Seasonal Changes of the Metabolites in the Leaves, Bark and Xylem Tissues of Olive Tree (Olea europaea. L) II. Carbohydrates

Seasonal changes of starch and soluble carbohydrates in leaves,bark and xylem tissues of olive tree were examined during acomplete annual cycle. Leaf starch and soluble carbohydrateswere detected at high levels during the spring and autumn metabolicallyactive periods. The low level of leaf starch in combinationwith the drastic reduction of soluble carbohydrates and mannitol,defined the summer period of the low metabolic state of thetree. The low leaf starch level in conjunction with the risensoluble carbohydrate levels in leaves in winter were associatedwith cold acclimation processes. The bark and xylem tissueswere performing as starch deposition sites, and differencesin the extent of starch accumulation in these tissues were detectedduring the seasons. The starch fluctuations in bark and xylemwere discussed in relation to the translocation of metabolitesand other physiological processes. Mannitol, the most abundantleaf carbohydrate, was examined in relation to the reducingsugars exported to the bark. The bark mannitol was examinedin conjunction with the sucrose, glucose and starch levels inthe maturing bark tissues and was correlated to the low wintertemperatures. During the winter there was a drastic reductionof mannitol circulation from the bark to xylem. Olive tree, Olea europaea, L, carbohydrates     

Morphological, Anatomical and Physiological Responses Related to Differential Shoot vs. Root Growth Inhibition at Low Temperature in Spring and Winter Wheat

Several morphological, anatomical and physiological changesand their relationship with differential root vs. shoot growthinhibition at low temperature (5°C) were studied in springand winter wheat cultivars. Root:shoot ratios, expressed eitheras a function of root and shoot fresh weight or as a functionof root and leaf areas, increased at low temperature and thisincrement was more pronounced in spring cultivars than in winterones. Although winter cultivars developed relatively smallerroot systems at 5°C, this characteristic was counterbalancedby a lower stomatal frequency and increased thickness of epidermalcell walls in leaves unfolded at this temperature, relativeto spring cultivars. Likewise, at 5°C a decrease in theosmotic potential of shoots and roots was observed in parallelwith sugar accumulation; this decrease was more marked in wintercultivars. These results indicate a differential morpho-anatomicaland physiological plasticity of winter and spring cultivarsduring development at low temperature. The possible associationbetween these changes and plant water economy at low temperaturesis discussed. Copyright 2001 Annals of Botany Company Spring wheat, winter wheat, Triticum aestivum, low temperature, root:shoot ratio, root surface area, stomatal frequency, osmotic potential     

Analysis of Growth and Yield of Winter and Spring Wheats

In a field experiment to investigate the physiological causesof variation in yield between autumn- and spring-sown wheatand between old and new varieties, the grain yields of the winterwheats were 3-15 per cent, greater than of the spring ones andthe new varieties Cappelle-Desprez and Jufy I yielded 40-70per cent, more than Squarehead's Master and Atle. Nitrogen fertilizerincreased the yields of Cappelle-Desprez and Jufy I more thanof Atle, and decreased the yield of Squarehead's Master by makingit lodge. Until ear emergence the winter varieties had greater leaf-areaindices (L) and dry weights, but smaller net assimilation rates(E), than the spring varieties. Square-head's Master had greaterL but smaller E, and similar dry weight to Cappelle-Desprez.Jufy I had similar E to Atlc, but greater L and dry weight.Nitrogen increased L and dry weight, but decreased E. All thedifferences in E between varieties and nitrogen treatments couldbe explained by the opposite effects on L, that is to say, thedifferences in E were caused by variation in mutual shadingarising from the differences in L and not by changes in leafphysiology. L of winter wheat reached its maximum at the end of May, butL of spring wheat continued to increase until ear emergence.Afterwards Ldecreased more rapidly for winter than for springwheat, so that eventually spring wheat had the greater L. Thesedifferences in the time changes of L partially compensated forthe shorter growth period of spring wheat, and tended to equalizethe grain yield from winter and spring sowings. After ear emergence total dry weight of winter varieties continuedto be greater than of spring ones, but the difference in dryweight of ears was much smaller because ear: shoot dry-weightratio was greater for the spring varieties. Total dry weight,ear dry weight and ear: shoot ratio were all greater in thenew than in the old varieties. Leaf area duration (D) afterear emergence was slightly greater for the winter than for thespring varieties and similar for old and new. The apparent efficiencyof this leaf area in grain production, measured by the grainleaf ratio (ratio of grain dry weight to D), was similar forwinter and spring varieties but greater for new than for old.This suggests that Cappelle-Desprez and Jufy I have higher grainyields because their ears photosynthesize more than do the earsof Squarehead's Master and Atle. Before ear emergence winter varieties had more shoots than springones, and old varieties more than new. After ear emergence therewere only small differences in numbers of ears; percentage survivalwas greater for spring than for winter and for new than forold varieties. Differences in dry weight between varieties were not causedby differences in nitrogen uptake.     

Water relations of climbing ivy in a temperate forest

Ivy (Hedera helix) is the most important liana in temperate European forests. We studied water relations of adult ivy in a natural, 35 m tall mixed deciduous forest in Switzerland using a construction crane to access the canopy. Predawn leaf water potential at the top of climbing ivy ranged from −0.4 to −0.6 MPa, daily minima ranged from −1.3 to −1.7 MPa. Leaf water potentials as well as relative sap flow were held surprisingly constant throughout different weather conditions, suggesting a tendency to isohydric behaviour. Maximum stomatal conductance was 200 mmol m⁻² s⁻¹. The use of a potometer experiment allowed us to measure absolute transpiration rates integrated over a whole plant of 0.23 mmol m⁻² s⁻¹. Nightly sap flow of ivy during warm, dry nights accounted for up to 20% of the seasonal maximum. Maximum sap flow rates were reached at ca. 0.5 kPa vpd. On the other hand, the host trees showed a less conservative stomatal regulation, maximum sap flow rates were reached at vpd values of ca. 1 kPa. Sap flow rates of ivy decreased by ca. 20% in spring after bud break of trees, suggesting that ivy profits strongly from warm sunny days in early spring before budbreak of the host trees and from mild winter days. This species may benefit from rising winter temperatures in Europe and thus become a stronger competitor against its host trees.     

Early Developments in RNA, Protein, and Sugar Levels during Cold Stress in Winter Rye (Secale cereale) Leaves

Changes in freezing tolerance of winter rye (Secale cerealeL. cv. Voima) were determined for leaf tissues during a 1-weekcold stress, which was performed by transferring the 7-d-oldseedlings from a greenhouse (25°C, long day) to 3°Cand short day conditions. The development of cold hardeningwas shown by using an ion leakage test and by determining theamounts of carbohydrates, soluble proteins and RNA. The firstevidence of the development of freezing resistance was foundafter 1 d at low temperature, i.e. an LT₅₀ value increased from-5 to -7°C. Plants cold treated for 7 d reached an LT₅₀value of -9°C. This increase in freezing tolerance was foundto be associated with the increased levels of soluble carbohydrates,total RNA and soluble proteins. These metabolic changes indicatethe association with adjustment of growth and cell metabolismto low temperatures at the beginning of cold acclimation ofwinter rye.Copyright 1994, 1999 Academic Press Secale cereale L., winter rye, cold stress, proteins, RNA, sugars     

The Effect of the Fruit and Exogenous Hormones on Leaf Expansion and Composition in Citrus

Sanz, A., Martinez Cortina, C. and Guardiola, J. L. 1987. Theeffect of the fruit and exogenous hormones on leaf expansionand composition in Citrus.—J. exp. Bot. 38: 2033-2042. The effect of the developing flowers and fruitlets on leaf expansionand composition has been determined in leafy inflorescencesof Citrus sinensis L. Osbeck. During leaf expansion the developingflowers do not compete with the leaves, and their early removaldoes not affect leaf size and composition. Competition for mineralelements is established after flower opening, once leaf expansionis complete. No effect of the fruit on metabolizable carbohydratesin the leaves was found up to day 22 after flower opening. The response to exogenously applied growth regulators suggeststhat the differences in weight and composition between inflorescenceleaves and leaves from vegetative sprouts may be due to hormonally-mediateddifferences in sink strength. Gibberellic acid enhances laminaexpansion and increases the sink strength of the leaves. Kinetinenhances lamina expansion without affecting sink strength. Leafgrowth is directly related to both soluble and wall-bound acidinvertase activities; however, the GA₃ effects on leaf growthand sink strength are unrelated to invertase activity and tothe rate of starch accumulation. Key words: Acid invertase, amylase, carbohydrates, Citrus, leaf growth     

Sink Activity Estimation by Sink Size and Dry Matter Increase During the Ripening Stage of Barley (Hordeum vu/gare) and Rice (Oryza sativa)

During the ripening stage of barley and rice, the sink activitywas defined as the dry matter increase per units sink size,leaf area and time, as follows: NAR = A.SinkW+NAR', where NAR is the net assimilation rate (g d.wt dm^–2d^–1);A is the sink activity [g d.wt g^–1d.wt (ear) dm^–2d^–1]; Sink W is ear wt per plant at heading (g d.wt);and NAR' is net assimilation rate excluding the assimilate ofsink organ (g d.wt dm^–2 d^–1). Plant material with 16 combinations of mutually different sink(ear) and source (leaf) size were produced at heading for eachcrop: parts of each leaf and ear were removed to produce fourgrades in barley, and also a part of each leaf was removed producingfour grades for four rice varieties showing different ear size.NAR and NAR' were determined during 26 and 21 d in barley andrice after heading, respectively. Sink activity (A), representedas the assimilation rate induced by the sink organ, was estimatedfrom the relationship between SinkW and NAR using the previousequation. The sink activity was significantly higher in ricewith a value of 0–0.028 g d.wt g^–1 d.wt (ear) dm^–2d^–1 vs. 0–0.0017 in barley, suggesting that therelative role of leaves for grain filling is considerably higherin rice than in barley. The sink activity obtained in the studymight be introduced into a model to predict the yields of barleyand rice. Hordeum vulgare L, barley, Oryza saliva L, rice, dry matter, NAR, sink, source, sink activity, model     

Dynamics of Fructan and Sucrose Biosynthesis in Crested Wheatgrass

Fructan metabolism occurs in many temperate grasses when ambienttemperatures are cool. Fructan is believed to influence thecold hardiness of grasses and to have osmoregulatory and carbohydratestorage functions. In the cold deserts of the western UnitedStates, crested wheatgrass (Agropyron spp.) usually maintainsmetabolically active leaves throughout the winter. The investigationreported here concerns nonstructural carbohydrate content ofcrested wheatgrass during a growing season (September-June).Fructan accumulated in plant parts during the fall and springwhen temperatures were near 15?C. However, fructan content waslowest when temperatures were coldest. Surose content peakedwhen fructan levels were low and when maximum daily temperaturesremained below 0?C. We propose that fructan biosynthesis inleaf vacuoles provides a sink for photosynthates when temperaturesare too cold for translocation, and growth. Stored fructan thenprovide a readily available substrate for sucrose synthesisand plant growth. Because crested wheatgrass maintains greenleaves during the winter and is capable of photosynthesis attemperatures near 0?C, less stored carbohydrates are requiredfor respiratory maintenance and spring growth than for warm-seasongrasses. ¹Cooperative investigations of the USDA-Agricultural ResearchService and the Utah Agricultural Experiment Station, Logan,Utah 84322, U.S.A. Approved as Journal Paper No. 3755. ²Plant Physiologists, USDA-ARS-Forage and Range Research, Logan,UT 84322-6300, U.S.A. (Received March 25, 1988; Accepted July 11, 1988)     

The Effect of Soil Phosphate on Injury to Winter Barley Caused by Mildew Infection (Erysiphe graminis f.sp. Hordei)

Populations of winter barley were sown in autumn in large tubsof soil to half of which additional phosphate was supplied.Half the plants of each phosphate treatment were infected withpowdery mildew (Erysiphe graminis D.C. f. sp. hordei Marchal)and all plants were transferred to the-field. Infection inducedextensive leaf injury during mid-winter in plants at low phosphate,but injury was greatly reduced in the high soil phosphate treatment.The extent of winter injury had a marked effect on the increasein leaf area in spring, and the accumulation of plant d. wtwas positively correlated with the percentage of total leafarea remaining undamaged at the end of winter. This, in turn,was strongly influenced by the interaction between powdery mildewand soil phosphate. High soil phosphate may act as a ‘buffer’to the effects of infection, minimizing the combined effectsof infection and abiotic stresses suffered by plants in winter. Barley, powdery mildew (Erysiphe graminis hordei), overwinter, phosphate, temperature     

Rhizome dynamics and resource storage in Phragmites australis

Seasonal changes in rhizome concentrations of total nonstructural carbohydrates (TNC), water soluble carbohydrates (WSC), and mineral nutrients (N, P and K) were monitored in two Phragmites australis stands in southern Sweden. Rhizome biomass, rhizome length per unit ground area, and specific weight (weight/ length ratio) of the rhizomes were monitored in one of the stands.Rhizome biomass decreased during spring, increased during summer and decreased during winter. However, changes in spring and summer were small (< 500 g DW m-2) compared to the mean rhizome biomass (approximately 3000 g DW m^–2). Winter losses were larger, approximately 1000 g DW m-2, and to a substantial extent involved structural biomass, indicating rhizome mortality. Seasonal changes in rhizome length per unit ground area revealed a rhizome mortality of about 30% during the winter period, and also indicated that an intensive period of formation of new rhizomes occurred in June.Rhizome concentrations of TNC and WSC decreased during the spring, when carbohydrates were translocated to support shoot growth. However, rhizome standing stock of TNC remained large (> 1000 g m^–2). Concentrations and standing stocks of mineral nutrients decreased during spring/ early summer and increased during summer/ fall. Only N, however, showed a pattern consistent with a spring depletion caused by translocation to shoots. This pattern indicates sufficient root uptake of P and K to support spring growth, and supports other evidence that N is generally the limiting mineral nutrient for Phragmites.The biomass data, as well as increased rhizome specific weight and TNC concentrations, clearly suggests that reloading of rhizomes with energy reserves starts in June, not towards the end of the growing season as has been suggested previously. This resource allocation strategy of Phragmites has consequences for vegetation management.Our data indicate that carbohydrate reserves are much larger than needed to support spring growth. We propose that large stores are needed to ensure establishment of spring shoots when deep water or stochastic environmental events, such as high rhizome mortality in winter or loss of spring shoots due to late season frost, increase the demand for reserves.     

Enhancement of Drought-Induced Senescence by the Reproductive Sink in Fertile Lines of Wheat and Sorghum

The leaf senescence pattern was examined in water-stressed malesterile and fertile lines of wheat (Triticum aestivum) and sorghum(Sorghum vulgare). The study was conducted at the seedling stageand during grain development. The loss of leaf area and chlorophyllcontent induced by water stress was similar in the male sterileand fertile lines of wheat at the seedling stage. At the grainfilling stage, leaf senescence occurred at a faster rate inthe fertile lines as compared to sterile lines of both wheatand sorghum. The study indicates that a reproductive sink accentuatesdrought-induced leaf senescence. Drought resistance, leaf senescence, male sterile, sink     

Modulation of Competition between Fruits and Leaves by Flower Pruning and Water Fogging, and Consequences on Tomato Leaf and Fruit Growth

The effects of water fogging and reducing plant fruit load werestudied in a tomato crop grown in a glasshouse under Mediterraneansummer conditions. The objective of these treatments was toreduce competition between leaves and fruits for carbohydratesand water. Flower pruning increased plant leaf area and increasedfruit, stem, lamina and petiole dry mass (DM). This indicatesthat leaf area growth was limited during the summer due to competitionbetween fruits and leaves for assimilates. In contrast, reducingthe air vapour pressure deficit (VPD) by water fogging had noeffect on plant leaf area or aerial plant DM. Interestingly,there was a significant interaction between plant fruit loadand VPD: the higher the leaf[ratio]fruit ratio the greater theresponses to a reduction in VPD (increase in fruit DM, fruitdiameter, fruit and leaf expansion rate). The data suggest thatunder high fruit loads, water and carbohydrates limit growthunder Mediterranean summer conditions. However, reducing VPDwas not always sufficient to enhance fruit and leaf growth.This might be due to the lower leaf area under high fruit load.In contrast, reducing VPD under low fruit load triggered higherrates of leaf and fruit expansion; this is probably linked toa greater availability of water and carbohydrates. Copyright2001 Annals of Botany Company Assimilate competition, assimilate supply, flower pruning, fruit load, fruit growth, generative/vegetative growth, leaf growth, Lycopersicon esculentum, specific leaf weight, tomato, vapour pressure deficit, water stress     

Some Effects of General Yellow Rust (Puccinia striiformis) Infection on 14Carbon Assimilation, Translocation and Growth in a Spring Wheat

A general, heavy infection of Yellow Rust(Puccinia StriiformisWestend.) on the leaf laminas of the spring wheat (Triticumvulgare Host) Jufy I, unlike an infection on one leaf only,modified the distribution pattern of ¹⁴C-labelled assimilatetranslocated from the second leaf: the proportion moving tothe roots (in older plants also to the tillers) was decreased,and that moving to the leaves was increased. The proportionof the assimilate translocated out of an infected leaf of asuch plant was, however more than that observed when that leafwas the only one infected, though still less than that froma corresponding leaf in a healthy plant. Age of leaf did notgreatly affect the distribution pattern. The effect of infection on the distribution pattern of assimilatefrom other leaves 15 days after inoculation was comparable tothe effect on that from the second leaf at the same intervalafter inoculation. In the case of the upper leaves the proportionmoving to the tillers was appreciably reduced by infection.These results are considered in relation to data obtained froma parellel growth analysis experiment, with which they are ingood agreement.     

Seasonal Onset and Disappearance of Diurnal Rhythmicity in Melatonin Secretion in Female Reindeer

The reindeer (Rangifer tarandus tarandus) is a semidomesticatedholarctic ruminant subject to economic activity. Our researchwas carried out in Northern Finland, at latitude 69°10'N,where the daily light-dark rhythm has a polar pattern: constantdarkness starts on November 26th and lasts about 10 weeks, whilethe polar day of about 10 weeks starts on May 15th. We had previouslyfound distinct daily rhythms in reindeer melatonin secretionin autumn, winter and spring but not at all in summer. Herewe determine how the daily melatonin pattern develops afterthe period of polar day and how it disappears at the beginningof that period. Melatonin showed increased concentrations verysoon after the first sunset. Thereafter the daily pattern developedgradually and was fully developed around the autumn equinox.Its shape was asymmetric and the maximum amplitude occurrednear the end of the dark period. The disappearance of this dailypattern in spring was also gradual. The maximal concentrationsdepended on ambient illumination, especially the duration ofthe dark period. In spring the reindeer appeared to be moresensitive to light than in autumn. Additionally illuminationof the same magnitude suppressed serum melatonin levels moreeffectively before midnight than afterwards, which is in accordancewith the asymmetric secretion pattern. Melatonin secretion wasalways suppressed when the ambient illumination exceeded 1,0001x. The pattern of melatonin secretion in reindeer is differentfrom those described earlier and hence the reindeer may serveas a model for melatonin secretion at high latitudes. We suggestthat, in addition to the duration of the melatonin secretion,changes in amplitude are also of importance in the reindeer.     

Why does Viola hondoensis (Violaceae) shed its winter leaves in spring?

? Premise of the study: Viola hondoensis is a perennial herb that inhabits the understory of temperate, deciduous forests. It is an evergreen plant with a leaf life span that is shorter than a year. Its summer leaves are produced in spring and shed in autumn; winter leaves are produced in autumn and shed in spring. Here we asked why the plant sheds its winter leaves in spring, though climate conditions improve from spring to summer. We proposed four hypotheses for the cause of shedding: (1) changes in seasonal environment such as day length or air temperature, (2) shading by canopy deciduous trees, (3) self-shading by taller summer leaves, and (4) competition for nutrients between summer and winter leaves. ? Methods: To test these hypotheses, we manipulated the environment of winter leaves: (1) plants were transplanted to the open site where there was no shading by canopy trees. (2) Petioles of summer leaves were anchored to the soil surface to avoid shading of winter leaves. (3) Sink organs were removed to eliminate nutrient competition. ? Key results: Longevity of winter leaves was extended when shading by summer leaves was eliminated and when sink organs were removed, but not when plants were transplanted to the open site. ? Conclusion: We conclude that the relative difference in light availability between summer and winter leaves is a critical factor for regulation of leaf shedding, consistent with the theory of maximization of the whole-plant photosynthesis.     

Life cycle strategies and seasonal variations in distribution and population structure of four dominant calanoid copepod species in the eastern Weddell Sea, Antarctica

The dominant Antarctic copepod species Calanoides acutus, Calanuspropinquus, Rhincalanus gigas and Metridia gerlachei were investigatedwith respect to their abundance, vertical distribution, developmentalstage composition, dry weight and lipid content. The specimenswere sampled during three expeditions to the eastern WeddellSea in summer (January/February 1985), late winter/early spring(October/November 1986) and autumn (April/May 1992) between0 and 1000 m depth to follow the seasonal development of thepopulations. Three species were most abundant in April, onlyC.propinquus reached highest concentrations in February. A seasonalmigration pattern was evident in all four species, but was mostpronounced in C.acutus. In October/November, they inhabiteddeeper water layers, their ascent started by mid-November andin mid-February the species concentrated in the upper 50 m,except for M.gerlachei (50–100 m). Their descent was observedin April/May. The stage composition changed dramatically withseason, the older developmental stages (CIII–CVI) dominatedthe populations in late winter/early spring, whereas youngerstages (CI and CII) prevailed during summer (C.acutus, C.propinquus)or autumn (R.gigas, M.gerlachei). Only C.acutus ceased feedingin autumn and diapaused at depth. Strong differences betweenseasons were also detected in dry weight and lipid levels, withminima in late winter/early spring and maxima in summer (C.acutus,R.gigas) or autumn (C.propinquus, M.gerlachei). Lipid reservesseem to be most important for the older stages of C.acutus andC.propinquus. Based on these seasonal data, different life cyclestrategies are suggested for the four species.     

Distribution of Assimilates from Various Source Leaves During the Development of Gladiolus grandiflorus

The distribution pattern of the products of photosynthesis wasstudied in gladiolus plants (Gladiolus grandiflorus cv Eurovision)in four stages of development I, plants having a very younginflorescence still enclosed between the leaves; II, plantswith a young inflorescence just emerged from the leaves, III,plants at full bloom, IV, plants with young fruits. The first,third or sixth foliage leaf was labelled with ¹⁴CO₂, and subsequentdistribution in the plant was determined Results were expressedas a percentage of translocated ¹⁴C accumulated by each partof the plant which gives a measure of its ‘sink strength’,or as ‘relative sink activity’ (RSA) which is independentof the size of the indicated organ. There are two competing sinks in the developing gladiolus—theinflorescence and the new corm. When RSA is the criterton theinflorescence constitutes the main sink irrespective of thesource leaf from the first stage until flowering. With the subsequentwilting of the flowers and fruit set RSA of the inflorescencedeclines rapidly and the new corm becomes the main sink When‘sink strength’ is the criterton it appears thatthe inflorescence acts as a very weak sink when it is youngand becomes increasingly stronger until flowering and then declinessteeply. Sink strength of the corm declines during the developmentof the inflorescence and then increases again steeply with wiltingof the flowers and fruit set. There are small differences betweenthe various source leaves. The young new corm acts as a strongsink for the lower foliage leaf and progressively weaker forupper leaves. Gladiolus grandiflorus, flower development, corm, assimilates distribution, sink strength, relative sink activity     

Low Temperature Affects Pattern of Leaf Growth and Structure of Cell Walls in Winter Oilseed Rape (Brassica napus L., var. oleifera L.)

Three-week acclimation of winter oilseed rape (Brassica napusL. var. oleifera L.) plants in the cold (2 °C) resultedin a modified pattern of leaf cell enlargement, indicated bythe increased thickness of young leaf blades and modified dimensionsof mesophyll cells, as compared with non-acclimated tissuesgrown at 20/15 °C (day/night). The thickness of leaf cellwalls also increased markedly during cold acclimation but itdecreased in response to a transient freezing event (5 °Cfor 18 h followed by 6 or 24 h at 2 °C, in the dark). Cellwalls of the upper (adaxial) epidermis were most affected. Theirultrastructure was modified by cold and freezing treatmentsin different ways, as revealed by electron microscopy. Possiblereasons for the cold- and freezing-induced modifications inthe leaf and cell wall morphology and their role in plant acclimationto low temperature conditions are discussed. Copyright 1999Annals of Botany Company Acclimation, Brassica napus var. oleifera, cell wall ultrastructure, cold, freezing, leaf structure, winter oilseed rape.     

Leaf Survival and Evolution in Betulaceae

Studies on the changes in leaf number of 12 species of Betulaceaewere carried out by repeated observations during several years.The inner structure of the winter buds of these species wasalso examined. The periods of leaf emergence were long in Alnusand Betula, intermediate in Corylus and short in Ostrya andCarpinus. A heavy summer leaf fall is characteristic only ofthe Gymnothyrsus subgenus of Alnus. One lamina and two stipulesis the basic unit constituting the winter buds. Only the budsof Gymnothyrsus are composed of several of these units. In theAlnaster subgenus of Alnus, Betula and Corylus, there are oneor two scales that seem to have originated from the two stipulesremaining after reduction of the lamina. Eight and 24 scalesof similar origin were found in Ostrya and Carpinus respectively.A common ancestral species having the following primitive charactersis proposed: shoot constituted only of the equal-sized units,period of leaf emergence long, and leaf fall usually occurs.Alnus (Gymnothyrsus) is assumed to be the most primitive typeas it has many characters similar to those of the proposed ancestralspecies. Carpinus is assumed to be the most advanced group.The leaf survivorship curve is assumed to have changed fromthe primitive bell-shaped to an advanced trapezoid concurrentwith an increase in the number of bud scales. Betulaceae, Alnus, Betula, Carpinus, Corylus, Ostrya, leaf survival, leaf emergence, stipules, winter buds, evolution     

Turnover of Carbohydrates in Relation to Growth in Apple Trees. I. Seasonal Variation of Growth and Carbohydrate Reserves

Growth in young apple trees of the rootstocks MM. 106 and M.7 was estimated by changes in d. wt., and growth in the differentregions of the two rootstocks was compared. Changes in d. wtwere compared with changes in extractable carbohydrates in MM.106 trees. The seasonal variations in d. wt, extractable carbohydratesand residues, are discussed in relation to utilization of reserveand current assimilates in the different regions of plant duringwinter, autumn, spring and summer. Malus sylvestris L, apple, carbohydrate, growth