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Past concepts and synonymies of Anadenobolus monilicornis (Porat, 1876) (Spirobolida: Rhinocricidae), including the implied synonymy of Rhinocricus ectus Chamberlin, 1920, are consolidated into a formal account with the fi rst illustrations of the holotype. Prior to 1492, A. monilicornis was probably indigenous to an unknown number of southern Antillean islands, but through modern commerce, man has introduced it to Florida, Bermuda, Barbados, the Cayman Islands, and Jamaica, and probably repeatedly (re)introduced conspecifi c material to all the Lesser Antilles, resulting in subcontinuous gene pool mixing and reticulate evolution. A broad species concept is necessary to encompass the multitudinous variants, some of which have been recognized as species; only one true Caribbean species of Anadenobolus Silvestri, 1897, may exist, for which arboreus (Saussure, 1859) is the oldest name. The distribution of A. monilicornis presently extends from Bermuda and southern coastal Florida through the Greater and Lesser Antilles (excepting Cuba) to eastern coastal Venezuela and central Suriname, with outlier populations in Jamaica, the Cayman Islands, and Tampa Bay and the eastern Floridian panhandle; excepting Barbados, the indigenous range may have extended from Hispaniola through the same area. Introductions into Manitoba, Canada, and North Carolina, USA, have not yielded viable populations. Localities are newly recorded from St. Thomas, US Virgin Islands.
A consistent muscle activation strategy underlies crawling and swimming in Caenorhabditis elegans
(2014)
Although undulatory swimming is observed in many organisms, the neuromuscular basis for undulatory movement patterns is not well understood. To better understand the basis for the generation of these movement patterns, we studied muscle activity in the nematode Caenorhabditis elegans. Caenorhabditis elegans exhibits a range of locomotion patterns: in low viscosity fluids the undulation has a wavelength longer than the body and propagates rapidly, while in high viscosity fluids or on agar media the undulatory waves are shorter and slower. Theoretical treatment of observed behaviour has suggested a large change in force–posture relationships at different viscosities, but analysis of bend propagation suggests that short-range proprioceptive feedback is used to control and generate body bends. How muscles could be activated in a way consistent with both these results is unclear. We therefore combined automated worm tracking with calcium imaging to determine muscle activation strategy in a variety of external substrates. Remarkably, we observed that across locomotion patterns spanning a threefold change in wavelength, peak muscle activation occurs approximately 45° (1/8th of a cycle) ahead of peak midline curvature. Although the location of peak force is predicted to vary widely, the activation pattern is consistent with required force in a model incorporating putative length- and velocity-dependence of muscle strength. Furthermore, a linear combination of local curvature and velocity can match the pattern of activation. This suggests that proprioception can enable the worm to swim effectively while working within the limitations of muscle biomechanics and neural control.
The riparian rainforest on the streamside levees of the coastal floodplain of the Clarence River on the North Coast of New South Wales was cleared during the 1860s by small landholders seeking fertile land. Only three small remnants remain. Using a combination of historical species lists, corner trees from surveyors’ portion plans, habitat information and the NSW Scientific Committee’s (1999) determination for lowland rainforest on floodplain a conceptual model of the original distribution of rainforest suballiances on the levees of the Clarence River coastal floodplain is proposed.
Immersion freezing is the most relevant heterogeneous ice nucleation mechanism through which ice crystals are formed in mixed-phase clouds. In recent years, an increasing number of laboratory experiments utilizing a variety of instruments have examined immersion freezing activity of atmospherically relevant ice nucleating particles (INPs). However, an inter-comparison of these laboratory results is a difficult task because investigators have used different ice nucleation (IN) measurement methods to produce these results. A remaining challenge is to explore the sensitivity and accuracy of these techniques and to understand how the IN results are potentially influenced or biased by experimental parameters associated with these techniques.
Within the framework of INUIT (Ice Nucleation research UnIT), we distributed an illite rich sample (illite NX) as a representative surrogate for atmospheric mineral dust particles to investigators to perform immersion freezing experiments using different IN measurement methods and to obtain IN data as a function of particle concentration, temperature (T), cooling rate and nucleation time. Seventeen measurement methods were involved in the data inter-comparison. Experiments with seven instruments started with the test sample pre-suspended in water before cooling, while ten other instruments employed water vapor condensation onto dry-dispersed particles followed by immersion freezing. The resulting comprehensive immersion freezing dataset was evaluated using the ice nucleation active surface-site density (ns) to develop a representative ns(T) spectrum that spans a wide temperature range (−37 °C < T < −11 °C) and covers nine orders of magnitude in ns.
Our inter-comparison results revealed a discrepancy between suspension and dry-dispersed particle measurements for this mineral dust. While the agreement was good below ~ −26 °C, the ice nucleation activity, expressed in ns, was smaller for the wet suspended samples and higher for the dry-dispersed aerosol samples between about −26 and −18 °C. Only instruments making measurement techniques with wet suspended samples were able to measure ice nucleation above −18 °C. A possible explanation for the deviation between −26 and −18 °C is discussed. In general, the seventeen immersion freezing measurement techniques deviate, within the range of about 7 °C in terms of temperature, by three orders of magnitude with respect to ns. In addition, we show evidence that the immersion freezing efficiency (i.e., ns) of illite NX particles is relatively independent on droplet size, particle mass in suspension, particle size and cooling rate during freezing. A strong temperature-dependence and weak time- and size-dependence of immersion freezing efficiency of illite-rich clay mineral particles enabled the ns parameterization solely as a function of temperature. We also characterized the ns (T) spectra, and identified a section with a steep slope between −20 and −27 °C, where a large fraction of active sites of our test dust may trigger immersion freezing. This slope was followed by a region with a gentler slope at temperatures below −27 °C. A multiple exponential distribution fit is expressed as ns(T) = exp(23.82 × exp(−exp(0.16 × (T + 17.49))) + 1.39) based on the specific surface area and ns(T) = exp(25.75 × exp(−exp(0.13 × (T + 17.17))) + 3.34) based on the geometric area (ns and T in m−2 and °C, respectively). These new fits, constrained by using an identical reference samples, will help to compare IN measurement methods that are not included in the present study and, thereby, IN data from future IN instruments.
Analysis of whole cell lipid extracts of bacteria by means of ultra-performance (UP)LC-MS allows a comprehensive determination of the lipid molecular species present in the respective organism. The data allow conclusions on its metabolic potential as well as the creation of lipid profiles, which visualize the organism's response to changes in internal and external conditions. Herein, we describe: i) a fast reversed phase UPLC-ESI-MS method suitable for detection and determination of individual lipids from whole cell lipid extracts of all polarities ranging from monoacylglycerophosphoethanolamines to TGs; ii) the first overview of a wide range of lipid molecular species in vegetative Myxococcus xanthus DK1622 cells; iii) changes in their relative composition in selected mutants impaired in the biosynthesis of α-hydroxylated FAs, sphingolipids, and ether lipids; and iv) the first report of ceramide phosphoinositols in M. xanthus, a lipid species previously found only in eukaryotes.
At the forefront of those who tenaciously pondered this issue are, I would claim, Walter Benjamin and Ludwig Wittgenstein. Benjamin and Wittgenstein both are philosophers of language who tried to establish in unique ways the doctrine of resemblance respectively: "Lehre vom Ähnlichen" and "[Lehre der] Familienähnlichkeit." What they see and find in language are not communication and mutual understanding but instead one of the weirdest phenomena in/of the world, viz., resemblance (likeness) in/of language. This phenomenon, I would insist, indicates the correlation of appearing and disappearing, of differentiating and integrating, and of dividing and imparting of language as such. For Benjamin and Wittgenstein, to sum up, language is a paradigmatic paradoxical site of (dis)appearance, differentiating integrity, and divisive imparting. For this reason, it is worthwhile to pin down where their thoughts on language converge and where they diverge.
Serial quantification of BCR–ABL1 mRNA is an important therapeutic indicator in chronic myeloid leukaemia, but there is a substantial variation in results reported by different laboratories. To improve comparability, an internationally accepted plasmid certified reference material (CRM) was developed according to ISO Guide 34:2009. Fragments of BCR–ABL1 (e14a2 mRNA fusion), BCR and GUSB transcripts were amplified and cloned into pUC18 to yield plasmid pIRMM0099. Six different linearised plasmid solutions were produced with the following copy number concentrations, assigned by digital PCR, and expanded uncertainties: 1.08±0.13 × 106, 1.08±0.11 × 105, 1.03±0.10 × 104, 1.02±0.09 × 103, 1.04±0.10 × 102 and 10.0±1.5 copies/μl. The certification of the material for the number of specific DNA fragments per plasmid, copy number concentration of the plasmid solutions and the assessment of inter-unit heterogeneity and stability were performed according to ISO Guide 35:2006. Two suitability studies performed by 63 BCR–ABL1 testing laboratories demonstrated that this set of 6 plasmid CRMs can help to standardise a number of measured transcripts of e14a2 BCR–ABL1 and three control genes (ABL1, BCR and GUSB). The set of six plasmid CRMs is distributed worldwide by the Institute for Reference Materials and Measurements (Belgium) and its authorised distributors (https://ec.europa.eu/jrc/en/reference-materials/catalogue/; CRM code ERM-AD623a-f).
The types of nominal species of Diapriinae in the collection of the Natural History Museum, London, are catalogued. Lectotypes are designated for the following taxa: Diapria peraffinis Ashmead, 1896; D. smithii Ashmead, 1896; Galesus bipunctatus Ashmead,1894; G. (G.) foersteri var. nigricornis Kieffer, 1911; G. sexpunctatus Ashmead, 1893; G. walkeri Kieffer, 1907; Idiotypa nigriceps Kieffer, 1909; I. nigriceps Kieffer, 1911; I. pallida Ashmead, 1893; I. pallida Ashmead in Riley, Ashmead & Howard, 1894; Paramesius angustipennis Kieffer, 1911; P. cameroni Kieffer, 1911; Phaenopria cameroni Kieffer, 1911; P. halterata Kieffer, 1911; P. magniclavata Ashmead, 1896; Tropidopsis clavata Ashmead, 1893; T. clavata Ashmead in Riley, Ashmead & Howard, 1894. New combinations are proposed: Aneuropria bifurcata comb. nov. for Mantara bifurcata Dodd, 1920; Basalys quadridens comb. nov. for Microgalesus quadridens Kieffer, 1912; Coptera cratocerus comb. nov. for Galesus cratocerus Cameron, 1912; Coptera sexpunctata comb. nov. for Galesus sexpunctatus Ashmead, 1893; Doliopria magniclavata comb. nov. for Phaenopria magniclavata Ashmead, 1896; Spilomicrus aterrimus comb. nov. for Hoplopria aterrima Dodd,
1920; Spilomicrus campbellanus comb. nov. for Antarctopria campbellana Yoshimoto, 1964; Spilomicrus coelopae comb. nov. for Antarctopria coelopae Early, 1978; Spilomicrus diomedeae comb. nov. for Antarctopria diomedeae Early, 1978; Spilomicrus helosciomyzae comb. nov. for Malvina helosciomyzae Early & Horning, 1978; Spilomicrus insulae comb. nov. for Malvina insulae Early, 1980; Spilomicrus latigaster comb. nov. for Antarctopria latigaster Brues in Tillyard, 1920; Spilomicrus punctatus comb. nov. for Malvina punctata Cameron, 1889; Spilomicrus rekohua comb. nov. for Antarctopria rekohua Early, 1978; Trichopria bouceki comb. nov. for Oxypria bouceki Masner, 1959; Trichopria nigriceps comb. nov. for Tropidopria nigriceps Ashmead in Riley, Ashmead & Howard, 1894; Trichopria nigriceps comb. nov. for Xyalopria nigriceps Kieffer, 1907; Trichopria spinosiceps comb. nov. for Acidopria spinosiceps Dodd, 1920; Trichopria walkeri comb. nov. for Diapria walkeri Dalla Torre, 1890. New replacement names are proposed: Coptera mosselensis nom. nov. for C. nigricornis Nixon, 1930 preocc.; Coptera pijiguaorum nom. nov. for C. sexpunctata Montilla & García, 2008 preocc.; Spilomicrus kozlovi nom. nov. for S. punctatus Kozlov, 1978 preocc.; Trichopria fluminis nom. nov. for T. nigriceps (Kieffer, 1907) preocc.; T. thermarum nom. nov. for T. nigriceps (Kieffer, 1913) preocc. New specific synonyms are proposed: Basalys cursitans (Kieffer, 1911) = B. pedisequa (Kieffer, 1911) syn. nov. (the former removed from synonymy with B. parvus Thomson, 1858); B. iphicla Nixon, 1980 = B. macroptera (Kieffer, 1911) syn. nov.; Coptera bipunctata (Ashmead in Riley, Ashmead & Howard, 1894) = C. sexpunctata (Ashmead, 1893) syn. nov.; Idiotypa nigriceps Kieffer, 1911 = I. nigriceps Kieffer, 1909 syn. nov.; I. pallida Ashmead in Riley, Ashmead & Howard, 1894 = I. pallida Ashmead, 1893 syn. nov.; Psilus nigricornis (Kieffer, 1911) = P. fuscipennis (Curtis, 1831) syn. nov.; P. walkeri (Kieffer, 1907) = P. fuscipennis (Curtis, 1831) syn. nov.; T. bouceki (Masner, 1959) = T. conotoma (Kieffer, 1911) syn. nov.; Trichopria halterata (Kieffer, 1911) = T. halterata (Kieffer, 1909) syn. nov. New generic synonyms are proposed: Antarctopria Brues in Tillyard, 1920 = Spilomicrus Westwood, 1832 syn. nov.; Malvina Cameron, 1889 = Spilomicrus Westwood, 1832 syn. nov.; Mantara Dodd, 1920 = Aneuropria Kieffer, 1905 syn. nov.; Microgalesus Kieffer, 1912 = Basalys Westwood, 1833 syn. nov.; Xyalopria Kieffer, 1907 = Trichopria Ashmead, 1893 syn. nov. (Xyalopria is removed from synonymy with Megaplastopria Ashmead, 1903). A brief account of some aspects of the history of these types is given.
A third Supplement to the 1992 Catalog of the Scolytidae and Platypodidae (Coleoptera) of the World (Wood and Bright 1992) is presented. This Supplement updates the taxonomy, distribution, and biology pertaining to these families of Coleoptera from 2000 to the end of 2010. A few 2011 taxonomic references are included in order to make the nomenclature as current as possible. The format of this Supplement differs slightly from the format of the original 1992 Catalog and the two previous Supplements. Only references relating to general biology, systematics and distribution were selected to be included. Tribal arrangement follows the scheme established in the 1992 World Catalog, with additions. Each genus is listed alphabetically under the current tribe and the species are listed alphabetically under the current genus. Additional information on figures, distribution, hosts, and references relating to the above are given. The bibliography used with this Supplement lists 580 references, most published from 2000 to the end of 2010. New synonymy proposed: Phloeotribus carinatus Burgos and Equihua, 2003 (= Phloeotribus ebeneus Wood, 2007). New combinations proposed: Phloeosinus kinabaluensis Bright to Hyledius; Phloeosinus phyllocladus Bright to Hyledius.
An argument is made for the retention of the family status of the Scolytidae and Platypodidae as members of the superfamily Curculionoidea. A new subfamily and tribal arrangement is proposed: SCOLYTIDAE comprising 13 subfamilies, Hylesininae, with 12 tribes, Hyorrhynchinae, with one tribe; Scolytinae, with one tribe; Hexacolinae, with one tribe; Cylindrobrotinae, with one tribe; Scolytoplatypodinae, with one tribe; Cactopininae, with one tribe; Carphodicticinae, with one tribe; Micracidinae, with one tribe; Crypturginae, with one tribe; Ipinae, with six tribes; Cryphalinae, with one tribe and Corthylinae, with two tribes and PLATYPODIDAE comprising three subfamilies, Coptonotinae, with three tribes; Tesserocerinae, with two tribes and Platypodinae, with one tribe.
A Book of Rooms
(2014)
Kobus Moolman has published six previous collections of poetry, and several plays. He has been awarded the Ingrid Jonker prize, the PANSA award, the South African Literary Award, the DALRO poetry prize and the Sol Plaatje European Union Poetry award. He teaches creative writing at the University of KwaZulu-Natal.
The article reviews distribution records of Deroceras invadens (previously called D. panormitanum and D. caruanae), adding significant unpublished records from the authors’ own collecting, museum samples, and interceptions on goods arriving in the U.S.A. By 1940 D. invadens had already arrived in Britain, Denmark, California, Australia and probably New Zealand; it has turned up in many further places since, including remote oceanic islands, but scarcely around the eastern Mediterranean (Egypt and Crete are the exceptions), nor in Asia. Throughout much of the Americas its presence seems to have been previously overlooked, probably often being mistaken for D. laeve. New national records include Mexico, Costa Rica, and Ecuador, with evidence from interceptions of its presence in Panama, Peru, and Kenya. The range appears limited by cold winters and dry summers; this would explain why its intrusion into eastern Europe and southern Spain has been rather slow and incomplete. At a finer geographic scale, the occurrence of the congener D. reticulatum provides a convenient comparison to control for sampling effort; D. invadens is often about half as frequently encountered and sometimes predominates. Deroceras invadens is most commonly found in synanthropic habitats, particularly gardens and under rubbish, but also in greenhouses, and sometimes arable land and pasture. It may spread into natural habitats, as in Britain, South Africa,
Australia and Tenerife. Many identifications have been checked in the light of recent taxonomic revision, revealing that the sibling species D. panormitanum s.s. has spread much less extensively. A number of published or online records, especially in Australia, have turned out to be misidentifications of D. laeve.
In this concise volume, author and legal scholar Michael Stolleis provides an overview of the development of the modern German welfare state. Stolleis’ analysis focuses on labor law and social policy, while acknowledging the influence of economic, social, and cultural factors thereon. Origins of the German Welfare State does not emphasize a complete understanding of its subject; rather it seeks to provide insight into the development of German social policy in relation to the political/ historical eras in which it finds itself, leading to a deeper understanding of the foundations of social policy. ...
The volume under review contains the published proceedings of a conference held in 2009 with the challenging title, "Merowingische Monetarmünzen und der Beginn des Mittelalters". These Merovingian "Monetarmünzen" are a distinctive group of coins of which less than 10 000 are currently known. Quite suddenly, in the late sixth century, this type of gold coinage appears, with the name of a moneyer ( monetarius ) on the obverse and the place name on the reverse (presumably, but not necessarily in all instances, the mint). Thus, over a thousand moneyers and 722 place names are recorded, many only attested once or twice. In the late 7 th c. these coins slowly give way to a system based on the silver penny/denier, no longer showing names of moneyers. Who were these moneyers? What was their relationship with the court and the kings? To what ends were those coins produced, and how were they used in daily commerce? Why are so many different mints attested? These questions have occupied scholars for several generations now. However, Jarnut and Strothmann have added a new perspective: in how far are these coinages and the associated monetary policy a continuation of late Roman practices, or do they represent something altogether different and can, therefore, be understood as an expression of a fundamentally altered society that could be termed medieval? ...
Published in good time for the 2014 "Karlsjahr", marking 1200 years since the emperor’s death, Johannes Fried’s latest book is intended to make specialist scholarship on Charlemagne accessible to a broad audience. Judging by the impressive sales figures, it has admirably fulfilled that purpose. That is not however to say that it is an anodyne synthesis of current research. The picture of the Frankish ruler it provides is very much the author’s own, as he himself emphasises, so there is little danger that it might be lost to sight amongst the many other biographies currently available. ...
Andreas Fahrmeir’s history of the first half of the "long nineteenth century" begins with a disdainful Arthur Young travelling through France at the beginning of 1790 and ends with London’s Great Exhibition of 1851. The contrasting fortunes of France and Great Britain exemplify the contrasting concepts of the title. While the former experienced at least eleven contested regime changes – 1789, 1792, 1793, 1794, 1799, 1814, 1815 (twice), 1830, 1848 and 1850 – the British political system endured, albeit modified by reforms. Moreover, revolutionary-Napoleonic France was responsible for numerous revolutions from above elsewhere, uprooting old regimes and creating satellite states right across the continent, from the Batavian Republic to the Grand Duchy of Warsaw. Old Europe was not restored in 1815. With the Holy Roman Empire gone for good, the Low Countries combined in a single kingdom, Poland expunged from the map once again and the Habsburg Empire much more of an Italian and Balkan power than in the past, quite a new order had emerged. The shallow roots of the new creations ensured their future fragility. ...
For faunistic research on a certain animal group, knowledge of the situation in surrounding countries is a necessity. The presence of certain species in neighbouring regions, together with notes on their distribution and trends, offers valuable information for the interpretation of the status of these species in one’s own study area. Changes in the national fauna – e.g. the discovery of a new species – can often better be explained when integrating information on the status of species in nearby countries. Distribution atlases are therefore not only valuable publications for the country of concern, but also for other countries in the same region.
In the title compound, C19H24N2O2, a di-Mannich base derived from 2-methylphenol and 1,3,6,8-tetraazatricyclo[4.4.1.13,8]dodecane, the imidazolidine ring adopts a twist conformation, with a twist about the ring N—C bond [C—N—C—C torsion angle = −44.34 (14)°]. The two 2-hydroxy-3-methylbenzyl groups are located in trans positions with respect to the imidazolidine fragment. The structure displays two intramolecular O—H⋯N hydrogen bonds, which each form an S(6) ring motif. In the crystal, the molecules are linked by weak C—H⋯O interactions with a bifurcated acceptor, forming a three-dimensional network.
The radiative capture cross section of 238U is very important for the developing of new reactor technologies and the safety of existing ones. Here the preliminary results of the 238U(n,γ) cross section measurement performed at n_TOF with C6D6 scintillation detectors are presented, paying particular attention to data reduction and background subtraction.