Answer:
hey...im not sure about the answer but i think it is the 2nd option which is: rocks buried deeply and melted by intrusion rock erodedaway and deposited in ocea n base
hope it helps
The correct answer is - D) covered by warm shallow seas.
The fact that the crinoids are have an abundance in the fossil records in Pennsylvania in the Mississippian Period, tells us that this area was covered with shallow and warm seas. The reason why we can get that conclusion is that the crinoids live only in that kind of environment, so it simply a logical conclusion.
The geological data is also confirming this, as it is easily noticeable in the layers that during this period of the geologic past, what is now Pennsylvania, was covered with shallow sea waters. Also, this waters were warm too, as the climate was warm and humid and that period, so it was a perfect environment for the crinoids to flourish.
A. C2H6 I am positive it’s a
Nivel subatómico: lo integran las partículas más pequeñas de la materia, como son los protones, los neutrones y los electrones.
Nivel atómico: lo componen los átomos, que son la parte más pequeña de un elemento químico que puede intervenir en una reacción.
Nivel molecular: está formado por las moléculas, que se definen como unidades materiales formadas por la unión, mediante enlaces químicos, de dos o más átomos, como por ejemplo una molécula de oxígeno (O2) o de carbonato cálcico (CaCO3).
Espero te sirva
Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.