There are three ways you can solve this problem:
1.- You can guide yourself through knowledge, and therefore know the answer. There isn´t much to explain here.
2.- You can eliminate obvious options such as sarcodina or apicomplexa. Euglenoid isn´t an extremely obvious removal since it has a flagela, which can be mistook by a hairy-structure. But, if you do things correctly, obtaining your answer wont be a problem.
3.- You can do an etymologic-guess, which works really well in biology. If you guide yourself this way, you´ll bump into the answer quickly --> "cilio" means hair and according to the description the specimen was covered in hairy structures.
Hope it helped,
BiologiaMagister
The average is 60-100.................
Answer:
8.800s
Explanation:
When the performer swings, she oscillates in SHM about Lo of the string with time period To = 8.90s.
First, determine the original length Lo, where for a SHM the time period is related to length and the gravitational acceleration by the equation
T = 2π×√(Lo/g)..... (1)
Let's make Lo the subject of the formulae
Lo = gTo^2/4π^2 ..... (2)
Let's put our values into equation (2) to get Lo
Lo = gTo^2/4π^2
= (9.8m/s^2)(8.90s)^2
------------------------------
4π^2
= 19.663m
Second instant, when she rise by 44.0cm, so the length Lo will be reduced by 44.0cm and the final length will be
L = Lo - (0.44m)
= 19.663m - 0.44m
= 19.223m
Now let use the value of L into equation (1) to get the period T after raising
T = 2π×√(L/g)
= 2π×√(19.223m/9.8m/s^2)
= 8.800s
Normal colour vision (trichromacy) refers to vision that uses all three types of light cones. People with defected trichromatic vision will be colour blind to some extent and these conditions are called anomalous trichromacy. Three types anomalous trichromacy ( one type of cone perceives light slightly) :
1. Protanomaly – phenotype: reduced sensitivity to red light
2. Deuteranomaly - phenotype: reduced sensitivity to green light
3. Tritanomaly – phenotype: reduced sensitivity to blue
People can also have color blindess as the result of mutation, when loss of function of one cone occurs. This condition is called dichromacy. If there is complete color blindness or monochromacy, the person can’t distinguish any color from grey.
Color blindness is an inherited genetic disorder resulted from mutations on the X chromosome.
