On Diversified Design Education in an Information Age

Multi-layer and poly-directional development trend is the inevitable situation for contemporary design education development. This is influenced and determined jointly by the intersectionality features of the design disciplinary, the status quo of information society development, and the history of design education development. This article summarizes the currently available educational study results and research experience in the field of design education. It makes discussions on the development significance to the design education. The article also offers preliminary discussions on how to go out of the design education dilemma in the information age so as to make its due contributions to the progress of the design education cause in China.

Short-Term Traffic Flow Local Prediction Based on Combined Kernel Function Relevance Vector Machine Model

Short-term traffic flow prediction is one of the most important issues in the field of adaptive traffic control system and dynamic traffic guidance system. In order to improve the accuracy of short-term traffic flow prediction, a short-term traffic flow local prediction method based on combined kernel function relevance vector machine (CKF-RVM) model is put forward. The C-C method is used to calculate delay time and embedding dimension. The number of neighboring points is determined by use of Hannan-Quinn criteria, and the CKF-RVM model is built based on genetic algorithm. Finally, case validation is carried out using inductive loop data measured from the north–south viaduct in Shanghai. The experimental results demonstrate that the CKF-RVM model is 31.1% and 52.7% higher than GKF-RVM model and GKF-SVM model in the aspect of MAPE. Moreover, it is also superior to the other two models in the aspect of EC

Chesapeake Bay Nitrogen Fluxes Derived From a Land-Estuarine Ocean Biogeochemical Modeling System: Model Description, Evaluation, and Nitrogen Bonds

The Chesapeake Bay plays an important role in transforming riverine nutrients before they are exported to the adjacent continental shelf. Although the mean nitrogen budget of the Chesapeake Bay has been previously estimated from observations, uncertainties associated with interannually varying hydrological conditions remain. In this study, a land-estuarine-ocean biogeochemical modeling system is developed to quantify Chesapeake riverine nitrogen inputs, within-estuary nitrogen transformation processes and the ultimate export of nitrogen to the coastal ocean. Model skill was evaluated using extensive in situ and satellite-derived data, and a simulation using environmental conditions for 2001-2005 was conducted to quantify the Chesapeake Bay nitrogen budget. The 5 year simulation was characterized by large riverine inputs of nitrogen (154 x 109 g N yr-1) split roughly 60: 40 between inorganic: organic components. Much of this was denitrified (34 x 109 g N yr-1) and buried (46 x 109 g N yr-1) within the estuarine system. A positive net annual ecosystem production for the bay further contributed to a large advective export of organic nitrogen to the shelf (91 x 109 g N yr-1) and negligible inorganic nitrogen export. Interannual variability was strong, particularly for the riverine nitrogen fluxes. In years with higher than average riverine nitrogen inputs, most of this excess nitrogen (50-60%) was exported from the bay as organic nitrogen, with the remaining split between burial, denitrification, and inorganic export to the coastal ocean. In comparison to previous simulations using generic shelf biogeochemical model formulations inside the estuary, the estuarine biogeochemical model described here produced more realistic and significantly greater exports of organic nitrogen and lower exports of inorganic nitrogen to the shelf

Chesapeake Bay nitrogen fluxes derived from a land-estuarine ocean biogeochemical modeling system: Model description, evaluation, and nitrogen budgets

The Chesapeake Bay plays an important role in transforming riverine nutrients before they are exported to the adjacent continental shelf. Although the mean nitrogen budget of the Chesapeake Bay has been previously estimated from observations, uncertainties associated with interannually varying hydrological conditions remain. In this study, a land-estuarine-ocean biogeochemical modeling system is developed to quantify Chesapeake riverine nitrogen inputs, within-estuary nitrogen transformation processes and the ultimate export of nitrogen to the coastal ocean. Model skill was evaluated using extensive in situ and satellite-derived data, and a simulation using environmental conditions for 2001-2005 was conducted to quantify the Chesapeake Bay nitrogen budget. The 5 year simulation was characterized by large riverine inputs of nitrogen (154 x 10(9) g N yr(-1)) split roughly 60: 40 between inorganic: organic components. Much of this was denitrified (34 x 10(9) g N yr(-1)) and buried (46 x 10(9) g N yr(-1)) within the estuarine system. A positive net annual ecosystem production for the bay further contributed to a large advective export of organic nitrogen to the shelf (91 x 10(9) g N yr(-1)) and negligible inorganic nitrogen export. Interannual variability was strong, particularly for the riverine nitrogen fluxes. In years with higher than average riverine nitrogen inputs, most of this excess nitrogen (50-60%) was exported from the bay as organic nitrogen, with the remaining split between burial, denitrification, and inorganic export to the coastal ocean. In comparison to previous simulations using generic shelf biogeochemical model formulations inside the estuary, the estuarine biogeochemical model described here produced more realistic and significantly greater exports of organic nitrogen and lower exports of inorganic nitrogen to the shelf

Reply to comment on “Current separation and upwelling over the southeast shelf of Vietnam in the South China Sea”

Author Posting. © American Geophysical Union, 2013. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 118 (2013): 1624, doi:10.1002/jgrc.20114.2013-09-3

Comparative studies on single-layer reduced graphene oxide films obtained by electrochemical reduction and hydrazine vapor reduction

The comparison between two kinds of single-layer reduced graphene oxide (rGO) sheets, obtained by reduction of graphene oxide (GO) with the electrochemical method and hydrazine vapor reduction, referred to as E-rGO and C-rGO, respectively, is systematically studied. Although there is no morphology difference between the E-rGO and C-rGO films adsorbed on solid substrates observed by AFM, the reduction process to obtain the E-rGO and C-rGO films is quite different. In the hydrazine vapor reduction, the nitrogen element is incorporated into the obtained C-rGO film, while no additional element is introduced to the E-rGO film during the electrochemical reduction. Moreover, Raman spectra show that the electrochemical method is more effective than the hydrazine vapor reduction method to reduce the GO films. In addition, E-rGO shows better electrocatalysis towards dopamine than does C-rGO. This study is helpful for researchers to understand these two different reduction methods and choose a suitable one to reduce GO based on their experimental requirements

Synthesis, photophysical properties and two-photon absorption study of tetraazachrysene-based N-heteroacenes

Three novel N‐heteroacene molecules (SDNU‐1, SDNU‐2 and SDNU‐3) based on tetraazachrysene units as cores have been designed, synthesized and fully characterized. Their photophysical, electrochemical and fluorescence properties were investigated, and they exhibited blue to green emission in the solid state. Interestingly, SDNU‐2 exhibited high solid photoluminescence quantum efficiencies (75.3 %), which is the highest value of N‐heteroacenes derivatives to date. Two‐photon absorption studies have been conducted by using the open and close aperture Z‐san technique. SDNU‐3 showed a significant enhancement in the two‐photon absorption cross‐section with magnitudes as high as about 700 GM (1 GM=1×10−50 cm4 s/photon) when excited with 800 nm light, which is the largest value based on a heteroacene system measured by using a Z‐scan experiment so far. We attribute the outcome to sufficient electronic coupling between the strong charge transfer of quadrupolar substituents and the tetraazachrysene core. Our result would provide a new guideline to design novel efficient two‐photon materials based on N‐heteroacene cores