106,872 research outputs found
Halliday, G H, VX63
This record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete.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/389873Surname: HALLIDAY. Given Name(s) or Initials: G H. Military Service Number or Last Known Location: VX63. Missing, Wounded and Prisoner of War Enquiry Card Index Number: 3289.214487
Item: [2016.0049.22166] "Halliday, G H, VX63
Dawn and photoperiod sensing by phytochrome A
In plants, light receptors play a pivotal role in photoperiod sensing, enabling them to track seasonal progression. Photoperiod sensing arises from an interaction between the plant's endogenous circadian oscillator and external light cues. Here, we characterize the role of phytochrome A (phyA) in photoperiod sensing. Our metaanalysis of functional genomic datasets identified phyA as a principal regulator of morning-activated genes, specifically in short photoperiods. We demonstrate that PHYA expression is under the direct control of the PHYTOCHROME INTERACTING FACTOR transcription factors, PIF4 and PIF5. As a result, phyA protein accumulates during the night, especially in short photoperiods. At dawn, phyA activation by light results in a burst of gene expression, with consequences for physiological processes such as anthocyanin accumulation. The combination of complex regulation of PHYA transcript and the unique molecular properties of phyA protein make this pathway a sensitive detector of both dawn and photoperiod. © 2018 Proceedings of the National Academy of Sciences of the United States of America. All rights reserved
Personal Papers (MS 80-0002)
Letter from G. R. Halliday to Harris L. Kempner enclosing a card and requesting it be fingerprinted, signed, and returned and notifying that the original card is in the process of lamination
Utah Broadcasters Association Officers and Board of Directors: George Hatch, Vice-President (Intermountain Network); Eugene M. Halliday, President (KSL); Arch Webb, Secretary-Treasurer (KVOG); Harold Van Wagenen (KIXX); Artur Higbee (KSUB); G. Bennet Larson (KDYL). Salt Lake City, Utah.
Photo of Utah Broadcasters Association Officers and Board of Directors: George Hatch, Vice-President (Intermountain Network); Eugene M. Halliday, President (KSL); Arch Webb, Secretary-Treasurer (KVOG); Harold Van Wagenen (KIXX); Artur Higbee (KSUB); G. Bennet Larson (KDYL). Salt Lake City, Utah
Sessiluncus G. Canestrini 1898
Genus Sessiluncus G. Canestrini, 1898 Sessiluncus G. Canestrini, 1898: 486. Gamasellus (Sessiluncus).— Berlese, 1905a: 168. Sessiluncus.— Vitzthum, 1931a: 142; 1943: 758; Ryke, 1962b: 160; Lee, 1970: 175; Bregetova, 1977a: 311; Nasr & Afifi, 1986: 17; Zaher, 1986: 30. Type species: Gamasus heterotarsus G. Canestrini, 1897, by subsequent monotypy.Published as part of Castilho, Raphael C., Silva, Edmilson S., De, Gilberto J. & Halliday, Bruce, 2016, Catalogue of the family Ologamasidae Ryke (Acari: Mesostigmata), pp. 1-147 in Zootaxa 4197 (1) on page 100, DOI: 10.5281/zenodo.16844
Binodoxys angelicae Halliday 1833
Binodoxys angelicae (Halliday, 1833) Aphis gossypii Glover on Pyrus communis 12 Ψ Athens, 25 April 1996 (GRE), † Prunus domestica var. insititia 7 Ψ 7 ɗ Athens, 0 2 May 2001 (GRE). Aphis pomi de Geer on † Cydonia oblonga 3 Ψ 2 ɗ Sykaminon, 25 May 2005 (GRE); Malus domestica 1 Ψ 2 ɗ Belgrade, 22 June 1995, 1 Ψ 25 June 1998, 10 Ψ 5 ɗ 0 2 May 2006 (SER). Dysaphis plantaginea (Passerini) on Pyrus communis 26 Ψ 25 ɗ Athens, 25 April 1996 (GRE). Ovatus insitus (Walker) on Cydonia oblonga 2 Ψ Belgrade, 13 May 1998 (SER).Published as part of Kavallieratos, Nickolas G., Tomanović, Ž Eljko & Starý, Petr, 2008, Parasitoids (Hymenoptera: Braconidae: Aphidiinae) attacking aphids feeding on Prunoideae and Maloideae crops in Southeast Europe: aphidiine-aphid-plant associations and key, pp. 47-64 in Zootaxa 1793 on page 53, DOI: 10.5281/zenodo.18256
Gamasiphoides lootsi Halliday, 2005, sp. nov.
<i>Gamasiphoides lootsi</i> sp. nov. (Figs 29–36) <p> <i>Specimens examined</i></p> <p> Holotype female, Hermanus, 28.viii.1994, T. K. Qin, clover and weeds, site 30­31 (= <b>94­31</b>). Paratypes, 1 female, same data as holotype; 4 females, 2 males, Humansdorp, 18.viii.1994, T. K. Qin, clover and weeds, site 30–14 (= <b>94­14</b>); 8 females, 3 males, 42 km north of Cape Town, Kalbaskraal turnoff, 25.viii.1994, grass and vetch, site 30–30 (= <b>94­ 30).</b></p> <p> <i>Description</i></p> <p>Female</p> <p> <i>Dorsal idiosoma</i> (Fig. 29). Dorsal shield length 722–781 µm, width 462–525 µm (n=13); oval shaped, surface smooth, with 37 pairs of smooth pointed setae visible dorsally; setae short, not long enough to reach the base of the next most posterior seta; arrangement of pairs slightly irregular in places.</p> <p> <i>Ventral idiosoma</i> (Fig. 30). Tritosternum with bell­shaped base and pilose laciniae. Pre­sternal area with two pairs of plates, the anterior pair smaller and irregularly shaped. Sternal shield with indistinct polygonal ornamentation anteriorly, posteriorly smooth; with four pairs of smooth pointed setae and three pairs of pores. Epigynial shield semi­circular, smooth, with one pair of smooth setae, flanked anteriorly by a pair of triangular endopodal plates, and posteriorly by a pair of oval­shaped metapodal plates each bearing a pore. Ventri­anal shield heart­shaped, approximately as wide as long (length 344–386 µm, width 353–378 µm), not fused to dorsal shield, with polygonal ornamentation medially, margins smooth, with 8 pairs of smooth pointed setae and a post­anal seta; para­anal setae inserted slightly anterior to anus. Exopodal plates split opposite coxa III; peritrematal plates extending from level of seta s1 to stigmata at a level between coxae III and IV, fused with broad exopodal plates behind coxae IV; dorsal shield encroaching onto ventral surface, with 2–3 pairs of setae not visible dorsally.</p> <p> <i>Gnathosoma</i>. Epistome triangular, with a long medial point and two small lateral points, length of medial point 60 µm, width at base 80 µm (Fig. 31). Fixed digit of chelicera with two small distal teeth, conspicuous pilus dentilis, two large triangular proximal teeth and a small basal tooth. Movable digit with a small distal tooth, a very large robust medial tooth, and two low proximal teeth, arthrodial brush very short (Fig. 32). Hypostomal groove with 8 transverse rows of denticles, the posterior two of which extend well outside the groove. Palp coxal seta, internal and external posterior hypostomal setae and anterior hypostomal seta subequal in length (ca. 45 µm); corniculae very short, heavy, and robust; internal malae long and fine, external malae fringed, salivary styli conspicuous (Fig. 33). Palp tarsal claw 2­tined, seta <i>al</i> 2 on palp genu spatulate, other palp setae smooth and pointed.</p> <p> <i>Legs</i>. Chaetotaxy: Leg I: coxa 0 0/1 0/1 0; trochanter 1 1/1 0/2 1; femur 2 3/1 2/3 2; genu 2 3/2 3/1 2; tibia 2 3/2 3/2 2. Leg II: coxa 0 0/1 0/1 0; trochanter 1 0/1 0/2 1; femur 2 3/1 2/2 1; genu 2 3/1 2/1 2; tibia 2 2/1 2/1 2; tarsus 3 3/2 3/2 3 + <i>mv</i>, <i>md</i>. Leg III: coxa 0 0/ 1 0/1 0; trochanter 1 0/1 0/2 1; femur 1 2/1 2/0 0; genu 2 2/1 2/0 1; tibia 2 1/1 2/1 1; tarsus 3 3/2 3/2 3 + <i>mv</i>, <i>md</i>. Leg IV: coxa 0 0/1 0/0 0; trochanter 1 0/1 0/2 1; femur 1 2/1 2/0 0; genu 2 2/0 3/1 1; tibia 2 1/1 3/1 2; tarsus 3 3/2 3/2 3 + <i>mv</i>, <i>md</i>. All leg setae fine, smooth pointed. All tarsi with a pair of claws and a rounded membranous pulvillus projecting slightly beyond the claws.</p> <p>Male</p> <p> <i>Dorsal idiosoma</i>. Dorsal shield length 676–727 µm, width 412–458 µm (n=5), structure and chaetotaxy as for female.</p> <p> <i>Ventral idiosoma</i> (Fig. 34). As for female, except sternal and epigynial shields fused to form a sterniti­genital shield, with five pairs of setae and three pairs of pores, large genital aperture at anterior margin of shield.</p> <p> <i>Gnathosoma</i>. As for female except fixed digit of chelicera with a small distal tooth, a small tooth adjacent to the pilus dentilis, and three large proximal teeth; movable digit with a single medial tooth, spermatodactyl fused with movable digit for most of its length, with a robust distal projection extending slightly beyond the tip of the movable digit, arthrodial brush modified into a membranous flap (Fig. 35).</p> <p> <i>Legs</i>. As for female, except femur II with a prominent ventral spur, genu II with a smaller capitate spur, and tibia II with a short thick spur­like seta (Fig. 36).</p> <p> <i>Notes</i></p> <p> In the key to species of <i>Gamasiphoides</i> given by Karg (1993b), <i>G. lootsi</i> runs to <i>G. octosetae</i> Karg 1976, on the basis of the shape of the ventri­anal shield (length = width), short dorsal shield setae, shape of the epistome, and the presence of 8 pairs of setae on the ventri­anal shield. However, <i>G. l o o t s i</i> differs from <i>G. o c t o s e t a e</i> in having sternal shield setae st1 and st2 smooth and pointed (pilose in <i>G. o c t o s e t a e</i>). The leg chaetotaxy of <i>G. lootsi</i> agrees with that for African species of <i>Gamasiphoides</i> described by Lee (1970).</p> <p> <i>Etymology</i></p> <p>This species is named in honour of South African acarologist Dr G. C. Loots.</p>Published as part of <i>Halliday, R. B., 2005, Predatory mites from crops and pastures in South Africa: potential natural enemies of redlegged earth mite Halotydeus destructor (Acari: Penthaleidae), pp. 11-64 in Zootaxa 1079</i> on pages 42-45, DOI: <a href="http://zenodo.org/record/170355">10.5281/zenodo.170355</a>
- …
