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Different environmental drivers influence the reproduction of a tropical sponge (Tedania ignis) along a latitudinal gradient
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00047641openalex-snapshot
A review of the reproductive bionomics of aquatic gammaridean amphipods: variation of life history traits with latitude, depth, salinity and superfamily
inferredcites →https://doi.org/10.1007/bf01320227openalex-snapshot
Influence of sponges on invertebrate recruitment: A field test of allelopathy
inferredcites →https://doi.org/10.1007/s00227-007-0793-yopenalex-snapshot
Temperature cues gametogenesis and larval release in a tropical sponge
inferredcites →https://doi.org/10.1007/s00227-016-2842-xopenalex-snapshot
Reproductive biology of the sea cucumber Holothuria grisea in Brazil: importance of social and environmental factors in breeding coordination
inferredcites →https://doi.org/10.1007/s00227-018-3294-2openalex-snapshot
Latitudinal variation in maternal investment traits of the kelp crab Taliepus dentatus along the coast of Chile
inferredcites →https://doi.org/10.1007/s002270050495openalex-snapshot
Reproduction in the Red Sea soft coral Heteroxenia fuscescens : seasonality and long-term record (1991 to 1997)
inferredcites →https://doi.org/10.1007/s002270100661openalex-snapshot
Latitudinal variation in the reproductive biology of the commensal crab Pinnaxodes chilensis (Decapoda: Pinnotheridae) along the Chilean coast
inferredcites →https://doi.org/10.1007/s00435-018-0429-4openalex-snapshot
Comparative ultrastructure of the spermatogenesis of three species of Poecilosclerida (Porifera, Demospongiae)
inferredcites →https://doi.org/10.1007/s10750-018-3562-7openalex-snapshot
Is the Orton’s rule still valid? Tropical sponge fecundity, rather than periodicity, is modulated by temperature and other proximal cues
inferredcites →https://doi.org/10.1007/s12526-019-01013-2openalex-snapshot
Influence of endogenous and exogenous factors on the reproductive output of a cryptogenic calcareous sponge
inferredcites →https://doi.org/10.1016/0022-0981(89)90045-2openalex-snapshot
Low-salinity tolerance of and salinity-induced dormancy in the estuarine sponge Microciona prolifera (Ellis et Solander) under long-term laboratory culture
inferredcites →https://doi.org/10.1016/0022-0981(94)90155-4openalex-snapshot
The reproductive cycle of the sponge Halichondria panicea Pallas (1766) and its relationship to temperature and salinity
inferredcites →https://doi.org/10.1016/j.bmc.2009.09.010openalex-snapshot
Tedanol: A potent anti-inflammatory ent-pimarane diterpene from the Caribbean Sponge Tedania ignis
inferredcites →https://doi.org/10.1016/s0022-0981(00)00181-7openalex-snapshot
Observations in ecology: you can’t make progress on processes without understanding the patterns
inferredcites →https://doi.org/10.1016/s0044-8486(01)00813-4openalex-snapshot
Latitudinal variation in reproductive behavior in the pearl oyster, Pinctada albina sugillata
inferredcites →https://doi.org/10.1016/s0065-2881(02)43004-0openalex-snapshot
Fecundity and life-history strategies in marine invertebrates
inferredcites →https://doi.org/10.1017/s0025315400000102openalex-snapshot
Sea-Temperature, Breeding and Distribution in Marine Animals
inferredcites →https://doi.org/10.1017/s0025315416001223openalex-snapshot
Reproductive patterns of musselPerumytilus purpuratus(Bivalvia: Mytilidae), along the Chilean coast: effects caused by climate change?
inferredcites →https://doi.org/10.1038/s41598-017-02196-zopenalex-snapshot
A decadal analysis of bioeroding sponge cover on the inshore Great Barrier Reef
inferredcites →https://doi.org/10.1038/s41598-018-26535-wopenalex-snapshot
The bioeroding sponge Cliona orientalis will not tolerate future projected ocean warming
inferredcites →https://doi.org/10.1080/00785236.2001.10409473openalex-snapshot
Latitudinal variation in the reproductive biology ofBetaeus truncatus(Decapoda: Alpheidae) along the Chilean coast
inferredcites →https://doi.org/10.1086/284716openalex-snapshot
Parental Investment in Offspring in Variable Environments: Theoretical and Empirical Considerations
inferredcites →https://doi.org/10.1086/409052openalex-snapshot
Life-History Tactics: A Review of the Ideas
inferredcites →https://doi.org/10.1086/bblv216n3p226openalex-snapshot
Egg Size as a Life History Character of Marine Invertebrates: Is It All It's Cracked Up to Be?
inferredcites →https://doi.org/10.1093/icesjms/fsv108openalex-snapshot
Marked variations in reproductive characteristics of snapper (Chrysophrys auratus, Sparidae) and their relationship with temperature over a wide latitudinal range
inferredcites →https://doi.org/10.1093/plankt/fbh173openalex-snapshot
The dynamics of sponge larvae assemblages from northwestern Mediterranean nearshore bottoms
inferredcites →https://doi.org/10.1111/brv.12189openalex-snapshot
Matrotrophy and placentation in invertebrates: a new paradigm
inferredcites →https://doi.org/10.1111/ele.12402openalex-snapshot
Deconstructing environmental predictability: seasonality, environmental colour and the biogeography of marine life histories
inferredcites →https://doi.org/10.1111/evo.13559openalex-snapshot
Thorson's rule, life‐history evolution, and diversification of benthic octopuses (Cephalopoda: Octopodoidea)
inferredcites →https://doi.org/10.1111/geb.12748openalex-snapshot
Global environmental drivers of marine fish egg size
inferredcites →https://doi.org/10.1111/geb.13245openalex-snapshot
Growth of marine ectotherms is regionally constrained and asymmetric with latitude
inferredcites →https://doi.org/10.1111/j.1439-0485.2008.00234.xopenalex-snapshot
Quantitative trends in sponge ecology research
inferredcites →https://doi.org/10.1111/j.1439-0485.2008.00244.xopenalex-snapshot
Reproductive output in a Mediterranean population of the homosclerophoridCorticium candelabrum(Porifera, Demospongiae), with notes on the ultrastructure and behavior of the larva
inferredcites →https://doi.org/10.1111/j.1439-0485.2011.00493.xopenalex-snapshot
Environmental cues and seasonal reproduction in a temperate estuary: a case study of Owenia collaris (Annelida: Polychaeta, Oweniidae)
inferredcites →https://doi.org/10.1111/j.1469-185x.1950.tb00585.xopenalex-snapshot
REPRODUCTIVE and LARVAL ECOLOGY OF MARINE BOTTOM INVERTEBRATES
inferredcites →https://doi.org/10.1111/j.1744-7410.2008.00128.xopenalex-snapshot
Differences in reproductive timing among sponges sharing habitat and thermal regime
inferredcites →https://doi.org/10.1111/maec.12202openalex-snapshot
Environmental effects on the reproduction and fecundity of the introduced calcareous sponge Paraleucilla magna in Rio de Janeiro, Brazil
inferredcites →https://doi.org/10.1111/maec.12524openalex-snapshot
Mind your neighbourhood: Biotic and abiotic factors shaping the small‐scale spatial distribution of sponges (Demospongiae) in tropical urban beaches
inferredcites →https://doi.org/10.1126/science.1241981openalex-snapshot
Surviving in a Marine Desert: The Sponge Loop Retains Resources Within Coral Reefs
inferredcites →https://doi.org/10.1139/z06-019openalex-snapshot
Ecological interactions of marine sponges
inferredcites →https://doi.org/10.1371/journal.pone.0042392openalex-snapshot
Life-Cycle Traits of Paraleucilla magna, a Calcareous Sponge Invasive in a Coastal Mediterranean Basin
inferredcites →https://doi.org/10.1371/journal.pone.0073800openalex-snapshot
Phylogeny Drives Large Scale Patterns in Australian Marine Bioactivity and Provides a New Chemical Ecology Rationale for Future Biodiscovery
inferredcites →https://doi.org/10.1371/journal.pone.0155266openalex-snapshot
The Effect of Latitudinal Variation on Shrimp Reproductive Strategies
inferredcites →https://doi.org/10.1590/1678-4766e2016007openalex-snapshot
Temporal variation of epi- and endofaunal assemblages associated with the red sponge Tedania ignis on a rocky shore (São Sebastião Channel), SE Brazil
inferredcites →https://doi.org/10.1641/b570707openalex-snapshot
Marine Ecoregions of the World: A Bioregionalization of Coastal and Shelf Areas
inferredcites →https://doi.org/10.1651/s-2788.1openalex-snapshot
Latitudinal Variation in Population Structure and Reproductive Pattern of the Endemic South American Shrimp Artemesia Longinaris (Decapoda: Penaeoidea)
inferredcites →https://doi.org/10.2307/1540468openalex-snapshot
THE REPRODUCTION OFHALICLONA LOOSANOFFIAND ITS APPARENT RELATIONSHIP TO WATER TEMPERATURE
inferredcites →https://doi.org/10.2307/1542466openalex-snapshot
Transport and Metabolism of Alanine and Palmitic Acid by Field-Collected Larvae of Tedania ignis (Porifera, Demospongiae): Estimated Consequences of Limited Label Translocation
inferredcites →https://doi.org/10.2307/2390028openalex-snapshot
Reproductive Trade-Offs in Caridean Shrimps
inferredcites →https://doi.org/10.32614/rj-2017-066openalex-snapshot
glmmTMB Balances Speed and Flexibility Among Packages for Zero-inflated Generalized Linear Mixed Modeling
inferredcites →https://doi.org/10.3354/meps07274openalex-snapshot
Quantile regression models for fish recruitment–environment relationships: four case studies
inferredcites →https://doi.org/10.3354/meps138169openalex-snapshot
Effects of physical factors on larval behavior, settlement and recruitment of four tropical demosponges
inferredcites →https://doi.org/10.7717/peerj.2623openalex-snapshot
A 12-year record of intertidal barnacle recruitment in Atlantic Canada (2005–2016): relationships with sea surface temperature and phytoplankton abundance
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4664470openalex-extracted
The Use of Shipwrecks as Stepstones of Non-Native Species in an Area of the Western Atlantic
inferred← citeshttps://doi.org/10.1007/s12526-021-01257-xopenalex-snapshot
Population dynamics of three species of the genus Aplysina (Porifera, Demospongiae, Verongiida) in a tropical bay in the Western Atlantic Ocean
inferred← citeshttps://doi.org/10.1111/ivb.12386openalex-snapshot
Reproductive cycles of the oviparous sponges Cinachyrella apion (Spirophorida) and Tethya maza (Tethyida) in a tropical intertidal environment
inferred← citeshttps://doi.org/10.7287/peerj.14685v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Life-cycle traits in the demosponge Hymeniacidon perlevis in a land-based fish farm (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14685v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Life-cycle traits in the demosponge Hymeniacidon perlevis in a land-based fish farm (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14685v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Life-cycle traits in the demosponge Hymeniacidon perlevis in a land-based fish farm (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.14685openalex-snapshot
Life-cycle traits in the demosponge Hymeniacidon perlevis in a land-based fish farm
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