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Curculionoidea (Coleoptera) of the West Indian island of Dominica are composed of 111 genera and 214 species and subspecies. Some of the species listed are morphospecies, or are known to be undescribed, but all are identified at least to genus. Previously the fauna was recorded as 31 species. Numbers presented herein represent a seven-fold increase in species diversity. Furthermore, the widespread nature of many species demonstrates that the supposedly endemic faunas of many West Indian islands may be based on collecting biases or a lack of people capable of providing species level identifications.
The beetles of Martinique, Lesser Antilles (Insecta: Coleoptera); diversity and distributions
(2011)
This paper summarizes the published information on the beetle fauna of the island of Martinique, in the Lesser Antilles. The fauna is known to contain 42 families, with 201 genera, and 270 species. The families with the largest numbers of species are Cerambycidae (57), Curculionidae (43), Scarabaeidae (42), Tenebrionidae (18), and Staphylinidae (17). At least 15species (5.5%) were probably accidentally introduced to the island by human activities. Forty six species (17.0%) are endemic (restricted) to the island and likely speciated on the island. Sixty seven species (24.8%) are shared only with other islands of the Lesser Antilles (Lesser Antillean endemics), and 26 species (9.6%) are more widespread Antilles endemics. The remaining 116 species (42.8%) in the fauna are otherwise mostly widely distributed in the Antilles and the Neotropical Region. The Martinique beetle fauna has mostly originated elsewhere than on Martinique and is largely an immigrant fauna from other islands of the West Indies or the continental Neotropics. The numbers of Martinique species shared with other larger islands of the Lesser Antilles are (north to south) Montserrat (73), Guadeloupe (175), Dominica (98), St. Lucia (68), St. Vincent (93), and Grenada (88). Undoubtedly, the real number of species on Martinique is much higher than now reported and may actually be around 1600 or more species.
Saba Island (Caribbean Netherlands) is one of the northernmost islands of the Lesser Antilles. It is only 13 square kilometers but contains a wide variety of potential spider habitats including dry, moist, and elfin forests. As part of a collaborative effort between Conservation International and Saba Conservation Foundation, during a several week period in March and May 2008 we briefly surveyed the island for spiders and other arthropods. This survey, the first for spiders of Saba, resulted in the identification of 18 families and 76 spider species, including six new species that will be described elsewhere and may be endemic to Saba. The species richness of Saba’s spider fauna is considerably higher than that reported from other small Caribbean islands. We conclude this is probably a combined result of undersampling and lower habitat diversity on these other islands.
A list of taxa belonging to Xylotrupes Hope (Scarabaeidae: Dynastinae: Dynastini) is presented which incorporates several taxonomic actions: X. australicus darwinia Rowland comb. nov.; X. damarensis Rowland stat. nov.; X. lorquini zideki Rowland comb. nov.; X. macleayi szekessyi Endrödi comb. nov.; X. pachycera Rowland stat. nov.; X. philippinensis philippinensis Endrödi stat. nov.; X. philippinensis peregrinus Rowland comb. nov.; X. sumatrensis tanahmelayu Rowland comb. nov.; X. tadoana Rowland stat. nov.; X. telemachos Rowland stat. nov.; X. wiltrudae Silvestre stat. nov. Two new taxa are described: X. carinulus sp. nov. and X. clinias buru ssp. nov. Lectotypes are designated for X. lamachus Minck and X. clinias Schaufuss. Xylotrupes lamachus is found to be a junior subjective synonym of X. ulysses (Guérin-Méneville), new synonymy.
Neoma, a new genus of Cerambycidae (Coleoptera: Cerambycidae: Prioninae: Macrotomini) is described for Mallodonopsis corrosus Bates, 1879, compared to related genera (Aplagiognathus Thomson, 1861; Archodontes Lameere, 1903; and Mallodonopsis Thomson, 1861), and its tribal position discussed. A lectotype for Mallodonopsis corrosus is here designated with the species redescribed and figured.
Wie entsteht Schmerz? Und wie kann man ihn lindern? Um diese Fragen beantworten zu können, untersuchen Forscher eine Gruppe von Schlüsselmolekülen, die Eicosanoide, und ihre Abbauprodukte. Dabei machen sie immer wieder überraschende Entdeckungen: Blockiert man etwa durch Schmerzmittel wie Acetylsalicylsäure gezielt die Entstehung des Abbauprodukts Prostaglandin, schützt dies auch vor Krebs. Verhindert man die Entstehung von Leukotrienen, lassen sich allergische Reaktionen wie Asthma, aber auch Krebs, Osteoporose und Herz-Kreislauf-Erkrankungen beeinflussen.
Over the past two decades the “one drug – one target – one disease” concept became the prevalent paradigm in drug discovery. The main idea of this approach is the identification of a single protein target whose inhibition leads to a successful treatment of the examined disease. The predominant assumption is that highly selective ligands would avoid unwanted side effects caused by binding to secondary non-therapeutic targets. In recent years the results of post-genomic and network biology showed that proteins rarely act in isolated systems but rather as a part of a highly connected network [1]. In addition this connectivity leads to more robust systems that cannot be interfered by the inhibition of a single target of that network and consequently might not lead to the desired therapeutic effect [2]. Furthermore studies prove that robust systems are rather affected by weak inhibitions of several parts than by a complete inhibition of a single selected element of that system [3]. Therefore there is an increasing interest in developing drugs that take effect on multiple targets simultaneously but is concurrently a great challenge for medicinal chemists. There has to be a sufficient activity on each target as well as an adequate pharmacokinetic profile [4]. Early design strategies tried to link the pharmacophors of known inhibitors, however these methods often lead to high molecular weight and low ligand efficacy. We present a new rational approach based on a retrosynthetic combinatorial analysis procedure [5] on approved ligands of multiple targets. These RECAP fragments are used to design a large combinatorial library containing molecules featuring chemical properties of each ligand class. The molecules are further validated by machine learning models, like random forests and self-organizing maps, regarding their activity on the targets of interest.
Introduction: Systemic inflammation (e.g. following surgery) involves Toll-like receptor (TLR) signaling and leads to an endocrine stress response. This study aims to investigate a possible influence of TLR2 and TLR4 single nucleotide polymorphisms (SNPs) on perioperative adrenocorticotropic hormone (ACTH) and cortisol regulation in serum of cardiac surgical patients. To investigate the link to systemic inflammation in this context, we additionally measured 10 different cytokines in the serum. Methods: 338 patients admitted for elective cardiac surgery were included in this prospective observational clinical cohort study. Genomic DNA of patients was screened for TLR2 and TLR4 SNPs. Serum concentrations of ACTH, cortisol, interferon (IFN)-, interleukin (IL)-1, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, tumor necrosis factor (TNF)- and granulocyte macro-phage-colony stimulating factor (GM-CSF) were determined before surgery, immediately post surgery and on the first postoperative day. Results: 13 patients were identified as TLR2 SNP carrier, 51 as TLR4 SNP carrier and 274 pa-tients as non-carrier. Basal levels of ACTH, cortisol and cytokines did not differ between groups. In all three groups a significant, transient perioperative rise of cortisol could be ob-served. However, only in the non-carrier group this was accompanied by a significant ACTH rise, TLR4 SNP carriers had significant lower ACTH levels compared to non-carriers ((mean[95% confidence intervals]) non-carriers: 201.9[187.7 to 216.1]pg/ml; TLR4 SNP car-riers: 149.9[118.4 to 181.5]pg/ml; TLR2 SNP carriers: 176.4[110.5 to 242.3]pg/ml). Compared to non-carriers, TLR4 SNP carriers showed significant lower serum IL-8, IL-10 and GM-CSF peaks ((mean[95% confidence intervals]): IL-8: non-carriers: 42.6[36.7 to 48.5]pg/ml, TLR4 SNP carriers: 23.7[10.7 to 36.8]pg/ml; IL-10: non-carriers: 83.8[70.3 to 97.4]pg/ml, TLR4 SNP carriers: 54.2[24.1 to 84.2]pg/ml; GM-CSF: non-carriers: 33.0[27.8 to 38.3]pg/ml, TLR4 SNP carriers: 20.2[8.6 to 31.8]pg/ml). No significant changes over time or between the groups were found for the other cytokines. Conclusions: Regulation of the immunoendocrine stress response during systemic inflamma-tion is influenced by the presence of a TLR4 SNP. Cardiac surgical patients carrying this ge-notype showed decreased serum concentrations of ACTH, IL-8, IL-10 and GM-CSF. This finding might have impact on interpreting previous and designing future trials on diagnosing and modulating immunoendocrine dysregulation (e.g. adrenal insufficiency) during systemic inflammation and sepsis.