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This paper is part of a project of studying benthic diatom biodiversity on marine coastal regions of Sweden with focus on rare and less known species. Two new species of Cocconeis Ehrenb. are described from Vrångö, a small island in the west coast of Sweden. Both species were found as epiphytic on the green alga Ulva intestinalis L. Cocconeis magnoareolata Al-Handal, Riaux-Gob., R.Jahn & A.K.Wulff sp. nov. is a small species not exceeding 9 μm in length and characterized by having large subquadrangular areolae on the sternum valve. Cocconeis vrangoensis Al-Handal & Riaux-Gob. sp. nov. appears similar to some taxa of the 'Cocconeis scutellum complex', but differs by its stria density on both valves and variable features of the areola and valvocopula ultrastructure. Detailed descriptions based on light and electron microscopy examination, a comparison with closely related taxa, as well as a description of the habitat of both species are here presented.
Race has been a term avoided in the Swedish debates, while at the same time, protections with respect to unlawful discrimination on the basis of race or ethnic origins have not been vigilantly upheld by the courts. This paper looks at the treatment of race by the Swedish legislature, as well as the treatment by the courts, specifically the Labour Court, with respect to claims of unlawful discrimination in employment on the basis of ethnic origins, against the background of Critical Race Theory. The disparities between the intent of the legislature and the outcome of the cases brought to the Swedish courts can be in least in part explained through the lens of Critical Race Theory, particularly with respect to the liberal approach taken by the courts when applying the law.
The Åland Islands archipelago enjoys a special international status sui generis, which essentially encompasses demilitarisation, neutralisation, and autonomy. This status is guaranteed under international law by the agreements of 1921, 1940, and 1947, which are still in force. Furthermore, there are convincing reasons to assume that the Åland Islands regime has grown into European customary law. By virtue of her international (treaty) obligations, Finland cannot unilaterally change this status under the present conditions, irrespective of domestic (constitutional) decisions. While integration into NATO’s collective defence system and the EU’s Common Security and Defence Policy structures is compatible with the special status of the Åland Islands, care must be taken by Finland and her partners to ensure that the obligations arising from these developments are fulfilled in accordance with the demilitarised and neutralised status of the archipelago. This includes that the use by Finnish troops for preventive defence, beyond the exceptions laid down in the 1921 Åland Agreement, is only permitted in the case (of threat) of an immediate and clearly identifiable attack.
The autonomous character of the Åland Islands was established under a League of Nations dispute settlement and implemented, inter alia, in Finnish legislation. Its essence even grew into customary law. The arrangements of 1921, however, do not constitute a bilateral treaty between Finland and Sweden. The UN assumes that the international mechanism to protect Åland’s autonomy did not become obsolete with the demise of the League of Nations, but was only “suspended until such time as an express decision has been taken by the United Nations to put it back into force”. A corresponding proposal could be submitted, in any case, both by Finland and/or Sweden or possibly even by any other UN member state, for discussion in the Sixth Committee. However, the final decision to re-activate this special mechanism would have to be adopted by the UN General Assembly.
EU Law applies to the Åland Islands in principle; however, Finland’s Accession Treaty to the EU to which Protocol No. 2 on the Åland Islands was annexed, established a number of specific rules which are still in force today. This, most notably, results in the limited application of value added tax and excise duties in the Åland Islands. Therefore, the rules on customs procedures apply with respect to the movement of goods to and from the Åland Islands. In addition, other provisions of Union law, in particular those relating to fundamental freedoms and European state aid law, may be relevant in view of the special fiscal status of the Åland Islands. However, assessing individual cases would require further information and in-depth studies. Irrespective of the requirements set out in the said Protocol, the EU is obliged to respect the national identity of Member States pursuant to Article 4 para. 2 TEU; this obligation includes respect for the special status of the Åland Islands under both international and Finnish constitutional law.
Glemparon Jaschhof, 2013, a previously monotypic genus confined to Sweden, is shown here to be considerably richer in species, with most species found to occur in the Australasian region. Eighteen new species are described: G. tomelilla sp. nov. (from Sweden); G. aotearoa sp. nov., G. birhojohmi sp. nov., G. cervus sp. nov., G. didhami sp. nov, G. kaikoura sp. nov., G. nativitas sp. nov., G. orautahi sp. nov., G. otago sp. nov., G. pureora sp. nov., G. rakiura sp. nov., G. rotoiti sp. nov., G. rotoroa sp. nov., G. tewaipounamu sp. nov., G. waipapa sp. nov., G. waipoua sp. nov. (all from New Zealand); G. manuka sp. nov. and G. warra sp. nov. (both from Tasmania, Australia). Glemparon sagittifer Jaschhof, 2013 is redescribed. Genitalic illustrations are provided allowing for the effective identification of all the species known thus far. Morphological data obtained here are used for revising the generic definition. Dicerura Kieffer, 1898 is hypothesized as the sister group to Glemparon. The case of Glemparon is discussed as a perfect example of the fact that our collective ignorance of porricondyline diversity in most parts of the world is a major impediment to a better understanding of the European species.
The Swedish species of Enicospilus are reviewed. Three species are described from Swedish material; Enicospilus cederbergi sp. nov., Enicospilus intermedius sp. nov. and Enicospilus ryrholmi sp. nov. Four species: Enicospilus cerebrator Aubert, 1966, Enicospilus combustus (Gravenhorst, 1829), Enicospilus merdarius (Gravenhorst, 1829) and Enicospilus myricae Broad & Shaw, 2016, are reported from Sweden for the first time. An illustrated key to the Swedish species of Enicospilus is provided. Validity of the new species is supported by DNA barcoding.
The Swedish species of Ophion Fabricius, 1798 are revised. More than 4800 specimens and relevant type material were studied; 234 sampled specimens produced COI sequences. The study recognises 41 species, 18 of which are described as new to science, mainly from Fennoscandian material: Ophion angularis Johansson & Cederberg sp. nov., Ophion arenarius Johansson sp. nov., Ophion autumnalis Johansson sp. nov., Ophion borealis Johansson sp. nov., Ophion broadi Johansson sp. nov., Ophion brocki Johansson sp. nov., Ophion confusus Johansson sp. nov., Ophion ellenae Johansson sp. nov., Ophion inclinans Johansson sp. nov., Ophion kallanderi Johansson sp. nov., Ophion matti Johansson sp. nov., Ophion norei Johansson sp. nov., Ophion paraparvulus Johansson sp. nov., Ophion paukkuneni Johansson sp. nov., Ophion splendens Johansson sp. nov., Ophion sylvestris Johansson sp. nov., Ophion tenuicornis Johansson sp. nov. and Ophion vardali Johansson sp. nov. Barcoding analysis also indicated the possible presence of at least three additional, partly cryptic species, but these cannot be separated morphologically with certainty at this point. Ophion costatus Ratzeburg, 1848 and Ophion artemisiae Boie, 1855 are interpreted and defined. Ophion slaviceki Kriechbaumer, 1892 is excluded from synonymy with Ophion luteus Linnaeus, 1758 stat. rev. Ophion polyguttator (Thunberg, 1824) stat. rev. and Ophion variegatus Rudow, 1883 stat. rev. are excluded from synonymy with O. obscuratus Fabricius, 1798. Ophion variegatus is redescribed and a neotype is designated. Ophion albistylus Szépligeti, 1905 (syn. nov.) is synonymized with Ophion pteridis Kriechbaumer, 1879 and Ophion frontalis Strobl, 1904 (syn. nov.) is synonymized with Ophion areolaris Brauns, 1889 syn. nov. Eleven species are reported from Sweden for the first time: Ophion artemisiae, Ophion crassicornis Brock, 1982, Ophion costatus, Ophion dispar Brauns, 1895, Ophion forticornis Morley, 1915, Ophion kevoensis Jussila, 1965, Ophion ocellaris Ulbricht, 1926, Ophion perkinsi Brock, 1982, Ophion subarcticus Hellén, 1926, Ophion variegatus Rudow, 1883 and Ophion wuestneii Kriechbaumer, 1892. The study shows that a number of species that previously have been treated as highly variable taxa, actually consist of several valid species that are separable using morphological characters. An illustrated key for the determination of the Swedish Ophion species is provided.
This paper compares the boom-bust cycle in Finland and Sweden 1984-1995 with the average boom-bust pattern in industrialized countries as calculated from an international sample for the period 1970-2002. Two clear conclusions emerge. First, the Finnish-Swedish experience is much more volatile than the average boom-bust pattern. This holds for virtually every time series examined. Second, the bust and the recovery in the two Nordic countries differ markedly more from the international pattern than the boom phase does. The bust is considerably deeper and the recovery comes earlier and is more rapid. We explain the highly volatile character of the Finnish and Swedish boom-bust episode by the design of economic policies in the 1980s and 1990s. The boom-bust cycle in Finland and Sweden 1984-1995 was driven by financial liberalization and a hard currency policy, causing large pro-cyclical swings in the real rate of interest transmitted via the financial sector into the real sector and then into the public finances. JEL Classification: E32, E62, E63
Aims: Carotid intima media thickness (CIMT) predicts cardiovascular (CVD) events, but the predictive value of CIMT change is debated. We assessed the relation between CIMT change and events in individuals at high cardiovascular risk.
Methods and results: From 31 cohorts with two CIMT scans (total n = 89070) on average 3.6 years apart and clinical follow-up, subcohorts were drawn: (A) individuals with at least 3 cardiovascular risk factors without previous CVD events, (B) individuals with carotid plaques without previous CVD events, and (C) individuals with previous CVD events. Cox regression models were fit to estimate the hazard ratio (HR) of the combined endpoint (myocardial infarction, stroke or vascular death) per standard deviation (SD) of CIMT change, adjusted for CVD risk factors. These HRs were pooled across studies.
In groups A, B and C we observed 3483, 2845 and 1165 endpoint events, respectively. Average common CIMT was 0.79mm (SD 0.16mm), and annual common CIMT change was 0.01mm (SD 0.07mm), both in group A. The pooled HR per SD of annual common CIMT change (0.02 to 0.43mm) was 0.99 (95% confidence interval: 0.95–1.02) in group A, 0.98 (0.93–1.04) in group B, and 0.95 (0.89–1.04) in group C. The HR per SD of common CIMT (average of the first and the second CIMT scan, 0.09 to 0.75mm) was 1.15 (1.07–1.23) in group A, 1.13 (1.05–1.22) in group B, and 1.12 (1.05–1.20) in group C.
Conclusions: We confirm that common CIMT is associated with future CVD events in individuals at high risk. CIMT change does not relate to future event risk in high-risk individuals.
High seroprevalence of Babesia antibodies among Borrelia burgdorferi-infected humans in Sweden
(2018)
In northern Europe, tick-borne diseases such as Lyme borreliosis (LB) and tick-borne encephalitis (TBE) are well known. The actual incidence of Babesia infections, however, has remained elusive. In this study, the prevalence of antibodies against two Babesia spp. was investigated in a cohort of patients that were seropositive for Borrelia (B.) burgdorferi sensu lato (s.l.). Data were compared to a control group of healthy individuals. Sera were collected from 283 individuals residing in the southernmost region of Sweden, Skåne County. Almost one third of the sera were from patients with a confirmed seropositive reaction against B. burgdorferi s.l. All sera samples were assessed for IgG antibodies against Babesia (Ba.) microti and Ba. divergens by indirect fluorescent antibody (IFA) assays. Seropositive IgG titers for at least one of the Babesia spp. was significantly more common (p < 0.05) in individuals seropositive for Borrelia (16.3%) compared to the healthy control group (2.5%). Our findings suggest that Babesia infections may indeed be quite common among individuals who have been exposed to tick bites. Furthermore, the results indicate that human babesiosis should be considered in patients that show relevant symptoms; particularly for splenectomized and other immunocompromised individuals. Finally, the data challenges current blood transfusion procedures and highlights the current lack of awareness of the parasite in northern Europe.