Content-Length: 408298 | pFad | https://link.springer.com/10.1007/978-3-031-71190-9_4

86400 Zooplanktonic Crustacea and Ichthyoplankton of the Patagonian Shelf-Break Front | SpringerLink
Skip to main content

Zooplanktonic Crustacea and Ichthyoplankton of the Patagonian Shelf-Break Front

  • Chapter
  • First Online:
The Patagonian Shelfbreak Front

Abstract

This chapter reviews information from the 1970s to the present day about zooplankton and ichthyoplankton occurring at the Patagonian shelf-break front (PSBF), aiming to establish a baseline of knowledge for both groups. Zooplankton information focuses on copepods, hyperiid amphipods, and euphausiids because of their abundance and relevance to the food web. General patterns of species diversity and biogeographic zonation of these zooplanktonic groups are described. Copepod diversity roughly increases northward, and the shelf-break front does not represent a sharp boundary between shelf and oceanic zooplankton species. Key species are defined, and data about their seasonal distribution, abundance, and life-history traits indicate that the same few species dominate the composition of these taxa all year round. The presence of larvae of some demersal and mesopelagic fish typical of cold sub-Antarctic waters denotes reproductive activity in the PSBF surroundings. Ichthyoplankton can be classified, according to bottom depths, as pertaining to the shelf-edge (80–200 m); slope (200–800 m); or oceanic regions (800–3100 m). Larvae show higher abundances immediately offshore of the front, especially above the thermocline. Copepods, especially their larval stages, constitute the main feeding source for fish larvae inhabiting along the shelf-break. Zooplankton and ichthyoplankton composition and abundance along the shelf-break are compared with those of the adjacent shelf. We finally go over open questions and prospects for future work on zooplankton and ichthyoplankton along the shelf-break.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 149.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 179.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Similar content being viewed by others

Abbreviations

ACS:

Argentine continental shelf

DVM:

daily vertical migrations

FAO:

Food and Agriculture Organization

OF:

occurrence frequency

PSBF:

Patagonian shelf-break front

INIDEP:

National Institute for Fisheries Research and Development

MCW:

Malvinas Current Waters

RII:

relative importance index

SASW:

Subantarctic Shelf Water

References

  • Acha EM, Ehrlich MD, Muelbert JH et al (2018) Ichthyoplankton associated to the frontal regions of the Southwestern Atlantic. In: Plankton ecology of the Southwestern Atlantic. Springer, Cham, pp 219–246. https://doi.org/10.1007/978-3-319-77869-3_11

    Chapter  Google Scholar 

  • Acha EM, Viñas MD, Derisio C et al (2020) Large-scale geographic patterns of pelagic copepods in the southwestern South Atlantic. J Mar Syst 204:103–281. https://doi.org/10.1016/j.jmarsys.2019.103281

    Article  Google Scholar 

  • Angelescu V (1982) Ecología trófica de la anchoíta del Mar Argentino (Engraulidae, Engraulis anchoita): parte II, Alimentación, comportamiento y relaciones tróficas en el ecosistema. Ser Contrib Inst Nac Invest Desarr Pesq 409:83

    Google Scholar 

  • Angelescu V Prenski LB (1987) Ecología trófica de la merluza común del Mar Argentino (Merlucciidae, Merluccius hubbsi). Parte 2. Dinámica de la alimentación analizada sobre la base de las condiciones ambientales, la estructura y las evaluaciones de los efectivos en su área de distribución. Contrib. INIDEP, Mar del Plata, 561, p 205

    Google Scholar 

  • Antacli JC (2011) Estrategias de vida de los copépodos Drepanopus forcipatus y Calanus australis en relación con los recursos tróficos en la plataforma patagónica austral (Argentina, 47°-55°S). Dissertation, Universidad Nacional de Mar del Plata

    Google Scholar 

  • Atkinson A (1998) Life cycle strategies of epipelagic copepods in the Southern Ocean. J Mar Syst 15(1–4):289–311. https://doi.org/10.1016/S0924-7963(97)00081-X

    Article  Google Scholar 

  • Atkinson A, Sinclair JD (2000) Zonal distribution and seasonal vertical migration of copepod assemblages in the Scotia Sea. Polar Biol 23(1):46–58

    Article  Google Scholar 

  • Bakun A (1996) Patterns in the ocean. Ocean processes and marine population dynamics. University of California Sea Grant, California

    Google Scholar 

  • Bakun A, Parrish RH (1991) Comparative studies of coastal pelagic fish reproductive habitats: the anchovy (Engraulis anchoita) of the southwestern Atlantic. ICES J Mar Sci 48(3):343–361. https://doi.org/10.1093/icesjms/48.3.343

    Article  Google Scholar 

  • Baldoni AG, Molinari G, Reta R, Guerrero RA (2015) Atlas de temperatura y salinidad de la plataforma continental del Atlántico Sudoccidental: períodos cálido y frío. INIDEP, Mar del Plata

    Google Scholar 

  • Balech E, Ehrlich MD (2008) Esquema Biogeográfico del Mar Argentino. Rev Invest Des Pesq 19:45–75

    Google Scholar 

  • Benedetti F, Gasparini S, Ayata SD (2015) Identifying copepod functional groups from species functional traits. J Plankton Res 38(1):159–166. https://doi.org/10.1093/plankt/fbv096

    Article  PubMed  PubMed Central  Google Scholar 

  • Benedetti F, Vogt M, Righetti D et al (2018) Do functional groups of planktonic copepods differ in their ecological niches? J Biogeogr 45(3):604–616. https://doi.org/10.1111/jbi.13166

    Article  Google Scholar 

  • Bertolotti MI, Brunetti NE, Carreto JI et al (1996) Influence of shelf-break fronts on shellfish and fish stocks off Argentina. Contribution to ICES annual science conference. Reykjavik, Iceland

    Google Scholar 

  • Bi H (2005) Population dynamics of Clausocalanus furcatus (Copepoda, Calanoida) in the northern Gulf of Mexico. Dissertation, Louisiana State University and Agricultural & Mechanical College

    Google Scholar 

  • Björnberg T (1981) Copepoda. In Boltovskoy D (ed) Atlas del Zooplancton del Atlántico Sudoccidental y Métodos de Trabajo con el Zooplancton Marino. Publicaciones Especiales INIDEP, Mar del Plata, Argentina, p 587–679

    Google Scholar 

  • Bollens SM, Frost BW (1991) Diel vertical migration in zooplankton: rapid individual response to predators. J Plankton Res 13(6):1359–1365

    Article  Google Scholar 

  • Boltovskoy D (ed) (1999) South Atlantic Zooplankton. Backhuys Publishers, Leiden

    Google Scholar 

  • Bradford-Grieve JM, Markhaseva EL, Rocha CEF et al (1999) Copepoda. In: Boltovskoy D (ed) South Atlantic Zooplankton. Backhuys Publishers, Leiden, pp 869–1098

    Google Scholar 

  • Brickle P, Arkhipkin AI, Laptikhovsky V et al (2009) Resource partitioning by two large planktivorous fishes Micromesistius australis and Macruronus magellanicus in the Southwest Atlantic. Estuar Coast Shelf Sci 84(1):91–98. https://doi.org/10.1016/J.ECSS.2009.06.007

    Article  Google Scholar 

  • Brickle P, Laptikhovsky V, Arkhipkin A (2011) The reproductive biology of a shallow water morid (Salilota australis Günther, 1878), around The Falkland Islands. Est Coast Shelf Sci 94:102–110

    Article  Google Scholar 

  • Burridge AK, Tump M, Vonk R et al (2017) Diversity and distribution of hyperiid amphipods along a latitudinal transect in the Atlantic Ocean. Progr Oceanogr 158:224–235. https://doi.org/10.1016/J.POCEAN.2016.08.003

    Article  Google Scholar 

  • Carreto JI, Lutz V, Carignan MO et al (1995) Hydrography and chlorophyll a in a transect from the coast to the shelf-break in the Argentinian Sea. Cont Shelf Res 15(2–3):315–336. https://doi.org/10.1016/0278-4343(94)E0001-3

    Article  Google Scholar 

  • Carreto JI, Montoya NG, Benavides HR et al (2003a) Characterization of spring phytoplankton communities in the Río de La Plata maritime front using pigment signatures and cell microscopy. Mar Biol 143(5):1013–1027. https://doi.org/10.1007/s00227-003-1147-z

    Article  Google Scholar 

  • Carreto JI, Montoya NG, Carignan MO et al (2003b) La campaña “Prospección ambiental del Río de la Plata y su frente marítimo (EH-09/01, 2da etapa)”. I. Caracterización de las comunidades fitoplanctónicas utilizando marcadores pigmentarios (HPLC-CHEMTAX). Informe técnico del Proyecto “Protección ambiental del Río de la Plata y su Frente Marítimo. Prevención y control de la contaminación y restauración de hábitats”, p 56

    Google Scholar 

  • Carreto JI, Montoya NG, Carignan MO et al (2016) Environmental and biological factors controlling the spring phytoplankton bloom at the Patagonian shelf-break front – degraded fucoxanthin pigments and the importance of microzooplankton grazing. Progr Oceanogr 146:1–21. https://doi.org/10.1016/j.pocean.2016.05.002

    Article  Google Scholar 

  • Cepeda GD, Temperoni B, Sabatini ME et al (2018) Zooplankton communities of the Argentine continental shelf (SW Atlantic, ca. 34°-55°S), an overview. In: Plankton ecology of the Southwestern Atlantic. Springer, Cham, pp 171–199. https://doi.org/10.1007/978-3-319-77869-3_9

    Chapter  Google Scholar 

  • Ciechomski JD, Sánchez RP (1983) Relationship between ichthyoplankton abundance and associated zooplankton biomass in the shelf waters off Argentina. Biol Oceanogr 3(1):77–101. https://doi.org/10.1080/01965581.1983.10749472

    Article  Google Scholar 

  • Ciechomski JD, Ehrlich MD, Lasta CA et al (1981) Distribución de huevos y larvas de peces en el Mar Argentino y evaluación de los efectivos desovantes de anchoíta y de merluza. Contrib Inst Nac Invest Des Pesq 383:59–79

    Google Scholar 

  • Cousseau MB, Perrotta RG (1998) Peces marinos de Argentina. INIDEP, Mar del Plata

    Google Scholar 

  • Curtolo LM, Dadon JR, Mazzoni HE (1990) Distribution and abundance of euphasids off Argentina in spring 1978. Revista Nerítica 5(1):1–14

    Google Scholar 

  • Derisio C, Acha M (2015) Efecto del sistema frontal de Península Valdés sobre la actividad reproductiva del copépodo Calaniodeo Ctenocalanus vanus. Inf Invest INIDEP N° 87/2015, p 8

    Google Scholar 

  • Derisio C, Alemany D, Acha M et al (2014) Influence of a tidal front on zooplankton abundance, assemblages and life histories in Península Valdés, Argentina. J Mar Syst 139:475–482. https://doi.org/10.1016/j.jmarsys.2014.08.019

    Article  Google Scholar 

  • Falabella V, Campagna C, Croxall J (2009) Atlas of the Patagonian Sea: Species and spaces. Buenos Aires: Wildlife Conservation Society and BirdLife International, Buenos Aires, Argentina, 15, 303

    Google Scholar 

  • Figueroa DE (2019) Clave de peces marinos del Atlántico Sudoccidental, entre los 33°S y 56°S. INIDEP, Mar del Plata

    Google Scholar 

  • Gibbons MJ, Gugushe N, Boyd AJ et al (1999) Changes in the composition of the non-copepod zooplankton assemblage in St Helena Bay (southern Benguela ecosystem) during a six day drogue study. Mar Ecol 180:111–120

    Article  Google Scholar 

  • Gomes Fisher L (2012) Distribuição, biomassas e ecologia de Macrouridae (Teleostei, Gadiformes) no Talude Continental do Sul do Brasil, com ênfase em Coelorinchus marinii Hubbs 1934 e Malacocephalus occidentalis Goode & Bean 1885. Dissertation, Universidade Federal do Rio Grande

    Google Scholar 

  • Ivanovic ML (2010) Alimentación del calamar Illex argentinus en la región patagónica durante el verano de los años 2006, 2007 y 2008. Rev Invest Desarr Pesq 20:51–63

    Google Scholar 

  • Jónasdóttir S, Visser AW, Richardson K et al (2015) Seasonal copepod lipid pump promotes carbon sequestration in the deep North Atlantic. Proc Natl Acad Sci 112(39):12122–12126. https://doi.org/10.1073/pnas.1512110112

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kiørboe T (2008) Optimal swimming strategies in mate-searching pelagic copepods. Oecologia 155(1):179–192. https://doi.org/10.1007/s00442-007-0893-x

    Article  PubMed  Google Scholar 

  • Kiørboe T (2011) How zooplankton feed: mechanisms, traits and trade-offs. Biol Rev 86(2):311–339. https://doi.org/10.1111/j.1469-185X.2010.00148.x

    Article  PubMed  Google Scholar 

  • Kiørboe T, Sabatini M (1994) Reproductive and life cycle strategies in egg-carrying cyclopoid and free-spawning calanoid copepods. J Plankton Res 16(10):1353–1366. https://doi.org/10.1093/plankt/16.10.1353

    Article  Google Scholar 

  • Lutz VA, Segura V, Dogliotti AI et al (2010) Primary production in the Argentine sea during spring estimated by field and satellite models. J Plankton Res 32(2):181–195. https://doi.org/10.1093/plankt/fbp117

    Article  CAS  Google Scholar 

  • Marí N, Sánchez F (2002) Espectros tróficos específicos de varias especies de peces demersales de la región austral y sus variaciones anuales entre 1994 y 2000. Inf Téc Int INIDEP 88:19

    Google Scholar 

  • Mauchline J (1998) The biology of calanoid copepods. Academic, London

    Google Scholar 

  • Mauchline J, Fisher LR (1969) The biology of euphausiids. Adv Mar Biol 7:1–421

    Google Scholar 

  • Mazzocchi MG, Paffenhöfer GA (1998) First observations on the biology of Clausocalanus furcatus (Copepoda, Calanoida). J Plankton Res 20(2):331–342

    Article  Google Scholar 

  • Mazzocchi MG, Paffenhöfer GA (1999) Swimming and feeding behaviour of the planktonic copepod Clausocalanus furcatus. J Plankton Res 21(8):1501–1518

    Article  Google Scholar 

  • Menni RC, Gosztonyi AE (1982) Benthic and semidemersal fish associations in the Argentine Sea. Studies Neotrop Fauna Environ 17:1–29. https://doi.org/10.1080/01650528209360599

    Article  Google Scholar 

  • Montú M (1977) Eufáusidos de la plataforma Argentina y adyacencias. I. Distribución estacional en el sector patagónico. Ecosur 4(8):187–225

    Google Scholar 

  • Olivar MP, Contreras T, Hulley PA et al (2018) Variation in the diel vertical distributions of larvae and transforming stages of oceanic fishes across the tropical and equatorial Atlantic. Prog Oceanogr 160:83–100

    Article  Google Scholar 

  • Padovani LN (2013) Biodiversidad y ecología de los anfípodos hiperideos del Mar Argentino y aguas adyacentes: Themisto gaudichaudii, una especie clave. Dissertation, Universidad Nacional de Mar del Plata

    Google Scholar 

  • Peralba À, Mazzocchi MG, Harris RP (2017) Niche separation and reproduction of Clausocalanus species (Copepoda, Calanoida) in the Atlantic Ocean. Prog Oceanogr 158:185–202. https://doi.org/10.1016/J.POCEAN.2016.08.002

    Article  Google Scholar 

  • Pillar SC, Stuart V, Barange M et al (1992) Community structure and trophic ecology of euphausiids in the Benguela ecosystem. Afr J Mar Sci 12(1):3935–3409. https://doi.org/10.2989/02577619209504714

    Article  Google Scholar 

  • Piola AR, Martínez Avellaneda N, Guerrero RA et al (2010) Malvinas-slope water intrusions on the northern Patagonia continental shelf. Ocean Sci 6(1):345–359. https://doi.org/10.5194/os-6-345-2010

    Article  Google Scholar 

  • Prenski LB, Sánchez F (1988) Estudio preliminar sobre asociaciones ícticas en la Zona Común de Pesca Argentino-Uruguaya. Publicaciones de la Comisión Técnica Mixta del Frente Marit 4:75–87

    Google Scholar 

  • Ramírez FC (1970) Copépodos planctónicos del sector patagónico. Resultados de la Campaña Pesquería XI. Physis 79:473–476

    Google Scholar 

  • Ramírez FC (1971a) Copépodos planctónicos de los sectores bonaerense y norpatagónico. Resultados de la Campaña Pesquería III. Rev Mus La Plata Sec Zool 11:73–94

    Google Scholar 

  • Ramírez FC (1971b) Eufáusidos de algunos sectores del Atlántico Sudoccidental. Physis 30(81):385–405

    Google Scholar 

  • Ramírez FC (1973) Eufáusidos de la expedición oceanográfica “Walther Herwig” 1966. Buenos Aires: Asociación Argentina de Ciencias Naturales. Physis 32(84):105–114

    Google Scholar 

  • Ramírez FC (1981) Zooplancton y producción secundaria. Parte I. Distribución y variación estacional de los copépodos. In: Angelescu V (ed) Campañas de investigación pesquera realizadas en el Mar Argentino por los B/I “Shinkai Maru” y “Walter Herwig” y el B/P “Marburg”, años 1978 y 1979. Resultados de la parte Argentina. Ser Contrib Inst Nac Invest Desarr Pesq, vol 383, p 202–212

    Google Scholar 

  • Ramírez FC, Björnberg T (1981) Distribución horizontal por masas de agua de los copépodos más frecuentes y abundantes (indicadores hidrológicos) en el Atlántico Sudoccidental. In: Boltovskoy D (ed) Atlas del Zooplancton del Atlántico Sudoccidental y Métodos de Trabajo con el Zooplancton Marino. Publicaciones Especiales INIDEP, Mar del Plata, Argentina, p 595

    Google Scholar 

  • Ramírez FC, Dato C (1983) Seasonal changes in population structure and gonadal development of three euphausiid species. Oceanol Acta 6(4):427–433

    Google Scholar 

  • Ramírez FC, Sabatini ME (2000) The occurrence of Calanidae species in waters off Argentina. Hydrobiologia 439(1):21–42. https://doi.org/10.1023/A:1004193401931

    Article  Google Scholar 

  • Ramírez FC, Santos BA (1994) Análisis del zooplancton de la plataforma bonaerense en relación con algunas variables ambientales: campañas “transección” de 1987. Frente Marit 15:141–156

    Google Scholar 

  • Ramírez FC, Viñas MD (1985) Hyperiid amphipods found in Argentine shelf waters. Physis 43(104):25–37

    Google Scholar 

  • Ramírez, FC, Mianzan H, Santos B (1990) Synopsis on the reproductive biology and early life of Engraulis anchoita, and related environmental conditions in vertical distribution and mortality of Engraulis anchoita eggs and larvae. 10C Worksh. Rep., 65, Annex V:5–49

    Google Scholar 

  • Rivas AL, Pisoni JP (2010) Identification, characteristics and seasonal evolution of surface thermal fronts in the Argentinean Continental Shelf. J Mar Syst 79(1–2):134–143. https://doi.org/10.1016/j.jmarsys.2009.07.008

    Article  Google Scholar 

  • Romero SI, Piola AR, Charo M et al (2006) Chlorophyll-a variability off Patagonia based on SeaWiFS data. J Geophys Res 111:CO5021. https://doi.org/10.1029/2005JC003244

    Article  Google Scholar 

  • Runge JA (1985) Relationship of egg production of Calanus pacificus to seasonal changes in phytoplankton availability in Puget Sound, Washington. Limnol Oceanogr 30(2):382–396

    Article  Google Scholar 

  • Sabatini ME (2008) Life history trends of copepods Drepanopus forcipatus (Clausocalanidae) and Calanus australis (Calanidae) in the southern Patagonian shelf (SW Atlantic). J Plankton Res 30:981–996. https://doi.org/10.1093/plankt/fbn062

    Article  Google Scholar 

  • Sabatini ME, Akselman R, Reta R et al (2012) Spring plankton communities in the southern Patagonian shelf: hydrography, mesozooplankton patterns and trophic relationships. J Mar Syst 94:33–51. https://doi.org/10.1016/j.jmarsys.2011.10.007

    Article  Google Scholar 

  • Sabatini ME, Reta R, Lutz VA et al (2016) Influence of oceanographic features on the spatial and seasonal patterns of mesozooplankton in the southern Patagonian shelf (Argentina, SW Atlantic). J Mar Syst 157:20–38. https://doi.org/10.1016/J.JMARSYS.2015.12.006

    Article  Google Scholar 

  • Sánchez RP, Ciechomski JD (1995) Spawning and nursery grounds of pelagic fish species in the sea-shelf off Argentina and adjacent areas. Sci Mar 59(3–4):455–478

    Google Scholar 

  • Saunders RA, Collins MA, Schreeve R et al (2018) Seasonal variation in the predatory impact of myctophids on zooplankton in the Scotia Sea (Southern Ocean). Progr Ocean 168:123–144. https://doi.org/10.1016/j.pocean.2018.09.017

    Article  Google Scholar 

  • Schnack-Schiel SB, Niehoff B, Hagen W et al (2008) Population dynamics and life strategies of Rhincalanus nasutus (Copepoda) at the onset of the spring bloom in the Gulf of Aqaba (Red Sea). J Plankton Res 30(6):655–672. https://doi.org/10.1093/plankt/fbn029

    Article  CAS  Google Scholar 

  • Segura V, Lutz VA, Dogliotti A et al (2013) Phytoplankton types and primary production in the Argentine Sea. Mar Ecol Prog Ser 491:15–31. https://doi.org/10.3354/meps10461

    Article  Google Scholar 

  • Severo A, Cepeda GD, Acha EM (2024) The effects of the Patagonian shelf-break front on copepod abundance, biodiversity, and assemblages. J Mar Syst 103921:103921. https://doi.org/10.1016/j.jmarsys.2023.103921

    Article  Google Scholar 

  • Tarling GA, Ward P, Sheader M et al (1995) Distribution patterns of macrozooplankton assemblages in the Southwest Atlantic. Mar Ecol Prog Ser 120(1/3):29–40

    Article  Google Scholar 

  • Turner JT (2004) The importance of small planktonic copepods and their roles in pelagic marine food webs. Zool Stud 43(2):255–266

    Google Scholar 

  • Verona C, Carreto JI, Ramirez F et al (1972) Plancton y condiciones ecológicas en las aguas de la plataforma bonaerense frente a Mar del Plata. Campaña “Transeccion l”. Doc tec Prel Proy Des pesq 24:1–35

    Google Scholar 

  • Weiss G (1974) Hallazgo y descripción de larvas de la polaca Micromesistius australis en aguas del sector patagónico argentino. Physis 33(87):537–542

    Google Scholar 

  • Weiss G (1975) Hallazgo, descripción y distribución de las postlarvas del bacalao criollo, Salilota australis y del pez sable, Lepidotus caudatus en aguas de la plataforma Argentina. Physis 34(89):319–325

    Google Scholar 

  • Yamaguchi A, Ikeda T, Hirakawa K (1999) Diel vertical migration, population structure and life cycle of the copepod Scolecithricella minor (Calanoida: Scolecitrichidae) in Toyama Bay, southern Japan Sea. Plankton Biol Ecol 46(1):54–61

    Google Scholar 

  • Zeidler W, De Broyer C (2009) Catalogue of the Hyperiidean Amphipoda (Crustacea) of the Southern Ocean with distribution and ecological data. Bull Séances Inst Roy Colon Belge 79(1):1–104. https://doi.org/10.15468/99f6q0

    Article  Google Scholar 

Download references

Acknowledgments

The authors thank infinitely to Drs. F.C. Ramírez, M.E. Sabatini, M.D. Viñas, and J.D. de Ciechomski for all the knowledge transmitted over so many years along diverse academic instances, which was essential for tackling this chapter. Also, we wish to thank the scientists, technicians, and research vessel crews of INIDEP, CONICET, and other international agencies who got the plankton samples, which were indispensable and valuable material for building our present understanding of the crustacean zooplankton and ichthyoplankton along the Patagonian shelf-break. Special thanks must be given to G.L. Álvarez-Colombo and L.N. Padovani for amphipods data, to the heads of the several assessment groups at INIDEP for receiving and helping plankton researchers on board their stock assessment cruises, to INIDEP facilities, and to the financial support from all the institutions involved and the grants held by all the authors. This is INIDEP contribution No. 2308.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Georgina D. Cepeda .

Editor information

Editors and Affiliations

4.1 Electronic Supplementary Material

Rights and permissions

Reprints and permissions

Copyright information

© 2024 The Author(s), under exclusive license to Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Cepeda, G.D. et al. (2024). Zooplanktonic Crustacea and Ichthyoplankton of the Patagonian Shelf-Break Front. In: Acha, E.M., Iribarne, O.O., Piola, A. (eds) The Patagonian Shelfbreak Front. Aquatic Ecology Series, vol 13. Springer, Cham. https://doi.org/10.1007/978-3-031-71190-9_4

Download citation

Publish with us

Policies and ethics









ApplySandwichStrip

pFad - (p)hone/(F)rame/(a)nonymizer/(d)eclutterfier!      Saves Data!


--- a PPN by Garber Painting Akron. With Image Size Reduction included!

Fetched URL: https://link.springer.com/10.1007/978-3-031-71190-9_4

Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy