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Synthesis of species distributions and hotspots of endangerment is critical for setting conservation priorities to address the acute worldwide biodiversity crisis (Feeley and Silman 2011). Such a synthesis requires enormous efforts to access and unite widely dispersed biodiversity data and to establish open data archiving as a standard scientific practice. The essential first steps in this endeavor are locating primary biodiversity data—where, when, how, and by whom species have been observed or collected—and mak- ing this basic data available to the scientific community. Here, we report on a coordinated initiative of freshwater journals to stimulate a culture of publishing primary biodiversity data. Although freshwaters are tiny in their extent, they harbor a very large fraction of the global species richness, and they have experienced alarming rates of biodiversity decline (Dudgeon et al. 2006). However, freshwater biodiversity is generally neglected or grossly underrepresented in data- mobilization efforts. The importance of broad biodiversity compilations, however, has been increasingly recognized, especially in light of the establishment of the Intergovernmental Science–Policy Platform on Biodiversity and Ecosystem Services and the Group on Earth Observations’ Biodiversity Observation Network, and standards and tools have already been put in place to manage large sets of primary biodiversity data. In particular, the Global Biodiversity Information Facility (GBIF; www.gbif.org) collates and centralizes biodiversity information through its participant nodes, which include large topical initiatives such as the Ocean Biogeographic Information System (Costello and Vanden Berghe 2006) and the distributed database network for vertebrates, VertNet (Constable et al. 2010). BioFresh (www.freshwaterbiodiversity.eu), a European Union–funded project, serves the same purpose for the freshwater realm. Recent calls for data archiving in ecology (Whitlock 2011), together with the increasingly common requirement by funding agencies to deposit research data, will be instrumental in making primary biodiversity data available. There is no doubt, however, that scientific journals can and should also play a key role in promoting data-sharing policies (Huang and Qiao 2011). Consequently, we developed the following statement in collaboration with freshwater journal editors to strongly encourage the submission of species-distribution data: “Authors are encouraged to place all species distribution records in a publicly accessible database such as the national Global Biodiversity Information Facility (GBIF) nodes (www.gbif.org) or data centers endorsed by GBIF, including BioFresh (www.freshwaterbiodiversity.eu).” This statement is posted on http:// data.freshwaterbiodiversity.eu/submit data.html along with further instructions and will be widely published in the journals’ instructions for authors and on their Web sites. The editors and publishers of the following journals have approved the statement: Aquatic Botany, Aquatic Conservation: Marine and Freshwater Ecosystems, Aquatic Ecology, Aquatic Sciences, Ecology of Freshwater Fish, Freshwater Biology, Freshwater Reviews, Fundamental and Applied Limnology, Hydrobiologia, Inland Waters, the International Review of Hydrobiology, Freshwater Science (formerly, the Journal of the North American Benthological Society), the Journal of Fish Biology, the Journal of Limnology, the Journal of Plankton Research, Limnetica, Limnologica, Marine and Freshwater Research, and River Systems. Discussions are in prog- ress with an additional nine major journals in the field. What is the benefit to authors in following the recommendations for publishing primary biodiversity data? Certainly, promoting large-scale bio- diversity syntheses is an important idealistic motivation. However, as was outlined by Costello (2009), embrac- ing data-publishing practices also leads to increased recognition of scientists’ work. Papers connected to publicly available data are cited significantly more often, because the data become available for inclusion in broad-scale analyses (Piwowar et al. 2007), which are increasingly gaining importance. Importantly, the publication of primary biodiversity data is technically straightforward and quick, which minimizes the burden on authors. This is achieved by restricting submissions to a minimal standard set of fields, similar to the requirements for sequence submission to GenBank, a hugely successful database with great potential for supporting biodiversity science as well. Endorsement of the proposed data-publishing policy by most major freshwater journals will doubtlessly spur submission of primary biodiversity data, because it would raise awareness and could establish a culture of data publication. It should also encourage a wider range of journals in other areas of ecology and related fields to join the initiative. This would be of great benefit to scientific progress and to biodiversity conservation alike.

The Dababiya corehole was drilled in the Dababiya Quarry (Upper Nile Valley, Egypt), adjacent to the GSSP for the Paleocene/ Eocene boundary, to a total depth of 140 m and bottomed in the lower Maastrichtian Globotruncana aegyptiaca Zone of the Dakhla Shale Formation. Preliminary integrated studies on calcareous plankton (foraminifera, nannoplankton), benthic foraminifera, dinoflagellates, ammonites, geochemistry, clay mineralogy and geophysical logging indicate that: 1) The K/P boundary lies between 80.4 and 80.2 m, the Danian/Selandian boundary between ~ 41 and 43 m, the Selandian/Thanetian boundary at ~ 30 m (within the mid-part of the Tarawan Chalk) and the Paleocene/Eocene boundary at 11.75 m (base [planktonic foraminifera] Zone E1 and [calcareous nannoplankton] Zone NP9b); 2) the Dababiya Quarry Member (=Paleocene/Eocene Thermal Maximum interval) extends from 11.75 to 9.5 m, which is ~1 m less than in the adjacent GSSP outcrop.; 3) the Late Cretaceous (Maastrichtian) depositional environment was nearshore, tropical-sub tropical and nutrient rich; the latest Maastrichtian somewhat more restricted (coastal); and the early Danian cooler, low(er) salinity with increasing warmth and depth of water (i.e., more open water); 4) the Paleocene is further characterized by outer shelf (~ 200 m), warm water environments as supported by foraminifera P/B ratios > 85% (~79-28 m), whereas benthic foraminifera dominate (>70%) from ~27-12 m (Tarawan Chalk and Hanadi Member) due, perhaps, in part to increased dissolution (as observed in nearby outcrop samples over this interval); 5) during the PETM, enhanced hydrodynamic conditions are inferred to have occurred on the sea-floor with increased river discharge (in agreement with sedimentologic evidence), itself a likely cause for very high enhanced biological productivity on the epicontinental shelf of Egypt; 6) correlation of in situ measured geophysical logs of Natural Gamma Ray (GR), Single-Point Resistance (PR), Self-Potential (SP), magnetic susceptibility(MS), and Resistivity, and Short Normal (SN) and Long Normal (LN) showed correspondence to the lithologic units. The Dababiya Quarry Member, in particular, is characterized by very high Gamma Ray and Resistivity Short Normal values.

The number of described species on the planet is about 1.9 million, with ca. 17,000 new species described annually, mostly from the tropics. However, taxonomy is usually described as a science in crisis, lacking manpower and funding, a politically acknowledged problem known as the Taxonomic Impediment. Using data from the Fauna Europaea database and the Zoological Record, we show that contrary to general belief, developed and heavily-studied parts of the world are important reservoirs of unknown species. In Europe, new species of multicellular terrestrial and freshwater animals are being discovered and named at an unprecedented rate: since the 1950s, more than 770 new species are on average described each year from Europe, which add to the 125,000 terrestrial and freshwater multicellular species already known in this region. There is no sign of having reached a plateau that would allow for the assessment of the magnitude of European biodiversity. More remarkably, over 60\% of these new species are described by non-professional taxonomists. Amateurs are recognized as an essential part of the workforce in ecology and astronomy, but the magnitude of non-professional taxonomist contributions to alpha-taxonomy has not been fully realized until now. Our results stress the importance of developing a system that better supports and guides this formidable workforce, as we seek to overcome the Taxonomic Impediment and speed up the process of describing the planetary biodiversity before it is too late.

Many, mostly older, names of animal species are nomenclaturally problematic, either because their orthography is unstable, or they cannot be linked reliably to a taxonomic identity, due to the lack of recognisable descriptions and/or types. Yet, they represent available (sensu International Code of Zoological Nomenclature) names and must be taken into account in zoological works. This situation, with available senior, yet dubious names confounding nomenclature, is undesirable. It creates uncertainties at a time when molecular approaches are revolutionizing our concepts of species diversity, and fails us when the current extinction crisis calls for efficient, accurate, and constructive approaches to document, monitor, and conserve biodiversity. The International Code of Zoological Nomenclature (The Code) provides a means to address this issue by restricting availability, application and orthography of names to those included in the List of Available Names in Zoology (LAN). The Code (Art. 79) allows an international body of zoologists in consultation with the Commission to propose a candidate part of the LAN for a major taxonomic field. We explore this possibility for 3570 species-group names of Phylum Rotifera (of which 665 are problematic), by presenting such a candidate Rotifera part of the LAN. The web site of the International Commission on Zoological Nomenclature (http://www.iczn.org) will hold both the candidate list and a forum to facilitate consultation on the candidate list, while the list itself also can already be freely downloaded from three other Internet sites: http://fada.biodiversity.be, http://rotifer.ansp.org/LAN, and www.hausdernatur.at/rotifera. We give here an overview of the general approach and procedures applied in preparation of the candidate list, and anticipate that our effort will promote the process as well as result in a standard list of names for use in taxonomy, the Global Names Architecture and other biodiversity information initiatives.

Five new species of Homoscleromorpha (Porifera) of four genera, Oscarella, Plakortis, Plakina and Corticium, are described from vertical walls of reef caves at depths ranging from 23 to 28 m in the Caribbean Sea. Oscarella nathaliae sp. nov. has a leaf-like thinly encrusting, flat body, loosely attached to the substrate and a perforated, not lobate surface. Oscarella nathaliae sp. nov. contains two bacterial morphotypes and is characterized by two mesohylar cell types with inclusions. Plakortis myrae sp. nov. has diods of two categories: abundant large ones (83–119 mm long) and rare small ones (67–71 mm long) with sinuous, S-bent centres; triods Y- or T-shaped (18–5 mm long), and abundant microrhabds (5–12 mm long). Plakortis edwardsi sp. nov. has diods of one category with thick, sinuous, S-bent centres (110 to 128 mm long); triods T-shaped (actines 28–59 mm long). It is the only species of this genus showing small diods (22–31 mm long). Plakortis dariae sp. nov. has diods of two categories: large ones (67–112 mm long) and small, rare, irregular ones, slightly curved, often deformed with one end blunt (30–59 mm long); triods rare and regular (actines 20–44 mm long long). Corticium diamantense sp. nov. has oscula situated near its border, regular non-lophose calthrops of one size class, very rare tetralophose calthrops and candelabra with the fourth actine ramified basally in 4–5 microspined rays. In addition, a re-description of Plakina jamaicensis Lehnert & van Soest 1998 is based on newly collected material and the type specimen. P. jamaicensis has a convoluted brainlike surface; well developed sub-ectosomal cavities; irregular sinuous diods, triods, calthrops, rare monolophose calthrops, rare dilophose calthrops, rare trilophose calthrops and common tetralophose calthrops. Molecular ‘barcoding’ sequences for mitochondrial cob are given for Plakortis edwardsi sp. nov., P. dariae sp. nov., Plakina jamaicensis and Corticium diamantense sp. nov. An identification key for all western Atlantic Homoscleromorpha is provided.