124,431 research outputs found
Lepthyphantes rossitsae Dimitrov 2018, sp. n.
No full textLepthyphantes rossitsae sp. n. Figs 1-6, 10-12, 16-22 Types: Male holotype, 1 male paratype, 7 females paratypes; Turkey, Çamlik village, Beyşehir district, Maǧarasi cave; 10.07.1993; P. Beron leg. Etymology: I dedicate the species to my wife Rossitsa Dimitrova. Diagnosis: The new species is very similar to Lepthyphantes leprosus in somatic and genital characters. The male of L. rossitsae sp. n. can be distinguished by the shape of the narrow branch of the lamella characteristica, which is shorter and wider apically (Figs 1, 4, 16, 18), while in L. leprosus it is longer, narrower and forked at the end (Fig. 7). The embolus in both species is very similar, but in L. rossitsae sp. n. the teeth at its base are less numerous and tiny (Figs 2, 5, 17), while in L. leprosus they are more numerous and slightly bigger (Fig. 8). Also the big tubercle of the cymbium (Figs 3, 6, 19) is shorter and wider than in L. leprosus (Fig. 9). The female epigyne (Figs 10-12, 20-22) has almost the same lateral wall and lateral lobe as in L. leprosus, but the scape in L. rossitsae sp. n. is thinner and longer and there are no lateral teeth (Figs 13-15). Description of male (holotype): Measurements: Total length 3.85; cephalothorax length 1.48, width 1.25; sternum length 0.68, width 0.45; chelicera length 0.72, width 0.30; abdomen length 2.35, width 1.45; leg I length 11.75 (0.80 + 3.00 + 0.45 + 3.00 + 3.00 + 1.50); leg II length 10.75 (0.60 + 2.80 + 0.45 + 2.70 + 2.85 + 1.35); leg III length 8.45 (0.55 + 2.35 + 0.40 + 1.90 + 2.25 + 1.00); leg IV length 10.70 (0.62 + 2.70 + 0.40 + 2.63 + 3.00 + 1.35). Eyes: Both eye rows straight; AME smaller than other eyes, touching each other. Other eyes approximately equal in size. AME diameter 0.05; ALE, PLE, PME diameter 0.09; ALE separated from AME by 0.03. PME separated from PLE and each other by 0.08, ALE touching PLE. Chelicerae with 2 large distal and 2 small apical teeth on promargin and with 1 large distal tooth on retromargin. Coloration: carapace, sternum, chelicerae and legs yellow-brown. Abdomen grey, with white pattern (not very well preserved). Leg chaetotaxy: leg I (1p, 1d, 2d2p1v1r, 1d1r); leg II (-, 1d, 2d1r1v, 1d1p); leg III (-, 1d, 2d1r, 1d); leg IV (-, 1d, 2d1r, 1d). Palps (Figs 1-6, 16-19): Cymbium with one big and one small tubercle in its basal part, visible in dorsal view (Figs 3, 6, 19). Paracymbium connected to cymbium with its flat internal part. Lamella characteristica broad and incised, bifid. It’s narrow distal branch gradually widening to a fan shaped apical part (Figs 1, 4, 16). Embolus bent, sickle-shaped, bearing small teeth near its base (Figs 4-5, 17). Description of female (paratype): Measurements: Total length 4.05; cephalothorax length 1.60, width 1.25; sternum length 0.85, width 0.75; chelicera length 0.72, width 0.30; abdomen length 2.66, width 1.70; leg I length 10.47 (0.65 + 2.95 + 0.47 + 2.50 + 2.50 + 1.40); leg II length 9.45 (0.63 + 2.40 + 0.47 + 2.30 + 2.40 + 1.25); leg III length 7.00 (0.54 + 2.00 + 0.40 + 1.35 + 1.85 + 0.86); leg IV length 9.35 (0.56 + 2.40 + 0.40 + 2.25 + 2.52 + 1.22). Eye arrangement and coloration as in male. Chelicerae with 4 large teeth on promargin and 4 small apical teeth on retromargin. Leg chaetotaxy: leg I (1p, 1d, 2d1p2v1r, 1d1p1r); leg II (-, 1d, 2d1v2r, 1d1p1r); leg III (-, 1d, 2d1v1r, 1d); leg IV (-, 1d, 2d1r, 1d). Epigyne (Figs 10-12, 20-22): Lateral wall without teeth (Figs 10-11, 20-21). Scape long and narrow, widening at the end (Figs 10, 20). Two lateral lobes on each side of scape (Figs 10-11, 20-21). Distribution: Known only from the type locality. Remarks: As already stated by Helsdingen (2009), the splitting of Lepthyphantes s. l. into several distinct genera by Saaristo & Tanasevitch (1996, 1999, 2000, 2001) not only makes species identification difficult and user-unfriendly, but also leaves Lepthyphantes s. str. as a heterogeneous group containing all species that could not be placed with certainty in any of the present genera close to Lepthyphantes. This is also the case with Lepthyphantes leprosus. Previously it was listed as part of the Lepthyphantes nebulosus group. Meanwhile most of the species from this group have been transferred to Megalepthyphantes Wunderlich, 1994, but Lepthyphantes leprosus remained in Lepthyphantes along with some other species, most of which are clearly not related to each other. Since the new species described here is very close to Lepthyphantes leprosus, it is provisionally also placed in Lepthyphantes.Published as part of Dimitrov, Dragomir, 2018, Description of Lepthyphantes rossitsae sp. n. from Turkey (Arachnida: Araneae: Linyphiidae), pp. 277-281 in Revue suisse de Zoologie 125 (2) on pages 277-280, DOI: 10.5281/zenodo.141422
Regrouping of endowments in exchange markets with indivisible goods
No full textDimitrov D, Haake C-J. Regrouping of endowments in exchange markets with indivisible goods. Working Papers. Institute of Mathematical Economics. Vol 367. Bielefeld: Universität Bielefeld; 2005.In this paper we are interested in efficient and individually rational exchange rules for markets with heterogeneous indivisible goods that exclude the possibility that an agent benefits by regrouping goods in her initial endowment. We present a suitable environment in which the existence of such rules can be analysed, and show the incompatibility of efficiency, individual rationality and regrouping-proofness even if agents' preferences are additive separable
Studies on homogeneous and immobilized metal carbonyl clusters on inorganic oxide
No full textA detailed investigation of the reaction between Os3(C))12 and Ru3(CO)12 with HOR (R = CH3, SiPh3), HOOCR (R = H, CH3) and 2,4-pentanedione was undertaken and the products of the form (μ-H)M3(CO)10(L) and [ M3(CO)10L^-] were characterized by i.r. and n.m.r. spectroscopies. The substitution of (μ-H)Os3(CO)10(O2CCH3) with phosphines is studied and the resulting cluster compounds (μ-H)Os3(CO)9(O2CCH3)(PPh3) isolated and characterized by i.r. and n.m.r. spectroscopies. Infrared and Raman spectroscopic studies of triosmium and triruthenium hydride carbonyl clusters were carried out to determine the hydrogen vibrational frequencies. The hydride modes of vibration in (μ-H)2M3(CO)10, (μ-H)2M3(CO)9(E), (E = S, PPh) and (μ-H) (μ-E')Os3(CO)10 (E' = OR, O2CR and acac) clusters were compared and the ability to identify particular co-ordination modes of hydrogen established. The immobilization of metal carbonyl clusters onto inorganic oxide and phosphine functionalized supports was investigated by i.r. and solid state magic angle spinning n.m.r. The triosmium and triruthenium carbonyls were shown to react with silica and alumina to form [(μ-H)M3(CO)10-O O-silica/alumina] or [(μ-H)M3(CO)10-O-silica/alumina] in mild conditions. The reaction of Os3(CO)11(L) and H20s3(CO)10(L) (L =PPh2(CH)2Si(OEt)3) with silica was shown to give intact supported species, while a surface attached cluster (μ-H)Os3(CO)9(L)break (O O-silica) is proposed to result in the case of (μ-H)_2Os_3(CO)9(L). The rhodium carbonyls Rh4(CO)_11(L) and Rh6(CO)15(L) were found to form initially [ Rh_4(CO)11(L')] and Rh6(CO)15(L') (L' = PPh_2(CH2)2Si-(OEt)3-x(OSi≡)x) which decompose on exposure to air to a common surface containing L'Rh(I)(O)2and Rh(I)(CO2)2. The direct interaction of Rh4(CO)12 and RH6(CO)16, at room temperature, with phosphinated silica was shown to result in initial formation of Rh (CO)12-x(L')x' x = 1,2 and complex surface, containing Rh6(CO)16-x(L')x x = 1, LRh(I)(CO)2, Rh(I)(CO)2 fragments and CO covered metallic rhodium. (D74035/87)</p
Maimuna anatolica Dimitrov 2022, sp. n.
No full textMaimuna anatolica sp. n. Figs 1–6, 13–16, 21–25, 28 M. cariae: Logunov, 2012: 376 [examined, misidentification] Type material. ♂ holotype, 2♀ paratypes; Turkey, Muðla, 7 km east of Dalaman, pine forest, 06.03.1977, leg. R. Kinzelbach (SMF); 1♂ 1♀ paratypes, with the same data as for the holotype (NMNHS). 1♂ paratype; Turkey, Antalya Province, near Kalkan village, 04.2003, L. Cook leg. (MMUE, collection number G7535.36) Etymology. Named after the Anatolian Peninsula, where the type material was collected. Diagnosis. The species is morphologically close to Maimuna cariae Brignoli, 1978 by the shape of the conductor of the male palp, and especially by the twisted lamellar terminal end of its ventral part, as well as by the shape of the epigynal hood and the notched epigynal field. The two species can be separated by (1) the shape of the median apophysis of the male palp that is narrow and pointed apically in Maimuna anatolica sp. n. (Figs 4, 21) vs. more massive and with irregular shape in M. cariae (Figs 7, 26); and (2) the wider receptacles (Figs 16, 25) than in M. cariae (Fig 18). Description. Male (Figs 1–2, 4–6, 21–23). Measurements. Total length 7.10; carapace length 3.74, width 2.42; sternum length 1.74, width 1.56; labium length 0.44, width 0.46; maxilla length 0.75, width 0.54; chelicera length 1.39, width 0.67; clypeus height (under AME) 0.34; palp cymbium length 1.47; eye diameters: AME 0.09, ALE 0.09, PME 0.20, PLE 0.09; interdistances between the eyes AME–AME 0.09, AME–ALE 0.04, AME–PME 0.05, ALE–PLE 0.08, PME–PME 0.11; abdomen length 3.36, width 2.00; PLS basal segment length 0.62, distal segment length 1.23; leg I—10.38 (1.48, 2.22, 0.93, 1.91, 2.36, 1.48), leg II—10.64 (1.47, 2.39, 1.05, 1.83, 2.37, 1.53), leg III—10.51 (1.43, 2.28, 0.97, 1.83, 2.63, 1.37), leg IV—12.89 (1.66, 2.78, 1.16, 2.37, 3.46, 1.48). Spination. Chaetotaxy typical for the genus. Coloration (Fig 1). Carapace yellow to light brown, with an indistinct lighter area at the middle of the dorsal side and slightly darker cephalic area and chelicerae. Fovea represented by a short dark stripe. Legs yellowish, without pattern, slightly lighter than the carapace. Sternum yellow, with slightly visible darker pattern. Palpal segments colored as legs. Abdomen dorsally light brown-gray with narrow yellowish longitudinal strip and 7–8 short yellowish radial strips. The ventral side uniformly light gray. Spinnerets yellowish. Other somatic characters. The cephalic area distinctly narrower and more elevated than thoracic area. The PER recurved (as seen from dorsal view). Chelicerae massive, bulged frontally, with opistognathic position. Three short promarginal and 2 very small retromarginal cheliceral teeth present. The retromarginal teeth positioned against the prolateral ones. Fovea smooth, black, well visible. Trochanters straight or slightly convex. Palp (Figs 2, 4–6, 21–23). Without patellar or tibial apophyses. Femur with distinct perpendicular ridge on the retrolateral side (Fig 2). Tibia with elongated ventral ridge. Tegulum brown, with well sclerotized basal part. Embolus thin, starting at 13 o’clock. Conductor large and complex, with wide latero-dorsal projection. Lateral margin wide, forming a deep groove that extends into the lateral projection. The terminal end of the ventral part of the conductor modified in twisted lamellar extension. Median apophysis long with wider triangular base, narrowing apically, with a thin pointed tip. Female (Figs. 3, 13–16, 24–25). Measurements. Total length 8.50; carapace length 3.78, width 2.36; sternum length 1.81, width 1.54; chelicera length 1.60, width 0.84; clypeus height (under AME) 0.24; eye diameters: AME 0.15, ALE 0.18, PME 0.26, PLE 0.17; interdistances between the eyes as in male; abdomen length 4.72, width 3.18; epigyne width 0.37; PLS basal segment length 0.63, distal segment length 1.55; leg I—9.96 (1.50, 2.39, 1.03, 1.71, 2.04, 1.29), leg II—9.99 (1.63, 2.22, 0.97, 1.71, 2.06, 1.40), leg III—9.73 (1.33, 2.29, 1.03, 1.64, 2.19, 1.25), leg IV—12.49 (1.67, 2.65, 1.15, 2.34, 3.18, 1.50). Coloration and other somatic characters as in male, abdomen slightly paler (Fig 3). Epigyne (Figs 13–15, 24) with wide epigynal hood. The epigynal field deeply notched. The notch long and narrow, reaching half of the epigynal field. Copulatory openings situated under the epigynal hood. Vulva (Figs 16, 25). Receptacles large, with irregular shape. Fertilization ducts ribbon-shaped. Distribution (Fig 28). Known only from the two type localities in the easternmost Anatolia, Turkey.Published as part of Dimitrov, Dragomir, 2022, A review of the genus Maimuna Lehtinen, 1967 (Araneae, Agelenidae) in Turkey with a description of a new species, pp. 383-390 in Zootaxa 5124 (3) on pages 384-388, DOI: 10.11646/zootaxa.5124.3.7, http://zenodo.org/record/641104
Il processo di Lipsia e la figura di Georgi Dimitrov
No full textL�articolo offre una breve ricostruzione del Processo di Lipsia (1933), dall�antefatto dell�incendio del Reichstag, all�incarcerazione degli imputati, comprese le differenti fasi processuali. Particolare attenzione è data al contributo di uno degli accusati, il bulgaro Georgi Dimitrov (membro di spicco del Comintern) il quale fu in grado, grazie ad una strenua quanto ardita autodifesa, di smascherare le macchinazioni della polizia e del sistema giudiziario nazista, all�interno di un processo di rottura politica
Going Beyond Counting First Authors in Author Co-citation Analysis
No full textThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Pinkfloydia harveii Dimitrov & Hormiga 2011, SP. NOV.
No full text<i>PINKFLOYDIA HARVEII</i> DIMITROV & HORMIGA SP. NOV. (FIGS 8–16) <p> <i>Types:</i> <i>Holotype</i>: male from Australia, Western Australia, Stirling Range National Park, Wedge Hill; 34°23′17″S, 118°10′18″E; 02.v.1996, Harvey, M. S., Waldock, J. M., Main, B. Y. Legit (Leg). (AUSTMUS T66621).</p> <p> <i>Paratypes:</i> 1 female, same data as holotype (in the same vial). Australia, Western Australia: 1 female, Walpole, Tinglewood Road, 35°00′S, 116°40′E, 13.vi.1987, Main, B. Y. Leg. (AUSTMUS 93/2124); 4 females, Mt Cooke, 32°25′S, 116°18′E, 27.iv.1992, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2080, 93/2081; 93/2082, 93/2083); 1 male, Boddington Bauxite Mine, site SSB02, 32°59′36″S, 116°28′23″E, vi.2003, Graby, G. Leg. (AUSTMUS T71617); 1 female, Stirling Range National Park, Toolbrunup Peak Track, 34°24′S, 118°04′E, 2.iv.1993, Harvey, M. S. Leg. (AUSTMUS T66619); 1 female, Bold Park, site BP1, 31°57′07″S, 115°45′30″E, 20.v.– 20.vii.1993, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2075); 1 female, Bold Park, site BP3, 31°56′33″S, 115°46′13″E, 20.v.–20.vii.1993, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2076); 2 males, Bold Park, site BP4, 31°56′29″S, 115°46′01″E, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2077, 93/2078); 1 male, Perth Airport, site PA5, 31°58′03″S, 115°58′11″E, 24.vi.–28.vii.1993, Harvey, M. S., Waldock, J. M., Sampey, A. Leg. (AUSTMUS 93/2085); 1 male, 1 female, Talbot Road Reserve, site TR2, 31°52′24″S, 116°02′52″E, 24.vi.–28.vii.1993, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2086, 93/2087).</p> <p> <i>Etymology:</i> The species epithet is a patronym after the Australian arachnologist Mark S. Harvey, collector of this and many other new species of arachnids from Western Australia.</p> <p> <i>Diagnosis:</i> As this genus is monotypic the diagnosis of <i>P. harveii</i> coincides with the diagnosis given for the genus (see above under Diagnosis).</p> <p> <i>Description (male holotype):</i> Total body length 2.77. Cephalothorax 1.36 long, 0.93 wide, 1.11 high. Sternum almost as long as wide; 0.67 long, 0.65 wide. Abdomen 1.41 long, 0.90 wide, 0.98 high. Cephalothorax, chelicerae, and sternum brown; dorsally sternum with darker markings laterally. Fovea well marked, with darker coloration. Eyes placed on a conically elevated and slightly projected forward cephalic region; PME on short elevations, much larger than the rest of the eyes (Figs 9B, 12A, B, D). Lateral eyes juxtaposed. Distance between AME 1.5 times one AME diameter; between AME and ALE about one AME diameter. Distance between PME almost two PME diameters. Lateral eyes placed close to the PME. Clypeus height 1.85 times one AME diameter. Chelicerae slender, elongated, and cylindrical (Figs 9B, 12D), with three anterior and two posterior teeth, and two small denticles between the anterior and posterior margins, adjacent to the fang joint (Fig. 12I). Cheliceral cuticle rugose (Fig. 12D). Abdomen oval, longer than wide, with grey-brownish coloration and very few remains of guanine patches. Dorsally with a darker band medially delimited by two clearer dorsolateral bands. Caudal tubercle more darkly pigmented (Fig. 9A, C). Ventrally abdomen lighter in colour, with few small darker dots medially. Legs yellowish. Femur I 1.78 long; 1.30 times the length of the cephalothorax. Femur I with a conspicuous line of oval markings prolaterally (Fig. 12E, G) that extend over the tibia. Similar markings also present on femur IV (under the SEM these markings seem to be made of adhered particles). Palp (Figs 8A–E, 13A–C, E, 14A) with a very long tibia, as long as or slightly longer than the cymbium (Fig. 12A, B). Patella without macrosetae (Fig. 12A, B, D). Paracymbium large and ventrally displaced with two distinctive black, long, and thick macrosetae (Figs 8A, C, 13G, 14A). Cymbial ecto-basal process very long with pointed tip and strongly chitinized (Figs 8B, 13A, D). Cymbial ecto-median process with transparent rim and numerous cuspules dorsally (Figs 8B, E, 13D, H, I). Embolus with large metine embolic apophysis, rectangular, with a pointed and folded laminar distal edge (Figs 8A–C, 13B, F, 14A). Conductor with blunt tip narrower than its base (Fig. 13B, E, F). Epiandrous fusules as in Figure 14D.</p> <p>E, prolateral; G, detail. Abdomen: F, ventral; H, lateral. I, cheliceral denticles. Adt, distal tubercle of the abdomen. Scale bars: A, B, C, D, F, H = 100 Mm; E = 30 Mm; I = 10 Mm; G = 2 Mm.</p> <p>fertilization duct; S, spermatheca; UE, uterus externus. Scale bars: A, B, C = 100 Mm; D, E, F, G, H = 10 Mm.</p> <p> <i>Female (paratype, AUSTMUS 93/2124):</i> Total body length 4.51. Cephalothorax 1.86 long, 1.16 wide, 1.15 high. Sternum almost as long as wide; 0.77 long, 0.70 wide. Abdomen 2.65 long, 2.15 wide, 1.86 high. Coloration pattern and eyes distribution as in males. Sternum slightly more elongated than in males; 0.77 long, 0.70 wide. Abdomen wider than in males, which gives it more rounded appearance (Fig. 10A, B, D). Chelicerae shorter and more robust than in male, with smooth cuticle (Figs 10C, 14E). Clypeus height 1.40 times one AME diameter. Legs brown-yellowish; femur I 1.83, 0.98 times the length of the cephalothorax. Epigynum well sclerotized, dark brown (Figs 8F, 10D, 15D–E). Epigynal plate flattened, with numerous cuticular pores (Fig. 15D, E, G). Remains of a ‘resinous’ secretion forming a genital plug are visible around the edges of the epigynum (Fig. 10E). Copulatory ducts well chitinized, opening on the ventral side of the epigynum and entering the spermathecae at their base (Figs 8G, H, 15F, 16C). Fertilization ducts membranous, originating very close to the copulatory duct entrance in the spermathecae but much wider than it (Figs 8G, H, 15F, H, 16A). Spermathecae oval, weakly sclerotized, and sack like (Fig. 15F, H).</p> <p> <i>Variation:</i> Male cephalothorax ranges in length from 1.36 to 1.61 (<i>N</i> = 7). Female cephalothorax length varies from 1.68–186 (<i>N</i> = 14). Male total body length ranges from 2.77 to 3.75 (<i>N</i> = 7). Female total body length ranges from 3.54 to 4.51 (<i>N</i> = 14). The male abdominal tubercle varies in height and length, in some specimens being very short, which gives the distal edge of the abdomen a more rounded appearance.</p> <p> <i>Natural history:</i> Very poorly known. Many of the specimens that we studied were collected by pitfall traps. We photographed the webs of four juvenile specimens of <i>P. harveii</i> in the Walpole area (Darling Range). Their horizontal webs were built on the leaf litter in a disturbed area and had a maximum frame width between 52 and 92 mm. These orbs were relatively densely spun, as they had many radii (17–28, mean 22, <i>N</i> = 4), lack split radii, and have numerous spiral turns (Fig. 11). The hub is closed and the temporary spiral is removed in the final web (see Fig. 11D). We observed one of the webs being built at night time.</p> <p> <i>Distribution:</i> Southern Western Australia (see map in Fig. 17).</p> <p> <i>Additional specimens studied:</i> Australia, Western Australia: 1 female, Chesapeake Road at Gardner River, 34°48′S, 116°11′E, 1.v.1990, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2079); 1 juvenile (juv.), Perth Airport, site PA5, 31°58′03″S, 115°58′11″E, 10.v.–20.vi.1993, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2084); 1 juv., Talbot Road Reserve, site TR2, 31°52′24″S, 116°02′52″E, 24.vi.–28.vii.1993, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2088); 1 male, Talbot Road Reserve, site TR3, 31°52′25″S, 116°03′03″E, 24.vi.–28.vii.1993, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS 93/2089); 1 juv., Kings Park, site J(E1), 31°58′S, 115°50′E, 26.iii.1981, UWA Zoology students, and B. Y. Main Leg. (AUSTMUS T66615); 1 female, Mt Cooke, 32°25′S, 116°18′E, 24.iv.1992, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS T66616, used for SEM); 1 male, Carabooda area, A. Lombardo’s property, un-named cave, YN-515, twilight zone, 31°35′S, 115°42′E, 22.v.1999, Foulds, R. Leg. (AUSTMUS T66617 used for SEM); 1 juv, Stirling Range National Park, Toolbrunup Peak Track, scree slope, 34°24′S, 118°04′E, 31.iii.1993, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS T66618); 1 female, Stirling Range National Park, S. of Bluff Knoll, 34°23′S, 118°15′E, 1.v.1996, Harvey, M. S., Waldock, J. M., Main, B. Y. Leg. (AUSTMUS T66620 used for dissection and SEM); 1 juv., Glenbourne, S. of Gracetown, site 5, 33°53′S, 115°00′E, 18.iv.–20.iv.1998, Marsh, L. <i>et al</i>. Leg. (AUSTMUS T66622); 1 juv., Karri Valley Resort, 34°26′S, 115°51′E, 21.x.1997, Waldock, J. M. Leg. (AUSTMUS T66623). 3 juv., forest near Tinglewood Cabins, 34°54′51.0″S, 116°43′50.9″E, elevation 185 m, G. Hormiga Leg. (GH0111, one of the specimens sequenced); 1 female, Talbot Road Nature Reserve, 31°52′24″S, 116°03′04″E, 29.viii.2006, Waldock, J. M., Edward, K. Leg. (AUSTMUS T79005); 2 juv., Jandakot Airport, site JK1, 32°05′36″S, 115°52′39″E, 4.v.– 6.vii.1995, Waldock, J. M., Harvey, M. S. Leg. (AUSTMUS T98587); 1 juv., Jandakot Airport, site JK1, 32°05′36″S, 115°52′39″E, 21.ii.–4.v.1995, Waldock, J. M., Harvey, M. S. Leg. (AUSTMUS T98588); 1 juv., Perth Airport, site PA6, 31°58′05″S, 115°58′05″E, 6.i.–18.iii.1994, Harvey, M. S., Waldock J. M. Leg. (AUSTMUS T98589); 1 juv., Woodman Point, site WO2, 32°07′50″S, 115°45′28″E, 04.xi.1994 – 19.i.1995, Waldock, J. M., Harvey, M. S. Leg. (AUSTMUS T98590); 1 juv., Woodman Point, site WO1, 32°07′47″S, 115°45′23″E, 19.i.–21.iii.1995, Harvey, M. S., Waldock, J. M. Leg. (AUSTMUS T98591); 1 female, Rottnest Island, near Lake Timperley, 32°00′23″S, 115°31′11″E, 13.vi.2007, Rix, M. G. Leg. (AUSTMUS T98592); 1 male, 1 female, Porongurup National Park, deep gully west of Waddy’s Hut, 34°40′55″S, 117°50′55″E, 29.iv.2008, Rix, M. G., Harvey, M. S. Leg. (AUSTMUS T98593); 1 male, Boonarring Nature Reserve, off Wannamel West Road, 31°10′27″S, 115°50′57″E, 15.vi.2007, Rix, M. G.Leg. (AUSTMUS T98594); 2 males, 1 female, Austin Bay Nature Reserve, E. of Peel Inlet, end of Beacham Road, 32°36′42″S, 115°47′11″E, 12.vi.2007, Rix, M. G.Leg. (AUSTMUS T98595); 1 female, Sand Patch Beach Reserve, Cuthbert, W of Roberts Road, 35°01′59″S, 117°47′47″E, 18.iii.2008, Rix, M., Harvey, M. S. Leg. (AUSTMUS T98596); 2 males, 1 female, S. of Bremer Bay, near Yate Road, 34°24′10″S, 119°22′43″E, 02.v.2008, Rix, M. G., Harvey, M. S., Newell, J. Leg. (AUSTMUS T98597); 1 male, Two Peoples Bay Nature Reserve, Sinker Reef Road, 34°59′12″S, 118°08′56″E, 01.v.2008, Rix, M., Harvey, M. S. Leg. (AUSTMUS T98598); 1 male, Stirling Range National Park, base of Pyongurup Peak, 34°21′54″S, 118°19′44″E, 05.viii.2008, Rix, M., Harvey, M. S. Leg. (AUSTMUS T98599); 1 female, Lesueur National Park, north of Mt Lesueur, 30°09′59″S, 115°12′06″E, 19.vi.2007, Rix, M. G. Leg. (AUSTMUS T98600); 1 female, 1 juv., Torndirrup National Park, Salmon Hole Road, 35°06′07″S, 117°58′03″E, 30.iv.2008, Rix, M. G., Harvey, M. S. Leg. (AUSTMUS T98601); 1 female, Badgingarra National Park, off Bibby Road, 4.4 km W of Brand Highway, 30°29′14″S, Lon; 115°26′05″E, 19.vi.2007, Rix, M. G. Leg. (AUSTMUS T98602); 1 male, Two Peoples Bay Nature Reserve, near Picnic Area, 34°58′27″S, 118°10′42″E, 01.v.2008, Rix, M., Harvey, M. S. Leg. (AUSTMUS T98603); 1 male, Buller Nature Reserve, 9.5 km SW of Waroona, 32°52′04″S, 115°49′43″E, 22.vii.2007, Rix, M. G. Leg. (AUSTMUS T98604); 1 male, Modong Nature Reserve. 1.5 km NE of Rockingham, 32°13′10″S, 115°54′09″E, 5.vi.2007, Rix, M. G. Leg. (AUSTMUS T98605).</p>Published as part of <i>Dimitrov, Dimitar & Hormiga, Gustavo, 2011, An extraordinary new genus of spiders from Western Australia with an expanded hypothesis on the phylogeny of Tetragnathidae (Araneae), pp. 735-768 in Zoological Journal of the Linnean Society (Zool. J. Linn. Soc.) (Zool. J. Linn. Soc.) 161 (4)</i> on pages 756-763, DOI: 10.1111/j.1096-3642.2010.00662.x, <a href="http://zenodo.org/record/5440041">http://zenodo.org/record/5440041</a>
Figure 273. The unique most parsimonious tree found with Pee-Wee with K in The genus Pholcus (Araneae, Pholcidae) in the Canary Islands
No full textFigure 273. The unique most parsimonious tree found with Pee-Wee with K = 4 (L = 254, CI = 41, RI = 65) based on the COMPLETE matrix.Published as part of Dimitrov, Dimitar & Ribera, Carles, 2007, The genus Pholcus (Araneae, Pholcidae) in the Canary Islands, pp. 59-114 in Zoological Journal of the Linnean Society 151 (1) on page 105, DOI: 10.1111/j.1096-3642.2007.00316.x, http://zenodo.org/record/543238
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