front 1 multicellularity | back 1 complex multicellular organisms can have upwards a trillion more cells |
front 2 complex multicellularity | back 2 has occurred upwards (evolved) to half a dozen times |
front 3 prokaryotic organisms | back 3 unicellular, however live in colonies (filaments) |
front 4 bacteria | back 4 does not develop macroscopic bodies with functionally differentiated tissues |
front 5 simple multicellular organisms | back 5 36 of the 119 major groups of eukaryotes are multicellular (filaments, hollow balls, or sheets of little-differentiated cells) |
front 6 the 83 unicellular organisms properties | back 6 eat other microorganisms or ingest small organic particles, live suspended in water columns, or are parasites within other organisms |
front 7 properties or simple multicellularity organisms | back 7
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front 8 coenocyte organisms | back 8 multinucleate cell which can result from multiple nuclear divisions without accompanied cytokinesis |
front 9 six groups have evolved coenocytic organization | back 9 nuclei evolved many times, not divided into individual cells, and results in very large cells with many nuclei |
front 10 pros and cons of coenocyte multicellularity | back 10
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front 11 complex multicellularity | back 11 land plants, animals, red/brown algae, fungi |
front 12 common features | back 12
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front 13 evolution occurred 6 times | back 13
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front 14 diffusion (important mechanism to transport substances in multicellular organisms) | back 14 random motion of molecules with net movement from areas of high to low concentration (entropy shiet) |
front 15 bulk transport (important mechanism to transport substances in multicellular organisms) | back 15 once an organism gets large enough diffusion doesn’t cut it for the movement of material; Bulk Transport is any means that are used to move material at rates higher than that of diffusion! |
front 16 diffusion limitations | back 16
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front 17 sponges | back 17 circumvent this by placing metabolically active cells in close contact with their external environment, hence their size |
front 18 jellyfish | back 18 have thin layers of metabolically active tissue above inactive material |
front 19 bulk transport in humans | back 19 we use a high ration of surface area to volume in lung tissue in order to bypass diffusion restrictions. We pump blood through the circulatory system to oxygenate tissues! |
front 20 bulk transport in plants | back 20 vascular tissues transport water from roots to photosynthetic sources, wherein other vascular tissues transport sugar from the leaves to other parts |
front 21 bulk transport in fungi | back 21 rely upon osmosis to pump material (hyphae) |
front 22 bulk transport in animals | back 22 pumping blood through the circulatory system to oxygenate tissues that are great distances from the lungs, during digestion, and during hormone signaling |
front 23 main components required for complex multicellularity (functional key) | back 23
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front 24 cell adhesion in animals | back 24 cadherins, integrins, and addn. Transmembrane proteins provide the molecular mechanisms for adhesion |
front 25 cell adhesion in plants | back 25 use adhesion molecules called pectins (where we get jelly from) |
front 26 choanoflagellates | back 26
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front 27 cell adhesion in choanoflagellates | back 27 signals caused by their pray (bacteria) , form a multicellular structure, support hypothesis that they facilitate predation |
front 28 communication | back 28 molecular signals found in animals, plants, and some protistan relatives |
front 29 gap junctions | back 29 protein channels allows ions and signaling molecules to move from one cell into another, help cells communicate with neighbor cells and targeted (specific) cells |
front 30 plasmodesmata | back 30 intracellular strands of cytoplasm that extend to neigh cell and allow same type of cell communication, permit signaling molecules to pass between cells (important step in evolution of complex multicellularity) |
front 31 complex multicellularity involves the | back 31 genetic programming of cells so that they can differentiate in space (3D organism) |
front 32 genes are turned off or on depending | back 32 molecular signals the cell receives number of gene families play a role in life cycle differentiation |
front 33 Plant multicellularity | back 33 plant cell wall (cellulose) -> structural and mechanical support, enables trees to grow, also for plant rigidity (developmental consequences)
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front 34 Animal Multicellularity | back 34 no cell wall, can move with each other, sperm + egg -> fertilized egg -> w/mitosis -> blastula (ball of undifferentiated cells) -> blastula migration, cell reorganization -> gastrula (hollow ball, folds inward at one location to form layered structure)
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front 35 Evolution of Complex Multicellularity | back 35 natural selection favors increase/diversification of genes regulating growth/development (more complex over time) |
front 36 Fossils do not preserve molecular features, but can show phylogenetic pattern | back 36 Complex multicellularity from 575-555 mya, oldest being rangeomorphs (found in newfoundland) showing no evidence of head or tail, no limbs, no opening as mouth , appeared to be very simple organisms that obtained both carbon and oxygen by diffusion Same time, preserved tracks showing movement, a bit later, animals get more complex(identifiable heads, tails, etc.) |
front 37 Oxygen enrichment vs. first appearance of complex animals | back 37 more oxygen = greater size permitted, greater size leads to evolution of bulk transport and signaling = even larger size allowance |
front 38 Complex multicell and land plants | back 38 origin about 465 mya (much later than marine animals and algae) Two challenges led to later evolution:
400 mya, plants evolved specialized tissue for bulk transport, plant biomass increased, created new opportunities for multicell organisms, specifically fungi |
front 39 Regulatory Genes (played a role in multicellular complex evolution) | back 39
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front 40 Distalless | back 40 regulatory genes account for coloration, mutation in genes creates variation within species, Distalless responsible for “eye” pattern on wing (linked to protein GFP), expression of gene traced to GFP visualization (affects number and size of eyes) |
front 41 Evo-Devo (evolutionary-developmental biology) | back 41 new field, growing understanding of how developmental genes underpin evolutionary change, illuminates long-suspected relationship between individual development and patterns of evolutionary relatedness among different species |