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1,153 results for “Fern”
Ferns Cemetery Grave Marker 3
A grave marker in Ferns Cemetery, St. Edan's Church, Ireland. The headstone marks the resting place of two people. Source: Objaverse 1.0 / Sketchfab
Supplemental Data for: Lineage diversification and rampant hybridization among subspecies explain taxonomic confusion in the endemic Hawaiian fern Polypodium pellucidum
<p><strong><span>Premise:</span></strong><span> <em>Polypodium pellucidum</em>, a fern endemic to the Hawaiian Islands, encompasses a broad spectrum of morphological and ecological variation, suggesting a complex history involving divergence and hybridization. In contrast to angiosperm systems, spore dispersal in ferns presents a unique opportunity to study how highly dispersible organisms diversify in the dynamic landscape of the archipelago.</span></p> <p><strong><span>Key Results: </span></strong><span>We infer <em>P. pellucidum</em> is monophyletic, dispersing to the Hawaiian archipelago 11.53 to 7.77 Mya, with diversification into extant clades 5.66 to 4.73 Mya. We identify four non-hybrid clades with unique morphologies, ecological niches, and distributions. Additionally, we elucidate several intraspecific hybrid combinations and evidence for undiscovered or extinct 'ghost' lineages contributing to extant hybrids populations. </span></p> <p><strong><span>Conclusions:</span></strong><span> We provide a roadmap for revising the taxonomy of <em>P. pellucidum</em> to account for cryptic lineages and intraspecific hybrids. Geologic succession of the Hawaiian Islands through cycles of volcanism, vegetative succession, and erosion has determined the available habitats and distribution of ecologically specific divergent clades within <em>P. pellucidum, </em>with intraspecific hybrids arising as a result of ecological and or geological transitions, often persisting after the local extinction of their progenitors. This research contributes to our understanding of the evolution of Hawaii's diverse fern flora and allows for better conservation efforts that are often complicated by the presence of cryptic taxa and hybridization.</span></p>
Fig. 7 in Typification and nomenclature of the ferns described in N.L. Burman's Flora Indica
Fig. 7. – Lectotype of Polypodium simplex Burm. f. in G-PREL.
Fig. 5 in Typification and nomenclature of the ferns described in N.L. Burman's Flora Indica
Fig. 5. – Lectotype of Polypodium glabrum Burm. f. in G-PREL.
Fig. 4 in Typification and nomenclature of the ferns described in N.L. Burman's Flora Indica
Fig. 4. – Lectotype of Polypodium adianthoides Burm. f. in G-PREL.
Fig. 1 in Lectotypification of the N.L. Burman's fern name Adiantum denticulatum
Fig. 1. – Lectotype of Adiantum denticulatum Burm. f. in G-PREL.
Fig. 6 in Typification and nomenclature of the western Indian Ocean islands ferns and lycophytes described in Linnaeus filius's Supplementum plantarum
Fig. 6. – Lectotype of Adiantum furcatum L. f. in LINN-HS). [© Linnean Society of London]
Fig. 4 in Typification and nomenclature of the western Indian Ocean islands ferns and lycophytes described in Linnaeus filius's Supplementum plantarum
Fig. 4. – Lectotype of Acrostichum punctatum L. f. in LINN-HS. [© Linnean Society of London]
Antheridiogen controls spatial dynamics of sex‐expression in naturally occurring gametophytes of the tree fern Cyathea multiflora
<p>Background and aims: Antheridiogen systems are an important and widespread mechanism by which sex expression is controlled and genetic diversity maintained in fern gametophyte populations. However, antheridiogens have rarely been studied outside of the laboratory and little is known about their function in natural populations. Combining predictions based on field and laboratory study, we document the sexual structure of tree fern gametophyte populations and test the effects of antheridiogen <em>in situ</em>. </p> <p>Key results: In all populations, sex ratios indirectly indicate antheridiogen activity. No hermaphroditic gametophytes were identified in any population. Female gametophytes are randomly distributed in each population while male gametophytes tend to cluster. In two of the populations, male sex expression is spatially dependent on females, providing direct evidence of antheridiogen function <em>in situ</em>.</p> <p>Conclusions: This study provides the first documentation of spatial sex expression in natural gametophyte populations of an antheridiogen-producing tree fern species. The profound impact of antheridiogen on gametophyte sex expression in field settings suggests this system is intimately tied to mating systems, fitness, and genetic diversity in <em>Cyathea multiflora</em>.</p>
Target capture methods offer insight into the evolution of rapidly diverged taxa and resolve allopolyploid homeologs in the fern genus Polypodium s.s.
<p><span></span></p> <p>Like many fern lineages comprising reticulate species complexes, <em>Polypodium</em> s.s. (Polypodiacaeae) has a history shaped by rapid diversification, hybridization, and polyploidy that poses substantial challenges for phylogenetic inference with plastid and single-locus nuclear loci. Using target capture probes for 408 nuclear loci developed by the GOFlag project and a custom bioinformatic pipeline, SORTER, we constructed multi-locus nuclear datasets for diploid temperate and Mesoamerican species of <em>Polypodium</em> and five allotetraploid species belonging to the well-studied <em>Polypodium</em> <em>vulgare</em> complex. SORTER employs a clustering approach to separate putatively paralogous copies of targeted loci into orthologous matrices and haplotype phasing to infer allopolyploid haplotypes across loci, resulting in datasets amenable to both concatenated maximum likelihood and multi-species coalescent phylogenetic analyses. By comparing phylogenies derived from maximum likelihood and multi- species coalescent analyses of unphased and phased datasets, as well as evaluating discordance among gene trees and species trees, we recover support for incomplete lineage sorting within <em>Polypodium</em> s.s., novel relationships among diploid taxa of the <em>Polypodium</em> <em>vulgare</em> complex and its Mesoamerican sister clade, and the placement of several <em>Polypodium</em> species within other genera. Additionally, we were able to infer well-supported phylogenies that identified the hypothesized progenitors of the allotetraploid species, indicating that SORTER is an effective and accurate tool for reconstructing homeolog haplotypes of allopolyploids in fern taxa and other non-model organisms from target capture data.</p>
Figure 7 in A New Species of Teratomyza, the First Fern Fly from New Guinea (Diptera, Teratomyzidae)
Figure 7. Teratomyza ismayi sp. nov., right prothoracic leg of male, lateral view.
Figure 4 in A New Species of Teratomyza, the First Fern Fly from New Guinea (Diptera, Teratomyzidae)
Figure 4. Teratomyza ismayi, inner claw of left prothoracic tarsus of male.
Figure 3 in A New Species of Teratomyza, the First Fern Fly from New Guinea (Diptera, Teratomyzidae)
Figure 3. Teratomyza ismayi, outer claw of left prothoracic tarsus of male.
Data from: Quantitative plant taphonomy: the cosmopolitan Mesozoic fern Weichselia reticulata as a case study
<p>A quantitative approach to plant taphonomy focusing on preservation type and fragment size is tested by comparing 3338 <em>Weichselia reticulata </em>fragments from 25 Lower Cretaceous localities of different ages and depositional environments. Moreover, palaeobiological insights are also obtained from the taphonomic analyses. In the case of the specimens of <em>Weichselia reticulata</em> included in this work, charred remains are the most frequent preservation type. They are the smallest and most homogeneous in size, probably due to the fragmentation of the fronds while burning and to the fact that burnt fragments are more fragile and break easily during the initial abrasion and attrition produced by transport. The sizes of charred fragments vary depending on the depositional environment, suggesting that biostratinomic processes, and not fire temperature, are the main cause for size differences, and providing valuable insight into the distance the remains might have traveled from production to final deposition. The taphonomic analyses suggest that <em>Weichselia reticulata</em> is allochthonous in all the localities analysed, and that its habitat would have been prone to fire and not far from freshwater systems. This case study shows promising results that can be implemented on different plant groups and chronostratigraphic ages, allowing for the proposal of a taphonomic model.</p>
Ferns Kiln
This is a partially unexcavated Kiln from Cutting Four that was unearthed during the Discovering Saint Aiden's Monastary IAFS field school project. This is the first excavated pottery kiln in Co. Wexford, Ireland. Source: Objaverse 1.0 / Sketchfab
Ferns Cemetery Grave Marker 2
A grave marker in Ferns Cemetery, St. Edan's Church, Ireland. As grave markers age, they deteriorate and break. It's stone being reclaimed by the earth once more. Source: Objaverse 1.0 / Sketchfab
Ferns Cutting Four
Cutting Four from the Discovering Saint Aiden's Monastary IAFS field school project. This cutting includes the first excavated kiln in Co. Wexford, Ireland. Source: Objaverse 1.0 / Sketchfab
Fig. 1 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.
Fig. 1. Collecting sites of Calicotis used in the present studies.
Fig. 12 in Figs. 23-34 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.
Fig. 12. Total body mass as a function of post-settlement age in C. venezuelae.
Fig. 52 in Plant Type Materials from Kanagawa Prefecture (Japan) in the Herbarium of the Komarov Botanical Institute (LE; Russia): Lycophytes, Ferns, Gymnosperms, and Angiosperms (Monocots and some Dicots)
Fig. 52. Isolectotype of Carex scita Maxim. (LE 10012387; KPM-NX0001328).
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