Answer:
Pupillary light reflex refers to the contraction that the pupils present when they light up. In cases of injury to the optic nerve, when the eye where the injured optic nerve is illuminated, since it cannot conduct the stimulus to the brain, neither pupil closes.
Explanation:
Pupillary light reflex refers to the reaction that causes the pupil to close with light thanks to the contraction of the sphincter of the pupil and to open in the dark thanks to the relaxation of that muscle by not receiving any stimulus. A light stimulus reaches the eye and in the retina it is transformed, through a chemical reaction, into an electrical stimulus that will be transmitted through the optic nerve and the visual pathways to the brain. The visual cells of the retina, rods and cones, also act as light receptors that control the pupil's motor activity. Thus, pupil-motor thresholds to light follow the same spectral sensitivity deviations as visual thresholds, which are a function of the state of light adaptation of the retina.
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Answer:
What is neuroscience---------------->any or all of the sciences, such as neurochemistry and experimental psychology, which deal with the structure or function of the nervous system and brain.
Explanation:
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Fossils provide solid evidence that organisms from the past are not the same as those found today; fossils show a progression of evolution. Fossils, along with the comparative anatomy of present-day organisms, constitute the morphological, or anatomical, record. By comparing the anatomies of both modern and extinct species, paleontologists can infer the lineages of those species. This approach is most successful for organisms that had hard body parts, such as shells, bones or teeth. The resulting fossil record tells the story of the past and shows the evolution of form over millions of years.
Answer:
1. Map-based genome sequencing: a; c; f; g
2. Whole-genome shotgun sequencing: b
3. Both sequencing methods: d; e
Explanation:
Map-based genome sequencing is a method that makes use of a reference genome sequence in order to determine the relative position of the DNA fragments before they are sequenced. This method is useful to determine the position of repetitive DNA fragments (for example, duplicated genes, repetitive non-coding regions, etc.) and Transposable Elements. Therefore, map-based genome sequencing is a suitable approach for large genomes (which are usually composed of repetitive sequences). On the other hand, in whole-genome shotgun sequencing, DNA sequences are obtained before the correct order of these DNA fragments is known. In this method, the genome is fragmented randomly into small DNA sequences (between 100 and 1000 base pairs), which are subsequently sequenced through the chain-termination sequencing approach (i.e., Sanger sequencing) and finally ordered by using bioinformatic tools that assemble overlapping reads.