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Fig. 1 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 1: The non-linear relationship between CO and Ca2+ con2 centrations in H 2O-CO2-CaCO3 solution. Each mixture (e.g. C) of the saturated solutions A and B lies on the straight line between them in the zone of undersaturation with respect to calcite, producing an aggressive solution that dissolves the surrounding carbonate (after Gabrovšek & Dreybrodt (2010)).

Fig. 8 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 8: Temperature, salinity and depth profiles recorded with the CTD probe during a dive inside the Y-Cave (August 27, 2003), 1 – vertical profile at the cave opening; 2 – vertical profile inside the cave entrance part; 3 – vertical profile at the turning point, section C-C'; 4 to 6 – vertical profiles in the inner part of the cave: 4 at approximately section E-E', 5 at approximately section G-G' and 6 at approximately section H-H'.

Fig. 3 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 3: The positions of temperature and light intensity data loggers inside the Y-Cave (dark circles - temperature data loggers; white circles - light intensity data loggers). Four loggers with their photosensitive cell facing upwards are marked with a black dot; the remaining cells were positioned to face the entrance of the cave.

Fig. 9 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 9: Variation of light intensity over a period of 11 days (June 19–30, 2006) at representative sites within the Y-Cave (Fig. 3): logger 1 – the entrance of the cave; logger 4 – the central part of the cave; logger 10 – the innermost part of the cave.

Fig. 6 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 6: The comparison of the tidal (solid line) and temperature (dashed line) fluctuation from February 2–8, 2004. Temperature records are from logger 4 (Fig. 3), and tides from the nearest tide gauge in Zadar port.

Fig. 7 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 7: Vertical temperature profiles inside and outside the YCave taken with the CTD probe (August 27, 2003); the profile labelled with a dotted line was taken at approximately section H-H', the profile labelled with a solid line at approximately section G-G'.

Fig. 2 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 2: The location, cross-section and layout of the Y-Cave on Dugi Otok Island, Croatia, with characteristic profiles.

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Figure 2 in "One is the loneliest number"; are we witnessing the death throes of the single-author research paper in the field of biological invasions?

Figure 2. Changes in % of research papers published over time by single-authors (white circles and grey line) and four or more authors (black circles and black line) in issues of (a) BioInvasions Records, (b) Aquatic Invasions and (c) Management of Biological Invasions.

opencc-by-4.0Jan 2019View details →

Figure 1 in "One is the loneliest number"; are we witnessing the death throes of the single-author research paper in the field of biological invasions?

Figure 1. Mean (± SE) % of research papers published in each issue of BioInvasions Records, Aquatic Invasions and Management of Biological Invasions categorised by number of authors.

opencc-by-4.0Jan 2019View details →

Figure 1 in Effects of Palmer Amaranth (Amoronthus polmeri) Establishment Time and Distance from the Crop Row on Biological and Phenological Characteristics of the Weed: Implications on Soybean Yield

Figure 1. Schematic representation of the experimental setup depicting the distance of Amoronthus polmeri (AMAPA) from the crop (i.e., 0, 24, and 48 cm from the soybean row) and the sequence of A. polmeri establishment time (i.e., 0, 1, 2, 4, 6, and 8 wk after soybean emergence [WAE] or AMAPA-0, AMAPA-1, AMAPA-2, AMAPA-4, AMAPA-6, and AMAPA-8, respectively). Each treatment combination (i.e., establishment time × distance from the crop) was applied only to one randomly selected experimental plot per replication.

Figure 9 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.

Figure 9. Relationships between embryo volume (mm3) and body size (CL3 = carapace length3) for females of Trypaea australiensis and Biffarius arenosus. Embryos were from females collected from March 2006 to May 2007 at Warneet and Crib Point, Western Port.

Figure 8 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.

Figure 8. Carapace length (CL) size frequency distributions for Biffarius arenosus collected at Crib Point, Western Port in 2006-2007. Non-ovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows show mean CL for cohorts as calculated in FISAT II.

Figure 7 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.

Figure 7. Carapace length (CL) size frequency distributions for Biffarius arenosus collected at Warneet, Western Port in 2006-2007. Non-ovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows indicate mean CL of cohorts calculated in FISAT II.

Figure 5 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.

Figure 5. Proportion of ovigerous females for April 2004 to March 2005 (a. Trypaea australiensis, b Biffarius arenosus) and March 2006 to May 2007 (c. T. australiensis, d. B. arenosus) at Warneet, Western Point. Proportion of ovigerous females for April 2006, October 2006 - February 2007 and April 2007 (e. T. australiensis, f. B. arenosus) at Crib Point, Western Port. Solid line is total proportions of ovigerous females, triangles with dashed line is proportion of ovigerous females with uneyed embryos and squares with dashed line is proportion of ovigerous females with eyed embryos.

Figure 4 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.

Figure 4. Carapace length (CL) size frequency distributions for Trypaea australiensis collected at Crib Point, Western Port in 2006-2007. Nonovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows show mean CL of the cohorts using FISAT II.

Figure 2 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.

Figure 2. Carapace length (CL) size frequency distributions for Trypaea australiensis collected at Warneet, Western Port in 2004-2005. Non-ovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows show mean CL length of the cohorts identified using FISAT II

Figure 3 in Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria.

Figure 3. Carapace length (CL) size frequency distributions for Trypaea australiensis collected at Warneet, Western Port in 2006-2007. Non-ovigerous females are shown by black bars, ovigerous females by grey bars and males by open bars (n = number of shrimp collected). Individuals are grouped into size classes by rounding to the closest mm from two decimal places. Arrows show the mean CL length of cohorts identified using FISAT II.

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Figure 2 in Endemic and enigmatic: the reproductive biology of Aegla (Crustacea: Anomura: Aeglidae) with observations on sperm structure

Figure 2. Light micrographs of Aegla rostrata Jara, 1977. A, Spermatophoric lobes; B–G, Squash of spermatophoric lobe contents showing spermatozoa (arrowheads) scattered amongst assorted cells (Asterisk in E and G indicate individual spermatozoa with three microtubular arms).

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Figure 1 in Endemic and enigmatic: the reproductive biology of Aegla (Crustacea: Anomura: Aeglidae) with observations on sperm structure

Figure 1. Occurrence of ovigerous females of Aegla species obtained from literature sources and USNM specimens. Total USNM specimens examined = 958 (40 ovigerous females). Symbols: 1 Bahamonde and López (1961); 2 Jara (1989); 3 Bueno and Bond-Buckup (2000); 4 Swiech-Ayoub and Masunari (2001a, 2001b); 5 Rodrigues and Hebling (1978); 6 Jara (1977); 7 Lopéz (1965). Shading = range from literature sources indicated. Solid black bar = number from USNM collection for that month.