Estimating sampling effort for early detection of non-indigenous benthic species in the Toledo Harbor Region of Lake Erie
Development of an automated ballast water treatment verification system utilizing fluorescein diacetate hydrolysis as a measure of treatment efficacy
Methods for verifying ballast water treatments in foreign vessels are needed to protect the Great Lakes from the discharge of live non-native organisms or pathogens. A prototype automated viability test system using fluorescein diacetate (FDA), a membrane permeable fluorogen, to differentiate live from dead bacteria and algae is described. The automated fluorescence intensity detection device (AFIDD) captures cultured algae or organisms in Detroit River water (simulated ballast water) on 0.2 μm filters, backwashes them from the filter into a cuvette with buffer and FDA for subsequent fluorescence intensity measurements, and washes the filters with sterile water for serial automated reuse. Preliminary manual versions of these procedures were also tested. Tests of various buffers determined N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid, N,N-Bis(2-hydroxyethyl)taurine (BES) and 3-(N-morpholino)propanesulfonic acid (MOPS) at pH 7.0 to be the best buffers, causing the least spontaneous FDA breakdown without inhibiting enzymatic activity. Fluorescence in the presence of live organisms increased linearly over time, and the rate of increase was dependent on the sample concentration. Following simulated ballast water treatments with heat or chlorine, the fluorescence produced by Detroit River samples decreased to near control (sterile water) levels. Automated measurements of FDA hydrolysis with a reusable filter backwash system should be applicable to near real-time remote-controlled monitoring of live organisms in ballast water. Copyright © 2014 Elsevier Ltd. All rights reserved.
Invading the invaders: Reproductive and other mechanisms mediating the displacement of zebra mussels by quagga mussels
Dreissenids are invasive bivalves, native to water bodies of the Ponto-Caspian region of southwestern Asia. Following dispersion in Europe in the early nineteenth century, they were accidentally introduced into the Great Lakes region of North America in the 1980s and 1990s. Recently, they were discovered in the southwestern USA. Initially, Dreissena polymorpha (zebra mussel, ZM) spread more rapidly than Dreissena rostriformis bugensis (quagga mussel, QM); however, QM is becoming predominant in many areas of the Great Lakes and was the first to appear west of the Continental Divide, in Lake Mead. In Europe, as well, ZM was the first species to spread widely in western Europe from its endemic range; however, QM have recently been found in areas previously colonized only by ZM. This article reviews the dynamics of this double dreissenid invasion and considers the question: what mechanisms mediate the displacement of ZM by QM? Despite their similar appearance, QM differ from ZM in temperature and salinity tolerance, byssal thread attachment, growth, respiration rates, assimilation efficiency, enzymes such as thiaminase, depth of occurrence, and reproduction. Differences in reproduction include the depth at which reproductively active animals are found, the temperature at which spawning can be initiated, number of gametes produced, and length and timing of their annual reproductive cycle. A hypothetical role of hybrids between the species mediating species change is suggested. Future investigations of the displacement of ZM by QM should consider the role of reproductive differences (hybrids, responses to environmental chemicals, etc.) in mediating the change.