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146 results for “sessile”
Figure 4. Zoothamnium sinense Song, 1991. A, C in The first finding of sessile ciliates Vorticella pyriforme Stiller, 1939 and Zoothamnium sinense Song, 1991 (Ciliophora, Peritrichia) in the Black Sea
Figure 4. Zoothamnium sinense Song, 1991. A, C – original, in vivo, scale bar: 35 µm; В – modified from Ji et al., 2006, scale bar: 20 µm.
Figure 4. Praethecacineta halacari Schultz, 1933. A, C in First finds of sessile ciliates (Ciliophora) in artificial and natural caverns on the Crimean coast of the Black Sea
Figure 4. Praethecacineta halacari Schultz, 1933. A, C – Ciliates attached to Halacarida; B, D – Magnified view of zooids.
Figure 3 in First finds of sessile ciliates (Ciliophora) in artificial and natural caverns on the Crimean coast of the Black Sea
Figure 3. Zoothamnium sp. 2. A – General view of Zoothamnium sp. attached to Halacarida; B – Type of branching; C, D – Zooids when contracted.
Figure 2 in First finds of sessile ciliates (Ciliophora) in artificial and natural caverns on the Crimean coast of the Black Sea
Figure 2. Zoothamnium sp. 1. A, C – General view of Zoothamnium sp.; B – Type of branching of Zoothamnium sp.; D – Zooid of Zoothamnium sp.
Figure 1. Cothurnia ovalis Kahl, 1933. A, B in First finds of sessile ciliates (Ciliophora) in artificial and natural caverns on the Crimean coast of the Black Sea
Figure 1. Cothurnia ovalis Kahl, 1933. A, B – Original; C – General view of Cothurnia ovalis attached to Oligochaeta; D – After Kahl, 1933, scale bar: 50 µm.
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i).
Text-fig. 46. Scanning electron microscope (SEM) images of "Rugulate fruit"; Catefica locality, Portugal. a, b) Lateral (a) and ventral (b) views of a rugulate fruit showing the short extension of the sessile stigma at the apex (arrows); c) Irregular surface of fruit that probably reflects an irregular endocarp; note the isodiametric outlines of the epidermal cells; d) Semi-tectate reticulate pollen grains embedded in the remains of a secretion on the stigmatic surface. Specimen, Catefica 154-S101291 (a–d). Scale bars = 300 Μm (a, b), 100 Μm (c), 6 Μm (d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 46. Scanning electron microscope (SEM) images of "Rugulate fruit"; Catefica locality, Portugal. a, b) Lateral (a) and ventral (b) views of a rugulate fruit showing the short extension of the sessile stigma at the apex (arrows); c) Irregular surface of fruit that probably reflects an irregular endocarp; note the isodiametric outlines of the epidermal cells; d) Semi-tectate reticulate pollen grains embedded in the remains of a secretion on the stigmatic surface. Specimen, Catefica 154-S101291 (a–d). Scale bars = 300 Μm (a, b), 100 Μm (c), 6 Μm (d).
Text-fig. 13. Scanning electron microscope (SEM) images of "Staminate inflorescence fragment with Clavatipollenites-type pollen sp. 4"; Catefica locality, Portugal. a) Fragment of stamen whorl from staminate inflorescence showing several closely packed, almost sessile stamens that lack a well-developed filament; b, c) Distal and proximal views of pollen grains showing poorly defined aperture with verrucate aperture membrane; d) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered columellae supporting the narrow muri with finely verrucate supratectal ornamentation. Specimen, Catefica 49-S107782 (a–d). Scale bars = 600 Μm (a), 6 Μm (b, c), 1.5 Μm (d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 13. Scanning electron microscope (SEM) images of "Staminate inflorescence fragment with Clavatipollenites-type pollen sp. 4"; Catefica locality, Portugal. a) Fragment of stamen whorl from staminate inflorescence showing several closely packed, almost sessile stamens that lack a well-developed filament; b, c) Distal and proximal views of pollen grains showing poorly defined aperture with verrucate aperture membrane; d) Detail of pollen wall showing the semitectate-reticulate tectum and long, scattered columellae supporting the narrow muri with finely verrucate supratectal ornamentation. Specimen, Catefica 49-S107782 (a–d). Scale bars = 600 Μm (a), 6 Μm (b, c), 1.5 Μm (d).
Text-fig. 29. Scanning electron microscope (SEM) images of stamens and pollen grains of cf. Endressistemon sp. 1 (a, b), cf. Endressistemon sp. 2 (c, d) and cf. Endressistemon sp. 3 (e–g); Catefica locality, Portugal. a) Two adhering stamens, each with a long, pointed extension of the connective; b) Monocolpate, reticulate pollen in situ in stamen from stamen pair in (a); c) Fragment of stamen with prominent apical extension of the connective; d) Reticulate, apparently monocolpate, pollen in situ in stamen fragment in (c); e) Stamen with basifixed anther, perhaps sessile, and with prominent, wing-like apical extensions of the connective; note the dehisced thecae with the anther wall curved back; f, g) Monocolpate, reticulate pollen in situ in stamen in (e). Specimens, Catefica 49-S107780 (a, b), Catefica 49-S107784 (c, d), Catefica 49-S107781 (e–g). Scale bars = 600 Μm (a, c, e), 6 Μm (b, d, f, g). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 29. Scanning electron microscope (SEM) images of stamens and pollen grains of cf. Endressistemon sp. 1 (a, b), cf. Endressistemon sp. 2 (c, d) and cf. Endressistemon sp. 3 (e–g); Catefica locality, Portugal. a) Two adhering stamens, each with a long, pointed extension of the connective; b) Monocolpate, reticulate pollen in situ in stamen from stamen pair in (a); c) Fragment of stamen with prominent apical extension of the connective; d) Reticulate, apparently monocolpate, pollen in situ in stamen fragment in (c); e) Stamen with basifixed anther, perhaps sessile, and with prominent, wing-like apical extensions of the connective; note the dehisced thecae with the anther wall curved back; f, g) Monocolpate, reticulate pollen in situ in stamen in (e). Specimens, Catefica 49-S107780 (a, b), Catefica 49-S107784 (c, d), Catefica 49-S107781 (e–g). Scale bars = 600 Μm (a, c, e), 6 Μm (b, d, f, g).
Text-fig. 28. Scanning electron microscope (SEM) images of stamens and pollen of Endressistemon cateficensis gen. et sp. nov.; Catefica locality, Portugal. a, b) Staminal structure with two lateral stamens and one median structure seen in ventral and dorsal view (orientation unknown) showing that each stamen has a prominent apical extension and two pairs of pollen sacs separated by a narrow connective; both stamens are borne on a common base together with the median structure and their anthers are sessile on the common stalk; note the apical projection of the median structure (asterisk) between the two stamens and the ribs over probable vascular bundles that extend from the common base into the apical projections of both stamens and the median structure (arrows); c) Staminal structure showing two stamens with prominent apical projections and median axis-like structure between the two stamens (arrow); d) Staminal structure showing two stamens with prominent apical projections borne on a common base; e) Staminal structure in (a) and (b), from the same orientation as (b), showing the ribs over probable vascular bundles (yellow) that extend into the apical projections; f) Detail of staminal structure in (a) and (b) showing the fused or strongly adhering apical projections of the two lateral stamens and the median structure (asterisk); g) Monocolpate, reticulate pollen grains from the pollen sacs of stamen in (d). Specimens, Catefica 49-S107778 (holotype, a, b, e, f), Catefica 49-S107769 (c), Catefica 49-S107751 (d, g). Scale bars = 600 Μm (a–d), 300 Μm (e), 100 Μm (f), 6 Μm (g). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 28. Scanning electron microscope (SEM) images of stamens and pollen of Endressistemon cateficensis gen. et sp. nov.; Catefica locality, Portugal. a, b) Staminal structure with two lateral stamens and one median structure seen in ventral and dorsal view (orientation unknown) showing that each stamen has a prominent apical extension and two pairs of pollen sacs separated by a narrow connective; both stamens are borne on a common base together with the median structure and their anthers are sessile on the common stalk; note the apical projection of the median structure (asterisk) between the two stamens and the ribs over probable vascular bundles that extend from the common base into the apical projections of both stamens and the median structure (arrows); c) Staminal structure showing two stamens with prominent apical projections and median axis-like structure between the two stamens (arrow); d) Staminal structure showing two stamens with prominent apical projections borne on a common base; e) Staminal structure in (a) and (b), from the same orientation as (b), showing the ribs over probable vascular bundles (yellow) that extend into the apical projections; f) Detail of staminal structure in (a) and (b) showing the fused or strongly adhering apical projections of the two lateral stamens and the median structure (asterisk); g) Monocolpate, reticulate pollen grains from the pollen sacs of stamen in (d). Specimens, Catefica 49-S107778 (holotype, a, b, e, f), Catefica 49-S107769 (c), Catefica 49-S107751 (d, g). Scale bars = 600 Μm (a–d), 300 Μm (e), 100 Μm (f), 6 Μm (g).
Text-fig. 9. Scanning electron microscope (SEM) images of stamens and pollen of Proencistemon portugallicus gen. et sp. nov. (a–g) and Proencistemon sp. (h–j); Catefica locality, Portugal. a) Fragment of stamen whorl from staminate inflorescence showing almost sessile anthers; note short bracts at the base of the stamen whorl (arrow) and apparent paired arrangement of the stamens; b) Fragment of stamen whorl showing almost sessile anthers and apparent paired arrangement of the stamens; c) Pollen in situ from stamen whorl in (b) showing poorly defined trichotomocolpate aperture and semitectate-reticulate tectum; d–g) Distal views of pollen in situ from pollen clump showing poorly defined trichotomocolpate aperture, semitectate-reticulate tectum (d–f), and fractured pollen wall with long, scattered columellae supporting narrow muri (g); h) Fragment of staminate inflorescence with narrow, almost sessile, stamens; i, j) Pollen from fragment of staminate inflorescence in (h) showing poorly defined trichotomocolpate aperture (i), semitectate-reticulate tectum (i, j) and long, scattered columellae supporting narrow muri (j). Specimens, Catefica 49-S266015 (a), Catefica 342-S122086 (b, c), Catefica 50-S170394 (d–g), Catefica 49-S107783 (h–j). Scale bars = 600 Μm (a, b, h), 6 Μm (c–f, i), 1.5 Μm (g, j). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 9. Scanning electron microscope (SEM) images of stamens and pollen of Proencistemon portugallicus gen. et sp. nov. (a–g) and Proencistemon sp. (h–j); Catefica locality, Portugal. a) Fragment of stamen whorl from staminate inflorescence showing almost sessile anthers; note short bracts at the base of the stamen whorl (arrow) and apparent paired arrangement of the stamens; b) Fragment of stamen whorl showing almost sessile anthers and apparent paired arrangement of the stamens; c) Pollen in situ from stamen whorl in (b) showing poorly defined trichotomocolpate aperture and semitectate-reticulate tectum; d–g) Distal views of pollen in situ from pollen clump showing poorly defined trichotomocolpate aperture, semitectate-reticulate tectum (d–f), and fractured pollen wall with long, scattered columellae supporting narrow muri (g); h) Fragment of staminate inflorescence with narrow, almost sessile, stamens; i, j) Pollen from fragment of staminate inflorescence in (h) showing poorly defined trichotomocolpate aperture (i), semitectate-reticulate tectum (i, j) and long, scattered columellae supporting narrow muri (j). Specimens, Catefica 49-S266015 (a), Catefica 342-S122086 (b, c), Catefica 50-S170394 (d–g), Catefica 49-S107783 (h–j). Scale bars = 600 Μm (a, b, h), 6 Μm (c–f, i), 1.5 Μm (g, j).
Key triggers of adaptive genetic variability of sessile oak [Q. petraea (Matt.) Liebl.] from the Balkan refugia: outlier detection and association of SNP loci from ddRAD-seq data
<p>Knowledge on the genetic composition of <em>Quercus petraea</em> in south-eastern Europe is limited despite the species' significant role in the re-colonisation of Europe during the Holocene, and the diverse climate and physical geography of the region. Therefore, it is imperative to conduct research on adaptation in sessile oak to better understand its ecological significance in the region. While large sets of SNPs have been developed for the species, there is a continued need for smaller sets of SNPs that are highly informative about the possible adaptation to this varied landscape. By using double digest restriction site associated DNA sequencing data from our previous study, we mapped RAD-tag sequences to the <em>Quercus robur</em> reference genome and identified a set of SNPs putatively related to drought stress-response. A total of 179 individuals from eighteen natural populations at sites covering heterogeneous climatic conditions in the southeastern natural distribution range of <em>Q. petraea</em> were genotyped. The detected highly polymorphic variant sites revealed three genetic clusters with a generally low level of genetic differentiation and balanced diversity among them but showed a north–southeast gradient. Selection tests showed nine outlier SNPs positioned in different functional regions. Genotype-environment association analysis of these markers yielded a total of 53 significant associations, explaining 2.4–16.6% of the total genetic variation. Our work exemplifies that adaptation to drought may be under natural selection in the examined <em>Q. petraea</em> populations.</p>
Data from: The effect of external flow on 3D orientation of a microscopic sessile suspension feeder, Vorticella convallaria
Open the record for dataset details and reuse information.
Impact of the 2011 Tohoku earthquake on the species diversity of rocky intertidal sessile assemblages
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Data for the paper "Dispersion of particles in a sessile droplet evaporating on a heated substrate"
<p><span><span>This file contains the data generated for each case demonstrated in the paper titled "Dispersion of particles in a sessile droplet evaporating on a </span>heated substrate" <br>Authors: Aman Kumar Jain, Fabian Denner, and Berend van Wachem. <br><br>The repository contains the 7 folders for 7 cases performed in stage 2 of the simulation described in table 4 of the paper. Cases C1 and C2 involve a droplet on a substrate at Ts = 25 ◦ C, while C3 and C4 involve a substrate at Ts = 50 ◦C. Marangoni stresses are considered in the even-numbered cases and neglected in the odd-numbered ones. The case names ending with suffix S denotes the standard silica particles and the case names ending with suffix N denotes neutrally buoyant articles. <br></span></p> <p><span>Along with these folders a python script "ParticleCombined.py" is added which uses the particle position data in each case folder to calculate the particle surface density. <br><br>Each case folder contains: <br>The fluid fields, mesh, and particle information are stored in folders Fields, DMs, Meshes and Particles. <br>A .xmf wrapper file is provided to read the simulation results in Paraview. <br>The "results.xmf" file shows the fluid data such as velocity, pressure and liquid volume fraction. The liquid volume fraction value, alpha, tracks the interface of an evaporating sessile droplet. <br>The "results_DEM.xmf" shows the particle data such as the position, velocity and other data sets associated with the particles. <br><br>Each case folder contains five *.csv files which contain the information of particle position for 5-time instances and are processed using the python script "ParticleCombined.py". <br><br>This research was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation), grant number 452916560.<br></span></p>
Shifts in dominance and complementarity between sessile oak and beech along ecological gradients
<p>Whether tree species benefit from growing in a mixed forest depends on the relative importance of positive versus negative interactions, which varies according to abiotic conditions. In mixture with sessile oak (Quercus petraea (Matt.) Liebl.), European beech (Fagus sylvatica L.) is often competitively dominant. Sessile oak, however, is more resistant to water deficit stress. Under water-limiting conditions, facilitation or even competition exerted by oak may gain in importance.</p> <p>We investigated the relative importance of dominance and complementarity in 7 triplets of pure and mixed forests in Belgium's temperate oceanic climate. We analysed ring width data of 145 oaks and 138 beech trees along three distinct gradients: a spatial (i) and a temporal (ii) water availability gradient and a temporal gradient in growing conditions (iii). Gradient (ii) was represented by a precipitation variable, obtained by defining a large set of candidate climate variables over variable time frames, narrowed down using a species and site-specific lasso model. Growing conditions on a temporal gradient (iii) were represented by standardized tree growth. Two sets of linear mixed-effects models were used. Growth models assess mixing effects on ring width along gradients (i) and (ii). Mixing index models test for all three gradients how they affect the relative difference in average ring width of trees in mixed and pure stands.</p> <p>Beech trees grew faster than oak trees, and mixing further increased beech growth while decreasing oak growth, except on drier sites where the negative effect on oak growth disappeared. Low precipitation years, in contrast, reduced the beneficial effect of mixing on beech. In years of low growth, the positive mixing effect on beech growth was reinforced, and the negative mixing effect on oak growth decreased.</p> <p>Synthesis. Mixing buffered against growth limitations in general, though this depends on the nature of the limitation and the gradient over which it is measured. On dry sites, competitive dominance of beech was replaced by higher complementarity between species. During dry years, however, oak did not profit from a decreased mixing benefit of beech.</p>
Greater functional similarity in mobile compared to sessile assemblages colonizing artificial coastal habitats
<p><span>Among anthropogenic habitats built in the marine environment, floating and non-floating structures can be colonized by distinct assemblages. However, there is little knowledge whether these differences are also reflected in the functional structure. This study compared the functional diversity of sessile and mobile invertebrate assemblages that settle over 3 months on floating vs. non-floating artificial habitats, in two Chilean ports. Using morphological, trophic, behavioral, and life history traits, we found differences between mobile and sessile assemblages regarding the effect of the type of habitat on the functional diversity. Compared to sessile assemblages, a greater functional similarity was observed for mobile assemblages, which suggests that their dispersal capacity enables them to balance the reduced connectivity between settlement structures. No traits, prevailing or selected in one or the other habitat type, were however clearly identified; a result warranting further studies focusing on more advanced stages of community</span><span> development.</span></p>
Figure 1 in The first finding of sessile ciliates Vorticella pyriforme Stiller, 1939 and Zoothamnium sinense Song, 1991 (Ciliophora, Peritrichia) in the Black Sea
Figure 1. Map of sampling area (September 2020).
Molecular phylogenetics of sessile Dolium sedentarium, a petalomonad euglenid
<p>The euglenids are a species-rich group of flagellates with varying modes of nutrition that can be found in diverse habitats. Phagotrophic members of this group gave rise to phototrophs and hold the key to understanding the evolution of euglenids as a whole, including the evolution of complex morphological characters like the euglenid pellicle. Yet to understand the evolution of these characters, a comprehensive sampling of molecular data is needed to correlate morphological and molecular data and to estimate a basic phylogenetic backbone of the group. While the availability of SSU rDNA and, more recently, multigene data from phagotrophic euglenids has improved, several 'orphan' taxa remain without any molecular data whatsoever. <em>Dolium</em> <em>sedentarium</em> is one such taxon: It is a rarely-observed phagotrophic euglenid that inhabits tropical benthic environments and is one of the few known sessile euglenids. Based on morphological characters, it has been thought of as part of the earliest branch of euglenids, the Petalomonadida. We report the first molecular sequencing data for <em>Dolium</em> using single-cell transcriptomics. Both SSU rDNA and multigene phylogenies confirm it as a solitary branch within Petalomonadida.</p>
Use of a Distal Colonoscope Attachment to Increase Detection of Sessile Serrated Adenomas
ClinicalTrials.gov study NCT03560037. IPD Sharing: YES. Countries: 1. Publications: 6.
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Annotated Behaviour and Observability Dataset (ABODe)
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