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Institution

Chinese Academy of Fishery Sciences

NonprofitBeijing, China
About: Chinese Academy of Fishery Sciences is a nonprofit organization based out in Beijing, China. It is known for research contribution in the topics: Population & Gene. The organization has 8107 authors who have published 7929 publications receiving 92095 citations. The organization is also known as: Zhōngguó shuǐchǎn Kēxuéyánjiūyuàn & Chinese Academy of Fishery Sciences.
Topics: Population, Gene, Shrimp, Genome, Mitochondrial DNA


Papers
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Journal ArticleDOI
TL;DR: Assessment of the relative contributions of traffic emission and other potential sources to high levels of atmospheric ammonia (NH3) in urban areas in the wintertime in northern China found that NH3 released from water evaporation is an important source.
Abstract: To assess the relative contributions of traffic emission and other potential sources to high levels of atmospheric ammonia (NH3) in urban areas in the wintertime, atmospheric NH3 and related pollutants were measured at an urban site, ∼300 m from a major traffic road, in northern China in November and December 2015 Hourly average NH3 varied from 03 to 108 ppb with an average of 24 ppb during the campaign Contrary to the common perspective in literature, traffic emission was demonstrated to be a negligible contributor to atmospheric NH3 Atmospheric NH3 correlated well with ambient water vapor during many time periods lasting from tens of hours to several days, implying NH3 released from water evaporation is an important source Emissions from local green space inside the urban areas were identified to significantly contribute to the observed atmospheric NH3 during ∼60% of the sampling times Evaporation of predeposited NHx through wet precipitation combined with emissions from local green space likely

72 citations

Journal ArticleDOI
TL;DR: The analyses suggest that environmental preferences of the large Jellyfish may enable prediction of jellyfish population sizes and distributions in Chinese waters, which is essential in order to address ecological problems caused by large jellyfish blooms in East Asia Waters.
Abstract: Climate change may contribute to the increasing frequency and intensity of jellyfish blooms around the world. To test the null hypotheses that distributions did not differ among species of jellyfish or according to temperature salinity, we sampled large jellyfishes using bottom trawl surveys during 2006–2007 in the Yellow Sea (YS) and East China Sea (ECS). The total biomass of large jellyfish in the YS was low in April 2006 in cool waters, increased with warming waters, peaked in early September 2006 (22,891 ± 25,888 kg km–2), and then decreased with cooling to minimal biomass during March 2007. During its peak early September 2006, Nemopilema nomurai was relatively eurythermal and distributed throughout the YS. Cyanea spp. occurred in warmer waters and attained maximum biomass in May 2007 in the ECS. Ulmaridae, which preferred colder temperatures, reached maximum biomass in October 2006 and occurred mainly in the central YS. Aequorea spp. usually occurred in colder waters, with maximum biomass in May 2007 mainly north of 30°N. Our analyses suggest that environmental preferences of the large jellyfish may enable prediction of jellyfish population sizes and distributions in Chinese waters, which is essential in order to address ecological problems caused by large jellyfish blooms in East Asia Waters.

72 citations

Journal ArticleDOI
TL;DR: Transcriptome analysis of hepatopancreas from black tiger shrimp treated with ammonia stress clarifies shrimp defensive response to ammonia toxicity and should benefit efforts to breed more ammonia‐tolerant varieties.

72 citations

Journal ArticleDOI
01 Aug 2012-PLOS ONE
TL;DR: Astaxanthin biosynthesis in the presence of JA appeared to be up-regulated mainly by psy, pds, crtR-B, lyc, bkt2 and crtO at the transcriptional level and ipi,1, ipi-2 at both transcriptional and post-transcriptional levels.
Abstract: Haematococcus pluvialis is an organism that under certain conditions can produce astaxanthin, an economically important carotenoid. In this study, the transcriptional expression patterns of eight carotenogenic genes of H. pluvialis in response to jasmonic acid (JA) were evaluated using real-time PCR. Astaxanthin accumulation action and photosynthesis flourescence were monitored at the same time. The results showed all eight genes exhibited higher transcriptional expression significantly under JA treatments. JA25 (25 mg/L) induction had greater effect (>10-fold up-regulation) on the transcriptional expression of pds, crtR-B and lyc than on ipi-1, ipi-2, psy, bkt2, and crtO. JA50 (50 mg/L) treatment had greater impact on the transcriptional expression of ipi-1, ipi-2, psy, crtR-B and crtO than on pds, lyc and bkt2. Astaxanthin biosynthesis in the presence of JA appeared to be up-regulated mainly by psy, pds, crtR-B, lyc, bkt2 and crtO at the transcriptional level and ipi-1, ipi-2 at both transcriptional and post-transcriptional levels. Under JA induction, the photosynthetic efficiency [Y (II)] and the maximum quantum efficiency of PS II (Fv/Fm) decreased significantly, but the non-photochemical quenching of chlorophyll fluorescence (NPQ) increased drastically with the accumulation of astaxanthin.

72 citations

Journal ArticleDOI
TL;DR: A facile droplet microfluidic platform was developed to dispense individual microbial cells into conventional standard containers for downstream analysis and showed that the individual cells isolated can be used in high-quality DNA and RNA analyses at both gene-specific and whole-genome levels.
Abstract: Wider application of single-cell analysis has been limited by the lack of an easy-to-use and low-cost strategy for single-cell isolation that can be directly coupled to single-cell sequencing and single-cell cultivation, especially for small-size microbes. Herein, a facile droplet microfluidic platform was developed to dispense individual microbial cells into conventional standard containers for downstream analysis. Functional parts for cell encapsulation, droplet inspection and sorting, as well as a chip-to-tube capillary interface were integrated on one single chip with simple architecture, and control of the droplet sorting was achieved by a low-cost solenoid microvalve. Using microalgal and yeast cells as models, single-cell isolation success rate of over 90% and single-cell cultivation success rate of 80% were demonstrated. We further showed that the individual cells isolated can be used in high-quality DNA and RNA analyses at both gene-specific and whole-genome levels (i.e. real-time quantitative PCR and genome sequencing). The simplicity and reliability of the method should improve accessibility of single-cell analysis and facilitate its wider application in microbiology researches.

71 citations


Authors

Showing all 8142 results

NameH-indexPapersCitations
Yu Huang136149289209
Meilin Liu11782752603
Lin Li104202761709
Jian Xu94136652057
Xiaolong Wang8196631455
Sheng Luan7627221253
Peng Xu75115125005
Qiang Li7385630598
Deliang Chen6846116966
Chao Li6456117253
Min Du6132611328
Lei Wang5998814887
Quan Chen5215416697
Jun Li5056212002
James P. Barry4916210687
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202311
2022147
2021894
2020763
2019734
2018653