Oospila falcata Lindt & Hausmann & Viidalepp 2018, sp. n.

Oospila falcata sp. n.
(Figs 5, 41, 73)

 Holotype: 1♂, French Guiana, Envorons de Cayenne, 1989 (de Toulgoet, Navatte, Lalanne Cassou; ZSM / Herbulot) (slide ZSM G 17198; barcode ID 69637, failure)

 Paratype: 1♀, French Guiana, St. Jean du Maroni, Piste Plateau des Mines PK 1 / PK 6, 0 1.02.1986 (de Toulgoet, Lalanne Cassou, Gibeaux; ZSM /Herbulot) (slide ZSM G 20344).

 Diagnosis. In wing colour and pattern reminiscent of O. flavilimes and O. cristae sp. n. but having fore wing apex shape and tornus of fore- and hind wing angulate and distal margin of both wings straighter. Hind wing discal spot black. Male genitalia similar to those of O. nigripunctata, in the short costa and membranized valvula, differing in the long sacculus curved to a 90° angle (almost straight in O. nigripunctata). The bursa copulatrix is very long.

 Description (Fig. 5): Wingspan, ♂ 14.5, ♀ 15.5 mm. Fore wing apex pointed. Ground colour bright green. Fore wing costa and fringe yellow, apical streak present, blackish. Black cell spots sharp and very fine, present on all wings, but on hind wing almost invisible. Frons and palpi of O. falcata are pale brown, the interantennal fillet contrasting white. The male antennae are bipectinate in the basal two-thirds, the length of the external and inner pectinations reaching 0.55 and 0.35 mm, accordingly. Female antennae thick filiform. The palpi are short and slender in the male, not reaching the frons. Female palpi slightly longer, slightly exceeding diameter of eye.

Male genitalia (Fig. 41): Uncus with tapered distal projection. The costa of valva is reduced to a stub which is connected to the valvula via a thin membrane, the sacculus and valvula are completely fused to a long process, tapering and curved to an angle of 90° at tip. Length of aedeagus 1.45 mm, with a short cornutus on the vesica. The sternite A8 is not sclerotized, posteriorly convex.

Female genitalia (Fig. 73): The papillae anales are subacute, apophyses posteriores about three times length of the apophyses anteriores. Antrum broadly bulbed, ductus bursae short. Corpus bursae very long (2.7 mm) and narrow, signum absent.

 Genetic data. Not yet DNA barcoded (DNA barcode specimenID BC ZSM Lep 69637: failure).

 Distribution. French Guiana, Guiana (cf. Cook & Scoble 1995).

 Biology. Collected in lowland tropical forest, in February.

 Etymology. The name refers to the rectangularly curved (falcate) valva.

Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Lepidoptera
Geometridae
Oospila
Oospila falcata

Published as part of Lindt, Aare, Hausmann, Axel & Viidalepp, Jaan, 2018, Review of some species groups of the genus Oospila Warren, with descriptions of nine new species (Lepidoptera: Geometridae: Geometrinae), pp. 151-194 in Zootaxa 4497 (2) on pages 157-158, DOI: 10.11646/zootaxa.4497.2.1, http://zenodo.org/record/1452101

Cook, M. A. & Scoble, M. J. (1995) Revision of the neotropical genus Oospila Warren (Lepidoptera: Geometridae). Bulletin of The Natural History Museum. Entomology Series, 64, 1, 115.


Observations of the new variable Z Herculis


Sedum acre L. (BR0000011913733)

Belgium Herbarium image of Meise Botanic Garden.

Biodiversity Taxonomy Terrestrial Herbarium Crassulaceae


Nordostdeutsche dermatologische Vereinigung: Sitzung am 29. März 1914


Teucrium montanum L. (BR0000010254141)

Biodiversity Taxonomy Terrestrial Herbarium Labiatae


GAIA 5G: A Multi-Access Smart-Campus Architecture

Smart-campuses are an emerging ecosystem that permit to enhance the performance and efficiency of academic facilities. Besides, they are also adopted as research, development, and testing platforms for the integration of novel management and governance mechanisms in complex ICT infrastructures. In this line, they are considered as small smart-city-like scenarios which can be used as a playground prior to large-scale deployments. This work presents the GAIA 5G smart-campus, located in the Espinardo campus of the University of Murcia (Spain). In the first place, its technological architecture is presented, detailing the multi-access platform that provides 5G, Internet of Things (IoT), and vehicular communications connectivity. Also, the virtualized computation environment is described. Thanks to these two pillars, GAIA 5G has the potential to host diverse use cases in multiple verticals, such as 5G connectivity, Network Function Virtualization (NFV) management and orchestration, or cybersecurity, which are also described. As discussed along the paper, GAIA 5G is an operative smart-campus infrastructure ready to support state-of-the-art research and accommodate novel 5Gand-beyond (B5G) test cases.

Ortiz, Jordi

University Center of Defense at the Spanish Air Force Academy

This work has been supported by Fundación Séneca—Agencia de Ciencia y Tecnología de la Región de Murcia—under the FPI Grant 21429/FPI/20, and co-funded by Odin Solutions S.L., Región de Murcia (Spain); by the Spanish Ministry of Science and Innovation under the DIN2019-010827 Industrial PhD Grant, and co-funded by Odin Solutions S.L.; by the European Commission under the 5GASP (Grant No. 101016448) and INSPIRE-5Gplus (Grant No. 871808) projects; by the ONOFRE-3 project (Grant No. PID2020-112675RB-C44) funded by MCIN/AEI/10.13039/501100011033; and by the 5G
Huerta project (Grant No.EQC2019-006364-P) funded by the Spanish Ministry of Science, Innovation and Universities, with ERDF funds.


LXXVI. Note on the energy of scattered X-radiation


An Alternative Antimicrobial Approach to Fight Bacterial Pathogens from Phellinus linteus

The objective of this research was focused on investigating in vitro antimicrobial activity of Phellinus linteus fruiting body extracts on Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus and Methicillin-resistant Staphylococcus aureus. Phellinus linteus fruiting body was extracted with ethanol and ethyl acetate and was vaporized. The disc diffusion assay was used to assess antimicrobial activity against tested bacterial strains. Primary screening of chemical profile of crude extract was determined by using thin layer chromatography. The positive control and the negative control were used as erythromycin and dimethyl sulfoxide, respectively. Initial screening of Phellinus linteus crude extract with the disc diffusion assay demonstrated that only ethanol had greater antimicrobial activity against Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus and Methicillin-resistant Staphylococcus aureus. The MIC assay showed that the lower MIC was observed with 0.5 mg/ml of Pseudomonas aeruginosa and Methicillin-resistant Staphylococcus aureus and 0.25 mg/ml. of Escherichia coli and Staphylococcus aureus, respectively. TLC chemical profile of extract was represented at Rf ≈ 0.71-0.76.

A.S. Haddadin, S.A. Fappiano, and P.A. Lipsett, "Methicillin resistant Staphylococcus aureus (MRSA) in the intensive care unit" Postgrad. Med. J. 2002, Vol. 78, pp. 385-392.

C.M. Kang, D.H. Han, H.K. Hwang, S.H. Choi, and W.J. Lee, "Anticancer effect of Phellinus linteus; potential clinical application in treating pancreatic ductal adenocarcinoma" J. Carcinogene Mutagene. 2013, pp. 13:1-8.

P. Toopmuang, C. Khamchum, and V. Punsuvon, "Detection and confirmation of hispolon in the mushroom Phellinus linteus" 2014, J. Sci. Asia. Vol. 40, pp. 141-144.

B.K. Yang, S.L. Hwang, I.K. Yun, E.J. Do, W.H. Lee, Y.M. Jung, S.C. Hong and D.C. Park, "Antitumor effects and immunodulating activities of Phellinus linteus extract in a CT-26 cell-injected colon cancer mouse model" Mycobiol. 2009, Vo. 37, pp 128-132.

D.S. Šeklić, M.S. Stanković, M.G. Milutinović, M.D. Topuzović, A. Š. Štajn and S.D. Marković, "Cytotoxic, antimigratory, pro-and antioxidative activities of extracts from medicinal mushrooms on colon cancer cell lines" Arch. Biol. Sci. 2016, Vol.68, pp. 93-105.

C.J. Lin, H.M. Lien, H.Y. Chang, C.L. Huang, J.J. Liu, Y.C. Chang, C.C. Chen and C.H. Lai, "Biological evaluation of Phellinus linteus-fermented broths as anti-inflammatory agents" J. Biosci. Bioeng. 2014. Vo. 118, pp. 88-93.

M. Balouiri, M. Sadiki, and S.K. Ibnsouda, "Methods for in vitro evaluating antimicrobial activity: A review" J. Pharm. Anal. 2016, Vol. 6, pp. 71-19.

H. Chen, Tian, T. Miao, H. and Zhao, Y.Y. "Traditional uses, fermentation, phytochemistry and pharmacology of Phellinus linteus: A review" Fitoterapia, Vol. 113, pp 6-26.

C. Valgas, S.M. Souza, E.F.A. Smânia, and A. Smânia-Jr, "Screening methods to determine antibacterial activity of natural products" Bra. J. Microbiol. 2007, pp. 369-379.
[10]	W.S. Jo, R. Y.H., Choi, S.G., Seo, G.S., Sung, J.M. and Uhm, J.Y. "the culture conditions for mycelial growth of Phellinus spp." Mycobiol. 2006, pp. 200-205.
[11]	Samchai, S., Seephonkai, P., Sangdee, A., Puntumchai, A. and Klinhom, U. Antioxidant, cytotoxic and antimalarial activities from crude extracts of mushroom Phellinus linteus. J. Biol. Sci. 2009;783-778.
[12]	C. Sittiwet, and D. Puangpronpitag, "Anti-Streptococcus aureus activity of Phellinus igniarius aqueous extract" In. J. Pharm. 2008, Vol. 4, PP. 503-505.
[13]	S.B. Hong, M.H. Rhee, B.S. Yun, Y.H. Lim, H.G. Song, and K.S. Shin, "Synergistic anti-bacrteial effects of Phellinus baumii ethyl acetate extracts and lactam antimicrobial agents against methicillin-resistant Staphylococcus aureus" Ann. Lab. Med. 2016, Vol. 36, pp. 111-116.
[14]	M.J. Alves, I.C.F.R. Ferreira, H.J.C. Froufe, R.M.V. Abreu, A. Martins, and M. Pintado, "Antimicrobial activity of phenolic compounds identified in wild mushrooms, SAR analysis and docking studies" J. Appl. Microbiol. 2013, pp. 1-12.


gaberosenfield/Glass-Lab-Flow-Cytometry-Analysis: First Release of Glass Lab Flow Cytometry Data Analysis Scripts

This release contains the scripts required to reproduce the analysis used in Goncalves et al "Allorecognition upon cell-cell contact determines social cooperation and acquisition of multicellularity" (2019).


KUR'ÂN'DA ŞİRKİN İPTALİNDE VÂRİT OLAN İFADELERİN DİLSEL ÖZELLİKLERİ

Öz

Kur’ân’ın indirilişindeki birinci gaye, insanları tevhîd inancına ulaştırmak, bu inancı benimsemelerini ve özümsemelerini sağlamaktır. Bu ise ilkin tevhîde zıt fikir ve inanışları ortadan kaldırmakla mümkündür. Tabiî olarak Kur’ân bunlarla mücadele etmeye yönelmiş ve toplumu bütün yönleriyle saran şirk anlayışını bertaraf etmeye çalışmıştır. Kur’ân, müşriklerin toplumsal yapılarını, temayüllerini ve ruh hallerini göz önünde bulundurarak, şirki ve şirk tanrılarını iptal için muhataplarıyla muhtelif usûllerle mücadele etmiştir. Bu cümleden olarak, Arapların öteden beri alışageldikleri üslubu da muhafaza etmiş, bildikleri bir üslupla onlarla mücadele etmeye ihtimam göstermişir. Sıklıkla kullandıkları ifadeleri Kur’ân da en mükemmel biçimde kullanmış ve bu yolla da onları ikna etmeyi hedeflemiştir. Örneğin, Araplar kasemi sıklıkla kullanmışlardır. Baktığımızda kasem Kur’ân’da da çok gelmiştir. Aynı şekilde te’kid, istifham, teşbih ve tekrar gibi kullanımlar sıklıkla gelmiştir. Gayemiz bu tür kullanımların şirk tanrılarının iptalinde ifade ettikleri mana ya da manaları ortaya çıkarmak ve çıkan bu manaların şirk tanrılarının iptalinde oynadığı rolü dikkatlere sunmaktır.

KUR’ÂN’DA ŞİRKİN İPTALİNDE VÂRİT OLAN İFADELERİN DİLSEL ÖZELLİKLERİ.pdf


Solar-vortex power plants: Principles of effective work and technical requirements on the preparation of initial data for design

This article discusses the conceptual problems of the energy conversion process from radiant radiation into the energy of flows and electric energy in solar convective-vortex power plants. Moreover, this research includes the analysis of the factors that can contribute to the achievement of the optimal conditions for the control of the thermal energy concentration processes of solar radiation into the energy of tornado-like flows. Also, this article will discuss the results of the development of appropriate technical requirements for the design and construction of the building foundations and structures of solar-vortex power systems.

Shilova, Liubov

Moscow State University of Civil Engineering (National Research University)

Seminar 2018, Web of Conferences "Theoretical Foundation of Civil Engineering"


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Amid the dust storms and economic depression of Dustbowl Era Oklahoma, Eugene Evans finds his family farm on the brink of foreclosure. His last bet to save the farm is the bounty on the head of fugitive bank robber Allison Wells.


Tiphia (Tiphia) nathani Allen 1975

  27. Tiphia (Tiphia) nathani Allen, 1975

(Figs 362–384)

 Tiphia (Tiphia) nathani Allen, 1975: 52–54. Holotype, ♂. Kadamparai, Anamalai Hills, Tamil Nadu (RNHM).

 Material examined: 2♀, INDIA: Andaman & Nicobar Islands, South Andaman district, Port Blair, Attam Pahar (11°38′00″N & 92°41′49″E, 27 m), 7.vii.2021, Coll. A.K. Dubey, (ZSIK) Regd. Nos. ZSI / WGRC /IR/INV.18385 & 18386. 2♀, Karnataka, Shimoga district, Mookambika Wildlife Sanctuary, Hulikal FRH (13°43′45″N & 75°01′08″E, 579 m), 7.ix.2021, Coll. V. D. Hegde & Party, (ZSIK) Regd. Nos. ZSI / WGRC /IR/INV.18853 & 18854. 2♂, Kerala, Idukki district, Chinnar (10°18′22″N & 77°12′24″E, 596 m), 28.xi.2018, Coll. M. Jafer Palot & Party, (ZSIK) Regd. Nos. ZSI / WGRC /IR/INV.16925 & 16926; 1♂, Wayanad district, Kuruva Island, Palkulam (1149′02″N & 7605′36″E, 714 m), 22.iii.2021, Coll. K.A. Subramanian & Party, (ZSIK) Regd. No. ZSI / WGRC / IR/INV.18565. 3♀, Maharashtra, Thane district, Mumbai (19°06′15″N & 72°53′40″E, 34 m), 14.viii.2017, Coll. A. Ramesh Kumar, (ZSIK) Regd. Nos. ZSI / WGRC /IR/INV.18156–18158. 1♂, Tamil Nadu, Coimbatore district, Sadivayal, Siruvani (10°56′22″N & 76°44′52″E, 458 m), 5.i.2019, Coll. P. Girish Kumar, (ZSIK) Regd. No. ZSI / WGRC /IR/INV.18564. 2♀, Uttarakhand, Dehradun district, WII Campus (30°16′55″N & 77°58′24″E, 605 m), 12.viii.2017, Coll. P. Girish Kumar, (ZSIK) Regd. Nos. ZSI / WGRC /IR/INV.18154 & 18155; 1♀, Dehradun district, WII Campus (30°16′55″N & 77°58′24″E, 605 m), 8.x.2017, Coll. K. Ramesh Kumar, (ZSIK) Regd. No. ZSI / WGRC /IR/INV.18217; 1♀, Dehradun district, Doon Nursery, near Ballupur (30°20′02″N & 78°00′18″E, 673 m), 10.viii.1991, Coll. S.K. Gupta, (ZSIK) Regd. No. ZSI / WGRC /IR/INV.18159.

 Diagnosis. Male. Body length 6.9–9.1 mm. Clypeus fully punctured with median extension bidentate (Fig. 364); dorsal pronotal carina buttressed with distinct ridges (Fig. 366); lateral side of pronotum with groove not complete across disk (Fig. 367); upper half of lateral side of propodeum with widely spaced rugulae (Fig. 367); metanotum coarsely punctate (Fig. 366); fore wing densely infumated with marginal cell moderately longer than second cubital cell in apical extension (Fig. 369); Gt 1 without transverse carina (Fig. 370); Gs 5 with lateral denticle; Gs 6 with short, sparse setae.

 Genitalia. Paramere spatula-shaped and covered with long hairs; cuspis not clearly visible; digitus basally with beak like projection; aedeagus folded completely (Figs 372–374).

 Female. Body length 10.3–14.1 mm. Clypeus with basal half punctured, apical half smooth and median extension rounded (Fig. 377); lateral side of pronotum with distinct groove (Fig. 380); metanotum densely set with large punctures (Fig. 379); dorsal side of propodeum with elongate areola, lateral carina convex towards base (Fig. 379); posterior side of propodeum without median carina (Fig. 379); fore wing darkly infumated (Fig. 382); marginal cell of fore wing without terminal spur (Fig. 382); femora of mid and hind legs bright red to orange (Fig. 378); hind basitarsus without groove; Gt 1 without anterior transverse carina (Fig. 383).

 Distribution. India: Andaman & Nicobar Islands (new record), Karnataka, Kerala (new record), Maharashtra (new record), Tamil Nadu, Uttarakhand (new record). Elsewhere: Thailand.

Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Hymenoptera
Tiphiidae
Tiphia
Tiphia nathani

Published as part of Hanima, Raveendran K. P., Kumar, Girish & Hegde, Vishwanath D., 2022, Additions to the knowledge on the genus Tiphia Fabricius (Hymenoptera: Tiphiidae: Tiphiinae) from India with the description of ten new species, pp. 1-106 in Zootaxa 5204 (1) on page 71, DOI: 10.11646/zootaxa.5204.1.1, http://zenodo.org/record/7285194

Allen, H. W. (1975) The genus Tiphia of the Indian Subcontinent. Bulletin of United States Department of Agriculture, 1509, 1 - 96, 6 pls.


XXIV. Note on a paper on electromagnetic waves


Hide-and-seek with hoverflies: Merodon aureus – a species, a complex or a subgroup?

In order to disentangle the currently confused interpretations and nomenclature of Merodon aureus and M. aeneus, we have reviewed all existing type material and species names known to us as assigned synonyms of these taxa. We resolve M. aeneus as being a junior synonym of M. aureus. We designate a lectotype for M. aureus and a neotype for M. aeneus. Additionally, we provide evidence that M. aureus, together with two newly discovered taxa (M. calidus sp. nov. and M. ortus sp. nov.), represent a complex of cryptic species named the M. aureus species complex. This complex, together with the M. unicolor species complex and the species M. pumilus, is part of the M. aureus subgroup. The M. unicolor species complex comprises two cryptic species: M. unicolor and M. albidus sp. nov. The new species are described by applying an integrative taxonomic approach using several data types (COI and 28S rRNA genes, geometric morphometry of the wings, ecological and distributional data). Based on the COI gene sequence analysis and distributional data, the pupa previously described as an immature stage of the species M. aureus is redefined as an immature stage of the new species M. calidus. Speciation within the M. aureus subgroup is discussed in the context of the phylogeographic history in the studied region.

Vujić Ante

University of Novi Sad, Faculty of Sciences, Trg Dositeja Obradovića 3, 21000 Novi Sad, Serbia

Šašić Zorić Ljiljana

University of Novi Sad, BioSense Institute, Dr Zorana Đinđića 1, 21000 Novi Sad, Serbia

Khaghaninia Samad

University of Tabriz, Faculty of Agriculture, Department of Plant Protection, Tabriz, Iran

cryptic taxa, distribution, DNA sequences, environmental niche modelling, geometric morphometry, identification key, new species, Palaearctic

The study was supported by the Ministry of Education, Science and Technological Development, Republic of Serbia, Grant No. 173002, III43002, 451-03-68/2020-14/200358 and 451-03-68/2020-14/200125, and the European Commission, Horizon 2020 project 'ANTARES' (Grant No. 739570). We also thank TÜBİTAK (The Scientific and Technological Research Council of Turkey) for financial support for the project 213O243 within the scope of which some type specimens were collected from Turkey.

Zoological Journal of the Linnean Society


Complexes of Cobalt(III) with Violuric and Thiovioluric  Acids. Synthesis and Characterisation

Department of Chemistry, M.D. University, Rohtak-124 001 (India)

Department of Chemistry, Delhi University, Delhi-110 007 (India)

Manuscript received 24 May 1978, accepted 20 October 1978

Complexes of the type Co(H3L).5H2O, where L =violuric acid (VA) or thiovioluric acid (TVA) have been synthesised and characterised. Their deprotonation equilibria in aqueous solution has been studied and it has been observed that they behave as triprotic acid giving the complex anions [Co(H2L)2(HL)]-9 [Co(H2L)(HL)2]2- and (Co(HL)3]2- ,which have been isolated by selective precipitation and characterised.

Cobalt(lll) Violuric Thiovioluric Synthesis

Journal of Indian Chemical Society


Fig. 5 in Rare Snakes-Five New Species from Eastern Panama: Reviews of Northern Atractus and Southern Geophis (Colubridae: Dipsadinae)

Fig. 5. Hemipenis of Atractus clarki (MCZ 133013). Uneverted left organ opened midventrally, ×10.

Published as part of MYERS, CHARLES W., 2003, Rare Snakes-Five New Species from Eastern Panama: Reviews of Northern Atractus and Southern Geophis (Colubridae: Dipsadinae), pp. 1-48 in American Museum Novitates 3391 on page 15, DOI: 10.1206/0003-0082(2003)391<0001:RSFNSF>2.0.CO;2, http://zenodo.org/record/5372761

American Museum Novitates


Botrychium lunaria (L.) Swartz (BR0000011035480)

Biodiversity Taxonomy Terrestrial Herbarium Ophioglossaceae


Beiträge zur Kiefer- und Gaumenplastik


Figure 2 from: Constantinescu IC, Chişamera G, Mukhim DKB, Adam C (2016) A new species of the genus Timalinyssus Mironov, 2001 (Acarina, Psoroptidia) with a key to known species. ZooKeys 557: 45-57. https://doi.org/10.3897/zookeys.557.7098

Figure 2 -

            Timalinyssus wahlangi
           sp. n., male holotype: ventral view of idiosoma.

Constantinescu, Ioana Cristina

"Grigore Antipa" National Museum of Natural History, Bucharest, Romania

Pteronyssidae
Timalinyssus wahlangi
new species
systematics


The rate of dialysis of diabetic blood-sugar


ЧИЧИБАБИНСКИЙ ИНТЕРТЕКСТ В ПОЭЗИИ ЗИНОВИЯ ВАЛЬШОНКА

Стаття присвячена дослідженню впливу лірики Бориса Олексійовича Чичибабіна на творчість Зиновія Михайловича Вальшонка – ліричного поета, пародиста, мемуариста, життя та творчість якого пов’язані з Харковом. Проблема творчого діалогу двох знаних харків’ян, інтерекстуального переклику їхніх творів ніколи ще не ставала предметом самостійного літературознавчого аналізу. Метою статті є дослідження чичибабінського інтертексту у поетичній творчості Вальшонка, характеристика окремих форм його присутності та основних функцій. Об’єктом аналізу стала книга Вальшонка «Мой друг Борис Чичибабин. Поэты и безвременье», до якої увійшли твори різних жанрів – вірші, поеми, мемуари.

У статті аналізуються особливості використання Вальшонком цитат з творів Чичибабіна, зокрема у функції епіграфа, пародії на чичибабінські вірші, які, з точки зору авторів статті, не мають на меті висміювання оригіналу, а є дружніми творами гумористичного характеру, які імітують його словник, стиль, тональність і т. п. Автори доходять висновку, що чичибабінський «дух» и чичибабінське слово пронизують всю структуру книги Вальшонка, змістоутворюючим центром якої стала особистість його старшого друга та вчителя – харківського поета Бориса Олексійовича Чичибабіна.

А. Г. Козлова

кандидат филологических наук, доцент Харьковского национального педагогического университета имени Г. С. Сковороды

Е. Д. Козлов

кандидат филологических наук, доцент Национального технического университета «Харковский политехнический институт»

творчість вплив лірика вірш поема інтертекстуальність цитата епіграф пародія

Русская филология: Вестник Харьковского национального педагогического университета имени Г.С. Сковороды


Figures 64-68 from: Espeland M, Sjöberg T, Johanson KA (2020) Description of 47 new species of the New Caledonian endemic caddisfly genus Agmina Ward & Schefter (Trichoptera, Ecnomidae). ZooKeys 956: 49-162. https://doi.org/10.3897/zookeys.956.51592

Figures 64-68 Agmina campanula sp. nov. male holotype 64 genitalia, left lateral view 65 genitalia, dorsal view 66 genitalia, ventral view 67 phallus, lateral view 68 phallus, ventral view.

Espeland, Marianne

Zoological Research Museum Alexander Koenig, Bonn, Germany

Sjöberg, Tin

Swedish Museum of Natural History, Stockholm, Sweden

Circumscriptional names of the taxon under

caddisflies diversity New Caledonia new species rivers streams


Agabus bipustulatus Linnaeus 1767

Agabus bipustulatus (Linnaeus, 1767)
 Material. OnE AdUlT SpEcImEn And TWO lArVAE. COllEcTEd On 13/VII/2011. "CAldEIrãO" - COrVO ISlAnd. UTM: 25 S 662065 4397306.

 Habitat. ThIS SpEcIES IS A cOmmOn SpEcIES InhAbITIng A lArgE VArIETY Of AQUATIc hAbITATS InclUdIng SmAll rIVErS, pOndS, lAkES And EnVIrOnmEnTS WITh pEbblY dEpThS, SIlT And mArgInAl VEgETATIOn. ThIS TAxOn AlSO InhAbITS TEmpOrArY pOndS And hUmAn-mAdE rESErVOIrS (FrIdAY 1988; DOnISThOrpE 1913; PIcAzO et al. 2010; DrOTz et al. 2012).

 Azorean habitat. ThIS SpEcIES hAS bEEn fOUnd In pErmAnEnT And TEmpOrArY pOndS, frEQUEnTlY lOcATEd In mEdIUm-hIgh AlTITUdES (bETWEEn 500 TO 912 m. A.S.l.), AlThOUgh IT hAS AlSO bEEn ObSErVEd In lOW AlTITUdES (390 m. A.S.l. "CAldEIrãO - COrVO) And In cATTlE TAnkS. A. bipustulatus USUAllY OccUrS In AcIdIc WATErS (pH VAlUES rAngIng frOm 4.4 TO 7.1) And OxYgEnATEd WATErS (dISSOlVEd OxYgEn cOncEnTrATIOn VAlUES rAngIng frOm 6.7 TO 8.1 mg L–1).

 World distribution. Agabus bipustulatus hAS A PAlEArcTIc dISTrIbUTIOn. WIdESprEAd And ExTEndEd In EUrOpE, NOrTh AfrIcA And SOmE rEgIOnS Of AfrIcA (SErrAnO & BOrgES 1987; DrOTz et al. 2003; DrOTz et al. 2012).

 Azorean distribution. AzOrES IS ThE WESTErnmOST ArEA In ThE dISTrIbUTIOnAl rAngE Of ThIS SpEcIES. IT IS prESEnT In FlOrES, PIcO, SãO JOrgE And TErcEIrA ISlAndS. OUr nEW rEcOrd cOnfIrmS ThE prESEncE In COrVO ISlAnd (SEE FIg. 1).

Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Coleoptera
Dytiscidae
Agabus
Agabus bipustulatus

Published as part of Lamelas-López, Lucas, Raposeiro, Pedro Miguel, Borges, Paulo A. V. & Florencio, Margarita, 2017, Annotated checklist of aquatic beetles (Coleoptera) and true bugs (Heteroptera) in the Azores Islands: new records and corrections of colonization status, pp. 117-132 in Zootaxa 4353 (1) on page 123, DOI: 10.11646/zootaxa.4353.1.7, http://zenodo.org/record/1064562


Revisions of the genera Lurama Schaus, 1928 and Ulmara Schaus, 1928 (Lepidoptera, Mimallonoidea, Mimallonidae) with the descriptions of three new Ulmara species and a new genus

The Andean genera Lurama Schaus, 1928 and Ulmara Schaus, 1928 are revised. Lurama poses difficulty for revision due to lost male genitalia of the types of both described species. Ulmara conjuncta sp. n., U. azurula sp. n., and U. dombroskiei sp. n. are described as new in the genus Ulmara. A lectotype is designated for Lurama quindiuna Schaus, 1928 and Ulmara rotunda (Dognin, 1916). A new monotypic genus, Cunicumara gen. n., which is externally similar to Ulmara, is described to include the new species Cunicumara anae sp. n. from low elevations of Bolivia and Paraguay. Male genital morphology does not support a close association of Cunicumara with Lurama or Ulmara. The latter two genera, however, are closely related based on similarities of male genitalia and biogeography.

Andean
Bolivia
Colombia
Cunicumara anae
Ecuador
Peru
Ulmara azurula
Ulmara dombroskiei
Ulmara conjuncta

ZooKeys


Fig. 19 in A New Protocetid Whale (Cetacea: Archaeoceti) from the Late Middle Eocene of South Carolina

Fig. 19. Anterior views of sixth (A) and seventh (B) cervical vertebrae of Carolinacetus gingerichi

Biodiversity Taxonomy Animalia Chordata Mammalia Cetacea Protocetidae Carolinacetus

Published as part of GEISLER, JONATHAN H., SANDERS, ALBERT E. & LUO, ZHE-XI, 2005, A New Protocetid Whale (Cetacea: Archaeoceti) from the Late Middle Eocene of South Carolina, pp. 1-66 in American Museum Novitates 3480 (1) on page 34, DOI: 10.1206/0003-0082(2005)480[0001:ANPWCA]2.0.CO;2, http://zenodo.org/record/5383082

American Museum Novitates


Figs 65-71 in On the Cephennium fauna of the Iberian Peninsula and the Atlantic Islands (Coleoptera, Staphylinidae, Scydmaeninae)

Figs 65-71: Cephennium cujonicum (65), C. verrens (66), C. segurae (67-69), and C. malagae (70- 71): (65-71) aedeagus in lateral and in ventral view. Scale bars: 65-71: 0.1 mm.

Biodiversity Taxonomy Animalia Arthropoda Insecta Coleoptera Staphylinidae Cephennium

Published as part of Assing, Volker, 2021, On the Cephennium fauna of the Iberian Peninsula and the Atlantic Islands (Coleoptera, Staphylinidae, Scydmaeninae), pp. 891-931 in Linzer biologische Beiträge 52 (2) on page 913, DOI: 10.5281/zenodo.5039032

Linzer biologische Beiträge


Abbottella (Abbottella) abbotti Bartsch 1946

Abbottella (Abbottella) abbotti Bartsch, 1946
Figures 3 A–E, 7 F

 Type material. USNM 504108, holotype.

 Type locality. Near Laguna, Samaná Bay [sic, probable error for Samaná Peninsula, see below], Dominican Republic.

 Other material examined. UF 215981, El Valle, Samaná Province, Dominican Republic; UF 215983, 2 km S of El Valle, Samaná Province, Dominican Republic, at 20 m; UF 215980, 2 km S of El Valle, Samaná Province, Dominican Republic; UF 215982, hills E and W of El Valle, Samaná Province, Dominican Republic; GTW 10829 a, Cayo Levantado, Samaná Province, Dominican Republic.

 Distribution and habitat. This species occurs in the Sierra de Samaná of the Cordillera Septentrional. Bartsch (1946) did not give any additional information on the type locality in his description of this species. However, under his description of Lagopoma lagopoma, he stated that Laguna was 4 miles north of Samaná. This is probably Punta Laguna Salada, which is adjacent to El Valle, the source of most of our material. Contrary to Bartsch’s description, Laguna is not on Samaná Bay but on the north coast of the peninsula; this was probably an error for Samaná Peninsula. All of our records are for the El Valle and the Las Galeras areas on the northeast coast of the peninsula. This species is probably distributed around the base of the outcrop between these two areas, a distance of ca. 20 km. Snails occur on and at the base of the steep limestone walls in cool, shaded areas with abundant vegetation and mosses.

 Comparison with other species. Abbottella abbotti is one of a group of small species on the Samaná Peninsula characterized by thorny sculpture. It differs from similar species in its deeply fimbriated outer lip and coarse sculpture arranged in prominent keels.

Biodiversity
Taxonomy
Animalia
Mollusca
Gastropoda
Neotaenioglossa
Pomatiidae
Abbottella
Abbottella abbotti

Published as part of Watters, G. Thomas, 2013, New taxa and distributional notes on Abbottella and related taxa (Gastropoda: Littorinoidea: Annulariidae), pp. 1-22 in Zootaxa 3646 (1) on page 11, DOI: 10.11646/zootaxa.3646.1.1, http://zenodo.org/record/283728


Anemone nemorosa L. (BR0000011139966)

Belgium Herbarium image of Meise Botanic Garden.

Biodiversity Taxonomy Terrestrial Herbarium Ranunculaceae


Nazeris yanyingae Hu, Li & Zhao 2011

Nazeris yanyingae Hu, Li & Zhao, 2011
 Nazeris yanyingae Hu, Li & Zhao, 2011: 5.

 Additional material examined. China, Zhejiang, Lishui City, Qingyuan Hsien, Baishanzu: 1 male, 27°45′14′′N, 119°11′55′′E, mixed forest, leaf litter, sifted, 1.V.2014, 1560– 1750 m, Peng et al. leg. (SNUC); 3 males, Station to peak, 27°45′20′′N, 119°11′78′′E, leaf litter, wood, sifted & beating, 1721 m, 22.V.2015, Song & Yan leg. (SNUC); China, Zhejiang, Lishui City, Fengyangshan: 6 males, 7 females, Huangmaojian, 27°53′23′′N, 119°10′32′′E, mixed leaf litter, sifted, 1580 m, 1.V.2016, Jiang, Liu & Zhou leg. (SNUC).

 Comparative notes. Nazeris yanyingae is similar to N. furcatus Hu, Li & Zhao, 2011 in appearance and aedeagal characters, but can be distinguished by all the abdominal segments with fine microsculpture; and by dorso-lateral apophyses lacking projection at middle.

 Distribution and habitat data. Specimens were found in two localities in south Zhejiang. The specimens were collected by sifting leaf litter at altitudes of 1500–1750 m.

Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Coleoptera
Staphylinidae
Nazeris
Nazeris yanyingae

Published as part of Hu, Jia-Yao, Tu, Yue-Ye & Li, Li-Zhen, 2016, On the Nazeris fauna of Zhejiang, China (Coleoptera, Staphylinidae, Paederinae), pp. 361-373 in Zootaxa 4169 (2) on page 368, DOI: 10.11646/zootaxa.4169.2.5, http://zenodo.org/record/266665

Hu, J. Y., Li, L. Z. & Zhao, M. J. (2011) Twelve new species of the genus Nazeris Fauvel from Zhejiang Province, China (Coleoptera, Staphylinidae, Paederinae). Zootaxa, 2797, 1 - 20.


Aerosol 3-DVAR source code and Lidar data

The code of this system can be obtained on request from the corresponding author


FIGURE 1. Berothidae indet., larva A in First fossil larvae of Berothidae (Neuroptera) from Baltic amber, with notes on the biology and termitophily of the family

FIGURE 1. Berothidae indet., larva A, whole larva as preserved. A, photograph. B, drawing (both dorsal view). Scale bar is 0.5 mm.

Biodiversity Taxonomy Animalia Arthropoda Insecta Neuroptera Berothidae

Published as part of Wedmann, Sonja, Makarkin, Vladimir N., Weiterschan, Thomas & Hörnschemeyer, Thomas, 2013, First fossil larvae of Berothidae (Neuroptera) from Baltic amber, with notes on the biology and termitophily of the family, pp. 236-258 in Zootaxa 3716 (2) on page 238, DOI: 10.11646/zootaxa.3716.2.6, http://zenodo.org/record/248083

Zootaxa


Melaloncha pilidorsata Brown 2006, new species

Melaloncha pilidorsata new species
Fig. 11

 Recognition. This yellowish species can be recognized by the shortened foretarsal segments and the dense dorsal setae of the ovipositor. The common and widespread species M. maculata is similar in general appearance, but has tarsal claws of the apical foretarsomere with a basal lobe, narrower foretarsomeres, and the ovipositor dorsally curved (straight in M. pilidorsata).

 Description. Female (male unknown) Body length 1.5–1.8 mm. Frons yellow, bare of setulae except few along eye margin; each ocellus surrounded by black. Mean frontal width 0.46 head width, range 0.45–0.47. Medial furrow absent. Ocular and genal setae light brown. Flagellomere 1, aristomeres 1, 2 and base of 3 yellow; rest of 3 brown. Palpus white; palpal setulae brown. Scutum yellowishbrown with posterolateral dark brown spot. Scutellum yellowishbrown with anterolateral round black spot. Pleuron yellowishbrown, except basalare dark brown. Legs yellowishbrown. Combined length of foretarsomeres 0.8 length of foretibia; foretarsomeres short, flat. Foretarsal claws unmodified, without basal lobe. Mean costal length 0.49 wing length, range 0.45–0.51. Halter yellow. Abdominal tergites yellow anteriorly, black posteriorly. Venter of abdomen yellow. Ovipositor yellow basally, mostly black; relatively straight, tubular, but flattened dorsally; with dense mediumlength setae dorsally.

 Host. Unknown.

 Geographical distribution. Peru and Bolivia.

 Derivation of specific epithet. Latin pilus for hair and dorsum for back, referring to the dorsally setose ovipositor.

 Holotype. ♀, PERU: Madre de Dios: Tambopata Research Center, 13.14°S, 69.61°W, 22.vii.2001, B. Brown, G. Kung, honeysprayed leaves [LACM ENT 075455] (MUSM).

 Paratypes. BOLIVIA: La Paz: Alto Rio Beni, south of Rio Inicua, 1100 m, 2♀, 15–18.i.1976, L. E. Peña (AMNH). PERU: Madre de Dios: Tambopata Research Center, 13.14°S, 69.61°W, 1♀, 24.vii.2001, B. Brown, G. Kung, honeysprayed leaves (LACM).

Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Diptera
Phoridae
Melaloncha
Melaloncha pilidorsata

Published as part of Brown, Brian V., 2006, Revision of the untreated taxa of Melaloncha s. s. bee-killing flies (Diptera: Phoridae), pp. 1-68 in Zootaxa 1280 (1) on page 25, DOI: 10.11646/zootaxa.1280.1.1, http://zenodo.org/record/5070710


Cocaine.


FIGURE 8 in The synopsis of the genus Tulipa (Liliaceae) in Uzbekistan

FIGURE 8. Species of Tulipa sect. Vinistriatae: A. T. greigii, B. T. vvedenskyi, C. T. butkovii. Scale bars, 1 cm.

Tojibaev, Komiljon

Flora of Uzbekistan laboratory, Institute of Botany of the Academy of Sciences of the Republic of Uzbekistan, 32 Durmon Yuli Str., Tashkent, 100125, Uzbekistan. & ktojibaev@mail.ru; https://orcid.org/0000-0003-2846-5777

Dekhkonov, Davron

Laboratory of Molecular Phylogeny and Biogeography, Institute of Botany of the Academy of Sciences of the Republic of Uzbekistan,32 Durmon Yuli Str., Tashkent, 100125, Uzbekistan. & Namangan state University, Boburshox str., 161, 60107161, Namangan, Uzbekistan. & davron-b@bk.ru; https://orcid.org/0000-0002-2762-5268

Ergashov, Ibrokhimjon

Laboratory of Molecular Phylogeny and Biogeography, Institute of Botany of the Academy of Sciences of the Republic of Uzbekistan,32 Durmon Yuli Str., Tashkent, 100125, Uzbekistan. & Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China. & University of Chinese Academy of Sciences, Beijing, China. & ibrohim8905@mail.ru; https://orcid.org/0000-0002-0991-1076

Sun, Hang

Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China. & hsun@mail.kib.ac.cn; https://orcid.org/0000-0001-5127-4579

Deng, Tao

Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China. & dengtao@mail.kib.ac.cn; https://orcid.org/0000-0003-4163-3368

Yusupov, Ziyoviddin

Laboratory of Molecular Phylogeny and Biogeography, Institute of Botany of the Academy of Sciences of the Republic of Uzbekistan,32 Durmon Yuli Str., Tashkent, 100125, Uzbekistan. & Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China. & Yunnan International Joint Laboratory for Biodiversity of Central Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China. & yusupov@mail.kib.ac.cn; https://orcid.org/0000-0003-2278-542X

Biodiversity Taxonomy Plantae Tracheophyta Liliopsida Liliales Liliaceae Tulipa

Published as part of Tojibaev, Komiljon, Dekhkonov, Davron, Ergashov, Ibrokhimjon, Sun, Hang, Deng, Tao & Yusupov, Ziyoviddin, 2022, The synopsis of the genus Tulipa (Liliaceae) in Uzbekistan, pp. 163-214 in Phytotaxa 573 (2) on page 187, DOI: 10.11646/phytotaxa.573.2.2, http://zenodo.org/record/7349887

Phytotaxa


Download Zip : Mp3 Empire Cast - Empire (Original Soundtrack from Season  @Full Album Download

Empire Cast - Empire (Original Soundtrack from Season 1) [Deluxe] mp3 Torrent rar Zippyshare m4a Album

DOWNLOAD ALBUM HERE: http://tinybit.cc/65b3b306

Empire (Original Soundtrack from Season 1) [Deluxe] is the new album by Empire Cast. This album has been released on 2015-11-20 and contains 18 tracks. Newest single from the album is Remember the Music (feat. Jennifer Hudson).

DOWNLOAD ALBUM HERE: http://tinybit.cc/65b3b306

Tracklist:
1. Good Enough (feat. Jussie Smollett)
2. What Is Love (feat. V. Bozeman)
3. No Apologies (feat. Jussie Smollett, Yazz)
4. Keep It Movin' (feat. Serayah McNeill and Yazz)
5. Keep Your Money (feat. Jussie Smollett)
6. Drip Drop (feat. Yazz and Serayah McNeill)
7. Can't Truss 'Em (feat. Yazz)
8. I Wanna Love You (feat. Jussie Smollett)
9. Money for Nothing (feat. Jussie Smollett and Yazz)
10. Walk Out on Me (feat. Courtney Love)
11. You're So Beautiful (feat. Jussie Smollett and Yazz)
12. Conqueror (feat. Estelle and Jussie Smollett)
13. Remember the Music (feat. Jennifer Hudson)
14. Shake Down (feat. Mary J. Blige and Terrence Howard)
15. Power of the Empire (feat. Yazz)
16. Nothing to Lose (feat. Jussie Smollett)
17. Whatever Makes You Happy (feat. Jennifer Hudson and Juicy J)
18. New York Raining (feat. Charles Hamilton and Rita Ora)

#zippymp3now


Data files for IEEE MMSP 2021 paper

Data files for the paper Hui Yuan, Raouf Hamzaoui, Ferrante Neri, Shengxiang Yang, Tingting Wang, Global rate-distortion optimization of video-based point cloud compression with differential evolution, in: Proc. 23rd International Workshop on Multimedia Signal Processing (IEEE MMSP 2021), Tampere, Oct. 2021.

Point cloud compression
Rate-distortion optimization
Rate control
Video coding
Differential evolution

These files are part of the OPT-PCC project, which has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 836192


Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid - Black magic – the powerful tool of astrology is being used since ancient times to solve self-purpose. It is nothing other than the worship of evil spirits and negative energies. In this country, black magic is being practiced for a long time by tantriks and sadhus but now astrologers are also using this art for the betterment of human life. Many of us don't believe in this trick and will discourage you about it but if you meet any real black magic specialist, you will see how it works and how fast you can achieve success. If you are failed to get what you want by the help of all other tricks, then you can try it ones. It has the ultimate power to deal with supernatural powers by which you can do anything. Previously, people use this trick to harm others but in recent days, astrologers don't use it for negative purposes. A specialist knows very well how to perform black magic to remove issues from human life. It can be love related, career-related, marriage related, or financial issues; black magic has a solution for everything. You just have to keep faith in it.

" Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid "

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115Molana Jabid - As black magic can be applied to someone by an expert, it also can be removed by those experts. We are living in a fast world where you can't avoid problems and troubles in our life. It can come in many ways, like financial, legal, and emotional and if not handled with care, it can be dangerous and we may have life risk. Many of us don't believe in astrology or black magic but it is proved since ages that black magic has the power to bring success in your life. If you go through any old book about black magic, you will be amazed to know its effects in life. Our life is surrounded by love, career, education, marriage, etc and sometimes we face issues in getting what we want. We all have friends as well as enemies. If any enemy applied black magic on you to harm you or to achieve his or her self purpose and you are being affected for that, then you must need to remove black magic from your life. If you hire an expert astrologer, you will definitely get rid of this.

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115Molana Jabid - If you are unable to solve problems from your life alone, then you must need a promising person who can give you support to recover from a bad situation. A famous black magic specialist can help you to trace the root of your problems and will guide you accordingly to heal those negative vibes. Black magic contains the powerful mantra and totkas by which you can take control of other's mind or you can force them to act according to your demand. Some people think that black magic only creates negativity in the environment but this is not true.

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115Molana Jabid - Although it contains negative powers and people use it to create damages but it also can be used to solve many issues in life. Black magic can solve your love related issues easily. Suppose you are in love with someone for a long time but suddenly feel that your partner is cheating on you, and then it is a hard situation to tackle. At that point, you may think to break up for ego but by heart, you want your partner in life, then black magic is the only way to bring back your lost love in life forever.

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115Molana Jabid - Black magic is now widely used in this country by the expert astrologers to solve difficult problems in human life. Black magic is a useful trick to solve family clash, career-related problems, legal issues, and marriage-related issues and many more. Suppose, you are running a business and making the profit but suddenly you started facing troubles in that business and instead of making the profit, you are having a loss then that is really a mess for you.

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Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid - So, this wazifa for controlling husband is verified remedy that's still getting used by many sisters to cure their crazy husbands and to form them hear their wife. If you are feeling that you simply actually need something strong and which features a long impact on your husband in order that he can become obedient towards you then look no further, try the wazifa for controlling husband now only.

The wazifa to remove husband’s anger is mentioned below –

The wife should recite the wazifa after the obligatory prayer of the night.

Keep two almonds on your tongue.

Recite DuroodShareef 11 times.

And while reicitng it, keep the almonds on your tongue and think about your husband.

Recite the verse #39 from Surah Taha 41 times.

Then recite the dua to bring husband and wife closer. “Bismillah Hi AlwasaoJallahJalaloho”

Recite DuroodShareef 11 times in the end.

Take out the almonds from your mouth and blow on it.

Now mix it any of the sweet dishes cooked by you and give it to your husband.

Pray to Allah (Swt) to calm the anger level of your husband and lower his rudeness

Insha Allah, slowly your husband will stop getting angry on you.

Perform this wazifa and dua for anry person for 7 days.

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid -  Marriage may be a bicycle where the husband and wife are the front and back wheel. And, with anyone not performing their duties and responsibilities right, the cycle will never run and therefore the relationship will fail. Sometimes, your marriage begins to experience problems. Whether it's from any of the partners, the opposite has got to attempt to reserve it . If you would like to save lots of your marriage from breaking, then you ought to recite wazifa for marriage problem. once you perform the wazifa with right intentions and purity in your heart, your relationship will start flourishing and every one the sadness, fights and misunderstandings will go from your marriage.

You might be thinking that how few spiritual words and procedure can change the behaviour of an individual . Well it's true! Many sisters who faced trouble in adjusting with their husbands are now enjoying a cheerful life with their spouse and therefore the credit goes to the wazifa for controlling husband only.

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If you are feeling that your husband has too many female friends then you'll simply encourage him to interrupt his relations with the other women apart from you with the assistance of the wazifa to regulate your husband. If you would like that your husband should leave his family to start out a fresh and separate life with you and your kids, then you would like to practice the wazifa to regulate your husband for few weeks as guided by our Islamic Guru, and you'll have it too.

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid -  So, regardless of whatever thing is troubling you or in whatever subject you're unable to control your husband, every motive are often achieved easily, with the assistance of our wazifa to regulate your husband. Try it now and see its impact on your husband in only few days.

On the opposite hand, it's totally wrong to mention that men don't feel insecure in their marriage. A husband might feel that his wife is giving others more importance than him. The responsibilities she has towards the entire family might overpower the love she has for him. this example is additionally one among the most important reason behind the differences a marriage faces in their life. The remedy to mapped out this difference is that the dua for removing differences between a husband and wife.

The best thanks to skills to perform the dua to get rid of differences between husband and wife is by lecture an Islamic scholar. The couple should first attempt to mapped out their differences by lecture one another and clearing out their insecurities and fears. If the ego clash is making it hard to try to to so, then they ought to consult an Islamic scholar. He will help them with the simplest dua which will remove all the differences and distance between the husband and wife. Their marriage will once more become happy and healthy.

Before marriage, every man and woman dreams of getting the right relationship with their spouse. Most the couples are capable of making an understanding between one another . This understanding becomes the strongest foundation of their relationship. This successively becomes the rationale that these couples don't fight or argue unnecessarily.

On the opposite side, there are few couples unable to make a bond of understanding between one another . When two people during a marriage aren't compatible with one another , arguments are sure to happen. there's no way that these people will prioritize their spouse before themselves. this example are often stressful not just for the couple but also for his or her families. and therefore the best thanks to make it stop is that the dua to prevent arguments between husband and wife.

Dua to prevent arguments between husband and wife is additionally helpful for those people that want to vary their spouse’s aggressive behavior. There are people that get frustrated because their husband or wife always wants to argue. rather than understanding their partner’s thoughts, they prefer to fight and make a scene. This dua is that the best thanks to make the short tempered spouse, a relaxed person.

The dua to prevent arguments between marriage may be a life altering remedy. There are couples who prefer to break their marriage due to unnecessary fights and arguments. This dua is that the best thanks to stop that from happening. This dua will change the dynamics of the bond between the couple instantly.

All marriages require love, affection and a spotlight to achieve success . But many an times, it's been seen that emotions like anger, frustration, lack of trust and misunderstanding between husband and wife make the connection poor and weak. If the wife is sweet and submissive but the husband features a rash nature, then the wife literally suffers in it. In Islam, most of the husbands are dominant in nature. They get angry on their wives for no mistake of their own. If your husband gets angry irrationally, then you ought to recite the wazifa to get rid of husband’s anger. The wazifa will calm your husband from inside and he will stop getting angry on you for little things.

wazifa for brief tempered husband

Every wife only wants lover, care and affection of her husband and zip more. However, some husbands don't even care about the emotions of their wives. If your husband gets angry on petty little things and is extremely short tempered, then you ought to recite the wazifa for brief tempered husband. The wazifa for husband’s irascibility will control your husband from getting angry on small things. He will learn to be silent and patient. He will treat you well and never misbehave with you. The wazifa to get rid of husband’s anger is extremely effective and it'll affect both the mind and heart of your husband and eventually he will become a perfect husband for you.

Because of ill temper , a number of the marital relationships get pathetic with every passing day. The antagonism of husbands reaches a replacement level because nothing overpowers them. But the dua for bad tempered husband will assist you control the anger of your husband. you'll witness a change in their nature and behavior and he will transform into a totally new person. All you would like to try to to is recite the wazifa for brief tempered husband and you'll see how phenomenally Allah (Swt) eases your life.

If your husband isn't taking interest in you and with time you are feeling that his love for you has diminished, then you ought to perform wazifa for marriage problem. The wazifa will re-create the lost love and affection in your husband’s heart and make him love you wish he did on the primary day of the wedding . If your husband has been taking interest in another woman and he want to go away you due to it, but you don’t want it to happen, then recite wazifa for marriage problem. Insha Allah, very soon Allah SubhanaWa’ Talah will make things okay between you and your husband which woman will haven't any role in your husband’s life.

If you are feeling that off lately there are tons of fights between you and your spouse and you think that that if these fights continue, then you both will part, then you ought to practice wazifa for problems in marriage. Allah Talah has blessed every man and woman on this earth with infinite dua and wazifa to cure their relationship. once you perform wazifa for problems in marriage, then you'll see that gently all the misunderstandings and problems will wipe out from your marriage and your relationship will rejuvenate and flourish.

You can acquire the wazifa for problems in marriage from our experienced Molvi Ji. With years of knowledge and experience, he has gained skills to resolve marital issues with effective wazifas. All you need to do is explain him the complete situation and why your marriage is in danger and Insha Allah, with the will and grace of Allah Talah, he will guide you with the best wazifa for problems in marriage.

Wazifa for marriage problem is given below:

Perform this wazifa after the namaz of Fajr.

Recite Surah Muzammil once and then recite all the four Kul. Recite Ayat-ul-Kursi 11 times and blow it on a glass of water.

Now make your husband drink that water.

Make sure you include DuroodSharee 11 times in the beginning and end of the wazifa.

Insha Allah, very soon you will see a change in your marital relationship. Perform this wazifa without a gap for 11 days. Remember the water should not fall on the ground. If there is any left over water, then throw it in the garden.

Black magic specialist in Hyderabad Telangana Call/WhatsApp on  +919784694115 Molana Jabid

All problem solution expert Molana Jabid Call/WhatsApp on +919784694115 to get quick solutions.

Black magic specialist in Hyderabad Telangana +919784694115

Black magic specialist in Hyderabad Telangana +919784694115

Black magic specialist in  Hyderabad Telangana.jpg


An Investigation Into the Clinical Significance of Albumosuria and Its Value in Diagnosis and Prognosis.


FIGURE. Varieties of Dicorynia paraensis. A. Dicorynia paraensis var. paraensis; B. Dicorynia paraensis var. macrophylla; C. Dicorynia paraensis var. uaupensis; D. Dicorynia paraensis var. ingens. A: Spruce, R. 1918; B: Ducke, A. s.n. RB23321; C: Amaral, I.L. 574; D: Ducke, A. s.n. MG15707(S). Images by: A: Paris Virtual Herbarium; B-D: Reflora. Scale bar: 5cm. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)

Torke, Benjamin Marland

Institute of Systematic Botany, The New York Botanical Garden, 2900 Southern Blvd., Bronx, NY, 10458-5126, USA. & btorke@nybg.org; https://orcid.org/0000-0001-8823-3519

Mansano, Vidal De Freitas

Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, DIPEQ. Rua Pacheco Leão 915, Jardim Botânico, Rio de Janeiro, RJ, 22460-030, Brazil. & vidalmansano@gmail.com; https://orcid.org/0000-0002-7204-0744

Published as part of Falcão, Marcus José De Azevedo, Torke, Benjamin Marland & Mansano, Vidal De Freitas, 2022, A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae), pp. 1-31 in Phytotaxa 554 (1) on page 20, DOI: 10.11646/phytotaxa.554.1.1, http://zenodo.org/record/6809750

Phytotaxa


Ueber die Capacität von Condensatoren


Report of a Case of Multiple Abscss of the Brain, Operaytion, Rcovery.*:


Cash management bij multinationale ondernemingen in de eurozone

In dit artikel wordt de invloed van liberalisering, deregulering en de introductie van de euro op het cash management van multinationale ondernemingen besproken. Door ontwikkelingen in de eurozone nemen de financiële marktimperfecties af. Tevens vermindert de noodzaak voor afzonderlijke liquiditeitsposities per land. Dat maakt centralisatie van het cash management gemakkelijker en de financiële controle van het hoofdkantoor kan toenemen. Door het uitbuiten van deze mogelijkheden kunnen multinationale ondernemingen in de eurozone voordelen van interne financiering behalen. Dat biedt ook weer kansen voor disintermediatie. Conglomeraatkortingen op aandelen ('conglomerate discounts') kunnen daarmee verminderen.

Maandblad Voor Accountancy en Bedrijfseconomie


Crafted With Durable & Child-Pleasant Features - Extra Large Unicorn Stuffed Animal

Ideal USE FOR UNICORN PLUSH STUFFED ANIMAL - Unicorn teddy bear will make an awesome add to a kid’s plush collection while couples & adults can express their love by surprising their beloved ones with a plush animal. Unicorn toy will be your little one’s huggable plush doll BFF when taking part in, touring, studying & will function a bedtime cuddly companion.


The Galliambic Metee


XLIV.— Description of a new species of Mantidæ with pointed eyes


Estímulo para o engajamento de estudantes de graduação nas atividades das disciplinas através da gamificação

English title: Promoting the engagement of undergraduate students in the class activities through gamification.

This presentation discusses the use of gamification techniques to stimulate the participation of undergraduate students in the classes activities. In addition, the presentation shows the results of the application of gamification in the Operating Systems and Computer Architecture classes.

gamification
undergraduate students
engaging

Inovações em Atividades Curriculares


Myosotis sylvatica Ehrh. ex Hoffm. (BR0000010681381)

Biodiversity Taxonomy Terrestrial Herbarium Boraginaceae


Habrobathynella adishankara Elia, Shaik & Reddy, 2016, n. sp.

Habrobathynella adishankara n. sp.
(Figs. 7–12)

 Type locality. The River Periyar at Kalady village (1010'60''N, 7613'0''E, elevation 10 m), Kerala State, southwestern India. This is the longest river (228 km) and one of the few perennial rivers in Kerala. Originating in the Western Ghats, one of the three biodiversity hotspots in India, at an elevation of 2438 m above sea level, the river has a total catchment area of over 5284 km 2. The influence of tectonism is evident from the stream pattern and presence of structural valleys. The river basin is ecologically sensitive owing to widespread erosion and mass movements. The average rainfall in the basin varies from 444 cm to 508 cm in the mountains to about 304 cm in the coastal fringes (Water Resources of Kerala, 1958). At the sampling site, the riverbed has a deposit of fine sand and detritus particles, but with little or no clay, and with patches of macrophytic vegetation.

 Type material examined. Holotype Ƌ (ZSI-C5867/2/a–l), dissected on 12 slides; allotype ♀ (ZSI-C5868/2/a– l), dissected on 12 slides; 1 paratype ♀, mounted whole on 1 slide (ZSI-C5869/2); 1 paratype Ƌ (MNHN-IU-2013- 11983), dissected on 1 slide. 3 February 2005, Coll. Y. Ranga Reddy.

 Diagnosis. Uropodal sympod with inhomonomous row of 6 spines, penultimate spine largest and ultimate spine similar to proximal spines. Pleotelson seta shorter than caudal furca. Male Th VIII small, subglobular, with protopod expanded distally in latero-external view; dentate lobe wide and with truncate distal margin; outer lobe conical and short, barely reaching midlength of balloon-shaped basipod. Antennule with 3 long and equal aesthetascs on fifth segment. Antennary proximal segment nearly as long as distal segment. Paragnaths with thumb-like smooth coupler and short triangular lateral lobes. Labrum with somewhat vaulted dentate margin. Maxilla with 1 seta on first segment as well as on mid-inner margin of second segment. Anal operculum deeply concave medially.

 Description of adult male. Total body length of holotype 0.73 mm. Body elongate, 11 times longer than maximum width; cuticle thin and imperforate. In lateral view, pleomeres wider than thoracomeres (Fig. 7); in dorsal view, body vermiform and uniformly narrow. Head 1.2 times as long as wide and about as long as first 2 thoracomeres combined.

Antennule (Fig. 8 A): 6-segmented, measuring 41.3% longer than head, no sexual dimorphism. First segment with 3 plumose setae near outer margin, 1 plumose dorsal seta subdistally, and 1 small plumose seta on ventral surface subdistally. Second segment with 3 unequal plumose setae in a row on dorsal surface of subdistal outer margin, 1 ventral plumose seta and 1 dorsal simple seta at inner distal corner. Third segment with 1 plumose seta and 1 long simple seta at outer distal corner, 1 ventral simple seta near distal inner corner. Inner flagellum subquadrate, with 3 unequal setae. Fourth segment with apophysis, reaching about midlength of next segment and with 2 unequal plumose setae; 2 plumose setae on small protuberance on distal margin. Fifth segment with 3 equal aesthetascs, overreaching sixth segment, 3 unequal simple setae and 1 short modified seta at inner distal corner. Sixth segment with 3 relatively short equal aesthetascs and 4 slightly unequal setae.

Antenna (Fig. 8 B): small, 2-segmented; proximal segment bare and 0.8 times as long as distal one; distal segment 1.3 times as long as wide, with 1 apical plumose seta, 2 subapical unequal simple setae and 1 simple seta on outer proximal margin.

Labrum (Fig. 8 C): dentate margin somewhat vaulted on both sides, though not deeply, and bearing 12 main pointed teeth, and one smaller tooth on either side

Mandible (Fig. 8 D): distal part of pars incisiva with 4 unequal teeth, proximal tooth smallest; distal tooth large, curved and pointed. Tooth of ventral edge lying close to the base of pars molaris. Pars molaris developed into pyriform outgrowth, carrying 2 isolated teeth on inner margin and 3 straight pointed unequal teeth in a group at proximal end; all teeth articulate and multicusped (Fig. 8 E). Palp completely absent.

Paragnaths (Fig. 8 F): coupler thumb-like, moderately developed and without ornamentation; lateral lobes small, triangular, disto-laterally directed and without ornamentation.

Maxillule (Fig. 8 G): consisting of 2 endites; proximal endite small, elongately oval, carrying 3 long unequal claw-like serrulate spines, 2 apical and 1 subapical setae and 1 simple setiform element at inner distal corner. Distal endite cylindrical, 2.6 times as long as proximal endite and with 2 apical claws and 1 subapical claw and 2 unequal claws on inner distal margin; 3 simple setae on subapical outer margin.

Maxilla (Fig. 8 H): 3-segmented; basal segment 1.5 times as long as wide with 1 long simple seta at inner distal corner; second segment 1.3 times as long as basal segment and armed with 13 simple setae. Third segment small, somewhat squarish, carrying 1 stout claw.

Thoracopods (Th) I–VII (Figs. 9 A–D, 10A–C): well-developed, Th I–III gradually increasing in size and Th IV–VII nearly similar in size, well-developed; epipod on Th II–VII biarticulate, club-shaped, slightly longer than basis. Coxa of Th I–VII with distinct conical projection at distal inner corner and basis with 1 simple seta slightly overreaching midlength of first endopodal segment. Exopod 2-segmented, 1.4 times as long as endopod on Th I and about as long as endopod on Th II–VII; segment 1 only slightly longer than segment 2, with 2 unequal plumose setae; dorsal seta as long as second segment on Th I, but ventral seta longer on Th II–VII. Segment 2 with 2 apical unequal setae, outer seta plumose, inner one spiculated. Ctenidia present at base of inner seta. Endopod 4- segmented, segment 4 smallest. Setal formulae of endopod: Th I 1 +0/0+1/0+1/2(0); Th II–VII 0+0/ 0+1/0+1/1(0).

Thoracopod VIII (Fig. 11 A–D): small, sub-globular, with protopod expanded distally (Fig. 11 A); dentate lobe wide and with truncate, finely denticulate distal margin. Outer lobe conical and short, barely reaching midlength of basipod. Inner lobe large and rectangular in latero-external view. Basipod balloon-like and 1.3 times as wide as long, carrying 1 simple seta at outer distal margin. Exopod small, somewhat hook-like, with minute denticles at distal margin. Endopod represented by a small seta.

Pleopod 1 absent

Uropod (Fig. 12 A, C): sympod 3.3 times as long as wide, bearing inhomonomous row of 6 serrulate spines; penultimate spine longer and thicker than proximal spines; ultimate spine slightly shorter than proximal spines; exopod cylindrical, 3.5 times as long as wide and half as long as sympod length and with 1 apical seta and 1 subapical outer seta; both setae plumose; outer seta half as long as apical seta. Endopod falcate, 0.7 times as long as sympod, bearing 2 equal short, plumose setae at proximal fourth of outer margin.

Pleotelson (Fig. 12 B, C): produced into small rounded lobe at postero-lateral angle (Fig. 12 A); 1 seta on either side at base of caudal furca; seta bare, shorter than caudal furca. Anal operculum deeply concave medially in dorsal view (Fig. 12 C).

Caudal furca (Fig. 12 A, C) as in preceding new species.

 Description of adult female. Total body length 1.03 mm. Body and all appendages except Th VIII as in male.

Thoracopod VIII (Fig. 12 D): small, broadly triangular lobe.

 Etymology. The specific epithet alludes to Adi Shankara, a renowned exponent of Advaita Vedanta philosophy (monism); used here as a noun in apposition to the generic name.

 Variation. Body size varies from 0.85–1.07 mm, mean 1.01 mm (n = 7). Uropodal sympod with 6 or, rarely, 7 spines. No variation in the number of spines on caudal furca.

 Ecology. H. adishankara n. sp. is so far known from the type locality, most probably endemic to Kerala State. The fauna that co-occurred with the new species included the following taxa: Serbanibathynella sp., unidentified harpacticoid and cyclopoid copepods, cladocerans, chironomid larvae, mayfly nymphs, oligochaetes, nematodes and rotifers.

 Remarks. Both H. muvattupuzha n. sp. and H. adishankara n. sp. perfectly fit the diagnosis of Habrobathynella Schminke, 1973, as recently revised by Ranga Reddy & Totakura (2010) and “slightly modified by Schminke (2011). Going by the essential features of the complex penile appendage, i. e. the male Th VIII, which is crucially important in the systematics of Parabathynellidae (Schminke 1973, 1976; Delamare Deboutteville & Serban 1974; Ranga Reddy & Totakura 2010), the two new species may be said to be more closely related to each other that than to their hitherto known 12 Indian and two Madagascan congeners. As for its size and shape, the said appendage in both taxa is small and the protopod is expanded distally, resulting in a somewhat cup- or bowl-like appearance, in latero-external view–reminiscent of the generality of Atopobathynella species besides some resemblance to the Indian Habrobathynella plenituda Ranga Reddy & Schminke, 2009, and H. pseudoindica Totakura & Ranga Reddy, 2014. Similarly, the penile lobes in both new species are only moderately produced and the outer lobe is short and conical. Further, the overall spine configuration on the uropodal sympod, as already described, is the same in both species except that the number of proximal spines is three in H. muvattupuzha n. sp. as against four or five in H. adishankara n. sp. The other points of similarity, inter alia, include: the poorly chitinised body; the equally long aesthetascs on fifth and sixth antennulary segments; the smooth couplers as well as small lateral lobes on the paragnaths; and the presence of a single seta on the mid-inner margin of the second maxillary segment. However, H. muvattupuzha n. sp. can be distinguished from H. adishankara n. sp., inter alia, by the following features: the uropodal sympod has three vs. four or five proximal spines; the pleotelson seta is long vs. short; the maxillule has six vs. five claws on the distal endite; the maxilla has two setae vs. one seta on the first segment, and the seta at the inner distal corner of the second segment strong vs. weak; the antennule has two vs. three aesthetascs on fifth segment; the antenna has short vs. long first segment; the paragnaths with minaret-like vs. thumb-like coupler; and the anal operculum flat vs. medially deeply concave. Both the new species stand out in the genus by their unique constellation of characters (see Diagnosis).

The salient morphological characters and their states among the then known species of Habrobathynella had been analysed by Ranga Reddy & Totakura (2010), Totakura & Ranga Reddy (2014), and Ranga Reddy et al. (2014). Now, we briefly mention the newly recognised and phylogenetically important character states in the present new species, and also refer to the parallel conditions in the allied lineages, wherever relevant.

Antennule. The fifth antennular segment in H. muvattupuzha n. sp. has two long aesthetascs, overreaching the sixth antennular segment. This character state is shared only with the Indian H. nagarjunai and both Madagascan species. All other species have three long or short aesthetascs on the said segment.

Antenna. In the Parabathynellidae as a whole, two-segmented antenna occurs only in three genera besides Habrobathynella: Kimberleybathynella Cho, Park & Humphreys, 2005, Nipponbathynella Schminke, 1973, and Nunubathynella Schminke, 1976. The proximal segment tends to be reduced among various species of these genera, and this is particularly true of Habrobathynella species (see Ranga Reddy & Totakura 2010). On the other hand, the segment is nearly half as long as the next segment in H. muvattupuzha n. sp. much like what is seen in H. vidua, and it is almost as long as the next segment in H. adishankara n. sp., somewhat similar to the condition seen in certain species of Kimberleybathynella. The as-yet known most derived one-segmented condition is present only in Atopobathynella Schminke, 1973.

Labrum. The vaulting is very vague in H. muvattupuzha n. sp. as in H. indica and H. ajraoi, whereas it is moderate in H. adishankara n. sp. as in H. pseudoindica. Among Habrobathynella species, the vaulting is most prominently developed in H. jeanneli, and the teeth are remarkably large and widely spaced in H. ajraoi. Interestingly, the vaulting is so deep that it has resulted almost in a bilobed condition of the labrum in the monotypic Haplophallonella Serban & Coineau, 1975.

Mandible. Both H. muvattupuzha n. sp. and H. adishankara n. sp. conform to typical pattern of Habrobathynella in which the mandible is generally conservative. However, the unarticulated tooth on the ventral edge and the reduced and fork-like pars molaris with only four fused teeth (claws) in H. ajraoi are reminiscent of the closely allied, African Haplophallonella (Totakura & Ranga Reddy 2014).

Paragnaths. The relative size, shape and ornamentation of the median coupler together with the size, shape, orientation and ornamentation of the lateral lobes constitute an important species-specific criterion (Ranga Reddy et al. 2014). While the coupler is ornamented in all species of Habrobathynella in which the paragnath morphology has been depicted, it is smooth in the two new species; the lateral lobes are also smooth and posteriorly directed in both new species. However, the form of the coupler is distinct in the two species being minaret-like in H. muvattupuzha n. sp. and thumb-like in H. adishankara n. sp.

Maxillule. In H. muvattupuzha n. sp., the proximalmost claw on inner margin of the distal endite is reduced to a spiniform structure, somewhat like in H. parakrishna, H. vaitarini, H. savitri and H. vidua (see Ranga Reddy & Totakura 2010). In H. adishankara n. sp., as also in H. ajraoi, the said claw is completely absent.

Maxilla. The number of armature elements at the inner distal corner of the first segment varies between one and three among the congeners (Ranga Reddy et al. 2014). H. muvattupuzha n. sp. has two strongly unequal setae as in H. schminkei, H. krishna and H. pseudoindica, but only a single seta in H. adishankara n. sp., H. milloti, H. jeanneli, H. savitri, H. vidua, H. borraensis, and H. parakrishna. The most plesiomorphic state of three setae occurs in H. nagarjunai, H. indica, H. plenituda, H. vaitarini and H. ajraoi. Similarly, the mid-inner margin of the second segment in the two new species has only one seta, as in H. parakrishna, H. pseudoindica, H. schminkei, H.

 savitri and H. borraensis. A maximum of three setae occurs in same position in H. indica and H. plenituda. The apical seta at the inner distal corner of the second segment shows several character states (see Totakura & Ranga Reddy 2014). In H. muvattupuzha n. sp., the seta is spiniform and about 80% as long as the apical claw whereas it is relatively slender, 55% as long as apical seta, and bulbous at the base in H. adishankara n. sp. In the two new species, the third segment is distinct from the apical claw as in the case of H. jeanneli, H. nagarjunai, H. schminkei, and H. plenituda whereas it is fused with the apical claw in all other species.

Thoracopod I. The two new species are no different from most of the Habrobathynella species in having a seta at the inner distal corner of the first endopodal segment. It is only in H. ajraoi and H. pseudoindica that this seta is missing –a novel apomorphic feature in Habrobathynella (Totakura & Ranga Reddy 2014). The seta, when present, shows different character states in its length. It is short, being less than half as long as the second endopodal segment in H. nagarjunai and H. parakrishna, whereas in all the remaining species including the new species, it is at least half as long as, or slightly longer (e. g. H. plenituda) than the second segment. So, the presence or absence of the afore-mentioned seta, and when present, its length relative to second endopodal segment merit attention at species-level decisions.

Thoracopod VIII male. The length of the basipodal seta generally varies between species (Totakura & Ranga Reddy 2014). It is moderately developed in the two new species whereas it is longest in H. ajraoi. The basipod is without ornamentation in the two new species whereas it is ornamented in H. schminkei, H. plenituda and H. krishna. Totakura & Ranga Reddy (2014) mentioned the ascending order of the length of penile region in Habrobathynella species. With the addition of the two new species, its ascending order is as follows: jeanneli ˂ vaitarini ˂ nagarjunai < borraensis < plenituda < muvattupuzha n. sp. ˂ adishankara n. sp. ˂ pseudoindica ˂ krishna <parakrishna ˂ savitri ˂ schminkei ˂ milloti ˂ ajraoi ˂ vidua < indica. The inner lobe in the two new species is shorter than the dentate lobe, as is the case in most species of Habrobathynella. However, it is longer in H. milloti, H. indica and H. krishna and as long as the dentate lobe in H. schminkei and H. ajraoi.

Uropod. Both H. muvattupuzha n. sp. and H. adishankara n. sp. have a similar configuration of a inhomonomous spine row, except that they have, respectively, three and four (rarely five) proximal spines, closely resembling the condition of H. krishna and H. vidua (see Totakura & Ranga Reddy 2014). The relative lengthwidth ratios of the uropodal exopod and endopod and also the relative lengths of their setae vary between certain species (Totakura & Ranga Reddy 2014; Ranga Reddy et al. 2014).

Biodiversity
Taxonomy
Animalia
Arthropoda
Malacostraca
Bathynellacea
Parabathynellidae
Habrobathynella
Habrobathynella adishankara

Published as part of Elia, Bandari, Shaik, Shabuddin & Reddy, Yenumula Ranga, 2016, Two new species of the genus Habrobathynella Schminke, 1973 (Syncarida, Parabathynellidae) from the southwestern peninsular India, pp. 149-167 in Zootaxa 4150 (2) on pages 157-165, DOI: 10.11646/zootaxa.4150.2.4, http://zenodo.org/record/267073

Schminke, H. K. (1973) Evolution, System und Verbreitungsgeschichte der Familie Parabathynellidae (Bathynellacea, Malacostraca). Akademie der Wissenschaften und der Literatur Mainz, mathematisch-naturwissenschaftliche Klasse, Mikrofauna Meeresboden, 24, 1 - 192.

Ranga Reddy, Y. & Totakura, V. R. (2010) A taxonomic revision of the genus Habrobathynella Schminke, 1973, with the description of four new species from southeastern India (Crustacea, Malacostraca, Bathynellacea). Zootaxa, 2532, 1 - 54.

Schminke, H. K. (2011) Arthropoda: Crustacea: Malacostraca: Bathynellacea Parabathynellidae, In, Invertebrate Fauna of the World, vol. 21. National Institute of Biological Resources, Seo-gu Incheon, Republic of Korea, 1 - 244.

Schminke, H. K. (1976) Systematische Untersuchungen an Grundwasserkrebsen - eine Bestandsaufnahme (mit der Beschreibung zweier neuer Gattungen der Familie Parabathynellidae, Bathynellacea). International Journal of Speleology, 8, 195 - 216. http: // dx. doi. org / 10.5038 / 1827 - 806 X. 8.1.18

Delamare Deboutteville, C. & Serban, E. (1974) Contribution la connaissance des pereiopodes VIII males des Habrobathynella milloti (Delamare et Paulian) Parabathynellidae, Bathynellacea. Annales de Speleologie, 29 (3), 381 - 387.


A Case of So-Called Chronic Neurasthenia Due to Abdominal Adhesions; Operation; Recovery.


Scrapter Lepeletier de Saint-Fargeau & Audinet-Serville 1828

Genus Scrapter Lepeletier & Serville, 1828
 Scrapter Lepeletier & Serville, 1828: 403 (not Scrapter Lepeletier, 1841: 260). Type species: Scrapter bicolor Lepeletier and Serville, 1828, by subsequent designation in Vachal (1897: 63). (For later type designations and confusion with Scrapter Lepeletier, see Michener 1997.)

 Polyglossa Friese, 1909: 123. Type species: Polyglossa capensis Friese, 1909, by subsequent designation in Cockerell (1921: 203). (For a later type designation by Sandhouse, see Michener 1997.)

 Strandiella Friese, 1912: 181. Type species: Strandiella longula Friese, 1912 = Scrapter niger Lepeletier & Serville, 1828, by subsequent designation in Cockerell (1916: 430).

 Polyglossa (Parapolyglossa) Brauns, 1929: 134. Type species: Polyglossa heterodoxa Cockerell, 1921, by subsequent designation in Sandhouse (1943: 584) (see Michener 1997).

 Detailed diagnoses and descriptions of Scrapter were provided by Eardley (1996), Engel (2005), Davies & Brothers (2006) and Michener (2007), so they are not repeated here. Regarding the availability of Scrapterini versus Scraptrinae see Ascher & Engel (2006). Scrapter shows an unusual level of intrageneric diversity, described in detail by Davies & Brothers (2006), so various authors suggested that after revision the genus could be split up into several (sub)genera (Engel 2005; Melo & Gonçalves 2005; Michener 2007). The current system of species-groups suggested by Eardley (1996) does not convincingly reflect this diversity, as it partly contains morphologically heterogenous and presumably paraphyletic species-groups. The S. flavostictus -group is an example of such an inhomogeneous assemblage and includes the first described "euryglossiform" Scrapter, S. albitarsis. This species and its relatives are here transferred to a new species-group.
    The group of "euryglossiform" Scrapter
 The term "euryglossiform" Scrapter is introduced here for a group of morphologically monotonous species, including the smallest bees of the genus (3.5–7.0 mm), that are predominantly black, often with yellow markings on the legs. This species-group can also be referred to as the S. albitarsis -group, named after the first described species. In their body shape, sparse pilosity, surface sculpture and narrow groove-like facial fovea they superficially resemble andreniform Euryglossinae. These similarities might be convergent (Michener 2007: 171) but potentially reflect the presumed sister-group relationship of the Australian Euryglossinae and Scraptrinae (Almeida & Danforth 2009).

 The species of the "euryglossiform" Scrapter are characterized by a) a sulcus-like facial fovea with an invisible bottom as in Hylaeus (e.g., Fig. 1D), b) basitibial plate of female with simple marginal carinae, c) body small, without metasomal hair bands in females and most males, and d) membraneous apicolateral lobes on male S7 (e.g., Fig. 5D), sometimes reduced to small structures, in nine of the 14 species where the males are known. In other Scrapter species these lobes, that are a common feature in many colletid genera, are only known in a much more reduced form from some species of the S. nitidus -group. This group also shares the narrow facial fovea and the shape of male genitalia with the "euryglossiform" Scrapter and might be their closest relatives as Davies et al. (2005) already suggested in their description of S. acanthophorus.

 As relationships of species within the "euryglossiform" Scrapter are not clear, they are listed in alphabetical order.
    Species of "euryglossiform" Scrapter

Biodiversity Taxonomy Animalia Arthropoda Insecta Hymenoptera Colletidae Scrapter

Published as part of Kuhlmann, Michael, 2014, Revision of the euryglossiform species of the Afrotropical bee genus Scrapter Lepeletier & Serville, 1828 (Hymenoptera: Apoidea: Colletidae), pp. 1-69 in European Journal of Taxonomy 95 on pages 3-4, DOI: 10.5852/ejt.2014.95, http://zenodo.org/record/3860596

Lepeletier de Saint-Fargeau A. L. M. & Serville A. 1828. In: M. Diderot et al. (eds) Encyclopedie Methodique, Histoire Naturelle. Insectes, Vol. 10: 345 - 832. Paris.

Lepeletier de Saint-Fargeau A. L. M. 1841. Histoire Naturelle des Insectes-Hymenopteres. Vol. 2, Roret, Paris.

Vachal, J. 1897. Eclaircissements sur de genre Scrapter et description d'une espece nouvelle de Dufourea. Bulletin de la Societe Entomologique de France 1897: 61 - 64.

Michener C. D. 1997. Genus-group names of bees and supplemental family group names. Scientific Papers, Natural History Museum, University of Kansas 1: 1 - 81.

Friese H. 1909. Die Bienen Afrikas nach dem Stande unserer heutigen Kenntnisse. In: Schultze L. (ed.) Zoologische und Anthropologische Ergebnisse einer Forschungsreise im westlichen und

Cockerell T. D. A. 1921. Descriptions and records of bees-XC. Annals and Magazine of Natural History (9) 7: 201 - 212. http: // www. biodiversitylibrary. org / item / 53357  page / 227 / mode / 1 up

Friese H. 1912. Neue und wenig bekannte Bienen Sud-Afrikas. Archiv fur Naturgeschichte, Abt. A 78 (5): 181 - 189.

Cockerell T. D. A. 1916. Descriptions and records of bees-LXXII. Annals and Magazine of Natural History (8) 17: 428 - 435. http: // www. biodiversitylibrary. org / item / 61721  page / 440 / mode / 1 up

Brauns H. 1929. Neue und auffallende Apiden aus Sud-Afrika. Zeitschrift fur Wissenschaftliche Insektenbiologie 24: 130 - 143.

Sandhouse G. A. 1943. The type species of the genera and subgenera of bees. Proceedings of the United States National Museum 92: 519 - 619. http: // www. biodiversitylibrary. org / item / 53694  page / 585 / mode / 1 up

Eardley C. D. 1996. The genus Scrapter Lepeletier & Serville (Hymenoptera: Colletidae). African Entomology 4: 37 - 92.

Engel, M. S. 2005. Family-group names for bees (Hymenoptera: Apoidea). American Museum Novitates 3476: 1 - 33.

Davies G. B. P. & Brothers D. J. 2006. Morphology of Scrapter (Hymenoptera: Anthophila: Colletidae), with description of three new species and taxonomic status of five Cockerell taxa. African Invertebrates 47: 135 - 183.

Michener C. D. 2007. The Bees of the World. 2 nd edition, Johns Hopkins University Press, Baltimore, Maryland.

Ascher J. S. & Engel M. S. 2006. On the availability of family-group names based on Scrapter (Hymenoptera: Colletidae). Entomological News 117: 117 - 119.

Melo G. A. R. & Goncalves R. B. 2005. Higher level bee classifications. Revista Brasileira de Zoologia 22: 153 - 159.

Almeida E. A. B. & Danforth B. N. 2009. Phylogeny of colletid bees (Hymenoptera: Colletidae) inferred from four nuclear genes. Molecular Phylogenetics and Evolution 50: 290 - 309.

Davies G. B. P., Eardley C. D. & Brothers D. J. 2005. Eight new species of Scrapter (Hymenoptera: Apoidea: Colletidae), with descriptions of S. albifumus and S. amplispinatus females and a major range extension of the genus. African Invertebrates 46: 141 - 179.


FIGURE 12 in Deep-sea Rhachotropis (Crustacea: Amphipoda: Eusiridae) from New Zealand and the Ross Sea with key to the Pacific, Indian Ocean and Antarctic species

FIGURE 12. Rhachotropis rossi sp. nov., holotype, 11.8 mm, female, NIWA 45813: a, uropod 1; b, uropod 2; c, uropod 3; d, telson; e, pleopod 2. Scale bars 1 mm.

Biodiversity Taxonomy Animalia Arthropoda Malacostraca Amphipoda Eusiridae Rhachotropis

Published as part of Lörz, Anne-Nina, 2010, Deep-sea Rhachotropis (Crustacea: Amphipoda: Eusiridae) from New Zealand and the Ross Sea with key to the Pacific, Indian Ocean and Antarctic species, pp. 22-48 in Zootaxa 2482 on page 38, DOI: 10.5281/zenodo.195450

Zootaxa


FIGURE 65. Distribution maps. A Nops minas n in A revision of the Neotropical spider genus Nops MacLeay (Araneae: Caponiidae) with the first phylogenetic hypothesis for the Nopinae genera

FIGURE 65. Distribution maps. A Nops minas n. sp.; B Nops nitidus Simon.

Biodiversity Taxonomy Animalia Arthropoda Arachnida Araneae Caponiidae Nops

Published as part of Sánchez-Ruiz, Alexander & Brescovit, Antonio D., 2018, A revision of the Neotropical spider genus Nops MacLeay (Araneae: Caponiidae) with the first phylogenetic hypothesis for the Nopinae genera, pp. 1-121 in Zootaxa 4427 (1) on page 97, DOI: 10.11646/zootaxa.4427.1.1, http://zenodo.org/record/1271779

Zootaxa


Survey of India Topo sheet 46J8 1978 1st edition

Survey of India Topo sheet 46/J8 1978 1st edition


Relatório Anual de Gestão da UEPA - Exercício 2019

O Relatório Anual de Gestão da Universidade do Estado do Pará é parte integrante do Relatório Anual de Prestação de Contas de Gestão, o qual é avaliado pelo Tribunal de Contas do Estado do Pará. Este Relatório é dividido em 8 secções,  sendo que o último corresponde ao Relatório da Ouvidoria da Uepa.

Secção 1  aborda o escopo do relatório  e breve apresentação do exercício 2019,

Secção 2  apresenta as ações que foram destaque no exercício de 2019.

Secção 3 – Ações de Gestão e Planejamento aborda o desempenho da execução de programas, ações e metas  física e regionalizadas definidas no Plano Plurianual de Governo (PPA 2016-2019);  demonstrativo da Execução Orçamentária por fonte de recurso; a evolução da  constituição do Capital Humano período 2016-2019  no que concerne ao quadro efetivo e temporário, a titulação dos docentes, e  evolução do número de servidores capacitados; Detalhamento da MODERNIZAÇÃO E INVESTIMENTO abordando a Aquisição de Material Permanente, investimento em Tecnologia, Evolução do Acervo,  e estratificação do investimento realizado em obras por região de integração.

Secção 4  apresenta Ações de Graduação englobando as oportunidades de acesso ao Ensino Superior através da isenção de taxas de inscrição ao processo seletivo,  o crescimento da oferta de vagas, a evolução das vagas de graduação pela estruturas de Centros que constituem a Uepa, comparativo das matriculas por gênero, relação entre matriculas e concluintes no PARFOR;  a Política de Assistência Estudantil expressa por meio  do Programa Institucional de Bolsas de Iniciação à Docência – PIBID,  do Programa de Bolsas de Monitoria,  do Programa Iniciação Científica – PIBIC, do Programa Campus Avançado, do Programa de Assistência Estudantil.

Secção 5  aborda as Ações de Pós-Graduação com a evolução do número de cursos e vagas ofertadas estratificadas por tipo (especialização, mestrado acadêmico, mestrado profissional, doutorado próprio, doutorado em rede); e com o detalhamento das publicações realizadas pela ADUEPA.

Secção 6  aborda as Ações de Pesquisa com o detalhamento dos programas de pesquisa com o quantitativo de pessoas envolvidas, bolsistas e docentes estratificados por município; os grupos de pesquisa ativos segundo o Diretório de Grupos de Pesquisa 5.0 do CNPQ ;  número de proteções à propriedade intelectual de inovações das pesquisas e detalhamento das proteções no período de 2013 – 2019 segundo o tipo (Marca, Desenho Industrial, Patente e Programa de Computador).

Secção 7  aborda as Ações de Extensão com a evolução de atendimentos à sociedade realizados nos programas e  unidades Planetário, Núcleo de Arte e Cultura; serviços ofertados à sociedade por meio do Centro de Saúde Escola do Marco (CSE-Marco) e seus anexos (Centro Saúde Escola, UEAFTO,  Unidade de Referência, Dermatologia e Laboratório)

Secção 8  Relatório de Gestão da Ouvidoria da Uepa que consolida estatísticas de reclamações, sugestões, denúncias, elogios, críticas e solicitações de informações, da sociedade,  relativas às atividades e serviços da Universidade do Estado do Pará.

Relatório Anual de Gestão - UEPA 2019.pdf

Plano Plurianual do Governo do Estado do Pará 2016-2019


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RB1372 nlp-18(ok1557)II | 2009-06-15T12:19:11+01:00

This experiment is part of the C.elegans behavioural database. For more information and the complete collection of experiments visit http://movement.openworm.org

preview link : https://www.youtube.com/watch?v=_5VBN21tVAo

strain : RB1372

timestamp : 2009-06-15T12:19:11+01:00

gene : nlp-18

chromosome : II

allele : ok1557

strain_description : nlp-18(ok1557)II

sex : hermaphrodite

stage : adult

ventral_side : clockwise

media : NGM agar low peptone

arena :

style : petri

size : 35

orientation : away

food : OP50

habituation : 30m wait

who : Laura Grundy

protocol : Method in E. Yemini et al. doi:10.1038/nmeth.2560. Worm transferred to arena 30 minutes before recording starts.

lab :

name : William R Schafer

location : MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 0QH, UK

software :

name : tierpsy (https://github.com/ver228/tierpsy-tracker)

version : cbfc23eb4f1ac2f29be75ade7a937eed58a5b219

featureID : @OMG

base_name : nlp-18 (ok1557)II on food L_2009_06_15__12_19_11__16

total time (s) : 299.62

frames per second : 26.9542

video micrometers per pixel : 4.57251

number of segmented skeletons : 5811