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Warfarin-Induced Developmental Toxicity: Insights into Embryogenesis, Teratogenicity, and Molecular Pathways
Evelyn Magee
,Grace Kuhnel
,Poongodi Geetha-Loganathan
Posted: 15 June 2026
Graph-Based Epidemic Intelligence: Explainable Neural Models for Pandemic Control and Zoonotic Transmission
Francesco Branda
,Annamaria Defilippo
,Ugo Lomoio
,Patrizia Vizza
,Fabio Scarpa
,Massimo Ciccozzi
,Pierangelo Veltri
,Pietro Hiram Guzzi
Posted: 15 June 2026
An Ensemble Multi-Task Learning Model for Predictive Performance Evaluation of Air Handling Units in HVAC Systems
Tobi Micheal Alabi
,Adedayo Johnson Ogungbile
,Favour David Agbajor
Posted: 15 June 2026
Transforming Lives: U‑Rock’s Restorative Pedagogy with Youth in Conflict with the Law
Edgar R. Eslit
Posted: 15 June 2026
A Trusted Execution Environment for Secure Reasoning on Large-Scale Models in the Power Industry
Zhibo Zhang
Posted: 15 June 2026
Temporal Patterns of Natural Infection of Grapevine Pruning Wounds by Botryosphaeriaceae, Diaporthe, and Cytospora in a Two-Year Multi-Site Field Study
Katherine Ashley
,Catarina Leal
,Rebeca Bujanda
,Valérie Didier
,Mélanie Duvillet
,David Gramaje
Posted: 15 June 2026
LeJEPA-FGP: Factorized Gaussian Process Regularization for Identifiable Joint-Embedding World Models
Yuan-Hao Wei
Posted: 15 June 2026
Transcriptomic Profiling Identifies a Subset of Renal Tumours with Overlapping Features of Clear Cell Papillary Renal Cell Tumour and Renal Cell Carcinoma with Fibromyomatous Stroma
Rasmus Jakobsson
,Martin Lindström
,Yvonne Arvidsson
,Iva Johansson
,Jonas A. Nilsson
,Niels Marcussen
,Joakim Karlsson
,Martin E. Johansson
Posted: 15 June 2026
Mapping the Mediascape in Motion: A Systematic Literature Review of Emerging Trends and Persistent Research Gaps in International Communication Studies, 2000–2026
Safran Safar Almakaty
Posted: 15 June 2026
Technical Aspects of Commercial Prebiotic Manufacturing
Sandra Saville
,Koen Venema
,Bradley A. Saville
,Helena Baric
,Sami M. Derya
Posted: 15 June 2026
Geometric Structure of Vector Fields on Surfaces—Toward a Nonlocal Definition of Vortex
Zhen Li
Posted: 15 June 2026
Genetic Approach in Diagnosis and Follow-Up of Patients with Thalassemia: A Comprehensive Narrative Review
Ashraf T. Soliman
,Fawzia Alyafei
,Nada Alaaraj
,Noor Hamed
,Shayma Ahmed
,Ahmed Elawwa
Posted: 15 June 2026
Harmonic Forecasting of Annual Peak Snow Water Equivalent at SNOTEL Monitoring Stations Across the Western United States
Joseph Higginbotham
,John Walker
Posted: 15 June 2026
Microbiota Profiling of Cerebrospinal Fluid in Bacterial Meningitis Using 16S rRNA Metagenomic Sequencing
Oral Oncul
,Lutfiye Oksuz
,Fatma Erdem
,Ugur Sezerman
,Zerrin Aktas
Posted: 15 June 2026
Post-Quantum Cryptography Migration for Agentic AI Systems
Robert Campbell
Posted: 15 June 2026
Training Frontline Providers in Basic Obstetric Ultrasound to Promote Healthy Pregnancy in Zimbabwe: Trainer and Trainee Experiences from a Qualitative Phenomenological Study
Cladious Verenga
,Shalote Chipamaunga-Bamu
,Farai Madzimbamuto
,Sunanda C. Ray
Posted: 15 June 2026
An Adaptive Shooting and Bouncing Ray Method Based on Q-Learning for Efficient Synthetic Aperture Radar Imaging Simulation
Dayong Tian
,Shuo Wang
,Md. Gazi Salahuddin
,Xiaoyang Li
Posted: 15 June 2026
Toxoplasma gondii in Wild Cervids and Wild Canids: Feeding Ecology, Environmental Exposure, and Trophic Transmission
Vy Dinh Bao Tran
,Dong-Hyuk Jeong
Toxoplasma gondii is a zoonotic protozoan transmitted by environmentally persistent oocysts and by tissue cysts in infected prey or meat. This structured narrative review compares infection evidence in five wild cervid species and three wild canid species to examine how feeding ecology shapes exposure and to assess their complementary value in wildlife surveillance. Peer-reviewed literature published between 2004 and 2025 was retrieved from PubMed, Scopus, ScienceDirect, and Google Scholar. Studies reporting evidence of T. gondii exposure or infection in wild cervids or wild canids were included, with serological evidence evaluated separately from molecular or histological detection. Cervids showed geographically variable exposure consistent with ingestion of oocysts from contaminated vegetation, soil, and water, supporting their use as sentinels of environmental contamination. Wild canids often showed higher reported seropositivity, although direct comparisons were limited by assay, sampling, and demographic heterogeneity. Their predatory, scavenging, and omnivorous diets allow access to both environmental oocysts and tissue cysts. Cervids and canids should therefore be treated as complementary rather than interchangeable indicators: cervids primarily reflect environmental exposure, whereas canids integrate environmental and trophic transmission. Standardized diagnostics, paired host–environment sampling, and explicit ecological metadata are needed to strengthen One Health surveillance and food-safety assessment.
Toxoplasma gondii is a zoonotic protozoan transmitted by environmentally persistent oocysts and by tissue cysts in infected prey or meat. This structured narrative review compares infection evidence in five wild cervid species and three wild canid species to examine how feeding ecology shapes exposure and to assess their complementary value in wildlife surveillance. Peer-reviewed literature published between 2004 and 2025 was retrieved from PubMed, Scopus, ScienceDirect, and Google Scholar. Studies reporting evidence of T. gondii exposure or infection in wild cervids or wild canids were included, with serological evidence evaluated separately from molecular or histological detection. Cervids showed geographically variable exposure consistent with ingestion of oocysts from contaminated vegetation, soil, and water, supporting their use as sentinels of environmental contamination. Wild canids often showed higher reported seropositivity, although direct comparisons were limited by assay, sampling, and demographic heterogeneity. Their predatory, scavenging, and omnivorous diets allow access to both environmental oocysts and tissue cysts. Cervids and canids should therefore be treated as complementary rather than interchangeable indicators: cervids primarily reflect environmental exposure, whereas canids integrate environmental and trophic transmission. Standardized diagnostics, paired host–environment sampling, and explicit ecological metadata are needed to strengthen One Health surveillance and food-safety assessment.
Posted: 15 June 2026
A Review of Standards for Artificial Intelligence Compliance in Nuclear Instrumentation Control System
Alberto Monici
Posted: 15 June 2026
Local-Time Sensitivity and Burst Instability for Threshold Functionals of One-Dimensional Diffusions
Tristan Guillaume
Let \(X = \left( X_{t} \right)_{0 \leq t \leq T}\) be a real-valued continuous process. For a threshold \(a\), the sub-threshold time set \[E_{T}(a) = \{ t \in \lbrack 0,T\rbrack:X_{t} \leq a\}\] encodes several different threshold observables. The most elementary one is the cumulative occupation time \[A_{T}(a) = \int_{0}^{T}\mathbf{1}_{\{ X_{t} \leq a\}}\, dt.\] For a regular one-dimensional diffusion, the classical occupation density formula gives \[A_{T}(a) = \int_{- \infty}^{a}\frac{L_{T}^{y}(X)}{\sigma^{2}(y)}\, dy,\] and hence \[\frac{\partial A_{T}}{\partial a}(a) = \frac{L_{T}^{a}(X)}{\sigma^{2}(a)}.\] Thus additive threshold occupation admits a local-time sensitivity calculus. In the terminology of barrier contracts, this additive clock is the cumulative, non-resetting Parisian clock, also called the Parasian clock. The purpose of this paper is to contrast this additive/Parasian regime with the behavior of resetting Parisian burst functionals. The connected components of \(E_{T}(a)\) represent sub-threshold episodes. We study in particular the longest burst \[M_{T}(a) = \sup\{|I|:I\text{ is a connected component of }E_{T}(a)\}.\] While \(A_{T}\) is locally controlled by local time, \(M_{T}\) is governed by the connectivity of the sub-threshold time set. We prove that \(M_{T}\) is monotone, that its supremum is attained, and that the weak-sublevel version is right-continuous with left limits, while the strict-sublevel version is its left-continuous regularization. The jump at a level is the increase in the maximal connected-component length produced by adjoining the level set. This gives a deterministic càdlàg/càglàd calculus for longest-burst profiles. For regular one-dimensional diffusions, this yields a sharp structural contrast. At deterministic levels which are almost surely not local-extreme values, the weak and strict longest bursts agree almost surely. Whenever the path has a unique interior maximum, the level-indexed longest-burst profile has a positive jump at the maximum level and is therefore not absolutely continuous. Brownian motion satisfies this criterion almost surely. We further identify the deterministic mechanism behind this instability: small threshold increases may fill short temporal bridges and merge large sub-threshold components. Finally, we show that the longest burst is exactly a one-sided continuous Parisian functional. This yields an exact Laplace-transform representation of its Brownian law through the Chesney--Jeanblanc-Picqué--Yor [1] Parisian transform, and an excursion-measure formulation in which local time enters only as the Itô excursion intensity. We also discuss smoothed burst statistics, moving thresholds, and diffusion examples. The paper is intended as a threshold-sensitivity comparison: local time controls cumulative Parasian occupation, whereas resetting Parisian burst observables are controlled by component mergers and excursion structure.
Let \(X = \left( X_{t} \right)_{0 \leq t \leq T}\) be a real-valued continuous process. For a threshold \(a\), the sub-threshold time set \[E_{T}(a) = \{ t \in \lbrack 0,T\rbrack:X_{t} \leq a\}\] encodes several different threshold observables. The most elementary one is the cumulative occupation time \[A_{T}(a) = \int_{0}^{T}\mathbf{1}_{\{ X_{t} \leq a\}}\, dt.\] For a regular one-dimensional diffusion, the classical occupation density formula gives \[A_{T}(a) = \int_{- \infty}^{a}\frac{L_{T}^{y}(X)}{\sigma^{2}(y)}\, dy,\] and hence \[\frac{\partial A_{T}}{\partial a}(a) = \frac{L_{T}^{a}(X)}{\sigma^{2}(a)}.\] Thus additive threshold occupation admits a local-time sensitivity calculus. In the terminology of barrier contracts, this additive clock is the cumulative, non-resetting Parisian clock, also called the Parasian clock. The purpose of this paper is to contrast this additive/Parasian regime with the behavior of resetting Parisian burst functionals. The connected components of \(E_{T}(a)\) represent sub-threshold episodes. We study in particular the longest burst \[M_{T}(a) = \sup\{|I|:I\text{ is a connected component of }E_{T}(a)\}.\] While \(A_{T}\) is locally controlled by local time, \(M_{T}\) is governed by the connectivity of the sub-threshold time set. We prove that \(M_{T}\) is monotone, that its supremum is attained, and that the weak-sublevel version is right-continuous with left limits, while the strict-sublevel version is its left-continuous regularization. The jump at a level is the increase in the maximal connected-component length produced by adjoining the level set. This gives a deterministic càdlàg/càglàd calculus for longest-burst profiles. For regular one-dimensional diffusions, this yields a sharp structural contrast. At deterministic levels which are almost surely not local-extreme values, the weak and strict longest bursts agree almost surely. Whenever the path has a unique interior maximum, the level-indexed longest-burst profile has a positive jump at the maximum level and is therefore not absolutely continuous. Brownian motion satisfies this criterion almost surely. We further identify the deterministic mechanism behind this instability: small threshold increases may fill short temporal bridges and merge large sub-threshold components. Finally, we show that the longest burst is exactly a one-sided continuous Parisian functional. This yields an exact Laplace-transform representation of its Brownian law through the Chesney--Jeanblanc-Picqué--Yor [1] Parisian transform, and an excursion-measure formulation in which local time enters only as the Itô excursion intensity. We also discuss smoothed burst statistics, moving thresholds, and diffusion examples. The paper is intended as a threshold-sensitivity comparison: local time controls cumulative Parasian occupation, whereas resetting Parisian burst observables are controlled by component mergers and excursion structure.
Posted: 15 June 2026
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