0:01 hello everyone and welcome to this
0:03 year's last minute crash review for your
0:05 end of course biology exam this video is
0:07 for students who are about to take a
0:10 final course test EOC or state exam in
0:12 biology that means you might be in 9th
0:14 or 10th grade right now but that may
0:16 vary depending on your school or state
0:17 in this video I'm going to quickly
0:19 review some really important content
0:21 that's commonly questioned on the end of
0:23 course biology exams and review some
0:25 basic skills that might pop up on your
0:27 test remember this is a fast review so
0:29 it won't cover everything you learned in
0:31 biology and I do talk fast so feel free
0:33 to change the speed on your video player
0:35 if you need if you need to go back and
0:36 do a deeper dive on any of these topics
0:37 make sure to check out the other
0:40 resources on my channel let's get
0:42 started very briefly remember all matter
0:44 on earth is made of different elements
0:46 elements are composed of different atoms
0:48 and in biology we really want to focus
0:50 on molecules called organic compounds
0:52 now these are special molecules that all
0:54 contain carbon that are essential for
0:56 life and the forming categories are
0:59 nucleic acids proteins carbohydrates and
1:00 lipids so we look at what they're made
1:03 of the monomers or the basic units of
1:05 nucleic acids are nucleotides the basic
1:08 monomers of proteins are amino acids and
1:10 carbohydrates the monomers are
1:12 monosaccharide and the basic monomers of
1:14 lipids are often fatty acids and
1:16 glycerol now up here I have the basic
1:17 structure as well this is actually a
1:18 phospholipid which makes up the cell
1:20 membrane of all living things and we'll
1:22 get to that in a little bit now to
1:24 remember all of these organic compound
1:26 groups I like the pneumonic clean later
1:28 party now for carbohydrates lipids
1:30 proteins and nucleic acid acids one
1:32 thing I like to add to this is clean
1:34 later party especially now to remember
1:37 that enzymes for that e are a type of
1:39 protein which is really important
1:41 enzymes are really important biological
1:43 macro molecules and they belong in the
1:45 protein category now let's talk about
1:46 water really quick water is the
1:49 universal solvent it is polar that means
1:51 it's partially positive and partially
1:54 negative on opposite ends so some
1:56 molecules are water loving we call these
1:58 hydrophilic and they interact easily
2:00 they're soluble with water
2:02 hydrophobic or water fearing molecules
2:05 like oils and fats are insoluble in
2:07 water now water has special properties
2:09 it has cohesion meaning water is
2:11 attracted to itself adhesion is the
2:13 attraction of water molecules to other
2:15 molecules or other things thinking
2:18 adding something on capillary action is
2:20 when cohesion and adhesion work together
2:22 pulling up against gravity we can see
2:25 this in stems in plants or in a straw
2:27 even and water also has a high surface
2:29 tension meaning it's more attracted to
2:31 itself then the air around it which
2:33 allows certain bugs like Strider bugs
2:36 and leaves to float on the surface of
2:38 water now let's get microscopic and go
2:40 down to the cell remember cells are the
2:43 basic units of life so all living things
2:45 have cells all cells are surrounded by a
2:47 cell membrane which is a phospholipid
2:49 bilayer we talked about lipids all
2:51 living things contain genetic
2:53 information DNA and all cells have
2:55 cytoplasm now if we look just at the
2:56 cell membrane let's zoom in really
2:58 closely it is actually a layer of two
3:01 rows of phos phospholipids so are Bayer
3:03 uh the heads of these fosol lipids are
3:05 hydrophilic so they are able to interact
3:07 with water easily the inner parts the
3:09 Tails here they're ranging themselves
3:11 away from the water because they are
3:13 hydrophobic now there's two main types
3:15 of cells we have eukaryotic cells which
3:19 have a nucleus and membranebound organel
3:21 like the mitochondria and then we have
3:23 procaryotic cells which also are
3:25 surrounded by membrane and also have DNA
3:27 but they do not have a nucleus and they
3:30 do not have membrane bound organel they
3:32 do have ribosomes they do have a
3:34 cytoplasm but we notice here the DNA
3:36 which is the scribbles on the diagram is
3:38 just floating freely in the cytoplasm
3:41 unlike the DNA and eukaryotic organisms
3:43 which is in the nucleus now eukaryotic
3:45 organisms can be animals they can be
3:47 plants and procaryotic organisms are
3:50 mostly bacteria we have archa as well
3:52 within our eukariotic cells we have
3:54 different types for example animal cells
3:56 over here which have a cell membrane and
3:58 plant cells which are also surrounded by
4:00 a cell wall for extra protection and
4:02 support another key difference between
4:04 plant and animal cells is the presence
4:06 of a chloroplast which is shown right
4:08 here chloroplasts are the location of
4:10 photosynthesis which plants perform
4:12 animal cells do not plant cells also
4:15 have one rather large vacu and animal
4:18 cells also have a vacu but um it's not
4:19 as big and they may have several
4:21 different vacul as well and remember
4:24 both plant and animal cells plant and
4:26 animal cells are both eukaryotic now
4:28 let's zoom in once again on that cell
4:30 membrane remember it is made made of a
4:32 phospholipid Bayer now different
4:34 molecules can get in and out of the cell
4:35 membrane in different ways we have
4:37 simple diffusion which is the movement
4:39 of particles from a higher concentration
4:42 to a lower concentration we have
4:43 facilitated diffusion which allows
4:45 particles to move from a higher
4:47 concentration to a lower concentration
4:50 but across a membrane facilitated being
4:52 helped this protein channel is helping
4:54 the molecules get through the membrane
4:56 then we have active transport which
4:58 allows molecules to move from a low
4:59 concentration to a higher con
5:02 concentration with the help of energy in
5:05 the form of ATP so a way I like to
5:07 remember this is kids going down the
5:09 slide so simple diffusion requires no
5:11 energy it's just a kid going down the
5:13 slide from high to low by themselves
5:15 facilitated diffusion might have a
5:16 parent or a friend which is
5:18 representative of our protein and
5:19 they're going from high to low as well
5:22 still requiring no energy themselves and
5:24 then active transport think of a child
5:26 going from low to high going up the
5:28 slide so against the concentration
5:30 gradient but they have to use energy to
5:33 do that so they're using ATP all right
5:35 when water moves across a membrane this
5:37 is called osmosis this is water moving
5:39 from a higher concentration of water
5:42 particles to a lower concentration of
5:44 water and when we think about where the
5:46 water is moving and comparison to the
5:48 solute or the other particles dissolved
5:51 in the water solution here we have kind
5:53 of an equal balance of particles in and
5:55 out of the cell that are not water so we
5:58 would call this an isotonic solution and
5:59 water would move freely in both
6:02 directions and about the same amounts in
6:03 this situation we have a higher
6:05 concentration of particles or solute
6:07 inside the cell but a higher
6:09 concentration of water particles which
6:11 is the blue here outside of the cell so
6:13 where would the water move the water
6:14 would move into the cell this is a
6:17 situation called a hypotonic solution
6:19 where there are fewer solute particles
6:21 outside the cell more inside the cell
6:23 more water outside the cell a lower
6:25 concentration of water inside the cell
6:27 so water would move in and now here we
6:29 have more solute particles out outside
6:31 the cell or a higher concentration of
6:33 solute particles so remember where is
6:35 water going to move from a high
6:36 concentration of water so that means it
6:38 would move outside the cell this is
6:41 called a hypertonic environment now in a
6:43 hypertonic environment there is a chance
6:45 that if a lot of water moves out of the
6:47 cell the cell could actually shrink and
6:49 the opposite would happen in a hypotonic
6:51 environment a lot of water may move into
6:53 the cell causing it to swell or burst
6:55 let's get back to enzymes remember these
6:56 are a type of proteins they are
6:59 extremely important to living things
7:01 they are biological catalysts meaning
7:03 they get things going they get reactions
7:05 started things like ligase helicase
7:08 polymerase amase these are all enzymes
7:09 notice all of these words and in the
7:12 letters as e which makes it easy to
7:13 recognize an enzyme even if you've never
7:15 seen it before some things that can
7:17 affect enzymes are temperature or pH if
7:20 enzymes get too hot they can denature or
7:22 unfold and then they'd be unable to act
7:24 with their substrate because they no
7:27 longer have the shape of the active site
7:29 which is where a protein or an enzyme
7:31 usually interacts with the substrate the
7:33 molecule that it's going to do something
7:35 to or interact with all right let's jump
7:37 over to cellular respiration now all
7:40 living things need energy and one of the
7:41 main ways they get that is through
7:43 cellular respiration which occurs in the
7:45 mitochondria this is the process where
7:48 organisms take glucose sugar and oxygen
7:50 and go through reactions to transform it
7:52 into ATP energy in that process carbon
7:55 dioxide and water are also generated so
7:57 if we think about this on a larger scale
7:59 when we eat we consume glucose when we
8:02 inhale we take in oxygen and when we
8:04 exhale that CO2 is a byproduct of
8:06 cellular respiration we exhale water
8:08 vapor as well you can see that coming
8:10 out of your mouth on a cold day and then
8:12 ATP is also generated which gives us the
8:15 energy to perform our daily activities
8:17 and survive all eukaryotic organisms are
8:19 going to perform some type of
8:22 respiration another important reaction
8:24 we need to be aware of is photosynthesis
8:27 this is how plants get the food they
8:28 need and they use sunlight energy to
8:31 convert the carbon and carbon dioxide
8:33 into food molecules like glucose so
8:35 carbon dioxide in the sunlight energy
8:37 and water can be transformed into
8:40 glucose and oxygen remember the plants
8:42 need that glucose and oxygen to perform
8:44 cellular respiration themselves so these
8:46 processes are complimentary and they
8:47 feed each other which is why
8:49 photosynthesis is crucial to life on
8:52 Earth another type of respiration is
8:54 fermentation this is often called
8:56 anerobic respiration it's a type of
8:58 anerobic respiration but that means it
9:01 occurs without oxygen so bacteria some
9:03 yeast perform this process and
9:05 fermentation is not as efficient as
9:06 cellular respiration cellular
9:09 respiration produces 36 molecules of ATP
9:11 where fermentation only produces two
9:14 molecules of ATP so even though we can
9:16 also perform fermentation in our muscle
9:18 cells for example when we run out of
9:20 oxygen cellular respiration is a much
9:22 more efficient efficient process for
9:24 producing energy molecules so like I
9:26 said the type of fermentation that we
9:28 can do in our muscle cells is called
9:30 lactic acid ferment ation and that's
9:32 because we take glucose and we generate
9:34 energy molecules ATP but also lactic
9:36 acid as a byproduct now yeast can do
9:37 another type of fermentation called
9:40 alcoholic fermentation and here the
9:42 yeast produce ethanol as a byproduct or
9:45 a type of alcohol and carbon dioxide so
9:47 that carbon dioxide we can see as
9:49 bubbles forming if you've ever done an
9:51 experiment with yeast and fermentation
9:53 it's why Bakers use yeast in their
9:55 baking because that carbon dioxide can
9:57 help bread rise and then also of course
9:59 ATP is generated in this process let's
10:02 get down to the DNA in our cells
10:04 remember all living things contain DNA
10:07 now DNA is organized it is wound up into
10:08 chromosomes and condenses into
10:10 chromosomal form before the cell can
10:13 divide remember each double-sided
10:15 chromosome that looks like this actually
10:17 is a duplicated set of DNA so we have
10:20 two sister chromatids here they're
10:22 connected at the center by a centrr but
10:24 usually within the cell if the cell is
10:26 not preparing for cell division it may
10:28 not be condensed into these chromosome
10:31 forms it may may just be in chromatin
10:33 form which sounds similar to chromosome
10:35 but it kind of is represented as this
10:36 like spaghetti like drawing where the
10:39 DNA is Unwound it's not condensed as the
10:41 cell prepares for cell division we may
10:43 see the chromosomes begin to look like
10:44 this that means the DNA has already been
10:46 duplicated and the chromosomes are
10:48 arranging themselves so they can prepare
10:51 for cell division mitosis is a type of
10:54 asexual reproduction where cells make
10:57 exact copies of themselves one cell can
10:59 generate two identical daughter cells
11:00 you might have learned the phases of
11:03 mitosis as Pat which stands for prophase
11:06 metaphase anaphase and telophase and
11:08 then at the end there's cyto Kinesis
11:10 where the cytoplasm actually divides now
11:12 in prophase the nuclear envelope
11:14 dissolves and the chromosomes condense
11:16 they start to move to the middle of the
11:18 cell and metaphase they align along that
11:21 cellular equator or the center of the
11:23 cell and these spindle fibers on
11:24 opposite ends of the cell come and
11:28 attach the cir in anaphase think a for
11:30 away the cytochrom are separated they
11:32 start to get pulled away from each other
11:34 towards opposite ends of the cell in
11:36 telophase new nuclear envelopes start to
11:39 form the cell starts to separate and
11:41 inside a Kinesis we have the exact
11:44 separation of the cytoplasm now with
11:46 mitosis you've probably also studied
11:48 meiosis which is a different type of
11:51 cell division mitosis remember will copy
11:53 body cells make exact duplicates of
11:56 cells so one parent cell will create two
11:58 identical daughter cells whereas meiosis
12:00 is the process used to generate sex
12:02 cells so one parent cell that goes
12:04 through meiosis will generate four
12:05 daughter cells but they'll only have
12:08 half the genetic information as the
12:10 parent cell so meiosis takes a little
12:12 bit longer it goes through pmac twice
12:13 and you don't need to memorize what
12:16 happens in every single stage but the
12:18 results are important so at the end of
12:19 meiosis there are going to be four
12:21 daughter cells each with half the
12:24 genetic information as the parent cell
12:26 and this genetic information has been
12:27 mixed up a little bit so it's a
12:29 different combination in each cell so
12:31 the genetic information is different at
12:33 the end of meiosis which is going to be
12:35 helpful in the diversity of life on
12:38 Earth as organisms reproduce sexually
12:40 now as organisms reproduce we pass on
12:42 our genetic traits Gregor Mandel was
12:44 often called the father of genetics he
12:46 did studies that recognize that a lot of
12:49 traits are controlled by two different
12:52 alals or versions of a gene and alals
12:54 can be dominant or recessive meaning one
12:57 can cover up a particular trait so we
13:00 have these words heterozygous homozygous
13:02 to talk about genotypes or combinations
13:05 of genes so for example this big T Big T
13:09 would be a homozygous dominant genotype
13:11 and each of these letters represents a
13:14 version of that Gene so you could pause
13:16 and try to fill this in for yourself but
13:18 here we go we have big T Big T would be
13:21 homozygous dominant Big B little B would
13:22 be heterozygous because it's two
13:25 different versions of the same gene and
13:27 Little T Little T is homozygous
13:29 recessive two different versions of the
13:31 recessive gene remember a big T often
13:34 represents a dominant Al and a little or
13:36 a lowercase letter would represent a
13:39 recessive Al so for example if yellow
13:41 body color is dominant to Blue in these
13:44 fish if we have a Big Y and a little y
13:47 that would result in a fish being yellow
13:49 that's the phenotype so if we write the
13:51 phenotypes here we would see what would
13:53 happen with each of these genotypes
13:55 remember genotypes are the combination
13:58 of genes phenotypes are the actual
14:00 physical character istics that we get
14:02 from the genotype so you can pause this
14:04 and go through each of the examples if
14:05 you want and you might have also
14:08 practiced punet squares in biology where
14:10 you have to separate the alals of both
14:13 parents on this table and figure out the
14:15 possible combinations that could result
14:18 from this Cross or from when these
14:20 parents mate what their offspring could
14:22 potentially have and remember what
14:23 happens in a punet square is just a
14:26 probability it is a potential outcome we
14:29 won't know for sure until the off spring
14:31 are born what the actual genotypes and
14:34 phenotypes are and remember most human
14:35 traits most genetics are very
14:37 complicated so it's not as simple as
14:38 Gregor mandelle said there's different
14:41 types of dominance like incomplete
14:43 dominance where there's a blending of
14:44 traits co-dominance where we see
14:47 representations of both traits so for
14:49 example if a purple and a pink flower
14:51 were co-dominant for flower color we
14:54 might see both purple and pink petals in
14:56 their flowers and of course there's also
14:57 sex linked traits which are traits that
14:59 are carried on the ex and the Y
15:02 chromosomes now humans have 23 pairs of
15:04 chromosomes that 23rd pair is going to
15:07 be the sex chromosomes and females have
15:10 two X chromosomes males have an X and A
15:12 Y we talk about traits like color
15:13 blindness these are traits that are
15:16 carried on the chromosomes that are sex
15:18 chromosomes so when we perform genetic
15:21 crosses with sex linked traits we'll
15:23 also write the X and the Y there and the
15:26 alil as an exponent and make sure we
15:28 carry all of the letters together in our
15:30 punet Square cross process now genes can
15:31 also be influenced by the environment
15:33 for example these hydrangeas can have
15:36 different colors based on the pH of the
15:37 soil and this can go for a lot of
15:39 different traits sometimes there's
15:41 temperature differences that can change
15:43 the color of fur of different mammals
15:45 and of course chromosomes can have
15:47 problems separating during meiosis or
15:48 mitosis and when we have that
15:50 non-disjunction or those sister
15:52 chromatids not going to the opposite end
15:54 of the cell correctly we could end up
15:55 with a cell with different numbers of
15:59 chromosomes for example triom 21 would
16:01 mean that we have three copies of the
16:03 21st chromosome and triom 21 is also
16:05 known as Down syndrome and that mean
16:07 that person would have a condition that
16:09 affects their physical characteristics
16:10 some of their development because of
16:12 that extra copy of that chromosome now
16:14 let's talk about DNA a little bit closer
16:17 now remember that in DNA we have four
16:20 different bases A's T's G's and C's a is
16:22 always pair with t g is always pair with
16:25 C DNA replicates during the S phase of
16:27 the cell cycle and in DNA replication we
16:30 have the DNA strand separating and new
16:32 strands of DNA are built off the templat
16:34 so it's called semiconservative
16:37 replication each new strand of DNA has
16:39 half the old Strand and half brand new
16:42 if we look back at our organic compound
16:44 structure each nucleotide has a
16:47 phosphate a sugar and a base atg or C
16:48 and so when we put these together A's
16:50 and T's we can see always pair together
16:52 with these are little hydrogen bonds in
16:54 the middle G's and C's always pair
16:56 together and the backbone of the DNA
16:58 molecule is made of phosphate and sugar
17:00 molecules so how do we get exactly from
17:03 our DNA to our actual trait well the
17:05 process is called protein synthesis and
17:07 in the nucleus where the DNA is the DNA
17:10 will separate and then an mRNA sequence
17:12 will be built off of the DNA template
17:15 that mRNA will leave the nucleus and
17:17 that process is transcription then we'll
17:19 go through translation where the MRNA
17:22 will go to a ribosome and tRNA molecules
17:24 a different type of RNA will match up
17:27 with the codons or the different groups
17:30 of mRNA and bring over a matching amino
17:31 acid and then those amino acids will
17:33 start to link up and remember amino
17:36 acids make proteins and so that is how
17:38 we deliver the message to build the
17:40 protein that is going to give us some
17:43 trait in our bodies like the protein
17:45 that influences eye color or the protein
17:46 that gives us our hair shape so some
17:48 differences to remember between DNA and
17:50 RNA DNA is double stranded RNA is single
17:53 stranded DNA has actually a deoxy ribo
17:55 sugar that's where its name comes from
17:57 deoxy ribonucleic Acid where RNA is made
18:00 of a ribo sugar and then DNA's bases are
18:02 A's T's G's and C's where RNA actually
18:04 has a u instead of a t so if you're
18:06 creating an RNA strand based off DNA
18:09 remember to replace wherever a t would
18:11 go with a u let's do a little practice
18:12 so if we're transcribing a sequence of
18:15 DNA this purple is the DNA here the
18:18 sequence is a g t g t c the
18:21 complimentary RNA would be a pairs with
18:25 u g pairs with C T pairs with a G pairs
18:27 with C T pairs with A and C pairs with G
18:29 so again try this on your own go ahead
18:31 and pause real quick the correct mRNA
18:35 sequence here would be a ug CG auu and
18:37 then don't forget the next step is
18:38 translation where we build that protein
18:40 and to do this by hand you might see a
18:41 codon chart where you're asked to find
18:43 the codon and then the matching amino
18:44 acids so let's say we were looking at a
18:46 codon that was CCC so we'd start in the
18:49 center find the C then find the next C
18:51 in the next Circle and then go to the
18:52 final Circle here find that c that
18:55 refers to Pro which is short for Proline
18:57 one of our amino acids you do not need
18:59 to memorize all your amino acids and if
19:01 you're ever asked to do translation on a
19:02 biology exam you will be provided with a
19:04 codeon chart codeon charts can also look
19:07 like this so let's look at CCC again C
19:09 is our first base here we would go to
19:10 the top for our second base here's
19:12 another C and then find that third base
19:14 C that also corresponds to Proline on
19:17 this chart it is a universal genetic
19:18 code let's talk really quickly about
19:20 biotechnology now there's lots of
19:22 different growing and emerging new
19:23 technologies in the field of
19:26 biotechnology from lab grown meat to DNA
19:28 tests to genetically engineered
19:30 organisms to resurrecting woly man
19:32 Mammoth to crisper DNA and so of course
19:34 there's ethical questions that go along
19:35 with all these new techniques one
19:37 technique you might see on your exam
19:39 would be gel electropheresis which is a
19:41 way to identify different parts of DNA
19:43 so gel electropheresis can be used to
19:45 study evolutionary relationships
19:47 identify DNA found at crime scenes or
19:50 maternity or paternity testing so here
19:52 we have a simple gel in the gel DNA is
19:55 loaded at these Wells at the top DNA is
19:56 negatively charged so it'll be attracted
19:58 towards the positive and then these DNA
20:01 samples will travel down this gel as we
20:03 run an electric current through the gel
20:06 and we can see which pairs match up so
20:07 here we have a mother which matches with
20:10 child a and child B child C though does
20:12 not have any matches with the mother so
20:14 we can say that child C is not related
20:16 to this particular mother and on a much
20:18 larger scale remember that evolution is
20:20 the change in genetic makeup of a
20:22 population over time natural selection
20:25 is the major mechanism behind Evolution
20:26 and when we talk about an organism Being
20:29 evolutionarily Fit that means means how
20:30 well they are able to survive and
20:32 reproduce not how strong they are not
20:35 how fast they are it's really about how
20:36 they can survive and pass on their
20:38 traits to their offspring and remember
20:40 that environments are a huge factor in
20:42 evolution and they can act as a
20:43 selective pressure and different
20:45 organisms will have better rates of
20:47 survival in different types of
20:48 environments an adaptation is an
20:51 inherited trait that is favorable to an
20:53 organism that helps an organism survive
20:55 and Charles Darwin was one of our main
20:57 scientists that created this idea of
20:59 natural selection we have lots of
21:01 evidence now to support this idea of
21:03 evolution from the fossil record to
21:05 biochemical and DNA evidence embryology
21:07 we can see how different organisms
21:09 develop very similarly through the study
21:12 of their embryos a philogenetic tree or
21:14 a cladogram is a way to look at
21:16 different evolutionary relationships
21:18 over time and when we see branches on a
21:20 tree we can see where their last common
21:22 ancestor might have been and we can also
21:24 add traits to this tree so if we look at
21:26 a tree like this we can read it as
21:28 anytime there's a trait that appears any
21:30 organism that comes after that trait
21:32 developed that trait so for example the
21:34 organisms on this tree that have
21:37 vascular tissue are ferns pine trees and
21:40 flowering plants but not mosses and the
21:42 organisms or the groups of organisms
21:44 that have seeds are pine trees and
21:45 flowering plants but not Ferns and
21:47 mosses now backing all the way up to the
21:49 biosphere remember different levels of
21:52 organization in biology go from molecule
21:54 all the way up to all life on Earth and
21:55 at the population community and
21:57 ecosystem level we can talk about
21:59 biodiversity which is a measure of the
22:01 variety of different types of organisms
22:04 in an ecosystem and biodiversity is very
22:06 important to living things because the
22:08 more biodiverse an ecosystem is the more
22:10 resilient it will be now of course
22:12 environments are always changing large
22:13 scale changes that can influence
22:16 ecosystem can be maybe the addition of
22:18 different nutrients to a system we could
22:20 have forest fires we could have droughts
22:22 we could have floods earthquakes there's
22:25 so many things that could influence and
22:27 create major changes to an ecosystem in
22:30 a food chain we can see that organisms
22:32 that produce their food often come first
22:34 so producers like these autot tropes or
22:36 grass are here and we always drew the
22:38 arrow pointing towards the organism that
22:40 is doing the eating so think about this
22:42 food going into this Elk's stomach
22:43 that's the direction of arrows for a
22:46 food chain or a food web now we have our
22:48 producers or our autotrophs here are
22:50 heterotrophs are organisms that get
22:51 their food from something else so they
22:53 don't make it on their own they consume
22:55 their food this is also a heter trro and
22:57 this is also a hetro and when we go up a
22:59 food chain or a food web we can also
23:01 identify organisms as producers or
23:03 consumers so this is a producer this is
23:05 a primary consumer because it's the
23:07 first organism that eats the producer
23:09 this is a secondary consumer and this is
23:11 a tertiary consumer if the human were to
23:14 eat the Bobcat on a trophic pyramid
23:16 remember that the most energy is found
23:19 at the bottom of the pyramid and as you
23:21 go up a level most of that energy is
23:22 lost to the environment so it's more
23:25 efficient to consume lower on at trophic
23:27 pyramid if you're an organism there are
23:29 tons of different mod molecules and
23:31 atoms cycling throughout our environment
23:33 carbon is one of them and the carbon
23:35 cycle involves both photosynthesis the
23:38 plants harnessing sunlight energy in
23:40 order to take the carbon dioxide from
23:42 the air and create glucose molecules
23:44 respiration we take that glucose and we
23:46 use it to create energy and then we
23:48 exhale the carbon dioxide decomposition
23:50 can break down carbon in organisms
23:52 bodies and combustion also releases
23:54 carbon dioxide into the environment now
23:56 there are tons of resources on Earth
23:57 some are renewable which means they can
24:00 be replaced quickly by natural processes
24:01 some are non-renewable meaning they
24:03 cannot be replaced generally within
24:05 human lifetimes or as fast as they are
24:08 being used and so we need to consider
24:10 the our use of resources as the
24:13 population of humans continues to boom
24:15 on planet Earth a hole in the ozone
24:18 layer is a problem that we've identified
24:20 recently but it's actually getting
24:23 better but this hole produced by the use
24:25 of cfc's or a chemical called
24:27 chlorofluorocarbons was pretty dangerous
24:29 cuz it was letting in armful UV
24:30 radiation into the earth now this is
24:32 separate from the issue of global
24:34 warming which is predominantly affected
24:37 by the combustion or burning of fossil
24:39 fuels because that adds gases to the
24:40 atmosphere that cause it to hold more
24:43 heat and continued global warming can
24:45 lead to rising sea levels coastal
24:47 flooding but there are other human
24:49 impacts plenty of human impacts on the
24:50 environment such as introduction of
24:52 invasive species introduction of
24:55 diseases changing habitats
24:58 deforestation industrialization all of
25:00 these things but humans can also have a
25:02 positive impact on the environment by
25:04 reducing our consumption of resources
25:06 recycling planting native species
25:08 protecting wildlife and habitats and
25:11 supporting sustainable practices wo
25:12 we're coming to the end I hope this has
25:14 been helpful as you cram for your
25:15 biology exam I have lots of other
25:18 biology AP biology and other life
25:20 science resources on this channel so be
25:21 sure to subscribe so you don't miss out
25:23 best of luck on your biology exam let me
25:24 know if you have any more questions in
25:26 the comments below thanks so much for
25:27 watching and give this video a like if
25:29 it's been help helpful I'll see you later