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3. Environmental drivers of herring growth and how the perception shifts with time series length

5. Otolith morphogenesis during the early life stages of fish is temperature‐dependent: Validation by experimental approach applied to European seabass (Dicentrarchus labrax).

12. Can exploited fish in the North Sea withstand climate change through evolution?

14. Cause or consequence? Exploring the role of phenotypic plasticity and genetic polymorphism in the emergence of phenotypic spatial patterns of the European eel

16. Predictive systems ecology

23. The Role of Fisheries-Induced Evolution [with Response]

25. Managing Evolving Fish Stocks

26. Directional Bilateral Asymmetry in Fish Otolith: A Potential Tool to Evaluate Stock Boundaries?

29. The logic of skipped spawning in fish

30. Complementarity and discriminatory power of genotype and otolith shape in describing the fine-scale population structure of an exploited fish, the common sole of the Eastern English Channel

31. Maturation trends indicative of rapid evolution preceded the collapse of northern cod

32. Can fisheries-induced evolution shift reference points for fisheries management?

34. Coupling individual natural tracers to assess the connectivity within a flatfish metapopulation

35. Etude de l'effet du cantonnement de Flamanville sur la communauté des crustacés

36. Measuring sensitivity of two OSPAR indicators for a coastal food web model under offshore wind farm construction

37. Directional bilateral asymmetry in otolith morphology may affect fish stock discrimination based on otolith shape analysis

38. Depth gradient on the resource use of a fish community from a semi-enclosed sea

43. Benthic and fish aggregation inside an offshore wind farm: Which effects on the trophic web functioning?

45. Directional bilateral asymmetry in otolith morphology may affect fish stock discrimination based on otolith shape analysis.

48. La plasticité phénotypique

50. Size-selective fishing gear and life history evolution in the Northeast Arctic cod

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