110,649 research outputs found
Isabella Jane Kell
No full textDate:1852-04Isabella Jane was born on 1 April 1852 to Ann and George Birkett in Liverpool, Lancashire, six years earlier than sister, Annie (later to become Annie Holtze). Isabella married William Rattray, a merchant mariner, on 19 August 1877. They married at sea on the Angola. Isabella was 25 and her husband 31 when they married. Isabella and William had a son, George Stanley Birkett Rattray, born 5 June 1878 in Liverpool. Isabella worked as a nurse at the Adelaide Hospital before she was transferred to Burra. Isabella arrived in Palmerston on 1 December 1888 to take over the position of Matron at the Palmerston Hospital from Jane Meissner. The hospital had no laundry, operating theatre or proper kitchen; all the while servicing 130 people a year. Matron Birkett had to seek permission from the Government Resident G L Parsons to employ a washerwoman in 1889. Her time at the hospital was not without controversy the Hospital Board was subject to an inquiry because a leper patient was nursed there and the Government Medical Officer had not been told. Known as the ?Marcus Baker Case', Isabella Birkett gave evidence. This case resulted in The Leprosy Ordinance of the Northern Territory. From nursing the leper patient the staff learned much about the diagnosis and treatment of the disease. After six years Matron Birkett was replace by Matron Freda Reinhardt who had arrived from Adelaide in February 1892. In 1893 Isabella's son George and her sister Margaret arrived in Adelaide on 19 November 1893 on the ?Gulf of Venice' from Liverpool and later joined her in Palmerston. Isabella left her position as matron to marry Walter Kell at Palmerston on Monday 8 January 1894. The couple left for Burrundie the morning after the wedding, where Walter had been gazetted as the Post and Telegraph Master at the Burrundie Overland Telegraph Station. In 1895, when Isabella was 43, she was one of the 82 women who enrolled to vote after the franchise was granted to South Australian and Territory women in 1894. She registered at Burrundie and her occupation was listed as 'married woman'. In 1896, Walter was Stationmaster at Powell's Creek where he was also appointed Inspector of Stock from 1900. The couple was removed from the Powell's Creek Roll on 20 December 1905 because they left the district for Wallaroo in South Australia. Walter died suddenly at home on 3 November 1919 aged 58. Isabella died at home in Wallaroo aged 74 in 1926. The couple are buried together in Wallaroo Cemetery.NurseEnglis
The regime of Isabella and Mortimer 1326 - 1330
No full textThe rule of the Despensers was brought to an end in 1326 by a coalition of magnates, churchmen and Londoners, drawn together by the invasion of Isabella and Mortimer. A carefully orchestrated demand for the removal of Edward II led to his deposition and ultimately to his murder at Mortimer's direction. Power was centralised in the hands of Isabella and Mortimer who took no steps to broaden the basis of their government. While returning confiscated lands to their supporters, they offered them little else in the way of reward but accumulated land to their own use, Crown land in the case of Isabella and an empire on the Welsh March in the case of Mortimer. Disillusioned by this and by their exclusion from government, the constituent parts of the coalition fell apart. Active opposition which had begun in Edward II's lifetime culminated in Lancaster's abortive rebellion of 1328-29. The effective suppression of this meant that opposition was stifled by the imposition of recognisances and because several barons fled abroad. This success merely served to increase Mortimer's arrogance and in 1330 he successfully engineered the downfall of Edward III's uncle, the earl of Kent. In foreign affairs, the failure of the Weardale campaign against the Scots and the unpopular peace of Northampton, coupled with a temporising and indecisive policy towards France over the questions of Gascony and homage, increased hostility towards the government. At home violent unrest continued and an improvident and irresponsible attitude to national finance involved heavy borrowing at a time when Mortimer lived in extravagant state. Faced by this misgovernment and fearing that Mortimer now aimed at royal power, Edward III built his own supporting group around him. When the opportunity came he struck swiftly at Mortimer, sending him to execution and Isabella into retirement
O paradis sorti de l'onde
No full textPays merveilleux, jardins fortunasO ridente suol, vago e bel giardinO thou smiling land, garden wide and fairFrom L'Africaine (1860); English version by Isabella G. Parke
Canova, Elena e Isabella
No full textConferenza a margine della mostra "Canova. I volti ideali", dal titolo "Canova, Elena e Isabella" (5 febbraio 2020, Galleria d'Arte Moderna di Milano, sala da ballo).
Un approfondimento sulla scultura canoviana incentrato su quella che fu all’epoca la più celebre e ammirata delle “teste ideali” realizzate da Antonio Canova: il busto di Elena. Dedicato alla più bella delle donne, il busto è l’emblema della bellezza ideale canoviana e al centro di un complesso intreccio che unisce arte, letteratura, poesia e politica. Donato da Canova a Isabella Teotochi Albrizzi, fu ammirato da scrittori e poeti di tutta Europa e cantato da George Byron
Il problema dell’autore in Simone Weil. La dialettica tra personale e impersonale.
No full textC’è un legame tra vita e pensiero? È opportuno interrogarsi sull’identità di chi scrive, sul suo carattere, indagare gli accadimenti più importanti della sua esistenza al fine di comprenderne l’opera? O è meglio mettere l’autore fra parentesi e concentrarsi sul messaggio che il testo veicola, occupandoci solo della sua veridicità? Questo problema è ormai da diversi anni entrato in modo prepotente nel dibattito letterario e filosofico, un dibattito a cui Simone Weil ha partecipato a modo suo. La soluzione proposta dalla filosofa francese è complessa in quanto presuppone la relazione dialettica tra la dimensione personale e quella impersonale presenti entrambe nell’autore.
Weil suggerisce che, se da un lato l’opera va oltre la singola individualità dell’autore, dall'altro non si può negare l’esistenza di un legame tra vita e pensiero. Pur riconoscendo che la biografia non può
spiegare completamente l’opera, ritiene che tra le due permanga pur sempre un rapporto. Secondo la filosofa francese, le opere di prim’ordine sono quelle in cui l’autore, mediante una rigorosa ascesi dell'attenzione e dello sguardo, riesce a superare il suo punto di vista parziale e ad accedere a una visione obiettiva. Pertanto, pur mantenendo l’opera al centro dell'attenzione, non si può trascurare il contesto personale dell’autore nel processo di comprensione e interpretazione.Is there a connection between life and thought? Is it appropriate to inquire into the identity of the author, their character, and investigate the most significant events of their existence to understand their work? Or is it better to put aside the author and focus solely on the message conveyed by the text, concerning itself only with its truthfulness? This issue has forcefully entered the literary and philosophical debate in recent years, a debate in which Simone Weil participated in her own way. The solution proposed by the French philosopher is complex, as it presupposes the dialectical relationship between the personal and impersonal dimensions present in the author.
Weil suggests that, on the one hand, the work transcends the individuality of the author, but on the other hand, the existence of a connection between life and thought cannot be denied. While acknowledging that a biography cannot fully explain the work, she believes that a relationship between the two always persists. According to the French philosopher, outstanding works are those in which the author, through a rigorous asceticism of attention and perception, manages to transcend their partial point of view and access an objective vision. Therefore, while keeping the work at the center of attention, one cannot overlook the personal context of the author in the process of understanding and interpretation
Funisciurus isabella
No full textFunisciurus isabella (Gray, 1862). Proc. Zool. Soc. Lond., 1862:180. TYPE LOCALITY: Cameroon, "... from the Camaroon Mountains, 7000 feet (2100 m) above the level of the sea... " DISTRIBUTION: Cameroon, Central African Republic, Congo. SYNONYMS: dubosti Eisentraut, 1969; duchaillui Sanborn, 1953.Published as part of Robert S. Hoffmann & Charles G. Anderson, 1993, Order Rodentia - Family Sciuridae, pp. 419-465 in Mammal Species of the World (2 nd Edition), Washington and London :Smithsonian Institution Press on page 427, DOI: 10.5281/zenodo.735313
Isabella tanoa Ekins, Erpenbeck, Wörheide & Hooper, 2016, n. sp.
No full textIsabella tanoa n. sp. (Figs 6–12, Table 1) Material examined. Holotype - MNHN DCL 4111 (fragment of holotype QM G 318737) Antigonia seamount, Norfolk Ridge, 23.367 S, 168.034 E, 180–250 m, RV Alis, 26 /06/ 2001, Waren dredge, coll. Bertrand Richer de Forges, Tin-Yam Chan, Bernard Cohen, Enrique MacPherson, Marie-Catherine Boisselier, Pierre Lozouet. Paratypes - QM G 318765, G 335130 Jumeau West seamount, Norfolk Ridge 23.669 S 168.009 E, 237–250 m, RV Alis, 21 /06/ 2001, Waren dredge, coll. Bertrand Richer de Forges, Tin-Yam Chan, Bernard Cohen, Enrique Mac- Pherson, Marie-Catherine Boisselier, Pierre Lozouet. G 318803 Blanc Nouveau 2 seamount, Norfolk Ridge, 23.302 S, 168.247 E, 185–207m, RV Alis, 27 /06/ 2001, Waren dredge, coll. Bertrand Richer de Forges, Tin-Yam Chan, Bernard Cohen, Enrique MacPherson, Marie-Catherine Boisselier, Pierre Lozouet. Description. Growth Form. Massive shallow cup like sponge, with a broad base and an even margin. Dimensions of the holotype are 59 mm long, 49 mm wide and 31 mm high. The other specimens range from 50–82 mm in diameter and 16–42 mm high. As one of the paratypes (G 335130) appears to be a triangular sector from a circular dish, we suspect this species could grow significantly larger than recorded here (Fig. 6). Colour. Wine dark purple on deck and wine dark purple/brown in ethanol (Fig. 6). Oscules. There are numerous microscopic exhalant oscules 0.05–0.2mm in diameter (Fig. 6), also seen to be minute under scanning electron microscopy (Fig. 7). Texture. Hard, stony but compressible and slightly hispid with a brittle compressible ectosomal crust. Surface ornamentation. Slightly hispid caused by oxeas protruding several millimetres above the surface every couple of millimetres (Fig. 7). Ectosomal skeleton. There is a thin (1mm) ectosomal crust of microscleres with smooth dichotriaenes perpendicular to the surface. The microscleres consist of abundant asymmetrical microspinose spiraster streptasters with short thick arms, and microxeas. The microxeas consist of thin microspinose centrotylote microxeas and microspinose microxeas. There are also brushes of long smooth oxeas, which originate in the choanosome and punctuate the surface by several millimetres. There is occasionally detritus embedded in the ectosome. Choanosomal skeleton. The skeleton in the subectosomal region of the choanosome consists of a 3 D matrix of regular and slightly curved dicranoclone desmas with some tubercles. Further into the choanosome the desmas change from long thin graceful dicranoclones into heavier interlocked dicranoclones with multiple zygosis. Choanosomal microscleres consist of microspinose spiraster streptasters with slender arms and occasional centrotylote oxeas. There are bundles of smooth very long curved oxeas that extend through the ectosome to the surface. Megascleres. There are two main smooth ectosomal dichotriaenes, one has delicate long shafted dichotriaenes with acerate rhabdome tips. There are also and slightly more commonly encountered delicate short-shafted dichotriaenes with smooth rounded rhabdome tips. Subectosomal choanosomal dicranoclone desmas are smooth and slender with small terminal tubercules. Dicranoclone desmas deep within the choanosome are thicker, interlocking, with more numerous tubercles with saddle zygoses. Oxeas are very long thin and sharp originating in the choanosome and extending in bundles out to the exterior of the sponge (see Fig. 7). Microscleres. Centrotylote microacanthoxeas are very common. The microscleres consist of abundant symmetrical microspinose spirasters with long thin arms and asymmetrical microspinose streptasters with short thick arms. DNA signature sequence. CO 1 sequences are deposited in NCBI Genbank (Accession number KX 267961 – KX 267963) and the Sponge Barcoding Database (Accession number 1643–1645). Etymology. Tanoa is the name of the mixing bowl used in the Yangona drinking ceremony in the Pacific Islands. The morphology of the sponge shares the basic bowl shape of the Tanoa. Isabella tanoa sp nov QM G Isabella tanoa sp nov QM G Isabella tanoa sp nov QM G Isabella harborbranchi KM Isabella harborbranchi KM Isabella harborbranchi KM Isabella harborbranchi KM Isabella mirabilis genotype F QM G Isabella mirabilis genotype F QM G Isabella mirabilis genotype F QM G Isabella mirabilis genotype F QM G Isabella mirabilis genotype F QM G Isabella mirabilis genotype F QM G Isabella mirabilis genotype F QM G Isabella mirabilis genotype F QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype C QM G Isabella mirabilis genotype D QM G Isabella mirabilis genotype D QM G Isabella mirabilis genotype E QM G Isabella mirabilis genotype E QM G Isabella mirabilis genotype E QM G Isabella mirabilis genotype E QM G Isabella mirabilis genotype E QM G Isabella mirabilis genotype E QM G Neoaulaxinia zingiberadix QM G Neoaulaxinia zingiberadix QM G Neoaulaxinia zingiberadix QM G Neoaulaxinia zingiberadix QM G Neoaulaxinia zingiberadix QM G Neoaulaxinia zingiberadix QM G Neoaulaxinia zingiberadix QM G Neoaulaxinia zingiberadix QM G 12 I. tanoa I.mirabilis 10 genotype F I. mirabilis 8 genotype C I. mirabilis genotype D Spicule width (µm) 6 I. mirabilis genotype E 4 2 0 0 20 40 60 80 100 120 140 160 Spicule Length (µm) 35 I. tanoa 30 I. mirabilis genotype F 25 I. mirabilis genotype C 20 I. mirabilis genotype D Spicule Width I. mirabilis genotype E (µm) 15 10 5 0 0 5 10 15 20 25 30 35 Spicule Length (µm) Remarks. Morphological distinction of Isabella spp. Isabella tanoa’s overall morphology resembles a Tanoa or Yangona bowl or mortar. The two paratypes resemble shallow bowls, and have similar colour and texture to both I. mirabilis and I. harborbranchi, whereas the holotype of I. tanoa lacks the characteristic warts that give I. mirabilis its warty appearance. Isabella tanoa differs from both I. mirabilis and I. harborbranchi in not having any smooth microxeas. Although microxeas are not specifically mentioned in the description of Carvalho et al. (2015), they include in their table oxeas whose smallest size is 100 µm long. The centrotylote microacanthoxeas are listed as rare in I. harborbranchi but abundant in I. tanoa and I. mirabilis. Isabella mirabilis also has smooth centrotylote microxeas. The microspined microxeas in I. tanoa are generally more slender than those in I. mirabilis and I. harborbranchi. I. tanoa lacks the fusiform microacanthoxeas found in I. mirabilis and I. harborbranchi and the long thin blunt oxeas found in I. harborbranchi. Isabella tanoa and I. mirabilis both have extremely long and slightly curved oxeas. However they are longer and thicker in I. tanoa. Both I. tanoa and I. mirabilis species have long oxeas, which pierce the surface in brushes, extending several millimetres above the sponge surface. Isabella tanoa does not have either of the shorter oxeas found in I. harborbranchi. Isabella tanoa lacks the long and short-shafted triaenes present in I. mirabilis and I. harborbranchi. Isabella tanoa has short-shafted dichotriaenes with rounded rhabdome tips, that are also present in I. mirabilis, however the dichotriaenes in I. tanoa are delicate and slender and only half the width of the stouter I. mirabilis dichotriaenes. All three species have similar large spirasters with long thin arms. Isabella mirabilis contain thick streptasters ‘Jacks’ that do not occur in either I. tanoa or I. harborbranchi. However, only I. tanoa and I. harborbranchi have the long spirasters with short thick thorny arms. Isabella tanoa has a combination of both graceful desmas in the subectosome region and the interlocking desmas as in I. mirabilis in the choanosomal skeleton. Both I. tanoa and I. mirabilis have an ectosomal skeleton which is easily differentiated and separable from the choanosomal skeleton, unlike in the skeleton of I. harborbranchi. Molecular distinction of I. tanoa sp. nov. The final data set consisted of 56 taxa and resulted in a dataset of 563 characters of which eleven (= 2 %) were variable among the Isabella spp (see Table 2). In I. mirabilis the CO 1 sequences differentiated specimens into four distinct genotypic groups labelled here as genotype C to F (see Ekins et al. (2015) with 0.2–0.5 % (uncorrected p-) difference. CO 1 sequences were identical for all the specimens of I. tanoa, but differed from sequences of I. mirabilis by 0.9–1.1 % and I. harborbranchi by 1.1 % (see Table 2). Maximum likelihood reconstructs the three species as highly supported monophyletic with a sister group relationship between I. harborbranchi and I. tanoa. Taxon\Position* 318 406 408 410 411 420 426 438 456 618 654 I. mirabilis C A G A A A T A G T G G I. mirabilis D A G A A A T A G T T G I. mirabilis E A G A A A T T G T G G I. mirabilis F A G A A A G T G T G G I. tanoa sp. nov. A C T C C G T G T G T I. harborbranchi G A T C A G T A C G G * referring to A. queenslandica CO 1 (NCBI Genbank NC 008944) Comparative morphometric analysis and variability. The length and width measurements of the spirasters of I. mirabilis and I. tanoa (Fig. 11), show a large overlap with I. tanoa at the smaller end of the scale. However, the differences between the two species, I. mirabilis and I. tanoa, are highly significant (P <0.001) across all of the genotypes for both measurements. There are also some slight variations within and between some genotypes of I. mirabilis. Dichotriaenes are extremely variable in shape and size in I. mirabilis (Fig. 12), with variation between individuals being more pronounced than the variation between the genotypes. However, the differences between the two species are very obvious despite these shape and size variations, as shown in Figure 12, where the major differences are in the thickness of the rhabdome and dichotriaene arms (P <0.001). There are also significant differences in the diameter of the cladome (P <0.05) and length of the rhabdome (P <0.001) between I. tanoa and all the genotypes of I. mirabilis. The delicate dichotriaenes of I. tanoa dichotriaenes also separate readily into short and long shafted dichotriaenes as seen in Figure 12. 90 I. mirabilis genotype C 80 I. mirabilis genotype D 70 I. mirabilis genotype E ) µm 60 ( I. mirabilis genotype F width 50 I. tanoa long shafted Rhabdome 40 30 I dichotriaenes dichotriaenes. tanoa short shafted 20 10 0 0 200 400 600 800 1000 1200 1400 Rhabdome length (µm) 12 I. mirabilis genotype C 10 I. mirabilis genotype D I. mirabilis genotype E 8 I. mirabilis genotype F Spicule Width 6 (µm) 4 2 0 0 50 100 150 Spicule Length (µm) Some significant differences were found in measurements of lengths and widths of the centrotylote microacanthoxeas for I. mirabilis and I. tanoa (as shown in Figure 10). However, the differences between the two species I. mirabilis and I. tanoa, are unique in that they are highly significant across all of the genotypes (P <0.001). Measurements of centrotylote microacanthoxeas for individual specimens of I. mirabilis show that significant differences were found within the four genotypes of this species (see Table 2), overshadowing any significant differences between the genotypes, such that morphometric differences between specimens were masked. Some specimens also had a larger number of centrotylote microacanthoxeas than non-centrotylote microacanthoxeas, some had triaenes, and some showed differences in the shape of their dichotriaenes, but these trends cut across the different genotypes. The variation within and between the specimens highlights the variability of these spicules within this species. 10 9 I. mirabilis genotype C 8 7 I. mirabilis genotype D 6 I. mirabilis genotype E Spicule Width 5 (µm) I. mirabilis genotype F 4 3 2 1 0 0 5 0 1 0 0 150 200 250 300 Spicule Length (µm) 10 I. mirabilis genotype C 9 8 I. mirabilis genotype D 7 I. mirabilis genotype E 6 I. mirabilis genotype F Spicule Width 5 (µm) 4 3 2 1 0 0 100 200 300 400 Spicule Length (µm) 25 I. mirabilis genotype C 20 I. mirabilis genotype D I. mirabilis genotype E 15 I. mirabilis genotype F Spicule Width (µm) 10 5 0 0 5 10 15 20 25 Spicule Length (µm) Comparisons of lengths and widths of the non-centrotylote microacanthoxeas, smooth centrotylote microxeas, smooth non-centrotylote microxeas and ‘Jack’ streptasters spicule types between and within the four genotypes of I. mirabilis indicate that they are similar to each other (Figs 13–16). Whilst significant differences do exist between some combinations of genotypes, there are never any consistent significant differences between any two genotypes (see Appendix/ Supplementary Material). Moreover there are significant differences between individuals within each genotype for these spicule types, indicating that measurements within this species are insufficient to justify the separation into four separate species. The absence of any triaene in genotype D of I. mirabilis is the most obvious difference between the four genotypes of this species. However, there are only two specimens of this genotype and the reality is that triaenes were not observed in all specimens of the other genotypes either (including the holotype) (see Table 2), and as such this character is interpreted as a secondary loss within specimens of this species.Published as part of Ekins, Merrick, Erpenbeck, Dirk, Wörheide, Gert & Hooper, John N. A., 2016, A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge, pp. 433-460 in Zootaxa 4136 (3) on pages 444-455, DOI: 10.11646/zootaxa.4136.3.2, http://zenodo.org/record/26736
G. Imbriano, Der Begriff der Politik. Die Moderne als Krisenzeit im Werk von Reinhart Koselleck
No full textRecensione a G. Imbriano, Der Begriff der Politik. Die Moderne als Krisenzeit im Werk von Reinhart Kosellec
Isabella County (Michigan), Greendale oil field
No full textGeneral view in Greendale field, Isabella Co., Michigan. (1934)GrayscaleClapp Nitrate Negative, Box 1
Clinical correlates of human leucocyte antigen (HLA)-G in systemic sclerosis
No full textHuman leucocyte antigen (HLA)-G has a tolerogenic function and could play a role in the pathogenesis of immune-mediated diseases, including systemic sclerosis (SSc). The aim of this study was to evaluate HLA-G serum expression (sHLA-G) and the HLA-G gene 14 base pairs (bp) insertion/deletion (del(-)/del(+)) polymorphism in patients with Ssc, to search for possible associations with clinical and laboratory variables. sHLA-G was measured by enzyme-linked immunosorbent assay (ELISA) in sera from 77 patients with SSc and 32 healthy donors (HD); the 14 bp del(-)/del(+) polymorphism was evaluated by polymerase chain reaction (PCR) amplification of peripheral blood mononuclear cells (PBMC) genomic DNA. Receiver operating characteristics (ROC) analysis identified the HLA-G cut-off that best discriminated dichotomized clinical and serological variables, that was subsequently employed to subdivide SSc patients into HLA-G high (HLA-G(+)) and low (HLA-G(-)) profile groups. sHLA-G were not statistically different between SSc patients and HD, nor between distinct SSc autoantibody subsets. Subdividing SSc patients by HLA-G positivity or negativity yielded significant differences for the modified Rodnan skin score (mRss) (P = 0.032), 'general' (P = 0.031) and 'kidney' (P = 0.028) Medsger severity scores (MSS) and disease activity index, and especially Δ heart/lung (P = 0.005). A worse 'general' MSS (P = 0.002) and Δ heart/lung (P = 0.011) were more frequent in the low sHLA-G group. These two variables and mRss were associated with sHLA-G levels at logistic regression analysis. Treatment had no influence on sHLA-G. Moreover, a higher frequency of scleredema was detected in the del(+)/del(+) than the del(-)/del(+) group (P = 0.04). These data suggest modulatory effects of sHLA-G on SSc. Prospective studies are needed to investigate a role in predicting the disease course.
© 2015 British Society for Immunology
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