Challenges in video based object detection in maritime scenario using computer vision

This paper discusses the technical challenges in maritime image processing and machine vision problems for video streams generated by cameras. Even well documented problems of horizon detection and registration of frames in a video are very challenging in maritime scenarios. More advanced problems of background subtraction and object detection in video streams are very challenging. Challenges arising from the dynamic nature of the background, unavailability of static cues, presence of small objects at distant backgrounds, illumination effects, all contribute to the challenges as discussed here

Visualisation of an entangled channel spin-1 system

Co-variance matrix formalism gives powerful entanglement criteria for continuous as well as finite dimensional systems. We use this formalism to study a mixed channel spin-1 system which is well known in nuclear reactions. A spin-j state can be visualized as being made up of 2j spinors which are represented by a constellation of 2j points on a Bloch sphere using Majorana construction. We extend this formalism to visualize an entangled mixed spin-1 system.Comment: 4 pages,4 figure

Arbitrarily large families of spaces of the same volume

In any connected non-compact semi-simple Lie group without factors locally isomorphic to SL_2(R), there can be only finitely many lattices (up to isomorphism) of a given covolume. We show that there exist arbitrarily large families of pairwise non-isomorphic arithmetic lattices of the same covolume. We construct these lattices with the help of Bruhat-Tits theory, using Prasad's volume formula to control their covolumes.Comment: 9 pages. Syntax corrected; one reference adde

MELAS: A multigenerational impact of the MTTL1 A3243G MELAS mutation

Background: the maternally inherited MTTL1 A3243G mutation in the mitochondrial genome causes MelaS (Mitochondrial encephalopathy lactic acidosis with Stroke-like episodes), a condition that is multisystemic but affects primarily the nervous system. Significant intra-familial variation in phenotype and severity of disease is well recognized. Methods: retrospective and ongoing study of an extended family carrying the MTTL1 A3243G mutation with multiple symptomatic individuals. tissue heteroplasmy is reviewed based on the clinical presentations, imaging studies, laboratory findings in affected individuals and pathological material obtained at autopsy in two of the family members. Results: there were seven affected individuals out of thirteen members in this three generation family who each carried the MTTL1 A3243G mutation. the clinical presentations were varied with symptoms ranging from hearing loss, migraines, dementia, seizures, diabetes, visual manifestations, and stroke like episodes. three of the family members are deceased from MelaS or to complications related to MelaS. Conclusions: the results of the clinical, pathological and radiological findings in this family provide strong support to the current concepts of maternal inheritance, tissue heteroplasmy and molecular pathogenesis in MelaS. neurologists (both adult and paediatric) are the most likely to encounter patients with MelaS in their practice. genetic counselling is complex in view of maternal inheritance and heteroplasmy. newer therapeutic options such as arginine are being used for acute and preventative management of stroke like episodes. © 2014 Canadian Journal of neurologiCal sciences inc