Bioluminescence in the Monterey Submarine Canyon: image analysis of video recordings from a midwater submersible

Video images of bioluminescence were recorded in situ during a 1985 study of the midwater environment of the Monterey Canyon, using a single-person, untethered submersible. Gelatinous organisms were responsible for the most brilliant bioluminescent displays, often exhibiting elaborate kinetics in response to mechanical stimulation. Images of bioluminescent displays recorded from identified organisms are shown and display patterns are described. All bioluminescence emission spectra from captured specimens were blue, with peak emissions between 460 and 494 nm. Image-analysis of recordings of mechanically stimulated bioluminescence revealed source densities between 43 and 175 m^-3 and intensities between 2.5 and 37.3 W sr^-1 m^-3. The predominant display type at all depths studied (between 100 and 560 m) was luminous secretions. Despite high intensities of mechanically stimulated bioluminescence, no spontaneous light production was recorded in the absence of mechanical stimulation.     

Correlation of bioluminescence emissions with ventral photophores in the mesopelagic squidAbralia veranyi (Cephalopoda: Enoploteuthidae)

Specimens of the squidAbralia veranyi were collected off the Bahamas in 1989. The bioluminescence of the ventral photophores was recorded on videotape at 11 to 12°C and 24°C, in conjunction with measurements of the spectral emission at the same temperatures. At 11 °C, the spectrum was unimodal, peaking at 490 nm with a narrow bandwidth. At the higher temperature a shoulder at about 440 nm appeared in the emission spectrum. The short, bright flashes from the subocular photophores had a broader bandwidth and a shorter wavelength emission maximum (475 nm) than that of the ventral photophores. Video recordings at the two temperatures showed no changes in either the identities of the luminescing photophores or their relative intensities. One structurally distinct type of photophore was not illuminated. We conclude that the observed spectral changes were produced within one group of photophores, and that recruitment of the unilluminated photophores would produce an additional spectral component, previously reported from another species ofAbralia (A. trigonura).     

Identification of marine organisms using kinetic and spectral properties of their bioluminescence

We have used a polychromator consisting of six photomultiplier tubes, each filtered to a different wavelength with narrow band-pass interference-filters, to study bioluminescence. Spectral and kinetic data collected from ten marine species in the laboratory describe their luminous flashes. These data suggest that the concept of luminous signatures, within the limits of our studies, is a valid one, with potential uses for future biological studies both in the laboratory and in situ. The kinetic parameters considered were rise time (RT), decay time (DT) and total time (TT), while the spectral parameters consisted of ratios of light intensities at 480 and 520 nm to the intensity at 500nm. Oneway analysis of variance (ANOVA) demonstrated significant heterogeneity among species for all variables. A posteriori analysis performed with the ANOVA for TT indicated that mean TT for most species is significantly different from all other species. Canonical discriminant analysis was performed to estimate the value of kinetic and spectral parameters for species' identification. Kinetic data were somewhat more valuable in species' classification than spectral data. Discriminant analysis with RT and DT alone gave 83.1% correct species-classifications. Classification success based only on relative intensities at 480 and 520 nm was 77.5%. When all four variables were included, classification success was 100%.     

In situ characterization of phytoplankton from vertical profiles of fluorescence emission spectra

Vertical profiling of the upper ocean with a laser/fiber optic fluorometer enabled the determination of fluorescence emission spectra of photosynthetic pigments over small vertical scales. Simultaneous acquisition of phycoerythrin (PE) and chlorophyll (chl) emission spectra allowed in situ differentiation between PE-containing cells (cryptomonads and cyanobacteria) and other chl-containing autotrophs. Further, fluorescence spectral peak shifts associated with different species of PE-containing cells resulted in even finer scale in situ taxonomic differentiation. We found that the phycoerythrin fluorescence emission maxima shifted from 578 nm near the surface, to 585 m at the base of the shallow thermocline (30% light level), and to 590 nm below the thermocline at the base of the euphotic zone (1% light level). These shifts in peak emission coincided with a taxonomic change in the PE-containing cells (as determined from analysis of discrete bottle samples) from a greater proportion of Synechococcus spp. in the upper water column to a greater proportion of cryptomonads at the base of the euphotic zone. These results indicate that the composition of the phytoplankton assemblage may be assessed in situ without sample collection.     

Photopigment and spectral sensitivity in the bioluminescent fish Porichthys notatus

Digitonin extracts from retinas of the marine fish Porichthys notatus, from California and Puget Sound (USA), contain a single photopigment with maximum absorbance at 498 nm. In the presence of hydroxylamine the final product of bleaching absorbs maximally at 367 nm, indicating that the photopigment is based on retinal. Spectral sensitivity measurements performed on intact eyes and eye-cup preparations in darkadapted and selectively light-adapted states yield curves which suggest that the retina of P. notatus contains at least 3 different types of receptors. In the darkadapted state, the spectral sensitivity curve has a broad peak, with a maximum between 480 and 500 nm. In the blue and red light-adapted states, in addition to depressing the sensitivity, the shape of the sensitivity curve also changes. Under these conditions new peaks appear which suggest the presence of at least two different types of cones, with sensitivity maxima in the blue and the green regions of the spectrum, respectively. Comparison of the spectral sensitivity curves with the in vivo bioluminescence emission spectrum of the fish gives an especially good correspondence and suggests that the fish is able to perceive the bioluminescence of its own species.     

Bioluminescence spectra of shallow and deep-sea gelatinous zooplankton: ctenophores, medusae and siphonophores

We have examined the variability and potential adaptive significance of the wavelengths of light produced by gelatinous zooplankton. Bioluminescence spectra were measured from 100 species of planktonic cnidarians and ctenophores collected between 1 and 3500 m depth. Species averages of maximal wavelengths for all groups ranged from 440 to 506 nm. Ctenophores (41 species) had characteristically longer wavelengths than medusae (34 species), and the wavelengths from siphonophores (25 species) had a bimodal distribution across species. Four species each produced two different wavelengths of light, and in the siphonophore Abylopsistetragona these differences were associated with specific body regions. Light from deep-dwelling species had significantly shorter wavelengths than light from shallow species in both ctenophores (p = 0.010) and medusae (p = 0.009). Although light production in these organisms was limited to the blue-green wavelengths, it appears that within this range, colors are well-adapted to the particular environment which the species inhabit. Received: 27 April 1998 / Accepted: 27 October 1998     

Green and blue fluorescing dinoflagellates in Bahamian waters

At three stations in Bahamas waters, in 1989, 15 to 30% of all the dinoflagellates >20µm diameter observed in near-surface waters fluoresced green under blue excitation light, 55 to 66% fluoresced red, and the remainder did not fluoresce at all. The abundance of these green-fluorescing dinoflagellates ranged from ca 5 to 10 cells l^–1 at the study sites. Under UV excitation, however, the dinoflagellates had a blue to blue-green appearance. Almost all the blue-green fluorescing dinoflagellates appeared to be heterotrophic, except for one species,Phalacroma rapa Stein, which also contained red-fluorescing (under blue light) chlorophylla. The emission spectra from all species examined were of three basic types. Type 1 typically had two fluorescence emission peaks (ca 440 and ca 510 nm). Type 2 spectra possessed one sharp peak at 495 nm. Spectra belonging to Type 3 had a broad peak around 470 to 480 nm. The green fluorescence thus is likely caused by different substances in individual species. The attempt to reconstitute observed spectra with nicotinamide adenine dinucleotide (NADH) and riboflavin 5-phosphate (FMN) solutions was unsuccessful.     

Quantification of emission variability for off-road equipment in China based on real-world measurements

• Emissions from 53 in-use diesel-fueled off-road equipment were measured. • There exists a large off-road equipment variability in emissions. • Engine operations have significant impacts on real-world tailpipe emissions. • Emission inventory development should take into account job duties and operations. The objective of this paper is to quantify the variability in emissions of off-road equipment using a portable emission measurement system. A total of 53 commonly used equipment for agriculture, base construction, paving construction, and material handling were selected. Time-based and fuel-based emissions were quantified by different duty and engine modes. Three duty modes (idling, moving, and working) were used. Ten engine modes were defined based on normalized engine revolutions-per-minute and manifold absolute pressure, respectively. Composite emission factors taking into account both duty modes and its corresponding time percentage during a typical duty cycle were estimated. Results showed that there existed a large off-road equipment variability in emissions. Depending on duty and engine modes, time-based NO emissions ranged from 3.1 to 237.9, 29.1‒1475.6, 83.2‒681.6, and 3.2‒385.2 g/h for agriculture, base construction, paving construction and material handling equipment, respectively while for fuel-based NO emissions these ranges were 5.3‒52.0, 11.7‒69.0, 4.8‒30.8, and 11.0‒54.6 g/kg, respectively. Furthermore, emission factors derived from this study exhibited a much larger variability compared to those used in NONROAD by US EPA and National Guideline for Off-road Equipment of China. This implied that localized measurements of emissions are needed for improvement of accuracy of emission inventory. Furthermore, both equipment types and operations should be considered for development of emission inventory and control strategy.     

Disparate forms of bioluminescence from the amphipodsCyphocaris faurei,Scina crassicornis andS. borealis

Bioluminescence from the gammarid amphipodCyphocaris faurei Barnard and the hyperiid amphipodsScina crassicornis (Fabricius) andScina borealis (Sars) was measured with a photomultiplier coupled to an integrating sphere, and with a video camera.C. faurei andS. crassicornis were collected in July 1986 and 1987 off Oahu, Hawaii;S. crassicornis was also collected in May 1987 in the northern Sargasso Sea, and in October 1988 north of Hawaii, andS. borealis was obtained in September 1989 off the southern California coast. Emission spectra were obtained with an optical multichannel analyzer. Bioluminescence ofC. faurei appeared as a secretion through integumentary pores on the telson and uropods, and as a glow from a single location on the cephalothorax. The emission spectrum was bimodal or unimodal, with distinct blue-green and orange peaks. In contrast, the bioluminescence ofS. crassicornis andS. borealis was internal and of significantly shorter duration and lower quantum emission, with a unimodal, bluegreen emission spectrum. Appropriate repetitive stimulation in all species induced temporally summated flashes with greater rise times, durations, and total quantum emission than luminescence induced by a single stimulus. The emission spectrum, flash kinetics, quantum emission, and mode of luminescence ofC. faurei are unique compared with those of all other previously investigated amphipod species.     

Comparative study of crustacean larval photoresponses

Ovigerous females of four brachyuran (Cancer gracilis, Lophopanopeus bellus bellus, Hemigrapsus oregonensis and Scyra acutiforns) and two anomuran (Pagurus beringanus and P. granosimanus) species, which live as adults in coastal areas, were collected near Friday Harbor, Washington, USA, in 1985, and spectral sensitivity and phototactic pattern of their larvae were measured. Responses were compared with previous measurements on estuarine species to determine whether responsiveness varies with adult habitat. Estuarine and coastal species have similar photoresponses. Spectral sensitivity of the test brachyran species had two maxima, one near 400 to 420 nm and another around 500 nm. The anomuran species were similar, but had an additional peak in the region of 580 to 620 nm. This sensitivity is adapted to daytime light conditions in the adult environment, and available spectra at the time of larval movement during diel vertical migration. Upon light adaptation and stimulation with a narrow light field, all six species showed positive phototaxis to high light intensities and a pronounced negative response to low intensities. Only the negative response will occur in natural underwater light conditions, and it is part of a predator-avoidance shadow-response which operates in areas of higher light intensity. The same phototactic pattern is observed in all species when darkadapted except H. oregonensis. If nocturnal vertical migration occurs, this negative response may be responsible for the descent at sunrise and depth maintenance during the day.     

Determination of photosynthetic pigment composition in an individual phytoplankton cell in seas and lakes using fluorescence microscopy; properties of the fluorescence emitted from picophytoplankton cells

To develop a method for the determination of photosynthetic pigment species in individual phytoplankton cells, especially natural picophytoplankton cells, the fluorescence spectra of intact cells were studied with cultured phytoplankton. The study was made mainly with phycoerythrin-containing picophytoplankton collected off Japan in 1982 with reference to diatomal species and phycoerythrin-free cyanophycean species. The spectra were measured for cell suspensions with an ordinary spectrofluorometer, and for individual cells with a microscope spectrofluorometer, paying special attention to the effect of cell-fixation. Results indicated that: (1) the cell-fixation with the glutaraldehyde and paraformaldehyde mixture modified phycoerythrin emission from picophytoplankton markedly in its wavelength location and intensity, but (2) the emission from phycocyanin was affected far less, and (3) the emission from chlorophyll a was not altered. However, the phycoerythrin emission modified by the fixation was found to be easily distinguished from other emissions, and kept its intensity high enough for detection with a fluorescence microscope. The fluorescence properties after the fixation were kept unaltered for a long period of time. Based on the results, we propose a simple method for the determination of photosynthetic pigments in individual phytoplankton cells in seas and lakes using fluorescence microscopy. Results of our tests with natural samples of phytoplankton are presented, and problems for further improvement are also discussed.     

Light harvesting in the green alga Ostreobium sp., a coral symbiont adapted to extreme shade

Ostreobium sp. (Chlorophyta: Siphonales) can be found as green bands within the skeletal material of a number of stony corals in the Indo-Pacific and Caribbean regions. Many of these corals also contain symbiotic dinoflagellates in the overlaying coral polyps that effectively screen out all the typical photosynthetically active radiation from the algae in the green bands below. Ostreobium sp., nevertheless, grows photosynthetically. Its action spectrum and absorption spectrum have been shown to extend much further into the near infra-red compared to other green algae. In the present study, carried out in 1987, fluorescence excitation and emission spectra were measured in Ostreobium sp. and compared to spectra obtained from the green alga Ulva sp. and the brown alga Endarachne sp. Xanthophylls, probably siphonein and an unidentified xanthophyll probably related to siphonaxanthin, are photosynthetically active in Ostreobium sp., and can sensitize Photosystem II fluorescence at 688 nm and Photosystem I (PS I) fluorescence at 718 nm. The fluorescence emission spectra of Ostreobium sp. measured at 25° C and 77 K were not remarkably different from those of the green alga Ulva sp. Absorbance changes induced by light were measured in Ostreobium sp. from 670 to 750 nm and were like those normally seen in green plants except that, in addition to the minimum expected for the reaction-center chlorophyll of PS I (P700) at 703 nm, another minimum was seen at 730 nm. It is possible that this spectrumreflects the functioning of a reaction center of Photosystem I that has adapted to function in light highly enriched in far-red wavelengths.CIW-DPB Publication No. 1021     

Planktonic bioluminescence in the pack ice and the marginal ice zone of the Beaufort Sea

An icebreaker cruise into the Beaufort Sea in the fall of 1986 provided a unique opportunity for studying planktonic bioluminescence in ice fields and in the marginal ice zone. Bathyphotometer casts (bioluminescence intensity, seawater temperature, beam attenuation coefficient, and salinity) and biological collections were made to a depth of 100 m. A light budget, which describes the planktonic species responsible for the measured bioluminescence, and a dinoflagellate species budget were constructed from the mean light output from luminescent plankton and plankton counts. The vertical distribution of bioluminescence among the ice stations was similar. The maximum intensities were 2 to 8×10⁶ photons s^-1 cm^-3 in the upper 50 m of the sea-ice interface. The marginal ice zone station (MIZ) exhibited a maximum intensity of 2 to 3×10⁸ photons s^-1 cm^-3 between 5 and 30 m depth. At Ice Station 2, Metridia longa and their nauplii contributed approximately 80% of stimulable bioluminescence in the upper 10 m but, overall, Protoperidinium spp. dinoflagellates contributed most of the light to a depth of 100 m. In the MIZ, Protoperidinium spp. dinoflagellates contributed 90% of the light within the upper 10 m, decreasing to 43% of the contributed light at a depth of 40 m. Below 40 m, dinoflagellate bioluminescence decreased to a few percent of the total to a depth of 90 m. Metridia spp. copepods contributed more than 50% of the light at depths from 40 to 90 m. Ostracods, larvaceans, and euphausiid furcilia contributed <1% of all bioluminescence at all depths sampled. Correlation analyses between measured bioluminescence (photons s^-1 cm^-3), the number of bioluminescent dinoflagellates and the light budget for the MIZ indicated highly significant associations: r=0.919, p=0.001, and r=0.912, p<0.001, respectively (Student's two-tailed t-tests). Bioluminescence was negatively correlated with seawater salinity at all stations (p=0.001). Maximum bioluminescence was measured in the less saline surface waters at all stations.     

Comparative study of behavioral-sensitivity thresholds to near-UV and blue-green light in deep-sea crustaceans

The behavioral sensitivities of five species of deep-sea crustaceans (order Decapoda: Acanthephyra curtirostris, A. smithi, Notostomus gibbosus, Janicella spinacauda and Oplophorus gracilirostris) to near-UV and blue-green light were studied during a research cruise off the coast of Hawaii in 1993. Two of the five species have electrophysiologically-measured spectral sensitivity peaks at 400 and 500 nm, while the remaining three species have a single sensitivity peak at 490 to 500 nm. In the current study, behavioral mean threshold sensitivities (defined as the lowest irradiance change to which the shrimp would give a behavioral response) were determined for tethered specimens of each species at two wavelengths, 400 and 500 nm. The mean behavioral threshold sensitivities of the two species with putative dual visual-pigment systems were approximately the same to near-UV and blue-green light, while the other three species were significantly less sensitive to near-UV vs blue-green light. Results from these experiments indicate that (1) behavioral information obtained from tethered shrimp accurately reflects their spectral sensitivity, and (2) the sensitivity of the putative dichromats to near-UV light is sufficiently low to detect calculated levels of near-UV light remaining in the down-welling field at their daytime depth of 600 m. Possible functions of this high sensitivity to short wavelength light are discussed.     

Variability of spectral absorption efficiency within living cells of Pyrocystis lunula (Dinophyta)

This study examines variability in the spectral absorption efficiency in various parts of living Pyrocystis lunula cells. changes in spectral absorption efficiency measured within cells are attributed to light-induced chloroplast migration as well as reorganization of cellular material during the process of asexual reproduction. During the dark cycle, major pigment peaks were well resolved in those spectra measured in the distal cytoplasmic strands where chloroplasts were concentrated. In contrast, the absorption efficiencies measured in the granular central area that did not contain chloroplasts decreased gradually from the blue to the red portions of the spectrum and are similar to those published for detrital particles. When chloroplasts migrated toward the center of the cell in response to light, absorption efficiency curves for the granular central area were flatter than the curves measured in cytoplasmic strands containing chloroplasts. This was due to the combined absorption properties of the central area and the chloroplasts. Absorption efficiency spectra were also flattened in aplanospores within the parent vegetative cells because of the concentration of cellular material into smaller areas. These findings suggest that shapes of spectral absorption curves measured for the major phytoplankton groups cannot be assumed to remain constant over time. Furthermore, changes in cell structure may account for some of the reported diel changes in beam attenuation and stimulated fluorescence in natural waters.     

Photoreactivity of humic substances: relationship between fluorescence and singlet oxygen production

Humic substances are natural compounds abundantly present in the environment. They play a significant role in the natural attenuation of pollution in surface water due to their capacity to generate reactive species upon solar light excitation. Finding physico chemical parameters related to this property would be of a great help in the prediction studies of the organic pollutants fate. In this work, we investigated relationships between the ability of the humic substances to produce singlet oxygen and their fluorescence properties. For this, a series of sixteen humic acids, fulvic acids, and water-extractable organic matter from soils were studied. The steady-state singlet oxygen concentrations in the irradiated humic substances solutions were measured by monitoring the loss of furfuryl alcohol added as a singlet oxygen scavenger. The emission spectra of the sixteen samples were also recorded. Values of the steady-state singlet oxygen concentrations and the emission intensities showed significant variations among the humic samples and a parallel increase. Thus, here we demonstrate that the rate of singlet oxygen production and the emission intensity of the humic samples are correlated, the best correlation being obtained for emission wavelengths between 500 and 580 nm. This correlation which was never reported until now can be used to estimate the singlet oxygen-production capacity of the humic substances based on their fluorescent properties.     

Action spectra and spectral quantum yield of photosynthesis in marine macroalgae with thin and thick thalli

Net photosynthesis at 10mol photons m^-2 s^-1 in each of 24 wavelengths was measured in absolute units by an O₂-electrode and corrected for dark respiration to construct action spectra for gross photosynthesis in nine species of algae, which included plants with thin and thick thalli from each of four major pigment groups. The photosynthesis of green and brown algae with thin thalli decreased in green light, but species with thick thalli from these two groups had action spectra which were almost flat, and matched the optical blackness of the thalli but did not reflect the pigment differences between the species. Among the red algae, on the other hand, there was little difference between the action spectra for thin and thick algae. Only wavelengths absorbed by the phycobilin pigments were effective in photosynthesis, even in species (e.g. Chondrus, Phyllophora) which absorbed all visible wavelengths strongly. Maximal quantum yields of 0.10 to 0.12 O₂ molecules per absorbed photon were recorded for thin green and brown algae, but thicker algae in these two groups had lower values. Red algae exhibited maximal values close to 0.10 O₂ molecules per absorbed photon, irrespective of thallus thickness or phycocyanin content, but the quantum yields of phycoerythrin-rich species in the 600 to 650 nm waveband were lower than those of phycocyanin-rich species.     

Interacting effects of ambient light and plumage color patterns in displaying Wire-tailed Manakins (Aves,Pipridae)

Sending color signals to conspecifics may attract predators, leading to opposing selection pressures on the evolution of signal expression and display behavior in animals. The costs of signaling can be reduced, however, because conspicuousness is the combined result of the reflectance spectra of the displayer's color pattern and the spectra of ambient light illuminating the animal. Changes in ambient light can alter conspicuousness, even when chemical and structural color-generating mechanisms remain constant, potentially allowing animals to display their colors most fully in light environments where the benefits are greatest relative to the costs. Using spectroradiometric methods, we determined how light habitat use affects conspicuousness in adult males of the Wire-tailed Manakin Pipra filicauda, a lekking bird species with vivid plumage colors. We studied three aspects of visibility, including properties of the entire color pattern, visual contrast within an individual's plumage and a bird's contrast relative to its visual background. Wire-tailed Manakins usually displayed in forest shade environments, which reduced their conspicuousness at larger viewing distances, while maximizing visual contrast within the plumage color pattern at close viewing distances. Compared to sunspots, ambient light in forest shade reduces the contrast of individual bird colors with the background at close viewing distance. However, background contrast of individual bird colors in the shade was still relatively higher during sunny than during cloudy weather which may explain why males were more active when the sun was not blocked by clouds. Assuming that the visual perceptions of predators and other manakins do not differ from the reflectance patterns we measured, Wire-tailed manakins tend to display in light environments that reduce the conflicts between avoiding long distance detection by predators and displaying conspicuous color signals to visiting females.     

细菌SOD对微生物紫外光辐射损伤的恢复作用

将培养至对数中期的大肠杆菌、钝齿棒杆菌和啤酒酵母等３种微生物的细胞适度稀释液，分别涂布于培养皿上使受紫外光照射，在细胞受辐射后死亡率大于９０％时停止照射，立即加入一定剂量的细菌超氧化物岐化酶（ＳＯＤ），以观察ＳＯＤ对微生物活力的恢复效应．结果表明，ＳＯＤ可使受辐照的细胞存活率显著提高，且量效关系明显，而照前添加ＳＯＤ则无上述效应．检测表明，紫外光照射可引发细菌的超弱发光，且该种超弱发光可因氧气的充入而瞬间增强，鲁米诺也能增强这种超弱发光，加入甘露醇对发光无影响．当紫外光照射后加入ＳＯＤ能使发光强度大为减弱，表明此种超弱发光与的活动有关，并对ＳＯＤ拮抗紫外线杀菌的机理作了讨论．     

Evolutionary variation in the expression of phenotypically plastic color vision in Caribbean mantis shrimps, genus Neogonodactylus

Many animals have color vision systems that are well suited to their local environments. Changes in color vision can occur over long periods (evolutionary time), or over relatively short periods such as during development. A select few animals, including stomatopod crustaceans, are able to adjust their systems of color vision directly in response to varying environmental stimuli. Recently, it has been shown that juveniles of some stomatopod species that inhabit a range of depths can spectrally tune their color vision to local light conditions through spectral changes in filters contained in specialized photoreceptors. The present study quantifies the potential for spectral tuning in adults of three species of Caribbean Neogonodactylus stomatopods that differ in their depth ranges to assess how ecology and evolutionary history influence the expression of phenotypically plastic color vision in adult stomatopods. After 12 weeks in either a full-spectrum “white” or a narrow-spectrum “blue” light treatment, each of the three species evidenced distinctive tuning abilities with respect to the light environment that could be related to its natural depth range. A molecular phylogeny generated using mitochondrial cytochrome oxidase C subunit 1 (CO-1) was used to determine whether tuning abilities were phylogenetically or ecologically constrained. Although the sister taxa Neogonodactylus wennerae and N. bredini both exhibited spectral tuning, their ecology (i.e. preferred depth range) strongly influenced the expression of the phenotypically plastic color vision trait. Our results indicate that adult stomatopods have evolved the ability to undergo habitat-specific spectral tuning, allowing rapid facultative physiological modification to suit ecological constraints.