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Sources and Locations of Sea Turtle Mortality along the Coast of El Salvador DEVELOPMENT ALTERNATIVES INC. (DAI) PREPARÓ ESTE PUBLICACIÓN POR LA AGENCIA PARA EL DESARROLLO INTERNACIONAL DE LOS ESTADOS UNIDOS (USAID)

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Page 1: Sea Turtle Mortality - ICAPO · species, sea turtle mortality, class size, and primary sources and areas of mortality. We documented a total of 55 sea turtle strandings: 76% were

Sources and Locations

of Sea Turtle Mortality

along the Coast of El Salvador

DEVELOPMENT ALTERNATIVES INC. (DAI) PREPARÓ ESTE P UBLICACIÓN POR LA AGENCIA PARA EL DESARROLLO INTERNACIONAL DE

LOS ESTADOS UNIDOS (USAID)

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Title: Sources and Locations of Sea Turtle Mortality along the Coast of El Salvador

Program, activity, or project name and number: USAID Improved Management and

Conservation of Critical Watersheds

Contract No. Epp-I-00-04-00023-0

Strategic objective number: 519-022 Contractor name: Development Alternatives (DAI)

Christopher Kernan

Project Director Improved Management and Conservation of Critical Watersheds

Avenida Dr. José Zablah, 4-6 Col. Utila Sta. Tecla, La Libertad, El Salvador

Phone (503) 2288-4198, (503) 2288-4318 Cell (503) 7468-1125 Email: [email protected]

This report is made possible by the support of the American People through the United States Agency for International Development (USAID). The contents of this report are the sole responsibility of DAI and do not necessarily reflect the views of USAID or the United States Government.

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Sources and Locations

of Sea Turtle Mortality

along the Coast of El Salvador

AUTHORS:

MICHAEL LILES

CARLOS THOMAS

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TABLE OF CONTENTS

EXECUTIVE SUMMARY....................................................................................................................................... 1

ACKNOWLEDGEMENTS ...................................................................................................................................... 2

1. INTRODUCTION .................................................................................................................................................... 3

2. MATERIALS AND METHODS ...................................................................................................................... 4 2.1. Sea turtle beach stranding surveys .............................................................................................................5 2.2. Interviews with marine resource users ....................................................................................................6

3. RESULTS ..................................................................................................................................................................... 9 3.1. Sea turtle beach stranding data ....................................................................................................................9 3.2. Sea turtle mortality sources and areas of concern identified by marine resource users 12

3.2.1. Industrial shrimp trawls...................................................................................................................... 14 3.2.2. Blast fishing ............................................................................................................................................... 16 3.2.3. Long-lines ................................................................................................................................................... 19 3.2.4. Bottom-set lobster gillnets ................................................................................................................. 21

4. RECOMMENDATIONS ................................................................................................................................... 24 4.1. General.................................................................................................................................................................. 24 4.2. Industrial shrimp trawls ............................................................................................................................... 26 4.3. Blast fishing ........................................................................................................................................................ 26 4.4. Long-lines ............................................................................................................................................................ 26 4.5. Bottom-set lobster gillnets .......................................................................................................................... 27

5. LITERATURE CITED ....................................................................................................................................... 28 A.1. Sea turtle stranding protocol used to document stranding events. .......................................... 33 A.2. Sea turtle reference sheets used during interviews with marine resource users. ............. 34

A.2.1. Olive ridley turtle reference sheet .................................................................................................. 34 A.2.2. East Pacific green turtle reference sheet...................................................................................... 35 A.2.3. Hawksbill turtle reference sheet ..................................................................................................... 36 A.2.4. Leatherback turtle reference sheet. ............................................................................................... 37

A.3. Interview protocol developed and used to interview marine resource users along the coast of El Salvador.................................................................................................................................................. 38

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FIGURES

Figure 1. Species composition of sea turtles stranded along the coast of El Salvador. ......... 10 Figure 2. Composition of probable mortality of sea turtles stranded along the coast of El

Salvador. ................................................................................................................. 10 Figure 3. Reponses of marine resource users regarding the primary sea turtle mortality

sources in their area................................................................................................. 14 Figure 4. Shrimp and camaroncillo capture by industrial and artisanal fisheries in El

Salvador from 1960 through 2005. Source: FAO 2009. ......................................... 15 Figure 5. Blast fishing and sea turtle priority conservation areas in the Bahía de Jiquilisco. 18 Figure 6. Overlap of long- line fishing and the high-priority conservation area for olive ridley

and East Pacific green turtles lying between 50 m and 100 m depth along the coast

of El Salvador.......................................................................................................... 21 Figure 7. Distribution and overlap with sea turtle distributions of lobster gillnets in Los

Cóbanos................................................................................................................... 23 Figure 8. Distribution and overlap with sea turtle distributions of lobster gillnets in El

Maculís.................................................................................................................... 24 Figure 9. Circle hook alternatives to J-hooks currently in use. Source: Mug et al. 2008. ..... 27

TABLES

Table 1. The 3 geographic zones of study, including priority beaches for conservation and corresponding department.................................................................................................. 5

Table 2. Characteristics of marine resource users interviewed in the 3 geographic zones of

El Salvador. ........................................................................................................................ 8 Table 3. Morphometric information and sex of stranded sea turtles by species in the 3

geographic zones.............................................................................................................. 11 Table 4. Incidental capture of sea turtles by fishing method along the coast of El Salvador

according to marine resource users. ................................................................................. 13

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EXECUTIVE SUMMARY

Four species of sea turtles occur in El Salvador: leatherback (Dermochelys coriacea),

hawksbill (Eretmochelys imbricata), green (Chelonia mydas), and olive ridley

(Lepidochelys olivacea). The objective of this study is to identify the sources and areas of

sea turtle mortality along the coast of El Salvador, and to identify protection areas to

reduce mortality.

From April through July 2010 we collected sea turtle stranding data from 31 sites, and

from June through August 2010 we used a semi-structured interview to capture

information from local marine resource users on fishing areas, fishing methods, target

species, sea turtle mortality, class size, and primary sources and areas of mortality. We

documented a total of 55 sea turtle strandings: 76% were olive ridley turtles; 11% were

hawksbill turtles; 6% were East Pacific green turtles; and 7% were unknown. Based on

the nature of the injuries we attributed the majority of strandings (65%) to shrimp

trawling vessels and 12% attributed to artisanal fisheries. Of the 115 marine resource

users we interviewed, 79% said that industrial fisheries, specifically shrimp trawling

vessels, killed sea turtles during their operations and 77% said that artisanal fishing

activities using long- lines, blast fishing, and bottom-set lobster gillnets were responsible

for sea turtle deaths. Using information from these interviews we were able to map the

locations and frequency of adult sea turtle sightings by species and the location and

intensity of industrial and artisanal fishing. The overlap identified areas of greatest

mortality and therefore highest priority for special conservation protection.

As long- lived organisms with slow reproductive rates, sea turtles are particularly

vulnerable to human-caused mortality. It is known that incidental deaths of sub-adults

and adults in industrial and artisanal fisheries is the leading source of sea turtle mortality

throughout the world, with shrimp trawls, gill-nets, and long- lines as the primary culprits.

Evidence from the present study suggests that, while industrial fishing is the most

important source of adult sea turtle mortality in El Salvador, artisanal blast fishing and

long- lining may be relatively more important than elsewhere in the world. We discuss the

implications of this for designing the protection and recovery of sea turtle populations in

El Salvador

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ACKNOWLEDGEMENTS

The authors thank and are indebted to the local marine resource users who participated in

this study and voluntarily assisted with data collection – this work would not have been

possible without their support and in-depth knowledge of industrial and artisanal fishing

practices, as well as interactions with sea turtles. We gratefully acknowledge the

organizations and entities that were integral to the success of this work, particularly

MARN (Barra de Santiago), FUNDARRECIFE, FUTECMA, Asociación Mangle,

CODEPA, and the many fishing cooperatives along the coast of El Salvador. We thank

Wallace J. Nichols for guidance on the development of the project’s methodology.

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1. INTRODUCTION

Of the seven species of sea turtles recognized worldwide, six are considered to be

critically endangered, endangered, or vulnerable to extinction. Kemp’s ridley

(Lepidochelys kempii ), leatherback (Dermochelys coriacea), and hawksbill

(Eretmochelys imbricata) turtles are listed as critically endangered; loggerhead (Caretta

caretta) and green (Chelonia mydas) turtles as endangered; and the olive ridley

(Lepidochelys olivacea) turtle as vulnerable under the IUCN Red List of Threatened

Species (IUCN 2010). As long- living organisms with slow reproductive rates (Musick

1999), sea turtles are particularly vulnerable to anthropogenic sources of mortality,

especially the incidental capture of sub-adults and adults in marine fisheries (Lutcavage

et al. 1997). High survival rates of large juvenile and adult turtles are needed for long-

term population growth and recovery, especially for populations at already reduced levels

(Heppell 1998, Heppell et al. 2003, Lewison & Crowder 2008). The widespread,

persistent, human-caused deaths of sub-adult and adult sea turtles worldwide contribute

largely to the precarious conservation status of many populations and their inab ility to

recover (Lutcavage et al. 1997, Lewison et al. 2004, Watson et al. 2005, Frazier et al.

2007).

The incidental capture of sea turtles by industrial and artisanal fisheries is the

leading source of mortality throughout the world (Wallace et al. 2010), with shrimp

trawls (Magnuson et al. 1990), gill-nets (Cheng & Chen 1997, Lee Lum 2006), and long-

lines (Witzell 1999, Lewison & Crowder 2008) as the primary culprits. Industrial shrimp

trawls have long been identified as the single most important cause of sea turtle mortality

(Magnuson et al. 1990, Caillouet et al. 1991) resulting in approximately 150,000 deaths

per year globally (Oravetz 1999). By employing the Turtle Excluder Device (TED) on

trawls, the incidental capture of some species of sea turtles can be reduced by nearly 45%

(Crowder et al. 1995); however, some countries do not require TEDs or do not enforce

the requirement (Spotila 2004). Turtles captured in trawls without TEDs are likely to be

submerged and prevented from surfacing to breathe for lengths of time greater than their

average dive times, which caused them to become comatose and eventually drown

(Lutcavage & Lutz 1997).

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Although artisanal fishers account for more than 95% of fishers globally (Pauly

2006), the impact of artisanal fisheries incidental capture on sea turtle populations

received little attention for many years (Soykan et al. 2008). Growing evidence suggests

that mortality caused by artisanal fisheries may be more significant than previously

thought (Lee Lum 2006, Koch et al 2006, Peckham et al. 2007, Gilman et al. 2009).

Regional variations in sea turtle mortality are expected due to differences in fishing

methods, intensity, and species-specific patterns (Polovina et al. 2003). The implications

of sea turtle deaths from artisanal fishing activity are important and deserve more focused

attention (Moore et al. 2010).

The waters and beaches of El Salvador are important nesting and/or feeding

grounds for olive ridley, East Pacific green, hawksbill, and leatherback turtles (Hasbun &

Vasquez 1999, Vasquez et al. 2008, Liles et al. 2010, Liles et al. In review). At the same

time, El Salvador is also the smallest and most densely-populated country in Central

America, with a total area of 21,040 km2 and an estimated population density of 342

people km-1. Both industrial and artisanal fisheries exist in El Salvador, but overfishing

has led to dwindling yields of certain target species (FAO 2009). Although human-turtle

interactions are common in shared spaces and human-caused sea turtle deaths have been

reported in El Salvador (e.g. Vasquez et al. 2008), the areas and importance of the

various potential sources of human-caused sea turtle mortality remain unclear. The

objectives of this study were to identify these sources, map the areas where they are most

likely to be occurring along the coast of El Salvador, and recommend measures to

minimize them.

2. MATERIALS AND METHODS

The study area consisted of the entire 321 km extension of Salvadoran coastline,

from 0 to 200 m of depth, with particular emphasis at the 31 beach sites identified by the

USAID Improved Management and Conservation of Critical Watersheds Project

(IMCCW) as priority areas for sea turtle nesting protection (Liles et al 2010).

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2.1. Sea turtle beach stranding surveys

In collecting sea turtle stranding data, we collaborated with the technical staff of

the Fundación Zoológica de El Salvador (FUNZEL) and with residents of coastal

communities. To facilitate the logistics, this work was organized within 3 geographic

zones: Western (Bola de Monte-Toluca), Central (Boca Poza-El Espino), and Eastern (El

Cuco-El Tamarindo) (Table 1).

Table 1. The 3 geographic zones of study, including priority beaches for conservation and corresponding

department.

Zone Beach Name Department Length (km)

Western Bola de Monte Ahuachapán 3.97

Garita Palmera Ahuachapán 6.68 Barra de Santiago Ahuachapán 5.61 Costa Azul Sonsonate 1.71

Los Cóbanos (El Almendro-Los Cóbanos Centro) Sonsonate 4.10 Playa Dorada Sonsonate 4.87

El Zonte La Libertad 1.85 El Palmarcito La Libertad 0.30 El Majahual La Libertad 1.54

San Blas La Libertad 1.64 San Diego La Libertad 9.00

El Amatal La Libertad 1.02 Toluca La Libertad 3.89

Total 46.18

Central Boca Poza La Libertad 1.50 Cangrejera-Los Pinos La Libertad 4.13

Amatecampo La Paz 1.75 La Zunganera La Paz 2.79

El Pimental La Paz 4.49 Isla Tasajera La Paz 6.77 Isla Montecristo Usulután 7.14

San Juan del Gozo Usulután 15.05 Isla de Mendez Usulután 8.53

Corral de Mulas Usulután 4.81 El Icaco Usulután 8.94 Isla San Sebastián Usulután 12.57

El Espino Usulután 6.53

Total 85.00

Eastern El Cuco San Miguel 4.86 El Icacal La Unión 9.40

Las Tunas La Unión 0.59 El Maculís La Unión 3.83

El Tamarindo La Unión 1.91

Total 20.59

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Between 1 April 2010 and 31 July 2010 six technical staff of FUNZEL, in

partnership with coastal communities and local institutions, recorded sea turtle stranding

events along 152 km of Salvadoran coastline using an approved national stranding

protocol (Appendix A.1). At each of the 31 selected beaches, the local hatchery manager

was responsible for documenting all mortality events according to protocol requirements,

which were collected weekly by FUNZEL technical staff. Only carcasses confirmed by

FUNZEL staff or hatchery managers were included in this study. To maintain the

anonymity of specific coastal community residents that collaborated with data collection,

stranding data were presented per geographic zone. When possible, the species, curved

carapace length (CCL), sex, and cause of death were reported for each individual.

2.2. Interviews with marine resource users

Interviews have been successfully employed to collect useful information on the

incidental capture of sea turtles in both industrial and artisanal fisheries when collecting

observer data was not feasible (Godley et al. 1998, Lee Lum 2006, Moore et al. 2010).

This is particularly true with dynamic artisanal fisheries, where thousands of fishers may

shift methods and target species frequently, and smaller boat sizes logistically restrict the

collection of observer data. In the absence of such empirical data, researchers have relied

upon the experience and knowledge of local fishers to assess the interplay between

artisanal fisheries and the marine environment (Godley et al. 1998, Drew 2005, Close &

Hall 2006, Moore et al. 2010).

We conducted marine resource user interviews at Estero Barra de Santiago, Los

Cóbanos Reef Marine Protected Area (MPA), Estero Jaltepeque, Bahia de Jiquilisco-

Xiriualtique Biosphere Reserve, and Golfo de Fonseca. We developed a semi-structured

interview format and sea turtle reference sheets (Appendix A.2) to capture information

from local fishers on fishing areas, fishing methods, target species, sea turtle mortality,

class size (small <30 cm, medium 30-50 cm, large >50 cm), and primary sources and

areas of mortality. We field-tested the interview protocol with 8 local fishers from

different coastal communities which produced the following results:

None of the fishers stated that they themselves had incidentally captured sea

turtles, even though their fishing methods were similar to those fishers and/or

fishing methods that they claimed did capture turtles;

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Few fishers were able to orient themselves confidently with maps;

Most fishers had varying ways of measuring distance from shore and depth;

Few fishers could distinguish between the olive ridley and East Pacific green

turtles; and

Few fishers fished deeper than 100 m.

In accordance with these conclusions, the methodology and interview protocol

(Appendix A.3) were adjusted to reflect the on-the-ground reality of the study area and its

inhabitants:

our interview questions did not ask the interviewees about their individual fishing

experiences, rather the questions were directed toward a certain fishing method

and/or groups of fishers in general (e.g. long- line fishers);

we interviewed other local marine resource users (e.g. mangrove cockle

harvesters) along with fishers to incorporate individuals with diverse experiences,

fishing methods, and marine habitats into the study; and

we used sea turtle reference sheets to determine reliability in interviewee

knowledge of species and behaviors (fishers that were unable to accurately

distinguish between species were noted).

Trusted coastal community leaders in each zone identified and introduced project

staff to highly experienced marine resource users in their area, with the assurance that all

names would remain confidential. We interviewed those willing to share their knowledge

about industrial and artisanal fishing methods and sea turtle mortality using the interview

protocol in groups of no more than 3 individuals to ensure that each person interviewed

maintained his/her voice without fear of repercussions. From 1 June through 27 August

2010, we interviewed a total of 115 experienced marine resource users in the 3

geographic zones (Table 2). We categorized marine resources users that were active in

more than one resource use activity by their primary activity.

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Table 2.Characteristics of marine resource users interviewed in the 3 geographic zones of El S alvador.

Zone Communities ----------------------------------------- No. of Interviewees ----------------------------------------- Fishers Cockle harvesters Oyster harvesters Egg harvesters Total Experience (yr)

Western Garita Palmera 2 0 0 0 2 22

Barra de Santiago 9 0 0 2 11 28 Los Cobanos 8 0 0 0 8 30

Barra Salada 8 0 0 0 8 12 Mizata 2 0 2 0 4 32 Taquillo 3 0 0 0 3 10

El Zonte 0 0 1 0 1 33 SUB-TOTAL 32 0 3 2 37 24

Central Isla Tasajera 5 0 0 0 5 18 El Icaco 6 5 0 5 16 21

Puerto El Triunfo 1 0 0 0 1 32 La Pirraya 9 1 0 0 10 19 El Cojollon 5 2 0 1 8 20

Puerto Ceiba 2 1 0 2 5 23 El Espino 2 0 0 0 2 27

SUB-TOTAL 30 9 0 8 47 23

Eastern Las Tunas 4 0 5 0 9 16 El Maculis 1 0 5 1 7 25

El Tamarindo 11 0 2 2 15 29 SUB-TOTAL 16 0 12 3 31 23

TOTAL 78 9 15 13 115 23

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3. RESULTS

3.1. Sea turtle beach stranding data

Beach strandings (i.e. dead sea turtles washed ashore) are not necessarily an

accurate predictor of adult sea turtle mortality because they may account for only 7-13%

of total morality due to the variety of factors such as current regimes, wind, and distance

from shore, that determine the final resting place of a carcass. But stranding data do

indicate that deaths have occurred (Epperly et al. 1996) and provide useful life-history

information for sea turtle species (Magnuson et al. 1990). The absence of beach

strandings does not mean that mortality is not occurring (Epperly et al. 1996).

Between 1 April 2010 and 31 July 2010, we documented 55 sea turtle strandings

along the coast of El Salvador: 76% (42) were olive ridley turtles, 11% (6) were

hawksbill turtles, 6% (3) were East Pacific green turtles, and 7% (4) were unknown

(Figure 1). Table 3 provides the morphometric and sex information of the stranded sea

turtles per species in the 3 geographic zones. Nearly 50% of the 42 olive ridley turtle

strandings occurred in the western zone, the majority of which were large individuals

(mean CCL=67.7 cm). 45% of these carcasses were male turtles. Of the 6 hawksbill

carcasses, 2 were medium sized from the western zone (mean CCL=46 cm), 3 carcasses

were large and from the central and western zones (mean CCL=76 cm), and 1 carcass

could not yield reliable measurements. All stranded hawksbill turtles were female. The 3

stranded East Pacific green turtles in the central and eastern zones were large individuals

(mean CCL=82.3 cm). Based on observation and interpretation of outward injuries and

marks, we attributed 65% of strandings of the 3 species to shrimp trawls, 12% to artisanal

fishing, and 17% to unknown sources (Figure 2). The “other” category of mortality

sources included sea turtles that were cut open to remove eggs, turtles hit by boats or

propellers, and those attacked by dogs. We generally were not able to perform necropsies

on the carcasses.

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Figure 1. Species composition of sea turtles stranded along the coast of El Salvador.

76%

11%

6%7%

Olive Ridley

Hawksbill

East Pacific Green

Unknown

Figure 2. Composition of probable mortality of sea turtles stranded along the coast of El Salvador.

65%

12%

6%

17%

Shrimp Trawls

Artisanal Fisheries

Other

Unknown

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Table 3. Morphometric information and sex of stranded sea turtles by s pecies in the 3 geographic zones. n=sample size; SD=standard deviation;

F=female; M=male; U=unknown; ST=shrimp trawls; AF=artisanal fisheries; O=other.

Species Zone n % --------- CCL (cm) --------- ---- Sex (%) ---- Source of Mortality (%)

Min Max Mean SD F M U ST AF O U

Olive Ridley Western 20 48 55.0 85.0 67.7 9.1 35 45 20 75 15 5 5

Central 12 28 58.0 85.0 72.5 9.1 50 42 8 50 8 8 33

Eastern 10 24 60.0 75.0 66.7 7.5 78 11 11 70 0 10 20

Total 42 100 55.0 85.0 69.3 8.8 51 34 15 67 10 7 17

Hawksbill Western 2 33 44.0 48.0 46.0 2.8 100 0 0 50 0 0 50

Central 2 33 74.5 85.0 79.8 7.4 100 0 0 0 100 0 0

Eastern 2 33 69.0 69.0 69.0 N/A 100 0 0 50 0 0 50

Total 6 99 44.0 85.0 64.1 17.6 100 0 0 33 33 0 33

East Pacific Green Western 0 0 N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A

Central 1 33 86.0 86.0 86.0 N/A 0 0 100 100 0 0 0

Eastern 2 67 70.0 91.0 80.5 14.8 100 0 0 100 0 0 0

Total 3 100 70.0 91.0 82.3 11.0 67 0 33 100 0 0 0

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In addition to the sea turtle strandings described above, hundreds of unconfirmed

but potentially stranded turtles were reported by local egg collectors and fishers to

FUNZEL staff, including at least 1 leatherback turtle (~1.25 m CCL) at Corral de Mulas

and 4 hawksbill turtles (2 individuals ~60 cm CCL at Playa Dorada, 1 male 76 cm CCL

at Barra de Santiago, and 1 individual 25-30 cm CCL in the Bahia de Jiquilisco).

However, carcasses not observed by FUNZEL staff or hatchery managers were not

included in the stranding database and we have not included them in this study.

Considering the critically endangered status of the leatherback and hawksbill turtles,

properly documenting all stranding events and identifying sources of mortality involving

these two species is of critical importance to direct conservation action and prevent

further reductions of their populations in the eastern Pacific Ocean.

3.2. Sea turtle mortality sources and areas of concern identified by marine resource users

During our interviews, all marine resource users mentioned that incidental capture

and death of sea turtles from fishing activity occurred along the coast of El Salvador. A

“mention” refers to the indication of sea turtle capture and/or mortality by a given fishing

method or other non-fishing source, where one marine resource user may have multiple

mentions. For example, an interviewee may have stated that bottom-set gillnets and long-

lines capture hawksbills and olive ridleys. We counted this as two mentions: 1 mention

being that bottom-set gillnets capture hawksbill turtles and 1 mention being that long-

lines capture olive ridley turtles. However, an interviewee may have stated that one

fishing method, such as bottom-set gillnets, capture olive ridley and hawksbill turtles. We

counted this as only 1 mention.

Of the 115 marine resource users we interviewed along the Salvadoran coast, 79%

(91) said that industrial fisheries incidentally captured sea turtles, while 77% (88) said

that sea turtles were incidentally captured in artisanal fisheries. As shown in Table 4,

shrimp trawls were blamed for capturing sea turtles in 100% of all industrial fisheries

incidental capture mentions, while long- lines (60%), blast fishing (30%), bottom-set

lobster gillnets

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Table 4. Incidental capture of sea turtles by fishing method along the coast of El Salvador according to marine resource users.

Fishery Fishing Method Target Species Mentions ---------- Sea Turtle Species Captured (% of Mentions) ---------- Olive Ridley Green Hawksbill Leatherback Unknown

Industrial Trawls Shrimp 91 55 8 1 0 45

Artisanal Long-lines Shark, snapper, mahi-mahi 53 34 4 2 0 49 Blast fishing All commercially valuable 26 12 15 81 0 15 Bottom-set gillnets Spiny lobster 14 21 0 79 0 21

Drift nets Snook 12 17 0 0 0 83 Trammel/gillnets Corvina, shrimp, snapper 12 25 0 33 0 58

Hand-lines Snapper 6 33 0 0 0 67

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(16%), drift nets (14%), trammel/gillnets (14%), and hand-lines (7%) were blamed for capturing

sea turtles in artisanal fisheries incidental capture mentions. Marine resource users said that

mortality was also caused by non-fishing activities: hit by boats/propellers (11%, 13);

contamination of marine environment (10%, 12); eggs cut out of live female turtles (6%, 7);

intoxication from “chichicaste” (6%, 7); red tide (4%, 4); and dogs on the beach (4%, 4).

During interviews with marine resource users, we asked interviewees what the primary

source of sea turtle mortality was in their area. 90% blamed some form of interaction between sea

turtles and fisheries: 61% (70) blamed industrial shrimp trawls, 20% (23) blast fishing, 9% (10)

long- lines, 3% (3) bottom-set lobster gillnets, and 7% (9) were uncertain (Figure 3). Over 70%

(83) said that stranded female turtle carcasses were found with eggs having been cut out, which

was blamed on fishers killing incidentally captured sea turtles during the nesting seasons. We

describe each primary source of mortality below.

Figure 3. Reponses of marine resource users regardi ng the primary sea turtle mortality sources in their area.

61%20%

9%

3%7%

Shrimp Trawls

Blast Fishing

Longlines

Bottom-set Lobster Gillnets

Uncertain

3.2.1. Industrial shrimp trawls

Since the 1950s, the industrial shrimping industry has been operating along the Pacific

coast of Central America with 55 to 80 foot vessels pulling one standard 50 to 65 foot headrope

length with two sea balloon trawls from each outrigger, or a standard flat net (Arauz 1996). In El

Salvador, target species include white (Litopenaeus vannamei, Litopenaeus stylirostris, L.

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esengancha), brown (F. californiensis), and pink (F. brevirostris) shrimp, as well as

camaroncillos (Xiphopenaeus rivetti, Trachipenaeus byrdi) (López 2009). As Figure 4

demonstrates, persistent overfishing has reduced existing stock (FAO 2009), and the effects of

natural and man-made indirect stresses (e.g. Hurricane Mitch, mangrove deforestation,

contamination) have suppressed the population recovery of these target species. Shrimp and

camaroncillo exports have fallen from $40 million in 1995 to less than $4 million in 2007 (López

2009).

Figure 4. Shrimp and camaroncillo capture by industrial and artisanal fisheries in El Salvador from 1960

through 2005. Source: FAO 2009.

Industrial fishing, particularly shrimp trawls, has enormous impacts on sea turtle

populations worldwide (Spotila 2004) and has long been identified as an important source of sea

turtle mortality (Magnuson et al. 1990, Oravetz 1999). The industrial shrimp fishery of the eastern

central Pacific has been of particular concern. In 1990, Arauz (1996) repo rted an extremely high

incidental capture mortality of up to 60,000 sea turtles along the Pacific coast of Central America ;

El Salvador’s 70 industrial shrimp trawling vessels accounted for 21,280 (35%) of those captures

(66% were olive ridley turtles and 33% were East Pacific green turtles).

Interactions between shrimp trawls and sea turtles occur when fishing activities overlap

with areas of sea turtle congregation. Such is the case in El Salvador, where olive ridley and East

Pacific green turtles inhabit waters that are trawled for shrimp and camaroncillos at depths of 10

to 80 m (Arauz 1996, López 2009, Liles et al. 2010). Over 60% of marine resource users we

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interviewed identified shrimp trawls as the most important mortality source of sea turtles in El

Salvador. To minimize sea turtle captures and mortality, the Turtle Excluder Device (TED) is

required on all active shrimp trawls (CENDEPESCA/MAG 1996). The Salvadoran fishing

authority, Centro de Desarrollo de la Pesca y la Acuicultura (CENDEPESCA), says that using

TEDs by the industrial fishing sector is an institutional priority (López 2009, Barahona &

Pacheco 2009). However, 33% (38) of the marine resource users we interviewed said that all

vessels did not use TEDs during all hours of operation at sea, and 37% (14) of these said that they

had personally seen trawls operating without TEDs or TEDs that had been sewn closed. In August

2010 a vessel inspected by CENDEPESCA was found operating without a TED (E. Ramirez per.

comm. to M. Liles).

Industrial shrimp trawling effort has decreased considerably in El Salvador over the last

decade, from 76 vessels operating a total of 18,713 days in territorial waters in 1999 to 28 vessels

operating 5,070 days in 2006 (FAO 2009). Sea turtle captures by shrimp trawling vessels can be

expected to have decreased as well, which may explain that 90% (104) of our marine resource

users informants said fewer sea turtle carcasses are washing up on beaches today than in the past,

with many attributing this to fewer shrimp trawlers operating along the coast. By employing the

catch per unit effort (CPUE) of 0.0511 turtles/hr that was used to determine 20,280 sea turtles

were captured in Salvadoran waters in 1990 (Arauz 1996) with the adjusted level of effort (5,070

days or 121,680 hours), a total of approximately 6,200 sea turtles would have been captured in

2006 if TEDs were not used by shrimp trawling vessels. However, with 18% (21) of marine

resource users saying that TEDs were used on shrimp trawls, it is likely that at least some

operating vessels employ TEDs, thus reducing the number of captured sea turtles.

Olive ridley turtles appear to be the species most impacted by shrimp trawling activities,

with 55% of mentions and 78% (28) of reported trawl-related beach strandings. Their larger

population size (Márquez 2000) and higher reproductive and growth rates compared to other sea

turtle species (Márquez et al. 1982) may allow their populations to recover faster if deaths from

shrimp trawls were reduced in El Salvador.

3.2.2. Blast fishing

Fishing with explosives, or blast fishing, is an unselective and destructive practice that can

have widespread and devastating effects on marine habitats and biodiversity. Although exact

methods may be country- or habitat-specific, blast fishers typically use contraband military-grade

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explosives or homemade devices to target aggregations of commercially valuable fish. Blast

fishing indiscriminately stuns or kills all size classes of target and non-target species, with the

majority of fish sinking to the bottom, many of which are not collected (Fox & Erdmann 2000).

In El Salvador, blast fishing is illegal as established by Article 31 of the Ley General de

Ordenación y Promoción de Pesca y Acuicultura, which states that, “se prohíbe el ejercicio de la

extracción usando venenos, explosivos u otros de similar efecto destructivo”. However, 20% of

the marine resource users we interviewed along the coast of El Salvador said that blast fishing

occurred in the Bahia de Jiquilisco-Xiriualtique. This is particularly worrisome, as the Bahia was

designated a Ramsar wetland in 2005 and a UNESCO Biosphere Reserve in 2007. With an area of

63,500 hectares, it is the largest brackish and saltwater forest in El Salvador and includes

numerous estuaries, canals, beaches, and various isles of different sizes.

The impacts of blast fishing on tropical coral reef ecosystems are well documented (e.g.

Alcala & Gomez 1987, Jennings & Polunin 1996, Gray 1997, Wells 2009) and to a lesser extent

on mangrove estuaries (e.g. Corcoran et al. 2007, Adekanmbi & Ogundipe 2009), but little

information exists on blast fishing in mangrove estuaries as a source of sea turtle mortality (but

see Liles et al. In review). Of the 47 marine resource users we interviewed in the central zone,

55% said that blast fishing was killing sea turtles in the Bahia. 81% of these mentions were

hawksbill, 15% were East Pacific green turtles, and 12% were olive ridley turtles. This is

particularly concerning for the hawksbill turtle, as the population of the eastern Pacific Ocean is

one of the most endangered sea turtle populations in the world and the Bahia is a critical nesting

and foraging ground for this population (Gaos et al. unpublished data, Gaos et al. 2010). As

shown in Figure 5, blast fishing regularly occurs in areas inhabited by hawksbill turtles along

mangrove- lined channels and estuaries throughout the Bahia, of which El Rincon Grande and

Estero Arcos have been designated high priority areas for hawksbill conservation due to the

presence of high-densities of large and medium size individuals (Liles et al. 2010).

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Figure 5. Blast fishing and sea turtle priori ty conservation areas in the Bahía de Jiquilisco.

All hawksbill turtle mentions by marine resource users said that large individuals were

killed by blast fishing, with an average of 13 large hawksbill turtles killed per year (n=15;

median=8). Figure 6 shows a large hawksbill turtle that was killed by blast fishing in the Bahia in

2008. As long-term sea turtle population growth and recovery requires high survival rates of sub-

adult and adult turtles, particularly for populations at already reduced levels (Heppell 1998,

Heppell et al. 2003), the annual loss of 13 large hawksbill turtles from a remnant population

whose status “is clearly of a highest concern for the Pacific” (NMFS & USFWS 1998) is

disastrous and unsustainable should be addressed with urgency.

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Figure 6. Hawksbill turtle killed by blast fishing in the Bahía de Jiquilisco.

3.2.3. Long- lines

In the eastern Pacific Ocean, industrial and artisanal fisheries target pelagic and coastal

fish species of high commercial value using long- lines that may extend from hundreds of meters

to kilometers in length, and employ hundreds to thousands of hooks. Shallow-set long- lines

typically target larger pelagic species such as billfish, tuna, shark, and mahi-mahi, whereas deep-

set long- lines are often directed towards snapper, grouper, and catfish, with both methods

commonly utilizing baited J-hooks.

Pelagic long-lines are under intense scrutiny for their impact on sea turtle populations,

particularly shallow-set long- lines the eastern Pacific Ocean, as they tend to incidentally capture

higher numbers of older age classes (NMFS 2004, Lewison & Crowder 2008) that are critical for

population growth and recovery (Heppell 1998). As reproductively active olive ridley turtles

aggregate in large numbers offshore from nesting beaches (Kalb 1999), recent growth in long- line

fisheries in the region pose a serious and growing threat to this species and have the potential to

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capture hundreds of thousands of individuals annually (Frazier et al. 2007). Along the Pacific

coast of Latin America, the artisanal long- line fleet is estimated to contain between 10,000 and

16,000 boats with the number of hooks used at an order of magnitude similar to the industrial

long- line fleet, indicating a level of sea turtle incidental capture that is likely significant (Mug et

al. 2008).

In El Salvador, a total of 762 long- line fishers employ nearly 345,000 hooks (90% of

which are J-hooks) to capture target fish species, with shallow-set and deep-set long- line fishers

dedicating 288 days and 144 days per year to fishing activities, respectively

(CENDEPESCA/MAG 2007). As Figure 7 demonstrates, preferred long- line fishing sites overlap

with areas inhabited by sea turtles, including the area between 50 m and 100 m with a high

frequency of large, reproductively active individuals of both olive ridley and East Pacific green

turtles (Liles et al. 2010). Of the 123 mentions by marine resource users of sea turtles captured in

artisanal fishing, 43% (53) said that the captures occurred during long-line fishing, with 34% of

these stating that olive ridley turtles that were captured (49% did not know the species). A recent

study on the incidental capture of sea turtles by the artisanal long-line fishery of El Salvador

reported that of 4,443 hooks sampled, 11 olive ridley turtles were hooked and 6 were entangled

(De Paz & Siu 2008). This same study calculated the following incidental capture rate: 10

turtles/1000 J4-hooks, 4 turtles/1,000 C13-hooks, 1.2 turtles/1,000 C15-hooks, and 0.7

turtles/1,000 C14-hooks (De Paz & Siu 2008). All olive ridley turtles captured in the study were

reportedly released alive, which is consistent with global long- line incidental capture patterns,

where only between 4 to 27% of captured turtles die on the line prior to retrieval (Aguilar et al.

1995, McCracken 2000, Camiñas 2004). However, the potential for high rates of post-release

mortality exists, particularly when turtles are released with hooks or lines remaining in their

mouths, throats, or gastrointestinal tracts that can lead to infection (Aguilar et al. 1995, Chaloupka

et al. 2004), which is the case for the many of turtles captured with swallowed J-hooks (Mug et al.

2008), or when captured turtles are not handled properly (Watson et al. 2005). 90% (311,981) of

the hooks currently used by artisanal long-line fishers in El Salvador are J-hooks, which suggests

that thousands of incidental sea turtle captures from long-line fishing are occurring annually, with

a potentially high post-release mortality rate. Of the marine resource user mentions saying that

artisanal long-line fishing captured sea turtles, 34% (18) said that turtles were released alive (line

cut or unhooked), 21% (11) said that turtles were drowned, 4% (2) said that they were entangled

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in the buoys or line, and 42% (22) did not respond. The use of circle hooks would result in fewer

and less dangerous captures than J-hooks, thus reducing mortality (Gilman et al. 2005, Swimmer

et al. 2006), while maintaining similar or greater target species catch rates (Read 2007, Mug et al.

2008). The proper handling and unhooking of captured sea turtles by long- line fishers is also

critical in lowering the mortality rate of released turtles.

Figure 6. Overlap of long-line fishing and the high-priority conservation area for olive ridley and East Pacific

green turtles lying between 50 m and 100 m depth along the coast of El Salvador.

3.2.4. Bottom-set lobster gillnets

In low-income countries such as El Salvador, the extraction and direct use of natural

resources remains an essential livelihood strategy for many people (Hutton & Leader-Williams

2003), particularly in rural and coastal areas where poverty is most acute (Lehoucq et al. 2004).

Where expanding human populations are placing increasing pressure on diminishing marine

resources, there is growing evidence that small-scale, passive net fisheries are a significant

mortality source for some sea turtle populations (Gilman et al. 2009), particularly in low-income

nations where management and enforcement are limited (Peckham et al. 2007).

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The rock reef ecosystems of Los Cóbanos and El Maculís are inhabited by the Pacific

green spiny lobster (Panulirus gracilis), a species of high commercial value targeted by artisanal

fishers in both areas. Los Cóbanos Reef (13°31’26”N 89°48’23”W), situated near to Acajutla in

the western zone of the country, is a marine protected area that contains 260 km of marine and

terrestrial habitat, with dominant features being a rocky coastline and submerged volcanic reef

formations ranging from 0 m to 30 m in depth. Los Cóbanos Reef is home to approximately 15

coral species and it boasts the highest diversity of marine algae, invertebrates, and fish in the

country. El Maculís Reef is located in the eastern zone of the country and borders the Salvadoran

portion of the Golfo de Fonseca (13°9´ and 13°20´N, and 87°45´ and 88°00´W). With a length of

approximately 5 km, little is known of the biophysical characteristics of this reef ecosystem.

To capture spiny lobsters, bottom-set gillnets (300 m long by 1 to 1.5 m deep; mesh size,

10 cm; line-test, 4 lbs) are set at preferred fishing sites once daily with a 12-hr soak time at depths

of between 3 m and 7 m (López et al. unpublished data). Gillnet characteristics and employment

may vary per site, depending on the biophysical conditions of specific fishing areas. Of the 14

marine resource user mentions that said that sea turtle incidental capture occurred in bottom-set

lobster gillnets along rock reefs, nearly 80% said that hawksbill turtles were captured. As the

reliance of hawksbill turtles on coral reefs as primary foraging grounds is well documented (e.g.

Meylan 1988, León & Bjorndal 2002, Spotila 2004), it is likely that the rock reef habitats of Los

Cóbanos (Figure 7) and El Maculís (Figure 8) preferred by spiny lobsters are also used as feeding

areas by hawksbill turtles (Liles et al. 2010). Potentially deadly incidental captures of hawksbill

turtles by bottom-set lobster gillnets will occur when gillnets are set in areas used by foraging

turtles (Liles et al. In review). In some parts of the world, sea turtle mortality rates in gillnet

fisheries has been reported to be 50% (Laurent et al. 1991; Argano et al. 1992). Nearly 65% (9) of

marine resource user mentions that said that lobster gillnets captured turtles also said that

captured turtles died, with an average of 12 medium size hawksbill turtles killed per year (n=9;

median=4). Population modeling has demonstrated that high survivorship of sub-adults may be

critical to the maintenance and recovery of sea turtle populations (Crouse et al. 1987, Crouse

1999), so the probable loss of this number of sub-adults in lobster gillnets in Los Cóbanos and El

Maculís is alarming for a population as severely depleted as the hawksbill turtle of the eastern

Pacific Ocean.

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Figure 7. Distribution and overlap with sea turtle distributions of lobster gillnets in Los Cóbanos.

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Figure 8. Distribution and overlap with sea turtle distributions of lobster gillnets in El Maculís.

4. RECOMMENDATIONS

As the leading source of sea turtle mortality throughout the world, incidental capture in industrial

and artisanal fisheries has severe impacts on populations and impedes their recovery. However,

modifications to fishing gear and methods can mitigate (avoid, reduce, and offset) deaths from

incidental capture in marine fisheries. We provide the following recommendations to reduce sea

turtle deaths from incidental capture in Salvadoran fisheries, to raise public awareness of the

impacts of incidental capture mortality on sea turtle populations, and to document incidental

capture deaths.

4.1. General

Quantify and map sea turtle incidental capture in industrial and artisanal fisheries using

independent observers on board fishing vessels to record data on fishing effort per-vessel,

target catch, and sea turtle captures (NMFS 2004, Moore et al. 2010)

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Quantify and document the practice by marine fishers of illegally killing captured female

turtles and cutting or their eggs

Prosecute violators of existing laws protecting sea turtles from incidental capture

Strictly regulate or prohibit fishing activities in high-density sea turtle habitats,

particularly areas inhabited by the critically endangered hawksbill turtle.

Ban the use of bottom-set gillnets in areas used by foraging hawksbill turtles.

Establish industrial and artisanal fishing “vedas” (bans) in specific marine areas at times

when a high probability exists for incidental capture deaths of sea turtles

Organize seminars with the industrial and artisanal fishing sectors to discuss effective

measures to reduce incidental capture deaths of sea turtles in Salvadoran fisheries

Encourage the active participation of the fishing community and offer financial support

for the implementation (experimentation) of agreed upon approaches

Encourage community regulation and protection of marine resources

Encourage community denuncias of illegal fishing activities

Train fishers on best practices in handling, unhooking, and resuscitating captured sea

turtles that are brought aboard alive

Review and, when necessary, revise fisheries regulation and legislation to provide better

protection for sea turtles in Salvadoran waters

Empower and strengthen sea turtle beach stranding network, including egg collectors,

local fishers, and other concerned coastal community residents, to ensure the proper

documentation and reporting of all stranded turtles along the coast of El Salvador

Train sea turtle beach stranding network on best practices for performing in-field

necropsies on carcasses and for mortality source identification

Raise public awareness of the effect of sea turtle incidental capture on sea turtle

populations, particularly populations that are severely reduced in the eastern Pacific

Ocean, such as hawksbill and leatherback turtles

Promote public action by clarifying the link between an individual’s daily choices (i.e.

consumption of unsustainably caught sea food products) and sea turtle mortality, while

offering more preferable alternatives

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4.2. Industrial shrimp trawls

Enforce the proper use of Turtle Excluder Devices (TEDs) on all operating shrimp

trawling vessels in El Salvador, as required by CENDEPESCA/MAG Resolution No. 112,

by deploying on-board observers and prosecuting violators

Establish a voluntary network of local fishers and fishing cooperatives to monitor the use

of TEDs by shrimp trawling vessels while at-sea and report violations to appropriate

authorities

Adopt as a high-priority policy of MARN and CENDEPESCA/MAG the enforcement of

sea turtle protection legislation

Reduce tow times of shrimp trawls

4.3. Blast fishing

Adopt as a high-priority policy of CENDEPESCA/MAG the enforcement of legislation

banning blast fishing in the Bahia de Jiquilisco-Xirihualtique Biosphere Reserve

Strictly enforce Article 31 of CENDPESCA/MAG Ley General de Ordenación y

Promoción de Pesca y Acuicultura and prosecute violators

Establish a baseline and annual monitoring of blast fishing practices and resulting sea

turtle deaths in the Bahia de Jiquilisco-Xirihualtique Biosphere Reserve

Engage blast fishers in discussions on the implications of blast fishing to the marine

environment and biodiversity, with an emphasis on sea turtle mortality, and jointly

develop potential income-generating alternatives and offer financial support for their

implementation

4.4. Long- lines

Replace J-hooks with circle hooks in the artisanal long- line fishery along the coast of El

Salvador (Figure 8). The use of circle hooks would result in fewer and less dangerous

captures than J-hooks, thus reducing mortality (Gilman et al. 2005, Swimmer et al. 2006),

while maintaining similar or greater target species catch rates (Read 2007, Mug et al.

2008)

Ban the use of shallow-set long- lines. This should substantially reduce the incidental

capture of olive ridley turtles, as they spend only about 10% of their time deeper than 100

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m (Polovina et al. 2003). However, the mortality rate of turtles captured on deep-set long-

lines may be higher than sea turtles captured near the surface.

Figure 9. Circle hook alternatives to J-hooks currently in use. Source: Mug et al. 2008.

4.5. Bottom-set lobster gillnets

Prohibit the use of bottom-set gillnets in areas where hawksbill turtle foraging occurs.

Regulate the soak time of gillnets at less than the maximum dive times of the most

vulnerable sea turtle species (olive ridley). Although hawksbill turtles can remain

submerged longer than other species of sea turtles (mean=56 min; max=74 min) (Spotila

2004), the 12-hr soak time commonly employed for bottom-set lobster gillnets surpasses

their maximum dive times.

Experiment with lobster fishing gear and methods, particularly cage traps that do not

incidentally capture sea turtles.

Establish a baseline and annual monitoring of the bottom-set lobster gillnet fisheries at

Los Cóbanos Reef MPA, Costa Acantilada, and El Maculis Reef, including quantifying

sea turtle incidental captures, fishing methods employed, and fishing intensity at mapped

fishing sites.

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APPENDIX A

A.1. Sea turtle stranding protocol used to document stranding events.

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A.2. Sea turtle reference sheets used during interviews with marine resource users.

A.2.1. Olive ridley turtle reference sheet

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A.2.2. East Pacific green turtle reference sheet

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A.2.3. Hawksbill turtle reference sheet

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A.2.4. Leatherback turtle reference sheet.

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A.3. Interview protocol developed and used to interview marine resource users along the coast of El Salvador.

A. Datos del informante local:

1) Fecha_____________ 2) Nombre_______________________________________

3) Sexo ______

4) Edad ______ 5) Comunidad _________________________________

6) A que se dedica?_____________________________

7) Desde hace cuanto?________años

B. Especies de tortugas marinas presentes en el área:

8) Cuantos tipos de tortugas marinas hay en su comunidad?______ Cuales son?__________________________________________________

*Muéstrele fotos de las 4 especies y anote cuales pudo identificar correctamente*

Golfina Prieta Carey Baule

Si o No Si o No Si o No Si o No

9) Ha visto tortugas en alta mar? Si o No

Especie Tamaño En que áreas Profundidad Meses Que están haciendo

Frecuencia (de 10 veces)

Observaciones___________________________________________________________________________

**Marque las áreas en el mapa y anote el nombre del área POR ESPECIE y POR TAMANO de las

tortugas**

10) Ha visto tortugas en el estero/manglar? Si o No

Especie Tamaño En que áreas Profundidad Meses Que están haciendo

Frecuencia (de 10 veces)

Si se esta alimentando, de que se alimenta (por

especie)?______________________________________________ Como lo sabe?________________________________

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Observaciones_______________________________________________________________________

**Marque las áreas en el mapa y anote el nombre del área POR ESPECIE y POR TAMANO de las

tortugas**

11) Hay pastos marinos? Si o No

Donde están ubicados?________________________________________________________________________

Ha visto tortugas en los pastos? Si o No

Especie Tamaño En que áreas Profundidad Meses Que están haciendo

Frecuencia (de 10 veces)

Si se están alimentando, de que se alimenta (por especie)?____________________________________ Como lo sabe?________________________

Observaciones_______________________________________________________________________

**Marque las áreas en el mapa y anote el nombre del área POR ESPECIE y POR TAMANO de las

tortugas** 12) Ha visto tortugas en los arrecifes? Si o No

Especie Tamaño En que áreas Profundidad Meses Que están

haciendo

Frecuencia

(de 10 veces)

Si se están alimentando, de que se alimenta (por especie)?____________________________________

Como lo sabe?________________________ Observaciones_______________________________________________________________________

**Marque las áreas en el mapa y anote el nombre del área POR ESPECIE y POR TAMANO de las tortugas**

Se observa mas, menos, o la misma cantidad de tortugas hoy en día que cuando empezó a pescar/ostrear/etc.

(por especie)?________________________________

C. La pesca: Alta Mar □ Estero/Manglar □ Arrecife □

13) Se dedican muchas personas de su comunidad a la pesca? Si o No Cuantas personas?_______

14) Cuantas lanchas se dedican a la pesca en su comunidad?___________ Cuantos pescadores hay por lancha (si depende del tipo de pesca, anote por tipo)?________________________

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Tipo de equipo (por especie de pez) En que áreas Profundidad

1.

2.

3.

En que meses (por especie de pez)?_________________________________________________________________

__________________________________________________________________________________________

___ 15) Cual tipo de equipo de pesca es lo mas utilizado?__________________________

El segundo mas utilizado?____________________________________________

16) Operan barcos camaroneros en frente de la pla ya de su comunidad? Si o No En que meses?___________________________

Cuantos barcos por mes (promedio)?__________________________ 17) Capturan tortugas marinas? Si o No

Cuantas

capturan

Especies Tamaño Que les pasa Como lo sabe Usan TED Como lo sabe

___ por año Si o No

Observaciones_______________________________________________________________________________

18) Hay otros tipos de pesca que accidentalmente capturan tortugas marinas? Si o No

Cuales Se

ocupan

Cuantas

capturan

Especies Tamaños En que áreas Que les pasa Como lo

sabe

Si o No __ por año

Observaciones______________________________________________________________________________

_

**Marque las áreas en el mapa y anote el nombre del área POR EQUIPO, POR ESPECIE y POR TAMANO

de las tortugas**

19) Hay tortugas que mueren dentro de los manglares? Si o no?

20) Hay tortugas que mueren por la pesca con bombas/explosivos? Si o No

Cuantas Especies Tamaños En que áreas

_____ por año

21) Hay tortugas que mueren por causas ajenas a la pesca? Si o No

Causa Cuantas Especies Tamaños En que áreas

____ por año

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Causa Cuantas Especies Tamaños En que áreas

____ por año

22) Tortugas que salen muertas

Cuantas normalmente No menos de No mas de En que playas

______ por mes ______ por mes ______ por mes

Salen mas, menos, o la misma cantidad de tortugas muertas que cuando empezó a pescar (por

especie)?___________

23) Cuales son las principales causas de muerte de las tortugas en su área?_____________________________________