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26 pages, 20364 KiB  
Article
Seasonal Mathematical Model of Salmonellosis Transmission and the Role of Contaminated Environments and Food Products
by Mohammed H. Alharbi, Fawaz K. Alalhareth and Mahmoud A. Ibrahim
Mathematics 2025, 13(2), 322; https://doi.org/10.3390/math13020322 - 20 Jan 2025
Abstract
Salmonellosis continues to be a global public health priority in which humans, livestock, and the contaminated environment interact with food to create complex interactions. Here, a new non-autonomous model is proposed to capture seasonal dynamics of Salmonella typhimurium transmission with key compartments that [...] Read more.
Salmonellosis continues to be a global public health priority in which humans, livestock, and the contaminated environment interact with food to create complex interactions. Here, a new non-autonomous model is proposed to capture seasonal dynamics of Salmonella typhimurium transmission with key compartments that include humans, cattle, and bacteria in environmental and food sources. The model explores how bacterial growth, shedding, and ingestion rates, along with contamination pathways, determine disease dynamics. Some analytical derivations of the basic reproduction number (R0) and threshold conditions for disease persistence or extinction are derived by using the spectral radius of a linear operator associated with the monodromy matrix. Parameter estimation for the model was accomplished with the aid of Latin hypercube sampling and least squares methods on Salmonella outbreak data from Saudi Arabia ranging from 2018 to 2021. The model was able to conduct an analysis based on the estimated 0.606 value of R0, and this meant that the model was able to fit reasonably well for both the cumulative and the new individual case data, which in turn, suggests the disease is curable. Predictions indicate a gradual decline in the number of new cases, with stabilization anticipated at approximately 40,000 cumulative cases. Further simulations examined the dynamics of disease extinction and persistence based on R0. When R0 is less than 1, the disease-free equilibrium is stable, resulting in the extinction of the disease. Conversely, when R0 exceeds 1, the disease persists, exhibiting endemic characteristics with recurrent outbreaks. Sensitivity analysis identified several parameters as having a significant impact on the model’s outcomes, specifically mortality and infection rates, along with decay rates. These findings highlight the critical importance of precise parameter estimation in understanding and controlling the transmission dynamics of Salmonella. Sensitivity indices and contour plots were employed to assess the impact of various parameters on the basic reproduction number and provide insights into the factors most influencing disease transmission. Full article
(This article belongs to the Special Issue Dynamics and Differential Equations in Mathematical Biology)
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<p>Diagram illustrating the flow of the model (<a href="#FD1-mathematics-13-00322" class="html-disp-formula">1</a>).</p>
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<p>Fitting results of the model to data from Saudi Arabia (2018–2021), showing cumulative infected cases (<b>left</b>) and newly infected cases (<b>right</b>). The parameter values used for the fitting are provided in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a>.</p>
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<p>The predicted trajectory of new Salmonella infections in Saudi Arabia is illustrated using the parameter values detailed in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a>.</p>
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<p>Extinction of Salmonella when <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="script">R</mi> <mn>0</mn> </msub> <mo>=</mo> <mn>0.6066</mn> <mo>&lt;</mo> <mn>1</mn> </mrow> </semantics></math>, given the specific parameter values specified in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a> (extinction).</p>
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<p>Persistence of Salmonella when <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="script">R</mi> <mn>0</mn> </msub> <mo>=</mo> <mn>6.97762</mn> <mo>&gt;</mo> <mn>1</mn> </mrow> </semantics></math>, given the specific parameter values specified in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a> (persistence).</p>
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<p>Positive periodic solutions when <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="script">R</mi> <mn>0</mn> </msub> <mo>=</mo> <mn>6.97762</mn> <mo>&gt;</mo> <mn>1</mn> </mrow> </semantics></math>, given the specific parameter values specified in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a> (persistence).</p>
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<p>Positive periodic solutions when <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="script">R</mi> <mn>0</mn> </msub> <mo>=</mo> <mn>6.97762</mn> <mo>&gt;</mo> <mn>1</mn> </mrow> </semantics></math>, given the specific parameter values specified in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a> (persistence).</p>
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<p>Sensitivity analysis for <math display="inline"><semantics> <mrow> <mo stretchy="false">[</mo> <msub> <mi mathvariant="script">R</mi> <mn>0</mn> </msub> <mo stretchy="false">]</mo> </mrow> </semantics></math>, using the parameter values specified in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a>. Sensitivity indices are presented in descending order of magnitude.</p>
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<p>Contour plots of the time-average basic reproduction number (<math display="inline"><semantics> <mrow> <mo stretchy="false">[</mo> <msub> <mi mathvariant="script">R</mi> <mn>0</mn> </msub> <mo stretchy="false">]</mo> </mrow> </semantics></math>) are presented as functions of <math display="inline"><semantics> <msub> <mi>β</mi> <mi>h</mi> </msub> </semantics></math>, <math display="inline"><semantics> <msub> <mi>α</mi> <mi>h</mi> </msub> </semantics></math>, <math display="inline"><semantics> <msub> <mi>α</mi> <mi>c</mi> </msub> </semantics></math>, <math display="inline"><semantics> <mrow> <mo stretchy="false">[</mo> <msub> <mi>β</mi> <mrow> <mi>b</mi> <mi>h</mi> </mrow> </msub> <mo stretchy="false">]</mo> </mrow> </semantics></math>, <math display="inline"><semantics> <msub> <mi>β</mi> <mi>c</mi> </msub> </semantics></math>, <math display="inline"><semantics> <mrow> <mo stretchy="false">[</mo> <msub> <mi>β</mi> <mrow> <mi>b</mi> <mi>c</mi> </mrow> </msub> <mo stretchy="false">]</mo> </mrow> </semantics></math>, <math display="inline"><semantics> <mrow> <mo stretchy="false">[</mo> <msub> <mi>β</mi> <mi>f</mi> </msub> <mo stretchy="false">]</mo> </mrow> </semantics></math>, <math display="inline"><semantics> <mi>η</mi> </semantics></math>, <math display="inline"><semantics> <msub> <mi>μ</mi> <mi>f</mi> </msub> </semantics></math>, and <math display="inline"><semantics> <msub> <mi>μ</mi> <mi>b</mi> </msub> </semantics></math>, with all other parameters set to the values given in <a href="#mathematics-13-00322-t002" class="html-table">Table 2</a>.</p>
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<p>Prediction of new Salmonella infections in Saudi Arabia.</p>
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15 pages, 18148 KiB  
Article
Fast 3D Transmission Tower Detection Based on Virtual Views
by Liwei Zhou, Jiaying Tan, Jing Fu and Guiwei Shao
Appl. Sci. 2025, 15(2), 947; https://doi.org/10.3390/app15020947 (registering DOI) - 19 Jan 2025
Viewed by 290
Abstract
Advanced remote sensing technologies leverage extensive synthetic aperture radar (SAR) satellite data and high-resolution airborne light detection and ranging (LiDAR) data to swiftly capture comprehensive 3D information about electrical grid assets and their surrounding environments. This facilitates in-depth scene analysis for target detection [...] Read more.
Advanced remote sensing technologies leverage extensive synthetic aperture radar (SAR) satellite data and high-resolution airborne light detection and ranging (LiDAR) data to swiftly capture comprehensive 3D information about electrical grid assets and their surrounding environments. This facilitates in-depth scene analysis for target detection and classification, allowing for the early recognition of potential hazards near transmission towers (TTs). These innovations present a groundbreaking strategy for the automated inspection of electrical grid assets. However, traditional 3D target detection techniques, which involve searching the entire 3D space, are marred by low accuracy and high computational demands. Although deep learning-based 3D target detection methods have significantly improved detection precision, they rely on a large volume of 3D target samples for training and are sensitive to point cloud data density. Moreover, these methods demonstrate low detection efficiency, constraining their application in the automated monitoring of electricity networks. This paper proposes a fast 3D target detection method using virtual views to overcome these challenges related to detection accuracy and efficiency. The method first utilizes cutting-edge 2D splatting technology to project 3D point clouds with diverse densities from a specific viewpoint, generating a 2D virtual image. Then, a novel local–global dual-path feature fusion network based on YOLO is applied to detect TTs on the virtual image, ensuring efficient and accurate identification of their positions and types. Finally, by leveraging the projection transformation between the virtual image and the 3D point cloud, combined with a 3D region growing algorithm, the 3D points belonging to the TTs are extracted from the whole 3D point cloud. The effectiveness of the proposed method in terms of target detection rate and efficiency is validated through experiments on synthetic datasets and outdoor LiDAR point clouds. Full article
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<p>Overall pipeline of the proposed method. The detected TTs are highlighted in red rectangles in the virtual image and are rendered in red within the 3D point cloud.</p>
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<p>Comparison of two projection strategies on the TT.</p>
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<p>Illustration of a portion of a generated virtual view.</p>
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<p>Local–global dual-path feature fusion network.</p>
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<p>Illustration of a TT extracted from the LiDAR data.</p>
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<p>Seven selected scenarios from TTPLA. All TTs are photographed from different angles.</p>
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<p>Example of airborne LiDAR data.</p>
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<p>Illustration of 2D detection results on airborne LiDAR data.</p>
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<p>Illustration of 3D detection results on airborne LiDAR data.</p>
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16 pages, 5748 KiB  
Article
Probabilistic Analysis of Infinite Slope Stability Considering Variation in Soil Depth
by Taejin Kim, Taeho Bong and Donggeun Kim
Appl. Sci. 2025, 15(2), 936; https://doi.org/10.3390/app15020936 (registering DOI) - 18 Jan 2025
Viewed by 324
Abstract
In probabilistic slope stability analysis, soil depth has been treated as a deterministic variable, although it is a highly variable parameter. This study aims to identify soil depth variability using seismic refraction survey data and to analyze its impact on probabilistic analysis of [...] Read more.
In probabilistic slope stability analysis, soil depth has been treated as a deterministic variable, although it is a highly variable parameter. This study aims to identify soil depth variability using seismic refraction survey data and to analyze its impact on probabilistic analysis of slope stability. Seismic refraction survey data were collected from 70 slopes in South Korea and employed to identify the variability of soil depth within natural slopes. As a result, the average soil depth across 70 slopes was 2.5 m, with an average coefficient of variation (COV) of 29%, indicating high variability. To investigate the influence of soil depth variability on the probability of slope failure, probabilistic slope stability analysis was conducted by considering the shear strength parameters of soil and soil depth as random variables. Accordingly, the influences of the variability of soil depth on the probabilistic analysis of slope stability were evaluated by comparing the probability of slope failure and distribution of the failure occurrence frequency by depth. Additionally, global sensitivity analysis was conducted to understand the relative contribution of input parameters on the probability of slope failure. Consequently, the probability of slope failure can vary significantly depending on soil depth variability, emphasizing the importance of considering this factor in probabilistic slope stability analysis. Full article
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<p>Schematic diagram of research process.</p>
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<p>Location of surveyed slopes in South Korea.</p>
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<p>Estimation of slope depth by P-wave velocity.</p>
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<p>Cross-section for slope stability analysis.</p>
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<p>Flowchart for the probabilistic slope stability analysis.</p>
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<p>Soil depth extraction at 5 m intervals to determine the variability in depth along the slope.</p>
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<p>Examples of slopes based on the average soil depth and its COV.</p>
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<p>Box plots of statistics of soil depth.</p>
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<p>Comparison of change in <span class="html-italic">P<sub>f</sub></span> according to saturation depth for each case.</p>
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<p>Comparison of frequency distribution of failure occurrences with depth: (<b>a</b>) saturation depth = 1.5 m and (<b>b</b>) saturation depth = 2.5 m.</p>
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<p>CDF of the minimum <span class="html-italic">F</span><sub>S</sub> for a saturation depth of 1.5 m.</p>
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<p>CDF of the minimum <span class="html-italic">F</span><sub>S</sub> for a saturation depth of 2.5 m.</p>
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<p>Changes in sensitivity of random variables according to saturation depth: (<b>a</b>) Case 2; (<b>b</b>) Case 3; and (<b>c</b>) Case 4.</p>
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29 pages, 597 KiB  
Article
The Impact and Mechanisms of State-Owned Shareholding on Greenwashing Behaviors in Chinese A-Share Private Enterprises
by Xinru Li, Zengrui Tian, Qian Liu and Beiquan Chang
Sustainability 2025, 17(2), 741; https://doi.org/10.3390/su17020741 - 18 Jan 2025
Viewed by 349
Abstract
In response to the increasing global emphasis on environmental accountability, the issue of greenwashing requires urgent resolution. This research investigates how state ownership affects greenwashing behaviors in Chinese A-share private companies over the period from 2010 to 2021, utilizing resource support and supervisory [...] Read more.
In response to the increasing global emphasis on environmental accountability, the issue of greenwashing requires urgent resolution. This research investigates how state ownership affects greenwashing behaviors in Chinese A-share private companies over the period from 2010 to 2021, utilizing resource support and supervisory governance as analytical frameworks. Empirical analysis reveals that state-owned shareholder holdings significantly inhibit greenwashing practices in private enterprises, with this result remaining robust across various sensitivity tests. Furthermore, it is demonstrated that these holdings reduce greenwashing through both resource support and supervisory governance pathways. This study enhances the scholarly understanding of how state capital impacts private firms and underscores the distinctive roles and benefits that state-owned shareholders bring to the mixed-ownership reform process. The results suggest new pathways for fostering the sustainable development of private enterprises and offer crucial insights for policymakers focused on advancing mixed-ownership reforms and ensuring corporate accountability. Full article
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<p>Conceptual framework illustrating the influence of state-owned shareholders’ equity holdings on greenwashing practices in private firms.</p>
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19 pages, 2632 KiB  
Article
A Novel Mobile Phase for Green Chromatographic Determination of Haloperidol: Application to Commercial Pharmaceutical Products and Forced Degradation Studies
by Khadidja Djilali, Rachida Maachi, Mohammed Danish, Sabrina Lekmine, Mohamed Hadjadj, Zohra Ait Mesbah, Ouided Benslama, Hichem Tahraoui, Mohammad Shamsul Ola, Ahmad Ali, Jie Zhang and Abdeltif Amrane
Processes 2025, 13(1), 260; https://doi.org/10.3390/pr13010260 - 17 Jan 2025
Viewed by 292
Abstract
The target molecule of this study is haloperidol, a neuroleptic from the butyrophenone family. It is one of the most widely used psychotropic drugs globally and is considered as effective as other low-potency psychotropic medications. The RP-HPLC method employed in this study utilizes [...] Read more.
The target molecule of this study is haloperidol, a neuroleptic from the butyrophenone family. It is one of the most widely used psychotropic drugs globally and is considered as effective as other low-potency psychotropic medications. The RP-HPLC method employed in this study utilizes a novel mobile phase composed of a 90:10 mixture of methanol and phosphate buffer (pH = 9.8) for isocratic elution. This method has been validated with a correlation coefficient (R) of 0.999 across a concentration range of 2.5 to 50 µg/mL. It exhibits excellent sensitivity, with a relative standard deviation (RSD) of less than 2% for both precision and accuracy. The method is highly effective for the analysis of haloperidol in oral commercial formulations. The mobile phase is cost-efficient, environmentally friendly, and simple to use, making it suitable for analyzing haloperidol in both liquid and powder forms. Additionally, the method is applied to monitor haloperidol degradation under various stress conditions. For powder samples, the maximum degradation observed was 6.20% after 48 h of sunlight exposure. For liquid haloperidol samples, stability was retained only under oxidative stress conditions, with the highest degradation (57.36%) occurring after 48 h of sunlight exposure and the lowest degradation (10.03%) observed under thermal stress at 60 °C over seven days. Full article
(This article belongs to the Section Pharmaceutical Processes)
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<p>Structure of haloperidol and its degradation products [<a href="#B22-processes-13-00260" class="html-bibr">22</a>].</p>
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<p>Chromatogram of haloperidol.</p>
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<p>(<b>A</b>) Linearity of the method; (<b>B</b>) residual graph showing the method’s linearity.</p>
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<p>Chromatograms of proposed RP-HPLC method for placebo (<b>A</b>), haloperidol (<b>B</b>), and commercial product (haloperidol oral solution 2 mg/mL) (<b>C</b>).</p>
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<p>Forced degradation of haloperidol in the presence of (<b>A</b>) HCl 0.1 N, 60 °C and 7 days; (<b>B</b>) HCl 1.0 N, 60 °C and 7 days; (<b>C</b>) NaOH 0.1 N, 60 °C and 7 days; (<b>D</b>) NaOH 1.0 N, 60 °C and 7 days; (<b>E</b>) H<sub>2</sub>O<sub>2</sub> 0.3%, 25 °C and 7 days; (<b>F</b>) H<sub>2</sub>O<sub>2</sub> 3.0%, 25 °C and 7 days; (<b>G</b>) H<sub>2</sub>O<sub>2</sub> 0.3%, 60 °C and 7 days; (<b>H</b>) H<sub>2</sub>O<sub>2</sub> 3.0%, 60 °C and 7 days.</p>
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<p>Forced degradation of haloperidol through (<b>A</b>) thermal degradation of active principal (PA) powder at 60 °C in 15 days; (<b>B</b>) thermal degradation of PA powder at 80 °C in 15 days; (<b>C</b>) thermal degradation of PA solution at 60 °C in 7 days; (<b>D</b>) thermal degradation of PA solution at 80 °C in 7 days; (<b>E</b>) photolytic degradation of PA powder in the presence of sunlight in 48 h; (<b>F</b>) photolytic degradation of PA solution in the presence of sunlight in 48 h (<b>G</b>) photolytic degradation of PA powder in the presence of UV light in 48 h; (<b>H</b>) photolytic degradation of PA solution in presence of UV light in 48 h.</p>
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19 pages, 675 KiB  
Article
Assessing the Role of Vaccination in the Control of Hand, Foot, and Mouth Disease Transmission
by Zuhur Alqahtani, Mahmoud H. DarAssi, Yousef AbuHour and Areej Almuneef
Mathematics 2025, 13(2), 268; https://doi.org/10.3390/math13020268 - 15 Jan 2025
Viewed by 374
Abstract
The impact of vaccination on the dynamics of hand, foot, and mouth disease (HFMD) transmission is explored in this paper, considering a fractional-order derivative system of equations. This model provides vaccination strategies and characterizes local and global stability using Lyapunov functions. This work [...] Read more.
The impact of vaccination on the dynamics of hand, foot, and mouth disease (HFMD) transmission is explored in this paper, considering a fractional-order derivative system of equations. This model provides vaccination strategies and characterizes local and global stability using Lyapunov functions. This work computes the basic reproduction number (R0) to represent the endemic and epidemic scenarios. Additionally, sensitivity analysis was performed to identify the most critical parameters responsible for the disease dissemination. Our results indicate that vaccination plays a crucial role in controlling HFMD, significantly reducing its prevalence. These findings align with existing research, supporting the importance of effective vaccination strategies and public health interventions against HFMD. The fractional-order model captures the memory effect in infectious disease dynamics, providing further insight into modeling HFMD transmission compared to a traditional integer-order model. The results would contribute to effective vaccination strategies and public health interventions against HFMD. Full article
(This article belongs to the Section E3: Mathematical Biology)
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<p>Links between compartments in the HFMD model.</p>
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<p>Comparative dynamics of foot, hand, and mouth disease: endemic states with fractional derivatives: (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>α</mi> <mo>=</mo> <mn>0.3</mn> </mrow> </semantics></math> vs. (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>α</mi> <mo>=</mo> <mn>0.8</mn> </mrow> </semantics></math>, and (<b>c</b>) pandemic potential with basic reproduction number <math display="inline"><semantics> <mrow> <msub> <mi>R</mi> <mn>0</mn> </msub> <mo>&gt;</mo> <mn>1</mn> </mrow> </semantics></math>.</p>
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<p>Modeling foot, hand, and mouth disease dynamics: a comparative analysis of short-term vs. long-term infection spread using alpha fractional derivatives.</p>
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<p>Trajectories of foot, hand, and mouth disease spread: convergence at the pandemic point.</p>
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<p>Controlling foot, hand, and mouth disease: recovery rate vs. vaccination efficiency.</p>
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<p>Parameter sensitivity: PRCC analysis.</p>
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25 pages, 1993 KiB  
Article
Hacking Exposed: Leveraging Google Dorks, Shodan, and Censys for Cyber Attacks and the Defense Against Them
by Abdullah Alabdulatif and Navod Neranjan Thilakarathne
Computers 2025, 14(1), 24; https://doi.org/10.3390/computers14010024 - 15 Jan 2025
Viewed by 334
Abstract
In recent years, cyberattacks have increased in sophistication, using a variety of tools to exploit vulnerabilities across the global digital landscapes. Among the most commonly used tools at an attacker’s disposal are Google dorks, Shodan, and Censys, which offer unprecedented access to exposed [...] Read more.
In recent years, cyberattacks have increased in sophistication, using a variety of tools to exploit vulnerabilities across the global digital landscapes. Among the most commonly used tools at an attacker’s disposal are Google dorks, Shodan, and Censys, which offer unprecedented access to exposed systems, devices, and sensitive data on the World Wide Web. While these tools can be leveraged by professional hackers, they have also empowered “Script Kiddies”, who are low-skill, inexperienced attackers who use readily available exploits and scanning tools without deep technical knowledge. Consequently, cyberattacks targeting critical infrastructure are growing at a rapid rate, driven by the ease with which these solutions can be operated with minimal expertise. This paper explores the potential for cyberattacks enabled by these tools, presenting use cases where these platforms have been used for both offensive and defensive purposes. By examining notable incidents and analyzing potential threats, we outline proactive measures to protect against these emerging risks. In this study, we delve into how these tools have been used offensively by attackers and how they serve defensive functions within cybersecurity. Additionally, we also introduce an automated all-in-one tool designed to consolidate the functionalities of Google dorks, Shodan, and Censys, offering a streamlined solution for vulnerability detection and analysis. Lastly, we propose proactive defense strategies to mitigate exploitation risks associated with such tools, aiming to enhance the resilience of critical digital infrastructure against evolving cyber threats. Full article
(This article belongs to the Special Issue Multimedia Data and Network Security)
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<p>Distribution of detected worldwide cyberattacks by type in 2022.</p>
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<p>Key steps involved in executing a cyberattack.</p>
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<p>Example of a Google dork query.</p>
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<p>Example of a Shodan query that returns a list of IP addresses for devices running Apache within the specified country: United States.</p>
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<p>Example of a Shodan query with filtered options.</p>
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<p>Example of a Censys search to find all devices with a software product with the word “Windows” in it.</p>
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<p>Automated Cyber Threat Hunting Tool V1.0.</p>
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15 pages, 4628 KiB  
Article
Evaluating the Impact of Climate Change on the Asia Habitat Suitability of Troides helena Using the MaxEnt Model
by Fengrong Yang, Quanwei Liu, Junyi Yang, Biyu Liu, Xinqi Deng, Tingjiang Gan, Xue Liao, Xiushan Li, Danping Xu and Zhihang Zhuo
Insects 2025, 16(1), 79; https://doi.org/10.3390/insects16010079 - 14 Jan 2025
Viewed by 477
Abstract
Butterflies are highly sensitive to climate change, and Troides helena, as an endangered butterfly species, is also affected by these changes. To enhance the conservation of T. helena and effectively plan its protected areas, it is crucial to understand the potential impacts [...] Read more.
Butterflies are highly sensitive to climate change, and Troides helena, as an endangered butterfly species, is also affected by these changes. To enhance the conservation of T. helena and effectively plan its protected areas, it is crucial to understand the potential impacts of climate change on its distribution. This study utilized a MaxEnt model in combination with ArcGIS technology to predict the global potential suitable habitats of T. helena under current and future climate conditions, using the species’ distribution data and relevant environmental variables. The results indicated that the MaxEnt model provided a good prediction accuracy for the distribution of T. helena. Under the current climate scenario, the species is primarily distributed in tropical regions, with high suitability areas concentrated in tropical rainforest climates. In future climate scenarios, the suitable habitat areas for T. helena in medium and high suitability categories generally show an expansion trend, which increases over time. Especially under the SSP5-8.5 scenario, by the 2090s, the area of high suitability for T. helena is projected to increase by 42.85%. The analysis of key environmental factors revealed that precipitation of the wettest quarter (Bio16) was the most significant environmental factor affecting the distribution of T. helena. The species has high demands for precipitation and temperature and can adapt to future climate warming. This study is valuable for identifying the optimal conservation areas for T. helena and provides a reference for future conservation efforts. Full article
(This article belongs to the Section Insect Ecology, Diversity and Conservation)
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<p>Evaluation of the modeling results for <span class="html-italic">T. helena</span> using the ROC curve and AUC.</p>
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<p>Variable importance, as determined via the folding jackknife test, for <span class="html-italic">T. helena</span>.</p>
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<p>Potential distribution and occurrence records of <span class="html-italic">T. helena</span> under current climate conditions. The red triangles represent the occurrence records of <span class="html-italic">T. helena</span>.</p>
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<p>Potential distribution of <span class="html-italic">T. helena</span> in future periods (2050s, 2090s) under the SSP1-2.6, SSP2-4.5, and SSP5-8.5 climate change scenarios. (<b>A</b>) represents the potential suitable habitat under the SSP1-2.6 scenario in the 2050s, (<b>B</b>) represents the potential suitable habitat under the SSP2-4.5 scenario in the 2050s, (<b>C</b>) represents the potential suitable habitat under the SSP5-8.5 scenario in the 2050s, (<b>D</b>) represents the potential suitable habitat under the SSP1-2.6 scenario in the 2090s, (<b>E</b>) represents the potential suitable habitat under the SSP2-4.5 scenario in the 2090s, and (<b>F</b>) represents the potential suitable habitat under the SSP5-8.5 scenario in the 2090s.</p>
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<p>Changes in the High Suitability Habitat of <span class="html-italic">T. helena</span> from the Present to the Future; “Gain” indicates areas where high suitability habitats have increased, “Lost” indicates areas where high suitability habitats have decreased, “Abs” indicates the area where non-high suitability habitats (unsuitable, low, and medium suitability) remain unchanged, and “Pres” indicates the area where high suitability habitats remain unchanged. (<b>A</b>) represents the changes in potential suitable habitat from the current scenario to the SSP1-2.6 scenario in the 2050s, (<b>B</b>) represents the changes in potential suitable habitat from the current scenario to the SSP2-4.5 scenario in the 2050s, (<b>C</b>) represents the changes in potential suitable habitat from the current scenario to the SSP5-8.5 scenario in the 2050s, (<b>D</b>) represents the changes in potential suitable habitat from the current scenario to the SSP1-2.6 scenario in the 2090s, (<b>E</b>) represents the changes in potential suitable habitat from the current scenario to the SSP2-4.5 scenario in the 2090s, and (<b>F</b>) represents the changes in potential suitable habitat from the current scenario to the SSP5-8.5 scenario in the 2090s.</p>
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<p>Response curves of <span class="html-italic">T. helena</span> to the five dominant environmental variables. The blue area represents the range of occurrence probability, while the red curve represents the average occurrence probability.</p>
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18 pages, 19968 KiB  
Article
How Do Changes in Grassland Phenology and Its Responses to Extreme Climatic Events in Central Asia?
by Xinwei Wang, Jianhao Li, Jianghua Zheng, Liang Liu, Xiaojing Yu, Ruikang Tian and Mengxiang Xing
Land 2025, 14(1), 160; https://doi.org/10.3390/land14010160 - 14 Jan 2025
Viewed by 298
Abstract
Extreme climate events have become more frequent under global warming, significantly affecting vegetation phenology and carbon cycles in Central Asia. However, the mediating effects of intensity of compound drought and heat events (CDHEs) and compound moisture and heat events (CMHEs) on grassland phenology [...] Read more.
Extreme climate events have become more frequent under global warming, significantly affecting vegetation phenology and carbon cycles in Central Asia. However, the mediating effects of intensity of compound drought and heat events (CDHEs) and compound moisture and heat events (CMHEs) on grassland phenology and their trends in the relative contributions to grassland phenology over time have remained unclear. Based on the calculation results of grassland phenology and compound events (CEs), this study used trend analysis, partial least squares regression structural equation modeling (PLS-SEM), and ridge regression analysis to investigate the mediating effect and the temporal trend in relative contribution of CEs to grassland phenology in Central Asia, and the magnitude of sensitivity of grassland phenology to CEs. This study revealed that the start of season (SOS) was advanced by 0.4 d·a−1, end of season (EOS) was delayed by 0.5 d·a−1, and length of season (LOS) extended by 0.8 d·a−1 in 1982–2022. The duration of the CDHEs (0−37 days) was greater than that of the CMHEs (0−9 days) in Central Asia. The direct effects of CDHEs and CMHEs on grassland phenology were generally negative, except for the direct positive effect of CDHEs on LOS. The indirect effects of temperature and precipitation on grassland phenology through CDHEs and CMHEs were greater than their direct effects on phenology. The relative contribution of CDHEs to grassland phenology was consistently greater than that of CMHEs, and both the relative contribution curves showed a significant upward trend. The sensitivity of grassland phenology to CDHEs was higher than its sensitivity to CMHEs at 0.79 (SOS), 1.18 (EOS), and 0.72 (LOS). Our results emphasize the mediating effects of CDHEs and CMHEs on grassland phenology. Under the influence of CDHEs and CMHEs, the LOS will further lengthen in the future. Full article
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<p>(<b>a</b>) Geographic location, elevation and (<b>b</b>) aridity index (AI) classification. The AI classification is based on the unit-free AI values calculated from the precipitation and reference evapotranspiration datasets, and the results are obtained according to different categories.</p>
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<p>Scatter density plot of the grassland phenology (<b>a</b>) SOS, (<b>b</b>) EOS, and (<b>c</b>) LOS test results. x-axis is the results based on NDVI, <span class="html-italic">y</span>-axis represents the phenology extraction results based on CSIF.</p>
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<p>Spatial distribution and temporal profile of multi-year means of grassland phenology (<b>a</b>,<b>b</b>) SOS, (<b>c</b>,<b>d</b>) EOS, and (<b>e</b>,<b>f</b>) LOS in 1982−2022. The box represents the interquartile range; the centerline represents the median; the whisker line represents 1.5 times the value of the object, which is an outlier; and the long-term trends (ΔSOS, ΔEOS and ΔLOS) were obtained from a linear fit.</p>
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<p>Spatial distribution and temporal curves of intensity of CDHEs and CMHEs for (<b>a</b>–<b>c</b>) SOS, (<b>d</b>–<b>f</b>) EOS and (<b>g</b>–<b>i</b>) LOS in 1982−2022.</p>
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<p>Spatial distribution of the long-term trends in grassland phenology (<b>a</b>) SOS, (<b>b</b>) EOS, and (<b>c</b>) LOS, along with the trend results for different AI zones. Trends above 0 indicate advanced phenology, while trends below 0 indicate delayed phenology.</p>
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<p>Spatial distribution of the long-term trends in (<b>a</b>–<b>c</b>) CDHEs and (<b>d</b>–<b>f</b>) CMHEs, along with the trend results for different AI zones. Trends above 0 indicate increasing trend in intensity, while trends below 0 indicate decreasing trend in intensity.</p>
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<p>Effect pathways between mean climate states (TEM and PRE), extreme climate events (DEs, TX90p and WEs), CEs (CDHEs and CMHEs), and grassland phenology for (<b>a</b>) SOS, (<b>b</b>) EOS, and (<b>c</b>) LOS in Central Asia. Solid lines indicate direct effects between factors, with red lines representing positive effects and blue lines representing negative effects. The coefficients in this study passed the <span class="html-italic">p</span> &lt; 0.05 significance test. The model was tested by GFI and RMSEA to determine the appropriateness of the fit.</p>
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<p>Spatial and temporal changes in the relative contribution of climate change to grassland phenology (<b>a</b>) SOS, (<b>b</b>) EOS, and (<b>c</b>) LOS over time. The bar chart shows the statistics of the share of the maximum impact factor in each AI zones. Equation is the result of the trend statistics.</p>
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<p>Spatial distribution of sensitivity of (<b>a</b>–<b>c</b>) CDHEs and (<b>d</b>–<b>f</b>) CMHEs to grassland phenology.</p>
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21 pages, 9488 KiB  
Article
Identification of Immune Infiltration-Associated CC Motif Chemokine Ligands as Biomarkers and Targets for Colorectal Cancer Prevention and Immunotherapy
by Minghao Liu, Teng Wang and Mingyang Li
Int. J. Mol. Sci. 2025, 26(2), 625; https://doi.org/10.3390/ijms26020625 - 13 Jan 2025
Viewed by 345
Abstract
Colorectal cancer (CRC) is the third most common cancer globally, with limited effective biomarkers and sensitive therapeutic targets. An increasing number of studies have highlighted the critical role of tumor microenvironment (TME) imbalances, particularly immune escape due to impaired chemokine-mediated trafficking, in tumorigenesis [...] Read more.
Colorectal cancer (CRC) is the third most common cancer globally, with limited effective biomarkers and sensitive therapeutic targets. An increasing number of studies have highlighted the critical role of tumor microenvironment (TME) imbalances, particularly immune escape due to impaired chemokine-mediated trafficking, in tumorigenesis and progression. Notably, CC chemokines (CCLs) have been shown to either promote or inhibit angiogenesis, metastasis, and immune responses in tumors, thereby influencing cancer development and patient outcomes. However, the diagnostic and prognostic significance of CCLs in CRC remains unclear. In this study, multiple online tools for bioinformatics analyses were utilized. The findings revealed that the mRNA expression levels of CCL3, CCL4, and CCL26 were significantly elevated in CRC tissues compared to normal tissues, whereas CCL2, CCL5, CCL11, CCL21, and CCL28 mRNA levels were markedly downregulated. Additionally, dysregulation of CCL4, CCL5, and CCL21 was strongly associated with clinical staging, and elevated levels of CCL4, CCL11, and CCL28 were linked to significantly prolonged survival in CRC patients. Functional enrichment analysis indicated that the cellular roles of CCLs were predominantly associated with the chemokine, Wnt, and Toll-like receptor signaling pathways, as well as protein kinase activity. Furthermore, transcriptional regulation of most CCLs involved RELA and NFKB1. Key downstream targets included members of the SRC family of tyrosine kinases (HCK, LYN, and LCK), serine/threonine kinases (ATR and ATM), and others such as CSNK1G2, NEK2, and CDK2. Moreover, CCLs (CCL2, CCL3, CCL4, CCL5, CCL11, CCL21, and CCL28) exhibited strong correlations with major infiltration-related immune cells, including B cells, CD8+ T cells, CD4+ T cells, macrophages, neutrophils, and dendritic cells. In conclusion, our study provides novel insights into the potential utility of CCLs as biomarkers and therapeutic targets for CRC prevention and immunotherapy. Full article
(This article belongs to the Section Molecular Informatics)
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<p>mRNA levels of CCLs in CRC. (<b>A</b>) The numbers of datasets with significant CCL mRNA overexpression (red) or downregulated expression (blue) based on ONCOMINE. (<b>B</b>) mRNA levels of CCLs in CRC compared with normal tissues from the TCGA database; data were expressed as medians (*, <span class="html-italic">p</span> &lt; 0.05; ***, <span class="html-italic">p</span> &lt; 0.001; ****, <span class="html-italic">p</span> &lt; 0.0001). (<b>C</b>) The relative level of CCLs in CRC using GEPIA.</p>
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<p>Correlation of CCLs with pathological stage and clinical outcomes in CRC. (<b>A</b>) The expression differences in CCLs among various pathological stages of CRC patients based on GEPIA. (<b>B</b>) The prognostic value of these indicators in CRC patients was assessed by drawing the overall survival curve on data from HPA.</p>
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<p>Genetic alteration, mutual expression, and protein–protein interaction of CCLs in CRC. (<b>A</b>) Summary of alterations in CCLs in CRC based on samples from cBioPortal (n = 1510). (<b>B</b>) Heat map showing the correlations among these CCLs in CRC (*, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001). (<b>C</b>) Gene–gene interaction network of different expressed CCLs using GeneMANIA. (<b>D</b>) Venn diagram gathering the common genes that were simultaneously mutated and co-expressed with CCLs. (<b>E</b>) Protein–protein interaction network of these CCLs and the expression products of these co-expressed mutated genes by searching STRING.</p>
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<p>The enrichment analysis of CCLs and co-expressed mutated genes in CRC. (<b>A</b>) Bubble diagram of KEGG-enriched terms using Shbio. (<b>B</b>) Bar plot of GO enrichment in cellular component terms, biological process terms, and molecular function terms based on Metascape.</p>
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<p>The correlation between CCLs and immune cell infiltration in CRC. The correlation between the abundance of immune cells and the expression of (<b>A</b>) CCL1, (<b>B</b>) CCL2, (<b>C</b>) CCL3, (<b>D</b>) CCL4, (<b>E</b>) CCL5, (<b>F</b>) CCL11, (<b>G</b>) CCL21, and (<b>H</b>) CCL28 in CRC using Sanger Box (ns, <span class="html-italic">p</span> &gt; 0.05; *, <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001; ****, <span class="html-italic">p</span> &lt; 0.0001). “TIMER_Neutrophil” and “TIMER_Macrophage” are metrics of immune infiltration correlation.</p>
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25 pages, 5527 KiB  
Article
Molecular Epidemiological Characteristics of Staphylococcus pseudintermedius, Staphylococcus coagulans, and Coagulase-Negative Staphylococci Cultured from Clinical Canine Skin and Ear Samples in Queensland
by Sara Horsman, Julian Zaugg, Erika Meler, Deirdre Mikkelsen, Ricardo J. Soares Magalhães and Justine S. Gibson
Antibiotics 2025, 14(1), 80; https://doi.org/10.3390/antibiotics14010080 - 13 Jan 2025
Viewed by 657
Abstract
Background/Objectives: Infections in dogs caused by methicillin-resistant staphylococci (MRS) present limited treatment options. This study’s objective was to investigate the molecular epidemiology of Staphylococcus spp. cultured exclusively from clinical canine skin and ear samples in Queensland, Australia, using whole-genome sequencing (WGS). Methods: Forty-two [...] Read more.
Background/Objectives: Infections in dogs caused by methicillin-resistant staphylococci (MRS) present limited treatment options. This study’s objective was to investigate the molecular epidemiology of Staphylococcus spp. cultured exclusively from clinical canine skin and ear samples in Queensland, Australia, using whole-genome sequencing (WGS). Methods: Forty-two Staphylococcus spp. isolated from clinical canine skin and ear samples, from an unknown number of dogs, were sourced from two veterinary diagnostic laboratories between January 2022 and May 2023. These isolates underwent matrix-assisted laser desorption ionisation– time of flight bacterial identification, minimum inhibitory concentration testing using SensititreTM plates and WGS. Phylogenetic trees and core genome multilocus sequence typing (cgMLST) minimum spanning trees (MSTs) were constructed. Results: The isolates included methicillin-resistant and -sensitive S. pseudintermedius (MRSP: 57.1%, 24/42; and MSSP: 19.1%, 8/42), methicillin-resistant and -sensitive S. coagulans (MRSC: 14.3%, 6/42; and MSSC: 2.4%, 1/42) and methicillin-resistant coagulase-negative staphylococci (MR-CoNS: 7.1%, 3/42). Thirty-nine isolates were included after WGS, where all MRS harboured the mecA gene. Eighteen sequence types (STs) were identified, including three novel MRSP and six novel MSSP STs. MRSP ST496-V-VII (23%; 9/39) and MRSP ST749-IV-(IVg) (12.8%; 5/39) were commonly isolated. Phylogenetic analysis of single nucleotide polymorphisms showed that MRSP, MRSC and MSSC were similar to globally isolated staphylococci from canine skin and ear infections. Using cgMLST MSTs, MRSP isolates were not closely related to global strains. Conclusions: Our findings revealed a genotypically diverse geographical distribution and phylogenetic relatedness of staphylococci cultured from clinical canine skin and ear samples across Queensland. This highlights the importance of ongoing surveillance to aid in evidence-based treatment decisions and antimicrobial stewardship. Full article
(This article belongs to the Special Issue Antimicrobial Resistance and Infections in Animals)
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<p>The maximum likelihood phylogenetic tree based on the core-alignment of single nucleotide polymorphisms (SNPs) of the 23 methicillin-resistant <span class="html-italic">Staphylococcus pseudintermedius</span> and 8 methicillin-sensitive <span class="html-italic">S. pseudintermedius</span> isolates cultured from clinical canine skin and ear samples. Included in the tree are 109 clinically relevant <span class="html-italic">S. pseudintermedius</span> genomes from the literature. The genome sequence of <span class="html-italic">S. pseudintermedius</span> LMG 22219 (GCA_001792775.2) was used as the reference for the SNP analysis. The isolates in this study are identified by ‘canine_#’, coloured in red. The presence of a <span class="html-italic">mecA</span> gene, SCC<span class="html-italic">mec</span> type, sample site, country and year the isolate was cultured, number of viruses and plasmids and multilocus sequence types (MLSTs) is annotated in the outer rings.</p>
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<p>The maximum likelihood phylogenetic tree based on the core-alignment of single nucleotide polymorphisms (SNPs) of the five methicillin-resistant <span class="html-italic">Staphylococcus coagulans</span> and one methicillin-sensitive <span class="html-italic">S. coagulans</span> isolates cultured from clinical canine skin and ear samples. Included in the tree are 124 clinically relevant <span class="html-italic">S. coagulans</span> genomes from the literature. The genome sequence of <span class="html-italic">S. coagulans</span> DSM 6628 (GCA_002901995.1) was used as the reference for the SNP analysis. The isolates in this study were identified by ‘canine_#’, coloured in red. The presence of a <span class="html-italic">mecA</span> gene, SCC<span class="html-italic">mec</span> type, sample site, country and year the isolate was cultured and the number of viruses and plasmids is annotated in the outer rings.</p>
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<p>GrapeTree minimum spanning tree showing core genome multilocus sequence types (cgMLST) of the methicillin-resistant and -sensitive <span class="html-italic">Staphylococcus pseudintermedius</span> sequenced isolates in this study (n = 31). The name for each isolate from this study is shown next to the corresponding node or circle (canine_#). The blue numbers refer to the allelic differences between two isolates. Each node represents a unique cgMLST. Canine_49 is a MSSP ST749. Isolates with closely related genotypes (≤25 allelic differences) are shaded in grey. The lines are scaled logarithmically.</p>
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<p>GrapeTree minimum spanning tree showing core genome multilocus sequence type (cgMLST) of the methicillin-resistant and -sensitive <span class="html-italic">Staphylococcus pseudintermedius</span> sequenced isolates in this study (n = 31), and the <span class="html-italic">S. pseudintermedius</span> reference genomes (n = 109). The name for each isolate from this study is shown next to the corresponding node or circle (canine_#). The reference genome nodes are only labelled if the isolates were closely related, denoted as RG_# (n = 31 reference genomes with ≤25 allelic differences). The list of corresponding reference genomes is in the table under the tree. The blue numbers refer to the allelic differences between genomes. Each node represents a unique cgMLST. Canine_49 is a MSSP ST749. Isolates and reference genomes with closely related genotypes (≤25 allelic differences) are shaded in grey. The lines are scaled logarithmically.</p>
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<p>Heatmap displaying the distribution of the <span class="html-italic">Staphylococcus</span> spp. multilocus sequence types (MLSTs), staphylococcal cassette chromosome <span class="html-italic">mec</span> (SCC<span class="html-italic">mec</span>) types, canine demographic factors, sample site, phenotypic antimicrobial resistance (AMR) profiles and AMR and virulence genes of the <span class="html-italic">Staphylococcus</span> spp. isolates (ordered from top to bottom by species and MLST: two methicillin-resistant coagulase-negative staphylococci (MR-CoNS), five methicillin-resistant <span class="html-italic">S. coagulans</span> (MRSC), one methicillin-sensitive <span class="html-italic">S. coagulans</span> (MSSC), 23 methicillin-resistant <span class="html-italic">S. pseudintermedius</span> (MRSP), and eight methicillin-sensitive <span class="html-italic">S. pseudintermedius</span> (MSSP) isolates). Mutations in the fluoroquinolone and mupirocin genes were also identified as an amino acid substitution. The presence and absence of the genes (or mutations) or elements is represented by the coloured and grey blocks, respectively. The horizontal colour bar on the bottom from left to right represents the canine demographic data, antimicrobials/antimicrobial classes for the phenotypic AMR profiles, AMR genes and specific virulence factors. SE-QLD = southeast Queensland; QLD = Queensland; NA = not applicable.</p>
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<p>Heatmap displaying the distribution of the <span class="html-italic">Staphylococcus</span> spp. multilocus sequence types (MLSTs), presence of the <span class="html-italic">mecA</span> gene, staphylococcal cassette chromosome <span class="html-italic">mec</span> (SCC<span class="html-italic">mec</span>) types, canine demographic factors, sample site, efflux pumps, quaternary ammonium compound, heavy metal genes and insertion sequence elements with the cluster identification of the <span class="html-italic">Staphylococcus</span> spp. isolates (ordered from top to bottom by species and MLST: two methicillin-resistant coagulase-negative staphylococci (MR-CoNS) isolates, five methicillin-resistant <span class="html-italic">S. coagulans</span> (MRSC), one methicillin-sensitive <span class="html-italic">S. coagulans</span> (MSSC), 23 methicillin-resistant <span class="html-italic">S. pseudintermedius</span> (MRSP), eight methicillin-sensitive <span class="html-italic">S. pseudintermedius</span> (MSSP) isolates). The presence and absence of the genes or elements is represented by the coloured and grey blocks, respectively. The horizontal colour bar on the bottom from left to right represents the canine demographic data and specific heavy metals including arsenic, cadmium and copper. SE-QLD = southeast Queensland; QLD = Queensland; NA = not applicable.</p>
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36 pages, 1986 KiB  
Review
Exploring Innovative Approaches for the Analysis of Micro- and Nanoplastics: Breakthroughs in (Bio)Sensing Techniques
by Denise Margarita Rivera-Rivera, Gabriela Elizabeth Quintanilla-Villanueva, Donato Luna-Moreno, Araceli Sánchez-Álvarez, José Manuel Rodríguez-Delgado, Erika Iveth Cedillo-González, Garima Kaushik, Juan Francisco Villarreal-Chiu and Melissa Marlene Rodríguez-Delgado
Biosensors 2025, 15(1), 44; https://doi.org/10.3390/bios15010044 - 13 Jan 2025
Viewed by 745
Abstract
Plastic pollution, particularly from microplastics (MPs) and nanoplastics (NPs), has become a critical environmental and health concern due to their widespread distribution, persistence, and potential toxicity. MPs and NPs originate from primary sources, such as cosmetic microspheres or synthetic fibers, and secondary fragmentation [...] Read more.
Plastic pollution, particularly from microplastics (MPs) and nanoplastics (NPs), has become a critical environmental and health concern due to their widespread distribution, persistence, and potential toxicity. MPs and NPs originate from primary sources, such as cosmetic microspheres or synthetic fibers, and secondary fragmentation of larger plastics through environmental degradation. These particles, typically less than 5 mm, are found globally, from deep seabeds to human tissues, and are known to adsorb and release harmful pollutants, exacerbating ecological and health risks. Effective detection and quantification of MPs and NPs are essential for understanding and mitigating their impacts. Current analytical methods include physical and chemical techniques. Physical methods, such as optical and electron microscopy, provide morphological details but often lack specificity and are time-intensive. Chemical analyses, such as Fourier transform infrared (FTIR) and Raman spectroscopy, offer molecular specificity but face challenges with smaller particle sizes and complex matrices. Thermal analytical methods, including pyrolysis gas chromatography–mass spectrometry (Py-GC-MS), provide compositional insights but are destructive and limited in morphological analysis. Emerging (bio)sensing technologies show promise in addressing these challenges. Electrochemical biosensors offer cost-effective, portable, and sensitive platforms, leveraging principles such as voltammetry and impedance to detect MPs and their adsorbed pollutants. Plasmonic techniques, including surface plasmon resonance (SPR) and surface-enhanced Raman spectroscopy (SERS), provide high sensitivity and specificity through nanostructure-enhanced detection. Fluorescent biosensors utilizing microbial or enzymatic elements enable the real-time monitoring of plastic degradation products, such as terephthalic acid from polyethylene terephthalate (PET). Advancements in these innovative approaches pave the way for more accurate, scalable, and environmentally compatible detection solutions, contributing to improved monitoring and remediation strategies. This review highlights the potential of biosensors as advanced analytical methods, including a section on prospects that address the challenges that could lead to significant advancements in environmental monitoring, highlighting the necessity of testing the new sensing developments under real conditions (composition/matrix of the samples), which are often overlooked, as well as the study of peptides as a novel recognition element in microplastic sensing. Full article
(This article belongs to the Special Issue Micro-nano Optic-Based Biosensing Technology and Strategy)
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<p>Chemical structure of the most common polymers present in MPs and NPs.</p>
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<p>Scheme of the current methods for analyzing microplastics and nanoplastics.</p>
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<p>Scheme of electrochemical (bio)sensing approaches (with or without receptors) for the analysis of microplastics.</p>
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<p>Scheme of plasmonic and fluorescence sensing approaches: (<b>a</b>) colorimetric methods, (<b>b</b>) surface plasmon resonance, (<b>c</b>) localized surface plasmon resonance, (<b>d</b>) surface-enhanced Raman spectroscopy, and (<b>e</b>) fluorescence for the analysis of microplastics.</p>
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22 pages, 3947 KiB  
Article
Enhancing Soybean Salt Tolerance with GSNO and Silicon: A Comprehensive Physiological, Biochemical, and Genetic Study
by Meshari Winledy Msarie, Nusrat Jahan Methela, Mohammad Shafiqul Islam, Tran Hoang An, Ashim Kumar Das, Da-Sol Lee, Bong-Gyu Mun and Byung-Wook Yun
Int. J. Mol. Sci. 2025, 26(2), 609; https://doi.org/10.3390/ijms26020609 - 13 Jan 2025
Viewed by 316
Abstract
Soil salinity is a major global challenge affecting agricultural productivity and food security. This study explores innovative strategies to improve salt tolerance in soybean (Glycine max), a crucial crop in the global food supply. This study investigates the synergistic effects of [...] Read more.
Soil salinity is a major global challenge affecting agricultural productivity and food security. This study explores innovative strategies to improve salt tolerance in soybean (Glycine max), a crucial crop in the global food supply. This study investigates the synergistic effects of S-nitroso glutathione (GSNO) and silicon on enhancing salt tolerance in soybean (Glycine max). Two soybean cultivars, Seonpung (salt-tolerant) and Cheongja (salt-sensitive), were analyzed for various physiological, biochemical, and genetic traits under salt stress. The results showed that the combined GSNO and Si treatment significantly improved several key traits, including plant height, relative water content, root development, nodule numbers, chlorophyll content, and stomatal aperture, under both control and salt stress conditions. Additionally, this treatment optimized ion homeostasis by enhancing the Na/K ratio and Ca content, while reducing damage markers such as electrolyte leakage, malondialdehyde, and hydrogen peroxide. The stress-responsive compounds, including proline, ascorbate peroxidase, and water-soluble proteins, were elevated under stress conditions, indicating improved tolerance. Gene expression analysis revealed significant upregulation of genes such as GmNHX1, GmSOS2, and GmAKT1, associated with salt stress response, while GmNIP2.1, GmNIP2.2, and GmLBR were downregulated in both varieties. Notably, the salt-sensitive variety Cheongja exhibited higher electrolyte leakage and oxidative damage compared to the salt-tolerant Seonpung. These findings suggest that the combination of GSNO and silicon enhances salt tolerance in soybean by improving physiological resilience, ion homeostasis, and stress-responsive gene expression. Full article
(This article belongs to the Special Issue Nitric Oxide Signalling in Plants)
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<p>The combined application of GSNO and Si enhanced plant growth in the soybean cultivars Seonpung and Cheongja under salt stress. (<b>A</b>) The plant phenotype of Cheongja and Seonpung, (<b>B</b>) plant height, (<b>C</b>) shoot relative water content, (<b>D</b>) shoot fresh weight, and (<b>E</b>) shoot dry weight. Plants were treated with control, GSNO, Si, and GSNO + Si under two factors: water and salt conditions. Sampling was performed at 28 days of age. The bar graph displays the standard error of the mean, with each data point representing the average of three replicates. The letters on the bars indicate significant differences determined using the DMRT at <span class="html-italic">p</span> ≤ 0.05. The same letters indicate no significant differences.</p>
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<p>The combined GSNO and Si treatment improved root traits in the soybean cultivars Seonpung and Cheongja under salt stress. (<b>A</b>) The root morphology of Cheongja, (<b>B</b>) root morphology of Seonpung, (<b>C</b>) total root length, (<b>D</b>) average root diameter, (<b>E</b>) root fresh weight, (<b>F</b>) root dry weight, (<b>G</b>) root relative water content, and (<b>H</b>) number of root tips. The bar graph displays the standard error of the mean, with each data point representing the average of three replicates. The letters on the bars indicate significant differences determined using DMRT at <span class="html-italic">p</span> ≤ 0.05. The same letters indicate no significant differences.</p>
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<p>Combined GSNO and Si treatment increased nodule numbers in the soybean cultivars Seonpung and Cheongja under salt-induced stress. (<b>A</b>) Nodules in Cheongja, (<b>B</b>) nodules in Seonpung, (<b>C</b>) nodule weight, and (<b>D</b>) nodule number. A centimeter (cm) ruler in A and B is shown in for scale reference. The bar graph displays the standard error of the mean, with each data point representing the average of three replicates. The letters on the bars indicate significant differences determined using DMRT at <span class="html-italic">p</span> ≤ 0.05. The same letters indicate no significant differences.</p>
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<p>Combined GSNO and Si treatment promoted plant growth in Seonpung and Cheongja under salt stress. (<b>A</b>) <span class="html-italic">Chlorophyll a</span>, (<b>B</b>) <span class="html-italic">chlorophyll b</span>, (<b>C</b>) stomatal aperture, and (<b>D</b>) leaf stomata under a light microscope. The scale bar represents 5 µm. The bar graph displays the standard error of the mean, with each data point representing the average of three replicates. The letters on the bars indicate significant differences determined using DMRT at <span class="html-italic">p</span> ≤ 0.05. The same letters indicate no significant differences.</p>
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<p>The combined GSNO and Si treatment regulates ion homeostasis in Seonpung and Cheongja under salt stress. (<b>A</b>) Na content, (<b>B</b>) K content, (<b>C</b>) Na/K ratio, (<b>D</b>) Ca content, and (<b>E</b>) Si accumulation. The bar graph displays the standard error of the mean, with each data point representing the average of three replicates. The letters on the bars indicate significant differences determined by DMRT at <span class="html-italic">p</span> ≤ 0.05. The same letters indicate no significant differences.</p>
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<p>The combined GSNO and Si treatment reduced cell leakage, MDA, and H<sub>2</sub>O<sub>2</sub> levels by increasing APX activity and proline accumulation in Seonpung and Cheongja under salt stress. (<b>A</b>) Electrolyte leakage in Cheongja, (<b>B</b>) electrolyte leakage in Seonpung, (<b>C</b>) proline content, (<b>D</b>) MDA content, (<b>E</b>) H<sub>2</sub>O<sub>2</sub> content, and (<b>F</b>) APX activity. The bar graph displays the standard error of the mean, with each data point representing the average of three replicates. The letters on the bars indicate significant differences determined using DMRT at <span class="html-italic">p</span> ≤ 0.05. The same letters indicate no significant differences.</p>
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<p>Heatmap of relative gene expression in response to treatments: (<b>A</b>) Cheongja and (<b>B</b>) Seonpung. The heatmap was generated using TBtools based on the mean expression values from three biological replicates. Red indicates high expression levels, while blue represents low expression levels, reflecting the correlation strength between gene expression and treatments. The genes analyzed include <span class="html-italic">GmNHX1</span>, <span class="html-italic">GmSOS2</span>, <span class="html-italic">GmNIP2.1</span>, <span class="html-italic">GmNIP2.2</span>, <span class="html-italic">GmAKT1</span>, and <span class="html-italic">GmLbR</span>, with treatments such as GSNO, Si, salt, and their combinations.</p>
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17 pages, 1363 KiB  
Article
Phenotypic Antibiotic Resistance Patterns of Escherichia coli Isolates from Clinical UTI Samples and Municipal Wastewater in a Grenadian Community
by Makeda Matthew-Bernard, Karla Farmer-Diaz, Grace Dolphin-Bond, Vanessa Matthew-Belmar, Sonia Cheetham, Kerry Mitchell, Calum N. L. Macpherson and Maria E. Ramos-Nino
Int. J. Environ. Res. Public Health 2025, 22(1), 97; https://doi.org/10.3390/ijerph22010097 - 12 Jan 2025
Viewed by 454
Abstract
Antimicrobial resistance (AMR) is a growing global health threat. This study investigated antibiotic resistance in E. coli isolates from municipal wastewater (86 isolates) and clinical urinary tract infection (UTI) cases (34 isolates) in a Grenadian community, using data from January 2022 to October [...] Read more.
Antimicrobial resistance (AMR) is a growing global health threat. This study investigated antibiotic resistance in E. coli isolates from municipal wastewater (86 isolates) and clinical urinary tract infection (UTI) cases (34 isolates) in a Grenadian community, using data from January 2022 to October 2023. Antibiogram data, assessed per WHO guidelines for Critically Important antimicrobials (CIA), showed the highest resistance levels in both clinical and wastewater samples for ampicillin, followed by amoxicillin/clavulanic acid and nalidixic acid, all classified as Critically Important. Similar resistance was observed for sulfamethoxazole-trimethoprim (highly important) in both groups, with nitrofurantoin showing resistance in the important category. According to the WHO AWaRe classification, ampicillin (ACCESS group) had the highest resistance, while nitrofurantoin had the lowest across all samples. The WATCH group antibiotics, cefuroxime and cefoxitin, showed comparable resistance levels, whereas aztreonam from the RESERVE group (tested only in wastewater) was 100% sensitive. Multiple Antibiotic Resistance (MAR) index analysis revealed that 7% of wastewater and 38.2% of clinical samples had MAR values over 0.2, indicating prior antibiotic exposure in clinical isolates. These parallel patterns in wastewater and clinical samples highlight wastewater monitoring as a valuable tool for AMR surveillance, supporting antibiotic stewardship through ongoing environmental and clinical assessment. Full article
(This article belongs to the Section Environmental Sciences)
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<p>WHO AWaRe classification.</p>
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<p>Susceptibility patterns of <span class="html-italic">E. coli</span> strains to WHO Medically Important Antimicrobials for Human Medicine rom wastewater: (BLUE) Critically Important antimicrobials, (PURPLE) Highly Important, and (Green) Important to human medicine. The WHO CIA list used was as a reference to help formulate and prioritize risk assessment and risk management strategies for containing antimicrobial resistance: (A) Critically Important: Antibiotics that meet both criteria: (1) they are the sole or limited therapeutic option for treating life-threatening infections, and (2) they are used to treat infections caused by bacteria from non-human sources or carry resistance genes originating from non-human sources. (B) Highly Important: Antibiotics that meet only one of the following criteria: (1) they are the sole or limited treatment option for life-threatening infections, or (2) they are used for infections caused by bacteria from non-human sources or with resistance genes from non-human sources. (C) Important: Antimicrobial classes used in humans that do not meet criteria (1) or (2) [<a href="#B41-ijerph-22-00097" class="html-bibr">41</a>].</p>
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<p>Susceptibility pattern of <span class="html-italic">E. coli</span> strains to WHO Medically Important Antimicrobials for Human Medicine from clinical samples: (BLUE) Critically Important antimicrobials, (PURPLE) Highly Important, and (Green) Important to human medicine.</p>
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<p>WHO AWaRe ACCESS classification for <span class="html-italic">E. coli</span> isolated from wastewater and clinical urinary tract isolates. The classification is based, in part, on the risk of developing antibiotic resistance and their importance to medicine. The ACCESS category of this classification includes empiric first or second choice for treatment of most common infection and generally available [<a href="#B42-ijerph-22-00097" class="html-bibr">42</a>].</p>
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<p>WHO AWaRe: WATCH classification for <span class="html-italic">E. coli</span> isolated from wastewater and clinical urinary tract isolates. AWaRe classification: The classification is based, in part, on the risk of developing antibiotic resistance and their importance to medicine. WATCH category: Antibiotics that have higher toxicity issues and higher potential to negatively impact AMR. They should only be prescribed for specific infections [<a href="#B42-ijerph-22-00097" class="html-bibr">42</a>].</p>
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18 pages, 5370 KiB  
Article
The Effect of Climatic Variability on Consumer Prices: Evidence from El Niño–Southern Oscillation Indices
by Joohee Park and Seongjoon Byeon
Sustainability 2025, 17(2), 503; https://doi.org/10.3390/su17020503 - 10 Jan 2025
Viewed by 528
Abstract
This study aimed to identify the correlation between global climate phenomena, such as the ENSO, and South Korea’s Consumer Price Index (CPI) for a climate-sustainable economy. South Korea’s CPI has shown a linear upward trend, prompting a trend analysis and the subsequent removal [...] Read more.
This study aimed to identify the correlation between global climate phenomena, such as the ENSO, and South Korea’s Consumer Price Index (CPI) for a climate-sustainable economy. South Korea’s CPI has shown a linear upward trend, prompting a trend analysis and the subsequent removal of the linear trend for further examination. The correlation analysis identified statistically significant cases under the study’s criteria, with the Southern Oscillation Index (SOI) displaying the highest contribution and sensitivity. When comparing general correlations, the strongest relationship was observed with a 27-month lag. The Granger Causality Test, however, revealed causality with a 9-month lag between the CPI and El Niño–Southern Oscillation (ENSO) indices. This indicates the feasibility of separate analyses for long-term (27 months) and short-term (9 months) impacts. The correlation analysis confirmed that the ENSO contributes to explainable variations in the CPI, suggesting that CPI fluctuations could be predicted based on ENSO indices. Utilizing ARIMA models, the study compared predictions using only the CPI’s time series against an ARIMAX model that incorporated SOI and MEI as exogenous variables with a 9-month lag. Using the ARIMA model, this study compared predictions based solely on the time series of CPI with the ARIMAX model, which incorporated SOI and MEI as exogenous variables with a 9-month lag. Furthermore, to investigate nonlinear teleconnections, the neural network model LSTM was applied for comparison. The analysis results confirmed that the model reflecting nonlinear teleconnections provided more accurate predictions. These findings demonstrate that global climate phenomena can significantly influence South Korea’s CPI and provide experimental evidence supporting the existence of nonlinear teleconnections. This study highlights the meaningful correlations between climate indices and CPI, suggesting that climate variability affects not only weather conditions but also economic factors in a country. Full article
(This article belongs to the Section Air, Climate Change and Sustainability)
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<p>Monthly variation in CIs (1995~2023).</p>
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<p>Overall research framework.</p>
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<p>Value of CPI with its trend and detrended CPI (1995~2023).</p>
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<p>Correlation among national CPI and regional CPIs: (<b>a</b>) correlation among national CPI and CPIs of metropolitan cities; (<b>b</b>) correlation among national CPI and CPIs of provinces in Korea.</p>
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<p>Time range for CPI and CIs.</p>
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<p>Overview of CPI (detrended) and CIs (SOI and MEI).</p>
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<p>Cross-correlation coefficients 0–60 months lags.</p>
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<p>Linear model ARIMA-based forecasting results: (<b>a</b>) ARIMA model results (Case 1); (<b>b</b>) ARIMAX model results (Case 2-1, exogenous variables: SOI, MEI); (<b>c</b>) ARIMAX (Case 2-2, exogenous variable: SOI); and (<b>d</b>) ARIMAX (Case 2-3, exogenous variable: MEI).</p>
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<p>Nonlinear neural network-based time-series model LSTM forecasting results: (<b>a</b>) Case 3-1 results (exogenous variables: SOI, MEI); (<b>b</b>) Case 3-2 (exogenous variable: SOI); (<b>c</b>) Case 3-3 (exogenous variable: MEI); and (<b>d</b>) Case 3-4 (no endogenous variables, exogenous variables: SOI, MEI).</p>
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