FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1834142451> ?p ?o ?g. }

• W1834142451 endingPage "490" @default.
• W1834142451 startingPage "468" @default.
• W1834142451 abstract "1. During laboratory maintenance, G. zacae from the Gulf of California molts during neap tides or the transition from spring to neap tides; oviposition probably occurs during neap tides or the transition from spring to neap tides. G. falcatus from Hawaii tends to molt during spring tides or the transition from neap to spring tides; oviposition occurs during neap tides or the transition from spring to neap tides. Strong evidence suggests that H. glyptocercus from Eniwetok molts during neap tides or their approach. P. ciliata from three populations molt during the last lunar phase, providing the only substantive evidence for lunar rather than tidal control of molting in stomatopods. While P. ciliata from Hawaii and Florida lays eggs during neap or waxing neap tidal phases, those maintained in Thailand deposit eggs during waning neap tidal cycles. G. falcatus and G. graphurus from Australia molt in opposite tidal cycles; G. graphurus molts during neap tides but reproduces during spring tides. The five species of Gonodactylidae from Australia oviposit during spring tides.2. Field data demonstrate significantly more molting during spring than neap tidal cycles in a gonodactylid community comprised of seven species in Phuket, Thailand. Laboratory maintenance increases variation in the pattern of molting across tidal cycles, although molting still occurs significantly more frequently in spring than neap tidal cycles. G. chiragra molts significantly more frequently than expected during spring than neap tides in the field. Both field and laboratory data demonstrate significant correlation of oviposition with spring tides among the species in 1973 but not 1974.3. These data support a temporal selfish herd hypothesis that synchrony of molting in the population reduces mortality due to conspecific and congeneric aggression in stomatopods. Observed data do not support predictions from alternative hypotheses that physical factors, feeding, or predation impose molting and reproductive rhythms. Molting synchrony is more consistent with the idea that stomatopod populations are limited by the availability of burrows than by food. The initiation of molting synchrony in the population can be explained by selection for response to environmental cues, by chance, and/or by small, local populations with synchronous hatching of young. Oviposition rhythms therefore may subserve the primary molting rhythm." @default.
• W1834142451 created "2016-06-24" @default.
• W1834142451 creator A5013104749 @default.
• W1834142451 date "1976-06-01" @default.
• W1834142451 modified "2023-10-01" @default.
• W1834142451 title "LUNAR AND TIDAL PERIODICITY OF MOLTING AND REPRODUCTION IN STOMATOPOD CRUSTACEA: A SELFISH HERD HYPOTHESIS" @default.
• W1834142451 cites W125333009 @default.
• W1834142451 cites W1562702058 @default.
• W1834142451 cites W1591347119 @default.
• W1834142451 cites W172714659 @default.
• W1834142451 cites W174633338 @default.
• W1834142451 cites W1906424671 @default.
• W1834142451 cites W1909094053 @default.
• W1834142451 cites W1983437861 @default.
• W1834142451 cites W1991662322 @default.
• W1834142451 cites W1998143474 @default.
• W1834142451 cites W2002664886 @default.
• W1834142451 cites W2003222503 @default.
• W1834142451 cites W2004318660 @default.
• W1834142451 cites W2005961008 @default.
• W1834142451 cites W2018651611 @default.
• W1834142451 cites W2043945644 @default.
• W1834142451 cites W2044887640 @default.
• W1834142451 cites W2071894611 @default.
• W1834142451 cites W2083272826 @default.
• W1834142451 cites W2085185344 @default.
• W1834142451 cites W2113710617 @default.
• W1834142451 cites W2161627394 @default.
• W1834142451 cites W2167020585 @default.
• W1834142451 cites W2177555117 @default.
• W1834142451 cites W2252743040 @default.
• W1834142451 cites W2261963055 @default.
• W1834142451 cites W2317700371 @default.
• W1834142451 cites W2327628472 @default.
• W1834142451 cites W2332458435 @default.
• W1834142451 cites W2464160896 @default.
• W1834142451 cites W2897955617 @default.
• W1834142451 cites W2913335677 @default.
• W1834142451 cites W356259956 @default.
• W1834142451 cites W38281800 @default.
• W1834142451 cites W396844444 @default.
• W1834142451 cites W612836844 @default.
• W1834142451 cites W2740607387 @default.
• W1834142451 doi "https://doi.org/10.2307/1540686" @default.
• W1834142451 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/953074" @default.
• W1834142451 hasPublicationYear "1976" @default.
• W1834142451 type Work @default.
• W1834142451 sameAs 1834142451 @default.
• W1834142451 citedByCount "54" @default.
• W1834142451 countsByYear W18341424512012 @default.
• W1834142451 countsByYear W18341424512013 @default.
• W1834142451 countsByYear W18341424512014 @default.
• W1834142451 countsByYear W18341424512015 @default.
• W1834142451 countsByYear W18341424512016 @default.
• W1834142451 countsByYear W18341424512018 @default.
• W1834142451 countsByYear W18341424512020 @default.
• W1834142451 crossrefType "journal-article" @default.
• W1834142451 hasAuthorship W1834142451A5013104749 @default.
• W1834142451 hasBestOaLocation W18341424512 @default.
• W1834142451 hasConcept C111368507 @default.
• W1834142451 hasConcept C127313418 @default.
• W1834142451 hasConcept C127413603 @default.
• W1834142451 hasConcept C173758957 @default.
• W1834142451 hasConcept C18903297 @default.
• W1834142451 hasConcept C2778163872 @default.
• W1834142451 hasConcept C2778712887 @default.
• W1834142451 hasConcept C41905685 @default.
• W1834142451 hasConcept C78519656 @default.
• W1834142451 hasConcept C84766238 @default.
• W1834142451 hasConcept C86803240 @default.
• W1834142451 hasConcept C88160329 @default.
• W1834142451 hasConceptScore W1834142451C111368507 @default.
• W1834142451 hasConceptScore W1834142451C127313418 @default.
• W1834142451 hasConceptScore W1834142451C127413603 @default.
• W1834142451 hasConceptScore W1834142451C173758957 @default.
• W1834142451 hasConceptScore W1834142451C18903297 @default.
• W1834142451 hasConceptScore W1834142451C2778163872 @default.
• W1834142451 hasConceptScore W1834142451C2778712887 @default.
• W1834142451 hasConceptScore W1834142451C41905685 @default.
• W1834142451 hasConceptScore W1834142451C78519656 @default.
• W1834142451 hasConceptScore W1834142451C84766238 @default.
• W1834142451 hasConceptScore W1834142451C86803240 @default.
• W1834142451 hasConceptScore W1834142451C88160329 @default.
• W1834142451 hasIssue "3" @default.
• W1834142451 hasLocation W18341424511 @default.
• W1834142451 hasLocation W18341424512 @default.
• W1834142451 hasLocation W18341424513 @default.
• W1834142451 hasOpenAccess W1834142451 @default.
• W1834142451 hasPrimaryLocation W18341424511 @default.
• W1834142451 hasRelatedWork W1886111637 @default.
• W1834142451 hasRelatedWork W1965981894 @default.
• W1834142451 hasRelatedWork W1990296635 @default.
• W1834142451 hasRelatedWork W1994460652 @default.
• W1834142451 hasRelatedWork W2007945551 @default.
• W1834142451 hasRelatedWork W2053228967 @default.
• W1834142451 hasRelatedWork W2055326011 @default.
• W1834142451 hasRelatedWork W2061169238 @default.
• W1834142451 hasRelatedWork W2370809130 @default.

• next