Find research datasets worth reusing

Figs 3–14 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Figs 3–14. Cyclophoridae: (3) Cyathopoma diegoense, 1.8×2.5 mm, stn 7. Maizaniidae: (4) Maizania wahlbergi, 11.5×15.2 mm, stn 3. Pomatiidae: (5) Tropidophora nyasana, 16.7×17.7 mm, stn 7; (6) T. ligata, 17.5×18.3 mm, stn 17; (7) T. insularis, 17.2×17.0 mm, stn 4; (8) T. zanguebarica, 11.0×10.8 mm, stn 9. Truncatellidae: (9) Truncatella marginata, 6.0×2.5 mm, stn 7. Pupillidae: (10) Pupoides coenopictus, 4.3×2.2 mm, stn 7. Gastrocoptidae: (11) Gastrocopta klunzingeri, 1.8×1.0 mm, stn 7. Vertiginidae (stn 7): (12) Nesopupa peilei, 1.7×1.0 mm; (13) Nesopupa corrugata, 2.0×1.0 mm; (14) Nesopupa bisulcata, 1.3×0.8 mm. Scale bar 1 mm in Figs 3, 10–14; 10 mm in Figs 4–8; 2 mm in Fig. 9.

Fig. 2 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Fig. 2. Cumulative graph of the number of species recorded sequentially at the stations in the sampled area.

Figs 46–52 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Figs 46–52. Euconulidae: (46) Microcystina minima, 0.68×1.20 mm, stn 7; (47) Afroguppya rumrutiensis, 1.3×1.9 mm, stn 7; Helicarionidae: (48) "Sitala" jenynsi, 10.5×16.0 mm, stn 12; (49) Trochonanina albopicta, 7.5×11.5 mm, stn 5; (50) T. bloyeti, 5.8×12.0 mm, stn 17; (51) Trochozonites crenulata, 9.3×12.0 mm, subadult, stn 7; (52) Quickia concisa, 6.0×3.9 mm, stn 7. Scale bar 1 mm in Figs 46–47; 5 mm in Figs 48–52.

Figs 26–29 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Figs 26–29. Subulinidae: (26) Curvella nyasana, 10.6×5.7 mm, stn 1; (27) Euonyma tugelensis, 7.2×2.6 mm, subadult, stn 1; (28) Opeas hannense, 5.4×1.8 mm, stn 1; (29) Allopeas? cf. acmella, 4.0×1.2 mm, stn 7.

Figs 56–61 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Figs 56–61. Pomatiidae: (56) Tropidophora ligata, shell 15.5×15.3 mm, stn 7; (57) T. zanguebarica, shell 10.0×9.5 mm, stn 7; Cerastidae: (58) Rhachistia catenata, shell 10.0×6.3 mm, subadult, stn 1; Achatinidae: (59) Achatina immaculata, shell 102×56 mm, stn 1; Subulinidae: (60) Kempioconcha boivini, shell 16.0×8.4 mm, stn 1; (61) K. conradti, shell 13.7×6.2 mm, stn 8.

Figs 15–25 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Figs 15–25. Cerastidae: (15) Gittenedouardia metuloides, 6.0×3.6 mm, subadult, stn 1; (16) Rhachistia catenata, 13.2×7.8 mm, stn 11; (17) Rachis cunctatoris, 19.1×8.6 mm, stn 5; (18) Limicena nyasana, 11.8×9.1 mm, subadult, stn 7. Achatinidae: (19) Achatina immaculata, 11.3×9.3 mm, juvenile, stn 1; (20) A. randabeli, 43.8×23.0 mm, stn 9. Subulinidae: (21) Kempioconcha cf. obtusa, 39.1×17.5 mm, two shells composite subadult, stn 14; (22) K. kirki, 30.2×13.9 mm, stn 6; (23) K. boivini, 17.8×9.1 mm, stn 5; (24) K. cf. subolivacea, 19.6×7.3 mm, stn 19; (25) K. conradti (von Martens, 1895), 15.4×6.4 mm, stn 5.

Figs 39–45 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Figs 39–45. Gulella delgada sp.n., stn 7: (39–43) 1st syntype, 4.0×1.8 mm, five views; (44) 2nd syntype, 3.8×1.8 mm; (45) 3rd syntype, 2.7×1.8 mm.

Fig. 1 in Terrestrial molluscs of Cabo Delgado and adjacent inland areas of north-eastern Mozambique

Fig. 1. Map of the sampled area with the plotted stations and the base camp. See Table 1 for additional information.

opencc-zeroDec 2023View details →

dryad40/100

Lake effect on summer cooling of shorelines and adjacent inland forests on Lake Superior's north shore

Climate refugia, or areas that are projected to remain relatively stable under climate change, can serve as remnant habitat or steeping stones for species dispersal. The largest freshwater lake in the world by surface area, Lake Superior, serves as a model system for understanding cooling-mediated local refugia, as its cool summer water temperatures and wave action have maintained shoreline habitats suitable for disjunct opulations for arctic-alpine plants since deglaciation. It is known to affect local climates by providing a summer cooling effect near its shorelines, however, the inland gradient of change and spatial patterns of cooling has not been quantified. Here, we describe the extent of the inland cooling gradient, the degree of temperature buffering, and patterns of cooling for Lake Superior's north shore over a 3-year period. Specifically, we established 7 transects along Lake Superior's north shore, with temperature data loggers placed at 10 m, 100 m, 1 km, 10 km, and 100 km inland. We analyzed temperature data by year, month, summer maximum, and growing degree days (GDD0) for each site. Summertime cooling at shore sites (10m) was ~5 °C cooler than inland control sites (100 km), while sites 10 km from the shore were still 1.6 °C cooler than control sites. Magnitude of cooling varied geographically, with sites further west and southeast showing little to no cooling effect. Site on the exposed north and northeast shore where disjunct arctic-alpine plants are most common showed the highest degree of temperature buffering. We also found that shoreline sites on the north and northeast shore had shorter growing seasons compared to inland control sites. Finally, the number of days per year warmer than 16 °C, a maximum temperature threshold associated with arctic-alpine plant occurrences, averaged 65 days per year at 10 m sites and 82 days per year at control sites. The north shore of Lake Superior serves as a transition zone between temperate deciduous forests and boreal forests and is predicted to transition to deciduous forests under climate change. An understanding of the extent of lake-mediated cooling on adjacent forests can better inform risk to arctic-alpine disjunct species, inland forests, and overall vegetation transition models on Lake Superior's north shore.

opencc-by-4.0Dec 2023View details →

Supplemental Movie 3: Simultaneous dual-color imaging of ICC-SM in the colon and adjacent SMCs.

Supplemental Movie 3: Simultaneous dual-color imaging of ICC-SM in the colon and adjacent SMCs.   Video shows spontaneous, propagating Ca2+ waves through an ICC-SM network along the submucosal surface of the CM in the proximal colon.  FOVs are from a muscle of a mouse expressing GCaMP6f in ICC (left FOV; colored green) and RCaMP1.07 in SMCs (right FOV; colored red) imaged simultaneously with a 20x objective. The characteristics of the fluorophores are such that there is minimal spectral overlap. Signals in ICC-SM and SMCs are coordinated, showing initiation of each cycle of Ca2+ transients in the ICC-SM network followed by activation of SMCs adjacent to ICC-SM. Bottom panel shows traces from fluorescence images:  ICC-SM transients (green trace) preceded Ca2+ signals in SMCs (red trace). Copied with permission from Reference (133).

dryad40/100

Distance functions of carabids in crop fields depend on functional traits, crop type and adjacent habitat: a synthesis

Natural pest and weed regulation are essential for agricultural production, but the spatial distribution of natural enemies within crop fields and its drivers are mostly unknown. Using 28 datasets comprising 1,204 study sites across eight Western and Central European countries, we performed a quantitative synthesis of carabid richness, activity densities and functional traits in relation to field edges (i.e. distance functions). We show for the first time that distance functions of carabids strongly depend on carabid functional traits, crop type and, to a lesser extent, adjacent non-crop habitats. Richness of both predators and granivores and activity densities of small and granivorous species decreased towards field interiors, whereas the densities of large species increased. We found strong distance decays in maize and vegetables whereas richness and densities remained more stable in cereals, oilseed crops and legumes. We conclude that carabid assemblages in agricultural landscapes are driven by the complex interplay of crop types, adjacent non-crop habitats and further landscape parameters with great potential for targeted agroecological management. In particular, our synthesis indicates that a higher edge-interior ratio can counter the distance decay of carabid richness per field and thus likely benefits natural pest and weed regulation, hence contributing to agricultural sustainability.

opencc-zeroDec 2023View details →

opencc-by-4.0Feb 2024View details →

Station Data and Earthquake Catalogs - Distinct yet adjacent earthquake sequences near the Mendocino Triple Junction: 20 December 2021 Mw 6.1 and 6.0 Petrolia, and 20 December 2022 Mw 6.4 Ferndale

Supplemental Material for publication from The Seismic Record (TSR): <div> <div> <div> Yoon, C. E. and D. R. Shelly (2024). Distinct Yet Adjacent Earthquake Sequences near the Mendocino Triple Junction: 20 December 2021 Mw 6.1 and 6.0 Petrolia, and 20 December 2022 Mw 6.4 Ferndale, The Seismic Record. 4(1), 81–92, doi: 10.1785/0320230053. Data Sets S0-S4 with station data and earthquake catalogs in text format See README_Data_Supplement.pdf for more details about contents of each data file.  Please refer to the accompanying publication and its supplement for figures, tables, and equations. </div> </div> </div>

opencc-by-4.0Oct 2023View details →

Figs 139–152 in Taxonomy of the katydids (Orthoptera: Tettigoniidae) from East Asia and adjacent islands. Communication 16

Figs 139–152. Elbenia: 139 – E. (Elbenia) eudigitata sp. n.; 140–149 – E. (Aequapteron) appressa sp. n.; 150–152 – E. (Ae.) bispinosa Karny. Teeth of left male stridulatory vein from below (139, 140); left (141) and right (142) dorsal fields of male tegmina; male abdominal apex from above (143, 150), from below (144, 151), from side and slightly below (145), and from side (152); distal parts of male last tergite lobes and male genital plate from side (146); apex of latter plate from behind (147); female last tergite with genital plate from below (148); female abdominal apex with ovipositor from side (149). [150–152, after Karny (1926a).]

opencc-by-4.0Oct 2023View details →

Figs 63–79 in Taxonomy of the katydids (Orthoptera: Tettigoniidae) from East Asia and adjacent islands. Communication 16

Figs 63–79. Elbenia (Elbenia), male: 63–68 – E. (E.) carinata sp. n.; 69 – E. (E.)?nigrosignata (Stål); 70–74 – E. (E.) apicata sp. n.; 75–79 – E. (E.) semicarinata sp. n. Male abdominal apex from above (63, 70, 75), from below (64, 71, 76), from side (65, 72, 77) and from behind (66, 67, 69, 73, 78); left lobe (68, 74) or both lobes (79) of genital plate from behind. [69, after Karny (1923).]

opencc-by-4.0Oct 2023View details →

Figs 1–12 in Taxonomy of the katydids (Orthoptera: Tettigoniidae) from East Asia and adjacent islands. Communication 16

Figs 1–12. Elbenia, male: 1–3 – E. (Tamdaopteron) ryabovi sp. n.; 4–6 – E. (T.) daedala sp. n.; 7–9 – E. (T.) subrecta sp. n.; 10–12 – E. (Elbenia) carinata sp. n. Stridulatory apparatus of left (1, 5, 7, 11) and right (2, 6, 8, 12) dorsal tegminal fields from above; teeth of stridulatory vein of left tegmen from below (3, 4, 9, 10).

Fig. 4 in Four new species of the genus Thinophilus Wahlberg, 1844 (Diptera: Dolichopodidae) with new records and a key to species known from India and adjacent regions

Fig. 4. Thinophilus sambharensis sp. n. (holotype): A – habitus; B – head; C – antenna; D – fore leg; E – wing; F – hypopygium, lateral view, after maceration; G – surstylus, lateral view; H – cerci, dorsal view.

Fig. 3 in Four new species of the genus Thinophilus Wahlberg, 1844 (Diptera: Dolichopodidae) with new records and a key to species known from India and adjacent regions

Fig. 3. Thinophilus poinguinimensis sp. n. (holotype): A – habitus; B – head; C – antenna; D – wing; E – hypopygium, lateral view, after maceration; F – phallosoma and surstylus, ventral view; G – cerci, dorsal view.

Fig. 2 in Four new species of the genus Thinophilus Wahlberg, 1844 (Diptera: Dolichopodidae) with new records and a key to species known from India and adjacent regions

Fig. 2. Thinophilus somnathensis sp. n. (holotype): A – habitus; B – head; C – antenna; D – hind femur; E – wing; F – hypopygium, lateral view, after maceration; G – cerci, dorsal view.

Fig. 1 in Four new species of the genus Thinophilus Wahlberg, 1844 (Diptera: Dolichopodidae) with new records and a key to species known from India and adjacent regions

Fig. 1. Thinophilus calangutensis sp. n. (holotype): A – habitus; B – head; C – palpus; D – antenna; E – wing; F – hypopygium, lateral view, after maceration; G – cerci, dorsal view.