scholarly journals Homing behaviour by destructive crown-of-thorns starfish is triggered by local availability of coral prey

2020 ◽  
Vol 287 (1938) ◽  
pp. 20201341
Author(s):  
S. D. Ling ◽  
Z.-L. Cowan ◽  
J. Boada ◽  
E. B. Flukes ◽  
M. S. Pratchett

Corallivorous crown-of-thorns starfishes ( Acanthaster spp.) can decimate coral assemblages on Indo-Pacific coral reefs during population outbreaks. While initial drivers of population irruptions leading to outbreaks remain largely unknown, subsequent dispersal of outbreaks appears coincident with depletion of coral prey. Here, we used in situ time-lapse photography to characterize movement of the Pacific crown-of-thorns starfish ( Acanthaster cf. solaris ) in the northern and southern Great Barrier Reef in 2015, during the fourth recorded population outbreak of the starfish, but prior to widespread coral bleaching. Daily tracking of 58 individuals over a total of 1117 h revealed all starfish to move a minimum of 0.52 m, with around half of all tracked starfish showing negligible daily displacement (less than 1 m day −1 ), ranging up to a maximum of 19 m day −1 . Movement was primarily nocturnal and daily displacement varied spatially with variation in local availability of Acropora spp., which is the preferred coral prey. Two distinct behavioural modes emerged: (i) homing movement, whereby tracked paths (as tested against a random-walk-model) involved short displacement distances following distinct ‘outward' movement to Acropora prey (typically displaying ‘feeding scars') and ‘homebound' movement to nearby shelter; versus (ii) roaming movement, whereby individuals showed directional movement beyond initial tracking positions without return. Logistic modelling revealed more than half of all tracked starfish demonstrated homing when local abundance (percentage cover) of preferred Acropora coral prey was greater than 33%. Our results reveal facultative homing by Acanthaster with the prey-dependent behavioural switch to roaming forays providing a mechanism explaining localized aggregations and diffusion of these population irruptions as prey is locally depleted.

2016 ◽  
Vol 57 (72) ◽  
pp. 118-127 ◽  
Author(s):  
Kristin M. Schild ◽  
Robert L. Hawley ◽  
Blaine F. Morriss

ABSTRACTMarine-terminating outlet glaciers discharge most of the Greenland ice sheet's mass through frontal ablation and meltwater runoff. While calving can be estimated by in situ and remote sensing observations, submarine melting and subglacial meltwater transport are more challenging to quantify. Here we investigate the subglacial hydrology of Rink Isbræ, a fast-flowing West Greenland tidewater glacier, using time-lapse photography, modeled runoff estimates and daily satellite imagery from 2007 to 2011. We find that sediment plumes appear episodically at four distinct locations across the terminus, and last between 2 h and 17 d. This suggests short-term variability in discharge and the existence of persistent pathways. The seasonal onset of sediment plumes occurs before supraglacial lake drainages, shortly after the onset of runoff, and only after the wintertime ice mélange has begun disintegrating. Plumes were also visible after the cessation of runoff (23 ± 5 d), which is indicative of subglacial storage. The lack of either a seasonal velocity change or a correspondence between meltwater availability and plume occurrence suggests that the subglacial system persists in a state of inefficient drainage. Subglacial hydrology at tidewater glaciers is of critical importance in understanding dynamics at the ice front.


2020 ◽  
Author(s):  
Dominic Franco C. Belleza ◽  
Yuuki Kawabata ◽  
Tatsuki Toda ◽  
Gregory N. Nishihara

ABSTRACTTrophic cascades exerts a powerful effect between predator and prey relationships in an ecosystem. In aquatic environments, the signals associated with predators and predation are used by prey as a cue to avoid encountering predators when foraging for food. These cues are powerful enough to control prey populations and indirectly protect primary producers. We evaluated the effects of cues associated with predation on the purple urchin, Heliocidaris crassispina and examined effects of hunger state and season using time-lapse photography, we conducted a series of manipulative and in situ behavior experiments to determine foraging behavior patterns which demonstrate behavior modification. The results suggest that starved urchins were less sensitive to predation cues when compared to normally fed urchins. Field experiments indicated that 70% of fed urchins fled when exposed to a predation cue (presence of a dead urchin), whereas all starved urchins remained regardless of the cue, supporting the results from the laboratory using the dead urchin and algae treatment cues. Sea urchin activity and feeding rates were lower in winter-spring than in summer-autumn. We suggest that hunger state has a large influence over the behavioral-response of sea urchins, while also being affected by season due to metabolic control. In general, starvation overrides predator avoidance behaviors and exposes prey species to higher risks of predation.


2021 ◽  
Vol 664 ◽  
pp. 133-148
Author(s):  
DFC Belleza ◽  
Y Kawabata ◽  
T Toda ◽  
GN Nishihara

Trophic cascades are a powerful result of predator-prey relationships in an ecosystem. In aquatic environments, the signals associated with predators and predation are used by prey as a cue to avoid encountering predators when foraging for food. These behavioral cues can be powerful enough to control prey populations and indirectly protect primary producers. Here, we evaluated the effects of cues associated with predation on the purple urchin Heliocidaris crassispina and examined effects of hunger state and season, using time-lapse photography. A series of laboratory and in situ manipulative experiments were conducted to determine patterns of foraging behavior and behavioral modifications. We showed that starved urchins were less sensitive to predation cues compared to normally fed urchins. Field experiments indicated that 70% of fed urchins fled when exposed to a predation cue (presence of a dead urchin) whereas starved urchins remained regardless of the cue, supporting results from the laboratory using dead urchin and algal cues. Sea urchin activity and feeding rates were lower in winter-spring than in summer-autumn. Results suggest that hunger state has a large influence over the behavioral response of sea urchins, while also being affected by season due to metabolic control. In general, starvation appears to override predator avoidance behaviors, which exposes prey species to higher risks of predation.


Development ◽  
1972 ◽  
Vol 27 (3) ◽  
pp. 623-637
Author(s):  
Alfredo Castro-Quezada ◽  
Bernardo Nadal-Ginard ◽  
María V. de la Cruz

The formation of the normal bulboventricular loop (convex to the right) and the inverted loop (convex to the left) produced by the Lepori technique in chick embryos was studied. The development of the loops was recorded by means of diagrams, photographs and microscopic time-lapse photography. Electron-microscope studies were also made. The normal loop was studied by means of labelling and removal experiments on the heart tube. The results demonstrated that the fusion of both cardiac primordia is made in stage 9 — in the mid-line of the embryo and that the first asymmetry of the heart tube appears in stage 10. The truncus region developed in situ directed towards the right after the fusion of both cardiac primordia, and in this region the electron-microscope study demonstrated a gradient of caudo-cephalic differentiation. In stage 10 the left caudal groove is the prospective interventricular groove, but the right caudal groove is not the right atrioventricular groove as had been stated by others. The asymmetric incorporation of both primordia begins in stage 11 —, when the curvature of the loop is already developing. In the removal experiments it was evident that the different portions of the cardiac tube in situ are orientated in space independently of the whole of the loop. The formation of the experimentally inverted loop is a mirror-image of the normal loop and appears to be originated through mechanic traction of the cardiac tube by the left splachnopleure and not by a faster displacement of the right cardiac primordia.


2019 ◽  
Vol 83 (1) ◽  
pp. 21-32
Author(s):  
Gesche Kohlberg ◽  
Anne Herbst ◽  
Gerd Niedzwiedz ◽  
Stefan Woelfl ◽  
Jorge Nimptsch ◽  
...  

2021 ◽  
Author(s):  
Koki Oikawa ◽  
Hirotaka Saito ◽  
Seiichiro Kuroda ◽  
Kazunori Takahashi

<p>As an array antenna ground penetrating radar (GPR) system electronically switches any antenna combinations sequentially in milliseconds, multi-offset gather data, such as common mid-point (CMP) data, can be acquired almost seamlessly. However, due to the inflexibility of changing the antenna offset, only a limited number of scans can be obtained. The array GPR system has been used to collect time-lapse GPR data, including CMP data during the field infiltration experiment (Iwasaki et al., 2016). CMP data obtained by the array GPR are, however, too sparse to obtain reliable velocity using a standard velocity analysis, such as semblance analysis. We attempted to interpolate the sparse CMP data based on projection onto convex sets (POCS) algorithm (Yi et al., 2016) coupled with NMO correction to automatically determine optimum EM wave velocity. Our previous numerical study showed that the proposed method allows us to determine the EM wave velocity during the infiltration experiment.</p><p>The main objective of this study was to evaluate the performance of the proposed method to interpolate sparse array antenna GPR CMP data collected during the in-situ infiltration experiment at Tottori sand dunes. The interpolated CMP data were then used in the semblance analysis to determine the EM wave velocity, which was further used to compute the infiltration front depth. The estimated infiltration depths agreed well with independently obtained depths. This study demonstrated the possibility of developing an automatic velocity analysis based on POCS interpolation coupled with NMO correction for sparse CMP collected with array antenna GPR.</p>


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