Answer:
secondary succession
Explanation:
<em>The kind of succession that will occur if no one mowed the grass at all is secondary succession.</em>
Succession generally refers to a gradual change in the structure of a community over a period of times. Succession could be primary or secondary.
Primary succession occur when a site that has not held any form of life before gets colonised by a new life. The new lives are referred to as pioneer species.
Secondary succession occur when a community that already has lives in it experiences a regime of disturbance. The structure of the community will change in response to the disturbance.
Both primary and secondary succession eventually lead to a relatively stable community, otherwise known as climax community.
<u>In this case, a baseball field that normal gets mowed every summer stops getting mowed. the community will experience secondary succession and keep changing till a level is reached where the structure hardly changes again. This level is the climax community.</u>
<h2>A) option is correct </h2>
Explanation:
Skin has two types of sweat glands: eccrine and apocrine
Eccrine glands occur over most of the body and open directly onto the surface of skin whereas apocrine glands open into the hair follicle, leading to the surface of the skin and develop in areas abundant in hair follicles, such as on scalp, armpits and groin
The eccrine gland is controlled by the sympathetic nervous system and regulates body temperature
In some animals, when internal temperature rises the eccrine glands secrete water to the skin surface, where heat is removed by evaporation
Eccrine glands when active are considered major thermoregulatory devices
Smaller mammals, such as rodents, cannot endure dehydration and hence possess no eccrine glands at all
Yes, it is true that Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.
Focal malformations of cortical development, including focal cortical dysplasia (FCD) and hemimegalencephaly (HME), are important causes of intractable childhood epilepsy.
Using targeted and exome sequencing on DNA from resected brain samples and non-brain samples from 53 patients with FCD or HME, we identified pathogenic germline and mosaic mutations in multiple PI3K/AKT pathway genes in 9 patients, and a likely pathogenic variant in 1 additional patient.
Our data confirm the association of DEPDC5 with sporadic FCD but also implicate this gene for the first time in HME. Our findings suggest that modulation of the mammalian target of rapamycin pathway may hold promise for malformation-associated epilepsy.
Learn more about mutations here : brainly.com/question/17031191
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The only possible phenotype is large ears.
This is because using a punnet square reveals that each option has a dominant allele of large ears, leaving no room for the recessive trait of small ears.
Hope this helps!
It a rock form from extrusive rock such as the follow of lava
