Plants absorb nutrients and water through their roots, but photosynthesis - the process by which plants create their fuel - occurs in the leaves. Therefore, plants need to get fluids and nutrients from the ground up through their stems to their parts that are above ground level.
Just as animals, plants also contain vascular tissues (xylem), which transports water and minerals up from the roots to the leaves, and phloem, which transports sugar molecules, amino acids, and hormones both up and down through the plant.
The leaves of plants also contain veins, through which nutrients and hormones travel to reach the cells throughout the leaf. Veins are easy to see some leaves (a maple tree, for instance). In some plants the veins are hard to see, but they're in there.
Sap is the mix of water and minerals that move through the xylem. Carbohydrates move through the phloem. There are several different "modes of transportation" through the xylem and phloem; their main function is to keep all cells of the plant hydrated and nourished.
Inside the cells of the root, there is a higher concentration of minerals than there is in the soil surrounding the plant. This creates root pressure, which forces water up out of the root through the xylem as more water and minerals are "pulled" into the root from the soil. This force results inguttation, which is the formation of tiny droplets on the ends of leaves or grass early in the morning.
The reason the droplets are seen in the morning is because transpiration - the loss of water from leaves - doesn't occur at night, so the pressure builds until morning. Those droplets are not just water, they're sap. And, those sap droplets are proof that water and minerals get pulled up from the soil and transported through the entire plant.
Guttation may work well for small plants, but gravity works against the upward movement through larger plants, so more active processes are involved.
Does the Y chromosome in Klinefelters syndrome look like the X chromosome?
No. People with Klinefelter's syndrome have a normal Y chromosome and 2 normal X chromosomes.
A carrier. This is usually a disease that requires two parts of a gene. The faulty gene is the recessive gene, and the healthy gene is the dominant gene. If two people with one dominant and one recessive gene each have a child they have a 25% chance of producing a child with two dominant genes, thereby resulting in that child having the disease.
Why would you use the amnicentesis test?
Amniocentesis is used for diagnosing foetal infections, Rh incompatibility, and chromosomal abnormalties and neural tube defects of the foetus
No, it does not have Klinefelter's syndrome. it is just a mix-breed cat, otherwise known as a mutt for cats. It is a tabby/calico mix-breed. It is not rare and it is not a disease. it is just an unusual color pattern found on a tabby/calico mix. So don't be worried your cat is perfectly fine. I hope this helped.
Because in males they have only 1 X chromosome. The other one is Y.
But in females they have 2 XX chromosomes so the chance that X chromosome will carry disease to cause illness is lower.
Example: lets say xx (recesssive) phenotype makes illness, whereas XX (dominant) is healthy.
A woman can have XX, Xx, xx right? Since Xx is a carrier and XX is healthy you wont see the illness. only xx can make illness. 1/3 chances she is sick.
However in males they have XY. so he can only have either XY or xY. No carrier form is present. The chances he will be sick is %50.
got it?
Im a genetic engineer and molecular biolog so count on me :)
What mutation causes bipolar disorder?
Bipolar means you have mixed emotions. For example, you can be super happy at one moment and then later you can feel depressed. Being bipolar isn't bad but, its better not to be.An international team of scientists, led by researchers at the University of California, San Diego School of Medicine, reports that abnormal sequences of DNA known as rare copy number variants, or CNVs, appear to play a significant role in the risk for early onset bipolar disorder.
The findings will be published in the December 22 issue of the journal Neuron.
CNVs are genomic alterations in which there are too few or too many copies of sections of DNA. Researchers have known that spontaneously occurring (de novo) CNVs - genetic mutations not inherited from parents - significantly increase the risk for some neuropsychiatric conditions, such as schizophrenia or the autism spectrum disorders. But their role was unclear in bipolar disorder, previously known as manic depression.
Principal investigator Jonathan Sebat, PhD, assistant professor of psychiatry and cellular and molecular medicine at UC San Diego's Institute of Genomic Medicine, and colleagues, found thatde novo CNVs contribute significant genetic risk in about 5 percent of early onset bipolar disorder, which appears in childhood or early adulthood.
In other words, said the study's first author Dheeraj Malhotra, assistant project scientist in Sebat's lab, "having a de novo mutation increases the chances of having an earlier onset of disease."
The cause or causes of bipolar disorder remain unclear. There is a clear genetic component - the disease runs in families - but previous studies that have focused mainly on common inherited variants have met with limited success in identifying key susceptibility genes.
How much for treatments for Marfan Syndrome cost?
The cost of treatments for Marfan Syndrome can vary depending on factors such as the specific treatments needed, healthcare providers, insurance coverage, and geographic location. Treatment may include medications, monitoring, surgeries, and ongoing specialist care. It's best to consult with a healthcare provider and insurance company for a personalized cost estimate.
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The chemical components of ammonia is one part of nitrogen and 3 parts of hydrogen. The chemical symbol is NH3.
Which genetic disease is it when someone only has a y chromosome but no x chromosome?
That isn't physically possible. All XO individuals are females with Turner's syndrome. Individuals with only a Y chromosome do not survive.
How many types of chlorophyll?
Tell me and i want to know more about in this topic can chlorophyll give us energy to build our body
Both parents are carriers of the recessive gene and if the child inherits that gene from both mother and father the child will have the disease even though the parents don't.
Does Williams syndrome occur in mild form?
William's Syndrome is commonly caused by micro deletions within the 7q11.23 chromosome, it is possible that a milder phenotype is evident through a very small deletion within a region that only spans a portion of the critical region.
What are the phentype of a person with klinefelter's syndrome?
47,XXY. This means that he has 47 chromosomes, including 2 X chromosomes and 1 Y chromosome.
What kinds of Raynaud's syndrome are there?
Raynaud's syndrome can be classified as one of two types: primary, or idiopathic (of unknown cause) disease; and secondary, which is also called Raynaud's phenomenon.
What is the most dangerous cancer in 2015?
all cancers are dangerous if not treated, however pancreatic cancer is the worst.
Cri du chat (French for "cry of the cat" or "cat's cry") syndrome is a rare genetic defect in humans. It is caused by a deletion of the short arrn of chromosome 5 (called 5p). Babies with this syndrome often have a characteristic high-pitched cry that sounds like a cat.
Jérôme Lejeune discovered the cause of cri du chat syndrome in 1964. Five years previously, he had discovered the chromosome abnormality that causes Down syndrome in humans.
It's called a "Punnet square".