The cost of being a caring mother: the ignored factor in the reproduction of marine invertebrates
By Miriam Fernández, C. Bock, H. Pörtner. 2000
130 citations recorded by the source corpus.
Subfields: Ecology, Global and Planetary Change
View Paper: https://www.semanticscholar.org/paper/810d2f6e2f9eafa0908eaea066e21adab59d29c4
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Citations in the corpus
- Effects of ocean acidification and warming on the larval development of the spider crab Hyas araneus from different latitudes (54° vs. 79° N) (2010, background): “This projection results from the principles of oxygen- and capacity-limited thermal tolerance: The brooding of the egg masses by crustacean females (Wheatly 1981, Fernández et al. 2000) enhances oxygen demand at constant oxygen supply capacity and, thereby, exacerbates any oxygen limitation.”
- Physiological basis for high CO2 tolerance in marine ectothermic animals: pre-adaptation through lifestyle and ontogeny? (2009, background): “…2 ra-tios, it seems likely that embryos from other marine taxa will also be surrounded by fluids of high p CO 2 and low pH. Decreased oxygen partial pressures have been measured for instance in shark eggs (Dietz and Davenport, 1987) and deca-pod crustacean egg masses (Fernandez et al., 2000, 2002).”
- Patterns of parental care in invertebrates (2012, background): “In aquatic environments, oxygen availability can be a fundamental constraint on the number of embryos that can be brooded and there can be considerable costs to making oxygen available to the centre of a large embryo mass (Fernández et al. 2000).”
- Meiobenthos at the Arctic Håkon Mosby Mud Volcano, with a parental-caring nematode thriving in sulphide-rich sediments (2006, background): “It ensures the temporary availability of oxygen to both embryos and juveniles which is necessary for proper growth (Fernandez et al. 2000).”
- Reproductive investment in the crab Cancer setosus along a latitudinal cline: egg production, embryo losses and embryo ventilation (2003, unknown): “Brooding species carry or protect the embryos throughout development, investing substantial amounts of energy in brood care (Menge 1974, Perron 1982, Clarke 1987, Pandian 1994, Fernández et al. 2000).”
- Abiotic conditions in cephalopod (Sepia officinalis) eggs: embryonic development at low pH and high pCO2 (2009, background): “…For example, Diez and Davenport (1987) showed that pO2 values in shark eggs decrease from ca. 18 kPa in early embryos to ca. 10 kPa in late embryos, Fernandez et al. (2000, 2002) measured water pO2 values \5 kPa in decapod crustacean egg masses, Cohen and Strathmann (1996) found pO2 values of less…”
- Active brood care in Cancer setosus (Crustacea: Decapoda): the relationship between female behaviour, embryo oxygen consumption and the cost of brooding (2002, background): “Only in rare cases have costs associated with brooding been estimated (cost of producing extra-embryonic material: Hughes & Roberts 1980; Perron 1981; Perron & Corpuz 1982; Lee & Strathmann 1998; cost of oxygen provision in crabs during early development of the embryos: Naylor, Taylor & Bennett 1997”
- Oxygen- and capacity-limitation of thermal tolerance: a matrix for integrating climate-related stressor effects in marine ecosystems (2010, background): “…be it in the limited capacity of adult specimens to ventilate their oxygen-limited egg masses (Cohen and Strathmann, 1996; Woods and Moran, 2008; Fernandez et al., 2000) or in the dependence of maximum body size of marine invertebrate phyla on temperature-dependent oxygen solubility and thus…”