Soral Crypsis:Protective Mimicry of a Coccid on an Indian Fern

Herbivory with crypsis is not well documented in ferns. The present record of cryptic coloration of coccid Saissetia filicum Boisduval （Homoptera： Coccidae） to the sori of a fern species Asplenium nidus L. （Aspleniaceae） is unique. Predatory beetles （Jauravia sp., Coleoptera： Coccinellidae） that feed on the coccids, are suggested to be selective pressure for the development of the present homopteran soral crypsis. A higher rate of effective predation is noticed in the vegetative leaves than the fertile leaves. Aggressive ants were found harvesting honeydew secretions from the coccids and defending the trophobionts as well as the host fern from their natural enemies. In addition, a possible three-way mutualistic relationship among the coccids, its host fern and the tending ant is suggested. Differential numbers of coccids on vegetative and fertile leaves is correlated with their phenol content and degree of predation by beetles. Such coloration mimicry by the coccids may enable them to obtain the necessary blend of sorus of the host fern needed to evade beetle detection and attack.

All‐metallic wide‐angle metasurfaces for multifunctional polarization manipulation

Optical camouflage is a magical capability of animals as first noticed in 1794 by Erasmus Darwin in Zoonomia,but current biomimetic camouflage strategies cannot be readily applied in complex environments involving multispectral and in particular multi-polarization detection.Here we develop a plasmonic approach toward broadband infrared polarimetric crypsis,where the polarized thermal emission near the pseudo-Brewster angle is the main signal source and no existing polarizing camouflage technique has been discovered in nature.Based on all-metallic subwavelength structures,an electrodynamic resistance-reduction mechanism is proposed to avoid the significant polarization-dependent infrared absorption/radiation.It is also found that the structured metal surface presents giant extrinsic anisotropy regarding the phase shift between orthogonal polarization states,which helps to realize ultrahigh-efficiency and tunable polarization conversion in an unprecedented manner.Finally,we note that the catenary optical theory may provide a useful means to explain and predict these unusual performances.

Australian cuckoos and their adaptations for brood parasitism

The strategies used by parasitic cuckoos to fool their hosts have intrigued naturalists and ornithologists for centuries. Here I review some of the tricks used by Australian parasitic cuckoos to increase host nest availability, access host nests, and fool their hosts into accepting their eggs and chicks. Some of these strategies are widely used by cuckoo species around the world, but other traits, such as cryptic eggs and mimetic chicks, appear to be largely restricted to the Australasian cuckoos. Generalist cuckoos face greater challenges than specialists if they must fool multiple host species, and this provides a possible explanation for why different species of cuckoos have evolved different strategies for host deception.

Does disruptive camouflage conceal edges and features？

Camouflage is ubiquitous in the natural world and benefits both predators and prey. Amongst the range of conceal- ment strategies, disruptive coloration is thought to visually fragment an animal＇s＇ outline, thereby reducing its rate of discovery. Here, I propose two non-mutually exclusive hypotheses for how disruptive camouflage functions, and describe the visual me- chanisms that might underlie them. （1） The local edge disruption hypothesis states that camouflage is achieved by breaking up edge information. （2） The global feature disruption hypothesis states camouflage is achieved by breaking up the characteristic features of an animal （e.g., overall shape or facial features）. Research clearly shows that putatively disruptive edge markings do increase concealment; however, few tests have been undertaken to determine whether this survival advantage is attributable to the distortion of features, so the global feature disruption hypothesis is under studied. In this review the evidence for global feature disruption is evaluated. Further, I address if object recognition processing provides a feasible mechanism for animals＇ features to influence concealment. This review concludes that additional studies are needed to test if disruptive camouflage operates through the global feature disruption and proposes future research directions [Current Zoology 61 （4）： 708-717, 2015].

Choosing between a rock and a hard place： Camouflage in the round-tailed horned lizard Phrynosoma modestum

The round-tailed homed lizard Phrynosoma modestum is cryptically colored and resembles a small stone when it draws legs close to its body and elevates its back. We investigated effectiveness of camouflage in P. modestum and its dependence on stones by placing a lizard in one of two microhabitats （uniform sand or sand with surface rocks approximately the same size as lizards）. An observer who knew which microhabitat contained the lizard was asked to locate the lizard visually. Latency to detec- tion was longer and probability of no detection within 60 s was higher for lizards on rock background than on bare sand. In arenas where lizards could choose to occupy rock or bare sand, much higher proportions selected rocky backgrounds throughout the day; at night all lizards slept among stones. A unique posture gives P modestum a rounded appearance similar to many natural stones. Lizards occasionally adopted the posture, but none did so in response to a nearby experimenter. Stimuli that elicit the posture are unknown. That P. modestum is better camouflaged among rocks than on bare sand and prefers to occupy rocky areas suggests that special resemblance to rocks （masquerade） enhances camouflage attributable to coloration and immobility.

Flight initiation distance, color and camouflage

Camouflage is widespread throughout the animal kingdom allowing individuals to avoid detection and hence save time and energy rather than escape from an approaching predator.Thus,camouflage is likely to have co-evolved with antipredator behavior.Here,we propose that camouflage results in dichotomous escape behavior within and among species with classes of individuals and species with cryptic coloration having shorter flight initiation distances(FIDs;the distance at which an individual takes flight when approached by a human).We report the results of 2 tests of this hypothesis.First,bird species with cryptically colored plumage have consistently shorter FID than closely related species without such color.Within species with sexually dimorphic plumage,brightly colored adult male common pheasants Phasianus colchicus and golden pheasants Chrysolophus pictus have long and variable FID,whereas cryptically colored juveniles and adult females have short and invariable FID.Second,FID in females was predicted by presence or absence of cryptic color,FID in males and their interaction.These findings are consistent with the hypothesis that risk-taking behavior has been attuned to camouflage,and that species with different levels of camouflage differ consistently in their FID.

Interactions between background matching and disruptive colouration： Experiments using human predators and virtual crabs

Interactions between disruptive colouration and the match between prey and background spot size were manipulated in two experiments that used time taken by human ＇predators＇ to find artificial prey （virtual crab morphs） against heterogeneous backgrounds as a measure of the their camouflage. Experiment 1, in which the spots and their placement imitated the arrangement on the crab Carcinus maenas, tested whether high and low contrast spots touching the body outline （disruptive ＇edge＇ morphs） made the artificial prey more difficult to detect than when the spots did not touch the outline （non-disruptive ＇inner＇ morphs） against three different backgrounds： ＇small＇, ＇middle＇ and ＇large＇ spot size. In Experiment 2, the range of spot sizes and their positions （＇edge＇ and ＇inner＇） on the crab morphs were varied to determine the most effective combination against the ＇mid- dle＇ background. Altogether, 640 volunteers participated in these computer trials, representing a high degree of independent replication. All patterned morphs were significantly harder to detect than plain morphs, indicating that possessing at least some degree of background matching can provide camouflage. Both experiments demonstrated that various morphs, though not having the same spot sizes as the background, had similar or better survivorship as those with matching spot sizes--indicating that opti- mal camouflage did not come from background matching alone. In Experiment 2, edge-disrupted morphs consistently took longer to find than their non-disruptive counterparts. The relative effects of edge disruption, contrast, and background/prey spot size are clearly context-dependent, highlighting the complexity of prey concealment [Current Zoology 61 （4）： 718-728, 2015].

Evolutionary implications of deception in mimicry and masquerade

Aggressive mimicry occurs when an organism resembles some aspect of another organism （the model） in order to obtain prey through its deceptive resemblance. This may function either through the overt response of the receiver or through the lack of response of the receiver. Reviewing selected examples, I discuss some of the difficulties in ascribing a model for the mimic. I also discuss how a single animal can have multiple ploys in its armoury of deceptive signals, thus belonging within two or more categories of deceptive signalling. In addition to aggressive mimicry, these may include crypsis or camouflage, mas- querade （mimicry of inanimate objects）, and Batesian or protective mimicry. Each of these examples of deception has multiple evolutionary pathways, and some deceptive signals may be more costly to receivers than others, but no single organism is subject to a single selection pressure, leading to the reality that many evolutionary pathways contribute to the diversity we see around us. New technologies are opening new channels of investigation into deceptive signaling in many different sensory modalities, and this is reflected in the recent increase in studies investigating the structure and function of deceptive signals. In turn, these studies are beginning to expose the fascinating complexity of deceptive signaling systems, allowing us to discover the myriad, non-mutually exclusive, solutions that can be selected for to obtain prey

Color change in a marine isopod is adaptive in reducing predation

Although background matching is a common form of camouflage across a wide diversity of animals, there has been surprisingly little experimental work testing the fitness consequences of this camouflage strategy, especially in marine ecosystems. In this study, we tested whether color camouflage enhances survival of the intertidal marine isopod Pentidotea （Idotea） wosnesenskii, quantified patterns of camouflage in different algal habitats, and examined how algal diet affected color change and growth using laboratory assays. In the field, isopods collected from two differently colored algal habitats （the brown alga Fucus distichus and the red alga Odonthaliafloccosa） matched the color of their respective algal habitats, and also differed significantly in body size： smaller red isopods were found on red algae, while larger brown isopods were found on brown algae. Predation ex- periments demonstrated these color differences had fitness benefits： brown isopods that matched their brown algae habitats sur- vived at higher rates than red unmatched isopods. Surprisingly, despite the propensity of isopods to match their algal habitats, algal diet had no effect on color change in color change experiments. Instead, isopods in all treatments turned browner, matching the color of the algal habitat that many isopods are found on as adults. In summary, our data supported our hypothesis that back- ground matching serves an adaptive function in reducing predation, with important evolutionary implications for explaining the wide variation in color change mechanisms in idoteid isopods [Current Zoology 61 （4）： 739-748, 2015].

Ecological significance of dorsal polymorphism in a Batesian mimic snake

Batesian mimicry is the process in which harmless species adopt the appearance of a dangerous, aposematic species.In some prey species,both Batesian mimetic and non-Batesian morphs coexist,presupposing that both morphs have to be evolutionarily advantageous.The viperine snake, Natrix maura,exhibits a zigzag dorsal pattern and antipredatory behavior that mimics European vipers.This snake also has a striped dorsal pattern that coexists with the zigzag pattern.We have examined whether individuals belonging to different geographically structured clades were more likely to exhibit a certain dorsal pattern,and whether the zigzag pattern has a protective function by exposing artificial snakes to predation in natural environments,in addition to comparing antipredatory behavior between zigzag and striped snakes also in natural environments.Our results indicate that the striped pattern was not geographically structured,but habitat-dependent.Aerial predators less frequently attacked zigzag plasticine models than striped or unpatterned models.We detected a shift in antipredator behavior between the 2 morphs,as Batesian mimicking N.maura responded to an approaching potential predator by remaining immobile or fleeing at shorter distances than did striped ones.We conclude that Batesian mimics maintain the cryptic and aposematic value by resembling vipers,whereas in open habitats the non-Batesian mimic has altered its antipredator behavior to maintain its fitness.