202,563 research outputs found
Licea nannengae Pando & Lado, Mycotaxon
No full text17. <i>Licea nannengae</i> Pando & Lado, Mycotaxon 31(2): 299 (1988) Figs. 14A–I <p>Sporophores sporocarpic, scattered to gregarious, sessile. Sporocarps subglosose, 0.05–0.2 mm diam., ridged, dark brown to yellow ochraceous. Peridium double, outer layer gelatinous, covered with refuse material, inner translucent and iridescent very thin, pale olive, smooth; dehiscence along ridges into platelets and lobes leaving a shiny base. Spores free, dark brown in mass, olivaceous brown by TL (Fig. 14 F), with a pale area, wall thick with thinner area, globose, 9.5–13.5 µm diam., smooth. By SEM the inner peridium surface is densely warted, with some warts joined in a loose reticulum, right up to the platelet margins (Figs. 14 G – H), with no prominent outgrowths; the epispore is smooth with a thinner area appearing wrinkled (Fig. 14 I).</p> <p> <i>Material examined</i>: Holotypus. SPAIN. Soria, Cubillos, 30TWM0421, 1080 m, corteza de <i>Juniperus thurifera</i> cultivado en cámara húmeda, 26-III-1986, 246 Pando (MA-Fungi 16056)!.</p> <p> <i>Habitat:</i> bark of living trees.</p> <p> <i>Distribution:</i> Norway (?), Lithuania, Russian Federation, Ireland, Germany, Spain, Kazakhstan, Mexico, Cuba, Argentina.</p> <p> <i>Icon.:</i> Pando & Lado (1988: 300, Fig. 1), Lado & Pando (1997: 122, Figs. 32a–b), Johannesen & Vetlesen (2020: 77, Figs. 39 A – C as <i>Licea</i> cf. <i>nannengae</i>), Nannenga-Bremekamp (2022: 533, Fig. 17).</p> <p> Notes. This species was described as having a smooth inner surface of the inner peridium by TL. However, by SEM, which was not available at the time of the description, the inner peridium looks densely warted (Fig. 14 H). In the collection of the holotype, that is marked with arrows (14 A), we have found sporocarps of a different species mixed in with <i>L. nannengae</i> Pando & Lado, with an almost smooth peridium and spiny spores. This may have lead to misidentification, such as reports from Colorado (Novozhilov <i>et al.</i> 2003) and Madagascar (Wrigley de Basanta <i>et al.</i> 2013) with a SEM image showing ornamented spores, and could affect distribution data. <i>Licea nannengae</i> resembles <i>L. belmontiana</i> Nann. -Bremek., however that species has darker brown sporocarps, not yellowish brown (compare Fig. 4 C with Fig. 14 B taken with the same optical instruments). The spores of <i>L. belmontiana</i> are lighter brown and not olivaceous and the inner peridial markings, as seen by SEM, are different in each species. In addition, the spores of <i>L. belmontiana</i> are ornamented, as seen by SEM, whereas those of <i>L. nannengae</i> are entirely smooth. <i>L. denudescens</i> H.W. Keller & T.E. Brooks differs from <i>L. nannengae</i> by darker, larger sporocarps (0.2–0.4 mm diam. vs. 0.05–0.2 mm diam.), sporocarps lacking ridges, and by darker spores.</p>Published as part of <i>Basanta, Diana Wrigley De, Mier, Carlos De & Lado, Carlos, 2023, A taxonomic revision of the species of Licea subg. Licea (Myxomycetes), pp. 95-128 in Phytotaxa 629 (2)</i> on pages 113-114, DOI: 10.11646/phytotaxa.629.2.1, <a href="http://zenodo.org/record/10276047">http://zenodo.org/record/10276047</a>
The role of gender in co-branding strategies of hi-tech brands and luxury brands
No full textWhat happens to male vis-à-vis female attitudes and behavioral intentions when hightech
and luxury products team up to form high-tech luxury co-branded products like HLCPs?
Our attention to HLCPs is mainly due to the fact that they represent an interesting case of brands
that are characterized by both functional attributes in which cognitive aspects are predominant,
and symbolic attributes where affective aspects are key. Provided that men and women seem to
assign different importance to both aspects, HLCPs represent a perfect setting to explore the
differences in consumer behavior between men and women
The Influence of High-Technology and Luxury Co-Branding Strategies on Cross-Cultural Consumer Evaluation and Purchase Intention
No full textGoing Beyond Counting First Authors in Author Co-citation Analysis
No full textThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
THE ELEVENTH AND TWELFTH DATA RELEASES OF THE SLOAN DIGITAL SKY SURVEY: FINAL DATA FROM SDSS-III
No full textCitation: Alam, S., Albareti, F. D., Prieto, C. A., Anders, F., Anderson, S. F., Anderton, T., . . . Zhu, G. T. (2015). THE ELEVENTH AND TWELFTH DATA RELEASES OF THE SLOAN DIGITAL SKY SURVEY: FINAL DATA FROM SDSS-III. Astrophysical Journal Supplement Series, 219(1), 27. doi:10.1088/0067-0049/219/1/12The third generation of the Sloan Digital Sky Survey (SDSS-III) took data from 2008 to 2014 using the original SDSS wide-field imager, the original and an upgraded multi-object fiber-fed optical spectrograph, a new near-infrared high-resolution spectrograph, and a novel optical interferometer. All of the data from SDSS-III are now made public. In particular, this paper describes Data Release 11 (DR11) including all data acquired through 2013 July, and Data Release 12 (DR12) adding data acquired through 2014 July (including all data included in previous data releases), marking the end of SDSS-III observing. Relative to our previous public release (DR10), DR12 adds one million new spectra of galaxies and quasars from the Baryon Oscillation Spectroscopic Survey (BOSS) over an additional 3000 deg(2) of sky, more than triples the number of H-band spectra of stars as part of the Apache Point Observatory (APO) Galactic Evolution Experiment (APOGEE), and includes repeated accurate radial velocity measurements of 5500 stars from the Multi-object APO Radial Velocity Exoplanet Large-area Survey (MARVELS). The APOGEE outputs now include the measured abundances of 15 different elements for each star. In total, SDSS-III added 5200 deg(2) of ugriz imaging; 155,520 spectra of 138,099 stars as part of the Sloan Exploration of Galactic Understanding and Evolution 2 (SEGUE-2) survey; 2,497,484 BOSS spectra of 1,372,737 galaxies, 294,512 quasars, and 247,216 stars over 9376 deg(2); 618,080 APOGEE spectra of 156,593 stars; and 197,040 MARVELS spectra of 5513 stars. Since its first light in 1998, SDSS has imaged over 1/3 of the Celestial sphere in five bands and obtained over five million astronomical spectra.Additional Authors: Berlind, A. A.;Beutler, F.;Bhardwaj, V.;Bird, J. C.;Bizyaev, D.;Blake, C. H.;Blanton, M. R.;Blomqvist, M.;Bochanski, J. J.;Bolton, A. S.;Bovy, J.;Bradley, A. S.;Brandt, W. N.;Brauer, D. E.;Brinkmann, J.;Brown, P. J.;Brownstein, J. R.;Burden, A.;Burtin, E.;Busca, N. G.;Cai, Z.;Capozzi, D.;Rosell, A. C.;Carr, M. A.;Carrera, R.;Chambers, K. C.;Chaplin, W. J.;Chen, Y. C.;Chiappini, C.;Chojnowski, S. D.;Chuang, C. H.;Clerc, N.;Comparat, J.;Covey, K.;Croft, R. A. C.;Cuesta, A. J.;Cunha, K.;da Costa, L. N.;Da Rio, N.;Davenport, J. R. A.;Dawson, K. S.;De Lee, N.;Delubac, T.;Deshpande, R.;Dhital, S.;Dutra-Ferreira, L.;Dwelly, T.;Ealet, A.;Ebelke, G. L.;Edmondson, E. M.;Eisenstein, D. J.;Ellsworth, T.;Elsworth, Y.;Epstein, C. R.;Eracleous, M.;Escoffier, S.;Esposito, M.;Evans, M. L.;Fan, X. H.;Fernandez-Alvar, E.;Feuillet, D.;Ak, N. F.;Finley, H.;Finoguenov, A.;Flaherty, K.;Fleming, S. W.;Font-Ribera, A.;Foster, J.;Frinchaboy, P. M.;Galbraith-Frew, J. G.;Garcia, R. A.;Garcia-Hernandez, D. A.;Perez, A. E. G.;Gaulme, P.;Ge, J.;Genova-Santos, R.;Georgakakis, A.;Ghezzi, L.;Gillespie, B. A.;Girardi, L.;Goddard, D.;Gontcho, S. G. A.;Hernandez, J. I. G.;Grebel, E. K.;Green, P. J.;Grieb, J. N.;Grieves, N.;Gunn, J. E.;Guo, H.;Harding, P.;Hasselquist, S.;Hawley, S. L.;Hayden, M.;Hearty, F. R.;Hekker, S.;Ho, S.;Hogg, D. W.;Holley-Bockelmann, K.;Holtzman, J. A.;Honscheid, K.;Huber, D.;Huehnerhoff, J.;Ivans, II;Jiang, L. H.;Johnson, J. A.;Kinemuchi, K.;Kirkby, D.;Kitaura, F.;Klaene, M. A.;Knapp, G. R.;Kneib, J. P.;Koenig, X. P.;Lam, C. R.;Lan, T. W.;Lang, D. T.;Laurent, P.;Le Goff, J. M.;Leauthaud, A.;Lee, K. G.;Lee, Y. S.;Licquia, T. C.;Liu, J.;Long, D. C.;Lopez-Corredoira, M.;Lorenzo-Oliveira, D.;Lucatello, S.;Lundgren, B.;Lupton, R. H.;Mack, C. E.;Mahadevan, S.;Maia, M. A. G.;Majewski, S. R.;Malanushenko, E.;Malanushenko, V.;Manchado, A.;Manera, M.;Mao, Q. Q.;Maraston, C.;Marchwinski, R. C.;Margala, D.;Martell, S. L.;Martig, M.;Masters, K. L.;Mathur, S.;McBride, C. K.;McGehee, P. M.;McGreer, I. D.;McMahon, R. G.;Menard, B.;Menzel, M. L.;Merloni, A.;Meszaros, S.;Miller, A. A.;Miralda-Escude, J.;Miyatake, H.;Montero-Dorta, A. D.;More, S.;Morganson, E.;Morice-Atkinson, X.;Morrison, H. L.;Mosser, B.;Muna, D.;Myers, A. D.;Nandra, K.;Newman, J. A.;Neyrinck, M.;Nguyen, D. C.;Nichol, R. C.;Nidever, D. L.;Noterdaeme, P.;Nuza, S. E.;O'Connell, J. E.;O'Connell, R. W.;O'Connell, R.;Ogando, R. L. C.;Olmstead, M. D.;Oravetz, A. E.;Oravetz, D. J.;Osumi, K.;Owen, R.;Padgett, D. L.;Padmanabhan, N.;Paegert, M.;Palanque-Delabrouille, N.;Pan, K. K.;Parejko, J. K.;Paris, I.;Park, C.;Pattarakijwanich, P.;Pellejero-Ibanez, M.;Pepper, J.;Percival, W. J.;Perez-Fournon, I.;Perez-Rafols, I.;Petitjean, P.;Pieri, M. M.;Pinsonneault, M. H.;de Mello, G. F. P.;Prada, F.;Prakash, A.;Price-Whelan, A. M.;Protopapas, P.;Raddick, M. J.;Rahman, M.;Reid, B. A.;Rich, J.;Rix, H. W.;Robin, A. C.;Rockosi, C. M.;Rodrigues, T. S.;Rodriguez-Torres, S.;Roe, N. A.;Ross, A. J.;Ross, N. P.;Rossi, G.;Ruan, J. J.;Rubino-Martin, J. A.;Rykoff, E. S.;Salazar-Albornoz, S.;Salvato, M.;Samushia, L.;Sanchez, A. G.;Santiago, B.;Sayres, C.;Schiavon, R. P.;Schlegel, D. J.;Schmidt, S. J.;Schneider, D. P.;Schultheis, M.;Schwope, A. D.;Scoccola, C. G.;Scott, C.;Sellgren, K.;Seo, H. J.;Serenelli, A.;Shane, N.;Shen, Y.;Shetrone, M.;Shu, Y. P.;Aguirre, V. S.;Sivarani, T.;Skrutskie, M. F.;Slosar, A.;Smith, V. V.;Sobreira, F.;Souto, D.;Stassun, K. G.;Steinmetz, M.;Stello, D.;Strauss, M. A.;Streblyanska, A.;Suzuki, N.;Swanson, M. E. C.;Tan, J. C.;Tayar, J.;Terrien, R. C.;Thakar, A. R.;Thomas, D.;Thomas, N.;Thompson, B. A.;Tinker, J. L.;Tojeiro, R.;Troup, N. W.;Vargas-Magana, M.;Vazquez, J. A.;Verde, L.;Viel, M.;Vogt, N. P.;Wake, D. A.;Wang, J.;Weaver, B. A.;Weinberg, D. H.;Weiner, B. J.;White, M.;Wilson, J. C.;Wisniewski, J. P.;Wood-Vasey, W. M.;Yeche, C.;York, D. G.;Zakamska, N. L.;Zamora, O.;Zasowski, G.;Zehavi, I.;Zhao, G. B.;Zheng, Z.;Zhou, X.;Zhou, Z. M.;Zou, H.;Zhu, G. T
Clastoderma confusum K. J. Knight & Lado 2020, sp. nov.
No full textClastoderma confusum K.J.Knight & Lado, sp. nov. (MB 832527). Type: Eagle Highway, 450 km north-east of Wiluna, Little Sandy Desert, Western Australia, 24 July 2018, K. J. Knight MC 154 [from moist chamber culture of bark of prone dead Acacia aneura, January 2019] (holo: PERTH 09078509; iso: CANB, K, MA-Fungi 90498). Clastoderma sp. Mungilli (K. J. Knight MC 154), Western Australian Herbarium, in FloraBase, https:// florabase.dpaw.wa.gov.au/ [accessed 3 October 2019]. Sporocarps gregarious, stalked, 0.25–0.46 mm high. Hypothallus bulbous and/or disc-like, sometimes insignificant, black, white or light brownish. Stalks c. 75% total height of the sporocarp, curved, frequently nodding, cylindrical, gently tapering from base to near the apex, with a slightly flared apex subtended by a small, straight section c. 10–40 × 5–10 µm; surface longitudinally rugose, dull, black or dark brown, sometimes with a pale, almost colourless section below the apex; walls pale ochraceous to colourless by transmitted light, grading to jet black c. 25 µm below the apex, densely filled with dark, granular refuse basally which becomes lighter and less dense distally. Sporotheca globose, 80–130 µm diam., dark brown or black. Peridium membranous, shiny, fugacious except for a collar and numerous minute and irregular fragments persisting either directly on the external surface of the capillitial mesh or on minute capillitial stubs of variable length along the capillitium, fragments forming an interrupted patterning of a shiny mesh with copper-coloured reflections; brown or violaceous-brown by transmitted light; collar relatively large, c. 30 µm diam., irregularly stellatewebbed between the capillitial threads, attached to the capillitium at the base and for a short distance up the threads, minutely striate. Columella absent. Capillitium with 4–6 threads radiating at almost right angles from the stalk apex; threads branching and anastomosing, forming a globose, rigid, complete, many-meshed net (the net sometimes collapsed in at the nodes but quickly expanding to globose in Hoyer’s medium); meshes mostly angular, (4–)5–7-sided, nodes not differentiated; threads straight, purple-brown or brown by transmitted light, hollow, thick-walled, flat, c. 2 µm wide throughout, without free ends, rarely with short, blunt branches within. Spores globose, (12–) 13–16 µm diam., dull brown-black or black in mass, mid-brown, brown or pink-brown by transmitted light; surface verruculose, with minute, variably sized and unevenly distributed warts, sometimes arranged in lax, short lines at ×100 with patchy areas of smooth surface, inconspicuous darker patches of warts seen at ×40; by SEM the spore surface is densely minutely ornamented with laxly sinuous ridges, the ridges decorated with struts from apex down to the spore wall and projections on the ridges forming undulating crests, ridges and struts are perforated in patches, warts rounded and occurring on the side of the ridges or between ridges in denser patches, with some thin projections emerging from the base of the wart forming fenestrations. (Figures 1, 2) Diagnostic features. This species is readily distinguished from all other species of Clastoderma by the following combination of features: a distinctive, rigid, capillitial net that arises at almost right angles from the top of the stalk; a mostly angular mesh that is ornamented with abundant, highly reflective, peridial fragments that resemble a shiny, copper-coloured net; a stellate-webbed peridial collar situated in close proximity to the capillitium; the absence of a columella; and patchy, verruculose spore ornamentation. Other specimens examined. WESTERN AUSTRALIA: Mt Caroline, 19 Apr. 2003, M. H. Brims 608 (PERTH); Giles Breakaway, 50 km NE of Laverton on Great Central Road, 1 Apr. 2019, K. J. Knight MC 169 (PERTH) . Ecology, distribution and habitat. Associated with acidic bark (bark of living Callitris columellaris, pH 4.4 – K. J. Knight MC 169, bark of prone dead Acacia aneura, pH 5.3 – K. J. Knight MC 154) and wood-based insect casings.The three known records are disjunct in WesternAustralia (WesternAustralian Herbarium 1998 –), occurring in semi-arid to arid areas in the Little Sandy Desert, Murchison and Avon Wheatbelt bioregions (Department of the Environment 2013). The type collection and K. J. Knight MC 169 are from sparse mulga over spinifex rangeland with summer rainfall, while M. H. Brims 608 is from a region characterised by eucalypt woodland or proteaceous scrub with winter rainfall. Etymology. From the Latin confusus (confused), in reference to its previous misidentification as a species of Cribraria. Vernacular name. Copper-netted Clastoderma. Conservation status. Although C. confusum is known from only three disjunct collections, it is not considered to be under conservation threat as its occurrence is likely to be more common and widespread. Myxomycetes in Western Australia are poorly known and rarely collected. Affinities. Clastoderma confusum appears to be most closely allied to C. microcarpum, a species that also has a complete, wide-meshed net and large spores, 13.5–15 µm diam. (Kowalski 1975). It can readily be distinguished from C. microcarpum by its dark brown or black sporocarps (vs ferruginous), black stalk apex (vs red-brown), patchy, verruculose spore ornamentation (vs evenly ornamented with numerous, scattered, minute papillae) and the absence of a columella. It also has a morphologically distinct capillitium with 4–6 threads that emerge at almost right angles from the stalk apex (vs branching from the columella apex into 2–4 main threads), and numerous persistent peridial fragments (vs peridial fragments entirely lacking or occasionally persisting as minute membranous expansions). Clastoderma confusum does not adhere to the most recent diagnosis of the genus and new order Clastodermatales Leontyev, Schnittler, S.L. Stephenson, Novozhilov & Shchepin proposed by Leontyev et al. (2019). These authors describe the columella as always ‘present, gradually turning into the capillitium’ and the capillitial threads as ‘branched and anastomosed, merging at the periphery to form plate-like swellings’. We note, however, that previous studies have observed that the columella may be lacking in C. debaryanum (Martin & Alexopolous 1969; Eliasson & Keller 1996; Poulain et al. 2011). Furthermore, the peridial fragments in C. confusum are shiny like the collar and irregularly shaped and thus appear to be of peridial rather than capillitial origin. As such, this contradicts what is indicated by Frederick et al. (1986) for C. debaryanum. The new species, therefore, seems to fit the broader concept of the genus Clastoderma, but an exhaustive review of their species is necessary to clarify its distinctive features. Notes. The collection M. H. Brims 608 is in poor condition due to an attack by a filamentous fungus and depauperate since it was split to confirm identification in 2004. It is somewhat atypical in having sporotheca that have mostly collapsed inwards at the capillitial nodes (as some have in the other two collections), slightly darker and smaller spores (brown and c. 12 µm diam. vs mid-brown or pinkbrown and 13–16 µm diam.), and a stalk with a distinctly paler section distally rather than black or dark-brown as in the other collections where the paler section can only be seen by transmitted light. These differences are minor and not considered to be taxonomically significant. The type substrate was not originally collected for use in a moist chamber but rather it was forwarded to the Western Australian Herbarium with the fungi Gloeophyllum abietinum growing on it. It is of interest to note that the substrate for the type species of the genus, C. debaryanum, is probably G. odoratus (Eliasson & Keller 1996), and although this new species was not growing directly on the hymenium of the fungi as per G. odoratus, there is a possibility of a relationship with this genus of fungus. For Herbarium quarantine purposes, the material was frozen at -18° C for seven consecutive days and accordingly the viability of spores was expected to be low, yet five species of slime mould were harvested, confirming that this procedure is a safe practice prior to moist chamber culture.Published as part of Knight, Karina J. & Lado, Carlos, 2020, Clastoderma confusum (Myxomycetes: Amoebozoa), a remarkable new species of slime mould from Western Australia, pp. 35-40 in Nuytsia 31 on pages 36-39, DOI: 10.5281/zenodo.406484
Mitomycin C in highly myopic eyes - Author reply
No full textOphthalmology. 2005 Feb;112(2):208-18; discussion 219.
Mitomycin C modulation of corneal wound healing after photorefractive keratectomy in highly myopic eyes.
Gambato C, Ghirlando A, Moretto E, Busato F, Midena E.
SourceRefractive Surgery Service and Antimetabolite Therapy Research Unit, Department of Ophthalmology, University of Padova, Padova, Italy.
Abstract
PURPOSE: To evaluate the role of topical mitomycin C in corneal wound healing (CWH) after photorefractive keratectomy (PRK) in highly myopic eyes.
DESIGN: Prospective, double-masked, randomized clinical trial.
PARTICIPANTS: Seventy-two eyes of 36 patients affected by high (>7 diopters) myopia.
METHODS: In each patient, one eye was randomly assigned to PRK with intraoperative topical 0.02% mitomycin C application, and the fellow eye was treated with a placebo. Postoperatively, mitomycin C-treated eyes received artificial tears (3 times daily, tapered in 3 months), whereas the fellow eye was treated with fluorometholone sodium 2% and artificial tears (3 times daily, tapered in 3 months).
MAIN OUTCOME MEASURES: Uncorrected visual acuity (UCVA) and best-corrected visual acuity (BCVA), contrast sensitivity, manifest refraction, and biomicroscopy. Contrast sensitivity was determined using the Pelli-Robson chart. Corneal confocal microscopy documented CWH.
RESULTS: Mean follow-up was 18 months (range, 12-36). No side effects or toxic effects were documented. At 12-month follow-up examination, UCVAs (logarithm of the minimum angle of resolution) were 0.4+/-0.48 and 0.5+/-0.53 (P = .03) in mitomycin C-treated eyes and corticosteroid-treated eyes, respectively. At 1 year, corneal haze developed in 20% of corticosteroid-treated eyes, versus 0% of mitomycin C-treated eyes. At 12, 24, and 36 months, corneal confocal microscopy showed activated keratocytes and extracellular matrix significantly more evident in untreated eyes (Ps = 0.004, 0.024, and 0.046, respectively).
CONCLUSION: Topical intraoperative application of 0.02% mitomycin C can reduce haze formation in highly myopic eyes undergoing PRK.
Comment in
Ophthalmology. 2006 Feb;113(2):357; author reply 357-8
Dispelling the Myths Behind First-author Citation Counts
No full textWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
Lado C : o arranjador e produtor musical na música instrumental
No full textEste trabalho apresenta os bastidores do processo de construção do álbum inédito “Lado C”, evidenciando os processos de arranjo e produção musical, com o objetivo de compreender melhor as possíveis formas de atuação nestas duas áreas dentro da música instrumental. Este trabalho, por conta do atravessamento da pandemia da COVID-19, também se propõe a demonstrar possíveis caminhos da gravação à distância, onde cada músico grava em seu home studio. O álbum “Lado C” tem o intuito de apresentar uma produção de música instrumental mais distante dos padrões de sonoridade e estética comuns ao gênero, pois quando se fala em jazz e/ou música instrumental o padrão é uma visão de que se deve gravar ao vivo, obedecendo um som mais acústico. Buscando modernizar estas concepções mais tradicionais, foram estudados aspectos de produção musical e de arranjo que pudessem proporcionar no conjunto do resultado final uma textura sonora mais processada e irreverente, com o objetivo de chegar em um produto mais original. O repertório do álbum é composto por seis composições autorais: Seventango, Percurtindo, Vendo a Vida Passar, Subliminar, Elo (parceria com Mateus Alves) e Lado C. As gravaçõs contam com a participação de vários músicos: Sandro Bonato gravou todas as Baterias, Leandro Santos gravou contrabaixo elétrico na faixa “Lado C”, Cri Ramos participou gravando contrabaixo na faixa “Vendo a Vida Passar”, Caio Maurente gravou contrabaixo acústico em “Seventango” e “Percurtindo”, e gravou contrabaixo elétrico na faixa “Subliminar”, Antônio Flores gravou guitarra em “Vendo a Vida Passar”, “Seventango” e “Percurtindo”, Adriano Sperandir gravou guitarra em “Elo” e violão em “Seventango”, Julio Herrlein gravou o violão em “Subliminar” e Bruno Coelho gravou percussões nas faixas “Elo”, “Seventango” e “Lado C”, os demais instrumentos foram gravados por mim, através de instrumentos virtuais, timbres eletrônicos de teclado, samples, etc.This paper showcases the making of the new album "Lado C", showing the processes of arrangement and musical production, in order to better understand the possible ways of acting in these two areas within instrumental music. This work, due to the COVID-19 pandemic, also proposes to demonstrate possible paths of distance recording, where each musician records in his home studio. The album “Lado C” aims to present an instrumental music production that is farther from the sound and aesthetic standards common to the genre, because when it comes to jazz and / or instrumental music, the standard approach is that it should be recorded at the same time, in a live setting, usually with more acoustic sounds. Seeking to modernize these more traditional conceptions, aspects of musical production and arrangement that could provide the final result with a more processed and irreverent sound texture were studied, in order to reach at a more original product. The album's repertoire consists of six original compositions: Seventango, Percurtindo, Vendo a Vida Passar, Subliminar, Elo (in partnership with Mateus Alves) and Lado C. The recordings have the contribution of several musicians: Sandro Bonato recorded all the Drums, Leandro Santos recorded electric bass on the track “Lado C”, Cri Ramos participated by recording bass on the track “Vendo a Vida Passar”, Caio Maurente recorded acoustic bass on “Seventango” and “Percurtindo”, and electric bass on the track “Subliminar”, Antônio Flores recorded the electric guitar in "Vendo a Vida Passar", "Seventango" and "Percurtindo", Adriano Sperandir recorded the electric guitar in "Elo" and guitar in "Seventango", Julio Herrlein recorded the guitar in "Subliminar", and Bruno Coelho recorded percussions in the tracks “Elo”, “Seventango” and “Lado C”, the other instruments were recorded by me, through virtual instruments, electronic keyboard tones, samples, etc
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