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Lophotrochozoans are protostomes or deuterostomes
Protostomes (they develop the mouth first in embryonic development)
Two larval features of lophotrochozoans
Trochophore larva (a tiny swimming larva covered in cilia); Lophophore (a ring of ciliated tentacles used for feeding)
What does the lophophore do
Uses cilia to create water flow and trap food particles
General traits of flatworms (platyhelminths)
Flat body (helps with diffusion); blind gut (only one opening); no circulatory or respiratory system; bilateral symmetry; simple nervous system
Why parasitism is considered an adaptation
Parasites evolved special body structures and life cycles through natural selection to live off hosts (not a choice, it's built into them)
Has parasitism evolved once or many times
Many times independently in different groups
Why many parasites use multiple hosts
Helps them spread, access more resources, avoid immune systems, and reach their final host
Cestode (tapeworm) adaptations
Scolex (head) with hooks/suckers to attach; no digestive system (absorb food through body); body segments full of reproductive organs
Where most mollusks live
Mostly in marine (ocean) environments
Why oceans have more mollusks
Oceans are stable, have lots of habitats, and have existed longer → more time to evolve diversity
3 main parts of a mollusk body
Muscular foot (movement); visceral mass (organs); mantle (covers body and can make shell)
Common mollusk evolutionary change
Loss or reduction of shell (like in slugs and octopus)
Phenotype vs genotype loss
Losing a trait doesn't mean the gene is gone—it might just be turned off
Cone snail hunting adaptation
They shoot a harpoon-like tooth that injects venom
How cone snail venom works
Contains strong neurotoxins that quickly paralyze prey
Cone snail toxin characteristics
Made of small proteins; each species has a mix ("cocktail"); targets specific nerve channels
Why cone snail venom is so diverse
Genes duplicated and mutated over time → lots of different toxins
Why cone snail venom is useful to humans
Very specific → good for making drugs (ex: pain medication like Prialt)
Did mollusks evolve one eye type or many
Many different eye types evolved (cup eyes, camera eyes, etc.)
Why similar eyes evolve multiple times
Same genes can be reused and slightly changed → leads to similar solutions (convergent evolution)
Echinoderm symmetry
Start as bilateral larvae but become radial as adults
Why echinoderm symmetry is important
Shows evolution changed body plan from bilateral ancestor
Echinoderm key features
Water vascular system (movement); tube feet; hard internal skeleton made of calcium plates
Pedicellariae
Small pincer-like structures that clean, protect, and catch tiny prey
Cephalochordates
Basic chordates (like lancelets) that share traits with us but lack a true brain and complex organs
Chordate defining traits
Notochord; dorsal hollow nerve cord; pharyngeal slits; post-anal tail
Why tunicates are interesting
Their larvae look like chordates but adults lose most of those traits
Escape variants
Viruses mutate so they can avoid the immune system and infect again
What fast-evolving pathogen trees look like
Long trunk with short branches (most lineages die quickly)
Red Queen hypothesis
Hosts and pathogens are constantly evolving against each other like an "arms race"
Why sex is important (Red Queen)
It creates genetic variation so organisms can keep up with evolving pathogens
MZT (maternal to zygotic transition)
The embryo switches from using mom's mRNA to its own DNA
Why MZT matters
Important for proper development
Lott lab discovery
There are core genes used in development that are conserved across species
Maternal vs zygotic genes
Maternal = more similar across species; zygotic = more different
DMIs (Dobzhansky-Muller incompatibilities)
When genes that evolved separately don't work together in hybrids
Why DMIs happen
Mutations are fine separately but clash when combined
Orr-Turelli model of DMIs
Depends on number of mutations, how they interact, and how harmful they are
Do more mutations always mean more DMIs
No—depends if mutations interact
Many mutations but no DMI
Mutations don't affect each other
Few mutations but strong DMI
Mutations strongly interfere with each other
Haerty & Singh finding
Reproductive genes (especially male ones) evolve fast and cause hybrid problems
Burton lab examples
Conflicts between mitochondrial and nuclear DNA; and between sex chromosomes and autosomes
Hybrid problems
Stress response activated, immune issues, low fertility
Polyploidy in plants
Extra sets of chromosomes can instantly create a new species
Why mules are infertile
Odd number of chromosomes (63) → can't pair in meiosis
Do all extra chromosomes have same effect
No—some survivable (Down syndrome), others usually fatal
Gonochore vs hermaphrodite
Gonochore = separate sexes; hermaphrodite = both sexes
Simultaneous hermaphrodite
Both sexes at the same time
Sequential hermaphrodite
Changes sex during life
Gynandromorph
Organism that is half male and half female
How meiosis creates variation
Independent assortment; crossing over; random fertilization
Size advantage model
Being one sex is better at a certain size, so organisms may change sex
Ecdysozoans
Animals that molt their outer layer (ex: arthropods, nematodes)
Key ecdysozoan trait
They have a cuticle (outer covering) that they shed to grow
Early ecdysozoan body plan
Worm-like with no appendages and fluid-based skeleton
Modern ecdysozoans
Segmented bodies, appendages, and chitin cuticle
Tardigrades
Crazy survival ability (cryptobiosis = metabolism stops)
Arthropod exoskeleton
Made of chitin and acts like armor
Why arthropods are so successful
Strong/light exoskeleton, flexible joints, waterproofing layer
Arthropod diversity
Most diverse animal group
Major arthropod groups
Crustaceans, chelicerates, insects, myriapods
Insect body plan
Head, thorax, abdomen
Where insect legs are attached
Thorax
Complete metamorphosis
Egg → larva → pupa → adult
Insect advantage
First animals to fly
Chelicerates
Arthropods with special mouthparts (chelicerae)
Chelicerae function
Used for grabbing or injecting venom
Spider silk
Produced in abdominal glands and released through spinnerets
Spinnerets
Movable structures that control silk release
Why silk is strong
Combines strength and stretch (toughness)
Spider venom
Used to capture prey and defend
Asexual reproduction
One parent, no gametes, fast population growth
Budding
New organism grows off parent (like a bump)
Fragmentation
Body breaks and each piece becomes a new organism
Sexual reproduction
Two parents and gametes → genetic variation
Iteroparous organisms
Reproduce many times
Semelparous organisms
Reproduce once then die
Sexual dimorphism
Males and females look different
Protogynous species
Female → male when needed
Protandrous species
Male → female when needed
Parthenogenesis
Mix of asexual and sexual reproduction
Spider web evolution
Many web types evolved independently (orb, sheet, trapdoor, etc.)
Spider venom evolution
Gene duplication created many different toxins
Human uses of spider silk
Medical materials like sutures
Human uses of venom
Medicines and insecticides
Sexual dimorphism
When males and females of the same species have different traits
Sex-specific trait
A trait that appears in only one sex (ex: only males or only females)
Example of a sex-specific structure
Modified bristles (like sex combs) used for mating behavior
Function of male-specific structures
Often help with mating success (grasping, attracting, competing)
Ancestral condition (before evolution of a new trait)
Males and females look similar with no special structures
Derived condition (after evolution)
One sex develops a new specialized structure
Main genes involved in sex-specific traits
Hox genes (like Scr) and sex-determination genes (like doublesex)
Hox genes
Genes that control body part identity (ex: which leg is which)
Role of Hox genes in traits
They define where a structure can form on the body
Sex-determination genes
Genes that control whether cells develop male or female traits
Doublesex gene function
Turns on male traits and turns off female traits (or vice versa)
Is doublesex active in all cells
No—only in cells that need to develop sex-specific traits
Why this matters
Only certain body parts become sexually dimorphic
Why most cells don't show sex differences
They don't express sex-determination genes like doublesex