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opencc-by-4.0Jul 2020View details →

Fig. 3 in Lady beetle oviposition site choices: maternal effects on offspring performance

Fig. 3. Reflectance spectrum for the elytra of Cycloneda sanguinea (n = 33) (A) and Hippodamia convergens (n = 18) (B) adults when fed with Uroleucon or Brevicoryne aphids during the immature stages. Each curve represents the average of 6 spectral measures (3 in each elytra) performed for each individual.

opencc-by-4.0Jul 2020View details →

Fig. 5 in Lady beetle oviposition site choices: maternal effects on offspring performance

Fig. 5. PCA graph performed for the following variables: development time (time), brightness, weight, and chroma derived from carotenoids, with the position of Hippodamia convergens (A) and Cycloneda sanguinea (B) adults which have emerged from the Uroleucon (grey) and Brevicoryne (black) diet during the immature stages, when sorted in function of the 2 main axes of data variation.

Fig. 5 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany

Fig. 5 Occurrence of mosquito taxa in relation to trap location. The number of analysable traps is given in brackets. For abbreviations, see Fig. 2

Fig. 4 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany

Fig. 4 Canonical correspondence analysis of land use types and mosquito taxa. Ae. j. japonicus occupied significantly more positive ovitraps in the settlement–forest transition zone than in other trap locations (Fisher's exact test: P = 0.0045 tested against arable land– forest, P <0.0001 tested against arable land–settlement)

Fig. 3 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany

Fig. 3 Percentages of mosquito-positive ovitraps (Traps positive), and air temperatures. Air temperature was calculated in the week before sampling in 2018. Sampling dates and the number of analysable ovitraps from a total of 270 ovitraps (in brackets) are shown on the x-axis. There was no statistically significant difference between the numbers of Aedes japonicus japonicus-positive ovitraps sampled in spring (April–May) and in autumn (October–November) (identical lowercase letters). By contrast, the numbers of Ae. japonicus japonicus-positive ovitraps in the summer (12 June to 25 September) were statistically significantly higher than in spring and autumn (different lowercase letters) (Fisher's exact test: P <0.0001. For all P-values, see Additional file 1: Table S2. For total numbers of emerged adults, see Additional file 2: dataset S1

Fig. 6 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany

Fig. 6 Logistic regression of probability proportion of adults hatched from larvae of Cx. pipiens s.l. vs. Ae. japonicus japonicus collected at the specified temperatures. Data from 2017 and 2018 (23 May to 25 September) for ovitraps located along the forest–settlement transect. Function jitter was used for taxa proportion data to improve visibility [85]

opencc-by-4.0Feb 2019View details →

Table 2 in Predation and oviposition potential of Brazilian populations of the predatory mite Amblyseius tamatavensis (Acari: Phytoseiidae) on eggs of Bemisia tabaci (Insecta: Hemiptera)

Table 2 Mean lengths (in micrometers ± standard error of the mean) of structures of populations of Amblyseius tamatavensis collected in different Brazilian municipalities (May 2015 to May 2016), and mean lengths given in the original description of the species (Blommers 1974).<table><tbody><tr><th>Parameter 1</th><th>Olho d’Água das Flores</th><th>Jataí</th><th>Nova- Crixás</th><th>Bom Repouso</th><th>Ituiutaba</th><th>Senador Amaral</th><th>Campinas</th><th>Cananéia</th><th>Mogi- Guaçu</th><th>Piracicaba (Areão)</th><th>Piracicaba (ESALQ)</th><th>Saltinho</th><th>Santa Maria da Serra</th><th>Lab.</th><th>Original descrip.</th></tr></tbody><tbody><tr><th>DSL</th><td>341±6 a</td><td>336±3 b</td><td>328±4 c</td><td>337±4 b</td><td>336±3 b</td><td>335 ± 7 b</td><td>333±3 b</td><td>338±5 b</td><td>337±5 b</td><td>333±2 c</td><td>336±4 b</td><td>324±6 c</td><td>325±2 c</td><td>342±5 a</td><td>340</td></tr><tr><th>DSW</th><td>231±4 a</td><td>226±4 b</td><td>223±3 bc</td><td>226±2 b</td><td>227±4 b</td><td>225±3 b</td><td>219±2 c</td><td>220±1 c</td><td>224±1 b</td><td>226±3 b</td><td>226±3 b</td><td>224±3 b</td><td>226 ± b</td><td>233±2 a</td><td>250</td></tr><tr><th>j1</th><td>32±0 a</td><td>31±0 a</td><td>32±0 a</td><td>32±0 a</td><td>32±0 a</td><td>32±1 a</td><td>30±3 a</td><td>31±1 a</td><td>33±0 a</td><td>32±1 a</td><td>31±2 a</td><td>31±1 a</td><td>31 ± 0 a</td><td>32±0 a</td><td>32</td></tr><tr><th>j3</th><td>51±1 b</td><td>54±2 a</td><td>50±4 b</td><td>52±3 b</td><td>54±1 a</td><td>55±2 a</td><td>52±1 b</td><td>51±5 b</td><td>55±2 a</td><td>52±1 b</td><td>55±1 a</td><td>52±1 b</td><td>51 ± 1 b</td><td>55±1 a</td><td>54</td></tr><tr><th>j4</th><td>5±0 a</td><td>5±0 a</td><td>5±0 a</td><td>5±0 a</td><td>5±0 a</td><td>6±0 a</td><td>5±0 a</td><td>5±1 a</td><td>5±0 a</td><td>5±0 a</td><td>5±0 a</td><td>5±0 a</td><td>5 ± 0 a</td><td>5±0 a</td><td>4</td></tr><tr><th>j5</th><td>4±0 a</td><td>3±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>3±0 a</td><td>3±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>3</td></tr><tr><th>J2</th><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>5±0 a</td><td>5±0 a</td><td>6±0 a</td><td>5±1 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6 ± 0 a</td><td>6±0 a</td><td>5</td></tr><tr><th>J5</th><td>8±0 a</td><td>7±1 a</td><td>7±1 a</td><td>7±0 a</td><td>7±1 a</td><td>7±0 a</td><td>7±1 a</td><td>8±0 a</td><td>7±1 a</td><td>8±0 a</td><td>7±1 a</td><td>7±0 a</td><td>7 ± 1 a</td><td>7±1 a</td><td>6</td></tr><tr><th>z2</th><td>6±0 a</td><td>6±1 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±1 a</td><td>6±0 a</td><td>6±0 a</td><td>7±0 a</td><td>7±0 a</td><td>6±1 a</td><td>7 ± 0 a</td><td>6±0 a</td><td>6</td></tr><tr><th>z4</th><td>7±0 a</td><td>7±0 a</td><td>6±0 a</td><td>7±0 a</td><td>6±1 a</td><td>7±0 a</td><td>6±1 a</td><td>6±0 a</td><td>7±0 a</td><td>7±0 a</td><td>7±0 a</td><td>6±0 a</td><td>6 ± 0 a</td><td>7±0 a</td><td>6</td></tr><tr><th>z5</th><td>4±0 a</td><td>4±1 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>3±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4±0 a</td><td>4 ± 0 a</td><td>4±0 a</td><td>3</td></tr><tr><th>Z1</th><td>6±0 a</td><td>6±1 a</td><td>7±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±1 a</td><td>6±0 a</td><td>6±0 a</td><td>7±0 a</td><td>6±0 a</td><td>7±0 a</td><td>6 ± 0 a</td><td>7±0 a</td><td>5</td></tr><tr><th>Z4</th><td>105±2 a</td><td>107±3 a</td><td>105±2 a</td><td>105±2 a</td><td>105±2 a</td><td>107±3 a</td><td>104±1 a</td><td>106±2 a</td><td>105±3 a</td><td>105±3 a</td><td>104±2 a</td><td>104±2 a</td><td>106 ±1 a</td><td>106±1 a</td><td>115</td></tr><tr><th>Z5</th><td>229±2 a</td><td>226±5 a</td><td>225±2 a</td><td>227±2 a</td><td>228±3 a</td><td>227±4 a</td><td>225±3 a</td><td>228±4 a</td><td>228±3 a</td><td>228±1 a</td><td>228±2 a</td><td>229±2 a</td><td>227±1a</td><td>229±2 a</td><td>250</td></tr><tr><th>s4</th><td>86±3 a</td><td>88±2 a</td><td>87±3 a</td><td>87±3 a</td><td>88±2 a</td><td>89±2 a</td><td>86±2 a</td><td>86±2 a</td><td>89±3 a</td><td>88±2 a</td><td>88±3 a</td><td>86±2 a</td><td>88±1 a</td><td>87±3 a</td><td>88</td></tr><tr><th>S2</th><td>7 ±0 a</td><td>6±1 a</td><td>7±0 a</td><td>6±0 a</td><td>7±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>7±0 a</td><td>7±0 a</td><td>6 ± 0 a</td><td>6±0 a</td><td>5</td></tr><tr><th>S4</th><td>6 ±1 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>7±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6 ± 0 a</td><td>6±0 a</td><td>6</td></tr><tr><th>S5</th><td>6 ±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6±0 a</td><td>6 ± 0 a</td><td>6±0 a</td><td>6</td></tr><tr><th>r3</th><td>14±1 a</td><td>15±1 a</td><td>13±1 a</td><td>14±1 a</td><td>14±1 a</td><td>14±1 a</td><td>13±2 a</td><td>14±1 a</td><td>15±1 a</td><td>15±1 a</td><td>15±1 a</td><td>14±1 a</td><td>14 ± 0 a</td><td>15±1 a</td><td>15</td></tr><tr><th>R1</th><td>7±0 a</td><td>7±1 a</td><td>7±0 a</td><td>7±0 a</td><td>7±0 a</td><td>7±0 a</td><td>7±0 a</td><td>7±1 a</td><td>7±1 a</td><td>7±1 a</td><td>7±0 a</td><td>7±0 a</td><td>7 ± 0 a</td><td>7±1 a</td><td>5</td></tr><tr><th>VASL</th><td>117±2 a</td><td>110±4 b</td><td>110±5 b</td><td>114±1 ab</td><td>110±2 b</td><td>108±4 b</td><td>111±3 b</td><td>112±3 b</td><td>113±2 b</td><td>113±2 b</td><td>108±3 b</td><td>109±3 b</td><td>111 ± 1 b</td><td>119±3 a</td><td>120</td></tr><tr><th>VASWant</th><td>99±3 a</td><td>97±4 a</td><td>94±3 b</td><td>95±3 b</td><td>95±2 b</td><td>93±2 b</td><td>91±4 b</td><td>98±4 a</td><td>97±3 a</td><td>95±2 b</td><td>97±2 a</td><td>91±3 b</td><td>92 ± 1 b</td><td>100±4 a</td><td>100</td></tr><tr><th>VASWpost</th><td>62±3 a</td><td>60±2 a</td><td>64±3 a</td><td>63±2 a</td><td>62±2 a</td><td>63±2 a</td><td>62±1 a</td><td>63±2 a</td><td>64±3 a</td><td>63±2 a</td><td>64±2 a</td><td>62±3 a</td><td>62± 2 a</td><td>62±4 a</td><td>-</td></tr><tr><th>St1-St2</th><td>32±0 a</td><td>32±0 a</td><td>32±1 a</td><td>33±1 a</td><td>33±0 a</td><td>32±0 a</td><td>32±1 a</td><td>32±0 a</td><td>34±0 a</td><td>32±1 a</td><td>32±1 a</td><td>32±1 a</td><td>33 ± 0 a</td><td>33±0 a</td><td>-</td></tr><tr><th>St2-St2</th><td>68±2 a</td><td>69±0 a</td><td>68±2 a</td><td>68±1 a</td><td>68±0 a</td><td>68±1 a</td><td>67±1 a</td><td>69±1 a</td><td>69±1 a</td><td>67±1 a</td><td>68±0 a</td><td>68±0 a</td><td>68 ± 1 a</td><td>70±0 a</td><td>-</td></tr><tr><th>St3-St3</th><td>76±2 a</td><td>77±2 a</td><td>76±2 a</td><td>78±3 a</td><td>76±2 a</td><td>78±1 a</td><td>75±1 a</td><td>77±2 a</td><td>77±2 a</td><td>76±2 a</td><td>76±2 a</td><td>76±1 a</td><td>77 ± 1 a</td><td>78±2 a</td><td>-</td></tr><tr><th>St1-St3</th><td>59±1 a</td><td>60±2 a</td><td>61±1 a</td><td>60±1 a</td><td>60±1 a</td><td>60±1 a</td><td>59±1 a</td><td>60±1 a</td><td>61±1 a</td><td>60±1 a</td><td>59±1 a</td><td>59±1 a</td><td>61 ± 0 a</td><td>62±1 a</td><td>-</td></tr><tr><th>St2-St3</th><td>27±1 a</td><td>27±1 a</td><td>28±1 a</td><td>27±1 a</td><td>28±1 a</td><td>28±0 a</td><td>27±1 a</td><td>28±1 a</td><td>28±1 a</td><td>28±1 a</td><td>28±1 a</td><td>27±0 a</td><td>28 ± 0 a</td><td>29±1 a</td><td>-</td></tr><tr><th>St4-St4</th><td>94±3 a</td><td>86±2 b</td><td>81±3 c</td><td>86±2 b</td><td>84±1 b</td><td>88±8 ab</td><td>81±3 c</td><td>84±2 b</td><td>84±3 b</td><td>86±3 b</td><td>86±2 b</td><td>81±3 c</td><td>85 ± 1 b</td><td>92±3 a</td><td>-</td></tr><tr><th>St5-St5</th><td>74±2 a</td><td>74±1 a</td><td>74±2 a</td><td>75±1 a</td><td>74±2 a</td><td>74±2 a</td><td>73±1 a</td><td>75±1 a</td><td>76±2 a</td><td>76±2 a</td><td>74±1 a</td><td>74±2 a</td><td>75 ± 2 a</td><td>76±2 a</td><td>-</td></tr><tr><th>Jv1</th><td>15±1 a</td><td>16±0 a</td><td>16±1 a</td><td>17±1 a</td><td>16±1 a</td><td>17±1 a</td><td>16±1 a</td><td>15±1 a</td><td>17±1 a</td><td>16±1 a</td><td>17±0 a</td><td>16±1 a</td><td>17 ± 0 a</td><td>17±1 a</td><td>-</td></tr><tr><th>Jv2</th><td>15±1 a</td><td>16±1 a</td><td>15±1 a</td><td>15±1 a</td><td>15±0 a</td><td>15±1 a</td><td>16±0 a</td><td>15±1 a</td><td>15±2 a</td><td>15±1 a</td><td>15±0 a</td><td>15±0 a</td><td>15 ± 0 a</td><td>16±1 a</td><td>-</td></tr><tr><th>Jv4</th><td>8±0 a</td><td>7±0 a</td><td>7±1 a</td><td>8±0 a</td><td>8±0 a</td><td>8±0 a</td><td>8±0 a</td><td>8±1 a</td><td>8±1 a</td><td>8±0 a</td><td>8±0 a</td><td>8±0 a</td><td>8 ± 0 a</td><td>7±0 a</td><td>-</td></tr><tr><th>Jv5</th><td>78±3</td><td>73±2</td><td>77±4</td><td>78±3</td><td>79±3</td><td>81±4</td><td>74±1</td><td>80±3</td><td>83±4</td><td>81±3</td><td>82±2</td><td>80±3</td><td>81 ± 2 a</td><td>82±3</td><td>84</td></tr><tr><th>Zv1</th><td>14±1 a</td><td>16±0 a</td><td>14±1 a</td><td>14±1 a</td><td>15±0 a</td><td>15±0 a</td><td>14±1 a</td><td>14±1 a</td><td>14±1 a</td><td>14±1 a</td><td>15±0 a</td><td>15±1 a</td><td>15 ± 0 a</td><td>14±0 a</td><td>-</td></tr><tr><th>Zv2</th><td>12±1 a</td><td>12±0 a</td><td>12±1 a</td><td>12±1 a</td><td>12±1 a</td><td>12±1 a</td><td>11±1 a</td><td>12±1 a</td><td>12±0 a</td><td>12±0 a</td><td>13±0 a</td><td>12±1 a</td><td>12 ± 0 a</td><td>13±1 a</td><td>-</td></tr><tr><th>Zv3</th><td>9±0 a</td><td>9±1 a</td><td>9±0 a</td><td>9±0 a</td><td>9±0 a</td><td>9±0 a</td><td>9±0 a</td><td>9±1 a</td><td>9±1 a</td><td>9±0 a</td><td>10±1 a</td><td>9±0 a</td><td>9 ± 0 a</td><td>10±0 a</td><td>-</td></tr><tr><th>SgeIV</th><td>98±2 a</td><td>97±3 a</td><td>97±3 a</td><td>98±3 a</td><td>97±2 a</td><td>99±2 a</td><td>98±2 a</td><td>100±2 a</td><td>100±4 a</td><td>100±1 a</td><td>98±2 a</td><td>98±3 a</td><td>99 ± 2 a</td><td>100±3 a</td><td>120</td></tr><tr><th>StiIV</th><td>66±4 a</td><td>65±3 a</td><td>66±2 a</td><td>66±3 a</td><td>67±4 a</td><td>64±2 a</td><td>65±1 a</td><td>66±4 a</td><td>65±4 a</td><td>64±3 a</td><td>66±3 a</td><td>64±3 a</td><td>65 ± 2 a</td><td>64±4 a</td><td>75</td></tr><tr><th>StIV</th><td>61±4 a</td><td>63±2 a</td><td>62±3 a</td><td>63±1 a</td><td>64±2 a</td><td>63±2 a</td><td>62±3 a</td><td>62±2 a</td><td>64±1 a</td><td>64±3 a</td><td>64±2 a</td><td>62±2 a</td><td>63 ± 0 a</td><td>65±2 a</td><td>73</td></tr><tr><th>Calyx</th><td>20±1 a</td><td>19±1 a</td><td>19±1 a</td><td>20±1 a</td><td>19±1 a</td><td>18±2 a</td><td>19±1 a</td><td>20±1 a</td><td>19±1 a</td><td>19±1 a</td><td>19±0 a</td><td>20±1 a</td><td>19±1 a</td><td>21±1 a</td><td>16</td></tr></tbody></table>1 DSL: dorsal shield length along the midline; DSW: dorsal shield width at the widest level of the podonotal region; VASL: length of the ventrianal shield along the midline; VSWant and VSWpost: anterior (at level of ZV2) and posterior (at level of anal opening) width of the ‘ventrianal shield; SgeIV, StiIV and StIV: lengths of macrosetae of genu, tibia and tarsus of leg IV; calyx: length of calyx of spermatheca. In a same line, means followed by the same letters are not statistically different (Tukey´s test; P> 0.05); (-) Not given.

opencc-by-4.0Oct 2024View details →

Different effects of Drosophila suzukii oviposition and larval activity on fruit rot and mold

Understanding symbioses and the selective pressures on symbionts requires elucidating how the different behaviors and phenotypes of hosts affect microbes. When female fruit-flies of the genus Drosophila deposit their eggs, they trigger substantial rots (i.e. the development of yeasts and bacteria) and molds (i.e. the development of filamentous fungi). It is however unknown whether these microbial growths are due to female oviposition per-se, or the activity of the larvae that emerge from the eggs. We investigated the specific effects of Drosophila suzukii (Diptera: Drosophilidae) female oviposition and larval activity on rot and mold development in fresh, on-plant strawberry and raspberry. To disentangle the effects of egg deposition from that of larval presence some females were mated with sterile males, as occurs when the Sterile Insect Technique (SIT) is deployed.   This “sterile treatment” without larvae produced intermediate intensities of rot and mold development, greater than “controls” unexposed to flies, but lower than the “fertile treatment” exposed to fertile flies. The proportion of berries too rotten for market access 3 days post-exposure was however equivalent in the sterile and the fertile treatments. But mold after 3 days was only pervasive in the fertile treatment and on strawberry. These results show specific effects of oviposition and larval activity on the development of yeast, bacteria and molds. The study indicates that when D. suzukii females are present in the field, damages to crops cannot be reduced by the release of sterile males. Instead, the sterile insect technique should be used to prevent population build-up.

opencc-by-4.0Jul 2017View details →

Fig. 4 in Dependence of daily oviposition activity and total fecundity on body mass in the house cricket Acheta domesticus (L.) (Insecta: Orthoptera)

Fig. 4: Total fecundity (mean + sd) measured for female crickets belonging to mass category (MC) 1, 2, and 3. Asterisks indicate highly significant differences between adjacent mean values (p <0.001).

opencc-by-4.0Jul 2017View details →

Fig. 3 in Dependence of daily oviposition activity and total fecundity on body mass in the house cricket Acheta domesticus (L.) (Insecta: Orthoptera)

Fig. 3: Temporal course of daily fecundity (mean + sd) in Acheta domesticus and its dependence on body mass. Three mass categories (MC) have been distinguished: MC1 ‒ 600-800 mg, MC2 ‒ 801- 100 mg, MC3 ‒ 1001-1200 mg; (a) 1st to 7th day of oviposition period; (b) 8th to 14th day; (c) 15th to 21st day, (d) 22nd to 28th day, (e) 29th to 35th day. Between most adjacent values significant differences (p <0.05) could be determined.

opencc-by-4.0Jul 2017View details →

Fig. 2 in Dependence of daily oviposition activity and total fecundity on body mass in the house cricket Acheta domesticus (L.) (Insecta: Orthoptera)

Fig. 2: Equipment for the culture of the house cricket Acheta domesticus: (a) climate chamber with plastic boxes containing cricket nymphs, (b) glass vessels containing adults separated by gender, (c) small oviposition vessels for the investigation of daily fecundity.

Figure 2. A in Oviposition behavior and host records for the parasitic midge Trichochilus lacteipennis (Johannsen) (Chironomidae: Orthocladiinae)

Figure 2. A female Trichochilus lacteipennis with egg string fully extruded, as it descended toward the water surface just prior to releasing the eggs.

Figure 3. A in Oviposition behavior and host records for the parasitic midge Trichochilus lacteipennis (Johannsen) (Chironomidae: Orthocladiinae)

Figure 3. A string of Trichochilus lacteipennis eggs suspended in water near the bottom of a glass rearing vessel.

Figure 1 in Oviposition behavior and host records for the parasitic midge Trichochilus lacteipennis (Johannsen) (Chironomidae: Orthocladiinae)

Figure 1. Two adult female Trichochilus lacteipennis hovering over Lake Umbagog, in the process of extruding strings of eggs.

Figure 4 in Oviposition behavior and host records for the parasitic midge Trichochilus lacteipennis (Johannsen) (Chironomidae: Orthocladiinae)

Figure 4. Four Trichochilus lacteipennis pupae revealed by incision of the outer lamella (marsupium) of the right gill of an Elliptio complanata.

opencc-by-4.0Jul 2023View details →

The influence of prey density and pollen on the predation and oviposition rate of Amblyseius swirskii on Echinothrips americanus

Data set of the research: "The influence of prey density and pollen on the predation and oviposition rate of Amblyseius swirskii on Echinothrips americanus". The dataset contains observations of predation and oviposition of Amblyseius swirskii on Echinothrips americanus. The different conditions were leaf area and prey density.