To Acclimate or Not to Acclimate? Simultaneous Positive and Negative Effects of Acclimation on Susceptibility of Tribolium confusum (Coleoptera: Tenebrionidae) and Oryzaephilus surinamensis (Coleoptera: Silvanidae) to Low Temperatures

2019 ◽  
Vol 112 (5) ◽  
pp. 2441-2449 ◽  
Author(s):  
Christos G Athanassiou ◽  
Frank H Arthur ◽  
Nickolas G Kavallieratos ◽  
Kris L Hartzer

Abstract Laboratory tests on acclimated and nonacclimated life stages of Tribolium confusum Jacquelin du Val (Coleoptera: Tenebrionidae) (adults, pupae, larvae, and eggs) and Oryzaephilus surinamensis (L.) (Coleoptera: Silvanidae) (adults, larvae, and eggs) were conducted at 0, –5, –10, and –15°C to evaluate effects of acclimation on susceptibility to cold treatment. Acclimation of all tested life stages for 7 d at 15°C affected susceptibility of both species to the cold temperatures. After 1 d exposures for ≥2 h, acclimated adults had a noticeable increase in cold tolerance compared with nonacclimated adults for both tested species. Nonacclimated pupae of T. confusum were equally susceptible to cold compared with acclimated pupae at short exposures to low temperatures. Exposure of nonacclimated life stages of T. confusum, at –10°C for 1 d gave 0% survival. Similarly, almost all (99.6%) nonacclimated individuals of O. surinamensis died at –10°C. At 0°C, nonacclimated larvae were more cold tolerant than acclimated larvae, but this trend was reversed when larvae were exposed to –5°C. Mixed results were obtained for larvae of O. surinamensis because in some of the combinations tested, nonacclimated larvae were more tolerant, even at temperatures that were lower than 0°C. In contrast to O. surinamensis, eggs of T. confusum that had not been exposed to cold were not affected by acclimation, while exposure to cold showed increased cold hardiness in acclimated eggs. Results show that individual stored-product insect species may have mixed susceptibility to cold temperatures, which must be taken into account when using cold treatment as a management strategy.

Author(s):  
Alireza Rahemi ◽  
Helen Fisher ◽  
Adam Dale ◽  
Toktam Taghavi ◽  
John M. Kelly

In recent years, new vineyards have been established in southwestern Ontario. The open water of Lake Erie provides some winter protection for Vitis hybrids and winter-hardy Vitis vinifera L. cultivars in this area. However, winter damage is possible when vines are grown distant from the open water or when lakes are frozen. To better understand the risks to winter survival, the dormancy and chilling phenology were studied over three winters from 2013-2016. Ten dormant canes of two V. vinifera cultivars, ‘Chardonnay’ and ‘Riesling’, were collected weekly from September 1 until March 30 from the mature vines in a commercial vineyard located at St. Williams (Ontario). The canes defoliated in early October, and the endodormancy was completed by the end of December. The cumulative chilling hours (0-7.2 °C) from defoliation until the completion of endodormancy were averaged 606 hours for ‘Chardonnay’ and 665 hours for ‘Riesling’. ‘Chardonnay’ buds were slightly less hardy than ‘Riesling’ to cold temperatures, with a threshold of about -24 °C for ‘Chardonnay’ and -25 °C for ‘Riesling’. Most primary buds of both cultivars died after February 16, 2015, and more than half died after February 12, 2014, due to severe low temperatures of -33.1 and -26 °C, respectively.


1981 ◽  
Vol 113 (9) ◽  
pp. 795-800 ◽  
Author(s):  
G. H. Gerber

AbstractEggs of the red turnip beetle, Entomoscelis americana Brown, were exposed to temperatures of 0°, −5°, −10°, −15°, and −20°C for 1–8 wk and for 200 days in the laboratory. At −5° and −10°C, there was no death attributable to the cold treatment. At −20°C, the cold treatment caused approximately 15% mortality in the 6- to 8-wk samples and 100% mortality in the 200-day samples. At 0° and −15°C, mortality in the 200-day samples was 39% and 23%, respectively. The data indicate that the embryos of E. americana are able to withstand cold temperatures for long periods and that the optimum temperature range for hibernation (between 0°C and −15°C) is similar to the one this beetle normally experiences in the subnivean air space once the hiemal threshold is established. For Canada, an evaluation of the snow cover and atmospheric air temperature data suggested that egg mortality due to exposure to temperatures of −20°C or lower in the subnivean air space should not occur in the various parts of the red turnip beetle’s range, except possibly the grassland region of the Prairie climatic zone.


1978 ◽  
Vol 58 (3) ◽  
pp. 915-916 ◽  
Author(s):  
L. G. PUTNAM

Microplitis plutellae, one of the principal parasites of the larvae of the diamondback moth Plutella xylostella, has a diapause in a portion of each of its several annual generations, occurring in the cocooned pupae or prepupae. In experiments, development resumed and adults emerged from most insect material in diapause after exposure to 0 °C for a period equal to the duration of a Saskatchewan winter, about 160 days. Of diapausing insects that did not respond to such a period of cold treatment, some did so after subjection to a further period of low temperatures of a similar duration. Diapausing M. plutellae were shown to tolerate sub-freezing temperatures in the laboratory and to survive Saskatchewan winter temperatures under snow cover in the field. There is no evidence that the other major parasite of diamondback larvae, Diadegma insularis, enters diapause or winters in Saskatchewan.


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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