Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
398
datasets available to search
ShareScore release 0.9.0
Dataset results
398 results for “morphotype”
FIGURE 4. Caddisfly larva morphotype 1 in Unique fossils of caddisfly larvae from Baltic amber and in situ amber formation in aquatic ecosystems
FIGURE 4. Caddisfly larva morphotype 1, Lepidostomatidae; specimen 3 from amber piece PED 1383. A–D. Volume renders of µCT-scan. A, Head in lateral view. B, Frontal view of the larva in the case. C, Dorsal view, "roof" of the case digitally removed. D, Frontal view slightly different angle than in B. E–G, Surface reconstruction of µCT-scan, case removed. E, Dorsal view. F, Lateral view. G, Antero-lateral view. Abbreviations: lh = lateral hump of abdomen unit 1.
FIGURE 2. Caddisfly larva morphotype 1 in Unique fossils of caddisfly larvae from Baltic amber and in situ amber formation in aquatic ecosystems
FIGURE 2. Caddisfly larva morphotype 1, Lepidostomatidae; specimen 2 from amber piece PED 1383, volume renders of µCT-scan A, Habitus, antero-ventral view. B, Colour-marked version of A. C, Head in frontal view. D, Thorax and head in dorsal view. E, Head in ventral view with mouthparts. F, Head in lateral view. Abbreviations: ad = abdomen; an = antenna; hc = head capsule; la = labium; lb = labrum; md = mandible; mp = maxillary palps; pt = prothorax; t3 = trunk appendage 3.
FIGURE 3. Caddisfly larva morphotype 1 in Unique fossils of caddisfly larvae from Baltic amber and in situ amber formation in aquatic ecosystems
FIGURE 3. Caddisfly larva morphotype 1, Lepidostomatidae; specimen 1 from amber piece PED 1383. Colourmarked version of Figure 1B. Abbreviations: at = antenna; frc = frontoclypeus; lr = labrum; md = mandible. Small brown dots on the labrum are marking labral setae bases. Images obtained with digital microscopy, white transmitted light.
FIGURE 6. Caddisfly larva morphotype 3 in Unique fossils of caddisfly larvae from Baltic amber and in situ amber formation in aquatic ecosystems
FIGURE 6. Caddisfly larva morphotype 3, Leptoceridae, PED 1635, volume renders of µCT-scans. A, Lateral view. B, Lateral view, other side. C, Fronto-lateral view, case partially removed. D, Frontal view. E, Colour-marked version of D. F, labeled head. Abbreviations: at = antenna; md = possible mandibles.
Figure 2 in DNA barcoding of two amphidromous goby postlarvae ('penja') morphotypes from Mandar River, West Sulawesi, Indonesia
Figure 2. – Neighbour-joining phylogenetic tree of amphidromous gobiid post-larvae ('penja') from the Mandar River based on Cytochrome oxydase I (COI) sequences.
Figure 3 in DNA barcoding of two amphidromous goby postlarvae ('penja') morphotypes from Mandar River, West Sulawesi, Indonesia
Figure 3. – Penja gobiid post-larvae from the Mandar River: A. 'penja alus' (Stiphodon semoni), B. 'penja mawassar' (Sicyopterus longifilis).
Fig. 3 in New Insights into the Male Morphotypes of the Amphidromous Shrimp (Weigmann, 1836) (Caridea: Palaemonidae) and a Discussion on Social Dominance Hierarchies.
Fig. 3. Macrobrachium olfersii (Wiegmann, 1836). Discrimination of juveniles and adult morphotypes (M1, M2, and M3) according to the most explanatory morphometric variables from the principal component analysis, propodus length (PrL), and major cheliped length (ChL).
Fig. 4 in New Insights into the Male Morphotypes of the Amphidromous Shrimp (Weigmann, 1836) (Caridea: Palaemonidae) and a Discussion on Social Dominance Hierarchies.
Fig. 4. Macrobrachium olfersii (Wiegmann, 1836). (A) Regression of the morphometric relationship of the propodus length (PrL) Vs. carapace length (CL) demonstrates the separation between juvenile and adult males. (B) A logistic curve shows the size at which 50% of males reach sexual maturity (CL50).
Fig. 2 in New Insights into the Male Morphotypes of the Amphidromous Shrimp (Weigmann, 1836) (Caridea: Palaemonidae) and a Discussion on Social Dominance Hierarchies.
Fig. 2. Macrobrachium olfersii (Wiegmann, 1836). Principal Component Analysis (PCA) of morphometric variables. Values indicate the projection of components 1 and 2 (PC1 and PC2).
Fig. 1 in New Insights into the Male Morphotypes of the Amphidromous Shrimp (Weigmann, 1836) (Caridea: Palaemonidae) and a Discussion on Social Dominance Hierarchies.
Fig. 1. (A) Carapace of Macrobrachium olfersii (Wiegmann, 1836). Dimension of carapace length (CL) measurements. (B) Major cheliped of Macrobrachium olfersii. Exemplification of the dimensions used to measure the length and height of the articles of the larger cheliped. The same measurements were used for the smaller cheliped. (C) Propodus of the larger cheliped of Macrobrachium olfersii in the standard position used in the geometric morphometric analyses. Red and blue circles are the landmarks and semilandmarks, respectively. CL = Carapace length; IL = Ischium length; ML = Merus length; CaL = Carpus length; PrL = Propodus length; DL = Dactylus length; PrH = Propodus height.
Fig. 5 in New Insights into the Male Morphotypes of the Amphidromous Shrimp (Weigmann, 1836) (Caridea: Palaemonidae) and a Discussion on Social Dominance Hierarchies.
Fig. 5. Macrobrachium olfersii (Wiegmann, 1836). Specimens and chelipeds of the male morphotypes, (A and B) Juvenile, (C and D) Morphotype 1, (E and F) Morphotype 2, and (G and H) Morphotype 3. All scale bars correspond to 10 mm, except for the scale bar present in 6B, which corresponds to 5 mm.
Fig. 6 in New Insights into the Male Morphotypes of the Amphidromous Shrimp (Weigmann, 1836) (Caridea: Palaemonidae) and a Discussion on Social Dominance Hierarchies.
Fig. 6. Macrobrachium olfersii (Wiegmann, 1836). (A) Scatter plot of canonical variation analysis (CVA) performed with the coordinates of variation in the propodus shape of the male morphotypes. (B) Variation in the propodus shape of each male morphotype. M3 presents evident differences in the shape of the palm region and also in the fixed finger in relation to the other morphotypes.
Figs. 1–6 in Insect galls on Bauhinia cupulata (Fabaceae): morphotypes characterization and description of a new species of Schizomyia (Cecidomyiidae, Diptera)
Figs. 1–6. Different development stages of galls induced by Schizomyia barreirensis, sp. n. (1) First stage. (2) Second stage. (3) Third stage. (4) Fourth stage. (5) Fifth stage. (6) Last stage (gall cut open to show the larval chamber).
Figs. 19 and 20 in Insect galls on Bauhinia cupulata (Fabaceae): morphotypes characterization and description of a new species of Schizomyia (Cecidomyiidae, Diptera)
Figs. 19 and 20. Schizomyia barreirensis, sp. n. (19) Female, abdominal segments 7–8 (lateral view); (20) Ovipositor (ventral view). Scale bars in mm.
Figs. 13–18 in Insect galls on Bauhinia cupulata (Fabaceae): morphotypes characterization and description of a new species of Schizomyia (Cecidomyiidae, Diptera)
Figs. 13–18. Schizomyia barreirensis sp. n. (13) Male, head (frontal view); (14) Male, flagellomere 3; (15) Female, flagellomere 2; (16) Tarsal claws and empodium; (17) Male, abdominal segments 3–8 (lateral view); (18) Male, terminalia (dorsal view). Scale bars in mm.
Fig. 3 in Isotopic discrimination and persistence of the C marker in adults of Anastrepha fraterculus (Diptera: Tephritidae) Brazilian-1 morphotype
Fig. 3. Stable carbon isotopic signature of Anastrepha fraterculus adults switched from different adult diets (sugar, mixture of sugar plus hydrolyzed yeast, or Gainesville diet) to apple (C3-based diet) over time.
Fig. 2 in Isotopic discrimination and persistence of the C marker in adults of Anastrepha fraterculus (Diptera: Tephritidae) Brazilian-1 morphotype
Fig. 2. Stable carbon isotopic signature of Anastrepha fraterculus adults switched from papaya slices (C3-based adult diet) to sugar (C4-based adult diet) over time.
Fig. 5. Sauria indet. morphotype X in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 5. Sauria indet. morphotype X from the Lower Triassic of Czatkowice, southern Poland. A. ZPAL RV/1991, adult left MttV in plantar (A1) and lateral-slightly plantar (A2) views. B. ZPAL RV/1354, juvenile left MttV in medial (B1) and plantar (B2) views. C. ZPAL RV/1992, adult left MttV in dorsal view. SEM stereo-pairs.
Fig. 5. A–E. Morphotype 9. A. P2−LV in Early ontogeny of Jurassic bakevelliids and their bearing on bivalve evolution
Fig. 5. A–E. Morphotype 9. A. P2−LV, arrows indicate pd−outlet, BGR X10868−7; A1, entire valve, × 175; A2, close up of dorsal−posterior segment with pd−outlet, × 500; A3, close up of the two rows of gear wheel type, secondary denticles, typical of the LV, × 1250. B. P2, external; note that the valve was mounted before the significance of the pd−outlet was known; left or right cannot be established, therefore, BGR X10865−7, × 175. C. P2−RV, arrows indicate pd−outlet, BGR X10868−1; C1, entire valve, × 175; C2, close up of "gothic window frame" secondary denticles, × 1250. D. Articulated P2 valves viewed from back, left and right cannot be distinguished, BGR X10868−5, × 175. E. P2−RV, arrow indicates pd−outlet, BGR X10865−5; E1, close up of posterior valve margin, × 500; E2, entire valve from back, × 175. F. Pinnid (?Atrina sp.), recent, Mediterranean, P2−RV, BGR X10848−8; F1, close up of posterior valve margin, note interruption (black arrows) of interlocking margin type, × 400; F2, entire valve, arrow shows postion of pd−outlet, × 100; F3, close up of hinge, arrow indicates detached position of resilium, growing anteriorly, × 400.
Fig. 2. Morphotype 3. A. P2 in Early ontogeny of Jurassic bakevelliids and their bearing on bivalve evolution
Fig. 2. Morphotype 3. A. P2−RV, arrow indicates slight shell deflection in postero−dorsal margin, which corresponds to growth track of pd−outlet, BGR X10864−3, × 100. B, G. P2−RV, BGR X10864−5. B. Arrow indicates position of pd−outlet, × 100. G. Close up of posterior−dorsal shell margin with outlet, × 500. C. P2, articulated shell, RV on top, dorsal view, note equivalve condition, BGR X10861−3, × 100. D. P2−RV, BGR X10861−8, × 100. E. P2−LV, BGR X10849−8; E1, arrow indicates growth track and position of pd−outlet, × 100; E2, dorsal view, × 100; E3, close up of hinge area, arrow indicates leading edge of ligament, × 250. F. LV nepioconch with P2, BGR X10860−1. F1, dorsal view, position of ligament pits indicated (1−3), × 40; F2, ventral view of ligament area, 1st ligament pit broken, × 40; F, close up of P2, × 100. G. RV nepioconch with P2, BGR X10862−2. G, ventral view, × 40; G, dorsal view onto P2, × 40.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.