Answer: Polychlorinated biphenyls (PCBs) are a group of manmade chemicals. They are oily liquids or solids, clear to yellow in color, with no smell or taste. PCBs are very stable mixtures that are resistant to extreme temperature and pressure. PCBs were used widely in electrical equipment like capacitors and transformers. They also were used in hydraulic fluids, heat transfer fluids, lubricants, and plasticizers. The primary company that made PCBs in the United States was Monsanto Inc., mainly using the name Aroclor. Commercial production of PCBs ended in 1977 because of health effects associated with exposure. In 1979, the U.S. Environmental Protection Agency (USEPA) banned the use of PCBs; however, PCBs are still present in many pre-1979 products.
Answer: Right inferior frontal gyrus was also activated for both reading and listening comprehension. The common areas of activation are shown in white in Figure 1. Listening comprehension showed large clusters of activation in bilateral (posterior and anterior) superior temporal and middle temporal gyri.
Explanation:
Answer:
Water's extensive capability to dissolve a variety of molecules has earned it the designation of “universal solvent,” and it is this ability that makes water such an invaluable life-sustaining force. On a biological level, water's role as a solvent helps cells transport and use substances like oxygen or nutrients.
Explanation:
Global warming / climate change resulting in the melting of glaciers causing a rise in sea level.
Answer:
Because the leading strand is synthesized continuously while the lagging strand is discontinuously synthesized.
Explanation:
Two DNA strands have opposite polarity, that is, the 5' end of one strand lies opposite to the 3' end of the other strand. However, DNA replication can occur in 5' to 3' direction only since the formation of phosphodiester bonds require the presence of nucleophile 3' OH to attack the 5' phosphate of an incoming deoxyribonucleotide.
The problem is solved by the synthesis of the leading strand continuously and the synthesis of the lagging strand in a discontinuous manner. Lagging strand synthesis requires the formation of primers and their elongation to form Okazaki fragments that may have few hundreds to few thousands of nucleotides. Removal of primers from Okazaki fragments is followed by joining them together to make the long lagging strand. The discontinuous replication of the lagging strand makes the replication at the leading strand ahead of it.