407 research outputs found

    Lyle Nelson Folder

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    33 pages of family history documents containing and related to Lyle Nelson - including: Statesman and Star News accounts and photos of Lyle Nelson, biathlon competitor from McCall; National Meets; Olympics; Author; Speaker; NBC ancho

    Katie Letcher Lyle, 3rd Annual ODU Literary Festival

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    While Katie Letcher Lyle is best known as the author of acclaimed novels for young people— I Will Go Barefoot All Summer For You, Fair Day, and Another Step Begun, — she has also published poems and nonfiction. She has written articles on popular music, the language arts, and food, in addition to producing four half-hour television scripts for the series Footsteps, now being aired nationally on PBS. She teaches at Southern Seminary and has appeared at many schools and conferences. A forthcoming novel, Scott\u27s Marathon, is scheduled for October publication

    Profile - Lyle Dick CHA Vice-President

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    Lyle Dick is the author of 90 publications on topics in Canadian and American history, historiography, and Arctic history, including the book Muskox Land: Ellesmere Island in the Age of Contact(University of Calgary Press, 2001), which was awarded the Harold Adams Innis Prize for Canada’s best-English-language book in the social sciences in 2003, and Farmers “Making Good”(Revised edition, University of Calgary Press, 2008), co-awarded the Canadian Historical Association’s Clio Prize in 1990 for the best book on the history of the prairie provinces

    Stasimopus finni Brandt & Sole & Lyle 2023, sp. nov.

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    Stasimopus finni sp. nov. (Figures 5B, 11B, 13A, 14, 15) Type material: Holotype Ô SOUTH AFRICA: Eastern Cape Province, Somerset East (-32.9386, 25.6612), 14.v.2018, S. Brandt, C. Sole, E. Engelbrecht and E. Brand, (NCA 2019/605). Etymology: The specific epithet is patronym in honour of Finn Robert Pirk the son of the third author, who loves all creepy crawlies. Diagnosis: The males of S. finni sp. nov. are distinguishable from other members of the genus occurring in the Karoo based on the following combination of characters. It is differentiated from S. astutus, S. erythrognathus, S. malesociatus sp. nov., S. patersonae, S. steynsbergensis, S. karooensis sp. nov. and S. mandelai based on the pedipalp not reaching the tarsus of leg I. Distinguished from S. palpiger as the pedipalp is longer than leg I, which S. finni sp. nov. is not. The species has denser cheliceral denticles (>11) than S. schrieneri (<5), S. ignis sp. nov. (<5) and S. maraisi (<10). Stasimopus finni sp. nov. is in general more spinose on the legs than S. dylani sp. nov. (Tibia of leg I and IV). Description: Based on the holotype Ô (NCA 2019/605). Remarks: Ô: The left AME is reduced in size, making some eye measurements unreliable. &female;: Known only from the type male. General: Ô: (Fig 5B) Medium bodied spider, 10.84 total length. Carapace: Ô: Carapace length 4.76; width 4.05. Deep red-brown colouration, thoracic region with rugose texture. Fovea procurved, 0.81 in length. Ocelli: Ô: (Fig 11B) AME diameter 0.14, PME diameter 0.19, MOQ anterior width 1.22 (may not be accurate due to deformity), MOQ posterior width 1.71; AME-AME 0.31 (may not be accurate due to deformity)., AME-ALE 0.10, ALE-ALE 0.65, PME-PME 0.79, PME-PLE 0.16, PLE-PLE 1.14. AER procurved, PER recurved. Chelicerae: Ô: (Fig 13A) Two teeth rows present, 4 teeth proventral row, 4 in retroventral row; 11–13 cuspules between rows. Sternum, labium and maxillae: Ô: (Fig 14C) Sternum length 2.66; sternum width 2.19. Sternum shape has distinct impressions of where the coxa are situated. Sigilla in the shape of a fused arrow, distal end fused, proximal end 0.69 apart; cuspules on labium absent; maxilla absent. Abdomen: Ô: (Fig 5B) Abdomen length 6.08; width 4.30. Pale beige colouration with dark grey banding, smaller band near carapace, followed by broader and wider band, then a narrower band, lastly two shorter bands next to one another. Pedipalps: Ô: (Fig 14A, B) Total length 16.03; Segment lengths 1.57, 5.42, 4.15, -, 4.88. Spines absent. Bulb oval, embolus elongated, tapering retrolaterally into sharp point. Legs: Ô: Length order: I, IV, II, III. I Total length 17.40; Segment lengths 5.54, 2.36, 4.22, 3.93, 1.35; Spination: spines absent on femur, with sparse setae. Patella v - 2–3 spines distally. Tibia (Fig 14D) v - 16–18 large spines extend pl & rl, denser distally. Metatarsus (Fig 14D) v - 15–16 large spines extend pl & rl. Tarsus (Fig 14D) pl & rl - 1–2 small spines, v - scopulate. II Total length 15.53; Segment lengths 4.77, 2.23, 3.63, 3.57, 1.33; Spination: spines absent on femur, with sparse setae. Patella v - 2–3 spines distally. Tibia v - 16 large spines extend pl & rl, denser distally. Metatarsus v - 14–16 large spines, 1 distinctly large spine distally on pl and rl aspects. Tarsus pl & rl - 2–3 small spines, v - scopulate. III Total length 11.75; Segment lengths 3.01, 1.54, 1.38, 3.68, 2.14; Spination: spines absent on femur, with sparse setae. Patella do - 11 small spines. Tibia pl - 1 spine, almost v, do - 2 unorganised rows of red spinules (11 pl / do; 8–9 rl / do). Metatarsus do - 8 spines in two 2, v (Fig 14E)—18 spines, 3 are large and distal. Tarsus v (Fig 14E)—7 small spines, extend pl & rl, dense setae covering spines. IV Total length 17.38; Segment lengths 4.27, 2.31, 3.66, 4.85, 2.29; Spination: spines absent on femur, with sparse setae. Patella do - short dense red spines proximally, less dense distally; interspersed with fine black setae. Tibia pl / v - 2–3 small spines. Metatarsus pl - 8 spines, v (Fig 14F)—I5 spines (4 large spines distally), spines extend pl. Tarsus (Fig 14F) pl - 11–14 spines, extend v, v - 7 small spines. Distribution and environment notes: The species is found in the localities indicated in Figure 15. The species is only known from the type locality near Somerset East in the Eastern Cape province. The location was a flat between small hills. The vegetation was dominated by low shrubs and aloe plants. The soil was very hard, chalky and pale. The specimen was found in a short burrow (Approx. 10cm deep). FIGURE 15. Map of the locality where the Stasimopus finni sp. nov. specimen was collected. Numbers match the site numbers in Figure 1. Map created in QGIS version 3.4.8-Madeira (2019), available at: http://qgis.osgeo.org.Published as part of Brandt, Shannon, Sole, Catherine & Lyle, Robin, 2023, An integrative taxonomy of the genus Stasimopus Simon 1892 (Araneae: Mygalomorphae) of the Karoo with the description of nine new species and a Stasimopus maraisi Hewitt 1914 male, pp. 1-60 in Zootaxa 5341 (1) on pages 24-27, DOI: 10.11646/zootaxa.5341.1.1, http://zenodo.org/record/832374

    Stasimopus dylani Brandt & Sole & Lyle 2023, sp. nov.

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    Stasimopus dylani sp. nov. (Figures 3B, 5A; 8, 9, 10, 11A) Type material: Holotype Ô SOUTH AFRICA: Western Cape Province: Murraysburg (-31.8884, 23.7310), 21.v.2018, S. Brandt, C. Sole, E. Engelbrecht and E. Brand, (NCA 2019/663). Paratypes. Same data, 21.v.2018, 1Ô (NCA 2019/664); Eastern cape Province: Jansenville (-32.8772, 24.4952), 17.vii.2015, I. Engelbrecht and D. Kambas, 4ÔÔ (NCA 2019/697, NCA 2019/698, NCA 2019/699, NCA 2019/702), Willowmore (-33.0423, 23.1958), 15.v.2018, S. Brandt, C. Sole, E. Engelbrecht and E. Brand, 1&female; juv. (NCA 2019/676). Etymology: This species is a patronym in recognition of Dylan Cecil Brandt, for his unending support and encouragement of the first author during her postgraduate studies. Diagnosis: The males of S. dylani sp. nov. are distinguishable from other members of the genus occurring in the Karoo based on the following combination of characters. Differentiated from S. astutus, S. erythrognathus, S. malesociatus sp. nov., S. patersonae, S. steynsbergensis, S. karooensis sp. nov. and S. mandelai based on the pedipalp not extending beyond the tarsus of leg I. It is distinguished from S. palpiger by the pedipalp that is longer than leg I, which is not the case with S. dylani sp. nov. The species can be distinguished from S. schrieneri, S. ignis sp. nov., S. finni sp. nov. and S. maraisi based on the largest eye, which in these species is the ALE, whereas in S. dylani sp. nov. it is the AME. Description: Based on the holotype Ô (NCA 2019/663) and paratypes 5Ô (NCA 2019/664, NCA 2019/697, NCA 2019/698, NCA 2019/699, NCA 2019/702). Remarks: &female;: Known only from males. General: Ô: (Fig 5A) Medium bodied spiders, ranging between 10.68–13.03 (13.03) total length. Carapace: Ô: Carapace length 4.78–6.28 (6.28); width 4.42–5.74 (5.74). Black colouration, thoracic region with rugose texture. The fovea strongly procurved, between 1.00–1.38 (1.11) in length. Ocelli: Ô: (Fig 11A, Fig 3B) AME diameter 0.26–0.28 (0.28), PME diameter 0.16–0.20 (0.19), MOQ anterior width 1.30–1.67 (1.67), MOQ posterior width 1.72–2.09 (2.05); AME-AME 0.25, AME-ALE 0.15, ALE-ALE 1.08, PME-PME 1.02, PME-PLE 0.16, PLE-PLE 1.62. AER arrangement slightly recurved, PER recurved. Chelicerae: Ô: (Fig 8B) Two teeth rows present, 4 teeth in proventral row, 5 teeth in retroventral row; 12 cuspules in between. Sternum, labium and maxillae: Ô: (Fig 8A) Sternum length 2.27–3.48 (3.48); sternum width 2.47–3.05 (3.05). Sternum shape has distinct impressions of where the coxa are situated. Sigilla in the shape of a fused arrow, distal end fused, proximal end 1.06–1.45 (1.12) apart; cuspules absent on labium and maxilla. Abdomen: Ô: (Fig 5A) Abdomen length 5.56–6.75 (6.75); width 3.45–4.63 (4.63). Colour, do - dark grey, v - and laterally beige. Pedipalps: Ô: (Fig 10A, B) Total length 19.01; Segment lengths 1.77, 6.41, 4.82, -,6.02. Spination: spines absent. Bulb compact, embolus elongated, tapering into sharp point, extending downwards, almost parallel to tibia. Legs: Ô: Length order: I, IV, II, III. I Total length 22.94; Segment lengths 7.07, 3.23, 4.86, 5.62, 2.16; Spination: spines absent on femur and patella, with sparse setae. Tibia v - 19 large spines (extending pl & rl), covering only distal half. Metatarsus (Fig 10C) pl - 19 large spines extending v, 21 large spines rl (slightly v). Tarsus (Fig 10C) pl - 4 spines, rl - 4 spines, v - scopulate. II Total length 20.88; Segment lengths 6.42, 2.86, 4.32, 5.21, 2.07; Spination: spines absent on femur and patella, with sparse setae. Tibia v - 5–7 spines distally. Metatarsus pl - 12–13 large spines extending v, rl - 10–11 large spines extending v. Tarsus pl - 4 spines, rl- 3–4 spines, v - scopulate. III Total length 16.45; Segment lengths 4.64, 2.26, 2.55, 4.35, 2.66; Spination: spines absent on femur, with sparse setae. Patella, do (slightly pl)- 7 small spines. Tibia (Fig 10F), do - Distally dense patch of spines (approx. 25), extend to metatarsus. Metatarsus (Fig 10D), pl - 11 spines, do - small patch of spines proximally (approx. 15) connecting to tibia, rl - 3 spines, v - 5 spines. Tarsus (Fig 10D) pl - 8 spines, rl - 7 spines. IV Total length 22.85; Segment lengths 5.32, 2.65, 4.50, 7.42, 2.96; Spination: spines absent on femur, with sparse setae. Patella (Fig 10G), do - short red spines proximally, less dense distally, interspersed with black setae. Tibia short black setae. Metatarsus (Fig 10E) pl - 5 spines, rl - 6 spines. Tarsus (Fig 10E) pl - 10 spines, rl - 9 spines. Distribution and environment notes: The species is found in the localities indicated in Figure 9. The species appears to have a broader distribution in the Western and Eastern Cape provinces of South Africa. The areas typically had sandy soils. The juvenile female was collected from a flat pan. All the males were collected while they were crossing quite roads. The SUOJ locality had no rain on the day collected, but a slight drizzle did occur after collection, whereas the males from FRE were collected after very heavy rain.Published as part of Brandt, Shannon, Sole, Catherine & Lyle, Robin, 2023, An integrative taxonomy of the genus Stasimopus Simon 1892 (Araneae: Mygalomorphae) of the Karoo with the description of nine new species and a Stasimopus maraisi Hewitt 1914 male, pp. 1-60 in Zootaxa 5341 (1) on pages 19-24, DOI: 10.11646/zootaxa.5341.1.1, http://zenodo.org/record/832374

    Schurian-finiteness of blocks of type AA Hecke algebras

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    For any algebra AA over an algebraically closed field F\mathbb{F}, we say that an AA-module MM is Schurian if EndA(M)F\mathrm{End}_A(M) \cong \mathbb{F}. We say that AA is Schurian-finite if there are only finitely many isomorphism classes of Schurian AA-modules, and Schurian-infinite otherwise. By work of Demonet, Iyama and Jasso it is known that Schurian-finiteness is equivalent to τ\tau-tilting-finiteness, so that we may draw on a wealth of known results in the subject. We prove that for the type AA Hecke algebras with quantum characteristic e3e\geq 3, all blocks of weight at least 22 are Schurian-infinite in any characteristic. Weight 00 and 11 blocks are known by results of Erdmann and Nakano to be representation finite, and are therefore Schurian-finite. This means that blocks of type AA Hecke algebras (when e3e\geq 3) are Schurian-infinite if and only if they have wild representation type if and only if the module category has finitely many wide subcategories. Along the way, we also prove a graded version of the Scopes equivalence, which is likely to be of independent interest.Comment: 40 pages. v4 combines the paper with its sequel arXiv:2208.05711 by Lyle and Speyer, adding Lyle as an author. v5 is the final version, to appear in The Journal of the London Mathematical Societ

    Ideas for justice

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    As part of the wider ‘What is Justice?’ symposium, the Ideas for Justice project is speaking to people about their understanding and experience of justice today. The interviews are being conducted by Harry Annison and Philippa Budgen. In this update on the ‘Ideas for Justice’ project, we reflect on the interviews that have been published so far

    A model for energy pricing with stochastic emission costs

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    Data source: Figures and tables, https://doi.org/10.1016/j.eneco.2009.11.001 Link to a related website: https://prism.ucalgary.ca/bitstream/1880/48998/1/Elliott_Model_Energy_2009_postprint_file.pdf, Open Access via UnpaywallWe use a supply-demand approach to value energy products exposed to emission cost uncertainty. We find closed form solutions for a number of popularly traded energy derivatives such as: forwards, European call options written on spot prices and European Call options written on forward contracts. Our modeling approach is to first construct noisy supply and demand processes and then equate them to find an equilibrium price. This approach is very general while still allowing for sensitivity analysis within a valuation setting. Our assumption is that, in the presence of emission costs, traditional supply growth will slow down causing output prices of energy products to become more costly over time. However, emission costs do not immediately cause output price appreciation, but instead expose individual projects, particularly those with high emission outputs, to much more extreme risks through the cost side of their profit stream. Our results have implications for hedging and pricing for producers operating in areas facing a stochastic emission cost environment.Robert J. Elliott, Matthew R. Lyle and Hong Mia

    Assembly of a novel cavitand utilizing dynamic covalent bond formation

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    Molecular assembly which utilizes dynamic covalent bonding is reported. Previously unreported cavitand 19 was synthesized and is shown to assemble into structure 20 which is composed of four cavitands and eight ethylenediamine by the formation of sixteen imine bonds.M.S.Includes bibliographical references (p. 42)
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