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Figure 9 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 9. PCA biplot of environmental parameters and abundance of microarthropods with treatment as grouping factor. sav ctrl: savanna, mb: maize bare, mbnpk: maize with chemical NPK fertilizer, mmdom: maize with dead organic matter.

Figure 8 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 8. Oribatida and Gamasina abundance (tsd. ind./m2) in plots (mb: maize bare, mmdom: maize with DOM). Abundances being significantly different from each other are marked by different letters for each microarthropod group (Wilcoxon signed rank test [p ˂ 0.05]). Error bars = standard error.

Figure 7 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 7. Collembola, Oribatida and Gamasina abundance (tsd. ind./m2) in plots (mb: maize bare, mbnpk: maize with chemical NPK). Abundances being significantly different from each other are marked by different letters (Wilcoxon signed rank test [p ˂ 0.05]). Error bars = standard error.

Figure 6 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 6. Effect of Maize cultivation on Collembola, Oribatida and Gamasina in control plots (sav ctrl: savanna, mb: maize bare). Abundances being significantly different from each other are marked by different letters for each microarthropod group (Wilcoxon signedrank test [p ˂ 0.05]). Error bars = standard error.

Figure 5 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 5. Temporal variation of Collembola, Oribatida and Gamasina abundance (tsd. ind./m2) in savanna and experimental field in (A) 2017 and (B) 2018. Abundance being significantly different from each other in time per treatment are marked by different letters for each microarthropod group (Wilcoxon signed-rank test [p ˂ 0.05]). Months not sampled are marked by asterisks. Error bars = standard error. sav ctrl: savanna, mb: maize bare, mbnpk: maize with chemical NPK fertilizer, mmdom: maize with dry organic matter (DOM).

Figure 2 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 2. Completely randomized block design of the experimental field; experimental field before sowing (A: 08/05/17) and with maize crop (B: 28/06/17); sav ctrl: savanna untreated (outside). mb(1): maize bare = maize plot without mulch or NPK fertilizer; mbnpk(2): maize bare with NPK = Maize plot treated with NPK fertilizer only and mmdom(3): maize mulch = maize plot treated with mulch only.

FIGURE 3 Holotype NMNS-8130-001 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea

FIGURE 3 Holotype NMNS-8130-001 of Pheronemoides curvipentactin sp. nov. A, the external morphology of dermal areas (scale bar = 5 cm); B, the external morphology of atrial areas.

Figure 1 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 1. Weather data for the Ngaoundéré area, Jan. to Dec. 2017 and 2018, provided by Ngaoundéré airport meteorological station; t: temperature, p: precipitation, h: relative humidity; h: averages per month; p: sum per month.

Figure 3 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 3. Abundances (mean ± S.E.) of Acari and Collembola for the rainy seasons of 2017 (n = 4) and 2018 (n = 4) as well as for the dry season of 2017/18 (n = 2). n sampling campaigns with 9 samples per plot [sav ctrl: savanna; mb: maize bare; mbnpk: maize with chemical NPK fertilizer; mmdom: maize with dead organic matter (DOM)].

Figure 4 in Effect of three different land use types on the temporal dynamics of microarthropod abundance in the high Guinean savanna of Ngaoundéré (Adamawa, Cameroon)

Figure 4. Abundances (mean ± S.E.) of Oribatida and Gamasina for the rainy seasons of 2017 (n = 4) and 2018 (n = 4) as well as for the dry season of 2017/18 (n = 2). n sampling campaigns with 9 samples per plot [sav ctrl: savanna; mb: maize bare; mbnpk: maize with chemical NPK fertilizer; mmdom: maize with dead organic matter (DOM)].

FIGURE 4 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea

FIGURE 4 Spicules of holotype NMNS-8130-001 of Pheronemoides curvipentactin sp. nov. A, choanosomal pentactin; B–C, dermal pinular pentactins; D–H, atrialia: D–E, pinular pentactins; F, crooked pentactin; G–H, special pentactins; I, shaft of macrouncinate; J, microuncinate; K, shaft of microuncinate; L, terminal of microuncinate; M, micramphidisc; N, microdiactin; O–Q, the anchor of basalia; R–S; marginalia.

FIGURE 5 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea

FIGURE 5 Bayesian inference trees of pheronematid species based on the 16S rDNA and 28S rDNA sequence data. Numbers at each node are Bayesian posterior probabilities (left) and ML analysis bootstrap values (right).

FIGURE 1 Holotype MBM286618 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea

FIGURE 1 Holotype MBM286618 of Pheronemoides crustiformis sp. nov. A, photograph showing the specimen in its natural habitat; B, the external morphology of atrial areas; C, the external morphology of dermal areas and basalia; D, mesh structure of dermal areas; E, mesh structure of atrial areas.

FIGURE 2 in Phylogeny of two new pheronematid sponges from the Caroline Seamount and South China Sea

FIGURE 2 Spicules of holotype MBM286618 of Pheronemoides crustiformis sp. nov. A, choanosomal pentactin; B, the anchor of basalia; C, atrial pinular pentactin; D, dermal pinular pentactin; E–G, micramphidiscs; H, microdiactin I; I, microdiactin II; J, shaft of macrouncinate; K, shaft of mesouncinate; L–N, Sceptre; O–P, the anchor of basalia.

Figures 169–187 in Revision of the genus Olivierus in Xinjiang, China, with comments on Mesobuthus thersites (Scorpiones: Buthidae)

Figures 169–187: Dentate margin of movable finger in Olivierus, showing complex (blue) and simple (green) subrows defined here; note: for clarity of explanation, the EAD is included within each complex subrow, but by definition it should be excluded. Figs. 169–183 are modified from Fet et al. (2018: figs. 304–313) and Fet et al. (2021: figs. 32, 43, 73, 84, 107). Figure 169. O. brutus, male paratype from Alamut, Qazvin Province, Iran. Figure 170. O. caucasicus, male from Melekli, Iğdir Province, Turkey. Figure 171. O. elenae, female holotype from Angor, Surxondaryo Province, Uzbekistan. Figure 172. O. gorelovi, male holotype from Tejen, Akhal Province, Turkmenistan. Figure 173. O. fuscus, female from Khuroson, Khatlon Province, Tajikistan. Figure 174. O. kaznakovi, male from Romit State Nature Reserve, Khatlon Province, Tajikistan. Figure 175. O. kreuzbergi, male holotype from Uzun, Surxondaryo Province, Uzbekistan. Figure 176. O. mischi, male holotype from Hazara Toghai, Balkh Province, Afghanistan. Figure 177. O. nenilini, male holotype from Mingbulak, Namangan Province, Uzbekistan. Figure 178. O. parthorum, male from Afghanistan. Figures 179–180. O. mikhailovi, paratype male (179) and female (180) from Bel'tau Mts., Turkistan Province, Kazakhstan.

Figures 157–162 in Revision of the genus Olivierus in Xinjiang, China, with comments on Mesobuthus thersites (Scorpiones: Buthidae)

Figures 157–162: Exemplar specimens of Olivierus martensii (Karsch, 1879) in vivo habitus. Figures 157–158. Adult male (157) and female (158) of typical phenotype from Luoyang City, Henan Province, China. Figures 159–160. Hypomelanistic (159; adult male) and piebaldistic (160; immature males) phenotypes. Figures 161–162. Leucistic (161; immature male) and albino (162; adult female) phenotypes.

Figures 155–156 in Revision of the genus Olivierus in Xinjiang, China, with comments on Mesobuthus thersites (Scorpiones: Buthidae)

Figures 155–156: Comparison between Olivierus longichelus, O. przewalskii and Mesobuthus thersites (left to right). Figure 155. Adult females. Figure 156. Adult males.

Figures 163–168 in Revision of the genus Olivierus in Xinjiang, China, with comments on Mesobuthus thersites (Scorpiones: Buthidae)

Figures 163–168: Raw stacked photos (unmatted) of typical adult male and female O. martensii from Luoyang City, Henan Province, China, under white light: chelae in external view (163, 166), metasoma V in ventral view (164, 167), and telo- and basitarsi of right 3rd leg in retrolateral view (165, 168). Figures 163–165. Male. Figures 166–168. Female.

Figures 150–151 in Revision of the genus Olivierus in Xinjiang, China, with comments on Mesobuthus thersites (Scorpiones: Buthidae)

Figures 150–151: Additional Olivierus longichelus populations used for DNA sequencing. Figure 150. Juvenile male from Korgas County (left) and adult male from Khorgos City (right). Figure 151. Adult male from Shawan City (left) and adult female from Wujiaqu City (right).

Figures 152–154 in Revision of the genus Olivierus in Xinjiang, China, with comments on Mesobuthus thersites (Scorpiones: Buthidae)

Figures 152–154. Olivierus longichelus from Korgas County (152–153) and its natural habitat (154). Photo: Yizun Wang.