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370 results for “Seasonal variations”
Figure 2 in Seasonal variations in immunoreactive cortisol and fecal immunoglobulin levels in Sichuan golden monkey (Rhinopithecus roxellana)
Figure 2. Immunoreactive cortisol concentrations in males (M1 was the dominant male; M2 and M3 were all-male units) within seasons (ng/g). Sp: Spring; Su: summer; Au: autumn; Wi: winter. a,b,c,d: Histograms that share the same letters do not differ from each other, whereas histograms with different letters are different at P <0.05. *,#: P <0.05, bar with # was significantly higher than bar with *.
Figure 1 in Seasonal variations in immunoreactive cortisol and fecal immunoglobulin levels in Sichuan golden monkey (Rhinopithecus roxellana)
Figure 1. Immunoreactive cortisol concentrations in nonpregnant (F1 and F2) and pregnant (F3) females within seasons (ng/g). Sp: spring; Su: summer; Au: autumn; Wi: winter. a,b,c,d: Histograms that share the same letters do not differ from each other, whereas histograms with different letters are different at P <0.05. *,#: P <0.05, bar with * was significantly higher than bar with #.
Figure 4 in Seasonal variations in immunoreactive cortisol and fecal immunoglobulin levels in Sichuan golden monkey (Rhinopithecus roxellana)
Figure 4. The immunoreactive cortisol concentrations of Sichuan golden monkeys over the year (ng/g). FM refers to mean of nonpregnant females (F1 and F2); MM refers to mean of males (M1, M2, and M3).
Figure 3 in Seasonal variations in body length and fecundity of 2 copepod species: Thermocyclops crassus (Fischer, 1853) and Eudiaptomus drieschi (Poppe & Mrázek, 1895
Figure 3. Monthly variations in mean egg numbers and lengths of females and males of 2 copepod species in Lake Yenişehir during the study period (broken lines show that no E. drieschi was found in this period).
Figure 2 in Seasonal variations in body length and fecundity of 2 copepod species: Thermocyclops crassus (Fischer, 1853) and Eudiaptomus drieschi (Poppe & Mrázek, 1895
Figure 2. Monthly variations of temperature, phosphate, nitrate, dissolved oxygen, and chlorophyll-a during the study in Lake Yenişehir, from May 2003 to June 2004 (±SD).
Figure 3 in Composition and seasonal variation of epigeic arthropods in field margins of NW Portugal
Figure 3. Mean abundance per pitfall for each guild in spring and autumn. Seasons were compared using a Kruskal–Wallis test followed by a Dunn's post hoc test (P <0.05). Bars represent means ± standard deviation. Distinct letters indicate statistical differences.
Figure 1. a in Composition and seasonal variation of epigeic arthropods in field margins of NW Portugal
Figure 1. a) Mean abundance per pitfall in autumn and spring. Seasons were compared using a Mann–Whitney U test; b) mean group richness per pitfall in autumn and spring. Seasons were compared using a Mann–Whitney U test. Bars represent means ± standard deviation. Distinct letters between seasons indicate statistical differences (P <0.001).
Figure 2 in Composition and seasonal variation of epigeic arthropods in field margins of NW Portugal
Figure 2. Nonmetric multidimensional scaling (nMDS) ordination in 2 dimen- sions computed for the 4 sites in spring and autumn. Lines group fields with a similarity of 35% or higher based on a group average cluster analysis. The value of stress is represented.
Figure 6 in Seasonal variations of abundance and live/dead compositions of copepods in Mersin Bay, northeastern Levantine Sea (eastern Mediterranean)
Figure 6. Percentage of dead copepods at the coastal and open water stations (a), and the percentage of dead copepods at 0–100 and 100–195 m at the open water station (b).
Figure 5 in Seasonal variations of abundance and live/dead compositions of copepods in Mersin Bay, northeastern Levantine Sea (eastern Mediterranean)
Figure 5. Cluster diagram of abundance data sets of monthly sampling based on the Bray– Curtis similarity matrix (1 represents coastal station, 2 represents open water station).
Figure 4 in Seasonal variation and taxonomic composition of mesozooplankton in the southern Black Sea (off Sinop) between 2005 and 2009
Figure 4. Percentage composition of the main mesozooplankton groups in terms of abundance and biomass off Sinop for 2005–2009.
Figs 4-8 in Influence of environmental variables on seasonal abundance and relative growth of Macrobrachium amazonicum (Crustacea: Decapoda: Caridea): variations of a continental population
Figs 4-8. Percentage distribution of the independent effect of the abiotic factor on the total abundance (Fig. 4), and on the abundance by demographic category (Figs 5-8) of Macrobrachium amazonicum (Heller, 1862). Grey bars indicate a significant effect (p<0.05), determined by the randomization test. Positive and relative relationships are shown by the bars above and under the horizontal aXis, respectively (EC, conductivity; DO, dissolved oXygen; PI, precipitation; T, water temperature).
Figs 2, 3 in Influence of environmental variables on seasonal abundance and relative growth of Macrobrachium amazonicum (Crustacea: Decapoda: Caridea): variations of a continental population
Figs 2, 3. Percentage of total abundance (Fig. 2) and juveniles, males, non-ovigerous females and ovigerous females (Fig. 3) of Macrobrachium amazonicum (Heller, 1862) along the study period (J, juveniles; M, males; NOF, non-ovigerous female; OF, ovigerous females).
Fig. 5 in Seasonal variation of the crustacean fauna in the belowground and aboveground strata in a Halodule wrightii meadow of northeastern Brazil
Fig. 5. Similarity among samples from aboveground stratum of Halodule wrightii meadow on Goiabeiras Beach, city of Fortaleza, state of Ceará, northeastern Brazil; Legend: I) samples collected in predominantly dry months; II) samples collected in predominantly rainy months.
Fig. 2 in Seasonal variation of the crustacean fauna in the belowground and aboveground strata in a Halodule wrightii meadow of northeastern Brazil
Fig. 2. Abundance of crustacean fauna captured in belowground and aboveground strata of Halodule wrightii meadow on Goiabeiras Beach, city of Fortaleza, state of Ceará, northeastern Brazil.
Fig. 4 in Seasonal variation of the crustacean fauna in the belowground and aboveground strata in a Halodule wrightii meadow of northeastern Brazil
Fig. 4. Similarity among samples from belowground stratum of Halodule wrightii meadow on Goiabeiras Beach, city of Fortaleza, state of Ceará, northeastern Brazil; Legend: I) samples collected in predominantly dry months; II) samples collected in predominantly rainy months; III) samples collected in both climatic periods.
Fig. 1 in Seasonal variation of the crustacean fauna in the belowground and aboveground strata in a Halodule wrightii meadow of northeastern Brazil
Fig. 1. Location of study area. Goiabeiras Beach, city of Fortaleza, state of Ceará, northeastern Brazil.
Fig. 3 in Seasonal variation of the crustacean fauna in the belowground and aboveground strata in a Halodule wrightii meadow of northeastern Brazil
Fig. 3. Mean Shannon diversity and Pielou evenness indices of crustacean fauna associated with belowground and aboveground strata of Halodule wrightii meadow in dry and rainy seasons on Goiabeiras Beach, city of Fortaleza, state of Ceará, northeastern Brazil (a, indices for community associated with belowground stratum; b, indices for community associated with aboveground stratum).
Fig. 7 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan
Fig. 7. Number of Mothocya parvostis collected at tidal levels: low tide, 1/3 tide, 2/3 tide, and high tide during the three days of sampling.
Fig. 6 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan
Fig. 6. Temporal variation in water temperature from October 2020 to December 2021. The gap in data is due to faulty logging equipment.
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