scholarly journals Infestation of Early- and Late-Flushing Trees by Spring Caterpillars: An Associational Effect of Neighbouring Trees

Forests ◽  
2021 ◽  
Vol 12 (9) ◽  
pp. 1281
Author(s):  
Lenka Sarvašová ◽  
Peter Zach ◽  
Michal Parák ◽  
Miroslav Saniga ◽  
Ján Kulfan

In temperate forests within Europe, early-flushing (EF) deciduous trees are often heavily infested by early spring leaf-eating Lepidoptera, while late-flushing (LF) trees are better protected in a phenological manner against such heavy infestations, as spring moth larvae begin to appear before their bud burst. The associational effects of EF trees on LF ones are only poorly known. We studied whether or not the infestation of LF trees by spring Lepidoptera can be affected by EF ones if they grow in the immediate vicinity. We compared spring assemblages of leaf-eating larvae of Lepidoptera on LF Quercus cerris L. with those on EF Q. pubescens Willd. in several microhabitats in Slovakia, Central Europe. Larvae were collected from mature and young trees. Mature trees sampled were growing: (1) in a closed-canopy forest; (2) in small groups; or (3) as a lone tree. Forest and tree groups are both constituted by oak species. Tree groups and lone trees were 20–50 m distant from forest edges. Young trees were growing (1) under mature Q. pubescens trees in a forest or (2) as a lone tree within forest gaps or near the edges. In the closed-canopy forest where LF trees (Q. cerris) were surrounded by EF ones (Q. pubescens), the caterpillars on mature LF trees were in abundance, almost as on mature EF ones. The species composition of larval assemblages on the two oak species was similar. In contrast, on small groups and on lone trees, the lepidopteran larvae were significantly less abundant on LF trees than EF ones. In the case of young trees, the abundance of larvae and their composition assemblages on both oaks were comparable in the forest. In the open habitat, LF trees were less infested by larvae than EF ones and the assemblages of moth larvae differed between the two. Our results reveal the effect (associational susceptibility) of EF trees on LF ones when growing in a close vicinity. It means that the phenological protection of LF trees may not be sufficient if they grow close to or are surrounded by EF ones.

IAWA Journal ◽  
2016 ◽  
Vol 37 (2) ◽  
pp. 315-331 ◽  
Author(s):  
Peter Kitin ◽  
Ryo Funada

This paper reviews the development of xylem vessels in ring-porous dicots and the corresponding leaf phenology. Also included are our original observations on the time-course of vessel element growth, secondary wall deposition, and end wall perforation in the deciduous hardwood Kalopanax septemlobus. Different patterns of xylem growth and phenology serve different strategies of the species for adaptation to seasonal climates. Trees with ring-porous xylem form wide earlywood vessels (EWV) in spring and narrow latewood vessels in summer. The wide EWV become embolized or blocked with tyloses by the end of the growing season while the narrow vessels may remain functional for many years. The co-occurrence of wide and narrow vessels provides both efficiency and safety of the water transport as well as a potentially longer growing season. It has for a long time been assumed that EWV in ring-porous hardwoods are formed in early spring before bud burst in order to supply sap to growing leaves and shoots.However, the full time-course of development of EWV elements from initiation of growth until maturation for water transport has not been adequately studied until recently. Our observations clarify a crucial relationship between leaf maturation and the maturation of earlywood vessels for sap transport. Accumulated new evidence shows that EWV in branches and upper stem parts develop earlier than EWV lower in the stem. The first EWV elements are fully expanded with differentiated secondary walls by the time of bud burst. In lower stem parts, perforations in vessel end walls are formed after bud burst and before the new leaves have achieved full size. Therefore, the current-year EWV network becomes functional for water transport only by the time when the first new leaves are mature.


1960 ◽  
Vol 51 (1) ◽  
pp. 175-201 ◽  
Author(s):  
P. B. Cornwell

The aerial dispersal of the Pseudococcid vectors of virus diseases of cacao in Ghana and the possible influence on it of wind speed was studied at Tafo. Seasonal variations in wind speed in Ghana are slight, particularly inland in the cacao-growing areas. Observations at Tafo during 1955 showed that air movement was maximal between 12.30 and 3.0 p.m. and minimal during the hours of darkness. Daily wind speeds in the open, from April to November 1955, averaged 1·1 m.p.h., 4 ft. above ground. About 80 per cent, of wind speeds measured in one-minute periods on two days in February 1955 were within the range 1–5 m.p.h. and 11–12 per cent, between 5 and the maximum recorded speed of 7 m.p.h.In cacao, wind speed is reduced by a factor of 10–20 times; daily speeds averaged 0·09 m.p.h., at 8 ft. above ground during April and May 1955. The highest daily averages under a closed canopy (400–650 ft./hr.) were recorded 2 ft. above ground-level; speeds fell to a minimum (25–125 ft./hr.) in the canopy at 15–25 ft., and rose again above the canopy at 30 ft. to a speed (250–350 ft./hr.) comparable with that just below the branches at 10 ft. At breaks in the canopy caused by the removal of diseased trees, daily averages were lowest (125–150 ft./hr.) 2 ft. above the ground. They rose to a peak (400–600 ft.) on a level with the lower branches of the canopy, dropped markedly (250–450 ft./hr.) at the level of the middle canopy and rose to a maximum (650–1,000 ft./hr.) at 30 ft.All instars of Pseudococcus njalensis Laing walking on pieces of cacao wood in the laboratory withstood removal at air speeds of 10 m.p.h., but these and corresponding stages of three other species could be dislodged by gently tapping the wood. The late nymphs and adults of Ps. njalensis and Ps. gahani Green were more easily removed than their ‘crawlers’, though this difference was not found between the developmental stages in Planococcus citri (Eisso) and Ferrisiana virgata (Ckll.). Amongst the four species tested, first-instar nymphs of Pl. citri were most easily dislodged, and those of Ps. njalensis or F. virgata more so than those of Ps. gahani.Airborne mealybugs were caught on adhesive traps, on bait twigs pinned to mature trees, and on cacao seedlings. Eight vector species became established on cacao after dispersal by air currents.Under a closed canopy, more airborne mealybugs were caught at two and ten feet above ground than at levels in and above the canopy. At breaks in the canopy, catches averaged about 13 per cent, of those obtained under a continuous canopy and were insufficient to show changes in aerial density with height. The distribution of catches over the surface of traps would suggest that mealybugs drop from the branches, are carried by air currents when falling, and become laterally dispersed at levels a few feet above the ground.In a clearing where cacao had been removed to simulate conditions following the routine cutting out of virus-infected trees, airborne mealybugs became established on seedlings at a distance of 45 ft. from infested cacao trees. The ratios of boxes of seedlings which became infested by aerially dispersed Ps. njalensis at increasing distances from infested standing cacao, in relation to those beneath it (unity), were: 0·86 at 10–20 ft., 0·57 at 30 ft. and 0·14 at 40–100 ft. Under conditions of high insolation, the maximum recorded distance of mealybug aerial dispersal from surrounding vegetation to cacao seedlings was 340 ft. Aerial catches on seedlings 40 to 165 ft. from cacao showed an over-all decrease with distance.Aerial dispersal is more pronounced during dry conditions, particularly during the main dry season, December–February, and to a lesser extent during the brief dry period experienced in July or August.The infestation rate of cacao seedlings by windborne mealybugs (predominantly Pl. citri and F. virgata) was increased by 50 per cent, when plants were protected from weather by artificial shade. These traps, insulated from ants, failed to become infested by Ps. njalensis.Out of 64 young cacao trees, 22 per cent, became infested by airborne vectors during the five-month period May to September 1955; when, for similar trees, normal dispersal was augmented by an initial artificial colonisation with Ps. njalensis, the corresponding figure was 41 per cent. The infestation rate, after either augmented or natural dispersal, was not significantly affected by attempts to establish on the trees nests of the ant, Grematogaster striatula Emery, or by affording protection from the weather in the form of artificial shade. It was evident, however, that the presence of mealybug-attending ants is almost essential for infestations of Ps. njalensis to develop, but there must be other limiting factors, since establishment failed on 58 per cent, of trees on which coccidophilic species were present.The part played by airborne vectors in extending infection by radial and ‘jump spread’ is discussed, together with the possible use of insecticidal measures to prevent their establishment on the trunks of healthy cacao.


1973 ◽  
Vol 105 (4) ◽  
pp. 605-612 ◽  
Author(s):  
David Evans

AbstractErannis vancouverensis Hulst occurs from northern British Columbia to central California, and has been occasionally reported at infestation levels. The larvae feed on young leaves of several species of deciduous trees; winter is passed in the egg or sometimes in the pupal stage; adults emerge during late autumn or occasionally during winter or early spring; females are wingless. The life stages, including larval instars, are described here in detail. Virus disease and parasitism by tachinid flies help control the species.


1979 ◽  
Vol 19 (96) ◽  
pp. 122 ◽  
Author(s):  
RA Sarooshi ◽  
EA Roberts

Effects of trellising together with the use of various foliage wire arrangements on the production and quality of harvest-pruned sultanas were studied over 4 years. In one experiment a single wire and four narrow 0.4 m 'T' trellis systems, and in a second experiment four 0.9 m wide 'T' trellis and one 0.4 m narrow 'T' trellis system, were tested. Other treatments superimposed on all trellises included crown bunch removal in early spring or at harvest pruning, one and two alkaline oil-in-water sprays (oil sprays) and gibberellic acid (GA) or no GA spray. There were no differences between the four narrow trellises. Dried fruit yield of these four trellises was greater than that of the single wire by an average of 27%, because of higher bunch and cane numbers. There were also no differences between the four wide trellises except that two of the complex ones had more canes. The narrow trellis NTI (used in both experiments) yielded 27% less than the wide trellises because of fewer bunches per vine, caused by lower cane numbers and fruitfulness. Trellising had no effect on fruit quality and only marginal effects on rate of fruit drying, most probably due to low vigour of the experimental vines. As the complex trellis systems had no advantage over the simpler two wire 'T' trellises, their use in harvest pruning is not advocated. In both experiments two oil sprays produced slightly better fruit quality with faster drying of fruit. Use of two oil sprays is warranted where fruit has to be dried rapidly to minimise risk due to rain damage. Early crown bunch removal did not reduce yield and the best time for bunch removal was 6 weeks after bud burst. Use of GA in harvest pruning is not recommended as it does not improve fruit quality and in some years leads to slower fruit drying.


1987 ◽  
Vol 65 (3) ◽  
pp. 466-475 ◽  
Author(s):  
Alastair D. Macdonald ◽  
D. H. Mothersill

Reproductive buds and developing inflorescences were collected weekly from mature trees during three successive growing seasons in northwestern Ontario. Material was prepared to show all stages of inflorescence and flower development and meiosis. Male inflorescence induction, involving the long-shoot bud apex and one or two proximal axillary apices, occurred in early May, before bud burst. Female induction involved the short-shoot bud apex and occurred in late June – early July. Both male and female partial inflorescences resembled a simple dichasium. The male flower consisted of usually two stamens and two or three tepals variably arranged. Meiosis occurred in late July – early August. Each female flower consisted of two stigmas, two connate tepals that were not noticeable at maturity, and a parietal placenta bearing two unitegmic ovules. Meiosis occurred in mid-June, after pollination in mid-May. It is concluded that developmental data do not help elucidate whether the inferior portion of the gynoecial wall is cauline or appendicular and whether the placenta is derived from axial or carpellary tissue. It is suggested that the trigger(s) evoking male and female inflorescence induction may be different and that the metabolic prerequisites for induction and early development would be supplied by winter-stored material for male development and by current metabolic processes for female development.


HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1077D-1077
Author(s):  
Wol-Soo Kim ◽  
Xiu-Yu Wu ◽  
Soon-Ju Chung

During the early spring, embolism symptoms may be observed on the leaves of kiwi trees after a severe, cold winter. The morphological character of embolism in young leaves in early spring is typically parachute shaped, at the basal part of kiwi shoots. Deformed leaves were observed at the beginning stage of development. To test the factors, we used water stress, low temperature, and xylem bubble treatments on kiwi vines during the winter season. Low temperature treatments on trees were carried out in a –15 °C chamber for 0, 12, 24, and 48 hours. For the xylem bubble treatment, the trees were injected with 3.5 MPa compressed air at –15 °C for 24 hours. For water stress treatments, the trees were not irrigated until dry soil conditions reached as little as 50% soil moisture. Treated kiwi trees planted in plastic pots (20 cm × 25 cm) were moved into the growth chamber at 25 °C with 12 hours of light, and the rate of deformed leaf symptoms was observed. In all treatments, deformed leaves were observed and bud burst rates were lower than for the control. Therefore, we confirmed that the main factors for deformed leaves were low temperature, xylem bubbles, and water stress.


2020 ◽  
Author(s):  
Yuko Kurita ◽  
Satomi Kanno ◽  
Ryohei Sugita ◽  
Atsushi Hirose ◽  
Miwa Ohnishi ◽  
...  

Summary(1) the research conducted, including the rationalePhosphorus (P) is an essential macronutrient for plant growth. In deciduous trees, P is remobilized from senescing leaves and stored in perennial tissues during winter for further growth. To clarify how deciduous trees utilize the internal P through a year, seasonal re-translocation routes and the reuse of P over winter were investigated.(2) methodsWe analyzed the seasonal re-translocation and accumulation of P in poplar trees (Populus alba. L) cultivated under “a shortened annual cycle system”, which mimicked seasonal phenology in a laboratory. The real-time radioisotope imaging and the macro- and micro-autoradiography with 32P and 33P were used to reveal the organ and tissue level P allocation.(3) key resultsThe direction of phosphate re-translocation changed seasonally. In the growing season, P was mainly re-translocated from a leaf to upper parts via phloem. During senescence, P was re-translocated to lower perennial parts, and also to inner xylem parenchyma cells. Phloem-xylem exchange of re-translocated P occurred in the stem. After bud burst in spring, stored P was re-translocated to the whole plant and mainly accumulated in new shoots.(4) the main conclusion, including the key points of discussionPoplar trees change the routes of P re-translocation longitudinally and radially depending on the season, and recycle internal P throughout the year.


2020 ◽  
Author(s):  
Bertold Mariën ◽  
Inge Dox ◽  
Hans J. De Boeck ◽  
Patrick Willems ◽  
Sebastien Leys ◽  
...  

Abstract. Severe droughts are expected to become more frequent and persistent. However, their effect on autumn leaf senescence, a key process for deciduous trees and ecosystem functioning, is currently unclear. We hypothesized that (I) severe drought advances the onset of autumn leaf senescence in temperate deciduous trees and that (II) tree species show different dynamics of autumn leaf senescence under drought. We tested these hypotheses using a manipulative experiment on beech saplings and three years of monitoring mature beech, birch and oak trees in Belgium. The autumn leaf senescence was derived from the seasonal pattern of the chlorophyll content index and the loss of canopy greenness using generalized additive models and piece-wise linear regressions. Drought did not affect the onset of autumn leaf senescence in both saplings and mature trees, even if the saplings showed a high mortality and the mature trees a high leaf mortality (due to accelerated leaf senescence and early leaf abscission). We did not observe major differences among species. Synthesis: The timing of autumn leaf senescence appears conservative across years and species, and even independent on drought stress. Therefore, to study autumn senescence, seasonal chlorophyll dynamics and loss of canopy greenness should be considered separately.


1983 ◽  
Vol 61 (12) ◽  
pp. 3049-3065 ◽  
Author(s):  
Alastair D. Macdonald ◽  
D. H. Mothersill

Buds and developing branches of Betula papyrifera were collected weekly from mature trees during three successive growing seasons. Material was prepared to show stages of bud inception, development, and flushing and female inflorescence inception. Short shoots develop from (i) proximal axillary buds on long shoots (ii) short-shoot terminal buds, or (iii) axillary buds on flowering short shoots. An axillary bud apex forms a terminal bud after bud burst. An axillary bud possesses one outer rudimentary leaf, but all other short-shoot buds have three outer rudimentary leaves. All short-shoot buds possess, in addition, one–three embryonic foliage leaves and, distally, three primordial rudimentary leaves which form the outermost appendages of the succeeding terminal bud. Rudimentary leaf stipules form the cataphylls. Foliage leaf primordia are initiated in May – early June and rudimentary leaves arise in late June – July. If a bud apex is initiated in year n, female inflorescence induction occurs in late June of year n + 1 or any succeeding year. An axillary bud develops on a short shoot as a consequence of flowering; it is initiated concurrently with inflorescence development and its development is completed during flowering and seed maturation. Short- and long-shoot buds can be distinguished, upon dissection, in mid-July when buds are forming. Hence, determination of potential long and short shoots occurs the year before bud burst.


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