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83 results for “Labiatae”
Fig. 3a-j in Physico-chemical characteristics of habitats colonized by the pond snail Radix labiata (Gastropoda, Basommatophora, Lymnaeidae): a model approach
Fig. 3a-j: Graphical presentation of essential parameters associated with logistic regression: white vertical line: position of the maximum probability of occurrence (xmax), black bar: optimum range of the given variable, grey-shaded area: range of the given variable that is still tolerated by the species; a) water temperature, b) pH, c) electric conductivity, d) oxygen content in the water, e) nitrate concentration in the water, f) water depth, g) biological oxygen demand within five days, h) content of ammonium nitrogen, i) geographic altitude, j) current velocity.
Fig. 1 in Physico-chemical characteristics of habitats colonized by the pond snail Radix labiata (Gastropoda, Basommatophora, Lymnaeidae): a model approach
Fig. 1: General habitus of the shell of R. labiata as well as the living animal: a) Front view of the shell (height: 1.4 cm, width: 0.75 cm), b) back view of the shell, c) living animal with its typical triangular tentacles.
Fig. 2a-j in Physico-chemical characteristics of habitats colonized by the pond snail Radix labiata (Gastropoda, Basommatophora, Lymnaeidae): a model approach
Fig. 2a-j: Results of the logistic regression procedure carried out for ten environmental variables: a) water temperature, b) pH, c) electric conductivity, d) oxygen content in the water, e) nitrate concentration in the water, f) water depth, g) biological oxygen demand within five days, h) content of ammonium nitrogen, i) geographic altitude, j) current velocity.
Figure 2 in FLORA OF NEPAL NOTULAE II: PHLOMOIDES LONGIDENTATA PENDRY, A NEW SPECIES OF LABIATAE FROM NEPAL AND BHUTAN
Figure 2. Phlomoides longidentata Pendry, sp. nov. (from DNEP3 BY205). A, Upper part of plant (DNEP3 BX36); B, close-up of inflorescence; C, side view of flower. All photographs by C. A. Pendry.
Figure 1 in FLORA OF NEPAL NOTULAE II: PHLOMOIDES LONGIDENTATA PENDRY, A NEW SPECIES OF LABIATAE FROM NEPAL AND BHUTAN
Figure 1. Phlomoides longidentata Pendry, sp. nov. A, Inflorescence and bracts; B, basal leaf, upper surface; C, detail of stellate indumentum of lower leaf surface; D, bracteole; E, side view of flower; F, opened calyx, outer view; G, opened corolla; H, ovary and style. Scale bars: A and B, 4 cm; C, 0.05 mm; D–H, 5 mm. Drawn from DNEP3 BX36 by Claire Banks.
Figure 5 in Portia labiata (Araneae: Salticidae: Spartaeini) as predator and prey of a synanthropic Parasteatoda sp. (Araneae: Theridiidae: Theridiinae)
Figure 5. Prominent arachnologists responsible for the naming of Portia labiata. 1, Tord Tamberlan Teodor Thorell (1830-1901), Swedish arachnologist who first described a female Portia labiata (as Linus labiatus) from Burma in 1887. 2, Ferdinand Anton Franz Karsch (1853-1936), German arachnologist who named the genus Portia in 1878. It was only much later (Wanless 1978) that labiata was recognized as a Portia by Fred Wanless (1940-2017).
Figure 4 in Portia labiata (Araneae: Salticidae: Spartaeini) as predator and prey of a synanthropic Parasteatoda sp. (Araneae: Theridiidae: Theridiinae)
Figure 4 (continued from previous page). 6, Male feeding on a captured spider. 7, Penultimate male feeding on a captured spiderling. This male feed on a series of immatures from this brood. 8, Frontal view of adult male. Note the prominent retrolateral tibial apophysis and basal cymbial apophysis of each pedipalp. Male and female P. albimana have a much more extensive cover of white setae on their face and pedipalps.
Figure 3 in Portia labiata (Araneae: Salticidae: Spartaeini) as predator and prey of a synanthropic Parasteatoda sp. (Araneae: Theridiidae: Theridiinae)
Figure 3. Sequential photos (1-3) showing a nesting female Parasteatoda sp. feeding on a male Portia labiata (Karnataka, 20 JUN 2022). Photo credits: 1-3, Sanath R M.
Figure 2 in Portia labiata (Araneae: Salticidae: Spartaeini) as predator and prey of a synanthropic Parasteatoda sp. (Araneae: Theridiidae: Theridiinae)
Figure 2. Sequential photos (1-12) showing the capture of a female Portia labiata by a female Parasteatodes (Karnataka). The Portia approached this Parasteatodes from a distance but became entangled in her silk as the Parasteatodes wrapped her with more silk (1-3). Subsequently the Portia was bitten (4), then wrapped with more silk, and eaten (9, 11). Photo credits: 1-12, Vipin Baliga.
Figure 4 in Portia labiata (Araneae: Salticidae: Spartaeini) as predator and prey of a synanthropic Parasteatoda sp. (Araneae: Theridiidae: Theridiinae)
Figure 4 (continued on next page). Female (1-2) and male (3-8) Portia labiata from Karnataka. 1, Female guarding her brood. 2, Female feed on a captured spider. 3, Adult male (missing leg L4). 4-5, Adult male feeding on a nematoceran. Note the broad, white bands on the margins of the carapace,
Figure 1 in Portia labiata (Araneae: Salticidae: Spartaeini) as predator and prey of a synanthropic Parasteatoda sp. (Araneae: Theridiidae: Theridiinae)
Figure 1. Sequential photos (1-3) showing a female Portia labiata feeding on a female Parasteatoda sp. that she has captured (Karnataka, 2 FEB 2021). Note the presence of a small kleptoparasitic spider (arrows). Photo credits: 1-3, Abhijith APC.
Figure 1 in Portia cf. labiata (Araneae: Salticidae: Spartaeini) as predator and prey of cellar spiders (Araneae: Pholcidae: Crossopriza) in Karnataka, India
Figure 1. Female Portia representing three species that have been found in India. 1, P. albimana, Kundannor, Maradu, Ernakulam, Kerala, India (21 JUL 2013). 2, P. albimana, Halanayakanahalli, Karnataka, India (8 MAY 2021). 3, P. fimbriata, Daintree Forest, Queensland, Australia (9 DEC 2018). 4, P. labiata, Singapore (17 NOV 2021). 5, P. labiata, Malaysia (SEP 2019). 6, P. labiata with spider prey, Penang, Malaysia (FEB 2018). Species names have not been confirmed by microscopic examination. Photo credits (all from iNaturalist): 1, Sunny Josef; 2, Thomas Job; 3, martisma; 4, budak; 5-6, Richard Ong. Photographs used under either a CC BY 4.0 license (1), or a CC BY-NC 4.0 license (2-6).
Figure 3 in Portia cf. labiata (Araneae: Salticidae: Spartaeini) as predator and prey of cellar spiders (Araneae: Pholcidae: Crossopriza) in Karnataka, India
Figure 3. Female Portia cf. labiata near her nest and emergent (second instar) young. 1, Dorsal view of female on vertical wall. 2, Female beneath her nest. 3, Female clinging to her nest. Note emergent young above the nest. 4, Female concealed by debris, suspended with silk lines (detail of 5). 5, Female position in debris (yellow rectangle), near nest (arrow). 6-7, Two more views of female at nest, with emergent young. 8, Detail of emergent Portia above nest. 9-11, Three views of an emergent Portia feeding on a small, immature Crossopriza. Photographs by Abhijith A. P. C., taken at his Indraprastha Organic Farm, Kalalwadi Village, Karnataka, India.
Figure 2 in Portia cf. labiata (Araneae: Salticidae: Spartaeini) as predator and prey of cellar spiders (Araneae: Pholcidae: Crossopriza) in Karnataka, India
Figure 2. Adult female Portia cf. labiata. 1, Portia (at right) watching a nearby pholcid spider of the genus Crossopriza. 2-4, Three sequential images of a Portia feeding on a captured Crossopriza. Photographs by Abhijith A. P. C., taken at his Indraprastha Organic Farm, Kalalwadi Village, Karnataka, India.
Santa Barbara Coastal site, station Arroyo Quemado Reef, Santa Barbara Channel, study of animal cover of Phidolopora labiata in units of percent on a yearly timescale
The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Santa Barbara Coastal (SBC) contains animal cover of Phidolopora labiata measurements in percent units and were aggregated to a yearly timescale.
FIGURE 5 in New records of family Hormathiidae (Cnidaria: Actiniaria) from Brazilian coast with description of Paraphelliactis labiata n. sp.
FIGURE 5. Cnidae of Paraphelliactis labiata n. sp. A) Robust spirocyst. B) Gracile spirocyst. C, D, F, H, I, K, L, M, N) Basitrichs. E, G, J) Microbasic p-mastigophore. Scale bar: 10 μm.
FIGURE 4 in New records of family Hormathiidae (Cnidaria: Actiniaria) from Brazilian coast with description of Paraphelliactis labiata n. sp.
FIGURE 4. External view and histology of Paraphelliactis labiata n. sp. A) Longitudinal section of the uppermost part of the column showing the marginal sphincter muscle (arrow). B) Cross section of a tentacle showing the ectodermal longitudinal musculature (arrow). C) Top view of the body, evidencing the oral disc and one of the two siphonoglyphs (arrow) D) Cross section of the column at actinopharynx level showing cycles of mesenteries (roman numbers), and unpaired mesentery of the fourth and fifth cycle (asterisk) E) Scheme of the mesenterial arrangement shown in D (mesenteries of fifth cycle indicated by asterisks). Abbreviations: Lm, longitudinal muscle; Me, mesoglea; Ms, marginal sphincter; Pa, parietobasilar muscle; Re, retractor muscle; S, siphonoglyph. Scale bars: A, D, 500 µm; B, 200 µm; C, 10 mm.
FIGURE 3 in New records of family Hormathiidae (Cnidaria: Actiniaria) from Brazilian coast with description of Paraphelliactis labiata n. sp.
FIGURE 3. External view of Paraphelliactis labiata n. sp. Holotype: A) Lateral view of the holotype. Note the distinct pedal disc coloration and its complete absence of tubercles. B) Oral view of the holotype revealing a pronounced flattening of the column due to the overlapping lobes. Paratypes: C) Detail of the oral disc of the medium-sized individual, showing small and large tubercles. D) Smaller paratype. Abbreviations: Od, oral disc; Tu, tubercles. Scale bars: A, B, 30 mm; C, 3 mm; D, 2 mm.
FIGURE 2. A in New records of family Hormathiidae (Cnidaria: Actiniaria) from Brazilian coast with description of Paraphelliactis labiata n. sp.
FIGURE 2. A) Paraphelliactis labiata n. sp., holotype. B) Monactis vestita on Drillia sp. empty shell. C) Phelliactis robusta. D) Phelliactis sp. Abbreviations: Mn, manganese nodule. Scale bars: A, 30 mm; B, 10 mm; C, 20 mm.
FIGURE 6 in New records of family Hormathiidae (Cnidaria: Actiniaria) from Brazilian coast with description of Paraphelliactis labiata n. sp.
FIGURE 6. External view and histology of the sea anemones in this paper. A, E–F) A, E–F) Phelliactis sp. A) Detail of the distended base holding a manganese nodule. B–C) Monactis vestita. B) Individual with base greatly distended, evidencing the arrangement of mesenteries. C) Cross section through the midcolumn, showing the four cycles of mesenteries (represented in roman letters). D) Individual of Phelliactis robusta attached to hexactinellid sponge fibers. E) Detail of the tubercles at distal column, near the oral disc. F) Cross section at the midcolumn showing a pair of mesenteries from the second cycle and the diffuse musculature of the retractor (arrows). Abbreviations: Re, retractor muscle. Scale bars: A and D, 10 mm; B, 5 mm; C, 0.5 mm; and E, 2 mm; F, 200 μm.
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