In the field of forensic imaging, it is important to be able to extract a camera fingerprint from one or a small set of images known to have been taken by the same camera (or image sensor). Note that we are using the word fingerprint because it is a piece of information extracted from images that can be used to identify an individual source camera. This technique is very important for certain security and digital forensic situations. Camera fingerprint is based on a certain kind of random noise present in all image sensors that is due to manufacturing imperfections and is, thus, unique and impossible to avoid. Photo response nonuniformity (PRNU) has become the most widely used method for source camera identification (SCI). In this paper, a set of attacks is designed and applied to a PRNU-based SCI system, and the success of each method is systematically assessed both in the case of still images and in the case of video. An attack method is defined as any processing that minimally alters image quality and is designed to fool PRNU detectors or, in general, any camera fingerprint detector. The success of an attack is assessed as the increment in the error rate of the SCI system. The PRNU-based SCI system was taken from an outstanding reference that is publicly available. Among the results of this work, the following are remarkable: the use of a systematic and extensive procedure to test SCI methods, very thorough testing of PRNU with more than 2000 test images, and the finding of some very effective attacks on PRNU-based SCI.
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http://dx.doi.org/10.3390/s23073462 | DOI Listing |
PLoS One
January 2025
Nanjing University of Information Science and Technology, Nanjing, China.
The forensic examination of AIGC(Artificial Intelligence Generated Content) faces poses a contemporary challenge within the realm of color image forensics. A myriad of artificially generated faces by AIGC encompasses both global and local manipulations. While there has been noteworthy progress in the forensic scrutiny of fake faces, current research primarily focuses on the isolated detection of globally and locally manipulated fake faces, thus lacking a universally effective detection methodology.
View Article and Find Full Text PDFVoid spot assay (VSA) noninvasively evaluates urination. VSA is often not performed in rats due to difficulty analyzing larger papers compared with mouse. This study optimizes VSA for rats by comparing post-assay visualization techniques: bright field light (BF), ultraviolet light (UV), and ninhydrin spray (N).
View Article and Find Full Text PDFAdv Sci (Weinh)
January 2025
PASTEUR, Département de chimie, École normale supérieure, PSL University, Sorbonne Université, CNRS, 24, rue Lhomond, Paris, 75005, France.
Imaging luminescence kinetics is invaluable in many fields, including biology and chemistry. However, the luminescence lifetime of most photo-activated states is in the low ns-µs range and its measurement requires adding costly image intensifiers to cameras to access the fast phenomena present. Here, the Rectified Imaging under Optical Modulation (RIOM) and Heterodyne Imaging under Optical Modulation (HIOM) protocols make this possible with standard low-cost cameras only, even under ambient light.
View Article and Find Full Text PDFJ Forensic Sci
January 2025
Department of Mathematics, Iowa State University, Ames, Iowa, USA.
ACS Chem Neurosci
October 2024
Department of Chemistry, Sharif University of Technology, Tehran 111559516, Iran.
Dopaminergic agents are compounds that modulate dopamine-related activity in the brain and peripheral nerves within the pathways on both sides of the blood-brain barrier. Atypical levels of them can precipitate a multitude of neurological disorders, whose timely diagnosis signifies not only stopping the advancement of the illness but also surmounting it. A silver metallized gold nanorod (AuNRs) conditional sensor array, designed to detect dopaminergic agents for assessing nervous system disorders, yielded significant results in simultaneous detection and discrimination of Benserazide (Benz), Levodopa (L-DOPA), and Carbidopa (Carb).
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