No, bigger organisms have more cells.
❤️Hello!❤️ In my opinion, i'm against GMO's. First of all you need to understand what GMO stands for, GMO means (Genetically Modified Organisms) and does that REALLY sound appealing to eat (Be honest). So now we have that covered i'm going to tell you some reasons why YOU should avoid Genetically Modified Organisms (GMO's). First of all GMO's are unhealthy, according to the American Academy of Environmental Medicine. They cite animal studies showing organ damage, gastrointestinal and immune system disorders, accelerated aging, and infertility. Second of all, GMO's contaminate forever. GMO's cross pollinate and their seeds can travel. It is impossible to fully clean up our contaminated gene pool. Self propagating GMO pollution will outlast the effects of global warming and nuclear waste. The impact is huge, threatening the health of future generations. Third of all, GMO's increase herbicide use, most GMO crops are engineered to be “Herbicide tolerant”―they deadly weed killer. Monsanto, for example, sells Roundup Ready crops, designed to survive applications of their Roundup herbicide. Between 1996 and 2008, US farmers sprayed an extra 383 million pounds of herbicide on GMO's. Overuse of Roundup results in “superweeds,” resistant to the herbicide. This is causing farmers to use even more toxic herbicides every year. ♒️ Hope this helps!♒️ ↪️ Autumn ↩️
Answer:
During transpiration, water will evaporate from tiny holes in the surfaces of leaves into the air (the tiny holes are called stomata). As the water molecules evaporate from plant leaves, they attract the water molecules still in the plant, helping to pull water up through the stems from the roots.
Hope this helps! *please mark me as brainliest :)
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
.
Answer:
A. Urethra
Explanation:
The part highlighted below is also known as the Urethra, or the tube in which the urine or semen travels in the male reproductive system! :)
