Temperature-dependent sugar accumulation in interspecific Capsicum F1 plants showing hybrid weakness

2021 ◽  
Author(s):  
Kumpei Shiragaki ◽  
Hajime Furukawa ◽  
Shuji Yokoi ◽  
Takahiro Tezuka
Keyword(s):  
Sugar Accumulation ◽  
Temperature Dependent ◽  
Hybrid Weakness

Establishing the temperature dependency of vegetative and reproductive growth processes and their threshold temperatures of vineyard-grown Vitis vinifera cv. Semillon vines across the growing season

2016 ◽  
Vol 43 (10) ◽  
pp. 986 ◽  
Author(s):  
Dennis H. Greer ◽  
Mark M. Weedon
Keyword(s):  
Vitis Vinifera ◽  
Biomass Accumulation ◽  
Growing Season ◽  
Leaf Expansion ◽  
Sugar Accumulation ◽  
Temperature Dependent ◽  
Growth Processes ◽  
Reproductive Growth ◽  
Vegetative And Reproductive Growth ◽  
Dependent Processes

A hydrocooling system provided canopy temperature control of Vitis vinifera L. cv. Semillon vines at set points of 30, 35 and 40°C. The impacts on vegetative and reproductive growth over the growing season were assessed. Dynamics and rates of leaf expansion, bunch biomass and sugar accumulation were strongly affected by canopy temperatures – being highest at 30°C and lowest at 40°C. Leaf and stem biomass accumulation at 40°C was detrimentally affected but was otherwise little affected by temperature. Leaf expansion was earliest, leaf sizes greatest and rates of expansion all optimal at 30°C and all were strongly temperature dependent. Bunch biomass accumulation was earliest at 35°C but amount of biomass in bunches and rates were both highly temperature dependent and optimal at 30°C. Rates of sugar accumulation and total amounts accumulated at harvest were both highly temperature-dependent processes: fastest and greatest at 30°C. Many of the temperature-dependent processes decreased in rates and amounts linearly between 30 and 40°C. Despite the effects of temperature on bunch and berry growth, there were no treatment effects on the yield per vine. The study confirms that the threshold temperature for most processes was 35°C, where some depreciation in dry matter and sugar accumulation occurred, whereas 40°C was detrimental to all growth processes.

scholarly journals Genetic and Cytological Analysis of a Novel Type of Low Temperature-Dependent Intrasubspecific Hybrid Weakness in Rice

PLoS ONE ◽  
2013 ◽  
Vol 8 (8) ◽  
pp. e73886 ◽  
Author(s):  
Chong-Yun Fu ◽  
Feng Wang ◽  
Bing-Rui Sun ◽  
Wu-Ge Liu ◽  
Jin-Hua Li ◽  
...  
Keyword(s):  
Low Temperature ◽  
Cytological Analysis ◽  
Temperature Dependent ◽  
Hybrid Weakness

(111) Monocrystalline Nickel Films

1972 ◽  
Vol 30 ◽  
pp. 512-513
Author(s):  
T.E. Pratt ◽  
R.W. Vook
Keyword(s):  
Film Thickness ◽  
Deposition Rate ◽  
Room Temperature ◽  
Narrow Range ◽  
High Vacuum ◽  
Residual Pressure ◽  
Temperature Dependent ◽  
Deposition Parameters ◽  
Transmission Electron ◽  
Substrate Temperatures

(111) oriented thin monocrystalline Ni films have been prepared by vacuum evaporation and examined by transmission electron microscopy and electron diffraction. In high vacuum, at room temperature, a layer of NaCl was first evaporated onto a freshly air-cleaved muscovite substrate clamped to a copper block with attached heater and thermocouple. Then, at various substrate temperatures, with other parameters held within a narrow range, Ni was evaporated from a tungsten filament. It had been shown previously that similar procedures would yield monocrystalline films of CU, Ag, and Au.For the films examined with respect to temperature dependent effects, typical deposition parameters were: Ni film thickness, 500-800 A; Ni deposition rate, 10 A/sec.; residual pressure, 10-6 torr; NaCl film thickness, 250 A; and NaCl deposition rate, 10 A/sec. Some additional evaporations involved higher deposition rates and lower film thicknesses.Monocrystalline films were obtained with substrate temperatures above 500° C. Below 450° C, the films were polycrystalline with a strong (111) preferred orientation.

In Vitro Effects of Urokinase — Prevention by Different Inhibitors

1990 ◽  
Vol 64 (03) ◽  
pp. 402-406 ◽  
Author(s):  
M D Oethinger ◽  
E Seifried
Keyword(s):  
In Vitro Study ◽  
Thrombin Time ◽  
Plasma Samples ◽  
Temperature Dependent ◽  
Chloromethyl Ketone ◽  
Control Value ◽  
Dose Time ◽  
In Vitro Effects ◽  
Full Protection

SummaryThe present in vitro study investigated dose-, time- and temperature-dependent effects of two-chain urokinase plasminogen activato(u-PA, urokinase) on normal citrated plasma. When 10 μg/ml u-PA wereadded to pooled normal plasma and incubated for 30 min at an ambient temperature (25° C), α2-antiplas-min decreased to 8% of the control value. Incubation on ice yielded a decrease to 45% of control,whereas α2-antiplasmin was fully consumed at 37° C. Fibrinogen and plasminogen fell to 46% and 39%, respectively, after a 30 min incubation at 25° C. Thrombin time prolonged to 190% of control.Various inhibitors were studied with respect to their suitability and efficacy to prevent these in vitro effects. Aprotinin exhibited a good protective effect on fibrinogen at concentrations exceeding 500 KlU/ml plasma. Its use, however, was limited due to interferences with some haemostatic assays. We could demonstrate that L-Glutamyl-L-Glycyl-L-Arginyl chloromethyl ketone (GGACK) and a specific polyclonal anti-u-PA-antibody (anti-u-PA-IgG) effectively inhibited urokinase-induced plasmin generation without interfering with haemostatic assays. The anti-u-PA-antibody afforded full protection ofα2-antiplasmin at therapeutic levels of u-PA.It is concluded that u-PA in plasma samples from patients during thrombolytic therapy may induce in vitro effects which should be prevented by the use of a suitable inhibitor such as GGACK or specific anti-u-PA-antibody.

Interventional Thermal Injury of the Arterial Wall: Unfolding of von Willebrand Factor and Its Increased Binding to Collagen after 55° C Heating

1996 ◽  
Vol 75 (03) ◽  
pp. 515-519 ◽  
Author(s):  
Mark J Post ◽  
Anke N de Graaf-Bos ◽  
George Posthuma ◽  
Philip G de Groot ◽  
Jan J Sixma ◽  
...  
Keyword(s):  
Von Willebrand Factor ◽  
Conformational Changes ◽  
Arterial Wall ◽  
Platelet Adhesion ◽  
Type I ◽  
Temperature Dependent ◽  
Collagen Types ◽  
Electron Microscopic ◽  
Von Willebrand ◽  
Willebrand Factor

Summary Purpose. Thermal angioplasty alters the thrombogenicity of the arterial wall. In previous studies, platelet adhesion was found to increase after heating human subendothelium to 55° C and decrease after heating to 90° C. In the present electron microscopic study, the mechanism of this temperature-dependent platelet adhesion to the heated arterial wall is elucidated by investigating temperature-dependent conformational changes of von Willebrand factor (vWF) and collagen types I and III and the binding of vWF to heated collagen. Methods. Purified vWF and/or collagen was applied to electron microscopic grids and heated by floating on a salt-solution of 37° C, 55° C or 90° C for 15 s. After incubation with a polyclonal antibody against vWF and incubation with protein A/gold, the grids were examined by electron microscopy. Results. At 37° C, vWF was coiled. At 55° C, vWF unfolded, whereas heating at 90° C caused a reduction in antigenicity. Collagen fibers heated to 37° C were 60.3 ± 3.1 nm wide. Heating to 55° C resulted in the unwinding of the fibers, increasing the width to 87.5 ± 8.2 nm (p < 0.01). Heating to 90° C resulted in denatured fibers with an enlarged width of 85.1 ± 6.1 nm (p < 0.05). Heating of collagen to 55° C resulted in an increased vWF binding as compared to collagen heated to 37° C or to 90° C. Incubation of collagen with vWF, prior to heating, resulted in a vWF binding after heating to 55° C that was similar to the 37° C binding and a decreased binding after 90° C. Conclusions. After 55° C heating, the von Willebrand factor molecule unfolds and collagen types I and III exhibit an increased adhesiveness for von Willebrand factor. Heating to 90° C denatures von Willebrand factor and collagen. The conformation changes of von Willebrand factor and its altered binding to collagen type I and III may explain the increased and decreased platelet adhesion to subendothelium after 55° C and 90° C heating, respectively.

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