Nemerteans of the Great Barrier Reef 5. Enopla Hoplonemertea (Monostilifera)

Three new species of monostiliferous hoplonemerteans from the Great Barrier Reef province of Australia are described and illustrated. These are, with their families indicated in parentheses, Poseidonemertes bothwellae sp. nov. (Amphiporidae), Nemertes hermaphroditicus sp. nov. (Emplectonematidae) and Pantinonemertes mooreae sp. nov. (Prosorhochmidae).     

Larval development of nemerteans of the genus Quasitetrastemma (Nemertea: Monostilifera)

Data on the larval development of Quasitetrastemma stimpsoni and Q. nigrifrons are presented. In both species, fertilization is external; the development passes through a free-swimming larval stage, the “hidden larva.” The larva has three pairs of eyes. After settling, the eyes of the second pair fuse with eyes of the first pair or are completely reduced. The basis and stylets are formed in 7–8 days after fertilization. Larvae of Q. stimpsoni settle on day 9–10 after fertilization; and Q. nigrifrons, on day 7–8.     

Morphology and systematics in mesopsammic nemerteans of the genus Ototyphlonemertes (Nemertea,Hoplonemertea, Ototyphlonemertidae)

Interstitial nemerteans of the genus Ototyphlonemertes are difficult to organize into traditional morphospecies. They occur in a multitude of slightly different local varieties that form a seemingly continuous morphological cline. In this paper, we summarize most published morphological data on the group, plus 73 new records of geographic varieties from the Mediterranean Sea in the East to the Sea of Japan in the West. We summarize morphological variation, partition traits into character and character states, propose a standardized protocol for examination of live specimens and discuss the phylogenetic structure of the group. The phylogenetic discussion leads to a hypothesis that partitions all varieties (including the established species) into six groups. These are the smallest morphologically homogenous sets of varieties (corresponding to traditional morphospecies) we can diagnose on phylogenetically reliable traits. Variation within the groups appears to be unreliable phylogenetic markers that may distinguish ecological forms rather than relatedness. However, we distinguish four of the groups by combinations of two traits, one apomorphy for a more inclusive group and one plesiomorphy, and the remaining two by one trait each that may be either a unique plesiomorphy or an apomorphy depending on the rooting, and most of them may thus join paraphyletic groups of cryptic monophyletic units. We call this kind of group phylomorph and name them the Duplex-, Pallida-, Cirrula-, Fila-, Lactea- and Macintoshi-morph (referring to the first established species within each group, i.e. Ototyphlonemertes duplex, O. pallida, O. cirrula, O. fila, O. lactea and O. macintoshi respectively). The phylogenetic scheme provides a simple tool to allocate geographical varieties to a group of possible `species' and a phylogenetic null-hypothesis for further tests with genetic data.     

Global diversity of nemerteans (Nemertea) in freshwater

Most ribborn worms (phylum Nemertea) are marine and only 22 of the currently named around 1,200 species are known from freshwater habitats (mainly lakes/ponds). They are all free-living benthic forms found in all continents except Antarctica. The vast majority of species have been recorded from the Palearctic region, but this may reflect sampling efforts rather than biogeography. Guest editors: E.V. Balian, C. Lévêque, H. Segers & K. Martens Freshwater Animal Diversity Assessment     

Potamostoma shizunaiense gen. et sp. nov. (Nemertea: Hoplonemertea: Monostilifera): a new brackish-water nemertean from Japan

Potamostoma shizunaiense gen. et sp. nov. (Nemertea: Hoplonemertea: Monostilifera) is described from the mouth of the River Shizunai, Hokkaido, Japan. This genus is readily distinguished from other monostiliferans by an oesophagus opening far anteriorly into the rhynchodaeum, a well developed excretory system extending the whole body length, terminals of the excretory collecting tubules situated between the body wall circular muscle layer and the dermis, and bilobed testes in males.     

Exploring the molecular diversity of Eleotridae (Gobiiformes) using mitochondrial DNA

Species with wide geographic distributions can consist of different lineages or even of different species. The present study evaluated the molecular diversity of the family Eleotridae by analyzing sequences of the COI gene from species collected in different locations in a Neotropical region as well as sequences from BOLD and GenBank. The analysis revealed the distinction and differentiation of a variety of species with high statistical support, including Gobiomorus dormitor (two lineages), Dormitator maculatus (three lineages) and Eleotris fusca (three lineages), and a number of different lineages of Microphilypnus. This indicates the existence of a number of unknown cryptic species that have not been reported previously, increasing the potential diversity of eleotrid species in the Neotropics.     

Phylogenetic relationships and genetic distances between some monostiliferous interstitial nemerteans (Ototyphlonemertes, Hoplonemertea, Nemertea) indicated from the 16s rRNA gene

Part of the 16s rRNA mitochondrial gene is used to reconstruct the relationships within five populations (representing three currently recognized species) of interstitial nemerteans ( Ototyphlonemertes , Hoplonemertea, Nemertea), and to assess genetic divergence between representatives of these populations. The non-helicophoran individuals form a monophyletic sister-group to the helicophoran taxon, which further resolves a previous hypothesis based on morphological characters. The small nucleotide differences between some of the populations are within levels expected for panmictic populations and fail to distinguish them genetically; without applying a phylogenic perspective, some of the populations may be allocated into paraphyletic species assemblages.     

Exploring the relationship between canopy height and terrestrial plant diversity

A relatively small number of broad-scale patterns describe the distribution of biodiversity across the earth. All of them explore biodiversity focusing on a mono or bi-dimensional space. Conversely, the volume of the forests is rarely considered. In the present work, we tested a global correlation between vascular plant species richness (S) and average forest canopy height (H), the latter regarded as a proxy of volume, using the NASA product of Global Forest Canopy Height map and the global map of plant species diversity. We found a significant correlation between H and S both at global and macro-climate scales, with strongest confidence in the tropics. Hence, two different regression models were compared and discussed to provide a possible pattern of the H–S relation. We suggested that the volume of forest ecosystems should be considered in ecological studies as well as in planning and managing natural sites, although in this first attempt, we cannot definitively prove our hypothesis. Again, high-resolution spatial data could be highly important to confirm the H–S relation, even at different scales.     

Molecular and morphological data reveal cryptic taxonomic diversity in the terrestrial slug complex Arion subfuscus/fuscus (Mollusca, Pulmonata, Arionidae) in continental north-west Europe

The importance and abundance of cryptic species among invertebrate taxa is well documented. Nowadays, taxonomic, phylogenetic and conservation biological studies frequently use molecular markers to delineate cryptic taxa. Such studies, however, often face the problem of the differential resolution of the molecular markers and techniques involved. This issue is explored in the present study of cryptic taxa within the terrestrial slug complex Arion subfuscus/fuscus in continental north-west Europe. To this end, morphological, allozyme and mitochondrial 16S rDNA sequence data have been jointly evaluated. Using allozyme data and gonad type, two distinct groups were consistently delineated, even under sympatric conditions. The 16S rDNA data strongly supported both those groups and even suggested the presence of three distinct taxa within one of them. However, in view of: (1) the allopatric distribution of three OTUs, (2) the lack of allozyme or morphological differentiation, and (3) the extremely high degree of intraspecific mtDNA variation reported in pulmonate gastropods, they are, for the time being, not regarded as valid species under the biological species concept. By means of 16S rDNA and allozyme data, the position of type and topotype material of A. subfuscus s.s. and A. fuscus relative to the newly defined OTUs was determined, thus clarifying the nomenclature of this species complex. Additionally, gonad type proved to be a useful character for distinguishing the two species in north-west Europe.  © 2004 The Linnean Society of London, Biological Journal of the Linnean Society , 2004, 83 , 23–38.     

Molecular analysis of the diversity of terrestrial planarians (Platyhelminthes, Tricladida, Continenticola) in the Iberian Peninsula

This work is a prospective study to estimate the potential species diversity of terrestrial planarians in the Iberian Peninsula. Live specimens were collected from several Iberian localities and assigned to different morphotypes on the basis of their external morphological characteristics. From the same specimens, sequences from the mitochondrial Cytochrome Oxidasa subunit I (COI) and from the nuclear ribosomal gene 18S rRNA were obtained. Sequences from GenBank of the families Dendrocoelidae, Planariidae, Bipaliidae, Geoplanidae and Rhynchodemidae have been used as outgroups in the phylogenetic analysis. The results showed that terrestrial planarians have a wide distribution in the Peninsula, with all individuals found belonging to the Rhynchodemidae family. Morphological observations indicated the presence of 10 morphospecies confirmed by the molecular analyses. At the same time, COI sequences were successfully used as a molecular marker for species identification in the barcoding mode, which is of great use in groups like this with few external morphological characteristics. The combined data strongly suggest the presence of at least 15 species in the Iberian Peninsula, a number that nearly doubles previous estimates, indicating that terrestrial planarians are more diverse than expected in the region and, as proposed, may be a good biodiversity indicator and model for biogeographical studies.     

The nemerteans (Nemertea) of Rottnest Island, Western Australia

Seventeen species of marine nemerteans are reported from Rottnest Island, Western Australia. Eight new species and four new genera are described and illustrated; these are the heteronemerteans Kohnia rottnestensis gen. et sp. n., Lineus bioculatus sp. n., Lineus gilviceps sp. n., Micrura callima sp. n. and Uricholemma nigricans gen. et sp. n., and the monostiliferous hoplonemerteans Aenigmanemertes norenburgi gen. et spn. n., Crybelonemertes arenicolus gen. et sp. n. and Tetrastemma tristibruna sp. n. A key for the field identification of the nemerteans of Rottnest Island is provided.     

Polymorphism hides cryptic species in Oerstedia dorsalis (Nemertea, Hoplonemertea)

The marine hoplonemertean Oerstedia dorsalis is considered to be a highly polymorphic species with extensive geographic distribution. We show, based on mitochondrial cytochrome c oxidase subunit I, 16S and nuclear internal transcribed spacer sequences, that there are genetic subsets withing this species. Seventy-one specimens of various colours from different geographic localities (in Europe) were sequenced and analysed using statistical parsimony and Bayesian analysis. Both analyses supported nine major clades. We conclude that O. dorsalis hides different species with geographic resolution. These species, however, appear to be polymorphic as well, and we find no diagnostic features in pigmentation or external characters to separate species within this complex.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 98 , 556–567.