scholarly journals Parameterization of temperature sensitivity of spring phenology and its application in explaining diverse phenological responses to temperature change

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Huanjiong Wang ◽  
Quansheng Ge ◽  
This Rutishauser ◽  
Yuxiao Dai ◽  
Junhu Dai
Author(s):  
Sung-Chang Lee ◽  
George W. Tyndall ◽  
Mike Suk

Flying clearance distribution with thermo-mechanical actuation is characterized. Especially, what factors contributing to variation of flying clearance are identified based on thermo-mechanical actuation profiles taken from burn-in process of hard disk drives and Gage R&R test of touch down repeatability. In addition, the effect of static temperature compensation scheme on flying clearance distribution is investigated and disadvantages of static adaptation to temperature change are identified. In order to avoid catastrophic early HDI failures due to poor static temperature compensation, we need to dynamically adjust flying clearance whenever environmental change is detected. Otherwise we need to utilize individual temperature sensitivity values of each flying head to adjust thermo-mechanical actuation amount accordingly with temperature change.


2011 ◽  
Vol 63-64 ◽  
pp. 732-735
Author(s):  
Gui Hua Zhang

According to the Bragging equation, the general mathematical formulas of the temperature change error and the strain error are got under the consideration of the second-order temperature sensitivity and the second-order strain sensitivity. The two error curves are given in the conditions of T = 20°C and e = 1000me.


2020 ◽  
Author(s):  
Haoming Yu ◽  
Yunting Fang ◽  
Ronghua Kang

<p>N<sub>2</sub>O and N<sub>2</sub> Emissions from soil in terrestrial ecosystems is a crucial component of the global nitrogen (N) cycle. The response of these two gases emissions from forest soil to temperature change and its underlying mechanisms are essential for predicting N cycle to global warming. Despite the warming-induced effects on soil N cycle is considered to be positive in general, our understanding of temperature sensitivity (Q<sub>10</sub>) of N<sub>2</sub>O and N<sub>2</sub> emissions is rather limited. We quantified the Q<sub>10</sub> of N<sub>2</sub>O and N<sub>2</sub> emissions in forest soils and explored their major driving factors by conducting an incubation experiment using <sup>15</sup>N tracer (Na<sup>15</sup>NO<sub>3</sub>) with soil samples from nineteen forest sites from temperate to tropical zones. The environmental conditions largely varied: mean annual temperature (MAT) ranging from -5.4 to 21.5<sup>o</sup>C and mean annual precipitation (MAP) ranging from 300 to 2449 mm. The soil pH varied between 3.62 to 6.38. We incubated soil samples under an anaerobic condition with temperature from 5 to 35<sup>o</sup>C with an interval of 5<sup>o</sup>C for 12 or 24 hours, respectively. Soil temperature strongly affected the production of N<sub>2</sub>O and N<sub>2</sub>. N<sub>2</sub>O and N<sub>2</sub> production rates showed a positive exponential relation with incubate time and temperature for all forest soils. Our results showed that the Q<sub>10</sub> values ranged from 1.31 to 2.98 for N<sub>2</sub>O emission and 1.69 to 3.83 for N<sub>2</sub> emission, indicating a generally positive feedback of N<sub>2</sub>O and N<sub>2</sub> production to warming. Higher Q<sub>10</sub> values for N<sub>2</sub> than N<sub>2</sub>O implies that N<sub>2</sub> emission is more sensitive to temperature increase. The N<sub>2</sub>O/(N<sub>2</sub>O+N<sub>2</sub>) decreased with increasing temperature in fifteen of nineteen forest soils, suggesting that warming accelerates N<sub>2</sub> emission. Strong spatial variation in Q<sub>10</sub> were also observed, with tropical forest soils exhibiting high Q<sub>10</sub> values and relatively low Q<sub>10</sub> in temperate forest soils. This variation is attributed to the inherent differences in N biogeochemical cycling behavior between the microbial communities among sites. Despite soil temperature primarily controls the N<sub>2</sub>O and N<sub>2</sub> emissions, we  explored the effects of other factors such as pH, C/N, DOC and related functional genes. In addition, we partitioned N<sub>2</sub>O and N<sub>2</sub> emissions to different microbial processes (e.g., denitrification, co-denitrification and anammox). The results indicated that denitrification was the main pathway of N<sub>2</sub>O and N<sub>2</sub> production under anaerobic environment and the contribution increased as temperature rise.</p><p>Key words: Temperature sensitivity, N<sub>2</sub>O, N<sub>2</sub>, Forest soil, Nitrogen cycle, Global warming, Denitrification</p>


2017 ◽  
Vol 23 (12) ◽  
pp. 5189-5202 ◽  
Author(s):  
Sabine Güsewell ◽  
Reinhard Furrer ◽  
Regula Gehrig ◽  
Barbara Pietragalla

PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e88178 ◽  
Author(s):  
Miaogen Shen ◽  
Yanhong Tang ◽  
Jin Chen ◽  
Xi Yang ◽  
Cong Wang ◽  
...  

2017 ◽  
Vol 30 (8) ◽  
pp. 2921-2935 ◽  
Author(s):  
Dana Ehlert ◽  
Kirsten Zickfeld ◽  
Michael Eby ◽  
Nathan Gillett

The ratio of global mean surface air temperature change to cumulative CO2 emissions, referred to as transient climate response to cumulative CO2 emissions (TCRE), has been shown to be approximately constant on centennial time scales. The mechanisms behind this constancy are not well understood, but previous studies suggest that compensating effects of ocean heat and carbon fluxes, which are governed by the same ocean mixing processes, could be one cause for this approximate constancy. This hypothesis is investigated by forcing different versions of the University of Victoria Earth System Climate Model, which differ in the ocean mixing parameterization, with an idealized scenario of 1% annually increasing atmospheric CO2 until quadrupling of the preindustrial CO2 concentration and constant concentration thereafter. The relationship between surface air warming and cumulative emissions remains close to linear, but the TCRE varies between model versions, spanning the range of 1.2°–2.1°C EgC−1 at the time of CO2 doubling. For all model versions, the TCRE is not constant over time while atmospheric CO2 concentrations increase. It is constant after atmospheric CO2 stabilizes at 1120 ppm, because of compensating changes in temperature sensitivity (temperature change per unit radiative forcing) and cumulative airborne fraction. The TCRE remains approximately constant over time even if temperature sensitivity, determined by ocean heat flux, and cumulative airborne fraction, determined by ocean carbon flux, are taken from different model versions with different ocean mixing settings. This can partially be explained with temperature sensitivity and cumulative airborne fraction following similar trajectories, which suggests ocean heat and carbon fluxes scale approximately linearly with changes in vertical mixing.


Author(s):  
Helfried Scheifinger

Phenology is the study of the seasonal timing of life cycle events. The Belgian botanist Charles Morren introduced the term in 1853, which is a combination of two Greek words, φαίνω, which means to show, to bring to light, make to appear, and λόγος, which means study, discourse, or reasoning. The global change discussion has stimulated phenological research, which as a consequence greatly advanced as science and evolved to one of the main climate impact indicators. Many of the earliest systematic efforts to collect phenological observations took place in countries sharing the Alps, most of which are still operating phenological networks. These phenological data sets are generally freely available to researchers, and numerous essential contributions to the topic of phenology and climate have been built on those data sets. Plant physiological processes underlying the ability of the plants to adapt to the year-to-year variability of the climate still constitutes largely a black box. Since the experiments of René Antoine Ferchault de Reaumur in the 18th century, it is known that temperature constitutes the main environmental driver of the seasonal development of the mid- to high-latitude plants. Second to temperature, day length governs the seasonal cycle of some species as an additional factor. Therefore, temperature-driven phenological models are able to simulate the year-to-year variability of phenological entry dates accurately enough for various applications, such as climate change impact research or numerical pollen forecast models, where the beginning of flowering of some plants is linked with the release of allergic pollen into the atmosphere. Large-scale circulation patterns, like the North Atlantic Oscillation, determine the frequency and intensity of warm and cold spells and decadal temperature trends over Europe. Combined anthropogenic and natural forcings explain the advance of spring phenology over the last 50 years, which is also clearly discernible in the area of the Alps. The early phenological spring starts in Western Europe, whereas later in the season it makes progress with a stronger southerly component across the Alps. The combined temporal and spatial trends have been studied along elevational gradients. Trends toward earlier entry dates are stronger at higher elevations, which indicates that the elevational phenological gradient has weakened since the mid-20th century. Similarly, the vegetation response to temperature is observed to decrease when moving from high to low latitudes. In contrast, the temporal response of plant phenology to increasing temperatures is less clear. Some works indeed demonstrate a decreasing temperature sensitivity with increasing temperature, which is explained as a result of a reduced winter chilling that delays spring phenology or of a limiting effect due to a shorter photoperiod. Other works report no change of temporal temperature sensitivity with increasing temperatures. Indigenous midlatitude vegetation is able to withstand large temperature variations during winter and spring. The safety margin between last frost events, budding, and leaf emergence was found to be uniform across elevations and taxa, except for beech trees. The probability of freezing damage to natural vegetation is almost nil, but late frost risk constitutes a real threat to fruit growers. The ratio of phenological and last frost trends is ambiguous. An increase or decrease in frost risk depends on regions, elevations, and species. Vegetation at high altitudes is exposed to a harsh climate with a long-lasting snow cover, low temperatures, and a short growing season. Snowmelt is a necessary but insufficient requirement for the start of the growing season, which has to be supplemented by plant-specific temperature sums to activate the growth of most alpine and subalpine species. The seasonal cycle has to be completed within a short time. Advances in remote sensing technology have provided access to high-resolution landscape scale phenological information. Especially in remote areas, like the Alps, in situ observations could be supplemented by satellite observations. Observations from both methods, I -situ and remote sensing, have been applied to describe spring vegetation dynamics, but the correlation between these data sets have typically been weak because of differences in temporal and spatial scales and resolutions. A successfully combined description of the seasonal vegetation cycle is still lacking. The area of the European Alps offers a wealth of long chronicles, containing historical phenological observations some of which have been extracted and digitized. Grape harvest dates belong to the most readily available historical phenological observations, which have helped reconstruct summer temperatures as far back as the 15th century.


2014 ◽  
Vol 20 (5) ◽  
pp. 1473-1480 ◽  
Author(s):  
Tao Wang ◽  
Catherine Ottlé ◽  
Shushi Peng ◽  
Ivan A. Janssens ◽  
Xin Lin ◽  
...  

2018 ◽  
Author(s):  
Xiyan Xu ◽  
William J. Riley ◽  
Charles D. Koven ◽  
Gensuo Jia

Abstract. The timing of spring greenup (SG) as inferred by remotely sensed vegetation indices have showed contrasting dynamics across the same region and periods. Assessing the uncertainty in SG associated with different Normalized Difference Vegetation Index (NDVI) products is essential for robustly interpreting the links between climate and phenological dynamics. We compare SG inferred from two NDVI products over the period 2001–2013: (1) Terra Moderate Resolution Imaging Spectroradiometer (MODIS) and (2) National Oceanic and Atmospheric Administration's (NOAA's) Advanced Very High Resolution Radiometer (AVHRR) instruments processed by the Global Inventory Monitoring and Modeling Studies (GIMMS) to explore confidence and uncertainty in the NDVI-inferred SG trend and its links to climate variability. Both MODIS and GIMMS agreed in showing an advancement of SG in northern Canada, the eastern United States, and Russia, as well as a delay in SG in western North America, parts of Baltic Europe and East Asia. In the regions with advanced SG, GIMMS inferred much weaker advancement whereas in the regions with delayed SG, GIMMS inferred much stronger delay than MODIS. This resulted in a GIMMS SG delay in both North America and Eurasia. MODIS data show no significant SG shift in North American for spatial heterogeneity in SG shift, but dominant SG advancement in Eurasia. The SG advancement inferred from MODIS is associated with a stronger coupling between SG and temperature and a stronger sensitivity across biomes as compared to GIMMS. The main uncertainty in the SG trend and SG-temperature sensitivity are in northern high latitudes (>50° N) where GIMMS and MODIS show different magnitude and sign of the annual SG anomalies. Compared to 1988–2000, inter-biome GIMMS SG-temperature sensitivity is stable and the SG-temperature sensitivity increased in the boreal and Arctic biomes despite a slight reduction in the SG-temperature coupling over the period 2001–2013. The explanation for the increased SG-temperature sensitivity remains unclear and requires further investigation. We suggest broader evaluation of the NDVI products against field measurements and inter-validation for robust assessment of vegetation dynamics.


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