Eastern deciduous tree seedlings advance spring phenology in response to experimental warming,but not wetting,treatments

Changing global climate, particularly rising temperatures, has been linked through observations with advanced spring phenology in temperate regions. We experimentally tested if regional climate change predictions of increased temperature and precipitation alter the spring phenology of eastern US tree seedlings. This study reports the results of a 3-year-field experiment designed to study the responses of eastern deciduous tree species planted in a post-harvest environment to a 2 °C increase in temperature and a 20 % increase in precipitation. Species were monitored for timing of germination and leaf out in four treatment combinations (ambient, warmed, irrigated, and warmed + irrigated) on 16 plots located in a recently harvested central Pennsylvania forest. The 2 °C warming advanced day of seed germination by an average of 2 weeks and seedling leaf out by 10 days among all species (both p < 0.001). However, increased precipitation did not result in a significant change in spring phenology. Species responded uniquely to treatments, with germination advancing in three of five species in response to warming and leaf out advancing in six of six species. Southern species projected to expand northward into the study region with rising temperatures did not show responses to warming treatments that would provide them an advantage over current resident species. Timing of germination and leaf out varied among years of the experiment, most likely driven by year-to-year variability in spring temperatures. The climate change experiment highlighted the potential of a moderate 2 °C temperature increase to advance spring phenology of deciduous tree seedlings by up to 2 weeks, with a lack of a phenological response to a 20 % increase in precipitation.     

Germination Strategy of a Woodland Grass: Milium effusum L.

Caryopses of Millum effusum L. were collected from wild plantsin south-east England Laboratory tests established that germination immediately followingharvest occurred relatively slowly at a narrow range of temperatures;optima occurred at 16 °C in the first weeks of experimentsand subsequently at 21 °C, at which the highest proportionof germination occurred Levels of germination increased aftercaryopses had been stored at 25 °C over anhydrous calciumchloride, when tests were done at fluctuating temperatures;or after chilling treatments at 2 °C, or high temperature(26 and 31 °C) conditioning treatments of imbibed seed Freshlyharvested caryopses displayed an inverse relationship betweentemperature and time taken to germinate resulting from variationsin the speed at which after-ripening processes were completedat different temperatures These responses were used to construct a model representativeof all populations of M effusum throughout its natural range.The results suggested that a coherent and plausible interpretationof the responses could be arrived at by suggesting that adaptationto local conditions depends largely on phenotypic plasticityarising from interactions between the germination characterand a variety of differing climatic conditions Millum effusum L wood millet, germination, temperature response     

Gap-detecting mechanism in the seed germination ofMallotus japonicus (Thunb.) Muell. Arg., a common pioneer tree of secondary succession in temperate Japan

Germination responses ofMallotus japonicus (Thumb). Muell. Arg. seeds to temperature revealed a gap-detecting mechanism in the seed germination of the species. Among various constant and alternating temperatures examined in the range from 12–40°C, only very limited temperature regimes were found to be favourable for seed germination, specifically, alternating temperatures between 18–32°C and 28–40°C. A single several-hour higher-temperature (32–40°C) treatment could also induce the germination of seeds which had been imbibed for several days at a constant temperature in the range of 20–26°C, suggesting that there is a process requiring higher temperature among the overal germination processes. Seeds located at or near the surface of denuded soil would have a good chance of experiencing such a temperature change when several rainy days are followed by fine weather, while seeds beneath close vegetation would not. On the other hand, the pressence or absence of light or a simulated ‘canopy ligh’ had little effect on the germination. Therefore, it was concluded that the seeds ofM. japonicus have a ‘gapdetecting mechanism’ in the form of a higher-temperature requirement of a certain process involved in the overall germination processes.     

Relative importance of temperature and other factors in determining geographic boundaries of seaweeds: Experimental and phenological evidence

Experimentally determined ranges of thermal tolerance and requirements for completion of the life history of some 60 seaweed species from the North Atlantic Ocean were compared with annual temperature regimes at their geographic boundaries. In all but a few species, thermal responses accounted for the location of boundaries. Distribution was restricted by: (a) lethal effects of high or low temperatures preventing survival of the hardiest life history stage (often microthalli), (b) temperature requirements for completion of the life history operating on any one process (i.e. [sexual] reproduction, formation of macrothalli or blades), (c) temperature requirements for the increase of population size (through growth or the formation of asexual propagules). Optimum growth/reproduction temperatures or lethal limits of the non-hardiest stage (often macrothalli) were irrelevant in explaining distribution. In some species, ecotypic differentiation in thermal responses over the distribution range influenced the location of geographic boundaries, but in many other species no such ecotypic differences were evident. Specific daylength requirements affected the location of boundaries only when interacting with temperature. The following types of thermal responses could be recognised, resulting in characteristic distribution patterns: (A) Species endemic to the (warm) temperate eastern Atlantic had narrow survival ranges (between ca 5 and ca 25°C) preventing occurrence in NE America. In species with isomorphic life histories without very specific temperature requirements for reproduction, northern and southern boundaries in Eur/Africa are set by lethal limits. Species with heteromorphic life histories often required high and/or low temperatures to induce reproduction in one or both life history phases which further restricted distribution. (B) Species endemic to the tropical western Atlantic also had narrow survival ranges (between ca 10 and ca 35°C). Northern boundaries are set by low, lethal winter temperatures. Thermal properties would potentially allow occurrence in the (sub) tropical eastern Atlantic, but the ocean must have formed a barrier to dispersal. No experimental evidence is so far available for tropical species with an amphi-Atlantic distribution. (C) Tropical to temperate species endemic to the western Atlantic had broad survival ranges (<0 to ca 35°C). Northern boundaries are set by low summer temperatures preventing (growth and) reproduction. Thermal properties would permit occurrence in the (sub)tropical eastern Atlantic, but along potential “stepping stones” for dispersal in the northern Atlantic (Greenland, Iceland, NW Europe) summer temperatures would be too low for growth. (D) In most amphi-Atlantic (tropical-) temperate species, northern boundaries are set by low summer temperatures preventing reproduction or the increase of population size. On European shores, species generally extended into regions with slightly lower summer temperatures than in America, probably because milder winters allow survival of a larger part of the population. (E) Amphi-Atlantic (Arctic-) temperate species survived at subzero temperatures. In species with isomorphic life histories not specifically requiring low temperatures for reproduction, southern boundaries are set by lethally high summer temperatures on both sides of the Atlantic. None of the species survived temperatures over 30°C which prevents tropical occurrence. Species with these thermal responses are characterized by distribution patterns in which southern boundaries in Eur/Africa lie further south than those in eastern N America because of cooler summers. In most species with heteromorphic life histories (or crustose and erect growth forms), low temperatures were required for formation of the macrothalli (either directly or through the induction of sexual reproduction). These species have composite southern boundaries in the north Atlantic Ocean. On American coasts, boundaries are set by lethally high summer temperatures, on European coasts by winter temperatures too high for the induction of macrothalli. Species with this type of thermal responses are characterized by distribution patterns in which the boundaries in Eur/Africa lie further north than those in eastern N America because of warmer winters. Paper presented at the XIV International Botanical Congress (Berlin, 24 July–1 August, 1987), Symposium 6-15, “Biogeography of marine benthic algae”.     

The interaction of temperature, water availability and fire cues regulates seed germination in a fire-prone landscape

Ambient temperature and water availability regulate seasonal timing of germination. In fire-prone landscapes, the role of fire-related cues in affecting the range of temperatures and water potentials (ψs) across which germination can occur is poorly known, especially in non-Mediterranean landscapes. We examined interactive effects of temperature (15 or 25°C), ψ (0 to −0.9 MPa), and fire-related cues (heat and smoke) on germination for seeds of three shrub species from fire-prone southeastern Australia. Incubation temperature affected germination of untreated seeds of Kunzea ambigua and Kunzea capitata (Myrtaceae) (reduction at 25°C), but germination was uniformly low in Epacris obtusifolia (Ericaceae). Decreasing ψ reduced germination across both incubation temperatures. Fire cues increased germination at both incubation temperatures and across ψs, although in Kunzea the increase was smaller and occurred over a narrower range of ψs at 25°C. Hydrotime analysis suggested that fire cues reduced the amount of water necessary for germination of Kunzea seeds. Post-fire germination of the three study species may occur during the warm season, although it is reduced and confined to wet periods for the two Kunzea species. Warm season germination of the study species is consistent with a trade-off between the increased risk of failure of a cohort of seedlings, and benefits of early establishment of a cohort that may survive in an environment with aseasonal rainfall.     

‘Safe sites’ for the seed germination ofRhus javanica: A characterization by responses to temperature and light

Germination responses ofRhus javanica L. seeds to temperature and light were investigated with special reference to their gap-detecting mechanisms in germination, i.e., responses to elevated and/or fluctuating temperatures and sensitivity to leaf-canopy transmitted light. The seeds, which have water-impermeable coats to prevent imbibition, were shown to become permeable and germinable after exposure to higher temperatures of 48–74°C for a brief period depending on the temperature. Once the coat impermeability had been removed by such heat treatment, the seeds became readily germinable over a wide range of temperature and light conditions. The lower and higher temperature limits for germination were around 8° and 36°C, respectively, with an optimal temperature of around 25°C. Simple linear relationships were observed between the temperature and germination rates, i.e., the reciprocals of the time taken by the seed subpopulations to show 10–70% germination in the sub-optimal temperature range, where the required ‘thermal time’ for germination was 2300–3600 Kh. The presence or absence of light or a simulated ‘canopy light’ had little effect on the germination of this species. It was concluded that the seeds ofR. javanica are furnished with a gap-detecting mechanism in the form of a heat requirement for the breakage of water-impermeable seed dormancy, which may be fulfilled by either daytime elevation of the surface temperature of exposed soil, or more effectively by fire.     

Germination responses to temperature responsible for the seedling emergence seasonality ofPrimula sieboldii E. Morren in its natural habitat

Temperature requirements for the breaking of seed dormancy and germination inPrimula sieboldii E. Morren and the annual surface-soil temperature regime in one of its natural habitats were investigated in order to clarify the germination responses determining the seedling emergence seasonality of the species. In a grassland nature reserve in an abandoned flood plain of the Arakawa River, natural seedling emergence of the species was shown to be restricted to mid- to late-spring before the closure of seasonal vegetational gaps, when the daily mean soil surface temperature reached about 15°C, accompanied by large daily fluctuations of about 10°C. Mature seeds collected in late June were never able to germinate at any constant temperature in the range of 8–40°C unless they had been previously subjected to moist-chilling treatment. The proportion of seeds which were released from dormancy increased with increasing duration of the moist-chilling treatment at 2°C, 70–85% of seeds becoming germinable at 16–28°C after 12 weeks of pretreatment at 2°C. The thermal time required for the germination of the thus-pretreated seed population was 905–1690 Kh with a base temperature of around 5°C. Fluctuating temperatures between 24°C and 16 or 12°C had a remarkable dormancy-breaking effect, inducing considerably quick germination in most of the seeds previously subjected to 2°C moist-chilling for 8 weeks.     

Effects of environmental factors on basidiospore germination of ammonia fungi <Emphasis Type="Italic">Coprinopsis</Emphasis> spp. collected from different geographical areas

Effects of pH, NH₄-N, and temperature on basidiospore germination in Coprinopsis austrophlyctidospora from New Zealand, C. phlyctidospora from Japan, C. aff. rugosobispora from Canada, and C. echinospora from Canada were investigated. The Coprinopsis spp. required the presence of ammonium-nitrogen under weak alkaline to neutral conditions for germination, regardless of their different areas of occurrence. The former two species had a wider concentration of NH₄Cl solution and pH range for germination in comparison to the latter two species. The optimum concentration of NH₄Cl solution for the germination was 0.01 M in C. austrophlyctidospora and 0.1 M in the other three species. The pH optimum for germination in the former two species was 8.0 whereas that for germination in the latter two species was 8.0–8.5. The temperature range (5.0–40.0°C) for the former two species was wider than that (5–30°C) for the latter two species. Temperature optima for the germination in the former two species, C. aff. rugosobispora and C. echinospora, were 30, 20–25 and 15°C, respectively. The germination abilities of these Coprinopsis species in a wide range of temperatures are relevant to their natural temperature regime, showing their potential ability to propagate in tropical to subarctic regions.     

Heat and smoke pre‐treatment of seeds to improve restoration of an endangered Mediterranean climate vegetation type

Invasive alien plants impact ecosystems, which often necessitates their removal. Where indigenous species recovery fails following removal alone, an active intervention involving reintroduction of seed of native species may be needed. This study investigated the potential for a combination of the fire cues of smoke and heat as a pre‐treatment of seeds in breaking dormancy and facilitating increased germination. Species were selected to represent different functional types within Cape Flats Sand Fynbos; a fire‐prone, critically endangered vegetation type in South Africa. Seeds were exposed to either a heat pulse (temperatures between 60 and 300°C for durations of between 30 s and 20 min) or dry after‐ripening (1 or 2 months at milder temperatures of 45°C or less). Thereafter, seeds were soaked in smoke solution for 18 h and subsequently placed on agar at 10/20°C for germination. Most species fell into one of two main groups: Seed germination in the first group was greatest following a lower temperature (60°C) heat pulse, an extended period of mild temperature (20/40°C or 45°C) exposure, or no pre‐treatment with heat. Seed germination in the second group was promoted after brief exposure to higher (100°C) temperatures. No germination occurred in any species following heat treatments of 150°C or higher. Species which responded better to higher temperatures were mainly those possessing physical dormancy, but seed morphology did not correlate with germination success. This study showed that heat stimulation of seeds is more widespread in fynbos plant families than previously known and will enable the development of better seed pre‐treatment protocols before large‐scale sowing as an active restoration treatment after alien plant clearing.     

Dormancy in Rice Seed: IV. VARIETAL RESPONSES TO STORAGE AND GERMINATION TEMPERATURES

Serial germination tests were carried out on dormant seeds ofsix rice varieties (four varieties of Oryza sativa L. and twovarieties of O. glaberrima Steud.) stored at several differentconstant temperatures within the range 27° C to 57°C. Probit analyses of the results were carried out to determmethe mean dormancy period for each variety at each temperature.Regression lines fitted to these data showed that there is adirect negative relationship between storage temperature andlog mean dormancy period over the range 27° C to 47°C, thus confirming a previous result obtained on a single variety.At 7° C there were indications of a slight departure fromthis relationship in that the mean dormancy periods at thistemperature were slightly longer than would have been predictedby extrapolation of the regressions calculated from the resultsobtained at lower temperatures. In all cases where the resultswere unambiguous (i.e. in all the sativa varieties and one ofthe glaberrima varieties) a constant Q₁₀ of 3.13 was shown forthe rate of loss of dormancy over the range of storage temperaturesfrom 27° C to 47° C. In the remaining glaberrima variety,where the results were less reliable, a Q₁₀ of 2.54 was found. Germination tests on all varieties were carried out at 32°C, but in the case of one sativa variety germination tests forall storage treatments were also duplicated at 27° C. Thisinvestigation showed that, in contrast to the effect of storagetemperature, the higher temperature during the germination testconsistently resulted in a lower percentage germination. Inaddition the results demonstrated that there is no interactionbetween storage temperature and germination temperature: consequentlythe storage-temperature coefficient has the same value irrespectiveof germination temperature. Some theoretical implications ofthe results are discussed.     

THE EFFECT OF ENVIRONMENTAL VARIABLES ON THE OXYGEN CONSUMPTION OF THE PROTOBRANCH BIVALVE NUCULA TURGIDA (LECKENBY AND MARSHALL)

The oxygen consumption of the protobranch bivalve Nucula turgidawas measured in relation to size and to variation in temperatureand ambient oxygen tension. The slope of the line relating logsize and log oxygen uptake varied from 0.539 to 0.884 over therange 5°C to 40°C in summer – conditioned (S)animals but for winter – conditioned (W) animals the slopevaried from 0.561 to 0.762 over the range 5°C to 15°Conly; from 20°C to 35°C the values for the slope fellfrom 0.298 to 0.092. There was evidence of reverse acclimation,since the absolute rate of oxygen consumption was greater inS animals than in W over the temperature range studied. Thelethal limit for both groups appeared to be between 30°Cand 35°C. At all temperatures (5°C–25°C) N. turgida wasfound to be a near complete oxyconformer with b₂ x 10³ valuesranging from +0.0754 to –0.0234. The responses to temperature differ little from those of eulamellibranchbivalves, but the lack of ability to oxyregulate does demonstratea difference which may be linked to the different gill structure. (Received 13 January 1983;     

Can seed characteristics or species distribution be used to predict the stratification requirements of herbs in the Australian Alps?

The germination requirements of 19 herbs in the Australian Alps were investigated to determine which species may be sensitive to predicted climate changes. Seeds were subjected to factorial treatments of cold stratification for 0, 4, 8 and 12 weeks, followed by incubation at constant temperatures of 10, 15, 20 and 25 °C and alternating temperatures of 20/5 and 20/10 °C. Germination responses were used to identify stratification‐dependent species, to classify dormancy and to determine optimum conditions for laboratory germination. Ordinal logistic regression was used to determine whether the duration of stratification required for ≥ 50% germination could be predicted by seed weight, seed length, embryo : seed ratio or species distribution (latitudinal range, altitudinal range and maximum altitude). The Kruskal–Wallis test was used to determine any significant differences in stratification requirement between endospermic and non‐endospermic seeds. Species varied considerably in their response to the treatment combinations, and therefore their dormancy class. No significant predictors of stratification requirement were identified by ordinal logistic regression (P > 0.9); however, there was a significant difference in stratification requirement between endospermic and non‐endospermic seeds (P = 0.003). Species with non‐endospermic seeds did not require any stratification to germinate well over a range of temperatures, and appear most likely to remain stable or expand in range in response to climate warming. Conversely, the need for ≥ 8 weeks of cold stratification was associated with the presence of endosperm and either a restricted distribution or upland ecotypes of widely distributed species. Alpine species with endospermic seed and a restricted distribution are most likely to contract in range under climate change and would be appropriate to prioritize for ex situ conservation. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013, 172 , 187–204.     

The Germination of the Seeds of Rhinanthus Crista-galli

The germination of the seeds of Rhinanthus Crista-galli hasbeen induced by exposing them to moisture at 2° C. for periodsof from 17 weeks to over a year, depending on the amount ofdry storage to which the seeds had previously been subjected.Germination could not be brought about by moisture-treatmentat 20° C. During moisture-treatment at 2° C. the respirationrate falls significantly after an initial increase, and thengradually rises, after which germination takes place. Generally,respiration is significantly lower during moisture-treatmentat 20° C. Analyses of the treated seeds suggest that therespiratory substrate might be protein. It was found by paperchromatography that during moisture-treatment at 2° C. thenumber of amino-acids in the alcohol extract first diminishesand then increases, reaching a maximum in the ungerminated seedjust before germination becomes apparent. Differences were detectedin the amino-acids found in the alcohol extracts of seeds treatedat 2° C. compared with those moisture-treated at 20°C. Reasons are given which suggest that the limiting factorin the germination process may be the nature and rate of thehydrolysis of the reserve proteins of the seeds.     

Comparative ecology of seedling recruitment in an oligotrophic wet meadow

Abstract. For the regeneration niche to contribute to the maintenance of species diversity interspecific differences in sensitivity of seedling recruitment to environmental conditions is assumed. We experimentally tested differences between meadow species for the response of seed germination to chilling, and sensitivity of seedling recruitment to microscale heterogeneity. We also compared the dynamics of seedling recruitment in gaps. Seed germination was tested in standard laboratory germination tests, comparing control seeds with seeds chilled at +4 °C, and at –14°C for one month. Species responses varied from significant increases in germinability after chilling (e.g. Cirsium palustre, Betonica officinalis, Angelica sylvestris) to significant decreases (e.g. Hieracium umbellatum, Succisa pratensis, Selinum carvifolia). In some species, chilling at + 4 °C has a similar effect to chilling at –14 °C, in others the effect of chilling at + 4°C was intermediate, and in some, there was no effect of chilling at + 4°C, but an effect of chilling at –14°C. Different chilling temperatures also affect timing and speed of seed germination under greenhouse conditions. The dynamics of seed germination under field conditions was studied by sowing seeds into artificially created gaps and following their germination, both where the seedlings were removed after emergence and where they were not removed. Species differ in their germination dynamics: they all start late April, but then differentiate from an abrupt maximum and early finish of germination (in the second half of May), to prolonged germination without a marked maximum. Seedling removal increased the total number of germinated seeds, with a marked density dependence at this stage. Seeds were also sown into plots with treatments (1) gaps, sod stripped, above-ground vegetation removed; (2) mown, moss layer removed; (3) mown; (4) untouched control. Seedling emergence was monitored for 3 yr. Seedling recruitment decreased from treatments (1) to (4), but sensitivity differed between species. With increasing seed weight, the difference between gaps and other treatments decreased. The results show that there are considerable differences in seedling recruitment sensitivity between species.     

Predicting patterns of post-fire germination in 35 eastern Australian Fabaceae

Germination in 35 species from 15 legume genera of southeastern Australia was promoted by a heat treatment which broke the seed coatcaused dormancy. Once the critical temperature was reached, most seeds had their dormancy broken, independent of the duration of heating. Species fell into three classes according to whether their dormancy was broken by a temperature of 40, 60 or 80°C. Highest germination in all species was achieved by heating in the temperature range 80–100°C, although long durations (120 min) at 100°C caused seed death in several species. At 120°C, seeds of most species were killed at all but one minute's duration. A proportion of seeds from 7 species (Acacia myrtifolia, Pultenaea daphnoides, P. incurvata, P. linophylla, P. polifolia, Dillwynia floribunda and Sphaerolobium vimineurn) was not killed at 120°C and had their dormancy broken. This proportion varied markedly and resultant germination levels were significantly less than those at 80 and 100°C, except in S. vimineum. Between-site variations in the 4 species tested (A. myrtifolia, A. suaveolens, A. terminalis and A. ulicifolia) were small. These variations concerned: (i) the minimum temperature required to break seed dormancy in 2 species: 60°C in one population of A. myrtifolia and A. suaveolens, and 80°C in the other; and (ii) the intensity of the germination response. Duration of heating was less important than temperature as a determinant of germination. Ordination techniques revealed that results from one duration across temperatures were comparable with data from multiple durations. This has significant applications in studying rare species, where seed may be in short supply. Predicted germination levels after a moderate intensity fire should far exceed those after a low intensity fire. Little germination was predicted for many species after a low intensity fire and for one species, A. elongata, no germination was predicted. The potential role of indicator species in relation to the maintenance of species in a community is suggested.     

The Interaction of Heat and Smoke in the Release of Seed Dormancy in Seven Species from Southwestern Western Australia

Exposure to high temperatures (40–60 °C) over severaldays to months (simulating summer soil conditions) or to extremelyhigh temperatures (80–120 °C) for periods rangingfrom minutes to several days (simulating the heat of an extremefire) promoted germination in five (including one legume species)of the seven species tested from southwestern Australia. Heat,a collective term for high temperature (HT) and extremely hightemperature (EHT), has previously been used to promote germinationin species with impermeable seed coats (many of which are legumes).If heat is found to promote germination in species with permeableseed coats, it could be of use in the release of dormancy forcommercial development of native plants. Here we report thatelevated storage temperatures (50 °C for 45 and 90 d or60 °C for 45 d) and EHT (100 °C for 3 h and 120 °Cfor 30 min) alone, and in addition to smoke, directly promotegermination of the refractory species Actinotus leucocephalus,Anigozanthos manglesii, Gompholobium knightianum, Loxocaryastriatus and Stylidium affine. Germination of Sowerbaea laxifloraseed was not improved with heat alone but was improved by thecombination of heat and smoke. Seed of Schoenus unispiculatusdid not germinate in response to any of the treatments. Interactionsbetween the effect of temperature, the duration of heat exposureor smoke were detected in all species. Whilst most species demonstratedan interaction between heat and time, not all species were affectedby smoke alone. This was illustrated by an interaction betweensmoke and HT found only in Actinotus leucocephalus, Anigozanthosmanglesii and Stylidium affine or smoke and EHT in A. manglesiiandS. affine . Smoke and exposure time to heat influenced thegermination of Actinotus leucocephalus,Anigozanthos manglesiiand L. striatus in response to HT and only S. affine appearedto demonstrate an interaction between smoke and EHT. The variationsfound in the interactions between treatments suggest that germinationevents occur over a range of conditions both spatially and temporallywhich may facilitate seedling survival and limit competitionbetween emergents. Copyright 2001 Annals of Botany Company Smoke, heat, fire, seedbank, seed dormancy, seed germination, Western Australia     

Germination of Stored Cassava Seed at Constant and Alternating Temperatures

Cassava seed is only capable of germinating over a restrictedrange of constant temperatures. During storage the optimum constanttemperature for germination decreases from about 35 to 30 °Cor possibly less. The rate at which the optimum temperaturechanges during dry storage increases with increase in storagetemperature over the range 0 to 40 °C. Some alternating-temperatureregimes (16 h at the lower temperature; 8 h at the higher temperature)can provide conditions as favourable for germination as theoptimum constant temperatures. Furthermore, it has been shownthat temperature alternation itself is stimulatory because whenthe range of the alternation does not include the optimum constanttemperature value, percentage germination is often higher thancould be obtained at any constant temperature within the range,though this stimulatory response declines during storage. Forthese reasons it is provisionally recommended that cassava seedshould be germinated at 25/35 °C which is as stimulatorya treatment as any which has so far been investigated and hasthe advantage of encompassing the range over which the optimumconstant temperature changes during storage. Manihot esculenta Crantz, cassava, germination, dormancy, seed viability, storage of seeds, after-ripening     

Effects of Cultivation on the Germination Character of the Corn Cockle (Agrostemma githago L.)

Germination tests were done on 19 populations of Agrostemmagithago to examine their responses in relation to the culturalhistory of the plant and to try to determine what changes mayhave accompanied cultivation and the part these may have playedin the establishment and subsequent decline of the species asa weed. Differences found from one population to another were foundto be relatively minor, and the responses of all the collectionsresembled those of other species of Silenoideae distributednaturally around the Mediterranean basin. Differences were establishedbetween adventive populations of A. githago and species naturallydistributed in deciduous woodland and steppeland zones of Europe,even when growth patterns and habitat preferences were relativelysimilar. It was concluded that A. githago had originated in an area witha Mediterranean climate and that there had been few changesin the germination responses of the species during its periodof association with man as a weed of cultivation. The significanceof this result is discussed in relation to the decline of thespecies in Europe during the last hundred years, and with respectto the effects of cultivation on the germination of species,including crop plants, of Mediterranean origin which possessgermination responses similar to those of Agrostemma.     

Germination responses of native and invasive Cerrado grasses to simulated fire temperatures

Background: Fire is an important ecological factor in the Cerrado (Brazilian savanna). However, comparative studies on the effect of high temperatures experienced during fires on seed germination of native and invasive grass species are few.

Aims: To assess germination responses to simulated fire temperatures by seeds of invasive and native Cerrado grasses.

Methods: Heat-shock treatments (50 °C, 70 °C, 90 °C, 110 °C, 130 °C or 150 °C) were applied to seeds of 10 species of native and invasive grasses. For each temperature, the seeds were heated in a dry-air flow for 2 or 5 min. This combination of temperatures and exposure times simulated the soil conditions during typical Cerrado fires.

Results: Temperature treatment was significantly related to germination, and the effect varied according to species. Heat shock did not increase germination in either the native or the invasive species. Exposure time was important for only two species, and four species showed a significant increase in mean germination time.

Conclusions: Species showed different tolerances to high temperatures. It was not possible to differentiate the native and invasive grasses only by their tolerance to high temperatures, suggesting that fire alone may not be an efficient management tool to control the invasive species studied here.