6,180 research outputs found
Sophonia longicephala Ahmed & Mahmood
Sophonia longicephala (Ahmed & Mahmood) Quercinirvana longicephala Ahmed & Mahmood, 1970: 261. Status revived (see S. orientalis). Pakistan. Sophonia longicephala (Ahmed & Mahmood), Viraktamath & Wesley, 1988: 201, figs 112–121. India.Published as part of Webb, M. D. & Viraktamath, C. A., 2004, On the identity of an invasive leafhopper on Hawaii (Hemiptera, Cicadellidae, Nirvaninae), pp. 1-6 in Zootaxa 692 on page 4, DOI: 10.5281/zenodo.15849
Doggerella angustata Mahmood, Quicke & Papp, sp. nov.
Doggerella angustata Mahmood, Quicke & Papp sp. nov. (Figs 2 a–f, 12 a–f) Female: Body length 4.4 mm, fore wing length 4.4 mm. Head: Antenna 31 segmented, as long as head, mesosoma and first tergite of metasoma, terminal segment pointed, simple (not acuminate), 2.0 times longer than wide, penultimate segment, 2.0 times longer than wide, first flagellomere 1.2 times longer than second and third. Scape 3.3 times as long as pedicel. Inter-tentorial distance 2.0 times tentorio-ocular distance. Face setose, quadrate in facial view, as wide as high (Figs 2 b, 12 b), with of face 0.43 times width of head. Head entirely coriaceous (Figs 2 a, 12 c), sub-cubic in dorsal view, 1.5 times as broad as long, head extended considerably above to level of eyes. Eye height 1.2 times width of face, eye glabrous in dorsal view. Temple not strongly receding behind eye. Stemmaticum with round edges, posterior ocellar line: transverse diameter of posterior ocellus: shortest distance between posterior ocellus to eye= 2.5:1.0: 4.5. Mesosoma: Almost entirely setose (Fig. 12 d), mostly black, 1.6 times longer than maximally high. Pronotum smooth laterally. Mesoscutum setose. Notauli weakly but distinctly impressed on anterior 0.85 of mesoscutum. Mesopleural sulcus absent. Scutellar sulcus narrow and finely crenulated. Propodeum coriaceous, with sparsely distributed long setae. Wings: Fore wing (Fig. 12 e). Ratio of length of veins SR 1: 3 -SR:r= 2.75: 1.38:1.0. Ratio of length of veins 2 - SR: 3 -SR:r-m= 1.5: 1.75:1.0. Veins 2 -M & 3 -SR, 3.75 times & 2.25 times as long as r-m, respectively. Vein 1 -M straight. Vein 1 -SR+M straight, distinctly less sclerotized near the origin of 1 -SR. Vein cu-a interstitial to marginally post furcal. Veins 1 -M and m-cu distinctly curving towards anterior wing margin. Ratio of length of veins 1 - M:m-cu=2.0:1.0. Vein 3 -CU 1 curved posteriorly. Hind wing. Evenly setose. Vein SC+R 1 2.5 times length of 1 rm.Vein 1 r-m 1.5 times length of R 1. Legs: Claw simple. Ratio of length of hind femur:tibia:basitarsus= 2.5: 3.2:1.0. Hind femur (excluding trochantellus) 2.7 times longer than maximally deep, broadest at middle, rather flattened laterally, setose. Hind tibia entirely setose. Hind basitarsus 2.9 times longer than maximally deep. Outer hind tibial spur reaching approximately 0.44 of distance along basitarsus. Metasoma: Sparsely setose and foveolate (Fig. 12 f). First tergite sparsely setose, weakly crenulated. Second tergite entirely setose, finely and weakly crenulated, 1.4 times longer medially than third. Second and third tergites transverse, second tergite 1.75 times and third tergite 2.4 times as wide apically as long medially. Second metasomal suture narrow. Third tergite sparsely setose, crenulated. Fourth and fifth tergites sparsely setose, crenulated. Hypopygium large and protruding beyond apex of tergites. Ovipositor sheath 1.9 mm long. Coloration: Head black with face, malar space and frons (around eyes) yellow brown. Mesosoma entirely dark brown to black. Wings almost clear, venation and pterostigma brownish. All legs black with yellow brown joints. Metasoma yellow brown. Sternites with black markings. Etymology: Named after narrow face Material examined: Holotype: female, South Africa, Cape Province, Queenstown, 16.i.- 10.ii. 1923, R.E. Turner, BMNH. Paratypes female, Kenya, Diani Beach, xi. 1951, N. L. H. Krauss, BMNH; female, Botswana, Kalkfontein (18 miles north east), 12–13.iv. 1972, BMNH; male, South Africa, Cape peninsula, Camps Bay, 1– 20.x. 1920, R.E. Turner, BMNH; female, South Africa, Limpopo (Northern) Province, 5 km, SSW Bandelierskop (23.21 S 29.47 E), 6.iv. 1997, S. Neser & M. Stiller, SANC.Published as part of Mahmood, Khalid, Papp, Jeno & Quicke, Donald L. J., 2011, A new Afrotropical genus Doggerella gen. nov. of braconine wasp (Hymenoptera: Braconidae) with twelve new species, pp. 1-37 in Zootaxa 2927 on pages 4-5, DOI: 10.5281/zenodo.27797
Doggerella mishkati Mahmood, Quicke & Papp, sp. nov.
Doggerella mishkati Mahmood, Quicke & Papp sp. nov. (Figs 19 a–f) Male: Body length 3.90 mm, fore wing length 3.10 mm. Head: Antenna 32 segmented, as long as head, mesosoma and first tergites of metasoma, terminal segment pointed, simple (not acuminate), 2.00 times longer than wide, penultimate segment 1.75 times longer than wide, first flagellomere 1.2 times longer than second and third. Scape 2.8 times as long as pedicel. Inter-tentorial distance 2.0 times tentorio-ocular distance. Face setose, quadrate in frontal view, as wider as high (Fig. 19 b), width of face 0.41 times width of head. Head entirely coriaceous (Fig. 19 c), in dorsal view cubic, 1.3 times as broad as long, head extended considerably above to level of eyes. Temple rather rounded. Eye height almost equal to width of face, eye glabrous in dorsal view. Stemmaticum with round edges, posterior ocellar line: transverse diameter of posterior ocellus: shortest distance between posterior ocellus to eye=3.0:1.0:3.0. Mesosoma: Almost entirely setose (Fig. 19 d), shiny, 1.7 times longer than maximally high. Pronotum smooth laterally. Mesoscutum setose. Notauli weakly but distinctly impressed on anterior 0.80 of mesoscutum. Mesopleural sulcus absent. Scutellar sulcus narrow and finely crenulate. Propodeum smooth, shiny, with sparsely distributed long setae. Wings: Fore wing (Fig. 19 e). Ratio of length of veins SR 1: 3 -SR:r= 3.7: 2.1:1.0. Ratio of length of veins 2 - SR: 3 -SR:r-m= 2.3: 2.1:1.0. Veins 2 -M & 3 -SR 3.57 times & 2.0 times as long as r-m respectively. Vein 1 -M straight. Vein 1 -SR+M straight, distinctly less sclerotized near the origin of 1 -SR. Vein cu-a interstitial to marginally post furcal. Veins 1 -M and m-cu distinctly curving towards anterior wing margin. Ratio of length of veins 1 -M:mcu=2.0:1.0. Vein 3 -CU 1 slightly curved posteriorly. Hind wing. Evenly setose. Vein SC+R 1 2.6 times length of 1 rm. Vein 1 r-m 1.5 times length of R 1. Legs: Claw simple. Ratio of length of hind femur:tibia:basitarsus=2.0: 2.3:1.0. Hind femur (excluding trochantellus) 3.33 times longer than maximally deep, broadest at middle, densely setose. Hind tibia entirely setose. Hind basitarsus 5.0 times longer than maximally deep. Outer hind tibial spur reaching approximately 0.4 of distance along basitarsus. Metasoma: Sparsely setose and foveolate (Fig. 19 f). First tergite sparsely setose, weakly crenulated. Second tergite entirely setose, finely and weakly crenulated, 2.0 times medially longer as third. Second and third tergites transverse second tergite 1.9 times and third tergite 3.9 times as wide apically as long medially. Second metasomal suture narrow. Third tergite sparsely setose, crenulated. Fourth and fifth tergites sparsely setose, crenulated. Coloration: Head mostly pale yellow except vertex and temple black. Face with a black spot in the middle. Mesosoma yellow brown with black markings. Scutum mostly black with a clear yellow brown rectangular spot in middle. All legs dark brown with yellow brown markings. Wings almost clear, venation and pterostigma brownish. Metasoma mostly pale yellow, tergites 4 & 5 brown. Sternites with black markings. Etymology: Named after Mishkat Ullah a colleague of KM for his contribution to Hymenoptera research in Pakistan Museum of Natural History. Material examined: Holotype: female, Madagascar, Tulear Province, Andohahela National Park, Tsimelahy (24 ° 56.21 ’ S, 46 ° 37.60 ’ E), 16–17.xii. 2002, M. Irwin, F. Parker, R. Harin’Hala (malaise trap in transitional forest)Published as part of Mahmood, Khalid, Papp, Jeno & Quicke, Donald L. J., 2011, A new Afrotropical genus Doggerella gen. nov. of braconine wasp (Hymenoptera: Braconidae) with twelve new species, pp. 1-37 in Zootaxa 2927 on pages 9-10, DOI: 10.5281/zenodo.27797
Singapora Mahmood
Key to adult males of Singapora Mahmood 1. Aedeagal shaft with processes (Figs 1 g, h, 2 f, 3 h, 4 h, 6 h, 10 h, 11 h).............................................. 2 - Aedeagal shaft without process (Figs 5 i, m, 7 e, 8 h, 9 i)........................................................ 9 2. Aedeagal shaft compressed (Figs 1 g-i, 2 f, g)................................................................ 3 - Aedeagal shaft tubular, not compressed (Figs 3 h, i, 4 h, j, 6 h, j, 10 h, i, 11 h, i)....................................... 4 3. Aedeagal shaft with apical processes lamellate, longer than shaft (Fig. 2g)..................... S. bannaensis Song & Li - Aedeagal shaft with apical processes slim, shorter than shaft (Fig. 1 i)................................. S. arifi Ghauri 4. Aedeagal shaft with three processes apically (Fig. 10 h)........................... S. triacantha Yang & Zhang sp. nov. - Aedeagal shaft with paired processes apically or subapically (Figs 3 h, 4 h, 6 h, 11 h).................................. 5 5. Aedeagal shaft with paired processes directed dorsad (Fig. 6 h)....................... S. candela Yang & Zhang sp. nov. - Aedeagal shaft with paired processes directed ventrad (Figs 3 h, 4 h, 11 h).......................................... 6 6. Anal tube appendage without apical hook, aedeagal shaft with paired processes subapically.............. S. diversa Ghauri - Anal tube appendage with distinct apical hook, aedeagal shaft with paired processes apically (Figs 3 b, h, 4 b, h, 11 b, h)..... 7 7. Inner protrusion of style subapical, aedeagal shaft with tiny process terminally (Figs 4 e, i)....... S. nigropunctata Mahmood - Inner protrusion of style near center, aedeagal shaft without tiny process terminally (Figs 3 e, h, 11 e, h).................. 8 8. Anal tube appendage with apex arcuate, aedeagal shaft with paired processes curved laterad apically (Figs 3 b, h)........................................................................................... S. fopingensis Chou & Ma - Anal tube appendage with apex sinuate, aedeagal shaft with paired processes almost straight apically (Figs 11 b, h)................................................................................ S. yingjiangica Cao & Zhang sp. nov. 9. Pronotum with yellow brownish markings................................................. S. cyclops (Kuznezov) - Pronotum without markings............................................................................ 10 10. Aedeagal shaft with smooth lateral sides (Figs 5 j, n, 7 e, 8 i, 9 i)................................................ 11 - Aedeagal shaft with serrated lateral sides.................................................................. 15 11. Style with apex sharply curved laterad, inner protrusion near center (Figs 8 e, f, 9 e, f)............................... 12 - Style with apex gradually curved laterad, inner protrusion subapical (Figs 5g, 7 c, d)................................ 13 12. Anal tube appendage rounded apically, aedeagal preatrial process curved dorsad (Figs 8 b, j)...................................................................................................... S. falcata Cao & Zhang sp. nov. - Anal tube appendage pointed apically, aedeagal preatrial process curved ventrad apically (Figs 9 b, j).......................................................................................... S. longiantrosa Yang & Zhang sp. nov. 13. Aedeagal preatrial process tapering to apex gradually (Figs 5 l, p)............................ S. shinshana (Matsumura) - Aedeagal preatrial process tapering towards midlength, apical half even in thickness (Fig. 7g)........................ 14 14. Anal tube appendage short, not reached hind margin of pygofer side, manubrium of connective broad, aedeagal preatrial pro- cess straight in distal half....................................................... S. victoreena Chiang & Knight - Anal tube appendage long, exceeding hind margin of pygofer side, manubrium of connective narrow, aedeagal preatrial pro- cess curved dorsad in distal half (Figs 7 a, c, g).................................... S. excedens Yang & Zhang sp. nov. 15. Body larger than 3.7mm, anal tube appendage blunt ventro-caudally......... S. karnatakana Viraktamath & Dworakowska - Body smaller than 3.4mm, anal tube appendage pointed ventro-caudally......................................... 16 16. Abdominal apodemes short, extended to anterior margin of 4 th sternite, aedeagal shaft T-shaped apically in caudal view....................................................................................... S. shivae Dworakowska - Abdominal apodemes long, extended to 5 th sternite, apex of aedeagal shaft not T-shaped in caudal view................ 17 17. Apex of aedeagal shaft truncate apically in caudal view..................................... S. viridis Dworakowska - Apex of aedeagal shaft rounded and serrated apically in caudal view................. S. indica (Ramakrishnan & Menon)Published as part of Cao, Yanghui, Yang, Meixia & Zhang, Yalin, 2014, Review of the leafhopper genus Singapora Mahmood (Hemiptera: Cicadellidae: Typhlocybinae: Erythroneurini), pp. 333-350 in Zootaxa 3774 (4) on pages 334-335, DOI: 10.11646/zootaxa.3774.4.3, http://zenodo.org/record/23057
The white matter of the human cerebrum: Part I The occipital lobe by Heinrich Sachs
This is the first complete translation of Heinrich Sachs' outstanding white matter atlas dedicated to the occipital lobe. This work is accompanied by a prologue by Prof Carl Wernicke who for many years was Sachs' mentor in Breslau and enthusiastically supported his work
Bio-bibliometric Study of Dr. Khalid Mahmood’s Contributions to LIS Field in Pakistan
This paper presents bio-bibliometric analysis of the contributions of Dr. Khalid Mahmood in the field of Library and Information Science through his publications. The analysis includes geographical and year wise distribution of publications; collaboration for publication; publications by type; language and journal preferences for the publication; and coverage of different subject areas. Results of the study indicate that Dr. Khalid Mahmood is a prolific writer in the field of library and information science. He contributed 115 items including 99 articles, six books, eight conference papers and two papers in newsletters till December 31, 2011. Research work by Dr. Khalid Mahmood is well accepted in developed countries like United Kingdom and United States of America. He used English language to disseminate majority of his research work. He believes in teamwork and about two third of his
research work was result of collaboration
Bactrocera (Zeugodacus) zahadi Mahmood 1999
Bactrocera (Zeugodacus) zahadi Mahmood Bactrocera (Zeugodacus) zahadi Mahmood, 1999: 232 (holotype male in BMNH); Drew & Raghu, 2002: 350. Material examined. – BHUTAN: 1 male (12 Apr.2000), 1 male (5 Oct.2000), Rimchu 1, coll. C. Dorji; 1 male, Tsirang, Damphu Orchard, 20 Apr.2000; 1 male, Suntalay, 28 Jun.2000, coll. S. Wangdi. All specimens attracted to cue lure. Specimens in NPPC and QDPI. Diagnosis. – A medium sized species; face fulvous with a pair of large irregularly oval black spots; postpronotal lobes and notopleura yellow; scutum black with areas of red-brown; lateral and medial postsutural vittae present; small yellow spot anterior to mesonotal suture; mesopleural stripe just slightly wider than notopleuron dorsally; scutellum entirely yellow; wing with a narrow fuscous costal band expanding into a tau - like spot in apex of wing, a broad fuscous cubital streak; cells bc and c colourless; microtrichia in outer corner of cell c only; legs with femora fulvous except for subapical dark fuscous spots on fore and mid femora and dark fuscous around apical 1/4 of hind femora; abdominal terga III-V fulvous with a ‘T’ pattern consisting of a narrow transverse black band across anterior margin of tergum III and a moderately broad medial longitudinal black band over all three terga, large anterolateral black corners on terga IV and V. Attractant. – Cue lure. Distribution. – Southern Sri Lanka, India, Myanmar, Pakistan and Bhutan. Hosts. – No known record. Remarks. – Bactrocera (Zeugodacus) zahadi Mahmood is extremely close to Bactrocera (Zeugodacus) tau (Walker) and may be a synonym of the latter. After studying large numbers of B. tau from across southeast Asia, it is clear that the lateral dark colour patterns on abdominal terga IV and V vary from small dark anterolateral corners to broad lateral longitudinal dark bands over both terga. Also, the femora colour varies from entirely fulvous to fulvous with preapical dark spots on some or all femora. One sound characteristic of B. tau is that it possesses a large keel shaped supernumerary lobe in the male wing which also is present in the holotype of B. zahadi. No good characters can be found to separate B. tau and B. zahadi. It is not a pest species.Published as part of Drew, R. A. I., Romig, M. C. & Dorji, C., 2007, Records Of Dacine Fruit Flies And New Species Of Dacus (Diptera: Tephritidae) In Bhutan, pp. 1-21 in Raffles Bulletin of Zoology 55 (1) on page 13, DOI: 10.5281/zenodo.533115
Reducing uncertainties of mercury loading into the Everglades nutrient removal project
Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Civil and Environmental Engineering, 1998.Includes bibliographical references (leaf 65).by Haseeb Mahmood and Carolyn E. Metzger.M.Eng
Transition in Primary and Secondary Schooling in Pakistan: Gender and Age Cohort Analysis
This study assesses the changing pattern of school attendance through age cohort analysis for both males and females in Pakistan. Based on the 1998 census data on educational attainment, the results indicate a profound rise in school attendance among younger age cohorts contributing to elimination of gender gap in primary-level schooling in urban areas only. The disadvantaged situation of rural females is reflected by a combination of low school entries/attendance to begin with, and high chance of discontinuing education before completing primary levels. The pattern of school transition reveals that among those few who have completed Class Five, the chances of staying through the secondary level are much higher—after which dropout accelerates rapidly. Two overall conclusions emerge from these results. First, the bulk of the deficit from universal primary education comes from females population, especially in rural areas. Second, the key to reducing dropouts and gender gap in school attendance lies in actions that raise the demand for schooling of girls, with equally matched availability of quality primary- and secondarylevel schools. It appears that achieving universal primary education by 2015, as mandated in the Millennium Development Goals (MDGs), remains a tall order for Pakistan.Primary Education, Secondary Education, Schooling, Pakistan
Influence of growth temperature and measuring temperature on isoprene emission, diffusive limitations of photosynthesis and respiration in hybrid poplars
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