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Answer:</h2>
Option C) All species with similar anatomical structures are related.
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Explanation:</h2>
- Homologous Structure: A homologous structure is an example of an organ or bone that appears in different animals, which are anatomically similar structure demonstrating descent from a common ancestor.
- All species with similar anatomical structures which means they have homologous structures and are related as they have evolved from a common ancestor.
- Homologous structures shows divergent evolution.
Result: Option C is the correct scientific inference for homologous structures.
Answer:
The three-chambered hearts of amphibians and nonbird reptiles are facultative, allowing variation in blood flow through the heart.
Explanation:
In Anatomy, cardiac cycle can be defined as a complete heartbeat of the human heart which comprises of sequential alternating contraction and relaxation of the atria and ventricles, therefore causing blood to flow unidirectionally (one direction) throughout the human body.
Generally, the cardiac cycle occurs in two (2) stages;
I. Diastole : in this stage, the ventricles is relaxed and would be filled with blood.
II. Systole: at this stage, the muscles contracts and thus, allow blood to be pushed through the atria.
All amphibians and reptiles except for crocodiles (having four-chambered heart) have three-chambered hearts, which typically comprises of a partially divided ventricle and two atria.
Hence, the correct statement about the three-chambered hearts of amphibians and nonbird reptiles is that, the three-chambered hearts of amphibians and nonbird reptiles are facultative, allowing variation in blood flow through the heart due to the partially divided ventricle.
<span>The correct answer is C.stability is genetic and cannot be improved. This is incorrect. Just think of when you ride a bike, it's not a genetic thing and anyone can learn it if they learn how to balance their center of gravity and their movement. It's not a genetic thing so only a few chosen people can ride a bike.</span>
Answer:
There are three main classes of parasites that can cause disease in humans: protozoa, helminths, and ectoparasites. Protozoa are microscopic, one-celled organisms that can be free-living or parasitic in nature.
Explanation:
Answer:
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/ dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.
1. The C. elegans embryo as a system to study cell division
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the syncytial gonad makes it possible to use RNA interference (RNAi) to generate oocytes whose cytoplasm is reproducibly (>95%) depleted of targeted essential gene products. Introduction of dsRNA rapidly catalyzes the destruction of the corresponding mRNA in many different systems. However, depletion of pre-existing protein is generally a slow process that depends on the half-life of the targeted protein. In contrast, in the C. elegans gonad, the protein present when the dsRNA is introduced is depleted by the continual packaging of maternal cytoplasm into oocytes (Figure 1). Since depletion relies on the rate of embryo production instead of protein half-life, the kinetics tend to be similar for different targets. By 36-48 hours after introduction of the dsRNA, newly formed oocytes are typically >95% depleted of the target protein.
Explanation:
