Fishermen Advocates: Disclosing Forgery in Fishing Industries





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Animal responses to holographic patterns

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 ( were used.

Small holograpic fields


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.


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.


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Category: Lures | Views: 227 | Added by: nickyurchenko | Date: 2017-01-04

Responses of freshwater fish to fluorescent lures at daylight

Many companies manufacture fishing lures and baits of bright fluorescent colors and position these products in the consumer markets as effective tools to attract and catch fish. However, numerous scientific, technical and applied investigations and recreational fishing practice show that these assertions are, as minimum, exaggerated.

In general case, fluorescence is an optical phenomenon when molecules of some substances absorb light in the ultraviolet or visual parts of the electromagnetic spectrum and immediately re-emit it with the longer wavelength. Because the falling light is partly reflected by these substances and the reflected light is mixed with the light of fluorescence, the eyes of human and animals (if they have color vision) perceive the total colors of these substances as “more bright”.

Spectral sensitivity

Fresh waters are optically more turbid than sea waters, so the maximum of spectral sensitivity in freshwater fish is shifted to the red part of the visual spectrum. In bluegill sunfish, Lepomis macrochirus, for example, the maximum of spectral sensitivity is shifted to 620-640 nm (orange part of the spectrum) (Hawryshyn et al., 1988). According to Kawamura & Kishimoto (2002), the maximum of spectral sensitivity in largemouth bass, Micropterus salmoides, is shifted even to 673 nm (red part of the spectrum). It means that for freshwater fish red and orange colors are brighter than other colors, in full contradiction with the perception of saltwater fish and human.

This red or orange shift of the maximum of spectral sensitivity is typical for other freshwater fish (Protasov, 1978).


Turbid waters decrease overall intensity of ambient light, decrease via scattering an ability of receivers to resolve silhouettes and more (for review, see Utne-Palm, 2002). In particular, turbidity affects color perception of freshwater fish, their color patterns and communication with the assistance of color signals.

For example, with an increase in turbidity of habitat males of red shiners, Cyprinella lutrensis, develop more intensive red fins (Dugas & Franssen, 2011). According to Kelley et al. (2012), rainbowfish, Melanotaenia australis, in the dissolved organic matter treatment show an increase in the area and brightness of their orange striped patterns.

More generally, turbidity weakens color signals in inter-sexual selection (Seehausen et al. 1997), even limiting species recognition in mate choice.

Fluorescent colors underwater

Overall, fluorescent colors are brighter than ordinary colors and are more visible underwater (Kinney et al., 1967). In turbid water (like Thames river), orange fluorescent color is most visible for the human’s eye than other colors.

Other animals

For fruit fly, Anastrepha suspensa, traps of orange fluorescent color are more attractive than traps of ordinary orange color (Greany et al., 1978).

Dull males versus bright males

Accustomed to think that females, in fish and other animals with the sexual dimorphism, prefer to mate with bright males than with dull males. In turn, generally recognized that bright males are more vulnerable to predation risks than dull males. However, special and most detailed investigations of these questions reveal that these “generally accepted rules” are not  universal.

For example, Breden & Stoner (1987) have shown that females of guppy, Poecilia reticulata, from high-predation populations show genetically determined, lower preference for brightly colored males than do females from areas of low predation. In turn, predatory pike cichlid, Crenicichla alta, prefer to attack in sex-mixed schools of guppy dull and most profitable females than bright and less profitable males (Pocklington & Dill, 1995).

In other words, detection of potential prey even from the longer distance and the real attack on prey need the different decisions making and are separated in time.

Transgenic fluorescent zebrafish

The development of transgenic zebrafish, Danio rerio, and other fish with green, yellow, orange, red and other fluorescent colors has opened an opportunity to study the role of fluorescence in intraspecific and interspecific relations in fish and their predators under the control conditions. Note that under the day light transgenic zebrafish have slightly more intensive colors than wildtype zebrafish (usually with the longitudinal bluish and yellowish stripes), but under the special ultraviolet illumination (invisible for human) they become extremely bright (for example, see photos given by Gong et al., 2003).

In our context, Cortemeglia & Beitinger (2006) have found that under the day light predatory largemouth bass, M. salmodes, consume red fluorescent zebrafish and wildtype zebrafish approximately in an equal proportion. According to Jha (2010), snakehead, Channa striatus, consume under the day conditions both red fluorescent zebrafish and wildtype zebrafish, but try to avoid red fluorescent zebrafish. However, Hill et al. (2011) have found that largemouth bass consume under the day conditions about two times more red fluorescent zebrafish than wildtype zebrafish and concluded that transgenic fish are more susceptible to predation.

In boreal countries (like Ukraine), wildtype and transgenic zebrafish are not survive in the nature due to the cold winters. So, in our experiments we used common perch, Perca fluviatilis, as native predators (about 5-7 cm total length) and aquarium forms of wildtype and red fluorescent zebrafish as popetial prey.

An experimental aquarium was located near the large laboratory windows and was illuminated with the ambient light, which varied from daylight to twilight and nightlight. Because perch were not familiar with both forms of zebrafish, they learnt to hunt novel prey (note, perch are diurnal and crepuscular predators). Briefly, perch passed from the first observations for prey to approaches, chases and the first prey captures (about mutual learning in predators and prey, see Lescheva & Zhuykov, 1989). Under the day and crepuscular illuminations, no preferences of perch towards wildtype or red fluorescent zebrafish (relatively dull under these illuminations) were observed. However, under additional ultraviolet illumination red fluorescent zebrafish became very bright, and perch avoided them (during 3 days of observations none of bright prey were eaten).


Fig. 1. Transgenic fluorescent danios (


According to our abservations, pike, Esox lucius, another diurnal and crepuscular predator, does not avoid dull red fluorescent zebrafish but avoid bright (UV illuminated) prey.

In the wild nature, visually guided fish may include in their diets new and brightly colored prey but only after long-term testing of these prey and formation of search image in respect to these prey. For example, Hope (1984) has informed that wild trout included in their diet an invasive species of beetles with bright coloration only through about month of acquaintance with this new prey and their testing.

Large fluorescent objects versus small fluorescent implants

It is necessary to distinguish large fluorescent objects and small fluorescent implants used to tag fish. It is shown (e.g., Catalano et al., 2001; Roberts & Kilpatrick, 2004) that small but bright fluorescent implants may attract predators and thus decrease the recapture rate of tagged fish in the nature.

Fluorescent fishing lines

It is shown that largemouth bass may distiguish white, yellow and green fluorescent fishing lines but only after several trials with attached worms to these lines (Miller & Janzow, 1979).

Fishing practice. Part 1

There are fish habitats that allow to confirm the attractiveness of red or orange fluorescent lures at the stati ... Read more »

Category: Lures | Views: 284 | Added by: nickyurchenko | Date: 2016-12-29




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