Return Of The Native: Historical Comparison Of Invasive And Indigenous Crab Populations Near The Mouth Of Delaware Bay

An invasive population of the Asian shore crab Hemigrapsus sanguineus was discovered in 1988 near the mouth of Delaware Bay, and populations now occur from North Carolina to Maine. The shore crab H. sanguineus competes with indigenous species and has displaced resident crabs throughout its invasive range. However, there have been few studies that document changes in populations of H. sanguineus after the species has become established. We compare sympatric populations of the Asian shore crab and a native mud crab (Panopeus herbstii) that were monitored initially in 2001 and again in 2011 and 2012. The historical study was conducted in a rocky habitat near Cape Henlopen at the southern terminus of Delaware Bay (38.793 degrees N, 75.158 degrees W). Results showed large differences in the relative abundance of the two species throughout the duration of the study. The Asian shore crab H. sanguineus accounted for 75% of total crab abundance in 2001, but abundance had decreased to less than 25% in both 2011 and 2012. Similar results were obtained when we compared the two species in terms of biomass. Additional sampling in 2012 showed comparable low values for H. sanguineus when compared with P. herbstii at two stations about 25 km and 50 km farther south along the coast. In contrast, H. sanguineus was strongly dominant at a station 50 km north of the historical sampling site. Percentage rock cover and size of rocks varied little among sampling locations, and all sites were proximal to the coastal ocean. However, basal sediment at the northern station was coarser than sediments at the other sites, which may have restricted the occurrence of mud crabs. Overall results of the study indicate a resurgence of native mud crabs at sites where sedimentary characteristics provide adequate habitat

Expanding dispersal studies at hydrothermal vents through species identification of cryptic larval forms

Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Springer for personal use, not for redistribution. The definitive version was published in Marine Biology 157 (2010): 1049-1062, doi:10.1007/s00227-009-1386-8.The rapid identification of hydrothermal vent-endemic larvae to the species level is a key limitation to understanding the dynamic processes that control the abundance and distribution of fauna in such a patchy and ephemeral environment. Many larval forms collected near vents, even those in groups such as gastropods that often form a morphologically distinct larval shell, have not been identified to species. We present a staged approach that combines morphological and molecular identification to optimize the capability, efficiency, and economy of identifying vent gastropod larvae from the northern East Pacific Rise (NEPR). With this approach, 15 new larval forms can be identified to species. A total of 33 of the 41 gastropod species inhabiting the NEPR, and 26 of the 27 gastropod species known to occur specifically in the 9° 50’ N region, can be identified to species. Morphological identification efforts are improved by new protoconch descriptions for Gorgoleptis spiralis, Lepetodrilus pustulosus, Nodopelta subnoda, and Echinopelta fistulosa. Even with these new morphological descriptions, the majority of lepetodrilids and peltospirids require molecular identification. Restriction fragment length polymorphism digests are presented as an economical method for identification of five species of Lepetodrilus and six species of peltospirids. The remaining unidentifiable specimens can be assigned to species by comparison to an expanded database of 18S ribosomal DNA. The broad utility of the staged approach was exemplified by the revelation of species-level variation in daily planktonic samples and the identification and characterization of egg capsules belonging to a conid gastropod Gymnobela sp. A. The improved molecular and morphological capabilities nearly double the number of species amenable to field studies of dispersal and population connectivity.Funding was provided by as Woods Hole Oceanographic Institution Deep Ocean Exploration Institute grant to L.M and S. Beaulieu, National Science Foundation grants OCE-0424953, OCE-9712233, and OCE-9619605 to L.M, OCE-0327261 to T.S., and OCE-0002458 to K. Von Damm, and a National Defense Science and Engineering Graduate fellowship to D.A

Methods for isolation, purification and structural elucidation of bioactive secondary metabolites from marine invertebrates

In the past few decades, marine natural products bioprospecting has yielded a considerable number of drug candidates. Two marine natural products have recently been admitted as new drugs: Prialt (also known as ziconotide) as a potent analgesic for severe chronic pain and Yondelis (known also as trabectedin or E-743) as antitumor agent for the treatment of advanced soft tissue sarcoma. In this protocol, methods for bioactivity-guided isolation, purification and identification of secondary metabolites from marine invertebrates such as sponges, tunicates, soft corals and crinoids are discussed. To achieve this goal, solvent extraction of usually freeze-dried sample of marine organisms is performed. Next, the extract obtained is fractionated by liquid-liquid partitioning followed by various chromatographic separation techniques including thin layer chromatography, vacuum liquid chromatography, column chromatography (CC) and preparative high-performance reversed-phase liquid chromatography. Isolation of bioactive secondary metabolites is usually monitored by bioactivity assays, e.g., antioxidant (2,2-diphenyl-1-picryl hydrazyl) and cytotoxicity (microculture tetrazolium) activities that ultimately yield the active principles. Special care should be taken when performing isolation procedures adapted to the physical and chemical characteristics of the compounds isolated, particularly their lipo- or hydrophilic characters. Examples of isolation of compounds of different polarities from extracts of various marine invertebrates will be presented in this protocol. Structure elucidation is achieved using recent spectroscopic techniques, especially 2D NMR and mass spectrometry analysis