a. Bindin ![]() |
||
b. Vitelline envelope ![]() |
||
c. Cortical granules ![]() |
||
d. Dynein ![]() |
a. Bindin ![]() |
||
b. Vitelline envelope ![]() |
||
c. Cortical granules ![]() |
||
d. Dynein ![]() |
a. The activation of egg metabolism ![]() |
||
b. The primary binding of sperm to the zona pellucida ![]() |
||
c. The secondary binding of sperm to the zona pellucida ![]() |
||
d. The absorption of nutrients into the egg’s cytoplasm ![]() |
a. The activation of egg metabolism ![]() |
||
b. The slow reaction to prevent polyspermy ![]() |
||
c. The fast reaction to prevent polyspermy ![]() |
||
d. The binding of sperm and egg ![]() |
a. Hertwig and Fol ![]() |
||
b. Leeuwenhoek ![]() |
||
c. Aristotle ![]() |
||
d. Both B and C ![]() |
a. It is most important in species with external fertilization. ![]() |
||
b. It involves chemicals that have powerful effects at very low concentrations. ![]() |
||
c. It involves chemicals that are present in sperm at higher and higher doses as they mature. ![]() |
||
d. It involves the creation of a concentration gradient. ![]() |
a. The blood vessels of chicks form before the heart. ![]() |
||
b. The intestinal tube forms by the folding of tissue that was once flat. ![]() |
||
c. Each generation organisms are created anew. ![]() |
||
d. Embryonic organs develop from different tissues than their adult counterparts. ![]() |
a. Fertilization occurs as a fusion of a sperm and an egg. ![]() |
||
b. Cleavage occurs through either the entire egg dividing into smaller cells or a small portion of the egg dividing and forming the embryo. ![]() |
||
c. All animals, even mammals, derive from eggs. ![]() |
||
d. The intestinal tube forms by the folding of tissue that was once flat. ![]() |
a. Calcium ![]() |
||
b. Sodium ![]() |
||
c. Potassium ![]() |
||
d. Hydrogen ![]() |
a. Yes, because you will ensure that these proteins are able to function properly in binding sperm to the egg. ![]() |
||
b. No, because these proteins are only marginally involved in chemoattraction and will not affect fertilization success. ![]() |
||
c. No, because while you might increase fertilization success, you will block the egg’s ability to prevent polyspermy. ![]() |
||
d. Yes, because you will ensure that the cumulus does not thicken too early in fertilization. ![]() |
a. Vertebrate embryos in their early stages of development are difficult to tell apart. ![]() |
||
b. As the embryos of “higher” (more recently evolved) vertebrate species develop, they resemble the adult stages of various ancestral forms. ![]() |
||
c. Early vertebrate embryos all have the same type of skin, only later growing scales, hair, or feathers. ![]() |
||
d. Vertebrate embryos resemble one another early in development but later do not resemble other species, only their own. ![]() |
a. RNA processing ![]() |
||
b. Post-translational modification ![]() |
||
c. Transcription ![]() |
||
d. Translation ![]() |
a. RNA processing ![]() |
||
b. Post-translational modification ![]() |
||
c. Transcription ![]() |
||
d. Translation ![]() |
a. RNA processing ![]() |
||
b. Post-translational modification ![]() |
||
c. Transcription ![]() |
||
d. Translation ![]() |
a. Promoters ![]() |
||
b. Enhancers ![]() |
||
c. Transcription factors ![]() |
||
d. Introns ![]() |
a. Pax6 works in combination with Sox2 to allow the transcription of the gene in the appropriate tissues. ![]() |
||
b. The lens gene is transcribed but is prevented from transport into the cytoplasm; it remains in the nucleus until it is degraded. ![]() |
||
c. The gene is stabilized in cells fated to become the lens by the addition of a longer poly(A) tail. ![]() |
||
d. The enzyme deltaEF1 phosphorylates the otherwise-inactive crystalline-lens protein, after it has been translated. ![]() |
a. Northern blot ![]() |
||
b. Making a quail-chick chimera ![]() |
||
c. In situ hybridization ![]() |
||
d. PCR ![]() |
a. Northern blot ![]() |
||
b. Making a quail-chick chimera ![]() |
||
c. In situ hybridization ![]() |
||
d. PCR ![]() |
a. Genetic knockout ![]() |
||
b. Insertion via retroviral vector ![]() |
||
c. Making a transgenic mouse ![]() |
||
d. Antisense RNA ![]() |
a. Northern blot ![]() |
||
b. Making a quail-chick chimera ![]() |
||
c. In situ hybridization ![]() |
||
d. PCR ![]() |
a. Genetic knockout ![]() |
||
b. Insertion via retroviral vector ![]() |
||
c. In situ hybridization ![]() |
||
d. PCR ![]() |
a. Genetic knockout ![]() |
||
b. Insertion via retroviral vector ![]() |
||
c. In situ hybridization ![]() |
||
d. PCR ![]() |
a. Autonomous ![]() |
||
b. Syncytial ![]() |
||
c. Semelparous ![]() |
||
d. Conditional ![]() |
a. Autonomous ![]() |
||
b. Syncytial ![]() |
||
c. Semelparous ![]() |
||
d. Conditional ![]() |
a. Sea urchins ![]() |
||
b. Amphibians ![]() |
||
c. Birds ![]() |
||
d. Mammals ![]() |
a. It serves as a buffer, preventing cells below it from affecting cells above it. ![]() |
||
b. It has no function and occurs as a byproduct of the cleavage process. ![]() |
||
c. It induces the formation of the blastopore. ![]() |
||
d. It forms the gut in later development. ![]() |
a. Veg1 ![]() |
||
b. β-catenin ![]() |
||
c. Veg2 ![]() |
||
d. Micromeres ![]() |
a. During early cleavage, stored maternal proteins and mRNAs control development, and virtually no activity is undergone by the zygote’s genome. ![]() |
||
b. Division occurs without any increase in the volume of the cell. ![]() |
||
c. The initiation of cleavage is inhibited by MPF. ![]() |
||
d. All of the above ![]() |
a. It provides nutrients for developing embryos. ![]() |
||
b. It helps determine the pattern and distribution of cleavage. ![]() |
||
c. It inhibits cleavage. ![]() |
||
d. None of the above ![]() |
a. Compaction ![]() |
||
b. Rotational cleavage ![]() |
||
c. Early activation of the zygotic genome ![]() |
||
d. Asynchronous cell division ![]() |
a. The animal pole ![]() |
||
b. The vegetal pole ![]() |
||
c. Neither has yolk ![]() |
||
d. Both have the same amount of yolk ![]() |
a. Your eggs undergo meroblastic cleavage. ![]() |
||
b. Your eggs divide at a slower rate than those with a great deal of yolk. ![]() |
||
c. Your young go through a larval stage in which they eat a great deal. ![]() |
||
d. Your eggs undergo discoidal cleavage. ![]() |
a. Autonomous ![]() |
||
b. Syncytial ![]() |
||
c. Semelparous ![]() |
||
d. Conditional ![]() |
a. Frog and avian gastrulation events are nearly identical. ![]() |
||
b. Mammalian gastrulation events are very similar to avian and reptilian events in spite of their eggs no longer having large amounts of yolk. ![]() |
||
c. Gastrulation events in amphibians are initiated by the same cell signals that are used in sea-urchin gastrulation. ![]() |
||
d. Gastrulation in birds goes through stages that reiterate the development of all earlier vertebrate groups. ![]() |
a. Involution ![]() |
||
b. Ingression ![]() |
||
c. Delamination ![]() |
||
d. Epiboly ![]() |
a. Involution ![]() |
||
b. Ingression ![]() |
||
c. Delamination ![]() |
||
d. Epiboly ![]() |
a. Involution ![]() |
||
b. Ingression ![]() |
||
c. Delamination ![]() |
||
d. Epiboly ![]() |
a. Invagination ![]() |
||
b. Involution ![]() |
||
c. Ingression ![]() |
||
d. Epiboly ![]() |
a. Blastocoel ![]() |
||
b. Cytotrophoblast ![]() |
||
c. Archenteron ![]() |
||
d. Epiblast ![]() |
a. The primitive groove, because it provides the opening through which cells migrate into the blastocoel. ![]() |
||
b. The scatter factor, because it defines the dorsal portion of the embryo. ![]() |
||
c. The germinal crescent, because it initiates gastrulation. ![]() |
||
d. There is no avian equivalent to the frog blastopore because of their different patterns of cleavage and gastrulation. ![]() |
a. Sea urchins ![]() |
||
b. Frogs ![]() |
||
c. Birds and mammals ![]() |
||
d. Mammals ![]() |
a. It is the point at which gastrulation is initiated. ![]() |
||
b. The cells opposite it will become the blastopore. ![]() |
||
c. It induces the necessary movement of the egg cytoplasm. ![]() |
||
d. It marks the future dorsal portion of the embryo. ![]() |
a. VegT ![]() |
||
b. Sonic hedgehog ![]() |
||
c. Distal ![]() |
||
d. Cortical cytoplasm ![]() |
a. Ectoderm ![]() |
||
b. Mesoderm ![]() |
||
c. Endoderm ![]() |
||
d. Neural crest ![]() |
a. Nanos ![]() |
||
b. Caudal ![]() |
||
c. Gurken ![]() |
||
d. Bicoid ![]() |
a. Two normal frog embryos ![]() |
||
b. One normal frog embryo and one mass of tissue ![]() |
||
c. One conjoined-twin frog embryo ![]() |
||
d. A mutant, non-viable embryo ![]() |
a. Two normal frog embryos ![]() |
||
b. One normal frog embryo and one mass of tissue ![]() |
||
c. One conjoined-twin frog embryo ![]() |
||
d. A mutant, non-viable embryo ![]() |
a. Two normal frog embryos ![]() |
||
b. One normal frog embryo and one mass of tissue ![]() |
||
c. One conjoined-twin frog embryo ![]() |
||
d. A mutant, non-viable embryo ![]() |
a. Left-right axis formation ![]() |
||
b. Dorsal-ventral axis formation ![]() |
||
c. Anterior-posterior axis formation ![]() |
||
d. Specification of the ectoderm ![]() |
a. Block the factors that inhibit ectoderm from developing into its “default fate” ![]() |
||
b. Overexpress the inhibitory factors within the organizer (e.g. follistatin, chordin) ![]() |
||
c. Block the factors that inhibit BMP4 expression ![]() |
||
d. Both A and B ![]() |
a. It is specified but not determined. ![]() |
||
b. It is composed of the dorsal-most vegetal cells. ![]() |
||
c. It induces the organizer. ![]() |
||
d. It occurs opposite the point of sperm entry. ![]() |
a. Both rely upon gradients of proteins and mRNAs to induce appropriate structures in appropriate regions along the anterior-posterior axis. ![]() |
||
b. Both have homeotic genes whose expression patterns control the development of regions of the body. ![]() |
||
c. Both form their anterior-posterior axis after dorsal-ventral axis formation has been induced. ![]() |
||
d. All of the above ![]() |
a. pH ![]() |
||
b. Nanos ![]() |
||
c. Gravity ![]() |
||
d. β-catenin ![]() |
a. Transplanting the dorsal lip of the blastopore from an untreated embryo to the same site on a treated embryo ![]() |
||
b. Transplanting the dorsal-most blastomeres from an untreated embryo to the same site on a treated embryo ![]() |
||
c. Rotating the embryo 180 degrees before the 32-cell stage ![]() |
||
d. Either A or B would allow you to rescue the embryo. ![]() |
a. Both are influenced by the asymmetric expression of the genes iv and inv. ![]() |
||
b. Both are influenced by the presence of a nodal gene on the left side of the embryo which activates pitx2. ![]() |
||
c. In both, right-side structures are initiated by the activation of snail, and left-side structures are initiated by the activation of pitx2. ![]() |
||
d. In both, left-right axis patterning is initiated by the presence of Noggin and Cerberus proteins. ![]() |
a. The AER ![]() |
||
b. BMP ![]() |
||
c. Retinoic acid (RA) ![]() |
||
d. Noggin ![]() |
a. Pax6 expression is not downregulated in the center of the brain. ![]() |
||
b. The migration of ectoderm to the developing face is not initiated. ![]() |
||
c. Hox gene constellations in the head are not expressed. ![]() |
||
d. The gradient of TGF-β proteins in the face is not established. ![]() |
a. Upside-down digits ![]() |
||
b. Development of hind-limb structures in forelimb area ![]() |
||
c. Webbing and/or no separation of digits ![]() |
||
d. Absence of distal limb structures ![]() |
a. Upside-down digits ![]() |
||
b. Development of hind-limb structures in forelimb area ![]() |
||
c. Webbing and/or no separation of digits ![]() |
||
d. Absence of distal limb structures ![]() |
a. Upside-down digits ![]() |
||
b. Development of hind-limb structures in forelimb area ![]() |
||
c. Webbing and/or no separation of digits ![]() |
||
d. Absence of distal limb structures ![]() |
a. Upside-down digits ![]() |
||
b. Development of hind-limb structures in forelimb area ![]() |
||
c. Webbing and/or no separation of digits ![]() |
||
d. Absence of distal limb structures ![]() |
a. Autonomous development ![]() |
||
b. Pluripotency ![]() |
||
c. Differentiation ![]() |
||
d. Syncytial development ![]() |
a. Paraxial mesoderm ![]() |
||
b. Intermediate mesoderm ![]() |
||
c. Neural crest ![]() |
||
d. Lateral-plate mesoderm ![]() |
a. Paraxial mesoderm ![]() |
||
b. Intermediate mesoderm ![]() |
||
c. Neural crest ![]() |
||
d. Lateral-plate mesoderm ![]() |
a. Mesonephros ![]() |
||
b. Metanephros ![]() |
||
c. Pronephros ![]() |
||
d. Germinativum ![]() |
a. Chorion ![]() |
||
b. Archenteron ![]() |
||
c. Blastocoel ![]() |
||
d. Coelom ![]() |
a. Juvenile hormone (JH) ![]() |
||
b. 20-hydroxyecdysone ![]() |
||
c. Imaginal discs ![]() |
||
d. Pupae ![]() |
a. Juvenile hormone (JH) ![]() |
||
b. 20-hydroxyecdysone ![]() |
||
c. Imaginal discs ![]() |
||
d. Pupae ![]() |
a. Juvenile hormone (JH) ![]() |
||
b. 20-hydroxyecdysone ![]() |
||
c. Imaginal discs ![]() |
||
d. Pupae ![]() |
a. The fly would develop as a fertile female. ![]() |
||
b. The fly would develop as a fertile male. ![]() |
||
c. The fly would develop as a sterile male. ![]() |
||
d. The fly would develop as a sterile female. ![]() |
a. The mammal would develop as a fertile female. ![]() |
||
b. The mammal would develop as a fertile male. ![]() |
||
c. The mammal would develop as a sterile male. ![]() |
||
d. The mammal would develop as a sterile female. ![]() |
a. Drosophila fruit-flies ![]() |
||
b. Mammals ![]() |
||
c. Most turtles and all crocodilians ![]() |
||
d. Crepidula fornicata snails ![]() |
a. A pollutant that blocks the transcription of Sry ![]() |
||
b. A pollutant that blocks the action of aromatase ![]() |
||
c. A pollutant that mimics Sox9 ![]() |
||
d. A pollutant that mimics Sex-lethal (Sxl) ![]() |
a. Epimorphosis, hydra ![]() |
||
b. Epimorphosis, newts ![]() |
||
c. Compensatory regeneration, liver ![]() |
||
d. Morphallaxis, newts ![]() |
a. Epimorphosis, hydra ![]() |
||
b. Epimorphosis, newts ![]() |
||
c. Compensatory regeneration, liver ![]() |
||
d. Morphallaxis, hydra ![]() |
a. It involves a reorganization of virtually every organ. ![]() |
||
b. It relies on a threshold response with different tissues responding to different concentrations of hormones. ![]() |
||
c. It can be inhibited by the removal of the pancreas. ![]() |
||
d. The hormones involved in it primarily regulate gene transcription. ![]() |
a. Juvenile hormone (JH) ![]() |
||
b. 20-hydroxyecdysone ![]() |
||
c. Thyroxine ![]() |
||
d. PTTH ![]() |
a. Turtle eggs must be raised at a fluctuating temperature in order to develop functioning gonads; these turtles were all sterile. ![]() |
||
b. The high temperature inactivated the transcription factors involved in initiating gonadal development from the turtles’ X and Y chromosomes. ![]() |
||
c. The high temperatures stimulated the hormonal induction of female sex development; the turtles were fertile but all female. ![]() |
||
d. The turtles’ gonads developed normally, but the constant temperature prevented the hormonal induction of secondary sex characteristics, and they could not display mating behaviors. ![]() |
a. Duplication and divergence ![]() |
||
b. Co-option ![]() |
||
c. Dissociation (allometry) ![]() |
||
d. Dissociation (heterochrony) ![]() |
a. Duplication and divergence ![]() |
||
b. Co-option ![]() |
||
c. Dissociation (allometry) ![]() |
||
d. Dissociation (heterochrony) ![]() |
a. Duplication and divergence ![]() |
||
b. Co-option ![]() |
||
c. Dissociation (allometry) ![]() |
||
d. Dissociation (heterochrony) ![]() |
a. Physical ![]() |
||
b. Phyletic ![]() |
||
c. Morphogenetic ![]() |
||
d. Heterochronic ![]() |
a. Physical ![]() |
||
b. Phyletic ![]() |
||
c. Morphogenetic ![]() |
||
d. Heterochronic ![]() |
a. It suggests that there has been a leap in complexity from invertebrates to vertebrates. ![]() |
||
b. The formation of the central nervous system and the limb are examples of pathways that exhibit it. ![]() |
||
c. When pathways exhibit it, it suggests that there has been only one way in which a particular development process has ever evolved. ![]() |
||
d. It occurs in pathways that not only involve the same proteins but use them for the same function. ![]() |
a. Pax6 ![]() |
||
b. Hox genes ![]() |
||
c. Tinman ![]() |
||
d. Dax1 ![]() |
a. Macroevolutionary events can be studied and explained by examining microevolution. ![]() |
||
b. The evolution of complex structures like the eye is more easily understood when the processes of Pax6 pathways, modularity, and correlated progression are explained. ![]() |
||
c. The environment, as well as genotype, influences an individual’s phenotype, and development is the means through which this relationship is mediated. ![]() |
||
d. Homologous genes have been found in very disparate, distantly related organisms. ![]() |
a. The early stage, because changes during that time will dramatically alter the embryo and create non-viable phenotypes. ![]() |
||
b. The early stage, because changes during that time are reversed or halted by developmental-repair factors. ![]() |
||
c. The middle stage, because changes during that time will affect processes of global induction and organogenesis. ![]() |
||
d. The late stage, because changes during that time will only disrupt the normal development of tissues that have already been differentiated. ![]() |
a. Organisms that display modular growth are those that are still in existence today, while those without it only exist in the fossil record. ![]() |
||
b. Because portions of the body are somewhat independent from one another, changes can alter one portion without affecting the entire organism. ![]() |
||
c. Because dramatic evolutionary changes can only occur when several modules are altered, genes that are expressed globally are the likeliest evolutionary candidates. ![]() |
||
d. Modularity is what allows for the sequestration of imaginal discs and the evolution of metamorphosis in insects. ![]() |
a. Physical ![]() |
||
b. Phyletic ![]() |
||
c. Morphogenetic ![]() |
||
d. Heterochronic ![]() |
a. An increase in the number of water fleas (Daphnia) with large head helmets ![]() |
||
b. A higher rate of early hatching in treefrog embryos ![]() |
||
c. A reduction in the number of insects entering diapause ![]() |
||
d. A change in the number of parthenogenetic vs. sexual aphids ![]() |
a. Snails exhibiting “imposex” ![]() |
||
b. Frogs exhibiting sex abnormalities ![]() |
||
c. Salmon exhibiting an inability to develop from parr (freshwater form) to smolt (saltwater form) ![]() |
||
d. Birds exhibiting beak abnormalities and soft eggshells ![]() |
a. Snails exhibiting “imposex” ![]() |
||
b. Frogs exhibiting sex abnormalities ![]() |
||
c. Salmon exhibiting an inability to develop from parr (freshwater form) to smolt (saltwater form) ![]() |
||
d. Birds exhibiting beak abnormalities and soft eggshells ![]() |
a. They would all be female. ![]() |
||
b. They would not develop functional abdomens. ![]() |
||
c. They would have a small sac behind their mantle, but it would not function as a light organ. ![]() |
||
d. They would have neither a light organ nor a sac designed to house one. ![]() |
a. In persistent ponds, tadpoles grow at faster rates and metamorphose sooner. ![]() |
||
b. In ponds that begin drying up, tadpoles metamorphose into larger juveniles. ![]() |
||
c. In ponds that begin drying up, tadpoles increase their assimilation efficiency of algae to speed up metamorphosis. ![]() |
||
d. In persistent ponds, tadpoles grow at normal rates with only a single phenotype and metamorphose later. ![]() |
a. Overcrowding ![]() |
||
b. Increasing water temperature ![]() |
||
c. Decreasing oxygen concentration ![]() |
||
d. Proximity to bottom (increasing shallowness) ![]() |
a. Retinoic acid (RA). ![]() |
||
b. Quinine. ![]() |
||
c. Ethanol (alcohol). ![]() |
||
d. Caffeine. ![]() |
a. Molts (from instar to instar vs. to pupa or eclosion) ![]() |
||
b. The development of queen bees and ants ![]() |
||
c. The development of short-winged or long-winged morphs in locusts ![]() |
||
d. The switch between parthenogenetic and sexual forms in female aphids ![]() |
a. The development of eyespots in different morphs of African butterflies ![]() |
||
b. The development of queen bees and ants ![]() |
||
c. The development of light-winged and dark-winged morphs of Pieris and Colias butterflies (the cabbage whites and sulphurs) ![]() |
||
d. The switch between parthenogenetic and sexual forms in female aphids ![]() |
a. These traits are caused by the presence of trout predators. ![]() |
||
b. These traits are heritable. ![]() |
||
c. Chub with these traits are eaten less. ![]() |
||
d. Both A and C ![]() |
a. Snails exhibiting “imposex” ![]() |
||
b. Frogs exhibiting sex abnormalities ![]() |
||
c. Salmon exhibiting an inability to develop from parr (freshwater form) to smolt (saltwater form) ![]() |
||
d. Birds exhibiting beak abnormalities and soft eggshells ![]() |