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Whyte, J B, 404473
This record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/425602Surname: WHYTE. Given Name(s) or Initials: J B. Military Service Number or Last Known Location: 404473. Missing, Wounded and Prisoner of War Enquiry Card Index Number: 49319.251711
Item: [2016.0049.57863] "Whyte, J B, 404473
Whyte, B D, 39410
This record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/425601Surname: WHYTE. Given Name(s) or Initials: B D. Military Service Number or Last Known Location: 39410. Missing, Wounded and Prisoner of War Enquiry Card Index Number: SEA-3332.251709
Item: [2016.0049.57862] "Whyte, B D, 39410
Going Beyond Counting First Authors in Author Co-citation Analysis
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
Maratus julianneae Baehr & Whyte, sp. nov.
<i>Maratus julianneae</i> Baehr & Whyte, sp. nov. <p>(FIGURES 7 B, E, H, 8A‒N, 9)</p> <p> <b>Material examined.</b> MALE HOLOTYPE (QM-S96325) from Australia, Queensland, Bush Blitz, Carnarvon Station Tussock grass with Silver-leaved Ironbark (<i>Eucalyptus melanophloia</i>), 783 m, 24°45’S, 147°44’E, 783 m, B. Baehr, 9‒16 Oct. 2014, hand coll. PARATYPES: 1 male (QM-S96326), same data as holotype, pitfall; 1 male (QM- S96327), Bush Blitz, Carnarvon Station Lyons Rd., Callitris grass, Cycad, 24°50’S, 147°45’E, 884 m, C. Lambkin, 8‒9 Oct. 2014, yellow pans; 1 male (QM-S96328), same as previous, C. Lambkin, N. Starick, B. Hawkins, 13 Oct. 2014, hand coll.</p> <p> <b>Etymology.</b> The specific name is a patronym in honour of Julianne Waldock, for her contributions to <i>Maratus</i> systematics over more than two decades. She also provided excellent support for Madeline Girard in finding <i>Maratus</i> localities.</p> <p> <b>Diagnosis.</b> This species belongs to the <i>Maratus anomalus</i> group, sharing a pair of large patches of white setae on the posterior sides of the prosoma, with an embolic disc which has a smooth narrow front with a retrobasal knee-shaped structure and a long narrow embolic tip with the embolic opening at the posterior distal part and a thin semicircular lateral process of embolic disc with a narrow retrolateral fold.</p> <p> <i>Maratus julianneae</i> can be separated from <i>M. michaelorum</i> and <i>M. anomalus</i> by the pattern of the opisothosoma. <i>M. michaelorum</i> has a pattern of a heart-shaped circle and two elongated patches of golden orange setae in the centre and <i>M. anomalus</i> has a completely bluish iridescent opisthosoma, whereas <i>Maratus julianneae</i> has a grey-whitish opisthosoma with bluish iridescent sides at the posterior third.</p> <p> <b>Description. Male</b> (QM-S96325). Total length 4.21. Prosoma 2.05 long, 1.60 wide, pl/pw 1.28; sternum 1.01 long, 0.71 wide, sl/sw 1.42; opisthosoma 2.16 long, 1.56 wide; opisthosoma longer than wide: ol/ow1.38. Ocular quadrangle 0.77 long. Anterior eye row 1.35, posterior eye row 1.49 wide. AME largest; posterior eye group width 0.97 of caput width; AME 0.40; ALE 0.24; PME 0.19; PLE 0.06; AME‒AME 0.05; AME‒ALE 0.05; PME‒PME 1.30; PME‒PLE 0.18; ALE‒PLE 0.29. Clypeus 0.22 high. Paturon with no promarginal teeth and one retromarginal tooth. Length of leg III, femur: 1.65, patella: 0.71, tibia: 0.99, metatarsus: 0.73, tarsus: 0.58, length of metatarsus III 0.74 the length of tibia III. Leg formula: 3421. Dorsal part of the prosoma dark brown, sides pale with dark reticular pattern, margin black. Ocular quadrangle covered with white setae. Front and half of the sides covered with golden setae. Posterior sites of the prosoma with large patches of white setae. Endites, labium and chelicerae pale with dark markings, sternum pale; opisthosoma pale, dotted with black and with one larger pair of black dots posteriorly, sparsely covered with longer black setae and white setae, bluish iridescent at posterior 1/3 of the opisthosoma lateraly. Lateral shoulders with longer white setae, venter pale. Male palp (Figs 7 B, E, H, 8H‒N): cymbium short, 1.6 times longer than wide, covered with long black setae, tip stout with distal scopula. Embolic disc as wide as long with smooth rim and no tooth-like projections centrally, embolus with narrow v-shaped tip, opening at the posterior part (Fig. 7 E); lateral process of embolic disc a long semicircular spur fitting into the retrolateral groove of the embolus (Fig. 7 H); tegular shoulder with cone-shaped lamella (LTS); retrobasal tegular lobe (TL) with narrow tip both sides concave (Fig. 8 J); tibia about as long as wide, prolaterally with long white setae covering 2/3 of the cymbium; retrolateral tibial apophysis (RTA) triangular (Fig. 8 K).</p> <p> <b>Female.</b> Unknown</p> <p> <b>Distribution.</b> Known only from Carnarvon Station in central Queensland.</p>Published as part of <i>Baehr, Barbara C. & Whyte, Robert, 2016, The Peacock Spiders (Araneae: Salticidae: Maratus) of the Queensland Museum, including six new species, pp. 501-525 in Zootaxa 4154 (5)</i> on page 511, DOI: 10.11646/zootaxa.4154.5.1, <a href="http://zenodo.org/record/255783">http://zenodo.org/record/255783</a>
Maratus eliasi Baehr & Whyte, sp. nov.
<i>Maratus eliasi</i> Baehr & Whyte, sp. nov. <p>(FIGURES 11 A, D, G, 12A‒I)</p> <p> <b>Material examined.</b> MALE HOLOTYPE (QM-S96335) from Australia, Queensland, Nuga Nuga National Park, 24°59’S, 148°40’E, M. Girard and D. Elias, 20 Oct. 2015, hand coll. PARATYPES: 1 male (QM-S73641) from Australia, Queensland, Boomer Ra. Mongrel Scub, 23°12’S, 149°46’E, G. Monteith, 16 Dec. 1999 ‒ 22 Mar. 2000, intercept.</p> <p> <b>Records.</b> 1 male, Australia, Queensland, Tregole National Park, 26°29’S, 147°06’E, M. Girard and D. Elias, 20 Oct. 2015, hand coll, deposited in M. Girard’s collection.</p> <p> <b>Etymology.</b> The specific name is a patronym in honour of Dr Damian Elias, who helped to discover new populations of <i>M. eliasi</i> while assisting his wife, Madeline Girard who was collecting specimens for her PhD work.</p> <p> <b>Diagnosis.</b> <i>M. eliasi</i> belongs to the <i>digitatus</i> group in having inflatable spinnerets (Fig. 12 A) <i>M. eliasi</i> is closely related to <i>M. digitatus</i> (mentioned in Otto & Hill, 2015: fig. 37 as <i>Maratus</i> cf. <i>digitatus</i>) sharing a nearly identical prosomal colour pattern and in having a larger pair of semicircular, iridescent, flaps which are uniformly dark green in <i>M. digitatus</i>.</p> <p> <i>M. eliasi</i> can be separated from <i>M. digitatus</i> by its opisthosomal colour pattern (golden and striped flaps) (Fig. 12 A) and its shorter embolic tip (Figs 11 B, E).</p> <p> <b>Description. Male</b> (Holotype, QM-S96335). Total length 3.98. Prosoma 2.12 long, 1.60 wide, pl/pw 1.32; sternum 0.91 long, 0.52 wide, sl/sw 1.75; abdomen 1.86 long, 1.44 wide; abdomen wider than long when inflated, (ol/ow 0.68; QM-S73641). Ocular quadrangle 0.93 long. Anterior eye row 1.51, posterior eye row 1.54 wide. AME largest; posterior eye group width 0.92 of caput width; AME 0.47; ALE 0.27; PME 0.23; PLE 0.08; AME‒AME 0.04; AME‒ALE 0.03; PME‒PME 1.19; PME‒PLE 0.180; ALE‒PLE 0.22. Clypeus 0.22 high. Paturon with no promarginal teeth and one retromarginal tooth. Length of leg III, femur: 1.54, patella: 0.65, tibia: 0.88, metatarsus: 0.75, tarsus: 0.52; metatarsus III 0.85 the length of tibia III. Leg formula: 3421. Prosoma dark brown; ocular quadrangle covered with golden setae scattered with white setae forming three bands, sides with a fringe, a posterior median patch and two lateral patches of white setae; AME and ALE dorsally with a fringe of golden setae, ventrally with a fringe of white setae. Endites distally pale; labium, chelicerae and sternum medium brown with darker reticulation; opisthosoma bluish iridescent, a dancing monster with a red head and arms and blue eyes when seen from the front, flaps golden with one black and two white stripes; venter pale. Leg I‒IV covered with white setae; tibiae and metatarsi I‒IV dark brown tarsi I‒IV pale. Male palp (Figs 11 A, D, G, 12G‒I): cymbium short, 1.6 times longer than wide, covered with white setae, prolateral distal half with stronger dark satae; tip stout with distal scopula. Embolic disc wider than long, with broad, flat front and flat retrolateral groove; with few small tooth-like denticules at the retrocentral part of the disc; embolus tip with triangular retrolateral ridge embolic opening pipe or chimney-shaped; finger-like lateral process of embolic disc with pancake-stack shaped retrolateral ridges; tegular shoulder with cone-shaped lamella (LTS); retrobasal tegular lobe (TL) with broader tip only prolateral side concave (Fig. 12 H); patella and tibia covered with long white setae covering 1/2 of the cymbium retolaterally; retrolateral tibial apophysis narrow, finger-shaped.</p> <p> <b>Female.</b> Unknown.</p> <p> <b>Distribution.</b> Known only from Queensland.</p>Published as part of <i>Baehr, Barbara C. & Whyte, Robert, 2016, The Peacock Spiders (Araneae: Salticidae: Maratus) of the Queensland Museum, including six new species, pp. 501-525 in Zootaxa 4154 (5)</i> on pages 515-518, DOI: 10.11646/zootaxa.4154.5.1, <a href="http://zenodo.org/record/255783">http://zenodo.org/record/255783</a>
Dispelling the Myths Behind First-author Citation Counts
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
Continuity and change in a partitioned civil society : Whyte revisited
Revised version of a paper presented at the final conference of the Mapping frontiers, plotting pathways: routes to North-South cooperation in a divided island programme, City Hotel, Armagh, 19-20 January 2006.This paper revisits John Whyte’s seminal 1983 article “The permeability of the United Kingdom-Irish border: a preliminary reconnaissance” (Whyte, 1983). The objective
is to explore hypotheses Whyte put forward as to why some private organisations are all-Ireland while others follow the international boundary. He suggested that two variables are crucial in explaining this: the nature of the organisation’s activities and the date of its foundation. He also identified a lack of readily available information on foundation dates. To overcome this lacuna we carried out a survey of private organisations to ascertain their foundation date, area of activity and what if any territorial reconfiguring they have undergone. Using the same functional categories as Whyte our research is generally supportive of his initial findings. Civil society can act as a counter-force to the boundary reinforcing dynamics of separate state developments.Not applicableti ke se - 100706 RB
Maratus kiwirrkurra Baehr & Whyte, sp. nov.
Maratus kiwirrkurra Baehr & Whyte, sp. nov. (FIGURES 1 A, D, G, 2A‒K, 3) Material examined. MALE HOLOTYPE (WAM-T138587) from Australia, Western Australia, Bush Blitz, Kiwirkurra indigenous protected area, S03, Lake Mackay, salt lake, 22°29'S, 128°22'E, 367 m, B. Baehr, 8‒18 Sep. 2015, pitfall traps. Etymology. The specific name in apposition refers to the type locality and recognises the community of the Kiwirrkurra indigenous protected area. Diagnosis. This small species belongs to the Maratus chrysomelas group, having a wide rimmed embolic disc covered with frontal ridges. There is no retrolateral process of the embolic disc. M. kiwirrkurra can be separated from other species of this group by the prosoma and opisthosoma being covered with cinnamon and white setae in a mottled manner, an adaptation for crypsis in the sand of the Gibson Desert (Fig. 2 C). Description. Male (Holotype, WAM-T138587). Total length 2.84. Prosoma 1.49 long, 1.13 wide, pl/pw 1.11; sternum 0.63 long, 0.47 wide, sl/sw 1.34; opisthosoma 1.35 long, 1.06 wide; opisthosoma longer than wide, ol/ ow1.27. Ocular quadrangle 0.67 long. Anterior eye row 0.95, posterior eye row 1.01 wide. AME largest; posterior eye group width 0.99 of caput width; AME 0.31; ALE 0.19; PME 0.16; PLE 0.06; AME‒AME 0.03; AME‒ALE 0.04; PME‒PME 0.91; PME‒PLE 0.14; ALE‒PLE 0.16. Clypeus 0.21 high. Paturon with no promarginal teeth and one retromarginal tooth. Length of leg III, femur: 1.08, patella: 0.45, tibia: 0.70, metatarsus: 0.61, tarsus: 0.43, length of metatarsus III 0.87 the length of tibia III. Leg formula: 3421. Dorsal part and sides of prosoma cinnamon brown, with faint reticular pattern, margin black. Ocular quadrangle darker around eyes black, covered with white and cinnamon setae. AME and ALE with cinnamon fringe (Figs 2 A, C, E, F). Endites, labium, chelicerae pale and sternum pale; opisthosoma cinnamon with darker patches, covered with white and cinnamon setae, with longer white setae posteriorly; venter cinnamon with darker brown book-lung covers, covered with white setae. Leg III pale cinnamon covered with white setae. Male palp (Figs 1 A, D, G, 2H‒K): cymbium short, 1.6 times longer than wide, covered with long black setae at prolateral margin and white setae dorsally, tip stout with distal scopula. Embolic disc longer than wide (Fig. 1 D), with narrow retrolateral groove (Fig. 1 G), frontally a few half-moon shaped ridges at anterior part and longitudinal ridges at posterior part reaching the end of the embolus (Fig. 1 D); embolus broad, flattened, embolus tip twisted, opening at frontal part (Fig. 1 A); retrobasal tegular lobe (TL) broad (Fig. 2 I); retrolateral tibial apophysis broadly conical (Fig. 2 K). Female. Unknown Distribution. Known only from Lake Mackay (Fig. 3) at Kiwirrkurra indigenous protected area, in the Gibson Desert, Eastern Western Australia.Published as part of Baehr, Barbara C. & Whyte, Robert, 2016, The Peacock Spiders (Araneae: Salticidae: Maratus) of the Queensland Museum, including six new species, pp. 501-525 in Zootaxa 4154 (5) on pages 503-504, DOI: 10.11646/zootaxa.4154.5.1, http://zenodo.org/record/25578
Ariadna kiwirrkurra Baehr & Whyte, sp. nov.
Ariadna kiwirrkurra Baehr & Whyte, sp. nov. (FIGURE 1 A–C, 2, 3 A–I, 4 A–F) Material examined. Holotype male (WAM-T138053) from Australia: Western Australia, Kiwirrkurra, SSS1, 22°51'56"S, 127°45'41"E, 449m, B. Baehr et.al., 8–18 Sep. 2015, vertebrate traps. Paratypes: 3 males (WAM-T138054) same as previous; 2 males (WAM-T138052), Kiwirrkurra SSS2, 22°48'42"S, 127°49'52"E, 436m, B. Baehr, et al. 8–18 Sep. 2015, vertebrate traps; 1 male (QM-S96340) same as previous. Etymology. The specific name is a noun in apposition taken from the type locality. Kiwirrkurra in the Gibson Desert is one of Australia's most recent Indigenous Protected Areas (IPA). Diagnosis. Ariadna kiwirrkurra can be separated from A. decatetracantha Main, 1954 in having a fovea as an indented pit (A. decatetracantha has no fovea); from A. thyrianthina Simon, 1908 by the oval opisthosoma (opisthosoma cylindrical in A. thyrianthina); from Ariadna burchelli (Hogg, 1900) by the absence of any opisthosomal pattern (A. burchelli has an opisthosomal pattern); from A. octospinata (Lamb, 1911) by PME in line of PLE (PME placed behind the line of PLE in A. octospinata) and from A. dysderina L. Koch, 1873 by the round PME (PME oval in A. dysderina). A. kiwirrkurra can be separated from the remaining non mainland Australian Ariadna species, in having the long paturon forward directed with lateral condyle; and a large globular palpal bulb at least twice the diameter of the tibia. Description. Male (Holotype, WAM-T138053). Total length 7.18. Prosoma 3.72 long, 2.84 wide, pl/pw 1.31; sternum 2.55 long, 1.29 wide, sl/sw 1.97, nearly 2 x as long as wide; opisthosoma 3.46 long, 2.56 wide. Eyes, anterior eye row narrower than posterior eye row; lateral and median eyes contiguous; eyes arranged in 3 closely spaced diads; PME largest; ALE 0.18; PME 0.19; PLE 0.18; ALE-ALE 0.33; PME-PLE 0.13. Clypeus 0.14 high. Prosoma dark brown, oval, reticulated, posteriorly concave (Fig. 3 A), sides rebordered and slightly undulated, fovea an indented pit. Chelicerae dark brown, directed forward; paturon twice as long as wide with lateral condyles, promargin with 3 (Fig. 4 B), retromargin with 1 tiny tooth, fangs short directed medially (Fig. 4 A). Endites, labium, medium brown, tips of endites white (Fig. 4 B); sternum pale sides darker (Fig. 3 A); opisthosoma oval, dark brown without any pattern; venter medium brown, booklungs pale (Fig. 38). Endites: serrula a single row of teeth (Fig. 3 D). Legs robust, yellow; leg I, II: distal part of femur, patella and tibia dark brown; metatarsus I with prolateral tubercle (Fig. 3 F, 4C, D), superior tarsal claw I and II with about 13 teeth (Fig. 4 E), claw III and IV with about 7 medially situated teeth (Fig. 4 F), inferior claw tiny, without teeth (Fig. 4 F). Tarsus IV ventrally swollen (Fig. 4 F). Leg formula: II-I-IV-III. Leg measurements: I, femur 3.36, patella 1.15, tibia 2.90, metatarsus 2.60, tarsus 1.02, total 10.13; II, 3.07, 1.26, 2.75, 2.73, 0.93, 10.74; III, 2.54, 0.73, 1.72, 1.66, 0.85, 7.50; IV, 3.17, 1.08, 2.33, 1.98, 0.96, 9.16. Leg spination (only surfaces bearing spines are listed): I: femur d1-1-1, p3ap,dr1ap; patella p1ap; tibia p1-1-1-1-1, vp2-2-2-1, vr1-1-1-1, r1-1-1-1-1-1-1; metatarsus p1-0-0-1, r1-0-0-1; II: femur d1-1-1-1, dp2ap,dr2ap; tibia p1-1-1, vp1-1-1, vr1-1-1-1, r1-1-1-1-1-1-1; metatarsus p1-1-1, v1, r1-1- 1-1; III: femur d1-1-1-1, dp2ap,dr2ap; tibia p1-1-1, v1, r1-1-1-1; metatarsus p1-1-1, v1, vr1-1, r1-1; IV: femur d1-1-1-1- 1; metatarsus r1. Male palp (Figs 3 G-I): cymbium short, dorsally indented about as long as wide, covered with black setae (Fig. 3 H); large globular palpal bulb twice the diameter of the tibia (Figs 3 G, I), embolus long and thin; tip s-shaped (Figs 3 G, I). Female. Unknown Distribution. Known only from the Kiwirrkurra IPA in the Gibson Desert in Western Australia (Fig. 1 A–C).Published as part of Baehr, Barbara C. & Whyte, Robert, 2016, The first described male Tube-web Spider for mainland Australia: Ariadna kiwirrkurra sp. nov. (Araneae: Segestriidae), pp. 595-599 in Zootaxa 4189 (3) on pages 595-597, DOI: 10.11646/zootaxa.4189.3.11, http://zenodo.org/record/16623
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