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18 results for “body height”

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zenodo40/100

Text-fig. 2. The methods of measurements. H – horizontal plane, HB – body height, SL – skull length, TL – total body length, 1 – the angle which the dorsal lobe of the caudal fin forms with the horizontal plane, 2 – the angle which the ventral lobe of the caudal fin forms with the horizontal plane, 3 – the angle which the scale row in front of the anal fin forms with the horizontal plane. in Actinopterygians Of The Broumov Formation (Permian) In The Czech Part Of The Intra-Sudetic Basin (The Czech Republic)

Text-fig. 2. The methods of measurements. H – horizontal plane, HB – body height, SL – skull length, TL – total body length, 1 – the angle which the dorsal lobe of the caudal fin forms with the horizontal plane, 2 – the angle which the ventral lobe of the caudal fin forms with the horizontal plane, 3 – the angle which the scale row in front of the anal fin forms with the horizontal plane.

opencc-by-4.0Dec 2021View details →
zenodo40/100

Fig. 11 in Shoulder height, body mass, and shape of proboscideans

Fig. 11. Left humerus of giant Mosbach mammoth (MNHM PW1947/23) from Middle Pleistocene, Mosbach, Germany; in lateral view.

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 10 in Shoulder height, body mass, and shape of proboscideans

Fig. 10. Different growth curves for Loxodonta africana from average-sized to world record specimens based on isometric growth (red), Laws' (1975) equations for wild population in good conditions up to average size (brown), Homo sapiens (in optimal conditions) allometric growth (grey), and the proposed allometric growth curve for proboscideans in this study (black).

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 6 in Shoulder height, body mass, and shape of proboscideans

Fig. 6. Femur length vs. skeletal shoulder height ratio of selected proboscideans based on the data collected in this study (Appendix 1, SOM: table 2; AL unpublished data).

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 3 in Shoulder height, body mass, and shape of proboscideans

Fig. 3. Humerus lengths vs. skeletal shoulder height ratio of selected proboscideans based on the data collected in this study (Appendix 1, SOM: table 2; AL unpublished data). The ratios shaded in grey correspond to the maximal length of the humerus and the white ones to the articular length of the humerus.

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 9 in Shoulder height, body mass, and shape of proboscideans

Fig. 9. Plot of height vs. weight for 561 male Homo sapiens in optimal conditions from 170 cm (low average) to 225 cm tall. Average growth curve (red line).

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 2 in Shoulder height, body mass, and shape of proboscideans

Fig. 2. Scapula lengths vs. skeletal shoulder height ratio of selected proboscideans based on the data collected in this study (Appendix 1, SOM: table 2; AL unpublished data). The ratios shaded in grey correspond to the maximal length of the scapula and the white ones to the articular length of the scapula.

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 5 in Shoulder height, body mass, and shape of proboscideans

Fig. 5. Radius length vs. skeletal shoulder height ratio of selected proboscideans based on the data collected in this study (Appendix 1, SOM: table 2; AL unpublished data).

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 1 in Shoulder height, body mass, and shape of proboscideans

Fig. 1. Reconstruction of the forelimb of the Zhalainuoer III mammoth in anatomical position. The actual shoulder height (black): total height in anatomical position 3690 mm. The height obtained by adding the articular (green): manus (500 mm) + ulna (960 mm) + humerus (1233 mm) + scapula (1075 mm) = 3768 mm. Maximal lengths of different bone elements (red): manus (500 mm) + radius (985 mm) + humerus (1274 mm) + scapula (1115 mm) = 3874 mm. The actual shoulder height can be calculated by multiplying the result by 0.98 in the case of the sum of articular lengths and by 0.95 in the case of maximal lengths.

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 4 in Shoulder height, body mass, and shape of proboscideans

Fig. 4. Ulna lengths vs. skeletal shoulder height ratio of selected proboscideans based on the data collected in this study (Appendix 1, SOM: table 2; AL unpublished data). The ratios shaded in grey correspond to the maximal length of the humerus, and the white ones to the articular length of the humerus.

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 8 in Shoulder height, body mass, and shape of proboscideans

Fig. 8. Fibula length vs. skeletal shoulder height ratio of selected proboscideans based on the data collected in this study (Appendix 1, SOM: table 2; AL unpublished data).

opencc-by-4.0Jul 2015View details →
zenodo40/100

Fig. 7 in Shoulder height, body mass, and shape of proboscideans

Fig. 7. Tibia length vs. skeletal shoulder height ratio of selected proboscideans based on the data collected in this study (Appendix 1, SOM: table 2; AL unpublished data).

opencc-by-4.0Jul 2015View details →
ClinicalTrials.gov36/100

Comparing the Effect of Under the Tongue Olanzapine Versus Swallowed Olanzapine on Body Mass Index (A Ratio of Weight to Height)

ClinicalTrials.gov study NCT00303602. IPD Sharing: Not stated. Countries: 5. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Predator community and resource use jointly modulate the inducible defense response in body height of crucian carp

<p>Phenotypic plasticity can be expressed as changes in body shape in response to environmental variability. Crucian carp (<i>Carassius carassius</i>), a widespread cyprinid, displays remarkable plasticity in body morphology and increases body depth when exposed to cues from predators, suggesting the triggering of an anti-predator defense mechanism. However, these morphological changes could also be related to resource use and foraging behavior, as an indirect effect of predator presence. In order to determine whether phenotypic plasticity in crucian carp is driven by a direct or indirect response to predation threat, we compared twelve fish communities inhabiting small lakes in southeast Norway grouped by four categories of predation regimes: no predator fish, or brown trout (<i>Salmo trutta</i>), perch (<i>Perca fluviatilis</i>) or pike (<i>Esox lucius</i>) as main piscivores. We predicted the body shape of crucian carp to be associated with the species composition of predator communities, and that the presence of efficient piscivores results in a deeper body shape. We use stable isotope analyses to test if this variation in body shape was related to a shift in individual resource use – i.e., littoral rather than pelagic resource use would favor the development of a specific body shape - or other environmental characteristics. The results showed that increasingly efficient predator communities induced progressively deeper body shape, larger body size and lower population densities. Predator maximum gape size and individual trophic position were the best variables explaining crucian carp variation in body depth among predation categories, while littoral resource use did not have a clear effect. The gradient in predation pressure also corresponded to a shift in lake productivity. These results indicate that crucian carp have a fine-tuned morphological defense mechanism against predation risk, triggered by the combined effect of predator presence and resource availability.</p>

opencc-zeroDec 2021View details →
dryad32/100

Predator community and resource use jointly modulate the inducible defense response in body height of crucian carp

Open the record for dataset details and reuse information.

publicDec 2021View details →
dryad28/100

Data from: Body height and immune efficacy: testing body stature as a signal of biological quality

According to the good genes hypothesis and energy allocation theory, human adult body height may reflect biological quality. An important aspect of this quality is immune system functioning (ISF). The aim of this study was to evaluate the relationship between ISF and body height in healthy people. The ISF was determined by several important innate (total complement and lysozyme activity, neutrophils function) and adaptive immune parameters (lymphocytes, IgA and IgG, and response to flu vaccine). Overall, 96 males and 97 females were subjected to flu vaccination, and of these 35 males and 34 females were subjected to tetanus. Blood samples were collected before and 4 weeks after vaccination. Immunomodulatory factors: participant's age, body fat and free testosterone levels, were controlled. There was no association between body height and all analysed immune parameters for both sexes. That might suggest that in western society, a women's preference for taller men is not related to "good genes for immune competence". We propose the novel Immunity Priority Hypothesis that explains the lack of relationship between adult body stature and ISF. This hypothesis, however, does not contradict the signalling role of a man's body height as a morphological marker of biological quality.

opencc-zeroDec 2016View details →
dryad28/100

Data from: Body height and immune efficacy: testing body stature as a signal of biological quality

Open the record for dataset details and reuse information.

publicJun 2017View details →
ClinicalTrials.gov24/100

Effects of GH on Body Proportions and Final Height in X-Linked Hypophosphatemic Rickets

ClinicalTrials.gov study NCT00473187. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →

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International Brain Laboratory public data

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