Time series monitoring in Japan (Introduction of Odate collection and Odate project) Hiroya Sugisaki ・ Kazuaki Tadokoro ・ Sanae Chiba.

Slides:



Advertisements
Similar presentations
Individual-based Models Three Examples
Advertisements

Particulate organic matter and ballast fluxes measured using Time-Series and Settling Velocity sediment traps in the northwestern Mediterranean Sea lead.
Biodiversity databases and database management systems for the world’s ocean: experience and outputs from five international projects Sergey Piontkovski.
Zooplankton variability on the Faroe Shelf and in the surrounding oceanic area in relation to phytoplankton and physical conditions E. Gaard, H. Debes,
Nekton – adaptations & communities. Defense and Camouflage Large size: Most have few predators Camouflage: –Cryptic Body Shape (alteration of body shape)
Trends in Early Spring Lake Superior Zooplankton Communities, Owen Gorman and Lori Evrard U.S. Geological Survey Lake Superior Biological Station.
Plankton changes and cod recruitment in the North Sea Plankton changes and cod recruitment in the North Sea Grégory Beaugrand 1,3*, Keith M. Brander 2,
NPAFC international cooperative research designates the distribution of Asian and North American chum salmon stocks in the Bering Sea and North Pacific.
The Oscillating Control Hypothesis Reassessment in view of New Information from the Eastern Bering Sea George L. Hunt, Jr. School of Aquatic and Fishery.
Zooplankton processes Puget Sound Oceanography Jan. 28, 2011.
Water column structure and zooplankton distribution along Trevor Channel, Barkley Sound Andrew Hamilton.
Growth and feeding of larval cod (Gadus morhua) in the Barents Sea and the Georges Bank Trond Kristiansen, Frode Vikebø, Svein Sundby, Geir Huse, Øyvind.
An Investigation of the Effect of Turbidity on the Diel Vertical Migration of Zooplankton in the Chincoteague Bay, VA. James Bergenti, Department of Biology,
Open Oceans: Pelagic Ecosystems II
Keith Brander IMBER-GODAE 12 June 2007 Variability and shifts in marine ecosytems Keith Brander ICES/GLOBEC Coordinator.
Prince William Sound Resurrection Bay Knight Island Passage Middleton Island The physical model is run in three dimensions and the data are used to drive.
Using fatty acids as physiological and ecological indicator of zooplankton in the Yellow Sea: with implications in relationships of biochemical indices.
IB 362 Lecture 12 Productivity and Food Webs.
Introduction Oithona similis is the most abundant copepod in the Gulf of Alaska, and is a dominant in many ecosystems from the poles to the sub-tropics.
How Does Climate Change Affect Biomass Accumulation in Boreal Ecosystems? Earth Science B Period 2012.
Introduction Greenland halibut (Reinhardtius hippoglossoides; GH) have declined significantly since the 1970’s in the eastern Bering Sea (EBS). The reasons.
> Inner Transitional Outer PWS 1.Large zooplankton were collected with 1-m2 square MOCNESS with 500  m mesh. Samples collected in 20 m depth increments.
Development of an oceanographic observatory in the Mexican Pacific Ocean to understand the pelagic ecosystem response to the climate variability and climate.
Some Thoughts on Ecology
Stratification on the Eastern Bering Sea Shelf, Revisited C. Ladd 1, G. Hunt 2, F. Mueter 3, C. Mordy 2, and P. Stabeno 1 1 Pacific Marine Environmental.
Centre for Ecological and Evolutionary Synthesis ICES/NAFO Decadal Symposium Santander, Spain May 12th 2011 The serial recruitment failure to North Sea.
Comparison of Synchronous Ecological Regime Shifts in the Humboldt and Kuroshio Currents Jürgen Alheit Baltic Sea Research Institute Warnemünde, Germany.
From Ocean Sciences at the Bedford Institute of Oceanography Temperature – Salinity for the Northwest.
Vertical distribution of ontogenetically migrating copepods in the Western Subarctic Gyre T. Kobari 1, D. K. Steinberg 2, S. Wilson 2, K. Buesseler 3,
Growth rates of Neocalanus species in the Gulf of Alaska R. R. Hopcroft, A.I. Pinchuk, & C. Clarke Institute of Marine Science, University of Alaska Fairbanks.
Long-Term Changes in the Biomass Yields of the Fish and Fisheries of the Yellow Sea LME Qisheng Tang Yellow Sea Fisheries Research Institute
Arctic Operational Oceanography at IMR Einar Svendsen Arctic GOOS planning meeting, September 2006 at NERSC, Bergen.
Summary Euphausiids (krill) are important food items of fish, seabirds and whales: consequently, it is important to understand their seasonal cycles. The.
A Survey of Diel-Vertical Migration of Freshwater Zooplankton at Pinchot Lake Eric Holtzapple Department of Biological Sciences, York College of Pennsylvania.
Interannual Time Scales: ENSO Decadal Time Scales: Basin Wide Variability (e.g. Pacific Decadal Oscillation, North Atlantic Oscillation) Longer Time Scales:
CMarZ Overarching question
OS36B-03 Growth and development of Metridia pacifica (Copepoda: Calanoida) in the northern Gulf of Alaska Hui Liu & Russell R. Hopcroft
Figure. Seasonally migrating copepods appeared at Station K2. We can identify two groups of the copepods by the life cycle. Red: surface spawning species,
Mesozooplankton-microbial food web interactions in a climatically changing sea ice environment Evelyn & Barry Sherr, Oregon State University Carin Ashjian,
Environmental surveys of the Nordic, North, and Barents Seas - by the Institute of Marine Research, Norway Webjørn Melle.
International Workshop for GODAR WESTPAC Global Ocean Data Archeology and Rescue: Scientific Needs from the Carbon Cycle Study in the Ocean Toshiro Saino.
LONG-TERM TALL TOWER CO 2 MONITORING IN HUNGARY László HASZPRA Hungarian Meteorological Service Zoltán BARCZA Eötvös Loránd University.
GODAR-WESTPAC Workshop March 5 – 7, 2002 Japan Oceanographic Data Center (JODC) Oceanographic Research & Data Management in Japan.
Time scales of physics vs. biology ENSO effects on biology Pacific Decadal Oscillation (PDO)
"The Gulf of Alaska Seward Line & 2006 Russell R. Hopcroft, Kenneth O. Coyle, Tomas J. Weigngartner, Terry E. Whitledge Institute.
Egg production rates of the larger copepods in the Gulf of Alaska: Calanus marshallae, Calanus pacificus, Eucalanus bungii and Neocalanus flemingeri Russell.
Ocean-scale modelling of Calanus finmarchicus
Physical-biological interactions: regional to basin scales I. Pseudocalanus spp.: MARMAP data II. P. moultoni and P. newmani: U.S. Globec Georges.
THE FOOD WEB DO NOW: What do you think is the most important
US GLOBEC NWA Program Phase 4B Synthesis Workshop 10/2-3/2006 – 507 Clark Laboratory, WHOI Logistics Logistics – Continental breakfast today & tomorrow.
Doney, 2006 Nature 444: Behrenfeld et al., 2006 Nature 444: The changing ocean – Labrador Sea Ecosystem perspective.
Global Biogeochemical Cycles (2014) 28 Annual net community production and the biological carbon flux in the ocean Steven Emerson School of Oceanography,
Introduction Egg production in copepod species may be the largest component of copepod production and is a parameter routinely monitored in ecosystem studies.
OEAS 604: Final Exam Tuesday, 8 December 8:30 – 11:30 pm Room 3200, Research Innovation Building I Exam is cumulative Questions similar to quizzes with.
Growth rates of Neocalanus flemingeri in the northern Gulf of Alaska in 2001 and 2002 H. Liu,C. Clarke & R.R.Hopcroft Institute of Marine Science, University.
Mesozooplankton component General objective: Quantitative assessment of its biomass and production and its impacts on phytoplankton stocks and vertical.
North Pacific Climate Regimes and Ecosystem Productivity (NPCREP) NOAA Fisheries Ned Cyr NOAA Fisheries Service Office of Science and Technology Silver.
Tracking life history of each particle Particles could be divided into three groups (Fig. 7) The red group’s period of copepodite stage shortened when.
Vertical Distribution of Larvae off the Coast of Assateague Island, Virginia Carlee Kaisen Department of Biological Sciences, York College of Pennsylvania.
Zooplankton biogeography as a measure of oceanographic change in Canada Basin (Arctic) Brian Hunt 1, John Nelson 2, Fiona McLaughlin 2, Eddy Carmack 2.
Climate Change Impacts on Estuarine Larval Fish Composition Jamie F. Caridad and Kenneth W. Able Institute of Marine and Coastal Sciences. Rutgers University.
Example #2: Northwest Pacific Zooplankton
Susan Hartman Richard Lampitt & others NOC
The Arctic Ocean Ecosystem
Climate change research in the Gulf of Alaska
Ken Coyle, Russ Hopcroft & Alexei Pinchuk
Critical and Compensation Depths Spring bloom and seasonal cycle
Department of Oceanography Sung-Chan Kang
Projected changes to ocean food webs and oceanic fisheries
CalCOFI.
Presentation transcript:

Time series monitoring in Japan (Introduction of Odate collection and Odate project) Hiroya Sugisaki ・ Kazuaki Tadokoro ・ Sanae Chiba

Regular sampling lines organized by Japan Meteorological Agency (from K.Tadokoro:TNFRI) Zooplankton has been collected seasonally since 1972 *P は pollution の略 PM-line PH-line PK-line PN-line PA-line winter/summer

Sampling stations organized by Fisheries Research Agency and local fisheries research institutes T,S and Zooplankton biomass has been researched since early1950s in order to forecast fisheries condition ODATE collection/data area

Active projects on field monitoring study in FRA,Japan A-Line(current: 1990~) O-Line(current: 2002~) Odate Project(retrospective :1950~2000)

A-Line well organized by HNF and TNFRI (PI: Tsuneo Ono) N1 N2 N3 N4 L a t i t u d e ( d e g r e e N ) Longitude (degree E) Hokkaido Honshu Akkeshi A1 A4 A11 A15 A7 5-8 cruises/yr. since1990 not only standard oceanographical monitoring, but also mechanisms of biological production or biological carbon transportation has been researched

What is Odate collection? More than zooplankton samples (formaline preserved) are stocked at Tohoku National Fisheries Research Institute, Fisheries Research Agency Japan. Long term variation of biomass (total wet weight) of this sample set was analyzed by Dr. Kazuko Odate (Odate, 1994). The samples are still available for identification of species, because preserved condition is good.

Sampling, Monitoring The purpose of the zooplankton sampling was routine monitoring of prey abundance of fishery ground and oceanic environment. Zooplankton samples have been collected by several public fisheries institutes in north eastern region of Japan since Sampling gears are conical standard plankton net (45cm diameter; 0.33mm mesh size). Net was towed vertically from 150m depth layer to the surface.

Long term variation of zooplankton biomass based on Odate collection Zooplankton biomass ( mgWW/m 3 ) low HIGH (revised from Odate,1994)

Analysis of species composition of zooplankton using Odate collection Mere monitoring on long-term variation of zooplankton Research on the mechanisms of long term variation of ecosystem Information on only total wet weight is not sufficient to analyze the interaction of biological phenomenon and climate change

Retrospective analysis of species composition of copepods using Odate collection = Odate Project FY Species composition data base from the Odate Collection reanalysis of species composition from Odate collection, establish the data base H.Sugisaki, T.Kobari, H.Itoh Long term variation of Climate/Physical oceanography analysis of physical effect on long term variation of pceanic ecosystem I.Yasuda, M.Noto Effect of biological production on the interaction between climate change and variation of ocean ecosystem interaction between physical and biological effect H.Saito Long term variation of zooplankton communities and the process of transportation of organic matter through biological processes analysis of mechanism of long term variation of copepods composition and establish the model S.Chiba, K.Tadokoro Financial supported by Japanese ministry of the Environment

Identification procedure Copepods were sorted out and identifies into species using newest information on copepod classification. Copepodite stages ( I-V ) of dominant copepods (Neocalanus, Eucalanus, Calanus and Metridia species) were identified. Total number of each classified species and life stage category were calculated.

Temperature of 100m depth # of Samples Year and season # of Detectedspecies OyashioColdcurrent Oyashio-Kuroshiotransition KuroshioWarmcurrent T 100 <5 o C 5 o C<T 100 <15 o C T 100 >15 o C (ca at the final result) January-November March-September ( result) (1960’s)

Interannual variations of mesozooplankton biomass

Hypothesis: top-down control (Tadokoro et al., 2005) Feeding rate of Japanese sardine was estimated % of Neocalanus production rate in Standing stock of sardine (million ton) Year (+1900) Migrate into the Oyashio during summer

OyashioMixed PO 4 (m mol m -3 ) Year(+1900) Sea surface Subsurface layer 18.6 yr tide cycle Hypothesis: bottom-up control (Tadokoro et al., PICES XV)

-56% -64% PO 4 (m mol m -3 ) PO Year (+1900) Oyashio Mixed biomass (g m -2 ) N. Plumchrus biomass had significant relationship with PO 4. Those relationships suggests the change in nutrients condition affect N. plumchrus biomass due to change the primary productively. -91% -92% Hypothesis: bottom-up control (Tadokoro et al., PICES XV)

Hypothesis: Phenological change (Chiba et al., 2006)

Lower tropic level responses to the 1976 and 1988 RS : (winter-spring processes) ( Chiba et al, submitted, PO ) After the mid 1970s After the late 1988s

World-wide Collaborative research is necessary CMarZ should be a good platform In order to reveal the mechanisms of variability of ecosystems,

The result will be open at the web site near future (Ex.) Long term variation of abundance of Neocalanus plumchrus (Ex.) distribution map of Neocalanus plumchrus