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Figure 37 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 37: Population structure of nase in Switzerland as inferred from microsatellite data. a) Individual population assign- ments estimated by STRUCTURE for K = 2. PCA based on population allele frequencies: b) with all populations included; c) P. toxostoma excluded. Populations Li, Wi, Mu, Bi, Su, Ro, Se and Do are from various Swiss river stations within Thur, Limmat, Reuss, Aare and Rhine downstream of Lake Constance. Ri is the Alpine Rhine, Da an Austrian inlet to Lake Constance, and Na is a Danubian population. The populations in tributaries to Lake Constance (Ri, Da) belong to the Danubian lineage, whereas all other Swiss populations belong to the Rhine lineage (from [143]).
Figure 36 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 36: Diversity of nose carps (Chondrostoma) in periapline systems. Top left: C. nasus Atlantic lineage (Wiese, Basel). Bottom left: C. nasus Atlantic lineage (Lake Sarnen, Projet Lac). Top right: C. nasus Danubian lineage (Alpine Rhine, Lake Constance inlet). Bottom right: C. soetta (Lake Mezzola, Projet Lac).
Figure 71 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 71: Species composition in the littoral zone by shallow-set vertical nets. Composition of fish catches among lakes in the littoral zone according to shallow-set (<3 m) vertical gillnets (excluding streams and rivers). Note that the high abundance of Barbatula barbatula in Lower Constance was caused by one action with 36 fish. The high biomass of Barbus barbus in Thun and Lower Constance was caused by eight and one fish respectively. The high biomass of Squalius cephalus was also caused by one fish in Joux and three fish in Walen.
Figure 35 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 35: Rutilus rutilus population genomic structure across northern perialpine lakes and phenotypic structure within Lake Brienz. Top left: Principal component analysis based on 3,865 polymorphic Single Nucleodide Polymorphisms: black = Lake Brienz, orange = Lake Walen, red = Lake Hallwill, green = Lake Geneva, blue = Lake Neuchatel. Top right: RAxML phylogeny tree depicting the genetic relationship among the individuals from the five lakes. Bottom left: Morphological (Mahalanobis) distances between roach caught over different substrates within Lake Brienz [145]. Bottom right: representative individuals from the five lakes.
Figure 34 b in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 34 b: Rutilus species hybrids. Left: phenotypic R. rutilus adult with mitochondrial barcode of R. pigus from Lake Lugano (a backcross to R. rutilus). Middle: phenotypic R. pigus subadult with barcode of R. aula from Lake Maggiore (a backcross to R. pigus). Right: a hybrid between Rutilus rutilus and Abramis brama from Lake Constance.
Figure 43 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 43: Comparison between the appearance of Esox lucius and Esox cisalpinus in lakes north (black text) and south (white text) of the Alps. Fish in each column are shown approximately to scale relative to each other. The two largest specimens display characteristic patterns for the two species respectively. * indicates that the species identity is based on genetic barcoding.
Figure 34a in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 34a: Rutilus species of the perialpine region. Rutilus aula (triotto) and Rutilus pigus (pigo) are native south of the Alps. Rutilus rutilus (roach) is native to the northern perialpine region and is introduced in many southern perialpine lakes, and invasive in several.
Figure 69 a in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 69 a): Species-abundance distributions (SADs) for each of 35 perialpine lakes and 1 lowland lake. a) The partial SADs obtained by sampling with the CEN netting protocol (lake plots in same order as in Fig. 6). b) The same but with the VERT net- ting protocol. c) The same but with the electrofishing protocol. Abundances are log2-transformed. Colours are the same as in Fig 6 and indicate drainage systems: green = Rhone, red = Rhine, orange = Po, blue = Danube. Lake Aulnes is a lowland lake in the southern Rhone drainage that we sampled but did not otherwise consider in this report. b) + c) see following page.
Figure 32 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 32: Silvery brown Carassius gibelio (Prussian carp) adults (Maggiore, Constance) and juvenile (Maggiore) with goldenbronze juvenile C. auratus (goldfish; Garda).
Figure 55 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 55: Phylogenetic relationships of Cottus from perialpine lakes (green labels) and streams/rivers (blue labels). RAxML tree with 100 bootstrap replicates. Grey dots on nodes indicate>50% bootstrap support. Adapted from Lucek et al. [41].
Figure 74 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 74: Composition of fish catches among lakes in open water, pelagic habitats according to deep-set (> 5 m) vertical gill- nets. Catches in the lowest 3 m of the nets were excluded to focus on fish caught in open-water. Note that the high relative biomass of Sander lucioperca in Upper Constance was caused by one 7.5 kg fish.
Figure 54 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 54: Phenotypic differences between littoral and profundal Cottus were consistent with the distinction between Cottus gobio (top) and Cottus ferrugineus (bottom) in Seeley [185].
Figure 65 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 65: Example of a hydroacoustic transect showing a cross-section of Lake Neuchatel from south-east, near Font (can- ton Fribourg/Freiburg; left side of figure) to north-west, near Vaumarcus (canton Neuchâtel; right side of figure). The red-brown band represents the lake floor. Hydroacoustic echoes of single fish are visible in the open water, particularly in the upper 25 m (depth-scale shown in green on the right hand side).
Figure 62 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 62: Retrieval of CEN gillnets. Photos: Andri Bryner, Eawag (left); Stefan Kubli, Eawag (right).
Figure 73 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 73: Composition of fish catches among lakes in open water, pelagic habitats (to 75 m deep) according to CEN pelagic gillnets. Note that only three and four fish were caught in pelagic CEN nets in Varese and Idro respectively.
Figure 59 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 59. Comparison between common phenotype of subadult Salaria fluviatilis and the new, rare phenotype in Lake Maggiore. The upper four photos were taken with the fish in cuvettes with (left) and without (right) gravel. Lower two photos are of additional individuals of the rare phenotype in their natural habitat. Note the marble pattern on the cheek on the rare phenotype, instead of the diagonal face stripes in the common phenotype. Also the broad, dark midlateral band running along the flank instead of paired vertical bars.
Figure 56 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 56: Variation in morphology, banding and fin colour in Perca fluviatilis. Figure 2 from [186].
Figure 63 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 63: Retrieval of vertical nets in open water. Photos: Andri Bryner, Eawag (left), Projet Lac (right).
Figure 29 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 29: Comparison of the number of instances a species was recorded in a lake by the different methods. All lakes where the three sampling methods (CEN gillnets, VERT gillnets, electrofishing) were applied are considered. The blue column represents the number of instances a species was recorded in a lake by each of the three methods. Green columns show the number of instances a species was recorded in a lake by only one method. Red columns show the number of instances a species was not recorded by one of the methods (but recorded in the other two methods) in a lake. The total number of fish populations considered was 533.
Figure 28 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report
Figure 28: Proportion of the lake shoreline in a near-natural state (green) and un-natural, modified or artificial state (red) as determined during littoral habitat mapping in Projet Lac.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.