Answer: Large molecules and wastes move through the membrane through forms of active transport- endocytosis and exocytosis.
Explanation:
Molecules are moved across the cell membrane via different mechanisms like diffusion, facilitated diffusion and passive transport; however, some very large molecules require specialized types of active transport to cross over- these are endocytosis and exocytosis.
During endocytosis large molecules cells and cell fragments moved across the plasma membrane through a process of <em>invagination;</em> piece of the external cell membrane falls into itself and forms a small pocket that surrounds the target molecule this breaks off from the membrane to form an intracellular vesicle. Different methods of endocytosis such as <em>phagocytosis, pinocytosis </em>and receptor-mediated <em>endocytosis</em>, take in cells, water and targeted substances respectively.
Like endocytosis, the particles (signal proteins, neurotransmitters and waste material) are surrounded by a phospholipid membrane. However, in exocytosis, this membrane is formed in the cytoplasm, and merges with the plasma membrane’s interior in a process <em>opposite to </em>endocytosis; material is removed from the cell and exported into the cell’s exterior called the extracellular space.
Homologous chromosome pairs are separated
Meiosis 1 refers to the initial stage of meiosis where one parent cell divides into two daughter cells. This stage is where homologous pairs of chromosomes will segregate and separate from each other and move into the two daughter cells which result in the division of the total chromosomal number by half.
<h3>What happens during Meiosis 1 ?</h3>
Meiosis I ends when the chromosomes of each homologous pair arrive at opposing poles of the cell.
- The microtubules disintegrate, and a new nuclear membrane forms around each haploid set of chromosomes.
- The chromosomes uncoil, forming chromatin again, and cytokinesis occurs, forming two non-identical daughter cells.
Learn more about Meiosis here:
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Growth and repair
creation of gametes (sex cells)
method of reproduction in unicellular organisms
Binary Fission - type of reproduction that occurs in bacterial cells, single celled organism splits and becomes two identical organisms
Chromosomes and DNA
Chromosomes are DNA wrapped around proteins to form an X-shaped structure.
The diagram will help you see the relationship.
1. Chromosomes are found in the nucleus
2. Chromosomes are made of DNA
3. Sections of chromosomes are called genes
DNA - deoxyribonucleic acid (it is the genetic code that contains all the information needed to build and maintain an organism)
Chromosome Structure
Chromosome Numbers
Each organism has a distinct number of chromosomes, in humans, every cell contains 46 chromosomes. Other organisms have different numbers, for instance, a dog has 78 chromosomes per cell.
Somatic Cells - body cells, such as muscle, skin, blood ...etc. These cells contain a complete set of chromosomes (46 in humans) and are called DIPLOID.
Sex Cells - also known as gametes. These cells contain half the number of chromosomes as body cells and are called HAPLOID
Chromosomes come in pairs, called Homologous Pairs (or homologs). Imagine homologs as a matching set, but they are not exacly alike, like a pair of shoes.
Diploid cells have 23 homologous pairs = total of 46
Haploid cells have 23 chromosomes (that are not paired) = total of 23
Homologous Chromosomes
Sex Determination
Chromosomes determine the sex of an offspring. In humans, a pair of chromosomes called SEX CHROMOSOMES determine the sex.
If you have XX sex chromosomes - you are female
If you have XY sex chromosomes - you are male
During fertilization, sperm cells will either contain an X or a Y chromosome (in addition to 22 other chromosomes - total of 23). If a sperm containing an X chromosome fertilizes an egg, the offspring will be female. If a sperm cell containing a Y chromosome fertilizes an egg, the offspring will be male.
Creation of a Zygote
When two sex cells, or gametes come together, the resulting fertilized egg is called a ZYGOTE
Zygotes are diploid and have the total 46 chromosomes (in humans)
Karyotype
A karyotype is a picture of a person's (or fetus) chromosomes. A karyotype is often done to determine if the offspring has the correct number of chromosomes. An incorrect number of chromosomes indicates that the child will have a condition, like Down Syndrome
Compare the Karyotypes below
Notice that a person with Down Syndrome has an extra chromosome #21. Instead of a pair, this person has 3 chromosomes - a condition called TRISOMY (tri = three)
Trisomy results when chromosomes fail to separate - NONDISJUNCTION - when sex cells are created. The resulting egg or sperm has 24 instead of the normal 23.
Other conditions result from having the wrong number of chromosomes:
Klinefelters Syndrome - XXY (sex chromosomes)
Edward Syndrome - Trisomy of chromosome #13
Littering, hunting specific endangered species, honestly there are tons of things so the easiest one would be littering because if animals eat certain things it can kill them.
