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Fig. 22 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 22. Paralosalda innova. Male abdominal morphology (scanning electron micrographs). A. Dorsal view of anterior region of abdomen. B. Detail of right laterotergite 2 showing setae of abdominal grasping organ. C. Detail of setae of abdominal grasping organ. D. Dorsolateral view of parandria showing absence of medial membranous region. aga, abdominal grasping apparatus.

Fig. 18 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 18. Pseudosaldula vulgaris (scanning electron micrographs). A. Lateral view of whole specimen using backscatter electrons. B. Frontolateral view of face showing condition of transverse swelling across base of clypeus. C. Lateral view of pronotum, scutellum, and base of hemelytron. D. Detail of clavus and row of punctures along claval suture, showing suberect simple setae and microtricha. E. Perspective view of gland pore on paramere. F. Detail of gland pore on paramere. tvs, transverse swelling.

Fig. 13 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 13. Pseudosaldula perula (scanning electron micrographs). A. Lateroventral view of left paramere. B. Apex of left paramere showing short setiform sensors. C. Detail of ventral face at level of processus sensualis showing perspective view of the gland pores. D. Detail of gland pore on paramere. glp, gland pore.

Fig. 12 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 12. Pseudosaldula huamachuco (scanning electron micrographs). A. General view of ventral face of right paramere. B. Detail of setae on processus sensualis as viewed from ventral face of paramere. C. Apex of left paramere showing short setiform sensors. D. Detail of gland pore on paramere.

Fig. 11 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 11. Pseudosaldula chilensis (scanning electron micrographs). A. Elongate seta on ventral surface of hind femur. B. Detail of base of elongate seta on ventral surface of hind femur. C. Ventral view of base of right forewing showing hypocostal ridge and wing coupling mechanism. D. Dorsal view of abdomen of male. E. Doral view of pygophore (detail) showing parameres in repose. F. Abdominal grasping organ in male, left side. G. Abdominal grasping organ in male, right side. aga, abdominal grasping apparatus.

Fig. 24 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 24. Saldula ablusa (scanning electron micrographs). A. Frontoventral view of left paramere. B. Apical view of left paramere. C. Detail of processus sensualis showing insertion of setae on moundlike area. D. Apex of paramere showing short setiform sensors. E. Dorsal view of parandria. F. Detail of gland pore on paramere.

Fig. 26 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 26. Cladogram of relationships of Pseudosaldula spp. Strict consensus of two equally most parsimonious cladograms. Ambiguity of relationships exists in the placement of P. aurea.

Fig. 5 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 5. Pseudosaldula andensis (scanning electron micrographs). A. Lateral view of whole specimen. B. Frontolateral view of face showing structure of transverse swelling across base of clypeus. C. Lateral view of pronotum, scutellum, and base of hemelytron showing erect setae on dorsum. D. Detail of scutellum and clavus showing erect setae and interface between areas of polished cuticle on scutellum and microtrichia on clavus. E. Detail of clavus and row of punctures along claval suture, showing suberect simple setae and microtricha. F. Detail of gland pore on paramere. mp, mandibular plate; tvs, transverse swelling.

Fig. 7 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 7. Pseudosaldula bergi (scanning electron micrographs). A. Lateral view of whole specimen. B. Lateral view of base of hemelytron showing short recumbent setae and dense covering of microtrichia on dorsum and polished radial vein. C. Microtricha on forewing. D. Membrane of forewing showing setae on veins. E. Ventral face of left paramere, apical half. F. Detail of ventral face of left paramere at level of processus sensualis. G. Apex of left paramere showing short setiform sensors.

Fig. 6 in Revision And Analysis Of Pseudosaldula Cobben (Insecta: Hemiptera: Saldidae): A Group With A Classic Andean Distribution

Fig. 6. Pseudosaldula andensis (scanning electron micrographs). Left paramere. A. Ventral face at level of processus sensualis. B. Dorsal face at level of processus sensualis. C. Apex of paramere, showing short setiform sensors. D. View of paramere from apical region along dorsal face of shaft. ps, processus sensualis.

Fig. 3. Lumbricus terrestris Linnaeus, 1758 in First Records from Japan of European Vermi-composter Dendrobaena veneta (Rosa, 1886) and of "Classical" Lumbricus terrestris Linnaeus, 1758 (Annelida, Oligochaeta, Megadrilacea, Lumbricidae)

Fig. 3. Lumbricus terrestris Linnaeus, 1758 diagram (modified from Blakemore 1997, 2000, 2020, 2021) compared to 2021 KPM specimens (KPM-NJL 79–80).

Fig. 6 in First Records from Japan of European Vermi-composter Dendrobaena veneta (Rosa, 1886) and of "Classical" Lumbricus terrestris Linnaeus, 1758 (Annelida, Oligochaeta, Megadrilacea, Lumbricidae)

Fig. 6. Eisenia fetida (author's camera lucida image) compared to D. veneta [after Sims & Gerard (1999: fig. 28) of"Eisenia veneta"with its cocoon]. TP = tubercula pubertatis.

Fig. 2 in First Records from Japan of European Vermi-composter Dendrobaena veneta (Rosa, 1886) and of "Classical" Lumbricus terrestris Linnaeus, 1758 (Annelida, Oligochaeta, Megadrilacea, Lumbricidae)

Fig. 2. Dendrobaena veneta (Rosa, 1886) dorsal and zoomed ventral habitus of mature specimen from Zama, Nov. 2020; fixed in 70 % EtOH (KPM-NJL 78 that provided small tissue samples for DNA analysis) (author's photo).

Fig. 4 in First Records from Japan of European Vermi-composter Dendrobaena veneta (Rosa, 1886) and of "Classical" Lumbricus terrestris Linnaeus, 1758 (Annelida, Oligochaeta, Megadrilacea, Lumbricidae)

Fig. 4. Striped body and pale or pinkish matured clitellum are shared characteristics, but closely paired setae are distinctive for Eisenia fetida as indicated (after Wiki image"close-up of red wiggler worm [sic] with visible bristles [sic]"Eisenia_fetida_HC1.jpg).

openJul 2024View details →

Recordings of classical music (voice with piano, piano solo) with smartphones and professional audio equipment

To investigate differences of performance rating and perception of classical music demo videos, two demos were recorded with six devices (four Smartphones with main cam video function, one field recorder, one professional setup). Video and Audio were separated for each file, only the audio files were used in the study and are thus presented here. The music of the voice demo is from the genres of romantic lied and romantic and modern opera, the piano solo music was composed in the 20th century. The documentation follows the recommendations of the German Society for Acoustics (DEGA), the information is as following: A 3D model of the recording situation. The audio files, normalised (as used in the corresponding study) and with original level. Geometric measurements of room dimensions. Pictures of the recording. A list of the equipment and recording system. Render statistics (provided by the DAW used, Reaper). Scores of two of the three pieces. A Takelist.

opencc-by-4.0Oct 2024View details →

Data Sets for "Efficient Solution of the Number Partitioning Problem on a Quantum Annealer: A Hybrid Quantum-Classical Decomposition Approach"

Open the record for dataset details and reuse information.

dryad28/100

Diet of the brown bear in Himalaya: combining classical and molecular genetic techniques

The ecological requirements of brown bears are poorly known in the Himalaya region, which complicates conservation efforts. We documented the diet of the Himalayan brown bear ( Ursus arctos isabellinus ) by combining classical scat analysis and a newly developed molecular genetic technique (the trn L approach), in Deosai National Park, Pakistan. Brown bears consumed over 50 plant species, invertebrates, ungulates, and several rodents. Eight plant families; Poaceae, Polygonaceae, Cyperaceae, Apiaceae, Asteraceae, Caryophyllaceae, Lamiaceae, and Rubiaceae were commonly eaten with graminoids comprising the bulk of the diet. Golden marmots comprised the major mammalian biomass in the park, and were also the main meat source for bears. Animal matter, making 36% of dietary content, contributed half of the digestible energy, due to its higher nutritious value. We did not find a significant temporal pattern in diet, perhaps because the availability of the major diet (graminoids) did not change over the foraging period. Male brown bears were more carnivorous than females, probably because of their larger size, which requires higher energy and also makes them more efficient in capturing marmots. Frequencies of three plant species were also significantly higher in male brown bears; Bistorta affinis , Carex diluta , and Carex sp. Diet of the brown bear differed significantly between the park and surrounding valleys. In valleys, diet consisted predominantly of graminoids and crops, whereas the park provided more nutritious and diverse food. The estimated digestible energy available to brown bears in Deosai was the lowest documented among brown bear populations, due to the lack of fruits and a relatively lower meat content. The low nutritious diet and high cost of metabolism in a high altitude environment, probably explains the very low reproductive potential of this population

opencc-zeroNov 2019View details →

dryad28/100

Data from: Transition from fractional to classical Stokes-Einstein behaviour in simple fluids

An optical technique for tracking single particles has been used to evaluate the particle diameter at which diffusion transitions from molecular behaviour described by the fractional Stokes-Einstein relationship to particle behaviour described by the classical Stokes-Einstein relationship. The results confirm a prior prediction from molecular dynamic simulations that there is a particle size at which transition occurs and show it is inversely dependent on concentration and viscosity but independent of particle density. For concentrations in the range 510-3 to 510-6mg/mL and viscosities from 0.8 to 150 mPa s, the transition was found to occur in the diameter range 150 to 300nm.

opencc-zeroDec 2016View details →

opencc-by-4.0Jan 2023View details →

Supplementary material to 'Hybrid Symmetry Breaking in Classical Spin Models With Subsystem Symmetries'

Data from numerical simulations of 3D Kitaev and AntiKitaev model on cubic lattice.