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22 pages, 5210 KiB  
Article
Revealing the Complexity of Host-Parasite Relationships Between Syringophilid Mites and Sunbirds in Their Global Range
by Bozena Sikora, Markus Unsoeld, Roland R. Melzer, Stefan Friedrich and Martin Hromada
Animals 2025, 15(1), 110; https://doi.org/10.3390/ani15010110 - 6 Jan 2025
Viewed by 532
Abstract
This article emphasises the importance of parasitological research in understanding ecological dynamics and biodiversity conservation through a global analysis of quill mites (Syringophilidae) parasitising Sunbirds (Nectariniidae). Data from 764 Sunbird individuals across seventy-six species revealed twelve quill mite species, including three newly described [...] Read more.
This article emphasises the importance of parasitological research in understanding ecological dynamics and biodiversity conservation through a global analysis of quill mites (Syringophilidae) parasitising Sunbirds (Nectariniidae). Data from 764 Sunbird individuals across seventy-six species revealed twelve quill mite species, including three newly described species: Aulonastus aethopygus Sikora and Unsoeld sp. n., Syringophiloidus haeckeli Sikora and Unsoeld sp. n., and Aulonastus arachnotherus Sikora and Unsoeld sp. n. A bipartite network analysis indicated a low connectance of 0.10, suggesting that only 10% of potential bird–parasite connections are realised. This high specialisation is further supported by an H2′ index of 0.94 and a C score of 0.83, indicating low co-occurrence among mite species. The temperature of nestedness at 13.49 suggests a well-organised network structure. Additionally, normalised specialisation (d’) ranged from 0.60 to 1, reflecting unique host–parasite interactions. High modularity (likelihood = 0.80) with nine modules was identified, with hosts ranging from one to seven. The study concludes by discussing the host–parasite dynamics and their ecological implications within this system. Full article
(This article belongs to the Section Birds)
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Figure 1
<p>Examples of bird species deposited in SNSB-ZSM and infested by quill mites. (<b>A</b>) <span class="html-italic">Anthreptes longuemarei</span> (Lesson); (<b>B</b>) <span class="html-italic">Cinnyris mariquensis</span> Smith; (<b>C</b>) <span class="html-italic">Cinnyris shelleyi</span> Alexander; (<b>D</b>) <span class="html-italic">Nectarinia tacazze</span> (Stanley); (<b>E</b>) <span class="html-italic">Aethopyga siparaja</span> (Raffles); (<b>F</b>) <span class="html-italic">Leptocoma zeylonica</span> (Linnaeus); (<b>G</b>) <span class="html-italic">Cinnyris mediocris</span> Shelley; (<b>H</b>) <span class="html-italic">Hedydipna collaris</span> (Vieillot); (<b>I</b>) <span class="html-italic">Cyanomitra olivacea</span> (Smith); (<b>J</b>) <span class="html-italic">Cinnyris venustus</span> (Shaw).</p>
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<p><span class="html-italic">Aulonastus aethopygus</span> Sikora and Unsoeld sp. n., female. (<b>A</b>)—dorsal view; (<b>B</b>)—ventral view; (<b>C</b>)—peritremes; (<b>D</b>)—fan-like seta <span class="html-italic">p’III</span>. Scale bars: (<b>A</b>,<b>B</b>) = 50 µm, (<b>C</b>,<b>D</b>) = 25 µm.</p>
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<p><span class="html-italic">Aulonastus arachnotherus</span> Sikora and Unsoeld sp. n., female. (<b>A</b>)—dorsal view; (<b>B</b>)—ventral view; (<b>C</b>)—peritremes; (<b>D</b>)—fan-like seta <span class="html-italic">p’III</span>. Scale bars: (<b>A</b>,<b>B</b>) = 50 µm, (<b>C</b>,<b>D</b>) = 25 µm.</p>
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<p><span class="html-italic">Syringophiloidus haeckeli</span> Sikora and Unsoeld sp. n., female. (<b>A</b>)—dorsal view; (<b>B</b>)—ventral view; (<b>C</b>)—peritremes; (<b>D</b>)—propodonotal seta <span class="html-italic">si</span>; (<b>E</b>)—solenidia of leg I; (<b>F</b>)—fan-like seta <span class="html-italic">p’III</span>; (<b>G</b>)—pseudanal setae <span class="html-italic">ps1–2</span>. Scale bars: (<b>A</b>,<b>B</b>) = 50 µm, (<b>C</b>–<b>G</b>) = 25 µm.</p>
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<p>Bipartite network graph of interactions between quill mite species (<b>left</b>) and their Sunbird hosts (<b>right</b>).</p>
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<p>Modules (1–8), generated for quill mite species and Sunbirds. The intensity of the colours of the squares indicates the strength of the interaction between particular parasite species (vertical axis) and their host species (horizontal axis).</p>
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<p>Potential distribution of quill mites of the genus <span class="html-italic">Aulobia</span> according to the host range.</p>
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<p>Potential distribution of quill mites of the genus <span class="html-italic">Syringophiloidus</span> according to the host range.</p>
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<p>Potential distribution of quill mites of the genus <span class="html-italic">Aulonastus</span> according to the host range.</p>
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<p>Potential distribution of quill mites of the genus <span class="html-italic">Neoaulonastus</span> according to the host range.</p>
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<p>Potential distribution of quill mites of the genus <span class="html-italic">Picobia</span> according to the host range.</p>
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15 pages, 5247 KiB  
Article
The Effects of Disturbance on Plant–Pollinator Interactions in the Native Forests of an Oceanic Island (Terceira, Azores)
by Mário Boieiro, Mariana Ferreira, Ana Ceia-Hasse, Fabiana Esposito, Renata Santos, Gabor Pozsgai, Paulo A. V. Borges and Carla Rego
Insects 2025, 16(1), 14; https://doi.org/10.3390/insects16010014 - 27 Dec 2024
Viewed by 1052
Abstract
The native biodiversity of oceanic islands is threatened by human-driven disturbance and by the growing number of species introductions which often interfere with natural ecological processes. Here, we aim to evaluate the effect of anthropogenic disturbance on plant–pollinator interactions in the native forest [...] Read more.
The native biodiversity of oceanic islands is threatened by human-driven disturbance and by the growing number of species introductions which often interfere with natural ecological processes. Here, we aim to evaluate the effect of anthropogenic disturbance on plant–pollinator interactions in the native forest communities of an oceanic island (Terceira, Azores, Portugal). We found that native species predominated in preserved sites compared to disturbed ones and that the extant plant–pollinator interactions were mostly dominated by generalist species. Dipterans, particularly hoverflies, emerged as the primary flower visitors, while introduced hymenopterans (Apis mellifera and Bombus terrestris) and native beetles were locally important, respectively, in disturbed and preserved sites. Human-driven disturbance seems to be responsible for the observed differences in flower abundance and species composition between sites and to drive changes in specific network metrics (namely nestedness, interaction strength asymmetry, and specialization), particularly in one of the study areas. Our findings also suggest that native generalist species provide ecological opportunities that can facilitate the establishment of introduced species through their broad interaction networks. Full article
(This article belongs to the Special Issue Current Advances in Pollinator Insects)
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<p>The native hoverflies <span class="html-italic">Episyrphus balteatus</span> (<b>a</b>), <span class="html-italic">Eristalis tenax</span> (<b>b</b>), and <span class="html-italic">Xanthandrus azorensis</span> (endemic to the Azores) (<b>c</b>) were found in all study sites, while the introduced honeybee <span class="html-italic">Apis mellifera</span> (<b>d</b>) was restricted to the disturbed ones.</p>
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<p>Percentage of visits made by the most important insect species (with &gt;5% of visits) in the study sites at Lomba (<b>A</b>) and Pico Galhardo (<b>B</b>). The distribution status of each insect species (endemic in light green, native non-endemic in green, and introduced in black) is shown jointly with insect visitor species names.</p>
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<p>Visitation networks from the preserved (<b>A</b>) and the disturbed (<b>B</b>) sites at Lomba. Selected plant and pollinator species names are listed at the bottom and at the top, respectively. Pollinators are categorized as native (green) or introduced (orange). Insect visitation to each plant species is proportional to the area of the interaction that connects them.</p>
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15 pages, 2567 KiB  
Article
Wild Bee Diversity and Bee–Plant Interactions in Tropical and Temperate Forest Clearings in a Natural Protected Area in Central West Mexico
by Alvaro Edwin Razo-León, Alejandro Muñoz-Urias, Claudia Aurora Uribe-Mú, Francisco Martín Huerta-Martínez, Hugo Eduardo Fierros-López, Miguel Vásquez-Bolaños, Gustavo Moya-Raygoza and Pablo Carrillo-Reyes
Insects 2024, 15(12), 1009; https://doi.org/10.3390/insects15121009 - 20 Dec 2024
Viewed by 953
Abstract
Background: Bees rely on plants for nutrition and reproduction, making the preservation of natural areas crucial as pollinator reservoirs. Seasonal tropical dry forests are among the richest habitats for bees, but only 27% of their original extent remains in Mexico. In contrast, temperate [...] Read more.
Background: Bees rely on plants for nutrition and reproduction, making the preservation of natural areas crucial as pollinator reservoirs. Seasonal tropical dry forests are among the richest habitats for bees, but only 27% of their original extent remains in Mexico. In contrast, temperate forests harbor fewer bee species and face high deforestation rates, with 40% of their area converted to other land uses. This study aimed to estimate the α and β diversities of wild bees and compare bee–plant interaction networks between these two vegetation types. Methods: Wild bees and their interactions with plants were monitored for one year in four sites within the Área de Protección de Flora y Fauna Sierra de Quila. Two sites corresponded to seasonal tropical dry forest and two to temperate forest. α and β diversity, connectance, nestedness, web asymmetry, and niche overlap were analyzed. Results: Sierra de Quila harbors high bee diversity, with 155 species in tropical dry forest and 103 in temperate forest. Species turnover between vegetation types was high, although nine species used floral resources in both forests, connecting the interaction networks. Conclusions: Sierra de Quila diverse habitats promote high bee diversity, with niche partitioning and low connectance facilitating coexistence across different vegetation types. Full article
(This article belongs to the Section Social Insects)
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Graphical abstract

Graphical abstract
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<p>Location of the APFFSQ (Sierra de Quila Flora and Fauna Protection Area) and sampling sites (SDTF—seasonally dry tropical forest, TF—temperate forest).</p>
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<p>Coverage—based rarefaction (solid line) and extrapolation (dashed line) plots with 95% confidence intervals (shaded areas) comparing (richness, q<sub>0</sub>), common species (q<sub>1</sub>), and dominant species (q<sub>2</sub>) on community bees between vegetation types (SDTF—seasonally dry tropical forest, TF—temperate forest).</p>
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<p>Bee plant interactions network (<b>a</b>) in SDTF1 and (<b>b</b>) SDTF2 of Sierra de Quila. Blue lines correspond to Apidae family, red lines to Megachilidae family, yellow lines to Halictidae, green lines to Colletidae, and orange lines to Andrenidae. (SDTF—seasonally dry tropical forest).</p>
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<p>Bee–plant interactions network (<b>a</b>) in TF<sub>1</sub> and (<b>b</b>) TF<sub>2</sub> of Sierra de Quila. Blue lines correspond to Apidae family, red lines to Megachilidae family, yellow lines to Halictidae, green lines to Colletidae, and orange lines to Andrenidae (TF—temperate forest).</p>
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15 pages, 2645 KiB  
Article
Drivers of Seasonal Change of Avian Communities in Urban Parks and Cemeteries of Latin America
by Lucas M. Leveau, Lucia Bocelli, Sergio Gabriel Quesada-Acuña, César González-Lagos, Pablo Gutierrez Tapia, Gabriela Franzoi Dri, Carlos A. Delgado-V, Alvaro Garitano-Zavala, Jackeline Campos, Yanina Benedetti, Rubén Ortega-Álvarez, Anotnio Isain Contreras-Rodríguez, Daniela Souza López, Carla Suertegaray Fontana, Thaiane Weinert da Silva, Sarah S. Zalewski Vargas, Maria C. B. Toledo, Juan Andres Sarquis, Alejandro Giraudo, Ada Lilian Echevarria, María Elisa Fanjul, María Valeria Martínez, Josefina Haedo, Luis Gonzalo Cano Sanz, Yuri A. Peña Dominguez, Viviana Fernandez-Maldonado, Veronica Marinero, Vinícius Abilhoa, Rafael Amorin, Juan Fernando Escobar-Ibáñez, María Dolores Juri, Sergio R. Camín, Luis Marone, Augusto João Piratelli, Alexandre G. Franchin, Larissa Crispim and Federico Morelliadd Show full author list remove Hide full author list
Animals 2024, 14(24), 3564; https://doi.org/10.3390/ani14243564 - 10 Dec 2024
Viewed by 1390
Abstract
Urban parks and cemeteries constitute hot spots of bird diversity in urban areas. However, the seasonal dynamics of their bird communities have been scarcely explored at large scales. This study aims to analyze the drivers of urban bird assemblage seasonality in urban parks [...] Read more.
Urban parks and cemeteries constitute hot spots of bird diversity in urban areas. However, the seasonal dynamics of their bird communities have been scarcely explored at large scales. This study aims to analyze the drivers of urban bird assemblage seasonality in urban parks and cemeteries comparing assemblages during breeding and non-breeding seasons in the Neotropical Region. Since cemeteries have less human disturbance than urban parks, we expected differences in bird community seasonality between habitats. The seasonal change of species composition was partitioned into species turnover and nestedness. At large scales, the seasonal change of species composition was positively related to temperature seasonality and was higher in the Northern Hemisphere. At the landscape scale, the seasonal change of composition decreased in sites located in the most urbanized areas. At the local scale, sites with the highest habitat diversity and pedestrian traffic had the lowest seasonal change of composition. The species turnover was higher in the Northern Hemisphere, augmented with increasing annual temperature range, and decreased in urban parks. The species nestedness was positively related to habitat diversity. Our results showed that a multi-scale framework is essential to understand the seasonal changes of bird communities. Moreover, the two components of seasonal composition dissimilarity showed contrasting responses to environmental variables. Although the surrounding urbanization lowered the seasonal dynamics of urban green areas, cemeteries seem to conserve more seasonal changes than urban parks. Thus, urban cemeteries help to conserve the temporal dynamics of bird communities in cities. Full article
(This article belongs to the Section Birds)
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<p>Schematic representation of (<b>a</b>) balanced variation in abundance, (<b>b</b>) abundance gradient, and (<b>c</b>) the presence of balanced variation and abundance gradient. In (<b>a</b>), some species lose individuals between seasons, whereas others gain individuals in the same proportion. In (<b>b</b>), all species lose individuals in the same proportion between breeding and non-breeding seasons. In (<b>c</b>), two species gain individuals whereas the other species lose individuals. Other hypothetical situations where species appear or disappear between seasons are also possible (see [<a href="#B36-animals-14-03564" class="html-bibr">36</a>]).</p>
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<p>Location of study sites (black dots) in Latin America.</p>
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<p>Relationship between environmental variables (<b>a</b>–<b>e</b>) and the seasonal change of bird composition (Bray–Curtis dissimilarity index) in urban parks and cemeteries of Neotropical cities. Blue lines are fitted models and grey bands are 95% confidence intervals. TRANGE: annual range of temperature (°C); Pedestrian: people/10 min; Habitat diversity: Shannon index (H′).</p>
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<p>Relationship between environmental variables and (<b>a</b>–<b>c</b>) the seasonally balanced variation dissimilarity, and (<b>d</b>) the abundance gradient dissimilarity in urban parks and cemeteries of Neotropical cities. Blue lines are fitted models and grey bands are 95% confidence intervals. TRANGE: annual range of temperature (°C). Habitat diversity: Shannon index (H′).</p>
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<p>Relationship between environmental variables (<b>a</b>–<b>c</b>) and the seasonal Sørensen abundance-based dissimilarity in urban parks and cemeteries of Neotropical cities. The Sørensen index considers unseen species between seasons. Blue lines are fitted models and grey bands are 95% confidence intervals. TRANGE: annual range of temperature (°C).</p>
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<p>Summary of the results found in our study. A multiscale framework shows the different drivers of bird assemblage seasonality in the Neotropics. The orange triangles represent the amount of seasonal change of species composition. At the large scale, the blue dashed line indicates the Equator. The seasonal change of bird composition increases with increasing annual range of temperature, which is positively related to latitude (r = 0.91, <span class="html-italic">p</span> &lt; 0.05). Moreover, the seasonal change in bird composition also increases in the Northern Hemisphere part of the Neotropics. At the landscape scale, the seasonal change is negatively related to urbanization (scales from grey to green), whereas at the local scale is negatively related to habitat diversity (yellow triangle).</p>
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18 pages, 3265 KiB  
Article
Long-Term Changes in Bird Communities in the Urban Parks of Mar del Plata City, Argentina
by Lourdes Galiano, Carlos M. Leveau and Lucas M. Leveau
Birds 2024, 5(4), 814-831; https://doi.org/10.3390/birds5040054 - 10 Dec 2024
Viewed by 911
Abstract
Urbanization is related to the loss of biodiversity and alteration of ecosystem processes. However, long-term changes in the southern hemisphere’s bird communities have been scarcely analyzed in urban areas. The general objective of this work was to analyze changes in bird species richness, [...] Read more.
Urbanization is related to the loss of biodiversity and alteration of ecosystem processes. However, long-term changes in the southern hemisphere’s bird communities have been scarcely analyzed in urban areas. The general objective of this work was to analyze changes in bird species richness, diversity, and composition in parks located in the urban and suburban landscapes of Mar del Plata City (Argentina) between 2003 and 2018. Additionally, we aimed to analyze whether these changes were associated with an increase in urbanization or with alterations in the parks’ habitat structure. Tree cover showed significantly lower coverage during 2018. The results showed increased species richness and diversity in all parks by 2018. Rarefaction curves showed that the park bird richness did not differ between the landscapes surrounding parks, but the Shannon and Simpson diversities were higher in parks in suburban landscapes than in parks in urban landscapes. The Shannon and Simpson diversities showed higher values in suburban parks during 2018. However, the diversity values were similar between years in parks in urban landscapes. The species composition was significantly different between landscapes and years. Species turnover was the most predominant pattern of species dissimilarity between landscapes, and species nestedness explained the most dissimilarity between years. Nestedness between years was related to the population increase in many bird species in 2018. In conclusion, we observed differences in the park bird communities between years and landscape types. However, the long-term community changes were not associated with an urbanization increase. Instead, the changes in the local bird community were more related to regional bird species population changes associated with climate warming and increased crop cover. Full article
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<p><b>Left</b>: Location of Mar del Plata City in Argentina. <b>Right</b>: Mar del Plata City and sampled parks.</p>
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<p>Landscape composition using ImageJ software (Version 1.54k), measuring the urban level within a 500 m radius of Urquiza Park in 2003.</p>
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<p>Box plots showing the percentage of tree, bush, grass, and concrete cover observed in urban and suburban parks in Mar del Plata in 2003 and 2018. The boxes represent the interquartile range (first, second, and third quartile). The horizontal lines in the middle of the box represent the median. The vertical lines represent the maximum and minimum coverage values. Points indicate outliers.</p>
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<p>Species richness, Shannon diversity, and Simpson diversity between years. The dots correspond to the average values per park, whereas the vertical lines are the 95% confidence intervals.</p>
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<p>Rarefaction curves of Hill numbers (species richness, q = 0; Shannon diversity, q = 1; and Simpson diversity, q = 2) with sample coverage for urban (urb) and suburban (sub) parks in 2003 and 2018 in Mar del Plata City, Argentina. The shaded bands represent the 84% confidence intervals.</p>
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<p>Nonmetric multidimensional scaling (NMDS) based on dissimilarity calculated with the Bray–Curtis index between urban and suburban parks in 2003 and 2018 in Mar del Plata City, Argentina. Sites marked with triangles correspond to urban parks, and those marked with circles correspond to suburban parks. The violet color represents parks in 2003, and the green color represents parks in 2018. Ellipses represent 95% confidence intervals between landscapes types and years. See <a href="#birds-05-00054-t001" class="html-table">Table 1</a> for species names.</p>
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18 pages, 3607 KiB  
Article
Rainfall and Soil Moisture Jointly Drive Differences in Plant Community Composition in Desert Riparian Forests of Northwest China
by Hengfang Wang, Zhengxian Mo, Wenjing Li, Hao Huang and Guanghui Lv
Forests 2024, 15(12), 2129; https://doi.org/10.3390/f15122129 - 1 Dec 2024
Viewed by 893
Abstract
Extreme rainfall and soil moisture play important roles in the survival, community composition, and ecosystem function of desert plants. This study focused on arid desert riparian forests ecosystems in the Ebinur Lake Basin of Xinjiang, China. We analyzed the effects of rainfall and [...] Read more.
Extreme rainfall and soil moisture play important roles in the survival, community composition, and ecosystem function of desert plants. This study focused on arid desert riparian forests ecosystems in the Ebinur Lake Basin of Xinjiang, China. We analyzed the effects of rainfall and soil moisture on species composition, indicator species, β diversity, species turnover, and nestedness using three consecutive years of community surveys. A zero-model combined with a Bayesian framework was used to explore the response of species turnover and nestedness to soil moisture and rainfall, and variance decomposition was used to quantify the relative importance of spatial distance, rainfall, and soil factors in determining species composition. The results indicated the following: (1) when rainfall was high, the richness and abundance of annual herbaceous plants increased. The proportion of the community based on richness (32%) and abundance (58.1%) of annual herbaceous plants in 2016 was higher than that in 2015 and 2017. The Jaccard, Bray–Curtis, and Chao indexes of the community in years with higher rainfall were significantly higher than in years with lower rainfall; however, a lag effect was also observed. (2) Soil factors explained 5% of the changes in community composition, rainfall explained 12% of the changes in community composition, and spatial distance, soil factors, and rainfall jointly explained 32% of the changes in community composition. (3) We also showed that high soil moisture leads to greater β diversity than low soil moisture. Rainfall had the greatest explanatory power on the measured values of β diversity (19.6%) and species turnover (38%), and the factor with the greatest explanatory power for species nestedness was the interaction between rainfall and soil moisture (26.2%). Our findings indicate that drought and rainfall drive differences in plant community composition, with rainfall playing a dominant role. These results provide a basis for understanding the impact of extreme rainfall events on arid ecosystem functions. Full article
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<p>Sketch map of the study area.</p>
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<p>Proportions of different life forms in different years. (<b>a</b>) Change of growth forms (Presence–Absence); (<b>b</b>) Change of growth forms (Abundance based).</p>
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<p>Indicator species from 2015 to 2017. Note: BC: <span class="html-italic">Nitraria sibirica</span>; DJC: <span class="html-italic">Horaninovia ulicina</span>; LBM: <span class="html-italic">Apocynum venetum</span>; LHYZZ: <span class="html-italic">Kalidium caspicum</span>; PPC: <span class="html-italic">Reaumuria songonica</span>; RJ: <span class="html-italic">Mulgedium tataricum</span>; SGZ: <span class="html-italic">Calligonum mongolicum</span>; SS: <span class="html-italic">Haloxylon ammodendron</span>; YDJP: <span class="html-italic">Suaeda salsa</span>; YSC: <span class="html-italic">Halogeton glomeratus</span>; YZZ: <span class="html-italic">Kalidium foliatum</span>; ZMC: <span class="html-italic">Kali collinum</span>.</p>
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<p>Non-metric multidimensional scale (NMDS) analysis of community’s β diversity from 2015 to 2017. NMDS analysis based on Jaccard differences (<b>a</b>); Horn differences (<b>b</b>); Morisita–Horn differences (<b>c</b>) Bray–Curtis differences (<b>d</b>); and Chao differences (<b>e</b>). Ellipse shows the 60% confidence interval of each year group.</p>
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<p>Dissimilarity analysis of community composition in different years and between years.</p>
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<p>The dissimilarity of β diversity of communities in different years. 2015–2017 average distance of the Jaccard similarity index (<b>a</b>); Horn similarity index (<b>b</b>); Morisita–Horn similarity index (<b>c</b>); Bray–Curtis similarity index (<b>d</b>); and Chao similarity index (<b>e</b>).</p>
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<p>Interpretation of environmental distance and spatial distance on community composition. (1) Soil factors include soil moisture and soil salinity. (2) Spatial factors represent the latitude and longitude of the sample. All are adjusted R<sup>2</sup>.</p>
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<p>The observed values of β diversity and its decomposition vary with time. (<b>a</b>,<b>c</b>,<b>e</b>) show the measured values of β diversity, species turnover, and species nestedness, respectively. (<b>b</b>,<b>d</b>,<b>f</b>) show the interpretation of the measured values of β diversity, species turnover, and nestedness, respectively. The circles represent the median of the model estimate, the error bar represents a 95% confidence interval. H: high water community; L: low water community.</p>
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15 pages, 3540 KiB  
Article
Exploring the Drivers Influencing Multidimensional Alpha and Beta Diversity of Macroinvertebrates in Mountain Streams
by Shudan Li, Xingzhong Wang, Lu Tan and Qinghua Cai
Water 2024, 16(20), 2915; https://doi.org/10.3390/w16202915 - 14 Oct 2024
Viewed by 2997
Abstract
Understanding the driving mechanisms of diversity across multiple dimensions is a fundamental task in biodiversity conservation. Here, we examined the alpha and beta diversity of macroinvertebrates in the taxonomic, functional, and phylogenetic dimensions in mountain streams of northwestern Hubei Province, China. We also [...] Read more.
Understanding the driving mechanisms of diversity across multiple dimensions is a fundamental task in biodiversity conservation. Here, we examined the alpha and beta diversity of macroinvertebrates in the taxonomic, functional, and phylogenetic dimensions in mountain streams of northwestern Hubei Province, China. We also assessed how much local environmental, land use, climatic, and spatial variables affected these diversities. We found that (1) there were generally weak or no correlations of alpha and beta diversity between taxonomic, functional, and phylogenetic dimensions; (2) compared to both functional and phylogenetic beta diversity, which was mainly determined by nestedness, taxonomic beta diversity was mostly molded by turnover and was much higher; and (3) local environmental variables predominantly influenced taxonomic and functional dimensions of alpha and beta diversity, while spatial factors primarily drove phylogenetic dimension. These results suggest that regulating local habitats is crucial for lotic biodiversity conservation efforts, though spatial processes cannot be overlooked. Furthermore, our findings verify the supplemental role of functional and phylogenetic data in enriching insights provided by taxonomic data alone. This underscores the importance of a multidimensional approach for a more nuanced understanding of community assembly mechanisms, which is crucial for efficient ecosystem management and biodiversity conservation. Full article
(This article belongs to the Section Biodiversity and Functionality of Aquatic Ecosystems)
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<p>Location of the mountain streams and sampling sites in northwestern Hubei Province (China). SNNR denotes Shennongjia National Nature Reserve.</p>
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<p>Correlations of alpha diversity between multiple dimensions —taxonomic, functional, and phylogenetic—based on Pearson correlation analysis. The Pearson correlation coefficients (r) and <span class="html-italic">p</span>-values are shown.</p>
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<p>Pure and joint effects of local environmental, land use, climate, and spatial factors on alpha diversity: (<b>a</b>) taxonomic richness, (<b>b</b>) functional alpha diversity, and (<b>c</b>) phylogenetic alpha diversity. Negative effects are omitted. The adjusted R<sup>2</sup> values are provided. ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05. Residuals denote unexplained variations of diversity.</p>
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<p>Decomposition of total beta diversity for the taxonomic, functional, and phylogenetic dimensions in mountain streams of northwestern Hubei Province.</p>
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<p>Correlations of beta diversity (including total beta diversity, turnover, and nestedness) between multiple dimensions—taxonomic, functional, and phylogenetic—based on Mantel tests. The Pearson correlation coefficients (r) and <span class="html-italic">p</span>-values are shown.</p>
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<p>Pure and joint effects of local environmental, land use, climatic, and spatial factors on beta diversity: (<b>a</b>) total taxonomic beta diversity, (<b>b</b>) taxonomic turnover, (<b>c</b>) taxonomic nestedness, (<b>d</b>) total functional beta diversity, (<b>e</b>) functional turnover, (<b>f</b>) functional nestedness, (<b>g</b>) phylogenetic turnover, and (<b>h</b>) phylogenetic nestedness. Negative effects are omitted. The adjusted R<sup>2</sup> values are provided. *** <span class="html-italic">p</span> &lt; 0.001, ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05. Residuals denote unexplained variations of diversity.</p>
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14 pages, 4000 KiB  
Article
Scale-Dependent Habitat Nestedness and Its Implications for Anuran Conservation in the Chengdu Region: A Multi-Extent Analysis
by Xiaoqin Shi, Xiaoke Liu and Youhua Chen
Animals 2024, 14(20), 2931; https://doi.org/10.3390/ani14202931 - 11 Oct 2024
Viewed by 718
Abstract
Nestedness in community ecology predicts that species in a species-poor site should be a subset of species of a species-rich site. A variety of ecological mechanisms have been offered to explain community nestedness; however, few studies have systematically discussed the issue of scale [...] Read more.
Nestedness in community ecology predicts that species in a species-poor site should be a subset of species of a species-rich site. A variety of ecological mechanisms have been offered to explain community nestedness; however, few studies have systematically discussed the issue of scale dependence when interpreting community nestedness. This study conducted surveys of anuran species data in the vicinity of Chengdu, Sichuan, in the summers of 2019–2020, using the transect method. The study area was divided into 23 sampling sites and 8 regions to explore the relationship between environmental factors and the nested distribution pattern of anuran communities under different sampling extents (with sampling buffers set at 1 km, 2 km, and 5 km). The WNODF (weighted-nestedness metric based on overlap and decreasing fill) results indicated that anurans exhibited a strong nested pattern at both the sampling sites scale and the regional scale. The habitat matrix test results suggested that a small-scale study area requires a correspondingly small habitat-sampling extent to effectively test for habitat nestedness. As the study area expands, the habitat-sampling range can be appropriately increased. The nested pattern of anurans in the vicinity of Chengdu can only be explained by habitat nestedness, as a Spearman’s correlation analysis showed that other environmental factors (area size, connectivity index, concentration index, proximity index, and distance to the city center) were not significantly correlated with the nested sequences of sampling points and regions. Therefore, regarding the conservation strategies for anurans in the vicinity of Chengdu, we recommend prioritizing the protection of areas with higher habitat diversity. Full article
(This article belongs to the Topic Land-Use Change, Rural Practices and Animal Diversity)
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<p>Transect line sampling locations in Sichuan, China (<b>left</b>), and eight regions divided (<b>right</b>).</p>
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<p>A schematic diagram for evaluating the influence of scale dependence on community structure. In our study, two scale-changing properties were evaluated: varying the study area extent (transect-site-region) and varying the sampling range (1 km, 2 km, and 5 km). Line transects are marked as red polylines.</p>
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<p>The relationships between species richness and relative area size predicted by the random placement model at sample-site (see subfigures (<b>a</b>–<b>c</b>)) and regional spatial scales (see subfigures (<b>d</b>–<b>f</b>)). Expected values and the 95% confidence interval (dashed lines), observed species richness of amphibians (black dots). Note that here, suitable habitat area sizes were determined by using 1 km, 2 km, and 5 km buffering circles.</p>
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12 pages, 7032 KiB  
Article
Vertical Stratification of Butterfly Assemblages Persists in Highly Disturbed Forest Fragments of the Brazilian Atlantic Forest
by Denise B. Silva, André V. L. Freitas, Oscar F. Junior and Jessie P. Santos
Diversity 2024, 16(10), 608; https://doi.org/10.3390/d16100608 - 1 Oct 2024
Viewed by 794
Abstract
Vertical stratification is a property of forest habitats related to the differential distribution of organisms according to the variation in the conditions, from the understory to the canopy. Here, we aimed to test whether butterfly assemblages from highly disturbed forests maintain the pattern [...] Read more.
Vertical stratification is a property of forest habitats related to the differential distribution of organisms according to the variation in the conditions, from the understory to the canopy. Here, we aimed to test whether butterfly assemblages from highly disturbed forests maintain the pattern of vertical stratification. We hypothesized that degraded forests would not exhibit vertical stratification due to the low variation in the microhabitat conditions along the vertical gradient, resulting from the canopy openness. To test this, we sampled fruit-feeding butterflies with bait traps, alternately disposed between the understory and canopy of three secondary forest fragments in a very fragmented Atlantic Forest landscape, for one year. We found that the vertical strata differed in terms of species composition, with a high contribution by the nestedness component on the beta diversity spatial variation. The understory assemblages had a higher abundance and were more diverse than the upper stratum. We demonstrated that vertical stratification is maintained even in disturbed forests; however, this does not necessarily provide support for a good quality and functioning ecosystem in these habitats. The butterfly assemblages recorded here are a subset of the species pool that inhabits conserved remnants. Thus, even being represented by species commonly found in disturbed habitats, the dynamic of vertical stratification of assemblages remains. Full article
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<p>(<b>A</b>) Map with the location of the three sampling transects (red circles) projected onto the forest remnants in the study site. The orange outline represents the Atlantic Forest domain, according to the integrative limit proposed by Muylaert et al. 2018; (<b>B</b>) sampling transect with a bait trap placed in the understory; (<b>C</b>) a transect photo to illustrate the canopy structure of the sampling site.</p>
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<p>Abundance of fruit-feeding butterflies recorded in each vertical stratum per month (mean ± SE).</p>
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<p>(<b>a</b>) Individual-based rarefaction curves comparing the species richness of fruit-feeding butterfly assemblages between the canopy and understory. The dashed line represents the interpolation where the number of individuals is the same for both vertical strata. The blue dashed line is the extrapolated number of individuals for the canopy. (<b>b</b>) Coverage-based curves comparing the species richness between the canopy and understory.</p>
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<p>Diversity profiles calculated with Hill numbers to compare the diversity between the canopy and understory in regard to different q values.</p>
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<p>Non-metric multidimensional scaling (NMDS) demonstrating the difference in species composition between the canopy (circles) and understory (triangles).</p>
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<p>SDR simplex approach for spatial beta diversity within each vertical stratum obtained through the Ruzicka dissimilarity matrix. Black lines inside each triangle represent the mean values for each component and the black points are the mean values for all the three components. Dashed lines represent the confidence intervals (0.95). (<b>a</b>) SDR simplex for pairwise canopy traps; (<b>b</b>) SDR simplex for pairwise understory traps.</p>
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18 pages, 3637 KiB  
Article
Diverging Elevational Patterns of Tree vs. Epiphyte Species Density, Beta Diversity, and Biomass in a Tropical Dry Forest
by Florian A. Werner and Jürgen Homeier
Plants 2024, 13(18), 2555; https://doi.org/10.3390/plants13182555 - 11 Sep 2024
Viewed by 1191
Abstract
There is evidence to suggest that vascular epiphytes experience low competition for resources (light, water, and nutrients) compared to terrestrial plants. We tested the hypothesis that low resource competition may lead to higher nestedness among vascular epiphyte assemblages compared to trees. We studied [...] Read more.
There is evidence to suggest that vascular epiphytes experience low competition for resources (light, water, and nutrients) compared to terrestrial plants. We tested the hypothesis that low resource competition may lead to higher nestedness among vascular epiphyte assemblages compared to trees. We studied the species composition and biomass of epiphytes and trees along an elevation gradient in a tropical dry forest in SW Ecuador. Both life-forms were inventoried on 25 plots of 400 m2 across five elevation levels (550–1250 m). Tree species density and total species richness increased with elevation, whereas basal area and biomass did not show significant trends. Epiphyte species density and richness both increased strongly with elevation, in parallel to biomass. Plot-level compositional changes were similarly strong for both life-forms. We attribute elevational increases in the species richness of trees and epiphytes to increasing humidity, i.e., more mesic growth conditions. We attribute the more pronounced elevational increase in epiphyte biomass, species density, and richness—the latter coupled with a higher degree of nestedness—to the greater moisture dependency of epiphytes and relatively low direct competition for resources. Our study provides a first comparison of elevational trends in epiphyte and tree diversity and biomass for a tropical dry forest. Full article
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<p>Aboveground biomass of vascular epiphytes (<b>top</b>) and trees (<b>bottom</b>) along the elevational gradient. Inserted are linear trendlines with 95% confidence intervals.</p>
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<p>Species density (species per plot) of epiphytes (<b>top</b>) and trees (<b>bottom</b>) vs. elevation. Species numbers are calculated through individual-based rarefaction at <span class="html-italic">n</span> = 13 (trees) and <span class="html-italic">n</span> = 125 (epiphytes), respectively. Inserted are second-degree polynomial (epiphytes) and linear (trees) trendlines with 95% confidence intervals. Raw species densities are plotted in <a href="#app1-plants-13-02555" class="html-app">Supplementary Figure S1</a>.</p>
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<p>Species accumulation curves across elevational levels (strata) for epiphytes (<b>top</b>) and trees (<b>bottom</b> panel) as yielded via sample-based rarefaction (5000 runs).</p>
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<p>NMDS ordinations of epiphyte (<b>top</b>) and tree assemblages (<b>bottom</b>), with fitted environmental vectors and regression surfaces. The length and direction of an arrow indicate the strength and sign of the linear correlation of an environmental variable with ordination scores. The contour lines show smooth trends in the relationship between elevation and plot scores. Vectors for epiphytes: tree AGB (not slope-corrected), mean stem lichen cover, and mean bryophyte cover (covers were taken as the average between understorey and canopy values); trees: soil pH, soil C/N, and soil P<sub>resin</sub>.</p>
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<p>Relationship between compositional dissimilarity and plot elevational distance among trees (<b>left</b> panels) and epiphytes (<b>right</b> panels). Shown are Sørensen dissimilarity (β<sub>sor</sub>; <b>top</b>) and its components turnover (β<sub>sim</sub>; <b>centre</b>) and nestedness (β<sub>sne</sub>; <b>bottom</b> panels). Linear regression lines with their corresponding R<sup>2</sup> and <span class="html-italic">p</span>-values are inserted in the panels. Differences between trees and epiphytes are significant for all three indices (paired <span class="html-italic">t</span>-test, df = 299): <span class="html-italic">t</span> = −12.2, <span class="html-italic">p</span> &lt; 0.001 (β<sub>sor</sub>); <span class="html-italic">t</span> = −14.8, <span class="html-italic">p</span> &lt; 0.001 (β<sub>sim</sub>); <span class="html-italic">t</span> = 8.5, <span class="html-italic">p</span> &lt; 0.001(β<sub>sne</sub>).</p>
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<p>Relative nestedness (β<sub>sne</sub>/β<sub>sor</sub>) among trees (green circles) and epiphytes (blue circles). Dashed lines are linear trend lines. Relative nestedness is significantly higher in epiphytes than in trees (paired <span class="html-italic">t</span>-test: <span class="html-italic">t</span> = 9.0, df = 299, <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>Map of the study area Reserva Natural Laipuna (reserve border: stippled blue line) and plot locations (orange dots).</p>
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16 pages, 1963 KiB  
Article
Taxonomic, Functional, and Phylogenetic Diversity of Bats in Urban and Suburban Environments in Southern México
by Miguel Briones-Salas, Gabriela E. Medina-Cruz and Cintia Natalia Martin-Regalado
Diversity 2024, 16(9), 527; https://doi.org/10.3390/d16090527 - 1 Sep 2024
Viewed by 1877
Abstract
Urbanization is one of the leading causes of habitat loss, which has increased significantly in tropical regions in recent years, leading to the loss of species, their ecological functions, and evolutionary history. To determine the effect of urbanization on the diversity of bat [...] Read more.
Urbanization is one of the leading causes of habitat loss, which has increased significantly in tropical regions in recent years, leading to the loss of species, their ecological functions, and evolutionary history. To determine the effect of urbanization on the diversity of bat communities in urban and suburban environments, we analyzed the α and β taxonomic, functional, and phylogenetic diversities at four sites along urbanization gradients surrounding a rapidly expanding city (Oaxaca City) in southern Mexico. We recorded bats using conventional techniques such as mist nets and acoustic monitoring. We calculated the diversity of bats in four sites with different urbanization conditions: urban (1), suburban (1), and rural (2). To assess the degree of total differentiation and components of bat turnover and nestedness between sites, we calculated the β taxonomic, functional, and phylogenetic diversities. A total of 33 bat species were recorded. The highest taxonomic and functional diversity was observed in the Center of Oaxaca (the site with the highest level of urbanization). In contrast, the highest phylogenetic diversity was found in the West (the site with the lowest level of urbanization). The total β taxonomic diversity was higher than the functional and phylogenetic diversity. Regarding the contributions of turnover and nestedness, turnover made a more significant contribution than nestedness to the taxonomic and phylogenetic β diversity. In contrast, functional nestedness contributed more to the functional β diversity than turnover. Tadarida brasiliensis, Desmodus rotundus, Sturnira hondurensis, and S. parvidens were recorded in all three urbanization conditions. In the most urbanized site, four Myotis species were recorded: M. fortidens, M. keaysi, M. thysanodes, and M. velifer. We suggest that the analysis of different dimensions of diversity is essential and should be considered to strengthen conservation strategies; moreover, we suggest the preservation of native vegetation mosaics and water bodies within the city to maintain bat diversity. Full article
(This article belongs to the Section Animal Diversity)
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<p>Geographic location of the study area in the Central Valleys of Oaxaca. The analyzed localities are indicated.</p>
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<p>Relationship between α taxonomic, functional, and phylogenetic diversities and the level of urbanization at four sites in the Central Valleys of Oaxaca, Mexico.</p>
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<p>Phylogenetic, functional, and taxonomic bats β diversities (i.e., total, turnover, and nestedness) in four sites in the Central Valleys of Oaxaca, México.</p>
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<p>UPGMA cluster analysis. The groups represent total taxonomic diversity (Taxoβjaccard), functional diversity (Funβjaccard), and phylogenetic diversity (Phyloβjaccard) of bats at four sites in the Central Valleys of Oaxaca, Mexico, based on Jaccard dissimilarity index and its turnover components (Taxoβturnover, Funβturnover, Phyloβturnover) and nestedness components (Taxoβnestedness, Funβnestedness, Phyloβnestedness).</p>
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14 pages, 888 KiB  
Article
Perinatal Outcomes of Immigrant Mothers and Their Infants Born Very Preterm across Germany
by Britta M. Hüning, Julia Jaekel, Nils Jaekel, Wolfgang Göpel, Egbert Herting, Ursula Felderhoff-Müser, Juliane Spiegler and Christoph Härtel
Healthcare 2024, 12(12), 1211; https://doi.org/10.3390/healthcare12121211 - 17 Jun 2024
Cited by 1 | Viewed by 1258
Abstract
Background: In Germany, more than 40% of infants are born to immigrant parents. Increased survival rates of very preterm (below 32 weeks gestation at birth; VP) infants have not resulted in equally improved life chances and quality of life. More information on perinatal [...] Read more.
Background: In Germany, more than 40% of infants are born to immigrant parents. Increased survival rates of very preterm (below 32 weeks gestation at birth; VP) infants have not resulted in equally improved life chances and quality of life. More information on perinatal variations in outcomes according to social inequalities, migration background, and language barriers is needed. We tested whether mothers’ immigrant status and language barriers are associated with perinatal health and short-term neonatal outcomes. Methods: The data are from the national multi-centre German Neonatal Network (GNN) cohort, including VP births from 2009 onwards. In total, 3606 (n = 1738 female) children were assessed, and 919 (n = 449 female) of these children had immigrant backgrounds. Immigrant status was operationalised as a binary variable based on the children’s mothers’ countries of birth (born in Germany vs. foreign-born). Self-reported home language (L1) was used to calculate the average linguistic distance to German as one continuous variable. Results: Mixed-effects models showed that two out of fourteen effects of interest survived the adjustment for known confounders and accounting for the nestedness of data within birth hospitals. Linguistic distance from mothers’ L1s to German was independently associated with diagnoses of preeclampsia (OR = 1.01, 95% CI = [1.00, 1.01]). Infants of foreign-born mothers had higher odds for amniotic infection syndrome (AIS; OR = 1.45 [1.13, 1.86]) than infants of German mothers. Conclusions: Our findings from this large multi-centre longitudinal cohort of VP-born children indicate that maternal immigrant status and language barriers have limited impact on perinatal health and severe neonatal outcomes. This suggests that, regardless of background or language skills, there may be few inequalities in the perinatal health of pregnant women and their newborn preterm infants. Full article
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<p>Linguistic distance variable scores among German and five selected immigrant languages.</p>
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<p>Study design flow chart of the GNN sample assessed to 5–6 years.</p>
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21 pages, 3583 KiB  
Article
Functional Alpha and Beta Diversity of Fish Communities and Their Relationship with Environmental Factors in the Huanghe River (Yellow River) Estuary and Adjacent Seas, China
by Shaowen Li, Yufang Huang, Fan Li, Yanfen Liu, Hongliang Ma, Xiaomin Zhang, Xiuxia Wang, Wei Chen, Guangxin Cui and Tiantian Wang
Fishes 2024, 9(6), 222; https://doi.org/10.3390/fishes9060222 - 12 Jun 2024
Viewed by 1498
Abstract
Fisheries and bottom seawater data were collected in July in 2022 and 2023 from 15 sampling stations in the Huanghe River estuary and adjacent seas in China. The patterns of functional alpha and beta diversity of fish communities in this area and their [...] Read more.
Fisheries and bottom seawater data were collected in July in 2022 and 2023 from 15 sampling stations in the Huanghe River estuary and adjacent seas in China. The patterns of functional alpha and beta diversity of fish communities in this area and their relationships with environmental factors were studied using trait-based analysis. Five functional classifications, which included 16 functional traits, four functional alpha diversity indices (functional richness, functional evenness, functional divergence, and community-weighted mean), three functional beta diversity indices (functional beta diversity and its turnover and nestedness components), and 14 bottom environmental factors were considered. The dominant traits of fish communities were the following: benthivorous feeding habits, small and front-facing mouths, high trophic level, demersal, anguilliform, low growth coefficient, medium resilience, low vulnerability, and adapted to warm temperate conditions. The dominant migration traits and types of fish eggs varied by year, and fish abundance was the main factor affecting the dominant traits of the communities. The results of multiple regression on distance matrices and variance partitioning analysis indicated that ammonia nitrogen content, total phosphorus content, and pH were the main environmental factors that affected fish functional diversity. The N/P ratio had a bottom-up control effect on fish functional diversity. Our findings also revealed that high pH gradients and distant geographical distances can inhibit trait turnover in fish communities. Full article
(This article belongs to the Special Issue Biodiversity and Spatial Distribution of Fishes)
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<p>Map showing the study area and locations of the fish sampling stations in the Huanghe River estuary and adjacent seas in China. The labels of stations represent the distance from the estuary. A is for 15–20 km from the estuary mouth, B for 25–35 km, and C for 40–55 km.</p>
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<p>Stacking plots of fish species and dominant species in the Huanghe River estuary seas in 2022 (<b>a</b>) and 2023 (<b>b</b>).</p>
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<p>Functional alpha diversity of fishes in the Huanghe River estuary and adjacent seas in 2022 and 2023. Asterisks denote a significant difference (* <span class="html-italic">p</span> &lt; 0.05); ns indicates no significant difference.</p>
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<p>Fish community <span class="html-italic">CWM</span> and variation in the Huanghe River estuary and adjacent seas. Asterisks denote significant difference (* <span class="html-italic">p</span> &lt; 0.05) or highly significant difference (** <span class="html-italic">p</span> &lt; 0.01), and ns indicates no significant difference.</p>
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<p>Functional beta diversity (<span class="html-italic"><sup>F</sup>β<sub>sor</sub></span>) and its turnover (<span class="html-italic"><sup>F</sup>β<sub>sim</sub></span>) and nestedness (<span class="html-italic"><sup>F</sup>β<sub>sne</sub></span>) components. (<b>a</b>) The 2022 values; (<b>b</b>) The 2023 values. Each red dot in the figure represents the data of one sample pair. The size of the red dot represents the <span class="html-italic"><sup>F</sup>β<sub>sor</sub></span> value of sample pair. The blue dots represent the mean values of the three components of functional beta diversity.</p>
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<p>VPA of the functional diversity explained by environmental factors and geographic distance variables. (<b>a</b>) the functional alpha diversity; (<b>b</b>) the functional beta diversity.</p>
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<p>Species accumulation curves in the Huanghe River estuary and adjacent seas. The red box represents the number of species that may be obtained at the sampling station. The blue area represents the range of the number of species surveyed during continuous sampling.</p>
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<p>Correlation of environmental factors based on a collinearity test.</p>
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9 pages, 399 KiB  
Article
An Entropic Analysis of Social Demonstrations
by Daniel Rico and Yérali Gandica
Entropy 2024, 26(5), 363; https://doi.org/10.3390/e26050363 - 25 Apr 2024
Cited by 1 | Viewed by 1394
Abstract
Social media has dramatically influenced how individuals and groups express their demands, concerns, and aspirations during social demonstrations. The study of X or Twitter hashtags during those events has revealed the presence of some temporal points characterised by high correlation among their participants. [...] Read more.
Social media has dramatically influenced how individuals and groups express their demands, concerns, and aspirations during social demonstrations. The study of X or Twitter hashtags during those events has revealed the presence of some temporal points characterised by high correlation among their participants. It has also been reported that the connectivity presents a modular-to-nested transition at the point of maximum correlation. The present study aims to determine whether it is possible to characterise this transition using entropic-based tools. Our results show that entropic analysis can effectively find the transition point to the nested structure, allowing researchers to know that the transition occurs without the need for a network representation. The entropic analysis also shows that the modular-to-nested transition is characterised not by the diversity in the number of hashtags users post but by how many hashtags they share. Full article
(This article belongs to the Special Issue Complex Systems Approach to Social Dynamics)
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<p>The number of unique hashtags and unique users in each one-hour temporal point are shown in the upper part. The bottom part depicts the values for modularity and nestedness on each one-hour temporal network. The background highlights in violet the temporal points that meet two conditions: high modularity and excluding inactive hours. In blue is signalled the points of low activity. A dashed-red line shows the point of highest nestedness. Results are shown for the demonstrations 9n, Noaltarifazo, and CharlieHebdo.</p>
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<p>From top to bottom are shown the number of hashtags, the number of users, the unique value of both numbers, the entropy for users along with the entropy of users per hashtag, and the entropy of hashtags along with the entropy of hashtags per user. All the plots correspond to the social demonstration 9n. With two different colours, the background highlights the temporal points of high modularity (violet), and a dashed-red line shows the point of highest nestedness.</p>
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<p>From top to bottom are shown the number of hashtags, the number of users, the unique value of both numbers, the entropy for users along with the entropy of users per hashtag, and the entropy of hashtags along with the entropy of hashtags per user. All the plots correspond to the social demonstration Noaltarifazo. With two different colours, the background highlights the temporal points of high modularity (violet), and a dashed-red line shows the point of highest nestedness.</p>
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<p>From top to bottom are shown the number of hashtags, the number of users, the unique value of both numbers, the entropy for users along with the entropy of users per hashtag, and the entropy of hashtags along with the entropy of hashtags per user. All the plots correspond to the social demonstration CharlieHebdo. With two different colours, the background highlights the temporal points of high modularity (violet), and a dashed-red line shows the point of highest nestedness.</p>
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13 pages, 1880 KiB  
Article
Patterns of Tadpole β Diversity in Temperate Montane Streams
by Da Kang, Zijian Sun, Jiacheng Tao, Yan Huang and Tian Zhao
Animals 2024, 14(8), 1240; https://doi.org/10.3390/ani14081240 - 20 Apr 2024
Cited by 1 | Viewed by 1766
Abstract
Understanding the spatial variation and formation mechanism of biological diversity is a hot topic in ecological studies. Comparing with α diversity, β diversity is more accurate in reflecting community dynamics. During the past decades, β diversity studies usually focused on plants, mammals, and [...] Read more.
Understanding the spatial variation and formation mechanism of biological diversity is a hot topic in ecological studies. Comparing with α diversity, β diversity is more accurate in reflecting community dynamics. During the past decades, β diversity studies usually focused on plants, mammals, and birds. Studies of amphibian β diversity in montane ecosystems, in particular, tadpoles, are still rare. In this study, Mount Emei, located in southwestern China, was selected as the study area. We explored the tadpole β diversity in 18 streams, based on a two-year survey (2018–2019). Our results indicated a high total β diversity in tadpole assemblages, which was determined by both turnover and nestedness processes, and the dominant component was turnover. Both the total β diversity and turnover component were significantly and positively correlated with geographical, elevational, and environmental distances, but no significant relationship was detected between these and the nestedness component. Moreover, the independent contributions of river width, current velocity, and chlorophyll α were larger than that of geographical and elevational distance. Overall, tadpole β diversity was determined by both spatial and environmental factors, while the contribution of environmental factors was larger. Future studies can focus on functional and phylogenetic structures, to better understand the tadpole assembly process. Full article
(This article belongs to the Section Aquatic Animals)
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<p>Map of the study area and the transects (The polygon represents the location of Mount Emei, and the triangles represent the positions of transects).</p>
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<p>Tadpole β diversity indices in Mount Emei. βsor: total β diversity; βsim: turnover component; βsne: nestedness component.</p>
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<p>Relationships between multifaceted β diversity indices and geographical (<b>a</b>–<b>c</b>), elevational (<b>d</b>–<b>f</b>), and environmental distances (<b>g</b>–<b>i</b>). Solid lines indicate significant relationships (<span class="html-italic">p</span> &lt; 0.05). Shallow area represents 95% confidence interval.</p>
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<p>Independent contribution of each explanatory distance matrix in the variations of tadpole β diversity. The meaning of the abbreviations can be found in <a href="#animals-14-01240-t002" class="html-table">Table 2</a>.</p>
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