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17 pages, 3347 KiB  
Article
Assessing Genetic Diversity and Population Structure of Western Honey Bees in the Czech Republic Using 22 Microsatellite Loci
by Aleš Knoll, Martin Šotek, Jan Prouza, Lucie Langová, Antonín Přidal and Tomáš Urban
Insects 2025, 16(1), 55; https://doi.org/10.3390/insects16010055 (registering DOI) - 9 Jan 2025
Abstract
To date, no study has been conducted to investigate the diversity in honeybee populations of Apis mellifera in the Czech Republic. Between 2022 and 2023, worker bees were collected from colonies distributed throughout the Czech Republic in 77 districts, and their genetic differences [...] Read more.
To date, no study has been conducted to investigate the diversity in honeybee populations of Apis mellifera in the Czech Republic. Between 2022 and 2023, worker bees were collected from colonies distributed throughout the Czech Republic in 77 districts, and their genetic differences were examined using 22 microsatellite loci. The samples were obtained from hives (n = 3647) and through the process of capture on flowers (n = 553). Genetic diversity parameters were assessed for both populations in all 77 districts. The findings demonstrated that honeybee populations exhibit moderate genetic diversity, as evidenced by the number of observed alleles, the Shannon index, and heterozygosity values. There was no discrepancy in diversity between hive and flower samples. Diversity characteristics were determined: mean observed heterozygosity 0.55 (hives) and 0.56 (flowers), and fixation index 0.58 for both populations. The average number of alleles per locus was 13.77 and 11.18 from hives and flowers, respectively. The low FST and FIS values (they measured the level of genetic differentiation between populations and the level of inbreeding, respectively) suggest the absence or minimal genetic diversity within and among studied populations. The genetic variation was calculated as 2% and 1% between populations, 8% and 6% between individuals within populations, and 91% and 93% between all individuals in samples from hives and flowers, respectively. Cluster and DAPC (discriminant analysis principal component) analysis classified the bee samples collected from across the country into three and five to six distinguishable groups, respectively. The honeybee population in the Czech Republic displays sufficient diversity and a partial structure. However, there appears to be no correlation between the genetic groups and the geographic regions to which they are assigned. Full article
(This article belongs to the Special Issue Biology and Conservation of Honey Bees)
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<p>The map of sampling sites in individual districts in the Czech Republic. Abbreviations of districts: BE Beroun; BI Brno-venkov; BK Blansko; BM Brno-město; BN Benešov; BR Bruntál; BV Břeclav; CB České Budějovice; CK Český Krumlov; CL Česká Lípa; CR Chrudim; CV Chomutov; DC Děčín; DO Domažlice; FM Frýdek Místek; HB Havlíčkův Brod; HK Hradec Králové; HO Hodonín; CH Cheb; JC Jičín; JE Jeseník; JH Jindřichův Hradec; JI Jihlava; JN Jablonec nad Nisou; KI Karviná; KH Kutná Hora; KD Kladno; KM Kroměříž; KO Kolín; KT Klatovy; KV Karlovy Vary; LI Liberec; LN Louny; LT Litoměřice; MB Mladá Boleslav; ME Mělník; MO Most; NA Náchod; NB Nymburk; NJ Nový Jičín; OC Olomouc; OP Opava; OV Ostrava-město; PU Pardubice; PB Příbram; PE Pelhřimov; PY Praha-východ; PHA Praha; PI Písek; PJ Plzeň-jih; PM Plzeň-město; PR Přerov; PS Plzeň-sever; PT Prachatice; PV Prostějov; PZ Praha-západ; RA Rakovník; RK Rychnov nad Kněžnou; RO Rokycany; SM Semily; SO Sokolov; ST Strakonice; SU Šumperk; SY Svitavy; TA Tábor; TC Tachov; TP Teplice; TR Třebíč; TU Trutnov; UH Uherské Hradiště; UL Ústí nad Labem; UO Ústí nad Orlicí; VS Vsetín; VY Vyškov; ZL Zlín; ZN Znojmo; ZR Žďár nad Sázavou.</p>
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<p>Principal component analysis (PCA) of 77 populations from hives (<b>a</b>,<b>b</b>) and from flower samples (<b>c</b>,<b>d</b>) based on Nei’s pairwise distances and <span class="html-italic">F<sub>ST</sub></span> pairwise distances. The population pairwise Nei’s and <span class="html-italic">F<sub>ST</sub></span> values for the samples from hives and flowers are presented in <a href="#app1-insects-16-00055" class="html-app">Tables S6 and S7</a>, respectively.</p>
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<p>Proportions of inferred STRUCTURE clusters (optimal K = 3, based on Puechmaille and Evanno method in <a href="#app1-insects-16-00055" class="html-app">Figure S1a</a>) from the individuals in samples from hives. Each vertical line denotes an individual sample, while the color indicates the probability of the individual belonging to a particular population district. The numbers (1–77) in the top chart represent districts (you can find the district designation in <a href="#app1-insects-16-00055" class="html-app">Table S1</a>). In the Sort by Q graph, individuals are sorted according to their estimated membership in each population.</p>
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<p>Proportions of inferred STRUCTURE clusters (optimal K = 3, based on the Puechmaille and Evanno method in <a href="#app1-insects-16-00055" class="html-app">Supplementary Figure S1b</a>) from the individuals in samples from flowers. Each vertical line denotes an individual sample, while the color indicates the probability of the individual belonging to a particular population district. The numbers (1–77) in the top chart represent districts (you can find the district designation in <a href="#app1-insects-16-00055" class="html-app">Supplementary Table S1</a>). In the Sort by Q graph, individuals are sorted according to their estimated membership in each population.</p>
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<p>(<b>a</b>) Discriminant analysis of principal components (DAPC) of samples from hives found six clusters distributed across districts (<a href="#app1-insects-16-00055" class="html-app">Figure S2a</a>). The plot describes the PCA eigenvalues, which explain how much variability is explained by the 1st and 2nd components, and the DA eigenvalues, which indicate how well each discriminant function separates clusters; (<b>b</b>) the plot shows the determination of the optimal number (K = 6) of clusters on the basis of the Bayes information criterion (BIC); and (<b>c</b>) the plot displays the densities of individuals on a discrimination function 1.</p>
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<p>(<b>a</b>) Discriminant analysis of principal components (DAPC) of samples from flowers found five clusters distributed across districts (<a href="#app1-insects-16-00055" class="html-app">Figure S2b</a>). The plot describes the PCA eigenvalues, which explain how much variability is explained by the 1st and 2nd components, and the DA eigenvalues, which indicate how well each discriminant function separates clusters; (<b>b</b>) the plot shows the determination of the optimal number (K = 5) of clusters on the basis of the Bayes information criterion (BIC); and (<b>c</b>) the plot displays the densities of individuals on a discrimination function 1.</p>
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20 pages, 5829 KiB  
Article
Research on Arc Extinguishing Characteristics of Single-Phase Grounding Fault in Distribution Network
by Yan Li, Jianyuan Xu, Peng Wang and Guanhua Li
Energies 2025, 18(2), 256; https://doi.org/10.3390/en18020256 (registering DOI) - 9 Jan 2025
Abstract
The development of a single-phase grounding fault arc is influenced by various environmental factors, which can result in the rapid extinction and reignition of the arc. This phenomenon can lead to accidents, such as resonant overvoltage. Current grounding arc models inadequately account for [...] Read more.
The development of a single-phase grounding fault arc is influenced by various environmental factors, which can result in the rapid extinction and reignition of the arc. This phenomenon can lead to accidents, such as resonant overvoltage. Current grounding arc models inadequately account for the effects of grounding current, arc length, environmental wind speed, and other variables on the characteristics of the arc. In response to this issue, this article establishes a three-dimensional single-phase grounding arc mathematical model grounded in magnetohydrodynamics. It simulates and analyzes the effects of arc length and environmental wind speed on both arc ignition and extinguishing. Furthermore, an artificial single-phase grounding test platform is constructed within the actual distribution network to validate the accuracy of the simulation model. Research has demonstrated that, under identical operating conditions for both simulation and experimentation, the error range between the simulated arc voltage and the measured data is within 8%. The three-dimensional single-phase grounding arc mathematical model effectively describes the dynamic development process of the grounding arc. At a gap of 12 cm, under windless conditions and with a grounding current of 40.0 A, the temperature of the arc column at the peak of the current reaches 2600 K, while the conductivity decreases to 2.1 × 10−4 S/m, resulting in the inability of the arc to sustain a burning state. At a gap of 2 cm and a wind speed of 7 m/s, the temperature of the arc column at the peak of the current reaches 2900 K, the conductivity drops to 4.3 × 10−3 S/m, leading to the extinction of the arc. Full article
(This article belongs to the Section F: Electrical Engineering)
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<p>Equivalent circuit of single-phase earth fault in a neutral grounded system by suppression coil.</p>
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<p>Multi-physical field coupling relationship of grounding arc.</p>
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<p>Mass flow rate through various interfaces of infinitesimal fluid microelements.</p>
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<p>Infinitesimal fluid microelements subjected to surface forces.</p>
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<p>Energy flux during the motion of infinitesimal microelements.</p>
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<p>Schematic diagram of grounding arc simulation model.</p>
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<p>Peak current moment, grounding current 20 A, 40 A, 80 A arc shape and temperature distribution.</p>
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<p>Arc shape and temperature distribution under ground current of 20 A, 40 A, and 80 A at peak current.</p>
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<p>A 220 kV substation circuit diagram.</p>
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<p>Air arc ignition device.</p>
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<p>(<b>a</b>) Gap distance of 12 cm, grounding current of 49.5 A, arc voltage and current test waveform; (<b>b</b>) gap distance of 16 cm, grounding current of 49.5 A, arc voltage and current test waveform; (<b>c</b>) gap distance of 16 cm, grounding current of 40.0 A, arc voltage and current test waveform.</p>
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<p>Spectrum of arc voltage test waveform under different operating conditions.</p>
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<p>(<b>a</b>) Simulation waveforms of arc voltage under different operating conditions; (<b>b</b>) spectral analysis of arc voltage simulation waveforms under different operating conditions.</p>
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<p>Arc voltage and current waveform under different gap distances.</p>
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<p>Arc shape and temperature distribution at different times and gap distances.</p>
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<p>Arc shape and temperature distribution at different wind speeds during the peak current moment in a 2 cm gap.</p>
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<p>Arc shape and temperature distribution at different times of 2 cm gap and 5 m/s.</p>
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11 pages, 363 KiB  
Article
Customers’ Preferences for Crape Myrtle (Lagerstroemia L.) Across Geographical Regions: Evidence from China
by Siwen Hao, Donglin Zhang and Yafeng Wen
Horticulturae 2025, 11(1), 61; https://doi.org/10.3390/horticulturae11010061 (registering DOI) - 9 Jan 2025
Abstract
Crape myrtle (Lagerstroemia L.), as a popular ornamental plant, holds significant importance in residents’ daily lives by supporting ecosystem services, enhancing urban aesthetics, and even impacting biological health. There are notable variations among crape myrtle species across different geographical distributions. However, potential [...] Read more.
Crape myrtle (Lagerstroemia L.), as a popular ornamental plant, holds significant importance in residents’ daily lives by supporting ecosystem services, enhancing urban aesthetics, and even impacting biological health. There are notable variations among crape myrtle species across different geographical distributions. However, potential differences in residents’ preferences for observing crape myrtle in various regions have not been thoroughly investigated. This study, based on a comprehensive analysis of 700 survey responses from diverse regions in China, sought to determine if discernible patterns exist in residents’ preferences for crape myrtle. The results revealed that residents across different regions exhibited distinct preferences for various ornamental characteristics of crape myrtle. These differences were particularly pronounced in intangible aspects such as cultural expression, ecological value, and economic value. Furthermore, the study demonstrated that the factors driving market demand for ornamental crape myrtle varied substantially across different regional populations. In north China, the flowering period and leaf size were identified as the primary factors influencing market interest. For south China, both the flowering period and flower size were crucial determinants. In central China, the key factors were the flowering period and flower color. The market demand in east China was largely driven by flower size and the flowering period. In northeast China, flower color and planting form played pivotal roles, while in northwest China, spatial ambiance and plant phenotype were significant in shaping preferences. Finally, in southwest China, landscape type and fruit color were the primary factors influencing market demand. These findings provide valuable insights into the relationship between regional preferences and the prevalence of crape myrtle, highlighting the potential factors that shape aesthetic choices in different parts of China. Full article
(This article belongs to the Section Floriculture, Nursery and Landscape, and Turf)
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<p>Regional variations in customer preferences for crape myrtle ornamentals.</p>
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22 pages, 4351 KiB  
Article
Assessing Climate Change Impact on Rainfall Patterns in Northeastern India and Its Consequences on Water Resources and Rainfed Agriculture
by Debasish Chakraborty, Aniruddha Roy, Nongmaithem Uttam Singh, Saurav Saha, Shaon Kumar Das, Nilimesh Mridha, Anjoo Yumnam, Pampi Paul, Chikkathimme Gowda, Kamni Paia Biam, Sandip Patra, Thippeswamy Amrutha, Braj Pal Singh and Vinay Kumar Mishra
Earth 2025, 6(1), 2; https://doi.org/10.3390/earth6010002 (registering DOI) - 9 Jan 2025
Abstract
To understand the impact of climate change on water resources, this research investigates long-term rainfall trends and anomalies across Northeastern India (NEI), covering Assam and Meghalaya (A&M); Nagaland, Manipur, Mizoram, and Tripura (NMMT); and Sub-Himalayan West Bengal and Sikkim (SHWB&S) using different statistical [...] Read more.
To understand the impact of climate change on water resources, this research investigates long-term rainfall trends and anomalies across Northeastern India (NEI), covering Assam and Meghalaya (A&M); Nagaland, Manipur, Mizoram, and Tripura (NMMT); and Sub-Himalayan West Bengal and Sikkim (SHWB&S) using different statistical tests including innovative trend analysis (ITA). The study scrutinizes 146 years of rainfall statistics, trend analyses, variability, and probability distribution changes to comprehend its implications. Furthermore, the change in the assured rainfall probabilities was also worked out to understand the impact on rainfed agriculture of Northeastern India. Comparative analysis between all India (AI) and NEI reveals that NEI receives nearly double the annual rainfall compared to AI (2051 mm and 1086 mm, respectively). Despite resembling broad rainfall patterns, NEI displays intra-regional variations, underscoring the necessity for region-specific adaptation strategies. Statistical characteristics like the coefficient of skewness (CS) and coefficient of kurtosis indicate skewed rainfall distributions, notably during the winter seasons in NMMT (CS~1.6) and SHWB&S (CS~1.5). Trend analyses reveal declining rainfall trends, especially conspicuous in NEI’s winter (−1.88) and monsoon (−2.9) seasons, where the rate of decrease was higher in the last three decades. The return periods of assured rainfall at 50% and 75% probability levels also increased sharply during the winter and monsoon seasons by over 30% during the recent half, posing challenges for rainfed upland hill farming. Furthermore, this study highlights increasing variability and negative anomalies in monsoon rainfall over NEI, exacerbating decreasing rainfall trends and significantly impacting agricultural productivity. These findings underscore the urgency for adaptive measures tailored to evolving rainfall patterns, ensuring sustainable agricultural practices and efficient water resource management. Full article
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<p>Map of the study area covering Northeastern India and its three meteorological sub-divisions.</p>
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<p>The mean (<b>upper row</b>) and coefficient of variation (<b>lower row</b>) of rainfall in the study regions of India (1871–2016).</p>
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<p>Rainfall distribution among the seasons as a percentage of the selected region’s annual rainfall (<b>a</b>) and their seasonal coefficient of variation (CV) (<b>b</b>).</p>
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<p>Trends (a: MKT and b: SRHO) in the rainfall series of the selected regions in India during different periods. *** for <span class="html-italic">p</span> ≤ 0.01, ** for 0.01&lt; <span class="html-italic">p</span> ≤ 0.05, and * for 0.05 &lt; <span class="html-italic">p</span> ≤ 0.1.</p>
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<p>Innovative trend analysis (<span class="html-italic">p</span> &lt; 0.01) of the rainfall series of the selected regions of India (Upward facing triangle indicated by “***” means statistically significant change while circle indicates non-significant values).</p>
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<p>Innovative trend analysis of the rainfall time series datasets (1871–2016) in the selected study regions.</p>
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<p>The changes in different characteristics of the rainfall series of the selected regions of India between the two periods (P1: 1871–1943 and P2: 1944–2016). *** for <span class="html-italic">p</span> ≤ 0.01, ** for 0.01&lt; <span class="html-italic">p</span> ≤ 0.05, and * for 0.05 &lt; <span class="html-italic">p</span> ≤ 0.1.</p>
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<p>The trend and variability in summer monsoon (JJAS) rainfall (1871–2016) in the selected study regions (AI-(<b>a</b>); NEI-(<b>b</b>), A&amp;M-(<b>c</b>), NMMT-(<b>d</b>), and SHWB&amp;S-(<b>e</b>); mean-M, standard deviation-SD; ***, **, and * denote trends at 1%, 5%, and 10% significance levels; green, red, and blue lines indicates excess, deficit and normal rainfall years, respectively; solid line and dotted lines represent the mean and deviation from mean, respectively).</p>
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<p>Percent change in return period of rainfall at different probability levels.</p>
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28 pages, 2771 KiB  
Article
Characterizing Groundwater Level Response to Precipitation at Multiple Timescales in the Lubei Plain Region Using Transfer Function Analysis
by Lewei Xu, Huili Gong, Beibei Chen, Chaofan Zhou, Xueting Zhong, Ziyao Ma and Dexin Meng
Remote Sens. 2025, 17(2), 208; https://doi.org/10.3390/rs17020208 - 8 Jan 2025
Abstract
Groundwater is essential for ecosystem stability and climate adaptation, with precipitation variations directly affecting groundwater levels (GWLs). Human activities, particularly groundwater exploitation, disrupt the recharge mechanism and the regional water cycle. In this study, we propose a new research framework: On the basis [...] Read more.
Groundwater is essential for ecosystem stability and climate adaptation, with precipitation variations directly affecting groundwater levels (GWLs). Human activities, particularly groundwater exploitation, disrupt the recharge mechanism and the regional water cycle. In this study, we propose a new research framework: On the basis of analyzing the spatiotemporal variability characteristics of precipitation and shallow GWL, we used transfer function analysis (TFA) to quantify the multi-timescale characteristics of precipitation–GWL response under the effects of climate change and human activities. In addition, we evaluated the GWL seasonality and seasonal response while also considering apportionment entropy. We applied this framework to the Lubei Plain (LBP), and the findings indicated the following: (1) Annual precipitation in the LBP decreased from southeast to northwest, with July and August contributing 51.5% of total rainfall; spatial autocorrelation of GWL was high and was influenced by geological conditions and cropland irrigation. (2) The coherence between GWL and precipitation was 0.96 in the high-precipitation areas but was only 0.6 in overexploited areas, and sandy soils enhanced the effective groundwater recharge, with a gain of 1.65 and a lag time of 2.1 months. (3) Over interannual scales, GWL response was driven by precipitation distribution and aquifer characteristics, while shorter timescales (4 months) were significantly affected by human activities, with a longer lag time in overexploited areas, which was nearly 60% longer than areas that were not overexploited. (4) Groundwater exploitation reduced the seasonality of GWL, and irrigation reduced the coherence between GWL and precipitation (0.5), with a gain of approximately 0.5, while a coherence of 0.8 and a gain of 3.5 were observed in the non-irrigation period. This study clarified the multi-timescale characteristics of the precipitation–GWL response, provided a new perspective for regional research on groundwater response issues, and proposed an important basis for the short-term regulation and sustainable development of water resources. Full article
25 pages, 2409 KiB  
Article
Phenotypic and Agronomic Variation Within Naturalized Medicago polymorpha L. (Burr Medic) in Subtropical Queensland, Australia, and Relationships with Climate and Soil Characteristics
by David L. Lloyd, John P. Thompson, Suzanne P. Boschma, Rick R. Young, Brian Johnson and Kemp C. Teasdale
Agronomy 2025, 15(1), 139; https://doi.org/10.3390/agronomy15010139 - 8 Jan 2025
Abstract
To characterize the naturalized population of burr medic (Medicago polymorpha L.), a valuable pasture legume, in subtropical Queensland, Australia, a collection of 1747 lines from 107 sites in 11 regions was grown, and 26 phenotypic and agronomic attributes were recorded. This data [...] Read more.
To characterize the naturalized population of burr medic (Medicago polymorpha L.), a valuable pasture legume, in subtropical Queensland, Australia, a collection of 1747 lines from 107 sites in 11 regions was grown, and 26 phenotypic and agronomic attributes were recorded. This data matrix was analyzed by cluster, principal co-ordinates, and discriminant and correlation analyses to examine line relationships based on plant attributes and their association with site characteristics of climate and soil. Among the wide polymorphism of attributes across the collection zone, there were a number of notable phenotypic associations. One of these, with large green leaves, minimally dentate leaf margins, and light purple petioles, was widely distributed. Three others, one with a distinctive magenta leaf mark, dark purple petioles, and an upright habit; one with those same attributes but with a prostrate habit; and one with grey-green leaves, high frost resistance, and the ability to stay green and to produce high pod yields, were associated with climatic and soil characteristics in the north, east, and south of the collection zone, respectively. Days to flowering were longer in lines from saline soils at lower altitude, and plant vigor was greatest in lines from more fertile soils with higher rainfall. A wide variation in time to flower of lines at all collection sites contributes to the adaptation of M. polymorpha in subtropical Queensland and potentially to its persistence with future climate change. Full article
(This article belongs to the Section Grassland and Pasture Science)
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<p><span class="html-italic">Medicago polymorpha</span> collection regions (defined by local government boundaries) in subtropical southern and central Queensland, Australia. Numbered regions are named with their acronym and number of lines collected in parentheses: 1. Central Highlands (CH, 71); 2. Central Queensland (CQ, 171); 3. Central West (CW, 55); 4. Darling Downs (DD, 260); 5. Maranoa North (MN, 119); 6. Maranoa South (MS, 168); 7. North Central Burnett (NCB, 128); 8. South Burnett Moreton (SBM, 121); 9. South West Queensland (SWQ, 94); 10. Western Downs North (WDN, 195); 11. Western Downs South (WDS,365). Isohyets represent average growing season rainfall (April to September).</p>
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<p>(<b>a</b>) Dendrogram of 1747 <span class="html-italic">Medicago polymorpha</span> lines depicting a cluster analysis based on 24 attributes. (<b>b</b>) The same dendrogram truncated at a similarity level of 0.65 delineating 15 clusters labelled A to O containing the following numbers of <span class="html-italic">M. polymorpha</span> lines given in parentheses: A (454); B (41); C (517); D (79); E (165); F (113); G (107); H (47); I (48); J (46); K (11); L (30); M (81); N (7) and O (1). Major furcations of the dendrogram are numbered 1 to 14.</p>
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<p>Scree plot of the percentage variation accounted for by latent roots from the PCoA of 1747 lines of <span class="html-italic">Medicago polymorpha</span>.</p>
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<p>Projections of the 1747 lines of <span class="html-italic">Medicago polymorpha</span> as points on the planes of (<b>a</b>) axes 1 and 2, and (<b>b</b>) axes 1 and 3 from the principal co-ordinates analysis (PCoA). Values in parentheses are the percentage of the total variation explained by each PCoA axis out of the 24 attribute axes.</p>
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<p>Scree plot of the percentage variation accounted for by latent roots from the discriminant analysis of regions based on phenotypic and agronomic attributes of 1747 lines of <span class="html-italic">Medicago polymorpha</span>.</p>
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<p>Distribution of the <span class="html-italic">Medicago polymorpha</span> lines grouped by region on the first discriminant axis from discriminant analysis based on plant attributes, which accounted for 23.5% of the variation. Region acronyms and numbers of lines are: Central Highlands (CH, 71); Central Queensland (CQ, 171); Central West (CW, 55); Darling Downs (DD, 260); Maranoa North (MN, 119); Maranoa South (MS, 168); North Central Burnett (NCB, 128); South Burnett Moreton (SBM, 121); South West Queensland (SWQ, 94); Western Downs North (WDN, 195); Western Downs South (WDS, 365).</p>
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<p>Distribution of the regional means of discriminant scores 1 and 2 from the discriminant analysis of regions based on plant attributes of 1747 lines of <span class="html-italic">Medicago polymorpha</span>. Region acronyms and numbers of lines are: Central Highlands (CH, 71); Central Queensland (CQ, 171); Central West (CW, 55); Darling Downs (DD, 260); Maranoa North (MN, 119); Maranoa South (MS, 168); North Central Burnett (NCB, 128); South Burnett Moreton (SBM, 121); South West Queensland (SWQ, 94); Western Downs North (WDN, 195); Western Downs South (WDS, 365).</p>
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<p>Box and whiskers plot of days to flowering of lines of <span class="html-italic">Medicago polymorpha</span> within regions. The upper and lower extremities of the box denote the upper and lower quartile values, respectively. The upper and lower extremities of the whiskers denote the maximum and minimum values, while the marked points are considered outliers. The median is shown as a horizontal line while the mean is shown as a cross. The maximum <span class="html-italic">Flsd</span> (<span class="html-italic">p</span> = 0.05) for difference between means is 3.1 days. Region acronyms and numbers of lines are: Central Highlands (CH, 71); Central Queensland (CQ, 171); Central West (CW, 55); Darling Downs (DD, 260); Maranoa North (MN, 119); Maranoa South (MS, 168); North Central Burnett (NCB, 128); South Burnett Moreton (SBM, 121); South West Queensland (SWQ, 94); Western Downs North (WDN, 195); Western Downs South (WDS, 365).</p>
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26 pages, 6157 KiB  
Article
Assessing the Impact of Climate Change on the Landscape Stability in the Mediterranean World Heritage Site Based on Multi-Sourced Remote Sensing Data: A Case Study of the Causses and Cévennes, France
by Mingzhuo Zhu, Daoye Zhu, Min Huang, Daohong Gong, Shun Li, Yu Xia, Hui Lin and Orhan Altan
Remote Sens. 2025, 17(2), 203; https://doi.org/10.3390/rs17020203 - 8 Jan 2025
Abstract
Global climate fluctuations pose challenges not only to natural environments but also to the conservation and transmission of human cultural and historical heritage. World Heritage Sites are pivotal regions for studying climate change impacts and devising adaptation strategies, with remote sensing technology showcasing [...] Read more.
Global climate fluctuations pose challenges not only to natural environments but also to the conservation and transmission of human cultural and historical heritage. World Heritage Sites are pivotal regions for studying climate change impacts and devising adaptation strategies, with remote sensing technology showcasing significant utility in monitoring these impacts, especially in the Mediterranean region’s diverse and sensitive climate context. Although existing work has begun to explore the role of remote sensing in monitoring the effects of climate change, detailed analysis of the spatial distribution and temporal trends of landscape stability remains limited. Leveraging remote sensing data and its derived products, this study assessed climate change impacts on the Causses and Cévennes Heritage Site, a typical Mediterranean heritage landscape. Specifically, this study utilized remote sensing data to analyze the trends in various climatic factors from 1985 to 2020. The landscape stability model was developed utilizing land cover information and landscape indicators to explore the landscape stability and its distribution features within the study area. Finally, we adopted the Geographical Detector to quantify the extent to which climatic factors influence the landscape stability’s spatial distribution across different periods. The results demonstrated that (1) the climate showed a warming and drying pattern during the study period, with distinct climate characteristics in different zones. (2) The dominance of woodland decreased (area proportion dropped from 76% to 66.5%); transitions primarily occurred among woodland, cropland, shrubland, and grasslands; landscape fragmentation intensified; and development towards diversification and uniformity was observed. (3) Significant spatiotemporal differences in landscape stability within the heritage site were noted, with an overall downward trend. (4) Precipitation had a high contribution rate in factor detection, with the interactive enhancement effects between temperature and precipitation being the most prominent. The present study delivers a thorough examination of how climate change affects the Causses and Cévennes Heritage Landscape, reveals its vulnerabilities, and offers crucial information for sustainable conservation efforts. Moreover, the results offer guidance for the preservation of similar Mediterranean heritage sites and contribute to the advancement and deepening of global heritage conservation initiatives. Full article
(This article belongs to the Section Environmental Remote Sensing)
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<p>Location (<b>a</b>), topography (<b>b</b>), and climatic zones (<b>c</b>) of the Causses and Cévennes World Heritage Site (Cf: temperate oceanic; Cs: Mediterranean; Df: temperate continental).</p>
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<p>Research framework.</p>
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<p>The annual cycle of temperature and precipitation in the heritage site (1985–2020).</p>
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<p>Temporal dynamics of climate factors in the heritage site from 1985 to 2020; (<b>a</b>) temperature, (<b>b</b>) precipitation, (<b>c</b>) potential evaporation, and (<b>d</b>) relative humidity.</p>
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<p>Spatial distribution of landscape types across different time periods in the Causses and Cévennes World Heritage Site; (<b>a</b>) 1985, (<b>b</b>) 2010, and (<b>c</b>) 2020.</p>
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<p>Landscape-type transition trajectory map of the heritage site, 1985–2020 (in km<sup>2</sup>).</p>
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<p>Spatial distribution of landscape-type transitions in the heritage site; (<b>a</b>) 1985–2010 and (<b>b</b>) 2010–2020.</p>
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<p>Changes in landscape indices.</p>
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<p>Spatial distribution of landscape stability in the heritage site from 1985 to 2020; (<b>a</b>) 1985, (<b>b</b>) 2010, and (<b>c</b>) 2020.</p>
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<p>Spatial dynamics of landscape stability from 1985 to 2020; (<b>a</b>) 1985–2010, (<b>b</b>) 2010–2020, and (<b>c</b>) 1985–2020.</p>
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<p>Contribution of climatic factors to the spatial divergence of landscape stability in the heritage site. (TMP, temperature; PRE, precipitation; RH, relative humidity; PET, potential evaporation).</p>
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<p>Climate trends and sub-regional variations in the heritage site (1985–2020); (<b>a</b>) temperature, (<b>b</b>) precipitation, (<b>c</b>) potential evaporation, (<b>d</b>) relative humidity.</p>
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21 pages, 6078 KiB  
Article
Analysis of the CHS Gene Family Reveals Its Functional Responses to Hormones, Salinity, and Drought Stress in Moso Bamboo (Phyllostachys edulis)
by Shiying Su, Xueyun Xuan, Jiaqi Tan, Zhen Yu, Yang Jiao, Zhijun Zhang and Muthusamy Ramakrishnan
Plants 2025, 14(2), 161; https://doi.org/10.3390/plants14020161 - 8 Jan 2025
Abstract
Chalcone synthase (CHS), the first key structural enzyme in the flavonoid biosynthesis pathway, plays a crucial role in regulating plant responses to abiotic stresses and hormone signaling. However, its molecular functions remain largely unknown in Phyllostachys edulis, which is one of the [...] Read more.
Chalcone synthase (CHS), the first key structural enzyme in the flavonoid biosynthesis pathway, plays a crucial role in regulating plant responses to abiotic stresses and hormone signaling. However, its molecular functions remain largely unknown in Phyllostachys edulis, which is one of the most economically and ecologically important bamboo species and the most widely distributed one in China. This study identified 17 CHS genes in Phyllostachys edulis and classified them into seven subgroups, showing a closer evolutionary relationship to CHS genes from rice. Further analysis of PeCHS genes across nine scaffolds revealed that most expansion occurred through tandem duplications. Collinearity analysis indicated strong evolutionary conservation among CHS genes. Motif and gene structure analyses confirmed high structural similarity, suggesting shared functional characteristics. Additionally, cis-acting element analysis demonstrated that PeCHS genes are involved in hormonal regulation and abiotic stress responses. RNA-Seq expression profiles in different bamboo shoot tissues and heights, under various hormone treatments (gibberellin (GA), naphthaleneacetic acid (NAA), abscisic acid (ABA), and salicylic acid (SA)), as well as salinity and drought stress, revealed diverse response patterns among PeCHS genes, with significant differential expression, particularly under hormone treatments. Notably, PeCHS14 consistently maintained high expression levels, suggesting its key role in stress response mechanisms. qRT-PCR analysis further validated the expression differences in five PeCHS genes under GA and ABA treatments. Subcellular localization analysis demonstrated that PeCHS14 and PeCHS15 proteins are localized in the nucleus. This study provides a foundation for investigating the potential functions of PeCHS genes and identifies candidate genes for future research on the responses of Phyllostachys edulis to abiotic stresses and hormone signaling. Full article
(This article belongs to the Special Issue The Genetic Architecture of Bamboo Growth and Development)
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<p>Phylogenetic analysis of interspecies relationships of PeCHS. The phylogenetic tree was constructed using MEGA 7.0 with the Neighbor-Joining (NJ) method. The evolutionary relationships among CHS sequences from <span class="html-italic">Phyllostachys edulis</span> (purple squares), <span class="html-italic">Arabidopsis thaliana</span> (orange triangles), and <span class="html-italic">Oryza sativa</span> (green circles) are illustrated. AtCHS represents CHS sequences from <span class="html-italic">Arabidopsis thaliana</span>, while OsCHS represents CHS sequences from <span class="html-italic">Oryza sativa</span>.</p>
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<p>Intraspecies and interspecies collinearity analysis of <span class="html-italic">PeCHS</span> genes. (<b>A</b>) Chromosomal distribution and interchromosomal relationships of <span class="html-italic">PeCHS</span> genes. (<b>B</b>) Interspecies collinearity analysis of CHS genes between <span class="html-italic">Phyllostachys edulis</span> and <span class="html-italic">Brachypodium distachyon.</span> (<b>C</b>) Interspecies collinearity analysis of <span class="html-italic">CHS</span> genes between <span class="html-italic">Phyllostachys edulis</span> and <span class="html-italic">Oryza sativa.</span> (<b>D</b>) Interspecies collinearity analysis of <span class="html-italic">CHS</span> genes between <span class="html-italic">Phyllostachys edulis</span> and <span class="html-italic">Zea mays</span>. Pe represents the chromosomes of <span class="html-italic">Phyllostachys edulis</span>, Bd represents the chromosomes of <span class="html-italic">Brachypodium distachyon</span>, Os represents the chromosomes of <span class="html-italic">Oryza sativa</span>, and Zm represents the chromosomes of <span class="html-italic">Zea mays</span>.</p>
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<p>Phylogenetic relationships, conserved motifs, and gene structures of <span class="html-italic">PeCHS</span> genes. (<b>A</b>) A Neighbor-Joining (NJ) phylogenetic tree of PeCHS proteins constructed using MEGA. (<b>B</b>) Conserved motifs in PeCHS proteins, with colored boxes representing motifs 1–5. (<b>C</b>) Gene structures of <span class="html-italic">PeCHS</span> genes, showing introns (gray lines), exons (blue rectangles), and untranslated regions (UTRs, gray rectangles). (<b>D</b>) Motif logo displaying the conserved sequences and relative frequencies of motifs in PeCHS proteins.</p>
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<p>Conserved domains and tertiary structure prediction of PeCHS proteins. (<b>A</b>) Conserved domains. Blue represents the Chal_sti_synt_N domain, and purple represents the Chal_sti_synt_C domain. (<b>B</b>) Tertiary structure.</p>
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<p><span class="html-italic">Cis</span>-regulatory elements in the promoter region (upstream 2000 bp) of <span class="html-italic">PeCHS</span> genes. (<b>A</b>) Different types of <span class="html-italic">cis</span>-regulatory elements upstream of <span class="html-italic">PeCHS</span> genes in <span class="html-italic">Phyllostachys edulis</span>, with the numbers inside the boxes representing the count of each element. (<b>B</b>,<b>C</b>) The number and proportion of different types of <span class="html-italic">cis</span>-regulatory elements upstream of <span class="html-italic">PeCHS</span> genes.</p>
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<p>Heatmap of <span class="html-italic">PeCHS</span> gene expression (log2<sup>(TPM+1)</sup>) in <span class="html-italic">Phyllostachys edulis</span>: (<b>A</b>) Expression in roots, stems, panicle inflorescences, and leaves. (<b>B</b>) Expression in shoots at different heights. (<b>C</b>) Expression under GA treatment. (<b>D</b>) Expression under NAA treatment. (<b>E</b>) Expression under SA treatment. (<b>F</b>) Expression under ABA treatment. (<b>G</b>) Expression under NaCl treatment. (<b>H</b>) Expression under PEG treatment. The relative expression levels are represented by a color scale, with blue indicating low expression and red indicating high expression.</p>
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<p>Top 20 most enriched GO terms for <span class="html-italic">PeCHS</span> genes. The horizontal axis represents the enrichment factor, and the size of the circles indicates the number of genes annotated with the given GO term.</p>
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<p>Correlation between <span class="html-italic">PeCHS</span> genes and transcription factor genes. The edge width of the lines represents the corresponding correlation strength, and the line color indicates statistical significance.</p>
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<p>Subcellular localization of GFP-fused PeCHS14 and PeCHS15 proteins. Bright: Bright-field image of <span class="html-italic">Nicotiana benthamiana</span> epidermal cells. GFP: Green fluorescence signal emitted by GFP. H2B-RFP: Red fluorescence signal emitted by nuclear H2B-RFP. Merge: Overlaid image of the two fluorescence signals, with yellow fluorescence indicating the overlap of green and red signals. Bars = 20 μm.</p>
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<p>Expression patterns of the <span class="html-italic">PeCHS</span> gene family under hormone treatments. (<b>A</b>) Expression patterns of the <span class="html-italic">PeCHS</span> gene family under GA treatment. (<b>B</b>) Expression patterns of the <span class="html-italic">PeCHS</span> gene family under ABA treatment. (*: <span class="html-italic">p</span> ≤ 0.05; **: <span class="html-italic">p</span> ≤ 0.01).</p>
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35 pages, 33466 KiB  
Article
Exploring the Influence of Microtopography on the Spatial Genes of Urban Historical Streets and Alleys in Xuzhou
by Yan Lin, Shuhan Zhang and Yi Jian
Sustainability 2025, 17(2), 427; https://doi.org/10.3390/su17020427 - 8 Jan 2025
Abstract
Spatial genes represent the fundamental interplay among the morphological characteristics of historical districts. Identifying and analyzing these morphological elements can enhance our understanding of urban spatial development, uncover spatial meanings, and provide informed recommendations for future development. This study focuses on the Xuzhou [...] Read more.
Spatial genes represent the fundamental interplay among the morphological characteristics of historical districts. Identifying and analyzing these morphological elements can enhance our understanding of urban spatial development, uncover spatial meanings, and provide informed recommendations for future development. This study focuses on the Xuzhou Huilongwo historical district, employing geographic information system, Global Mapper, and other digital technologies to determine the area’s microtopographic features. Qualitative methodologies extract the spatial genes of street segments, entry spaces, and node spaces. By summarizing the microtopography’s influence on street and alley characteristics, valuable spatial samples were selected and visually represented for analysis. This included examining the street segment interface, entry space sequences, and the planar morphology of node spaces. The findings reveal that Huilongwo architecture aligns with topographical features, exhibiting a multi-directional distribution. Height differences help establish street boundaries and enhance pathways’ experiential quality. Additionally, topography significantly influences street spaces, leading to undulating sequences in entry spaces. This study provides insights into the preservation and enhancement of streets and alleys within Xuzhou’s historical district. Full article
(This article belongs to the Special Issue Architecture, Urban Space and Heritage in the Digital Age)
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<p>Theoretical framework.</p>
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<p>The study area (the city of Xuzhou).</p>
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<p>Historical maps of Xuzhou and photos of Huilongwo.</p>
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<p>Functional distribution of Huilongwo district.</p>
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<p>Research framework.</p>
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<p>Elevation analysis of Huilongwo district.</p>
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<p>Huilongwo district gradient and slope analysis.</p>
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<p>Analysis perspective generation framework.</p>
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<p>Alley elevation distribution and marking.</p>
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<p>Lane 1: planar views and photo.</p>
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<p>Lane 5: planar views and photo.</p>
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<p>Lanes 8 and 9: planar views and photos.</p>
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<p>Elevated positions and flow lines for elevation as a site boundary.</p>
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<p>Lanes 7, 13, and 14.</p>
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<p>Lane 2: planar views and photos.</p>
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<p>Lane 4: planar views and photos.</p>
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<p>Lane 10: planar views and photos.</p>
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<p>Lane 11: planar views and photos.</p>
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<p>Elevated positions and flow lines for elevation as an enriching experience.</p>
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<p>Lane 3: planar views, elevated positions, flow lines, and photos.</p>
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<p>Relationship between façade profile and ground elevation.</p>
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<p>Lane 5 and 6 façades.</p>
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<p>Boundary extraction of a street segment.</p>
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<p>Lanes 6 and 7: planar views, elevated positions, flow lines, and photos.</p>
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<p>Entry space distribution.</p>
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<p>Courtyard spatial distribution.</p>
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<p>The Hotel of Flowers’ multi-perspective analysis.</p>
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<p>Pengcheng Gift Store’s multi-perspective analysis.</p>
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<p>Waku Teahouse’s multi-perspective analysis.</p>
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<p>The corridor’s spatial distribution.</p>
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<p>Hanfeng Cultural and Creative Store’s multi-perspective analysis.</p>
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<p>Banyunting Restaurant’s and Flower Stream Bookstore’s multi-perspective analyses.</p>
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<p>The platform’s spatial distribution.</p>
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<p>Platform entry space multi-perspective analysis.</p>
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<p>Distribution of node spaces.</p>
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<p>Node 1 multi-perspective analysis.</p>
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<p>Node 2 multi-perspective analysis.</p>
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<p>Nodes 3 and 5 multi-perspective analyses.</p>
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<p>Nodes 4 and 6 multi-perspective analyses.</p>
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<p>Node 7 multi-perspective analysis.</p>
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<p>Street segment spatial genes summary.</p>
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<p>Entry space genes summary.</p>
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<p>Node space genes summary.</p>
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<p>Spatial genetic system of streets and alleys.</p>
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22 pages, 6364 KiB  
Review
Review on the Application of Remote Sensing Data and Machine Learning to the Estimation of Anthropogenic Heat Emissions
by Lingyun Feng, Danyang Ma, Min Xie and Mengzhu Xi
Remote Sens. 2025, 17(2), 200; https://doi.org/10.3390/rs17020200 - 8 Jan 2025
Abstract
Anthropogenic heat is the heat generated by human activities such as industry, construction, transport, and metabolism. Accurate estimates of anthropogenic heat are essential for studying the impacts of human activities on the climate and atmospheric environment. Commonly applied methods for estimating anthropogenic heat [...] Read more.
Anthropogenic heat is the heat generated by human activities such as industry, construction, transport, and metabolism. Accurate estimates of anthropogenic heat are essential for studying the impacts of human activities on the climate and atmospheric environment. Commonly applied methods for estimating anthropogenic heat include the inventory method, the energy balance equation method, and the building model simulation method. In recent years, the rapid development of computer technology and the availability of massive data have made machine learning a powerful tool for estimating anthropogenic heat fluxes and assessing its effects. Multi-source remote sensing data have also been widely used to obtain more details of the spatial and temporal distribution characteristics of anthropogenic heat. This paper reviews the main approaches for estimating anthropogenic heat emissions. The typical algorithms of the abovementioned three methods are introduced, and their advantages and limitations are also evaluated. Moreover, the recent progress in the application of remote sensing data and machine learning are discussed as well. Based on big data and machine learning techniques, the research on feature engineering and model fusion will bring about major changes in data analysis and modeling of anthropogenic heat. More in-depth research of this issue is recommended to provide important support for curbing global warming, mitigating air pollution, and achieving the national goals of carbon peak and a carbon neutrality strategy. Full article
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<p>Time series graph of keywords and top articles of anthropogenic heat articles [<a href="#B4-remotesensing-17-00200" class="html-bibr">4</a>,<a href="#B6-remotesensing-17-00200" class="html-bibr">6</a>,<a href="#B9-remotesensing-17-00200" class="html-bibr">9</a>,<a href="#B10-remotesensing-17-00200" class="html-bibr">10</a>].</p>
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<p>Number of AH articles in the last decade (2010–2023).</p>
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<p>Flow chart of PRISMA for systematic review.</p>
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<p>Different methods and scales of AH estimation articles, 2010–2023. NCP refers to the North China Plain region. YRD refers to the Yangtze River Delta region. PRD refers to the Pearl River Delta region.</p>
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<p>The application of satellite remote sensing data in the inventory method.</p>
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<p>The process of building machine learning models.</p>
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<p>Flowchart of the article including regression factors and machine learning methods (Ao et al., 2024 [<a href="#B30-remotesensing-17-00200" class="html-bibr">30</a>]).</p>
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<p>Flowchart of the article, including regression factors and machine learning methods (Qian et al., 2024 [<a href="#B66-remotesensing-17-00200" class="html-bibr">66</a>]).</p>
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<p>Importance of the features for (<b>a</b>) building heat, (<b>b</b>) industrial heat, and (<b>c</b>) transportation heat (Qian et al., 2024 [<a href="#B66-remotesensing-17-00200" class="html-bibr">66</a>]).</p>
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12 pages, 212 KiB  
Article
Retrospective Analysis Comparing Lung-RADS v2022 and British Thoracic Society Guidelines for Differentiating Lung Metastases from Primary Lung Cancer
by Loredana Gabriela Stana, Alexandru Ovidiu Mederle, Claudiu Avram, Felix Bratosin and Paula Irina Barata
Biomedicines 2025, 13(1), 130; https://doi.org/10.3390/biomedicines13010130 (registering DOI) - 8 Jan 2025
Viewed by 92
Abstract
Background and Objectives: The current study aimed to compare the effectiveness of the Lung Imaging Reporting and Data System (Lung-RADS) Version 2022 and the British Thoracic Society (BTS) guidelines in differentiating lung metastases from de novo primary lung cancer on CT scans [...] Read more.
Background and Objectives: The current study aimed to compare the effectiveness of the Lung Imaging Reporting and Data System (Lung-RADS) Version 2022 and the British Thoracic Society (BTS) guidelines in differentiating lung metastases from de novo primary lung cancer on CT scans in patients without prior cancer diagnosis. Materials and Methods: This retrospective study included 196 patients who underwent chest CT scans between 2015 and 2022 without a known history of cancer but with detected pulmonary nodules. CT images characterized nodules based on size, number, location, margins, attenuation, and growth patterns. Nodules were classified according to Lung-RADS Version 2022 and BTS guidelines. Statistical analyses compared the sensitivity and specificity of Lung-RADS and BTS guidelines in distinguishing metastases from primary lung cancer. Subgroup analyses were conducted based on nodule characteristics. Results: Of the 196 patients, 148 (75.5%) had de novo primary lung cancer, and 48 (24.5%) had lung metastases from occult primary tumors. Lung-RADS Version 2022 demonstrated higher specificity than BTS guidelines (87.2% vs. 72.3%, p < 0.001) while maintaining similar sensitivity (91.7% vs. 93.8%, p = 0.68) in differentiating lung metastases from primary lung cancer. Lung metastases were more likely to present with multiple nodules (81.3% vs. 18.2%, p < 0.001), lower lobe distribution (58.3% vs. 28.4%, p < 0.001), and smooth margins (70.8% vs. 20.3%, p < 0.001), whereas primary lung cancers were associated with solitary nodules, upper lobe location, and spiculated margins. Conclusions: Lung-RADS Version 2022 provides higher specificity than the BTS guidelines in differentiating lung metastases from primary lung cancer on CT scans in patients without prior cancer diagnosis. Recognizing characteristic imaging features can improve diagnostic accuracy and guide appropriate management. Full article
(This article belongs to the Section Cancer Biology and Oncology)
13 pages, 1385 KiB  
Article
Emergence of Carbapenem-Resistant blaPOM-1 Harboring Pseudomonas otitidis Isolated from River Water in Ghana
by Frederick Ofosu Appiah, Samiratu Mahazu, Isaac Prah, Taira Kawamura, Yusuke Ota, Yohei Nishikawa, Mitsunori Yoshida, Masato Suzuki, Yoshihiko Hoshino, Toshihiko Suzuki, Tomoko Ishino, Anthony Ablordey and Ryoichi Saito
Antibiotics 2025, 14(1), 50; https://doi.org/10.3390/antibiotics14010050 - 8 Jan 2025
Viewed by 93
Abstract
Introduction: Pseudomonas otitidis, known for carrying the blaPOM-1 gene and linked to various diseases, is widely distributed. However, its prevalence in Ghana is unknown, mainly due to misidentification or inadequate research. In this study, for the first time, we characterized [...] Read more.
Introduction: Pseudomonas otitidis, known for carrying the blaPOM-1 gene and linked to various diseases, is widely distributed. However, its prevalence in Ghana is unknown, mainly due to misidentification or inadequate research. In this study, for the first time, we characterized P. otitidis from Densu river water in Ghana. Methods: The antimicrobial susceptibility and whole genome characteristics of two strains (Tg_9B and BC12) were determined. The resistance and virulence features were determined using ResFinder and the VFDB database, respectively. Maximum-likelihood phylogeny was conducted based on amino acid sequences of blaPOM-1 and P. otitidis core genomes. Results: The strains carried blaPOM-1 on the chromosome, with only Tg_9B showing intermediate resistance to meropenem. Tg_9B had a unique genetic make-up downstream of blaPOM-1, compared with BC12 and other reference strains. Both strains harbored virulence factors able to induce pathogenicity through immune evasion. The efflux pump genes (adeF, rsmA, and qacG) were present in the genomes of all the strains used in this study. The amino acid sequences of POM-1 in the strains shared a sequence homology with seven other sequences from different countries. Conclusions: This study highlights the emergence of blaPOM-1 harboring P. otitidis in Ghana and affirms the conservation of blaPOM-1 and adeF, rsmA, and qacG in the species. Full article
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<p>Graphical map of the sampling sites with a scale of 2 km. The red triangle denotes the location of Pakro Densu River, while the blue triangle indicates the position of Avaga Densu River.</p>
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<p>Maximum-likelihood phylogenetic tree of amino acid sequences (red highlights) isolated in this study (river water = 2), and 16 reference MBL amino acids sequences (10 POM subclass B3 MBL, 4 PAM-1 subclass B3 MBL, L1 subclass B3 MBL, and NDM-1 subclass B1 MBL) deposited to the NCBI from different sources and countries.</p>
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<p>Maximum-likelihood phylogenetic tree based on <span class="html-italic">P. otitidis</span> core genomes. The phylogeny of Tg_9B and BC12 with respect to the other <span class="html-italic">P. otitidis</span> strains is highlighted with red-colored branches. The occurrence of AMR genes in these genomes is also illustrated, as well as the genome data (accession number, country, source, and year of collection).</p>
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<p>Linearized comparison of the <span class="html-italic">bla</span><sub>POM-1</sub> genetic environment of our study strains (Tg_9B, BC12) and strains obtained from the NCBI database (MrB4 and TL17). Similar features are represented by the same color. Gray shading indicates regions of shared homology among different elements. The darker and lighter shadings represent 100% and 67% homology, respectively.</p>
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18 pages, 5042 KiB  
Article
The Influence of Different Land Uses on Tungstate Sorption in Soils of the Same Geographic Area
by Gianniantonio Petruzzelli and Francesca Pedron
Environments 2025, 12(1), 17; https://doi.org/10.3390/environments12010017 - 8 Jan 2025
Viewed by 76
Abstract
The growing use of tungsten (W) in industrial applications has made it a critical element in modern production processes. This increasing demand is also contributing to the element’s wider dispersion in the environment, including in soil. In addition to mining areas, it is [...] Read more.
The growing use of tungsten (W) in industrial applications has made it a critical element in modern production processes. This increasing demand is also contributing to the element’s wider dispersion in the environment, including in soil. In addition to mining areas, it is necessary to evaluate the possible environmental effects of tungsten even in non-contaminated areas. The mobility and bioavailability of W in soil are essentially determined by the sorption processes that regulate its distribution between the liquid and solid phases of the soil. In this study, the effect of different land uses—natural, agricultural, and urban—on the sorption of W in soils of the same geographical area was addressed. The results showed that the maximum sorption can be found in natural soils, with a value of 528 mg/kg, while for agricultural and urban soils, the mean values are 486 and 392 mg/kg, respectively. Anthropic interventions seem to reduce this capacity in agricultural soils by about 8%, probably due to agronomic practices, and by even more, 26%, in urban soils, where the use of different materials can modify the original characteristics of the soils. These results show that variations in some of the main characteristics of soils, such as pH and organic matter content, also derived from different land uses, influence the sorptive properties of the soils. Full article
(This article belongs to the Special Issue Environments: 10 Years of Science Together)
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<p>Map of the study area.</p>
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<p>Boxplots representing the distribution of pH values and organic matter content in the soils from different land uses, with central lines marking the median values. Values followed by different lowercase letters are significantly different at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Boxplots representing the distribution of clay, sand, and Fe content (%) in the soils from different land uses, with central lines marking the median values.</p>
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<p>Sorption isotherms for the different soil uses. Data refer to the soil samples with the highest qmax values for each land use: N, A, and U.</p>
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<p>Relationship between the soils’ pH and the sorption maxima of all the sampled soils.</p>
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<p>Relationship between the SOM content and sorption maxima of all the sampled soils.</p>
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<p>Relationship between the soils’ clay, sand, and total Fe content and the sorption maxima of all the sampled soils.</p>
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<p>Kd trends of N, A, and U soils versus equilibrium concentrations (C<sub>e</sub>).</p>
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21 pages, 3776 KiB  
Article
Spatial Distribution Characteristics of Micronutrients and Their Deficiency Effect on the Root Morphology and Architecture in Citrus Rootstock
by Gaofeng Zhou, Yiping Fu, Mei Yang, Yanhong Li and Jing Zhang
Plants 2025, 14(2), 158; https://doi.org/10.3390/plants14020158 - 8 Jan 2025
Viewed by 99
Abstract
Roots play essential roles in the acquisition of water and minerals from soils in higher plants. However, water or nutrient limitation can alter plant root morphology. To clarify the spatial distribution characteristics of essential nutrients in citrus roots and the influence mechanism of [...] Read more.
Roots play essential roles in the acquisition of water and minerals from soils in higher plants. However, water or nutrient limitation can alter plant root morphology. To clarify the spatial distribution characteristics of essential nutrients in citrus roots and the influence mechanism of micronutrient deficiency on citrus root morphology and architecture, especially the effects on lateral root (LR) growth and development, two commonly used citrus rootstocks, trifoliate orange (Poncirus trifoliata L. Raf., Ptr) and red tangerine (Citrus reticulata Blanco, Cre), were employed here. The analysis of the mineral nutrient distribution characteristics in different root parts showed that, except for the P concentrations in Ptr, the last two LR levels (second and third LRs) had the highest macronutrient concentrations. All micronutrient concentrations in the second and third LRs of Ptr were higher than those of Cre, except for the Zn concentration in the second LR, which indicates that Ptr requires more micronutrients to maintain normal root system growth and development. Principal component analysis (PCA) showed that B and P were very close in terms of spatial distribution and that Mo, Mn, Cu, and Fe contributed significantly to PC1, while B, Cu, Mo, and Zn contributed significantly to PC2 in both rootstocks. These results suggest that micronutrients are major factors in citrus root growth and development. The analysis of root morphology under micronutrient deficiency showed that root growth was more significantly inhibited in Ptr and Cre under Fe deficiency (FeD) than under other micronutrient deficiencies, while Cre roots exhibited better performance than Ptr roots. From the perspective of micronutrient deficiency, FeD and B deficiency (BD) inhibited all root morphological traits in Ptr and Cre except the average root diameter, while Mn deficiency (MnD) and Zn deficiency (ZnD) had lesser impacts, as well as the morphology of the stem. The mineral nutrient concentrations in Ptr and Cre seedlings under micronutrient deficiency revealed that single micronutrient deficiencies affected both their own concentrations and the concentrations of other mineral nutrients, whether in the roots or in stems and leaves. Dynamic analysis of LR development revealed that there were no significant decreases in either the first or second LR number in Ptr seedlings under BD and ZnD stress. Moreover, the growth rates of first and second LRs in Ptr and Cre did not significantly decrease compared with the control under short-term (10 days) BD stress. Altogether, these results indicate that micronutrients play essential roles in citrus root growth and development. Moreover, citrus alters its root morphology and biological traits as a nutrient acquisition strategy to maintain maximal micronutrient acquisition and growth. The present work on the spatial distribution characteristics and micronutrient deficiency of citrus roots provides a theoretical basis for effective micronutrient fertilization and the diagnosis of micronutrient deficiency in citrus. Full article
(This article belongs to the Special Issue Innovative Techniques for Citrus Cultivation)
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<p>Nutrient distribution in different root parts of trifoliate orange (Ptr) and red tangerine (Cre) seedlings. (<b>A</b>) P concentration; (<b>B</b>) K concentration; (<b>C</b>) Ca concentration; (<b>D</b>) Mg concentration; (<b>E</b>) Fe concentration; (<b>F</b>) Mn concentration; (<b>G</b>) B concentration; (<b>H</b>) Zn concentration; (<b>I</b>) Cu concentration; (<b>J</b>) Mo concentration. Data are presented as the mean ± SE of six biological replicates. Different lowercase and uppercase letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between the different root parts and the citrus rootstock species, respectively.</p>
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<p>Principal component analysis (<b>A</b>) and loading scatter plot (<b>B</b>) of 10 elements in different root parts of trifoliate orange and red tangerine seedlings. Green symbols in (<b>A</b>) represent red tangerine, and black symbols represent trifoliate orange; green symbols in (<b>B</b>) represent micronutrients, and red symbols represent macronutrients. The red circle in subfigure (<b>B</b>) indicated that the correlation between nutrient elements was significant.</p>
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<p>Scanned images of the root morphology of two types of citrus rootstocks under different micronutrient deficiency conditions. Ptr: trifoliate orange, Cre: red tangerine, CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency. Bar = 2 cm.</p>
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<p>Root system architecture response to micronutrient deficiency stress in trifoliate orange (Ptr) and red tangerine (Cre) seedlings. (<b>A</b>) Taproot length; (<b>B</b>) Total root length; (<b>C</b>) Root surface area; (<b>D</b>) Root volume; (<b>E</b>) Average root diameter. Data are presented as the mean ± SE of six biological replicates. Different lowercase letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between the different root parts and the citrus rootstock species, respectively. CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency.</p>
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<p>Effects of micronutrient deficiency on the distribution and ratio of root length and root surface area in trifoliate orange (Ptr, <b>A</b>,<b>C</b>) and red tangerine (Cre, <b>B</b>,<b>D</b>) seedlings. Data are presented as mean ± SE of six biological replicates. Different lowercase letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between the different root parts and the citrus rootstock species, respectively. Significance of analysis of variance (ANOVA): * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01. CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency.</p>
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<p>Effects of micronutrient deficiency on the distribution and ratio of root volume in trifoliate orange (Ptr) and red tangerine (Cre) seedlings. (<b>A</b>,<b>B</b>) Root volume distribution and their ratio of Ptr; (<b>C</b>,<b>D</b>) Root volume distribution and their ratio of Cre. Data are presented as mean ± SE of six biological replicates. Different lowercase letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between the different root parts and the citrus rootstock species, respectively. CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency.</p>
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<p>Effects of micronutrient deficiency on macronutrient concentrations (%) in the leaves and roots of trifoliate orange and red tangerine seedlings. P concentration in leaf (<b>A</b>) and root (<b>E</b>); K concentration in leaf (<b>B</b>) and root (<b>F</b>); Ca concentration in leaf (<b>C</b>) and root (<b>G</b>); Mg concentration in leaf (<b>D</b>) and root (<b>H</b>).Trifoliate orange (Ptr) and red tangerine (Cre) seedlings were grown under different micronutrient deficiency conditions for 12 weeks. Data are presented as means ± SE of nine replicates (n = 9, one plant for each replicate). Different lowercase letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between different growth conditions. CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency.</p>
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<p>Effects of micronutrient deficiency on the micronutrient concentrations (mg/kg DW) in the leaves and roots of trifoliate orange and red tangerine seedlings. Fe concentration in leaf (<b>A</b>) and root (<b>B</b>); Mn concentration in leaf (<b>C</b>) and root (<b>D</b>); B concentration in leaf (<b>E</b>) and root (<b>F</b>); Zn concentration in leaf (<b>G</b>) and root (<b>H</b>); Cu concentration in leaf (<b>I</b>) and root (<b>J</b>); Mo concentration in leaf (<b>K</b>) and root (<b>L</b>). Trifoliate orange (Ptr) and red tangerine (Cre) seedlings were grown under different micronutrient deficiency conditions for 12 weeks. Data are presented as means ± SE of nine replicates (n = 9, one plant for each replicate). Different lowercase letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between different growth conditions. CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency.</p>
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<p>Effects of micronutrient deficiency on the mineral nutrient concentrations in the stems of trifoliate orange and red tangerine seedlings. (<b>A</b>) P concentration; (<b>B</b>) K concentration; (<b>C</b>) Ca concentration; (<b>D</b>) Mg concentration; (<b>E</b>) Fe concentration; (<b>F</b>) Mn concentration; (<b>G</b>) B concentration; (<b>H</b>) Zn concentration; (<b>I</b>) Cu concentration; (<b>J</b>) Mo concentration. Trifoliate orange (Ptr) and red tangerine (Cre) seedlings were grown under different micronutrient deficiency conditions for 12 weeks. Data are presented as means ± SE of nine replicates (n = 9, one plant for each replicate). Different lowercase letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between different growth conditions. CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency.</p>
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<p>Dynamic analysis of the lateral root growth rates of trifoliate orange (Ptr) and red tangerine (Cre) seedlings under micronutrient deficiency conditions. (<b>A</b>) The primary lateral root growth rate of Ptr; (<b>B</b>) The secondary lateral root growth rate of Ptr; (<b>C</b>) The primary lateral root growth rate of Cre; (<b>D</b>) The secondary lateral root growth rate of Cre. Trifoliate orange and red tangerine seedlings were grown under different micronutrient deficiency conditions for 40 days. CK: control, FeD: iron deficiency, MnD: manganese deficiency, BD: boron deficiency, and ZnD: zinc deficiency. All results regarding the per-plant root growth rate data are the average value (±SD) from nine seedlings.</p>
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Article
Temporal–Spatial Dynamics and Collaborative Effects of Cropland Resilience in China
by Liang Luo, Yetong Li, Wenjie Ma, Jianbo Rong, Jie Wei, Yong Cui and Tingting Qu
Land 2025, 14(1), 108; https://doi.org/10.3390/land14010108 - 8 Jan 2025
Viewed by 202
Abstract
Cropland resilience is the ability of cropland systems to adapt and rebound from multiple stresses and disturbances. Cropland resilience is vital for ensuring national food security, promoting sustainable agricultural development, and adapting to global climate change. This study measures cropland resilience in China [...] Read more.
Cropland resilience is the ability of cropland systems to adapt and rebound from multiple stresses and disturbances. Cropland resilience is vital for ensuring national food security, promoting sustainable agricultural development, and adapting to global climate change. This study measures cropland resilience in China using the entropy method within the PSR framework. Additionally, it employs quantitative analysis methods, including kernel density estimation, the standard deviation ellipse, the Theil Index, and the geographical detector, to systematically examine the spatiotemporal dynamics of cropland resilience and its driving factors in China. The findings reveal the evolving trends of cropland resilience over time and space, highlighting regional differences and the spatial distribution of resilience. The study found the following: (1) The overall cropland resilience in China shows an upward trend, but there is uneven development among regions, particularly in the relatively lagging western areas. (2) There is a notable spatial imbalance in cropland resilience, primarily driven by intra-regional differences. (3) Stability of Grain Production; Total Grain Production; Fiscal Expenditure on Agriculture, Forestry, and Water; Soil–Water Harmony; and the Cropland Disaster Resistance Index are identified as key driving factors, with the influence of the Cropland Disaster Resistance Index notably increasing over time. (4) The study highlights the critical role of synergistic effects among these factors in enhancing cropland resilience, noting a significant strengthening of these synergies over time. The research results offer a fresh perspective on the role of cropland resilience in dynamic environments. They enhance our understanding of the spatiotemporal characteristics of cropland resilience, reveal its underlying dynamic processes, and provide a scientific basis for policymaking aimed at promoting the sustainable use and management of cropland. Full article
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<p>The PSR framework for cropland resilience.</p>
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<p>Legend of the zoning map.</p>
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<p>Results of the resilience measurement of cultivated land in China’s three major regions from 2013 to 2022.</p>
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<p>Illustration of the spatiotemporal measurement levels of China’s cropland resilience: (<b>a</b>) 2013; (<b>b</b>) 2016; (<b>c</b>) 2019; (<b>d</b>) 2022.</p>
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<p>Three-dimensional kernel density dynamic evolution map of the whole country and the eastern, central, and western regions.</p>
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<p>Comparison of the standard deviation ellipses for the development levels of resilience of cultivated land in 2013, 2016, 2019, and 2022.</p>
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<p>Comparison of factor changes from 2013 to 2017 and from 2018 to 2022.</p>
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<p>Results of the interaction of impact factors for 2013–2017 and 2018–2022.</p>
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