Tomato cultivation slamming three attention
Grasp a good time to fight in 1 day, it is best to choose sunny high-temperature hours to fight. In the morning, the snoring caused excessive flow of blood and caused the loss of nutrients. At noon the temperature was high. After the snoring, the wounds healed quickly and there was less wound flow. If the snoring occurred after 4 o'clock in the afternoon, the wounds were easily infected by bacteria during the night.
Disinfection work before snoring to prevent cross-infection Because the hands of people, especially smokers, often have tobacco mosaic virus and other harmful bacteria, such as incomplete disinfection can easily cause a large area of ​​infection. Therefore, beforehand, hands and scissors should be thoroughly cleaned with soapy water or disinfectant. When burping, be selective. That is to say, first hit a healthy and disease-free plant, then hit the affected plant, and the remaining debris should be piled up, then clean up and buried, and avoid throwing it away.
It is appropriate to keep many farmers from eradicating all defects from the base when they fight. The disadvantage of this approach is that in the event of pathogen infection, the pathogen quickly spreads along the wound to the trunk, and the wound is large, which is unfavorable for wound healing. The correct course of action is to leave 1 to 2 centimeters high at the base of the cockroach when it is snoring, which can effectively prevent the bacteria from invading the trunk from the wound and also make the wound smaller, which will help the wound heal.
LCZ696 (Valsartan/sacubitril) is a combination drug for use in heart failure developed by Novartis. It consists of the angiotensin receptor blocker valsartan and the neprilysin inhibitor sacubitril, in a 1:1 mixture by molecule count. It may be used instead of an ACE inhibitor or an angiotensin receptor blocker in people with heart failure with reduced ejection fraction. The combination is sometimes described as an "angiotensin receptor-neprilysin inhibitor" (ARNi).
It was approved under the FDA's priority review process on July 7, 2015. It is also approved in Europe.
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