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129 results for “Chinese waters”
Total Energy Expenditure in Healthy Chinese Populations: A Nationwide Study Using the Doubly Labelled Water Method
ClinicalTrials.gov study NCT07178054. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Conservation genetics of native and European-introduced Chinese Water Deer (Hydropotes inermis)
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FIGURE 3 in Records of the crangonid shrimp genus Pontocaris Bate, 1888 (Crustacea: Decapoda: Caridea) from Chinese waters, with notes on biology of P. pennata Bate, 1888
FIGURE 3. Distribution depths of Pontocaris pennata based on the material examined.
FIGURE 12. Sadayoshia acroporae Baba, 1972, MBM150129, female. A in First records of six galatheid species (Crustacea: Decapoda: Anomura) from Chinese waters
FIGURE 12. Sadayoshia acroporae Baba, 1972, MBM150129, female. A, dorsal view; B, ventral view.
FIGURE 1 in Phytocoetes sinensis n. sp. and Telmatactis clavata (Stimpson, 1855), two poorly known species of Metridioidea (Cnidaria: Anthozoa: Actiniaria) from Chinese waters
FIGURE 1. Sampling sites of Telmatactis clavata and Phytocoetes sinensis n. sp. in Chinese waters.
Potential distribution of seagrass meadows based on MaxEnt model in Chinese coastal waters
<p><span>Seagrass meadows are generally diverse in China and have the same essential ecosystem services as elsewhere. However, an evaluation of seagrass distribution across China is still lacking, and the magnitude and direction of changes in seagrass meadows remains unclear. Our primary objective was to provide a nationwide seagrass distribution map, and to explore the dynamic changes of seagrass population under global climate change. We use simulation studies within the modelling software MaxEnt with 58961 occurrence records and 27 marine environmental variables, to simulate the potential distribution of seagrasses and calculate the area. 7 environmental variables were deleted before the modelling processes based on a correlation analysis to ensure predicted suitability. The predicted area was 790.09 km<sup>2</sup>, which is much larger than the known seagrass distribution in China, and would be increased to 923.62 km<sup>2</sup> by the year 2100. However, the suitable habitat of almost all seagrass will shift northwest in the future. The sum of individual family will under-predict the national distribution of seagrass, showed a downward trend consistently in the future. Out of all environmental variables, the physical ones (e.g. depth, land distance and sea surface temperature) had the greatest contribution in predicting seagrass distributions, and nutrients (e.g. nitrate, phosphate) ranked among the key influential predictors for habitat suitability in our focal area. As this is a first effort to fill a gap in our understanding of the distribution of seagrass in China, further studies are necessary using both modeling and biological/ecological approaches. </span></p>
Figure 5 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 5 Median-joining networking drawn based on ODH gene haplotypes. Colours represent the corresponding population frequencies. Key: Dalian; Dongshan; Nantong; Qingdao; Shanghai; Wenzhou; Xiamen; Zhoushan.
Figure 2 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 2 Neighbour-joining phylogenetic tree constructed based on RD gene sequences. Key: DL = Dalian, N = Nantong, Q = Qingdao, S = Shanghai, W = Wenzhou, X = Xiamen, Z = Zhoushan.
Figure 4 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 4 Median-joining networking drawn based on RD gene haplotypes. Colours represent the corresponding population frequencies. Key: Dalian; Dongshan; Nantong; Qingdao; Shanghai; Wenzhou; Xiamen; Zhoushan.
Figure 3 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 3 Neighbour-joining tree constructed based on the ODH gene. Key: DL = Dalian, N = Nantong, Q = Qingdao, S = Shanghai, W = Wenzhou, X = Xiamen, Z = Zhoushan.
FIGURE 2 in A review of the genus Apocepon Nierstrasz & Brender à Brandis (Isopoda: Epicaridea: Bopyridae) parasitic on purse crabs (Decapoda: Brachyura: Leucosiidae) from Chinese waters, with description of a new species
FIGURE 2. Apocepon pulcher Nierstrasz & Brender à Brandis. Reference male, EL5208012. A,
FIGURE 5 in A review of the genus Apocepon Nierstrasz & Brender à Brandis (Isopoda: Epicaridea: Bopyridae) parasitic on purse crabs (Decapoda: Brachyura: Leucosiidae) from Chinese waters, with description of a new species
FIGURE 5. Apocepon digitatum Stock. Reference female, EL615001. A–E, right pleopods and
FIGURE 6 in Johnius taiwanensis, a new species of Sciaenidae from the Taiwan Strait, with a key to Johnius species from Chinese waters
FIGURE 6. Five mental pores of Johnius taiwanensis (148 mm SL) at lower jaw (ventral view).
FIGURE 5 in Johnius taiwanensis, a new species of Sciaenidae from the Taiwan Strait, with a key to Johnius species from Chinese waters
FIGURE 5. The first gill arch of Johnius taiwanensis (144 mm SL).
Fig. 2. Polymorphic sites from 386 in Pattern Of Genetic Variation Of Bottlenose Dolphins In Chinese Waters
Fig. 2. Polymorphic sites from 386-bp of mitochondrial control region of bottlenose dolphins determined in the present study in comparison with those Tursiops sequences downloaded from GenBank. Sequence identity to reference sequences of first haplotype (T1au) is indicated by dot, and indels indicated by dash. Individual number of each haplotype identified in the present study is also presented
Figure 1 in Conservation genetics of native and European-introduced Chinese water deer (Hydropotes inermis)
Figure 1. Chinese water deer (Hydropotes inermis). Credit: Jacquie Pringle.
Potential distribution of seagrass meadows based on MaxEnt model in Chinese coastal waters
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Expression profiling of wheat heads from spring wheat Chinese Spring (CS) and CS-7EL (CS with additional chromosome arm 7EL from Thinopyrum elongatum), after inoculation with either water (mock inocul
GEO Series GSE70797. Triticum aestivum. 12 samples. Type: Other.
Figure 1 from: Muhammad F, Lü Z-m, Liu L, Gong L, Du X, Shafi M, Kaleri HA (2018) Genetic structure of Octopus minor around Chinese waters as indicated by nuclear DNA variations (Mollusca, Cephalopoda). ZooKeys 775: 1-14. https://doi.org/10.3897/zookeys.775.24258
Figure 1 Map showing the collection locations.
Study on Water Turnover of the Chinese Population Based on Deuterium Dilution Method
ClinicalTrials.gov study NCT07028021. IPD Sharing: Not stated. Countries: 1. Publications: 0.
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International Brain Laboratory public data
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OpenNeuro
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