Find research datasets worth reusing

Fig. 4 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)

Fig. 4 Percentages of the Cerambycoidea species in 95 geographic regions of the western Palaearctic feeding on a broadleaved trees, b conifer trees and c roots

Fig. 5 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)

Fig. 5 Average linkage clustering with approximately unbiased bootstraps (black circle ≥90 %, white circle>90 ×>70) for 95 geographic regions of the western Palaearctic and their clusters and sub-clusters plotted to maps. a, b Sorensen similarity coefficients. c, d Simpson similarity coefficients

Fig. 8 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)

Fig. 8 Synthesis of assumed glacial refugia, dispersal barriers, filters and dispersal routes of longhorn beetles based on the analysis of regional species assemblages. R refugia of major importance, r refugia of minor importance, continuous red lines old dispersal barriers (more ancient than Postglacial), broken red lines postglacial dispersal barriers, dotted red lines postglacial filters, dotted blue arrows mostly ancient spreads, dashed blue arrows mostly recent spreads but including events before the postglacial and continuous blue arrows postglacial spreads

Fig. 5 in A vanishing hotspot-the impact of molecular insights on the diversity of Central European Bythiospeum Bourguignat, 1882 (Mollusca: Gastropoda: Truncatelloidea)

Fig. 5 Anterior part of the body of both sexes for representatives of all five Bythiospeum clades expect for clade II, renopericardial duct not shown, operculum in most specimens removed, mantle in males sometimes trimmed or pushed away to expose penis. Clade I, Degenfeld (A–C). Female, SMNS-ZI0098574-1 (A). Males, SMNS-ZI0098574-2/-4 (B, C). Clade III, Dossenbach (D–G). Female, SMNS-ZI0059270, pallial oviduct (D). Same specimen, stomach and intestine with oviduct (seen through the body wall) (E). Males, SMNS-ZI0059269/ 59268 (F, G). Clade V, La Balme d'Epy (H–J). Female, SMNSZI0079848 (H). Males, SMNSZI0079845/79844 (I, J). Clade IV, Source du Suran (K–M). Female, SMNS-ZI0079862 (K). Males, SMNS-ZI0079863/79864 (L, M). Scale bar: 0.5 mm

Fig. 1 in A vanishing hotspot-the impact of molecular insights on the diversity of Central European Bythiospeum Bourguignat, 1882 (Mollusca: Gastropoda: Truncatelloidea)

Fig. 1 Map of sampling sites of Bythiospeum in western and southern Germany, Switzerland and eastern France. Stars, type localities; circles, clade I; triangle pointing up, clade II; square, clade III; triangle pointing down, clade IV; rhomb, clade V (background map based on www. ginkgomaps.com)

Fig. 4 in A vanishing hotspot-the impact of molecular insights on the diversity of Central European Bythiospeum Bourguignat, 1882 (Mollusca: Gastropoda: Truncatelloidea)

Fig. 4 Network of haplotypes of the Bythiospeum clades connected applying the 95 % threshold, subclades with high support in light grey squares; circle size is proportional to the number of haplotypes

Fig. 9 in A vanishing hotspot-the impact of molecular insights on the diversity of Central European Bythiospeum Bourguignat, 1882 (Mollusca: Gastropoda: Truncatelloidea)

Fig. 9 Bythiospeum Balpinum^, Interlaken—part of the oviduct assumed to be diagnostic by Bernasconi (1988). A SMNSZI0098583-29. B, C Modified drawings of Bernasconi (1988: 788, Fig. 2e). D, E SMNSZI00583-29/-09. Abbreviations: bc, bursa copulatrix; gpd, gonopericardial duct; ov, oviduct; rs, receptaculum seminis. Scale bar: 0.5 mm

Fig. 1 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)

Fig. 1 Study area and its geographic sub-division. Numbers indicate the regions sensu Illies (1976) and letters indicate the sub-regions

opennotspecifiedJan 2014View details →

Fig. 3 a–m in Impact of habitat and life trait on character evolution of pallial eyes in Pectinidae (Mollusca: bivalvia)

Fig. 3 a–m Median sections of pectinid eyes from the ventral part of the mantle of investigated taxa stained after Masson-Goldner. a– c Aequipecten opercularis: overview of whole section (a), detail of pallial pigment epithelium, cornea and lens (b), detail of distal and proximal retina (c); d–f Pecten maximus, overview of whole section (d), detail of cornea and lens (e), detail of distal and proximal retina (f); g–i

opennotspecifiedJan 2014View details →

Fig. 4 a-m in Impact of habitat and life trait on character evolution of pallial eyes in Pectinidae (Mollusca: bivalvia)

Fig. 4 a-m Median sections of pectinid eyes from the ventral part of the mantle of investigated taxa stained after Masson-Goldner. a– c Talochlamys pusio, overview of whole section (a), detail of cornea and lens (b), detail of distal and proximal retina (c); d–f Palliolum incomparabile, overview of whole section (d), detail of cornea and lens (e), detail of distal and proximal retina (f); g–i Pseudamussium peslutrae,

opennotspecifiedJan 2014View details →

Fig. 5 in Impact of habitat and life trait on character evolution of pallial eyes in Pectinidae (Mollusca: bivalvia)

Fig. 5 Cladogram of BEAST analysis of investigated taxa (after Malkowsky and Klussmann-Kolb 2012) and character estimation with BayesTraits for life trait (pie chart) and morphological state changes for eye characters. Diagrams showing cross-sections of reconstructed eye for the discussed taxa (see text). Cf Flat cornea, Cc slightly convex cornea, Csc

opencc-by-4.0Jul 2024View details →

Impact of Salt Precipitation on Thermal conductivity of Sandy Soil

<p>This is the dataset form the study "<span>Impact of Salt Precipitation on Thermal conductivity of Sandy Soil", including test data and X-ray CT images.</span></p>

Fig. 4 in Stopped Dead in Their Tracks: The Impact of Railways on Gopher Tortoise (Gopherus polyphemus) Movement and Behavior

Fig. 4. Principal component analysis (PCA) with 95% confidence ellipses comparing tortoise behavior expressed over a one-hour observation period. Confidence ellipse fills are based on railway familiarity in addition to the control group. Control tortoises fall well outside the multivariate space of tortoises placed in the railway, demonstrating the inability of tortoises to cross railways.

Fig. 2 in Stopped Dead in Their Tracks: The Impact of Railways on Gopher Tortoise (Gopherus polyphemus) Movement and Behavior

Fig. 2. (A) The trench dug underneath the rails and between the railway ties. A game camera faces the entrance/exit on the west side of the railway to photograph Gopher Tortoises passing from one side to the other. (B) A series of pictures of a single Gopher Tortoise moving from the east side of the tracks to the west side.

Fig. 1 in Stopped Dead in Their Tracks: The Impact of Railways on Gopher Tortoise (Gopherus polyphemus) Movement and Behavior

Fig. 1. (A) The 20 m railway plot in which Gopher Tortoises were tested for crossing ability and behavioral differences between Habituated (n ¼ 12) and Naïve (n ¼ 12) railway familiarity. (B) The control plot in which tortoises (n ¼ 12) were tested for crossing ability and behavioral differences solely on the presence of a visual barrier.

Fig. 3 in Stopped Dead in Their Tracks: The Impact of Railways on Gopher Tortoise (Gopherus polyphemus) Movement and Behavior

Fig. 3. (A) Three simulated correlated random walks (CRWs) by a single tortoise (ID: 5233) confined to the coastal strand habitat. Each simulation is a different patterned line with the start point designated by the triangle (m) and the stop points designated by squares (&). Each simulation counted the number of times the tortoise crossed the railway (represented by the thick dotted line). (B) Histogram of the number of expected railway crosses based on 1000 simulated CRWs by a single tortoise (ID: 5233). The observed number of crosses is plotted with the dotted line and is significantly below the expected number of crosses.

FIG. 6 in Predicting Eco-evolutionary Impacts of Fishing on Body Size and Trophic Role of Atlantic Cod

FIG. 6. Demography and adaptation are predicted to interact to shape the abundance, body size distribution, and trophic role of Atlantic Cod.

FIG. 5 in Predicting Eco-evolutionary Impacts of Fishing on Body Size and Trophic Role of Atlantic Cod

FIG. 5. (A) Change in mean trophic level and (B) the abundance of fish with trophic level greater than 5.5, relative to the unfished population, with size-selective fishing mortality in both scenarios. In both panels, black lines are demography only, gray lines are demography with adaptation.

FIG. 2 in Predicting Eco-evolutionary Impacts of Fishing on Body Size and Trophic Role of Atlantic Cod

FIG. 2. (A) Age distribution of mature females in the unfished population. (B) Age distribution of mature females after size-selective fishing mortality. Note that growth, maturation, and fecundity functions are fixed functions of age and do not change with additional mortality (solid lines, Fig. 1B, C). Inset: Fishery selectivity (risk of fishing mortality) increases steeply with length. (C) Age distribution of mature females when maturation age decreases in response to size-selective fishing (dashed lines, Fig. 1B, C). Selectivity is identical to the inset in panel B.

FIG. 1 in Predicting Eco-evolutionary Impacts of Fishing on Body Size and Trophic Role of Atlantic Cod

FIG. 1. Functions describing (A) somatic growth, (B) maturation, and (C) fecundity with age of our representative species, the Georges Bank stock of Atlantic Cod (GADUS MORHUA). A maturation ogive is the cumulative probability that an individual is mature. Black lines represent fixed relationships; dashed lines are plastic or evolutionary changes that occur with the advent of size-selective mortality. The decrease in size and age at maturation (dashed line, panel B) could be due to selection for earlier reproduction or due to lower relative size or density.