scholarly journals Late to bed, late to rise – warmer autumn temperatures delay spring phenology by delaying dormancy

2021 ◽  
Author(s):  
Ilka Beil ◽  
Jürgen Kreyling ◽  
Claudia Meyer ◽  
Nele Lemcke ◽  
Andrey V. Malyshev
Keyword(s):  
2021 ◽  
Vol 124 ◽  
pp. 107286
Author(s):  
Cheng Li ◽  
Ranghui Wang ◽  
Xuefeng Cui ◽  
Fang Wu ◽  
Yu Yan ◽  
...  

2021 ◽  
Vol 41 (6) ◽  
pp. 3725-3742
Author(s):  
Jie Peng ◽  
Chaoyang Wu ◽  
Xiaoyue Wang ◽  
Linlin Lu

2021 ◽  
Author(s):  
John P. Severson ◽  
Heather E. Johnson ◽  
Stephen M. Arthur ◽  
William B. Leacock ◽  
Michael J. Suitor

2021 ◽  
Vol 310 ◽  
pp. 108630
Author(s):  
Zhaoqi Zeng ◽  
Wenxiang Wu ◽  
Quansheng Ge ◽  
Zhaolei Li ◽  
Xiaoyue Wang ◽  
...  

1987 ◽  
Vol 65 (7) ◽  
pp. 1597-1606 ◽  
Author(s):  
A. T. Bergerud ◽  
R. E. Page

Survival of caribou (Rangifer tarandus) calves until 4 months of age was monitored for 8 years in four herds in northern British Columbia, Canada. The chief cause of mortality was predation by wolves (Canis lupus) and grizzly bears (Ursus arctos) and this mortality was correlated within years between all herds. More calves died in years with late springs when extensive snow patches remained during calving in June than in early springs when larger snow-free areas existed. Before calving and after birth, caribou cows sought to space themselves out on snow-free areas in small aggregations at high elevations above treeline. By placing themselves at high elevations, the females increased the distance between themselves and wolves and bears travelling in the valley bottoms, as well as the main alternate prey, moose (Alces alces), which calved only in forest cover at lower elevations. In addition, the reduced snow in early springs meant that there was more space for dispersion. The variation in calf survival for three herds was negatively correlated with the heterogeneity of the calving area. Snow cover disappeared in smaller patches in more rugged mountains regardless of spring phenology, thereby providing a more constant search area for predators from year to year. More uniform mountains had either extensive areas of snow cover (late years) or brown substrates (early years), thus greatly varying the space that predators had to search between years. As stochastic variation in snow cover at calving time alters the searching ability of predators, the aggregation responses of prey, and the spatial overlap between predators and prey, it promotes short-term stability of the prey and lessens the probability of extinction.


2022 ◽  
Vol 505 ◽  
pp. 119911
Author(s):  
Wujun Dai ◽  
Huiying Jin ◽  
Tong Liu ◽  
Guangze Jin ◽  
Yuhong Zhang ◽  
...  

2021 ◽  
Author(s):  
Al Kovaleski

AbstractBudbreak is one of the most observed and studied phenological phases in perennial plants. Two dimensions of exposure to temperature are generally used to model budbreak: accumulation of time spent at low temperatures (chilling); and accumulation of heat units (forcing). These two effects have a well-established negative correlation: the more chilling, the less forcing required for budbreak. Furthermore, temperate plant species are assumed to vary in amount of chilling required to complete endodormancy and begin the transition to breaking bud. Still, prediction of budbreak remains a challenge. The present work demonstrates across a wide range of species how bud cold hardiness must be accounted for to study dormancy and accurately predict time to budbreak. Cold hardiness defines the path length to budbreak, meaning the difference between the cold hardiness buds attain during the winter, and the cold hardiness at which deacclimated buds are predicted to open. This distance varies among species and throughout winter within a species. Increases in rate of cold hardiness loss (deacclimation) measured throughout winter show that chilling controls deacclimation potential – the proportion of the maximum rate response attained at high chill accumulation – which has a sigmoid relationship to chilling accumulation. For forcing, rates of deacclimation increase non-linearly in response to temperature. Comparisons of deacclimation potential show a dormancy progresses similarly for all species. This observation suggests that comparisons of physiologic and genetic control of dormancy requires an understanding of cold hardiness dynamics and the necessity for an update of the framework for studying dormancy and its effects on spring phenology.


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