RESUMO
Existing distortion functions in steganography which achieved high undetectability are designed for unprocessed natural image. Nowadays, a large number of images are filtered before transmitting for the sake of beautification. In this situation, existing distortion functions should be improved to fit the properties of these beautified images. This paper proposes a distortion function optimization method for steganography on beautified images. Given an unprocessed image, a popular image beautification software is employed to produce two similar beautified images. One of them is used for embedding and the other one is employed as reference. Guided by the reference, existing distortion functions are improved by distinguishing the embedding costs for ±1 embedding. After embedding, the stego image is closer to the reference, which results in a higher undetectability against steganalysis. Experimental results also proved the increasing of undetectability when examined by modern steganalytic tools.
Assuntos
Segurança Computacional , Interpretação de Imagem Assistida por Computador/métodos , Processamento de Imagem Assistida por Computador/métodos , Informática/métodos , Algoritmos , Estética , Reprodutibilidade dos Testes , SoftwareRESUMO
The cooperativity effects between the O/N-HâââO hydrogen-bonding and NaâºâââO cation-molecule interactions in the 1: 2 (Naâº: N-(Hydroxymethyl)acetamide) systems were investigated at the B3LYP/6-311++G**, MP2(full)/6-311++G** and MP2(full)/aug-cc-pvtz levels. The thermodynamic cooperativity calculations were also carried out for two pathways of the ternary-complex formation. The result shows that, in most ternary complexes, the O/N-HâââO and NaâºâââO interactions are weakened in comparison with those in binary systems, leading to the anti-cooperativity effects, in particular in the complexes in which only the NaâºâââO interactions exist. Shifts of electron density confirm the existence of anti-cooperativity. The increase of favorable enthalpic contribution leads to the positive cooperativity effect with negative ΔG(coop.) on forming the ternary complex by initial N-(Hydroxymethyl)acetamide dimer followed by addition of Naâº. In forming the ternary complex by NaâºâââN-(Hydroxymethyl)acetamide with the second N-(Hydroxymethyl)acetamide unit, the large unfavorable entropy change leads to the negative cooperativity effect with positive ΔG(coop.). The ternary complex is more easily formed by the pathway in which Na⺠binds to N-(Hydroxymethyl)acetamide dimer.