MODES OF SEASONAL ADAPTATION IN THE INSECTS: I. WINTER SURVIVAL

1978 ◽  
Vol 110 (11) ◽  
pp. 1167-1205 ◽  
Author(s):  
H. V. Danks

AbstractFactors affecting the winter survival of temperate-zone insects are reviewed. Certain species suffer high winter mortality especially in cold years, or in years with below normal amounts of insulating snow.Survival depends on the choice of winter microhabitat and on cold-hardiness, but also on biological features that have not previously been emphasized. These include behaviour that results in placement of overwintering eggs in less severe sites and manufacture of cocoons or other structures that retard inoculation by ice, or desiccation. The possible role of habitat heterogeneity in facilitating population survival is stressed.Microhabitats are characterized mainly with respect to temperature. They differ markedly among geographic areas and not only in midwinter conditions (including the extent of variation), but also in the time at which entry to the microhabitat in fall is necessary to avoid the risk of frost. The cues that govern entry into these microhabitats include negative phototaxis in many species but have not been subjected to quantitative analysis. Deeper layers are warmer in winter but warm up more slowly in spring and therefore some species, especially in arctic habitats where rapid vernal development is advantageous because the season is short, overwinter in superficial or insolated sites.Supposed mechanisms of cold- and freezing-injury and its avoidance are reviewed. There are several theories of freezing-injury: many modem theories focus on damage to the cell membrane, apparently caused by changes in cell volume induced during freezing. Injury is avoided by suppression of haemolymph nucleators (enhancing supercooling); or by a variety of methods, especially those involving solutes, minimising damage to frozen tissues. Among these solutes, the prevalence of glycerol in overwintering insects is not unexpected since glycerol is a normal metabolite in animals and can play several possible roles in cryoprotection.Cold-hardiness is metabolically costly because of these solute adjustments. The cold-hardiness of a taxon depends partly on climatic history during its evolution. Faunal composition at the highest latitudes reflects this dependence.The winter survival of many high-latitude insects varies rather widely from year to year; but the many detailed studies on cold-hardiness that have been made in the laboratory have seldom been related to natural mortality.The overwintering stage depends partly on the taxon. It is often fixed within a genus, but less closely within higher taxa. Proportionately more species overwinter as larvae at higher latitudes, especially when the life cycle lasts more than one year. Habitat also influences the overwintering stage: aquatic species generally overwinter as larvae, although species of temporary pools frequently overwinter as eggs. Overwintering in more than one stage is not common.This review suggests that winter survival of a group depends on latitude (or its climatic equivalent), habitat, and evolutionary history. It might therefore be especially useful to compare cold-hardiness, developmental rates, control of the life cycle and other features among species at the same latitude from each extreme of a series, that contrasts cold-hardy groups in stable habitats (such as Chironomidae) with aerial or vegetation dwelling groups that are not cold-hardy (such as Orthoptera). Future study of winter survival also demands more ecological data (overwintering stage, microhabitat, and conditions experienced there) for a larger sample of the fauna, and the simultaneous measurement of cold-hardiness.

1997 ◽  
Vol 77 (3) ◽  
pp. 399-420 ◽  
Author(s):  
Pauliina Palonen ◽  
Deborah Buszard

This article gives an overview of the current state of cold hardiness research in fruit crops by reviewing the recently published studies on cold hardiness of both tree fruit and berry crops. Topics discussed include cold hardiness of fruit species, cultivars and different plant organs, biophysical and biochemical aspects of hardiness, evaluation of hardiness, as well as endogenous, cultural and environmental factors affecting cold hardiness in these species. Lack of cold hardiness is a major limiting factor for production of fruit crops in many regions of the world and improved cold hardiness one of the major objectives in numerous breeding programs and research projects. Screening cultivars or selections for cold hardiness is commonly done, and different methods applied to the evaluation of hardiness are discussed. The physical limit of deep supercooling may be a restricting factor for expanding the production of some fruit crops, such as Prunus species and pear. As for biochemical aspects, a relationship between carbohydrates and cold hardiness is most commonly found. Studies have also been made on different hardiness modifying cultural factors including rootstock, crop load, raised beds and application of growth regulators. The latter seems promising for some species. Cold hardiness is an extremely complex phenomenon and understanding different mechanisms involved is critical. Since hardiness is, however, primarily affected by genotype, developing cold-hardy fruit cultivars and effective screening methods for hardiness are essential. Finally, cultural practices may be improved to further enhance hardiness. Key words: Berries, cold hardiness, fruits, small fruits, stress, winter hardiness


1964 ◽  
Vol 96 (4) ◽  
pp. 617-625 ◽  
Author(s):  
A. W. MacPhee

AbstractIn Kings County, Nova Scotia, low temperatures in the coldest nights of winter can differ by as much as 10°F. from one area to another. This has an important bearing on winter survival of some arthropods. Overwintering sites of orchard arthropods range from exposed situations which remain at air temperature to well protected ones on the ground where temperatures rarely go below 20°F. The cold-hardiness of each of 24 species of arthropods was measured: seven were sufficiently cold-hardy to survive any winter conditions in Nova Scotia, five were less cold-hardy but overwinter in well protected sites and twelve had marginal cold-hardiness, their mortality varying with the winter and the locality.


2015 ◽  
Author(s):  
Stefanos S Andreadis ◽  
Yianna Poulia ◽  
Sofia Noukari ◽  
Barbara Aslanidou ◽  
Matilda Savopoulou-Soultani

The potato tuberworm, Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae), is a worldwide pest of solanaceous crops especially devastating to potatoes. In the present study we investigated the cold hardiness profile of short-term acclimated and non-acclimated immature and adult stages of a field population of P. operculella. Late instars displayed the lowest mean supercooling point, for both short-term acclimated and non-acclimated individuals, however, no significant differences were observed among developmental stages. Unlike supercooling capacity, acclimation at 5 oC for 5 days enhanced the ability to survive at subzero temperatures after a 2 h exposure. Mean lethal temperature (LTemp50) of all developmental stages (egg, late instar, pupa and adult) decreased after short-term acclimation, however only adults displayed a significant difference among acclimated and non-acclimated individuals concerning their LTemp50 (-11.1 and -8.3 oC, respectively). Generally, pupae were the most cold tolerant developmental stage followed in decreasing order by the eggs and adults, while interestingly late instars were the least ones. Non-freezing injury above the supercooling point was well documented for all developmental stages indicating a pre-freeze mortality and suggesting that P. operculella is considered to be chill tolerant rather than freeze intolerant. Nevertheless, given its high degree of cold hardiness, winter mortality of P. operculella due to low temperatures is not likely to occur and potential pest outbreak can take place following a mild winter.


1985 ◽  
Vol 65 (4) ◽  
pp. 893-900 ◽  
Author(s):  
D. W. A. ROBERTS

Nine cultivars of common wheat (Triticum aestivum L.) ranging from very cold hardy to tender were sprouted in vermiculite at 0.5–1.0 °C for 7 wk in the dark and then placed at 0.5 °C, −2.5 °C, −5 °C, −7.5 °C, or −10 °C for up to 20 wk. Plants held at 0.5 °C progressively lost hardiness. Little change occurred in the hardiness of plants moved to −2.5 °C. There was apparently a small initial increase in hardiness after transfer to −5 °C or −7.5 °C followed by a decline in hardiness. Plants transferred to −10 °C lost hardiness progressively after transfer. These results suggest that part of the reason for late-winter mortality of winter wheats in northern regions of the Canadian prairies is damage from long exposures to temperatures only slightly lower than −5 °C. This damage is manifested by higher LT50 values or lower cold hardiness in late winter and early spring.Key words: Triticum aestivum L., cold hardiness, winter survival


HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 448E-449
Author(s):  
Chon C. Lim ◽  
Rajeev Arora ◽  
Stephen L. Krebs

Few genetic studies have been conducted on the inheritance of cold hardiness (CH) in woody plants. An understanding of the genetic control of CH can greatly assist the breeder in reducing winter injury. This study was initiated to evaluate the distribution of CH phenotypes in segregating populations of evergreen rhododendrons. Naturally acclimated leaves from individual plants (parents, F1 and 47 F2 progeny) were subjected to controlled freeze–thaw regimes. Using slow cooling rates, leaf discs were cooled over a range of treatment temperatures from –10°C to –52°C. Freezing injury of leaf tissue was assessed by measuring ion-leakage and non-linear regression analysis (data fitted to Gompertz functions) was used to estimate Tmax, the temperature causing the maximum rate of injury. Tmax for the parent plants (R. catawbiense & R. fortunei) and the F1 cultivar Ceylon, were estimated to be –51.6°C, –30.1°C, and –40.4°C, respectively. CH estimates among F2 progeny (Ceylon, selfed) were normally distributed from –14.8°C to –41.5°C, with mean of –27.6°C. Most F2 progeny were less cold-hardy than the tender parent, R. fortunei. The apparent reduction in F2 CH may be caused by the differences in age between the parents (20-year-old mature plants) and F2 progenies (3-year-old juvenile seedlings). Currently, we are testing age-dependent CH responses in rhododendrons, and are also characterizing CH distributions in a backcross population.


HortScience ◽  
1992 ◽  
Vol 27 (12) ◽  
pp. 1262f-1262
Author(s):  
Danny L. Barney

During freezing studies of `Concord' grape (Vitis labrusca L.), bud viability significantly affected callus formation, adventitious root initiation, and root dry weight during regrowth assays conducted to assess freezing injury. Applying exogenous 1- H -indole-3-acetic acid (IAA) partially offset bud loss and stimulated root initiation. Further tests demonstrated that buds were less cold hardy than internode woody tissues in dormant `Concord' canes. Because of cold-hardiness differences between buds and wood and because bud viability affects callus formation, root initiation, and root dry weight, regrowth assays do not seem to be sensitive indicators of freezing injury in grape woody tissues. Regrowth assays, however, seem to be reliable indicators of overall viability for frozen `Concord' grape cuttings.


2015 ◽  
Author(s):  
Stefanos S Andreadis ◽  
Yianna Poulia ◽  
Sofia Noukari ◽  
Barbara Aslanidou ◽  
Matilda Savopoulou-Soultani

The potato tuberworm, Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae), is a worldwide pest of solanaceous crops especially devastating to potatoes. In the present study we investigated the cold hardiness profile of short-term acclimated and non-acclimated immature and adult stages of a field population of P. operculella. Late instars displayed the lowest mean supercooling point, for both short-term acclimated and non-acclimated individuals, however, no significant differences were observed among developmental stages. Unlike supercooling capacity, acclimation at 5 oC for 5 days enhanced the ability to survive at subzero temperatures after a 2 h exposure. Mean lethal temperature (LTemp50) of all developmental stages (egg, late instar, pupa and adult) decreased after short-term acclimation, however only adults displayed a significant difference among acclimated and non-acclimated individuals concerning their LTemp50 (-11.1 and -8.3 oC, respectively). Generally, pupae were the most cold tolerant developmental stage followed in decreasing order by the eggs and adults, while interestingly late instars were the least ones. Non-freezing injury above the supercooling point was well documented for all developmental stages indicating a pre-freeze mortality and suggesting that P. operculella is considered to be chill tolerant rather than freeze intolerant. Nevertheless, given its high degree of cold hardiness, winter mortality of P. operculella due to low temperatures is not likely to occur and potential pest outbreak can take place following a mild winter.


1990 ◽  
Vol 70 (4) ◽  
pp. 1033-1041 ◽  
Author(s):  
J. B. THOMAS ◽  
R. A. BUTTS

Russian wheat aphid (RWA) (Diruaphis noxia (Mordvilko)) is a new and cold-hardy pest of temperate cereals in western Canada. In view of the risk of fall infestation of winter wheat (Triticum aestivum L. em. Thell.), this study was made to establish whether feeding by RWA can interfere with cold hardening and plant survival of overwintering winter wheat. Feeding by RWA significantly increased the LT50 of field-hardened Norstar winter wheat by + 2 to + 4 °C. Application of 400 g (a.i.) ha−1 of the insecticide chlorpyrifos in mid-October to control severe RWA infestations in two different fields of Norstar winter wheat significantly improved winter survival of the crop. The pattern of winterkill within the two fields suggested that this protective effect of chlorpyrifos was greatest in areas where microtopography resulted in the least accumulations of snow and cold stress was most intense. It was concluded that heavy RWA infestation in the fall significantly reduced freezing tolerance of winter wheat and increased the likelihood of winterkilling of the crop by severe cold.Key words: Winter survival, cold hardening, Diuraphis noxia, insecticide, chlorpyrifos, Triticum aestivum, crop damage


Author(s):  
Neil O. M. Ravenscroft

AbstractThe marsh fritillary Euphydryas aurinia is declining across Europe and is of high conservation interest. Its ecology has been defined and its conservation status assessed primarily from the affinities and populations of young caterpillars in the autumn, before hibernation and high winter mortality. The possibility that caterpillars of E. aurinia can overwinter more than once was investigated on the Isle of Islay, Scotland after caterpillars were found to occur at some locations in the spring despite a pre-hibernation absence. Closely-related species in North America and Northern Europe can prolong larval development by diapausing for a year as does E. aurinia in Scandinavia. Measurements of development and manipulations of distribution confirmed that some caterpillars do extend the life-cycle in Scotland and may occur in areas devoid of larvae in their first year. Caterpillars attempting this life-cycle develop slowly in spring, attain the normal penultimate spring instar and then enter diapause while other caterpillars are pupating. They moult just before diapause, construct highly cryptic webs and on emergence the following spring are 5–6 times heavier than larvae emerging in their first spring, or the equivalent of a month or so ahead. They attain a final, extra instar as larvae in their first spring reach the penultimate instar. Knowledge of this life-cycle is confined in the UK to Islay but its occurrence in this mild climate implies that it is more widespread.Implications for insect conservation Conditions that permit long diapause are probably precise and may not be reflected in recognised qualities of habitat. The species may also be present despite a perceived absence in autumn, the standard period for monitoring. Assessments of the prevalence of the life-cycle and its contribution to the persistence of E. aurinia are required. Populations of E. aurinia are known to fluctuate greatly and do occur below the observation threshold for long periods.


1979 ◽  
Vol 57 (9) ◽  
pp. 997-999 ◽  
Author(s):  
R. J. Reader

In laboratory freezing trials, cold hardiness of six types of bog ericad flowers differed significantly (i.e., Chamaedaphne calyculata > Andromeda glaucophylla > Kalmia polifolia > Vaccinium myrtilloides > Ledum groenlandicum > Vaccinium macrocarpon) at air temperatures between −4 and −10 °C but not at temperatures above −2 °C. At the Luther Marsh bog in southern Ontario, low temperatures (−3 to −7 °C) would select against May flowering by the least cold hardy ericads. Availability of pollinators, on the other hand, would encourage May flowering by the most cold hardy species. Presumably, competition for insect pollinators has promoted the diversification of bog ericad flowering peaks, while air temperature, in conjunction with flower cold hardiness, determined the order in which flowering peaks were reached.


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