Plants,because in a plant there are little roots just like capillaries in a humans body which push water and nutrients like how our capillaries push blood through our veins which pushes it up through the rest of the plant just like how our veins and capillaries push blood through or body .
Answer:
The adaptation in owl butterfly helps it to camouflage and also protects it from predators. Adaptations allow organisms to be better suited to their environment. So the answer is both 'A' and 'B' .
Explanation:
Owl butterfly use the concept of mimicry. It is a form of <em>adaptation</em> in which they fool the predator in thinking that they are owls and not butterflies. These butterflies have eyespots under their wings. By flashing them they look like the <em>eyes </em>of an owl.
Since owls feed on small animals, and small animals feed on butterflies, the owl butterflies protect themselves from predators. The small animals thinking that the butterfly is an owl, run away instead of coming closer. This way these small insects camouflage and protect themselves.
<span>1. Reorient frequently to time, place, and situation.
2. Put the client in a quiet room furthest from the nursing station.
3.perform necessary producers quickly
4.Arrange for familiar pictures or special items at bedside.
5.Limit the client visitor's.
6.spend time with clients ,establishing a trusting.</span>
Answer:
As a result of photosynthesis oxygen and sugar
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.
