Next Article in Journal
Trichosanthes kirilowii Extract Promotes Wound Healing through the Phosphorylation of ERK1/2 in Keratinocytes
Previous Article in Journal
Microencapsulation of Lacticaseibacillus rhamnosus GG for Oral Delivery of Bovine Lactoferrin: Study of Encapsulation Stability, Cell Viability, and Drug Release
Previous Article in Special Issue
Measuring Photonics in Photosynthesis: Combined Micro-Fourier Image Spectroscopy and Pulse Amplitude Modulated Chlorophyll Fluorimetry at the Micrometre-Scale
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Perspective

Revealing the Wonder of Natural Photonics by Nonlinear Optics

1
Institute of General and Physical Chemistry, Studentski trg 12/V, 11158 Belgrade, Serbia
2
Center for Photonics, Institute of Physics, University of Belgrade, Pregrevica 118, 11080 Belgrade, Serbia
3
Molecular Imaging and Photonics, Department of Chemistry, KU Leuven, Celestijnenlaan 200D, 3001 Heverlee, Belgium
4
Department of Physics and Astronomy, University of Exeter, Stocker Road, Exeter EX4 4QL, UK
5
Department of Physics & Namur Institute of Structured Matter (NISM), University of Namur, Rue de Bruxelles 61, 5000 Namur, Belgium
6
Micro- and Nanophotonic Materials Group, University of Mons, Place du Parc 20, 7000 Mons, Belgium
*
Authors to whom correspondence should be addressed.
Biomimetics 2022, 7(4), 153; https://doi.org/10.3390/biomimetics7040153
Submission received: 28 July 2022 / Revised: 27 September 2022 / Accepted: 30 September 2022 / Published: 5 October 2022
(This article belongs to the Special Issue Photonic Structures in Nature and Biomimetic Materials)

Abstract

:
Nano-optics explores linear and nonlinear phenomena at the nanoscale to advance fundamental knowledge about materials and their interaction with light in the classical and quantum domains in order to develop new photonics-based technologies. In this perspective article, we review recent progress regarding the application of nonlinear optical methods to reveal the links between photonic structures and functions of natural photonic geometries. Furthermore, nonlinear optics offers a way to unveil and exploit the complexity of the natural world for developing new materials and technologies for the generation, detection, manipulation, and storage of light at the nanoscale, as well as sensing, metrology, and communication.

1. Introduction

It has been known for a long time that colors in nature are not designed for beauty but are of the utmost importance for communication. Structural colors belong to a special class of colors that have no chemical origin, but they arise from the interaction of light with structures, such as periodically arranged materials [1,2]. Structural colors are ubiquitous colors among insects, fish, and birds. In addition, they are a main topic of research in fields such as biophotonics and biomimetics. In this perspective article, we demonstrate the interest and impact of nonlinear optical studies of photonic structures. We highlight the benefit of nonlinear optical techniques for revealing the details of structured matter at the nanoscale and its interaction with light. We also emphasize that the control of structural colors is essential for various applications in materials science. After introducing the readers to basic concepts of nonlinear optics and natural photonics, we present different cases of natural photonic structures (sometimes combined with artificial materials) investigated by nonlinear optical techniques.

2. Basics of Nonlinear Optics

Nonlinear optics is a part of optics that studies light propagation in nonlinear media. In such media, the polarization P has a nonlinear response to the electric field E. Such optical behavior usually occurs at a high intensity of light, such as the one generated by a laser.
In the linear regime, when an electromagnetic wave interacts with some materials, e.g., a medium containing electric charges, a dipolar type of interaction appears between the dipoles in the medium and the incident electromagnetic fields at a frequency ω [3]. This interaction can be described by an induced polarization P ind that is linear with the electric field E of the incident light and acts as the source of radiation:
P ind = χ ( 1 ) E ,
with χ ( 1 ) , the linear susceptibility that is related to the refractive index. The response can be modelled by a classical harmonic oscillator, yielding a linear complex refractive index of the medium that scales with ω [3].
However, in the case of high-intensity incident electromagnetic fields, such as laser light (Figure 1), the harmonic oscillator response is not sufficient anymore to describe the observed phenomena [4,5,6,7]. The oscillations become anharmonic, i.e., they do not respond linearly to the incident electromagnetic wave. In the nonlinear regime, the induced polarization P ind is expanded in a Taylor series as a function of the total applied electric field. The induced polarization is then written as [7]:
P ind = P ( 1 ) + P ( 2 ) + P ( 3 ) + = χ ( 1 ) E + χ ( 2 ) E E + χ ( 3 ) E E E +
with P ( 1 ) , the linear part of the induced polarization; P ( 2 ) , the second-order nonlinear response; and P ( 3 ) , the third order nonlinear response. χ ( 1 ) , χ ( 2 ) , and χ ( 3 ) are the linear, the first nonlinear, and the second nonlinear susceptibilities, respectively. The latter two quantify the second-order and third-order nonlinear optical response. Since all susceptibilities are related to the refractive index, a nonlinear complex refractive index is obtained.
One of the advantages of nonlinear optical techniques is due to the nature of the nonlinear susceptibilities, which are tensors of third and fourth rank, respectively. Especially, second-order nonlinear optical effects, which are described by the third-rank tensor χ ( 2 ) , have extremely interesting symmetry properties. In general, χ ( 2 ) is a third-rank tensor with 27 components, but the number of independent and nonvanishing components is dependent on the symmetry of the medium. All of the components of χ ( 2 ) will vanish in a medium with inversion symmetry. On the other hand, any surface where the symmetry is necessarily broken will typically yield four independent susceptibility components [7]. Since the nonlinear susceptibility directly determines the magnitude and phase of the nonlinear response, the measured response can serve as a means to evaluate the symmetry of the sample.
In addition to the optical properties of matter that can be probed by linear techniques, much more information is available by exploiting the interaction of matter with higher-intensity laser beams. Multiphoton (including two-photon) excitation fluorescence is certainly the most used nonlinear optical technique. In the case of two-photon excitation fluorescence (TPEF), high-intensity photons illuminate a sample [7]. Because of this high intensity, two photons simultaneously interact with the sample, following different selection rules from the photons in the linear light–matter interaction regime. Since two photons are absorbed initially and give rise to only one emitted photon, the resulting photon has a higher energy than each of the two absorbed photons. Multiphoton absorption and fluorescence originate from a third-order nonlinear optical response [7].
In second harmonic generation (SHG), the material also interacts with two photons [7]. Unlike two-photon excitation fluorescence, a third photon is instantaneously emitted (within ca 10 15 s) with exactly twice the energy (and, thus, half the wavelength) of the two initial photons. Since SHG is a second-order nonlinear optical process, selection rules that are different from TPEF apply: symmetry requirements such as non-centrosymmetric samples are essential to observe SHG [4,5,6,7]. Similarly, third harmonic generation (THG) corresponds to the instantaneous emission of a single photon following the interaction of three incident photons [7]. The generated photon has three times the energy and a third of the wavelength of the three initial photons.
There are multiple advantages to nonlinear techniques with respect to linear optical techniques [8,9]. An important feature is the increase in imaging depth, which can be attributed to multiple factors: first, there is a low probability of multiple photons interacting simultaneously, resulting in a minimal imaging volume at the femtoliter scale by reducing out-of-focus fluorescence. It is therefore possible to image accurately at different depths, similarly to confocal microscopes, and to create 3D reconstructions of the investigated material without the use of a pinhole. Due to the absence of a pinhole, more light can be collected and thus a clearer image can be formed. This also results in an increase in the practical resolution as the pinhole of confocal microscopes is often opened to increase the amount of incoming light to image fluorescing samples. This results in a lower resolution. Practically, the resolution of a multiphoton microscope was shown to approach 250 nm, which equals the best possible resolution of the confocal fluorescence microscopy. Another significant advantage of nonlinear optical techniques is the use of near-infrared excitation light with wavelengths corresponding to the transparency window of biological tissue. This leads to an increase in penetration depth, and it is therefore possible to image sensitive samples without damaging the structure or with minimal damage. Furthermore, most multi-photon microscopes use femtosecond-lasers as an excitation source, which further reduces the risk of photodamage. In addition, no sample preparation is necessary. This constitutes the main advantage over more complicated microscopy techniques such as scanning electron microscopy (SEM) or transmission electron microscopy (TEM) [10,11]. Finally, another interesting application of multiphoton microscopy is the imaging of the local polarization anisotropy via SHG, enabling the user to seperately determine the orientation and degree of organization of each non-centrosymmetric component within a sample.

3. Introduction to Natural Photonics

Colours in nature originate from chemical or physical properties of matter, light sources, or combinations of them [1,2]. Chemical colours are caused by pigments. These molecules selectively absorb incident light within a given wavelength band. Examples are eumelanins and pheomelanins, which give rise to brown/black and yellow/red human skins, respectively [12,13]. Light that is not absorbed by pigments is scattered, giving rise to colours that an observer may perceive. Physical colours are due to interference between incident light and a physical structure. Hence, they are often called structural colours, as a synonym. Structures giving rise to such colours have geometrical dimensions at the micro- or nanoscale. They encompass optical thin films [14,15,16,17], diffraction gratings [18,19,20], Bragg mirrors [21,22,23,24,25,26], chirped multilayer reflectors [27,28], and photonic crystals [29,30,31,32,33,34], as well as quasi-ordered [35,36,37,38,39,40] and randomly disordered [41,42,43,44] photonic structures.
Natural photonics is the field of research that studies the interaction between light and such physical structures in nature. Natural structural colours occur in organisms ranging from mammals such as primates (including human blue eyes) and marsupials, fish, or birds such as hummingbirds and pigeons to insects such as butterflies and beetles (Figure 2) [1,2,45].
This section introduces key concepts and presents some selected case studies from natural photonics, in the linear regime.
One striking example is the case of the male beetle Hoplia coerulea (Figure 3). The blue-violet iridescent colour of its elytra and body observed in reflection with incident visible light arises from a photonic structure, namely, a porous periodic multilayer, within the round scales occurring on its body [46,47].
This multilayer is mainly composed of chitin, the building material of insects [1,2]. Upon contact with liquids and vapour, these scales change their colour to green [48,49,50,51,52]: the spectral reflectance peak red-shifts. This colour change arises from the penetration of some liquid into the pores of the scales, filling the pores and changing the refractive index.
Furthermore, one-photon excitation fluorescence (OPEF) emission was observed when the beetle was illuminated with UV light (Figure 3d) [53,54]. The colour of the scales covering the elytra and body of this insect is turquoise. This phenomenon arises in biological organisms, the integuments of which contain so-called fluorophores [55,56]. Examples include birds [44,57,58,59], insects [60,61,62,63,64,65,66,67,68,69,70,71], arachnids [72,73], mammals [74], amphibians [75,76], reptiles [77], marine animals [78,79], and plants [80,81] (Figure 2). These molecules emit longer-wavelength light (typically, visible photons) following the absorption of incident shorter-wavelength light (typically, UV, violet or blue photons).
Fluorescence emission results from transition between two real electron states with the same multiplicity of spin. The role, if any, of fluorescence (Figure 4) in visual communication is unclear [55,56]. Biopterin, the green fluorescent protein (GFP), papiliochrom II, psittacofulvin, and resilin are examples of fluorophores.
When light emission takes place in photonic structures, the structure may modify the directionality, the decay time, and the spectral intensity of the emitted light [82,83]. Light emission can be reduced or even inhibited if the emission wavelength is in the range of the photonic bandgap of the structure. The decay time of the excited is then increased and can, theoretically, be infinite. When such light emitted in a photonic structure originates from fluorescence, this phenomenon is often referred to as controlled fluorescence. The confinement of fluorophores in natural photonic structures was found in several species [84,85,86,87,88], including the male beetle H. coerulea [53,54]. Upon contact with water, the peak in the fluorescence emission spectrum from the scales of this beetle blue-shifts, giving rise to a navy blue colour (Figure 3d,f). Following the penetration of the porous structure by water, the local density of optical states (LDOS) is modified, leading to the observed colour change.
The interaction between fluorescent light and photonic structures was also highlighted in the scales covering the elytra of longhorn beetles Celosterna pollinosa sulfurea and Phosphorus virescens [68]. These scales exhibit yellow and turquoise colours under visible and UV incident light, respectively, with an underlying basal brown membrane (Figure 5a–d), akin to the beetles Euchroea auripigmenta and Trictenotoma childreni [69,70]. Through scatterograms and detailed series of simulations, it was demonstrated that the scales play the role of waveguides for light emitted by the embedded fluorophores (Figure 5e,f).

4. Nonlinear Optical Study of Natural Photonic Structures

Harnessing light–matter interaction in a nonlinear regime, researchers and engineers developed various tools for imaging and spectroscopy analyses of biological samples [8,62,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105]. Nonlinear optical imaging and spectroscopy have proved to be versatile and efficient techniques in biomedical and biological research, with many benefits, including an increase in analytic depth and a reduction in photodamage, with respect to classical linear optical techniques [8]. In general, nonlinear optical studies led to a better understanding of the link between the optical response and geometries of natural photonic structures that are essential for potential applications of these structures in biomimetics and quantum technology [9].
For instance, the multi-excited states character of the fluorophores embedded in the integuments of H. coerulea were revealed by comparing OPEF spectra with TPEF measurements [106] (Figure 6a–d).
This provided insight into the electron structure of the embedded fluorophores.
Furthermore, local-form anisotropy arising from local-direction-dependent subwavelength morphology was shown to influence both linear and nonlinear optical responses (in reflection and emission) thanks to THG spectroscopy [106]. The anisotropy is caused due to the subwavelength spacers located in the mixed air-chitin layers (Figure 3b). These spacers are locally parallel.
This finding highlighted the need to take a more accurate model into account for predicting some of the optical properties of the elytra of this beetle.
Similarly, the yellow and fluorescent elongated scales covering the elytra of the log-boring beetle Trictenotoma childreni were investigated by nonlinear optical methods, including OPEF, TPEF, and SHG microscopy and spectroscopy (Figure 7) [70]. These scales appear similar to the ones of the longhorn beetles Celosterna pollinosa sulfurea and Phosphorus virescens (Figure 5) [68]. They contain fluorophores that give rise to a yellow visual appearance upon UV illumination. These observations allowed one to highlight the non-centrosymmetric nature of the fluorophores embedded within these scales [70].
So far, various natural photonic structures from different insects, including butterflies and cicadas, have been investigated for sensing and materials-oriented applications. For example, corrugated natural photonic structures offer a unique possibility to develop new sensing platforms by combing corrugation at different scales, plasmonic properties, and surface-enhanced Raman spectroscopy (SERS) [107,108,109,110,111]. The work of Garrett and coworkers clearly shows the benefit of natural and bioinspired structuring, which can be used for different sensing applications (Figure 8) [108,109,110]. The development of such novel platforms relying on SERS will lead to the fast and accurate screening of chemical, biochemical, and pharmaceutical compounds, which is crucial for the growing fields of proteomics, genomics, molecular medicine, and biophysics, as well as for the development of assays for the detection of diseases [107,112].
The work of Stoddart and coworkers highlighted that practical applications of SERS for sensing depend on the development of manufacturing methods that will be used to mimic the complex morphology of insect integuments [107]. It pointed out the importance of biomimetics for the advancement of materials science [107]. In addition, it was shown that the enhancement of SERS also depends on the aspect ratio of metallic nanoparticles. The presence of different multiscale groove-like structures presented the possibility of developing smart surfaces for controlling optical response and wetting properties [113]. Structuring materials have a significant effect on the latter, as was demonstrated both theoretically and experimentally, specifically at different length scales [114,115,116].
Furthermore, the natural photonic structures occurring in the wings of the butterfly Cymothoe sangaris were used for tuning the upconversion luminescence of nanoparticles doped with lanthanide ( NaYF 4 : Yb 3 + , Er 3 + ) [117]. Upon illumination with a light at 980 nm, both red and green emission bands of NaYF 4 : Yb 3 + , Er 3 + could be controlled, producing different luminescent colours Figure 9. Doping natural photonic structures with materials including metals and oxides also presents the possibility of using these structures as templates to design nanocorrugated materials (with complex shapes and geometries) on demand for various material applications [118].

5. Conclusions

In this perspective article, we presented theoretical key concepts of nonlinear optics and discussed the results of nonlinear optical studies in the field of natural photonics. Because nonlinear optical techniques are inherently sensitive to symmetry; the presence of interfaces; and chirality, they offer a more detailed insight into the molecular properties of biomaterials. This is crucial for applications in different areas of material science. Even though, at the moment, nonlinear optical investigations of natural photonics are still at their infant stage of development, the primary aim of this article is to draw the attention of the broad material, photonic, and biological scientific communities to the capability of nonlinear optics, which could be used to forge new horizons in physical, biological and material research.

Author Contributions

Conceptualization, B.K. and S.R.M.; writing—original draft: S.R.M. and B.K.; and writing—review & editing: all authors. All authors have read and agreed to the published version of the manuscript.

Funding

DM acknowledges KU Leuven Postdoctoral Mandate Internal Funds (PDM) for a Postdoctoral fellowship (PDM/20/092). BB and BK acknowledge financial support of the Ministry of Education, Science, and Technological Development of the Republic of Serbia (grant III 45016). BB, BK, and DM acknowledge the support of the Office of Naval Research Global through the Research Grant N62902-22-1-2024. SRM was supported by a BEWARE Fellowship (Convention n°2110034) of the Walloon Region (Marie Skłodowska-Curie Actions of the European Union #847587), as a Postdoctoral Researcher. TV acknowledges financial support from the Hercules Foundation. BK acknowledges support from the Belgian National Fund for Scientific Research (FRS-FNRS).

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Kinoshita, S. Structural Colors in the Realm of Nature; World Scientific Publishing Co.: Singapore, 2008. [Google Scholar]
  2. Mouchet, S.R.; Deparis, O. Natural Photonics and Bioinspiration; Artech House: Boston, MA, USA, 2021. [Google Scholar]
  3. Hecht, E. Optics; Addison-Wesley Publishing Company: Reading, MA, USA, 2001. [Google Scholar]
  4. Stratton, J. Electromagnetic Theory; McGraw-Hill: New York, NY, USA, 1941. [Google Scholar]
  5. Böttcher, C. Theory of Electric Polarization, 2nd ed.; Elsevier: Amsterdam, The Netherlands, 1973. [Google Scholar]
  6. Zernike, F.; Midwinter, J. Applied Nonlinear Optics; Wiley: New York, NY, USA, 1973. [Google Scholar]
  7. Verbiest, T.; Clays, K.; Rodriguez, V. Second-Order Nonlinear Optical Characterization Techniques: An Introduction; CRC Press Taylor & Francis Group: Boca Raton, FL, USA, 2009. [Google Scholar]
  8. Zipfel, W.R.; Williams, R.M.; Webb, W.W. Nonlinear magic: Multiphoton microscopy in the biosciences. Nat. Biotechnol. 2003, 21, 1369. [Google Scholar] [CrossRef] [PubMed]
  9. Verstraete, C.; Mouchet, S.R.; Verbiest, T.; Kolaric, B. Linear and nonlinear optical effects in biophotonic structures using classical and nonclassical light. J. Biophotonics 2019, 12, e201800262. [Google Scholar] [CrossRef]
  10. Pathan, A.; Bond, J.; Gaskin, R. Sample preparation for scanning electron microscopy of plant surfaces—Horses for courses. Micron 2008, 39, 1049–1061. [Google Scholar] [CrossRef] [PubMed]
  11. Ayache, J.; Beaunier, L.; Boumendil, J.; Ehret, G.; Laub, D. Sample Preparation Handbook for Transmission Electron Microscopy; Springer: New York, NY, USA, 2010. [Google Scholar]
  12. Slominski, A.; Tobin, D.J.; Shibahara, S.; Wortsman, J. Melanin Pigmentation in Mammalian Skin and Its Hormonal Regulation. Physiol. Rev. 2004, 84, 1155–1228. [Google Scholar] [CrossRef]
  13. Ito, S.; Wakamatsu, K. Diversity of human hair pigmentation as studied by chemical analysis of eumelanin and pheomelanin. J. Eur. Acad. Dermatol. Venereol. 2011, 25, 1369–1380. [Google Scholar] [CrossRef] [PubMed]
  14. Stavenga, D.G.; Giraldo, M.A.; Leertouwer, H.L. Butterfly wing colors: Glass scales of Graphium sarpedon cause polarized iridescence and enhance blue/green pigment coloration of the wing membrane. J. Exp. Biol. 2010, 213, 1731–1739. [Google Scholar] [CrossRef] [Green Version]
  15. Stavenga, D.G.; Matsushita, A.; Arikawa, K.; Leertouwer, H.L.; Wilts, B.D. Glass scales on the wing of the swordtail butterfly Graphium sarpedon act as thin film polarizing reflectors. J. Exp. Biol. 2012, 215, 657–662. [Google Scholar] [CrossRef] [Green Version]
  16. Stavenga, D. Thin film and multilayer optics cause structural colors of many insects and birds. Mater. Today Proc. 2014, 1S, 109–121. [Google Scholar] [CrossRef]
  17. Siddique, R.; Vignolini, S.; Bartels, C.; Wacker, I.; Hölscher, H. Colour formation on the wings of the butterfly Hypolimnas Salmacis Scale Stacking. Sci. Rep. 2016, 6, 36204. [Google Scholar] [CrossRef] [Green Version]
  18. Vukusic, P.; Sambles, J.R.; Lawrence, C.R.; Wootton, R.J. Limited-view iridescence in the butterfly Ancyluris Meliboeus. Proc. R. Soc. Lond. Ser. B Biol. Sci. 2002, 269, 7–14. [Google Scholar] [CrossRef]
  19. Vukusic, P.; Kelly, R.; Hooper, I. A biological sub-micron thickness optical broadband reflector characterized using both light and microwaves. J. R. Soc. Interface 2009, 6, S193–S201. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Vigneron, J.P.; Simonis, P.; Aiello, A.; Bay, A.; Windsor, D.M.; Colomer, J.F.; Rassart, M. Reverse color sequence in the diffraction of white light by the wing of the male butterfly Pierella Luna (Nymphalidae: Satyrinae). Phys. Rev. E 2010, 82, 021903. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Biró, L.P.; Bálint, Z.; Kertész, K.; Vértesy, Z.; Márk, G.I.; Horváth, Z.E.; Balázs, J.; Méhn, D.; Kiricsi, I.; Lousse, V.; et al. Role of photonic-crystal-type structures in the thermal regulation of a Lycaenid butterfly sister species pair. Phys. Rev. E 2003, 67, 021907. [Google Scholar] [CrossRef] [PubMed]
  22. Yoshioka, S.; Kinoshita, S. Single-scale spectroscopy of structurally colored butterflies: Measurements of quantified reflectance and transmittance. J. Opt. Soc. Am. A 2006, 23, 134–141. [Google Scholar] [CrossRef] [PubMed]
  23. Noyes, J.A.; Vukusic, P.; Hooper, I.R. Experimental method for reliably establishing the refractive index of buprestid beetle exocuticle. Opt. Express 2007, 15, 4351–4358. [Google Scholar] [CrossRef] [PubMed]
  24. Kertész, K.; Molnár, G.; Vértesy, Z.; Koós, A.; Horváth, Z.; Márk, G.; Tapasztó, L.; Bálint, Z.; Tamáska, I.; Deparis, O.; et al. Photonic band gap materials in butterfly scales: A possible source of “blueprints”. E-MRS 2007 Spring Conference Symposium A: Sub-wavelength photonics throughout the spectrum: Materials and Techniques. Mater. Sci. Eng. B 2008, 149, 259–265. [Google Scholar] [CrossRef]
  25. Wilts, B.D.; Leertouwer, H.L.; Stavenga, D.G. Imaging scatterometry and microspectrophotometry of lycaenid butterfly wing scales with perforated multilayers. J. R. Soc. Interface 2009, 6, S185–S192. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Stavenga, D.G.; Wilts, B.D.; Leertouwer, H.L.; Hariyama, T. Polarized iridescence of the multilayered elytra of the Japanese jewel beetle, Chrysochroa Fulgidissima. Philos. Trans. R. Soc. B Biol. Sci. 2011, 366, 709–723. [Google Scholar] [CrossRef] [Green Version]
  27. Vigneron, J.P.; Pasteels, J.M.; Windsor, D.M.; Vértesy, Z.; Rassart, M.; Seldrum, T.; Dumont, J.; Deparis, O.; Lousse, V.; Biró, L.P.; et al. Switchable reflector in the Panamanian tortoise beetle Charidotella Egregia (Chrysomelidae: Cassidinae). Phys. Rev. E 2007, 76, 031907. [Google Scholar] [CrossRef] [Green Version]
  28. Pasteels, J.M.; Deparis, O.; Mouchet, S.R.; Windsor, D.M.; Billen, J. Structural and physical evidence for an endocuticular gold reflector in the tortoise beetle, Charidotella Ambita. Arthropod Struct. Dev. 2016, 45, 509–518. [Google Scholar] [CrossRef]
  29. Kertész, K.; Bálint, Z.; Vértesy, Z.; Márk, G.I.; Lousse, V.; Vigneron, J.P.; Rassart, M.; Biró, L.P. Gleaming and dull surface textures from photonic-crystal-type nanostructures in the butterfly Cyanophrys remus. Phys. Rev. E 2006, 74, 021922. [Google Scholar] [CrossRef] [PubMed]
  30. Michielsen, K.; Stavenga, D. Gyroid cuticular structures in butterfly wing scales: Biological photonic crystals. J. R. Soc. Interface 2008, 5, 85–94. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  31. Saranathan, V.; Osuji, C.O.; Mochrie, S.G.J.; Noh, H.; Narayanan, S.; Sandy, A.; Dufresne, E.R.; Prum, R.O. Structure, function, and self-assembly of single network gyroid (I4132) Photonic Cryst. Butterfly Wing Scales. Proc. Natl. Acad. Sci. USA 2010, 107, 11676–11681. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Pouya, C.; Vukusic, P. Electromagnetic characterization of millimetre-scale replicas of the gyroid photonic crystal found in the butterfly Parides Sesostris. Interface Focus 2012, 2, 645–650. [Google Scholar] [CrossRef] [Green Version]
  33. Mouchet, S.R.; Vigneron, J.P.; Colomer, J.F.; Vandenbem, C.; Deparis, O. Additive photonic colors in the Brazilian diamond weevil: Entimus imperialis. Proc. SPIE 2012, 8480, 848003. [Google Scholar] [CrossRef]
  34. Mouchet, S.; Colomer, J.F.; Vandenbem, C.; Deparis, O.; Vigneron, J.P. Method for modeling additive color effect in photonic polycrystals with form anisotropic elements: The case of Entimus Imp. Weevil. Opt. Express 2013, 21, 13228–13240. [Google Scholar] [CrossRef] [Green Version]
  35. Prum, R.O.; Torres, R.H.; Williamson, S.W.; Dyck, J. Coherent light scattering by blue feather barbs. Nature 1998, 396, 28–29. [Google Scholar] [CrossRef]
  36. Prum, R.O.; Torres, R.H. A Fourier Tool for the Analysis of Coherent Light Scattering by Bio-Optical Nanostructures1. Integr. Comp. Biol. 2003, 43, 591–602. [Google Scholar] [CrossRef]
  37. Prum, R.O.; Torres, R. Structural colouration of avian skin: Convergent evolution of coherently scattering dermal collagen arrays. J. Exp. Biol. 2003, 206, 2409–2429. [Google Scholar] [CrossRef] [Green Version]
  38. Prum, R.O.; Torres, R.H. Structural colouration of mammalian skin: Convergent evolution of coherently scattering dermal collagen arrays. J. Exp. Biol. 2004, 207, 2157–2172. [Google Scholar] [CrossRef]
  39. Henze, M.J.; Lind, O.; Wilts, B.D.; Kelber, A. Pterin-pigmented nanospheres create the colours of the polymorphic damselfly Ischnura Elegans. J. R. Soc. Interface 2019, 16, 20180785. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Mouchet, S.R.; Luke, S.; McDonald, L.T.; Vukusic, P. Optical costs and benefits of disorder in biological photonic crystals. Faraday Discuss. 2020, 223, 9–48. [Google Scholar] [CrossRef] [PubMed]
  41. Morehouse, N.I.; Vukusic, P.; Rutowski, R. Pterin pigment granules are responsible for both broadband light scattering and wavelength selective absorption in the wing scales of pierid butterflies. Proc. R. Soc. B Biol. Sci. 2007, 274, 359–366. [Google Scholar] [CrossRef] [PubMed]
  42. Stavenga, D.G.; Stowe, S.; Siebke, K.; Zeil, J.; Arikawa, K. Butterfly wing colours: Scale beads make white pierid wings brighter. Proc. R. Soc. Lond. Ser. B Biol. Sci. 2004, 271, 1577–1584. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Stavenga, D.G.; Giraldo, M.A.; Hoenders, B.J. Reflectance and transmittance of light scattering scales stacked on the wings of pierid butterflies. Opt. Express 2006, 14, 4880–4890. [Google Scholar] [CrossRef] [Green Version]
  44. Ladouce, M.; Barakat, T.; Su, B.L.; Deparis, O.; Mouchet, S.R. Scattering of ultraviolet light by avian eggshells. Faraday Discuss. 2020, 223, 63–80. [Google Scholar] [CrossRef]
  45. Mouchet, S.R.; Vukusic, P. Structural Colours in Lepidopteran Scales. Adv. Insect Physiol. 2018, 54, 1–53. [Google Scholar] [CrossRef]
  46. Vigneron, J.P.; Colomer, J.F.m.; Vigneron, N.; Lousse, V. Natural layer-by-layer photonic structure in the squamae of Hoplia Coerulea (Coleoptera). Phys. Rev. E 2005, 72, 061904. [Google Scholar] [CrossRef]
  47. Mouchet, S.; Lobet, M.; Kolaric, B.; Kaczmarek, A.; Van Deun, R.; Vukusic, P.; Deparis, O.; Van Hooijdonk, E. Photonic scales of Hoplia Coerulea Beetle: Any Colour You Like. Mater. Today Proc. 2017, 4, 4979–4986. [Google Scholar] [CrossRef]
  48. Rassart, M.; Simonis, P.; Bay, A.; Deparis, O.; Vigneron, J.P. Scale coloration change following water absorption in the beetle Hoplia Coerulea (Coleoptera). Phys. Rev. E 2009, 80, 031910. [Google Scholar] [CrossRef]
  49. Mouchet, S.R.; Su, B.L.; Tabarrant, T.; Lucas, S.; Deparis, O. Hoplia Coerulea, A Porous Nat. Photonic Struct. Template Opt. Vap. Sensor. Proc. SPIE 2014, 9127. [Google Scholar] [CrossRef]
  50. Mouchet, S.R.; Tabarrant, T.; Lucas, S.; Su, B.L.; Vukusic, P.; Deparis, O. Vapor sensing with a natural photonic cell. Opt. Express 2016, 24, 12267–12280. [Google Scholar] [CrossRef] [PubMed]
  51. Mouchet, S.; Van Hooijdonk, E.; Welch, V.; Louette, P.; Colomer, J.F.; Su, B.L.; Deparis, O. Liquid-induced colour change in a beetle: The concept of a photonic cell. Sci. Rep. 2016, 6, 19322. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Mouchet, S.; Van Hooijdonk, E.; Welch, V.; Louette, P.; Tabarrant, T.; Vukusic, P.; Lucas, S.; Colomer, J.F.; Su, B.L.; Deparis, O. Assessment of environmental spectral ellipsometry for characterising fluid-induced colour changes in natural photonic structures. Mater. Today Proc. 2017, 4, 4987–4997. [Google Scholar] [CrossRef]
  53. Van Hooijdonk, E.; Berthier, S.; Vigneron, J.P. Bio-Inspired approach of the fluorescence emission properties in the scarabaeid beetle Hoplia Coerulea (Coleoptera): Model. Transf.-Matrix Opt. Simulations. J. Appl. Phys. 2012, 112, 114702. [Google Scholar] [CrossRef]
  54. Mouchet, S.R.; Lobet, M.; Kolaric, B.; Kaczmarek, A.M.; Van Deun, R.; Vukusic, P.; Deparis, O.; Van Hooijdonk, E. Controlled fluorescence in a beetle’s photonic structure and its sensitivity to environmentally induced changes. Proc. R. Soc. Lond. B Biol. Sci. 2016, 283. [Google Scholar] [CrossRef] [Green Version]
  55. Lagorio, M.G.; Cordon, G.B.; Iriel, A. Reviewing the relevance of fluorescence in biological systems. Photochem. Photobiol. Sci. 2015, 14, 1538–1559. [Google Scholar] [CrossRef] [Green Version]
  56. Marshall, J.; Johnsen, S. Fluorescence as a means of colour signal enhancement. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2017, 372. [Google Scholar] [CrossRef] [Green Version]
  57. Arnold, K.E.; Owens, I.P.F.; Marshall, N.J. Fluorescent Signaling in Parrots. Science 2002, 295, 92. [Google Scholar] [CrossRef]
  58. McGraw, K.J.; Toomey, M.B.; Nolan, P.M.; Morehouse, N.I.; Massaro, M.; Jouventin, P. A description of unique fluorescent yellow pigments in penguin feathers. Pigment Cell Res. 2007, 20, 301–304. [Google Scholar] [CrossRef]
  59. Ladouce, M.; Barakat, T.; Su, B.L.; Deparis, O.; Mouchet, S.R. UV scattering by pores in avian eggshells. Proc. SPIE 2020, 11481, 101–109. [Google Scholar] [CrossRef]
  60. Cockayne, E.I. The Distribution of Fluorescent Pigments in Lepidoptera. Trans. R. Entomol. Soc. Lond. 1924, 72, 1–19. [Google Scholar] [CrossRef]
  61. Vukusic, P.; Hooper, I. Directionally Controlled Fluorescence Emission in Butterflies. Science 2005, 310, 1151. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Israelowitz, M.; Rizvi, S.H.; von Schroeder, H.P. Fluorescence of the “fire-chaser” beetle Melanophila Acuminata. J. Lumin. 2007, 126, 149–154. [Google Scholar] [CrossRef]
  63. Trzeciak, T.M.; Wilts, B.D.; Stavenga, D.G.; Vukusic, P. Variable multilayer reflection together with long-pass filtering pigment determines the wing coloration of papilionid butterflies of the Nireus Group. Opt. Express 2012, 20, 8877–8890. [Google Scholar] [CrossRef] [Green Version]
  64. Hooijdonk, E.V.; Vandenbem, C.; Berthier, S.; Vigneron, J.P. Bi-Functional photonic structure in the Papilio Nireus (Papilionidae): Model. Scatt.-Matrix Opt. Simulations. Opt. Express 2012, 20, 22001–22011. [Google Scholar] [CrossRef]
  65. Van Hooijdonk, E.; Berthier, S.; Vigneron, J.P. Contribution of both the upperside and the underside of the wing on the iridescence in the male butterfly Troïdes Magellanus (Papilionidae). J. Appl. Phys. 2012, 112, 074702. [Google Scholar] [CrossRef]
  66. Welch, V.L.; Van Hooijdonk, E.; Intrater, N.; Vigneron, J.P. Fluorescence in insects. Proc. SPIE 2012, 8480, 848004. [Google Scholar] [CrossRef]
  67. Wilts, B.D.; Trzeciak, T.M.; Vukusic, P.; Stavenga, D.G. Papiliochrome II pigment reduces the angle dependency of structural wing colouration in Nireus Group Papilionids. J. Exp. Biol. 2012, 215, 796–805. [Google Scholar] [CrossRef] [Green Version]
  68. Van Hooijdonk, E.; Barthou, C.; Vigneron, J.P.; Berthier, S. Yellow structurally modified fluorescence in the longhorn beetles Celosterna pollinosa sulfurea and Phosphorus virescens (Cerambycidae). J. Lumin. 2013, 136, 313–321. [Google Scholar] [CrossRef]
  69. Mouchet, S.R.; Kaczmarek, A.M.; Mara, D.; Deun, R.V.; Vukusic, P. Colour and fluorescence emission of Euchroea Auripigmenta Beetle. Proc. SPIE 2019, 10965, 72–82. [Google Scholar] [CrossRef]
  70. Mouchet, S.R.; Verstraete, C.; Kaczmarek, A.M.; Mara, D.; van Cleuvenbergen, S.; Van Deun, R.; Verbiest, T.; Maes, B.; Vukusic, P.; Kolaric, B. Unveiling the nonlinear optical response of Trictenotoma Child. Longhorn Beetle. J. Biophotonics 2019, 12, e201800470. [Google Scholar] [CrossRef] [PubMed]
  71. Mouchet, S.R.; Verstraete, C.; Bokic, B.; Mara, D.; Dellieu, L.; Orr, A.G.; Deparis, O.; Deun, R.V.; Verbiest, T.; Vukusic, P.; et al. Naturally occurring fluorescence in transparent insect wings. arXiv 2021, arXiv:2110.06086. [Google Scholar]
  72. Lawrence, R.F. Fluorescence in Arthropoda. J. Entomol. Soc. S. Afr. 1954, 17, 167–170. [Google Scholar]
  73. Pavan, M.; Vachon, M. Sur l’existence d’une substance fluorescente dans les téguments des Scorpions (Arachnides). Comptes Rendus L’Académie Sci. 1954, 239, 1700–1702. [Google Scholar]
  74. Tani, K.; Watari, F.; Uo, M.; Morita, M. Fluorescent Properties of Porcelain-Restored Teeth and Their Discrimination. Mater. Trans. 2004, 45, 1010–1014. [Google Scholar] [CrossRef] [Green Version]
  75. Taboada, C.; Brunetti, A.E.; Pedron, F.N.; Carnevale Neto, F.; Estrin, D.A.; Bari, S.E.; Chemes, L.B.; Peporine Lopes, N.; Lagorio, M.G.; Faivovich, J. Naturally occurring fluorescence in frogs. Proc. Natl. Acad. Sci. USA 2017, 114, 3672–3677. [Google Scholar] [CrossRef] [Green Version]
  76. Deschepper, P.; Jonckheere, B.; Matthys, J. A Light in the Dark: The Discovery of Another Fluorescent Frog in the Costa Rican Rainforests. Wilderness Environ. Med. 2018, 29, 421–422. [Google Scholar] [CrossRef] [Green Version]
  77. Mohd Top, M.; Puan, C.L.; Chuang, M.F.; Othman, S.N.; Borzée, A. First record of ultraviolet fluorescence in the Bent-toed Gecko Cyrtodactylus Quadrivirgatus Taylor, 1962 (Gekkonidae: Sauria). Herpetol. Notes 2020, 13, 211–212. [Google Scholar]
  78. Gruber, D.F.; Gaffney, J.P.; Mehr, S.; DeSalle, R.; Sparks, J.S.; Platisa, J.; Pieribone, V.A. Adaptive Evolution of Eel Fluorescent Proteins from Fatty Acid Binding Proteins Produces Bright Fluorescence in the Marine Environment. PLoS ONE 2015, 10, e0140972. [Google Scholar] [CrossRef]
  79. Gruber, D.F.; Loew, E.R.; Deheyn, D.D.; Akkaynak, D.; Gaffney, J.P.; Smith, W.L.; Davis, M.P.; Stern, J.H.; Pieribone, V.A.; Sparks, J.S. Biofluorescence in Catsharks (Scyliorhinidae): Fundamental Description and Relevance for Elasmobranch Visual Ecology. Sci. Rep. 2016, 6, 24751. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  80. Iriel, A.; Lagorio, M.G. Is the flower fluorescence relevant in biocommunication? Naturwissenschaften 2010, 97, 915–924. [Google Scholar] [CrossRef] [PubMed]
  81. Iriel, A.; Lagorio, M.G. Implications of reflectance and fluorescence of Rhododendr. Indicum Flowers Biosignaling. Photochem. Photobiol. Sci. 2010, 9, 342–348. [Google Scholar] [CrossRef] [PubMed]
  82. Purcell, E.M. Spontaneous emission probabilities at radio frequencies. Phys. Rev. 1946, 69, 681. [Google Scholar]
  83. Yablonovitch, E. Inhibited Spontaneous Emission in Solid-State Physics and Electronics. Phys. Rev. Lett. 1987, 58, 2059–2062. [Google Scholar] [CrossRef]
  84. Kumazawa, K.; Tanaka, S.; Negita, K.; Tabata, H. Fluorescence from Wing of Morpho Sulkowskyi Butterfly. Jpn. J. Appl. Phys. 1994, 33, 2119–2122. [Google Scholar] [CrossRef]
  85. Lawrence, C.R.; Vukusic, P.; Sambles, J.R. Grazing-incidence iridescence from a butterfly wing. Appl. Opt. 2002, 41, 437–441. [Google Scholar] [CrossRef] [Green Version]
  86. Vigneron, J.P.; Kertész, K.; Vértesy, Z.; Rassart, M.; Lousse, V.; Bálint, Z.; Biró, L.P. Correlated diffraction and fluorescence in the backscattering iridescence of the male butterfly Troides Magellanus (Papilionidae). Phys. Rev. E 2008, 78, 021903. [Google Scholar] [CrossRef] [Green Version]
  87. Van Hooijdonk, E.; Barthou, C.; Vigneron, J.P.; Berthier, S. Detailed experimental analysis of the structural fluorescence in the butterfly Morpho Sulkowskyi (Nymphalidae). J. Nanophotonics 2011, 5, 053525. [Google Scholar] [CrossRef]
  88. Hooijdonk, E.V.; Barthou, C.; Vigneron, J.P.; Berthier, S. Angular dependence of structural fluorescent emission from the scales of the male butterfly Troïdes Magellanus (Papilionidae). J. Opt. Soc. Am. B 2012, 29, 1104–1111. [Google Scholar] [CrossRef]
  89. Verbiest, T.; Kauranen, M.; Persoons, A.; Ikonen, M.; Kurkela, J.; Lemmetyinen, H. Nonlinear Optical Activity and Biomolecular Chirality. J. Am. Chem. Soc. 1994, 116, 9203–9205. [Google Scholar] [CrossRef]
  90. Campagnola, P.J.; Millard, A.C.; Terasaki, M.; Hoppe, P.E.; Malone, C.J.; Mohler, W.A. Three-dimensional high-resolution second-harmonic generation imaging of endogenous structural proteins in biological tissues. Biophys. J. 2002, 82, 493–508. [Google Scholar] [CrossRef] [Green Version]
  91. Friedl, P.; Wolf, K.; Harms, G.; Andrian, U.H. Biological Second and Third Harmonic Generation Microscopy. Curr. Protoc. Cell Biol. 2007, 34, 4.15.1–4.15.21. [Google Scholar] [CrossRef] [PubMed]
  92. Ries, R.S.; Choi, H.; Blunck, R.; Bezanilla, F.; Heath, J.R. Black Lipid Membranes: Visualizing the Structure, Dynamics, and Substrate Dependence of Membranes. J. Phys. Chem. B 2004, 108, 16040–16049. [Google Scholar] [CrossRef]
  93. Brown, D.J.; Morishige, N.; Neekhra, A.; Minckler, D.S.; Jester, J.V. Application of second harmonic imaging microscopy to assess structural changes in optic nerve head structure ex vivo. J. Biomed. Opt. 2007, 12, 5. [Google Scholar] [CrossRef]
  94. Lis, D.; Guthmuller, J.; Champagne, B.; Humbert, C.; Busson, B.; Tadjeddine, A.; Peremans, A.; Cecchet, F. Selective detection of the antigenic polar heads of model lipid membranes supported on metals from their vibrational nonlinear optical response. Chem. Phys. Lett. 2010, 489, 12–15. [Google Scholar] [CrossRef]
  95. Nguyen, T.T.; Conboy, J.C. High-Throughput Screening of Drug-Lipid Membrane Interactions via Counter-Propagating Second Harmonic Generation Imaging. Anal. Chem. 2011, 83, 5979–5988. [Google Scholar] [CrossRef] [Green Version]
  96. Theer, P.; Denk, W.; Sheves, M.; Lewis, A.; Detwiler, P.B. Second-Harmonic Generation Imaging of Membrane Potential with Retinal Analogues. Biophys. J. 2011, 100, 232–242. [Google Scholar] [CrossRef] [Green Version]
  97. Chen, X.; Nadiarynkh, O.; Plotnikov, S.; Campagnola, P.J. Second harmonic generation microscopy for quantitative analysis of collagen fibrillar structure. Nat. Protoc. 2012, 7, 654. [Google Scholar] [CrossRef]
  98. Akerboom, J.; Carreras Calderón, N.; Tian, L.; Wabnig, S.; Prigge, M.; Tolö, J.; Gordus, A.; Orger, M.B.; Severi, K.E.; Macklin, J.J.; et al. Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics. Front. Mol. Neurosci. 2013, 6, 2. [Google Scholar] [CrossRef] [Green Version]
  99. Rabasović, M.D.; Pantelić, D.V.; Jelenković, B.M.; Ćurčić, S.B.; Rabasović, M.S.; Vrbica, M.D.; Lazović, V.M.; Ćurčić, B.P.; Krmpot, A.J. Nonlinear microscopy of chitin and chitinous structures: A case study of two cave-dwelling insects. J. Biomed. Opt. 2015, 20, 016010. [Google Scholar] [CrossRef] [PubMed]
  100. Chen, Y.C.; Lee, S.Y.; Wu, Y.; Brink, K.; Shieh, D.B.; Huang, T.D.; Reisz, R.R.; Sun, C.K. Third-harmonic generation microscopy reveals dental anatomy in ancient fossils. Opt. Lett. 2015, 40, 1354–1357. [Google Scholar] [CrossRef]
  101. Lis, D.; Cecchet, F. Unique Vibrational Features as a Direct Probe of Specific Antigen–Antibody Recognition at the Surface of a Solid-Supported Hybrid Lipid Bilayer. ChemPhysChem 2016, 17, 2645–2649. [Google Scholar] [CrossRef] [PubMed]
  102. Rowlands, C.J.; Park, D.; Bruns, O.T.; Piatkevich, K.D.; Fukumura, D.; Jain, R.K.; Bawendi, M.G.; Boyden, E.S.; So, P.T. Wide-field three-photon excitation in biological samples. Light Sci. Appl. 2017, 6, e16255. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  103. Reynaud, C.; Thoury, M.; Dazzi, A.; Latour, G.; Scheel, M.; Li, J.; Thomas, A.; Moulhérat, C.; Didier, A.; Bertrand, L. In-place molecular preservation of cellulose in5,000-year-old archaeological textiles. Proc. Natl. Acad. Sci. USA 2020, 117, 19670–19676. [Google Scholar] [CrossRef]
  104. Raoux, C.; Schmeltz, M.; Bied, M.; Alnawaiseh, M.; Hansen, U.; Latour, G.; Schanne-Klein, M.C. Quantitative structural imaging of keratoconic corneas using polarization-resolved SHG microscopy. Biomed. Opt. Express 2021, 12, 4163–4178. [Google Scholar] [CrossRef]
  105. Schmeltz, M.; Robinet, L.; Heu-Thao, S.; Sintès, J.M.; Teulon, C.; Ducourthial, G.; Mahou, P.; Schanne-Klein, M.C.; Latour, G. Noninvasive quantitative assessment of collagen degradation in parchments by polarization-resolved SHG microscopy. Sci. Adv. 2021, 7, eabg1090. [Google Scholar] [CrossRef]
  106. Mouchet, S.R.; Verstraete, C.; Mara, D.; Cleuvenbergen, S.V.; Finlayson, E.D.; Deun, R.V.; Deparis, O.; Verbiest, T.; Maes, B.; Vukusic, P.; et al. Nonlinear optical spectroscopy and two-photon excited fluorescence spectroscopy reveal the excited states of fluorophores embedded in a beetle’s elytra. Interface Focus 2019, 9, 20180052. [Google Scholar] [CrossRef] [Green Version]
  107. Stoddart, P.R.; Cadusch, P.J.; Boyce, T.M.; Erasmus, R.M.; Comins, J.D. Optical properties of chitin: Surface-enhanced Raman scattering substrates based on antireflection structures on cicada wings. Nanotechnology 2006, 17, 680. [Google Scholar] [CrossRef]
  108. Garrett, N.L.; Vukusic, P.; Ogrin, F.; Sirotkin, E.; Winlove, C.P.; Moger, J. Spectroscopy on the wing: Naturally inspired SERS substrates for biochemical analysis. J. Biophotonics 2009, 2, 157–166. [Google Scholar] [CrossRef]
  109. Garrett, N.L. Naturally Inspired SERS Substrates: Datasheet from · Volume: “Raman Spectroscopy for Nanomaterials Characterization”; SpringerMaterials: Cham, Switzerland, 2012. [Google Scholar] [CrossRef]
  110. Garrett, N.L.; Sekine, R.; Dixon, M.W.A.; Tilley, L.; Bambery, K.R.; Wood, B.R. Bio-Sensing with butterfly wings: Naturally occurring nano-structures for SERS-based malaria parasite detection. Phys. Chem. Chem. Phys. 2015, 17, 21164–21168. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  111. Palmer, L.D.; Brooks, J.L.; Frontiera, R.R. Probing the coupling of butterfly wing photonic crystals to plasmon resonances with surface-enhanced Raman spectroscopy. J. Mater. Chem. C 2019, 7, 13887–13895. [Google Scholar] [CrossRef]
  112. Langer, J.; Jimenez de Aberasturi, D.; Aizpurua, J.; Alvarez-Puebla, R.A.; Auguié, B.; Baumberg, J.J.; Bazan, G.C.; Bell, S.E.; Boisen, A.; Brolo, A.G.; et al. Present and Future of Surface-Enhanced Raman Scattering. ACS Nano 2020, 14, 28–117. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  113. Zhang, G.; Zhang, J.; Xie, G.; Liu, Z.; Shao, H. Cicada Wings: A Stamp from Nature for Nanoimprint Lithography. Small 2006, 2, 1440–1443. [Google Scholar] [CrossRef]
  114. Dellieu, L.; Sarrazin, M.; Simonis, P.; Deparis, O.; Vigneron, J.P. A two-in-one superhydrophobic and anti-reflective nanodevice in the grey cicada Cicada Orni (Hemiptera). J. Appl. Phys. 2014, 116, 024701. [Google Scholar] [CrossRef] [Green Version]
  115. Deparis, O.; Mouchet, S.R.; Dellieu, L.; Colomer, J.F.; Sarrazin, M. Nanostructured Surfaces: Bioinspiration for Transparency, Coloration and Wettability. Mater. Today Proc. 2014, 1S, 122–129. [Google Scholar] [CrossRef]
  116. Kovačević, A.; Petrović, S.; Mimidis, A.; Stratakis, E.; Pantelić, D.; Kolaric, B. Molding Wetting by Laser-Induced Nanostructures. Appl. Sci. 2020, 10, 6008. [Google Scholar] [CrossRef]
  117. Gao, T.; Zhu, X.; Wu, X.J.; Zhang, B.; Liu, H.L. Selectively Manipulating Upconversion Emission Channels with Tunable Biological Photonic Crystals. J. Phys. Chem. C 2021, 125, 732–739. [Google Scholar] [CrossRef]
  118. Zhang, D. Morphology Genetic Materials Templated from Nature Species; Springer: Berlin/Heidelberg, Germany, 2012. [Google Scholar]
Figure 1. Depending on the intensity of the incident electric field (E), the electric polarization (P) will respond linearly or nonlinearly. As long as the intensity of the electric field is small, the electric polarization is linear to the electric field intensity. This case corresponds to the linear regime. When the intensity of the electric field is high, P is not proportional to E and the regime is nonlinear. Reproduced from Verbiest, T., Clays, K., and Rodriguez, V., 2009. Second-order Nonlinear Optical Characterization Techniques: An Introduction, with permission from Taylor and Francis Group, LLC, a division of Informa plc.
Figure 1. Depending on the intensity of the incident electric field (E), the electric polarization (P) will respond linearly or nonlinearly. As long as the intensity of the electric field is small, the electric polarization is linear to the electric field intensity. This case corresponds to the linear regime. When the intensity of the electric field is high, P is not proportional to E and the regime is nonlinear. Reproduced from Verbiest, T., Clays, K., and Rodriguez, V., 2009. Second-order Nonlinear Optical Characterization Techniques: An Introduction, with permission from Taylor and Francis Group, LLC, a division of Informa plc.
Biomimetics 07 00153 g001
Figure 2. Many examples of structural colours are found in the integuments of natural organisms. They include the wings of the common morpho Morpho peleides (a), the body of some dragonfly species (b), the thorax and elytra of the green rose chafer Cetonia aurata (c), the body of the Botany Bay diamond weevil Chrysolopus spectabilis (d), the integuments of some jumping spider species (e), the skin of the mandrill Mandrillus sphinx (f), the feathers of the Indian peafowl Pavo cristatus (g), the head of the mallard Anas platyrhynchos (h), and the body of the neon tetra fish Paracheirodon innesi (i). Reproduced from from https://pixabay.com/ accessed on 27 July 2022.
Figure 2. Many examples of structural colours are found in the integuments of natural organisms. They include the wings of the common morpho Morpho peleides (a), the body of some dragonfly species (b), the thorax and elytra of the green rose chafer Cetonia aurata (c), the body of the Botany Bay diamond weevil Chrysolopus spectabilis (d), the integuments of some jumping spider species (e), the skin of the mandrill Mandrillus sphinx (f), the feathers of the Indian peafowl Pavo cristatus (g), the head of the mallard Anas platyrhynchos (h), and the body of the neon tetra fish Paracheirodon innesi (i). Reproduced from from https://pixabay.com/ accessed on 27 July 2022.
Biomimetics 07 00153 g002
Figure 3. The blue-violet colour of the male beetle Hoplia coerulea (a) originates from a multilayer photonic structure. This porous periodic multilayer (b) occurs in the scales covering the elytra (c) and body of the insect. Upon UV light illumination, the scales display a turquoise colour through fluorescence (d). When in contact with water, the scales turn to green (e) and navy blue (f) under visible and UV lightillumination, respectively. Reproduced from Mouchet, S.R., Lobet, M., Kolaric, B., Kaczmarek, A.M., Van Deun, R., Vukusic, P., Deparis, O., and Van Hooijdonk, E., 2016. Controlled fluorescence in a beetle’s photonic structure and its sensitivity to environmentally induced changes. Proc. R. Soc. B 283, 20162334, with permission from The Royal Society.
Figure 3. The blue-violet colour of the male beetle Hoplia coerulea (a) originates from a multilayer photonic structure. This porous periodic multilayer (b) occurs in the scales covering the elytra (c) and body of the insect. Upon UV light illumination, the scales display a turquoise colour through fluorescence (d). When in contact with water, the scales turn to green (e) and navy blue (f) under visible and UV lightillumination, respectively. Reproduced from Mouchet, S.R., Lobet, M., Kolaric, B., Kaczmarek, A.M., Van Deun, R., Vukusic, P., Deparis, O., and Van Hooijdonk, E., 2016. Controlled fluorescence in a beetle’s photonic structure and its sensitivity to environmentally induced changes. Proc. R. Soc. B 283, 20162334, with permission from The Royal Society.
Biomimetics 07 00153 g003
Figure 4. Fluorescence is ubiquitous in the integuments of natural organisms. The integuments of some jellyfish species (a), some grasshopper species (b), some millipede species (c), and some greeneye fish species (d) are known for their fluorescent properties. (d) Top (bottom): greeneye fish under visible (UV) light. Reproduced from from pixabay.com.
Figure 4. Fluorescence is ubiquitous in the integuments of natural organisms. The integuments of some jellyfish species (a), some grasshopper species (b), some millipede species (c), and some greeneye fish species (d) are known for their fluorescent properties. (d) Top (bottom): greeneye fish under visible (UV) light. Reproduced from from pixabay.com.
Biomimetics 07 00153 g004
Figure 5. The elytra of longhorn beetles Celosterna pollinosa sulfurea and Phosphorus virescens are covered by elongated scales, in which fluorophores are embedded. These scales act as waveguides for the light emitted by the fluorophores. They display a yellow colour under visible light for C. pollinosa sulfurea (a) and P. virescens (b) (here, observation by optical microscopy). Under UV light, the observed colour is turquoise in both respective cases (c,d). Upon illumination with UV light (represented in magenta), embedded fluorophores mostly emitted within two emission cones (in green) (e) due to a waveguide effect taking place within the scales (f). Reproduced from Van Hooijdonk, E., Barthou, C., Vigneron, J.-P., and Berthier, S., 2013. Yellow structurally modified fluorescence in the longhorn beetles Celosterna pollinosa sulfurea and Phosphorus virescens (Cerambycidae). J. Lumin. 136, 313–321, with permission from Elsevier.
Figure 5. The elytra of longhorn beetles Celosterna pollinosa sulfurea and Phosphorus virescens are covered by elongated scales, in which fluorophores are embedded. These scales act as waveguides for the light emitted by the fluorophores. They display a yellow colour under visible light for C. pollinosa sulfurea (a) and P. virescens (b) (here, observation by optical microscopy). Under UV light, the observed colour is turquoise in both respective cases (c,d). Upon illumination with UV light (represented in magenta), embedded fluorophores mostly emitted within two emission cones (in green) (e) due to a waveguide effect taking place within the scales (f). Reproduced from Van Hooijdonk, E., Barthou, C., Vigneron, J.-P., and Berthier, S., 2013. Yellow structurally modified fluorescence in the longhorn beetles Celosterna pollinosa sulfurea and Phosphorus virescens (Cerambycidae). J. Lumin. 136, 313–321, with permission from Elsevier.
Biomimetics 07 00153 g005
Figure 6. TPEF microscopy and spectroscopy of the scales covering H. coerulea’s elytra. An intense TPEF response was detected from the elytra of the male beetle H. coerulea with an excitation wavelength equal to 900 nm (a) and 800 nm (b). TPEF excitation spectra were measured with various excitation wavelengths (c). Upon contact with water (d), the emitted intensity decreases and the peak wavelength red-shifts slightly (the excitation wavelength equals 800 nm). Scale bars: (a) 200 µm and (b) 100 µm. Reproduced from Mouchet, S. R., Verstraete, C., Mara, D., Van Cleuvenbergen, S., Finlayson, E. D., Van Deun, R., Deparis, O., Verbiest, T., Maes, B., Vukusic, P., and Kolaric, B., 2019 Nonlinear optical spectroscopy and two-photon excited fluorescence spectroscopy reveal the excited states of fluorophores embedded in a beetle’s elytra, Interface Focus 9(1), 20180052, with permission from The Royal Society.
Figure 6. TPEF microscopy and spectroscopy of the scales covering H. coerulea’s elytra. An intense TPEF response was detected from the elytra of the male beetle H. coerulea with an excitation wavelength equal to 900 nm (a) and 800 nm (b). TPEF excitation spectra were measured with various excitation wavelengths (c). Upon contact with water (d), the emitted intensity decreases and the peak wavelength red-shifts slightly (the excitation wavelength equals 800 nm). Scale bars: (a) 200 µm and (b) 100 µm. Reproduced from Mouchet, S. R., Verstraete, C., Mara, D., Van Cleuvenbergen, S., Finlayson, E. D., Van Deun, R., Deparis, O., Verbiest, T., Maes, B., Vukusic, P., and Kolaric, B., 2019 Nonlinear optical spectroscopy and two-photon excited fluorescence spectroscopy reveal the excited states of fluorophores embedded in a beetle’s elytra, Interface Focus 9(1), 20180052, with permission from The Royal Society.
Biomimetics 07 00153 g006
Figure 7. The yellow and fluorescent scales occurring on the elytra of the log-boring beetle T. childreni were investigated by nonlinear optical techniques, including OPEF, TPEF, and SHG microscopy and spectroscopy. The elytra exhibit a yellow colour under both incident visible white (a) and UV (b) light. This colour is due to the presence of elongated scales covering the elytra (c,d). Under visible (c) or UV light (d), they appear in shades of yellow. Upon excitation with a fundamental wavelength of 1000 nm, a SHG (e) and a TPEF (f) signal can be detected from the scales (here observed by microscopy in false colours). Multiphoton emission spectra of the log-boring beetle’s scales measured with various excitation wavelengths (g) exhibit SHG peaks at half the excitation wavelengths (thick lines). TPEF peaks were observed around 550 nm at most excitation wavelengths. Reproduced from Mouchet, S. R., Verstraete, C., Kaczmarek, A. M., Mara, D., van Cleuvenbergen, S., Van Deun, R., Verbiest, T., Maes, B., Vukusic, P., and Kolaric, B., 2019, Unveiling the nonlinear optical response of Trictenotoma childreni longhorn beetle, J. Biophot. 12(9), 12:e201800470, with permission from John Wiley and Sons.
Figure 7. The yellow and fluorescent scales occurring on the elytra of the log-boring beetle T. childreni were investigated by nonlinear optical techniques, including OPEF, TPEF, and SHG microscopy and spectroscopy. The elytra exhibit a yellow colour under both incident visible white (a) and UV (b) light. This colour is due to the presence of elongated scales covering the elytra (c,d). Under visible (c) or UV light (d), they appear in shades of yellow. Upon excitation with a fundamental wavelength of 1000 nm, a SHG (e) and a TPEF (f) signal can be detected from the scales (here observed by microscopy in false colours). Multiphoton emission spectra of the log-boring beetle’s scales measured with various excitation wavelengths (g) exhibit SHG peaks at half the excitation wavelengths (thick lines). TPEF peaks were observed around 550 nm at most excitation wavelengths. Reproduced from Mouchet, S. R., Verstraete, C., Kaczmarek, A. M., Mara, D., van Cleuvenbergen, S., Van Deun, R., Verbiest, T., Maes, B., Vukusic, P., and Kolaric, B., 2019, Unveiling the nonlinear optical response of Trictenotoma childreni longhorn beetle, J. Biophot. 12(9), 12:e201800470, with permission from John Wiley and Sons.
Biomimetics 07 00153 g007
Figure 8. The structures occurring on the wings of the purple spotted swallowtail butterfly (Graphium weiskei) coated with a metal thin film were found to be an excellent substrate for SERS, in terms of biocompatibility and sensitivity [108,109,110]. G. weiskei (a) exhibit conical microstructures on its wings (bd) as observed here by SEM. After coating by gold or silver, these structures can be used to detect protein binding from direct observation of the modifications in the SERS response. Reproduced from Garrett, N. L., Vukusic, P., Ogrin, F., Sirotkin, E., Winlove, C. P., and Moger, J., 2009, Spectroscopy on the wing: Naturally inspired SERS substrates for biochemical analysis, J. Biophot. 2(3), 157–166.
Figure 8. The structures occurring on the wings of the purple spotted swallowtail butterfly (Graphium weiskei) coated with a metal thin film were found to be an excellent substrate for SERS, in terms of biocompatibility and sensitivity [108,109,110]. G. weiskei (a) exhibit conical microstructures on its wings (bd) as observed here by SEM. After coating by gold or silver, these structures can be used to detect protein binding from direct observation of the modifications in the SERS response. Reproduced from Garrett, N. L., Vukusic, P., Ogrin, F., Sirotkin, E., Winlove, C. P., and Moger, J., 2009, Spectroscopy on the wing: Naturally inspired SERS substrates for biochemical analysis, J. Biophot. 2(3), 157–166.
Biomimetics 07 00153 g008
Figure 9. The upconversion luminescence of nanoparticles doped with lanthanide ( NaYF 4 : Yb 3 + , Er 3 + ) was controlled thanks to the natural photonic crystals occurring in the wings of the butterfly Cymothoe sangaris. With a 980 nm incident light, various luminescent colours were generated. Reproduced from Gao, T., Zhu, X., Wu, X. J., Zhang, B., and Liu, H. L., 2021, Selectively Manipulating Upconversion Emission Channels with Tunable Biological Photonic Crystals, J. Phys. Chem. C, 125(1), 732–739, with permission from ACS Publications.
Figure 9. The upconversion luminescence of nanoparticles doped with lanthanide ( NaYF 4 : Yb 3 + , Er 3 + ) was controlled thanks to the natural photonic crystals occurring in the wings of the butterfly Cymothoe sangaris. With a 980 nm incident light, various luminescent colours were generated. Reproduced from Gao, T., Zhu, X., Wu, X. J., Zhang, B., and Liu, H. L., 2021, Selectively Manipulating Upconversion Emission Channels with Tunable Biological Photonic Crystals, J. Phys. Chem. C, 125(1), 732–739, with permission from ACS Publications.
Biomimetics 07 00153 g009
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Mara, D.; Bokic, B.; Verbiest, T.; Mouchet, S.R.; Kolaric, B. Revealing the Wonder of Natural Photonics by Nonlinear Optics. Biomimetics 2022, 7, 153. https://doi.org/10.3390/biomimetics7040153

AMA Style

Mara D, Bokic B, Verbiest T, Mouchet SR, Kolaric B. Revealing the Wonder of Natural Photonics by Nonlinear Optics. Biomimetics. 2022; 7(4):153. https://doi.org/10.3390/biomimetics7040153

Chicago/Turabian Style

Mara, Dimitrije, Bojana Bokic, Thierry Verbiest, Sébastien R. Mouchet, and Branko Kolaric. 2022. "Revealing the Wonder of Natural Photonics by Nonlinear Optics" Biomimetics 7, no. 4: 153. https://doi.org/10.3390/biomimetics7040153

APA Style

Mara, D., Bokic, B., Verbiest, T., Mouchet, S. R., & Kolaric, B. (2022). Revealing the Wonder of Natural Photonics by Nonlinear Optics. Biomimetics, 7(4), 153. https://doi.org/10.3390/biomimetics7040153

Article Metrics

Back to TopTop