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Summary
In the "Stroll Through the Playlist," the Amoeba Sisters take you on an extensive review journey through their biology video collection, offering a fun and engaging refresher on key concepts ranging from the characteristics of life, cell biology, biomolecules, genetic makeup, to the principles of ecology and the complexity of body systems. This comprehensive video is designed to be paused frequently, allowing viewers to ponder questions that reinforce understanding. The Amoeba Sisters' playful approach not only educates but also inspires curiosity and a deeper appreciation for biology as an interconnected discipline.
Highlights
A fun and informative stroll through Amoeba Sisters' biology playlist! đ„
Quirky humor and engaging explanations make learning biology fun! đ
Frequent pauses provide opportunities to check your understanding! đ
Explore diverse biology topics, from cell theory to ecological succession! đż
Biology concepts are linked to create a comprehensive learning experience! đ
Key Takeaways
Discover the wonders of biology with a fun and engaging playlist stroll! đż
Pause and reflect with on-the-spot questions throughout the video! đ
Explore biological concepts from the microscopic to the ecological scale! đŹ
Connect biology with the real world, making learning exciting and relevant! đ
Enjoy the Amoeba Sisters' unique and humorous teaching style! đ
Overview
The Amoeba Sisters invite you to take a leisurely stroll through their biology video playlist, summarizing countless key concepts in a refreshingly entertaining manner. They start by revisiting the basics, such as the characteristics of life and cell theory, reminding us how everything is interconnected within the microscopic world. With Petunia, they cleverly use mnemonic devices, humor, and a little bit of nostalgia to make these foundational topics memorable.
As the stroll progresses, viewers are prompted to pause and engage in small quiz sessions to test their knowledge retention. From the biological levels of organization to complex processes like photosynthesis and cellular respiration, the video ties everything together in a seamless storytelling format. This just isn't biology as usual; itâs an intriguing narrative that keeps you captivated!
By the end of this educational stroll, the Amoeba Sisters have imparted a wealth of knowledge while maintaining a light-hearted tone. They've turned a potential cramming session into a motivational journey, encouraging students to stay curious and realize how these seemingly disparate concepts actually connect to form the tapestry of life. It's a delightful reminder of why biology matters beyond just exam preparation.
Chapters
00:00 - 01:00: Introduction and Video Overview In the introduction, the transcript features a casual conversation between individuals reminiscing about their collection of videos and pictures that serve as educational materials. A specific memory about 'the danger guppy,' associated with a classification video, highlights the importance of scientific names over common or fabricated names for reliability.
01:00 - 03:30: Characteristics of Life and Biological Organization This chapter discusses the challenges of retaining information from numerous educational videos, highlighting a common issue of forgetting details. It introduces the concept of a 'TL;DR' or summary version as a solution to improve retention by providing a quick refresher of the main points, suggesting the potential need for creating such summaries to aid learning.
03:30 - 07:30: Biomolecules and Enzymes This chapter discusses the concept of creating a comprehensive recap video for biology students, specifically focusing on biomolecules and enzymes. The chapter identifies that while the video will be longer than typical short videos, it will serve as a valuable study tool by connecting the main concepts and information. The chapter emphasizes including only the main points due to the vast amount of vocabulary and content in biology, suggesting that viewers frequently pause to absorb the information. Gus is mentioned as someone who can assist by indicating when to pause to better digest the material.
07:30 - 13:00: Cell Structure and Membrane Transport The chapter begins with an emphasis on interactive learning, encouraging viewers to ask questions and engage with the material. It briefly touches upon the characteristics of life and what distinguishes living organisms from non-living entities.
13:00 - 16:30: Photosynthesis and Cellular Respiration The chapter begins with a discussion on the complexity of defining life, noting exceptions when considering life's characteristics. It humorously references a comparison between a 'bathtub grown pony' and a real pony, emphasizing the challenge of quantifying life's traits. The text encourages reflection on the characteristics of life, prompting readers to consider their own list. The chapter also acknowledges the possibility of different terminologies for these characteristics.
16:30 - 19:30: DNA Structure and Replication The chapter begins with a discussion on the fundamentals of biology focusing on the biological levels of organization. It emphasizes that understanding starts with small units, specifically highlighting the cell as the smallest living unit, which is a cornerstone of cell theory. The cell theory is outlined, affirming that the cell is the smallest living unit in all organisms, all living organisms are composed of cells, and new cells arise from pre-existing ones.
19:30 - 27:00: Cell Cycle, Mitosis, and Meiosis This chapter provides an overview of the hierarchical organization of biological systems, starting from cells that combine to form tissues, which then form organs, organ systems, and entire organisms. It emphasizes the interconnectedness of these biological structures, leading up to the concept of populations, communities, and ecosystems, highlighting the complexity of biological organization.
27:00 - 37:00: Genetics and Heredity The chapter "Genetics and Heredity" starts by distinguishing abiotic (non-living) factors such as rocks and temperature from biotic (living) factors, which make up levels of ecological organization from biomes to the biosphere. The focus then shifts to living organisms and the biomolecules that are essential for life. Four major types of macromolecules are addressed: carbohydrates, lipids, proteins, and nucleic acids, including their building blocks.
37:00 - 46:00: Bacteria and Viruses The chapter "Bacteria and Viruses" focuses on the basic building blocks of life, namely monosaccharides, fatty acid & glycerol, amino acids, and nucleotides. These are true monomers for essential biomolecules such as carbohydrates, proteins, and nucleic acids. The text challenges readers to think about critical functions these biomolecules perform, which are vital for life. Additionally, the beauty of their structures is highlighted, along with a mnemonic to assist memory.
46:00 - 52:00: Plants and Photosynthesis This chapter delves into the fundamental role of enzymes in biological systems, particularly in plants and photosynthesis. It describes enzymes as proteins with active sites where substrates bind, highlighting their capability to accelerate reactions by breaking down or building up substrates. The chapter underscores the significance of enzymes in various biological processes, providing an example of digestive enzymes that specialize in breaking down complex molecules, thereby facilitating crucial biochemical reactions in organisms.
52:00 - 62:00: Ecological Succession and Ecosystems The chapter "Ecological Succession and Ecosystems" discusses the critical role that enzymes play within cells, emphasizing their dependence on specific temperature and pH ranges to function properly. A disruption in these conditions can lead to enzyme denaturation, impacting cellular functions. The chapter also hints at additional resources for understanding cellular components, particularly the distinctions between prokaryotic and eukaryotic cells.
62:00 - 69:00: Ecological Relationships and Human Body Systems The chapter begins with a mnemonic to differentiate between prokaryotic and eukaryotic cells, emphasizing that 'pro' rhymes with 'no' (indicating prokaryotic cells lack a nucleus and membrane-bound organelles) and 'eu' rhymes with 'do' (indicating eukaryotic cells do have these features). Prokaryotes, such as bacteria and archaea, contrast with eukaryotic organisms which include plants, animals, protists, and fungi. The chapter encourages thinking about commonalities between prokaryotic and eukaryotic cells.
69:00 - 73:00: Conclusion and Study Tips In the conclusion and study tips chapter, the focus is on understanding the basic components found in all cells, such as DNA, cytoplasm, ribosomes, and a cell membrane, which are common to both prokaryotic and eukaryotic cells. The chapter reiterates insights from the 'Intro to Cells' video, which delves into membrane-bound organelles unique to eukaryotes like the nucleus, endoplasmic reticulum, golgi apparatus, and mitochondria. It also hints at differences between plant and animal cells, starting with an introduction to the cell membrane or plasma membrane.
Stroll Through the Playlist (a Biology Review) Transcription
00:00 - 00:30 Captions are on! Click CC button at bottom right to turn off. Petunia, we have so many videos now. Every once in a while, Iâll come across
one of your pictures and be reminded all about the topic again ---I love them so much. Aw, thanks. Remember the danger guppy? I LOVE the danger guppy. Ha! Which video was that for? Classification. Remember, we were talking about how a scientific
name is much more reliable than a common name? Especially a made up common name? Oh yeeeah. Sometimes I forget what Iâve drawn.
00:30 - 01:00 YouâŠforget? Well, every video has like 200 pictures. If I donât go back and watch the videos,
I tend to forget. And I mean, we have like more than 50 videos
soooo that would take a long time. I guess Iâd be more inclined to do that
if we had like a TL;DR version. A what? You know â too long, didnât read? A summary of sorts? Like a refresher just covering the
main points. A refresher⊠Now wait a minute, I didn't mean that
we actually need to create â But we DO.
01:00 - 01:30 I mean, weâve made quite a few videos now
in our biology playlist. And if someone was reviewing, we could have
this recap video, this stroll through the playlist! Yeah butâ Now this one video would be way longer than
our short videos, obviously, but it could be a useful study tool to connect the main
pieces of the content together. Granted, it would only have main points. Not everything. I guess that would be helpful...I just don't think we- Also, this stroll would be meant to be paused a lot. Thereâs so much vocabulary in biology. Weâll get Gus in on this; he can hold up
the âpauseâ sign so people know when to
01:30 - 02:00 pause the video so we can even ask the viewer
questions. And if the questions are difficult to answer,
that may be a good indicator to check out the video it corresponds to. Are you ready to stroll, Petunia? Uhhhh⊠Actually this is going to be kind of
a brisk stroll. And because it only covers a short part of
each concept, never forget biology is full of more exceptions and details than we can
cover. But thatâs great for more exploring. We start with characteristics of life. What makes an organism alive or not alive
anyway?
02:00 - 02:30 Life is difficult to define, and there are
exceptions when looking at characteristics of life. We went through some characteristics between
my bathtub grown pony (a long story) and a real pony, but we didnât want to put numbers
on the characteristics of life because we didnât want to suggest that these are the
only characteristics that one could argue. So hereâs your first pause question- can
you think of some characteristics of life to include? [PAUSE] We also noted in the video they could
certainly be titled differently, but here
02:30 - 03:00 they are! But this may get you thinking of whatâs
living and whatâs not. When studying biology, the study of life,
itâs important to understand the biological levels of organization. Meaning these levels start small. The smallest living unit being the cell---thatâs
part of the cell theory after all. The cell theory includes that the cell is
the smallest living unit in all organisms, that all living things are made up of cells,
and what else? [PAUSE] Ah, yes, that all cells come from
pre-existing cells.
03:00 - 03:30 So cells combined together make up tissues,
tissues make up organs, organs make up organ systems, organ systems are part of an organism! An individual organism. Individuals can be part of a population- theyâre
all the same species. A community---now youâre including different
species. Can you keep leveling up? [PAUSE] So the next larger level after community
would be ecosystemâŠat that level youâre
03:30 - 04:00 including abiotic factors which are nonliving
factors. Rocks. Or temperature. Next level is biome. And then with biomes combined, all parts of
the living world- the biosphere. Letâs focus on living organisms. Biomolecules are part of living organisms. We mentioned four of these major macromolecules---can
you name them here with their building blocks? [PAUSE] Carbohydrates, lipids, proteins, and
nucleic acids.
04:00 - 04:30 And here are their building blocks: monosaccharides,
fatty acid & glycerol, amino acids, and nucleotides. These building blocks are considered true
monomers for carbs, proteins, and nucleic acids. Can you think of some important functions
for any of these biomolecules? [PAUSE] Ok, Petunia, bring out some functions. These are just SOME functions---we wouldnât
exist without these large molecules of life! And their structures are---just beautiful----we
included a popular mnemonic to remember some
04:30 - 05:00 of the major elements they contain in their
structures as well. Most enzymes are made of proteins. Can you describe some of the vocabulary associated
with the enzyme? [PAUSE] Well, you can see this enzyme has
an active site where a substrate binds. Enzymes can speed up reactions. Enzymes have the ability to break down or
build up the substrates that they act upon. And ta-da: products! An example of why we care? Well, consider the specific, different digestive
enzymes that are specific for breaking down
05:00 - 05:30 fats or sugars or proteins. But enzymes typically have a specific temperature
and pH range that they need to be in to work correctly. And what happens if enzymes canât stay in
their ideal temperature or pH range? [PAUSE] Thatâs right, they can denature. Enzymes play a major role within cells. We have oh so many videos on cells that you
may wish to explore. We explain the differences between prokaryotic
cells and eukaryotic cells using the popular
05:30 - 06:00 mnemonic that âproâ rhymes with no and
âeuâ rhymes with do but what does that actually reference to? [PAUSE] Prokaryotic cells have no nucleus
nor the other fancy membrane bound organelles. But âeuâ rhymes with do and eukaryotic
cells do have a nucleus and other membrane bound organelles. Prokaryotes include bacteria and archaea. Eukaryotes include plants, animals, protists,
and fungi. Can you think of some things that prokaryotic
cells would have in common with eukaryotic
06:00 - 06:30 cells? [PAUSE] So just to name a few: DNA, cytoplasm,
ribosomes and a cell membrane would be included in both. In our âIntro to Cellsâ video, we explore
a lot of membrane-bound organelles that would be found exclusively in eukaryotes such as
the nucleus, endoplasmic reticulum, golgi apparatus, and mitochondria. Plant cells and animal cells can have some
differences between them as well. Letâs consider the cell membrane, also known
as a plasma membrane.
06:30 - 07:00 It is a part of all living cells so why is
it so important? [PAUSE] Remember all cells have a membrane---regardless
of whether or not they may have a cell wall. The membrane is a big deal for homeostasis
because it controls what goes in and out of the cell. The membrane is made up of these phospholipids
which have polar heads and nonpolar tails. Some molecules move passively through the
membrane without a need for added energy- thatâs called passive transport.
07:00 - 07:30 Simple diffusion---and facilitated diffusion
(which is through a protein)---are examples of passive transport. In those cases, solutes travel with the gradient. Active transport though can involve using
ATP to force molecules to move in the opposite direction of the gradient. So is this example simple diffusion, facilitated
diffusion, or active transport and how do you know? [PAUSE] Well itâs not active transport---you
can tell the molecules are traveling with
07:30 - 08:00 the gradient without a need for ATP. Itâs not simple diffusion because it does
seem to require a protein. Itâs facilitated diffusion! And thatâs passive. Water molecules can travel directly across
a semi-permeable membrane as they are so small, or they can travel through proteins called
aquaporins â that is more efficient. Water traveling through the membrane is called
osmosis. Like diffusion, water molecules do travel
from an area where there is a high concentration
08:00 - 08:30 of water molecules to an area of low concentration
of water molecules. But we mention thereâs another way to look
at osmosis. You can also look at it as water traveling
to areas where there is a higher solute concentration---as the water concentration is less there. So to determine the net movement of water
in osmosis, look for the hypertonic area, the areas of high solute concentration. A cell that is placed in a salty solution
can lose water because the net movement of
08:30 - 09:00 water is to the area of high solute concentration. One reason why you should not drink a lot
of salt waterâŠitâs very dehydrating. Check to see if you can explain this graphic
using the vocabulary hypertonic, hypotonic, and isotonic. [PAUSE] Letâs move beyond the membrane here and
take a look at these organelles: the mitochondria and chloroplasts. In eukaryotes, cellular respiration involves
the mitochondria and photosynthesis involves
09:00 - 09:30 the chloroplasts. Cellular respiration involves the breakdown
of glucose (sugar) to yield ATP. All organisms must make ATP in some way or
another. Yes, this includes plants. And amoebas. If oxygen isnât available, some organisms---like
bacteria or yeast---can do anaerobic respiration or fermentation to make their ATP. So what do these chemical equations [cellular
respiration and photosynthesis] have in common?
09:30 - 10:00 [PAUSE] Well one thing that is interesting
is that these reactants and products are switched here. Although that doesn't mean they are simply
the reverse of each other. Keep in mind that they have many different
steps within them that make them very different. Photosynthesis produces glucose (sugar) using
sunlight energy. Not everything can do photosynthesis. In eukaryotic cells, it occurs in the chloroplasts. So moving beyond the mitochondria and chloroplasts,
letâs take a look at this nucleus of a eukaryotic
10:00 - 10:30 cell. Guess whatâs in here? DNA! DNA is a nucleic acid, and nucleic acids are
one of the types of biomolecules. It contains your genetic information, and
your entire DNA code is found in almost all of your body cells, although genes can be
turned on or off in different cells. Letâs zoom into the monomer of DNA, a nucleotide. Nucleotides have a phosphate, deoxyribose,
and a nitrogenous base.
10:30 - 11:00 Which part of these do you think is critical
for determining genetic information? [PAUSE] Yep, the base. Well, that is, the sequence of them. And this mnemonic, âApples in the Tree;
Car in the Garageâ can help you remember that the bases adenine and thymine pair together. Cytosine and guanine pair together. DNA can be tightly coiled and condensed into
these units called chromosomes. The number of chromosomes in humans is 46. How many do you receive from each parent?
11:00 - 11:30 [PAUSE] Well, you would receive 23 from the
female parent and 23 from the male parent. Thatâs really important later on when we
talk about cell division, because chromosomes are more portable when it comes to cells dividing. Zooming back out, DNA is made up of two anti-parallel
strands. One strand runs 5â to 3â---and the other
strand runs 3â to 5â. Now, your body cells have to make copies of
their DNA. Why?
11:30 - 12:00 [PAUSE] When you make a new body cell- which
you make body cells for growth and repair- you need DNA to go into that new body cell
as that is its genetic material. Hence the need for DNA replication. Making more DNA. We have some major key player enzymes here-
can you remember what these key players do? [PAUSE] DNA must be unwound by an enzyme called
helicase. Primase is an enzyme that sets down primers. Primers are needed because another enzyme
called DNA Polymerase requires them in order
12:00 - 12:30 to start building. DNA Polymerase builds the new strand in the
5â to 3â direction only. And because of that directional building,
one of these new strands will be a lagging strand as DNA polymerase has to keep racing
up here next to where the unwinding is going on. This causes fragments on the lagging strand
known as Okazaki fragments. Ligase can eventually be involved in sealing
those fragments together.
12:30 - 13:00 So we mentioned that you have to replicate
DNA before you make new cells. Thatâs a controlled event that happens in
something known as the cell cycle. Do you remember the cell cycle phases, often
shown in a pie chart like this? [PAUSE] The cell cycle includes G1 (the cell
is growing), S phase (synthesis of DNA- thatâs when the DNA replicates), G2 (cell grows some
more to prepare for dividing), and then M phase which includes mitosis and cytokinesis.
13:00 - 13:30 G1, S, and G2 are all part of interphase so
the cell is not dividing during that time. But once it enters M phase, it divides. There are checkpoints that control whether
a cell can continue through the cycle. If a cell doesnât meet the checkpoint requirements,
it is either fixed or it must undergo apoptosis which means the cell destroys itself. This highly regulated cell cycle is controlled
by many different proteins- some that we mentioned included Cdk, cyclin, and p53.
13:30 - 14:00 Cancer cells are body cells that do not respond
correctly to these checkpoints and tend to divide out of control. They can also have other problems such as
making too much of their own growth factors, not anchoring properly, and not functioning
correctly. Now, we mentioned this cell cycle has M phase
which includes mitosis. So what is mitosis? Mitosis is part of cell division.
14:00 - 14:30 What kind of cells does it make? [PAUSE] In humans and many other organisms,
it makes identical body cells. Like skin cells making skin cells or stomach
cells making stomach cells. Great for growth of an organism or replacement
of worn out cells. During mitosis, chromosomes- which are condensed
forms of DNA and protein- can be moved more easily into the newly formed daughter cell. We went over the PMAT mnemonic to remember
the stages- prophase, metaphase, anaphase,
14:30 - 15:00 and telophase. Cytokinesis splits the cytoplasm and completely
divides the actual cell. Whatâs really easy to confuse with mitosis? Meiosis. Kind of wish they didnât sound so close. Anyway what kind of cells does meiosis make? [PAUSE] In humans and many other organisms,
meiosis makes gametes which are critical for sexual reproduction. Otherwise known as sperm and egg cells, these
gametes have half the number of chromosomes
15:00 - 15:30 as a body cell. Gametes are haploid---meaning they have one
set of chromosomes. Body cells are diploid---meaning they have
two sets of chromosomes. PMAT happens twice here in meiosis. You have your starting cell here which is
diploid. It goes through prophase I, metaphase I, anaphase
I, and telophase I. Then cytokinesis happens and it makes 2 cells. Then those cells go through prophase 2, metaphase
2, anaphase 2, and telophase 2.
15:30 - 16:00 After cytokinesis, this results in 4 haploid
cells as these sperm cells shown here. These cells are all different from each other
due to independent assortment and a process known as crossing over. So what is crossing over again and when does
it happen? [PAUSE] Crossing over happens during prophase
I and itâs when pairs of homologous chromosome can transfer information between each other.
16:00 - 16:30 So since meiosis is an important process for
making sperm and egg cells for sexual reproduction in humans and many other organisms, how is
this involved with the alleles and genes that a baby organism may inherit? Remember that in humans, a sperm cell has
23 chromosomes and an egg cell has 23 chromosomes. When they come together in a fertilized egg,
that is 46 chromosomes. Portions of the chromosomes are genes that
can code for specific traits.
16:30 - 17:00 Many traits actually involve multiple genes. Genes can come in varieties known as alleles. Alleles are forms of a gene. For example, we talk about the trait of tasting
or not tasting the chemical PTC. If treating this as a single gene trait, we
would say the gene is a PTC tasting gene. But the allele that could be on a chromosome,
which is a form of the gene, could be tasting (in this case we used a capital letter T to
indicate itâs a dominant allele) or non-tasting
17:00 - 17:30 (in this case, we used a lowercase letter
t to indicate itâs a recessive allele). In Mendelian inheritance, recessive alleles
are expressed if the dominant allele is not present. So someone who inherits a homozygous dominant
genotype of TT would have a phenotype that is PTC tasting. What would the phenotypes be of these other
two? [PAUSE] Someone who inherits a heterozygous
Tt genotype would have a phenotype that is
17:30 - 18:00 also PTC tasting. Only someone who inherits a homozygous recessive
tt genotype would have a phenotype that is non PTC tasting. Again, assuming it is a single gene trait,
and as we mentioned in the video- it may be more complex than that. So speaking of alleles and genes, itâs time
for the super brisk stroll through different
18:00 - 18:30 types of genetics we have covered. We started with basic Mendelian monohybrid
and dihybrid crosses. Could you explain, in your own words, how
to complete these Punnett squares and how to write out the genotype and phenotype ratios
of the offspring? [PAUSE] To get help with the answer to these
questions, check out the videos on these two topics specifically because there are multiple
steps to solving these. Then we talked about some non-Mendelian inheritance
including sex-linked traits and multiple alleles
18:30 - 19:00 â if these look unfamiliar, you might want
to review those videos as well. We also mentioned incomplete dominance and
codominance. What is the difference between incomplete
dominance and codominance? [PAUSE] This graphic may help- notice in codominance
both alleles are expressed! In incomplete dominance, you can see how the
phenotype can have an almost âin-betweenâ appearance of the two traits---there is not
complete dominance when both of these alleles
19:00 - 19:30 are present. Finally, we have a video on pedigrees. Pedigrees can be used to track a trait of
interest whether it be a sex-linked trait or an autosomal trait. In a pedigree, individuals that are female
are represented by circles, males are represented by squares, and individuals that have the
trait being tracked are represented by circles or squares that are shaded. Now, when weâre talking about these fascinating
traits, you might wonder---how does DNA actually
19:30 - 20:00 code for your traits? Well DNA can code for proteins and proteins
are involved with many traits. Proteins are involved in transport, in structure,
in acting as enzymes that make all kinds of materials, in protecting the bodyâŠand so
much more. Your eye color is due to proteins involved
in pigment production. So protein synthesis- that is making proteins-
is a big deal. Do you remember the two major steps in protein
synthesis? [PAUSE] First step is transcription---which
makes mRNA within the nucleus.
20:00 - 20:30 The second step is translation---which takes
place in the ribosome and makes a chain of amino acids known as a polypeptide. Proteins can be made up of 1 or more of these
polypeptide chains. We also mention other forms of RNA such as
rRNA and tRNA as well as how to read a codon chart to determine which amino acids are produced. Proteins often need folding to be fully functional-
we have a video clip on protein folding and
20:30 - 21:00 structure too. Now on the subject of this codon chart, you
will notice that the bases are read in threes to determine a specific amino acid. These three bases on the mRNA are known as
a codon. tRNA has an anticodon on it that complements
the mRNA codon. tRNAs also carry the corresponding amino acid. But what if there is a mutation in the DNA
or mRNA?
21:00 - 21:30 When we talk about mutations, we first mentioned
gene mutations. This can include substitution, deletion, or
insertion. Do you remember which of these are more likely
to result in a frameshift mutation? [PAUSE] A frameshift is a shift in the reading
frame. Bases are read in threes so a frameshift mutation
is more commonly caused by an insertion or deletion. If you add or delete a base, itâs possible
to change the entire reading frame depending
21:30 - 22:00 on where it occurs. With substitution, you typically would only
affect one codon. Now not every change in the base means the
amino acid will be different. See how all of these codons still code for
the amino acid leucine? We also discussed chromosomal mutations. Can you name and describe some chromosomal
mutations? [PAUSE] We mentioned duplication, deletion,
inversion, and translocation. As mentioned, mutations can be neutral.
22:00 - 22:30 They can also be harmful or, potentially,
even beneficial. But the mutations are random- the organism
doesnât will itself to mutate or have some certain trait. This is a good time to talk about natural
selection. Take these frogs, sitting on logs. They are all the same species. There can be variety though within the species-
due to processes like independent assortment and crossing over during meiosis or from mutations.
22:30 - 23:00 The frogs in this population with a darker
color blend into this particular environment more easily. A predator may have a higher chance of consuming
the lighter, easier to see green frogs. The darker green frogs may have more fitness
than the lighter frogs. Fitness, in the biological sense, is determined
by not how strong they are or how long they live---but by how many offspring they have. These darker green frogs pass down their DNA
to their offspring.
23:00 - 23:30 The new baby frogs will have DNA from their
parents. The lighter green frogs are being selected
against since they are easier to see in this particular habitat. Over a long period of time, you could expect
to see a higher frequency of darker frogs in the population. This mechanism of evolution is known as natural
selection, which acts on populations. So how does natural selection compare to genetic
drift? <PAUSE> Well both genetic drift and natural
selection are mechanisms of evolution.
23:30 - 24:00 In natural selection, organisms with traits
that result in high reproductive fitness tend to be more frequent in a population over time. But with genetic drift, the organisms that
survive and have offspring were randomly selected---they are not necessarily more biologically fit-
instead itâs more that the organisms won the game of chance from an event. Check out the bottleneck effect and founder
effect which are forms of this.
24:00 - 24:30 We mention in our natural selection video
an example involving bacteria and antibiotic resistance that continues to be a great concern
in our world. But letâs talk more about bacteria in general. Bacteria are unicellular prokaryotes; some
can make their own food (theyâre autotrophs) and some consume organic material (theyâre
heterotrophs). Being prokaryotes, they donât have a nucleus
or other membrane-bound organelles, but they still have genetic material, cytoplasm, and
ribosomes.
24:30 - 25:00 Bacteria can come in a range of shapes. Bacteria often get a reputation for being
bad pathogens, and there are many that can be, although not all bacteria are harmful. Bacteria can also be very helpful for organisms
and ecosystems. Can you think of some examples of bacteria
being helpful? <PAUSE> Some examples of helpful bacteria
roles include breaking down food in our digestive system, acting as decomposers, making some
foods that we eat, and fixing nitrogen for
25:00 - 25:30 plants. But as for harmful bacteria, they can be treated
with antibiotics. Examples of bacterial infections include strep
throat, tooth decay, or tetanus. When we start thinking about bacteria, our
minds may wander to viruses. How are bacteria and viruses similar and how
are they different? <PAUSE> If you watch our viruses video, you
will hear some reasons why viruses are not
25:30 - 26:00 considered to be living organisms although
debate still exists on calling them non-living. Unlike bacteria, viruses are not prokaryotes;
viruses donât even consist of cells. But viruses do have genetic material (DNA
or RNA). Viruses typically have a protein coat known
as a capsid. Some viruses have envelopes, and some diseases
that viruses cause include the common cold, HIV, or influenza (the flu).
26:00 - 26:30 Unlike bacteria though, viruses donât respond
to antibiotics. While bacteria can reproduce by splitting
in something called binary fission, viruses actually require a host to reproduce. Viruses reproduce using the lytic or lysogenic
cycle- definitely something to revisit if you have forgotten. While viruses are not considered to be living
organisms, bacteria are. So are archaea, protists, fungi, plants, and
animals.
26:30 - 27:00 We mention that archaea are unicellular prokaryotes
and many can live in extreme environments; they can be either autotrophs or heterotrophs. Protists are mostly unicellular but can be
multicellular- this diverse group can be made up of autotrophs or heterotrophs. Fungi are typically multicellular but they
can be unicellular. Fungi are heterotrophs; many can act as decomposers. Weâll get to plants and animal systems a
bit later. So how do we classify living organisms?
27:00 - 27:30 Well, first of all, all of life can be organized
into three domains. Can you recall what those domains are? <PAUSE>
Those domains are Bacteria, Archaea, and Eukarya. Consider looking at the classification video
to refresh your memory of characteristics of these domains. But we can get more specific than domains,
right? Can you remember those taxonomy levels that
come after domain? <PAUSE> They are Kingdom, Phylum, Class, Order,
Family, Genus, and Species.
27:30 - 28:00 And this was our mnemonic to help you remember,
but you may have one that is more memorable. The thing about classification is that it
is changing as we learn more about relatedness from DNA evidence. Scientific names tend to be able to be used
everywhere, often having Latin or Greek roots, and they are definitely more reliable than
common names which can vary by language or location. OrâŠin this caseâŠbe completely made up. Letâs take some time to focus on a kingdom
that provides a significant amount of the
28:00 - 28:30 oxygen that we breathe. A talented kingdom of autotrophs, which means,
they make their own food. Plants. And if they are going to make their own food
using photosynthesis, they are definitely going to need to have structure that helps
them do so. To do photosynthesis, plants need water. How do they get water? Nonvascular plants get their water by osmosis. Kind of like soaking up water like a sponge. How is that different from a vascular plant? <PAUSE> Vascular plants have two major types
of vessels.
28:30 - 29:00 The xylem, which carries water, and the phloem,
which can carry photosynthesis products such as sugar, throughout the plant. How about light? We mention that plant cells have chloroplasts
to capture light energy. To do photosynthesis, plants need carbon dioxide. Many plants have these fascinating little
openingsâpores really---called âstomata.â Stomata have a major role in gas exchange. Gases like CO2 can flow in through these openings.
29:00 - 29:30 Guard cells can control the opening and closing
of the stomata. When might stomata need to be closed? <PAUSE> One example is on a very hot day when
the plant has low water. So staying on the topic of plants, how do
they reproduce? Well, many plants can reproduce asexually
as mentioned with my spider plants. But many plants, spider plants included, can
reproduce sexually. We only covered sexual reproduction in flowering
plants at the time of this stroll, otherwise
29:30 - 30:00 known as reproduction in angiosperms. Angiosperms typically have petals to attract
pollinators and many offer nectar to attract them as well. Many angiosperms have sepals which protect
the developing flower bud. Ok, so do you remember the male and female
parts that can be within a flower structure? <PAUSE> Male parts of the flower include the
anther and filament---this whole thing here is the stamen.
30:00 - 30:30 Female parts of the flower include the stigma,
style, and ovary---this whole thing here is the pistil. Can you describe the pollination and fertilization
process in angiosperms using those terms? <PAUSE> Simplified a bit, pollen is brought
from an anther to the sticky stigma. Possibly by a pollinator. Thatâs pollination. Next comes fertilization. For this to happen, a pollen tube is formed. A generative cell from within the pollen can
divide into two sperm cells which can travel
30:30 - 31:00 down the style to the ovary, into an ovule,
where one sperm cell will fertilize an egg---giving rise to a zygote. Inside the ovule, another sperm cell will
fertilize two polar nuclei which gives rise to the endosperm. The endosperm provides food for the baby plant. Because this fertilization process involved
sperm cells joining two different things (the egg and the polar nuclei)---we call this double
fertilization. These fertilized ovules can develop into seeds. The ovary can give rise to a fruit- and that
fruit can be very useful for helping the seeds
31:00 - 31:30 get dispersed. But, while angiosperms bear fruit- keep in
mind it may not be how you might imagine a fruit. So we talked about plant structure and how
some plants reproduce. We already mentioned how plants provide a
lot of the oxygen that we breathe. But itâs not just about oxygen. Plants are also critical as part of food chains
and food webs. As autotrophs, plants are producers. If you remember, in a food chain, we start
with producers.
31:30 - 32:00 Then we move into the consumers, which are
heterotrophs. Heterotrophs have to consume other things. So we have primary consumers, secondary consumers,
tertiary consumers---we could keep going. The arrows point to the direction of the energy
flow. We could arrange this into an energy pyramid. The producers at the base here---in trophic
level 1---- actually contain the most energy. The primary consumers here---in trophic level
2---actually only receive approximately 10% of the energy from the level below.
32:00 - 32:30 Meaning, letâs say you have plants here
that had 10,000 kilocalories of energy. Can you complete the rest of the pyramid with
approximately how much of the energy would be within each trophic level? <PAUSE> Well the next level here---the primary
consumers in trophic level 2, would only receive 1,000 kilocalories of energy. The secondary consumers in trophic level 3,
would receive 100 kilocalories of energy! Tertiary consumers in trophic level 4 would
receive approximately 10 kilocalories of energy.
32:30 - 33:00 Energy can be lost as heat or undigested. Ecosystems typically do not have a single
food chain. Instead, they tend to have a food web. A food web is made up of multiple food chains
that interact together. This can show the importance of biodiversity:
the variety of organisms living in a given area. Biodiversity can contribute to the sustainability
of a community. But how do they develop?
33:00 - 33:30 This takes us to our ecological succession
video. Ecological succession is a process---over
time--- of organisms in an ecological community. In primary succession, the area this is happening
in generally is brand new without soil. An example could be a volcano lava flow that
has cooled and left behind this new area with no soil present. Usually you have a pioneer species, which
is a name for the species that colonizes first. Lichen or moss for example.
33:30 - 34:00 After pioneer species colonize the area, they
slowly break down rock into smaller, more plant friendly substrate---and over time,
contributing more organic matter in newly formed soil which will support plants. Small vascular plants like grasses can come
in. Shrubs can follow. Then trees. Animals continue to move into the area. How long this takes can varyâŠbut itâs
often hundreds of years before you get a climax community going. So how is this different from secondary succession?
34:00 - 34:30 <PAUSE> With secondary succession, youâre
talking about an area that once had plants and animals and an ecological community going
on. But then there is an ecological disturbance
such as a forest fire or human activity. The soil is still there and thatâs kind
of the big key point here, because your initial species starting out could be small plants
as there is already soil there. Secondary succession can then follow a similar
sequence to primary succession after that point. See our video for more details and an understanding
of why this succession sequence tends to happen.
34:30 - 35:00 Communities make up ecosystems, and in order
for these ecosystems to function---weâve got to have cycling. You probably learned about the water cycle
in elementary school- learning about the carbon cycle and the nitrogen cycle tends to be explored
later on in junior high or high school. So letâs recap that from our Nitrogen and
Carbon cycle video. Carbon is often known as a building block
in life: you will find it in the four big
35:00 - 35:30 biomolecules. Can you think of examples where you might
find carbon? <PAUSE> Some examples: Carbon is dissolved
in the ocean. It is in rocks and fossil fuels. It is in living organisms. It can be in the atmosphere. Consider carbon dioxide in the atmosphere. It is taken in by organisms that perform photosynthesis. If the photosynthetic organism is eaten by
an animal, it becomes part of that animal too. And the animal that eat that animal. Both the plants and animals do cellular respiration
which releases carbon dioxide.
35:30 - 36:00 When the plants and animals die, the carbon
can be released and stored in sediment. Over a very long time, they can even be converted
into fossil fuels. The burning of fossil fuels produces carbon
dioxide, and this has also led to the concern of excessive carbon dioxide in the atmosphere. Now for nitrogen. Nitrogen is important in building proteins
and nucleic acids. Letâs look at how it can cycle. Nitrogen can be found in the atmosphere, but
it needs to be âfixedâ before it can be
36:00 - 36:30 used well. Some plants have nitrogen fixing bacteria
living in their roots---the nitrogen is fixed by these bacteria into a form of nitrogen
known as ammonia and ammonium. Nitrifying bacteria in the soil can convert
the ammonium to nitrates and nitrites, forms of nitrogen that plants can also easily use
and assimilate. Animals can eat those plants and obtain nitrogen. When both plants and animals decompose, decomposers
help return ammonia and ammonium to the soil
36:30 - 37:00 in a process known as ammonification where
it can be reused again. There are also denitrifying bacteria! In denitrification, they can convert nitrates
and nitrites back into nitrogen gas. This is just one example of cycling, but keep
in mind that this happens in both aquatic and terrestrial environments. So you can see thereâs a balance with these
elements and living organisms in an ecosystem. Letâs talk about some of the ecological
relationships among living organisms.
37:00 - 37:30 In the ecological relationships video, I mention
my fascination with antlions. Antlions are predators of ants. Ants are their prey. This is known as predation. Antlions have to compete with other predators-
like this jumping spider for example. Competing for a food resource is an example
of competition. We also mentioned three symbiotic relationships:
symbiotic relationships are specific types of relationships where different species live
together. Can you recall what occurs in the three symbiotic
relationships that we mention: commensalism,
37:30 - 38:00 parasitism, and mutualism? <PAUSE> In commensalism, one organism benefits
and the other is neither helped nor harmed: itâs neutral. Many barnacle species can attach themselves
to moving things. On a free whale ride, this barnacle can get
access to food since itâs a filter feeder and the whale may travel to nutrient rich
waters. However, in this example with this particular
whale and these barnacles, the whale was neither helped nor harmed. In parasitism, one organism benefits and the
other one is harmed by a parasite.
38:00 - 38:30 Parasites can live inside or on their host. Mutualism is an example of a symbiotic relationship
where both organisms involved benefit. Our example had been an acacia tree being
protected by acacia ants. The acacia tree provides a home- and possibly
nutrients. But you know, one of my favorite examples
of mutualism is the good bacteria. They can live in our digestive system and
help us digest our food.
38:30 - 39:00 So speaking of systems in the human body-
our short video on that topic only goes into basic functions of eleven body systems. Here they are up here for you in alphabetical
order---can you give a general function for each of these? <PAUSE> The circulatory system helps transport
gases and nutrients. The digestive system is involved with both
the mechanical and chemical breakdown of food. The endocrine system is involved with producing
important signals known as hormones. The excretory system is involved with excreting
waste material as done by the kidneys or skin.
39:00 - 39:30 The immune/lymphatic system helps defend our
body against pathogens such as viruses and harmful bacteria. The integumentary system---long, fancy word
for a large organ- your skin---can protect against water loss and serve as a barrier. The muscular system is involved with allowing
for movement. The nervous system coordinates both voluntary
and involuntary responses. The reproductive system allows for the ability
to reproduce.
39:30 - 40:00 The respiratory system is involved with gas
exchange. And the skeletal system is critical for structure
and support. Those are very basic functions mentioned and,
of course, this doesnât include structures. But the big takeaway we hope you have from
our body systems video is that these systems donât work in isolation! They work together. If youâre nervous about a test---which we
hope youâre not because we have confidence that youâre going to do great---but if you
were nervous, you can get an adrenaline rush. Your endocrine system secretes adrenaline,
a hormone, that can cause your heart---involved
40:00 - 40:30 in the circulatory systemâto speed up its
beating. Your breathing rate, which is involved with
your respiratory system, can increase. These are all systems working together. And thatâs relevant for the end. Because in this stroll through our playlist,
youâve seen how weâve been connecting these concepts together. Because thatâs the thing that is so cool
about biology: itâs all connected. We hope this video helps you to identify your
strengths and areas that you might want to go back and explore.
40:30 - 41:00 We also hope that you recognize that beyond
any test youâre studying: it is so important to be able to answer, âWhy does this content
matter?â If there is a topic in this video that still
doesnât seem to matter beyond just studying for a test---please check out our full video
on that topic---because thatâs something that we really try to address in each and
every video. Donât forget we also have a video with study
strategies that you may want to check out, and we have helpful GIF animations and comics
on our website that you might find useful. AndâŠif you are studying for something bigâŠ
it is our sincere amoebic wish that you will
41:00 - 41:30 feel confident about your learning. Well, thatâs it for the Amoeba Sisters,
and we remind you to stay curious.