169,886 research outputs found

    FIGURE 14 in Genus Acalvolia (Acari: Winterschmidtiidae), with the description of a new species from the USA

    No full text
    FIGURE 14. Acalvolia americana sp. nov. (tritonymph). A, leg I; B, leg II; C, leg III; D, leg IV; E, right tarsus IV.Published as part of Fan, Qing-Hai, George, Sherly & Kumarasinghe, Lalith, 2010, Genus Acalvolia (Acari: Winterschmidtiidae), with the description of a new species from the USA, pp. 41-61 in Zootaxa 2719 on page 59, DOI: 10.5281/zenodo.19984

    Acalvolia americana Fan, George & Kumarasinghe, 2010, sp. nov.

    No full text
    Acalvolia americana sp. nov. (Figs. 1–14, Plates 1–3) Material examined. Five slides stored in the PANZ (Plant Health & Environment Laboratory, Auckland, New Zealand) insect reference collection were studied. SLIDE 1: holotype female, a paratype female, intercepted on orange (Citrus sinensis) from the United States of America (USA), 18 May 2006 (Accession No. 09/ 2006 / 2528); SLIDE 2: a paratype male, a paratype tritonymph and a damaged protonymph, intercepted on orange from USA, 7 Apr 2003 (Accession No. 09/ 2003 / 1734); SLIDE 3: two paratype females and a paratype male, intercepted on orange from USA, 6 Apr 2009 (Accession No. 09/ 2009 / 1785); SLIDE 4: a paratype female, intercepted on orange from USA, 18 May 2005 (Accession No. 09/ 2005 / 2986); SLIDE 5: a paratype female, intercepted on orange from USA, 31 Mar. 2010 (Accession No. 09/ 2010 / 1820). The slide with holotype female and a paratype female will be deposited in NZAC (New Zealand Arthropod Collection). Other slides are retained in PANZ. Diagnosis. FEMALE. Supracoxal setae scx smooth, without barbs, tapering from base to tip; ratio sci: sce= 2.5 (2.5–2.8); setae c 1, d 1 and e 1 reaching or overlapping bases of setae in next row; coxal plates II large, extending far beyond apex of apodeme II, posterior margin concave; spermathecal duct a cylindrical tube, widening as it connects subterminally to spermathecal sac; sclerotised base of spermathecal sac blind ended, U-shaped, a pair of bell-shaped sclerites of oviducts situated at the end of spermathecal sac. MALE. Supracoxal setae, ratio sci: sce, comparative length and distances of setae c 1, d 1 and e 1 as in female; aedeagus medially curved, gradually tapering from base to tip; ventro-terminal sucker of tarsi I and II large, extending to bases of wa. Description. FEMALE (n= 5; Figs 1–5, Plate 1). Idiosomal length 465 (380–465), width at level between coxae II and III 297 (225–297); cuticle without obvious striation. Chelicerae (Fig 3 A) robustly chelate, 78 (68–78), movable digit 28 (25–30), cheliceral seta cha conical, spiniform, 4 (3–4); subcapitulum (Fig 3 B) bearing setae m, 23 (22–25); palpal supracoxal seta elcp absent; dorsal palptibial seta filiform, 22 (21–27), lateral palptibial seta filiform, 14 (12–15), dorsal palptarsal seta filiform, 9 (7–10), terminal palptarsal solenidion tiny, 4 (3–4). Dorsum (Fig 1). Prodorsal shield nearly trapezoidal, faintly and evenly punctate, 85 (76–88) long, width at anterior and posterior margins 63 (50–63) and 83 (83–94), respectively; lateral margins of anterior half slightly concave, posterior margin slightly convex. Supracoxal sclerite elongate, duct of supracoxal gland prominent and opens at midway of supracoxal sclerite; Grandjean’s organ (Fig 3 C) smooth and short, finger-shaped, 6 (5–6); supracoxal setae scx (Fig 3 C) smooth, setiform, tapering from base to tip, 27 (26–27). Opisthonotal gland openings gla closer to e 2 than to d 2. Opisthosoma with three pairs of tiny tubercles, first pair posteriad of h 1, second pair at level of rear end of anus and third pair posteriad of ps 1. External vertical setae ve represented by alveoli, distance between them 67 (64–76). All other dorsal idiosomal setae smooth; vi, sci, c 1, c 2, d 1, e 1, e 2 and h 1 subequal; sce obviously longer than sci, ratios: sce: sci= 2.5 (2.5–2.8), sci–sci: sci–sce= 1.1 (1.1–1.7); setal lengths: vi 78 (75– 78), sci 78 (71–81), sce 193 (176–196); distances: vi– vi 10, vi–ve 48 (42–49), sci–sci 38 (32–47), sci–sce 34 (27– 34). Hysterosomal setae, d 2 about 1.4 (1–1.4)× length of c 1; lengths: c 1 75 (75–100), c 2 84 (77–86), cp 135 (125– 135), c 3 70 (56 – 7 (73–100), d 2 103 (100–103), e 1 95 (81–103), e 2 90 (78–96), f 2 68 (61–68), h 1 81 (80–105), h 2 228 (196–260), h 3 absent; distances: c 1 –c 1 64 (49–64), c 1 –d 1 65 (50–71), d 1 –d 1 63 (48–64), d 2 –gla 85 (62–85), d 1 – e 1 75 (63–75), e 1 – e 1 75 (64–83). Venter (Fig 2). Coxal apodemes I joined at midline, forming a prosternal apodeme directed posteromedially; coxal plate I posteriorly extending beyond apex of prosternal apodeme and widely expanded laterally; coxal apodemes II directed posteromedially, plates large, extending far beyond apex of apodeme II, posterior margin concave; sejugal apodeme very faint, a simple suture; epigynal sclerite thickened, just anterior to genital opening; apodemes III and IV directed anteriomedially, apodeme IV medially connected with posterior sclerite of coxa III. Ventral setae 1 a inserted posterolaterad of coxal plate I, 3 a laterad of genital opening, g posterior to genital papillae, 4 a posterior to genital opening; lengths: 1 a = 43 (40–44), 3 a= 33 (25–33), 4 a= 30 (28–30), g= 30 (23– 30). Genital opening inverted V-shaped, situated centrally between coxae III–IV. Anal opening far posterior to genital opening, about as long as genital opening, surrounded by 3 pairs of pseudanal setae, ps 1 3.9 (3.9–4.2)× as long as ps 2 and 4.3 (4.2–5.3)× as long as ps 3, lengths: ps 3 = 50 (35–50), ps 2 = 55 (44–55), ps 1 = 215 (184–220). Copulatory opening posterior to anus (Fig 3 D); spermathecal duct a cylindrical tube, widening as it reaches spermathecal sac; sclerotised base of spermathecal sac narrowly U-shaped, a pair of bell-shaped sclerites of oviducts situated at end of spermathecal sac, 4 (4–5). Leg lengths (I–IV): 205 (172–208), 200 (165–200), 212 (182–230) and 250 (205–257); all setae on trochanters, femora, genua, tibiae and basal two thirds of tarsi smooth and attenuate. Leg I (Fig 4 A). Trochanter I with 8–12 minute teeth on anteromedial edge; femur I 45 (37–51), vF filiform, slightly longer (50 (48–54)) than femur I; genu I 35 (28–37), solenidia σ' 38 (32–38), σ" 58 (56–66); σ": σ'= 1.5 (1.5–2.1), setae cG and mG subequal, 35 (33–35) and 33 (30–37), respectively; tibia I 35 (30–35), φ 95 (95–98), gT and hT subequal, 28 (23–29) and 29 (26–32), respectively; tarsus I (excluding pretarsus, same as below) 69 (64– 72) long, about 4.3 (4.1–5.1)× as long as its basal width (16 (14–16)), ω 1 (Fig 5 A) parallel sided and gradually tapered at its apex, 19 (16–19) long, ε 5 (4–5), ω 2 6.5 (6–6.5), ω 3 28 (28–33), setae wa 47 (40–47), ra 27 (25–30), la 25 (20–30), d 21 (21–25), e 6 (5–6), f 8 (8–10); ventro-terminal spine s 5 (5–6), u basally merged with p, v basally merged with q, u = v = 3 (3–4), p = q = 5 (4–5); membranous empodium 13 (12–18), claw 6 (5–6). Leg II (Fig 4 B). As in trochanter I, trochanter II also has 8–12 minute teeth on anteromedial edge; femur II 45 (41–49), vF 55 (49–56); genu II 33 (28–34), σ 16 (16–22), cG 22 (20–26), mG 27 (24–30); tibia II 35 (28–35), φ whip-like, 126 (105–127), gT 27 (23–32), hT 25 (20–25); tarsus II 67 (61–71) long, about 4.5 (4.0– 5.1)× as long as its basal width (15 (14–17)); ω parallel sided and gradually tapered at its apex, 19 (19–20) long, wa 44 (37–44), ra 28 (24–32), la 25 (23–27), d 33 (29–35), e 5 (4–5), f 7 (6–8), s 5 (4–5), u basally merged with p, v basally merged with q, u = v = 3 (3–4), p = q = 5 (4–5), empodium 13 (11–16), claw 6 (5–6). Leg III (Fig 4 C). Femur III 42 (35–44); genu III 31 (26–32), σ 10, nG absent; tibia III 33 (28–37), φ whiplike, 117 (96–117), kT 36 (28–36); tarsus III 82 (73–82) long, 13 (12–15) wide at base, ratio length: width= 6.3 (5.4–6.3), w 39 (30–39), r 19 (15–18), d 48 (37–48), e 3 (3–4), f 4 (4–6), s 5 (4–5), u basally merged with p, v basally merged with q, u = v = 2 (2–3), p = q = 4, empodium 14 (12–16), claw 6 (5–6). Leg IV (Fig 4 D). Femur IV 47 (41–50), wF absent; genu IV 35 (30–39); tibia IV 36 (31–37), φ whip-like, 114 (98–117), kT 38 (34–40); tarsus IV 97 (91–198) long, 15 (13–17) wide at segment base, ratio length: width= 6.5 (5.8–7.4), w 33 (30–37) long, r 20 (18–22) long, d 44 (44–51), e and f absent, s 5 (5–6), u basally merged with p, v basally merged with q, u = v = 2, p = q = 4 (4–5), empodium 15 (12–16), claw 6 (6–6.5). MALE (n= 2; Figs. 6–10, Plate 2) Idiosomal length 350 (326–350), width at level between coxae II and III 205; cuticle without obvious striation. Chelicerae (Fig 8 A) robustly chelate, 75 (64–75), movable digit 28 (27–28), cheliceral seta cha conical, spiniform, 4; subcapitulum (Fig 8 B) bearing a pair of subcapitular setae m, 23; palpal supracoxal seta elcp normally at dorsolateral sides absent; dorsal palptibial seta filiform, 15 (12–15) long, lateral palptibial seta filiform, 14 (13–14), dorsal palptarsal seta filiform, 11, terminal palptarsal solenidion tiny, 4. Dorsum (Fig 6). Prodorsal shield as in female, faintly punctate, with posterior half wider than anterior half, 75 (75–76) long, width at anterior and posterior margins 59 and 86, respectively; Supracoxal sclerite elongate, duct of supracoxal gland prominent and opens at midway of supracoxal sclerite; Grandjean’s organ (Fig 8 C) smooth and short, finger-shaped, 4 long; supracoxal setae scx smooth, setiform, tapering from base to tip, 28 (27–28). Opisthonotal gland openings gla closer to e 2 than to d 2. One pair of tiny tubercles posteriad of h 1. External vertical setae ve represented by alveoli, distance between them 72. All other dorsal idiosomal setae filiform, without barbs; sce about 2.5 (2.5–2.7)× as long as sci; distance sci–sci 1.5 × as wide as sci–sce; lengths: vi 66 (66–69), sci 72 (67– 72), sce 181 (181–182); distances: vi– vi 9, sci–sci 39 (37–39), sci–sce 25. Hysterosomal setae, d 2 about 1.2 × length of c 1; lengths: c 1 75 (69–75), c 2 74 (74–76), cp 117 (110–117), c 3 54 (44–54), d 1 (69), d 2 89 (81–89), e 1 80 (80–81), e 2 84 (78–84), f 2 67 (67–71), h 1 78 (74–78), h 2 235 (232–235), h 3 absent; distances: c 1 –c 1 41 (41–44), c 1 –d 1 54, d 1 –d 1 45 (30–45), d 2 –gla 55 (54–55), d 1 – e 1 40 (40–44), e 1 – e 1 57 (44–57). PLATE 1. Acalvolia americana sp. nov. (female). A, prodorsal shield; B, supracoxal setae and ducts of supracoxal gland; C, coxae I and II; D, copulatory opening and spermatheca. Venter (Figs 7 and 8). Coxal apodemes I joined at midline as in female; coxal plates II larger than those in female, their posterior edges rounded, nearly reaching sejugal suture, sejugal apodeme represented by a simple suture; epigynal sclerite thickened, inverted U-shaped, its anterior rim contiguous with medial part of apodemes IV which is medially fused together. Ventral setae 3 a and 4 a absent, genital setae g anterior to genital papillae; lengths: 1 a = 32 (30–32), g= 30 (27–30). Genital opening situated between coxae IV, aedeagus (Figs 8 D and 8 E) gradually tapering from base to tip and medially curved. Anal opening surrounded by 3 pairs of pseudanal setae, about 1.3 × as long as distance between anterior rim of anus and posterior end of basal region of aedeagus: pseudanal setae ps 1 4.2 × as long as ps 2 and 4.0 (4.0– 4.6)× as long as ps 3, lengths: ps 3 = 43 (37–43), ps 2 = 41 (41–42), ps 1 = 172. Legs I and II slightly thicker than legs III and IV, tarsi I and II obviously shorter than those in female, each bearing a subterminal ventral sucker; lengths of legs I–IV: 165 (165–167), 165 (165–171), 202 (181–202) and 210 (198–210); all setae on trochanters, femora, genua and tibiae smooth and attenuate. Leg I (Figs 9 A and 10 A, B). Trochanter I with 8–12 minute teeth on anteromedial edge; femur I 42 (42–44), vF filiform, 53 (47–53); genu I 30, solenidia σ' 37 (34–37), σ" 55 (55–56); σ": σ'= 1.5 (1.5–1.6), setae cG 35 (34–35), mG 31 (27–31); tibia I 32, φ 100 (100–102), gT 27 (25–27), hT 25 (20–25); tarsus I 45 (44–45), about 2.3 (2.3– 2.6)× as long as its basal width (20 (17–20)), ω 1 parallel sided and gradually tapered at its apex, 18 (17–18) long, ε 4, ω 2 8 (7–8), ω 3 28 (28–32), setae wa 25 (25–30), ra 20, la 20, d 24 (22–24), e 6 (6–7), f 10; ventro-terminal sucker large, extending to base of wa, spine s indiscernible, u fully merged with p, v basally merged with q, about 4 (3.5– 4) in length; membranous empodium 15, claw 5.5 (5.5–6). Leg II (Figs 9 B and 10 C–E). Trochanter II with 8–12 minute teeth as in trochanter I; femur II 42 (42–44), vF 43 (42–43); genu II 32 (32–34), σ 22 (20–22), cG 30 (23–30), mG 19 (19–20); tibia II 32 (32–33), φ whip-like, 112 (112–124), gT 27 (23–27), hT 26 (22–26); tarsus II 43 long, about 2.5 (2.5–2.8)× as long as its basal width (17 (15–17)); ω parallel sided and gradually tapered at its apex, 17 (15–17) long, wa 26 (26–29), ra 21 (18–21), la 21 (17–21), d 37 (35–37), e 4 (4–5), f 8; ventro-terminal sucker large, extending to base of wa, spine s indiscernible, u fully merged with p and v basally merged with q, about 4 (3.5–4) in length; membranous empodium 16 (15–16), claw 5.5 (5.5–6). Leg III (Figs 9 C and 10 F, G). Femur III nude, 42 (35–42); genu III 27 (25–27), σ 10 (9–10), nG absent; tibia III 31 (30–31), φ whip-like, 119 (114–119), kT 34 (34–35); tarsus III 69 (69–72) long, 15 wide at base, ratio length: width= 4.6, w 35 (33–35), r 15 (11–15), d 45 (45–46), e 3, f 4, s 4, u fully merged with p and v with q, about 4.5 (4– 4.5) in length, empodium 14 (12–14), claw 5.5 (5.5–6). Leg IV (9 D and 10 H, I). Femur IV nude, 45 (42–45); genu IV nude, 30 (23–30); tibia IV 29 (29–31), φ whiplike, 120 (120–129), kT 40 (39–40); tarsus IV 77 (72–82) long, 15 wide at segment base, ratio length: width= 5.1 (5.1–5.5), w 36 (36–40) long, r 14 (13–14) long, d 51 (44–51), e and f absent, s 4 (3–4), u fully merged with p, v with q, about 4 (3–4) in length, empodium 12 (11–12), claw 5.5 (5.5–6). PLATE 2. Acalvolia americana sp. nov. (male). A, prodorsal shield and supracoxal setae; B, subcapitulum; C, genital area; D, tibia and tarsus of leg I; E, tibia and tarsus of leg II. TRITONYMPH (n= 1; Figs. 11–14) Idiosomal length 241, width at level between coxae II and III 156; cuticle without obvious striation. Chelicerae (Fig 13 A) robustly chelate, 54, movable digit 20, cheliceral seta cha conical, spiniform, 3; subcapitulum (Fig 13 B) bearing a pair of subcapitular setae m, 24; palpal supracoxal seta elcp normally at dorso-lateral sides absent; dorsal palptibial seta filiform, 18 long, lateral palptibial seta filiform, 12, dorsal palptarsal seta filiform, 7, terminal palptarsal solenidion tiny, 2.5. Dorsum (Fig 11). Prodorsal shield indiscernible. Supracoxal setae scx smooth, setiform, tapering from base to tip, 24. Opisthonotal gland openings gla very close to e 2. Opisthosomal tubercles perceptible. External vertical setae ve represented by alveoli, distance between them 63. All dorsal idiosomal setae (except ve) smooth, vi, sci, c 1, c 2, d 1, e 1, e 2 and h 1 subequal; sce obviously longer than sci, ratios: sce: sci= 3.1, sci–sci: sci–sce= 1.8; lengths: vi 55, sci 48, sce 147; distances: vi– vi 7, sci–sci 33, sci–sce 18. Hysterosomal setae, d 2 about 1.3 × length of c 1; lengths: c 1 50, c 2 51, cp 77, c 3 44 d 1 58, d 2 64, e 1 55, e 2 52, f 2 34, h 1 54, h 2 146, h 3 absent; distances: c 1 –c 1 33, c 1 –d 1 30, d 1 –d 1 30, d 2 –gla 38, d 1 – e 1 34, e 1 – e 1 38 Venter (Figs 12 and 13 c). Coxal apodemes I joined at midline, forming a prosternal apodeme directed posteromedially; coxal apodemes II directed posteromedially, plates large, extending far beyond apex of apodeme II, posterior margin convex; epigynal sclerite absent; apodemes III and IV directed medially, apodeme IV not connected with posterior sclerite of coxa III. Ventral 3 a anteriorad of genital opening, g at same level with anterior pair of genital papillae (Fig 13 C), 4 a absent; lengths: 1 a = 21, 3a= 29, g= 23. Genital opening a longitudinal slit, situated between coxae IV. Anal opening surrounded by 3 pairs of pseudanal setae, ps 1 4.4 × as long as ps 2 and 4.0× as long as ps 3, lengths: ps 3 = 35, ps 2 = 32, ps 1 = 141. Copulatory opening and spermathecal duct absent. Legs lengths (I–IV): 130, 129, 128 and 149; all setae on trochanters, femora, genua, tibiae and basal two thirds of tarsi smooth and attenuate. Leg I (Figs 14 A and 13 D). Trochanter I with 8–12 minute teeth on anteromedial edge; femur I 31, vF filiform, longer (45) than femur I; genu I 21, solenidia σ' 23, σ" 41; σ": σ'= 1.8, setae cG 29, mG 24; tibia I 22, φ 73, gT and hT subequal, 23 and 25, respectively; tarsus I 47 long, about 3.1 × as long as its basal width (15), ω 1 parallel sided and tapered at its apex, 15 long, ε 3.5, ω 2 6, ω 3 27, setae wa 33, ra 17, la 19, d 19, e 3, f 6; ventro-terminal spine s, 4.5, u basally merged with p and v basally merged with q, about 3 long; membranous empodium 10, claw 4.5. Leg II (Figs 14 B and 13 E). Trochanter II also has 8–12 minute teeth on anteromedial edge; femur II 27, vF 41; genu II 23, σ 15, cG 21, mG 16; tibia II 23, φ whip-like, 95, gT 15 hT 24; tarsus II 43 long, about 3.3 × as long as its basal width (13); ω parallel sided and gradually tapered at its apex, 18 long, wa 29 ra 16, la 16, d 18, e 3, f 6, s 4, u basally merged with p and v basally merged with q, about 3 long, empodium 11, claw 5.5. Leg III (Fig 14 C and 13 F). Femur III 25; genu III 21, σ 7, nG absent; tibia III 21, φ whip-like, 88, kT 24; tarsus III 51 long, 12 wide at base, length: width= 4.3, w 20, r 11, d 30, e 2.5, f 3, s 4, u basally merged with p and v basally merged with q, about 3.5 long, empodium 9, claw 5. Leg IV (Fig 14 D and 13 G). Femur IV 29, wF absent; genu IV 21; tibia IV 21, φ whip-like, 54, kT 19; tarsus IV 58 long, 12 wide at segment base, length: width= 4.8, w 17, r 14, d 31, e and f absent, s positioned close to midventral seta w, 3 long, u basally merged with p and v basally merged with q, u = v = 3, p = q = 2, empodium 9, claw 4.5. EGG (n= 9; Plate 3) Elongate-oval in shape, 136.5 (124.9–139.7) long, about 2.2 (1.9–2.2)× of width (61.3 (61.0– 72.3)); shell of newly formed egg smooth; shell of fully developed egg ornamented with scattered and linear tubercles and surmounted longitudinally by a crenulated band (8.7 wide). Distribution. USA (type locality not provided). Biology. This mite species was collected from orange fruit, near the calyx where mites were usually seen hiding. Conidia of Cladosporium sp. were found in the pigmented guts suggesting that this mite species is a fungus feeder. Etymology. The species name americana refers to the origin of this species in the United States of America. Remarks. Three characters (the well-developed duct of supracoxal gland, serrations on anteromedial edges of trochanters I and II in both sexes and the subterminal attachment of spermathecal duct to the spermatheca in female) with taxonomic importance at family level, are recognized in this paper. Acalvolia americana sp. nov. and specimens of the genera Calvolia, Czenspinskia, Neocalvolia and Oulenzia in PANZ share these characters. This species can be readily distinguished from the only known species, Acalvolia squamata (Oudemans, 1909), by the following key. PLATE 3. Acalvolia americana sp. nov. (fully developed egg). A, surface ornamentation and half view of the longitudinal circular band of unknown substance; B, surface ornamentation and the longitudinal circular band of unknown substance.Published as part of Fan, Qing-Hai, George, Sherly & Kumarasinghe, Lalith, 2010, Genus Acalvolia (Acari: Winterschmidtiidae), with the description of a new species from the USA, pp. 41-61 in Zootaxa 2719 on pages 42-60, DOI: 10.5281/zenodo.19984

    Acalvolia americana Fan, George & Kumarasinghe, 2010, sp. nov.

    No full text
    Acalvolia americana sp. nov. (Figs. 1–14, Plates 1–3) Material examined. Five slides stored in the PANZ (Plant Health & Environment Laboratory, Auckland, New Zealand) insect reference collection were studied. SLIDE 1: holotype female, a paratype female, intercepted on orange (Citrus sinensis) from the United States of America (USA), 18 May 2006 (Accession No. 09/ 2006 / 2528); SLIDE 2: a paratype male, a paratype tritonymph and a damaged protonymph, intercepted on orange from USA, 7 Apr 2003 (Accession No. 09/ 2003 / 1734); SLIDE 3: two paratype females and a paratype male, intercepted on orange from USA, 6 Apr 2009 (Accession No. 09/ 2009 / 1785); SLIDE 4: a paratype female, intercepted on orange from USA, 18 May 2005 (Accession No. 09/ 2005 / 2986); SLIDE 5: a paratype female, intercepted on orange from USA, 31 Mar. 2010 (Accession No. 09/ 2010 / 1820). The slide with holotype female and a paratype female will be deposited in NZAC (New Zealand Arthropod Collection). Other slides are retained in PANZ. Diagnosis. FEMALE. Supracoxal setae scx smooth, without barbs, tapering from base to tip; ratio sci: sce= 2.5 (2.5–2.8); setae c 1, d 1 and e 1 reaching or overlapping bases of setae in next row; coxal plates II large, extending far beyond apex of apodeme II, posterior margin concave; spermathecal duct a cylindrical tube, widening as it connects subterminally to spermathecal sac; sclerotised base of spermathecal sac blind ended, U-shaped, a pair of bell-shaped sclerites of oviducts situated at the end of spermathecal sac. MALE. Supracoxal setae, ratio sci: sce, comparative length and distances of setae c 1, d 1 and e 1 as in female; aedeagus medially curved, gradually tapering from base to tip; ventro-terminal sucker of tarsi I and II large, extending to bases of wa. Description. FEMALE (n= 5; Figs 1–5, Plate 1). Idiosomal length 465 (380–465), width at level between coxae II and III 297 (225–297); cuticle without obvious striation. Chelicerae (Fig 3 A) robustly chelate, 78 (68–78), movable digit 28 (25–30), cheliceral seta cha conical, spiniform, 4 (3–4); subcapitulum (Fig 3 B) bearing setae m, 23 (22–25); palpal supracoxal seta elcp absent; dorsal palptibial seta filiform, 22 (21–27), lateral palptibial seta filiform, 14 (12–15), dorsal palptarsal seta filiform, 9 (7–10), terminal palptarsal solenidion tiny, 4 (3–4). Dorsum (Fig 1). Prodorsal shield nearly trapezoidal, faintly and evenly punctate, 85 (76–88) long, width at anterior and posterior margins 63 (50–63) and 83 (83–94), respectively; lateral margins of anterior half slightly concave, posterior margin slightly convex. Supracoxal sclerite elongate, duct of supracoxal gland prominent and opens at midway of supracoxal sclerite; Grandjean’s organ (Fig 3 C) smooth and short, finger-shaped, 6 (5–6); supracoxal setae scx (Fig 3 C) smooth, setiform, tapering from base to tip, 27 (26–27). Opisthonotal gland openings gla closer to e 2 than to d 2. Opisthosoma with three pairs of tiny tubercles, first pair posteriad of h 1, second pair at level of rear end of anus and third pair posteriad of ps 1. External vertical setae ve represented by alveoli, distance between them 67 (64–76). All other dorsal idiosomal setae smooth; vi, sci, c 1, c 2, d 1, e 1, e 2 and h 1 subequal; sce obviously longer than sci, ratios: sce: sci= 2.5 (2.5–2.8), sci–sci: sci–sce= 1.1 (1.1–1.7); setal lengths: vi 78 (75– 78), sci 78 (71–81), sce 193 (176–196); distances: vi– vi 10, vi–ve 48 (42–49), sci–sci 38 (32–47), sci–sce 34 (27– 34). Hysterosomal setae, d 2 about 1.4 (1–1.4)× length of c 1; lengths: c 1 75 (75–100), c 2 84 (77–86), cp 135 (125– 135), c 3 70 (56 – 7 (73–100), d 2 103 (100–103), e 1 95 (81–103), e 2 90 (78–96), f 2 68 (61–68), h 1 81 (80–105), h 2 228 (196–260), h 3 absent; distances: c 1 –c 1 64 (49–64), c 1 –d 1 65 (50–71), d 1 –d 1 63 (48–64), d 2 –gla 85 (62–85), d 1 – e 1 75 (63–75), e 1 – e 1 75 (64–83). Venter (Fig 2). Coxal apodemes I joined at midline, forming a prosternal apodeme directed posteromedially; coxal plate I posteriorly extending beyond apex of prosternal apodeme and widely expanded laterally; coxal apodemes II directed posteromedially, plates large, extending far beyond apex of apodeme II, posterior margin concave; sejugal apodeme very faint, a simple suture; epigynal sclerite thickened, just anterior to genital opening; apodemes III and IV directed anteriomedially, apodeme IV medially connected with posterior sclerite of coxa III. Ventral setae 1 a inserted posterolaterad of coxal plate I, 3 a laterad of genital opening, g posterior to genital papillae, 4 a posterior to genital opening; lengths: 1 a = 43 (40–44), 3 a= 33 (25–33), 4 a= 30 (28–30), g= 30 (23– 30). Genital opening inverted V-shaped, situated centrally between coxae III–IV. Anal opening far posterior to genital opening, about as long as genital opening, surrounded by 3 pairs of pseudanal setae, ps 1 3.9 (3.9–4.2)× as long as ps 2 and 4.3 (4.2–5.3)× as long as ps 3, lengths: ps 3 = 50 (35–50), ps 2 = 55 (44–55), ps 1 = 215 (184–220). Copulatory opening posterior to anus (Fig 3 D); spermathecal duct a cylindrical tube, widening as it reaches spermathecal sac; sclerotised base of spermathecal sac narrowly U-shaped, a pair of bell-shaped sclerites of oviducts situated at end of spermathecal sac, 4 (4–5). Leg lengths (I–IV): 205 (172–208), 200 (165–200), 212 (182–230) and 250 (205–257); all setae on trochanters, femora, genua, tibiae and basal two thirds of tarsi smooth and attenuate. Leg I (Fig 4 A). Trochanter I with 8–12 minute teeth on anteromedial edge; femur I 45 (37–51), vF filiform, slightly longer (50 (48–54)) than femur I; genu I 35 (28–37), solenidia σ' 38 (32–38), σ" 58 (56–66); σ": σ'= 1.5 (1.5–2.1), setae cG and mG subequal, 35 (33–35) and 33 (30–37), respectively; tibia I 35 (30–35), φ 95 (95–98), gT and hT subequal, 28 (23–29) and 29 (26–32), respectively; tarsus I (excluding pretarsus, same as below) 69 (64– 72) long, about 4.3 (4.1–5.1)× as long as its basal width (16 (14–16)), ω 1 (Fig 5 A) parallel sided and gradually tapered at its apex, 19 (16–19) long, ε 5 (4–5), ω 2 6.5 (6–6.5), ω 3 28 (28–33), setae wa 47 (40–47), ra 27 (25–30), la 25 (20–30), d 21 (21–25), e 6 (5–6), f 8 (8–10); ventro-terminal spine s 5 (5–6), u basally merged with p, v basally merged with q, u = v = 3 (3–4), p = q = 5 (4–5); membranous empodium 13 (12–18), claw 6 (5–6). Leg II (Fig 4 B). As in trochanter I, trochanter II also has 8–12 minute teeth on anteromedial edge; femur II 45 (41–49), vF 55 (49–56); genu II 33 (28–34), σ 16 (16–22), cG 22 (20–26), mG 27 (24–30); tibia II 35 (28–35), φ whip-like, 126 (105–127), gT 27 (23–32), hT 25 (20–25); tarsus II 67 (61–71) long, about 4.5 (4.0– 5.1)× as long as its basal width (15 (14–17)); ω parallel sided and gradually tapered at its apex, 19 (19–20) long, wa 44 (37–44), ra 28 (24–32), la 25 (23–27), d 33 (29–35), e 5 (4–5), f 7 (6–8), s 5 (4–5), u basally merged with p, v basally merged with q, u = v = 3 (3–4), p = q = 5 (4–5), empodium 13 (11–16), claw 6 (5–6). Leg III (Fig 4 C). Femur III 42 (35–44); genu III 31 (26–32), σ 10, nG absent; tibia III 33 (28–37), φ whiplike, 117 (96–117), kT 36 (28–36); tarsus III 82 (73–82) long, 13 (12–15) wide at base, ratio length: width= 6.3 (5.4–6.3), w 39 (30–39), r 19 (15–18), d 48 (37–48), e 3 (3–4), f 4 (4–6), s 5 (4–5), u basally merged with p, v basally merged with q, u = v = 2 (2–3), p = q = 4, empodium 14 (12–16), claw 6 (5–6). Leg IV (Fig 4 D). Femur IV 47 (41–50), wF absent; genu IV 35 (30–39); tibia IV 36 (31–37), φ whip-like, 114 (98–117), kT 38 (34–40); tarsus IV 97 (91–198) long, 15 (13–17) wide at segment base, ratio length: width= 6.5 (5.8–7.4), w 33 (30–37) long, r 20 (18–22) long, d 44 (44–51), e and f absent, s 5 (5–6), u basally merged with p, v basally merged with q, u = v = 2, p = q = 4 (4–5), empodium 15 (12–16), claw 6 (6–6.5). MALE (n= 2; Figs. 6–10, Plate 2) Idiosomal length 350 (326–350), width at level between coxae II and III 205; cuticle without obvious striation. Chelicerae (Fig 8 A) robustly chelate, 75 (64–75), movable digit 28 (27–28), cheliceral seta cha conical, spiniform, 4; subcapitulum (Fig 8 B) bearing a pair of subcapitular setae m, 23; palpal supracoxal seta elcp normally at dorsolateral sides absent; dorsal palptibial seta filiform, 15 (12–15) long, lateral palptibial seta filiform, 14 (13–14), dorsal palptarsal seta filiform, 11, terminal palptarsal solenidion tiny, 4. Dorsum (Fig 6). Prodorsal shield as in female, faintly punctate, with posterior half wider than anterior half, 75 (75–76) long, width at anterior and posterior margins 59 and 86, respectively; Supracoxal sclerite elongate, duct of supracoxal gland prominent and opens at midway of supracoxal sclerite; Grandjean’s organ (Fig 8 C) smooth and short, finger-shaped, 4 long; supracoxal setae scx smooth, setiform, tapering from base to tip, 28 (27–28). Opisthonotal gland openings gla closer to e 2 than to d 2. One pair of tiny tubercles posteriad of h 1. External vertical setae ve represented by alveoli, distance between them 72. All other dorsal idiosomal setae filiform, without barbs; sce about 2.5 (2.5–2.7)× as long as sci; distance sci–sci 1.5 × as wide as sci–sce; lengths: vi 66 (66–69), sci 72 (67– 72), sce 181 (181–182); distances: vi– vi 9, sci–sci 39 (37–39), sci–sce 25. Hysterosomal setae, d 2 about 1.2 × length of c 1; lengths: c 1 75 (69–75), c 2 74 (74–76), cp 117 (110–117), c 3 54 (44–54), d 1 (69), d 2 89 (81–89), e 1 80 (80–81), e 2 84 (78–84), f 2 67 (67–71), h 1 78 (74–78), h 2 235 (232–235), h 3 absent; distances: c 1 –c 1 41 (41–44), c 1 –d 1 54, d 1 –d 1 45 (30–45), d 2 –gla 55 (54–55), d 1 – e 1 40 (40–44), e 1 – e 1 57 (44–57). PLATE 1. Acalvolia americana sp. nov. (female). A, prodorsal shield; B, supracoxal setae and ducts of supracoxal gland; C, coxae I and II; D, copulatory opening and spermatheca. Venter (Figs 7 and 8). Coxal apodemes I joined at midline as in female; coxal plates II larger than those in female, their posterior edges rounded, nearly reaching sejugal suture, sejugal apodeme represented by a simple suture; epigynal sclerite thickened, inverted U-shaped, its anterior rim contiguous with medial part of apodemes IV which is medially fused together. Ventral setae 3 a and 4 a absent, genital setae g anterior to genital papillae; lengths: 1 a = 32 (30–32), g= 30 (27–30). Genital opening situated between coxae IV, aedeagus (Figs 8 D and 8 E) gradually tapering from base to tip and medially curved. Anal opening surrounded by 3 pairs of pseudanal setae, about 1.3 × as long as distance between anterior rim of anus and posterior end of basal region of aedeagus: pseudanal setae ps 1 4.2 × as long as ps 2 and 4.0 (4.0– 4.6)× as long as ps 3, lengths: ps 3 = 43 (37–43), ps 2 = 41 (41–42), ps 1 = 172. Legs I and II slightly thicker than legs III and IV, tarsi I and II obviously shorter than those in female, each bearing a subterminal ventral sucker; lengths of legs I–IV: 165 (165–167), 165 (165–171), 202 (181–202) and 210 (198–210); all setae on trochanters, femora, genua and tibiae smooth and attenuate. Leg I (Figs 9 A and 10 A, B). Trochanter I with 8–12 minute teeth on anteromedial edge; femur I 42 (42–44), vF filiform, 53 (47–53); genu I 30, solenidia σ' 37 (34–37), σ" 55 (55–56); σ": σ'= 1.5 (1.5–1.6), setae cG 35 (34–35), mG 31 (27–31); tibia I 32, φ 100 (100–102), gT 27 (25–27), hT 25 (20–25); tarsus I 45 (44–45), about 2.3 (2.3– 2.6)× as long as its basal width (20 (17–20)), ω 1 parallel sided and gradually tapered at its apex, 18 (17–18) long, ε 4, ω 2 8 (7–8), ω 3 28 (28–32), setae wa 25 (25–30), ra 20, la 20, d 24 (22–24), e 6 (6–7), f 10; ventro-terminal sucker large, extending to base of wa, spine s indiscernible, u fully merged with p, v basally merged with q, about 4 (3.5– 4) in length; membranous empodium 15, claw 5.5 (5.5–6). Leg II (Figs 9 B and 10 C–E). Trochanter II with 8–12 minute teeth as in trochanter I; femur II 42 (42–44), vF 43 (42–43); genu II 32 (32–34), σ 22 (20–22), cG 30 (23–30), mG 19 (19–20); tibia II 32 (32–33), φ whip-like, 112 (112–124), gT 27 (23–27), hT 26 (22–26); tarsus II 43 long, about 2.5 (2.5–2.8)× as long as its basal width (17 (15–17)); ω parallel sided and gradually tapered at its apex, 17 (15–17) long, wa 26 (26–29), ra 21 (18–21), la 21 (17–21), d 37 (35–37), e 4 (4–5), f 8; ventro-terminal sucker large, extending to base of wa, spine s indiscernible, u fully merged with p and v basally merged with q, about 4 (3.5–4) in length; membranous empodium 16 (15–16), claw 5.5 (5.5–6). Leg III (Figs 9 C and 10 F, G). Femur III nude, 42 (35–42); genu III 27 (25–27), σ 10 (9–10), nG absent; tibia III 31 (30–31), φ whip-like, 119 (114–119), kT 34 (34–35); tarsus III 69 (69–72) long, 15 wide at base, ratio length: width= 4.6, w 35 (33–35), r 15 (11–15), d 45 (45–46), e 3, f 4, s 4, u fully merged with p and v with q, about 4.5 (4– 4.5) in length, empodium 14 (12–14), claw 5.5 (5.5–6). Leg IV (9 D and 10 H, I). Femur IV nude, 45 (42–45); genu IV nude, 30 (23–30); tibia IV 29 (29–31), φ whiplike, 120 (120–129), kT 40 (39–40); tarsus IV 77 (72–82) long, 15 wide at segment base, ratio length: width= 5.1 (5.1–5.5), w 36 (36–40) long, r 14 (13–14) long, d 51 (44–51), e and f absent, s 4 (3–4), u fully merged with p, v with q, about 4 (3–4) in length, empodium 12 (11–12), claw 5.5 (5.5–6). PLATE 2. Acalvolia americana sp. nov. (male). A, prodorsal shield and supracoxal setae; B, subcapitulum; C, genital area; D, tibia and tarsus of leg I; E, tibia and tarsus of leg II. TRITONYMPH (n= 1; Figs. 11–14) Idiosomal length 241, width at level between coxae II and III 156; cuticle without obvious striation. Chelicerae (Fig 13 A) robustly chelate, 54, movable digit 20, cheliceral seta cha conical, spiniform, 3; subcapitulum (Fig 13 B) bearing a pair of subcapitular setae m, 24; palpal supracoxal seta elcp normally at dorso-lateral sides absent; dorsal palptibial seta filiform, 18 long, lateral palptibial seta filiform, 12, dorsal palptarsal seta filiform, 7, terminal palptarsal solenidion tiny, 2.5. Dorsum (Fig 11). Prodorsal shield indiscernible. Supracoxal setae scx smooth, setiform, tapering from base to tip, 24. Opisthonotal gland openings gla very close to e 2. Opisthosomal tubercles perceptible. External vertical setae ve represented by alveoli, distance between them 63. All dorsal idiosomal setae (except ve) smooth, vi, sci, c 1, c 2, d 1, e 1, e 2 and h 1 subequal; sce obviously longer than sci, ratios: sce: sci= 3.1, sci–sci: sci–sce= 1.8; lengths: vi 55, sci 48, sce 147; distances: vi– vi 7, sci–sci 33, sci–sce 18. Hysterosomal setae, d 2 about 1.3 × length of c 1; lengths: c 1 50, c 2 51, cp 77, c 3 44 d 1 58, d 2 64, e 1 55, e 2 52, f 2 34, h 1 54, h 2 146, h 3 absent; distances: c 1 –c 1 33, c 1 –d 1 30, d 1 –d 1 30, d 2 –gla 38, d 1 – e 1 34, e 1 – e 1 38 Venter (Figs 12 and 13 c). Coxal apodemes I joined at midline, forming a prosternal apodeme directed posteromedially; coxal apodemes II directed posteromedially, plates large, extending far beyond apex of apodeme II, posterior margin convex; epigynal sclerite absent; apodemes III and IV directed medially, apodeme IV not connected with posterior sclerite of coxa III. Ventral 3 a anteriorad of genital opening, g at same level with anterior pair of genital papillae (Fig 13 C), 4 a absent; lengths: 1 a = 21, 3a= 29, g= 23. Genital opening a longitudinal slit, situated between coxae IV. Anal opening surrounded by 3 pairs of pseudanal setae, ps 1 4.4 × as long as ps 2 and 4.0× as long as ps 3, lengths: ps 3 = 35, ps 2 = 32, ps 1 = 141. Copulatory opening and spermathecal duct absent. Legs lengths (I–IV): 130, 129, 128 and 149; all setae on trochanters, femora, genua, tibiae and basal two thirds of tarsi smooth and attenuate. Leg I (Figs 14 A and 13 D). Trochanter I with 8–12 minute teeth on anteromedial edge; femur I 31, vF filiform, longer (45) than femur I; genu I 21, solenidia σ' 23, σ" 41; σ": σ'= 1.8, setae cG 29, mG 24; tibia I 22, φ 73, gT and hT subequal, 23 and 25, respectively; tarsus I 47 long, about 3.1 × as long as its basal width (15), ω 1 parallel sided and tapered at its apex, 15 long, ε 3.5, ω 2 6, ω 3 27, setae wa 33, ra 17, la 19, d 19, e 3, f 6; ventro-terminal spine s, 4.5, u basally merged with p and v basally merged with q, about 3 long; membranous empodium 10, claw 4.5. Leg II (Figs 14 B and 13 E). Trochanter II also has 8–12 minute teeth on anteromedial edge; femur II 27, vF 41; genu II 23, σ 15, cG 21, mG 16; tibia II 23, φ whip-like, 95, gT 15 hT 24; tarsus II 43 long, about 3.3 × as long as its basal width (13); ω parallel sided and gradually tapered at its apex, 18 long, wa 29 ra 16, la 16, d 18, e 3, f 6, s 4, u basally merged with p and v basally merged with q, about 3 long, empodium 11, claw 5.5. Leg III (Fig 14 C and 13 F). Femur III 25; genu III 21, σ 7, nG absent; tibia III 21, φ whip-like, 88, kT 24; tarsus III 51 long, 12 wide at base, length: width= 4.3, w 20, r 11, d 30, e 2.5, f 3, s 4, u basally merged with p and v basally merged with q, about 3.5 long, empodium 9, claw 5. Leg IV (Fig 14 D and 13 G). Femur IV 29, wF absent; genu IV 21; tibia IV 21, φ whip-like, 54, kT 19; tarsus IV 58 long, 12 wide at segment base, length: width= 4.8, w 17, r 14, d 31, e and f absent, s positioned close to midventral seta w, 3 long, u basally merged with p and v basally merged with q, u = v = 3, p = q = 2, empodium 9, claw 4.5. EGG (n= 9; Plate 3) Elongate-oval in shape, 136.5 (124.9–139.7) long, about 2.2 (1.9–2.2)× of width (61.3 (61.0– 72.3)); shell of newly formed egg smooth; shell of fully developed egg ornamented with scattered and linear tubercles and surmounted longitudinally by a crenulated band (8.7 wide). Distribution. USA (type locality not provided). Biology. This mite species was collected from orange fruit, near the calyx where mites were usually seen hiding. Conidia of Cladosporium sp. were found in the pigmented guts suggesting that this mite species is a fungus feeder. Etymology. The species name americana refers to the origin of this species in the United States of America. Remarks. Three characters (the well-developed duct of supracoxal gland, serrations on anteromedial edges of trochanters I and II in both sexes and the subterminal attachment of spermathecal duct to the spermatheca in female) with taxonomic importance at family level, are recognized in this paper. Acalvolia americana sp. nov. and specimens of the genera Calvolia, Czenspinskia, Neocalvolia and Oulenzia in PANZ share these characters. This species can be readily distinguished from the only known species, Acalvolia squamata (Oudemans, 1909), by the following key. PLATE 3. Acalvolia americana sp. nov. (fully developed egg). A, surface ornamentation and half view of the longitudinal circular band of unknown substance; B, surface ornamentation and the longitudinal circular band of unknown substance.Published as part of Fan, Qing-Hai, George, Sherly & Kumarasinghe, Lalith, 2010, Genus Acalvolia (Acari: Winterschmidtiidae), with the description of a new species from the USA, pp. 41-61 in Zootaxa 2719 on pages 42-60, DOI: 10.5281/zenodo.19984

    What can management accounting practitioners and academics do to improve risk measurement and forewarn of impending financial crises?

    No full text
    We discuss some perceived shortcomings of management accounting in the light of the financial crisis of 2008. We describe current trends in management accounting thinking and Japanese perspectives on the discipline. Our main focus is on the lack of reliable measurement of financial risk and its consequences. The importance of collaborative multi-disciplinary research through partnerships between academics and practitioners is emphasised.SubmittedAsada, T., Bailes, J. C. and Suzuki, K. (2000). “Implementing ABM with Hoshin Management”, Management Accounting Quarterly,Winter, 1-6 Beheshti, H. M. (2006). “What managers should know about ERP/ERP II’, Management Research News, 29 (4), 184-193 Bhimani, A. (2002). “European management accounting research: traditions in the making”,The European Accounting Review, 11(1), 99-117 Bromwich, M. (1999/2000). “Thoughts on management accounting and strategy”, Pacific Accounting Review, 11(2), 41-48 Davila, T. and Oyon, D. (2008). “Cross paradigm collaboration and the advancement of the management accounting knowledge”, Critical Perspectives on Accounting, 19, 8 87-893 Dercon, B. (2007). “Corporate governance after the Asian crisis”, Managerial Law, 49 (4),129-1 40 Dujuan, Y. (2009). “Inefficient American corporate governance under the financial crisis and China’s reflections”, International Journal of Law and Management, 51(3), 139-152 Falta, M., Gallagher, L. and Willett, R.J.(2006). “Modelling “hard-to-measure” costs in environmental management accounting”, Asia Pacific Journal of Management Accounting, 1, 76-91. Hopper, T., Koga, T., and Goto, J. (1999). “Cost accounting in small and medium sized Japanese companies: an exploratory study”, Accounting and Business Research, 30 (1), 73-86 “Japan Company Handbook”, (2009) Tokyo, Toyo Keizai Inc. Kakouris, A. P. And Polychronopoulos, G.(2005). “Enterprise resource planning (ERP)system: An effective tool for production management”, Management Research News, 28 (6), 66-7 8 Langfield-Smith, K. (2008). “Strategic Management Accounting: How far have we come in 25 years?” Accounting, Auditing, & Accountability Journal, 2 1(2), 204-228 Lewellyn, S. (2003). “What counts as “theory” in qualitative management and accounting research?” Accounting, Auditing & Accountability Journal, 16 (4), 662-708 Nishimura, A. (2007). “Conceptual analysis of value-based management and accounting: with reference to Japanese practice”, Asia-pacific Management Accounting Journal, 2(1), 71-88 Nishimura, A. and Willett, R. (2005). “Fundamental features and perspectives of Management Accounting in Asia” in Management Accounting in Asia, ed. Akira Nishimura and Roger Willett, Malaysia, Thomson Learning. Nishimura, A. (2003). “Management Accounting: feed forward and Asian perspectives”, New York, Palgrave Nishimura, A. and Willett, R. (1997). “Structures and features of Japanese Accounting” in Accounting in the Asia-Pacific Region, ed. Nabil Baydoun, Akira Nishimura, and Roger Willett, Singapore, John Wiley and Sons. Nobes, C. W. (1983). “A Judgemental International Classification of Financial Reporting Practices”, Journal of Business Finance & Accounting, Spring, 1-19 Otley, D. (2008). “Did Kaplan and Johnson get it right?” Accounting, Auditing, & Accountability Journal, 21(2), 229-239 Parker, S, Peters, G. F. and Turetsky, H. F. (2002). “Corporate governance and corporate failure; a survival analysis”, Corporate Governance, 2 (2), 4-12 Pretorius, M. (2008). “When Porter’s generic strategies are not enough: complementary strategies for turnaround situations”, Journal of Business Strategy, 29(6), 19-28 Pudelko, M. and Mendenhall, M. E. (2007). „What western executives need to know about current management practices”, Organizational Dynamics, 36 (3), 274-287 Riaz, S. (2009). “The global financial crisis: an institutional theory analysis”, Critical Perspectives on International Business, 5 (1/2), 26-3 5 Rosenzweig, E. G. (2009). “A contingent view of e-collaboration and performance in manufacturing”, Journal of Operations Management, 27, 462-47 8 Wong, L. (2009). “The crisis: a return to political economy?” Critical Perspective on International Business, 5 (1/2), 56-7

    Acalvolia

    No full text
    Key to the known species of genus Acalvolia 1. Ratio sce: sci = 4.6; dorsal idiosomal setae c 1, d 1 and e 1 length less than two thirds the distance between their bases and the bases of setae in next row; supracoxal setae barbed........................ Acalvolia squamata (Oudemans, 1909) Ratio sce: sci = 2.5 (Figs. 1 and 6); setae c 1, d 1 and e 1 reaching or overlapping bases of setae in next row (Figs. 1 and 6); supracoxal setae smooth (Figs. 3 and 8)................................................................... Acalvolia americana sp. nov.Published as part of Fan, Qing-Hai, George, Sherly & Kumarasinghe, Lalith, 2010, Genus Acalvolia (Acari: Winterschmidtiidae), with the description of a new species from the USA, pp. 41-61 in Zootaxa 2719 on page 60, DOI: 10.5281/zenodo.19984

    Going Beyond Counting First Authors in Author Co-citation Analysis

    No full text
    The 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

    Mitomycin C in highly myopic eyes - Author reply

    No full text
    Ophthalmology. 2005 Feb;112(2):208-18; discussion 219. Mitomycin C modulation of corneal wound healing after photorefractive keratectomy in highly myopic eyes. Gambato C, Ghirlando A, Moretto E, Busato F, Midena E. SourceRefractive Surgery Service and Antimetabolite Therapy Research Unit, Department of Ophthalmology, University of Padova, Padova, Italy. Abstract PURPOSE: To evaluate the role of topical mitomycin C in corneal wound healing (CWH) after photorefractive keratectomy (PRK) in highly myopic eyes. DESIGN: Prospective, double-masked, randomized clinical trial. PARTICIPANTS: Seventy-two eyes of 36 patients affected by high (>7 diopters) myopia. METHODS: In each patient, one eye was randomly assigned to PRK with intraoperative topical 0.02% mitomycin C application, and the fellow eye was treated with a placebo. Postoperatively, mitomycin C-treated eyes received artificial tears (3 times daily, tapered in 3 months), whereas the fellow eye was treated with fluorometholone sodium 2% and artificial tears (3 times daily, tapered in 3 months). MAIN OUTCOME MEASURES: Uncorrected visual acuity (UCVA) and best-corrected visual acuity (BCVA), contrast sensitivity, manifest refraction, and biomicroscopy. Contrast sensitivity was determined using the Pelli-Robson chart. Corneal confocal microscopy documented CWH. RESULTS: Mean follow-up was 18 months (range, 12-36). No side effects or toxic effects were documented. At 12-month follow-up examination, UCVAs (logarithm of the minimum angle of resolution) were 0.4+/-0.48 and 0.5+/-0.53 (P = .03) in mitomycin C-treated eyes and corticosteroid-treated eyes, respectively. At 1 year, corneal haze developed in 20% of corticosteroid-treated eyes, versus 0% of mitomycin C-treated eyes. At 12, 24, and 36 months, corneal confocal microscopy showed activated keratocytes and extracellular matrix significantly more evident in untreated eyes (Ps = 0.004, 0.024, and 0.046, respectively). CONCLUSION: Topical intraoperative application of 0.02% mitomycin C can reduce haze formation in highly myopic eyes undergoing PRK. Comment in Ophthalmology. 2006 Feb;113(2):357; author reply 357-8

    Dispelling the Myths Behind First-author Citation Counts

    No full text
    We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more sophisticated methods

    Structural properties of Silicon-Germanium and Germanium-Silicon Core-Shell Nanowires

    No full text
    Core-shell nanowires made of Si and Ge can be grown experimentally with excellent control for different sizes of both core and shell. We have studied the structural properties of Si/Ge and Ge/Si core-shell nanowires aligned along the [110] direction, with diameters up to 10.2 nm and varying core to shell ratios, using linear scaling Density Functional Theory (DFT). We show that Vegard's law, which is often used to predict the axial lattice constant, can lead to an error of up to 1%, underlining the need for a detailed ab initio atomistic treatment of the nanowire structure. We analyse the character of the intrinsic strain distribution and show that, regardless of the composition or bond direction, the Si core or shell always expands. In contrast, the strain patterns in the Ge shell or core are highly sensitive to the location, composition and bond direction. The highest strains are found at heterojunction interfaces and the surfaces of the nanowires. This detailed understanding of the atomistic structure and strain paves the way for studies of the electronic properties of core-shell nanowires and investigations of doping and structure defects

    A Multi-Language Comparison of Influences on Author Verification using Character N-Grams

    No full text
    We create a new multi-language corpus for author verification based on Wikipedia talkpages, and evaluate the influence that differences in topic and time have on character n-gram author profiles. Topic alignment between two texts is found to increase author verification precision, and an authors writing style is found to change over time, but not more significantly after 3 years than after 1 year.Information ArchitectureWISElectrical Engineering, Mathematics and Computer Scienc
    corecore