Contribution of a pathway through the Arctic Ocean to the re cent reduction in the ice cover

The sea ice cover in the Arctic Ocean has been reducing and hit the low record in the summer of 2007. The anomaly was extremely large in the Pacific sector. The sea level height in the Bering Sea vs. the Greenland Sea has been analyzed and compared with the current meter data through the Bering Strait. A recent peak existed as a consequence of atmospheric circulation and is considered to contribute to inflow of the Pacific Water into the Arctic Basin. The timing of the Pacific Water inflow matched with the sea ice reduction in the Pacific sector and suggests a significant increase in heat flux. This component should be included in the model prediction for answering the question when the Arctic sea ice becomes a seasonal ice cover.     

A coupled ice-ocean ecosystem model for 1-D and 3-D applications in the Bering and Chukchi Seas

Primary production in the Bering and Chukchi Seas is strongly influenced by the annual cycle of sea ice. Here pelagic and sea ice algal ecosystems coexist and interact with each other. Ecosystem modeling of sea ice associated phytoplankton blooms has been understudied compared to open water ecosystem model applications. This study introduces a general coupled ice-ocean ecosystem model with equations and parameters for 1-D and 3-D applications that is based on 1-D coupled ice-ocean ecosystem model development in the landfast ice in the Chukchi Sea and marginal ice zone of Bering Sea. The biological model includes both pelagic and sea ice algal habitats with 10 compartments： three phytoplankton （pelagic diatom, flagellates and ice algae： D, F, and Ai） , three zooplankton （copepods, large zooplankton, and microzooplankton ： ZS, ZL, ZP） , three nutrients （ nitrate ＋ nitrite, ammonium, silicon ： NO3 , NH4, Si） and detritus （Det）. The coupling of the biological models with physical ocean models is straightforward with just the addition of the advection and diffusion terms to the ecosystem model. The coupling with a multi-category sea ice model requires the same calculation of the sea ice ecosystem model in each ice thickness category and the redistribution between categories caused by both dynamic and thermodynamic forcing as in the physical model. Phytoplankton and ice algal self-shading effect is the sole feedback from the ecosystem model to the physical model.     

Summer fast ice evolution off Zhongshan Station,Antarctica

Based on the field data acquired in the program of fast ice observation off Zhongshan Station, Prydz Bay, East Antarctica during the austral summer 2005/ 2006, physical properties evolution of fast ice during the ice ablation season is analyzed in detail. Results show that the annual maximum ice thickness in 2005 occurred in later November, and then ice started to reek, and the ablation duration was 62 days; sea water under the ice became warmer synchronously; corresponding to the warming sea ice temperature, a ＂relative cold mid-layer＂ appeared in sea ice; the fast ice marginal line recoiled back to the shore observably, and the recoil distance was 20.9 km from 18 December 2005 through 14 January 2006. In addition, based on the data of sea ice thickness survey along the investigation course of MV Xuelong on December 18 of 2005, the ice thickness distribution paten in the marginal ice zone have been described ： sea ice thickness increased, but the diversity of floe ice thick-ness decreased from open water to fast ice zone distinctly.     

A coupled multi-category sea ice model and POM for Baffin Bay and the Labrador Sea

An overview of the seasonal variation of sea-ice cover in Baffin Bay and the Labrador Sea is given. A coupled ice-ocean model, CECOM, has been developed to study the seasonal variation and associated ice-ocean processes. The sea-ice component of the model is a multi-category ice model in which mean concentration and thickness are expressed in terms of a thickness distribution function. Ten categories of ice thickness are specified in the model. Sea ice is coupled dynamically and thermodynamically to the Princeton Ocean Model. Selected results from the model including the seasonal variation of sea ice in Baffin Bay, the North Water polynya and ice growth and melt over the Labrador Shelf are presented.     

Disease resistance and humoral immunomodulatory effects of vitamin C on grouper,Epinephelus awoara

The disease resistance and humoral immunomodulatory effects of vitamin C administered orally to grouper,Epinephelus awoara maintained on a frozen fish diet supplemented with vitamin C at 500, 1000, 1500 and 2000 mg/kg were investigated. After 20 weeks, the growth rates of the groups with high level of vitamin C apparently increased. The untreated fish had symptoms of vitamin C deficiency. The endogenous liver tissue vitamin C levels were found to reflect well the dietary treatments. After intraperitoneal injection or bath challenge with a virulent strain ofVibrio vulnificus, fish fed with high level vitamin C showed significantly higher survival rate compared with the normal control group. Vaccination with formalin inactivatedV. vulnificus significantly enhanced the specific antibody production in fish treated with vitamin C, and completely protected from strong bacterial challenge the groups fed on fish with vitamin C 1500 and 2000 mg/kg diet. Project 39500113 supported by NSFC and also by Guangdong Science Research Foundation (Grant No. 950711).     

Seasonal change of ice algal and phytoplankton assemblages in the Nella Fjord near Zhongshan Station, East Antarctica

The ice algal and phytoplankton assemblages were studied from Nella Fjord near Zhongshan Station, East Antarctica from April 12 to December 30, 1992. Algal blooms occurred about 3 cm thick on the bottom of sea ice in late April and mid November to early December respectively, and a phytoplankton bloom appeared in the underlying surface water in mid December following the spring ice algal bloom. The biomass in ice bottom was 1 to 3 orders of magnitude higher than that of surface water. Amphiprora kjellmanii, Berkeleya sp., Navicula glaciei, Nitzschia barkelyi, N. cylindrus /N. curta, N. lecointei and Nitzschia sp. were common in the sea ice temporarily or throughout the study period. The biomass in a certain ice segment was decreased gradually and the dominant species were usually succeeded as the season went on. Nitzschia sublineata and Dactyliosolen antarctica were two seasonal dominant species only observed in underlying water column. The assemblages between bottom of ice and underlying surface water were different except when spring ice algae bloomed. The evidence shows that the ice algal blooms occurred mainly by in situ growth of ice algae, and the phytoplankton bloom was mostly caused by the release of ice algae.     

脉宽调制型数字温度表

选择线性热敏电阻组成的脉宽电路 ,将脉宽作为控制计数的时间 ,由晶振产生某一标准频率的脉冲信号 ,通过分频以及计算译码驱动送显示。可直接显示温度数字。该设计省去 A/ D转换器 ,结构简单 ,成本低廉 ,灵敏度高 ,稳定可靠 ,使用方便。     

一种实用的铂热电阻温度巡检仪

介绍了一种经济实用的 16通道铂热电阻测温巡检显示仪 ,并论述了铂热电阻的引线消除和用正反馈实现非线性校正的方法。     

Spatiotemporal characteristics of Qinghai Lake ice phenology between 2000 and 2016

Journal of Geographical Sciences - Lake ice phenology is considered a sensitive indicator of regional climate change. We utilized time series information of this kind extracted from a series of...     

Transition Periods Between Sea Ice Concentration and Sea Surface Air Temperature in the Arctic Revealed by an Abnormal Running Correlation

This study used the synthetic running correlation coefficient calculation method to calculate the running correlation coefficients between the daily sea ice concentration(SIC) and sea surface air temperature(SSAT) in the Beaufort-Chukchi-East Siberian-Laptev Sea(BCEL Sea), Kara Sea and southern Chukchi Sea, with an aim to understand and measure the seasonally occurring changes in the Arctic climate system. The similarities and differences among these three regions were also discussed. There are periods in spring and autumn when the changes in SIC and SSAT are not synchronized, which is a result of the seasonally occurring variation in the climate system. These periods are referred to as transition periods. Spring transition periods can be found in all three regions, and the start and end dates of these periods have advancing trends. The multiyear average duration of the spring transition periods in the BCEL Sea, Kara Sea and southern Chukchi Sea is 74 days, 57 days and 34 days, respectively. In autumn, transition periods exist in only the southern Chukchi Sea, with a multiyear average duration of only 16 days. Moreover, in the Kara Sea, positive correlation events can be found in some years, which are caused by weather time scale processes.