True. The embryonic period is the second period of prenatal development and extends from the third week through the eighth week.
<h3>
What is embryonic period?</h3>
Your kid goes through a phase of rapid change after conception known as the embryonic stage. From the fifth through the tenth week of pregnancy, this phase lasts. The infant is referred to as an embryo at this point. The embryonic stage is when a lot of changes take place.
<h3>What happens during embryonic stage?</h3>
The heart starts to beat and the organs develop and start to work during the embryonic period.
<h3>Why is embryonic stage important?</h3>
The brain develops during the embryonic period, which is crucial.
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Characteristics of Living Organisms: Ability to reproduce independently, ability to grow
Characteristics of Viruses: Not made of cells, have a protein coat instead of a membrane.
Characteristics of Both: Can have a DNA genome, may mutate and evolve
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All of the above, here's an explanation. The sun helps the water cycle due to evaporation which causes it to turn into a steam/gas. Now for wind, it's because the sun heats up the air and causes thermal energy which later turns into wind. And finally, weather, obviously the sun evaporates water which causes it to be rainy/drowsy.
Answer:
Once the embryo sac has developed, pollination has occurred, and the pollen tube has grown into the ovary to make contact with the ovule, fertilization (fusion of egg and sperm) can occur.Typically, the pollen tube reaches the embryo sac via the micropyle (Greek, mikros + pyle = small opening), or opening, in the integuments of the ovule.. There, it discharges its sperm into the embry
Explanation:
The pollen tube enters into the ovule, through the micropyle. Inside the embryo sac, the tip of the pollen tube ruptures and the 2 male gametes are set free near the egg apparatus. Inside the embryo sac, one of the 2 male gametes fuses with the egg nucleus and forms a diploid zygote. This process is called syngamy or true fertilisation.
Explanation:
It is sex-linked: genetic red-green color blindness affects males much more often than females, because the genes for the red and green color receptors are located on the X chromosome, of which males have only one and females have two.