Trophic Ecology of Benthic Marine Invertebrates with Bi-Phasic Life Cycles: What Are We Still Missing?

Advances in Marine Biology

Volumn 71, Issue , 2015, Pages 1-70

  Calado, Ricardo ^a   Leal, Miguel Costa ^b  

^a UNIVERSITY OF AVEIRO   (Portugal)

^b SWISS FEDERAL INSTITUTE OF AQUATIC SCIENCE AND TECHNOLOGY   (Switzerland)

Author keywords

Carry over effects; Life history; Maternal effects; Metamorphosis; Phenotypic plasticity; Trophic interactions

Indexed keywords

INVERTEBRATA;

ANIMAL; AQUATIC SPECIES; CLASSIFICATION; FOOD CHAIN; INVERTEBRATE; LIFE CYCLE STAGE; PHYSIOLOGY; REPRODUCTION;

ANIMALS; AQUATIC ORGANISMS; FOOD CHAIN; INVERTEBRATES; LIFE CYCLE STAGES; REPRODUCTION;

EID: 84945484782     PISSN: 00652881     EISSN: 21625875     Source Type: Book Series    
DOI: 10.1016/bs.amb.2015.07.001     Document Type: Chapter

References (323)

1. Alfaro A.C. Diet of littoraria scabra, while vertically migrating on mangrove trees: gut content, fatty acid, and stable isotope analyses. Estuar. Coast. Shelf Sci. 2008, 79:718-726.
2. Alfaro A.C., Thomas F., Sergent L., Duxbury M. Identification of trophic interactions within an estuarine food web (northern New Zealand) using fatty acid biomarkers and stable isotopes. Estuar. Coast. Shelf Sci. 2006, 70:271-286.
3. Allen R.M., Marshall D.J. The larval legacy: cascading effects of recruit phenotype on post-recruitment interactions. Oikos 2010, 119:1977-1983.
4. Allen R.M., Marshall D.J. Phenotypic links among life-history stages are complex and context-dependent in a marine invertebrate: interactions among offspring size, larval nutrition and postmetamorphic density. Funct. Ecol. 2013, 27:1358-1366.
5. Allen R.M., Marshall D. Egg size effects across multiple life-history stages in the marine annelid Hydroides diramphus. PLoS One 2014, 9:e102253.
6. Allen J.D., Pernet B. Intermediate modes of larval development: bridging the gap between planktotrophy and lecithotrophy. Evol. Dev. 2007, 9:643-653.
7. Allen R.M., Buckley Y.M., Marshall D.J. Offspring size plasticity in response to intraspecific competition: an adaptive maternal effect across life-history stages. Am. Nat. 2008, 171:225-237.
8. Anger K. Effects of temperature and salinity on the larval development of the Chinese mitten crab Eriocheir sinensis (Decapoda: Grapsidae). Mar. Ecol. Prog. Ser. 1991, 72:103-110.
9. Anger K. Patterns of growth and chemical composition in decapod crustacean larvae. Invertebr. Reprod. Dev. 1998, 33:159-176.
10. Anger K. The Biology of Decapod Crustacean Larvae 2001, 300. A. A. Balkema Publishers, Lisse.
11. Anger K. Contributions of larval biology to crustacean research: a review. Invertebr. Reprod. Dev. 2006, 49:175-205.
12. Anger K., Dawirs R.R., Anger V., Costlow J.D. Effects of early starvation periods on zoeal developement of brachyuran crabs. Biol. Bull. 1981, 161:199-212.
13. Arendt J.D. Adaptive intrinsic growth rates: an integration across taxa. Q. Rev. Biol. 1997, 72:149-177.
14. Back J.A., King R.S. Sex and size matter: ontogenetic patterns of nutrient content of aquatic insects. Freshw. Sci. 2013, 32:837-848.
15. Back J.A., Taylor J.M., King R.S., Fallert K.L., Hintzen E.H. Ontogenic differences in mayfly stoichiometry influence growth rates in response to phosphorus enrichment. Fundam. Appl. Limnol. 2008, 171:233-240.
16. Baeza J.A., Fernandez M. Active brood care in Cancer setosus (Crustacea : Decapoda): the relationship between female behaviour, embryo oxygen consumption and the cost of brooding. Funct. Ecol. 2002, 16:241-251.
17. Baggett L.P., Heck K.L., Frankovich T.A., Armitage A.R., Fourqurean J.W. Stoichiometry, growth, and fecundity responses to nutrient enrichment by invertebrate grazers in sub-tropical turtle grass (Thalassia testudinum) meadows. Mar. Biol. 2013, 160:169-180.
18. Baptista M., Lopes V.M., Pimentel M.S., Bandarra N., Narciso L., Marques A., Rosa R. Temporal fatty acid dynamics in the octocoral Veretillum cynomorium. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 2012, 161:178-187.
19. Barile P.J., Lapointe B.E., Capo T.R. Dietary nitrogen availability in macroalgae enhances growth of the sea hare Aplysia californica (Opisthobranchia: Anaspidea). J. Exp. Mar. Biol. Ecol. 2004, 303:65-78.
20. Bas C.C., Spivak E.D. Effects of embryonic salinity exposure on larval development in two populations of the estuarine crab Chasmagnathus granulatus Dana, 1851 (Crustacea: Brachyura). Invertebr. Reprod. Dev. 2003, 43:117-123.
21. Bas C.C., Spivak E.D., Anger K. Seasonal and interpopulational variability in fecundity, egg size, and elemental composition (CHN) of eggs and larvae in a grapsoid crab, Chasmagnathus granulatus. Helgol. Mar. Res. 2007, 61:225-237.
22. Battaglene S.C., Seymour J.E., Ramofafia C. Survival and growth of culture juvenile sea cucumbers, Holothura scabra. Aquaculture 1999, 178:293-322.
23. Bell M.V., Tocher D.R. Biosynthesis of polyunsaturated fatty acids in aquatic ecosystems: general pathways and new directions. Lipids in Aquatic Ecosystems 2009, 211-236. Springer, Heidelberg. M.T. Arts, M.J. Kainz, M.T. Brett (Eds.).
24. Bernárdez C., Freire J., González-Gurriarán E. Feeding of the spider crab Maja squinado in rocky subtidal areas of the Ría de Arosa (north-west Spain). J. Mar. Biol. Assoc. UK 2000, 80:95-102.
25. Bishop C.D., Huggett M.J., Heyland A., Hodin J., Brandhorst B.P. Interspecific variation in metamorphic competence in marine invertebrates: the significance for comparative investigations into the timing of metamorphosis. Integr. Comp. Biol. 2006, 46:662-682.
26. Blankenship L.E., Yayanos A.A. Universal primers and PCR of gut contents to study marine invertebrate diets. Mol. Ecol. 2005, 14:891-899.
27. Blaxter J.H.S., Hempel G. The influence of egg size on herring larvae (Clupea harengus L.). J. Cons. Int. Explor. Mer 1963, 28:211-240.
28. Bode A., Fernandéz C., Mompeán C., Parra S., Rozada F., Valencia-Vila J., Viana I.G. Differential processing of anthropogenic carbon and nitrogen in benthic food webs of A Coruña (NW Spain) traced by stable isotopes. Deep-Sea Res. II Top. Stud. Oceanogr. 2014, 106:198-206.
29. Boecklen W.J., Yarnes C.T., Cook B.A., James A.C. On the use of stable isotopes in trophic ecology. Annu. Rev. Ecol. Syst. 2011, 42:411-440.
30. Boersma M., Aberle N., Hantzsche F.M., Schoo K.L., Wiltshire K.H., Malzahn A.M. Nutritional limitation travels up the food chain. Int. Rev. Hydrobiol. 2008, 93:479-488.
31. Botello G., Krug P.J. 'Desperate larvae' revisited: age, energy and experience affect sensitivity to settlement cues in larvae of the gastropod Alderia sp. Mar. Ecol. Prog. Ser. 2006, 312:149-159.
32. Bowen W.D., Iverson S.J. Methods of estimating marine mammal diets: a review of validation experiments and sources of bias and uncertainty. Mar. Mamm. Sci. 2013, 29:719-754.
33. Braeckman U., Provoost P., Sabbe K., Soetaert K., Middelburg J.J., Vincx M., Vanaverbeke J. Temporal dynamics in the diet of two marine polychaetes as inferred from fatty acid biomarkers. J. Sea Res. 2012, 68:6-19.
34. Budge S.M., Iverson S.J., Koopman H.N. Studying trophic ecology in marine ecosystems using fatty acids: a primer on analysis and interpretation. Mar. Mamm. Sci. 2006, 22:759-801.
35. Bullejos F.J., Carrillo P., Gorokhova E., Medina-Sánchez J.M., Balseiro E.G., Villar-Argaiz M. Shifts in food quality for herbivorous consumer growth: multiple golden means in the life history. Ecology 2014, 95:1272-1284.
36. Burgess S.C., Marshall D.J. Temperature-induced maternal effects and environmental predictability. J. Exp. Biol. 2011, 214:2329-2336.
37. Burgess S.C., Marshall D.J. Are numbers enough? Colonizer phenotype and abundance interact to affect population dynamics. J. Anim. Ecol. 2011, 80:681-687.
38. Burke R.D. The induction of metamorphosis of marine invertebrate larvae: stimulus and response. Can. J. Zool. 1983, 61:1701-1719.
39. Burnett N., Sulkin S. Characteristics of feeding on dinoflagellates by newly hatched larval crabs. Mar. Biol. 2006, 151:851-861.
40. Burress E.D., Duarte A., Serra W.S., Gangloff M.M., Siefferman L. Species-specific ontogenetic diet shifts among Neotropical Crenicichla: using stable isotopes and tissue stoichiometry. J. Fish Biol. 2013, 82:1904-1915.
41. Burrows M.T., Gontarek S.J., Nash R.D.M., Gibson R.N. Shrimp predation on 0-group plaice: contrasts between field data and predictions of an individual-based model. J. Sea Res. 2001, 45:243-254.
42. Byrne M. Impact of ocean warming and ocean acidification on marine invertebrate life history stages. Vulnerabilities and potential for persistence in a changing ocean. Oceanography and Marine Biology: An Annual Review 2011, vol. 49:1-42. Taylor & Francis, Boca Raton, FL.
43. Calado R. Marine Ornamental Shrimp: Biology, Aquaculture and Conservation 2008, Wiley-Blackwell, Oxford.
44. Calado R., Narciso L., Morais S., Rhyne A.L., Lin J. A rearing system for the culture of ornamental decapod crustacean larvae. Aquaculture 2003, 218:329-339.
45. Calado R., Figueiredo J., Rosa R., Nunes M.L., Narciso L. Effects of temperature, density, and diet on development, survival, settlement synchronism, and fatty acid profile of the ornamental shrimp Lysmata seticaudata. Aquaculture 2005, 245:221-237.
46. Calado R., Rosa R., Morais S., Nunes M.L., Narciso L. Growth, survival, lipid and fatty acid profile of juvenile monaco shrimp Lysmata seticaudata fed on different diets. Aquacult. Res. 2005, 36:493-504.
47. Calado R., Pimentel T., Vitorino A., Dionísio G., Dinis M.T. Technical improvements of a rearing system for the culture of decapod crustacean larvae, with emphasis on marine ornamental species. Aquaculture 2008, 285:264-269.
48. Calado R., Dionísio G., Bartilotti C., Nunes C., Dos Santos A., Dinis M.T. Importance of light and larval morphology in starvation resistance and feeding ability of newly hatched marine ornamental shrimps Lysmata spp. (Decapoda: Hippolytidae). Aquaculture 2008, 283:56-63.
49. Calado R., Olaguer-Feliú A.O., González-Gordillo J.I., Queiroga H. The capacity of crab megalopae to autotomize body appendages and the consequences upon their feeding ability-the price to pay to live another day. Mar. Freshw. Behav. Physiol. 2009, 42:329-341.
50. Calado R., Pimentel T., Cleary D.F.R., Dionisio G., Nunes C., Da Silva T.L., Dinis M.T., Reis A. Providing a common diet to different marine decapods does not standardize the fatty acid profiles of their larvae: a warning sign for experimentation using invertebrate larvae produced in captivity. Mar. Biol. 2010, 157:2427-2434.
51. Campbell D.B. Foraging movements of the sea star Asterias forbesi (Desor) (Echinodermata: Asteroidea) in Narragansett Bay, Rhode Island U.S.A. Mar. Behav. Physiol. 1984, 11:185-198.
52. Carabel S., Godínez-Domínguez E., Verísimo P., Fernandéz L., Freire J. An assessment of sample processing methods for stable isotope analyses of marine food webs. J. Exp. Mar. Biol. Ecol. 2006, 336:254-261.
53. Carpenter S.R., Armbrust E.V., Arzberger P.W., Chapin F.S., Elser J.J., Hackett E.J., Ives A.R., Kareiva P.M., Leibold M.A., Lundberg P., Mangel M., Merchant N., Murdoch W.W., Palmer M.A., Peters D.P.C., Pickett S.T.A., Smith K.K., Wall D.H., Zimmerman A.S. Accelerate synthesis in ecology and environmental sciences. Bioscience 2009, 59:699-701.
54. Carreón-Palau L., Parrish C.C., Angel-Rodríguez J.A., Pérez-España H., Aguiñiga-García S. Revealing organic carbon sources fueling a coral reef food web in the Gulf of Mexico using stable isotopes and fatty acids. Limnol. Oceanogr. 2013, 58:593-612.
55. Carroll D.J., Kempf S.C. Laboratory culture of the aeolid nudibranch Berghia verrucicornis (Mollusca, Opisthobranchia): some aspects of its development and life history. Biol. Bull. 1990, 179:243-253.
56. Casini M., Lövgren J., Hjelm J., Cardinale M., Molinero J.-C., Kornilovs G. Multi-level trophic cascades in a heavily exploited open marine ecosystem. Proc. R. Soc. B 2008, 275:1793-1801.
57. Chia F.-S., Buckland-Nicks J., Young C.M. Locomotion of marine invertebrate larvae: a review. Can. J. Zool. 1984, 62:1205-1222.
58. Clark P.F., Calazans D.K., Pohle G.W. Accuracy and standardization of Brachyuran larval descriptions. Invertebr. Reprod. Dev. 1998, 33:127-144.
59. Cleary A.C., Durbin E.G., Rynearson T.A. Krill feeding on sediment in the Gulf of Maine (North Atlantic). Mar. Ecol. Prog. Ser. 2012, 455:157-172.
60. Cocito S., Ferrier-Pagès C., Cupido R., Rottier C., Meier-Augenstein W., Kemp H., Reynaud S., Peirano A. Nutrient acquisition in four Mediterranean gorgonian species. Mar. Ecol. Prog. Ser. 2013, 473:179-188.
61. Coelho H., Calado R., Olaguer-Feliu A.O., Vieira S., Queiroga H., Serodio J. Nondestructive quantification of phytoplankton gut content of brachyuran crab megalopae using in vivo chlorophyll a fluorescence. J. Plankton Res. 2009, 31:577-581.
62. Coelho H., Lopes Da Silva T., Reis A., Queiroga H., Serôdio J., Calado R. Fatty acid profiles indicate the habitat of mud snails Hydrobia ulvae within the same estuary: mudflats vs. seagrass meadows. Estuar. Coast. Shelf Sci. 2011, 92:181-187.
63. Cowan J.H., Houde E.D. Growth and survival of bay anchovy Anchoa mitchilli larvae in mesocosm enclosures. Mar. Ecol. Prog. Ser. 1990, 68:47-57.
64. Cowen R.K., Sponaugle S. Larval dispersal and marine population connectivity. Ann. Rev. Mar. Sci. 2009, 1:443-466.
65. Czamanski M., Nugraha A., Pondaven P., Lasbleiz M., Masson A., Caroff N., Bellail R., Tréguer P. Carbon, nitrogen and phosphorus elemental stoichiometry in aquacultured and wild-caught fish and consequences for pelagic nutrient dynamics. Mar. Biol. 2011, 158:2847-2862.
66. Dalsgaard J., John M.S., Kattner G., Müller-Navarra D., Hagen W. Fatty acid trophic markers in the pelagic marine environment. Adv. Mar. Biol. 2003, 46:225-340.
67. Davidson E.H., Peterson K.J., Cameron R.A. Origin of bilaterian body plans: evolution of developmental regulatory mechanisms. Science 1995, 270:1319-1325.
68. Deagle B.E., Thomas A.C., Shaffer A.K., Trites A.W., Jarman S.N. Quantifying sequence proportions in a DNA-based diet study using Ion Torrent amplicon sequencing: which counts count?. Mol. Ecol. Resour. 2013, 13:620-633.
69. Deschaseaux E., Taylor A., Maher W. Measure of stress response induced by temperature and salinity changes on hatched larvae of three marine gastropod species. J. Exp. Mar. Biol. Ecol. 2011, 397:121-128.
70. Dewitt T.J., Sih A., Wilson D.S. Costs and limits of phenotypic plasticity. Trends Ecol. Evol. 1998, 13:77-81.
71. Diederich C.M., Jarrett J.N., Chaparro O.R., Segura C.J., Arellano S.M., Pechenik J.A. Low salinity stress experienced by larvae does not affect post-metamorphic growth or survival in three calyptraeid gastropods. J. Exp. Mar. Biol. Ecol. 2011, 397:94-105.
72. Dionísio G., Rosa R., Leal M.C., Cruz S., Brandão C., Calado G., Serôdio J., Calado R. Beauties and beasts: a portrait of sea slugs aquaculture. Aquaculture 2013, 408:1-14.
73. Dong S., Liang M., Gao Q., Wang F., Dong Y., Tian X. Intra-specific effects of sea cucumber (Apostichopus japonicus) with reference to stocking density and body size. Aquacult. Res. 2010, 41:1170-1178.
74. Dos Santos A., Santos A.P., Conway D.V. Horizontal and vertical distribution of cirripede cyprid larvae in an upwelling system off the Portuguese coast. Mar. Ecol. Prog. Ser. 2007, 329:145-155.
75. Duffy J.E., Cardinale B.J., France K.E., Mcintyre P.B., Thebault E., Loreau M. The functional role of biodiversity in ecosystems: incorporating trophic complexity. Ecol. Lett. 2007, 10:522-538.
76. Dupont S., Dorey N., Stumpp M., Melzner F., Thorndyke M. Long-term and trans-life-cycle effects of exposure to ocean acidification in the green sea urchin Strongylocentrotus droebachiensis. Mar. Biol. 2012, 160:1835-1843.
77. Durbin E.G., Casas M.C., Rynearson T.A. Copepod feeding and digestion rates using prey DNA and qPCR. J. Plankton Res. 2011, 34:72-82.
78. WoRMS Editorial Board World Register of Marine Species 2015, (online, accessed 31-05-2015).
79. Edwards M., Richardson A.J. Impact of climate change on marine pelagic phenology and trophic mismatch. Nature 2004, 430:881-884.
80. Elser J.J. Biological stoichiometry: a chemical bridge between ecosystem ecology and evolutionary biology. Am. Nat. 2006, 168:S25-S35.
81. Elser J.J., Dobberfuhl D.R., Mackay N.A., Schampel J.H. Organism size, life history, and N:P stoichiometry. Bioscience 1996, 46:674-684.
82. Fabricius K., Yahel G., Genin A. In situ depletion of phytoplankton by an azooxanthellate soft coral. Limnol. Oceanogr. 1998, 43:354-356.
83. Fenaux L., Strathmann M.F., Strathmann R.A. Five tests of food-limited growth of larvae in coastal waters by comparison of rates of development and form of echinoplutei. Limnol. Oceanogr. 1994, 39:84-98.
84. Ferrier-Pagès C., Rottier C., Beraud E., Levy O. Experimental assessment of the feeding effort of three scleractinian coral species during a thermal stress: effect on the rates of photosynthesis. J. Exp. Mar. Biol. Ecol. 2010, 390:118-124.
85. Ferrier-Pagès C., Peirano A., Abbate M., Cocito S., Negri A., Rottier C., Riera P., Rodolfo-Metalpa R., Reynaud S. Summer autotrophy and winter heterotrophy in the temperate symbiotic coral Cladocora caespitosa. Limnol. Oceanogr. 2011, 56:1429-1438.
86. Fischer J., Phillips N.E. Carry-over effects of multiple stressors on benthic embryos are mediated by larval exposure to elevated UVB and temperature. Glob. Chang. Biol. 2014, 20:2108-2116.
87. Folt C.L., Burns C.W. Biological drivers of zooplankton patchiness. Trends Ecol. Evol. 1999, 14:300-305.
88. Francis D.S., Salmon M.L., Kenway M.J., Hall M.R. Palinurid lobster aquaculture: nutritional progress and considerations for successful larval rearing. Rev. Aquac. 2014, 6:180-203.
89. Frischer M.E., Sanchez C.A., Walters T.L., Thompson M.E., Frazier L.M., Paffenhöfer G.A. Reliability of qPCR for quantitative gut content estimation in the circumglobally abundant pelagic tunicate Dolioletta gegenbauri (Tunicata, Thaliacea). Food Webs 2014, 1:18-24.
90. Fry B. Stable Isotope Ecology 2008, 308. Springer, New York.
91. Fusetani N. Biofouling and antifouling. Nat. Prod. Rep. 2004, 21:94-104.
92. Gattuso J.P., Lavigne H. Technical note: approaches and software tools to investigate the impact of ocean acidification. Biogeosciences 2009, 6:2121-2133.
93. Gebauer P., Paschke K., Anger K. Costs of delayed metamorphosis: reduced growth and survival in early juveniles of an estuarine grapsid crab, Chasmagnathus granulata. J. Exp. Mar. Biol. Ecol. 1999, 238:271-281.
94. Gebauer P., Paschke K., Barria A., Anger K. Seasonal variation in dry weight and elemental composition of the early developmental stages of Petrolisthes laevigatus (Guerin, 1835) (Decapoda: Porcellanidae) in the Seno de Reloncavi, southern Chile. Helgol. Mar. Res. 2013, 67:167-177.
95. Genard B., Pernet F., Lemarchand K., Boudry P., Moraga D., Tremblay R. Physiological and biochemical changes associated with massive mortality events occurring in larvae of American oyster (Crassostrea virginica). Aquat. Living Resour. 2011, 24:247-260.
96. Giangrande A. Polychaete reproductive patterns, life cycles and life histories: an overview. Oceanogr. Mar. Biol. Annu. Rev. 1997, 35:323-386.
97. Giangrande A., Geraci S., Belmonte G. Life-cycle and life-history diversity in marine invertebrates and the implications in community dynamics. Oceanogr. Mar. Biol. Annu. Rev. 1994, 32:305-333.
98. Gimenez L. Effects of prehatching salinity and initial larval biomass on survival and duration of development in the zoea 1 of the estuarine crab, Chasmagnathus granulata, under nutritional stress. J. Exp. Mar. Biol. Ecol. 2002, 270:93-110.
99. Giménez L. Phenotypic links in complex life cycles: conclusions from studies with decapod crustaceans. Integr. Comp. Biol. 2006, 46:615-622.
100. Giménez L. Relationships between habitat conditions, larval traits, and juvenile performance in a marine invertebrate. Ecology 2010, 91:1401-1413.
101. Giménez L. Exploring mechanisms linking temperature increase and larval phenology: the importance of variance effects. J. Exp. Mar. Biol. Ecol. 2011, 400:227-235.
102. Giménez L., Anger K. Larval performance in an estuarine crab, Chasmagnathus granulata, is a consequence of both larval and embryonic experience. Mar. Ecol. Prog. Ser. 2003, 249:251-264.
103. Gonzalez-Ortegón E., Giménez L. Environmentally mediated phenotypic links and performance in larvae of a marine invertebrate. Mar. Ecol. Prog. Ser. 2014, 502:185-195.
104. Greve W. Planktonkreisel a new device for culturing zooplankton. Mar. Biol. 1968, 1:201-203.
105. Grosholz E. Ecological and evolutionary cosequences of coastal invasions. Trends Ecol. Evol. 2002, 17:22-27.
106. Grosholz E.D., Ruiz G.M. Predicting the impact of introduced marine species: lessons from the multiple invasions of the European green crab Carcinus maenas. Biol. Conserv. 1996, 78:59-66.
107. Guerao G., Simeó C.G., Anger K., Urzúa Á., Rotllant G. Nutritional vulnerability of early zoea larvae of the crab Maja brachydactyla (Brachyura, Majidae). Aquat. Biol. 2012, 16:253-264.
108. Gurney R., Lebour M.-V. On the larvae of certain crustacea macrura, mainly from Bermuda. J. Linn. Soc. Lond. 1941, 41:89-181.
109. Hadfield M.G. Why and how marine-invertebrate larvae metamorphose so fast. Semin. Cell Dev. Biol. 2000, 11:437-443.
110. Hadfield M.G., Paul V.J. Natural chemical cues for settlement and metamorphosis of marine invertebrate larvae. Marine Chemical Ecology 2001, 431-461. CRC Press, Boca Raton, FL. J.B. McClintock, B.J. Baker (Eds.).
111. Hadfield M.G., Strathmann M.F. Variability, flexibility and plasticity in life histories of marine invertebrates. Oceanol. Acta 1996, 19:323-334.
112. Hadfield M.G., Carpizo-Ituarte E.J., Del Carmen K., Nedved B.T. Metamorphic competence, a major adaptive convergence in marine invertebrate larvae. Am. Zool. 2001, 41:1123-1131.
113. Hamel J.-F., Conand C., Pawson D.L., Mercier A. The sea cucumber Holothuria scabra (Holothuroidea: Echinodermata): its biology and exploitation as Beche-de-mer. Adv. Mar. Biol. 2001, 41:129-223.
114. Hamner W.M. Design developments in the planktonkreisel, a plankton aquarium for ships at sea. J. Plankton Res. 1990, 12:397-402.
115. Hampton S.E., Parker J.N. Collaboration and productivity in scientific synthesis. Bioscience 2011, 61:900-910.
116. Hansen B., Ockelmann K.W. Feeding behaviour in larvae of the opisthobranch Philine aperta. I. Growth and functional response at different developmental stages. Mar. Biol. 1991, 111:255-261.
117. Hargrove J.S., Parkyn D.C., Murie D.J., Demopoulos A.W.J., Austin J.D. Augmentation of French grunt diet description using combined visual and DNA-based analyses. Mar. Freshw. Res. 2012, 63:740-750.
118. Hart M.W. Particle captures and the method of suspension feeding by echinoderm larvae. Biol. Bull. 1991, 180:12-27.
119. Hendry A.P., Peichel C.L., Matthews B., Boughman J.W., Nosil P. Stickleback research: the now and the next. Evol. Ecol. Res. 2013, 15:1-31.
120. Henry J.J., Collin R., Perry K.J. The slipper snail, Crepidula: an emerging lophotrochozoan model system. Biol. Bull. 2010, 218:211-229.
121. Hessen D.O., Elser J.J., Sterner R.W., Urabe J. Ecological stoichiometry: an elementary approach using basic principles. Limnol. Oceanogr. 2013, 58:2219-2236.
122. Hickman C.P., Roberts L.S., Keen S.L., Larsaon A., L'anson H., Eisenhour D.J. Integrated Principles of Zoology 2007, 928. McGraw-Hill Higher Education, Cleveland. 14th ed.
123. Hoegh-Guldberg O., Pearse J.S. Temperature, food availability, and the development of marine invertebrate larvae. Am. Zool. 1995, 35:415-425.
124. Holmstrom C., Kjelleberg S. The effect of external biological factors on settlement of marine invertebrate and new antifouling technology. Biofouling 1994, 8:147-160.
125. Houlbrèque F., Ferrier-Pages C. Heterotrophy in tropical scleractinian corals. Biol. Rev. 2009, 84:1-17.
126. Houlbrèque F., Tambuttée E., Richard C., Ferrier-Pagès C. Importance of a micro-diet for scleractinian corals. Mar. Ecol. Prog. Ser. 2004, 282:151-160.
127. Houlbrèque F., Delesalle B., Blanchot J., Montel Y., Ferrier-Pagès C. Picoplankton removal by the coral reef community of La Prévoyante, Mayotte Island. Aquat. Microb. Ecol. 2006, 44:59-70.
128. Howard S.C., Hentschel B.T. Effects of short-term food variability on the plasticity of age and size at metamorphosis of porcelain crab larvae. Limnol. Oceanogr. 2005, 50:1960-1971.
129. Hughes A.D., Catarino A.I., Kelly M.S., Barnes D.K.A., Black K.D. Gonad fatty acids and trophic interactions of the echinoid Psammechinus militaris. Mar. Ecol. Prog. Ser. 2005, 305:101-111.
130. Hunt H.L., Scheibling R.E. Role of early post-settlement mortality in recruitment of benthic marine invertebrates. Mar. Ecol. Prog. Ser. 1997, 155:269-301.
131. Iverson S.J. Tracing aquatic food webs using fatty acids: from qualitative indicators to quantitative determination. Lipids in Aquatic Ecosystems 2009, 281-308. Springer, Heidelberg. M.T. Arts, M.J. Kainz, M.T. Brett (Eds.).
132. Iverson S.J., Field C., Bowen W.D., Blanchard W. Quantitative fatty acid signature analysis: a new method of estimating predator diets. Ecol. Monogr. 2004, 74:211-235.
133. Ives A.R., Cardinale B.J., Snyder W.E. A synthesis of subdisciplines: predator-prey interactions, and biodiversity and ecosystem functioning. Ecol. Lett. 2005, 8:102-116.
134. Jackson T.D., Torres G., Giménez L. Survival and development of larvae of two decapod crustaceans under limited access to prey across a thermal range. J. Plankton Res. 2014, 36:1476-1487.
135. Jaeckle W.B., Manahan D.T. Feeding by a "nonfeeding" larva: uptake of dissolved amino acids from seawater by lecithotrophic larvae of the gastropod Haliotis rufescens. Mar. Biol. 1989, 103:87-94.
136. Jeffrey S.W., Mantoura R.F.C., Bjørnland T. Data for the identification of 47 key phytoplankton pigments. Phytoplankton Pigments in Oceanography: Guidelines to Modern Methods 1997, 449-559. UNESCO, Paris. S.W. Jeffrey, R.F.C. Mantoura, S.W. Wright (Eds.).
137. Jeffs A.G., Willmott M.E., Wells R.M.G. The use of energy stores in the puerulus of the spiny lobster Jasus edwardsii across the continental shelf of New Zealand. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 1999, 123:351-357.
138. Jeffs A.G., Nichols P.D., Mooney B.D., Phillips K.L., Phleger C.F. Identifying potential prey of the pelagic larvae of the spiny lobster Jasus edwardsii using signature lipids. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 2004, 137:487-507.
139. Jeffs A.G., Montgomery J.C., Tindle C.T. How do spiny lobster post-larvae find the coast?. N. Z. J. Mar. Freshw. Res. 2005, 39:605-617.
140. Jeyasingh P.D., Cothran R.D., Tobler M. Testing the ecological consequences of evolutionary change using elements. Ecol. Evol. 2014, 4:528-538.
141. Johnson K.B., Shanks A.L. The importance of prey densities and background plankton in studies of predation on invertebrate larvae. Mar. Ecol. Prog. Ser. 1997, 158:293-296.
142. Jones D.A., Kumlu M., Le Vay L., Fletcher D.J. The digestive physiology of herbivorous, omnivoros and carnivorous crustacean larvae: a review. Aquaculture 1997, 155:285-295.
143. Kelly J.R., Scheibling R.E. Fatty acids as dietary tracers in benthic food webs. Mar. Ecol. Prog. Ser. 2012, 446:1-22.
144. Kennicutt M.C., Chown S.L., Cassano J.J., Liggett D., Peck L.S., Massom R., Rintoul S.R., Storey J., Vaughan D.G., Wilson T.J., Allison I., Ayton J., Badhe R., Baeseman J., Barrett P.J., Bell R.E., Bertler N., Bo S., Brandt A., Bromwich D., Cary S.C., Clark M.S., Convey P., Costa E.S., Cowan D., Deconto R., Dunbar R., Elfring C., Escutia C., Francis J., Fricker H.A., Fukuchi M., Gilbert N., Gutt J., Havermans C., Hik D., Hosie G., Jones C., Kim Y.D., Le Maho Y., Lee S.H., Leppe M., Leitchenkov G., Li X., Lipenkov V., Lochte K., Lopez-Martinez J., Luedecke C., Lyons W., Marenssi S., Miller H., Morozova P., Naish T., Nayak S., Ravindra R., Retamales J., Ricci C.A., Rogan-Finnemore M., Ropert-Coudert Y., Samah A.A., Sanson L., Scambos T., Schloss I.R., Shiraishi K., Siegert M.J., Simoes J.C., Storey B., Sparrow M.D., Wall D.H., Walsh J.C., Wilson G., Winther J.G., Xavier J.C., Yang H., Sutherland W.J. A roadmap for Antarctic and Southern Ocean science for the next two decades and beyond. Antarct. Sci. 2015, 27:3-18.
145. Keough M.J., Raimondi P.T. Responses of settling invertebrate larvae to bioorganic films: effects of dietary types of films. J. Exp. Mar. Biol. Ecol. 1995, 185:235-253.
146. Kimberly D.A., Salice C.J. If you could turn back time: understanding transgenerational latent effects of developmental exposure to contaminants. Environ. Pollut. 2014, 184:419-425.
147. Kimbro D.L., Grosholz E.D., Baukus A.J., Nesbitt N.J., Travis N.M., Attoe S., Coleman-Hulbert C. Invasive species cause large-scale loss of native California oyster habitat by disrupting trophic cascades. Oecologia 2009, 160:563-575.
148. King R.A., Read D.S., Traugott M., Symondson W.O. Molecular analysis of predation: a review of best practice for DNA-based approaches. Mol. Ecol. 2008, 17:947-963.
149. Kirby R.R., Beaugrand G., Lindley J.A., Richardson A.J., Edwards M., Reid P.C. Climate effects and benthic-pelagic coupling in the North Sea. Mar. Ecol. Prog. Ser. 2007, 330:31-38.
150. Klinzing M.S.E., Pechenik J.A. Evaluating whether velar lobe size indicates food limitation among larvae of the marine gastropod Crepidula fornicata. J. Exp. Mar. Biol. Ecol. 2000, 252:255-279.
151. Laspoumaderes C., Modenutti B., Balseiro E. Herbivory versus omnivory: linking homeostasis and elemental imbalance in copepod development. J. Plankton Res. 2010, 32:1573-1582.
152. Layman C.A., Winemiller K.O., Arrington D.A., Jepsen D.B. Body size and torphic position in a diverse tropical food web. Ecology 2005, 86:2530-2535.
153. Layman C.A., Araujo M.S., Boucek R., Hammerschlag-Peyer C.M., Harrison E., Jud Z.R., Matich P., Rosenblatt A.E., Vaudo J.J., Yeager L.A., Post D.M., Bearhop S. Applying stable isotopes to examine food-web structure: an overview of analytical tools. Biol. Rev. 2012, 87:545-562.
154. Leakey C.D.B., Attrill M.J., Jennings S., Fitzsimons M.F. Stable isotopes in juvenile marine fishes and their invertebrate prey from the Thames Estuary, UK, and adjacent coastal regions. Estuar. Coast. Shelf Sci. 2008, 77:513-522.
155. Leal M.C., Sá C., Nordez S., Brotas V., Paula J. Distribution and vertical dynamics of planktonic communities at Sofala Bank, Mozambique. Estuar. Coast. Shelf Sci. 2009, 84:605-616.
156. Leal M.C., Nunes C., Alexandre D., Da Silva T.L., Reis A., Dinis M.T., Calado R. Parental diets determine the embryonic fatty acid profile of the tropical nudibranch Aeolidiella stephanieae: the effect of eating bleached anemones. Mar. Biol. 2012, 159:1745-1751.
157. Leal M.C., Nunes C., Engrola S., Dinis M.T., Calado R. Optimization of monoclonal production of the glass anemone Aiptasia pallida (Agassiz in Verrill, 1864). Aquaculture 2012, 354-355:91-96.
158. Leal M.C., Puga J., Serodio J., Gomes N.C.M., Calado R. Trends in the discovery of new marine natural products from invertebrates over the last two decades-where and what are we bioprospecting?. PLoS One 2012, 7:e30580.
159. Leal M.C., Nunes C., Kempf S., Reis A., Da Silva T.L., Serôdio J., Cleary D.F.R., Calado R. Effect of light, temperature and diet on the fatty acid profile of the tropical sea anemone Aiptasia pallida. Aquacult. Nutr. 2013, 19:818-826.
160. Leal M.C., Pochelon P.N., Da Silva T.L., Reis A., Rosa R., Calado R. Variable within-brood maternal provisioning in newly extruded embryos of Homarus gammarus. Mar. Biol. 2013, 160:763-772.
161. Leal M.C., Ferrier-Pagès C., Calado R., Brandes J.A., Frischer M.E., Nejstgaard J.C. Trophic ecology of the facultative symbiotic coral Oculina arbuscula. Mar. Ecol. Prog. Ser. 2014, 504:171-179.
162. Leal M.C., Ferrier-Pages C., Calado R., Thompson M.E., Frischer M.E., Nejstgaard J.C. Coral feeding on microalgae assessed with molecular trophic markers. Mol. Ecol. 2014, 23:3870-3876.
163. Leal M.C., Berger S.A., Ferrier-Pagès C., Calado R., Brandes J., Frischer M.E., Nejstgaard J.C. Temporal changes in the trophic ecology of the asymbiotic gorgonian Leptogorgia virgulata. Mar. Biol. 2014, 161:2191-2197.
164. Leal M.C., Nejstgaard J.C., Calado R., Thompson M.E., Frischer M.E. Molecular assessment of heterotrophy and prey digestion in zooxanthellate cnidarians. Mol. Ecol. 2014, 23:3838-3848.
165. Leal M.C., Ferrier-Pagès C., Petersen D., Osinga R. Coral aquaculture: applying scientific knowledge to ex situ production. Rev. Aquacult. 2014, 2015. in press. 10.1111/raq.12087.
166. Leal M.C., Hoadley K., Pettay D.T., Grajales A., Calado R., Warner M.E. Symbiont type influences trophic plasticity of a model cnidarian-dinoflagellate symbiosis. J. Exp. Biol. 2015, 218:858-863.
167. Lihoreau M., Buhl J., Charleston M.A., Sword G.A., Raubenheimer D., Simpson S.J. Nutritional ecology beyond the individual: a conceptual framework for integrating nutrition and social interactions. Ecol. Lett. 2015, 18:273-286.
168. Limbourn A.J., Babcock R.C., Johnston D.J., Nichols P.D., Knott B. Post-settlement energy reserves in Panulirus cygnus: experimental effects of starvation on survival and nutritional condition. Mar. Biol. 2008, 153:445-456.
169. Mace G. Ecology must evolve. Nature 2013, 503:191-192.
170. Magnone L., Bessonart M., Gadea J., Salhi M. Trophic relationships in an estuarine environment: a quantitative fatty acid analysis signature approach. Estuar. Coast. Shelf Sci. 2015, in press. 10.1016/j.ecss.2014.12.033.
171. Maloy A.P., Culloty S.C., Slater J.W. Use of PCR-DGGE to investigate the trophic ecology of marine suspension feeding bivalves. Mar. Ecol. Prog. Ser. 2009, 381:109-118.
172. Maloy A.P., Culloty S.C., Slater J.W. Dietary analysis of small planktonic consumers: a case study with marine bivalve larvae. J. Plankton Res. 2013, 35:866-876.
173. Maloy A.P., Nelle P., Culloty S.C., Slater J.W., Harrod C. Identifying trophic variation in a marine suspension feeder: DNA- and stable isotope-based dietary analysis in Mytilus spp. Mar. Biol. 2013, 160:479-490.
174. Malzahn A.M., Hantzsche F., Schoo K.L., Boersma M., Aberle N. Differential effects of nutrient-limited primary production on primary, secondary or tertiary consumers. Oecologia 2010, 162:35-48.
175. Manahan D.T. Adaptations by invertebrate larvae for nutrient acquisition from seawater. Am. Zool. 1990, 30:147-160.
176. Marshall D.J. Transgenerational plasticity in the sea: context-dependent maternal effects across the life history. Ecology 2008, 89:418-427.
177. Marshall D.J., Keough M.J. Variation in the dispersal potential of non-feeding larvae: the desperate larva hypothesis and larval size. Mar. Ecol. Prog. Ser. 2003, 255:145-153.
178. Marshall D.J., Keough M.J. Variable effects of larval size on post-metamorphic performance in the field. Mar. Ecol. Prog. Ser. 2004, 279:73-80.
179. Marshall D.J., Keough M.J. Complex life cycles and offspring provisioning in marine invertebrates. Integr. Comp. Biol. 2006, 46:643-651.
180. Marshall D.J., Morgan S.G. Ecological and evolutionary consequences of linked life-history stages in the sea. Curr. Biol. 2011, 21:R718-R725.
181. Marshall D.J., Uller T. When is a maternal effect adaptive?. Oikos 2007, 116:1957-1963.
182. Marshall D.J., Bolton T.F., Keough M.J. Offspring size affects the post-metamorphic performance of a colonial marine invertebrate. Ecology 2003, 84:3131-3137.
183. Marshall D.J., Pechenik J.A., Keough M.J. Larval activity levels and delayed metamorphosis affect post-larval performance in the colonial, ascidian Diplosoma listerianum. Mar. Ecol. Prog. Ser. 2003, 246:153-162.
184. Marshall D.J., Allen R.M., Crean A.J. The ecological and evolutionary importance of maternal effects in the sea. Oceanogr. Mar. Biol. Ann. Rev. 2008, 46:203-250.
185. Marshall D.J., Bonduriansky R., Bussiere L.F. Offspring size variation within broods as a bet-hedging strategy in unpredictable environments. Ecology 2008, 89:2506-2517.
186. Marshall D.J., Monro K., Bode M., Keough M.J., Swearer S. Phenotype-environment mismatches reduce connectivity in the sea. Ecol. Lett. 2010, 13:128-140.
187. Marshall R., Mckinley S., Pearce C.M. Effects of nutrition on larval growth and survival in bivalves. Rev. Aquac. 2010, 2:33-55.
188. Marta-Almeida M., Dubert J., Peliz A., Queiroga H. Influence of vertical migration pattern on retention of crab larvae in a seasonal upwelling system. Mar. Ecol. Prog. Ser. 2006, 307:1-19.
189. Mather J.A., O'dor R.K. Foraging strategies and predation risk shape the natural history of juvenile Octopus vulgaris. Bull. Mar. Sci. 1991, 49:256-269.
190. Matthews B., Narwani A., Hausch S., Nonaka E., Peter H., Yamamichi M., Sullam K.E., Bird K.C., Thomas M.K., Hanley T.C., Turner C.B. Toward an integration of evolutionary biology and ecosystem science. Ecol. Lett. 2011, 14:690-701.
191. McConaugha J. Alternative feeding mechanisms in megalopae of the blue crab Callinectes sapidus. Mar. Biol. 2002, 140:1227-1233.
192. McEdward L. Ecology of Marine Invertebrate Larvae 1995, 480. CRC Press, Boca Raton.
193. Mcginley M.A., Temme D.H., Geber M.A. Parental investment in offspring in variable environments-theoretical and empirical considerations. Am. Nat. 1987, 130:370-398.
194. McKenzie J.D., Black K.D., Kelly M.S., Newton L.C., Handley L.L., Scrimgeour C.M., Raven J.A., Henderson R.J. Comparisons of fatty acid and stable isotope ratios in symbiotic and non-symbiotic brittlestars from Oban Bay, Scotland. J. Mar. Biol. Assoc. UK 2000, 80:311-320.
195. Menge B.A., Sutherland J.P. Community regulation: variation in disturbance, competition, and predation in relation to environmental stress and recruitment. Am. Nat. 1987, 130:730-757.
196. Mente E. Survival, food consumption and growth of Norway lobster (Nephrops norvegicus) kept in laboratory conditions. Integr. Zool. 2010, 5:256-263.
197. Metaxas A., Young C.M. Responses of echinoid larvae to food patches of different algal densities. Mar. Biol. 1998, 130:433-445.
198. Metcalfe N.B., Monaghan P. Compensation for a bad start: grow now, pay later?. Trends Ecol. Evol. 2001, 16:254-260.
199. Meunier C.L., Boersma M., Wiltshire K.H., Malzahn A.M. Zooplankton eat what they need: copepod selective feeding and potential consequences for marine systems. Oikos 2015, in press. 10.1111/oik.02072.
200. Meyer-Harms B., Harms J. Detection of phytoplankton pigments by HPLC in Hyas araneus larvae (Crustacea, Decapoda): comparison of field and labortory samples. J. Sea Res. 1993, 31:153-161.
201. Michener R.H., Kaufman L. Stable isotope ratios as tracers in marine food webs: an update. Stable Isotopes in Ecology and Environmental Science 2007, 238-282. Wiley-Blackwell, Oxford. R.H. Michener, K. Lajtha (Eds.).
202. Montory J.A., Chaparro O.R., Pechenik J.A., Diederich C.M., Cubillos V.M. Impact of short-term salinity stress on larval development of the marine gastropod Crepipatella fecunda (Calyptraeidae). J. Exp. Mar. Biol. Ecol. 2014, 458:39-45.
203. Moorhead J.A. Research-scale tank designs for the larval culture of marine ornamental species, with emphasis on fish. Aquac. Eng. 2015, 64:32-41.
204. Moran N.A. Adaptation and constraint in the complex life cycles of animals. Annu. Rev. Ecol. Syst. 1994, 25:573-600.
205. Moran A.L., Manahan D.T. Physiological recovery from prolonged 'starvation' in larvae of the Pacific oyster Crassostrea gigas. J. Exp. Mar. Biol. Ecol. 2004, 306:17-36.
206. Moran A.L., Mcalister J.S. Egg size as a life history character of marine invertebrates: is it all it's cracked up to be?. Biol. Bull. 2009, 216:226-242.
207. Mousseau T.A., Fox C.W. The adaptive significance of maternal effects. Trends Ecol. Evol. 1998, 13:403-407.
208. Nates S.F., Mckenney C.L. Ontogenetic changes in biochemical composition during larval and early postlarval development of Lepidophthalmuslouisianensis, a ghost shrimp with abbreviated development. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 2000, 127:459-468.
209. Nejstgaard J.C., Frischer M.E., Simonelli P., Troedsson C., Brakel M., Adiyaman F., Sazhin A.F., Artigas L.F. Quantitative PCR to estimate copepod feeding. Mar. Biol. 2008, 153:565-577.
210. Nielsen C. Origin and evolution of animal life cycles. Biol. Rev. Camb. Philos. Soc. 1998, 73:125-155.
211. Nielsen C. How did indirect development with planktotrophic larvae evolve?. Biol. Bull. 2009, 216:203-215.
212. O'Rorke R., Lavery S.D., Wang M., Nodder S.D., Jeffs A.G. Determining the diet of larvae of the red rock lobster (Jasus edwardsii) using high-throughput DNA sequencing techniques. Mar. Biol. 2014, 161:551-563.
213. Obermüller B.E., Truebano M., Peck L.S., Eastman J.T., Morley S.A. Reduced seasonality in elemental CHN composition of Antarctic marine benthic predators and scavengers. J. Exp. Mar. Biol. Ecol. 2013, 446:328-333.
214. Obrebski S. Larval colonization strategies in marine benthic invertebrates. Mar. Ecol. Prog. Ser. 1979, 1:293-300.
215. Olivotto I., Planas M., Simões N., Holt G.J., Avella M.A., Calado R. Advances in breeding and rearing marine ornamentals. J. World Aquacult. Soc. 2011, 42:135-166.
216. Olsen B.R., Dahlgren K., Schander C., Bamstedt U., Rapp H.T., Troedsson C. PCR-DHPLC assay for the identification of predator-prey interactions. J. Plankton Res. 2012, 34:277-285.
217. Olson R.R., Olson M.H. Food limitation of planktotrophic marine invertebrate larvae: does it control recruitment success?. Annu. Rev. Ecol. Syst. 1989, 20:225-247.
218. O'Rorke R., Jeffs A.G., Fitzgibbon Q., Chow S., Lavery S. Extracting DNA from whole organism homogenates and the risk of false positives in PCR based diet studies: a case study using spiny lobster larvae. J. Exp. Mar. Biol. Ecol. 2013, 441:1-6.
219. Osinga R., Delft S.V., Lewaru M.W., Janse M., Verreth J.A. Determination of prey capture rates in the stony coral Galaxea fascicularis a critical reconsideration of the clearance rate concept. J. Mar. Biol. Assoc. UK 2011, 92:713-719.
220. Padilla D.K., Mccann M.J., Glenn M.M., Hooks A.P., Shumway S.E. Effect of food on metamorphic competence in the model system Crepidula fornicata. Biol. Bull. 2014, 227:242-251.
221. Palardy J.E., Grottoli A.G., Matthews K.A. Effects of upwelling, depth, morphology and polyp size feeding in three species of Panamanian corals. Mar. Ecol. Prog. Ser. 2005, 300:79-89.
222. Palardy J.E., Rodrigues L.J., Grottoli A.G. The importance of zooplankton to the daily metabolic carbon requirements of healthy and bleached corals at two depths. J. Exp. Mar. Biol. Ecol. 2008, 367:180-188.
223. Pappalardo P., Fernández M. Mode of larval development as a key factor to explain contrasting effects of temperature on species richness across oceans. Glob. Ecol. Biogeogr. 2014, 23:12-23.
224. Pascal P.-Y., Bellemare C., Sterrer W., Boschker H.T.S., Gonzalez-Rizzo S., Gros O. Diet of Haplognathia ruberrima (Gnathostomulida) in a Caribbean marine mangrove. Mar. Ecol. 2015, 36:246-257.
225. Paschke K.A., Gebauer P., Buchholz F., Anger K. Seasonal variation in starvation resistance of early larval North Sea shrimp Crangon crangon (Decapoda : Crangonidae). Mar. Ecol. Prog. Ser. 2004, 279:183-191.
226. Pawlik J.R. Chemical ecology of the settlement of benthic marine invertebrates. Oceanogr. Mar. Biol. 1992, 30:273-335.
227. Pawlik J.R., Butman C.A., Starczak V.R. Hydrodynamic facilitation of gregarious settlement of a reef-building tube worm. Science 1991, 251:421-424.
228. Pechenik J.A. Ability of some gastropod egg capsules to protect against low-salinity stress. J. Exp. Mar. Biol. Ecol. 1982, 63:195-208.
229. Pechenik J.A. Delayed metamorphosis by larvae of benthic marine-invertebrates-does it occur-is there a price to pay. Ophelia 1990, 32:63-94.
230. Pechenik J.A. On the advantages and disadvantages of larval stages in benthic marine invertebrate life cycles. Mar. Ecol. Prog. Ser. 1999, 177:269-297.
231. Pechenik J.A. Larval experience and latent effects-metamorphosis is not a new beginning. Integr. Comp. Biol. 2006, 46:323-333.
232. Pechenik J.A., Cerulli T.R. Influence of delayed metamorphosis on survival, growth, and reproduction of the marine polychaete Capitella sp. I. J. Exp. Mar. Biol. Ecol. 1991, 151:17-27.
233. Pechenik J.A., Eyster L.S. Influence of delayed metamorphosis on the growth and metabolism of young Crepidula fornicata (Gastropoda) juveniles. Biol. Bull. 1989, 176:14-24.
234. Pechenik J.A., Wendt D.E., Jarrett J.N. Metamorphisis is not a new beginning. Bioscience 1998, 48:901-910.
235. Pechenik J.A., Jarrett J.N., Rooney J. Relationships between larval nutritional experience, larval growth rates, juvenile growth rates, and juvenile feeding rates in the prosobranch gastropod Crepidula fornicata. J. Exp. Mar. Biol. Ecol. 2002, 280:63-78.
236. Petchey O.L., Mcphearson P.T., Casey T.M., Morin P.J. Environmental warming alters food-web structure and ecosystem function. Nature 1999, 402:69-72.
237. Phillips N.E. Effects of nutrition-mediated larval condition on juvenile performance in a marine mussel. Ecology 2002, 83:2562-2574.
238. Phillips N.E. Variable timing of larval food has consequences for early juvenile performance in a marine mussel. Ecology 2004, 85:2341-2346.
239. Pilati A., Vanni M.J. Ontogeny, diet shifts, and nutrient stoichiometry in fish. Oikos 2007, 116:1663-1674.
240. Pitta P., Giannakourou A., Divanach P., Kentouri M. Planktonic food web in marine mesocosms in the eastern Mediterranean: bottom-up or top-down regulation?. Hydrobiologia 1998, 363:97-105.
241. Pochelon P.N., Calado R., Dos Santos A., Queiroga H. Feeding ability of early zoeal stages of the Norway lobster Nephrops norvegicus (L.). Biol. Bull. 2009, 216:335-343.
242. Pochelon P.N., Queiroga H., Rotllant G., Dos Santos A., Calado R. Effect of unfavorable trophic scenarios on amylase and protease activity of Nephrops norvegicus (L.) larvae during their first vertical migration: a laboratory approach. Mar. Biol. 2011, 158:2079-2085.
243. Podolsky R.D., Moran A.L. Integrating function across marine life cycles. Integr. Comp. Biol. 2006, 46:577-586.
244. Pompanon F., Deagle B.E., Symondson W.O., Brown D.S., Jarman S.N., Taberlet P. Who is eating what: diet assessment using next generation sequencing. Mol. Ecol. 2012, 21:1931-1950.
245. Price H.J. Feeding mechanisms in marine and freshwater zooplankton. Bull. Mar. Sci. 1988, 43:327-343.
246. Przeslawski R., Byrne M., Mellin C. A review and meta-analysis of the effects of multiple abiotic stressors on marine embryos and larvae. Glob. Chang. Biol. 2015, 21:2122-2140.
247. Qian P.Y. Larval settlement of polychaetes. Hydrobiologia 1999, 402:239-253.
248. Queiroga H., Blanton J.O. Interactions between behaviour and physical forcing in the control of horizontal transport of decapod crustaceans' larvae: an overview. Adv. Mar. Biol. 2005, 47:107-214.
249. Rahman M.A., Yusoff F.M., Arshad A., Uehara T. Effects of delayed metamorphosis on larval survival, metamorphosis, and juvenile performance of four closely related species of tropical sea urchins (Genus Echinometra). Sci. World J. 2014, 1-11. Article ID 918028. 10.1111/oik.02072.
250. Raimondi P.T., Keough M.J. Behavioural variability in marine larvae. Aust. J. Ecol. 1990, 15:427-437.
251. Raubenheimer D., Zemke-White W.L., Phillips R.J., Clements K.D. Algal macronutrients and food selection by the omnivorous marine fish Girella tricuspidata. Ecology 2005, 86:2601-2610.
252. Raubenheimer D., Simpson S.J., Mayntz D. Nutrition, ecology and nutritional ecology: toward an integrated framework. Funct. Ecol. 2009, 23:4-16.
253. Raven J.A., Walker D.I., Jensen K.R., Handley L.L., Scrimgeour C.M., Mcinroy S.G. What fraction of the organic carbon in sacoglossans is obtained from photosynthesis by kleptoplastids? An investigation using the natural abundance of stable carbon isotopes. Mar. Biol. 2001, 138:537-545.
254. Rey F., Silva Neto G.M., Rosa R., Queiroga H., Calado R. Laboratory trials reveal that exposure to extreme raining events prior to metamorphosis affect the post-settlement performance of an estuarine crab. Estuar. Coast. Shelf Sci. 2015, 154:179-183.
255. Ribes M., Coma R., Gili J.-M. Seasonal variation of in situ feeding rate by the temperate ascidian Halocynthia papillosa. Mar. Ecol. Prog. Ser. 1998, 175:201-213.
256. Ribes M., Coma R., Gili J.-M., Svoboda A., Julià A., Parera J. A 'semi-enclosed' recirculating system for the in situ study of feeding and respiration of benthic suspension feeders. Sci. Mar. 2000, 64:265-275.
257. Riebesell U., Fabry V.J., Hansson L., Gattuso J.-P. Guide to best practices for ocean acidification research and data reporting. Report of international research workshop on best practices for ocean acidification research (19-21 November 2008 in Kiel, Germany) 2009, 200. European Commission, Belgium.
258. Roberts R. A review of settlement cues for larval abalone (Haliotis spp.). J. Shellfish Res. 2001, 20:571-586.
259. Rocha R.J.M., Bontas B., Cartaxana P., Leal M.C., Ferreira J.M., Rosa R., Serôdio J., Calado R. Development of a standardized modular system for experimental coral culture. J. World Aquacult. Soc. 2015, 46:235-251.
260. Rodriguez S.R., Ojeda F.P., Inestrosa N.C. Settlement of benthic marine invertebrates. Mar. Ecol. Prog. Ser. 1993, 97:193-207.
261. Rosa R., Morais S., Calado R., Narciso L., Nunes M.L. Biochemical changes during the embryonic development of Norway lobster, Nephrops norvegicus. Aquaculture 2003, 221:507-522.
262. Rosa R., Calado R., Narciso L., Nunes M.L. Embryogenesis of decapod crustaceans with different life history traits, feeding ecologies and habitats: a fatty acid approach. Mar. Biol. 2007, 151:935-947.
263. Rosa R., Pimentel M.S., Baptista M., Trübenbach K., Calado R., Nunes M.L., Moreno A., Pereira J. Trophic and reproductive biochemistry of a deep-sea gelatinous octopus, Opisthoteuthis calypso. Mar. Biol. 2013, 160:263-275.
264. Rosa R., Trubenbach K., Pimentel M.S., Boavida-Portugal J., Faleiro F., Baptista M., Dionisio G., Calado R., Portner H.O., Repolho T. Differential impacts of ocean acidification and warming on winter and summer progeny of a coastal squid (Loligo vulgaris). J. Exp. Biol. 2014, 217:518-525.
265. Roura Á., González A.F., Pascual S., Guerra Á. A molecular approach to identifying the prey of cephalopod paralarvae. ICES J. Mar. Sci. 2010, 67:1408-1412.
266. Roura Á., González Á.F., Redd K., Guerra Á. Molecular prey identification in wild Octopus vulgaris paralarvae. Mar. Biol. 2012, 159:1335-1345.
267. Ryer C.H. Temporal patterns of feeding by blue crabs (Callinectes sapidus) in a tidal-marsh creek and adjacent seagrass meadow in the lower Chesapeake Bay. Estuar. Coast. Shelf Sci. 1987, 10:136-140.
268. Sanford E. Regulation of keystone predation by small changes in ocean temperature. Science 1999, 283:2095-2097.
269. Sanford E. Water temperature, predation, and the neglected role of physiological rate effects in rocky intertidal communities. Integr. Comp. Biol. 2002, 42:881-891.
270. Schellekens T., De Roos A.M., Persson L. Ontogenetic diet shifts result in niche partitioning between two consumer species irrespective of competitive abilities. Am. Nat. 2010, 176:625-637.
271. Segura C.J., Chaparro O.R., Pechenik J.A., Paschke K.A., Osores S.J.A., Navarro J.M., Cubillos V.M. Delayed effects of severe hypoxia experienced by marine gastropod embryos. Mar. Ecol. Prog. Ser. 2014, 510:59-71.
272. Sheppard S.K., Harwood J.D. Advances in molecular ecology: tracking trophic links through predator-prey food-webs. Funct. Ecol. 2005, 19:751-762.
273. Shumaway S.E., Frank D.M., Ewart L.M., Ward J.E. Effect of yellow loess on clearence rate in seven species of benthic, filter-feeding invertebrates. Aquacult. Res. 2003, 34:1391-1402.
274. Simith D.D.D., Diele K., Abrunhosa F.A. Carry-over effects of delayed larval metamorphosis on early juvenile performance in the mangrove crab Ucides cordatus (Ucididae). J. Exp. Mar. Biol. Ecol. 2013, 440:61-68.
275. Simpson S.J., Raubenheimer D. Assuaging nutritional complexity: a geometrical approach. Proc. Nutr. Soc. 1999, 58:779-789.
276. Simpson S.J., Raubenheimer D. A framework for the stuy of macronutrient intake in fish. Aquacult. Res. 2001, 32:421-432.
277. Simpson S.J., Raubenheimer D. The nature of nutrition: a unifying framework. Aust. J. Zool. 2011, 59:350-368.
278. Smith C.D. Diet of Octopus vulgaris in False Bay, South Africa. Mar. Biol. 2003, 143:1127-1133.
279. Soler-Membrives A., Rossi S., Munilla T. Feeding ecology of Ammothella longipes (Arthropoda: Pycnogonida) in the Mediterranean Sea: a fatty acid biomarker approach. Estuar. Coast. Shelf Sci. 2011, 92:588-597.
280. Spilmont N., Meziane T., Seuront L., Welsh D.T. dentification of the food sources of sympatric ghost shrimp (Trypaea australiensis) and soldier crab (Mictyris longicarpus) populations using a lipid biomarker, dual stable isotope approach. Austral Ecol. 2009, 34:878-888.
281. Stahlschmidt Z.R., Adamo S.A., Davidowitz G. Food-limited mothers favour offspring quality over offspring number: a principal components approach. Funct. Ecol. 2015, 29:88-95.
282. Stearns S.C. The Evolution of Life Histories 1992, Vol. 249:249. Oxford University Press, Oxford.
283. Stearns S.C. Life history evolution: successes, limitations, and prospects. Naturwissenschaften 2000, 87:476-486.
284. Sterner R.W., Elser J.J. Ecological Stoichiometry: The Biology of Elements from Molecules to the Biosphere 2002, pp. 439. Princeton University Press, Princeton.
285. Stevens B.G., Armstrong D.A., Cusimano R. Feeding habits of the Dungeness crab cancer magister as determined by the index of relative importance. Mar. Biol. 1982, 72:135-145.
286. Strathmann R.R. Feeding and nonfeeding larval development and life-history evolution in marine invertebrates. Annu. Rev. Ecol. Syst. 1985, 16:339-361.
287. Strathmann R.R., Strathmann M.F. Oxygen supply and limits on aggregation of embryos. J. Mar. Biol. Assoc. UK 1995, 75:413-428.
288. Sun X., Li Q. Effects of delayed first feeding on larval growth, survival and development of the sea cucumber Apostichopus japonicus (Holothuroidea). Aquacult. Res. 2014, 45:278-288.
289. Sutherland W.J., Freckleton R.P., Godfray H.C.J., Beissinger S.R., Benton T., Cameron D.D., Carmel Y., Coomes D.A., Coulson T., Emmerson M.C., Hails R.S., Hays G.C., Hodgson D.J., Hutchings M.J., Johnson D., Jones J.P.G., Keeling M.J., Kokko H., Kunin W.E., Lambin X., Lewis O.T., Malhi Y., Mieszkowska N., Milner-Gulland E.J., Norris K., Phillimore A.B., Purves D.W., Reid J.M., Reuman D.C., Thompson K., Travis J.M.J., Turnbull L.A., Wardle D.A., Wiegand T., Gibson D. Identification of 100 fundamental ecological questions. J. Ecol. 2013, 101:58-67.
290. Sutherland W.J., Clout M., Depledge M., Dicks L.V., Dinsdale J., Entwistle A.C., Fleishman E., Gibbons D.W., Keim B., Lickorish F.A., Monk K.A., Ockendon N., Peck L.S., Pretty J., Rockstrom J., Spalding M.D., Tonneijck F.H., Wintle B.C. A horizon scan of global conservation issues for 2015. Trends Ecol. Evol. 2015, 30:17-24.
291. Symondson W.O. Molecular identification of prey in predator diets. Mol. Ecol. 2002, 11:627-641.
292. Tewfik A., Rasmussen J.B., Mccann K.S. Anthropogenic enrichment alters a marine benthic food web. Ecology 2005, 86:2726-2736.
293. Thackeray S.J., Sparks T.H., Frederiksen M., Burthe S., Bacon P.J., Bell J.R., Botham M.S., Brereton T.M., Bright P.W., Carvalho L., Clutton-Brock T.I.M., Dawson A., Edwards M., Elliott J.M., Harrington R., Johns D., Jones I.D., Jones J.T., Leech D.I., Roy D.B., Scott W.A., Smith M., Smithers R.J., Winfield I.J., Wanless S. Trophic level asynchrony in rates of phenological change for marine, freshwater and terrestrial environments. Glob. Chang. Biol. 2010, 16:3304-3313.
294. Thomas A.C., Jarman S.N., Haman K.H., Trites A.W., Deagle B.E. Improving accuracy of DNA diet estimates using food tissue control materials and an evaluation of proxies for digestion bias. Mol. Ecol. 2014, 23:3706-3718.
295. Thorson G. Reproductive and larval ecology of marine bottom invertebrates. Biol. Rev. 1950, 25:1-45.
296. Toonen R.J., Pawlik J.R. Settlement of the gregarious tube worm Hydroides dianthus (Polychaeta : Serpulidae). II. Testing the desperate larva hypothesis. Mar. Ecol. Prog. Ser. 2001, 224:115-131.
297. Traugott M., Kamenova S., Ruess L., Seeber J., Plantegenest M. Empirically characterising trophic networks: what emerging DNA-based methods, stable isotope and fatty acid analyses can offer. Adv. Ecol. Res. 2013, 49:177-224.
298. Tremblay P., Fine M., Maguer J.F., Grover R., Ferrier-Pagès C. Photosynthate translocation increases in response to low seawater pH in a coral-dinoflagellate symbiosis. Biogeosciences 2013, 10:3997-4007.
299. Tremblay P., Maguer J.F., Grover R., Ferrier-Pagès C. Trophic dynamics of scleractnian corals: stable isotope evidence. J. Exp. Biol. 2015, 218:1223-1234.
300. Troedsson C., Simonelli P., Nägele V., Nejstgaard J.C., Frischer M.E. Quantification of copepod gut content by differential length amplification quantitative PCR (dla-qPCR). Mar. Biol. 2009, 156:253-259.
301. Troedsson C., Bouquet J.M., Skinnes R., Acuna J.L., Zech K., Frischer M.E., Thompson E.M. Regulation of filter-feeding house components in response to varying food regimes in the appendicularian, Oikopleura dioica. J. Plankton Res. 2009, 31:1453-1463.
302. Turner J.T. Zooplankton fecal pellets, marine snow and sinking phytoplankton blooms. Aquat. Microb. Ecol. 2002, 27:57-102.
303. Urzua A., Paschke K., Gebauer P., Anger K. Seasonal and interannual variations in size, biomass and chemical composition of the eggs of North Sea shrimp, Crangon crangon (Decapoda: Caridea). Mar. Biol. 2012, 159:583-599.
304. Van Der Meeren G.I. Potential of ecological studies to improve survival of cultivated and released European lobster, Homarus gammarus. N. Z. J. Mar. Freshw. Res. 2005, 39:399-424.
305. Villar-Argaiz M., Medina-Sánchez J.M., Carrillo P. Linking life history strategies and ontogeny in crustacean zooplankton: implications for homeostasis. Ecology 2002, 83:1899-1914.
306. Voigt W., Perner J., Davis A.J., Eggers T., Schumacher J., Bahrmann R., Fabian B., Heinrich W., Kohler G., Lichter D., Marstaller R., Sander F.W. Trophic levels are differentially sensitive to climate. Ecology 2003, 84:2444-2453.
307. Wacker A., Elert E. Food quality controls egg quality of the zebra mussel Dreissena polymorpha: the role of fatty acids. Limnol. Oceanogr. 2004, 49:1794-1801.
308. Wang M., O'Rorke R., Waite A.M., Beckley L.E., Thompson P., Jeffs A.G. Fatty acid profiles of phyllosoma larvae of western rock lobster (Panulirus cygnus) in cyclonic and anticyclonic eddies of the Leeuwin Current off Western Australia. Prog. Oceanogr. 2014, 122:153-162.
309. Webster N., Pantile R., Botte E., Abdo D., Andreakis N., Whalan S. A complex life cycle in a warming planet: gene expression in thermally stressed sponges. Mol. Ecol. 2013, 22:1854-1868.
310. Weis V.M., Davy S.K., Hoegh-Guldberg O., Rodriguez-Lanetty M., Pringle J.R. Cell biology in model systems as the key to understanding corals. Trends Ecol. Evol. 2008, 23:369-376.
311. Wendt D.E. Energetics of larval swimming and metamorphosis in four species of Bugula (Bryozoa). Biol. Bull. 2000, 198:346-356.
312. Wickins J.F., Beard T.W., Child A.R. Maximizing lobster, Homarus gammarus (L.), egg and larval viability. Aquacult. Res. 1995, 26:379-392.
313. Wijgerde T., Diantari R., Lewaru M.W., Verreth J.A., Osinga R. Extracoelenteric zooplankton feeding is a key mechanism of nutrient acquisition for the scleractinian coral Galaxea fascicularis. J. Exp. Biol. 2011, 214:3351-3357.
314. Wilcox M., Rochette R. Does claw morphology of the green crab Carcinus maenas vary in relation to its diet on rocky versus fine-sediment shores of southwest New Brunswick, Bay of Fundy, Canada?. J. Exp. Mar. Biol. Ecol. 2015, 465:121-129.
315. Williamson D.I. On a collection of planctonic decapoda and stomatopoda (Crustacea) from the Mediterranean coast of Israel. Bull. Sea Fish. Res. Sta. Haifa. 1970, 45:32-64.
316. Williamson D.I. Larvae of Stenopodidea (Crustacea, Decapoda) from the Indian Ocean. J. Nat. Hist. 1976, 10:497-509.
317. Wray G.A. Evolution of larvae and developmental modes. Ecology of Marine Invertebrate Larvae 1995, 413-447. CRC Press, Boca Raton, FL. L. McEdward (Ed.).
318. Wu L.X., Dong S.L. Compensatory growth responses in juvenile Chinese shrimp, Fenneropenaeus chinensis, at different temperatures. J. Crustac. Biol. 2002, 22:511-520.
319. Young C.M. Larval ecology of marine invertebrates: a sesquicentennial history. Ophelia 1990, 32:1-48.
320. Zimmerfaust R.K., Tamburri M.N. Chemical identity and ecological implications of a waterborne, larval settlement cue. Limnol. Oceanogr. 1994, 39:1075-1087.
321. Zimmerman K.M., Pechenik J.A. How do temperature and salinity affect relative rates of growth, morphological differentiation and time to metamorphic competence in larvae of the marine gastropod Crepidula plana. Biol. Bull. 1991, 180:372-386.
322. Zupo V., Messina P. How do dietary diatoms cause the sex reversal of the shrimp Hippolyte inermis Leach (Crustacea, Decapoda). Mar. Biol. 2007, 151:907-917.
323. Zupo V., Messina P., Carcaterra A., Aflalo E.D., Sagi A. Experimental evidence of a sex reversal process in the shrimp Hippolyte inermis. Invertebr. Reprod. Dev. 2008, 52:93-100.