Fig. 1. Food intake and body mass increase from day 1 in migratory dunnocks in two 12-day magnetic displacement experiments during autumn 2014. Food intake.

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P.464. Table 13-1, p.465 Fig. 13-1, p.466 Fig. 13-2, p.467.
Fig. 11-1, p p. 360 Fig. 11-2, p. 361 Fig. 11-3, p. 361.
Table 6-1, p Fig. 6-1, p. 162 p. 163 Fig. 6-2, p. 164.
CHAPTER 50 AN INTRODUCTION TO ECOLOGY AND THE BIOSPERE Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings Section D: The Spatial.
Analysis of covariance for feeding rate (rF) in H
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. External work and kinetic and potential energy of the whole body for the mean individual (individual 10) in the mean population (population 1)
Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.
Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.
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. 2. Long-term CCH increases SDH activity after 6 weeks and does not prevent an increase of the fibre cross-sectional area.Fish were kept for 3 or 6.
Foraging tracks of individuals from Point Danger and Pope's Eye
Fig. 4. Effects of ion deprivation on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effects of ion deprivation on percentage.
Fig. 4. Effect of royal jelly on silkmoth fat body cells and eggs.
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. 2. Body weight and size analysis of A1/A2-KO mice
Fig. 2. The effect of spatial enrichment on brain size.
Fig. 6. Schematic diagram showing distribution and dynamics of four E-cadherin populations within the ROI of a FRAP experiment. Schematic diagram showing.
Fig. 1. Lack of Hmga1 and Hmga2 expression in A1/A2-KO mice
Fig. 3. Changes of sugar- and malate-metabolic enzyme activities during fruit development under different K treatment conditions. Changes of sugar- and.
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. 1. Body weight gain in Cbx7-KO mice
Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.
Fig. 7. E2F1 acetylation in A1/A2-KO MEFs
Fig. 4. Brood size of four successive births by male seahorses Hippocampus erectus in the two groups (TR-1, TR-2).In TR-1 groups: male and female seahorses.
Fig. 2. Dispersal pattern and walking distances of the two wingless strains of Acyrthosiphon pisum in 24 h. Dispersal pattern and walking distances of.
Fig. 3. Low power hemi retinal image of the RPE surface showing the albino central and equatorial retina and pigment distribution in the periphery. Low.
Fig. 2. Mean oxygen consumption per metre (mL O2 m−1) of jump distance between springboards during horizontal jumping.Seven jumping conditions were generated.
Fig. 8. C. elegans susceptibility to α-terthienyl was affected by the activities of skn-1 and wdr-23. C. elegans susceptibility to α-terthienyl was affected.
Fig. 5. GFP fluorescence colocalization of Gcn5.
Fig. 3. Computer-assisted sperm analyses (CASA) of epididymal sperm collected from wild-type (WT), miR-34b/c knockout (KO), miR-449 KO, and miR-34b/c;miR-449.
24 h mean of body temperature plotted against 24 h mean of air temperature (A), and 24 h amplitude of body temperature plotted against 24 h range of air.
Fig. 7. Interaction between BAF60c and cardiac transcription factors.
Fig. 2. Effect of substrate orientation on growth rate of midwater tadpoles with different oral configurations. Effect of substrate orientation on growth.
Fig. 2. Soluble sugar and organic acid levels with different K fertilization during fruit development. Soluble sugar and organic acid levels with different.
Fig. 1. Aboveground biomass of Caragana and herbaceous plants, and proportional abundance of Caragana, under different grazing management treatments. Aboveground.
Fig. 4. BKA values for different species.
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.
Fig. 4. Co-immunostaining of nocodazole or ASNase treated RPE-1 cells with anti-hASNS and anti-alpha tubulin showed defect in both mitotic spindle formation.
Body density decreased and buoyancy increased as air sac volume increased with inflation pressure in the three species. Body density decreased and buoyancy.
Fig. 3. Effect of substrate orientation on growth rate for bottom-dwelling tadpoles with similar oral configuration. Effect of substrate orientation on.
Fig. 3. Urinary excretion of Na+ and K+ in WNK3 knockout mice
Distribution and extent of expression.
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 genomic distribution of essential and non-essential mouse genes, separated into known and predicted essentiality. The genomic distribution of essential.
Fig. 1. Expression of the five miRNAs encoded by two miRNA clusters in mouse sperm and oocytes.(A) qPCR analyses of levels of miR-16 (positive control),
Fig. 4. Spectra of monochromatic light from the OLS
Fig. 8. Tracking details and coordinate systems.
Amplicon sequencing analysis of on-target sites in trβ crispants
Delay of tail resorption in trβ crispants during natural metamorphosis
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.
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.
Morphological changes induced by T3 treatment in trβ crispants
Fig. 1. Expression of the five miRNAs encoded by two miRNA clusters in mouse sperm and oocytes.(A) qPCR analyses of levels of miR-16 (positive control),
A broken-stick O2-uptake function for male and female killer whales as used in the O2 model (model 3). A broken-stick O2-uptake function for male and female.
Fig. 1. Generation of induced pluripotent stem cells (iPSCs) from urine cells (UC). Generation of induced pluripotent stem cells (iPSCs) from urine cells.
Fig. 7. Eye defects in STK35 KO mouse.
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. 5. Behaviours of the wild-types Oregon-R at two temperatures.
Fig. 3. Changes in the total EPS/Chl a ratio and bend interval of trichomes before and after the removal of polysaccharide from the BG11-cultured N. flagelliforme.
Fig. 1. lgl interacts genetically with Argonaute 1 (AGO1) in the eye.
Fig. 1. Effects of royal jelly on silkmoth body size.
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Fig. 1. Food intake and body mass increase from day 1 in migratory dunnocks in two 12-day magnetic displacement experiments during autumn 2014. Food intake and body mass increase from day 1 in migratory dunnocks in two 12-day magnetic displacement experiments during autumn 2014. In the first experiment birds were displaced to the southern destination area (Control n=11; South n=12) from day 1 (Oct 5). In the second experiment birds were displaced both to the southern destination area and the northern limit of species distribution range (Control n=6; South n=8; North n=7). Moreover, the magnetic field was changed every day during 6-day period (until the dashed line) and then kept to a constant value. The geographical positions corresponding to the simulated magnetic displacements were Sweden (Control), southern France (South) and northwestern Russia (North) as reported in Fig. 2 and Table 2. Data represented as mean±s.e.m. Mihaela Ilieva et al. Biology Open 2016;bio.014779 © 2016. Published by The Company of Biologists Ltd