182,188 research outputs found

    C. S. Lewis Chapel: Rev. Dr. Laura A. Smit

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    Reverend Dr. Laura A. Smit, Professor of Theology, Calvin College, Grand Rapids, MI, speaks on an essay response and a visual response to the story of Mary and Martha for the C. S. Lewis Chapel

    Siamaxonopsis Smit 2016, n. gen.

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    Genus Siamaxonopsis n. gen. Diagnosis — Dorsal and ventral shields present. Dorsal shield fused anteriorly with ventral shield. Dorsal shield with A2, postocularia and four pairs of glandularia, the most posterior pair flanking the excretory pore (the latter fused with dorsal shield) and visible only in posteromedial view. Anterior coxal plates not extending to anterior idiosoma margin, without hook-like structures. Anterior to fourth leg sockets a ridge extending to lateral idiosoma margin. Between fourth leg sockets and genital field with two pairs of glandularia, lying closer to genital field than to fourth leg sockets. Genital field numerous pairs of acetabula. P2 with a large nose-shaped extension. Type species — Siamaxonopsis ypsilon n. sp. Remarks — The only known axonopsine genus with more than three or four pairs of acetabula is Omanaxonopsis Smit and Peši´c, 2010. However, this genus has one pair of glandularia between the fourth leg sockets and the genital field, has no dorsal glandularia flanking the excretory pore, has a truncate lateral projection of the ventral shield and leg claws with dorsal and ventral clawlets (Smit and Peši´c 2010).Published as part of Smit, H., 2016, The water mite family Aturidae Thor, 1900 from Southeast Asia (Acari: Hydrachnidia) with the description of one new genus and 14 new species, pp. 341-365 in Acarologia 56 (3) on page 360, DOI: 10.1051/acarologia/20162248, http://zenodo.org/record/539384

    Javalbia rotunda Smit 2016, n. sp.

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    Javalbia rotunda n. sp. (Figure 11) Material examined. Holotype male, Stream near Haewsai Waterfall, Nam Nao NP, Thailand, 16°40.668N 101°41.856E, alt. 425 m a.s.l., 16-xi-2007. Diagnosis — A2 not fused with dorsal shield; postocularia lying anteromedially of dgl-1; dgl-4 absent, only associated setae present; anterior coxae close to anterior idiosoma margin; gonopore nearly rounded. Description — Male: Idiosoma yellowish, dorsally 421 long and 275 wide, ventrally 413 long. Dorsal shield 405 long and 235 wide; excretory pore fused with dorsal shield. A2 not fused with dorsal shield, postocularia lying anteromedially of dgl-1; dgl-4 absent, only associated setae present. Glandularia platelets in dorsal furrow small. Coxae lying far anteriorly, but not reaching anterior idiosoma margin. Coxal suture lines incomplete. Cxgl-4 lying closer to fourth leg sockets than to genital field. Genital field with three pairs of acetabula, fused with ventral shield. Gonopore nearly rounded, 44 long and 40 wide. Vgl-4 fused with ventral shield. Length of P1-5: 20, 40, 30, 56, 29. Length of I-leg-4- 6: 70, 68, 66 (till tip of segment).Length of IV-leg-4-6: 88, 96, 72. Legs without swimming setae. Female: Unknown. Etymology — Named for the nearly rounded gonopore. Remarks — Few Javalbiopsis species have the postocularia anteromedially of dgl-1: Javalbia kinabaluensis Smit and Peši´c, 2014 has the genital field separate from the ventral shield, J. magniseta Smit and Peši´c, 2014 has very large dorsal setae and the coxae lying less anteriorly, J. reticulata Smit and Peši´c, 2014 has a less rounded gonopore and dgl-2 and -3 without glandularia and J. nova n. sp. has dgl-4 with glandularia.Published as part of Smit, H., 2016, The water mite family Aturidae Thor, 1900 from Southeast Asia (Acari: Hydrachnidia) with the description of one new genus and 14 new species, pp. 341-365 in Acarologia 56 (3) on page 357, DOI: 10.1051/acarologia/20162248, http://zenodo.org/record/539384

    M. C. Smit Collection. Handwritten Notes Collection. Fond 001-002

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    This is a collection of handwritten notes by M.C. Smit; generally written on Journal Articles and important essays in philosophy, history, and theology

    Arrenurus (Micruracarus) pesici Smit, 2010, n. sp.

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    Arrenurus (Micruracarus) pesici n. sp. (Figs. 13 A–C) Material examined. Holotype male, Little Llangothlin Nature Reserve, New South Wales, Australia, 30 ° 0 5.104 S 151 ° 46.564 E, alt. 1353 m a.s.l., 21 November 2003 (AMS). Diagnosis. Cauda not set off from remainder of idiosoma, cauda posteriorly with a shallow indentation. Description. Male: Idiosoma yellowish brown, 796 long and 680 wide. Dorsal shield incomplete, holotype also lacking lateral part of dorsal furrow, which must be considered as an anomaly. Width of dorsal shield therefore not measurable. Cauda not set off from remainder of idiosoma, posteriorly with a shallow indentation, inner margins of cauda with small irregularly shaped hyaline membranes (Fig. 13 A). Petiole hyaline, irregularly fork-shaped, left fork a little longer than right fork, attached to idiosoma by a hyaline membrane. Medial distance of third and fourth coxal plates relatively wide. Genital plates long, almost extending to lateral idiosoma margin, slightly sloping (Fig. 13 B). Lengths of PI-PV: 30, 68, 46, 92, 56; PII medially with five setae, three anteriorly, one more dorsally and more posteroventrally (Fig. 13 C). Antagonistic bristle of normal size, but looks short in illustration due to its position is slide. Lengths of I-leg- 4-6: 126, 118, 146. Lengths of IV-leg- 4-6: 150, 150, 156; IV-leg- 4 without spur. Third and fourth legs with numerous swimming setae. Female: Unknown. Etymology. Named after Dr. V. Pešić in appreciation of his acarological work. Remarks. The new species belongs to a group of water species with a hyaline fork-shaped petiole. In all other species (A. forpicatoides, A. perplexus Smit and A. queenslandicus Smit) the indentation of the cauda is narrow and deep.Published as part of Smit, Harry, 2010, Australian Arrenurus (Acari, Hydrachnidia) with the description of eleven new species, pp. 1-26 in Zootaxa 2541 on pages 19-20, DOI: 10.5281/zenodo.19669

    Torrenticola calliope Pešić & Smit, 2014, n. sp.

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    Torrenticola calliope n. sp. Synonymy. Torrenticola harrisoni K. Viets, 1956 sensu Motas & Tanasachi 1968: p. 175, figs. 4–6); Goldschmidt & Smit (2009: p. 191, fig. 5). Type material. Holotype male (RMNH: ZMA. ACAR. 32333), Ethiopia, Roby River, 9 º 44.996 N, 38 º 59.743 E, alt. 2507 m asl., 21.x. 2006, Smit; described and illustrated by Goldschmidt & Smit (2009) in fig. 5, dissected and slide mounted. Paratype (RMNH): 1 /0/0, same data as holotype, unmounted. Diagnosis. Cxgl- 4 far posterior at margin of Cx-I/II between I-L and II-L insertions, but approaching to I-L insertion; P- 2 and P- 3 with a subrectangular, apically serrated distoventral projection, moderately long ventral seta laterally at base of ventrodistal protrusion of P- 2, ventrodistal protrusion P- 4 stout with well developed ventral protuberance in distal half of segment. Description. Male as described by Goldschmidt & Smit (2009) from Ethiopia, and illustrated in their figure 5 as Torrenticola harrisoni K. Viets, 1956. Female as described and illustrated Motas & Tanasachi (1968) from River Takazé, Ethiopia, and illustrated in their figures 4–6 as Torrenticola harrisoni K. Viets, 1956. General features —Cxgl– 4 far posterior at margin of Cx-I/II between I-I and II-L insertions, but approaching I- L insertion; ventral margin of gnathosoma moderately curved, rostrum well developed and slender (see Fig. 5 B in Goldschmidt & Smit 2009); P- 2 shorter than P- 4, P- 2 ventral margin convex, moderately long ventral seta (longer than length of P- 2 ventral projection) laterally at base of ventrodistal protrusion of P- 2, P- 2 and P- 3 with a subrectangular, apically serrated distoventral projection, P- 4 with well developed ventral protuberance just in distal half of segment (see Figs. 5 B–C in Goldschmidt & Smit 2009). Male: medial suture line of Cx-II+III moderately long; ejaculatory complex with small proximal chamber (see Fig. 5 B in Goldschmidt & Smit 2009). Female: genital field pentagonal (see Fig. 4 in Motas & Tanasachi 1968). Etymology. The species is named after Calliope (Ancient Greek: Καλλιόπη), one of nine Muses from Greek mythology, who was a patron of epic poetry and song. The species name is a noun in apposition (in the nominative case), despite the Recommendation 31 A of the ICZN (1999) about avoidance of personal names as nouns in appositions, because there is no case for it being confusing or misleading. Discussion. Goldschmidt & Smit (2009) were aware that specimens from Ethiopia assigned to Torrenticola harrisoni, those described Motas & Tanasachi (1968) and their two males differ from the type specimen described by K.Viets (1956) from South Africa. Moreover, they mentioned that their specimens differ from those described by K. Viets (1956) as well as by Motas & Tanasachi (1968) in having a longer and slender ventrodistal protrusion of P- 2, a relatively shorter P- 2 and a relatively longer P- 4. Goldschmidt & Smit (2009) mentioned that the ventral seta on P- 2 of their specimen is longer than in the figure given by Motas & Tanasachi (1968), however, they considered that to be a case of intraspecific variability. In the light of newly discovered findings of Torrenticola harrisoni in Ghana, these morphological differences cannot be attributed to intraspecific variability. The specimens from Ethiopia described by Goldschmidt & Smit (2009) as well the specimens described by Motas & Tanasachi (1968) differ from the orginal description of T. harrisoni and specimens from our study in having a moderately long ventral seta laterally at the base of the ventrodistal protrusion of P- 2. In the figures given by K. Viets (1956) and K.O. Viets (1965) this seta is completely missing. In specimens in our study this seta is very short, denticle-like and inserted closely at distal edge of P- 2 ventrodistal protrusion (see Figs. 8 A–C, 10 B–C). This seta is hardly visible and sometimes not exceeding the serrate distal edge of the ventrodistal protrusion, so it is possible that it has been overlooked in the description of South African specimens. In our opinion the Ethiopian populations reported by Goldschmidt & Smit (2009) and Motas & Tanasachi (1968) differ from populations from South Africa and Ghana, and warrant the erection of a new species, Torrenticola calliope n. sp. Distribution. Ethiopia.Published as part of Pešić, Vladimir & Smit, Harry, 2014, Torrenticolid water mites (Acari: Hydrachnidia: Torrenticolidae) from Ghana, pp. 1-80 in Zootaxa 3820 (1) on page 21, DOI: 10.11646/zootaxa.3820.1.1, http://zenodo.org/record/28630

    Arrenurus (Brevicaudaturus) postmai Smit 2003

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    Arrenurus (Brevicaudaturus) postmai Smit, 2003 (Figs. 11 A–C) Material examined. Queensland. 1 /0/0, Rock pool Porcupine Creek, Porcupine Gorge NP, 20 ° 21.039 S 144 ° 27.852 E, 23 October 2005; 0/ 2 / 1, Porcupine Creek, Porcupine Gorge NP, same coordinates as previous location, 23 October 2005. Description. Female. Idiosoma 1508 (1447) long and 1411 (1367) wide, yellowish brown. Dorsal shield complete, somewhat angular laterally, 905 (844) long and 955 (925) wide. D 1 and D 3 on large humps (Fig. 11 A, C). Medial margin of fourth coxal plates larger than medial margin of third coxal plates. Medial distance of fourth coxal plates larger than width of gonopore. Gonopore 142 long and 168 wide, without chitinized patches. Genital plates long and bowed (Fig. 11 B), width of genital field 945. Lengths of PI-PV: 48, 134, 76, 144, 52. Palp as in male, PII medially with five heavy setae. Lengths of I-leg- 4-6: 235, 235, 300. Lengths of IV-leg- 4-6: 324, 300, 223. Second, third and fourth legs with numerous swimming setae, first legs with less swimming setae. Remarks. The female of A. postmai is close to A. laticodulus, but differs in smaller or absent humps of L 4 and V 3. Distribution. Previously only known from the holotype male from The Kimberley, Western Australia, and reported here for the first time from Queensland.Published as part of Smit, Harry, 2010, Australian Arrenurus (Acari, Hydrachnidia) with the description of eleven new species, pp. 1-26 in Zootaxa 2541 on page 17, DOI: 10.5281/zenodo.19669

    Cymothoa hermani Hadfield, Bruce & Smit 2011

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    Cymothoa hermani Hadfield, Bruce & Smit, 2011 Cymothoa hermani Hadfield, Bruce & Smit, 2011: 57 –68. Remarks. Cymothoa hermani can be identified by the unique bulbous ornamentation on pereonite 1, anterolateral angles on pereonite 1 rounded and produced past frontal margin of cephalon, long and slender dactyli and the numerous lobes on pleopods 4 and 5 in the ovigerous female. The only other Cymothoa species known from the region, C. eremita, differs from C. hermani by the lack of the characteristic bulbous ornamentation on pereonite 1 that is present in C. hermani. Cymothoa eremita also has a dorsally visible and wider cephalon with the anterolateral margin of pereonite 1 not produced past the cephalon; irregular posterior margins of the pleonites with pleonite 5 appearing to have very distinctly produced sub-medial points; and more acutely produced lateral pereonite margins than in C. hermani. Hosts. Only known from Leptoscarus vaigiensis (Quoy & Gaimard, 1824) (see Hadfield et al. 2011). Distribution. Known from the type location, off Miwi Island, Zanzibar, Tanzania (Hadfield et al. 2011).Published as part of Hadfield, Kerry A., Bruce, Niel L. & Smit, Nico J., 2013, Review of the fish-parasitic genus Cymothoa Fabricius, 1793 (Isopoda, Cymothoidae, Crustacea) from the southwestern Indian Ocean, including a new species from South Africa, pp. 152-176 in Zootaxa 3640 (2) on pages 163-164, DOI: 10.11646/zootaxa.3640.2.2, http://zenodo.org/record/21957

    Vicinaxonopsis costata Smit 2016, n. sp.

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    Vicinaxonopsis costata n. sp. (Figure 15) Material examined — Holotype female, Thorntip Waterfall, Kaeng Krachan NP, Thailand, 12°50.952N 99°18.498E, 29-xi-2007. Diagnosis — Eyes absent, venter with distinctive longitudinal ridges. Description — Female: Idiosoma brown coloured, dorsally 489 long and 373 wide, ventrally 467 long; eyes absent. Dorsal shield fused anteriorly with ventral shield, 373 wide; excretory pore fused with dorsal shield. Dorsal shield with A2, postocularia and four pairs of glandularia; due to rugosity of integument associated setae of dorsoglandularia not visible. Body pores of integument arranged in a rounded pattern in anterior part of dorsal shield; anterior part of dorsum with two pairs of large lateral papillae. Anterior coxae not extending to anterior idiosoma margin. Coxal suture lines obliterated. Apodemes of gnathosoma very long. Anterior to the fourth leg sockets a ridge extending to the lateral idiosoma margin. Venter with numerous distinctive longitudinal ridges. Between fourth leg sockets and genital field two pairs of glandularia, lying close to each other. Genital field with three pairs of acetabula; gonopore 60 long and 46 wide. Length of P1-5: 30, 50, 24, 50, 53. P4 stocky and ventrally somewhat bulging, with a long ventral seta; P5 long and slender. Length of I-leg-4-6: 52, 54, 56 (till tip of segment). Length of IV-leg-4-6: 80, 78, 56. Numbers of swimming setae: IV-leg-4 one, IV-leg-5 two. Male: Unknown. Etymology — Named for the distinctive ridges of the venter. Remarks — The combination of absence of eyes and the presence of longitudinal ridges is characteristic for the new species. Vicinaxonopsis caeca (Smit and Peši´c, 2014) from Borneo has reduced lateral eyes and a different patterns of the anterior dorsal shield (Smit and Peši´c 2014). Despite the absence of eyes, the distinctive brown colour of the idiosoma shows that this species is not hyporheic.Published as part of Smit, H., 2016, The water mite family Aturidae Thor, 1900 from Southeast Asia (Acari: Hydrachnidia) with the description of one new genus and 14 new species, pp. 341-365 in Acarologia 56 (3) on pages 362-364, DOI: 10.1051/acarologia/20162248, http://zenodo.org/record/539384

    Torrenticola neoindica Pešić & Smit 2014, n. sp.

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    Torrenticola neoindica n. sp. (Figs. 12A–D, 13A–D, 16C–D, 17C–D, 23F) Type series. Holotype male, dissected and slide mounted, Malaysia, Borneo, Mahua stream, downstream of national park entrance, Crocker Range, 5º46.491 N, 116º25.770 E, alt. 865 m asl., 22.ix.2012 Smit. Paratypes: 3/ 4[one juvenile]/0 (+ 5/0 in ethanol), same data as holotype, one female dissected and slide mounted. Further records. Borneo: Great Lumotok stream, Mt Kinabalu, 6º09.336 N, 116º08.417 E, alt. 433 m asl., 18.ix.2012 Smit 2/1[one juvenile]/0 (1/0/0 mounted); Mahua stream, Mahua, Crocker Range, 5º47.838 N, 116º24.510 E, alt. 1052 m asl., 21.ix.2012 Smit 0/3/1 (+ 4/0 in ethanol); Mahua stream at crossing with main road, Crocker Range, 5º45.225 N, 116º26.085 E, alt. 752 m asl., 22.ix.2012 Smit 3[one juvenile]/0/1; Kibamabangan River, Crocker Range, 5º51.28 N, 116º08.417 E, alt. 433 m asl., 18.ix.2012 Smit 1[juvenile]/0/0 (mounted); Little Lumotok stream, Sayap, 6º09.497 N, 116º34.027 E, alt. 1065 m asl., 17.ix.2012 Smit 0/1/0; small stream waterfall trail Inobong, 5º51.306 N, 116º08.292 E, alt. 482 m asl., 19.ix.2012 Smit 1/0/0; small stream Layang Layang, Mt Kinabalu, 6º02.711 N, 116º33.627 E, alt. 2697 m asl., 12.ix.2012 Smit 0/1/[juvenile]0; first stream Minduk Sirung Trail, Alab, Crocker Range, 5º45.225 N, 116º26.085 E, alt. 752 m asl., 22.ix.2012 Smit 4[one juvenile]/0/0; SilauSilau stream, upstream, Mt Kinabalu, 6º00.681 N, 116º32.417 E, alt. 1592 m asl., 2.ix.2012 Smit 1/1/0 (damaged). Diagnosis. Idiosoma elongated-oval (dorsal shield L/W ratio 1.2–1.4); shoulder platelets fused to the large dorsal plate; dorsal shield with colour pattern as illustrated in Figs. 16C–D; Cxgl-4 subapical, only slightly posterior of Cx-I tips; suture lines of Cx-IV extending posteriorly beyond posterior margin of genital field. Male: medial suture line of Cx-II+III short. Description General features —Idiosoma elongated-oval; shoulder platelets fused to the large dorsal plate; dorsal shield with colour pattern as illustrated in Figs. 16C–D; gnathosomal bay U-shaped; Cxgl-4 subapical, only slightly posterior of Cx-I tips; suture line of Cx-IV distinct, extending posteriorly beyond posterior margin of genital field; excretory and Vgl-2 pore away from the line of primary sclerotization, excretory pore slightly anterior or on the level with Vgl-2; gnathosoma with curved ventral margin; rostrum well developed (Fig. 12D); P-2 longer than P-4, P-2 ventral margin slightly convex, distally with a subrectangular, anteriorly directed and apically serrated hyaline extension (covering less than 30% of ventral margin) and a short seta laterally at base of projection; P-3 with a shorter, subrectangular, apically serrated ventrodistal projection, and a long seta laterally at base of projection; P-4 stout, with ventral tubercles pointed and separated, bearing one long and three short setae (Figs. 12C, 13C–D). Male: medial suture line of Cx-II+III short; genital field subrectangular in shape; ejaculatory complex normal in shape (Fig. 23F). Female: genital field pentagonal in shape. Measurements Male (holotype, in parentheses from Great Lumotok stream)—Idiosoma (ventral view: Figs. 12A, 13B, 17C) L 563 (596), W 411 (469); dorsal shield (Fig. 13A, 16C) L 477 (500), W 360 (404), L/W ratio 1.32 (1.24); dorsal plate L 453 (469); frontal plate L 105–111 (116–117), W 37–38 (44), L/W ratio 2.8–3.0 (2.6–2.7). Gnathosomal bay L 109 (109), Cx-I total L 231 (232), Cx-I mL 121 (123), Cx-II+III mL 62 (69); ratio Cx-I L/Cx-II+III mL 3.7 (3.4); Cx-I mL/Cx-II+III mL 2.0 (1.8). Genital field L/W 119 (130)/94 (98), ratio 1.27 (1.32); ejaculatory complex L 143 (177); distance genital field-excretory pore 116 (103), genital field-caudal idiosoma margin 150 (163). Gnathosoma vL 265 (305); chelicera total L 297 (328); palp total L 250 (271), dL/H, dL/H ratio: P-1, 28/26, 1.08 (32/29, 1.1); P-2, 86/50, 1.72 (95/48-49, 1.95); P-3, 46/45, 1.03 (48/45, 1.06); P-4, 72/26, 2.73 (80/25, 3.28); P-5, 18/12, 1.46 (16/11, 1.48); P-2/P-4 ratio 1.2 (1.18). Female (paratype from Mahua stream, downstream of national park entrance)—Idiosoma (ventral view: Figs. 12B, 17D) L 609, W 411; dorsal shield (Fig. 16D) L 508, W 350, L/W ratio 1.45; dorsal plate L 481; frontal plate L 115, W 40, L/W ratio 2.9–3.1. Gnathosomal bay L 113, Cx-I total L 229, Cx-I mL 116, Cx-II+III mL 55; ratio CxI L/Cx-II+III mL 4.2; Cx-I mL/Cx-II+III mL 2.1. Genital field L/W 134/116, ratio 1.16; distance genital fieldexcretory pore 122, genital field-caudal idiosoma margin 191. Gnathosoma vL 281; palp total L 271, dL/H, dL/H ratio: P-1, 31/29, 1.06; P-2, 93/52, 1.78; P-3, 53/46, 1.16; P-4, 79/26, 3.0; P-5, 15/11, 1.44; P-2/P-4 ratio 1.18. Etymology. Named after its similarity with T. indica. Discussion. The specimens from Borneo agree well in general morphology of the palp (P-2 and -3 with a subrectangular, anteriorly directed and apically serrated hyaline extensions) with Torrenticola indica Cook, 1967, a species described from India (Cook 1967). The latter species can be easily distinguished in a different colour pattern on the dorsal shield (see Cook 1967: fig. 222) and in the male having a longer medial suture line of CxII+III. Wiles (1999) reported T. indica from several sites in the catchment area of the Rivers Temburong and Belalong in Brunei Darussalem, without discussion on differences with the original description. Habitat. Sandy/bouldery streams, shaded by rain forest (Figs. 43A, C). Distribution. Borneo.Published as part of Pešić, Vladimir & Smit, Harry, 2014, Torrenticolid water mites (Acari: Hydrachnidia: Torrenticolidae) from Malaysian Borneo, pp. 1-72 in Zootaxa 3840 (1) on pages 20-22, DOI: 10.11646/zootaxa.3840.1.1, http://zenodo.org/record/492789
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