Find research datasets worth reusing

opencc-by-4.0Aug 2021View details →

Fig. 1 in Morphological and molecular identification of Cryptocotyle lingua metacercariae isolated from Atlantic cod (Gadus morhua) from Danish seas and whiting (Merlangius merlangus) from the English Channel

Fig. 1 Infected Atlantic cod (Gadus morhua) (a) and microscope observation of encysted metacercariae in caudal fin (b)

opencc-by-4.0Jun 2024View details →

Supplementary Material for "Can ZooMS help assess species abundance in highly fragmented bone assemblages? Integrating morphological and proteomic identifications for the calculation of an adjusted ZooMS-eNISP"

Supplementary Material for the article "Can ZooMS help assess species abundance in highly fragmented bone assemblages? Integrating morphological and proteomic identifications for the calculation of an adjusted ZooMS-eNISP" by Discamps et al., published in Palaeoanthropology. SI#1 Cassenade dataset (morphological and ZooMS identifications, sizes, masses, etc.) in RDS format. SI#2 Cassenade dataset (morphological and ZooMS identifications, sizes, masses, etc.) in CSV format. SI#3 R script used for making the figures and statistical tests

Figure 10 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 10. Nucleotide sequence alignment of the ITS (ITS1, 5.8S rDNA and ITS4) region of the C. sphaerospermum isolate 10 and the other isolates already recorded in NCBI.

Figure 8 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 8. Nucleotide sequence alignment of the ITS (ITS1, 5.8S rDNA and ITS4) region of the C. sphaerospermum isolate 9 and the other isolates already recorded in NCBI.

Figure 5. A phylogenetic tree was generated using the neighbor-joining method which shows the genetic relationship between C. sphaerospermum 2 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 5. A phylogenetic tree was generated using the neighbor-joining method which shows the genetic relationship between C. sphaerospermum 2 (as indicated in red circle) and the other C. sphaerospermum isolates deposited in GenBank (NCBI)

Figure 3. A in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 3. A phylogenetic tree constructed by the neighbor-joining method depending on a comparison of the nucleotide sequences obtained from the C. sphaerospermum isolates (1-13).

Figure 2 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 2. The similarity and difference in the nucleotide sequences of the C. sphaerospermum isolates (1-13) identified in the present study. Similar nucleotides are stated in dots. Numbers given on the right side of the figure represent the nucleotide sequences obtained from the C. sphaerospermum isolates.

Figure 1. 1 in Morphological and molecular identification of Cladosporium sphaerospermum isolates collected from tomato plant residues

Figure 1. 1% Agarose gel electrophoresis of PCR products amplified using the primer pair ITS1 and ITS4 from the C. sphaerospermum isolates (1-13) obtained from tomato plant residues collected from different regions of Najaf and Karbala provinces. M: 1Kbp DNA Ladder (Promega, USA).

Fig. 6 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 6. Molecular phylogenetic analysis of COI gene sequences of cyathostomine species using the maximum likelihood method in MEGA7. The percentage of trees in which associated taxa clustered together is shown next to the branches. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. GenBank accession numbers are indicated alongside taxa name.

Fig. 5 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 5. Photomicrographs of Quilonia travancra. A, anterior end of a male, showing head papillae (arrows) and mouth collars (*); B, head of a male, showing crown leaflets (arrow); C, bursa of a male, lateral view, showing two branches (arrows) and three sub-branches of the posterior branch at approximately the same length (*); D, posterior branch of dorsal ray of bursa of a male, showing an appearance of trifurcation although the median and internal sub-branches are fused (*).

Fig. 2 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 2. Photomicrographs of Murshidia indica. A, anterior end of a male, showing the appearance of plumose sculpturing on anterior portion of oesophagus (arrows); B, head of a male, showing coronal leaflets (*); C, copulatory bursa and spicules (arrow) of a male; D, dorsal ray of bursa of a male, showing two branches (arrows), in which the posterior branch has a pointed extremity (*).

Fig. 4 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 4. Photomicrographs of Quilonia renniei. A, anterior end of a female, showing cylindrical shape of oesophagus (arrow); B, head of a female, showing a small buccal capsule (arrow) and curved coronal leaflets project above head (*); C, posterior end of a female; D, dorsal ray of bursa of a male, showing two branches (arrows), in which the posterior branch divided two sub-branches and the inner sub-branch is slightly bifid at the extremity (*).

Fig. 3 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 3. Photomicrographs of Murshidia neveulemairei. A, anterior end of a female, showing the appearance of plumose sculpturing on anterior portion of oesophagus (arrows); B, posterior extremity of a female, showing anus (arrow) and vulva (*); C, dorsal ray of bursa of a male, showing two branches (arrows), in which the anterior branch is bifurcated in the distal half (*).

Fig. 1 in Morphological and molecular identification of cyathostomine gastrointestinal nematodes of Murshidia and Quilonia species from Asian elephants in Myanmar

Fig. 1. Photomicrographs of Murshidia falcifera. A, anterior end of a female, showing the appearance of two lateral lips of mouth collar with prominent head papillae (arrows) and coronal leaflets (*); B, head of a male, showing cuticular lining of buccal capsule (arrows) and funnel-shaped throat (*); C, dorsal ray of bursa of a male, showing three branches, in which anterior branch is composed of two sub-branches (arrows) and the posterior one is longer (*); D, posterior end of a female, showing anus (arrow).

Fig. 14 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.

Fig. 14. Phyllosoma larva of?Chelarctus sp-1, stage VII. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.

Fig. 11 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.

Fig. 11. Phyllosoma larva of Chelarctus crosnieri sub sp., stage V. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E, ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.

Fig. 5 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.

Fig. 5. Phyllosoma larva of Chelarctus virgosus, stage VI. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E, ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.

Fig. 4 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.

Fig. 4. Phyllosoma larva of Chelarctus virgosus, stage V. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.

Fig. 2 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.

Fig. 2. Neighbor-joining phylogenetic tree drawn using the Kimura-2-parameter distances for each of the partial COI sequences between the subfamily Scyllarinae species. Scyllarides brasiliensis was used as the outgroup. Closed squares indicate the phyllosoma specimens analyzed in this study. Bootstrap values of> 50% (from 1000 replicates) are shown at each node.

Fig. 1 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.

Fig. 1. Survey area and collection locations for the phyllosoma larvae sampled by the three research vessels: RV Shunyo-maru (SHU), Koyo-maru (KY), and RV Hakuho-maru (KH). Closed red circles indicate the sampling stations where Scyllarinae phyllosomas were collected. The specimens analyzed in this study were collected from the large circle stations. See table 1 for specimen ID.