SARSIM Model Output for the Distribution of Sardine in Canadian, US and Mexican Waters. Richard Parrish October 13, 2015

Similar documents
Spatial dynamics of small pelagic fish in the California Current system on the regime time-scale. Parallel processes in other species-ecosystems.

Changes in spatial distribution of chub mackerel under climate change: the case study using Japanese purse seine fisheries data in the East China Sea

over the Northern West Florida Shelf from SeaWinds and ASCAT

CICESE Update. S. G. Marinone Edgar G. Pavia. January 2017

Variability and trends in daily minimum and maximum temperatures and in diurnal temperature range in Lithuania, Latvia and Estonia

2001 State of the Ocean: Chemical and Biological Oceanographic Conditions in the Newfoundland Region

Characterizing the Physical Oceanography of Coastal Waters Off Rhode Island

2004 State of the Ocean: Physical Oceanographic Conditions in the Newfoundland and Labrador Region

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

Investigating the contribution of allochthonous subsidies to kelp forests in central California

TILT, DAYLIGHT AND SEASONS WORKSHEET

Modelling the biophysical dynamics of sardine and anchovy ichthyoplankton in the Canary Upwelling System: continent-archipelago interactions

The biological importance of the major ocean currents

Serial No. N4470 NAFO SCR Doc. 01/83 SCIENTIFIC COUNCIL MEETING SEPTEMBER 2001

Multivariate time-series forecasting of the NE Arabian Sea Oil Sardine fishery using satellite covariates

THE BC SHELF ROMS MODEL

What Maintains the Western Gulf of Maine Cod Stock?

PROGRESS ACCOMPLISHED THIS PERIOD

IPC 24th Session, Dehradun Nov 2012

Interannual Variability of Wind Induced Onshore Transport over the Northern West Florida Shelf

Agricultural Science Climatology Semester 2, Anne Green / Richard Thompson

UPPLEMENT A COMPARISON OF THE EARLY TWENTY-FIRST CENTURY DROUGHT IN THE UNITED STATES TO THE 1930S AND 1950S DROUGHT EPISODES

On the presence of tropical vortices over the Southeast Asian Sea- Maritime Continent region

Comparing walleye pollock dynamics across the Bering Sea and adjacent areas

53 contributors for 35 individual reports in 2009 show 5% of figures today

Climate also has a large influence on how local ecosystems have evolved and how we interact with them.

by co-chairs Lisa Hendrickson, Hassan Moustahfid and Alexander Arkhipkin

ONE-YEAR EXPERIMENT IN NUMERICAL PREDICTION OF MONTHLY MEAN TEMPERATURE IN THE ATMOSPHERE-OCEAN-CONTINENT SYSTEM

The Climate of Grady County

Global Climates. Name Date

RECENT CHANGES IN THE DISTRIBUTION OF HAKE LARVAE: CAUSES AND CONSEQUENCES

The Arctic Energy Budget

Modelling Denitrification

Present and Future Upwelling off the Entrance to Juan de Fuca Strait

Champaign-Urbana 2000 Annual Weather Summary

The Climate of Oregon Climate Zone 4 Northern Cascades

Physical Oceanography of the Northeastern Chukchi Sea: A Preliminary Synthesis

Chapter 5 Northern distribution of North Sea herring as a response to high water temperatures and/or low food abundance

DROUGHT IN MAINLAND PORTUGAL

Cross-shore exchange processes, and their effect on zooplankton biomass and community composition patterns in the Northeast Pacific

PYROGEOGRAPHY OF THE IBERIAN PENINSULA

CLIMATE OVERVIEW. Thunder Bay Climate Overview Page 1 of 5

The pattern determination of sea surface temperature distribution and chlorophyll a in the Southern Caspian Sea using SOM Model

DEPARTMENT OF EARTH & CLIMATE SCIENCES Name SAN FRANCISCO STATE UNIVERSITY Nov 29, ERTH 360 Test #2 200 pts

Climatic Conditions Around Greenland 1993

Faisal S. Syed, Shahbaz M.,Nadia R.,Siraj I. K., M. Adnan Abid, M. Ashfaq, F. Giorgi, J. Pal, X. Bi

PRELIMINARY DRAFT FOR DISCUSSION PURPOSES

Distributional changes of west coast species and impacts of climate change on species and species groups

Seasonal cycle of phytoplankton community composition off Newport, Oregon, in 2009

Local Ctimatotogical Data Summary White Hall, Illinois

Final Anchovy and Sardine TACs and TABs for 2016, Using OMP-14

Exemplar for Internal Achievement Standard. Mathematics and Statistics Level 3

Long term change in the abundances of northern Gulf of Mexico scyphomedusae Chrysaora sp. and Aurelia spp. with links to climate variability

Future of Kuroshio/Oyashio ecosystems: an outcome of the CFAME Task Team and WG20

IMPACTS OF A WARMING ARCTIC

ENSO UPDATE By Joseph D Aleo, CCM

Produced by Canadian Ice Service of. 2 December Seasonal Outlook Gulf of St Lawrence and East Newfoundland Waters Winter

The North Atlantic Oscillation: Climatic Significance and Environmental Impact

Will a warmer world change Queensland s rainfall?

Champaign-Urbana 2001 Annual Weather Summary

A Report on a Statistical Model to Forecast Seasonal Inflows to Cowichan Lake

Grade 6 Standard 2 Unit Test Astronomy

Seasonal Climate Watch July to November 2018

Early Period Reanalysis of Ocean Winds and Waves

Satellite-derived environmental drivers for top predator hotspots

Sierra Weather and Climate Update

A Comparison of the Anomalous Ocean Conditions observed off the West Coast of Canada in 2014 and 2015.

Here s what a weak El Nino usually brings to the nation with temperatures:

The Climate of Payne County

Oceanographic conditions in the JARPNII survey area from 2000 to 2013 using FRA-ROMS data

Final Anchovy TAC and Sardine TAB for 2011, Using OMP-08

CHAPTER 1: INTRODUCTION

Surface Anomalies Prior to Earthquakes

ALASKA REGION CLIMATE FORECAST BRIEFING. December 15, 2014 Rick Thoman NWS Alaska Region ESSD Climate Services

INDIAN OCEAN STATE February 14, 2018 MJO INDEX

Lecture Prepared By: Mohammad Kamrul Arefin Lecturer, School of Business, North South University

The Climate of Bryan County

THE INCORPORATION OF AN OCEAN TEMPERATURE PROFILE INTO AN EXISTING ICEBERG DETERIORATION MODEL CANADA CANADA

Arctic Climate Change. Glen Lesins Department of Physics and Atmospheric Science Dalhousie University Create Summer School, Alliston, July 2013

Identifying risks of geoduck aquaculture: the role of larval transport

that individual/local amplitudes of Ro can reach O(1).

Phytoplankton. Zooplankton. Nutrients

Seasonal Climate Watch June to October 2018

Spawning migration in fish: A case study of sockeye salmon from the Fraser River in British Columbia

Champaign-Urbana 1999 Annual Weather Summary

Environmental changes

Seasonal forecasting as a stepping stone to climate adaptation in marine fisheries and aquaculture

Climate of Columbus. Aaron Wilson. Byrd Polar & Climate Research Center State Climate Office of Ohio.

Technical note on seasonal adjustment for M0

The Climate of Pontotoc County

PICES W3 [D-504], Sep 22, 2017, 11:40-12:05

Long-term Change of Ocean Productivity: A case study in the Bay of Bengal

PRMS WHITE PAPER 2014 NORTH ATLANTIC HURRICANE SEASON OUTLOOK. June RMS Event Response

Spatio-temporal dynamics of Marbled Murrelet hotspots during nesting in nearshore waters along the Washington to California coast

The Climate of Kiowa County

REVIEW OF AERIAL SURVEY ESTIMATES FOR RINGED SEALS (PHOCA HISPIDA) IN WESTERN HUDSON BAY

State of the Ocean 2003: Physical Oceanographic Conditions in the Gulf of St. Lawrence

Recruitment variability in Norwegian spring-spawning herring (&pea harengus L.): the effect of temperature in larval drift trajectories

NatGasWeather.com Daily Report

Ecology Student Edition. A. Sparrows breathe air. B. Sparrows drink water. C. Sparrows use the sun for food. D. Sparrows use plants for shelter.

Transcription:

SARSIM Model Output for the Distribution of Sardine in Canadian, US and Mexican Waters. Richard Parrish October 13, 2015 Agenda Item H.1.c The information presented below was taken from a model that I presented at the 2004 CalCOFI Conference. The paper was submitted for publication in CalCOFI Reports and the editor informed me that the paper exceeded the normal page limits for CalCOFI Reports. Given the options available I withdrew the paper as I was shortly leaving for a consultation in Portugal and would not be able to make the major revisions necessary to meet the page limitation in time for the CalCOFI deadline. Shortly thereafter I retired from the NMFS so very few people have seen the MS; however, I have given several seminars in central California based on the paper. The distribution of biomass by Country was not presented in the original paper but the output described here was output from the 2004 model. Summary: I had not looked at the output data from a Country perspective and I was amazed to find that the model resulted in an average 88% of sardine biomass in US waters; almost identical to the 87% value used in the original and current harvest guidelines (Table 1). The minimum annual value for US waters was 66.6% in 1972 and the maximum was 96.6% in 1973. I also looked at 3 year running means to assess the multiyear affects of sea surface temperature on geographical distribution. The average 3 year percentage of sardines in USA waters was essentially the same at the annual percentage (88%); however, the minimum 3 year percentage was higher than the annual (76% vs 67%) and the maximum 3 year percentage was lower than the annual (93% vs 97%). The average annual percentage occurring in Canada was 2.45% and 9.5% in Mexico. Maximum percentages in Canada for the annual and 3 year averages were 16% and 8%; values for Mexico were 23% and 6%. Table 1 Annual and Three Year Percentage of Sardine in Canada, USA and Mexico from SARSIM Model. (model run TS F: 1967-2002 simulation with observed environmental data time-series and modeled fishery) Canada USA Mexico Annual Average 2.45% 88.05% 9.50% Minimum 0.00% 66.64% 2.99% Maximum 16.15% 96.59% 31.80% 3 Year Periods Average 1.79% 88.18% 10.03% Minimum 0.05% 76.35% 5.58% 1

Maximum 8.12% 93.37% 22.79% Agenda Item H.1.c The modeled average biomass distributions suggest that the current 87% distribution parameter was well selected. Interyear variation in the percentage of annual biomass in US waters is unlikely to be a problem for management. However, multiyear periods with a higher than average percentage of sardine biomass in Mexico, which occurred in the model during the cold regime in the early 1970s, could be a problem. The correlation analyses of SST vs the percentage of sardine biomass in US waters suggest that Southern California SST in the winter, i.e. the Nov-Feb preceeding the model year (R=0.70), is a reasonable predictor of an anomalously high percentage of biomass in Mexican waters. MODEL DESCRIPTION: The model has 9 roughly latitudinal regions; 2 in Canada, 5 in the USA and 2 in Mexico (Figure 1). Sardine are forced by sea surface temperature (SST), size, and nonlinear functions to move seasonally between regions. In addition, eggs, larvae and juveniles are advected by wind driven transport. The time step of the model is bi-monthly; 24 time steps per year. Monthly environmental data are used for two time steps for each month. Figure 1. Regions included in the sardine model. The model was designed for the northern sardine stock the critical sea surface temperatures which determine the direction of migration, north or south are 13 2

degrees C.in the feeding season and 17 degrees in the spawning season (Figure 2). So the model has the same 17 degree separation between the northern and southern stock as that in recent sardine analyses. as sardine in the model always migrate northwards if the regional SST is above 17 degrees. The simulation runs in this report were made with a starting biomass of 1 mmt in 1967 using the observed environmental variables and a fishery based on a CUTOFF of 150,000 mt a MAXCAT of 200,000 mt and a constant FRACTION of 0.15. The model has no spawner-recruit function and no density-dependence in recruitment, growth or reproductive output. The model simulates the sardine population from egg to death and the percentages of biomass by area listed below were calculated from a simulation with fishing occuring in regions 2, 3, 5.7.and 8. Figure 2. Temperature-dependent migration rates; positive northward and negative southward. A. Feeding migration. B. Spawning migration It should be noted that the period since 2002 has not had sea surface temperatures as cold as the period prior to 1977, so the model would result in a slightly larger Canadian average percentage and a moderately smaller Mexican percentage for the 1967-2014 period than for the 1967-2002 period. The present model cannot reproduce multi-year recruitment failures that are not associated with sea surface temperatures. The primary variable forcing population growth in the model, satellite chlorophyll, is the only environmental variable that uses climatology monthly means rather than a time-series of observed monthly data (Figure 3). This is because less than 7 years of satellite data were available when the model was developed. Obviously a time series of satellite chlorophyll would result in far less population stability and faster rates of change that simulations based on monthly climatology. The sea surface temperature affect on biomass is 3

caused by altering the geographical distribution of sardine and thereby altering their position in the phytoplankton field. Essentially the model results in biomass growth if a significant porportion of the biomass reaches the satellite chlorophyll maximum that occurs during the summer and fall in the Columbia and Vancouver areas and the biomass falls if the majority of the biomass stays south of the Figure 15. Satellite chlorophyll Sep97-Mar04 monthly means 4.5 4.0 3.5 3.0 mg/sq m 2.5 2.0 1.5 1.0 0.5 0.0 QCIs Van Col AREA Mend Mont Conc SCB NBC CBC Jan Mar May Jul Sep Nov MONTH 4.000-4.500 3.500-4.000 3.000-3.500 2.500-3.000 2.000-2.500 1.500-2.000 1.000-1.500 0.500-1.000 0.000-0.500 Mendocino area. Figure 3. Satellite chlorophyll Sep97-Mar04 monthly means. The early life history stages are planktonic and advected based on monthly upper mixed layer transports calculated with Jim Ingrams (OSCURS) surface drift model. July transports are relatively consistent (Figure 4), differing primarily in the offshore componet which is not included in the model structure. January wind diriven transport is much more variable between years with the northern regions having primariluy northward transport and the southern regions having southward transport. In the Mendocino, Monterey, and to a lesser degree, the Conception regions, the transport can be either northwards or southwards in individual years. In the principal spring spawning months northward transport only occurs in the areas from Mendocino northwards. Note that without the southerly advection of early life history stages, the average biomass distribution would be further north. 4

Figure 4. Bimonthly migration alongshore transport of eggs and larvae based on 1967-2002 monthly values from Jim Ingrams (OSCURS) surface drift model. (Three of 12 months shown). The initial (1 MMT) model biomass declines sharply during the early 1970s cold period reaching a minimum of 0.242 MMT in 1979; it then rises slowly until the early 1990s and then increases to a peak of 0.859 MMT in 2000 (Figure 5). Figure 5. Biomass with observed 1967-2002 environmental data and fishery. 5

Agenda Item H.1.c The SST regional matrices show the temporally coherent variability in the sardine habitat and the general increases in SST that occur after the 1976-77 regime shift (Figure 6). Figgure 6. Sea surface temperature fields used for migration (4 of 9 areas shown) 6

ADDITIONAL ANALYSIS OF THE PERCENTAGE OF BIOMASS BY COUNTRY: The minimum annual percentages in the USA and the maximum annual percentages in Mexico primarily occurred prior to the 1976-77 regime shift (Figure 7). The maximum percentages in Canada were after the regime shift and widely spread out in time. Figure 7. Annual percentage of biomass by Country Another way of looking at sardine distribution is to plot the percentage of sardine in each country using the bi-monthly distributions from the model output (Figure 8). The difference between the annual distribution and bi-monthly distribution is striking. In 10 of the 35 years there were periods lasting from 2 weeks to 4 months when less than 50% of the sardine biomass was in US waters. More than 50% of the biomass was in Canadian waters for two months in 1997 and more than 50% of the biomass was in Mexican waters for 4 months in 1972. The SARSIM model output suggests that there are years when it is physically possible that either Mexico or Canada could land a significant proportion of the USA Harvest Guideline even when the annual distribution percentage in the country is relatively low. Note: however, that a high percentage abundance in Mexico is associated with low abundance in Canada and visa versa so it is unlikely that both Canada and Mexico will have higher percentages of sardine biomass in the same year. A brief correlation search was made and the highest correlation found (R=0.70) was between the southern California winter SST and the annual percentage of sardine in US waters (Figure 9). The time series of the percentage of biomass in US 7

waters again shows the low percentages that occurred during the early 1970s (Figure 9.) Figure 8. Bi-monthly percentage of biomass by Country. Winter temperatures in all of the regions, except region 1, were correlated with the annual percentage of sardine in US waters at values above R=0.50 (Figure 9). The lowest percentage of sardine biomass in US waters was in the period before the 1976-77 regime shift and these low values were caused by increased percentages of sardine in Mexico during the very cold years of the early 1970s. Figure 9. Annual percentage of biomass in US waters vs winter SST and 1967-2002 percentage of biomass in US waters. 8