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Optical parameters of the eyes of some benthic decapods as a function of habitat depth (Crustacea, Decapoda)
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-642-66468-7_3openalex-snapshot
Adaptations to the Deep-Sea Environment
inferredcites →https://doi.org/10.1007/978-3-642-66907-1_4openalex-snapshot
Optics and Vision in Invertebrates
inferredcites →https://doi.org/10.1007/bf00220529openalex-snapshot
The eyes of mesopelagic crustaceans: I. Gennadas sp. (Penaeidae)
inferredcites →https://doi.org/10.1007/bf00225767openalex-snapshot
The microanatomy of the compound eye of Munida irrasa (Decapoda: Galatheidae)
inferredcites →https://doi.org/10.1007/bf00446350openalex-snapshot
Neue untersuchungen über sinnesorgane und nervensystem der crustaceen. I
inferredcites →https://doi.org/10.1007/bf00504738openalex-snapshot
Bacterial bioluminescence as an early indication of marine fish spoilage
inferredcites →https://doi.org/10.1007/bf00605034openalex-snapshot
Optics of the eyes ofPhronima and other deep-sea amphipods
inferredcites →https://doi.org/10.1007/bf00605230openalex-snapshot
Optical parameters of euphausiid eyes as a function of habitat depth
inferredcites →https://doi.org/10.1007/bf02582973openalex-snapshot
The optical geometry of euphausiid eyes
inferredcites →https://doi.org/10.1016/0011-7471(76)90810-xopenalex-snapshot
Adenosine triphosphate in the North Atlantic ocean and its relationship to the oxygen minimum
inferredcites →https://doi.org/10.1016/0040-8166(77)90010-6openalex-snapshot
Fine structure of the compound eyes of the midwater amphipod Phronima in relation to behavior and habitat
inferredcites →https://doi.org/10.1016/0042-6989(65)90082-9openalex-snapshot
The euphausiid eye—a re-evaluation
inferredcites →https://doi.org/10.1016/0300-9629(75)90146-2openalex-snapshot
The respiratory rates of midwater crustaceans as a function of depth of occurrence and relation to the oxygen minimum layer off Southern California
inferredcites →https://doi.org/10.1016/b978-0-08-091734-4.50010-xopenalex-snapshot
Ecology of Juvenile and Adult Homarus
inferredcites →https://doi.org/10.1080/00222938609460133openalex-snapshot
XVII.—The abyssal Decapod Crustacea of the ‘Albatross’ Dredgings in the North Atlantic
inferredcites →https://doi.org/10.1086/physzool.55.2.30155856openalex-snapshot
Effects of Temperature, Pressure, and Oxygen Concentration on the Oxygen Consumption Rate of the Hydrothermal Vent Crab Bythograea thermydron (Brachyura)
inferredcites →https://doi.org/10.1098/rspb.1972.0071openalex-snapshot
The angular distribution of the light produced by some mesopelagic fish in relation to their camouflage
inferredcites →https://doi.org/10.1098/rspb.1976.0029openalex-snapshot
Light, and photoreceptor degeneration in the Norway lobster, Nephrops norvegicus (L.)
inferredcites →https://doi.org/10.1126/science.203.4385.1109openalex-snapshot
Cryptic Bioluminescence in a Midwater Shrimp
inferredcites →https://doi.org/10.1139/z78-148openalex-snapshot
Comparative biology of four species of glyphocrangonid and crangonid shrimp from the continental slope of the middle Atlantic Bight
inferredcites →https://doi.org/10.1242/jeb.98.1.83openalex-snapshot
Light Organ and Eyestalk Compensation to Body Tilt in the Luminescent Midwater Shrimp, Sergestes Similis
inferredcites →https://doi.org/10.1515/znc-1974-9-1023openalex-snapshot
The Absolute Sensitivity of Lens and Compound Eyes
inferredcites →https://doi.org/10.2307/1541479openalex-snapshot
MARINE BIOLUMINESCENCE SPECTRA MEASURED WITH AN OPTICAL MULTICHANNEL DETECTION SYSTEM
inferredcites →https://doi.org/10.4319/lo.1971.16.1.0104openalex-snapshot
RESPIRATORY RATE AND DEPTH OF OCCURRENCE OF MIDWATER ANIMALS1
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.4202/app.2009.0036zenodo-depositor-declared
Ecological Significance of the Arthropod Fauna from the Jurassic (Callovian) La Voulte Lagerstätte
inferred← citeshttps://doi.org/10.5852/ejt.2020.604zenodo-depositor-declared
Thoridae (Crustacea: Decapoda) can penetrate the Abyss: a new species of Lebbeus from the Sea of Okhotsk, representing the deepest record of the family
inferred← citeshttps://doi.org/10.1007/s00227-005-1606-9openalex-snapshot
Correlation between photosensitivity and downwelling irradiance in mesopelagic crustaceans
inferred← citeshttps://doi.org/10.1007/s00227-009-1176-3openalex-snapshot
The structure and sensitivity of the eye of different life history stages of the ontogenetic migrator Gnathophausia ingens
inferred← citeshttps://doi.org/10.1007/s00359-014-0918-yopenalex-snapshot
Ecological constraints on sensory systems: compound eye size in Daphnia is reduced by resource limitation
inferred← citeshttps://doi.org/10.1007/s12562-014-0734-xopenalex-snapshot
Eye structure and function in the giant freshwater prawn Macrobrachium rosenbergii
inferred← citeshttps://doi.org/10.1007/s13199-019-00657-9openalex-snapshot
To see or to smell: the role of vision in host-recognition by an ectoparasitic crab
inferred← citeshttps://doi.org/10.1016/0042-6989(88)90047-8openalex-snapshot
Eye size of pelagic crustaceans as a function of habitat depth and possession of photophores
inferred← citeshttps://doi.org/10.1016/0198-0149(90)90104-4openalex-snapshot
Metabolic rates of benthic deep-sea decapod crustaceans decline with increasing depth primarily due to the decline in temperature
inferred← citeshttps://doi.org/10.1016/j.asd.2016.01.004openalex-snapshot
The Hunsrück biota: A unique window into the ecology of Lower Devonian arthropods
inferred← citeshttps://doi.org/10.1016/j.crpv.2014.03.001openalex-snapshot
The La Voulte-sur-Rhône Lagerstätte (Middle Jurassic, France)
inferred← citeshttps://doi.org/10.1016/j.isci.2021.103579openalex-snapshot
The remarkable visual system of a Cretaceous crab
inferred← citeshttps://doi.org/10.1016/s1873-0140(06)80035-4openalex-snapshot
Chapter 9 metabolic potentials of deep-sea fishes: A comparative approach
inferred← citeshttps://doi.org/10.1038/s41598-019-50961-zopenalex-snapshot
Distribution and quantification of bioluminescence as an ecological trait in the deep sea benthos
inferred← citeshttps://doi.org/10.1093/plankt/fbae058openalex-snapshot
Exposure to fungal infection decreases eye size in the zooplankton, Daphnia
inferred← citeshttps://doi.org/10.1098/rspb.2018.2625openalex-snapshot
Predation selects for smaller eye size in a vertebrate: effects of environmental conditions and sex
inferred← citeshttps://doi.org/10.1098/rspb.2025.0553openalex-snapshot
Plasticity in Daphnia eye size is determined by intra-generational environmental conditions
inferred← citeshttps://doi.org/10.1111/1365-2435.70107openalex-snapshot
At the edge of darkness: A framework for the evolution of visual systems in dim light
inferred← citeshttps://doi.org/10.1111/evo.13283openalex-snapshot
The evolution of vertebrate eye size across an environmental gradient: phenotype does not predict genotype in a Trinidadian killifish
inferred← citeshttps://doi.org/10.1111/evo.13748openalex-snapshot
Context‐dependent evolution of ostracod morphology along the ecogeographical gradient of ocean depth
inferred← citeshttps://doi.org/10.1111/jeb.14175openalex-snapshot
Experimental test of the influence of light availability on the evolution of eye size and behaviour in Daphnia
inferred← citeshttps://doi.org/10.1126/sciadv.abc6721openalex-snapshot
Disparate compound eyes of Cambrian radiodonts reveal their developmental growth mode and diverse visual ecology
inferred← citeshttps://doi.org/10.1159/000540491openalex-snapshot
Eye Size Does Not Change with Artificial Selection on Relative Telencephalon Size in Guppies (Poecilia reticulata)
inferred← citeshttps://doi.org/10.1186/s12862-016-0694-0openalex-snapshot
Evolution of body size, vision, and biodiversity of coral-associated organisms: evidence from fossil crustaceans in cold-water coral and tropical coral ecosystems
inferred← citeshttps://doi.org/10.1242/jeb.072033openalex-snapshot
Light and vision in the deep-sea benthos: II. Vision in deep-sea crustaceans
inferred← citeshttps://doi.org/10.1371/journal.pone.0099505openalex-snapshot
Linking Eye Design with Host Symbiont Relationships in Pontoniine Shrimps (Crustacea, Decapoda, Palaemonidae)
inferred← citeshttps://doi.org/10.1666/08-006.1openalex-snapshot
Ekalakia(Decapoda: Brachyura): the preservation of eyes links Cretaceous crabs to Jurassic ancestors
inferred← citeshttps://doi.org/10.2307/1542723openalex-snapshot
Compound Eye Fine Structure in Paralomis multispina Benedict, an Anomuran Half-Crab From 1200 m Depth (Crustacea; Decapoda; Anomura)
inferred← citeshttps://doi.org/10.2307/1548328openalex-snapshot
Multisensory Control of Eyestalk Orientation in Decapod Crustaceans: An Ecological Approach
inferred← citeshttps://doi.org/10.3389/fevo.2021.698041openalex-snapshot
Exploring the Evolution of Perception: An Agent-Based Approach
inferred← citeshttps://doi.org/10.7287/peerj.1176v0.1/reviews/1openalex-snapshot
Peer Review #1 of "External morphology of eyes and Nebenaugen of caridean decapods–ecological and systematic considerations (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.1176v0.1/reviews/2openalex-snapshot
Peer Review #2 of "External morphology of eyes and Nebenaugen of caridean decapods–ecological and systematic considerations (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.1176v0.1/reviews/3openalex-snapshot
Peer Review #3 of "External morphology of eyes and Nebenaugen of caridean decapods–ecological and systematic considerations (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.1176openalex-snapshot
External morphology of eyes and Nebenaugen of caridean decapods–ecological and systematic considerations
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