Macroparasites of angelfish Brama brama (Bonnaterre, 1788) in the southern Benguela Current ecosystem

The angelfish Brama brama is a mesopelagic species distributed circumglobally in temperate to warm-temperate waters, including continental-shelf-edge and upper-slope waters of the Benguela Current ecosystem. Little is known about the parasite assemblage of Benguela B. brama, with only three parasite taxa having previously been documented from this species in the southern Benguela. This study describes the macroparasites recorded from 35 B. brama collected during research surveys off the west coast of South Africa in 2015 and 2016. A total of six macroparasite taxa were documented, including the nematode Anisakis pegreffii, the copepod Hatschekia conifera, the cestode Hepatoxylon trichiuri, an acanthocephalan from the genus Rhadinorhynchus, a monogenean from the family Diclidophoridae, and an unidentified species. Three of these (He. trichiuri, Rhadinorhynchus sp. and the unidentified species) had not previously been found to infect B. brama. The most prevalent macroparasite taxa were A. pegreffii (94%), the unidentified species (71%) and Ha. conifera (60%). Two of the parasites, Ha. conifera and He. trichiuri, showed seasonal variation in infection, and infection with the latter was positively correlated with host length. These findings increase our knowledge of B. brama biology and contribute to our understanding of the biodiversity of the southern Benguela ecosystem.     

Reef fishes recruited at midwater coral nurseries consume biofouling and reduce cleaning time in Seychelles,Indian Ocean

In coral reef restoration, coral gardening involves rearing coral fragments in underwater nurseries prior to transplantation. These nurseries become fish-aggregating devices and attract biofouling. We hypothesised that: (1) the presence of corals at a nursery is critical to recruit fish assemblages and (2) the recruited fish assemblages control biofouling, reducing person-hours invested in nursery cleaning. Three midwater coral nurseries were deployed at 8?m depth for 27 months within the marine protected area of Cousin Island Special Reserve, Seychelles, Indian Ocean. Each nursery consisted of a 6?m×6?m PVC pipe frame, layered with a recycled 5.5-cm-mesh tuna net. Human cleaning effort was calculated based on daily dive logs. Nursery-associated fish assemblages and behaviour were video-recorded prior to harvesting corals after a 20-month growth period and seven months post-coral harvesting. The density (ind. m–2) of blue-yellow damselfish Pomacentrus caeruleus was 12–16 times higher when corals were present than when corals were absent at the nurseries. Fish assemblages recruited into the nurseries included three trophic levels, from herbivores to omnivores, in six families: Ephippidae, Pomacentridae, Labridae (Scarinae), Gobiidae, Siganidae and Monacanthidae. Higher abundance of large fish (total number of individuals) resulted in 2.75 times less person-hours spent in nursery cleaning. These results have important implications for cost-effective coral reef restoration.     

DELINEATION OF SHALLOW SALT DOMES AND SURFACE FAULTS BY TEMPERATURE MEASUREMENTS AT A DEPTH OF APPROXIMATELY 2 METRES*

The feasibility of using temperature measurements at a depth of about 2 m for locating and delineating salt domes and faults has been investigated both theoretically and in experimental field surveys. It is shown that measurable temperature anomalies in the soil are to be expected over shallow salt domes. In a field survey over a salt-dome area bordering the Groningen gas field, a large number of temperature measurements were made in small holes (2 m deep, 3 cm in diameter) within a relatively short time (some weeks). The results clearly indicate several temperature anomalies with differential temperatures of about 1°C. Comparison of our thermal contour map with interpretations of available seismic or gravity data, or with direct evidence from wells, showed an excellent correlation. Seismic data even support the shape of the thermal contours. Results in similar agreement with gravity or well data were obtained over salt ridges in a tropical area. Experiments showed that the technique worked as well in lakes and marshes as on dry land. In addition, some experimental evidence collected so far over shallow and surface faults is presented. In several cases, strong thermal anomalies coincided with known surface faults. A thermal model for a surface-fault zone is suggested which accounts satisfactorily for the observed thermal data. It suggests some diagnostic value for the fault's geometry. For shallow faults, however, lack of knowledge of subsurface detail prevented any unambiguous correlation with observed thermal anomalies. Accordingly any geological use of thermal analysis over shallow faults remains debatable. The field technique is simple, needs little correction and can, where useful, easily be included in routine gravity work to provide additional local information.     

LIGHT THROWN ON GENERAL PROBLEMS BY THE ROUMANIAN RESULTS

The sedimentological characteristics of typical flysch sediments are confirmed for the Roumanian flysch. The emplacement by turbidity currents of the coarse beds alternating with the shales and marls is again abundantly confirmed by the studies in the area under discussion.     

Paragenesis of Cretaceous to Eocene carbonate reservoirs in the Ionian fold and thrust belt (Albania): relation between tectonism and fluid flow

ABSTRACT This paper examines the diagenetic history of dual (i.e. matrix and fracture) porosity reservoir lithologies in Cretaceous to Eocene carbonate turbidites of the Ionian fold and thrust belt, close to the oil‐producing centre of Fier–Ballsh (central Albania). The first major diagenetic event controlling reservoir quality was early cementation by isopachous and syntaxial low‐Mg calcite. These cements formed primarily around crinoid and rudist fragments, which acted as nucleation sites. In sediments in which these bioclasts are the major rock constituent, this cement can make up 30% of the rock volume, resulting in low effective porosity. In strata in which these bioclasts are mixed with reworkedmicrite, isopachous/syntaxial cements stabilized the framework, and matrixporosity is around 15%. The volumetric importance of these cements, their optical and luminescence character (distribution and dull orange luminescence) and stable isotopic signal (δ¹⁸O and δ¹³C averaging respectively; ?0·5‰ VPDB and +2‰ VPDB) all support a marine phreatic origin. Within these turbidites and debris flows, several generations of fractures alternated with episodes of cementation. A detailed reconstruction of this history was based on cross‐cutting relationships of fractures and compactional and layer‐parallel shortening (LPS) stylolites. The prefolding calcite veins possess orange cathodoluminescence similar to that of the host rock. Their stable isotope signatures (δ¹⁸O of ?3·86 to ?0·85‰ VPDB and δ¹³C of – 0·14 to + 2·98‰ VPDB) support a closed diagenetic rock‐buffered system. A similar closed system accounts for the selectively reopened and subsequently calcite‐cemented LPS stylolites (δ¹⁸O of ?1·81 to ?1·14‰ VPDB and δ¹³C of +1·52 to +2·56‰ VPDB). Within the prefolding veins, brecciated host rock fragments and complex textures such as crack and seal features resulted from hydraulic fracturing. They reflect expulsion of overpressured fluids within the footwall of the frontal thrusts. After folding and thrust sheet emplacement, some calcite veins are still rock buffered (δ¹⁸O of ?0·96 to +0·2‰ VPDB and δ¹³C of +0·79 to +1·37‰ VPDB), whereas others reflect external (i.e. extraformational) and thus large‐scale fluid fluxes. Some of these veins are linked to basement‐derived fluid circulation or originated from fluid flow along evaporitic décollement horizons (δ¹⁸O around +3·0‰ VPDB and δ¹³C around +1·5‰ VPDB). Others are related to the maturation of hydrocarbons in the system (δ¹⁸O around ?7·1‰ VPDB and δ¹³C around +9·3‰ VPDB). An open joint system reflecting an extensional stress regime developed during or after the final folding stage. This joint system enhanced vertical connectivity. This open joint network can be explained by the high palaeotopographical position and the folding of the reservoir analogue within the deformational front. The joint system is pre‐Burdigalian in age based upon a dated karstified discordance contact. Sediment‐filled karst cavity development is linked to meteoric water infiltration during emergence of some of the structures. Despite its sediment fill, the karst network is locally an important contributor to reservoir matrix porosity in otherwise tight lithologies. Development of secondary porosity along bed‐parallel and bed‐perpendicular (i.e. layer‐parallel shortening) stylolites is interpreted as a late‐stage diagenetic event associated with migration of acidic fluids during hydrocarbon maturation. Development of porosity along the LPS system enhanced the vertical reservoir connectivity.     

EMPLACEMENT OF FLYSCH-TYPE SAND BEDS

Recently several attempts have been made to explain deep-sea sands or flysch-type sandstone beds by normal currents, instead of by turbidity currents. The arguments that are offered against turbidity currents and those in favour of normal currents are inconclusive. Current measurements and calculations indicate 1 m from the bottom on abyssal plains velocities are less than 30 cm/sec. The ubiquitous structures: sole markings, graded bedding, fine-grained ripple mark between a lower and a covering set of horizontal laminae, and convolution, are shown each in turn to be inexplicable on the basis of normal traction currents and the same holds for the uniform bed thickness. On the other hand these features develop readily in a circular flume from overloaded suspension currents. These experiments show that to support a heavy charge of fine sand in a clay suspension a current must exceed 100 cm/sec, and in clear water double that amount is needed. The inadequacy of normal currents both in velocity and kind is thus established. This lends powerful support to the case for turbidity currents. Many authors claim to have found evidence for the deflection of turbidity currents or for currents flowing across the paleo-slope. Explanations offered include the Coriolis force, normal currents, multiple turbidity currents, or surge waves. Analysis shows that all are open to serious doubts. The author suggests, quite tentatively, that the deflections may be only simulated by the development of lamination and grain orientation oblique and perpendicular to the current direction. Sagging of the trough floor may also play a part by confusing the determination of paleo-slope. Another possibility is that the turbidity current deviated from its original direction by “internal slope”, by momentum, by centrifugal force, or by lack of space. Admittedly, a problem remains, for the swift deposition deduced from the climbing ripples is in contradiction with the supposed stretching of the turbidity current inferred from grading.     

Integrated Futures for Europe’s Mountain Regions: Reconciling Biodiversity Conservation and Human Livelihoods

Introduction Europe's mountains cover nearly half of the continent's area (Price et al. 2004) and land cover varies significantly (European Commission 2004). In most massifs, except for Sicily, southern Greece, and the British Isles, forest cover is dominant. In northern Europe, grassland is proportionately more important, and much of the mountains of the British Isles is covered by moorland. In central and southern Europe, arable land is of far greater importance than grassland, with Med…