78 research outputs found
Psammoecus luchti Karner 2012, sp. nov.
No full textPsammoecus luchti sp. nov. (Fig. 6) Etymology The name is dedicated to Wilhelm Lucht (1922-2000), who provided the author with much helpful advice in the course of his first steps into entomology. Material examined Holotype ♂: ‘I.R.S.A.C. – Mus. Congo | N. Rhodesia: Mpika | (Muchinga Mts.) 1700 m. | VII.1960 N. Leleup’, ‘ Dans | l’humus’ [blue label], ‘ HOLOTYPUS | Psammoecus | luchti | des. Karner’ [red label] (MRAC). Paratypes 1♂ ‘COLL. MUS. TERVUREN | Kivu: Butembo | alt. 1740 m. III.1965 | M.J. Celis et collab.’, ‘sous | Dendrocalamus’, ‘ PARATYPUS | Psammoecus | luchti | des. Karner’ [red label] (MKF). 1♂ ‘COLL. MUS. CONGO | Katanga: gal. forest. | de la Kisanga IX- | N. Leleup 1948 | (Env. d’ Elisabethville)’, ‘Récolté dans | humus’ [blue label], ‘ PARATYPUS | Psammoecus | luchti | des. Karner’ [red label] (MKF). 1 spm ‘I.R.S.A.C. – Mus. Congo | N. Rhodesia: Abercorn, | 1800m. | VII.1960 N. Leleup’, ‘Galerie forestière | de la Mwengo, | dans l’humus’, ‘ PARATYPUS | Psammoecus | luchti | des. Karner’ [red label] (MRAC). 1 spm ‘I.R.S.A.C. – Mus. Congo | N. Rhodesia: Danger Hill | à 45 km. N. de Mpika | VII.1960 N. Leleup’, ‘Humus | de galerie | forestière’ [blue label], ‘ PARATYPUS | Psammoecus | luchti | des. Karner’ [red label] (MRAC). 3 spms ‘I.R.S.A.C. – Mus. Congo | N. Rhodesia: Mpika | (Muchinga Mts.) 1700 m. | VII.1960 N. Leleup’, ‘Dans | l’humus’ [blue label], ‘ PARATYPUS | Psammoecus | luchti | des. Karner’ [red label] (MRAC). Diagnosis Lateral margins of pronotum rounded, bearing five distinct teeth with wide bases. Elytra elongate-oval, bright reddish-brown with dark, transverse band at beginning of posterior portion, sometimes with darkened suture near elytral apex; striae on elytral disc slightly wider than interstices. Parameres small, elongate, spatula-shaped. Differential diagnosis Ps. luchti sp. nov. differs from Ps. simoni Grouvelle, 1892 by the elytral striae being only slightly wider than the interstices, elytra being more elongate, elytral basis not darkened. It differs from Ps. hacquardi and Ps. marginicollis by wider bases of lateral teeth of pronotum; from Ps. hacquardi also by wider elytral striae and elytral basis not darkened; from Ps. marginicollis, Ps. parallelus, Ps. leleupi sp. nov., Ps. simoni, and Ps. laetulus by spatula-shaped parameres. It further differs from Ps. leleupi sp. nov. and Ps. laetulus by elytral basis not darkened; from Ps. personatus by shorter lateral teeth of pronotum with wider bases; and from Ps. laetulus by more rounded lateral margin of pronotum. Description BODY. Elongate oval, total length 2.80-3.19 mm (Fig. 6A). Bright reddish-brown, elytra with dark, transverse band at beginning of posterior portion, some specimens also with darkened suture near elytral apex. Antennae with 7 th- 10 th antennomere blackish brown, some specimens with darkened apex of 6 th antennomere. 11 th antennomere, sometimes also 10 th antennomere, bright yellowish brown, brighter than basal antennomeres. HEAD. Very wide, with large, protuberant eyes, temples narrowed immediately behind eyes. Head width 0.79-0.88 mm, length 0.44-0.48 mm, 1.75-1.96 times as wide as long. Eyes 0.20-0.23 mm long, distance of inner margins 0.50-0.60 mm. Puncturation on vertex coarse, relatively dense, distance between punctures irregular; pubescence composed of long erect setae, directed anteriorly; microsculpture absent. Longitudinal impressions on vertex distinct, short, attaining second third of eyes. Antennae as in Fig. 6B, long and slender, 1.45-1.55 mm long, antennomere proportions of holotype as follows: 2.6: 1.1: 1.4: 1.3: 1.5: 1.4: 1.3: 1.1: 1.0: 1.1: 2.1. PRONOTUM. Broad, shallowly impressed near apical margin and apical angles, width 0.80-0.96 mm, length 0.60-0.73 mm, 1.28-1.40 times as wide as long. Anterior angles with group of very small teeth, lateral margins with five distinct, triangular teeth; tooth I small, tooth II larger, tooth III largest, tooth IV slightly smaller than tooth III, tooth V smallest; posterior angle with very small angular tooth. Puncturation and pubescence on disc as on vertex; microsculpture absent. ELYTRA. Elongate oval, length 1.85-2.05 mm, combined width 1.15-1.40 mm, 1.44-1.65 times as long as their combined width. Rows of punctures on disc slightly wider than interstices, pubescence composed of semierect setae that are somewhat shorter as on head and pronotum; microsculpture absent. PARAMERES. Small, elongate; base less than 2 times as wide as apical extension, inner margins with few short setae, inner portion of apex with four longer setae, outer portion with one shorter and one longer seta (Fig 6C).Published as part of Karner, Michael, 2012, A revision of African Psammoecus (Coleoptera, Silvanidae) and descriptions of two new species from the collection of the Musée royal de l'Afrique centrale, pp. 1-31 in European Journal of Taxonomy 17 on pages 14-16, DOI: 10.5852/ejt.2012.17, http://zenodo.org/record/385784
Upgrade of staching device for ceramic bases of CH tipe fuses
No full textNamen diplomskega dela je bil izdelati nadgrajeno različico obstoječe zlagalne naprave v podjetju ETI Elektroelement d. o. o., ki v industrijskem obratu služi kot avtomatski proces za zlaganje keramičnih osnov za varovalke tipa CH. Prvotna naprava je delovala z napakami, ki so povzročale neželene zastoje in posledično podaljšanje delovnega cikla naprave. Napake so se pojavljale v vakuumskem prijemalu. Diplomsko delo tako zajema opis prvotne naprave, opis tehnološkega postopka in pomanjkljivosti naprave. Za tem sledita snovanje novega vakuumskega prijemala in nadgradnja naprave z novo možnostjo zlaganja keramičnih osnov. Nato preidemo na pnevmatsko in deloma električno vezavo naprave ter na koncu opišemo postopek delovanja.The purpose of the diploma was to create an upgraded version of the stacking device in company ETI Elektroelement d. o. o., which serves as an automatic process for stacking ceramic bases for CH type fuses in the industrial plant. The original device operated with errors that caused undesirable downtimes and consequently extended the working cycle of the device. The errors occurred in the vacuum gripper. The diploma includes a description of the original device, a description of the technological process, and the deficiencies of the device. This is followed by the design of a new vacuum gripper and the upgrade of the device with a new option for stacking ceramic bases. Then we move on to the pneumatic and partly electrical wiring of the device and finally describe the operation process
Source-based morphometry reveals distinct patterns of aberrant brain volume in delusional infestation
No full textLittle is known about the neural correlates of delusional infestation (DI), the delusional belief to be infested with pathogens. So far, evidence comes mainly from case reports and case series. We investigated brain morphology in 16 DI patients and 16 healthy controls using structural magnetic resonance imaging and a multivariate data analysis technique, i.e. source-based morphometry (SBM). In addition, we explored differences in brain structure in patient subgroups based on disease aetiology. SBM revealed two patterns exhibiting significantly (p < 0.05, Bonferroni-corrected) lower grey and higher white matter volume in DI patients compared to controls. Lower grey matter volume was found in medial prefrontal cortex, anterior cingulate cortex, medial temporal lobe structures (parahippocampus and hippocampus), sensorimotor cortices, bilateral insula and thalamus and inferior parietal regions. Higher white matter volume was found in medial and middle frontal and temporal cortices, left insula and lentiform nucleus. Grey matter volume was abnormal in both "psychiatric" (primary DI and DI associated with an affective disorder) and "organic" DI (DI due to a medical condition). In contrast, aberrant white matter volume was only confirmed for the "organic" DI patient subgroup. These results suggest prefrontal, temporal, parietal, insular, thalamic and striatal dysfunction underlying DI. Moreover, the data suggest that aetiologically distinct presentations of DI share similar patterns of abnormal grey matter volume, whereas aberrant white matter volume appears to be restricted to organic case
Initial Plant Growth in Sand Mine Spoil Amended with Peat Moss and Fertilizer Under Greenhouse Conditions: Potential Species for Use in Reclamation
No full textThe Great Lakes Basin exhibits the largest collection of freshwater sand dunes in the world. Sand dunes are ecologically important and support a unique assemblage of flora and fauna. Sand dunes are also economically valuable. However, when sand dunes are mined, soil quality is drastically reduced. Therefore, soil quality improvements followed by revegetation maybe necessary for successful reclamation. This study evaluates the germination and initial growth of 2 legume species, sundial lupine (Lupinus perennis) and Illinois bundleflower (Desmanthus illinoensis), and 2 warm-season grass species, Indian grass (Sorghastrum nutans) and little bluestem (Schizachyrium scoparium), in the presence of 2 soil amendments (inorganic fertilizer and sphagnum peat moss) added to spoil from a local sand mine. We sowed species in pots and propagated them under greenhouse conditions. Results indicate that sundial lupine and Illinois bundleflower exhibited the greatest germination and growth among species. Peat moss had the greatest overall impact on germination and growth while the addition of fertilizer positively affected initial growth. Based on these results, sundial lupine is recognized as a primary candidate for sand mine reclamation, while Illinois bundleflower is also recommended as an appropriate species for revegetation efforts. We recommend using soil amendments that are functionally equivalent to peat in increasing soil water holding capacity. We further suggest that fertilization may be accomplished by including legumes in plant species mixes used for revegetation. Results presented here may help to identify appropriate species and soil amendments for the reclamation of former sand mines or restoration of freshwater sand dunes
Safe Space in Times of Post-Modernity: On the practice and dynamics of Neo-Diasporic Communities
No full textIn ihrem Buch Neo-diasporische Gemeinschaften: Blouzaniyye in Sydney, Australien stellt Marie Johanna Karner eine neue Diaspora-Theorie vor, die Dynamiken des 21. Jahrhunderts berücksichtigt und neue Perspektiven auf Akteur_innen, kollektive Erzählungen und gemeinschaftsstiftende Praktiken bietet. Die Autorin entwickelt die Theorie anhand einer empirischen, interdisziplinären und multimethodischen Untersuchung libanesischer maronitischer diasporischer Gemeinschaften.In her book, Neo-diasporische Gemeinschaften: Blouzaniyye in Sydney, Australien, Marie Johanna Karner presents a new diaspora theory that considers the dynamics of the 21st century and offers new perspectives on actors, collective narratives, and community-building practices. The author develops the theory through empirical, interdisciplinary, and multi-method research on Lebanese Maronite diasporic communities
Psammoecus trimaculatus Motschulsky 1858
No full text<i>Psammoecus trimaculatus</i> Motschulsky, 1858 <p> <i>Psammoecus excellens</i> Grouvelle, 1908a: 115. <b>syn. nov.</b></p> <p> <i>Psammoecus alluaudi</i> Grouvelle, 1912: 409. <b>syn. nov.</b></p> Material examined <p> 1♀ [round, red label]; [yellow label]; ‘Psammecus [sic!] | trimaculatus | Motch. | Ceylon’ [Motschulsky’s hand] (ZMUM). 3 spms ‘Af. or. All. | Eichelbaum’ [Grouvelle’s hand], ‘Type’ [red label], ‘MUSEUM PARIS | 1917 | Coll. GROUVELLE’ [blue label], ‘ Psammoecus | excellens | G Grouv’ [Grouvelle’s hand] (MNHN). One ♂ specimen was designated as lectotpyus of <i>Ps excellens</i> Grouvelle and labelled accordingly. Holotype of <i>Ps alluaudi</i>. ♂: ‘ Madagascar | Su[???]ieville’ [blue label, Grouvelle’s hand], ‘Type’ [red label], ‘MUSEUM PARIS | 1917 | Coll. GROUVELLE’ [blue label], ‘ Psammoecus | alluaudi | G. Grouv’ [Grouvelle’s hand] (MNHN).</p> Remarks <p> Pal (1985) gave a redescription of <i>Ps. trimaculatus</i> based on material from Motschulsky’s collection (Museum Moscow) that he accepted as type material. He did not designate a lectotype. The material consisted of five specimens mounted on a single label (Pal 1996, personal communication).</p> <p>It was not possible for the present author to see this material, but he had the opportunity to study a single, female specimen from Motschulsky’s collection (ZMUM). This specimen is not assumed to be a type, while the material mentioned by Pal may be discovered again.</p> <p> Pal (1985) provided detailed figures of <i>Ps. trimaculatus</i>, including the male genitalia, and gives an overview on the taxonomy. He states that it occurs in India, Nepal, Bhutan, Sri Lanka, Myanmar, Malaysia, Australia, Japan, and Madagascar. Recently, it has also been recorded as being established in Brasil (Thomas & Yamamoto 2007).</p> <p> Both <i>Ps. excellens</i> Grouvelle and <i>Ps. alluaudi</i> Grouvelle are conspecific and have to be synonymised with <i>Ps. trimaculatus</i> Motschulsky.</p>Published as part of <i>Karner, Michael, 2012, A revision of African Psammoecus (Coleoptera, Silvanidae) and descriptions of two new species from the collection of the Musée royal de l'Afrique centrale, pp. 1-31 in European Journal of Taxonomy 17</i> on page 24, DOI: 10.5852/ejt.2012.17, <a href="http://zenodo.org/record/3857844">http://zenodo.org/record/3857844</a>
Psammoecus simoni Grouvelle 1892
No full textPsammoecus simoni Grouvelle, 1892 (Fig. 11) Psammoecus simonis Grouvelle, 1892: 287. Psammoecus simoni – Grouvelle 1908c: 476.— Pal 1985. Material examined Lectotype ♂, by present designation: ‘ Antipolo | E. Simon’, ‘TYPE’ [red label], ‘MUSEUM PARIS | 1917 | Coll. GROUVELLE’ [yellow label], ‘ Psammoecus | Simoni | ty. A. Grouv’ [Grouvelle’s hand] (MNHN). Paralectotype 1 spm with identical data as lectotype (MNHN). Other material 5 spms ‘COLL: MUS. CONGO | Madagascar: Maroansetra | (à la lumière) II/ IV-1950 | J. Vadon’ (MRAC). 1spm ‘COLL. MUS. TERVUREN | N.E. Madagascar: | Ambodivoangy 1959 | J. Vadon’ (MRAC). Differential diagnosis Ps. simoni differs by its short oval habitus and the short, stout parameres that are fused with the basal piece from all other African Psammoecus. The wide-based pronotal teeth resemble Ps. luchti sp. nov., it differs by the elytral striae being considerably wider than interstices, elytra being shorter, darkened basis of elytra, parameres short, stout and fused with basal piece. Redescription BODY. Oval, total length 2.13-3.00 mm (Fig. 11A). Surface yellowish-brown, sometimes reddish-brown, elytra with brown or blackish-brown maculae: humeral swelling, a transverse band in the middle of the elytra, the elytral suture along the posterior two thirds and the elytral apex are dark. Base of antennae yellowish or reddish brown, 6 th to 10 th antennomere darkened, 11 th antennomere yellowish-white, some specimens with light apex of 10 th antennomere. HEAD. Broad, temples narrowed immediately behind eyes; width 0.64-0.71 mm, length 0.33-0.44 mm, 1.67-1.73 times as wide as long. Eyes protuberant, rounded, 0.17-0.20 mm long, distance of inner margins 0.38-0.45 mm. Puncturation on vertex coarse, density of punctures variable, pubescence composed of long, semierect setae, directed anteriorly; microsculpture absent. Longitudinal impressions on vertex very shallow, attaining the middle of the eyes, sometimes shorter. Antennae as in Fig. 11B, 1.17-1.40 mm long, stout, antennomere proportions of lectotype as follows: 2.9: 1.3: 1.8: 1.5: 1.8: 1.6: 1.4: 1.0:1.2: 1.4: 2.8. PRONOTUM. Broad; width 0.62-0.74 mm, length 0.48-0.56 mm, 1.22-1.35 times as wide as long. Surface smooth, without impressions. Anterior angles with distinct groups of small teeth; lateral margins with four distinct teeth; tooth I very small, tooth II a little larger, teeth III and IV largest. Posterior group of teeth consisting of a larger anterior tooth and a very small, almost obtuse posterior tooth. Puncturation coarser than on vertex, punctures sometimes adjoining. Pubescence as on vertex; microsculpture absent. ELYTRA. Oval, short, length 1.35-1.70 mm, combined width 1.00- 1.23 mm, 1.27-1.43 times as long as their combined width. Rows of punctures on disc wider than interstices. Pubescence consists of long, semierect setae. Microsculpture absent. PARAMERES. Short, stout, fused with basal piece; with distinct pattern of three large setae (Fig. 11 C). Remarks In his original description, Grouvelle (1892) spells the name ‘simonis’. However, on the labels that Grouvelle added to the syntypes as well as in a later paper (Grouvelle, 1908c), he spells the name ‘simoni’. Pal (1985) also uses the latter spelling. Hence the present author considers ‘simonis’ to be a misprint and proposes to spell the name in accordance with Grouvelle (1908c) and Pal (1985).Published as part of Karner, Michael, 2012, A revision of African Psammoecus (Coleoptera, Silvanidae) and descriptions of two new species from the collection of the Musée royal de l'Afrique centrale, pp. 1-31 in European Journal of Taxonomy 17 on pages 24-26, DOI: 10.5852/ejt.2012.17, http://zenodo.org/record/385784
Psammoecus personatus Grouvelle 1919
No full text<i>Psammoecus personatus</i> Grouvelle, 1919 <p>(Fig. 1)</p> Material examined <p> <b>Holotype</b></p> <p>♀: ‘ Funchal | Madère’, ‘Type’[red label],‘MUSEUM PARIS |1917 | Coll.GROUVELLE’, ‘ Psammoecus | personatus Grl. ’ [not Grouvelle’s hand] (MNHN).</p> <p> <b>Other material</b></p> <p>1♀ ‘MUSÉE DU CONGO | Haut-Uele: Moto | - 1923 | L. Burgeon’ (MRAC). 1♂ ‘ Congo Belge: P.N.A. | 7-9-IV-1955 | P. Vanschuytbroeck | 12.743-58’, ‘Secteur Nord | riv. Mukandwe, | affl. Talya, 1.200 m’ (MRAC). 1♂ ‘MUSÉE DU CONGO | Mombassa (36 km S. | Lubero VIII-1932 | L. Burgeon’ (MRAC). 2 spms ‘COLL. MUS. CONGO | Uganda: 1400 m. | savane boisée | 5/ 8-VIII-1957 ’, ‘Mission Zoolog. I.R.S.A.C. | en Afrique orientale | P. Basilewsky et | N. Leleup’ (MRAC, MKF). 1♀ ‘MUSÉE DU CONGO | Haut-Uele: Abimva | - V- 1925 | L. Burgeon’ (MRAC). 3♀♀ ‘MUSÉE DU CONGO | Haut-Uele | Watsa, XI-1919 | L. Burgeon’ (MRAC). 1♂ ‘MUSÉE DU CONGO | Ruvenzori: Kalonge | (2050 m.) 9-VIII-1932 | L. Burgeon’ (MKF). 1♂ ‘COLL. MUS. CONGO | Kivu: Ibanda | 1952 | M. Vandelanoite’ (MRAC). 1♂ ‘I.R.S.A.C.-MUS.CONGO | Kivu: Uvira | XI-1949 | N. Leleup’ (MRAC). 1♀ ‘I.R.S.A.C.-MUS.CONGO | Kivu: Marais de la basse | Kalimabenge (Uvira) | N. Leleup XI – 1955 ’ (MRAC). 1♀ ‘I.R.S.A.C.-MUS.CONGO | Maniema: Kabambare | (à la lumière) 16/18-X-54 | N. Leleup’ (MRAC). 1♀ ‘MUSÉE DU CONGO | Ifuri: Adia | 1935 | 1.a | (R. Belot.)’ (MRAC). 1♀ ‘COLL. MUS. CONGO | Elisabethville II/ IV-1949 | Ch. Seydel”, ‘A la lumière’ (MRAC). 1♂ ‘COLL. MUS. CONGO | Elisabethville, A la | lumière XI-50/VI-51 | Ch. Seydel’ (MRAC). 1♂ ‘Madeira 19- 24.4.1978 | Garajau | Th. Palm’, ‘ Psammoecus | personatus | Grouvelle | det. G.Israelson’ (MHNAF).</p> Differential diagnosis <p> <i>Ps. personatus</i> differs from <i>Ps. marginicollis</i> Grouvelle, 1908, <i>Ps. parallelus</i> Grouvelle, 1919, <i>Ps. laetulus</i> Grouvelle, 1914 and <i>Ps. luchti</i> sp. nov. by the longer lateral teeth of the pronotum. It differs from <i>Ps. leleupi</i> sp. nov. by the narrower elytral striae, narrower bases of lateral teeth of pronotum, and slender parameres with shorter and fewer setae; from <i>Ps. hacquardi</i> Grouvelle, 1889 by the 1 st antennomere being less than two times as long as 2 nd; from <i>Ps. laetulus</i> by the maximum pronotal width being closer to the middle, narrower elytral striae, and less extensive dark elytral markings.</p> Redescription <p> BODY. Elongate oval, total length 2.50-3.00 mm (Fig. 1A). Surface yellowish brown. Elytra with round brown or blackish-brown maculae on disc and narrow macula on posterior part of suture; some specimens without elytral maculae. Antennae as in Fig. 1B, yellowish brown, 7 th to 10 th and apex of 6 th antennomere brown or blackish brown, 11 th antennomere lighter than basal antennomeres.</p> <p>HEAD. Broad, temples rounded, immediately narrowed behind eyes; width 0.69-0.83 mm, length 0.36- 0.45 mm, 1.71-1.90 times as wide as long. Eyes protuberant, 0.21-0.24 mm long, distance of inner margins 0.43-0.54 mm. Puncturation on vertex variable, moderate to very dense, distance between punctures irregular, slightly increasing anteriorly. Pubescence composed of long, semierect setae, directed anteriorly; microsculpture absent. Longitudinal impressions on vertex distinct, attaining anterior third of eyes. Antennae 1.23-1.43 mm long; antennomere proportions of holotype as follows: 2.5: 1.4: 1.4: 1.6: 1.6: 1.4: 1.1: 1.1:1.1: 1.0: 2.3.</p> <p>PRONOTUM. Broad, width 0.71-0.88 mm, length 0.48-0.60 mm, 1.35-1.50 times as wide as long. Anterior angles with distinct group of small, short teeth; lateral margins with five teeth, tooth I small, tooth II larger, tooth III the largest, tooth IV a little smaller than tooth II, tooth V very small. Posterior angle diminutive. Puncturation on disc coarser than on vertex, punctures sometimes hardly separated. Pubescence as on vertex; microsculpture mostly not visible (holotypus), some specimens showing a very shallow reticulation.</p> <p>ELYTRA. Oval, length 1.63-2.00 mm, combined width 1.08-1.38 mm, 1.35-1.56 times as long as combined width. Rows of punctures on disc somewhat narrower than interstices. Pubescense composed of long, semierect setae, directed posteriorly; microsculpture absent.</p> <p>PARAMERES. Slender, curved basally, with small setae along the inner margins and single long seta at their apices (Fig. 1C).</p>Published as part of <i>Karner, Michael, 2012, A revision of African Psammoecus (Coleoptera, Silvanidae) and descriptions of two new species from the collection of the Musée royal de l'Afrique centrale, pp. 1-31 in European Journal of Taxonomy 17</i> on pages 3-5, DOI: 10.5852/ejt.2012.17, <a href="http://zenodo.org/record/3857844">http://zenodo.org/record/3857844</a>
From Interspace To Interface: Shaping Public Life
No full textSome public spaces in the Netherlands function exceptionally well and provide significant benefit to the wider society in areas such as public health, retail activity and community participation. However, the vast majority of public space does not perform as well. One example is Oude Noorden, where the public space has failed to provide a noticeable benefit for the community and contribute to a separation between the different cultural groups within the multicultural neighbourhood. Moreover, the transition zones between public and private spaces are absent or do not work well and this results in social disconnection and poor public life. This thesis looks at the question of how spatial interventions can enhance the quality and increase public life of public spaces within a multi-cultural neighbourhood like Oude Noorden in Rotterdam. I particularly look at the design of the intermediate zone between public and private spaces, named as interface. Architects create urban areas by situating an imposing structure and the public and private spaces occurs as leftover spaces. However, it is precisely this space that is one of the main components that influence public life in-between buildings and shape our movements and behaviour. I developed design criteria that can be translated to other contents and locations to create a successful public space and increase public life.Design of the Urban FabricUrbanismArchitecture and The Built Environmen
South Korea's experience with international capital flows
No full text노트 : I would like to thank Paul Karner for research assistance and participants in the NBER International Capital Flows conference for comments on an earlier draft.The views expressed herein are those of the author(s) and do not necessarily reflect the views of the National Bureau of Economic Research
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