We determine the mass of the metal in grams by weighing it using the balance.
Next we obtain the volume of the metal by measuring its displacement with a graduated cylinder and water in the following way:
1.measure amount of water in the graduated cylinder.
2. Place metal into the graduated cylinder
3. Measure the amount of water in the graduated cylinder
4. Subtract step 1 from step 3. The difference is the metal's volume.
Once we have found out the mass and the volume then we calculate the density using the formula:
Density = Mass/Volume.
We then check our answer from the known densities of metals in the table of densities that has been provided and determine the identity and purity of the metal by how close our answer is to the most probable value in the table.
Answer:
Both studies support the concept that species operate within a narrow optimum temperature range and are coupled to enzymatic activity.
Explanation:
The studies shown in the question above started from the same concept to establish the scientific experiment and had the same objective related to the investigation as temperature changes in the environment where these organisms live influences the enzymatic activity and, therefore, the functioning of their organism, being able to including modifying the environment around them. In summary, we can say that the studies sought to support the concept that species operate within a narrow range of optimal temperature and are coupled with enzymatic activity.
Large cactus finch, vampire finch, mangrove finch, ect. Any Darwin's finch.
Answer:
DNA ligase
Explanation:
DNA replication is a process whereby a particular DNA makes a copy of or synthesizes itself. It consists of several steps with some important enzymes for successful, error free replication. The various steps are as follows;
- Unwinding of the double helix structure of the DNA and formation of replication fork. The enzyme involved here is the DNA helicase.
- Primer, a short piece of RNA becomes synthesized and binds to the 3' end of one of the 2 strands of the DNA, the leading strand. The enzyme involved is the DNA primase.
- Replication of the <em>leading strand</em> then proceeds with the elongation of the primer through the addition of bases in the 5' to 3' direction leading to the formation of continuous strands.
- The other strand of the DNA, known as the <em>lagging strand </em>starts its own replication by binding with multiple primers at different regions of the strand. Bases are then added to each primer leading to the formation of several, short discontinuous DNA strands known as Okazaki fragments. The enzyme involved in the elongation process is the DNA polymerase.
- Next is the termination of the replication process after the formation of the continuous and discontinuous strands. Exonuclease enzyme removes primers from the synthesized strands. Primers are replaced by appropriate DNA bases and the Okazaki fragments are joined to form a unified DNA strand by an enzyme known as the DNA ligase.
The many, few nucleotides long DNA segments observed by the Biochemist are the Okazaki fragments that should have been joined together by the DNA ligase.
Hence, DNA ligase must have been the component left of the mixture.
Alleles. Alleles are the "same" genes, but provide a variation of the intended function.
