. Intermittent flooding protects bottomland forests by increasing groundwater supplies, transporting sediments necessary for creating favorable seedbeds, and regulating decomposition of organic matter. Major adaptations for flood tolerance of some woody plants include high capacity for producing adventitious roots that compensate physiologically for decay of original roots under soil anaerobiosis, facilitation of oxygen uptake through stomata and newly formed lenticels, and metabolic adjustments. Halophytes can adapt to saline water by salt tolerance, salt avoidance, or both. Cold hardiness: Environmental stresses that inhibit plant growth, including low temperature, drought, short days, and combinations of these, induce cold hardening and hardiness in many species. Cold hardiness develops in two stages: at temperatures between 10° and 20°C in the autumn, when carbohydrates and lipids accumulate; and at subsequent freezing temperatures. The sum of many biochemical processes determines the degree of cold tolerance. Some of these processes are hormone dependent and induced by short days; others that are linked to activity of enzyme systems are temperature dependent. Short days are important for development of cold hardiness in species that set buds or respond strongly to photoperiod. Nursery managers often expose tree seedlings to moderate water stress at or near the end of the growing season. This accelerates budset, induces early dormancy, and increases cold hardiness. Pollution tolerance: Absorption of gaseous air pollutants varies with resistance to flow along the pollutant’s diffusion path. Hence, the amount of pollutant absorbed by leaves depends on stomatal aperture, stomatal size, and stomatal frequency. Pollution tolerance is increased when drought, dry air, or flooding of soil close stomatal pores. Heat tolerance: Exposure to sublethal high temperature can increase the thermotolerance of plants. Potential mechanisms of response include synthesis of heat-shock proteins and isoprene and antioxidant production to protect the photosynthetic apparatus and cellular metabolism. Breaking of dormancy: Seed dormancy can be broken by cold or heat. Embryo dormancy is broken by prolonged exposure of most seeds to temperatures of 1° to 15°C. The efficiency of treatment depends on interactions between temperature and seed moisture content. Germination can be postponed by partially dehydrating seeds or altering the temperature during seed stratification. Seed-coat dormancy can be broken by fires that rupture seed coats or melt seedcoat waxes, hence promoting water uptake. Seeds with both embryo dormancy and seed-coat dormancy may require exposure to both high and low temperatures to break dormancy. Exposure to smoke itself can also serve as a germination cue in breaking seed dormancy in some species. Bud dormancy of temperate-zone trees is broken by winter cold. The specific chilling requirement varies widely with species and genotype, type of bud (e.g., vegetative or floral bud), depth of dormancy, temperature, duration of chilling, stage of plant development, and daylength. Interruption of a cold regime by high temperature may negate the effect of sustained chilling or breaking of bud dormancy. Near-lethal heat stress may release buds from both endodormancy and ecodormancy. Pollen shedding: Dehiscence of anthers and release of pollen result from dehydration of walls of anther sacs. Both seasonal and diurnal pollen shedding are commonly associated with shrinkage and rupture of anther walls by low relative humidity. Pollen shedding typically is maximal near midday (low relative humidity) and low at night (high relative humidity). Pollen shedding is low or negligible during rainy periods. Seed dispersal: Gymnosperm cones typically dehydrate before opening. The cones open and shed seeds because of differential shrinkage between the adaxial and abaxial tissues of cone scales. Once opened, cones may close and reopen with changes in relative humidity. Both dehydration and heat are necessary for seed dispersal from serotinous (late-to-open) cones. Seeds are stored in serotinous cones because resinous bonds of scales prevent cone opening. After fire melts the resinous material, the cone scales can open on drying. Fires also stimulate germination of seeds of some species. Some heath plants require fire to open their serotinous follicles and shed seeds. Fire destroys the resin at the valves of follicles, and the valves then reflex to release the seeds. Following fire the follicles of some species require alternate wetting and drying for efficient seed dispersal. Stimulation of reproductive growth: Vegetative and reproductive growth of woody plants are negatively correlated. A heavy crop of fruits, cones, and seeds is associated with reduced vegetative growth in the same or following year (or even years). Subjecting trees to drought during early stages of fruit development to inhibit vegetative growth, followed by normal irrigation, sometimes favors reproductive growth. Short periods of drought at critical times not only induce formation of flower buds but also break dormancy of flower buds in some species. Water deficits may induce flowering directly or by inhibiting shoot flushing, thereby limiting the capacity of young leaves to inhibit floral induction. Postharvest water stress often results in abundant return bloom over that in well-irrigated plants. Fruit yields of some species are not reduced or are increased by withholding irrigation during the period of shoot elongation. In several species, osmotic adjustment occurs during deficit irrigation. In other species, increased fruit growth by imposed drought is not associated largely with osmotic adjustment and maintenance of leaf turgor. Seedling storage: Tree seedlings typically are stored at temperatures just above or below freezing. Growth and survival of cold-stored seedlings depend on such factors as: date of lifting from the nursery; species and genotype; storage temperature, humidity, and illumination; duration of storage; and handling of planting stock after storage. Seedlings to be stored over winter should be lifted from the nursery as late as possible. Dehydration of seedlings before, during, and after storage adversely affects growth of outplanted seedlings. Long-term storage of seedlings may result in depletion of stored carbohydrates by respiration and decrease of root growth potential. Although many seedlings are stored in darkness, a daily photoperiod during cold storage may stimulate subsequent growth and increase survival of outplanted seedlings. For some species, rapid thawing may decrease respiratory consumption of carbohydrates (over slowly thawed seedlings) and decrease development of molds. Pollen storage: Preservation of pollen is necessary for insurance against poor flowering years, for gene conservation, and for physiological and biochemical studies. Storage temperature and pollen moisture content largely determine longevity of stored pollen. Pollen can be stored successfully for many years in deep freezers at temperatures near −15°C or in liquid nitrogen (−196°C). Cryopreservation of pollen with a high moisture content is difficult because ice crystals may destroy the cells. Pollens of many species do not survive at temperatures below −40°C if their moisture contents exceed 20–30%. Pollen generally is air dried, vacuum dried, or freeze dried before it is stored. To preserve the germination capacity of stored pollen, rehydration at high humidity often is necessary. Seed storage: Seeds are routinely stored to provide a seed supply during years of poor seed production, to maintain genetic diversity, and to breed plants. For a long time, seeds were classified as either orthodox (relatively long-lived, with capacity for dehydration to very low moisture contents without losing viability) or recalcitrant (short-lived and requiring a high moisture content for retention of viability). More recently, some seeds have been reclassified as suborthodox or intermediate because they retain viability when carefully dried. True orthodox seeds are preserved much more easily than are nonorthodox seeds. Orthodox seeds can be stored for a long time at temperatures between 2° and −20°C, with temperatures below −5°C preferable. Some orthodox seeds have been stored at superlow temperatures, although temperatures of −40°, −70°, or −196°C have not been appreciably better than −20°C for storage of seeds of a number of species. Only relatively short-term storage protocols have been developed for nonorthodox seeds. These treatments typically extend seed viability to as much as a year. The methods often require cryopreservation of excised embryos. Responses to cryopreservation of nonorthodox seeds or embryos vary with species and genotype, rate of drying, use of cryoprotectants, rates of freezing and thawing, and rate of rehydration. Fruit storage: Storing fruits at low temperatures above freezing, increasing the CO₂ concentration, and lowering the O₂ concentration of fruit storage delays senescence of fruits and prolongs their life. Fruits continue to senesce and decay while in storage and become increasingly susceptible to diseases. Both temperate-zone and tropical fruits may develop chilling injury characterized by lesions, internal discoloration, greater susceptibility to decay, and shortened storage life. Chilling injury can be controlled by chemicals, temperature conditioning, and intermittent warming during storage. Stored fruits may become increasingly susceptible to disease organisms. Fruit diseases can be controlled by cold, which inhibits growth of microorganisms and maintains host resistance. Exposure of fruits to high CO₂ and low O₂ during storage directly suppresses disease-causing fungi. Pathogens also can be controlled by exposing fruits to heat before, during, and after storage. Scald that often develops during low-temperature storage can be controlled by chemicals and by heat treatments.     

Effects of prescribed burning on leaves and flowering of Quercus garryana

Many woodland understories are managed with prescribed fire. While prescribed burns intended to manipulate understory vegetation and fuels usually do not cause excessive tree mortality, sublethal canopy damage may occur and can affect tree vigor and reproductive output. We monitored Quercus garryana trees in western Washington, USA with multiple canopy thermocouples during three prescribed burns. Peak temperatures recorded in tree canopies ranged from 36 to 649°C. We assessed leaf damage immediately after burning, and flower, leaf and acorn production in the following year in the vicinity of each thermocouple. Leaf scorch first occurred with peak thermocouple temperatures around 45°C, was variable up to 75°C, but above 75°C all leaves were killed. Buds, including their reproductive and leaf organs were more resistant to heat damage than leaves, but leaf scorch had predictive value in forecasting bud organ damage. Staminate and pistillate inflorescences and acorn production per bud decreased and bud mortality increased with maximum thermocouple temperature. In two burns where the highest peak temperatures reached 137°C, there was no difference in leaf production between burned and control plots in the spring following burning. However, no staminate or pistillate inflorescences were produced when thermocouple peak temperatures went above 55 or 68°C, respectively. While heat damage to bud organs was detected, production of reproductive organs was also curtailed at temperatures lower than could reasonably be attributed to heat damage. Thus, it is probable that some other fire-related factor, possibly smoke, was also involved.