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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
Proteomic Analysis of Retinas from Two Different Type-1 Diabetic Models
Gieth Alahdab
,Sonali Sharma
,Nandini Koneru
,Mohamed Moustafa
,Muhammad N. Haque
,Kaitlin Lowran
,Xiao Zhang
,Khaled Elmasry
,Mohamed Al-Shabrawey
Posted: 15 June 2026
Introduction to TinyML: The New Era of Low-Power AI for IoT Devices
Chandramouli Haldar
,Rishi Jain
Posted: 15 June 2026
Research on Deep Learning-Based User Experience Optimization Methods in the Digital Exhibition of Huizhou Intangible Cultural Heritage
Zhibo Zhang
Posted: 15 June 2026
From Environmental Pollutants to Electricity Generation: A Bibliometric Correlation Between Bioelectrochemistry and Pollutants in the Environment
Pavlos Tziourrou
,Evangelia E. Golia
,Stella Girousi
Posted: 15 June 2026
Bridging Healthcare and Community Physical Activity: The Emerging Role of Physical Activity for Health in Ireland
Stephen McNally
Posted: 15 June 2026
Corporate FinTech Adoption and ESG Disclosure in Saudi Arabia: A Textual Analysis for Sustainable Growth
Durga Prasad Samontaray
,Randheer Kokku
,Najeeb Muhammad Nasir
,Nasir Ali
Posted: 15 June 2026
Sustainable Service Practices and Revisit Intention in the Hospitality Industry: The Roles of Perceived Value, Customer Trust and Environmental Awareness
Mohammed Majeed
Posted: 15 June 2026
Tailoring the Electric Field Response of Porous BaTiO3 Ceramics Fabricated via a Sucrose-Assisted Process
Muhammad Wasim
,Evangelos Kordatos
,Antonio Feteira
,Iasmi Sterianou
Porous BaTiO3 (BTO) ceramics with controlled porosity were successfully fabricated using a simple and cost-effective sucrose-assisted route. Porosity was introduced by incorporating 10–50 vol% sucrose as a pore-forming agent, followed by sintering at 1350 °C for 2 h. The use of sucrose as an effective pore-forming agent is corroborated by the systematic reduction in bulk density from ~5.92 to ~4.1 g.cm-3. X-ray diffraction and Raman spectroscopy analysis revealed the retention of the tetragonal phase across all samples, indicating that the introduction of porosity does not alter either the average crystal or local structure. Microstructural analysis demonstrated well-developed grains with heterogeneously distributed and interconnected porosity upon sucrose addition, while maintaining good grain connectivity. Electrical characterisation showed a gradual decrease in maximum polarisation (Pmax) from ~21 µC.cm-2 for dense BTO to ~12 µC.cm-2 for 50 vol% sucrose samples. Despite increased porosity, the electric field-induced strain response exhibited only a marginal reduction (~0.137% to 0.10%), indicating preserved electromechanical functionality with enhanced large-signal piezoelectric coefficient ~468 pm.V-1 for the 20 vol% sucrose sample, whereas the 10 vol% counterpart shows the largest ɛRT ~1150 with tan δ = 0.005. These results demonstrate that sucrose-assisted fabrication enables effective porosity engineering in BTO without compromising its ferroelectric nature, offering a promising approach for the development of porous ferroelectric ceramics with tunable electromechanical properties.
Porous BaTiO3 (BTO) ceramics with controlled porosity were successfully fabricated using a simple and cost-effective sucrose-assisted route. Porosity was introduced by incorporating 10–50 vol% sucrose as a pore-forming agent, followed by sintering at 1350 °C for 2 h. The use of sucrose as an effective pore-forming agent is corroborated by the systematic reduction in bulk density from ~5.92 to ~4.1 g.cm-3. X-ray diffraction and Raman spectroscopy analysis revealed the retention of the tetragonal phase across all samples, indicating that the introduction of porosity does not alter either the average crystal or local structure. Microstructural analysis demonstrated well-developed grains with heterogeneously distributed and interconnected porosity upon sucrose addition, while maintaining good grain connectivity. Electrical characterisation showed a gradual decrease in maximum polarisation (Pmax) from ~21 µC.cm-2 for dense BTO to ~12 µC.cm-2 for 50 vol% sucrose samples. Despite increased porosity, the electric field-induced strain response exhibited only a marginal reduction (~0.137% to 0.10%), indicating preserved electromechanical functionality with enhanced large-signal piezoelectric coefficient ~468 pm.V-1 for the 20 vol% sucrose sample, whereas the 10 vol% counterpart shows the largest ɛRT ~1150 with tan δ = 0.005. These results demonstrate that sucrose-assisted fabrication enables effective porosity engineering in BTO without compromising its ferroelectric nature, offering a promising approach for the development of porous ferroelectric ceramics with tunable electromechanical properties.
Posted: 15 June 2026
Spatial Co-Location of Oil Extraction and Agricultural Storage Infrastructure: Implications for Sustainable Land-Use Planning in North Dakota
Edmond Loni M. Lisinge
,Raj Bridgelall
Posted: 15 June 2026
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