549 research outputs found
WELLINGTON AMORIM: Um olhar sobre a obra Amor Líquido de Zigmunt Bauman
No full textResumo - As tecnologias digitais enfraquecem as relações sociais? Essa é a pergunta que norteia uma das principais obras do autor polonês Zigmunt Bauman, nomeada Amor Líquido (2004). Com a consolidação da Internet, em especial das redes sociais digitais, as relações sociais, hoje, ganham novas interpretações. Assim, mostra-se importante discutir as consequências dessas formas de relacionamento, dos laços que hoje são construídos exclusivamente online. Para refletir sobre o pensamento do autor polonês, conversamos com o Prof. Dr. Wellington Amorim que nos ajuda a compreender o posicionamento de Bauman e seu lugar de fala.Palavras-chave: Bauman; Amor Líquido; Relações Sociais; Abstract - Do digital technologies weaken social relationships? This is the question that drives one of the major works of polish author Zygmunt Bauman, named Liquid Love (2004). With the consolidation of the Internet, particularly digital social media, social relationships today gain new interpretations. Thus, it proves salutary to discuss the consequences of these types of relationships, the ties that are now built exclusively online. To reflect on the thoughts of Bauman, we had a conversation with Prof. Dr. Wellington Amorim that helps us understand the positioning of the polish author and his place of speech.Keywords: Bauman; Liquid Love; Social Relationships
Neopleurophora kungi Ament & Amorim 2013, sp. nov.
No full textNeopleurophora kungi, sp. nov. (Figs. 2, 72–75, 175, 212, 240–241, 284–285) Diagnosis (males). Epandrial medial process not bifurcated, slightly curved, apically tapered. Epandrial right posterior margin with large, pointed projection. Material examined. Holotype ♂, BRAZIL: Amazonas: Manaus, Reserva Ducke, Igarapé Barro Branco, 12– 27.i.2005, Malaise trap, A. Henriques col. (MZUSP). Paratypes: ECUADOR: 1♂, Sucumbios: Sacha Lodge, 0.5ºS, 75.5ºW, 23.vi–3.vii.1994, Malaise trap, 270 m, P. Hibbs col. (LACM); BRAZIL: 1♂, same data as holotype, but 12–22.iv.2004 (INPA); 1♂, Rondônia: Guajará-Mirim, Rio Ouro Preto, Bananal, 20–27.x.1995, Malaise trap, J.A. Rafael & A. Henriques col. (MZUSP). Description. Male. Body length, 2.5 mm. Head. Frons black, anterior apex yellow, pubescent, without median furrow. Flagellomere 1 yellowish-brown, pubescent, oval. Arista pre-apical, pubescent. Palpus yellowish-brown, oval; one upper genal and two lower genal small setae. Thorax. Scutum and pleural sclerites light brown, sometimes scutum yellowish-brown anteriorly; anepisternum setulose dorsally, with one long seta; scutellum brown, posteriorly yellow. Legs yellowish-brown, hind femur brown at apex. Forefemur with ventral row of five strong setae near apex. Foretibia with one dorsal seta at basal fourth and an anterodorsal row of strong setae. Foremetatarsus ratio, 4.8. Midtibia with one anterodorsal and one posterodorsal setae at basal third (Fig. 175). Hind femur swollen (height/length ratio, 0.40), with ventral row of eight strong setae near base (Figs. 240–241). Hind tibia with one anterodorsal and four posterodorsal setae (Fig. 212). Wing. Costa 0.44 of the wing length, other wing features as for the genus. Halter yellow. Abdomen. Tergites dark brown, with lighter posterior band. Hypopygium light brown (Figs. 72–75). Epandrial medial process apically tapered, slightly curved, not bifurcated, esclerotized at apex. Epandrial right posterior margin with large, pointed projection, subepandrial setulose process present. Hypandrium left lobe large; right lobe narrow. Hypoproct with two setae. Phallus (Figs. 284–285). Basiphallus without dorsal process. Core plate flattened, bilobed. Epiphallus covered with medium size scales, connected to the right arm at the left of the phallus. Ventral plate well developed, bifurcated at apex into two dented processes. Female. Unknown. Geographic distribution. Southwestern and northern Amazonia in Brazil and in Amazonian Ecuador. Etymology. The specific epithet is given after Giar-Ann Kung, great friend and author of some papers on phorid taxonomy. With her help, together with the support from Weiping Xie and Dr. Brian Brown, it was possible to access most of the material used in this study, at the LACM. Comments. Neopleurophora kungi is hypothesized to be close to N. ptychodrilus and N. manauara based on the presence of the phallic ventral plate bearing apical teeth.Published as part of Ament, Danilo Cesar & Amorim, Dalton De Souza, 2013, Taxonomic revision of the genus Neopleurophora Brown (Diptera: Phoridae), with the description of thirty seven new species, pp. 1-93 in Zootaxa 3657 (1) on pages 33-34, DOI: 10.11646/zootaxa.3657.1.1, http://zenodo.org/record/526558
A produção de Francisco Gomes de Amorim sobre emigração em periódicos e cartas do século XIX
No full textFrancisco Gomes de Amorim (1827-1891), a Portuguese writer who emigrated to Amazonia in 1837, he lived several experiences that were later reported on his literary production and in the various contributions he made to periodicals, as well as in correspondence exchanges with his contemporaries. According to a compilation carried out by Costa Carvalho (2000), and in files available in Póvoa de Varzim, we can affirm that Gomes de Amorim had a broad vision on the themes he favored. Acording to a possible perspective for the 19th century, the author brought to light discussions that were boiling at that time, such as the social inequalities he experienced in Amazonia and the experience of Portuguese emigration to Brazil.Francisco Gomes de Amorim (1827-1891), escritor português que emigrou para Amazônia em 1837, viveu diversas experiências que, posteriormente, foram relatadas em sua produção literária e nas diversas contribuições em periódicos que realizou, bem como nas trocas de correspondência com seus contemporâneos. Conforme compilação realizada por Costa Carvalho (2000), e em arquivos disponíveis em seu espólio em Póvoa de Varzim, podemos afirmar que Gomes de Amorim tinha uma ampla visão sobre os temas que privilegiava. Dentro da perspectiva possível para o século XIX, o autor trouxe à tona discussões em ebulição naquele tempo, a exemplo das desigualdades sociais vivenciadas por ele na Amazônia e a experiência de emigração portuguesa para o Brasil
Au cœur de la tragédie brésilienne, l’espoir d’une défaite de Bolsonaro l'an prochain
No full textAlors que les décès dus au Covid augmentent, le président semble précipiter le pays dans un abîme sans issue. Le vaste remaniement ministériel auquel il vient de procéder, suivi de la démission des chefs d’état-major des armées, de la marine et de l’aviation ouvre une période d’instabilité dangereuse au pire moment de la pandémie due au Covid-19. Celso Amorim, ancien ministre des affaires étrangères (1993-1994 et 2003-2010) et de la défense (2011-2014) des gouvernements Lula et Dilma éclaire cette situation instable. Traduit par Gérard Wormser depuis son texte original anglais
Amid Brazil's tragedy, our hope is the prospect of Bolsonaro's defeat next year
cet article inaugure la chronique que son auteur accepte de nous donner.As Covid deaths climb the president seems to be throwing the country into an abyss that will be difficult to escape from. His recent extensive cabinet reshuffle, followed by the resignation of the chiefs of staff of the army, navy and air force, opens a period of dangerous instability at the worst moment of the Covid-19 pandemic. Celso Amorim, former Minister of Foreign Affairs (1993-1994 and 2003-2010) and Defense (2011-2014) of the Lula and Dilma governments, sheds light on this unstable situation. Translated by Gérard Wormser from Amorim's original English text
Amid Brazil's tragedy, our hope is the prospect of Bolsonaro's defeat next year
, this article inaugurates the chronicle that its author agrees to provide
CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish
No full textSince its first application for site-directed mutagenesis, the CRISPR-Cas9 system has revolutionized genome engineering. Here, we present a validated workflow for the generation of targeted genomic deletions in zebrafish, including the design, cloning, and synthesis of single-guide RNAs and Cas9 mRNA, followed by microinjection in zebrafish embryos and subsequent genotype screening for the establishment of a mutant line. The versatility and efficiency of this pipeline makes the generation of zebrafish models a widely used approach in functional genetics. For complete details on the use and execution of this protocol, please refer to Amorim et al. (2020).This work was supported by the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (grant agreement no. ERC_2015_StG _ 680156 _ZPR). J.B. acknowledges Fundação para a Ciência e a Tecnologia (FCT) for an FCT Scientific Stimulus Grant ( CEECIND/03482/2018 ). J.A. is a PhD fellow from FCT ( SFRH/BD/145110/2019 ). R.B.C. was funded by FCT ( ON2201403-CTO-BPD ) and EMBO (Short-Term Fellowship). We thank Joaquin Letelier, Ana Novoa, and Moises Mallo for important advice establishing the current protocol. We also thank Joana Marques for constant assistance in establishing the protocol
EU PREFERIA TER PERDIDO UM OLHO: A REPRESENTAÇÃO DO ESTUPRO, NA CRÔNICA DE PALOMA FRANCA AMORIM (2017)
No full textThis article aims to analyze the chronicle written by Paloma Franca Amorim (2017), entitled Eu preferia ter perdido um olho, primarily published in the newspaper O Liberal, in the state of Pará. The author offers a sensitive linguistic fabric when dealing with one of the violences against a woman and thematizes rape. She uses the chronicle’s resources to represent the social and historical problem and transport the discourse to the dimension that permeates literature and journalism. The study is based on the point of view of Nádia Battella Gotlib (1998), about literature written by women in Brazil, intertwined with the reports collected by Sohaila Abdulali (2019), who confronts the rape culture and culminates with Monique Wittig’s conceptions (2019) about what it means to be a woman in a sexist society.O presente artigo investiga a representação do estupro, na crônica de Paloma Franca Amorim (2017), intitulada Eu preferia ter perdido um olho, publicada primariamente no Jornal O Liberal, do estado do Pará. A autora oferece um tecido linguístico sensível ao representar uma das violências mais recorrentes contra as mulheres ao rememorar dois desses episódios traumáticos pelos quais a própria autora viveu e entrelaça a uma notícia sobre o tema, que estava em voga na época. Ela escolhe a crônica como narrativa do problema social e histórico, transportando o discurso para esta dimensão que permeia a Literatura e o Jornalismo. O estudo toma por base as discussões de Nádia Battella Gotlib (1998), a respeito da literatura feita por mulheres no Brasil, entrelaçadas aos relatos coletados por Sohaila Abdulali (2019), que faz frente à cultura do estupro e culmina nas concepções de Monique Wittig (2019) a respeito do que é ser mulher em uma sociedade sexista
Literatura infantil indígena: um olhar para a ancestralidade das crianças não indígenas no primeiro ciclo do ensino fundamental através dos contos indígenas
No full textThis monograph aims to analyze bibliographies on children's literature of indigenous tales as a way of promoting and strengthening the Brazilian child's view of their ancestry from the first year of the elementary cycle. By rescuing lost knowledge and values in relation to indigenous peoples over the times when non-indigenous peoples distanced themselves due to the lack of knowledge of this knowledge, they led to the construction of a society based on the instrumental rationality of technological progress and destruction of nature, causing damage all humanity. In addition, we intend bringing reflectionsthat can indirectly provoke the look at the pedagogical practice of teachers, who work in the early years of elementary school, and the treatment with children's literature through indigenous tales and the role of literature for the construction of identities of children. The recognition of traditions, customs, languages and knowledge can benefit the non-indigenous worldview with the other, in relation to themselves and the planet. Methodologically, this work has a qualitative approach and a bibliographic review with contributions from theorists such as PURI (2019), GRAÚNA (2012), AMORIM (2018), KABEMBA (2019), among others. We will discuss ancestry, children's literature and indigenous literature in the focus of re-signification of pedagogical practices to develop a future complete and upstanding citizen to act consciously in society. We will also analyze the book of indigenous children's literature “Meu Vô Apolinário: um mergulho no rio da (minha) memoria”,by author Daniel Munduruku, as well as websites, blogs and videos in line with indigenous ancestry, highlighting the importance of the teacher as a mediator of the process that aims at the formation of conscious readers and future social authors.Esta monografia tem como objetivo analisar bibliografias sobre a literatura infantil de contos indígenas como forma de promoção e fortalecimento do olhar da criança brasileira para a sua ancestralidade a partir do primeiro ano do ciclo fundamental.Ao resgatar saberes e valores perdidos em relação aos povos indígenas ao longo dos tempos em que os não indígenas se distanciaram pelo desconhecimento desses saberes, levaram à construção de uma sociedade pautada na racionalidade instrumental do progresso tecnológico e destruição da natureza, acarretando danos para toda a humanidade. Ademais, pretendemos trazer reflexões que possam provocar de forma indireta o olhar para a prática pedagógica de professores que atuam nos anos iniciais do ensino fundamental, e o trato com a literatura infantil por meio dos contos indígenas e do papel da literatura para a construção das identidades das crianças. O reconhecimento das tradições, costumes, línguas e saberes pode beneficiar a visão de mundo dos não indígenas com o outro, em relação a si e com o planeta. Metodologicamente, este trabalho é de abordagem qualitativa e revisão de cunho bibliográfico com aporte em teóricos tais como PURI (2019), GRAÚNA (2012), AMORIM (2018), KABEMBA (2019), dentre outros. Discutiremos a ancestralidade, literatura infantil e literatura indígena no enfoque de ressignificação das práticas pedagógicas para desenvolver um futuro cidadão completo e íntegro para atuar de forma consciente na sociedade. Também analisaremos o livro de literatura infantil indígena Meu Vô Apolinário: um mergulho no rio da (minha) memória,do autor Daniel Munduruku, além de sites, blogs e vídeos em consonância com a ancestralidade indígena, destacando a importância do professor como mediador do processo que visa à formação de leitores conscientes e futuros autores sociais
Manota williamsi Kurina & Hippa & Amorim 2019, sp. n.
No full textManota williamsi sp. n. Figs 1 A–C, 2A–F Male. Colour. Head brown, face somewhat paler. Antenna light brown, including scape and pedicel. Clypeus and mouthparts yellowish. Thorax brown to dark brown, medial part of scutum and scutellum somewhat darker due to their curvature on slide. Legs yellowish, mid- and hind femora basally infuscated. Wing with brownish tinge because of microtrichia; halter mostly yellow, with blackish knob. Abdomen brown to dark brown, tergites laterally and sternites lighter. All setosity pale, yellowish or brownish, thicker setae darker than finer ones. Head. Fourth antennal flagellomere 1.0–1.2 times as long as wide. Palpomere 3 of maxillary palpus with apicomesial thumb-like extension, with 3 curved apical sensillae; palpomere 4 with parasegment; palpomere 5 ca. 1.5 times longer than palpomere 4. Number of strong postocular setae 11. Thorax. Anepisternum with 11–17 setae; anterior basalare and laterotergite non-setose; preepisternum 2 with 11–18 setae; metepisternum with 19-28 setae. Legs. Mid tibial organ present, extending over about one third of tibial length (Fig. 1B). Hind tibial organ absent. Wing. R 1 meeting C within basal half of costal margin; sclerotized part of M 2 extending to level of tip of R 1; wing length 1.8–2.1 mm. Hypopygium (Figs. 1C, 2 A–F). Sternite 9 tapering, laterally free from gonocoxa, posteriorly blunt, extending to about middle between the bases of gonocoxa and gonostylus, anterior margin with deep and narrow V-shaped medial incision dividing sternite almost into two halves, anterior part non-setose, setae on posterior part similar to those on ventral side of gonocoxa. Parastylar lobe small, finger-like, with 2–3 setae apically. Paraapodemal lobe not observed. Ventral and dorsal medial margins of gonocoxa simple, both slightly bulging medially. Ventrally from dorsal medial margin of gonocoxa an anterior finger-like lobe with 5–6 apical setae and a large posterior lobe that is posteromedially drawn out, bearing ca. 30 apically curved setae. Dorsal setae on anterior half of gonocoxa similar to those on ventral side; dorsal setae on posterior half of gonocoxa somewhat longer. Two juxtagonostylar setae present, a flattened, sub-apically geniculate megaseta, with a sub-apical medially directed whip-like branch and a weak and shorter normal seta, both arising from a common basal body shorter than the megaseta. Gonostylus elongate-oval, setigerous, with 1–2 sub-apical, medially directed stronger setae. Aedeagus wide, with prominent lateral shoulders, apex curved ventrad. Hypoproct posteriorly extending near base of gonostylus, ventral part (sternite 10) with ca. 40 scattered setae on each half. Cerci medially separate, elongated, apically widening, with setae apically and medially. Female. Unknown. Etymology. The species is named after Geoff Williams, the owner of Lorien Wildlife Refuge and Conservation Area, northeast of Taree, New South Wales. Geoff Williams is an authority on the natural history of the northern New South Wales, and has been recognized nationally for his service to conservation as an ecologist, biologist, author and wildlife refuge custodian. Discussion. In having a setose anepisternum and a non-setose laterotergite, Manota williamsi sp. n. resembles M. gemella Hippa, 2007 (from Maluku Ultra, Indonesia) — into which it would run in the key by Hippa (2007). However, it differs in details of the male hypopygium as follows: (1) dorsal medial margin of gonocoxa with anterior finger-like lobe and large posterior lobe at a more ventral level (with small subapical lobe only in M. gemella); (2) juxtagonostylar megaseta flattened, with a subapical, medially directed whip-like branch (simple, without branch in M. gemella); (3) gonostylus elongate-oval, with 1–2 sub-apical setae stronger (with two small medial lobes in M. gemella); (4) hypoproct wide, with ca. 40 scattered ventral setae on each half (narrow, with ca. 8 ventral setae on each half); (5) aedeagus wide, with prominent lateral shoulders (narrow with weak lateral shoulders in M. gemella). The presence of the mid tibial organ in M. williamsi resembles the group of five species from New Zealand (cf. Jaschhof & Jaschhof 2010). Some characters in the male hypopygium of M. williamsi are also typical to the New Zealand species, e.g., sternite 9 laterally free from the gonocoxa and dorsal medial margin of the gonocoxa with anterior and posterior lobes (= positions I and II by Jaschhof & Jaschhof 2010). However, M. williamsi has the gonostylus elongate-oval without lobes, instead of being composed of several lobes as in New Zealand’s species. The similarities between M. williamsi and the New Zealand species could be homoplastic, although a similar distribution pattern is known from some other sciaroid groups, e.g., the keroplatid genus Arachnocampa Edwards (Baker et al. 2008). Type material. Holotype. Male, AUSTRALIA, N.S.W., Carrai State Forest, 30°54’33’’S 152°16’26’’E, 1075m, E. Tasker 3.xii–8.xii.1997, sticky trap on Eucalyptus saligna, CS-CR-127-2 (on slide, AMSA: K377226). Paratypes. 1 male, AUSTRALIA, N.S.W., Taree, Lorien Wildlife Refuge, 3 Km N of Landsdowne, sclerophyll forest, Malaise trap, 1–14.xi.2011, 31° 45’ 04” S, 152° 32’ 03” E. G. & B. Williams col. (on slide # 5, MZUSP); 1 male, same data except 14–31.xii.2011 (on slide # 4, MZUSP); 1 male, same data except 17.i–4.ii.2012 (on slide # 6, MZUSP); 1 male, AUSTRALIA, N.S.W., Carrai State Forest, 30°54’35’’S 152°16’26’’E, 1090m, 3.xii– 8.xii.1997, sticky trap on Eucalyptus obliqua E. Tasker leg., CC-FK-127-3 (AMSA: K377230); 2 males, AUSTRALIA, N.S.W., Carrai State Forest, 31°00’19’’S 152°16’24’’E, 940m; E. Tasker 3.xii–8.xii.1997; sticky trap on Eucalyptus campanulata, CS-GP-127-3 (on slides, AMSA: K377228); 1 male, AUSTRALIA, N.S.W., E. Kunderang Rd OWRNP, 30°49’19’’S 152°02’9’’E, 6.xi–14.xi. 2015, 850 m, pitfall trap SR1 (open eucalypt forest on ridge, westerly aspect), Bray, Lamb, Nzama & Smith leg., (on slide, AMSA: K379411). Additional material studied (all in alcohol). 5 males, AUSTRALIA, N.S.W., Carrai State Forest, 31°54’19’’S 152°17’36’’E, 1055m, 3.xii–8.xii.1997, sticky trap on E. cameronii, E. Tasker leg., CS-DP-127-6 (AMSA: K377135); 1 male, same data except 30°54’33’’S 152°16’28’’E, 1075m, sticky trap on E. campanulata, CC-CR-127-6 (K377206, in AMSA); 2 male s, same data except CC-CR-127-5 (AMSA: K377208); 1 male, same data except 30°54’35’’S 152°16’26’’E, 1090m, sticky trap on E. campanulata, CC-FK-127-2 (AMSA: K377209); 3 males, same data except 30°54’19’’S 152°17’36’’E, 1055m, sticky trap on E. obliqua, CS-DP-127-5 (AMSA: K377210); 2 males, same data except 30°59’45’’S 152°16’23’’E, 930m, 11.i–16.i.1998; sticky trap on E. campanulata, CS-FZ-018-4 (AMSA: K377211); 3 males, same data except 31°00’19’’S 152°16’24’’E, 940m, CS- GP-018-6 (AMSA: K377213); 3 males, same data except 3.xii–8.xii.1997, CS-GP-127-6 (AMSA: K377212); 2 males, same data except 30°59’45’’S 152°16’23’’E, 930m, 3.xii–8.xii.1997, sticky trap on E. saligna, CS-FZ-127- 1 (AMSA: K377215); 1 male, same data except CS-FZ-127-2 (AMSA: K377218); 3 males, same data except 30°0’19’’S 152°16’24’’E, 940m, 3.xii–8.xii.1997, sticky trap on E. campanulata, CS-GP-127-1 (AMSA: K377221); 2 males, same data except 30°58’48’’S 152°17’0’’E, 975m, sticky trap on E. obliqua, CS-RO-127-5 (AMSA: K377223); 3 males, same data except 30°54’33’’S 152°16’26’’E, 1075m, sticky trap on E. campanulata, CS-CR-127-2 (AMSA: K377226); 3 males, same data except 30°58’48’’S 152°17’6’’E, 975m, sticky trap on E. viminalia, CS-RO-127-1 (AMSA: K377229); 2 males, same data except 30°54’35’’S 152°16’26’’E, 1090m, sticky trap on E. campanulata, CC-FK-127-6 (AMSA: K377231); 3 males, same data except 30°54’19’’S 152°17’36’’E, 1055m, 11.i– 16.1.1998, sticky trap on E. campanulata, CC-DP-018-2 (AMSA: K377232); 1 male, same data except 30°54’19’’S 152°17’36’’E, 1055m, sticky trap on E. obliqua, CC-DP-018-4 (AMSA: K377235); 2 males, same data except 30°58’48’’S 152°17’6’’E, 975m, sticky trap on E. campanulata, CS-RO-018-2 (AMSA: K377236); 1 male, same data except 30°58’48’’S 152°17’36’’E, 975m, sticky trap on E. obliqua, CS-RO-018-5 (AMSA: K377239); 2 males, same data except 30°58’48’’S 152°17’6’’E, 975m, sticky trap on E. campanulata, CS-RO-018-1 (AMSA: K377243); 1 male, same data except 31°00’19’’S 152°16’24’’E, 940m, sticky trap on E. campanulata, CS-GP-018-5 (AMSA: K377244); 1 male, same data except 30°59’45’’S 152°16’23’’E, 930m, sticky trap on E. saligna, CS-FZ-018-3 (AMSA: K377246); 1 male, same data except 30°54’33’’S 152°16’28’’E, 1075m, sticky trap on E. campanulata, CC-CR-018-1 (AMSA: K377250); 1 male, same data except 30°59’45’’S 152°16’23’’E, 930m, sticky trap on E. saligna, CS-FZ-018-5 (AMSA: K377252); 2 males, same data except 30°58’48’’S 152°17’6’’E, 975m, sticky trap on E. obliqua, CS-RO-018-4 (AMSA: K377256); 1 male, same data except 30°59’45’’S 152°16’23’’E, 930m, sticky trap on E. campanulata, CS-FZ-018-6 (AMSA: K377257); 1 male, same data except 31°00’19’’S 152°16’24’’E, 940m, sticky trap on E. saligna, CS-FZ-018-3 (AMSA: K377258); 3 males, same data except 30°59’45’’S 152°16’23’’E, 930m, sticky trap on E. saligna, CS-FZ-018-1 (AMSA: K377264); 2 males, same data except 30°59’45’’S 152°16’23’’E, 930m, sticky trap on E. campanulata, CS-FZ-018-2 (AMSA: K379008); 2 males, same data except 30°54’33’’S 152°16’26’’E, 1090m, sticky trap on E. campanulata, CC-FK-018-1 (AMSA: K379010); 3 males, same data except 30°54’33’’S 152°16’28’’E, 1075m, 3.xii–8.xii.1997, sticky trap on E. obliqua, CC-CR-127-3 (AMSA: K377248); 2 males, same data except CC-CR- 127-4 (AMSA: K377249); 2 males, same data except 30°58’48’’S 152°17’6’’E, 975m, sticky trap on E. viminalia, CS-RO-127-3 (AMSA: K377251); 1 male, same data except 30°54’35’’S 152°16’26’’E, 1090m, sticky trap on E. obliqua, CC-FK-127-9 (AMSA: K379013); 3 males, same data except 30°58’48’’S 152°17’6’’E, 975m, sticky trap on E. viminalia, CS-RO-127-2 (AMSA: K379016 SA); 1 male, same data except 31°00’19’’S 152°16’24’’E, 940m, sticky trap on E. saligna, CS-GP-127-2 (AMSA: K379017); 2 males, same data except 30°59’49’’S 152°16’23’’E, 930m, sticky trap on E. campanulata, CS-FZ-127-3 (AMSA: K379105); 6 males, same data except 30°54’33’’S 152°16’28’’E, 1075m, sticky trap on E. obliqua, CS-CR-127-1 (AMSA: K379106); 2 males, same data except 30°54’19’’S 152°17’36’’E, 1055m, sticky trap on E. campanulata, CC-DP-127-4 (AMSA: K379107); 5 males, same data except 31°00’19’’S 152°16’24’’E, 940m, sticky trap on E. saligna, CS-GP-127-5 (AMSA: K379110); 5 males, same data except 30°58’48’’S 152°17’6’’E, 975m, sticky trap on E. campanulata, CS-RO-127-6 (AMSA: K379111); 2 males, N.S.W., Werrikimbe NP 31°16’42’’S 152°5’5’’E, 1040m; E. Tasker 1.xii–7.xii.1997; sticky trap on E. obliqua, WS-GB-127-4 (AMSA: K377207); 1 male, same data except 31°16’50’’S 152°3’19’’E, 1045m, sticky trap on E. viminalis, WS-FC-127-4 (AMSA: K377216); 1 male, same data except 31°16’42’’S 152°5’6’’E, 1040m, sticky trap on E. campanulata, WS-GB-127-5 (AMSA: K377220); 3 males, same data except 31°16’50’’S 152°3’19’’E, 1045m, WS-FC-127-1 (AMSA: K377222); 2 males, same data except 31°11’24’’S 152°9’39’’E, 1030m, 29.i–4.ii.1998, sticky trap on E. nobilis, WC-WT-018-5 (AMSA: K377225); 4 males, same data except 31°16’50’’S 152°3’19’’E, 1045m, 3.xii–7.xii.1997, sticky trap on E. saligna, WC-FC-127-6 (AMSA: K377227); 4 males, same data except 31°11’56’’S 152°10’23’’E, 1025m, 29.i–4.ii.1998, sticky trap on E. saligna, WC-WN- 018-03 (AMSA: K377233); 3 males, same data except 31°11’24’’S 152°9’39’’E, 1030m, sticky trap on E. obliqua, WC-WT-018-04 (AMSA: K377234); 2 males, same data except 31°11’56’’S 152°10’23’’E, 1025m, sticky trap on E. campanulata, WS-WIN-018-06 (AMSA: K377237); 2 males, same data except 31°16’42’’S 152°5’5’’E, 1040m, sticky trap on E. dives, WS-GB-018-06 (AMSA: K377238); 1 male, same data except 31°16’50’’S 152°3’19’’E, 1045m, sticky trap on E. campanulata, WS-FC-018-1 (AMSA: K377240); 3 males, same data except 31°12’0’’S 152°9’0’’E, 1060m, sticky trap on E. obliqua, WC-MR-018-2 (AMSA: K377241); 8 males, same data except 31°10’23’’S 152°9’46’’E, 1060m, sticky trap on E. campanulata, WS-KF-018-4 (AMSA: K377242); 3 males, same data except 31°10’23’’S 152°9’45’’E, 1060m, sticky trap on E. obliqua, WC-KF-018-2 (AMSA: K377245); 3 males, same data except 31°12’0’’S 152°9’0’’E, 1060m, sticky trap on E. nobilis, WC-MR-018-6 (AMSA: K377247); 2 males, same data except 31°16’42’’S 152°5’5’’E, 1040m, sticky trap on E. obliqua, WS- GB-018-1 (AMSA: K377253); 2 males, same data except 31°12’0’’S 152°5’5’’E, 1060m, sticky trap on E. obliqua, WS-GB-018-1 (AMSA: K377254); 2 males, same data except 31°10’23’’S 152°9’45’’E, 1060m, sticky trap on E. obliqua, WS-KF-018-5 (AMSA: K377255); 14 males, same data except 31°11’24’’S 152°9’39’’E, 1030m, sticky trap on E. campanulata, WS-WT-018-1 and WS-WT-018-3 (AMSA: K377259, K377260); 2 males, same data except 31°12’0’’S 152°9’0’’E, 1060m, sticky trap on E. campanulata, WC-MR-018-3 (AMSA: K377261); 4 males, same data except 31°11’56’’S 152°10’23’’E, 1025m, sticky trap on E. campanulata, WC- WIN-018-3 (AMSA: K377262); 5 males, same data except 31°10’23’’S 152°9’45’’E, 1060m, sticky trap on E. campanulata, WS-KF-018-3 (AMSA: K377263); 1 male, same data except 31°10’23’’S 152°9’45’’E, 1060m, sticky trap on E. nobilis, WS-KF-018-6 (AMSA: K377265); 1 male, same data except 31°16’50’’S 152°3’19’’E, 1045m, sticky trap on E. obliqua, WS-FC-018-2 (AMSA: K379011); 2 males, same data except 31°16’42’’S 152°5’5’’E, 1040m, sticky trap on E. dives, WS-GB-018-4 (AMSA: K379015); 5 males, same data except 31°16’50’’S 152°3’19’’E, 1045m, 1.xii–7.xii.1997, sticky trap on E. campanulata, WS-FC-127-3 (AMSA: K379104); 4 males, same data except 31°16’50’’S 152°3’19’’E, 1045m, 1.xii–7.xii.1997, sticky trap on E. saligna, WS-FC-127-5 (AMSA: K379108); 1 male, Werrikimbe NP, Gunny Bag, 31°16’42’’S 152°5’6’’E, 1040m, E. Tasker & R. German 29.i–4.ii.1998, sticky trap, WS-GB-018-2 (AMSA: K379012).Published as part of Kurina, Olavi, Hippa, Heikki & Amorim, Dalton De Souza, 2019, Notes on Manota Williston (Diptera: Mycetophilidae) from Australia and Papua New Guinea, with description of two new species, pp. 385-395 in Zootaxa 4555 (3) on pages 386-387, DOI: 10.11646/zootaxa.4555.3.7, http://zenodo.org/record/262452
The higher the propofol concentration needed for loss of consciousness the larger its difference to the concentrations required at maintenance, using TCI and BIS guided anesthesia: 9AP9-8
No full textRotinas de controlo de gestão e disciplina na execução da estratégia : estudo de caso da Amorim Florestal
No full textCom o passar dos anos, o controlo de gestão tem assumido um papel cada vez mais importante nas organizações. Este é o responsável por garantir que os objetivos da organização são alcançados através de um conjunto integrado de ferramentas, metodologias e processos de gestão. Para garantir que os objetivos são alcançados, as organizações implementaram rotinas de controlo de gestão, com a finalidade de acompanhar de forma contínua o progresso dos objetivos definidos. Essas rotinas são geralmente lideradas pela função organizacional de controlo de gestão (controllers), os quais têm a responsabilidade de supervisionar e garantir a eficácia dessas atividades. A função de controller tem sido marcada por uma crescente sofisticação e abrangência das responsabilidades, principalmente em empresas de maior dimensão. Enquanto no passado o papel do controller era principalmente o de monitorizar as transações financeiras da empresa e produzir relatórios financeiros, atualmente, não é apenas isso o esperado da função. Esta passou a incluir outras atividades, tais como, planeamento e análise. Passou então a existir uma ligação muito mais próxima à estratégia, o que permitiu atuarem em estreita colaboração com os líderes da organização. O presente estudo, tendo por base os contributos disponíveis na literatura, pretende analisar de que forma a evolução do contexto organizacional pode impactar na função de controlo de gestão e as suas rotinas. Para essa análise, foi estudada a evolução do papel dos controllers que, consequentemente, tem vindo a exigir outro tipo de competências para o desempenho da função. De forma a analisar o caso num contexto real, foi estudada a empresa onde o autor trabalha, a Amorim Florestal, uma das empresas do grupo Corticeira Amorim. Para a análise foram realizadas entrevistas aos profissionais da área na empresa. A vii análise empírica efetuada permitiu concluir que a função de controlo de gestão assume um papel preponderante na organização, com modelo e rotinas muito bem definidas, que são identificadas como um dos principais fatores de sucesso do grupo. Identifica-se também uma evolução ao longo do tempo na função de controller, em que não se restringe exclusivamente ao reporte, mas sim a um conjunto de processos mais abrangente, com intervenção ao longo de todo o modelo de planeamento e controlo de gestão.Over the years, management control has assumed an increasingly important role in organizations. It is responsible for ensuring that organisations objectives are achieved through an integrated set of management tools, methodologies and processes. To ensure that the objectives are achieved, organisations have implemented management control routines in order to continuously monitor the progress of the defined objectives. Such routines are usually led by the organizational function of management control (controllers) who have the responsibility of supervising and ensuring the effectiveness of these activities. The role of controller has been marked by a growing sophistication and broader scope of responsibilities, especially in larger companies. While in the past the controller’s role was primarily to monitor the company's financial transactions and produce financial reports, today it is not only this that is expected of the function. Now it includes other activities, such as planning and analysis. There is a much closer connection to the strategy, which allowed the controller to act in close collaboration with the leaders of the organisation. The present study, based on the contributions available in the literature, aims to analyze how the evolution of the organizational context can impact on the management control function and its routines. For this analysis, we studied the evolution of the role of controllers that, consequently, has been requiring another type of skills for function performance. In order to analyze the case in a real context, the company where the author works, Amorim Florestal, one of the companies of the Corticeira Amorim group, was studied. For the analysis, interviews were conducted with professionals in the company. The empirical analysis carried out allowed us to conclude that the management control function assumes a preponderant role in the organisation, ix with a very well defined model and routines, which are identified as one of the main success factors of the group. It’s also identified an evolution over time in the function of controller, in which it is not restricted exclusively to reporting, but rather to a more comprehensive set of processes, with intervention throughout the planning model and management control
- …
