Answer:
how changes in biodiversity impact an ecosystem
Explanation:
Water hyacinth is a free-floating perennial aquatic plant. This plant is native to tropical and sub-tropical South America. As an invasive species, when it grows in the new environment causes severe ecological or economic harm. By growing where it not native, it can spread extremely fast, blanketing a water surface in a very short period of time. It can limit boat traffic, swimming, and fishing, and it can deprive native plants and animals of sunlight and oxygen, thus reducing the local biodiversity.
This is how an ecosystem effects biodiversity impact. When a biological species grows in the new environment, It can affect the biodiversity or environment that can affect the biological species.
Answer:
Both speed and mass causes the kinetic energy to change.
Explanation:
The energy an object because of its motion is called as Kinetic energy. A object that moves be it horizontal or vertical direction possess kinetic energy. Some forms of kinetic energy are rotational, vibrational, translational. The kinetic energy(K) of the object depends on two components i.e., the mass (m) of the object involved and its speed(v)
The relation between the mass, speed of the object can be represented as
Kinetic energy$=\frac{1}{2} m \times v^{2}$
Thus when there is a increase in the mass and speed, the kinetic energy will also increase
Answer:
Several 2',3'-dideoxy-3'-thiapyrimidine nucleosides were studied for their ability to inhibit hepatitis B virus (HBV) DNA replication in a HBV-transfected cell line (2.2.15). 2',3'-Dideoxy-3'-thiacytidine (SddC) and 5-fluoro-2',3'-dideoxy-3'-thiacytidine(5-FSddC) were found to be the most potent anti-HBV compounds of those examined. Both compounds resulted in nearly complete cessation of viral DNA replication at 0.5 microM, as monitored by the absence of both intracellular episomal and secreted viral DNAs. The HBV-specific RNAs were not reduced at concentrations that completely blocked HBV DNA replication, suggesting that the inhibitory target is HBV DNA synthesis. The antiviral action of SddC and 5-FSddC was reversible. The concentration of SddC and 5-FSddC required to inhibit 50% of 4-day cell growth in culture was 37 microM and more than 200 microM, respectively. Unlike 2',3'-dideoxycytidine, these two compounds do not affect mitochondrial DNA synthesis in cells at concentrations lower than that required to inhibit cell growth. In view of the potent and selective antiviral activity, both SddC and 5-FSddC should be further evaluated for the treatment of human HBV infection.
Explanation:
