Find research datasets worth reusing

Supplementary material 1 from: Harper L, Watson H, Donnelly R, Hampshire R, Sayer C, Breithaupt T, Hänfling B (2020) Using DNA metabarcoding to investigate diet and niche partitioning in the native European otter (Lutra lutra) and invasive American mink (Neovison vison). Metabarcoding and Metagenomics 4: e56087. https://doi.org/10.3897/mbmg.4.56087

Appendix 1: Fish inventory

Supplementary material 2 from: Harper L, Watson H, Donnelly R, Hampshire R, Sayer C, Breithaupt T, Hänfling B (2020) Using DNA metabarcoding to investigate diet and niche partitioning in the native European otter (Lutra lutra) and invasive American mink (Neovison vison). Metabarcoding and Metagenomics 4: e56087. https://doi.org/10.3897/mbmg.4.56087

Appendix 2: Methods

Supplementary material 4 from: Harper L, Watson H, Donnelly R, Hampshire R, Sayer C, Breithaupt T, Hänfling B (2020) Using DNA metabarcoding to investigate diet and niche partitioning in the native European otter (Lutra lutra) and invasive American mink (Neovison vison). Metabarcoding and Metagenomics 4: e56087. https://doi.org/10.3897/mbmg.4.56087

Appendix 4: Samples from non-focal mammal predators

Supplementary material 5 from: Harper L, Watson H, Donnelly R, Hampshire R, Sayer C, Breithaupt T, Hänfling B (2020) Using DNA metabarcoding to investigate diet and niche partitioning in the native European otter (Lutra lutra) and invasive American mink (Neovison vison). Metabarcoding and Metagenomics 4: e56087. https://doi.org/10.3897/mbmg.4.56087

Appendix 5: Non-focal mammal diet

GITM-R paper

<p>The dataset related to the GITM-R paper. </p>

Supplementary material 1 from: Liu J, Jiang R, Zhang G (2020) Number and distribution of large old ginkgos in east China: Implications for regional conservation. Nature Conservation 42: 71-87. https://doi.org/10.3897/natureconservation.42.59284

The large old ginkgos in Jiangsu Province, east China

Figure 5 from: Di Pietro R, Conte AL, Fortini P, D'Amato G, Astuti G (2020) Chromosome numbers for the Italian flora: 10. Italian Botanist 10: 113-122. https://doi.org/10.3897/italianbotanist.10.61847

Figure 5 Sesleria caerulea (L.) Ard. from Bosco delle Tagliate (Capo di Ponte, Brescia), 2n = 28. Scale bar: 10 µm.

Figure 2 from: Di Pietro R, Conte AL, Fortini P, D'Amato G, Astuti G (2020) Chromosome numbers for the Italian flora: 10. Italian Botanist 10: 113-122. https://doi.org/10.3897/italianbotanist.10.61847

Figure 2 Plantago crassifolia Forssk. from Saline di Punta della Contessa (San Godenzo, Brindisi), 2n = 20. Scale bar: 10 µm.

Figure 1 from: Di Pietro R, Conte AL, Fortini P, D'Amato G, Astuti G (2020) Chromosome numbers for the Italian flora: 10. Italian Botanist 10: 113-122. https://doi.org/10.3897/italianbotanist.10.61847

Figure 1 Plantago albicans L. from Madonna delle Grazie (Pisticci, Matera), 2n = 20. Scale bar: 10 µm.

Figure 3 from: Di Pietro R, Conte AL, Fortini P, D'Amato G, Astuti G (2020) Chromosome numbers for the Italian flora: 10. Italian Botanist 10: 113-122. https://doi.org/10.3897/italianbotanist.10.61847

Figure 3 Plantago subulata L. from Isola di San Domino (Isole Tremiti, Foggia), 2n = 12. Scale bar: 10 µm.

Figure 2 from: Wang I-C, Lin H-D, Liang C-M, Huang C-C, Wang R-D, Yang J-Q, Wang W-K (2020) Complete mitochondrial genome of the freshwater fish Onychostoma lepturum (Teleostei, Cyprinidae): genome characterization and phylogenetic analysis. ZooKeys 1005: 57-72. https://doi.org/10.3897/zookeys.1005.57592

Figure 2 Comparison of codon usage in mitochondrial genomes of Onychostoma lepturuma Relative synonymous codon usage (RSCU) in the Onychostoma lepturum mitogenome. Codon families are provided on the X-axis, and the RSCU values, on the Y-axis b Codon distribution in the Onychostoma lepturum mitogenome. CDspT, codons per thousand codons. Codon families are provided on the X-axis.

Figure 1 from: Wang I-C, Lin H-D, Liang C-M, Huang C-C, Wang R-D, Yang J-Q, Wang W-K (2020) Complete mitochondrial genome of the freshwater fish Onychostoma lepturum (Teleostei, Cyprinidae): genome characterization and phylogenetic analysis. ZooKeys 1005: 57-72. https://doi.org/10.3897/zookeys.1005.57592

Figure 1 Gene map of the mitochondrial genome of Onychostoma lepturum. Two rRNA genes (in red); 13 coding genes (in green); 22 tRNA genes and control region (D-loop) (in yellow). (Color figure online).

Supplementary material 1 from: Wang I-C, Lin H-D, Liang C-M, Huang C-C, Wang R-D, Yang J-Q, Wang W-K (2020) Complete mitochondrial genome of the freshwater fish Onychostoma lepturum (Teleostei, Cyprinidae): genome characterization and phylogenetic analysis. ZooKeys 1005: 57-72. https://doi.org/10.3897/zookeys.1005.57592

Table S1

Figure 3 from: Wang I-C, Lin H-D, Liang C-M, Huang C-C, Wang R-D, Yang J-Q, Wang W-K (2020) Complete mitochondrial genome of the freshwater fish Onychostoma lepturum (Teleostei, Cyprinidae): genome characterization and phylogenetic analysis. ZooKeys 1005: 57-72. https://doi.org/10.3897/zookeys.1005.57592

Figure 3 Phylogenetic trees derived from Maximum-Likelihood (ML) and Neighbor Joining (NJ) approaches based on whole mitochondrial genomes. The numbers on the nodes are the bootstrap values of ML/NJ. The number after the species name is the GenBank Accession Number.

Figure 9 from: Buyck B, Hofstetter V, Ryoo R, Ka K-H, Antonín V (2020) New Cantharellus species from South Korea. MycoKeys 76: 31-47. https://doi.org/10.3897/mycokeys.76.58179

Figure 9 Cantharellus anzutakea, b Ka & Ryoo 3_Korea_1-2 [22/08/2012, Pyeongchang, Jungwangsan, 37°27'27.48"N, 128°29'04.35"E, 771 m asl, under Pinus koraiensis Siebold & Zucc.] c Antonín 16.140 (PC0142465). Note the very pale hymenophore in young specimens, remaining for a long time paler closer to the stipe when maturing. Scale bar: 20 mm.

Figure 7 from: Buyck B, Hofstetter V, Ryoo R, Ka K-H, Antonín V (2020) New Cantharellus species from South Korea. MycoKeys 76: 31-47. https://doi.org/10.3897/mycokeys.76.58179

Figure 7 Cantharellus anzutake, microscopic features. Hyphal extremities at the pileus surface, on the left near the pileus center, on the right closer to the pileus margin. Scale bar: 10 μm. Drawings B. Buyck.

Figure 8 from: Buyck B, Hofstetter V, Ryoo R, Ka K-H, Antonín V (2020) New Cantharellus species from South Korea. MycoKeys 76: 31-47. https://doi.org/10.3897/mycokeys.76.58179

Figure 8 Cantharellus anzutake. Microscopic features. Basidia, basidiola and spores. Scale bar: 10 μm, but only 5 μm for spores. Drawings B. Buyck.

Figure 4 from: Buyck B, Hofstetter V, Ryoo R, Ka K-H, Antonín V (2020) New Cantharellus species from South Korea. MycoKeys 76: 31-47. https://doi.org/10.3897/mycokeys.76.58179

Figure 4 a–cCantharellus citrinus, yellow, more common form a (VA 13.170) bC. citrinus, reddish orange form (VA 16.169) c (VA 13.156, holotype). Photos V. Antonín.

Figure 3 from: Buyck B, Hofstetter V, Ryoo R, Ka K-H, Antonín V (2020) New Cantharellus species from South Korea. MycoKeys 76: 31-47. https://doi.org/10.3897/mycokeys.76.58179

Figure 3 Cantharellus citrinus (holotype) a spores b basidia and basidiola c hyphal extremities of the pileipellis near mid-radius. Scale bar: 10 μm, but only 5 μm for spores. Drawings B. Buyck.

Figure 2 from: Buyck B, Hofstetter V, Ryoo R, Ka K-H, Antonín V (2020) New Cantharellus species from South Korea. MycoKeys 76: 31-47. https://doi.org/10.3897/mycokeys.76.58179

Figure 2 Most likely tree (-ln = 3254.82124) obtained by phylogenetic analyses of 48 tef-1 Cantharellus sequences. Supported branches are in bold with bootstrap values, when significant (≥ 70%), indicated along the branches. Sequences newly obtained for this study are in bold and highlighted in blue for the new species described in the present study. Extraction numbers and GenBank accession numbers for tef-1 sequences are reported before taxon names. Delimitation of Cantharellus subgenera Cinnabarini and Parvocantharellus (sensu lato) are indicated and C. goossensiae Heinem. and C. rubrosalmoneus (Buyck & V. Hofst.) Buyck & V. Hofst. (both in C. subg. Pseudocantharellus) are used as outgroup.