Fig. 2. Examples of changes in angular velocity and correlation coefficient during the O–O test. Examples of changes in angular velocity and correlation.

Slides:

Advertisements

Similar presentations

Interactions of movement and EODs for producing envelopes.

Advertisements

Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial cells using live-imaging. Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial.

Fig. 6. Ultrastructural changes in the glycocalyx of N

Fig. 5. Prip silencing enhances the co-localization of GABARAP with insulin vesicles and β-tubulin.Co-localization of GABARAP (green) with insulin (red)

Fig. 1. Overview of the nervous system of the adult S. roscoffensis.

Fig. 3. Effect of NH4Cl (0 or 30 mM) on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effect of NH4Cl (0 or 30 mM) on percentage.

Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.

Fig. 3. Hts and Dlg are in a complex at the postsynaptic membrane of larval NMJs.(A–B″) PLA with HtsM and Dlg antibodies (green) performed on third instar.

Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.

Fig. 4. E-cadherin expression level affects monomer dynamics.

Fig. 5. Effect of MPO on surface elasticity of human platelets

Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.

Fig. 2. Proportion of motile objects and track length

Fig. 6. Hts regulates par-1 and camkII mRNA distribution and levels in the muscle.(A–J) Views of muscles 6/7 in abdominal segment 4, probed for either.

Fig. 4. A primary screen based on scrape closure

Fig. 1. Blood lactate, blood glucose and blood corticosterone concentration from crawl until 4 hours of frenzy swimming in loggerhead (C. caretta) and.

Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.

Fig. 1. Lipid analysis.(a) HP-TLC analysis of DIMs of tobacco pollen tubes, using increasing detergent/protein ratios. Lipid analysis.(a) HP-TLC analysis.

Foraging tracks of individuals from Point Danger and Pope's Eye

Table 1. Menthol preference index (MPI) and average number of eggs laid per female (EPF) in F0 and F1 lines.The statistical significance of MPI was assessed.

Fig. 1. Mitochondrial internalization in cardiomyocytes.

Fig. 4. The model of malate metabolism in fruit cells under different K level conditions. The model of malate metabolism in fruit cells under different.

Fig. 7. E2F1 acetylation in A1/A2-KO MEFs

Fig. 3. Characterization of unclassified cells (UCs).

Fig. 1. Co-immunostaining of yeast spheroplasts with anti-hASNS and anti-alpha tubulin revealed that yeast asparagine synthetases formed filaments/foci.

Fig. 2. Two signal-producing behaviours of wild-type Canton-S males and per mutant males relative to whether the wild-type female is moving or immobile.

Fig. 2. The kar phenotype arises during metamorphosis

Fig. 3. The checkpoint proteins Mad2 and BubR1 remain associated with the kinetochores of unaligned chromosomes in cenp-metaΔ mutant cells entering anaphase.(A–C)

Fig. 5. GFP fluorescence colocalization of Gcn5.

Fig. 2. Morphological analysis of acentriolar mitotic spindles

The TER94-p47 complex isinvolved in Notch signaling regulation

Illustration of the hypothetical relationships among metabolic level, the intraspecific scaling exponent b and cell size. Illustration of the hypothetical.

Fig. 2. Soluble sugar and organic acid levels with different K fertilization during fruit development. Soluble sugar and organic acid levels with different.

Fig. 7. Representative images of control (Cas9+GFP) and Cas9+gRNA+GFP co-injected embryos on day 4 of culture, showing nuclear-imported GFP (green) and.

Bivariate plots of mean total scratches and mean total pits for natural grazers. Bivariate plots of mean total scratches and mean total pits for natural.

Comparison ofMyc-induced zebrafish liver tumors with different stages of human HCC and seven mouse HCC models. Comparison ofMyc-induced zebrafish liver.

Table 1. Average ± S.E. of level of dissimilarity scores of each feature per stripe per pattern comparison of sides of the same fish (“Same Individual”),

The idefix phenotype first becomes visible during metamorphosis

Fig. 3. Immunostaining for neural differentiation makers of the stage 29 optic cup.Immunoreactive signals are shown in green or red. Immunostaining for.

Statistical chart of significantly differentially expressed genes

Chronic phenytoin increases activity levels in Mecp2Null/Y mice.

Fig. 4. Spectra of monochromatic light from the OLS

Example of a putative bridging fiber.

Fig. 2. RGD and KGD motifs in N. vectensis thrombospondins

Fig. 1. Generation of binarized movies of medaka behavior during the O–O test using the UMATracker program. Generation of binarized movies of medaka behavior.

Exo70 is recruited to the plasma membrane at sites of mechanical wounding. Exo70 is recruited to the plasma membrane at sites of mechanical wounding. NRK.

Fig. 6. F1 trβ mutants accomplish natural metamorphosis.

Vertical ground reaction force–time waveforms for RFS trials.

Vertical ground reaction force–time waveforms for FFS trials.

Analysis of mutant Best1 protein (Y227N) in testis and sperm function

Fig. 2. Effects of pH on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effects of pH on percentage of motile spermatozoa.

Approach trajectories of squid and prey and angular velocity of squid.

Fig. 12. Overview of the molecular program essential to build mdDA neurons.The genes identified in this study (in red) have been added to the programming.

Fig. 3. Representive still images of typical pelagic foraging behaviour of Australaisan gannets. Representive still images of typical pelagic foraging.

Kinematic measurements recorded as squid approached shrimp and fish.

Morphological changes induced by T3 treatment in trβ crispants

Fig. 3. transparent is required cell-autonomously in iridophores

The occurrence of D calls on a dive profile.

Fig. 3. Mean force and velocity during jumping

Fig. 4. Representative still images of behaviour and characteristics typical of inshore foraging strategy of Australasian gannets. Representative still.

Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.

Table 1. Measurement of ring diameters of proteins localizing in ring-like patterns around centrioles.Consideration of the size of IgG (about 8 nm) raises.

Fig. 7. Nrf2-dependent enzyme activities in wild-type, Nrf2- and Keap1-deficient tissues.Hepatic (A,C,E) and cortical (B,D,F) enzyme activities of NQO1.

Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.

Fig. 7. Rho family GTPase signaling is required for cyst formation in Ptp4E Ptp10D mutants.(A–C) Expression of DN Rho1 and Rac1 mutants in wild-type (w1118)

Fig. 1. lgl interacts genetically with Argonaute 1 (AGO1) in the eye.

Membrane integration of the model constructs depends on protein sequence, not codon usage. Membrane integration of the model constructs depends on protein.

Instances during the time course of wake generation behind a steadily swimming eel (speed U=0.121 m s-1, sequence 1, see Table 1). Instances during the.

Example of swimming trajectories from three groups of fish from three different weeks along with the extracted behavioral parameters. Example of swimming.

Flow field adjacent to an eel (body length L=0

Presentation transcript:

Fig. 2. Examples of changes in angular velocity and correlation coefficient during the O–O test. Examples of changes in angular velocity and correlation coefficient during the O–O test. The values in the first clockwise, second counterclockwise, and third clockwise stripe rotations are shown in red, green, and blue, respectively. The angular velocity became ±36°/s and the correlation coefficient became +1.0 when fish followed the rotating stripes exactly. (A,B) A typical example of OMR-positive fish (control fish at λ=750 nm). The fish quickly started and stably continued following the stripes in all three rotations. (C,D) A typical example of OMR-negative fish (mutant fish at λ=850 nm). The fish continued swimming slowly in a clockwise direction (without any turning) throughout the 90 s O–O test. (E,F) Examples of fish that did not follow the stripes. Mutant fish at λ=760 nm (E) immediately started the OMR in the first rotation, but not in the second or third rotations. Whether the fish overlooked or intentionally ignored the changes in rotating direction is unknown. Control fish at λ=720 nm (F) restlessly swam back and forth in the first and second rotations, whereas the correlation coefficient became stably high for at least ∼10 s in the third rotation. These quick changes in swimming direction were rarely observed when fish could not follow the stripes (see Fig. 2D). (G,H) Examples of fish with an ambiguous behavior. Whether medaka did not or could not follow the stripes was unclear. A control fish at λ=850 nm (G) largely swam in the rotating direction, but the values fluctuated comparison with those shown in Fig. 2B. A mutant fish at λ=750 nm (H) seemed to start following the stripes at the end of each rotation, but this could be an accidental correlation. Megumi Matsuo et al. Biology Open 2018;7:bio033175 © 2018. Published by The Company of Biologists Ltd