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33 results for “Staging Area”
Alkanna tinctoria (L.) Tausch roots in different soils and developmental stages, HPLC peak areas of alkannins/shikonins
<p>Table of peak areas of alkannins detected in the HPLC-UV/Vis analysis of extracts of <em>Alkanna tinctoria</em> (L.) Tausch root samples cultivated in the greenhouse in various soils. Samples come from four different stages of plant growth.</p>
Year 2001, 15 minute measurements of stage, water temperature, conductivity, dissolved oxygen, and pH on the Ipswich R. mainstem at North Reading, just upstream of Rt. 28 (~48 km2 drainage area).
Year 2001, continuous measurements, every 15 minutes, were made of stage, water temperature, conductivity, dissolved oxygen, and pH in a small headwater stream draining a moderate sized, mixed land use watershed. Measurements are for part of the ice free season (June – December). Discharge is determined from stage using discharge vs stage regressions. Several day gaps occur periodically due to removal for recalibration.
Year 2002, 15 minute measurements of stage, water temperature, conductivity, dissolved oxygen, and pH on the Ipswich R. mainstem at North Reading, just upstream of Rt. 28 (~48 km2 drainage area).
Year 2002, continuous measurements, every 15 minutes, were made of stage, water temperature, conductivity, dissolved oxygen, and pH in a small headwater stream draining a moderate sized, mixed land use watershed. Measurements are for the ice free season (March – December). No Discharge was determined because beaver activity prevented rating curve estimate. Several day gaps occur periodically due to removal for recalibration.
Year 2003, 15 minute measurements of stage, water temperature, conductivity, dissolved oxygen, and pH on the Ipswich R. mainstem at North Reading, just upstream of Rt. 28 (~48 km2 drainage area).
Year 2003, continuous measurements, every 15 minutes, were made of stage, water temperature, conductivity, dissolved oxygen, and pH in a small headwater stream draining a moderate sized, mixed land use watershed. Measurements are for part of the ice free season (March – December). No Discharge was determined because beaver activity prevented rating curve estimate. Several day gaps occur periodically due to removal for recalibration.
Text-fig. 13. Zoophycos isp. a: BK 17, Layer No. 6; b: BK 27, Layer No. 8; c: lateral tunnel continuing from spreite side to the surrounding rock, BK 28, Layer No. 23; d: BK 22, Layer No. 1; e: "juvenile" stage of the structure on a horizontal winding tunnel, BK 21, Layer No. 26; f: BK 24, Layer No. 17; g: broad winding tunnel adjacent to spreite, BK 26, Layer No. 6; h: BK 15, Layer No. 18; i: BK 23, Layer No. 2. Scale bar = 1 cm. in Early Complex Tiering Pattern: Upper Ordovician, Barrandian Area, The Czech Republic
Text-fig. 13. Zoophycos isp. a: BK 17, Layer No. 6; b: BK 27, Layer No. 8; c: lateral tunnel continuing from spreite side to the surrounding rock, BK 28, Layer No. 23; d: BK 22, Layer No. 1; e: "juvenile" stage of the structure on a horizontal winding tunnel, BK 21, Layer No. 26; f: BK 24, Layer No. 17; g: broad winding tunnel adjacent to spreite, BK 26, Layer No. 6; h: BK 15, Layer No. 18; i: BK 23, Layer No. 2. Scale bar = 1 cm.
Text-fig. 2. Condylopyge cf. rex (BARRANDE, 1846), middle Cambrian, latest Cambrian Stage 5 and lower Drumian, Jince Formation, Příbram-Jince Basin. a. internal mould of isolated cephalon (Specimen CGS CW 17), Potůček near Rejkovice locality (= locality 12 in Fatka and Kordule 1992) in lower levels of the Paradoxides (Eccaparadoxides) pusillus Zone. b. latex cast of external mould of isolated pygidium (Specimen CGS FK 63), Potůček near Rejkovice locality (= locality 12 in Fatka and Kordule 1992) in lower levels of the Paradoxides (Eccaparadoxides) pusillus Zone. c. internal mould of isolated cephalon (Specimen CGS CW 18), foot of the slope known as Vinice near Jince (locality 20 in Fatka and Kordule 1992) in lower levels of the Onymagnostus hybridus Zone. Condylopyge rex (BARRANDE, 1846), middle Cambrian, lower Drumian, Buchava Formation, Paradoxides (Eccaparadoxides) pusillus Zone, Skryje-Týřovice Basin. d. internal mould of isolated cephalon (NM-L43011a), Karáskovská rokle - nad chatami. e. internal mould of isolated pygidium (NM-L43014), Lůmek u Týřovic. f. internal mould of isolated cephalon (NM-L43013), Lůmek u Týřovic. Whitened with ammonium chloride sublimate. All scale bars are 1 mm. Photographs by Martin Valent (National Museum Prague). in Condylopyge Hawle Et Corda, 1847 In The Příbram-Jince Basin (Barrandian Area, The Czech Republic, Agnostida)
Text-fig. 2. Condylopyge cf. rex (BARRANDE, 1846), middle Cambrian, latest Cambrian Stage 5 and lower Drumian, Jince Formation, Příbram-Jince Basin. a. internal mould of isolated cephalon (Specimen CGS CW 17), Potůček near Rejkovice locality (= locality 12 in Fatka and Kordule 1992) in lower levels of the Paradoxides (Eccaparadoxides) pusillus Zone. b. latex cast of external mould of isolated pygidium (Specimen CGS FK 63), Potůček near Rejkovice locality (= locality 12 in Fatka and Kordule 1992) in lower levels of the Paradoxides (Eccaparadoxides) pusillus Zone. c. internal mould of isolated cephalon (Specimen CGS CW 18), foot of the slope known as Vinice near Jince (locality 20 in Fatka and Kordule 1992) in lower levels of the Onymagnostus hybridus Zone. Condylopyge rex (BARRANDE, 1846), middle Cambrian, lower Drumian, Buchava Formation, Paradoxides (Eccaparadoxides) pusillus Zone, Skryje-Týřovice Basin. d. internal mould of isolated cephalon (NM-L43011a), Karáskovská rokle - nad chatami. e. internal mould of isolated pygidium (NM-L43014), Lůmek u Týřovic. f. internal mould of isolated cephalon (NM-L43013), Lůmek u Týřovic. Whitened with ammonium chloride sublimate. All scale bars are 1 mm. Photographs by Martin Valent (National Museum Prague).
Arctic migrating barnacle geese utilise accommodation fields in a new agricultural staging area
Open the record for dataset details and reuse information.
Data from: Migration routes and staging areas of trans-Saharan Turtle Doves appraised from light-level geolocators
The identification of migration routes, wintering grounds and stopover sites are crucial issues for the understanding of the Palearctic-African bird migration system as well as for the development of relevant conservation strategies for trans-Saharan migrants. Using miniaturized light-level geolocators we report a comprehensive and detailed year round track of a granivorous trans-Saharan migrant, the European Turtle Dove (Streptopelia turtur). From five recovered loggers, our data provide new insights on migratory journeys and winter destinations of Turtle Doves originating from a breeding population in Western France. Data confirm that Turtle Doves wintered in West Africa. The main wintering area encompassed Western Mali, the Inner Delta Niger and the Malian/Mauritanian border. Some individuals also extended their wintering ranges over North Guinea, North-West of Burkina Faso and the Ivory-Coast. Our results reveal that all individuals did not spend the winter period at a single location; some of them experienced a clear eastward shift of several hundred kilometres. We also found evidence for a loop migration pattern, with a post-breeding migration flyway lying west of the spring route. Finally, we found that on their way back to breeding grounds Turtle Doves needed to refuel after crossing the Sahara desert. Contrary to previous suggestions, our data reveal that birds used stopover sites for several weeks, presumably in Morocco and North Algeria. This later finding is a crucial issue for future conservation strategies because environmental conditions on these staging areas might play a pivotal role in population dynamics of this declining species.
FIGURE 64 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURE 64. Metarhombognathus nudus (Viets, 1928), genital opening, male. FIGURES 65–66. Mictognathus werthelloides Newell, 1984, 65. genital opening, female; 66. genital plate, deutonymph. FIGURE 67. Phacacarus flavellus Bartsch, 1992, genitoanal plate, female. FIGURE 68. Rhombognathides spinipes (Viets, 1933), genital opening, female. FIGURES 69–70. Scaptognathides hawaiiensis Bartsch, 1988, female, 69. posterior part of genitoanal plate; 70. left AE with epimeral pore. FIGURES 71–72. Simognathus maculatus Bartsch, 1994, 71. posterior part of genitoanal plate, female; 72. posterior idiosoma with genital plate, protonymph. FIGURE 73. Simognathus fuscus Viets, 1936, posterior idiosoma with genital plate, deutonymph. FIGURE 74. Simognathus sp., genital plate, deutonymph. FIGURE 75. Simognathus actius Otto, 2000, posterior idiosoma with genital plate, protonymph. (ep, epimeral tube; gac, genital acetabula) Scale = 50 µm
FIGURES 76–80 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURES 76–80. Thalassarachna basteri (Johnston, 1836), 76. genital opening, female; 77. tip of everted ovipositor, female, dorsal aspect (anteroapical part omitted); 78. everted ovipositor, female, ventral aspect (posteroapical part omitted); 79. genital opening, male; 80. detail of posterior part of genital opening, male. FIGURE 81. Thalassarachna longipes (Trouessart, 1888), genital opening, female. FIGURES 82–83. Thalassarachna dissimilis (Bartsch, 1979), 82. genital region, female; 83. genital opening, male. FIGURE 84. Tropihalacarus longirostris (Bartsch, 1995), genital opening, male (three posterior pairs of subgenital setae omitted). FIGURE 85. Werthelloides bathyalis Bartsch, 1986, genital opening, female. (bgsp, basal genital spine; gac, genital acetabula; sgs, subgenital setae) Scale = 50 µm.
FIGURES 28–31 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURES 28–31. Bradyagaue drygalskii (Lohmann, 1907), 28. genital opening, female; 29. genital opening, male (subgenital setae omitted); 30. genital plate, deutonymph; 31. genital plate, protonymph. FIGURES 32–33. Camactognathus tesselatus (Morselli & Mari, 1982), 32. genital opening, female; 33. genitoanal plate, deutonymph. FIGURES 34–35. Coloboceras longiusculus Trouessart, 1889, 34. genital opening, female; 35. genital plate, deutonymph. FIGURE 36. Copidognathides ampliatus Bartsch, 1999, genital opening, male. FIGURE 37. Copidognathus magniporus Bartsch, 1973, genital opening, female. FIGURE 38. Copidognathus magnipalpus (Police, 1909), genital opening, female. FIGURE 39. Copidognathus caelatus Bartsch, 1994, genital opening and everted ovipositor, ventral aspect. FIGURE 40. Copidognathus wadjemupis Bartsch, 1999, everted ovipositor, ventral aspect. (agsp, apical genital spines; bgsp, basal genital spine; gac, genital acetabula; pgs, perigenital setae; sgs, subgenital seta) Scale = 50 µm.
FIGURE 53. Isobactrus hartmanni Bartsch, 1972 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURE 53. Isobactrus hartmanni Bartsch, 1972, genital region, female. FIGURES 54–55. Isobactrus obesus Bartsch, 1992, 54. genital plate, female; 55. genital region, tritonymph. FIGURES 56–59. Isobactrus aspidotus Bartsch, 2009, 56. genital opening, male; 57. genital region, tritonymph; 58. genital region, deutonymph; 59. genital region, protonymph. FIGURE 60. Isobactrus uniscutatus (Viets, 1939), genital plate, male. FIGURE 61. Lohmannella falcata (Hodge, 1863), genital plate, protonymph. FIGURES 62–63. Makarovana spinosa (Bartsch, 1978), female, 62. posterior part of genitoanal plate; 63. genital opening with everted ovipositor and two genital spines (enlarged), lateral aspect. (bgsp, basal genital spine; pgs, perigenital setae; pogs, postgenital sclerite; prgs, pregenital sclerite) Scale = 50 µm.
FIGURES 16–18 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURES 16–18. Arhodeoporus gracilipes (Trouessart, 1889), 16. genital region, female; 17. everted ovipositor, ventrolateral aspect; 18. genital opening, male. FIGURES 19–20. Arhodeoporus corallinus Otto, 2000, 19. genital region, female; 20. genital opening, male. FIGURES 21–22. Arhodeoporus bonairensis (Viets, 1936), 21. genital opening, female; 22. genital plate, deutonymph. FIGURES 23–24. Atelopsalis pacifica Bartsch, 1985, 23. posterior part of genitoanal plate, female, ventrolateral aspect (genital acetabula of the other side not illustrated); 24. genital plate, protonymph. FIGURES 25–26. Australacarus pustulatus Bartsch, 1993, 25. genitoanal plate, female; 26. genitoanal plate, male. FIGURE 27. Bathyhalacarus acutus Bartsch, 1982, genital opening, female. (fo, foveate surface structure; gac, genital acetabula; ov, ovipositor; pa, porose surface structure) Scale = 50 µm.
FIGURES 1–2. Acanthohalacarus reticulatus Bartsch, 2001, 1 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURES 1–2. Acanthohalacarus reticulatus Bartsch, 2001, 1. genital opening, female; 2. genital opening, male. FIGURES 3–4. Acarochelopodia biunguis Bartsch, 1988, 3. genitoanal plate, male; 4. genital plate, deutonymph. FIGURES 5–6. Acaromantis armatus Bartsch, 1977, 5. genital opening, female; 6. genital plate, protonymph. FIGURE 7. Actacarus spinosus Otto, 2000, posterior part of genitoanal plate, female. FIGURE 8. Agaue galatea Otto, 1999, genital plate, deutonymph. FIGURES 9–10. Agauopsis arborea Bartsch, 2003, 9. genital opening, female; 10. genital opening, male. FIGURE 11. Agauopsis arabia Bartsch & Chatterjee, 2001, everted ovipositor and two genital spines (enlarged), ventral aspect, female. FIGURE 12. Agauopsis mokari Otto, 1994, genital opening, male. FIGURE 13. Agauopsis sp. (A. furcata group), genital opening, female. FIGURES 14–15. Agauopsis moorea Bartsch, 1992, 14. genital opening, female; 15. genital opening, male. (agsp, apical genital spine; bgsp, basal genital spine; gac, genital acetabula; GF, genital foramen; gsc, genital sclerite; gsp, genital spines; pgs, perigenital setae; sgs, subgenital seta) Scale = 50 µm
FIGURES 41–43. Enterohalacarus minutipalpus Viets, 1938, 41 in The genital area of Halacaridae (Acari), life stages and development of morphological characters and implication on the classification
FIGURES 41–43. Enterohalacarus minutipalpus Viets, 1938, 41. anterior part of genital plate, female; 42. genital opening, lateral aspect, female; 43. genital plate, nymph. FIGURE 44. Halacarellus capuzinus (Lohmann, 1893), genital region, female. FIGURES 45–46. Halacarellus balticus (Lohmann, 1889), female, 45. everted ovipositor, lateral aspect; 46. apex of ovipositor, posteroapical part, lateral aspect. FIGURE 47. Halacaropsis hirsuta (Trouessart, 1889), genital opening, female. FIGURES 48–49. Halacarus bisulcus Viets, 1927, 48. genital opening, female; 49. genital opening, male. FIGURES 50–52. Halixodes novaezelandiae Bartsch, 1986, male, 50. genitoanal plate; 51. genital sclerites with stump-like, spinose subgenital setae; 52. genital opening (subgenital setae omitted). (aagsp, anteroapical genital spines; bgsp, basal genital spine; gac, genital acetabulum; gsp, genital spines; ov, ovipositor (at rest); pagsp, posteroapical genital spines; sgs, subgenital seta) Scale = 50 µm.
FIGURES 11–15 in Descriptions of the immature stages and new host plant records of Notozulia entreriana (Berg) (Hemiptera: Cercopidae) pests of grasses in subtropical areas of the Americas
FIGURES 11–15. Apical portion of tibiae and tarsi of immature stages of Notozulia entreriana. (11) First instar. (12) Second instar. (13) Third instar. (14) Fourth instar. (15) Fifth instar. Scale bar= 1 mm.
FIGURES 6–10 in Descriptions of the immature stages and new host plant records of Notozulia entreriana (Berg) (Hemiptera: Cercopidae) pests of grasses in subtropical areas of the Americas
FIGURES 6–10. Antennae of Notozulia entreriana, nymphal instars. (6) First instar. (7) Second instar. (8) Third instar. (9) Fourth instar. (10) Fifth instar. Scale bar = 1 mm.
FIGURES 1–5 in Descriptions of the immature stages and new host plant records of Notozulia entreriana (Berg) (Hemiptera: Cercopidae) pests of grasses in subtropical areas of the Americas
FIGURES 1–5. Immature stages of Notozulia entreriana in dorsal view. (1) First instar, (2) Second instar, (3) Third instar. (4) Fourth instar. (5) Fifth instar. Scale bar = 1 mm.
FIGURE. Euphorbia fuscoclada in situ, Mandritsara area. A. branch and details of spination; B. inflorescence, pistillate flower stage; C. inflorescence, fruiting stage; D. habit. Credits: P.Pavelka (A–D). in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)
FIGURE. Euphorbia fuscoclada in situ, Mandritsara area. A. branch and details of spination; B. inflorescence, pistillate flower stage; C. inflorescence, fruiting stage; D. habit. Credits: P.Pavelka (A–D).
Life‐stage‐dependent supergene haplotype frequencies and metapopulation neutral genetic patterns of Atlantic cod, Gadus morhua, from Canada's Northern cod stock region and adjacent areas
<p class="BodyA">Among highly migratory fish species, nursery areas occupied by juveniles often differ from adult habitats. To better understand the spatial dynamics of Canada's Northern cod stock, juveniles caught off the east coast of Newfoundland and Labrador were compared to adults from the same region as well as individuals from other areas in Atlantic Canada using ddRAD-derived SNPs. A reduced proportion of homozygotes with a chromosomal inversion located in LG1 was detected between juvenile and adult samples in the Northern cod stock region, potentially indicating age-dependent habitat use or ontogenetic selection for attributes associated with the many genes located in LG1. No neutral genetic differences were found between samples from the Northern cod stock; however, significant differences were found between some of these samples and cod collected from St. Pierre Bank, Bay of Fundy, Browns Bank and the southern Scotian Shelf. Clustering analysis of variants at neutral loci provided evidence for three major genetic units: 1) the Newfoundland Atlantic Coast, 2) eastern and southern Gulf of St. Lawrence and Burgeo Bank, and 3) the Bay of Fundy, Browns Bank and southern Scotian Shelf. Both adaptive and neutral population structure within the Northern cod stock should be considered by managers to promote rebuilding.</p>
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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