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Four monoraphid taxa belonging to the genera Achnanthes, Psammothidium and Planothidium were found during the ongoing taxonomic revision of the freshwater and limno-terrestrial diatoms of the Maritime Antarctic region. The present paper describes these four taxa as new based on detailed light and scanning electron microscopy observations: Achnanthes kohleriana Kopalová, Zidarova & Van de Vijver sp. nov., Planothidium wetzelectorianum Kopalová, Zidarova & Van de Vijver sp. nov., Psammothidium confusoneglectum Kopalová, Zidarova & Van de Vijver sp. nov. and Psammothidium superpapilio Kopalová, Zidarova & Van de Vijver sp. nov. The morphology and ecology of all four taxa are discussed and the species are compared with morphologically similar taxa.
We revise the Panjange nigrifrons group in Borneo and document an unexpected diversity in western Sarawak forests. Five species occur within 80 km from Kuching, each species being known from its type locality only. Further species occur east until Niah, but the genus seems to be absent from Sabah. We contrast this with another pholcid genus (Aetana Huber, 2005), which is diverse in Sabah and westward until Niah, but does not seem to occur in central and western Sarawak. Five species are newly described: Panjange kapit Huber, sp. nov., Panjange kubah Huber, sp. nov., Panjange niah Huber, sp. nov., Panjange pueh Huber, sp. nov., Panjange seowi Huber, sp. nov.; Panjange tahai (Huber, 2011) comb. nov. is transferred from Pholcus.
The use of phylogenies in ecology is increasingly common and has broadened our understanding of biological diversity. Ecological sub-disciplines, particularly conservation, community ecology and macroecology, all recognize the value of evolutionary relationships but the resulting development of phylogenetic approaches has led to a proliferation of phylogenetic diversity metrics. The use of many metrics across the sub-disciplines hampers potential meta-analyses, syntheses, and generalizations of existing results. Further, there is no guide for selecting the appropriate metric for a given question, and different metrics are frequently used to address similar questions. To improve the choice, application, and interpretation of phylo-diversity metrics, we organize existing metrics by expanding on a unifying framework for phylogenetic information.
Generally, questions about phylogenetic relationships within or between assemblages tend to ask three types of question: how much; how different; or how regular? We show that these questions reflect three dimensions of a phylogenetic tree: richness, divergence, and regularity. We classify 70 existing phylo-diversity metrics based on their mathematical form within these three dimensions and identify ‘anchor’ representatives: for α-diversity metrics these are PD (Faith's phylogenetic diversity), MPD (mean pairwise distance), and VPD (variation of pairwise distances). By analysing mathematical formulae and using simulations, we use this framework to identify metrics that mix dimensions, and we provide a guide to choosing and using the most appropriate metrics. We show that metric choice requires connecting the research question with the correct dimension of the framework and that there are logical approaches to selecting and interpreting metrics. The guide outlined herein will help researchers navigate the current jungle of indices.
The genus Thlaspi has been variously subdivided since its description by Linnaeus in 1753, but due to similarities in fruit shape several segregates have still not gained broad recognition, despite the fact that they are not directly related to Thlaspi. This applies especially to segregates now considered to belong to the tribe Coluteocarpeae, which includes several well-studied taxa, e.g., Noccaea caerulescens (syn. Thlaspi caerulescens), and the widespread Microthlaspi perfoliatum (syn. Thlaspi perfoliatum). The taxonomy of this tribe is still debated, as a series of detailed monographs on Coluteocarpeae was not published in English and a lack of phylogenetic resolution within this tribe was found in previous studies. The current study presents detailed phylogenetic investigations and a critical review of morphological features, with focus on taxa previously placed in Microthlaspi. Based on one nuclear (ITS) and two chloroplast (matK, trnL-F) loci, four strongly supported major groups were recovered among the Coluteocarpeae genera included, corresponding to Ihsanalshehbazia gen. nov., Friedrichkarlmeyeria gen. nov., Microthlaspi s.str., and Noccaea s.l. In addition, two new species of Microthlaspi, M. sylvarum-cedri sp. nov. and M. mediterraneo-orientale sp. nov., were discovered, which are well supported by both morphological and molecular data. Furthermore, M. erraticum comb. nov. (diploid) and M. perfoliatum s.str. (polyploid) were shown to be distinct species, phylogenetically widely separate, but with some overlap in several morphological characters. Detailed descriptions, notes on taxonomy, geographical distribution, and line drawings for the new species and each species previously included in Microthlaspi are provided. In addition, the current taxonomic state of the tribe Coluteocarpeae is briefly discussed and it is concluded that while several annual taxa are clearly distinct from Noccaea, many perennial taxa, after thorough phylogenetic and morphological investigations, may have to be merged with this genus.
We provide the current holdings of Meropeidae in the Florida State Collection of Arthropods (FSCA). To date, FSCA holds a well-curated collection of extant meropeids representing 17 U.S. states and Western Australia (n = 316 Merope tuber Newman, fi ve Austromerope poultoni Killington). Merope tuber records from Vermont, Texas, and South Carolina are published here for the fi rst time. A total of 298 pinned M. tuber and four pinned
A. poultoni; six M. tuber specimens preserved in 95% ethanol; and 12 M. tuber and one A. poultoni sputter-coated with gold-palladium for SEM are available for researchers interested in studying this unique family of insects.
The island arc of the Lesser Antilles lies at the eastern margin of the Caribbean Sea in the Western Hemisphere, and stretches from the eastern end of the islands of the Greater Antilles (at the Virgin Islands), south to a position near the continental islands of Trinidad and Tobago at the north eastern corner of South America. The islands are a part of the West Indian Islands biodiversity “hotspot” and have been available for terrestrial colonization for about the past 15 million years. This is a status report on present knowledge of the beetle faunas of these islands, which is composed of 90 families, 1210 genera, and 2612 recognized species. Many additional species are not yet identified, or are unnamed, or remain to be discovered. Reported for the first time from the Lesser Antilles are four families, 49 genera, 105 species, and 1253 new island records. The largest families are Curculionidae (588 species), Staphylinidae (389 species), Chrysomelidae (181 species), Tenebrionidae (142 species), Cerambycidae (138 species), Scarabaeidae (127 species), and Carabidae (126 species). There are differing patterns of species distributions: 154 species are probably introduced by human activities; 985 are endemic species (limited to a single island); 465 are species endemic to more than one island of the Lesser Antilles; 212 are species limited to just islands of the West Indies; and 800 are native (naturally occurring) species which also have part of their distributional range in North, Central, or South America. Most of the widely distributed beetle fauna has probably come from South America by over-water dispersal. There is no compelling evidence for a vicariance origin of any part of the beetle fauna. Earlier colonists have had more time to form endemic genera (18) and endemic species. The more widely distributed species probably represent distributions achieved in and since the Pleistocene.