[go: up one dir, main page]
More Web Proxy on the site http://driver.im/
You seem to have javascript disabled. Please note that many of the page functionalities won't work as expected without javascript enabled.
 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (90,737)

Search Parameters:
Keywords = AT1R

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
22 pages, 1775 KiB  
Article
Classifications of Several Classes of Armendariz-like Rings Relative to an Abelian Monoid and Its Applications
by Jianwei He and Yajun Ma
Mathematics 2025, 13(5), 874; https://doi.org/10.3390/math13050874 - 5 Mar 2025
Abstract
Let M be an Abelian monoid. A necessary and sufficient condition for the class ArmM of all Armendariz rings relative to M to coincide with the class Arm of all Armendariz rings is given. As a consequence, we [...] Read more.
Let M be an Abelian monoid. A necessary and sufficient condition for the class ArmM of all Armendariz rings relative to M to coincide with the class Arm of all Armendariz rings is given. As a consequence, we prove that ArmM has exactly three cases: the empty set, Arm, and the class of all rings. If N is an Abelian monoid, then we prove that ArmM×N=ArmMArmN, which gives a partial affirmative answer to the open question of Liu in 2005 (whether R is M×N-Armendariz if R is M-Armendariz and N-Armendariz). We also show that the other Armendariz-like rings relative to an Abelian monoid, such as M-quasi-Armendariz rings, skew M-Armendariz rings, weak M-Armendariz rings, M-π-Armendariz rings, nil M-Armendariz rings, upper nil M-Armendariz rings and lower nil M-Armendariz rings can be handled similarly. Some conclusions on these classes have, therefore, been generalized using these classifications. Full article
(This article belongs to the Section A: Algebra and Logic)
Show Figures

Figure A1

Figure A1
<p>The multiplication table of <math display="inline"><semantics> <mrow> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>4</mn> <mo>}</mo> </mrow> <mo>⊆</mo> <mrow> <mo stretchy="false">(</mo> <msup> <mi mathvariant="double-struck">Z</mi> <mo>+</mo> </msup> <mo>,</mo> <mo>·</mo> <mo stretchy="false">)</mo> </mrow> </mrow> </semantics></math>.</p>
Full article ">Figure A2
<p>The multiplication table of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>4</mn> <mo>,</mo> <mn>6</mn> <mo>,</mo> <mn>7</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math>.</p>
Full article ">Figure A3
<p>The multiplication table of <math display="inline"><semantics> <mrow> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>4</mn> <mo>}</mo> </mrow> <mo>⊆</mo> <mrow> <mo stretchy="false">(</mo> <msup> <mi mathvariant="double-struck">Z</mi> <mo>+</mo> </msup> <mo>,</mo> <mo>·</mo> <mo stretchy="false">)</mo> </mrow> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A4
<p>The multiplication table of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>4</mn> <mo>,</mo> <mn>6</mn> <mo>,</mo> <mn>7</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A5
<p>The multiplication table of degree 3 of <math display="inline"><semantics> <mrow> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>4</mn> <mo>}</mo> </mrow> <mo>⊆</mo> <mrow> <mo stretchy="false">(</mo> <msup> <mi mathvariant="double-struck">Z</mi> <mo>+</mo> </msup> <mo>,</mo> <mo>·</mo> <mo stretchy="false">)</mo> </mrow> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A6
<p>The multiplication table of degree 3 of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>4</mn> <mo>,</mo> <mn>6</mn> <mo>,</mo> <mn>7</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A7
<p>The multiplication table of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>0</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>5</mn> <mo>,</mo> <mn>6</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A8
<p>The multiplication table of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>0</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>5</mn> <mo>,</mo> <mn>6</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math> with straight lines.</p>
Full article ">Figure A9
<p>The graph of <math display="inline"><semantics> <mrow> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>4</mn> <mo>}</mo> </mrow> <mo>⊆</mo> <mrow> <mo stretchy="false">(</mo> <msup> <mi mathvariant="double-struck">Z</mi> <mo>+</mo> </msup> <mo>,</mo> <mo>·</mo> <mo stretchy="false">)</mo> </mrow> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A10
<p>The graph we need.</p>
Full article ">Figure A11
<p>The graph of <math display="inline"><semantics> <mrow> <mrow> <mo stretchy="false">(</mo> <mn>0</mn> <mo>,</mo> <mn>1</mn> <mo>,</mo> <mn>1.5</mn> <mo>)</mo> </mrow> <mo>∈</mo> <mrow> <mo stretchy="false">(</mo> <msup> <mi mathvariant="double-struck">Q</mi> <mo>∗</mo> </msup> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </mrow> </semantics></math>.</p>
Full article ">Figure A12
<p>The graph of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>0</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math>.</p>
Full article ">Figure A13
<p>The multiplication table of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>0</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>4</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A14
<p>The multiplication table of degree 4 of <math display="inline"><semantics> <mrow> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mn>3</mn> <mo>}</mo> </mrow> <mo>⊆</mo> <mrow> <mo stretchy="false">(</mo> <msup> <mi mathvariant="double-struck">Z</mi> <mo>+</mo> </msup> <mo>,</mo> <mo>·</mo> <mo stretchy="false">)</mo> </mrow> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A15
<p>The multiplication table of degree 4 of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>0</mn> <mo>,</mo> <mn>3</mn> <mo>,</mo> <mn>5</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math> with curves.</p>
Full article ">Figure A16
<p>The graph of <math display="inline"><semantics> <mrow> <mrow> <mo>{</mo> <mn>1</mn> <mo>,</mo> <mn>2</mn> <mo>,</mo> <mo>⋯</mo> <mo>,</mo> <mn>10</mn> <mo>}</mo> </mrow> <mo>⊆</mo> <mrow> <mo stretchy="false">(</mo> <msup> <mi mathvariant="double-struck">Z</mi> <mo>+</mo> </msup> <mo>,</mo> <mo>·</mo> <mo stretchy="false">)</mo> </mrow> </mrow> </semantics></math>.</p>
Full article ">Figure A17
<p>The graph of <math display="inline"><semantics> <mrow> <mo>{</mo> <mn>0</mn> <mo>,</mo> <mn>41</mn> <mo>,</mo> <mn>65</mn> <mo>,</mo> <mn>82</mn> <mo>,</mo> <mn>95</mn> <mo>,</mo> <mn>106</mn> <mo>,</mo> <mn>115</mn> <mo>,</mo> <mn>123</mn> <mo>,</mo> <mn>130</mn> <mo>,</mo> <mn>136</mn> <mo>}</mo> <mo>⊆</mo> <mo stretchy="false">(</mo> <mi mathvariant="double-struck">N</mi> <mo>,</mo> <mo>+</mo> <mo stretchy="false">)</mo> </mrow> </semantics></math>.</p>
Full article ">
18 pages, 7850 KiB  
Article
Gastrointestinal Helminthofauna of Mediterranean Elasmobranchs
by Perla Tedesco, Enrico Liborio Quadrone, Linda Albonetti, Federica Marcer, Monica Caffara, Maria Letizia Fioravanti, Fausto Tinti and Andrea Gustinelli
J. Mar. Sci. Eng. 2025, 13(3), 512; https://doi.org/10.3390/jmse13030512 - 5 Mar 2025
Abstract
Elasmobranchs (Chondrichthyes, Elasmobranchii) are exposed to a variety of gastrointestinal parasites acquired through the ingestion of infected prey. An increasing amount of evidence suggests the usefulness of parasitological information to elucidate aspects of the biology and ecology of sharks and rays, to inform [...] Read more.
Elasmobranchs (Chondrichthyes, Elasmobranchii) are exposed to a variety of gastrointestinal parasites acquired through the ingestion of infected prey. An increasing amount of evidence suggests the usefulness of parasitological information to elucidate aspects of the biology and ecology of sharks and rays, to inform the correct management and conservation of their stocks and the appropriate husbandry of captive specimens. This study aims to identify at the morphological and molecular level the helminth parasites found in the stomachs and intestines of various elasmobranchs accidentally caught by Mediterranean fisheries, with the aim of updating and providing new information on the parasitic fauna of these species. Specimens of smooth-hound Mustelus mustelus, blackspotted smooth-hound Mustelus punctulatus, blue shark Prionace glauca, spiny dogfish Squalus acanthias, lesser-spotted dogfish Scyliorhinus canicula, pelagic stingray Pteroplatytrygon violacea and Mediterranean starry ray Raja asterias were examined. The parasitological examination allowed us to identify the nematode Acanthocheilus rotundatus in the two species of smooth-hounds analyzed, the tapeworm species Scyphophyllidium exiguum, S. prionacis, Anthobothrium caseyi and Nybelinia indica in P. glauca, the nematodes Hysterothylacium aduncum and Proleptus obtusus in S. acanthias and S. canicula, respectively, and finally the nematode Pseudanisakis rajae and the tapeworm Nybelinia sp. in Raja asterias. Some observations represent new reports at a geographical level, in particular, those on A. caseyi in P. glauca and H. aduncum in S. acanthias from the Adriatic Sea, or first host records, such as S. exiguum and N. indica in P. glauca or P. rajae. in R. asterias. The results of this survey represent a contribution to broadening the knowledge of the parasitic fauna of these elasmobranchs in the Mediterranean Sea. From more in-depth future studies, it will be possible to reach more solid evidence and general conclusions on aspects relating to the biology, ecology, and health of the investigated species, offering useful information for their conservation and management. Full article
(This article belongs to the Special Issue Parasites of Marine Fishes: Advances and Perspectives)
Show Figures

Figure 1

Figure 1
<p><span class="html-italic">Scyphophyllidium</span> spp. adult stages from <span class="html-italic">Prionace glauca</span>: (<b>A</b>) <span class="html-italic">S. exiguum</span>, anterior end showing the appearance of scolex and neck region; (<b>B</b>) <span class="html-italic">S. exiguum</span>, detail of neck with scutellate surface; (<b>C</b>) <span class="html-italic">S. prionacis</span>, scolex; (<b>D</b>) <span class="html-italic">S. prionacis</span>, detail of bothridial margin; (<b>E</b>) <span class="html-italic">S. prionacis</span>, detail of serrated microtriches and filiform microtriches over bothridial margin; and (<b>F</b>) <span class="html-italic">S. prionacis</span>, proglottids.</p>
Full article ">Figure 2
<p><span class="html-italic">Antobothrium caseyi</span> adult stage from <span class="html-italic">Prionace glauca</span>: (<b>A</b>) immature proglottids (scale bar 100 µm); (<b>B</b>) mature proglottids (scale bar 100 µm).</p>
Full article ">Figure 3
<p><span class="html-italic">Nybelinia indica</span> adult stage from <span class="html-italic">Prionace glauca</span>: (<b>A</b>) scolex (scale bar 500 µm); (<b>B</b>) detail of bothridial margin; (<b>C</b>) detail of microtriches over bothridial surface; (<b>D</b>) detail of microtriches over bothridial margin; (<b>E</b>) detail of hooked tentacle; and (<b>F</b>) mature proglottids (scale bar 100 µm).</p>
Full article ">Figure 4
<p><span class="html-italic">Nybelinia</span> sp. adult stage from <span class="html-italic">Raja asterias</span>: (<b>A</b>) and (<b>B</b>) scolex; (<b>C</b>) and (<b>D</b>) details of hooked tentacles.</p>
Full article ">Figure 5
<p><span class="html-italic">Acanthocheilus rotundatus</span> adult stages from <span class="html-italic">Mustelus</span> spp. (<b>A</b>) Anterior end (scale bar 100 µm); (<b>B</b>) details of anterior end showing bifid teeth (scale bar 50 µm); (<b>C</b>) scanning electron micrograph showing surface details of anterior end; (<b>D</b>) caudal end of male specimen (scale bar 100 µm); (E) Ventriculus (scale bar 100 µm); and (<b>F</b>) caudal end of female specimen (scale bar 500µm).</p>
Full article ">Figure 6
<p><span class="html-italic">Proleptus obtusus</span> female adult stage from <span class="html-italic">Scyliorhinus canicula</span>: (<b>A</b>) anterior end; (<b>B</b>) details of cephalic collar; (<b>C</b>) eggs; and (<b>D</b>) caudal end.</p>
Full article ">Figure 7
<p><span class="html-italic">Pseudanisakis</span> from <span class="html-italic">Raja asterias</span>: (<b>A</b>) anterior end; (<b>B</b>) scanning electron micrograph showing single ring of denticles surrounding the triradiate mouth; (<b>C</b>) excretory pore (arrow); (<b>D</b>) ventriculus (v); (<b>E</b>) caudal end of male specimen with everted spicules (sp); and (<b>F</b>) details of caudal papillae of male specimen.</p>
Full article ">Figure 8
<p><span class="html-italic">Hysterothylacium aduncum</span> larval stage from <span class="html-italic">Squalus acanthias</span>: (<b>A</b>) anterior end of third-stage larva; (<b>B</b>) excretory pore of fourth-stage larva (arrow); (<b>C</b>) anterior end of molting fourth-stage larva; and (<b>D</b>) posterior end of molting fourth-stage larva.</p>
Full article ">
19 pages, 704 KiB  
Review
Advances in Targeted and Chemotherapeutic Strategies for Colorectal Cancer: Current Insights and Future Directions
by Salique H. Shaham, Puneet Vij and Manish K. Tripathi
Biomedicines 2025, 13(3), 642; https://doi.org/10.3390/biomedicines13030642 - 5 Mar 2025
Abstract
Colorectal cancer (CRC) remains one of the leading causes of cancer-related mortality worldwide, necessitating the continuous evolution of therapeutic approaches. Despite advancements in early detection and localized treatments, metastatic colorectal cancer (mCRC) poses significant challenges due to low survival rates and resistance to [...] Read more.
Colorectal cancer (CRC) remains one of the leading causes of cancer-related mortality worldwide, necessitating the continuous evolution of therapeutic approaches. Despite advancements in early detection and localized treatments, metastatic colorectal cancer (mCRC) poses significant challenges due to low survival rates and resistance to conventional therapies. This review highlights the current landscape of CRC treatment, focusing on chemotherapy and targeted therapies. Chemotherapeutic agents, including 5-fluorouracil, irinotecan, and oxaliplatin, have significantly improved survival but face limitations such as systemic toxicity and resistance. Targeted therapies, leveraging mechanisms like VEGF, EGFR, and Hedgehog pathway inhibition, offer promising alternatives, minimizing damage to healthy tissues while enhancing therapeutic precision. Furthermore, future directions in CRC treatment include exploring innovative targets such as Wnt/β-catenin, Notch, and TGF-β pathways, alongside IGF/IGF1R inhibition. These emerging strategies aim to address drug resistance and improve patient outcomes. This review emphasizes the importance of integrating molecular insights into drug development, advocating for a more personalized approach to combat CRC’s complexity and heterogeneity. Full article
27 pages, 1899 KiB  
Article
Enhanced Adsorption of Methylene Blue in Wastewater Using Natural Zeolite Impregnated with Graphene Oxide
by Gabriela Tubon-Usca, Cyntia Centeno, Shirley Pomasqui, Amerigo Beneduci and Fabian Arias Arias
Appl. Sci. 2025, 15(5), 2824; https://doi.org/10.3390/app15052824 - 5 Mar 2025
Abstract
The use of graphene oxide (GO) in combination with mesoporous materials has gained interest in the development of adsorbents. In this study, GO was impregnated into zeolite at three concentrations (ZGO2.5, ZGO5, and ZGO10) through a simple thermal process to enhance the adsorption [...] Read more.
The use of graphene oxide (GO) in combination with mesoporous materials has gained interest in the development of adsorbents. In this study, GO was impregnated into zeolite at three concentrations (ZGO2.5, ZGO5, and ZGO10) through a simple thermal process to enhance the adsorption of methylene blue (MB). Characterization of the resulting materials was performed using spectroscopic techniques such as UV-Vis and FT-IR spectroscopy, SEM, and EDS, confirming the presence of GO on zeolite. Batch experiments were conducted to evaluate their performance, analyzing contact time, pH effect, and adsorption kinetics. Pseudo-first-order, pseudo-second-order, and Elovich kinetic models were applied, and the adsorption mechanism was studied using Langmuir, Freundlich, Temkin II, and Dubinin–Radushkevich (D-R) isotherms at different temperatures. Optimal adsorption was achieved at 273 K, 100 mg L−1 of MB, adsorbent mass of 100 mg, 250 rpm, and pH 5–9, with 90% removal efficiency after 70 min. The pseudo-second-order, Freundlich, and D-R models best described the process (R2 > 0.98), suggesting a mixed physisorption–chemisorption mechanism. The maximum adsorption capacity from the D-R isotherm reached 119 mg g−1 at 333 K. Thermodynamic studies showed that adsorption was a spontaneous and endothermic process. These findings highlight the potential of GO-impregnated zeolite as an effective adsorbent for MB. Full article
(This article belongs to the Section Materials Science and Engineering)
20 pages, 1752 KiB  
Article
Experimental Study of Wear Resistance Improvement of Modular Disk Milling Cutter by Preliminary Pre-Processing Method
by Karibek Sherov, Almat Sagitov, Gulim Tusupbekova, Aibek Sherov, Gulnara Kokayeva, Dinara Kossatbekova, Gulnur Abdugaliyeva and Nurgul Karsakova
Designs 2025, 9(2), 30; https://doi.org/10.3390/designs9020030 - 5 Mar 2025
Abstract
The problem of increasing the tool durability (service life) when machining hard-to-machine materials is one of the major practical problems of modern mechanical engineering. This paper aims to improve the wear resistance of modular disk mills using the pre-processing method. Second-order rotatable planning [...] Read more.
The problem of increasing the tool durability (service life) when machining hard-to-machine materials is one of the major practical problems of modern mechanical engineering. This paper aims to improve the wear resistance of modular disk mills using the pre-processing method. Second-order rotatable planning was applied for the experimental study of the pre-processing of modular disk mills. Experimental research on the pre-processing of modular disk mills was carried out on a vertical milling machine XH950A when milling a workpiece made of steel 45. It was revealed that the increase in pre-processing modes up to specific values (f = 60 mm/min; 𝑣𝑐 = 17 m/min; t = 6 min) on the tool durability period has a positive effect. At the same time, the tool durability period was increased up to T = 155 min. Tests of the machined modular disk mills were carried out in the conditions of the laboratory base to determine the durability period. After pre-processing at different modes, each modular disk mill was used to machine the workpiece until wear signs appeared on the cutting edge. At the same time, the time was recorded to determine the durability period. It was found that the optimum mode of tool preliminary pre-processing provides the best deformation and thermal conditions for hardening the tool cutting part. As a result of modeling with the ANSYS 2024 R1 program, it was found that a hardened layer is indeed formed on the cutting part of the modular disk mill after pre-processing. The results obtained show the possibility of using the preliminary pre-processing method to improve the wear resistance of other metal-cutting tools. Full article
(This article belongs to the Section Mechanical Engineering Design)
15 pages, 664 KiB  
Review
Optimizing Conservative Treatment for Femoroacetabular Impingement Syndrome: A Scoping Review of Rehabilitation Strategies
by Federica Giorgi, Daniela Platano, Lisa Berti, Danilo Donati and Roberto Tedeschi
Appl. Sci. 2025, 15(5), 2821; https://doi.org/10.3390/app15052821 - 5 Mar 2025
Abstract
Background: Femoroacetabular Impingement Syndrome (FAIS) is a musculoskeletal disorder characterized by hip pain, reduced range of motion (ROM), and functional impairment, particularly in young and physically active individuals. While surgery is generally not performed in individuals under 18 due to skeletal immaturity, [...] Read more.
Background: Femoroacetabular Impingement Syndrome (FAIS) is a musculoskeletal disorder characterized by hip pain, reduced range of motion (ROM), and functional impairment, particularly in young and physically active individuals. While surgery is generally not performed in individuals under 18 due to skeletal immaturity, it remains a standard treatment option for adults presenting with persistent symptoms and functional limitations. However, the overall effectiveness of physiotherapy-based interventions remains unclear. This review aimed to evaluate the effectiveness of conservative rehabilitation strategies for FAIS, assessing their impact on pain management, functional improvement, and quality-of-life outcomes, rather than directly comparing them to surgical interventions. Methods: This scoping review was conducted following the Joanna Briggs Institute (JBI) framework and PRISMA-ScR guidelines. A systematic literature search was performed in PubMed, Cochrane CENTRAL, Scopus, PEDro, and Web of Science. Studies were included if they examined conservative rehabilitation for FAIS, assessing outcomes such as pain reduction, functional improvement, range of motion (ROM), muscle strength, and quality of life. Data were extracted and synthesized narratively. Results: Both conservative rehabilitation and surgical intervention resulted in significant improvements in pain, function, and quality of life. Exercise-based physiotherapy, particularly programs incorporating core stability, progressive strengthening, and neuromuscular training, demonstrated positive outcomes. Surgery provided faster pain relief, ROM improvements, and earlier functional gains, particularly in activities requiring hip flexion. Given the variability in outcome measures, including pain, function, and quality of life, the interpretation of results must consider differences in treatment protocols across studies. Conclusions: Conservative rehabilitation should be considered a first-line treatment for Femoroacetabular Impingement Syndrome (FAIS), as it provides significant improvements in pain relief, function, and quality of life while mitigating the risks associated with surgery. Exercise-based physiotherapy, particularly programs incorporating core stabilization, progressive strengthening, and neuromuscular training, has demonstrated positive clinical outcomes. Although surgery may offer faster symptom relief and greater short-term functional gains, long-term differences between surgical and conservative management appear minimal in selected patient populations. Structured physiotherapy interventions should be prioritized before surgical consideration, except in cases where symptoms persist despite adequate rehabilitation. Future research should aim to establish standardized rehabilitation protocols, define optimal intervention parameters, and identify patient subgroups most likely to benefit from conservative management. Additionally, longitudinal studies with larger sample sizes are needed to clarify the long-term effects of non-surgical treatments on joint health and functional outcomes. Full article
Show Figures

Figure 1

Figure 1
<p>Preferred reporting items for systematic reviews and meta-analyses 2020 (PRISMA) flow-diagram.</p>
Full article ">
22 pages, 516 KiB  
Article
Evaluating Medical Students’ Satisfaction with E-Learning Platforms During the COVID-19 Pandemic: A Structural Equation Modeling Analysis Within a Multimodal Educational Framework
by Gheorghe-Dodu Petrescu, Andra-Luisa Preda, Anamaria-Cătălina Radu, Luiza-Andreea Ulmet and Andra-Victoria Radu
Soc. Sci. 2025, 14(3), 160; https://doi.org/10.3390/socsci14030160 - 5 Mar 2025
Abstract
The rapid advancement of digital technologies in education is revolutionizing learning environments and influencing the future of educational methodologies. This study seeks to determine the parameters affecting students’ satisfaction with e-learning platforms utilized during the COVID-19 pandemic, within a multimodal educational framework. A [...] Read more.
The rapid advancement of digital technologies in education is revolutionizing learning environments and influencing the future of educational methodologies. This study seeks to determine the parameters affecting students’ satisfaction with e-learning platforms utilized during the COVID-19 pandemic, within a multimodal educational framework. A Structural Equation Modeling (SEM) approach was used to examine the contributions of different components to students’ views of e-learning tools and the inter-relationships between them. Data were gathered from 314 students via a questionnaire, with the dependent variable being student satisfaction with e-learning platforms and the independent variables comprising the perceived benefits and disadvantages, ease of use, prior experience, perceptions of the platforms, perceived risks, and communication efficiency between students and professors. The results indicated that 78% of the variance in student satisfaction was explained by these parameters (R-squared = 0.78), underscoring the substantial impact of these features on the digital learning experience. This study enhances the comprehension of the influence of e-learning platforms within a multimodal educational framework on students’ learning experiences, especially with the challenges presented by the pandemic. The collected insights can guide the development of more effective, accessible, and user-focused educational tools. Full article
(This article belongs to the Special Issue Educational Technology for a Multimodal Society)
13 pages, 1269 KiB  
Article
Innovative Binocular Vision Testing for Phoria and Vergence Ranges Using Automatic Dual Rotational Risley Prisms
by Hui-Rong Su, Yu-Jung Chen, Yun-Shao Hu, Chi-Hung Lee, Shang-Min Yeh and Shuan-Yu Huang
Sensors 2025, 25(5), 1604; https://doi.org/10.3390/s25051604 - 5 Mar 2025
Abstract
This study evaluated binocular visual function using automatic dual rotational Risley prisms (ADRRPs) to measure phoria and vergence ranges. Thirty-nine (mean age: 21.82 ± 1.10 years; age range: 20–24 years) healthy adults with normal binocular vision participated. Each underwent baseline refraction exams followed [...] Read more.
This study evaluated binocular visual function using automatic dual rotational Risley prisms (ADRRPs) to measure phoria and vergence ranges. Thirty-nine (mean age: 21.82 ± 1.10 years; age range: 20–24 years) healthy adults with normal binocular vision participated. Each underwent baseline refraction exams followed by phoria and vergence tests conducted using both a phoropter with Maddox rods and the ADRRPs. The results revealed a strong positive correlation between the two instruments for distance phoria (r = 0.959, p < 0.001) and near-phoria measurements (r = 0.968, p < 0.001). For vergence testing, positive fusional vergence (PFV) at distance showed a moderate-to-strong correlation for break points (r = 0.758, p < 0.001) and a moderate correlation for recovery points (r = 0.452, p < 0.001). Negative fusional vergence (NFV) at distance demonstrated a strong correlation for break points (r = 0.863, p < 0.001) and a moderate correlation for recovery points (r = 0.458, p < 0.01). Near-vergence testing showed moderate-to-strong correlations for break points (r = 0.777, p < 0.001) and recovery points (r = 0.623, p < 0.001). The inclusion of Bland–Altman analysis provides a more comprehensive evaluation of agreement between ADRRPs and the phoropter. While strong correlations were observed, systematic bias and LoA indicate that these methods are not perfectly interchangeable. The ADRRPs demonstrated potential for binocular vision assessment but require further validation for clinical application. Full article
(This article belongs to the Special Issue Advances in Optical Sensing, Instrumentation and Systems: 2nd Edition)
22 pages, 5430 KiB  
Article
Multi-Omics Analysis Reveals the Negative Effects of High-Concentrate Diets on the Colonic Epithelium of Dumont Lambs
by Shufang Li, Hairong Wang, Boyang Li, Henan Lu, Jianxin Zhao, Aiwu Gao, Yawen An, Jinli Yang and Tian Ma
Animals 2025, 15(5), 749; https://doi.org/10.3390/ani15050749 - 5 Mar 2025
Abstract
Feeding HC diets has been found to induce metabolic dysregulation in the colon. However, the mechanisms by which changes in colonic flora and metabolites damage the colonic epithelium are poorly studied. Therefore, the present experiment used a multi-omics technique to investigate the mechanism [...] Read more.
Feeding HC diets has been found to induce metabolic dysregulation in the colon. However, the mechanisms by which changes in colonic flora and metabolites damage the colonic epithelium are poorly studied. Therefore, the present experiment used a multi-omics technique to investigate the mechanism of colonic injury induced by high-concentrate diets in lambs. Twelve male Dumont lambs were randomly split into two groups: a low-concentrate diet (LC = concentrate/forage = 30:70) group and a high-concentrate diet (HC = concentrate/forage = 70:30) group. The results showed that the HC group presented significantly increased lipopolysaccharide (LPS) concentrations in the colonic epithelium and significantly decreased serum total cholesterol (TC), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) levels (p < 0.05), which led to cavities and inflammatory cell infiltration in the colonic epithelium. The HC group had significantly lower pH and less VFAs in colon contents, as well as a significantly increased abundance of bacteria of the genera [Eubacterium]_coprostanoligenes_group, Rikenellaceae_RC9_gut_group, Treponema, Clostridia_UCG-014, Alistipes, Ruminococcus, Christensenellaceae_R-7_group, UCG-002, Bacteroidales_RF16_group and Lachnospiraceae_AC2044_group compared to the LC diet group. These microorganisms significantly increased the level of metabolites of cholic acid, chenodeoxycholic acid, LysoPA (P-16:0/0:0), methapyrilene, and fusaric acid. A transcriptome analysis showed that cytokine–cytokine receptor interaction, glutathione metabolism, and the peroxisome signaling pathway were downregulated in the colon epithelium of the lambs fed the HC diet. Therefore, the HC diet caused epithelial inflammation and oxidative damage by affecting the interaction between the microbial flora of the colon and metabolites and the host epithelium, which eventually disrupted colon homeostasis and had a negative impact on sheep health. Full article
Show Figures

Figure 1

Figure 1
<p>Effect of HC diet on colon epithelial lipopolysaccharide content and serum parameters in Dumont lambs. (<b>A</b>) The concentrations of colonic epithelial LPS, serum LPS, and SAA. (<b>B</b>) The concentrations of serum TG, TC, and GLU. (<b>C</b>) The concentrations of serum TP, ALB, and GLB. (<b>D</b>) The concentrations of serum TNF-α, IL-1β, and IL-6. (<b>E</b>) The concentrations of serum IgA, IgM, and IgG. (<b>F</b>) The concentrations of serum SOD and GSH-Px. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30. Not significantly different (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.</p>
Full article ">Figure 1 Cont.
<p>Effect of HC diet on colon epithelial lipopolysaccharide content and serum parameters in Dumont lambs. (<b>A</b>) The concentrations of colonic epithelial LPS, serum LPS, and SAA. (<b>B</b>) The concentrations of serum TG, TC, and GLU. (<b>C</b>) The concentrations of serum TP, ALB, and GLB. (<b>D</b>) The concentrations of serum TNF-α, IL-1β, and IL-6. (<b>E</b>) The concentrations of serum IgA, IgM, and IgG. (<b>F</b>) The concentrations of serum SOD and GSH-Px. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30. Not significantly different (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.</p>
Full article ">Figure 2
<p>Effects of HC diet on the morphology of the colonic epithelium and tight junction mRNA expression in Dumont lambs. (<b>A</b>) LC group, cavities and inflammatory cell infiltration appeared. (<b>B</b>) HC group. (<b>C</b>) The expression of ZO-1, Cloudin-1, and Occludin mRNA. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30. Significantly * <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 3
<p>Effect of HC diet on colonic fermentation parameters of Dumont lambs (colon contents collected post-mortem). (<b>A</b>) VFAs in the colon content. (<b>B</b>) Colon pH. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30. Not significantly different (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.</p>
Full article ">Figure 4
<p>Effect of HC diet on microbial composition in colon of Dumont lambs. (<b>A</b>) PCoA plot. (<b>B</b>) Bacterial phylum with relative abundance ≥ 0.1%. (<b>C</b>) Bacterial genus with relative abundance ≥ 0.1%. (<b>D</b>) Comparison of bacterial phylum abundance with relative abundance ≥ 0.1% between LC and HC groups. Bacterial abundance at phylum level. (<b>E</b>) Comparison of bacterial genus abundance with relative abundance ≥ 1% between LC and HC groups. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
Full article ">Figure 4 Cont.
<p>Effect of HC diet on microbial composition in colon of Dumont lambs. (<b>A</b>) PCoA plot. (<b>B</b>) Bacterial phylum with relative abundance ≥ 0.1%. (<b>C</b>) Bacterial genus with relative abundance ≥ 0.1%. (<b>D</b>) Comparison of bacterial phylum abundance with relative abundance ≥ 0.1% between LC and HC groups. Bacterial abundance at phylum level. (<b>E</b>) Comparison of bacterial genus abundance with relative abundance ≥ 1% between LC and HC groups. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
Full article ">Figure 5
<p>LEfSe analysis of microbial community in colon of lambs in LC and HC groups. (<b>A</b>) Cladogram of LDA scores. (<b>B</b>) Bar graph of the LDA value distribution.</p>
Full article ">Figure 6
<p>Correlation analysis between the relative abundances of colonic microbial genera and colonic fermentation parameters. Spearman’s correlation between VFAs and top 10 genera; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, R &gt; 0.60.</p>
Full article ">Figure 7
<p>Effect of high-concentrate diet on metabolites in colon content of Dumont lambs. (<b>A</b>) OPLS-DA based on the metabolite matrix of colon content. (<b>B</b>) Differential metabolite VIP value of LC and HC groups. (<b>C</b>) KEGG enrichment analysis of differential metabolites of LC and HC groups, where red represents upregulated, and blue represents downregulated. (<b>D</b>) Correlation network analysis between metabolites and the top 20 bacterial genera showed positive correlations (red squares) and negative correlations (blue squares). A significant correlation was defined as R &gt; 0.6, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30.</p>
Full article ">Figure 8
<p>Effect of a high-concentrate diet on transcriptional profile of colon epithelium in Dumont lambs. (<b>A</b>) Volcano plots from RNA-seq analysis of the HC and LC groups show upregulated DEGs in red and downregulated DEGs in blue. (<b>B</b>) The KEGG enrichment analysis of DEGs of LC and HC groups. GPX4 = glutathione peroxidase 4; IL1R1 = interleukin 1 receptor type 1; TLR2 = Toll-like receptor 2; MMP25 = matrix metalloproteinase 25; CXCL10 = chemokine (C-X-C motif) ligand 10; MMP9 = matrix metalloproteinase 9; MMP28 = matrix metallopeptidase 28; HSPA1A = heat shock protein 1A; TXN = thioredoxin; CXCL8 = chemokine (C-X-C motif) ligand 8; HSPB6 = heat shock protein beta 6; CDX2 = caudal-type homeobox 2; HSPB7 = heat shock protein beta 7; CD93 = cluster of differentiation 93; CXCL1 = chemokine (C-X-C motif) ligand 1; CD84 = cluster of differentiation 84; GSS = glutathione synthetase; BAX = Bcl-2-associated X protein. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30.</p>
Full article ">Figure A1
<p>Species accumulation curve. The horizontal axis represents the sample size and the vertical axis represents the number of ASVs detected.</p>
Full article ">Figure A2
<p>The comparison of α-diversity (Chao, Shannon, Simpson and observation index) of bacterial communities at ASVs level. LC and HC represent diets with concentrate/forage ratios of 30:70 and 70:30. Not significantly different (ns.) <span class="html-italic">p</span> &gt; 0.05.</p>
Full article ">Figure A3
<p>Classification of significantly different metabolites.</p>
Full article ">
19 pages, 3245 KiB  
Article
Isolation, Identification, and Characteristics of Aeromonas salmonicida subsp. masoucida from Diseased Starry Flounder (Platichthys stellatus)
by Soo-Ji Woo, So-Sun Kim, Ahran Kim, Mi-Young Cho and Jeong-Wan Do
Pathogens 2025, 14(3), 257; https://doi.org/10.3390/pathogens14030257 - 5 Mar 2025
Abstract
Aeromonas salmonicida is a predominant pathogen that infects fish. The pathogen A. salmonicida subsp. masoucida (ASM) was isolated for the first time from diseased starry flounders (Platichthys stellatus). Our study aimed to isolate, characterize, and investigate the pathogenicity of ASM. Bacterial [...] Read more.
Aeromonas salmonicida is a predominant pathogen that infects fish. The pathogen A. salmonicida subsp. masoucida (ASM) was isolated for the first time from diseased starry flounders (Platichthys stellatus). Our study aimed to isolate, characterize, and investigate the pathogenicity of ASM. Bacterial species were identified using 16s rRNA, gyrB, dnaJ, and vapA analyses. Phylogenetic tree analysis revealed that the ASM strains were clustered with the ASM ATCC strain and other strains isolated from black rockfish. In the antimicrobial susceptibility test, the three ASM strains were considered non-wild types for enrofloxacin, florfenicol, flumequine, oxolinic acid, and oxytetracycline susceptibility. Histopathological analysis revealed bacterial colonies in the secondary lamella and heart, indicating that ASM strains are highly virulent in fish. Comparative analysis and annotation via genome sequencing revealed that, among the 1156 factors, adherence factors were the most prevalent putative virulence determinants, followed by the effector delivery system and adherence. ASM was found to possess 43 type III secretion systems, 22 type VI secretion systems, 11 antimicrobial resistance genes, 3 stress genes, and prophage regions. These findings provide new insights into the virulence profile of ASM and highlight the risk posed by emerging pathogenic strains to starry flounders. Full article
(This article belongs to the Special Issue Emerging Pathogens in Aquaculture)
19 pages, 42632 KiB  
Article
Correlation Between the Growth Index and Vegetation Indices for Irrigated Soybeans Using Free Orbital Images
by Gildriano Soares de Oliveira, Jackson Paulo Silva Souza, Érica Pereira Cardozo, Dhiego Gonçalves Pacheco, Marinaldo Loures Ferreira, Marcelo Coutinho Picanço, João Rafael Silva Soares, Ana Maria Oliveira Souza Alves, André Medeiros de Andrade and Ricardo Siqueira da Silva
AgriEngineering 2025, 7(3), 67; https://doi.org/10.3390/agriengineering7030067 - 5 Mar 2025
Abstract
Soybeans are key in generating foreign currency for the world economy. Geotechnologies, through vegetation indices (VIs) generated by orbital images or remotely piloted aircraft, are essential tools for assessing the impact of climate on productivity and the ecoclimatic suitability of crops. This study [...] Read more.
Soybeans are key in generating foreign currency for the world economy. Geotechnologies, through vegetation indices (VIs) generated by orbital images or remotely piloted aircraft, are essential tools for assessing the impact of climate on productivity and the ecoclimatic suitability of crops. This study aimed to correlate the growth indices from the CLIMEX model, previously validated, with VIs derived from orbital remote sensing and ecological niche modeling for soybean cultivation in six irrigated pivots located in the northwest of Minas Gerais, Brazil. The maximum normalized difference vegetation index (NDVImax) and the maximum soil-adjusted vegetation index (SAVImax) were extracted from Landsat-8 OLI/TIRS sensor images for the 2016 to 2019 harvests during the R1 to R3 phenological stages. The maximum NDVI values varied across the study regions and crops, ranging from 0.27 to 0.95. Similarly, SAVI values exhibited variability, with the maximum SAVI ranging from 0.13 to 0.85. The growth index (GIw), derived from the CLIMEX model, ranged from 0.88 to 1. The statistical analysis confirmed a significant correlation (p < 0.05) between NDVImax and GIw only for the 2018/19 harvest, with a Pearson correlation coefficient of r = 0.86, classified as very strong. Across all harvests, NDVI consistently outperformed SAVI in correlation strength with GIw. Using geotechnologies through remote sensing shows promise for correlating spectral indices and climate suitability models. However, when using a valid model, all crops did not correlate. Still, our study has the potential to be improved by investigating new hypotheses, such as using drone images with better resolution (spatial, spectral, temporal, and radiometric) and adjusting the response of soybean vegetation indices and the phenological stage. Our results correlating the CLIMEX model of growth indices with vegetation indices have the potential for monitoring soybean cultivation and analyzing the performance of varieties but require a more in-depth view to adapt the methodology. Full article
Show Figures

Figure 1

Figure 1
<p>(<b>a</b>) Spatial location of the state of Minas Gerais within the national territory, (<b>b</b>) northwest region of Minas Gerais, (<b>c</b>) location of the study area with details of the altimetry for the regions (pivots) located in the municipalities of Buritis (Region 1), Arinos (Region 2), Cabeceira Grande (Region 3), Unaí (Region 4), Varjão de Minas (Region 5) and Vazante (Region 6).</p>
Full article ">Figure 2
<p>Flowchart of the work stages.</p>
Full article ">Figure 3
<p>Growth index for the six regions and four harvests, where (<b>A</b>,<b>E</b>,<b>I</b>,<b>M</b>,<b>Q</b>,<b>U</b>)—2016/2017 harvest; (<b>B</b>,<b>F</b>,<b>J</b>,<b>N</b>,<b>R</b>,<b>V</b>)—2017/2018 harvest; (<b>C</b>,<b>G</b>,<b>K</b>,<b>O</b>,<b>S</b>,<b>W</b>)—2018/2019 harvest; (<b>D</b>,<b>H</b>,<b>L</b>,<b>P</b>,<b>T</b>,<b>X</b>)—2019/2020 harvest. The green color shows the growth rate and the red color shows the soybean growing seasons.</p>
Full article ">Figure 4
<p>NDVI values (minimum, maximum, and average) for the 2016/17, 2017/18, 2018/19, and 2019/20 harvests in the different study regions.</p>
Full article ">Figure 5
<p>NDVI for the six regions for the 2016/2017 and 2017/2018 harvests.</p>
Full article ">Figure 6
<p>NDVI for the six regions for the 2018/2019 and 2019/2020 harvests.</p>
Full article ">Figure 7
<p>SAVI values (minimum, maximum, and average) for the 2016/17, 2017/18, 2018/19, and 2019/20 harvests in the different study regions.</p>
Full article ">Figure 8
<p>SAVI for the six regions for the 2016/2017 and 2017/2018 harvests.</p>
Full article ">Figure 9
<p>SAVI for the six regions for the 2018/2019 and 2019/2020 harvests.</p>
Full article ">Figure 10
<p>Variables measured in soybeans for irrigated soybean-producing Region 1, northwest Minas Gerais.</p>
Full article ">Figure 11
<p>Variables measured in soybeans for irrigated soybean-producing Region 2, northwest Minas Gerais.</p>
Full article ">Figure 12
<p>Variables measured in soybeans for irrigated soybean producing Region 3, northwest Minas Gerais.</p>
Full article ">Figure 13
<p>Variables measured in soybeans for irrigated soybean-producing Region 4, northwest Minas Gerais.</p>
Full article ">Figure 14
<p>Variables measured in soybeans for irrigated soybean-producing Region 5, northwest Minas Gerais.</p>
Full article ">Figure 15
<p>Variables measured in soybeans for irrigated soybean-producing Region 6, northwest Minas Gerais.</p>
Full article ">
14 pages, 1221 KiB  
Article
Concordance Between Estimated Fetal Weight by Ultrasound and Birth Weight and Its Association with Adverse Perinatal Outcomes
by Cinara Carvalho Silva, Artur Bizinotto, Edward Araujo Júnior, Taciana Mara Rodrigues da Cunha Caldas, Alberto Borges Peixoto and Roberta Granese
J. Clin. Med. 2025, 14(5), 1757; https://doi.org/10.3390/jcm14051757 - 5 Mar 2025
Abstract
Objective: The aim of this study was to analyze the concordance between estimated fetal weight (EFW) and birth weight among ultrasound examinations with fetal biometry considered adequate and inadequate according to the International Society of Ultrasound in Obstetrics and Gynecology (ISUOG) guidelines, and [...] Read more.
Objective: The aim of this study was to analyze the concordance between estimated fetal weight (EFW) and birth weight among ultrasound examinations with fetal biometry considered adequate and inadequate according to the International Society of Ultrasound in Obstetrics and Gynecology (ISUOG) guidelines, and its association with adverse perinatal outcomes. Methods: This was a retrospective and cross-sectional study carried out in two centers, involving parturients who delivered between 37 and 41 weeks. The following parameters were evaluated: biparietal (BPD), head circumference (HC), abdominal circumference (AC), and femur length (FL) measurement; EFW; the interval between the ultrasound and delivery; and the discrepancy between EFW and birth weight. A minimum of 140 participants were required to assess the association between EFW and birth weight. Results: A total of 305 ultrasound examinations were selected and divided into two groups: adequate (Group I n = 115) and inadequate (Group II n = 190) fetal biometry. The measurements of the cephalic pole (BPD + HC), AC, and FL were inadequate in 69.5% (132/190), 91.6% (175/190), and 72.1% (137/190) of participants, respectively. Group I had a lower gestational age at ultrasound examination (38.4 vs. 39.9 weeks, p < 0.001), a larger BPD measurement (93.9 vs. 91.6 mm, p = 0.001), a longer interval between ultrasound examination and delivery (3.8 vs. 2.0 days, p < 0.001), and a smaller discrepancy between EFW and birth weight (7.2 vs. 9.5%, p = 0.002) than Group II. In Group I, EFW was a strong significant predictor (AUC:0.94, 95%CI 0.85–0.99, p = 0.032) for identifying birth weight >4000 g. An EFW cut-off value of 4019.0 g was found to be a correct identifier for 85.7% of newborns with a birth weight >4000 g, with a false-positive rate of 13.7%. Group I had a lower risk of postpartum hemorrhage (7.0% vs. 15.8%, OR:0.39, 95%CI 0.17–0.90, p = 0.024) and composite adverse perinatal outcomes (13.0 vs. 23.3%, OR:0.49, 95%CI 0.26–0.94, p = 0.030) than Group II. In Group I patients, undergoing an ultrasound 7 days before delivery was an independent predictor of composite adverse perinatal outcomes [x2(1) = 4.9, OR:0.49, 95%CI: 0.26–0.94, R2 Nagelkerke:0.026, p = 0.030]. Conclusions: We observed a high rate of inadequate fetal biometry. There was poor concordance between EFW and birth weight. EFW was a strong significant predictor for identifying macrosomia. Ultrasound examination performed 7 days before delivery was an independent predictor of adverse perinatal outcomes. Full article
(This article belongs to the Section Obstetrics & Gynecology)
Show Figures

Figure 1

Figure 1
<p>Measurements of biparietal diameter (BPD) (<b>A</b>), head circumference (HC) (<b>B</b>), abdominal circumference (AC) (<b>C</b>), and femur length (FL) (<b>D</b>) according to the International Society of Ultrasound in Obstetrics and Gynecology (ISUOG) guidelines.</p>
Full article ">Figure 2
<p>Flowchart of the included cases.</p>
Full article ">Figure 3
<p>Receiver operating characteristics (ROC) curve for determining the best cut-off value of estimated fetal weight, performed 7 days before delivery, to predict birth weight &gt; 4000 g, among ultrasound examinations with adequate (<b>A</b>) and inadequate (<b>B</b>) fetal biometry.</p>
Full article ">Figure 4
<p>Correlation between estimated fetal weight and birth weight among ultrasound examinations with adequate (<b>A</b>) and inadequate (<b>B</b>) fetal biometry. Correlation between estimated fetal weight and birth weight discrepancy among ultrasound examinations with adequate (<b>C</b>) and inadequate (<b>D</b>) fetal biometry. Pearson correlation coefficient (r). <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 5
<p>Bland–Altman plot for birth weight among ultrasound examinations with adequate (<b>A</b>) and inadequate (<b>B</b>) fetal biometry.</p>
Full article ">
34 pages, 435 KiB  
Article
Optimal Almost Sure Rate of Convergence for the Wavelets Estimator in the Partially Linear Additive Models
by Khalid Chokri and Salim Bouzebda
Symmetry 2025, 17(3), 394; https://doi.org/10.3390/sym17030394 - 5 Mar 2025
Abstract
In this article, we examine a class of partially linear additive models (PLAM) defined via a measurable mapping Ψ:RqR. More precisely, we consider [...] Read more.
In this article, we examine a class of partially linear additive models (PLAM) defined via a measurable mapping Ψ:RqR. More precisely, we consider Ψ(Yi):=Yi=Ziβ+l=1dml(Xl,i)+εi,i=1,,n, where Zi=(Zi,1,,Zi,p) and Xi=(X1,i,,Xd,i) denote vectors of explanatory variables. The unknown parameter vector is β=(β1,,βp), and m1,,md are real-valued functions of a single variable whose forms are not specified. The error terms ε1,,εn are identically distributed with mean zero and finite variance σε, and they fulfill the condition E(εX,Z)=0 almost surely. These models are broadly applicable in finance, biology, and engineering, where capturing intricate nonlinear effects is essential. We propose an estimation method that leverages marginal integration in conjunction with linear wavelet-based techniques to obtain estimators for the unknown components m1,,md. Under suitable regularity conditions, we establish strong uniform convergence of these estimators, demonstrating that they achieve practically relevant convergence rates. Our theoretical results indicate that these estimators converge uniformly at rates that are favorable for practical applications, underscoring the adaptability and scope of this partially linear additive model. Full article
(This article belongs to the Section Mathematics)
10 pages, 4107 KiB  
Article
Whole Genome Analysis of Proteus mirabilis in a Poultry Breeder Farm Reveals the Dissemination of blaNDM and blaCTX-M Mediated by Diverse Mobile Genetic Elements
by Haibin Hu, Ke Wu, Tiejun Zhang, Yuhuan Mou, Luya Liu, Xiaoqin Wang, Wei Xu, Wenping Chen, Xiaojiao Chen, Hongning Wang and Changwei Lei
Agriculture 2025, 15(5), 555; https://doi.org/10.3390/agriculture15050555 - 5 Mar 2025
Abstract
Proteus mirabilis is a significant foodborne opportunistic pathogen associated with various nosocomial infections. Chicken farms may serve as an important reservoir for P. mirabilis. However, research on antibiotic resistance and genomic features of P. mirabilis in China’s poultry industry is limited. This [...] Read more.
Proteus mirabilis is a significant foodborne opportunistic pathogen associated with various nosocomial infections. Chicken farms may serve as an important reservoir for P. mirabilis. However, research on antibiotic resistance and genomic features of P. mirabilis in China’s poultry industry is limited. This study isolates P. mirabilis from a breeder farm in China and investigates the dissemination of P. mirabilis and clinically significant antibiotic resistance genes (ARGs), including blaNDM and blaCTX-M. From 510 samples, 69 isolates were obtained, classified into 11 sequence types (STs), with ST135 and ST175 predominating. A total of 39 ARGs were detected, including fosA3, floR, blaCTX-M-3, blaCTX-M-65, and blaNDM-1. Genetic analysis revealed that blaNDM-1 was exclusively located on Salmonella genomic island 1 (SGI1), while blaCTX-M was found in various mobile genetic elements (MGEs), including Tn7, SXT/R391 integrative conjugative elements (ICEs), Proteus mirabilis genomic resistance island 1 (PmGRI1), and SGI1. Notably, many isolates carried multiple MGEs, suggesting frequent horizontal transfer of ARGs in P. mirabilis. These findings underscore the role of P. mirabilis in carrying and spreading antibiotic resistance, posing significant risks to the poultry industry and public health. Full article
Show Figures

Figure 1

Figure 1
<p>Antibiotic resistance and antibiotic resistance genes (ARGs) of the <span class="html-italic">P. mirabilis</span> isolates. (<b>a</b>) Antibiotic resistance against the selected antimicrobial agents. (<b>b</b>) ARGs in the isolates, including aminoglycoside resistance genes <span class="html-italic">aac(</span>3<span class="html-italic">)-IV</span>, <span class="html-italic">aac(</span>3<span class="html-italic">)-lld</span>, <span class="html-italic">aadA1</span>, <span class="html-italic">aadA2</span>, <span class="html-italic">aadA2b</span>, <span class="html-italic">aadA3</span>, <span class="html-italic">aadA5</span>, <span class="html-italic">aph(</span>3″<span class="html-italic">)-Ⅰb</span>, <span class="html-italic">aph(</span>3′<span class="html-italic">)-Ia</span>, <span class="html-italic">aph(</span>3′<span class="html-italic">)-</span>VIa, <span class="html-italic">aph(</span>4<span class="html-italic">)-Ⅰa</span>, <span class="html-italic">and aph(</span>6<span class="html-italic">)-Id</span>; aminoglycoside and quinolone resistance genes <span class="html-italic">aac(</span>6′<span class="html-italic">)-Ib-cr</span>; rifampin resistance gene <span class="html-italic">ARR-3</span>; cephalosporin resistance genes <span class="html-italic">bla</span><sub>CTX-M-3</sub> and <span class="html-italic">bla</span><sub>CTX-M-65</sub>; carbapenem resistance gene <span class="html-italic">bla</span><sub>NDM-1</sub>; beta-lactam resistance genes <span class="html-italic">bla</span><sub>OXA-1</sub> and <span class="html-italic">bla</span><sub>TEM-1B</sub>; bleomycin resistance gene <span class="html-italic">bleO</span>; chloramphenicol resistance genes <span class="html-italic">catB3</span>, <span class="html-italic">cmlA1</span>, and <span class="html-italic">floR</span>; trimethoprim resistance genes <span class="html-italic">dfrA1</span>, <span class="html-italic">dfrA12</span>, <span class="html-italic">dfrA17</span>, and <span class="html-italic">dfrA32</span>; macrolide resistance genes <span class="html-italic">erm(</span>42<span class="html-italic">)</span>, <span class="html-italic">ere(</span>A<span class="html-italic">)</span>, <span class="html-italic">mph(</span>E<span class="html-italic">)</span>, and <span class="html-italic">msr(</span>E<span class="html-italic">)</span>; fosfomycin resistance gene <span class="html-italic">fosA3</span>; lincosamide resistance gene <span class="html-italic">lnu(</span>F<span class="html-italic">)</span>; quinolone resistance gene <span class="html-italic">qnrD1</span>; sulfonamide resistance genes <span class="html-italic">sul1</span>, <span class="html-italic">sul2</span>, and <span class="html-italic">sul3</span>; and tetracycline resistance genes <span class="html-italic">tet(</span>A<span class="html-italic">)</span> and <span class="html-italic">tet(</span>C<span class="html-italic">)</span>.</p>
Full article ">Figure 2
<p>Detection results of ARGs in the <span class="html-italic">P. mirabilis</span> isolates of different STs and isolation sources. The black squares indicate the presence of ARGs. The dendrograms on the left and top sides of the heatmap show hierarchical clustering of the isolates and ARGs, respectively.</p>
Full article ">Figure 3
<p>Phylogenetic analysis of 69 <span class="html-italic">P. mirabilis</span> strains: the origin, ST, and presence of key ARGs are represented using different colors. The clonal clusters (SNPs ≤ 10) are designated as I–VIII.</p>
Full article ">Figure 4
<p>Genetic environments of <span class="html-italic">bla</span><sub>CTX-M-65</sub>, including its association with Tn<span class="html-italic">7</span> transposons (<b>a</b>), SXT/R391 ICEs (<b>b</b>), and PmGRI1 (<b>c</b>) in <span class="html-italic">P. mirabilis</span> isolates. ORFs are depicted as arrows, with arrowheads indicating the direction of transcription. Integrase genes, resistance genes, and transposase genes are highlighted in yellow, red, and blue, respectively. Regions with &gt;85% nucleotide sequence identity are shaded in gray. HS1 to HS5 denote hotspots 1 to 5, and VRIII represents variable region III within the SXT/R391 integrative conjugative element (ICE). Direct repeats at the ends of genetic elements are labeled as DR-L and DR-R.</p>
Full article ">Figure 5
<p>Genetic environments of clinically important ARGs <span class="html-italic">bla</span><sub>NDM-1</sub> and <span class="html-italic">bla</span><sub>CTX-M-3</sub> associated with SGI1 variants in <span class="html-italic">P. mirabilis</span> isolates. Genes and ORFs are depicted as arrows, with arrowheads indicating the direction of transcription. Integrase genes, resistance genes, and transposase genes are highlighted in yellow, red, and blue, respectively. Regions with &gt;85% nucleotide sequence identity are shaded in gray. Direct repeats at the ends of genetic elements are labeled as DR-L and DR-R.</p>
Full article ">
19 pages, 2838 KiB  
Article
Comparison of Machine Learning Models for Real-Time Flow Forecasting in the Semi-Arid Bouregreg Basin
by Fatima Zehrae Elhallaoui Oueldkaddour, Fatima Wariaghli, Hassane Brirhet, Ahmed Yahyaoui and Hassane Jaziri
Limnol. Rev. 2025, 25(1), 6; https://doi.org/10.3390/limnolrev25010006 - 5 Mar 2025
Abstract
Morocco is geographically located between two distinct climatic zones: temperate in the north and tropical in the south. This situation is the reason for the temporal and spatial variability of the Moroccan climate. In recent years, the increasing scarcity of water resources, exacerbated [...] Read more.
Morocco is geographically located between two distinct climatic zones: temperate in the north and tropical in the south. This situation is the reason for the temporal and spatial variability of the Moroccan climate. In recent years, the increasing scarcity of water resources, exacerbated by climate change, has underscored the critical role of dams as essential water reservoirs. These dams serve multiple purposes, including flood management, hydropower generation, irrigation, and drinking water supply. Accurate estimation of reservoir flow rates is vital for effective water resource management, particularly in the context of climate variability. The prediction of monthly runoff time series is a key component of water resources planning and development projects. In this study, we employ Machine Learning (ML) techniques—specifically, Random Forest (RF), Support Vector Regression (SVR), and XGBoost—to predict monthly river flows in the Bouregreg basin, using data collected from the Sidi Mohamed Ben Abdellah (SMBA) Dam between 2010 and 2020. The primary objective of this paper is to comparatively evaluate the applicability of these three ML models for flow forecasting in the Bouregreg River. The models’ performance was assessed using three key criteria: the correlation coefficient (R2), Akaike Information Criterion (AIC), and Bayesian Information Criterion (BIC). The results demonstrate that the SVR model outperformed the RF and XGBoost models, achieving high accuracy in flow prediction. These findings are highly encouraging and highlight the potential of machine learning approaches for hydrological forecasting in semi-arid regions. Notably, the models used in this study are less data-intensive compared to traditional methods, addressing a significant challenge in hydrological modeling. This research opens new avenues for the application of ML techniques in water resource management and suggests that these methods could be generalized to other basins in Morocco, promoting efficient, effective, and integrated water resource management strategies. Full article
Back to TopTop