188 results on '"White, Ian M."'
Search Results
2. A New Dynamic Bandwidth Allocation Protocol with Quality of Service in Ethernet-based Passive Optical Networks
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An, Fu-Tai, Hsueh, Yu-Li, Kim, Kyeong Soo, White, Ian M., and Kazovsky, Leonid G.
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Computer Science - Networking and Internet Architecture - Abstract
Ethernet-based Passive optical network (E-PON) is the key for next generation access networks. It must have the property of high efficiency, low cost, and support quality of service (QoS). We present a novel media access control (MAC) protocol that maximizes network efficiency by using dynamic bandwidth allocation (DBA) algorithm suitable for E-PON. This protocol minimizes packet delay and delay variation for high priority traffic to ensure QoS. Simulation results show excellent network throughput. Simulation results also show low packet delay and packet delay variation for high priority traffic compare with traditional MAC protocol of E-PON. When the network performs ranging, this protocol ensures zero interruption of high priority traffic, such as audio or video applications., Comment: Proc. of IASTED International Conference on Wireless and Optical Communications (WOC 2003), Banff, Canada, Jul. 2003
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- 2014
3. Effect of heterogeneity in recombination rate on variation in realised relationship
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White, Ian M. S. and Hill, William G.
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- 2020
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4. Assessment of surfactants for efficient droplet PCR in mineral oil using the pendant drop technique
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Pandit, Kunal R., Rueger, Paul E., Calabrese, Richard V., Raghavan, Srinivasa R., and White, Ian M.
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- 2015
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5. Sample-to-Answer Immuno-Magnetic Assay Using Thermally Responsive Alkane Partitions
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Everitt, Micaela L., primary, Boegner, David J., additional, and White, Ian M., additional
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- 2022
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6. Sample-to-Answer Immuno-Magnetic Assay Using Thermally Responsive Alkane Partitions
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Everitt, Micaela L., Everitt, Micaela L., Boegner, David J., White, Ian M., Everitt, Micaela L., Everitt, Micaela L., Boegner, David J., and White, Ian M.
- Abstract
To combat pandemics, there is a need for rapid point-of-care diagnostics to identify infected patients and to track the spread of the disease. While recent progress has been made in response to COVID-19, there continues to be a need for point-of-care diagnostics capable of detecting biomarkers—such as antibodies—in whole blood. We have recently reported the development of thermally responsive alkane partitions (TRAPs) for the automation of point-of-care immuno-magnetic assays. Here, we demonstrate the use of TRAPs to enable sample-to-answer detection of antibodies against the SARS-CoV-2 virus in whole blood samples. We report a limit of detection of 84 pg/mL, well below the clinically relevant threshold. We anticipate that the TRAP-enabled sample-to-answer immunoassay can be used to track the progression of future pandemics, leading to a more informed and robust clinical and societal response.
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- 2022
7. High-sensitivity electrochemical enzyme-linked assay on a microfluidic interdigitated microelectrode
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Chen, I-Jane and White, Ian M.
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- 2011
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8. Estimation of Quantitative Genetic Parameters
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Thompson, Robin, Brotherstone, Sue, and White, Ian M. S.
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- 2005
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9. Label-free quantitative DNA detection using the liquid core optical ring resonator
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Suter, Jonathan D., White, Ian M., Zhu, Hongying, Shi, Huidong, Caldwell, Charles W., and Fan, Xudong
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- 2008
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10. Phage-based label-free biomolecule detection in an opto-fluidic ring resonator
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Zhu, Hongying, White, Ian M., Suter, Jonathan D., and Fan, Xudong
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- 2008
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11. Thermal characterization of liquid core optical ring resonator sensors
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Suter, Jonathan D., White, Ian M., Zhu, Hongying, and Fan, Xudong
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Sensors -- Research ,Sensors -- Thermal properties ,Resonators -- Research ,Astronomy ,Physics - Abstract
The liquid core optical ring resonator (LCORR) has recently shown promise as a high-sensitivity label-free lab-on-a-chip biological--chemical sensor. We investigate experimentally and theoretically the temperature dependence of the LCORR to establish a noise baseline, which will enable us to implement a temperature stabilization mechanism to reduce the thermally induced noise and to improve the sensor detection limit. Our studies involve analysis of the thermo-optic and thermomechanical effects of fused silica and aluminosilicate glass as they impact LCORR performance. Both thick-walled and thin-walled LCORRs are investigated to elucidate the contribution of water in the core to the thermal response of the LCORRs. Theoretical calculations based on Mie theory are used to verify the experimental observations. OCIS codes: 230.5750, 140.4780, 170.4520, 290.4020.
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- 2007
12. Increasing the enhancement of SERS with dielectric microsphere resonators
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White, Ian M., Oveys, Hesam, and Fan, Xudong
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Surface-enhanced Raman spectroscopy (SERS) is a widely studied technique capable of adding single-molecule detection capability to the rich information provided by Raman spectroscopy. In this article, we show an additional […]
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- 2006
13. Isothermal DNAzyme-Mediated Bicyclic Rolling Circle Amplification Enables Simple Colorimetric Detection of a Target Sequence
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Zimmermann, Alessandra C., primary, Kahn, Jason D., additional, and White, Ian M., additional
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- 2020
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14. Effect of heterogeneity in recombination rate on variation in realised relationship
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White, Ian M. S., primary and Hill, William G., additional
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- 2019
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15. A revision of the genus Chaetorellia Hendel (Diptera: Tephritidae) including a new species associated with spotted knapweed, Centaurea maculosa Lam. (Asteraceae)
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White, Ian M. and Marquardt, Kirsten
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Chaetorellia acrolophi sp. n. is associated with some European species of the subgenus Acrolophus of Centaurea. It is a potential biocontrol agent of some Acrolophus species that are adventive noxious weeds in North America. Ch. acrolophi sp. n. is described, and a key is provided to all nine species. The confirmed host-plants, knapweed, starthistles and related plants, belong to the genera Centaurea, Carthamus and Chartolepis (Asteraceae), and these are listed. Available biological data are reviewed, and some details of egg, larval and pupal morphology are described. Host-plant choice tests and canonical variates analysis were used to justify the separation of some species and to help identify some populations. The following nomenclatural changes are made (junior synonyms in brackets): Chaetorellia conjuncta (Becker) is removed from synonymy with Ch. succinea (Costa); Ch. hexachaeta australis Hering is raised to specific status; Ch. hestia Hering (=Ch. nigropicta Hering); Ch. loricata (Rondani) (= Ch. mara Hering and Ch. loricata septentrionalis Hering). Questionable synonyms include: Ch. australis Hering (?=Trypeta hexachaeta Loew); Ch. hestia (?= T. vittata Rondani); Chaetostomella cylindrica (Robineau-Desvoidy) (?= Tephritis algira Macquart, which is removed from Chaetorellia)
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- 2017
16. Tephritids of knapweeds, starthistles and safflower: results of a host choice experiment and the taxonomy of Terellia luteola (Wiedemann) (Diptera: Tephritidae)
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White, Ian M., Groppe, Kerstin, Sobhian, Rouhollah, White, Ian M., Groppe, Kerstin, and Sobhian, Rouhollah
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A host choice experiment was carried out to determine the host range of some potential biological control agents of yellow starthistle (Centaurea solstitialis), a Mediterranean plant which has become a serious rangeland weed in western USA. This paper describes the results of that experiment and discusses its taxonomic implications. The experiment confirmed the extreme host specificity of some species. However, two reputedly polyphagous species, Acanthiophilus helianthi (Rossi) and Urophora quadrifasciata (Meigen), attacked a narrower range of hosts than expected. The results of this and similar host choice experiments are discussed and it is concluded that this sort of anomaly can be caused by the existence of host races, unrecognized sibling species, or by varieties of plants naturally resistant to attack. These complex patterns of host relationship highlight the need to interpret host catalogue data cautiously, as they oversimplify complex biological systems. The identity of one species reared in the experiment, Terellia luteola (Wiedemann), is discussed; a key is presented for its separation from other Terellia species, and it is removed from synonymy with T. colon (Meigen)
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- 2017
17. Investigating the challenges of water governance in Oceania
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Daniell, Katherine Anne, Bouard, Séverine, Poelina, Anne, Ferrand, Nils, White, Ian M., Alexandra, Jason, Apithy, Leïla, Bois, Marion, Chevreux-Warode, Léa, Bouteloup, Perrine, Spencer, Michael, Perdrisat, Ian, Hassenforder, Emeline, Andrews, Kate, Rougier, Jean Emmanuel, Le Meur, Pierre-Yves, Sabinot, Catherine, Lejars, Caroline, Kaberiera, Teitibwebwe, Alberger Le Deunff, Helene, Fache, Elodie, Nabavi, Ehsan, and Kula, Taaniela
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E14 - Économie et politique du développement ,P10 - Ressources en eau et leur gestion - Published
- 2016
18. A Preliminary Notes on the Host-plants of Fruit Flies of the Tribe Dacini (Diptera, Tephritidae) in Sri Lanka
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Tsuruta, Kenji, White, Ian M., Bandara, H. M. J., Rajapakse, H., Sundaraperuma, S. A. H., Kahawatta, S. B. M. U. C., and Rajapakse, G. B. J. P.
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Dacini ,Diptera ,fruit flies ,host plants ,Biology ,Sri Lanka - Abstract
Host plants including a total of 22 families representing 45 species were recorded for 16 fruit flies of the tribe Dacini in Sri Lanka. Bactrocera kandiensis was found to be highly polyphagous, and its host range was as wide as that of B. dorsalis. Some host plants of B. dorsalis, B. kandiensis, B. correcta, B. cucurbitae, and B. trilineata were newly recorded. In addition, host plants of B. gavisa, B. sp. near nigrotibialis, B. sp. near tau, Dacus discophorus, and D. keiseri were recorded for the first time. Host plants of 46 % Sri Lankan Dacini are now known.
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- 1997
19. Dacus pleuralis Collart 1935
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Meyer, Marc De, White, Ian M., and F. M. Goodger, Kim
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus pleuralis ,Taxonomy - Abstract
Dacus pleuralis Collart, 1935 Among the material examined was a male specimen collected at Ibadan, Nigeria (4-8 Dec. 2003, cue lure traps, leg. G. Goergen), in addition to the male specimen studied earlier (White & Goodger 2009). It shows some morphological deviation from the earlier collected specimen and from the type material as redescribed in White (2006): the xanthines (katatergite and anatergite) are fused, while in the typical D. pleuralis the xanthines are clearly separated. The anterior supra-alar seta is absent or vestigial while well developed in the typical D. pleuralis. These differences, however, appear to be intraspecific variation and do not warrant separate description., Published as part of Meyer, Marc De, White, Ian M. & F. M. Goodger, Kim, 2013, Notes on the frugivorous fruit fly (Diptera: Tephritidae) fauna of western Africa, with description of a new Dacus species, pp. 1-17 in European Journal of Taxonomy 50 on page 12, DOI: 10.5852/ejt.2013.50, http://zenodo.org/record/3814414, {"references":["White I. M. & Goodger K. F. M. 2009. African Dacus (Diptera: Tephritidae); new species and data, with particular reference to the Tel Aviv University Collection. Zootaxa 2127: 1 - 49.","White I. M. 2006. Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology Memoir 2: 1 - 156."]}
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- 2013
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20. Dacus (Psilodacus) goergeni Meyer & White 2013, sp. nov
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Meyer, Marc De, White, Ian M., and F. M. Goodger, Kim
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Dacus ,Dacus goergeni ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Dacus (Psilodacus) goergeni sp. nov. urn:lsid:zoobank.org:act: 47F1AD2E-9183-4C0F-A65B-D9FDBB15DB1D Fig. 4 Etymology Named in honour of the collector, Dr Georg Goergen, who is also the founder and conservator of the entomological collections at the International Institute of Agriculture. Material Holotype ♂, TOGO, Kloto, Jan. 2006, ‘ on Solanum sp.’, leg. G. Goergen (deposited in collection of IITA). Paratypes TOGO: same locality as holotype, 1 ♂, Dec. 2005, ‘on Acacia auriculiformis ’; 2 ♂♂, 5 ♀♀, Jan. 2006; 1 ♂, 3 ♀♀, Jan. 2006, ‘on Solanum sp.’; 4 ♂♂, 1 ♀, Jan. 2008; 1 ♂, 1 ♀, Feb. 2008. BENIN: Lokossa, 1 ♂, 1 ♀, Jan. 2006. All leg. G. Goergen. Paratypes deposited in collections of IITA, NHM and RMCA. Description SIZE. 6.2-7.5 mm, wing length 4.8-6.6 mm. HEAD. Pedicel and 1st flagellomere not longer than ptilinal suture. Face (Fig. 4A): antennal furrow without a dark spot; upper area with a dark marking, tending to an inverted V-shaped dark marking (in some specimens this extends down each side of carina and may be mistaken for facial spots). Frons: frontal setae 0, orbital seta 0. THORAX. Scutum (Fig. 4B) predominantly fuscous, tending to red-brown antero-laterally; postpronotal lobe entirely pale, yellowish; notopleural callus pale posteriorly, anteriorly concolorous with scutum; notopleural xanthine probably isolated from notopleural callus but can appear almost joined (as in wedge form); lateral and medial postsutural vitta absent. Scutellum without any dark patterning (except for basal dark margin, which is very narrow). Anepisternum (Fig. 4C) with a stripe from notopleural callus to (or almost to) katepisternum; stripe very broad (anteriorly extending almost to postpronotal lobe); extended onto katepisternum. Laterotergal xanthine confined to katatergite. THORACIC SETAE. Anterior notopleural seta present; anterior supra-alar seta present. WING (Fig. 4E). Basal cell bc without microtrichia; cell c with an almost complete (> 90%) covering of microtrichia; cell bm without microtrichia. Narrow subbasal raised section of cell br with extensive covering of microtrichia; partly bare in apical half. Crossvein R-M beyond middle of cell dm. Costal band complete; shallow, not or barely extending below vein R 2+3, except in basal section (before crossvein R-M) and at wing apex; expanded into a small spot at apex. Anal streak absent (but with a trace of colour confined to cell bcu). Cells bc and c coloured (not as deep as costal band). Without any crossbanding. LEGS. Forefemur pale, yellowish, sometimes indistinctly darkened apically; midfemur bicoloured (pale basal half to two-thirds, red-brown apically); hindfemur pale, yellow, rarely distinctly darkened apically. ABDOMEN. Predominantly fuscous; shape and patterning, see Fig. 4D. Tergites I-V all fused. Male Tergite III with some very fine hairs (possible vestigial pecten); lacking hindtibia preapical “pad”. Basal costal sections without specialised setae. Female Aculeus pointed, similar to B. stylifer. Host No host records known (some material is indicated as being found on Solanum sp. or Acacia auriculiformis but there is no indication that either of these plants is a host). Distribution Reported from Benin and Togo. Remarks The new species is very similar to Dacus stylifer which is an East African species. It differs in the wing cell c having almost complete coverage of microtrichia in the males (50% in male stylifer); the midfemur bicoloured (pale in typical stylifer); the notopleuron bicoloured and sutural xanthine distinct, unlike typical stylifer. Dacus goergeni sp. nov. is placed in the ill-defined subgenus Psilodacus, based upon a combination of characters, which typify the grouping, including the lack of facial spots: the dark, almost inverted V-shaped, dark marking at the top of the face; lack of anal streak and male pectin; it differs from most Psilodacus spp. in having anterior supra-alar setae. The type specimens were captured in the Guinean Forest Savannah Mosaic and the Eastern Guinean Forest ecoregions. Label information indicates that the specimens were collected in forested areas., Published as part of Meyer, Marc De, White, Ian M. & F. M. Goodger, Kim, 2013, Notes on the frugivorous fruit fly (Diptera: Tephritidae) fauna of western Africa, with description of a new Dacus species, pp. 1-17 in European Journal of Taxonomy 50 on pages 10-12, DOI: 10.5852/ejt.2013.50, http://zenodo.org/record/3814414
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- 2013
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21. Dacus blepharogaster Bezzi 1917
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Meyer, Marc De, White, Ian M., and F. M. Goodger, Kim
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Dacus ,Dacus blepharogaster ,Insecta ,Arthropoda ,Diptera ,parasitic diseases ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Dacus blepharogaster Bezzi, 1917 A male specimen from Sérou, Benin (Dec. 2005, leg. G. Goergen) differs from D. blepharogaster, as described by White (2006) in having some red pattern on the third abdominal tergite. However, since this species belongs to a group that needs proper revision (Dacus (Lophodacus) brevis group as defined by White 2006) and since only one specimen was found in the collections studied, it is not described as a separate species. As the previous species, this is also predominantly an East African species (Kenya, Eritrea and Ethiopia) but was not included in the richness analysis., Published as part of Meyer, Marc De, White, Ian M. & F. M. Goodger, Kim, 2013, Notes on the frugivorous fruit fly (Diptera: Tephritidae) fauna of western Africa, with description of a new Dacus species, pp. 1-17 in European Journal of Taxonomy 50 on page 13, DOI: 10.5852/ejt.2013.50, http://zenodo.org/record/3814414, {"references":["White I. M. 2006. Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology Memoir 2: 1 - 156."]}
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- 2013
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22. Dacus mochii Bezzi 1917
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Meyer, Marc De, White, Ian M., and F. M. Goodger, Kim
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus mochii ,Taxonomy - Abstract
Dacus mochii Bezzi, 1917 Dacus mochii was described from Eritrea, but the type specimens were lost. White (2006) placed it in synonymy with D. annulatus Becker, based on the similarity of the original description. Subsequently, White & Goodger (2009) reported a specimen from Ethiopia, which was clearly not D. annulatus, but was a good match to the description of D. mochii, which they then removed from synonymy. Amongst the material examined here, there was a male specimen from Kloto, Togo (Mar. 2006, leg. G. Goergen), which is very similar to the D. mochii from Ethiopia, except that it has pallid face spots. Togo is a considerable westward expansion of the known distribution of a species otherwise known only from a restricted area of East Africa. Since it concerns a single specimen whose identity is uncertain, we excluded it from the richness analysis., Published as part of Meyer, Marc De, White, Ian M. & F. M. Goodger, Kim, 2013, Notes on the frugivorous fruit fly (Diptera: Tephritidae) fauna of western Africa, with description of a new Dacus species, pp. 1-17 in European Journal of Taxonomy 50 on page 13, DOI: 10.5852/ejt.2013.50, http://zenodo.org/record/3814414, {"references":["White I. M. 2006. Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology Memoir 2: 1 - 156.","White I. M. & Goodger K. F. M. 2009. African Dacus (Diptera: Tephritidae); new species and data, with particular reference to the Tel Aviv University Collection. Zootaxa 2127: 1 - 49."]}
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- 2013
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23. Case 3693 Cryptodacus Hendel, 1914 (Insecta: Diptera: tephritidae): proposed suppression of Cryptodacus Gundlach, 1862 (Reptilia, Serpentes, colubridae)
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Norrbom, Allen L., primary, McDiarmid, Roy, additional, Chen, Xiao-Lin, additional, David, K.J., additional, Meyer, Marc De, additional, Freidberg, Amnon, additional, Han, Ho-Yeon, additional, Hancock, David, additional, Steck, Gary J., additional, Thompson, F. Christian, additional, White, Ian M., additional, and Zucchi, Roberto A., additional
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- 2015
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24. Records of frugivorous fruit flies (Diptera: Tephritidae; Dacini) from the Comoro archipelago
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De Meyer, Marc, Quilici, Serge, Franck, Antoine, Chadhouliati, A.C., Issimaila, M.A., Youssoufa, M.A, Abdoul-Karime, Anli Liachouroutu, Attié, Marc, White, Ian M., De Meyer, Marc, Quilici, Serge, Franck, Antoine, Chadhouliati, A.C., Issimaila, M.A., Youssoufa, M.A, Abdoul-Karime, Anli Liachouroutu, Attié, Marc, and White, Ian M.
- Abstract
This paper summarizes current knowledge of the occurrence of Dacini fruit flies in the Comoro archipelago of the Indian Ocean. Ten species are confirmed as occurring in the archipelago: Bactrocera invadens Drew, Tsuruta & White, 2005, Dacus bivittatus (Bigot, 1858), D. ciliatus Loew, 1862, D. etiennellus Munro, 1984, D. punctatifrons Karsch, 1887, D. vertebratus Bezzi, 1908 (all Dacina), Ceratitis capitata (Wiedemann, 1824), C. malgassa Munro, 1939, Neoceratitis cyanescens (Bezzi, 1923), and Trirhithrum nigerrimum (Bezzi, 1913) (all Ceratitidina). Records of Bactrocera cucurbitae (Coquillett, 1899) remain unconfirmed. The fauna of the Comoros is briefly compared to that of other islands in the western Indian Ocean.
- Published
- 2014
25. Bactrocera latifrons
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White, Ian M. and Goodger, Kim F. M.
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Insecta ,Arthropoda ,Bactrocera ,Diptera ,Tephritidae ,Animalia ,Biodiversity ,Taxonomy ,Bactrocera latifrons - Abstract
Group Latifrons The Asian B. latifrons was not known in Africa before White (2006) was completed. Its name is here given to a species group for consistency of classsification., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 45, DOI: 10.5281/zenodo.274925, {"references":["White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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- 2009
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26. Dacus (Lophodacus) transversalis White & Goodger, 2009, sp.n
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy ,Dacus transversalis - Abstract
Dacus (Lophodacus) transversalis sp.n. Figures 91 ��� 96. Diagnosis. Differs from other Dacus spp. in lacking microtrichia in the narrow subbasal section of cell br, combined with the lack of a facial spot (fig. 93) and presence of a notopleural xanthine (fig. 91). It also has an unusual wing pattern (very broad dark band from sc to behind Cu 1; fig. 96), a dark triangle marking covering most of the scutellum (fig. 91) and the male lacks a pecten. Description. Size. Small, wing length, 4.6 ��� 4.8 mm. Head (fig. 93). Pedicel+first flagellomere not longer than ptilinal suture. Face, antennal furrow without a dark spot. Frons, frontal setae 2, orbital setae 1. Thorax (figs 91, 94). Scutum black; postpronotal lobe bicoloured (yellow confined to posterior third); notopleural callus yellow; notopleural xanthine wedge shaped (connected to notopleural callus); lateral and medial postsutural vitta absent. Scutellum with a basal black triangle, leaving only narrow yellow margin. Anepisternum with a very narrow yellow stripe from notopleural callus to (or almost to) katepisternum; not extended onto katepisternum. Lateroterga without a xanthine. Thoracic setae. Anterior notopleural seta present; anterior supra-alar seta absent. Wing (fig. 96). Basal cells bc and c without a complete covering of microtrichia; cell bm without microtrichia. Narrow subbasal raised section of cell br without microtrichia. Crossvein R-M beyond middle of cell dm. Costal band absent (reduced to a small apical spot). Anal streak absent (at most with a trace of colour confined to cell bcu). Cells bc and c hyaline. Crossbanding; broad crossband on R-M which continues across cell dm. Legs (fig. 95). Femora brown. Abdomen (fig. 92). Predominantly black, except sometimes for a red-brown submedial area on tergite V (one specimen lacks this). Tergites I ��� V all fused. Male. Tergite III without pecten; no dense microtrichia adjacent end A 1 +Cu 2; no hindtibia preapical pad. Female. Unknown. Etymology. Descriptive name for the broad crossband that traverses (transversus) most of the wing. Material. Holotype male, paratype male, MALAWI: Chitipa Distr., Jembya Resv., 18km. sse. Chisenga, 1870m., 10 o 8 ���S, 33 o 27 ���E, 11 ��� 20.i. 1989, J. Rawlins, S. Thompson (authors borrowed from TAU; expected to be returned to CMP by collection manager of TAU). Remarks. The complete lack of microtrichia in the narrow subbasal section of wing cell br places this species in sg. Lophodacus. It is similar to members of the Triater group (no face spot, triangular mark on scutellum, no male pecten) except in having the notopleural xanthine connected to the callus. The xanthine is medially narrowed, not in the form of a distinct wedge (as in Brevis group), which suggests doubtful homology. However, no species of sg. Lophodacus is known to have an isolated notopleural xanthine. Its unique wing pattern makes it an easy species to recognise., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on pages 36-38, DOI: 10.5281/zenodo.274925
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- 2009
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27. Didacus Collart
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White, Ian M. and Goodger, Kim F. M.
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Insecta ,Arthropoda ,Didacus ,Diptera ,Tephritidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Subgenus DIDACUS Collart Dacus (Didacus) Collart, 1935: 33. Type species Dacus ciliatus Loew, 1862, by original designation. Other synonyms: White (2006: 81), Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 10, DOI: 10.5281/zenodo.274925, {"references":["Collart, A. (1935) Les Dacinae du Congo Belge (Diptera: Trypetidae). Bulletin du Musee Royal d'Histoire Naturelle de Belgique, 11 (1), 1 - 45.","Loew, H. (1862) Bidrag till kannedomen om Afrikas Diptera. Ofversigt af Finska Vetenskaps-Societetens Forhandlingar. Afd. A. Matematik och Naturvetenskaper (Helsingfors), 19, 3 - 14.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
- Published
- 2009
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28. Dacus triater White & Goodger, 2009, sp.n
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Dacus triater ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Group Triater This group is now expanded to include D. apostata Hering, 1937 and D. nigriscutatus White, 2006; this removes the Apostata group name from the classification. White (2006) separated the Apostata and Triater groups by the presence or absence of a pecten. The strong similarity of D. pseudapostata sp.n. to D. apostata, from which it differs in the absence of a pecten, indicates that these two groups are inseparable. Additionally, known hosts of both groups are Zehneria spp. (Cucurbitaceae) (White 2006), and Virgilio et al. (in press) found that DNA studies muddled representatives of both groups into a single well defined clade., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 34, DOI: 10.5281/zenodo.274925, {"references":["Hering, [E.] M. (1937) Neue Bohrfliegen aus der Beckerschen Sammlung. (Dipt.) (16. Beitrag zur Kenntnis der Trypetidae). Mitteilungen aus dem Zoologischen Museum in Berlin, 22, 244 - 264.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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29. Dacus (Ambitidacus) mirificus Munro
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus mirificus ,Taxonomy - Abstract
Dacus (Ambitidacus) mirificus (Munro) Myrmecodacus mirificus Munro, 1984: 119 Material. KENYA: 1 male, West Pokot, Chepareria, 4 ��� 5.xi. 1983, A. Freidberg (TAU) Remarks. First record for Kenya. Differing from Congo specimens in wing cell r 4 + 5 being fumose brown almost throughout., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 10, DOI: 10.5281/zenodo.274925, {"references":["Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313."]}
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30. Dacus (Leptoxyda) yaromi White & Goodger, 2009, sp.n
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus yaromi ,Taxonomy - Abstract
Dacus (Leptoxyda) yaromi sp.n. Figures 33 ��� 38. Diagnosis. As D. attenuatus Collart, 1935, except: Wing. Costal band apically expanded into a spot which only reaches about mid-depth of cell r 4 + 5 (fig. 38). Legs. Femora bicoloured (fig. 37). Abdomen. Predominantly dark red-brown (fig. 34). Description. Size. Small, wing length, 5.6 mm. Head (fig. 35). Pedicel+first flagellomere not longer than ptilinal suture. Face, antennal furrow with a dark spot; slightly taller than broad, almost filling width of furrow. Frons, frontal setae 2, orbital setae 1. Thorax (figs 33, 36). Scutum red-brown; postpronotal lobe concolorous with scutum; notopleural callus red; notopleural xanthine wedge shaped and red (connected to notopleural callus); lateral and medial postsutural vitta absent. Scutellum without any dark patterning (except for basal red-brown margin). Anepisternum with a red subparallel stripe from notopleural callus to katepisternum; extended onto katepisternum. Laterotergal xanthine barely differentiated from red-brown body colour; confined to katatergite. Thoracic setae. Anterior notopleural seta present; anterior supra-alar seta absent. Wing (fig. 38). Basal cells bc and c without an almost complete covering of microtrichia; cell bm without microtrichia. Narrow subbasal raised section of cell br with extensive covering of microtrichia. Crossvein R-M beyond middle of cell dm. Costal band complete; shallow, not extending below vein R 2 + 3 before wing apex; apically expanded into a spot which reaches about mid-depth of cell r 4 + 5; and starts before end of vein R 2 + 3. Anal streak present (colour extending beyond cell bcu). Cells bc and c hyaline. Without any crossbanding. Legs (fig. 37). Femora bicoloured (pale basally, brown to black apical third to two-thirds). Abdomen (fig. 34). Syntergosternite I+II red-brown; terga III ��� V dark red-brown with a barely differentiated blackish medial stripe; shape similar to D. attenuatus. Tergites I ��� V all fused. Male. Tergite III with pecten, dense microtrichia adjacent end A 1 +Cu 2, and hindtibia preapical pad. Female. Unknown. Etymology. Patronym for Dr. (Mr.) I. Yarom, who collected the holotype. Material. Holotype male, ETHIOPIA: Gamo, Gofa, Arba Minch Springs, 1300m., 5.ii. 2000, I. Yarom & A. Freidberg (TAU). Remarks. This species shares with D. attenuatus the unusual feature of red xanthines and differs only in having a very much smaller costal band apical spot and a less extensively dark midfemur. There is a remote possibility that this is merely the dimorphic male form of D. attenuatus. It should also be noted that reddish xanthines are a known variant of some more common species., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 18, DOI: 10.5281/zenodo.274925, {"references":["Collart, A. (1935) Les Dacinae du Congo Belge (Diptera: Trypetidae). Bulletin du Musee Royal d'Histoire Naturelle de Belgique, 11 (1), 1 - 45."]}
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31. Dacus (Lophodacus) blepharogaster Bezzi
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Dacus blepharogaster ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Dacus (Lophodacus) blepharogaster Bezzi Dacus blepharogaster Bezzi, 1917: 68 Didacus zavattarianus Hering, 1952: 93 Other combinations: White (2006: 118) Material. KENYA: 1 female, Nyanza, Gembe Hills, 1362m., 0o 29.36 S, 34 o 14.60 E, 27.iv. ��� 11.v. 2006, malaise trap, R.S. Copeland (BMNH). Remarks. This is both new to Kenya and the first known female. The wing has a complete costal band, similar to the holotype of D. blepharogaster. Unlike both holotype males, the mid- and hindfemora are distinctly bicoloured, being almost black in the apical third. The abdomen differs in having a distinct black midline on terga IV and V; tergite IV is largely black with indistict red-brown areas posteriorly either side of the midline; tergite V is distinctly red-brown either side of the midline, implying a similarity to the description of the lost abdomen of the holotype of D. zavattarianus. The aculeus is well exposed; it lacks any torsion and is shaped like D. brevis Coquillett, 1901., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 28, DOI: 10.5281/zenodo.274925, {"references":["Bezzi, M. (1917) New Ethiopian fruit-flies of the genus Dacus. Bulletin of Entomological Research, 8, 63 - 71.","Hering, E. M. (1952 [dated 1951]) Missione biologica Sagan-Omo diretta dal Prof. Edoardo Zavattari. Diptera Trypetidae [36. Beitrag zur Kenntnis der Trypetidae]. Rivista di Biologia Coloniale (Rome), 11, 91 - 99.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156.","Coquillett, D. W. (1901 [dated 1902]) New Diptera from southern Africa. Proceedings of the United States National Museum, 24, 27 - 32."]}
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32. Ambitidacus Munro
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White, Ian M. and Goodger, Kim F. M.
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Insecta ,Arthropoda ,Diptera ,Tephritidae ,Animalia ,Biodiversity ,Ambitidacus ,Taxonomy - Abstract
Subgenus Ambitidacus Munro Ambitidacus Munro, 1984: 120. Type species, Dacus brevistriga Walker, 1861, by original designation. Other synonyms: White (2006: 77), Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 6, DOI: 10.5281/zenodo.274925, {"references":["Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313.","Walker, F. (1861) Characters of undescribed Diptera in the collection of W. W. Saunders, Esq., F. R. S. & c. [concl.]. Transactions of the Entomological Society of London (N. S.), 5, 297 - 334.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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33. Dacus magnificus
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus magnificus ,Taxonomy - Abstract
Group Magnificus New group for a single species that is assigned to s.g. Lophodacus because of its very reduced covering of microtrichia in the narrow raised subbasal section of wing cell br. Unlike other Lophodacus spp. whose males have a pecten, it lacks a xanthine on the lateroterga., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 28, DOI: 10.5281/zenodo.274925
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34. Bactrocera White & Goodger, 2009, s. str
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White, Ian M. and Goodger, Kim F. M.
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Insecta ,Arthropoda ,Bactrocera ,Diptera ,Tephritidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Subgenus BACTROCERA s. str. Dacus (Bactrocera) Macquart, 1835: 452. Type species B. longicornis Macquart, 1835, by monotypy. Other synonyms: White (2006: 137), Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 45, DOI: 10.5281/zenodo.274925, {"references":["Macquart, J. P. M. (1835) Histoire naturelle des Insectes. Dipteres. Roret, Paris. Tome deuxieme. IV, 1 - 710.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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35. Dacus (Didacus) ficicola Bezzi
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus ficicola ,Taxonomy - Abstract
Dacus (Didacus) ficicola Bezzi Dacus ficicola Bezzi, 1915: 100 Other synonyms: White (2006: 86) Material. KENYA: 3 females, Kinungi, Rt.A 104, nr. Naivasha, 80km Nakuru, 2250m., 24.viii. 2003, A. Freidberg (TAU). Remarks. White (2006) made a note in the description matrix (on CD-ROM) that some specimens of D. ficicola Bezzi, 1915 exhibit aculeus torsion. However, this was interpreted as artifact (possibly due to postmortem change) and not mentioned in the written description. A specimen in the TAU collection shows quite convincing torsion and the the description should be modified to indicate that this species may exhibit torsion, although the reason for the apparent variation remains uncertain., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on pages 13-14, DOI: 10.5281/zenodo.274925, {"references":["Bezzi, M. (1915) On the Ethiopian fruit-flies of the genus Dacus. Bulletin of Entomological Research, 6, 85 - 101.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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36. Dacus (Psilodacus) pergulariae Munro
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White, Ian M. and Goodger, Kim F. M.
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Dacus pergulariae ,Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Dacus (Psilodacus) pergulariae Munro Dacus (Metidacus) pergulariae Munro, 1938 b: 163 Dacus (Psilodacus) miniatus Munro 1948: 31 Other combinations: White (2006: 135) Material. ETHIOPIA: 1 male, 1 female, Bale, Bale Mountains, Micha River, 10km S. Goba, 3100m., 31.i. 2000, A. Freidberg & I. Yarom (TAU). Remarks. These specimens are somewhat larger than those reported by White (2006), being up to 7.2mm wing length, and may be confused in the key with D. stylifer (Bezzi, 1919), but they lack the dark lateral abdomen markings of that species (corrected in revised key; revised couplet 263). These specimens also have bicoloured femora, whereas typical D. pergulariae have entirely pale femora. The paratype female D. miniatus, a synonym of D. pergulariae, is teneral but shows signs of having a bicoloured hindfemur. Most specimens used in the description of D. pergulariae by White (2006) were reared and may also have been incompletely coloured. In the absence of better data these non-reared specimens are assumed to be more mature or a variant form, but further study may indicate that some Ethiopian populations represent a distinct species, possibly already described as D. miniatus., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on pages 42-43, DOI: 10.5281/zenodo.274925, {"references":["Munro, H. K. (1938 b) New Trypetidae from Kenya Colony. II. Journal of the East Africa and Uganda Natural History Society, 13, 159 - 167.","Munro, H. K. (1948) New African Dacinae (Trypetidae, Dipt.) with some preliminary statistical studies. Journal of the Entomological Society of Southern Africa, 11, 13 - 33.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156.","Bezzi, M. (1919) New Ethiopian fruit-flies of the genera Tridacus and Dacus (Dipt.). Bulletin of EntomologicalResearch, 9, 177 - 182."]}
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37. Dacus (Lophodacus) magnificus White & Goodger, 2009, sp.n
- Author
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus magnificus ,Taxonomy - Abstract
Dacus (Lophodacus) magnificus sp.n. Figures 64 ��� 70. Diagnosis. Separated from all other African Dacus spp. as follows: Thorax. Lateral and medial postsutural vittae absent (fig. 64); lateroterga without a xanthine (fig. 68). Wing. Costal band incomplete (fig. 70); cell c with an almost complete covering of microtrichia; narrow subbasal raised section of cell br with only a few microtrichia. Male. Tergite III with pecten (fig. 65). Description. Size. Medium, wing length, 6.7 ��� 6.9 mm. Head (fig. 67). Pedicel+first flagellomere not longer than ptilinal suture. Face, antennal furrow with a very small vertically elongate spot, adjacent lower facial margin; Frons, frontal setae 2, orbital setae 1. Thorax (figs 64, 68). Scutum red-brown, without any distinct darker areas; postpronotal lobe concolorous with scutum; notopleural callus white; notopleural suture xanthine absent; lateral and medial postsutural vittae absent. Scutellum dorsally concolorous with scutum, laterally white. Anepisternum with a narrow white stripe from notopleural callus to katepisternum; extended onto katepisternum. Lateroterga without a xanthine. Thoracic setae. Anterior notopleural seta present; anterior supra-alar seta absent. Wing (fig. 70). Basal cell bc without an almost complete covering of microtrichia; cell c with an almost complete (> 90 %) covering of microtrichia; cell bm without microtrichia. Narrow subbasal raised section of cell br with only a few microtrichia. Crossvein R-M in apical quarter of cell dm. Costal band reduced; cells c and sc coloured; large apical spot which extends below vein M and includes both R-M and DM-Cu crossveins. Anal streak absent (at most with a trace of colour confined to cell bcu). Cell bc hyaline. Without any crossbanding. Legs (fig. 69). Femora orange-brown. Abdomen (fig. 65). Orangebrown, without any distinct darker marks; broadest at tergite V (based on paratype female; holotype male distorted). Tergites I ��� V all fused. Ceromata present. Male. Tergite III with pecten, dense microtrichia adjacent end A 1 +Cu 2, and hindtibia preapical pad. Female (fig. 66). Aculeus pointed. Etymology. Descriptive name for its magnificent (magnificenti) appearance. Material. Holotype, male, TANZANIA: 35km. S. Mbeya, Rt.A 345, 2200m., 1.ix. 1996, A. Freidberg (TAU); paratype, 1 female, same data as holotype (TAU). Remarks. The wing of this fly is similar to that of D. attenuatus, notably in apical spot size and shape; but if differs in its almost complete lack of microtrichia in the narrow portion of cell br, its extensive covering in cell c, and the lack of a continuous costal band., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on pages 28-30, DOI: 10.5281/zenodo.274925
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38. Dacus (Didacus) africanus Adams
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy ,Dacus africanus - Abstract
Dacus (Didacus) africanus Adams Dacus africanus Adams, 1905: 169 Didacus africanus: Cogan & Munro 1980: 521 Dacus (Didacus) devure Hancock, 1985 b: 304; White (2006: 82); syn.n. Material. MOZAMBIQUE: 1 male, Gorongoza, 18.3 S, 34.02 E, 1 ��� 2.xii. 2006, trapped with mixed male lure (cue lure, methyl eugenol, trimedlure), P. Schule (MRAC). Remarks. White (2006) was not able to study the type of D. devure and similarly, Hancock (1985 b) did not study the type of D. africanus. The males of both these species are reported to be attracted to cue lure, i.e. 4 -(p -acetoxyphenyl)- 2 -butanone (White 2006). The discovery of a male from Mozambique which clearly ran to D. devure in the key by White (2006), and which was lure collected, prompted further consideration of the separation of D. devure from D. africanus, which was as follows: laterotergite xanthine completely confined to the katatergite in D. africanus, or slightly extended onto the anatergite in D. devure. A further 6 males were recently (2009) collected using cue lure in Mozambique by M. De Meyer (MRAC) and selected images were supplied to the authors. These show a continuous range of variation between the xanthine being confined to the katatergite, to it also covering one-third of the anatergite; the costal band in each case was narrower than normally observed in D. vertebratus, as indicated by couplet 167 of the key in White (2006). In conclusion, there is no evidence to support the continued listing of D. devure as a separate species, and it is here placed as a synonym to D. africanus. The continued separation of D. africanus from D. vertebratus is supported by the differing lure response of these species; males of D. vertebratus being attracted to methyl- 4 -hydroxybenzoate, which Hancock (1985 a) named as ���vert lure���., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on pages 11-13, DOI: 10.5281/zenodo.274925, {"references":["Adams, C. F. (1905) Diptera africana, I. Kansas University Science Bulletin, 3, 149 - 208.","Cogan, B. H. & Munro, H. K. (1980) 40. Family Tephritidae. In: Crosskey, R. W. (Ed.) Catalogue of theDiptera of the Afrotropical Region. British Museum (Natural History), London, pp. 518 - 554.","Hancock, D. L. (1985 b) New species and records of African Dacinae (Diptera: Tephritidae). Arnoldia Zimbabwe, 9, 299 - 314.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156.","Hancock, D. L. (1985 a) A specific male attractant for the melon fly Dacus vertebratus. Zimbabwe Science News (Causeway), 19, 118 - 119."]}
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39. Dacus (Didacus) insolitus White & Goodger, 2009, sp.n
- Author
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White, Ian M. and Goodger, Kim F. M.
- Subjects
Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus insolitus ,Taxonomy - Abstract
Dacus (Didacus) insolitus sp.n. Figures 20 ��� 26. Diagnosis. Differs from all other known African Dacus spp. in its lack of a facial spot (fig. 23), combined with an extensive covering of microtrichia in cell bc. Description. Size. Very small, wing length, 2.8 ��� 3.8 mm. Head (fig. 23). Pedicel+ 1 st flagellomere not longer than ptilinal suture. Face, antennal furrow without a dark spot. Frons, frontal setae 1, orbital setae 0. Thorax (figs 20, 24). Scutum red-brown; postpronotal lobe and notopleural callus concolorous with scutum; notopleural xanthine absent; lateral and medial postsutural vittae absent. Scutellum concolorous with scutum. Anepisternum without a yellow stripe. Katepisternum with a trace of a xanthine. Laterotergal xanthine absent. Setae. Anterior notopleural seta absent; anterior supra-alar seta absent. Wing (fig. 26). Basal cells bc and c with an almost complete covering of microtrichia; cell bm without microtrichia. Narrow subbasal raised section of cell br with extensive covering of microtrichia. Crossvein R-M beyond middle of cell dm. Costal band pale (but distinct) in cell r 1; reduced to a very narrow and pale band in cell r 2 + 3 (barely discernable); apically expanded into a distinctly coloured oblique spot, reaching vein M. Anal streak present (colour extending beyond cell bcu). Cells bc and c hyaline. Crossbanding; at most with a trace of a crossband on the anterior portion of R-M. Legs (fig. 25). Femora brown. Abdomen (fig. 21). Predominantly red-brown, with distinct black pear-drop shaped spots on each of terga III, IV and V, but not coalesced into a strip. Tergites I ��� V all fused. Male. Tergite III with pecten, dense microtrichia adjacent end A 1 +Cu 2, and hindtibia preapical pad. Female (fig. 22). Aculeus blunt and with preapical "shoulder"; complete torsion. Etymology. Named for its unusual (insolitus) combination of character states. Material. Holotype female (NMKE), KENYA: Nyanza, Nyamarandi Village, 1251m., 0o 30.535 ���S, 34 o 11.206 ���E, 6 ��� 20.vi. 2006, malaise trap, R.S. Copeland. Paratypes: 1 female (NMKE), KENYA: Nyanza, Rusinga Island, 1206m., 0o 23.430 ���S, 34 o 10.995 ���E, 15. ��� 21.xi. 2004, malaise trap, R.S. Copeland; 1 female (MRAC), same data except, 28.xi. ��� 5.xii. 2004; 1 male (BMNH), same data except, 29.xii. 2004 ��� 4.i. 2005; 1 female (BMNH), same data except, 21.iv. ��� 12.v. 2005. Remarks. The combination of aculeus torsion and lack of an anterior notopleural seta indicates an affinity to the Mulgens group; the abdomen pattern is similar to D. (Lophodacus) nairobensis but the dense covering of microtrichia in the narrowed portion of cell br rules out membership of sg. Lophodacus; the complete lack of vittae (save for a trace on the katepisternum) is unusual in specimens that show no trace of postmortem staining; an almost complete coverage of microtrichia in cell bc is otherwise only known in four other African species, namely D. (D.) bequaerti Collart, 1935, D. (Leptoxyda) arabicus White, 2006, D. (Neodacus) melanaspis (Munro, 1984) and D. (N.) xanthaspis (Munro, 1984)., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 14, DOI: 10.5281/zenodo.274925, {"references":["Collart, A. (1935) Les Dacinae du Congo Belge (Diptera: Trypetidae). Bulletin du Musee Royal d'Histoire Naturelle de Belgique, 11 (1), 1 - 45.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156.","Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313."]}
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40. Dacus (Lophodacus) chamun Munro
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Dacus chamun ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Dacus (Lophodacus) chamun (Munro) Nebrodacus chamun Munro, 1984: 141 Dacus (Leptoxyda) chamun: Norrbom et al. 1999: 136; White 2006: 120 Remarks. Following the discovery of the following additional species, D. chamun is here regarded as part of the Apoxanthus group, rather than being placed in a group of its own., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 24, DOI: 10.5281/zenodo.274925, {"references":["Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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41. Dacus (Leptoxyda) brunnalis White & Goodger, 2009, sp.n
- Author
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy ,Dacus brunnalis - Abstract
Dacus (Leptoxyda) brunnalis sp.n. Figures 39 ��� 44. Diagnosis. As D. lounsburyii Coquillett, 1901 except: Thorax. Scutellum with a narrow basal dark margin (fig. 39). Wing. Cells bc slightly coloured (almost as dark as costal band); wing other than costal band and anal streak with a brownish tint, darkening posteriorly (fig. 44). Legs. Fore- and midfemora bicoloured (fig. 43). Description. Size. Medium, wing length, 8.2 mm. Head (fig. 41). Pedicel+first flagellomere not longer than ptilinal suture. Face, antennal furrow with a dark spot; tear-drop shaped; occupying almost whole width and lower have of furrow. Frons, frontal setae 2, orbital setae 1. Thorax (figs 39, 42). Scutum predominantly dark red-brown, with a black mark anterior to notopleural xanthine and mesal of lateral vitta; postpronotal lobe yellow; notopleural callus yellow; notopleural xanthine wedge shaped (connected to notopleural callus); lateral (narrow) and medial postsutural vittae present. Scutellum without any dark patterning (except for narrow basal dark margin). Anepisternum with a stripe from notopleural callus to katepisternum; extended as a broad xanthine on katepisternum. Laterotergal xanthine confined to katatergite. Thoracic setae. Anterior notopleural seta present; anterior supra-alar seta absent. Wing (fig. 44). Basal cell bc without an almost complete covering of microtrichia; cell c with more than 75 % covering of microtrichia; cell bm without microtrichia. Narrow subbasal raised section of cell br with extensive covering of microtrichia. Crossvein R- M beyond middle of cell dm. Costal band complete; deep, extending to vein R 4 + 5 before wing apex; apically expanded into a large spot, reaching below vein M, and starts before end of vein R 2 + 3. Anal streak present (colour extending beyond cell bcu). Cells bc and c slightly coloured (almost as dark as costal band). Without any crossbanding. Remainder of wing with a brownish tint, darkening posteriorly. Legs (fig. 43). Femora bicoloured (pale basally and red-brown in apical two-thirds to three quarters, dorsally; more extensively redbrown ventrally). Abdomen (fig. 40). Predominantly red-brown to fuscous, paler apically on tergite II and submedially on terga IV ��� V; terga I ��� V with a medial black stripe; shape as D. lounsburyii. Tergites I ��� V all fused. Male. Tergite III with pecten, dense microtrichia adjacent end A 1 +Cu 2; hindtibia preapical pad apparently absent. Female. Unknown. Etymology. Descriptive name for the brown (brunneus) colour over most of the wing (ala). Material. Holotype male, CAMEROON: Mbalmayo, ix. 2004, cue lure, M. Tindo (MRAC). Remarks. Closest to D. fuscovittatus Graham, 1910, but differing from that species in the laterotergal xanthine being restricted to the katatergite and the longer narrower lateral vitta. Curiously, there is no indication of a raised tubercle near the apex of the male hind tibia, as normally seen in species with a pecten; however, there is flat area on which the setulae are finer than those on the rest of the tibia. The only other African species known to have a pecten but no hindtibia tubercle is D. notalaxus Munro, 1984., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 20, DOI: 10.5281/zenodo.274925, {"references":["Coquillett, D. W. (1901 [dated 1902]) New Diptera from southern Africa. Proceedings of the United States National Museum, 24, 27 - 32.","Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313."]}
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42. Dacus (Didacus) pusillator Munro
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus pusillator ,Taxonomy - Abstract
Dacus (Didacus) pusillator (Munro) Pycnodacus pusillator Munro, 1984: 140 Dacus (Leptoxyda) pusillator: Norrbom et al. 1999: 137 Remarks. This species is only known from a single female. White (2006) noted that in terms of overall similarity this species was similar to D. binotatus Loew, 1862, but that it had the group features of D. seguyi, and so placed it in the Seguyi group, then regarded as part of sg. Didacus. However, new evidence presented here indicates that D. seguyi should be placed in sg. Lophodacus, and D. pusillator is therefore moved to the Binotatus group, pending the discovery of a male specimen from which to clarify its true affinities., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 13, DOI: 10.5281/zenodo.274925, {"references":["Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156.","Loew, H. (1862) Bidrag till kannedomen om Afrikas Diptera. Ofversigt af Finska Vetenskaps-Societetens Forhandlingar. Afd. A. Matematik och Naturvetenskaper (Helsingfors), 19, 3 - 14."]}
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43. Dacus (Lophodacus) pseudapostata White & Goodger, 2009, sp.n
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus pseudapostata ,Taxonomy - Abstract
Dacus (Lophodacus) pseudapostata sp.n. Figures 84 ��� 90. Diagnosis. Differs from D. triater in lacking a black triangular mark on the scutellum (fig. 84). Differs from D. apostata in the male lacking a pecten and associated characters (no dense microtrichia adjacent end A 1 +Cu 2; no hindtibia preapical pad). Differs from both species in the apical wing spot being larger (fig. 90). Description. Size. Small, wing length, 4 ��� 4.8 mm. Head (fig. 87). Pedicel+first flagellomere not longer than ptilinal suture. Face, antennal furrow without a dark spot. Frons, frontal setae 1 ��� 2, orbital setae absent. Thorax (figs 84, 88). Scutum black; postpronotal lobe yellow (sometimes indistinctly brownish anteromesally); notopleural callus black; notopleural xanthine absent; lateral and medial postsutural vittae absent. Scutellum yellow, without any dark patterning (except for basal dark margin which is deep in the females). Anepisternum with a yellow subtriangular xanthine from notopleural callus to (or almost to) katepisternum; anteriorly almost reaching postpronotal lobe; not extended onto katepisternum. Laterotergal xanthine confined to katatergite. Thoracic setae. Anterior notopleural seta sometimes present (present in holotype male; absent in females); anterior supra-alar seta absent. Wing (fig. 90). Basal cells bc and c without a covering of microtrichia; cell bm without microtrichia. Narrow subbasal raised section of cell br without microtrichia. Crossvein R-M beyond middle of cell dm. Costal band absent; reduced to a trace of dark colour in cell r 1 and an apical spot which reaches about mid-depth of cell r 4 + 5. Anal streak absent. Cells bc and c hyaline. Crossbanding; sometimes with an isolated crossband on R-M (the females have this; the holotype male does not). Legs (fig. 89). Femora pale (yellow) coloured. Abdomen (fig. 85). Black, except apical half of tergite V (also antero-medial area of tergite V in male holotype). Tergites I ��� V all fused. Male. Tergite III without pecten; no dense microtrichia adjacent end A 1 +Cu 2; no hindtibia preapical pad. Female (fig. 86). Aculeus pointed; no torsion. Etymology. Descriptive name for its resemblance (pseudo) to D. apostata Hering, 1937. Material. Holotype male, paratype, 1 female, CAMEROON: Bali-Batibo, Rt. N 6, W. of Bamenda, 20.xi. 1987, A. Freidberg (TAU); paratype, 1 female, Bambalang area, 35km E. Bamenda, off Rt. N 11, 1200m., 8.xi. 1987, F. Kaplan (TAU). Remarks. Males of D. pseudapostata sp.n., from West Africa, are easily separated from D. apostata, from East Africa, by the lack of a pecten. There are some minor colour differences that may help differentiate females; D. apostata has a smaller apical wing spot and usually lacks any bright colour at the apex of the abdomen. This short series of specimens also suggests some sexual dimorphism with females having the wing crossband and the male not, and the male having more colour on the abdomen apex than the females., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on pages 34-36, DOI: 10.5281/zenodo.274925, {"references":["Hering, [E.] M. (1937) Neue Bohrfliegen aus der Beckerschen Sammlung. (Dipt.) (16. Beitrag zur Kenntnis der Trypetidae). Mitteilungen aus dem Zoologischen Museum in Berlin, 22, 244 - 264."]}
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44. Dacus (Lophodacus) seguyi Munro
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Dacus seguyi ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Dacus (Lophodacus) seguyi (Munro) Pycnodacus seguyi Munro, 1984: 140 Dacus (Leptoxyda) seguyi: Norrbom et al. 1999: 137 Material. CAMEROON: 1 male, Bamenda, 20km s., 1800m., 5 o 30 ���N, 10 o 10 ���E, 22.xi. 1987, F. Kaplan (TAU). Remarks. This specimen differs from the holotype female in having a narrower and darker (sublateral red-brown areas confined to tergite V) abdomen; the femora more extensively dark; and a deeper dark marginal band across the base of the scutellum. All of these features are within the bounds of likely variation. This male, which has a pecten (new data included in revised key; revised couplet 208), was collected within a short distance of the type locality (Bamoun region, Baigom; 5 o 34 ���N, 10 o 41 ���E Gazetteer data)., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 31, DOI: 10.5281/zenodo.274925, {"references":["Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313."]}
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45. Dacus velutifrons
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Biodiversity ,Dacus velutifrons ,Taxonomy - Abstract
Group Velutifrons This is a new group for this single species that lacks an anal streak, in common with the Longistylus and Marshalli groups; but differs from those in the male having a pecten., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 22, DOI: 10.5281/zenodo.274925
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46. Dacus (Leptoxyda) sphaeristicus Speiser
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Lauxaniidae ,Animalia ,Dacus sphaeristicus ,Biodiversity ,Taxonomy - Abstract
Dacus (Leptoxyda) sphaeristicus Speiser Dacus sphaeristicus Speiser, 1910: 183 Other synonyms: White (2006: 110), Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 22, DOI: 10.5281/zenodo.274925, {"references":["Speiser, P. G. E. (1910) Cyclorrhapha, Aschiza. In: Sjostedt, Y. (Ed.) Wissenschaftliche Ergebnisse der Schwedischen Zoologischen Expedition nach dem Kilimandjaro, dem Meru und den umgebenden Massaisteppen Deutsch- Ostafrikas 1905 - 1906 unter Leitung von Prof. Dr. Yngve Sjostedt. 2. Band [Abteilung] 10 (Diptera), 113 - 202.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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47. Dacus (Psilodacus) merzi White
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Dacus merzi ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Dacus (Psilodacus) merzi White Dacus (Psilodacus) merzi White, 2006: 132 Material. KENYA: 2 males, 1 female, Mt. Elgon Lodge, 1 ��� 6.xi. 1983, A. Freidberg (TAU) Remarks. White (2006) described this species from a single male which had an almost complete (c. 90 %) covering of microtrichia in cell c. These males are similar but the female has a considerably reduced covering of microtrichia in cell c (around 75 %) and will erroneously run to D. herensis Munro, 1984 using the key provided by White (2006) (corrected in revised key). The known males, including the holotype, all have a large inverted-V mark on the face, just below the antennal insertions. In the female this is reduced to a pair of very small dark marks., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 42, DOI: 10.5281/zenodo.274925, {"references":["White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156.","Munro, H. K. (1984) A taxonomic treatise on the Dacidae (Tephritoidea, Diptera) of Africa. Entomology Memoirs, Republic of South Africa, Department of Agriculture, 61, 1 - 313."]}
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48. Psilodacus Collart
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White, Ian M. and Goodger, Kim F. M.
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Insecta ,Arthropoda ,Diptera ,Psilodacus ,Tephritidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Subgenus PSILODACUS Collart Dacus (Psilodacus) Collart, 1935: 5. Type species D. annulatus Becker, 1903, by original designation. Other synonyms: White (2006: 124), Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 38, DOI: 10.5281/zenodo.274925, {"references":["Collart, A. (1935) Les Dacinae du Congo Belge (Diptera: Trypetidae). Bulletin du Musee Royal d'Histoire Naturelle de Belgique, 11 (1), 1 - 45.","Becker, T. (1903) Agyptische Dipteren. (Fortsetzung und Schluss). Mitteilungen aus dem Zoologischen Museum in Berlin, 2 (3), 67 - 195.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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49. Dacus kaplanae
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White, Ian M. and Goodger, Kim F. M.
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Dacus ,Insecta ,Arthropoda ,Diptera ,Dacus kaplanae ,Lauxaniidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Group Kaplanae A new group near to the Schoutedeni group, differing in the lack of an anal streak. Like D. schoutedeni Collart 1935 and D. merzi White, 2006, the males have a pecten and hindtibia swelling, but lack the area of microtrichia adjacent the end of wing vein A 1 +Cu 2, as seen in almost all other Dacus and Bactrocera spp. which have a pecten., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on page 40, DOI: 10.5281/zenodo.274925, {"references":["Collart, A. (1935) Les Dacinae du Congo Belge (Diptera: Trypetidae). Bulletin du Musee Royal d'Histoire Naturelle de Belgique, 11 (1), 1 - 45.","White, I. M. (2006) Taxonomy of the Dacina (Diptera: Tephritidae) of Africa and the Middle East. African Entomology, Memoir, 2, 1 - 156."]}
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50. Bactrocera (Bactrocera) latifrons Hendel
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White, Ian M. and Goodger, Kim F. M.
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Insecta ,Arthropoda ,Bactrocera ,Diptera ,Tephritidae ,Animalia ,Biodiversity ,Taxonomy ,Bactrocera latifrons - Abstract
Bactrocera (Bactrocera) latifrons (Hendel) Chaetodacus latifrons Hendel 1915: 425 [I.C.Z.N. priority rule suspended to validate established name; White & Liquido 1995: 251] Dacus parvulus Hendel 1912: 21 Chaetodacus antennalis Shiraki 1933: 56 Strumeta latifrons: Shiraki 1933: 63 Dacus (Strumeta) latifrons: Hardy & Adachi 1954: 171 Dacus (Bactrocera) latifrons: Hardy 1977: 50 Bactrocera (Bactrocera) latifrons: White & Elson-Harris 1992: 208 Material. TANZANIA: 2 male, 2 female, Morogoro, 11.v. 2006, ex Solanum aethiopicum, leg. Resta (R 825) (MRAC); 1 male, 2 females, same data (R 872) (MRAC); 1 female, Morogoro, Sokoine Univ.Agric., 22.v. 2006, leg. Resta (T 2770) (MRAC). Remarks. The discovery of this Asian species in East Africa has been discussed elsewhere (Mwatawala et al. 2007). It has been added to the revised key (after couplet 5)., Published as part of White, Ian M. & Goodger, Kim F. M., 2009, African Dacus (Diptera: Tephritidae); New Species and Data, with Particular Reference to the Tel Aviv University Collection, pp. 1-49 in Zootaxa 2127 on pages 45-46, DOI: 10.5281/zenodo.274925, {"references":["Hendel, F. G. (1915) H. Sauter's Formosa-Ausbeute. Tephritinae. Annales Historico-Naturales Musei Nationalis Hungarici, 13, 424 - 467.","White, I. M. & Liquido, N. J. (1995) Chaetodacus latifrons Hendel, 1915 (currently Bactrocera latifrons; Insecta, Diptera): Proposed precedence of the specific name over that of Dacus parvulus Hendel, 1912. Bulletin of Zoological Nomenclature, 52, 250 - 253.","Hendel, F. G. (1912) Genus Dacus, Fabricius (1805) (Dipt.). Supplementa Entomologica (Berlin-Dahlem), 1, 13 - 24.","Shiraki, T. (1933) A systematic study of the Trypetidae of the Japanese Empire. Memoires of the Faculty of Science and Agriculture, Taihoku Imperial University, 2, 1 - 509.","Hardy, D. E. & Adachi, M. S. (1954) Studies in the fruit flies of the Philippine Islands, Indonesia and Malaya. Part 1. Dacini (Tephritidae-Diptera). Pacific Science, 8, 147 - 204.","Hardy, D. E. (1977) Tephritidae (Trypetidae, Trupaneidae), In: Delfinado, M. D., Hardy, D. E. (eds), A Catalogue of the Diptera of the Oriental Region, Honolulu, 3, 44 - 134.","White, I. M. & Elson-Harris, M. M. (1992) Fruit Flies of Economic Significance; their Identification and Bionomics. CAB International, Wallingford, 601 pp.","Mwatawala, M., De Meyer, M., White, I. M., Maerere, A. & Makundi, R. H. (2007) Detection of the Solanum fruit fly, Bactrocera latifrons (Hendel) in Africa (Dipt., Tephritidae). Journal of Applied Entomology, 131, 501 - 503."]}
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