The Geonemertes problem (Nemertea)

A new genus of monostiliferous hoplonemerteans, Pantinonemertes gen. nov., provides evidence for the separate evolution of terrestrial nemerteans. The genus is established for two new species found in Australia, P. enalios sp. nov., an intertidal form, and P. winsori sp. nov., which lives in fallen timber in the supralittoral brackish water regions of mangrove swamps. One only of the known species of land nemerteans, Geonemertes agricola from Bermuda, closely resembles these two species morphologically and is transferred to the new genus as Pantinonemertes agricola .
A re-examination of all the known species of Geonemertes has shown that two major groups can be distinguished on the basis of morphological characters. In one group the rhynchocoel musculature is in two distinct layers, a frontal organ is present, the mid-dorsal blood vessel has a single vascular plug, and the flame cells are binucleate and reinforced with cuticular support bars. It comprises the genus Pantinonemertes gen, nov, and the Pelaensis or Indopacific group of terrestrial nemerteans, for which the generic name Geonemertes is retained. In the second major group the rhynchocoel musculature is composed of interwoven longitudinal and circular fibres, there is no frontal organ, the mid-dorsal blood vessel bears two vascular plugs, and the flame cells are mononucleate and lack support bars. Five genera, three of which are new, are distinguished in this group. Australian species are united in the genus Argonemertes gen. nov., and New Zealand forms comprise the genus Antiponemertes gen. nov., while Acteonemertes bathamae from New Zealand and the Auckland and Ocean Islands remains in a separate genus. Geonemertes nightingaleensis is transferred to a new genus, Katechonemertes gen. nov., and for Geonemertes chalicophora a previously used generic name, Leptonemertes , is adopted.
A key to the terrestrial, brackish-water and marine nemertean species described in the present paper is provided.     

A new semi-terrestrial nemertean from California

A new species of semi-terrestrial monostiliferous hoplonemertean from California, Pantinonemertes californiensis sp. nov., is described and illustrated. The genus Pantinonemertes, transitional between marine and terrestrial habitats, provides evidence for one evolutionary line towards the colonization of land by nemerteans.     

Terrestrial nemerteans thirty years on

The present paper records changes in the reported distribution and abundance of terrestrial nemerteans during the last 30 years. New records are reported from the Isles of Scilly, Bermuda and New Zealand of species previously only known elsewhere. Human activity, especially the increased importation and exportation of plants between countries, has probably led to terrestrial nemerteans, as well as other organisms, becoming introduced into many new localities. However, the conservation outlook is not hopeful because of a global loss of appropriate habitat, particularly forests. Today three species (Geonemertes rodericana Gulliver, 1879, Pantinonemertes agricola Willemoes-Suhm, 1874 and Antiponemertes allisonae Moore, 1973) are feared to be extinct, and none of the extant species seem to be as abundant as they once were. Behavioural changes in Antiponemertes pantini (Southgate, 1954) under arid conditions may be associated with heavy gregarine infestations.     

THE EVOLUTION AND COMPARATIVE PHYSIOLOGY OF TERRESTRIAL AND FRESHWATER NEMERTEANS

(1) Parallel evolution from separate marine ancestors has given rise to two groups of genera of terrestrial nemerteans, representative of at least two different family stocks. They have colonized land by the direct route, moving up the shore on widely separated oceanic islands. The relationships between the known terrestrial and semi-terrestrial nemerteans, comprising seven genera and 15 species, are defined and their geographic distribution is discussed.
(2) In fresh water, three heteronemertean and nine hoplonemertean species are known. The hoplonemerteans arise from two different families representing two different evolutionary routes to fresh water, one by way of estuaries and the other via land. The distribution of freshwater nemerteans and the characters common to all species are discussed.
(3) Very little is known about the comparative physiology of land and freshwater nemerteans. However, information about the physiology of marine forms is combined with morphological differences from them found in terrestrial and freshwater species to suggest profitable lines of future research.
(4) Water relations pose a major problem for both terrestrial and freshwater nemerteans. The role of the cerebral organs, the blood and the excretory system in the osmotic physiology of some littoral nemerteans is beginning to be understood. These systems in land and freshwater forms have clearly distinctive features which need to be thoroughly investigated.
(5) Suggestions are given for valuable lines of investigation of the mucous glands, digestive physiology and general behaviour of terrestrial and freshwater nemerteans.     

Phylogeny and Cladistic Classification of the Paramonostiliferous Family Plectonemertidae (Phylum Nemertea)

Abstract— Numerical phylogenetic analysis of nemertean species from the genera Plectonemertes, Katechonemertes and Acteonementes (marine), Argonemertes, Antiponemertes and Leptonemertes (terrestrial), Potamonemertes and Campbellonemertes (freshwater) in the family Plectonemertidae was carried out with the following aims. (1) To estimate the evolutionary relationships between and among these species. (2) To lest the hypothesis of Moore and Gibson that the analysed freshwater species originated from a terrestrial ancestor. (3) To classify the species in monophyletic genera. The analysis did not confirm the hypothesis that the freshwater habitat has been colonised via land. Instead, it suggests that both terrestrial and freshwater species within this family have evolved from a marine ancestor. The cladogram suggests that Antiponemetes is paraphyletic, and it is combined with Argonemertes to form a monophyletic genus.     

Aspects of the biology of Pantinonemertes californiensis,a high intertidal nemertean

I studied the distribution, feeding biology, and reproductive biology of Pantinonemertes californiensis, described as a semi-terrestrial nemertean, along the central California coast. At the sites used in this study, maximal tidal height is about 2 m, and P. californiensis typically occurred under boulders between 1.3 and 1.7 m tidal height. Worms fed primarily on the semi-terrestrial amphipod Traskorchestia traskiana. Distribution of nemerteans was similar to that of the prey, although prey extended higher on the beach than did the worms. Nemerteans were largest and most abundant at the site with highest abundance of T. traskiana and smallest and least abundant at the lowest prey abundance site. In laboratory feeding trials, nemerteans from the site with lowest prey abundance fed most readily. Non-reproductive nemerteans lived for at least a week when submerged in sea water; some prey died within a week of being submerged. Nemerteans only lived minutes when submerged in fresh water; 50% of prey lived 4.5 h. Eggs are approximately 90–100 μm in diameter and hundreds to thousands are shed per female. Larvae are planktonic and apparently planktotrophic, and are morphologically similar to other marine hoplonemertean larvae. At the sites studied life history characteristics of P. californiensis provided little evidence of adaptations to terrestrial life in these worms and were not helpful in elucidating the role of semi-terrestrial nemerteans in the evolution of terrestrial nemerteans.     

The Distribution and Evolution of Terrestrial Nemertines

The occurrence of terrestrial nemertines on widely separatedoceanic islands is described: there are three groups of species(in Australia, New Zealand and the Indopacific islands) andthree separate species on Atlantic islands. Parallel evolutionfrom separate marine ancestors is indicated. The evolutionaryrelationship between different species is established on securemorphological grounds, with particular reference to the genusPantinonemertes which comprises marine, semi-terrestrial andfully terrestrial species. The distribution of terrestrial nemertinesis discussed. Most species are extremely localised but a fewhave become widely dispersed, notably Argonemertes dendyi butalso Geonemertes pelaensis and to a lesser extent Leptonemerteschalicophora. At least two of these widespread species are hermaphrodite.     

Exploring the molecular diversity of terrestrial nemerteans (Hoplonemertea, Monostilifera, Acteonemertidae) in a continental landmass

We report the finding of terrestrial nemerteans of the family Acteonemertidae from the northern part of Spain. The specimens were studied using molecular data from the nuclear ribosomal 18S rRNA and the mitochondrial cytochrome c oxidase subunit I genes. The 18S rRNA data strongly suggest the presence of three species of terrestrial nemerteans in the Iberian Peninsula, an old landmass where terrestrial nemerteans had not previously been reported. These specimens originate from primarily undisturbed forests across a distance of c . 1000 km. Cytochrome c oxidase subunit I data also indicate the presence of multiple lineages of Iberian terrestrial nemerteans. Nonetheless, the pattern obtained from this marker is obscured most probably by deep genetic divergences. This molecular diversity, at least in some of the clades, suggests that the Iberian species are not the result of recent introductions, as proposed for other terrestrial nemerteans found in Europe. Our data also touch upon the question of a single origin of terrestriality in nemerteans, a hypothesis rejected by both data sets. Nevertheless, terrestriality seems to have had a single origin in the family Acteonemertidae.     

A new genus of freshwater hoplonemertean from New Zealand

Potamonemertes percivali , a new freshwater hoplonemertean from the Selwyn River, New Zealand, is described. It is more closely related to the antipodean prosorhochmid supralittoral and terrestrial genera Acteonemertes and Geonemertes than to the only other freshwater hoplonemertean genus Prostoma,* but possesses a distinctive combination of characters which establish it as a new genus and species.     

Patterns of trace metal accumulation in Swedish marine nemerteans

Total body burdens of Zn, Pb, Al and Cu were measured in Swedish marine nemerteans sampled from an area close to a major source of pollution. Accumulation patterns varied both seasonally and spatially. The results suggest that nemerteans may be useful bioindicator species in environmental monitoring programmes.     

Status of the Nemertea as prey in marine ecosystems

Nemerteans are predators of a wide variety of animals, but little is known of their role as prey for other animals. The presence of toxins in the tissues and secretions of these worms has led to the assumption usually suggested that they are ingested only rarely. However, analysis of a Food Habits Data Base from the United States National Marine Fisheries Service, compiled for fishes collected in the Atlantic Ocean from the Canadian border to Cape Hatteras, North Carolina (1973–1990), showed that nemerteans were recovered from the stomachs of 27 species of fishes in 14 families. They were found in 223 of 26 642 (0.84%) fish stomachs examined in the laboratory, but only in 0.09% of 58 812 fish examined in the field. Among species in the former category, for which 1000 were examined, the winter flounder, Pseudopleuronectes americanus(Walbaum), and the yellowtail flounder, Limanda ferruginea (Storer), had the greatest frequency of nemerteans, 71 of 1545 (4.6%) and 33 of 1045 (3.2%), respectively. These nemerteans were identified as Nemertea, Cerebratulus sp. or Micrura sp., but it is likely that they were all of a Cerebratulus-like type. Nemerteans have also been recorded from the guts of eight additional species (including four additional families) of fishes collected from the western Atlantic Ocean, Gulf of Mexico, eastern Pacific Ocean (Washington, Alaska), North Sea and Indian Ocean off South Africa. The black-bellied plover, Pluvialis squatarola(L.), semipalmated plover, Charadrius semipalmatus Bonapart and the herring gull, Larus argentatus Pontoppidan are the only three species known to feed on nemerteans (Cerebratulus lacteus (Leidy) and Paranemertes peregrina Coe by the black-bellied plover and C. lacteus by the other species). Several species of nemerteans are known to ingest other nemerteans, and several arthropods, a squid, and a few other invertebrates also feed on these worms. On the other hand, careful laboratory studies have shown that some members of the Palaeonemertea, Heteronemertea and Hoplonemertea, when fed to various species of fishes, crustaceans (Astacidea, Anomura, Brachyura and Amphipoda) and a polychaete, were rejected, usually violently. There is a history of using large nemerteans, e.g. Cerebratulus lacteus and Polybrachiorhynchus dayi, as bait by sport fishermen in the United States and South Africa. The incongruity of successfuly using these toxic animals to catch fish is discussed in relation to conclusions on the importance of nemerteans as prey in the marine environment.     

The syndermatan phylogeny and the evolution of acanthocephalan endoparasitism as inferred from 18S rDNA sequences

The phylogeny of the Syndermata (Rotifera: Monogononta, Bdelloidea, Seisonidea; Acanthocephala: Palaeacanthocephala, Eoacanthocephala, Archiacanthocephala) is key to understanding the evolution of acanthocephalan endoparasitism from free-living ancestors. In the present study, maximum likelihood, distance/neighbor-joining, and maximum parsimony analyses have been carried out based on 18S rDNA data of 22 species (four new sequences). The results suggest a monophyletic origin of the Eurotatoria (Monogononta+Bdelloidea). Seison appears as the acanthocephalan sistergroup. Palaeacanthocephala split into an "Echinorhynchus"-and a "Leptorhynchoides"-group, the latter sharing a monophyletic origin with the Eoacanthocephala and Archiacanthocephala. As inferred from the phylogeny obtained acanthocephalan endoparasitism evolved from a common ancestor of Seison and Acanthocephala that lived epizoically on an early mandibulate. Probably, an acanthocephalan stem species invaded the mandibulate host, thus establishing an endoparasitic lifestyle. Subsequently, vertebrates (or gnathostomes) became part of the parasite's life cycle. In the stem line of the Archiacanthocephala, a terrestrial life cycle has evolved, with an ancestor of the Tracheata (Insecta, Myriapoda) acting as intermediate host.     

Pushing the limits in marine species distribution modelling: lessons from the land present challenges and opportunities

Aim Species distribution models (SDMs) have been used to address a wide range of theoretical and applied questions in the terrestrial realm, but marine‐based applications remain relatively scarce. In this review, we consider how conceptual and practical issues associated with terrestrial SDMs apply to a range of marine organisms and highlight the challenges relevant to improving marine SDMs. Location We include studies from both marine and terrestrial systems that encompass many geographic locations around the globe. Methods We first performed a literature search and analysis of marine and terrestrial SDMs in ISI Web of Science to assess trends and applications. Using knowledge from terrestrial applications, we critically evaluate the application of SDMs in marine systems in the context of ecological factors (dispersal, species interactions, aggregation and ontogenetic shifts) and practical considerations (data quality, alternative modelling approaches and model validation) that facilitate or create difficulties for model application. Results The relative importance of ecological factors to be considered when applying SDMs varies among terrestrial and marine organisms. Correctly incorporating dispersal is frequently considered an important issue for terrestrial models, but because there is greater potential for dispersal in the ocean, it is often less of a concern in marine SDMs. By contrast, ontogenetic shifts and feeding have received little attention in terrestrial SDM applications, but these factors are important to many marine SDMs. Opportunities also exist for applying more advanced SDM approaches in the marine realm, including mechanistic ecophysiological models, where water balance and heat transfer equations are simpler for some marine organisms relative to their terrestrial counterparts. Main conclusions SDMs have generally been under‐utilized in the marine realm relative to terrestrial applications. Correlative SDM methods should be tested on a range of marine organisms, and we suggest further development of methods that address ontogenetic shifts and feeding interactions. We anticipate developments in, and cross‐fertilization between, coupled correlative and process‐based SDMs, mechanistic eco‐physiological SDMs, and spatial population dynamic models for climate change and species invasion applications in particular. Comparisons of the outputs of different model types will provide insight that is useful for improved spatial management of marine species.     

EVOLUTION OF SCAPULA SIZE AND SHAPE IN DIDELPHID MARSUPIALS (DIDELPHIMORPHIA: DIDELPHIDAE)

The New World family Didelphidae, the basal lineage within marsupials, is commonly viewed as morphologically conservative, yet includes aquatic, terrestrial, scansorial, and arboreal species. Here, I quantitatively estimated the existing variability in size and shape of the Didelphidae scapula (1076 specimens from 56 species) using geometric morphometrics, and compared size and shape differences to evolutionary and ecologic distances. I found considerable variation in the scapula morphology, most of it related to size differences between species. This results in morphologic divergence between different locomotor habits in larger species (resulting from increased mechanical loads), but most smaller species present similarly shaped scapulae. The only exceptions are the water opossum and the short-tailed opossums, and the functional explanations for these differences remain unclear. Scapula size and shape were mapped onto a molecular phylogeny for 32 selected taxa and ancestral size and shapes were reconstructed using squared-changed parsimony. Results indicate that the Didelphidae evolved from a medium- to small-sized ancestor with a generalized scapula, slightly more similar to arboreal ones, but strikingly different from big-bodied present arboreal species, suggesting that the ancestral Didelphidae was a small scansorial animal with no particular adaptations for arboreal or terrestrial habits, and these specializations evolved only in larger-bodied clades.     

The number and kinds of embryo-bearing plants which have become aquatic: a survey

The extant embryo-bearing plants (mosses, ferns and seed plants) have an aquatic ancestor or ancestors. Today they dominate the terrestrial vegetation of the world. Embryo-bearing plants which now live in water have, for a second or even third time, re-invaded water. Aquatic species are found in 440 genera from 103 families of embryo-bearing plants. This survey attempts to find out how often the Event of evolving from land back to water has taken place among the living plants of today. Analysing the morphological and phylogenetic affinities of all aquatics at taxonomic levels from divisio to varieties of species indicate the Event has taken place, at least 222 times but it could have happened 271 or even more times (bryophytes 10–19 times, ferns seven times, seed plants 205–245 times). Aquatic plants have evolved from often very different genetic and ecological backgrounds. Also, they have evolved at different times; some old ones are aquatic at the level of order or family, while others, more recent, are isolated species in otherwise terrestrial genera or races within species. It is, nevertheless, wonderful that such a large variety of plants have evolved solutions to the single problem of remastering life in water.     

Marine-terrestrial contrasts in the ecology of plant chemical defenses against herbivores

Small marine herbivores that live on the plants they consume often selectively eat seaweeds that are chemically defended from fishes. Their feeding is unaffected or stimulated by the plant metabolites that deter fishes, and these small herbivores dramatically reduce their susceptibility to predation by associating with host plants that are noxious to fishes. Ecological similarities between these small marine herbivores and numerous terrestrial insects suggest that herbivorous insects also may have evolved a preference for toxic plants because this diminishes their losses to predators, parasites and pathogens. Although marine and terrestrial plants and herbivores evolved in strikingly different environments, the ease of experimentation in some marine systems makes them ideal for addressing certain questions of fundamental importance to both terrestrial and marine workers.     

Why are there so few fish in the sea?

The most dramatic gradient in global biodiversity is between marine and terrestrial environments. Terrestrial environments contain approximately 75-85% of all estimated species, but occupy only 30 per cent of the Earth's surface (and only approx. 1-10% by volume), whereas marine environments occupy a larger area and volume, but have a smaller fraction of Earth's estimated diversity. Many hypotheses have been proposed to explain this disparity, but there have been few large-scale quantitative tests. Here, we analyse patterns of diversity in actinopterygian (ray-finned) fishes, the most species-rich clade of marine vertebrates, containing 96 per cent of fish species. Despite the much greater area and productivity of marine environments, actinopterygian richness is similar in freshwater and marine habitats (15 150 versus 14 740 species). Net diversification rates (speciation-extinction) are similar in predominantly freshwater and saltwater clades. Both habitats are dominated by two hyperdiverse but relatively recent clades (Ostariophysi and Percomorpha). Remarkably, trait reconstructions (for both living and fossil taxa) suggest that all extant marine actinopterygians were derived from a freshwater ancestor, indicating a role for ancient extinction in explaining low marine richness. Finally, by analysing an entirely aquatic group, we are able to better sort among potential hypotheses for explaining the paradoxically low diversity of marine environments.