Approaching merchant ships elicit behavioral changes in Atlantic sturgeon (Acipenser oxyrinchus) in the St. Lawrence River, Canada.

There are gaps in our understanding of sturgeon's response to anthropogenic sounds and the spatial scales at which they occur. We measured spatial displacement of Atlantic sturgeon in the St. Lawrence River at various distances of approaching merchant ships.

Automatic detection and classification of beluga whale calls in the St. Lawrence estuary.

The endangered beluga whale (Delphinapterus leucas) of the St. Lawrence Estuary (SLEB) faces threats from a variety of anthropogenic factors. Since belugas are a highly social and vocal species, passive acoustic monitoring has the potential to deliver, in a non-invasive and continuous way, real-time information on SLEB spatiotemporal habitat use, which is crucial for their monitoring and conservation.

Correction: Lagrois et al. Low-to-Mid-Frequency Monopole Source Levels of Underwater Noise from Small Recreational Vessels in the St. Lawrence Estuary Beluga Critical Habitat. 2023, , 1674.

There was an error in the original publication [...

Low-to-Mid-Frequency Monopole Source Levels of Underwater Noise from Small Recreational Vessels in the St. Lawrence Estuary Beluga Critical Habitat.

Anthropogenic noise from navigation is a major contributor to the disturbance of the acoustic soundscape in underwater environments containing noise-sensitive life forms. While previous studies mostly developed protocols for the empirical determination of noise source levels associated with the world's commercial fleet, this work explores the radiated noise emitted by small recreational vessels that thrive in many coastal waters, such as in the St. Lawrence Estuary beluga population's summer habitat.

Avoiding sharp accelerations can mitigate the impacts of a Ferry's radiated noise on the St. Lawrence whales.

Exposure to anthropogenic noise from the commercial fleet is one of the primary constituents of the acoustic pollution perturbing the environment of aquatic life. Merchant ships (e.g.

Machine-Learning Approach for Automatic Detection of Wild Beluga Whales from Hand-Held Camera Pictures.

A key aspect of ocean protection consists in estimating the abundance of marine mammal population density within their habitat, which is usually accomplished using visual inspection and cameras from line-transect ships, small boats, and aircraft. However, marine mammal observation through vessel surveys requires significant workforce resources, including for the post-processing of pictures, and is further challenged due to animal bodies being partially hidden underwater, small-scale object size, occlusion among objects, and distracter objects (e.g.

Extracting spatial networks from capture-recapture data reveals individual site fidelity patterns within a marine mammal's spatial range.

Estimating the impacts of anthropogenic disturbances requires an understanding of the habitat-use patterns of individuals within a population. This is especially the case when disturbances are localized within a population's spatial range, as variation in habitat use within a population can drastically alter the distribution of impacts.Here, we illustrate the potential for multilevel binomial models to generate spatial networks from capture-recapture data, a common data source used in wildlife studies to monitor population dynamics and habitat use.

Agent-based modelling reveals a disproportionate exposure of females and calves to a local increase in shipping and associated noise in an endangered beluga population.

Vessel underwater noise (VUN) is one of the main threats to the recovery of the endangered St. Lawrence Estuary Beluga population (SLEB). The 1% yearly population decline indicates that the cumulative threats are already beyond sustainable limits for the SLEB.

A voluntary conservation agreement reduces the risks of lethal collisions between ships and whales in the St. Lawrence Estuary (Québec, Canada): From co-construction to monitoring compliance and assessing effectiveness.

Lethal collisions with ships are limiting the recovery of several at-risk whale species worldwide. In the St. Lawrence Estuary (Quebec, Canada), the endangered blue whale and of special concern fin whale are among the migratory species subject to collisions with large ships.

A functional calcium-binding site in the metalloprotease domain of ADAMTS13.

ADAMTS13 regulates the multimeric size of von Willebrand factor (VWF). Its function is highly dependent upon Ca(2+) ions. Using the initial rates of substrate (VWF115, VWF residues 1554-1668) proteolysis by ADAMTS13 preincubated with varying Ca(2+) concentrations, a high-affinity functional ADAMTS13 Ca(2+)-binding site was suggested with K(D(app)) of 80 muM (+/- 15 muM) corroborating a previously reported study.

The central role of thrombin in hemostasis.

Following vascular injury, blood loss is controlled by the mechanisms of hemostasis. During this process, the serine proteinase, thrombin, is generated both locally and rapidly at sites of vessel damage. It plays a pivotal role in clot promotion and inhibition, and cell signaling, as well as additional processes that influence fibrinolysis and inflammation.

Further characterization of ADAMTS-13 inactivation by thrombin.

Background: The multimeric size and platelet-tethering function of von Willebrand factor (VWF) are modulated by the plasma metalloprotease, a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS-13). In vitro ADAMTS-13 is susceptible to proteolytic inactivation by thrombin.

Objectives: In this study, we aimed to characterize the inactivation of ADAMTS-13 by thrombin and to assess its physiological significance.

ADAMTS13 and von Willebrand factor and the risk of myocardial infarction in men.

Von Willebrand factor (VWF) mediates the tethering/adhesion of platelets at sites of vascular injury. This function depends on its multimeric size, which is controlled by ADAMTS13. We measured plasma ADAMTS13 and VWF antigen levels by enzyme-linked immunosorbent assay (ELISA) in a large population-based case-control study (Study of Myocardial Infarctions Leiden [SMILE]), consisting of 560 men with a first myocardial infarction (MI) and 646 control subjects.

Two protein trafficking processes at motor nerve endings unveiled by botulinum neurotoxin E.

The unique ability of a family of botulinum neurotoxins to block neuroexocytosis specifically-by selective interaction with peripheral cholinergic nerve endings, endocytotic uptake, translocation to the cytosol, and enzymic cleavage of essential proteins-underlies their increasing therapeutic applications. Although clinical use of type A is most widespread due to its prolonged inactivation of the synaptosomal-associated protein of 25 kDa, botulinum neurotoxin E cleaves this same target but at a different bond and exhibits faster onset of neuromuscular paralysis. Herein, insights were gained into the different dynamics of action of types A and E toxins, which could help in designing variants with new pharmacological profiles.

ADAMTS13 substrate recognition of von Willebrand factor A2 domain.

ADAMTS13 controls the multimeric size of circulating von Willebrand factor (VWF) by cleaving the Tyr1605-Met1606 bond in theA2 domain. To examine substrate recognition, we expressed in bacteria and purified three A2 (VWF76-(1593-1668), VWF115-(1554-1668), VWFA2-(1473-1668)) and one A2-A3 (VWF115-A3-(1554-1874)) domain fragments. Using high pressure liquid chromatography analysis, the initial rates of VWF115 cleavage by ADAMTS13 at different substrate concentrations were determined, and from this the kinetic constants were derived (Km 1.

Purification and characterization of two components of epoxypropane isomerase/carboxylase from Xanthobacter Py2.

Epoxypropane isomerase from Xanthobacter Py2 has been resolved into at least two components (A and B) by ion-exchange chromatography. Both components were required for the degradation of epoxypropane and were purified further. Component A was apparently homohexameric with a subunit M(r) of about 44,000, and possessed NAD(+)-dependent dihydrolipoamide dehydrogenase activity and lipoamide reductase activity.

Isolation of promoter sequences from Brevibacterium sp. R312.

Promoter sequences recognized by Escherichia coli RNA polymerase were isolated from Brevibacterium sp. R312, a coryneform strain producing nitrile hydratase and amidase. Ten Escherichia coli clones containing promoter sequences were selected for their ability to grow with chloramphenicol concentrations of up to 1500 micrograms/ml.

The N-terminal amino acid sequences of Brevibacterium sp. R312 nitrile hydratase.

Nitrile hydratase from Brevibacterium sp. R312 was purified to homogeneity. The isoelectric point was 5.

N-terminal amino acid sequence of Brevibacterium sp. R312 wide-spectrum amidase.

A wide-spectrum amidase from Brevibacterium sp. R312 was partially purified. The enzyme subunit was purified by reversed phase HPLC and the N-terminal amino acid sequence was found to be identical to that of Pseudomonas aeruginosa aliphatic amidase.

Cloning vectors and antibiotic-resistance markers for Brevibacterium sp. R312.

Replication of several cryptic plasmids from coryneform strains was investigated in Brevibacterium sp. R312. Only the Corynebacterium glutamicum pSR1 replicon was found to be suitable for establishing a host-vector system.