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Diversity, Volume 16, Issue 3 (March 2024) – 62 articles

Cover Story (view full-size image): Global warming is causing poleward expansion of species ranges, under a process known as “tropicalisation”, i.e., the combination of seawater warming and establishment of southern species. The Ligurian Sea is one of the coldest sectors of the Mediterranean and has been characterized by a dearth of warm-temperate species and a comparative abundance of cold-temperate ones. This paper uses a time series of sea surface temperature (SST) and new records of thermophilic fish to reconsider the biogeography of the Ligurian Sea. SST has increased significantly since the 1980s, favouring the arrival and establishment of thermophilic species. Concurrently, heat waves and climate-related diseases have caused mass mortality of native species. Recent changes in the biogeography of the Ligurian Sea call for re-defining its chorological spectrum. View this paper
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20 pages, 10936 KiB  
Article
Water Reserves for the Environment: A Strategic and Temporal Analysis (2012–2022) for the Implementation of Environmental Flows in Mexico
by Sergio A. Salinas-Rodríguez and Anuar I. Martínez Pacheco
Diversity 2024, 16(3), 190; https://doi.org/10.3390/d16030190 - 21 Mar 2024
Viewed by 2294
Abstract
In Mexico, the evaluations of environmental flows are regulated by the Mexican Norm NMX-AA-159-SCFI-2012, and they warrant the establishment of water reserves for the environment. However, the pressure or demand for water use limits the establishment of said reserves because their implementation is [...] Read more.
In Mexico, the evaluations of environmental flows are regulated by the Mexican Norm NMX-AA-159-SCFI-2012, and they warrant the establishment of water reserves for the environment. However, the pressure or demand for water use limits the establishment of said reserves because their implementation is generally conditioned to water availability. This research aimed to evaluate the changes through time of the variables that serve as a basis for the implementation strategy by the Mexican government. A geographical information system was built with updated information on water availability, conservation values, and pressures for all basins nationwide. Their desired conservation status was analyzed, and the potential reserves were estimated based on the reference values. The results were examined according to the ranking changes in environmental water reserves enactment feasibility and desired conservation status of Mexican basins, the progress achieved to date, and the potential contribution to the conservation of protected areas and their connectivity if the gaps of reserves were implemented. The outcomes point towards an administrative implementation strategy with positive results despite the growing demand for water use, with a change rate higher than the one for the creation of new protected areas. Currently, basins with low demand and high conservation value have the potential to meet people’s and the environment’s water needs, and contribute to 86% of the goal set by the present administration without affecting water availability. Finally, reserving water in the priority basins would guarantee the legal protection of the flow regime in 48–50% of the hydrographic network (63,760–66,900 km) in a desired conservation status, 43–49% of wetlands of international importance (48,650–49,600 km2) and other protected areas (128,700–136,500 km2) in 85–89% of the global ecoregions represented in Mexico (780,500–852,200 km2). Full article
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<p>Matrix for the classification of environmental objectives. Source: Mexican Norm NMX-AA-159-SCFI-2012.</p>
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<p>Geographic distribution of basins identified as potential water reserves.</p>
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<p>Geographic distribution of the environmental objectives’ classes by hydrological basin.</p>
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<p>Geographical locations of the country’s basins with current water reserves, and the surplus and deficit of water availability for the establishment of new reserves (volume of current water availability minus reserves).</p>
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<p>Exploratory analysis of water availability volumes in million cubic meters based on reference values for ecological reserve by class of environmental flow objectives (A = blue, B = green, C = yellow, D = red), with focus on (<b>a</b>) central frequency distribution values within upper and lower limits (quartile 3 and 1 ± 1.5 times the interquartile range, respectively) and (<b>b</b>) outliers.</p>
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14 pages, 1474 KiB  
Article
A Beacon in the Dark: Grey Literature Data Mining and Machine Learning Enlightening Historical Plankton Seasonality Dynamics in the Ligurian Sea
by Alice Guzzi, Stefano Schiaparelli, Maria Balan and Marco Grillo
Diversity 2024, 16(3), 189; https://doi.org/10.3390/d16030189 - 21 Mar 2024
Cited by 2 | Viewed by 1683
Abstract
The Mediterranean Sea, as one of the world’s most climate-sensitive regions, faces significant environmental changes due to rising temperatures. Zooplankton communities, particularly copepods, play a vital role in marine ecosystems, yet their distribution dynamics remain poorly understood, especially in the Ligurian Sea. Leveraging [...] Read more.
The Mediterranean Sea, as one of the world’s most climate-sensitive regions, faces significant environmental changes due to rising temperatures. Zooplankton communities, particularly copepods, play a vital role in marine ecosystems, yet their distribution dynamics remain poorly understood, especially in the Ligurian Sea. Leveraging open-source software and environmental data, this study adapted a methodology to model copepod distributions from 1985 to 1986 in the Portofino Promontory ecosystem using the Random Forest machine learning algorithm to produce the first abundance and distribution maps of the area. Five copepod genera were studied across different trophic guilds, revealing habitat preferences and ecological fluctuations throughout the seasons. The assessment of model accuracy through symmetric mean absolute percentage error (sMAPE) highlighted the variability in copepod dynamics influenced by environmental factors. While certain genera exhibited higher predictive accuracy during specific seasons, others posed challenges due to ecological complexities. This study underscores the importance of species-specific responses and environmental variability in predictive modeling. Moreover, this study represents the first attempt to model copepod distribution in the Ligurian Sea, shedding light on their ecological niches and historical spatial dynamics. The study adhered to FAIR principles, repurposing historical data to generate three-dimensional predictive maps, enhancing our understanding of copepod biodiversity. Future studies will focus on developing abundance distribution models using machine learning and artificial intelligence to predict copepod standing crop in the Ligurian Sea with greater precision. This integrated approach advances knowledge of copepod ecology in the Mediterranean and sets a precedent for integrating historical data with contemporary methodologies to elucidate marine ecosystem dynamics. Full article
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<p>Study area. Black dots are original sampling stations from Fabiano et al. (1988) [<a href="#B48-diversity-16-00189" class="html-bibr">48</a>]. Portofino MPA marine protection zones are shown on the map (red = zone A, No-Take Zone; yellow = zone B, Sustainable Use Zone; green = zone C, Transition Zone).</p>
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<p>Predictive map for <span class="html-italic">Acartia</span> spp., a filter feeder calanoid, during spring (sMAPE = 0.4105), along with the corresponding RA values (expressed as Individuals/m<sup>3</sup>). Black dots are original sampling stations from Fabiano et al. (1988) [<a href="#B48-diversity-16-00189" class="html-bibr">48</a>].</p>
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<p>Predictive map for <span class="html-italic">Oithona</span> spp., an ambush feeder cyclopoid, during winter (sMAPE = 0.4567), accompanied by the corresponding RA values (expressed as Individuals//m<sup>3</sup>). Black dots are the original sampling stations from Fabiano et al. (1988) [<a href="#B48-diversity-16-00189" class="html-bibr">48</a>].</p>
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14 pages, 3875 KiB  
Article
Feeding Ecology of Reintroduced Golden Parakeets (Guaruba guarouba, Psittacidae) in a Protected Area in the Amazon Forest
by Marcelo Rodrigues Vilarta, Thaís Tamamoto De Moraes, Maria Fernanda Naegeli Gondim, Crisomar Lobato, Mônica Nazaré Rodrigues Furtado Da Costa, Rubens de Aquino Oliveira and Luís Fábio Silveira
Diversity 2024, 16(3), 188; https://doi.org/10.3390/d16030188 - 21 Mar 2024
Viewed by 2063
Abstract
The Golden Parakeet is an endemic Brazilian flagship species that has suffered from poaching and habitat loss, leading to local extinctions in the urbanized parts of the Amazon. We reintroduced six groups of mostly captive-bred parakeets in a protected area. The birds were [...] Read more.
The Golden Parakeet is an endemic Brazilian flagship species that has suffered from poaching and habitat loss, leading to local extinctions in the urbanized parts of the Amazon. We reintroduced six groups of mostly captive-bred parakeets in a protected area. The birds were acclimatized for at least five months at the release site, where they were trained to recognize native foods and develop foraging skills. Subsequently, we conducted a soft release, followed by daily supplementation and monitoring. For three years following the release we recorded their diet, feeding behavior, and how they adapted to wild foraging. The reintroduced birds fed on 23 plant species, with 13 not being previously listed in past studies. The three most consumed species corresponded to 77% of their feeding records. Parakeets spent more time feeding in altered landscapes and secondary vegetation than in the preserved forest. Most of the feeding happened during the rainy season when most of their favorite plants are fruiting. The parakeets’ incorporation of new species in their diet and their transition from supplemental to natural feeding happened gradually, as we did not reduce food offerings. Parakeets that showed site fidelity were able to find native food rapidly following release, but individuals that dispersed immediately had more difficulty finding food. This study showed that captive-bred Golden Parakeets can transition to a wild diet following a gradual reintroduction process. Full article
(This article belongs to the Special Issue Ecology and Conservation of Parrots)
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<p>(<b>a</b>) Released Golden Parakeet feeding on unripe <span class="html-italic">Byrsonima crassifolia</span> by perching with one foot while processing the fruit and seed with the other. (<b>b</b>) Released Golden Parakeet feeding on <span class="html-italic">Elaeis guineensis</span> by peeling the oily fruit whilst holding it with its foot.</p>
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<p>Group of released Golden Parakeets foraging on a <span class="html-italic">Euterpe oleracea</span> palm. While three individuals feed on the fruits, four others remain vigilant at the top.</p>
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<p>Hourly distribution of feeding times of the released Golden Parakeets.</p>
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<p>Plant species accumulation curve in the diet of reintroduced Golden Parakeets, as documented during post-release monitoring campaigns. Each asterisk (*) refer to the first time a plant species provided in food training was used in the wild.</p>
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<p>Percentage of time that the group of released parakeets spent feeding in the wild (Natural) or at suspended feeders (Supplemental) throughout the monitoring period.</p>
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<p>(<b>a</b>) Time the released parakeets spent feeding on primary or secondary vegetation types. The park is mostly covered by primary vegetation, 60%, while secondary only covers 15% of the area. (<b>b</b>) Feeding time (observed feeding/total effort) of the released parakeets during the rainy and dry seasons.</p>
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<p>(<b>a</b>) Relative distribution of parakeets’ feeding time during the rainy season between primary and secondary vegetation. (<b>b</b>) Relative distribution of their feeding time during the dry season between primary and secondary vegetation physiognomies.</p>
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11 pages, 669 KiB  
Article
Population Reinforcement of the Endangered Freshwater Pearl Mussel (Margaritifera margaritifera): Lessons Learned
by Louise Lavictoire and Christopher West
Diversity 2024, 16(3), 187; https://doi.org/10.3390/d16030187 - 20 Mar 2024
Cited by 1 | Viewed by 2816
Abstract
Freshwater mussel populations are in sharp decline and are considered to be one of the most imperilled groups globally. Consequently, the number of captive breeding programmes has increased rapidly in recent years, coupled with subsequent reintroductions/population reinforcements to reverse these declines. The outcomes [...] Read more.
Freshwater mussel populations are in sharp decline and are considered to be one of the most imperilled groups globally. Consequently, the number of captive breeding programmes has increased rapidly in recent years, coupled with subsequent reintroductions/population reinforcements to reverse these declines. The outcomes of mussel conservation translocations are seldom reported in the primary literature, hindering opportunities for learning and for population recovery at pace. Here, we describe the methods employed to carry out a successful conservation translocation of the freshwater pearl mussel (Margaritifera margaritifera) in a declining population in northwest England. Following a small-scale pilot release in 2017, four release sites were identified for a population reinforcement of over 1300 tagged mussels in 2021. Monitoring during 2022 showed high levels of retention of juveniles at three out of the four release sites, despite the occurrence of a significant flood event during October 2021. Subsequent releases of 1100 juveniles were carried out across the three successful sites in 2023. Ongoing and regular monitoring is essential in order to provide data on the longer-term fate of propagated juveniles in the wild. This will allow for adaptive management of release activities in this river. These data will be useful to design conservation translocation strategies for other imperilled pearl mussel populations in the UK and throughout Europe. Full article
(This article belongs to the Special Issue Population Ecology and Protection of Freshwater Mussels)
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<p>Photographs to illustrate riparian land coverage and substrate characteristics at each release site.</p>
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10 pages, 610 KiB  
Article
Microclimatic Influences on the Abundance of Three Non-Troglobiont Species
by Luca Coppari, Raoul Manenti and Enrico Lunghi
Diversity 2024, 16(3), 186; https://doi.org/10.3390/d16030186 - 19 Mar 2024
Viewed by 1372
Abstract
Subterranean environments are often characterized by a natural gradient of microclimatic conditions and trophic resources, showing a higher trophic availability and a lower microclimatic stability in the shallowest area (close to the cave entrance), while the opposite occurs in the deepest sections. The [...] Read more.
Subterranean environments are often characterized by a natural gradient of microclimatic conditions and trophic resources, showing a higher trophic availability and a lower microclimatic stability in the shallowest area (close to the cave entrance), while the opposite occurs in the deepest sections. The shallowest areas of subterranean environments (e.g., the entrance and twilight zone, Mesovoid Shallow Substratum) act as ecotones between the surface habitats and the deep areas, creating a particular habitat which can be exploited by numerous species with different degrees of adaptation to subterranean environments. Species living in these ecotones may hold a key role in sustaining the entire ecosystem, as they are likely one of the major drivers of allochthonous organic matter. Indeed, these species are usually facultative cave-dwellers, meaning that they are able to exit and forage on the surface. Once these species are back inside the cave, they provide the local community with different typologies of organic matter (e.g., feces, eggs), which represent one of the most important sources of organic carbon. Therefore, studying which ecological features may exert significant effects on the abundance of these species may be of great help in understanding the ecosystem dynamics and the functional role of each species. In this study we analyzed the data collected through a year-round monitoring program, aiming to assess the potential effects that both abiotic and biotic features may have on the abundance of three facultative cave species. We focused on seven caves located in Monte Albo (Sardinia, Italy). The cave environments were divided into 3-meter sectors, and within each cave sector, microclimatic and biological data were seasonally recorded. We focused on the following facultative cave species: the spiders Metellina merianae and Tegenaria sp. and the snail Oxychilus oppressus. Different relationships were observed between the ecological features and the abundance of the three species. The two spiders were more abundant in warmer cave sectors closer to the cave entrance, especially the M. merianae. On the other hand, the snail tended to be more abundant farther from the cave entrance and in more illuminated cave sectors, probably because sunlight promotes the abundance of some of its trophic resources (e.g., lichens, vegetation). Furthermore, O. oppressus was the only species whose abundance and cave distribution was significantly affected by seasonality. This study provides useful and novel information to understand the population dynamics of facultative cave species and their role in subterranean ecosystems. Full article
(This article belongs to the Section Biodiversity Loss & Dynamics)
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<p>Differences in microclimatic conditions experienced by the studied species. Boxplots show the species’ range preferences for (<b>A</b>) temperature, (<b>B</b>) humidity, and (<b>C</b>) illuminance recorded within occupied cave sectors. The diagonal bar inside the box represents the median, dots indicate outliers. Significance of pairwise comparisons (Tukey’s HSD) is also shown.</p>
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32 pages, 10022 KiB  
Article
Two New Species of Elaphoidella (Copepoda, Harpacticoida) from Subterranean Waters in Northeast Thailand, with a Record of a Gynandromorphic Specimen and an Up-to-Date Key to Elaphoidella Species from Southeast Asia
by Chaichat Boonyanusith, Anton Brancelj and Laorsri Sanoamuang
Diversity 2024, 16(3), 185; https://doi.org/10.3390/d16030185 - 18 Mar 2024
Cited by 1 | Viewed by 2114
Abstract
Two new species of copepods of the genus Elaphoidella Chappuis, 1929 were discovered in a cave and a spring in northeastern Thailand. The first species, E. phuphamanensis sp. nov., belongs to species-group VII sensu Lang. It is most similar to E. turgisetosa Petkovski, [...] Read more.
Two new species of copepods of the genus Elaphoidella Chappuis, 1929 were discovered in a cave and a spring in northeastern Thailand. The first species, E. phuphamanensis sp. nov., belongs to species-group VII sensu Lang. It is most similar to E. turgisetosa Petkovski, 1980 in the armament of the male third exopod of the fourth swimming leg and the shape and armament of the fifth swimming leg in both sexes. However, it is easily distinguished from other congeners by the segmentation of the first swimming leg, the endopod of the fourth swimming leg, and the armature of the third exopod of swimming legs 2–4 in both sexes. The second species, E. propecabezasi sp. nov., is located in species-group I sensu Lang, where the male does not have a transformed seta on the third exopod of the fourth swimming leg and the female fifth swimming leg has four baseoendopodal robust setae, unequal in length. It is most similar to E. cabezasi Petkovski, 1982 and E. paraaffinis Watiroyram, Sanoamuang and Brancelj, 2017 in having the same armature formula as endopods 1–2 of female swimming legs 1–4. However, the ornamentation of the anal operculum, the shape of the caudal ramus, and the armature of the fifth swimming leg in both sexes distinguish them from each other. A rare gynandromorphic specimen of E. propecabezasi sp. nov. was recorded, and a revised key to Elaphoidella species in Southeast Asia is provided. Full article
(This article belongs to the Section Animal Diversity)
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<p>Geographical location and details on sampling sites. (<b>A</b>) map of Thailand and location of sampling sites in Khon Kaen and Loei provinces (indicated by black circle and square, respectively); (<b>B</b>) geographical details of sampling sites (Google Earth map); (<b>C</b>,<b>D</b>) sampling sites in which <span class="html-italic">Elaphoidella phuphamanensis</span> sp. nov. was collected; (<b>E</b>) sampling site in which <span class="html-italic">Elaphoidella propecabezasi</span> sp. nov. was collected.</p>
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<p><span class="html-italic">Elaphoidella phuphamanensis</span> sp. nov., paratypes (<b>A</b>,<b>B</b>), holotype (<b>C</b>–<b>E</b>), and allotype (<b>F</b>). (<b>A</b>) female habitus, dorsal view; (<b>B</b>) male habitus, dorsal view; (<b>C</b>) surface of female cephalothorax with refractile points and the distal part of the nuchal organ, dorsal view; (<b>D</b>) female P2- and P3-bearing somites, dorsal view; (<b>E</b>) female urosomite 4 and anal somite, dorsal view; (<b>F</b>) male P1, anterior view. Arrowheads on plates A, B, and D indicate middorsal pores. Scale bars: (<b>A</b>,<b>B</b>) 100 μm; (<b>C</b>–<b>F</b>) 25 μm.</p>
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<p><span class="html-italic">Elaphoidella phuphamanensis</span> sp. nov., female, holotype. (<b>A</b>) urosome, ventral view (arrowheads indicate integumental pores); (<b>B</b>) genital complex and P6, ventral view; (<b>C</b>) anal somite and caudal rami, dorsal view; (<b>D</b>) anal somite and caudal rami, lateral view; (<b>E</b>) caudal ramus, dorsal view (Roman numerals: setae numbers after Huys and Boxshall [<a href="#B18-diversity-16-00185" class="html-bibr">18</a>]). Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella phuphamanensis</span> sp. nov., female, holotype. (<b>A</b>) A1 without setae; (<b>B</b>) A1 with setae and aesthetascs (arrowheads indicate aesthetascs; II*, ventral view); (<b>C</b>) A2; (<b>D</b>) mandible; (<b>E</b>) maxillule; (<b>F</b>) maxilla; (<b>G</b>) maxilliped, posterior view. Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella phuphamanensis</span> sp. nov., female, holotype. (<b>A</b>) P1; (<b>B</b>) P2; (<b>C</b>) P3; (<b>D</b>) P4; (<b>E</b>) P5. Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella phuphamanensis</span> sp. nov., male, allotype. (<b>A</b>) urosomites 1–3, ventral view (arrowheads indicate integumental pores); (<b>B</b>) urosomites 4–6, ventral view; (<b>C</b>) A1, without setae; (<b>D</b>) A1, with setae and aesthetascs (arrowheads indicate aesthetascs, II*, ventral view). Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella phuphamanensis</span> sp. nov., male, allotype. (<b>A</b>) P1; (<b>B</b>) P2; (<b>C</b>) P3; (<b>D</b>) P4. Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella propecabezasi</span> sp. nov. paratypes (<b>A</b>,<b>B</b>) and holotype (<b>C</b>,<b>D</b>). (<b>A</b>) female habitus, dorsal view; (<b>B</b>) male habitus, dorsal view; (<b>C</b>) female anal somite, dorsal view; (<b>D</b>) urosomite 4 and anal somite, dorsal view. Scale bars: (<b>A</b>,<b>B</b>): 100 μm; (<b>C</b>): 25 μm; (<b>D</b>): 50 μm.</p>
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<p><span class="html-italic">Elaphoidella propecabezasi</span> sp. nov., female, holotype. (<b>A</b>) urosomites 2–5 and anal somite, ventral view (arrowhead indicates integumental pore); (<b>B</b>) P6 and genital complex, ventral view; (<b>C</b>) anal somite and caudal ramus, lateral view (an asterisk indicates seta I and an arrow indicates the posterior tip of the dorsal keel). Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella propecabezasi</span> sp. nov., female, holotype. (<b>A</b>) A1; (<b>B</b>) A2; (<b>C</b>) mandible; (<b>D</b>) maxillule; (<b>E</b>) maxilla; (<b>F</b>) maxilliped. Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella propecabezasi</span> sp. nov., female, holotype (<b>A</b>–<b>E</b>) and paratype (<b>F</b>). (<b>A</b>) P1; (<b>B</b>) P2; (<b>C</b>) P3; (<b>D</b>) P4; (<b>E</b>) P5; (<b>F</b>) P5 Exp (arrowhead indicates additional seta). Scale bars: (<b>A</b>–<b>E</b>): 50 μm; (<b>F</b>): 5 μm.</p>
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<p><span class="html-italic">Elaphoidella propecabezasi</span> sp. nov., male, allotype. (<b>A</b>) urosome, ventral view (arrowhead indicates integumental pore); (<b>B</b>) A1, left side, complete appendage with partial figured armature (arrowhead indicates aesthetasc on segment IX); (<b>C</b>) details of setation on segments I–VI (arrowhead indicates aesthetasc on segment V; II*, ventral view). Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella propecabezasi</span> sp. nov. male, allotype. (<b>A</b>) P2; (<b>B</b>) P3; (<b>C</b>) P4. Scale bars: 50 μm.</p>
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<p><span class="html-italic">Elaphoidella propecabezasi</span> sp. nov. gynandromorphic specimen. (<b>A</b>) genital double somite, dorsal view (arrow indicates the separation in the normal male); (<b>B</b>) genital double somite, ventral view (arrows indicate characteristics different from the normal male (♂) or female (♀)); (<b>C</b>) A1; left side, complete appendage with a partially figured armature (arrowhead indicates partly fused segment 8); (<b>D</b>) P4 Enp-2 (arrowhead indicates the spine, different from that of the normal male). Scale bars: 50 μm.</p>
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17 pages, 18811 KiB  
Article
Phylogeography of Dolichophis Populations in the Aegean Region (Squamata: Colubridae) with Taxonomic Remarks
by Adam Javorčík, Ilias Strachinis, Evanthia Thanou, Panagiotis Kornilios, Aziz Avcı, Nazan Üzüm, Kurtuluş Olgun, Çetin Ilgaz, Yusuf Kumlutaş, Petros Lymberakis, Zoltán T. Nagy and Daniel Jablonski
Diversity 2024, 16(3), 184; https://doi.org/10.3390/d16030184 - 18 Mar 2024
Cited by 1 | Viewed by 1795
Abstract
In this study, we investigate the phylogeographic patterns of Dolichophis species in the Aegean region, aiming to elucidate their genetic diversity and putative historical colonisation routes through mitochondrial and nuclear DNA data. Our findings revealed distinct phylogeographic patterns: D. caspius exhibited a [...] Read more.
In this study, we investigate the phylogeographic patterns of Dolichophis species in the Aegean region, aiming to elucidate their genetic diversity and putative historical colonisation routes through mitochondrial and nuclear DNA data. Our findings revealed distinct phylogeographic patterns: D. caspius exhibited a higher level of haplotypes within two shallow mitochondrial lineages, contrasting with D. jugularis, which displayed lower genetic variability in the area. Additionally, we identified evidence showing possible human-mediated historical translocation of D. caspius populations to Karpathos from the Balkans mainland. The mitochondrial variability in D. jugularis remained relatively uniform across southwestern Anatolia and Dodecanese, except for Rhodes Island. The evidence from mitochondrial and nuclear data confirming the previously described morphological differentiation of the Rhodes snakes, and thus the name D. j. zinneri Cattaneo, 2012, described on the island, could be applied to this isolated population. This result addresses the first genetic view on the long-standing taxonomic uncertainties regarding the subspecies status of Rhodes D. jugularis. Our results also raise questions regarding possible historical hybridisations between D. caspius and D. jugularis in the Dodecanese islands, prompting the need for further investigation using extensive field studies and genomic approaches. Ultimately, the Aegean islands, particularly Kos and Rhodes, seem to be important sites for the evolution of these colubrid snakes and their historical dynamics. Full article
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<p>The genotyped localities of <span class="html-italic">Dolichophis caspius</span> and <span class="html-italic">D</span>. <span class="html-italic">jugularis</span> in the Aegean region (<b>A</b>) together with the mitochondrial tree (<b>B</b>). Colourations on the map and the tree correspond to taxa. Underlined sequence codes in the mtDNA tree mark those used for nuDNA analysis. The orange shading of Rhodes and surrounding islands marks the range of <span class="html-italic">D</span>. <span class="html-italic">jugularis zinneri</span> according to Cattaneo [<a href="#B16-diversity-16-00184" class="html-bibr">16</a>]. The asterisk indicates the distribution of the eastern Aegean–Anatolian lineage of <span class="html-italic">D</span>. <span class="html-italic">caspius</span>. The line in the middle of the Aegean Sea represents the early formation of the Aegean barrier. Nuclear allele networks of the phased sequences of C-mos, BDNF, and Rag1 genes (<b>C</b>) presenting relationships between Rhodes (12204) and selected populations and taxa. Species colours in networks follow those used in the map (<b>A</b>) and tree (<b>B</b>). Circle sizes are proportional to the number of individuals that share a given allele. A small empty circle in networks indicates a missing or hypothetical allele. Different alleles of a single heterozygous sequence is coded as a and b, and without division, they represent homozygous sequences. Refer to <a href="#diversity-16-00184-t001" class="html-table">Table 1</a> for locality details and sample codes used in the tree and networks. Inset photographs: Daniel Jablonski (<span class="html-italic">D</span>. <span class="html-italic">caspius</span> from Bulgaria) and Ilias Strachinis (<span class="html-italic">D</span>. <span class="html-italic">jugularis</span> from Rhodes). The map was generated using QGIS 3.28, available at <a href="https://qgis.org/" target="_blank">https://qgis.org/</a>.</p>
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<p>The distribution of mitochondrial haplotypes of <span class="html-italic">Dolichophis caspius</span> in the Aegean area (<b>A</b>) and the haplotype network (<b>B</b>) defining haplogroups by colouration. The names in bold of the haplotype network highlight the Aegean islands. Refer to <a href="#diversity-16-00184-t001" class="html-table">Table 1</a> for locality details and sample codes used in the network. The line in the middle of the Aegean Sea represents the early formation of the Aegean barrier. The question mark indicates a place of unclear or possible occurrence of the species on Rhodes Island. The distribution range of the species in the studied area is highlighted in orange. The map was generated using QGIS 3.28, available at <a href="https://qgis.org/" target="_blank">https://qgis.org/</a>.</p>
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<p>The distribution of mitochondrial haplotypes of <span class="html-italic">Dolichophis jugularis</span> in the Aegean area (<b>A</b>) and the haplotype network (<b>B</b>) defining haplogroups by colouration. The names in bold of the haplotype network highlight the Aegean islands. Refer to <a href="#diversity-16-00184-t001" class="html-table">Table 1</a> for locality details and sample codes used in the network. The question mark indicates a place of possible occurrence of the species in the westernmost Anatolia [<a href="#B8-diversity-16-00184" class="html-bibr">8</a>]. The distribution range of the species in the studied area is highlighted in orange. The map was generated using QGIS 3.28, available at <a href="https://qgis.org/" target="_blank">https://qgis.org/</a>.</p>
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<p>The adult specimen NHMW 18618:1 (holotype; [<a href="#B20-diversity-16-00184" class="html-bibr">20</a>]) representing <span class="html-italic">Coluber caspius eiselti</span> Zinner 1972 from Lindos, Rhodes, Greece. (<b>A</b>,<b>B</b>) Dorsal and ventral view of the body. (<b>C</b>–<b>F</b>) Dorsal, ventral, and lateral view of the head. (<b>G</b>–<b>I</b>) Dorsal and ventral view of the body’s scalation, colouration, and pattern. Photos: Daniel Jablonski.</p>
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<p>The juvenile specimen NHMW 18618:3 (paratype; [<a href="#B20-diversity-16-00184" class="html-bibr">20</a>]) representing <span class="html-italic">Coluber caspius eiselti</span> Zinner 1972 from Lindos, Rhodes, Greece. (<b>A</b>,<b>B</b>) Dorsal and ventral view of the body. (<b>C</b>–<b>F</b>) Dorsal, ventral, and lateral view of the head. (<b>G</b>–<b>I</b>) Dorsal and ventral view of the body’s scalation, colouration, and pattern. Photos: Daniel Jablonski.</p>
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<p>The adult specimen ZFMK 92945 (holotype; [<a href="#B15-diversity-16-00184" class="html-bibr">15</a>]) from the type collection of <span class="html-italic">Dolichophis jugularis zinneri</span> Cattaneo, 2012. (<b>A</b>,<b>B</b>) Dorsal and ventral view of the body. (<b>C</b>–<b>F</b>) Dorsal, ventral, and lateral view of the head. (<b>G</b>–<b>I</b>) Dorsal and ventral view of the body’s scalation, colouration, and pattern. Photos: Morris Flecks (<b>A</b>–<b>D</b>) and Daniel Jablonski (<b>E</b>–<b>I</b>).</p>
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13 pages, 221 KiB  
Article
An Assessment of the Implementation of the Convention on International Trade in Endangered Species of Wild Fauna and Flora in Kenya
by Nicholus Kilonzo, Joel T. Heinen and Patrick Byakagaba
Diversity 2024, 16(3), 183; https://doi.org/10.3390/d16030183 - 18 Mar 2024
Cited by 1 | Viewed by 2089
Abstract
International trade is hastening extinction for many species of plants and animals despite the fact that many countries have ratified CITES. The adoption of treaties is often symbolic as many countries, especially in the developing world where most biodiversity is found, experience a [...] Read more.
International trade is hastening extinction for many species of plants and animals despite the fact that many countries have ratified CITES. The adoption of treaties is often symbolic as many countries, especially in the developing world where most biodiversity is found, experience a lack of fit between international agreements and national laws and institutions. Our main objective here is to assess the extent of jurisdictional and institutional fit in the implementation of CITES in Kenya, an important issue given the amount of international trade in wild products and the importance of wildlife tourism to the country. The specific objectives are to assess the following: the capacity and level of coordination among state actors and conservation mandates in national policy and law using a mixed methods approach involving a literature review and 38 key informant surveys representing professional expertise from various stakeholder groups. We found that over 60% of respondents indicated only moderate capacity for the implementation of CITES and coordination between local and central governments. Some participants indicated that judicial officers lack adequate conservation knowledge, thus hampering enforcement via low prosecution rates. A moderate (at best) structural fit involving inefficiencies such as conflicting processes, unequal enforcement, and suboptimal coordination implies a degree of failure in developing the implementation capacity of CITES within Kenya. Our results also show a mismatch between agency staffing and workload at several levels of government, and we make suggestions for improvement. Full article
(This article belongs to the Special Issue Biodiversity Conservation Planning and Assessment)
5 pages, 182 KiB  
Editorial
Ecology, Diversity, Conservation and Management of Ungulates
by Friedrich Reimoser and Ursula Nopp-Mayr
Diversity 2024, 16(3), 182; https://doi.org/10.3390/d16030182 - 17 Mar 2024
Viewed by 2350
Abstract
Wild ungulates are important drivers of the dynamics of many terrestrial ecosystems and impact biodiversity at different system levels [...] Full article
(This article belongs to the Special Issue Ecology, Diversity, Conservation and Management of Ungulates)
18 pages, 10965 KiB  
Article
Global Warming Drives Transitions in Suitable Habitats and Ecological Services of Rare Tinospora Miers Species in China
by Huayong Zhang, Zhe Li, Hengchao Zou, Zhongyu Wang, Xinyu Zhu, Yihe Zhang and Zhao Liu
Diversity 2024, 16(3), 181; https://doi.org/10.3390/d16030181 - 17 Mar 2024
Viewed by 1799
Abstract
Tinospora Miers is considered a valuable medicinal herb that is suffering from severe habitat degradation due to climate change and human activities, but the variations in its suitable habitats and ecological service values remain unclear, especially in the context of accelerating global warming. [...] Read more.
Tinospora Miers is considered a valuable medicinal herb that is suffering from severe habitat degradation due to climate change and human activities, but the variations in its suitable habitats and ecological service values remain unclear, especially in the context of accelerating global warming. In this study, we employed the MaxEnt model to estimate the suitable habitat changes and ecological service values of three rare Tinospora (T. craveniana, T. yunnanensis, and T. sinensis) species in China under four climate change scenarios (SSP126, SSP245, SSP370, and SSP585) from 2041 to 2100. The results show that the suitable habitats of T. craveniana, T. yunnanensis, and T. sinensis are mainly distributed in Sichuan, Yunnan, and Guangxi, respectively. Under the future climate scenarios, the suitable habitat of T. craveniana and T. sinensis is projected to expand toward the northeast and north, while that of T. yunnanensis will contract toward the northeast. The mean diurnal temperature range is the main environmental factor affecting T. craveniana and T. yunnanensis, while the annual mean temperature is a more important factor affecting T. sinensis. In the SSP245 scenario, T. craveniana and T. yunnanensis are expected to have the highest ecological service values from 2081 to 2100, while they will be relatively consistent in other climate scenarios and chronologies. The case of water protection accounts for the highest proportion of the total ecosystem service values, except for the economic value. This study provides a scientific reference for the diversity conservation of these rare species. Full article
(This article belongs to the Section Plant Diversity)
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<p>Distribution point data of <span class="html-italic">Tinospora</span> in China.</p>
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<p>Results of the Pearson’s correlation test for <span class="html-italic">Tinospora</span>. (<b>a</b>) <span class="html-italic">T. craveniana</span>; (<b>b</b>) <span class="html-italic">T. yunnanensis</span>; (<b>c</b>) <span class="html-italic">T. sinensis</span>.</p>
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<p>Suitable habitats for three species of <span class="html-italic">Tinospora</span> under the current climate scenario. (<b>a</b>) <span class="html-italic">T. craveniana</span>; (<b>b</b>) <span class="html-italic">T. yunnanensis</span>; (<b>c</b>) <span class="html-italic">T. sinensis</span>.</p>
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<p>Changes in suitable habitats for <span class="html-italic">T. craveniana</span> under four climate scenarios during three time periods.</p>
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<p>Changes in suitable habitats for <span class="html-italic">T. yunnanensis</span> under four climate scenarios during three time periods.</p>
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<p>Changes in suitable habitats for <span class="html-italic">T. sinensis</span> under four climate scenarios during three time periods.</p>
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<p>Detailed ecological service value of <span class="html-italic">T. craveniana</span>.</p>
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<p>Detailed ecological service value of <span class="html-italic">T. yunnanensis</span>.</p>
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<p>Detailed ecological service value of <span class="html-italic">T. sinensis</span>.</p>
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17 pages, 3202 KiB  
Article
Effects of Freshwater Inflow during the Rainy Season on the Benthic Polychaete Community in the Geum River Estuary, South Korea
by Sang Lyeol Kim, Kyung-Hee Oh, Kongtae Ra and Ok Hwan Yu
Diversity 2024, 16(3), 180; https://doi.org/10.3390/d16030180 - 16 Mar 2024
Cited by 1 | Viewed by 1416
Abstract
In the estuaries of Korea, the freshwater inflow increases rapidly due to the Changma (Korean summer rainy season). To elucidate the effect of this massive freshwater inflow on the benthic polychaete community, a survey was conducted before, during, and after the rainy season. [...] Read more.
In the estuaries of Korea, the freshwater inflow increases rapidly due to the Changma (Korean summer rainy season). To elucidate the effect of this massive freshwater inflow on the benthic polychaete community, a survey was conducted before, during, and after the rainy season. Comparing the environmental characteristics before and after the rainy season, the salinity and dissolved oxygen decreased, the sand content of sediment was significantly reduced, and silt increased. The number of species decreased sharply, and this change was more considerable at sites closer to the estuary. Loimia sp. and Pseudopotamilla sp., the dominant species before the rainy season, were not found after the rainy season. The massive freshwater inflow during the rainy season has been a tremendous stress on the benthic environment and significantly alters the species composition and distribution of benthic polychaetes. Full article
(This article belongs to the Special Issue Dynamics of Marine Communities)
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<p>Sampling area in the Geum River Estuary, Yellow Sea of Korea.</p>
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<p>Ternary plot of sediment composition at the sampling sites (X: clay, Y: silt, Z: sand).</p>
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<p>Vertical distributions of water temperature (°C), salinity (psu), and dissolved oxygen (mg/L) at the sampling sites.</p>
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<p>Density (individuals/m<sup>2</sup>) of polychaete dominant species at the sampling sites (<span class="html-italic">Heteromastus filiformis</span>, <span class="html-italic">Ampharete</span> cf. <span class="html-italic">finmarchica</span>, <span class="html-italic">Loimia</span> sp., <span class="html-italic">Pseudopotamilla</span> sp., <span class="html-italic">Sigambra tentaculata</span>).</p>
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<p>Cluster analysis and multidimensional scaling analysis (MDS) of the fourth-root transformed polychaetes species densities at the sampling sites.</p>
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<p><span class="html-italic">K</span>-dominance curves of the polychaete densities in pre- and post-rainy seasons at the sampling sites.</p>
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<p>Canonical correspondence analysis (CCA) between the nine most abundant polychaete species and seven environmental variables at the sampling sites.</p>
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16 pages, 4923 KiB  
Article
Two New and One First Recorded Species of Xylaria Isolated from Fallen Leaves in Hainan Tropical Rainforest National Park in China
by Xiaoyan Pan, Zongzhu Chen, Jinrui Lei, Xiaohua Chen, Tingtian Wu, Yuanling Li and Yiqing Chen
Diversity 2024, 16(3), 179; https://doi.org/10.3390/d16030179 - 14 Mar 2024
Cited by 1 | Viewed by 2112
Abstract
Xylaria is a widely distributed genus in the Ascomycota phylum that can decompose wood. It is an essential decomposer in ecosystems and a source of bioactive secondary metabolites. Based on morphological characteristics and molecular evidence, this article thoroughly describes two new species discovered [...] Read more.
Xylaria is a widely distributed genus in the Ascomycota phylum that can decompose wood. It is an essential decomposer in ecosystems and a source of bioactive secondary metabolites. Based on morphological characteristics and molecular evidence, this article thoroughly describes two new species discovered on the fallen leaves in Hainan Tropical Rainforest National Park, along with illustrations and comparisons with similar species. Xylaria diaoluoshanensis is characterized by filamentous stromata with long infertile apexes, ascospores sometimes with non-cellular appendages. Xylaria fulvotomentosa differentiates itself from other Xylaria species that grow on fallen leaves by its stroma surface, being yellow tomentose. These two new species of the genus Xylaria were found by phylogenetic analysis using the ITS-β-tubulin-RPB2 sequence dataset. Furthermore, a species first discovered in China, X. petchii, is described. Finally, a search table for 44 species related to fallen leaves and petioles in the world is established. Full article
(This article belongs to the Special Issue Microbiota Diversity in Plants and Forest)
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<p>The ML phylogenetic tree of <span class="html-italic">Xylaria</span> constructed with ITS-β-tubulin-RPB2 sequences. Support values of ML and BI analyses (bootstrap supports ≥ 70% and posterior probability values ≥ 0.95) are indicated above or below the branches. Species related to fallen leaves and petioles are in blue, and those described in this article are in bold.</p>
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<p><span class="html-italic">Xylaria diaoluoshanensis</span> (HAFFR 117). (<b>A</b>) Stromata on leaves; (<b>B</b>,<b>C</b>) stromatal surface and ostioles; (<b>D</b>) section through stroma, showing perithecia; (<b>E</b>,<b>F</b>) ascal apical apparatus in Melzer’s reagent; (<b>G</b>,<b>H</b>) asci in 1% SDS; (<b>I</b>,<b>L</b>,<b>M</b>,<b>Q</b>) ascospores in Melzer’s reagent; (<b>J</b>) ascospore in 1% SDS, with a slightly curved germ slit along almost half of the spore-length; (<b>K</b>) ascospore in water; (<b>N</b>) ascospore in 1% SDS; (<b>O</b>) ascospore in 1% SDS, with nearly spore-length germ slit; (<b>P</b>) ascospores in 1% SDS, presenting non-cellular appendages; (<b>R</b>) ascospore under SEM; scale bars: (<b>A</b>) = 0.5 cm; (<b>B</b>–<b>D</b>) = 200 µm; (<b>E</b>–<b>Q</b>) = 10 µm; (<b>R</b>) = 5 µm.</p>
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<p><span class="html-italic">Xylaria fulvotomentosa</span> (holotype HAFFR 124). (<b>A</b>–<b>C</b>) Stromata on leaves ((<b>C</b>), HAFFR 129); (<b>D</b>–<b>F</b>) stromatal tomentose surface and ostioles ((<b>F</b>), HAFFR 129); (<b>G</b>) section through stroma, showing perithecia; (<b>H</b>,<b>I</b>) asci in Melzer’s reagent; (<b>J</b>) ascus in 1% SDS; (<b>K</b>) ascal apical ring in Melzer’s reagent; (<b>L</b>) ascospores in 1% SDS, showing germ slit; (<b>M</b>,<b>N</b>) ascospores in 1% SDS, with non-cellular appendages; (<b>O</b>,<b>P</b>) ascospores in water; (<b>Q</b>) ascospore under SEM; scale bars: (<b>A</b>) = 0.5 cm; (<b>B</b>–<b>G</b>,<b>I</b>) = 200 µm; (<b>H</b>,<b>J</b>–<b>P</b>) = 10 µm; (<b>Q</b>) = 5 µm.</p>
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<p><span class="html-italic">Xylaria petchii</span> (HAFFR 118). (<b>A</b>,<b>B</b>) Stromata on leaves ((<b>B</b>), HAFFR 57); (<b>C</b>) stromata on branches (HAFFR 60); (<b>D</b>) stromatal surface; (<b>E</b>) ostioles; (<b>F</b>,<b>G</b>) section through stroma, showing perithecia; (<b>H</b>) ascal apical apparatus in Melzer’s reagent; (<b>I</b>,<b>J</b>) asci with apical apparatus in Melzer’s reagent; (<b>K</b>) asci in water; (<b>L</b>) ascospores in 1% SDS, presenting non-cellular appendages; (<b>M</b>) ascospores in Melzer’s reagent; (<b>N</b>) ascospore with a spore-length germ slit in water; (<b>O</b>) ascospore in water; (<b>P</b>) ascospore in Melzer’s reagent, showing a slightly sigmoid germ slit; (<b>Q</b>) ascospore under SEM; scale bars: (<b>A</b>–<b>C</b>) = 0.5 cm; (<b>D</b>–<b>G</b>) = 200 µm; (<b>H</b>,<b>I</b>,<b>L</b>–<b>P</b>) = 10 µm; (<b>J</b>,<b>K</b>) = 25 µm; (<b>O</b>) = 5 µm.</p>
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17 pages, 3383 KiB  
Article
Geography, Climate, and Habitat Shape the Microbiome of the Endangered Rock Gnome Lichen (Cetradonia linearis)
by Julianna Paulsen, Jessica L. Allen, Nathan Morris, Jenna Dorey, Jenifer B. Walke and S. Elizabeth Alter
Diversity 2024, 16(3), 178; https://doi.org/10.3390/d16030178 - 13 Mar 2024
Viewed by 1845
Abstract
Bacterial symbionts are essential components of healthy biological systems. They are increasingly recognized as important factors in the study and management of threatened species and ecosystems. Despite management shifts at the ecosystem level, microbial communities are often neglected in discussions of holobiont conservation [...] Read more.
Bacterial symbionts are essential components of healthy biological systems. They are increasingly recognized as important factors in the study and management of threatened species and ecosystems. Despite management shifts at the ecosystem level, microbial communities are often neglected in discussions of holobiont conservation in favor of the primary members of a symbiosis. In this study, we addressed the bacterial community knowledge gap for one of two federally endangered lichen species in the United States, Cetradonia linearis (Cladoniaceae). We collected 28 samples of the endangered rock gnome lichen (Cetradonia linearis) from 13 sites and characterized bacterial communities in thalli using 16S rRNA metabarcoding to investigate the factors influencing the microbiome composition and diversity within the thallus. We found that Proteobacteria (37.8% ± 10.3) and Acidobacteria (25.9% ± 6.0) were the most abundant phyla recovered. Cyanobacteria were a major component of the microbiome in some individuals, despite this species associating with a green algal symbiont. Habitat, climate, and geography were all found to have significant influences on bacterial community composition. An analysis of the core microbiome at a 90% threshold revealed shared amplicon sequence variants in the microbiomes of other lichens in the family Cladoniaceae. We concluded that the bacterial microbiome of Cetradonia linearis is influenced by environmental factors and that some bacterial taxa may be core to this group. Further exploration into the microbiomes of rare lichen species is needed to understand the importance of bacterial symbionts to lichen diversity and distributions. Full article
(This article belongs to the Section Biodiversity Conservation)
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<p><span class="html-italic">Cetradonia linearis</span> overall habit showing the squamules comprising the main body of the lichen (green and white), sexual reproductive structures called apothecia (Ap), and asexual reproductive structures called pycnidia (Py). The scale bar in the bottom right corner is 3 mm long.</p>
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<p>Global distribution of <span class="html-italic">Cetradonia linearis</span>, showing sampled sites (white circles) and all known occurrences for the species (black circles). The majority of sites from which <span class="html-italic">C. linearis</span> has been documented are in North Carolina in the United States of America.</p>
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<p>Relative abundances of bacterial phyla with &gt;0.1% mean abundance per sample and samples organized according to mountain range. All lineages with &lt;0.1% relative abundances were removed from the dataset.</p>
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<p>Relative abundance of Cyanobacterial orders in sampled individuals. Abundances range from zero (dark purple) to 0.214 (bright yellow).</p>
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<p>Prevalence of the core constituents of the microbiome of <span class="html-italic">Cetradonia linearis</span>, defined as any bacterial ASV that was present at any abundance in at least 90% of the samples. Taxonomic assignments were deduced according to the Silva classifier and are shown on the left. Prevalences ranged from 0.0 (blue) to 1.0 (red) and refers to the proportion of samples that contained an ASV at a given detection threshold, indicated by the X-axis.</p>
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<p>Habitat strongly shapes bacterial diversity and community structure. (<b>A</b>) Bacterial communities in cliff-dwelling individuals were more diverse than those in streams (cliff n = 18, stream n = 10, Kruskal-Wallis, <span class="html-italic">p</span>-value = 0.049). (<b>B</b>) Bacterial communities in each habitat type were significantly different from each other (PERMANOVA, <span class="html-italic">p</span>-value = 0.001).</p>
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17 pages, 1181 KiB  
Systematic Review
A Systematic Review of Population Monitoring Studies of Sea Turtles and Its Application to Conservation
by Haley Hendrix and Sílvia Pérez-Espona
Diversity 2024, 16(3), 177; https://doi.org/10.3390/d16030177 - 12 Mar 2024
Viewed by 5118
Abstract
Sea turtles are keystone species in marine environments due to their essential role as seagrass grazers and population regulation of jellyfish and sponges in coral reefs. However, due to their predominant presence in coastal areas, sea turtle populations face significant threats due to [...] Read more.
Sea turtles are keystone species in marine environments due to their essential role as seagrass grazers and population regulation of jellyfish and sponges in coral reefs. However, due to their predominant presence in coastal areas, sea turtle populations face significant threats due to the impact of human activities. In this systematic review, 655 peer-reviewed publications were analyzed to assess the extent of population monitoring for all seven sea turtle species. The analyses revealed that, although population monitoring studies have increased for sea turtles in the past four decades, these have been biased towards certain species and oceanic regions. Furthermore, sea turtle population monitoring has been undertaken primarily using field-based methods, with satellite tracking and nest surveys being the most commonly used methods; however, the implementation of genetic methods for population monitoring has increased since the 2000s. Direct conservation recommendations from this study include the urgent need to establish population monitoring studies in the Critically Endangered Kemp’s ridley and hawksbill and the Data Deficient flatback. Furthermore, population monitoring programs should be implemented in Southeast Asia and Northern and Central Africa, where knowledge on sea turtle populations is still limited. Finally, due to the long-distance movements of sea turtles, we also advocate for international cooperation and collaboration of local communities to protect these ecologically important and iconic marine species. Full article
(This article belongs to the Special Issue Genetic Diversity, Ecology and Conservation of Endangered Species)
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<p>Annual trends of the variables assessed from sea turtle population monitoring studies (including population characterization): the total number of publications/studies (<b>a</b>), oceanic regions (<b>b</b>), studies per IUCN conservation status (<b>c</b>), population parameters (<b>d</b>), top five most used field-based methods (<b>e</b>), use of genetic vs. field-based monitoring (<b>f</b>), top five most used genetic markers (<b>g</b>). Statistical significance for all the time series was confirmed by Mann–Kendall tests (<span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Heat map illustrating the sea turtle population monitoring (including population characterization) effort per coastal region. Colors range from green (low number of studies) to yellow to red (high number of studies). This heat map does not include far-reaching studies (i.e., migratory path studies), as these studies covered entire oceanic regions and cannot be pinpointed to one location. Map prepared with Maptive.</p>
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<p>Percentage of population monitoring studies (including population characterization) that indicated significant positive or stable population trends per species (top graph) or decreasing population trends (bottom graph). Grey bars indicate reporting of those trends before each species’ most recent IUCN Red List species assessment; black bars indicate reporting of significant population trends after the most recent IUCN Red List species assessment.</p>
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<p>Duration (in years) of sea turtle population monitoring studies employing field-based methods. The Y-axis represents the total number of studies per study duration time category.</p>
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12 pages, 5011 KiB  
Article
Effects of Invasive Smooth Cordgrass Degradation on Avian Species Diversity in the Dafeng Milu National Nature Reserve, a Ramsar Wetland on the Eastern Coast of China
by Taiyu Chen, Pan Chen, Bing Liu, Dawei Wu and Changhu Lu
Diversity 2024, 16(3), 176; https://doi.org/10.3390/d16030176 - 12 Mar 2024
Cited by 1 | Viewed by 1400
Abstract
Invasive smooth cordgrass (Spartina alterniflora) has been expanding rapidly through the coastal wetlands of eastern China and these changes negatively affect local birds. In the Dafeng Milu National Nature Reserve (henceforth referred to as DMNNR), rapid degradation of spartina occurs after [...] Read more.
Invasive smooth cordgrass (Spartina alterniflora) has been expanding rapidly through the coastal wetlands of eastern China and these changes negatively affect local birds. In the Dafeng Milu National Nature Reserve (henceforth referred to as DMNNR), rapid degradation of spartina occurs after an increase in milu (Elaphures davidianus; hereafter elk) numbers and ecological hydrological engineering. We evaluated the impact of such degradation on the abundance and species diversity of birds in the DMNNR during 2017–2021. We found that the area covered by S. alterniflora decreased significantly in the study area at a rate of 310 ha per year and by 62% during 2017–2021 (p < 0.01). With this decrease in the S. alterniflora area, the species richness and abundance of birds first increased and then decreased. Songbird density clearly decreased but species richness did not significantly do so. This research demonstrated that during the initial stages of vegetation degradation, there was a positive effect on bird diversity. With the increasing vegetation degradation increases, both songbirds and waterbirds experience negative impacts. The DMNNR is an important stopover site for waterbirds in the East Asian–Australasian Flyway, and additional measures are needed to control vegetation degradation and to restore the native habitats for birds. Full article
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<p>Study site in the Yancheng coastal wetland, Jiangsu Province, China.</p>
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<p>Vegetation coverage change during 2017–2021 in the DMNNR.</p>
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<p>The spartina area in the DMNNR was modeled via linear regression during 2017–2021.</p>
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<p>Species richness of birds in different groups observed over 5 years, from 2017 to 2021, in the DMNNR.</p>
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<p>Mean bird densities (±SE) of various bird groups in the five years.</p>
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<p>Correspondence analysis of habitat types and bird species in the DMNNR. The regular triangles represent habitat types; the solid circles represent different bird species. Waterbird species were classified into four groups: (<b>a</b>) swan, goose, and duck; (<b>b</b>) shorebird; (<b>c</b>) songbird; and (<b>d</b>) others.</p>
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13 pages, 3228 KiB  
Article
Structure from Motion Photogrammetry as an Effective Nondestructive Technique to Monitor Morphological Plasticity in Benthic Organisms: The Case Study of Sarcotragus foetidus Schmidt, 1862 (Porifera, Demospongiae) in the Portofino MPA
by Torcuato Pulido Mantas, Camilla Roveta, Barbara Calcinai, Fabio Benelli, Martina Coppari, Cristina Gioia Di Camillo, Ubaldo Pantaleo, Stefania Puce and Carlo Cerrano
Diversity 2024, 16(3), 175; https://doi.org/10.3390/d16030175 - 8 Mar 2024
Cited by 2 | Viewed by 2066
Abstract
Porifera are essential components of marine ecosystems, providing valuable ecological functions. Traditional approaches to estimating sponge growth and biomass are destructive and often not suitable for certain morphologies. The implementation of new innovative techniques and nondestructive methodologies have allowed for a more sustainable [...] Read more.
Porifera are essential components of marine ecosystems, providing valuable ecological functions. Traditional approaches to estimating sponge growth and biomass are destructive and often not suitable for certain morphologies. The implementation of new innovative techniques and nondestructive methodologies have allowed for a more sustainable approach. In this study, a population of Sarcotragus foetidus Schmidt, 1982 (Demospongiae, Dictyoceratida, Irciinidae), thriving inside the Portofino Marine Protected Area, was monitored using Structure from Motion photogrammetry over a period of 6 years, from September 2017 to October 2023. Of the 20 initial individuals, only 12 were still in place during the last monitoring, indicating 40% mortality. Through photogrammetry, the overall volume change and biomass production were estimated to be 9.24 ± 5.47% year−1 and 29.52 ± 27.93 g DW year−1, respectively, indicating a general decreasing trend between 2021 and 2023. Signs of necrosis were observed in some individuals, potentially related to the high temperature occurring during summer 2022 and 2023. Considering the current climate crisis, long-term monitoring efforts must be made to better understand the dynamics of this species, and photogrammetry has the potential to be a versatile monitoring tool that will contribute to the standardization of methodologies for sponge growth studies. Full article
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<p>(<b>a</b>) Map indicating the location of Punta del Faro (Portofino MPA, Italy). (<b>b</b>) Three-dimensional reconstruction of the submerged part of the area of interest. The boulder where the <span class="html-italic">Sarcotragus foetidus</span> population was monitored is outlined in red and indicated by a red arrow. (<b>c</b>) Details of the surveyed boulder and the exact location of each sponge individual marked with a white “X”. Sponges considered for the volume change analysis are circled in white, while individuals affected by mortality are circled in red.</p>
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<p>(<b>a</b>–<b>c</b>) Examples of the 3D reconstructions produced for three <span class="html-italic">Sarcotragus foetidus</span> individuals over three monitoring time steps (September 2017, t<sub>1</sub>; November 2021, t<sub>2</sub>; and October 2023, t<sub>3</sub>). Scale bars = 10 cm.</p>
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<p><span class="html-italic">(</span><b>a</b>–<b>c</b>) Distances calculated between the 3D models of <span class="html-italic">Sarcotragus foetidus</span> obtained for t<sub>1</sub>–t<sub>2</sub> (September 2017–November 2021) on the left and t<sub>2</sub>–t<sub>3</sub> (November 2021–October 2023) on the right. Comparisons calculated using point cloud distances in Cloud Compare. Scale bars = 10 cm.</p>
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<p>Particular cases regarding the 3D assessment of <span class="html-italic">Sarcotragus foetidus</span> changes during this study. (<b>a</b>) <span class="html-italic">S. foetidus</span> individual affected by necrosis during the t<sub>2</sub>–t<sub>3</sub> (November 2021–October 2023) period; (<b>b</b>) <span class="html-italic">S. foetidus</span> individual affected by a high level of epibiosis by <span class="html-italic">Padina pavonica</span>, preventing an accurate t<sub>1</sub>–t<sub>2</sub> (September 2017–November 2021) 3D change assessment. Scale bars = 10 cm.</p>
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<p>(<b>a</b>) <span class="html-italic">Sarcotragus foetidus</span> estimated yearly volume changes (%) for the two periods of this study: t<sub>1</sub>–t<sub>2</sub> (September 2017–November 2021) and t<sub>2</sub>–t<sub>3</sub> (November 2021–October 2023). (<b>b</b>) Boxplots depicting the sea surface temperatures (SSTs) recorded in the Portofino MPA during the summer periods (from 21 June to 22 September) of each monitoring year; the jittered points represent the underlying distribution of the SST data.</p>
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<p>Growth phases of <span class="html-italic">Sarcotragus foetidus</span>: (<b>a</b>) initial growth phase of a cushion-shaped specimen; (<b>b</b>) specimen where sediments accumulating in the center of the sponge trigger reshaping through a central depression; (<b>c</b>) with the enlargement of the cavity, sediments are released on the sea floor and the sponge takes on a ring shape; (<b>d</b>) the continuous growth of the sponge leads to a perforated horseshoe shape. Although observed in several other areas, (<b>c</b>,<b>d</b>) are virtually reconstructed images of the potential development of the monitored individuals.</p>
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11 pages, 3701 KiB  
Article
Spatial Distribution Pattern of the Mesozooplankton Community in Ross Sea Region Marine Protected Area (RSR MPA) during Summer
by Sung Hoon Kim, Wuju Son, Jeong-Hoon Kim and Hyoung Sul La
Diversity 2024, 16(3), 174; https://doi.org/10.3390/d16030174 - 8 Mar 2024
Cited by 1 | Viewed by 1245 | Correction
Abstract
The Ross Sea region Marine Protected Area (RSR MPA) is one of the most productive regions in the Southern Ocean. Mesozooplankton intermediates the primary product to the higher predators, such as penguins and seals, in this ecosystem. In this study, the mesozooplankton community [...] Read more.
The Ross Sea region Marine Protected Area (RSR MPA) is one of the most productive regions in the Southern Ocean. Mesozooplankton intermediates the primary product to the higher predators, such as penguins and seals, in this ecosystem. In this study, the mesozooplankton community structure and spatial pattern in the RSR MPA in January were investigated by using 505 μm-mesh-size bongo net samples. As a result, 37 mesozooplankton taxa with a total mean abundance of 35.26 ind./m3, ranging from 2.94 to 139.17 ind./m3, were confirmed. Of the 37 taxa, 7 occupied almost 84% of the total abundance, with copepods being the main dominant taxa. As shown by our hierarchical analysis, the mesozooplankton community was divided into four groups, each associated with a specific geographical distribution. Group A was composed of stations around Terra Nova Bay and showed relatively low abundance. Group B included stations around the continental slope region. Group D was composed of the Ross Sea continental shelf stations, while group C consisted of stations geographically located between those of groups B and D. These four groups were influenced by various environmental factors, such as water temperature, salinity, and nutrients. In summary, the mesozooplankton community can be separated according to geographical pattern. This pattern is related to several environmental factors. Full article
(This article belongs to the Special Issue Dynamics of Marine Communities)
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<p>Map showing the survey region (red frame) and sampling stations (blue circles) within the RSR MPA from 17 January to 1 February 2023.</p>
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<p>Spatial pattern of the surface environmental parameters in the RSR MPA.</p>
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<p>Spatial pattern of the average environmental parameters in the RSR MPA.</p>
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<p>Comparison of the abundance (ind./m<sup>3</sup>) values of the dominant taxa at each sampling station.</p>
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<p>A dendrogram (<b>A</b>) based on the mesozooplankton abundance and a map (<b>B</b>) showing the separated groups based on the CLUSTER analysis.</p>
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<p>Canonical analysis of principal coordinates (CAP) plots according to the mesozooplankton abundance data showing correlations with the dominant species (<b>A</b>) and environmental parameters (<b>B</b>). Ai, Appendicularia indet.; Ca, <span class="html-italic">Calanoides acutus</span>; Cn, Cirriped nauplius; Cp, <span class="html-italic">Calanus propinquus</span>; Ec, <span class="html-italic">Euphausia</span> calyptopis; Fl, Fish larvae; Lr, <span class="html-italic">Limacina rangii</span>; Mg, <span class="html-italic">Metridia gerlachei</span>; Oi, Ostracoda indet.; Os, <span class="html-italic">Oithona</span> spp.; Pa, <span class="html-italic">Paraeuchaeta antarctica</span>; Pl, Polychaeta larvae; Ss, <span class="html-italic">Sagitta</span> sp.; S2, Siphonophore 2; Ta, <span class="html-italic">Triconia antarctica</span>.</p>
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14 pages, 4320 KiB  
Review
Nanopore Sequencing Technology as an Emerging Tool for Diversity Studies of Plant Organellar Genomes
by Jakub Sawicki, Katarzyna Krawczyk, Łukasz Paukszto, Mateusz Maździarz, Mateusz Kurzyński, Joanna Szablińska-Piernik and Monika Szczecińska
Diversity 2024, 16(3), 173; https://doi.org/10.3390/d16030173 - 7 Mar 2024
Cited by 2 | Viewed by 3009
Abstract
In this comprehensive review, we explore the significant role that nanopore sequencing technology plays in the study of plant organellar genomes, particularly mitochondrial and chloroplast DNA. To date, the application of nanopore sequencing has led to the successful sequencing of over 100 plant [...] Read more.
In this comprehensive review, we explore the significant role that nanopore sequencing technology plays in the study of plant organellar genomes, particularly mitochondrial and chloroplast DNA. To date, the application of nanopore sequencing has led to the successful sequencing of over 100 plant mitochondrial genomes and around 80 chloroplast genomes. These figures not only demonstrate the technology’s robustness but also mark a substantial advancement in the field, highlighting its efficacy in decoding the complex and dynamic nature of these genomes. Nanopore sequencing, known for its long-read capabilities, significantly surpasses traditional sequencing techniques, especially in addressing challenges like structural complexity and sequence repetitiveness in organellar DNA. This review delves into the nuances of nanopore sequencing, elaborating on its benefits compared to conventional methods and the groundbreaking applications it has fostered in plant organellar genomics. While its transformative impact is clear, the technology’s limitations, including error rates and computational requirements, are discussed, alongside potential solutions and prospects for technological refinement. Full article
(This article belongs to the Special Issue 2024 Feature Papers by Diversity’s Editorial Board Members)
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<p>Comparison of mapping simplex and duplex reads onto <span class="html-italic">acc</span>D gene of <span class="html-italic">Riccia fluitans</span> plastome.</p>
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<p>Plant organellar genomes in GenBank database sequenced using nanopore technology.</p>
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<p>Coverage fluctuation of plastid genome assemblies using native and enriched DNA. The various bryophyte plastid genomes of similar lengths (ca 120 kbp) were sequenced using different approaches. From top to bottom: <span class="html-italic">Apopellia endiviifolia</span> (without enrichment), <span class="html-italic">Scapania undulata</span> (with organellar DNA enriched using bead-based method), <span class="html-italic">Orthotrichum cupulatum</span> (total DNA enrichment via standard PCR), <span class="html-italic">Riccia fluitans</span> (DNA enrichment using rolling circle amplification), and <span class="html-italic">Riccia glauca</span> (adaptative sampling using <span class="html-italic">Riccia fluitans</span> plastome as a reference).</p>
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<p>Possible workflows in sequencing plant organellar genomes using nanopore technology. Asterisk indicates optional samples multiplexing.</p>
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18 pages, 1747 KiB  
Article
Low Resource Competition, Availability of Nutrients and Water Level Fluctuations Facilitate Invasions of Australian Swamp Stonecrop (Crassula helmsii)
by Hein H. van Kleef, Janneke M. M. van der Loop and Laura S. van Veenhuisen
Diversity 2024, 16(3), 172; https://doi.org/10.3390/d16030172 - 7 Mar 2024
Cited by 1 | Viewed by 1386
Abstract
Australian swamp stonecrop (Crassula helmsii (Kirk) Cockayne) is invasive in Western Europe. Its small size and high potential for regeneration make it difficult to eliminate. Short-term experiments have demonstrated that the growth of C. helmsii depends on nutrient availability and resource competition. [...] Read more.
Australian swamp stonecrop (Crassula helmsii (Kirk) Cockayne) is invasive in Western Europe. Its small size and high potential for regeneration make it difficult to eliminate. Short-term experiments have demonstrated that the growth of C. helmsii depends on nutrient availability and resource competition. In order to confirm those mechanisms in the field, we studied the abundance of C. helmsii in Northern Europe over a longer period of time in relation to nutrient availability and co-occurring plant communities and plant species. C. helmsii impacted native species mainly by limiting their abundance. The native plant species present indicated that previous or periodic elevated nutrient availability were likely responsible for the proliferation of C. helmsii. When growing in submerged conditions, the dominance of C. helmsii depended on a high availability of CO2. A series of exceptionally dry summers allowed C. helmsii to increase in cover due to weakened biotic resistance and a loss of carbon limitation. Only Littorella uniflora (L.) Asch. and Juncus effusus L. were able to remain dominant and continue to provide biotic resistance. Based on our findings, minimizing nutrient (C and N) availability and optimizing hydrology provides native species with stable growth conditions. This optimizes resource competition and may prevent the proliferation of C. helmsii. Full article
(This article belongs to the Special Issue Emerging Alien Species and Their Invasion Processes)
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<p>Cover (%) and biomass (grams dry weight per m<sup>2</sup>, note: logarithmic scale on the y-axis) of <span class="html-italic">Crassula helmsii</span> in study sites (N = 71). Line describes relationship between <span class="html-italic">C. helmsii</span> cover and biomass (as in Equation (3)) with 95% confidence intervals.</p>
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<p>Relation between relative biomass of <span class="html-italic">Crassula helmsii</span> and nutrient availability of the ecosystem, as indicated by the identity and cover of the species present. (<b>A</b>) Aquatic sites; (<b>B</b>) terrestrial sites. Low: Mean Ellenberg value of N &lt; 4; high: Mean Ellenberg value of N ≥ 4. * <span class="html-italic">W</span>(32) = 215; <span class="html-italic">p</span> = 0.014 Wilcoxon rank-sum exact test. NS: <span class="html-italic">W</span>(35) = 134; <span class="html-italic">p</span> = 0.987 Wilcoxon rank-sum exact test.</p>
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<p>Bivariate plots between change in species richness (<b>A</b>), species- (<b>B</b>) and abundance-based turnover (<b>C</b>) and change in cover of <span class="html-italic">Crassula helmsii</span>.</p>
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16 pages, 1614 KiB  
Review
A Comprehensive Review of Disease-Causing Agents in Freshwater Turtles: Implications for Conservation and Public Health
by João Rato, Raquel Xavier, D. James Harris, Filipe Banha and Pedro Anastácio
Diversity 2024, 16(3), 171; https://doi.org/10.3390/d16030171 - 7 Mar 2024
Viewed by 2624
Abstract
Freshwater turtles comprise 81% of all chelonian species despite freshwater systems only occupying 1% of the earth’s surface, and they are commonly exploited as pets and food resources. This contact between humans and turtles may put both sides at risk of disease transmission. [...] Read more.
Freshwater turtles comprise 81% of all chelonian species despite freshwater systems only occupying 1% of the earth’s surface, and they are commonly exploited as pets and food resources. This contact between humans and turtles may put both sides at risk of disease transmission. Additionally, human impact on ecosystems can cause disease outbreaks in turtle populations. In this review, we focused on disease agents affecting freshwater turtles, intending to contribute to conservation and public health efforts. We analysed 423 articles and noted a post-SARS-COVID-19 peak, with most research originating from Asia, North America, and Europe. Emydidae was the most frequently studied family, and there was also a bias towards adults, live specimens, and native species. Since most of the studied turtles were wild-caught, we recommend that captive turtles should also be thoroughly studied since they can transmit diseases to other turtles and humans. We registered 2104 potential disease-causing agents, with Platyhelminthes dominating within Animalia, while Proteobacteria dominated bacterial agents. Viruses’ representation was low, highlighting gaps in reptile virology. Fungi, Chromista, and Protozoa were also underrepresented, but this is changing with the development of molecular tools. This synthesis serves as a foundation for targeted health assessments, conservation strategies, and future research, essential to mitigate ecosystem and public health threats. Full article
(This article belongs to the Special Issue 2024 Feature Papers by Diversity’s Editorial Board Members)
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<p>The process of the literature review, which includes three different stages: identification, screening, and inclusion. At the identification stage, all Google Scholar, Scopus, and Web of Science search results were gathered. Next, at the screening stage, all search results that did not meet the criteria were excluded. In the final analyses, only 423 were included.</p>
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<p>Yearly distribution of publications involving disease agents in freshwater turtles.</p>
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<p>World distribution of publications. The darker red represents a higher number of publications per square kilometer and the lighter red represents a lower number of publications per square kilometer. White-coloured countries did not have any publications.</p>
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<p>Number of publications for each family of freshwater turtles and the total number of turtle species in each family according to Uetz et al. [<a href="#B2-diversity-16-00171" class="html-bibr">2</a>]. The total number of hosts is more than the total number of publications because several publications refer to more than one turtle species.</p>
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<p>Number of publications for each potential disease agent. The combined number of publications is higher than the total number of publications because many publications refer to more than one disease agent.</p>
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<p>Yearly distribution of the cited disease agents for each 5 years period (e.g., 1935–1939). The number of disease agents is higher than the total number of publications because many publications refer to more than one disease agent.</p>
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52 pages, 3850 KiB  
Article
Checklist of Basidiomycota and New Records from the Azores Archipelago
by Martin Souto, Pedro Miguel Raposeiro, Ana Balibrea and Vítor Gonçalves
Diversity 2024, 16(3), 170; https://doi.org/10.3390/d16030170 - 7 Mar 2024
Viewed by 2854
Abstract
This paper presents an annotated checklist of the Basidiomycota taxa (including lichenicolous fungi and the subdivision Pucciniomycotina) from the Azores archipelago and reviews the published records to account for their taxonomic status. The number of Basidiomycota species recorded in the Azores has increased [...] Read more.
This paper presents an annotated checklist of the Basidiomycota taxa (including lichenicolous fungi and the subdivision Pucciniomycotina) from the Azores archipelago and reviews the published records to account for their taxonomic status. The number of Basidiomycota species recorded in the Azores has increased considerably during the 20th century and now stands at 544 species. This study provides distribution data and includes changes in the nomenclature of the listed taxa. Sampling campaigns contributed to 116 new records of Basidiomycota for the Azores archipelago. In addition, there were new records for eight islands: 162 species found for the first time on São Miguel Island, 55 species new to Santa Maria Island, 33 species new to Flores Island, 15 species new to Terceira Island, 9 species new to Pico Island, 17 species new to São Jorge Island, 4 species new to Graciosa Island, and 2 species new to Corvo Island. The transformation of vegetation cover in the archipelago has been very drastic, and this is reflected in the presence of many foreign fungal species on the islands. From these data, we conclude that within Macaronesia, the diversity of Basidiomycota in the Azores is more similar to that in Madeira than in the Canary Islands. Full article
(This article belongs to the Section Microbial Diversity and Culture Collections)
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<p>Location of the 45 sampling sites on the islands of the Azores archipelago.</p>
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<p>Basidiomycota diversity of the Azores archipelago: (<b>a</b>) Eocronartium muscicola; (<b>b</b>) Roridomyces roridus; (<b>c</b>) Entoloma chalybeum; (<b>d</b>) Tremellodendropsis tuberosa; (<b>e</b>) Phylloporus rhodoxanthus; (<b>f</b>) Myxarium nucleatum; (<b>g</b>) Boletus reticulatus; (<b>h</b>) Leucocoprinus cepistipes; (<b>i</b>) Mutinus ravenelii.</p>
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<p>Number of previous and new records of Basidiomycota for each Azorean Island and archipelago. STM—Santa Maria Island; SMG—São Miguel Island; TER—Terceira Island; GRA—Graciosa Island; SJG—São Jorge Island; PIC—Pico Island; FAI—Faial Island; FLO—Flores Island; COR—Corvo Island; AZO—Azores archipelago.</p>
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<p>Evolution of knowledge. The total number (line) and new records (bars) of Basidiomycota species in the Azores archipelago from 1874 to 2023. References: Bk [<a href="#B7-diversity-16-00170" class="html-bibr">7</a>], T [<a href="#B9-diversity-16-00170" class="html-bibr">9</a>], B [<a href="#B10-diversity-16-00170" class="html-bibr">10</a>], TW [<a href="#B11-diversity-16-00170" class="html-bibr">11</a>], A [<a href="#B12-diversity-16-00170" class="html-bibr">12</a>], V [<a href="#B13-diversity-16-00170" class="html-bibr">13</a>], CL [<a href="#B126-diversity-16-00170" class="html-bibr">126</a>], H [<a href="#B127-diversity-16-00170" class="html-bibr">127</a>], GD [<a href="#B14-diversity-16-00170" class="html-bibr">14</a>], D [<a href="#B8-diversity-16-00170" class="html-bibr">8</a>] GS [<a href="#B16-diversity-16-00170" class="html-bibr">16</a>], GH [<a href="#B128-diversity-16-00170" class="html-bibr">128</a>], SB [<a href="#B18-diversity-16-00170" class="html-bibr">18</a>], BA [<a href="#B47-diversity-16-00170" class="html-bibr">47</a>], RS [<a href="#B19-diversity-16-00170" class="html-bibr">19</a>,<a href="#B20-diversity-16-00170" class="html-bibr">20</a>], ME [<a href="#B23-diversity-16-00170" class="html-bibr">23</a>], BP [<a href="#B48-diversity-16-00170" class="html-bibr">48</a>], TE [<a href="#B24-diversity-16-00170" class="html-bibr">24</a>], A [<a href="#B129-diversity-16-00170" class="html-bibr">129</a>], C [<a href="#B33-diversity-16-00170" class="html-bibr">33</a>], BO [<a href="#B52-diversity-16-00170" class="html-bibr">52</a>], I [<a href="#B34-diversity-16-00170" class="html-bibr">34</a>], D [<a href="#B55-diversity-16-00170" class="html-bibr">55</a>], and S (Souto et al.; this paper).</p>
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<p>Venn diagram and Sørensen-Dice Quotient of Similarity (QS) showing Basidiomycota species diversity in the Macaronesia archipelagos.</p>
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<p>Relative species richness of Basidiomycota ecological groups in the Azores.</p>
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<p>Diagram representing the species number of the main groups of Basidiomycota in Macaronesia.</p>
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13 pages, 3442 KiB  
Article
Application of Univariate Diversity Metrics to the Study of the Population Ecology of the Lizard Lacerta bilineata in an Ecotonal Habitat
by Roger Meek and Luca Luiselli
Diversity 2024, 16(3), 169; https://doi.org/10.3390/d16030169 - 7 Mar 2024
Cited by 1 | Viewed by 1422
Abstract
The expansion of human activities across natural environments is now well known. This includes agricultural activities that effectively render many former natural environments sterile habitats for animals. Very often, what remains of the natural habitat are hedgerows that serve as habitat or pathways [...] Read more.
The expansion of human activities across natural environments is now well known. This includes agricultural activities that effectively render many former natural environments sterile habitats for animals. Very often, what remains of the natural habitat are hedgerows that serve as habitat or pathways for movement between habitats for many species, including reptiles. In this study, we describe population changes in the western green lizard, Lacerta bilineata, in a hedgerow system in western France. The results are derived from a univariate diversity analysis of photographic data to identify individual lizards over a 4-year study period. Lizards were sighted from March April to October early November but there was a midsummer gap in sightings during July–August. The annual presence of individual lizards was low, both between and within years, but based on the diversity analysis, the overall stability of the population was high. Female numbers varied and were highest in 2020, but juveniles were highest in 2023; the numbers of males present each year were approximately the same. Individual lizards that were present before the midsummer gap were mostly absent after the midsummer gap and were replaced by new individuals. Incidences of autotomy were low in males and juveniles and were not recorded in females. In general, the results suggest that the lizards move through hedgerow systems but remain in a specific section for reproduction from March to July. Through this study, we also highlight the importance of univariate diversity formulas to obtain robust results in investigations of the demographic aspects of animal populations that are easy to monitor. Full article
(This article belongs to the Special Issue Herpetofauna of Eurasia)
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<p>Google Earth map showing the section of study hedgerow surveyed (colored lines) and the extent of the adjoining hedgerow, woodland and extensive agriculture. A ground view is shown below with arrows indicating the direction of the photograph.</p>
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<p>Examples of the diversity of lizard markings used for identification. Males are in (<b>A</b>,<b>B</b>) with (<b>B</b>) showing a male with recent tail loss. At the bottom are a second year juvenile (<b>C</b>) and a female from 2023 (<b>D</b>).</p>
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<p>Annual numbers of lizards identified in each year (x-axis) plotted against the frequency of their sightings. Black bars represent males, grey represents females, and white bars represent juveniles.</p>
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<p>Annual sighting frequencies of individual lizards by month. Black bars represent males, grey bars represent females, and white bars represent juveniles.</p>
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<p>Graph on semi-logarithmic coordinates, showing the relationship between the number of sighting frequencies of individual lizards and the maximum number of days between their first and final annual sightings within each year. The line running through the data represent the regression equation derived from the pooled male/juvenile data. A number of data points at low numbers of sightings (e.g., below 5 on the x axis) represent more than one data point. See <a href="#diversity-16-00169-t003" class="html-table">Table 3</a> and the text for more details.</p>
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15 pages, 4750 KiB  
Article
The Potential of Foraging Chacma Baboons (Papio ursinus) to Disperse Seeds of Alien and Invasive Plant Species in the Amathole Forest in Hogsback in the Eastern Cape Province, South Africa
by Lwandiso Pamla, Loyd R. Vukeya and Thabiso M. Mokotjomela
Diversity 2024, 16(3), 168; https://doi.org/10.3390/d16030168 - 6 Mar 2024
Cited by 1 | Viewed by 2247
Abstract
The invasion of alien and invasive plants into the threatened Amathole Forest in Hogsback, Eastern Cape Province (South Africa) is an emerging priority conservation issue. The objective of this pilot study was to document and compare the foraging visits of two chacma baboon [...] Read more.
The invasion of alien and invasive plants into the threatened Amathole Forest in Hogsback, Eastern Cape Province (South Africa) is an emerging priority conservation issue. The objective of this pilot study was to document and compare the foraging visits of two chacma baboon (Papio ursinus) troops in their natural and human habitats and their foraging behavioural activities to understand their potential to disperse ingested alien seeds in Hogsback. We also estimated the number of seeds per faecal sample collected from the foraging trails of the two troops of baboons, and determined potential dispersal distances using allometric equations. Since the focal troops used preferred sleeping and foraging sites, we predicted that these sites would have a high concentration of propagules. We applied the normalised difference vegetation index (NDVI) to discern possible vegetation cover changes. Overall, the two chacma baboon troops showed a similar number of daily foraging visits, although they preferred to forage more in human-modified than natural habitats. Their feeding and moving activities were significantly greater than other activities recorded during the study. There were significant differences in the numbers of seeds of six different fruiting plant species: 82.2 ± 13.3% (n = 284) for Acacia mearnsii; 78.9 ± 12.1% (n = 231) for Pinus patula, and 64.0 ± 20.0% (n = 108) for Solanum mauritianum. The two baboon troops could transport about 445 536 seeds from the six focal fruiting plant species considered in this study. Baboons’ seed dispersal distances were long at > 5 km per daily foraging activity. The NVDI vegetation cover analysis (i.e., 1978–2023) shows that the dense vegetation cover expanded by 80.9 ha, while the moderate and sparse vegetation cover collectively decreased by 10.3 ha. Although the seed dispersal pattern was neither clumped nor displayed any recognisable pattern, against our prediction, the number of faecal samples containing alien seeds and the observed foraging movement patterns suggest that chacma baboons disperse alien plant seeds that may establish and facilitate the deterioration of the natural forest. Further quantitative studies investigating the diversity of the plant species dispersed, their germination rates after ingestion by baboons, and their seasonal patterns are required to understand the baboon seed dispersal systems in the Amathole forests of Hogsback. Full article
(This article belongs to the Special Issue Emerging Alien Species and Their Invasion Processes)
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<p>Map of Hogsback study site (red box) in Eastern Cape, South Africa (<b>A</b>). (<b>B</b>) shows the vegetation types, and (<b>C</b>) shows the natural and human environments within the study site.</p>
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<p>Male chacma baboon on the edge of the mountain, Hogsback in Eastern Cape Province, South Africa (picture: Ken Harvey).</p>
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<p>Foraging paths of the focal baboon troops. The red colour shows Nola’s troop’s range, and the blue colour shows Evie’s troop’s range. The orange polygon shows the overlap between the foraging home ranges of the two troops.</p>
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<p>Chacma baboon faecal sample that is not crushed (<b>above</b>) and crushed with a stick (<b>below</b>) containing seeds processed during foraging.</p>
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<p>Daily mean foraging visits frequency of Evie’s and Nola’s troops in the human-modified and natural habitats. The standard error is represented by the bars.</p>
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<p>Variation in the normalised difference vegetation index for Hogsback areas (the study site) between 1978 and 2023.</p>
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13 pages, 3691 KiB  
Article
Ascaridoid Nematodes Infection in Anadromous Fish Coilia nasus from Yangtze River
by Qingjie Zhou, Lijun Wang, Bingwen Xi, Congping Ying and Kai Liu
Diversity 2024, 16(3), 167; https://doi.org/10.3390/d16030167 - 6 Mar 2024
Viewed by 1728
Abstract
The longjaw tapertail anchovy Coilia nasus, which migrates from ocean to freshwater for spawning in spring, is an important anadromous fish with ecological and cultural significance. To determine parasite infection in anadromous C. nasus, a total of 103 fish from the [...] Read more.
The longjaw tapertail anchovy Coilia nasus, which migrates from ocean to freshwater for spawning in spring, is an important anadromous fish with ecological and cultural significance. To determine parasite infection in anadromous C. nasus, a total of 103 fish from the Yangtze River were collected and examined in 2021 and 2022. The overall infection prevalence of nematodes in C. nasus was 100%, with a mean intensity of 13.81 ± 16.45. The mean intensity of nematode infections in 2022 was significantly higher than that observed in 2021 across all sampling sites (p < 0.05). Nematodes were widely detected in the mesentery, pyloric cecum, stomach, and liver, among which the mesentery accounted for the highest proportion, reaching up to 53.52%. A total of eight ascaridoid nematodes belonging to the family Anisakidae and Raphidascarididae were identified by using morphological characters and molecular biological techniques, including two species of Anisakis, five species of Hysterothylacium, and one species of Raphidascaris. A. pegreffii was found as the predominant species, accounting for 48.65% of all identified parasitic nematodes in liver, while Raphidascaris sp. was the most common nematode in the mesentery, pyloric cecum, and stomach, reaching up to 39.81%, 36.21%, and 74.36%, respectively. The present study systematically investigated the parasitic status and community structure of the nematode in C. nasus during its migration in the Yangtze River. This research provides a foundation for studying the impact of nematode parasitism on the reproductive migration and population recruitment of C. nasus, and offers valuable insights for biomarker screening and nematode identification in C. nasus. Full article
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<p>The nematodes in the liver of <span class="html-italic">C. nasus</span>, indicated with arrows.</p>
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<p>The variations in the mean intensity of nematodes in <span class="html-italic">C. nasus</span> at each sampling site across different years. Abbreviations: SH2021—Shanghai section of the Yangtze River (2021), AQ2021—Anqing section of the Yangtze River (2021), SH2022—Shanghai section of the Yangtze River (2022), AQ2022—Anqing section of the Yangtze River (2022). The numbers enclosed in parentheses indicate sampling date. Bars represent standard deviation. The ‘*’ represents statistically significant disparities (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Relationship between the sex of <span class="html-italic">C. nasus</span> and the intensity of infection at various sampling time points. Bars represent standard deviation. The ‘*’ represents statistically significant disparities (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Number of individuals with different infection intensities of nematodes in <span class="html-italic">C. nasus</span> from two sampling years.</p>
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<p>Relationship between the body length of <span class="html-italic">C. nasus</span> and the intensity of infection in two sampling years.</p>
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<p>The distribution and mean infection intensity of parasitic nematodes in different tissues and organs of <span class="html-italic">C. nasus</span> at each sampling time and site. Bars represent standard deviation. The presence of distinct letters signifies statistically significant disparities (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The species composition of nematodes isolated from <span class="html-italic">C. nasus</span> (n = 26).</p>
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<p>The species composition of nematodes isolated from <span class="html-italic">C. nasus</span> at each sampling site in 2022.</p>
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<p>Bayesian inference phylogenetic tree based on the obtained sequences of ITS1-5.8s-ITS2.</p>
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<p>The proportion of parasitic nematode species identified in each organ and tissue of <span class="html-italic">C. nasus</span> in 2022.</p>
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30 pages, 7683 KiB  
Article
A Contribution to the Knowledge of Hydnum (Hydnaceae, Cantharellales) in China, Introducing a New Taxon and Amending Descriptions of Five Known Species
by Hua-Zhi Qin, Yu-Ting Liao, Yu-Zhuo Zhang, Wen-Fei Lin, Xin-Quan Yang and Nian-Kai Zeng
Diversity 2024, 16(3), 166; https://doi.org/10.3390/d16030166 - 6 Mar 2024
Cited by 1 | Viewed by 2451
Abstract
Hydnum (Hydnaceae, Cantharellales), one of the edible ectomycorrhizal mushrooms, is of considerable ecological and economic importance. Although previous studies have focused on the genus in China, the diversity still remains incompletely understood. In the present study, in addition to the known species from [...] Read more.
Hydnum (Hydnaceae, Cantharellales), one of the edible ectomycorrhizal mushrooms, is of considerable ecological and economic importance. Although previous studies have focused on the genus in China, the diversity still remains incompletely understood. In the present study, in addition to the known species from China being reviewed, six phylogenetic species from the country were described/redescribed, which included a new species: H. erectum, and five known taxa: H. cremeoalbum, H. minus, H. orientalbidum, H. tenuistipitum, and H. treui; H. treui is new to China. Detailed descriptions, color photographs of fresh basidiomata, and line drawings of microstructures of them are presented. A key to the accepted species of Hydnum in China is also provided. Full article
(This article belongs to the Section Microbial Diversity and Culture Collections)
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<p>A phylogram of <span class="html-italic">Hydnum</span> inferred from a two-locus (28S and ITS) dataset using RAxML. BS (≥70%) and PP (≥0.95) are indicated above the branches. Newly generated sequences are in color; SW: Southwestern, NE: Northeastern, NW: Northwestern, SE: Southeastern.</p>
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<p>A phylogram of <span class="html-italic">Hydnum</span> inferred from a two-locus (28S and ITS) dataset using RAxML. BS (≥70%) and PP (≥0.95) are indicated above the branches. Newly generated sequences are in color; SW: Southwestern, NE: Northeastern, NW: Northwestern, SE: Southeastern.</p>
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<p>A phylogram of <span class="html-italic">Hydnum</span> inferred from a two-locus (28S and ITS) dataset using RAxML. BS (≥70%) and PP (≥0.95) are indicated above the branches. Newly generated sequences are in color; SW: Southwestern, NE: Northeastern, NW: Northwestern, SE: Southeastern.</p>
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<p>Basidiomata of <span class="html-italic">Hydnum</span> species. (<b>a</b>,<b>b</b>) <span class="html-italic">Hydnum cremeoalbum</span> (<b>a</b>) from FHMU2404; (<b>b</b>) from FHMU1631); (<b>c</b>,<b>d</b>) <span class="html-italic">Hydnum erectum</span> (FHMU7689, holotype); (<b>e</b>,<b>f</b>) <span class="html-italic">Hydnum minus</span> (<b>e</b>) from FHMU2408; (<b>f</b>) from FHMU7603); (<b>g</b>,<b>h</b>) <span class="html-italic">Hydnum orientalbidum</span> (<b>g</b>) from FHMU6327; (<b>h</b>) from FHMU6361; (<b>i</b>,<b>j</b>) <span class="html-italic">Hydnum tenuistipitum</span> (<b>i</b>) from FHMU7642; (<b>j</b>) from FHMU7636); (<b>k</b>,<b>l</b>) <span class="html-italic">Hydnum treui</span> (<b>k</b>) from FHMU7690; (<b>l</b>) from FHMU7691. Scale bars = 1 cm. Photographs by N.K. Zeng.</p>
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<p>Microscopic features of <span class="html-italic">Hydnum cremeoalbum</span> (FHMU1631). (<b>a</b>) Basidiospores. (<b>b</b>) Basidia. (<b>c</b>) Pileipellis. Scale bars = 10 μm. Drawings by Y.Z. Zhang.</p>
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<p>Microscopic features of <span class="html-italic">Hydnum erectum</span> (FHMU7689, holotype). (<b>a</b>) Basidiospores. (<b>b</b>) Basidia. (<b>c</b>) Pileipellis. Scale bars = 10 μm. Drawings by H.Z. Qin.</p>
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<p>Microscopic features of <span class="html-italic">Hydnum minus</span> (FHMU2408). (<b>a</b>) Basidiospores. (<b>b</b>) Basidia. (<b>c</b>) Pileipellis. Scale bars = 10 μm. Drawings by Y.Z. Zhang.</p>
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<p>Microscopic features of <span class="html-italic">Hydnum orientalbidum</span> (FHMU3153). (<b>a</b>) Basidiospores. (<b>b</b>) Basidia. (<b>c</b>) Pileipellis. Scale bars = 10 μm. Drawings by Y.Z. Zhang.</p>
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<p>Microscopic features of <span class="html-italic">Hydnum tenuistipitum</span> (FHMU7644). (<b>a</b>) Basidiospores. (<b>b</b>) Basidia. (<b>c</b>) Pileipellis. Scale bars = 10 μm. Drawings by H.Z. Qin.</p>
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<p>Microscopic features of <span class="html-italic">Hydnum treui</span> (FHMU7690). (<b>a</b>) Basidiospores. (<b>b</b>) Basidia. (<b>c</b>) Pileipellis. Scale bars = 10 μm. Drawings by H.Z. Qin.</p>
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14 pages, 11888 KiB  
Article
Effective Field Collection of Pezizales Ascospores for Procuring Diverse Fungal Isolates
by Alassane Sow, Judson Van Wyk, Benjamin Lemmond, Rosanne Healy, Matthew E. Smith and Gregory Bonito
Diversity 2024, 16(3), 165; https://doi.org/10.3390/d16030165 - 6 Mar 2024
Viewed by 1952
Abstract
Pezizales are a diverse and economically important order of fungi. They are common in the environment, having epigeous form, such as morels and hypogeous, forms called truffles. The mature ascospores of most epigeous Pezizales are forcibly discharged through an opening at the ascus [...] Read more.
Pezizales are a diverse and economically important order of fungi. They are common in the environment, having epigeous form, such as morels and hypogeous, forms called truffles. The mature ascospores of most epigeous Pezizales are forcibly discharged through an opening at the ascus apex created with the lifting of the operculum, a lid-like structure specific to Pezizales. The axenic cultures of Pezizales fungi isolated from single ascospores are important for understanding the life cycle, development, ecology, and evolution of these fungi. However, obtaining single-spore isolates can be challenging, particularly for collections obtained in locations where sterile work environments are not available. In this paper, we introduce an accessible method for harvesting ascospores from fresh ascomata in the field and laboratory for obtaining single-spore isolates. Ascospores are harvested on the inside cover of Petri plate lids in the field, air dried, and stored. At a later date, single-spore isolates are axenically cultured through serial dilution and plating on antibiotic media. With this approach, we were able to harvest ascospores and obtain single-spore isolates from 12 saprotrophic and 2 ectomycorrhizal species belonging to six Pezizales families: Discinaceae, Morchellaceae, Pezizaceae, Pyronemataceae, Sarcosomataceae, and Sarcoscyphaceae. This method worked well for saprotrophic taxa (12 out of 19 species, 63%) and was even effective for a few ectomycorrhizal taxa (2 out of 13 species, 15%). This process was used to study the initial stages of spore germination and colony development in species across several Pezizales families. We found germination often commenced with the swelling of the spore, followed by the emergence of 1–8 germ tubes. This method is sufficiently straightforward that, provided with sterile Petri dishes, citizen scientists from distant locations could use this approach to capture spores and subsequently mail them with voucher specimens to a research laboratory for further study. The generated single-spore Pezizales isolates obtained through this method were used to generate high-quality genomic data. Isolates generated in this fashion can be used in manipulative experiments to better understand the biology, evolution, and ecogenomics of Pezizales. Full article
(This article belongs to the Special Issue Diversity in 2024)
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<p>Pezizales collections in the field and confirmation of spore dispersal in the laboratory. (<b>A</b>) <span class="html-italic">Pachyella</span> (FLAS-F-69780) collection still attached to woody substrate in a 60 × 15 mm plate. (<b>B</b>) <span class="html-italic">Sarcoscypha</span> sp. propped up using living leaves in a 60 × 15 mm plate. (<b>C</b>) Spores of <span class="html-italic">Legliana</span> (FLAS-F-68766), where the spore print was circled with a marker; the line separates the spore print from the surface without spores. (<b>D</b>) Spores of <span class="html-italic">Scutellinia</span> sp. (FLAS-F-68459), where the spore print was circled with a marker. (<b>E</b>) Confirming presence of <span class="html-italic">Legliana</span> sp. (FLAS-F-68766) spores within the marked circle shown in (<b>C</b>); note that spores (dark clusters) are present inside the circled area but are not present outside of the border. (<b>F</b>) Confirming presence of <span class="html-italic">Scutellinia</span> sp. (FLAS-F-68459) spores (dark specks) within the marked circle as shown in (<b>D</b>) = 500 µm, (<b>F</b>) = 500 µm.</p>
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<p>One of the most likely RAxML phylogenetic trees estimated from an LSU alignment showing the wide diversity of single-spore isolates among other Pezizales fungi. Significant support is denoted by bootstrap values ≥70% at nodes. Green taxa represent isolates that germinated and grew in axenic cultures in this study. Circled numbers represent the number of different isolates obtained of a given species.</p>
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<p><span class="html-italic">Gyromitra venenata</span> (MSC0286084) ascospores at 400× magnification. (<b>A</b>–<b>C</b>) Ascospores germinating, exhibiting dramatic swelling and multipolar germ tube formation. (<b>D</b>) Dormant and germinating ascospores. Bar = 50 µm.</p>
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<p>Spores and other survival structures that formed in Pezizales cultures. (<b>A</b>) Microsclerotia in <span class="html-italic">Morchella angusticeps</span> (MSC0286085). (<b>B</b>) Chlamydospores of <span class="html-italic">Morchella angusticeps</span> (MSC0286085). (<b>C</b>) Sclerotia of <span class="html-italic">Phylloscypha phyllogena</span> (MSC0286083), which only formed in multispore cultures. (<b>D</b>) Arthroconidia of <span class="html-italic">Phylloscypha phyllogena</span> (MSC0286083). (<b>E</b>) Conidia in <span class="html-italic">Peziza</span> sp. 1 (MSC0286080). Scale bars: (<b>A</b>) = 790 µm; (<b>B</b>) = 200 µm; (<b>C</b>) = 3.175 mm; (<b>D</b>) = 200 µm; (<b>E</b>) = 50 µm.</p>
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11 pages, 4515 KiB  
Article
Diversity of Fish and Decapod Fry in the Coastal Zone of Amvrakikos Gulf
by George Katselis, Nikolaos Vlahos, Constandin Koutsikopoulos and Dimitrios K. Moutopoulos
Diversity 2024, 16(3), 164; https://doi.org/10.3390/d16030164 - 6 Mar 2024
Viewed by 1913
Abstract
Amvrakikos Gulf and its surrounding coastal lagoons are of primary importance for the local biodiversity and fishing activities. Fish species inhabited the coastal lagoons based on the seasonal ongoing migration movements of fry and adult fish individuals from the sea towards the lagoons. [...] Read more.
Amvrakikos Gulf and its surrounding coastal lagoons are of primary importance for the local biodiversity and fishing activities. Fish species inhabited the coastal lagoons based on the seasonal ongoing migration movements of fry and adult fish individuals from the sea towards the lagoons. Information on the early stages of fish and decapod species in the Amvrakikos Gulf is limited only to the planktonic ontogenetic stages and reproduction biology, respectively. The aim of this study was to describe the spatial distribution of fry from commercially important fish and decapod species in the coastal zone of Amvrakikos Gulf. The seasonal appearance of the early stage of the most commercially important fish species caught in the coastal zone of the gulf ranged from one to four seasons, depending on the species. Individuals of all ontogenetic stages (fry, juveniles, and adults) were reported for several species (A. boyeri, A. fasciatus, S. abaster, S. tyfle, and B. ocellaris), indicating that these species may be regarded as residents in the coastal zone, providing habitats for their entire life cycle. The average relative abundance of the species/genera exhibited no differences compared to other Greek brackish waters. The species composition in the Amvrakikos Gulf at 10 cm and above was in agreement with the transitional nature of the area, with permanent and occasional species present. The present study emphasizes the importance of the coastal zone as a nursery habitat for commercially important species. Full article
(This article belongs to the Special Issue Diversity in 2024)
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<p>Map of the study area (<b>A</b>) and sampling station for early stages species in the coastal zone of Amvakikos Gulf, May 2016 to March 2017, station’s spatial clusters (SpC-i), and sampling period (<b>B</b>).</p>
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<p>Spatio-temporal distribution of Shannon–Weiner index (H′) and number of the species (blue numbers) of all stages in the study area.</p>
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<p>Ranking of species/genera according to their ecological profile for all ontogenetic stages (AS) and new recruits (NR): high spatial distribution, non-seasonality, and no microhabitat selection (score 222); high spatial distribution, non-seasonality, and microhabitat selection (total score 221); low spatial distribution, non-seasonality, and no microhabitat selection (total score 122); low spatial distribution, non-seasonality, and microhabitat selection (total score 121); low spatial distribution, seasonality, and no microhabitat selection (total score 112); and low spatial distribution, seasonality, and microhabitat selection (total score 111).</p>
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20 pages, 1536 KiB  
Review
Sturgeon Parasites: A Review of Their Diversity and Distribution
by György Deák, Elena Holban, Isabela Sadîca and Abdulhusein Jawdhari
Diversity 2024, 16(3), 163; https://doi.org/10.3390/d16030163 - 5 Mar 2024
Cited by 3 | Viewed by 2480
Abstract
Sturgeon species have inhabited the world’s seas and rivers for more than 200 million years and hold significant taxonomic significance, representing a strong conservation interest in aquatic biodiversity as well as in the economic sector, as their meat and eggs (caviar) are highly [...] Read more.
Sturgeon species have inhabited the world’s seas and rivers for more than 200 million years and hold significant taxonomic significance, representing a strong conservation interest in aquatic biodiversity as well as in the economic sector, as their meat and eggs (caviar) are highly valuable goods. Currently, sturgeon products and byproducts can be legally obtained from aquaculture as a sustainable source. Intensive farming practices are accompanied by parasitic infestations, while several groups of parasites have a significant impact on both wild and farmed sturgeons. The present article is a review of common sturgeon parasites from the genus: Protozoa, Trematoda, Crustacea, Nematodes, Monogenea, Hirudinea, Copepoda, Acanthocephala, Cestoda, Polypodiozoa, and Hyperoartia, while also addressing their pathology and statistical distribution. Full article
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<p>Percentage of parasite recurrence by affected organs (all taxonomic groups).</p>
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<p>Percentage of parasite taxonomic group identification in sturgeon species, based on the reviewed scientific literature.</p>
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<p>Percentage of infestation of each parasite taxonomic group on different organs.</p>
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16 pages, 2244 KiB  
Article
Shallow Hard-Bottom Benthic Assemblages of South Bay (Antarctic Peninsula): An Update 40 Years Later
by Sol Morales, César A. Cárdenas, Diego Bravo-Gómez and Cristian Lagger
Diversity 2024, 16(3), 162; https://doi.org/10.3390/d16030162 - 5 Mar 2024
Viewed by 1562
Abstract
This work completes and updates the information about the diversity and distribution of benthic assemblages in an Antarctic fjord (South Bay, Antarctic Peninsula) 40 years after the first and only community-level study was conducted there. To determine the community changes, a photographic survey [...] Read more.
This work completes and updates the information about the diversity and distribution of benthic assemblages in an Antarctic fjord (South Bay, Antarctic Peninsula) 40 years after the first and only community-level study was conducted there. To determine the community changes, a photographic survey was conducted at four sites with different substrate inclinations along a bathymetric gradient of 5–20 m depth. In total, 160 photoquadrats were analyzed, resulting in a total area of 40 m2. Sixty taxa represented by 12 phyla were identified, of which eight phyla corresponded to animals. The remaining species corresponded to macroalgae and benthic diatoms, both taxa presenting the highest coverages of the entire study area. The highest richness and diversity values were obtained at greater depths and at the sites with the steepest slopes. Here, we discuss the role of substrate inclination and depth in the structure of the benthic assemblages concerning possible variations in the presence and frequency of physical disturbances (e.g., ice disturbance and sedimentation). The abundances, densities, and distributions of all species found are detailed, updating the ecological data of the benthic ecosystem of this Antarctic fjord from the previously published assessment four decades ago. In a continent where rapid environmental changes are being experienced due to climate-induced processes, we discuss the first massive record of benthic diatoms in this fjord and the striking absence of the sea urchin Sterechinus neumayeri, an abundant species from previous records from the early 1980s. Full article
(This article belongs to the Section Marine Diversity)
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<p>Study area: (<b>A</b>) Map of the location of South Bay in the Antarctic Peninsula. (<b>B</b>) Doumer Island with the sampled sites in South Bay: Site 1 (64°52′12.0″ S; 63°33′50.5″ W); Site 2 (64°52′32.1″ S; 63°35′04.1″ W); Site 3 (64°51′53.0″ S; 63°35′25.2″ W); Site 4 (64°51′55.9″ S; 63°33′55.7″ W).</p>
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<p>Percentage coverage of each taxon and substrate in the four sampled sites at South Bay, Doumer Island (WAP). Due to the large number of taxa, they were grouped into five groups. The sessile included Porifera, Cnidaria, Bryozoa, Brachiopoda, and Chordata; mobiles included Mollusca, Nemertea, and Echinodermata; while green, red, and brown algae formed the group of macroalgae.</p>
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<p>Percentage coverage of benthic diatoms (±SE) at each depth of the four sampled sites at South Bay, Doumer Island (WAP).</p>
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<p>(<b>a</b>) Macroalgae, such as <span class="html-italic">Palmaria decipiens</span>, and mobile species, such as <span class="html-italic">Nacella concinna</span>, dominated the shallowest depths at the S4 site; (<b>b</b>) benthic filamentous diatoms presented the highest percentage of total coverage, especially in the shallowest depths, at the S3 site; (<b>c</b>) <span class="html-italic">Himantothallus grandifolius</span> was one the main contributors to the percentage of coverage at the S2 site; (<b>d</b>) the highest abundance and richness of fauna was found at S1, where filter-feeder animals, such as sponges and ascidians, dominated the vertical rock walls. Underwater photographs taken by Cristian Lagger.</p>
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<p>Non-metric multidimensional scaling biplot based on the Bray–Curtis similarity matrix for percentage coverage of registered taxa (square-root transformed data). Cluster analysis was obtained using the UPGMA method, classifying (<b>A</b>) the samples analyzed by site, showing two groups: S1–S2 and S3–S4; (<b>B</b>) classifying the samples analyzed by depths, showing two groups: 5–10 m and 15–20 m. 2D stress = 0.16.</p>
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13 pages, 4938 KiB  
Article
Revealing the Diversity of Thin Filamentous Cyanobacteria, with the Discovery of a Novel Species, Pegethrix qiandaoensis sp. nov. (Oculatellaceae, Oculatellales), in a Freshwater Lake in China
by Kaihui Gao, Yao Cheng, Rouzhen Geng, Peng Xiao, He Zhang, Zhixu Wu, Fangfang Cai and Renhui Li
Diversity 2024, 16(3), 161; https://doi.org/10.3390/d16030161 - 5 Mar 2024
Cited by 2 | Viewed by 1668
Abstract
During the study of diversity in filamentous cyanobacteria in China, two strains (WZU0719 and WZU0723) with the form of thin filaments were isolated from the surface of Qiandao Lake, a large freshwater lake in Zhejiang Province, China. A comprehensive analysis was conducted, incorporating [...] Read more.
During the study of diversity in filamentous cyanobacteria in China, two strains (WZU0719 and WZU0723) with the form of thin filaments were isolated from the surface of Qiandao Lake, a large freshwater lake in Zhejiang Province, China. A comprehensive analysis was conducted, incorporating morphological, ecological, and molecular data. The morphological examination provided an initial identification as a Leptolyngbya-like cyanobacterium. Genetic characterization was also performed by amplifying the 16S rRNA gene and the 16S-23S rRNA internal transcribed spacer (ITS) region. The phylogenetic grouping based on the 16S rRNA gene demonstrates that the examined strain is unequivocally assigned to the Pegethrix genus. However, it possesses distinct phylogenetic divergence from the six described Pegethrix species. Additionally, discrepancies in habitat further differentiate it from other members of this genus. Employing the polyphasic approach, we present a comprehensive account of the newly discovered taxa: Pegethrix qiandaoensis sp. nov. The novel taxonomic finding in this research significantly contributes to enhancing the comprehension of Pegethrix diversity across various habitats. Full article
(This article belongs to the Special Issue 2024 Feature Papers by Diversity’s Editorial Board Members)
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Figure 1

Figure 1
<p>Light microscopy of <span class="html-italic">Pegethrix qiandaoensis</span> strains. A single trichome with a sheath (<b>a</b>,<b>h</b>,<b>i</b>). Morphological photos confirm that the strains that were studied have no obvious nodules cells and no knots have been observed in the filaments (<b>a</b>–<b>i</b>). Observed obvious cell wall structure (<b>e</b>,<b>g</b>,<b>i</b>). Macro-culture status of <span class="html-italic">Pegethrix qiandaoensis</span> strains (<b>j</b>). Scale bars: 10 µm.</p>
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<p>Longitudinal section of vegetative cell (TEM), showing sheath (s) and parietal thylakoids (pt) (<b>A</b>,<b>C</b>,<b>D</b>), cyanophycin granules (cg) (<b>A</b>,<b>D</b>) and cell division—formation of new cell wall (cd) (<b>B</b>), and a lack of cell constriction. Scale bar: 0.5 μm.</p>
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<p>Maximum-likelihood (ML) phylogenetic tree of <span class="html-italic">Pegethrix qiandaoensis</span> strains based on 16S rRNA gene sequences. For MP/ML methods and Bayesian posterior probabilities, bootstrap values above 50% are displayed in the BI tree. * Indicates a bootstrap value of 100 and a posterior probability of 1.00 for MP, ML, and BI. The novel filamentous strains of this study are indicated in bold.</p>
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<p>Bayesian inference (BI) phylogenetic tree of <span class="html-italic">Pegethrix qiandaoensis</span> strains based on ITS rRNA gene sequences. For MP/ML methods and Bayesian posterior probabilities, bootstrap values above 50% are displayed in the BI tree. * Indicates a bootstrap value of 100 and a posterior probability of 1.00 for MP, ML, and BI. The novel filamentous strains of this study are indicated in bold.</p>
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<p>Secondary structures of the D1–D1′ helix in <span class="html-italic">Pegethrix</span> species. (<b>a</b>–<b>f</b>) D1–D1′ helices: (<b>a</b>) <span class="html-italic">Pegethrix qiandaoensis</span> WZU0719. (<b>b</b>) <span class="html-italic">Pegethrix convoluta</span>. (<b>c</b>) <span class="html-italic">Pegethrix bostrychoides</span>. (<b>d</b>) <span class="html-italic">Pegethrix indistincta</span>. (<b>e</b>) <span class="html-italic">Pegethrix sichuanica</span>. (<b>f</b>) <span class="html-italic">Pegethrix atlantica</span>.</p>
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<p>Secondary structures of the Box–B helix in <span class="html-italic">Pegethrix</span> species. (<b>a</b>–<b>f</b>) D1–D1′ helices: (<b>a</b>) <span class="html-italic">Pegethrix qiandaoensis</span> WZU0719. (<b>b</b>) <span class="html-italic">Pegethrix convoluta</span>. (<b>c</b>) <span class="html-italic">Pegethrix bostrychoides</span>. (<b>d</b>) <span class="html-italic">Pegethrix indistincta</span>. (<b>e</b>) <span class="html-italic">Pegethrix sichuanica</span>. (<b>f</b>) <span class="html-italic">Pegethrix atlantica</span>.</p>
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<p>Secondary structures of the V3 helix in Pegethrix species. (<b>a</b>–<b>f</b>) D1–D1′ helices: (<b>a</b>) <span class="html-italic">Pegethrix qiandaoensis</span> WZU0719. (<b>b</b>) <span class="html-italic">Pegethrix convoluta</span>. (<b>c</b>) <span class="html-italic">Pegethrix bostrychoides</span>. (<b>d</b>) <span class="html-italic">Pegethrix indistincta</span>. (<b>e</b>) <span class="html-italic">Pegethrix sichuanica</span>. (<b>f</b>) <span class="html-italic">Pegethrix atlantica</span>.</p>
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