In ethological literature, little is
known about responses of fish and other animals to holographic foils
which may be used in decoration of nests, sexual and schoolmate dummies,
artificial fishing lures and other objects.
To our knowledge, Östlund-Nilsson &
Holmlund (2003) offered colored metal foil sticks (15 mm length) to
males of three-spined stickleback, Gasterosteus aculeatus, to
decorate their nests and found that males preferred sticks of red color.
Even earlier, Darkov (1980) studied schooling behaviour of sunbleak, Leucaspius delineatus, and found that fish preferred to school with the silvery models than with the black models.
However, in both these works the influence of holographic patterns on the behavioural responses of fish has not been studied.
Experimental procedure
Our experiments were carried out in an
aquarium of 30 x 30 x 60 cm sizes under the daylight illumination. The
aquarium bottom was covered with the pebbles of medium size (10-15 mm).
At the distance of 3 cm from the side wall the lifting transparent glass
was located. This glass was used to stick holographic models (see
below). At the distance of 10 cm from this glass the frosted lifting
glass was located. When animals moved near this glass, this glass was
lifted and animals could see models.
This tank was used as aquarium to study fish and as terrarium to study lizards.
The experimental fish were wild perch, Perca fluviatilis (5-7 cm total length), wild roach, Rutilus rutilus (5-7 cm total length), and wild sunbleak, L. delineatus (about 4 cm total length). Fish were fed live bloodworms. The experimental lizards were sand lizards, Lacerta agilis (6-8 cm total length), which were fed live room flies and small grasshoppers (without one wing or one hind leg).
When animals discovered models, they
usually moved towards these models. Three types of responses were
fixated: 1) the first movement to the left or right model, 2) staying
near the left or right model during 30 min, and 3) the first attempt to
bite the left or right model. As animals observed both models at the
same time for free choice, the method of paired comparisons (sign test)
was used for statistics.
To make models, holographic foils produced by WTP Inc., USA (http://www.wtp-inc.com/color-card) were used.
Small holograpic fieldsFish
The sizes of models were 20 x 5 mm. Two
models were placed horizontally at the distance of 10 cm from each
other, at the height of 5 cm from the bottom and at the distance about
12-14 cm from the fish.
In the experiments of this type with
perch and roach, the left model made of red plain foil, WTP 45, and the
right model made of red holographic foil with large horizontal streaks,
WTP 825, were compared. In all experiments with permutation models from
left to right and vice versa, perch and roach preferred to approach,
stay and bite without hesitations the holographic model over the plain
model (sign test, P < 0,01).
However, fish were no able to
discriminate models with the similar holographic patterns like red prism
glitter, WTP 355, and red mini scale, WTP 185.
In general, fish can be trained to
discriminate visual abstract patterns (for review, see Northmore et al.,
1978), illusory patterns (Wyzisk & Neumeyer; 2007; Sovrano &
Bisazza, 2009; Agrillo et al., 2013), mirror patterns (Gierszewski et
al., 2013) and naturalistic forms (Schluessel et al., 2012). However, in
our experiments wild perch and roach were untrained for the aims of
visual discriminations and generalized similar holograpic patterns.
Lizards
Because lizards are more sensitive to
the light of shorter wavelengths, models of blue color were used. Models
made of blue plain foil, WTP 43, and blue holographic foil with large
horizontal streaks, WTP 823, were compared. In all cases, lizards
preferred the holographic model over the plain model (sign test, P <
0,01).
However, lizards were no able to
discriminate models with the similar holographic patterns like blue
prism glitter, WTP 353, and blue mini scale, WTP 183.
Basic wooden decoys
In this part of the experiments, we
considered how predatory fish responded in the field to the plain foils
and holographic foils with the different patterns.
Basic wooden decoys are lathed
practically of any timber, including an imported balsa, and have not any
concavities. Commonly, lures have an usable cylindric shape (with the
flat or roundish ends), an elongated oval shape, an elongated
barrel-like shape (with the flat ends) and an elongated drop-like shape
(with the most diameter in the tail, near to the hook). Decoys do not
equipped with self-righting ventral hooks, so their rostrums have not
skews for sinking or lifting.
To use 2D & 3D artificial eyes, recesses with the flat bottom are milled in the decoy bodies.
Each decoy has the central longitudinal
hole and is strung directly on the fishing line, resting on the treble
hook. To fish pike, Esox lucius, with sharp teeth, steel
leaders are used. The treble hook is decorated with the woolen or
synthetic material, commonly of white or light grey colors.
In our experiments, waterproof
cylindric wooden decoys of 5.0 cm length and 1.0 cm diameter were used.
Their bodies were enveloped with silvery plain foils and sivery
holographic foils described below. In addition, 2D eyes 7/32” with the
red iris, WTP 405, were sticked bilaterally in the head part of all
decoys.
Compared decoys were tested in pairs
using standard trolling technique on the two sides of the boat at the
same time. Trolling was carried out in daytime at the depth 2.5-3.0 m.
The distance between moving decoys was about 2 m. Visibility in the
water was 0.6-0.8 m for Secchi disk. Thus fish could not see both
compared lures simultaneously and therefore independent samples were
used for statistics.
The most abundant predatory fish like perch, P. fluviatilis, pikes, E. lucius, zanders, Stizostedion lucioperca, and asps, Aspius aspius, were catched and considered in the general pool.
In an aquarium when two flat foil
stripes (20 x 5 mm) are static, perch have enough time to study both
models and prefer (sign test, P < 0,01) the silvery holographic foil
with prism glitter, WTP 351, over the silvery plain foil, WTP 41.
In the field, however, perch and other
predatory fish are forced to attack potential prey very quickly (during
split second) and thus they have not enough time to study their visual
features. So approximately the same number of perch, pike, zander and
asp (Table 1) were caught on decoys enveloped with the plain and
holographic foils or with the different holographic foils.
In general (see Curio, 1976), the
process of prey-recognition (seconds, minutes, hours) and the process of
prey-attack (split second) are the different processes that are
separated in time.
Dodgers and flashers
Oscillating dodgers and rotating
flashers are special trolling devices. They have large sizes (up to 30
cm) and are frequently equiped with the holographic foils (Fig 1).
Fig. 1. Trolling flashers with the holographic foils.
Trolling gears with dodgers allow to
catch predatory fish of larger sizes than gears without dodgers (Dooley,
1989). It means that strongly vibrating and shining dodgers and flahers
repel relatively small predatory fish.
Nothing is known about the effect of holographic patterns.
Medium holographic fields
In the experiments of this type,
rectangular models, 4 x 1 cm, and sunbleak (about 4 cm length) had
approximately equal sizes to study schooling responses of fish. Three
randomly placed horizontal models made of silvery plain foil, WTP 41,
and three randomly placed horizontal models made of silvery holographic
foils with prism glitter, WTP 351, were compared. In all cases, highly
schooling sunbleak (1, 2 and 3 individuals) preferred to approach and to
stay near the holographic models over the plain models (sign test, P
< 0,01).
However, sunbleak were no able to
discriminate models with the similar holographic patterns like silvery
prism glitter, WTP 351, and silvery mini scale, WTP 181.
Large holographic fields
In these cases, the sizes of
holographic objects are much more than the sizes of the experimental
animals. The rectangular photos (20 x 10 cm) of underwater plants and
rectangular photos of grass at the level of sand on the one hand, and
the holographic panels (20 x 10 cm) of the various types on the second
hand were used to study the responses of fish and lizards, respectively.
Fish and lizards were introduced
individually in aquarium or terrarium in the center between photos and
holographic panels and released. In all cases, fish and lizards moved
immediately or after short confusion towards the natural backgrounds
avoiding thus the large holographic panels (sign test, P < 0,01).
All holographic patterns scare. In other words, fish and lizards are not able to distinguish scared holographic patterns.
These results are not new. It is known,
for example, that holographic foils are repellents for birds and
produced on an industrial scale (see https://www.shopwtp-inc.com/index.php?cPath=34).
Basic references
Agrillo C., Petrazzini M.E.M., Dadda M. 2013. Illusory patterns are fishy for fish, too. Frontiers in Neural Circuits 7, doi: 10.3389/fncir.2013.00137
Curio E. 1976. Ethology of predation. Zoophysiology and Ecology 7. Berlin, Springer
Darkov A.A. 1980. Ecological features of visual signalling in fishes. Moscow, Science Publishing
Dooley R.H.A. 1989. The response of rainbow trout (Salmo gairdneri) to lures with special reference to color preference. Master’s Thesis. University of British Columbia, Canada, 1-76
Gierszewski S., Bleckmann H., Schluessel V. 2013. Cognitive abilities in malawi cichlids (Pseudotropheus sp.): matching-to-sample and image/mirror-image discriminations. PLoS ONE 8: e57363. doi:10.1371/journal.pone.0057363
Northmore D., Volkmann F.C., Yager D. 1978. Vision in fishes: color and pattern. The Behavior of Fish and Other Aquatic Animals. Edited by D.I. Mostofsky. Academic Press, New York
Östlund-Nilsson S., Holmlund M. 2003. The artistic three-spined stickleback (Gasterosteus aculeatus). Behavioral Ecology and Sociobiology 53, 214-220
Schluessel V., Fricke G., Bleckmann H. 2012. Visual discrimination and object categorization in the cichlid Pseudotropheus sp. Animal Cognition 15:525-537
Siebeck U.E., Litherland L., Wallis G.M. 2009. Shape learning and discrimination in reef fish. Journal of Experimental Biology 212, 2113-2119
Sovrano V.A., Bisazza A. 2009. Perception of subjective contours in fish. Perception 38, 579-590
Wyzisk K., Neumeyer C. 2007. Perception of illusory surfaces and contours in goldfish. Visual neuroscience 24, 291-298
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Friday, July 27, 2018
Animal responses to holographic patterns
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