They both have similar environments, which show they have evolved similar behaviors and appearances. hope this helps <3
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Answer:
- time: 1.122 seconds
- range: 10.693 m
- maximum height: 1.543 m
Explanation:
<u>Given</u>:
runner is launched at 30° angle to horizontal at 11 m/s
acceleration due to gravity is g = -9.8 m/s²
<u>Find</u>:
runner's hang time
runner's distance to the landing point
runner's maximum height
<u>Solution</u>:
The (horizontal, vertical) speed components will be ...
(11 m/s)(cos(30°), sin(30°)) = (5.5√3 m/s, 5.5 m/s)
The time of flight can be found from the height formula:
h(t) = 1/2gt² +vt . . . . . . where v is the vertical speed at launch
The time we're concerned with is the time when h(t)=0 and t>0.
0 = -4.9t^2 +5.5√3t = t(-4.9t +5.5√3)
The second factor is zero when ...
t = (5.5√3)/4.9 ≈ 1.122 . . . seconds hang time
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The distance to the landing point will be the product of horizontal speed and hang time:
d = (5.5 m/s)(5.5√3/4.9 s) ≈ 10.693 m . . . . distance to landing
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The maximum height can be found from the formula (based on conversion of kinetic energy to potential energy) ...
h = v²/|2g| = (5.5 m/s)²/(2(9.8 m/s²)) ≈ 1.543 m . . . . maximum height
The outer core of Mars cooled too quickly and the magnetic field didn't have time to fully form so the solar winds destroyed the magnetic field and the atmosphere
Prader-Willi syndrome (PWS) is a gentic disorder which has an impact on numerous physiological systems. PWS affected individuals (specifically babies) experience delayed growth, significant hypotonia (low muscle tone), and feeding issues. It does effect circadian rhythms in mice models.
SNORD116, often referred to as HBII-85, is a non-coding RNA (ncRNA) molecule that contributes to the alteration of other small nuclear RNAs (snRNAs). Unlike the majority of other snoRNAs, SNORD116 is not significantly complementary to ribosomal RNA and is expressed widely in the brain (but not in PWS patients).
According to the studies, SNORD116 cause sleep defect in patients with Prader-Willi syndrome. Same observation was seen in mouse models too. Paternal expression of SNORD116 is thought to be a potential gene for the sleep disruptions/circadian rhythm’s that the majority of PWS sufferers.
To learn more about circadian rhythm click here
brainly.com/question/6434404
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