Which of the following is true regarding tissue? a)
An example of tissue is the digestive system, which helps break down food
particles for organisms to obtain energy and nutrients.
Ob) Tissue is a group of specialized cells that work together for a common
function and form organs.
O c) Sponges are the only animal made of tissue and made of haploid cells.
d) Tissue is a group of diploid molecules bonded together chemically.

True: b) Tissue is a group of specialized cells that work together for a common  function and form organs.

Explanation:

Cells are the smallest units of life, they may be either unicellular or multicellular. Unicellular organs have a single cell capable of carrying out all of the functions necessary for its survival. Multicellular organisms are more complex, and require the work of multiple different cell types.

Their cells become differentiated- where they undergo certain processes to become specialized, and gain maturity. Groups of specialized cell types form tissue; these each have varying functions over time. Organs consist of two or more tissue types that are specifically organized to carry out a function.

b) Tissue is a group of specialized cells that work together for a common

function and form organs.

Explanation:

Sponges are the simplest type of animal therefore they have a few different features than other animals. Like all animals, sponges are diploid, multicellular, heterotrophic, reproduce sexually, mobile, and don't have a cell wall. They are different in that their zygotes do not form into a blastula and they are not made of tissue.

Also, i took the quiz :)

oxygen +1 most likely

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.