Monitoring Spawning Activity in Cabo Pulmo National Park Using Molecular Identification of Fish Eggs and Larvae Ana Luisa M. Ahern1, Jaime Gomez-Gutiérrez2, David I. Castro Arvizú3, Arturo R. Sanchez-Uvera2, Ricardo J. Saldierna-Martínez2, Andrew F. Johnson1, Alice E. Harada1, Brad Erisman1,4, Carlos A. Sánchez-Ortiz5, Ronald S. Burton1, Octavio Aburto-Oropeza1 1Marine Biology Research Division, Scripps Institute of Oceanography, California, USA; 2Centro Interdisciplinario de Ciencias Marinas, IPN, La Paz, Baja California Sur, Mexico; 3Parque Nacional Cabo Pulmo, Baja California Sur, Mexico; 4The University of Texas at Austin, Marine Science Institute, College of Natural Sciences, Port Aransas, Texas, USA; 5Departamento de Biología Marina, Universidad Autónoma de Baja California Sur, La Paz, Baja California Sur, Mexico

Introduction Results Located in southern Baja • Identi ed 112 from 16 orders, 49 families and 94 genera California, Mexico, Cabo Pulmo • An additional 51 sequences did not match to existing voucher specimens in online databases, National Park’s 27 square miles of revealing even greater diversity teeming waters is a shining example • Identi ed species from diverse natural histories including reef-associated species and highly of a well-managed marine migratory pelagic species protected area. A recent study • Captured rare, understudied mesopelagic species such as Regalecus glesne (giant oar sh), determined that in just 14 years sh revealing new information regarding spawning location and timing biomass increased by 463%, the • Several popular recreational shery species were present, including Nematistius pectoralis largest measured in a marine (rooster sh) and Coryphaena hippurus (dolphin sh) reserve worldwide.1 While there is Total Number of Fish Eggs and Larvae Collected an abundance of data collected via traditional monitoring techniques such as diver surveys, little is known about the species speci c spawning activities that occur in Cabo Pulmo. is study monitors the sh spawning activity through molecular identi cation of eggs and larvae collected in the park.

1Aburto-Oropeza O, B. Erisman, G.R. Galland, I. Mascarenas-Osorio, E. Sala., E. Ezcurra. 2011. Large Recovery of Fish Biomass in a No-Take Marine Reserve. PLoSONE 6: 23601.

Why Ichthyoplankton? Why Genetics? Regalecus glesne egg Tetraodontiformes • Reveal the species composition, timing and location of spawning activities • Complement diver-conducted surveys • Can be used as a baseline to compare shiing populations and spawning patterns 44369 Anguilliformes • Provide evidence of the success of marine protected areas • Aid in the assessment and management of marine COLLECTED ecosystems • Molecular identi cation is more accurate and reliable than traditional morphological methods 4870 ANALYZED

Rarefaction Curves Eggs identi ed morphologically as one species; genetics revealed 8 dierent species SEQUENCED2929 Methods

Mugiliformes

Syngnathiformes

• Distinctive peaks in spawning activity were revealed for several ORDERS16 species, potentially triggered by full moons • Eggs of some species were present throughout the time series whereas others showed restricted spawning seasons • Weekly plankton tows in CPNP conducted by David • Revealed inaccuracy of morphological identi cation Castro, divemaster from Cabo Pulmo • Captured species and activities that would be missed in • Biologists at CICIMAR-IPN in La Paz, BCS separate eggs traditional survey methods utilized in Cabo Pulmo from zooplankton, make preliminary morphological identi cations, and send eggs and larvae to SIO for analysis Number of Species in Each Collection • Universal sh primers are used to amplify cytochrome oxidase subunit 1 (COI) or 16S ribosomal RNA through polymerase chain reaction (PCR) • Successfully ampli ed samples sent osite for sequencing • Results compared to sequences in GenBank and FishBOL, 49FAMILIES online databases of sequences from vouchered specimens

Aulopiformes

GENERA94 162 SPECIES Pleuronectiformes 6th International Zooplankton Production Symposium