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The Largetooth Sawfish, Pristis pristis (Linnaeus, 1758), is not extirpated from Peru: new records from Tumbes

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The Largetooth Sawfish, Pristis pristis, was for a long time considered extirpated from Peru. However, here we report the capture of 2 individuals from the north coast of Peru, indicating that this species is still extant in Peruvian waters. Both individuals were adult-sized and their encounters occurred during the austral summer, which could indicate a seasonal presence in those waters. Gillnets are still a major threat for the species as both specimens were incidentally captured with this gear. Our finding highlights the need for continuous research, awareness, and legal protection of this species.
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The Largetooth Sawsh, Pristis pristis (Linnaeus, 1758), is not
extirpated from Peru: new records from Tumbes
Alejandra Mendoza,1 Shaleyla Kelez,1 Wilmer Gonzales Cherres,2 Rossana Maguiño1
1 ecOceánica, Copernico 179, San Borja, Lima 41, Peru. 2 Asociacion de Pescadores Artesanales para Consumo Humano Directo de La Cruz,
Caleta La Cruz, Tumbes, Peru.
Corresponding author: Alejandra Mendoza, alejandra.mendoza@ecoceanica.org
Abstract
The Largetooth Sawsh, Pristis pristis, was for a long time considered extirpated from Peru. However, here we report
the capture of 2 individuals from the north coast of Peru, indicating that this species is still extant in Peruvian waters.
Both individuals were adult-sized and their encounters occurred during the austral summer, which could indicate a
seasonal presence in those waters. Gillnets are still a major threat for the species as both specimens were incidentally
captured with this gear. Our nding highlights the need for continuous research, awareness, and legal protection of
this species.
Key words
Tropical Eastern Pacic; bycatch; Pristidae; northern Peru; critically endangered species.
Academic editor: Arturo Angulo Sibaja | Received 15 March 2017 | Accepted 24 May 2017 | Published 4 August 2017
Citation: Mendoza A, Kelez S, Cherres WG, Maguiño R (2017) The Largetooth Sawsh, Pristis pristis (Linnaeus, 1758), is not extirpated from
Peru: new records from Tumbes. Check List 13 (4): 261–265. https://doi.org/10.15560/13.4.261
Check List 13 (4): 261–265
https://doi.org/10.15560/13.4.261
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261
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Mendoza et al
Copyright Mendoza et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted
use, distribution, and reproduction in any medium, provided the original author and source are credited.
Introduction
All extant sawshes belong to the family Pristidae,
which includes the genera Anoxypristis White & Moy-
Thomas, 1941 and Pristis Linck, 1790 (Compagno and
Cook 1995). The genus Anoxypristis only has 1 species:
the Knifetooth Sawsh, Anoxypristis cuspidata (Latham,
1794); the genus Pristis includes 4 species: Largetooth
Sawsh, Pristis pristis (Linnaeus, 1758); Smalltooth
Sawsh, Pristis pectinata Latham, 1794; Dwarf Sawsh,
Pristis clavata Garman, 1906); and Green Sawsh, Pris-
tis zijsron Bleeker, 1851 (Faria et al. 2013).
Sawshes live in shallow coastal waters usually at
depths up to 20 m but as deep as 122 m (Harrison and
Dulvy 2014). They can tolerate wide ranges of salinity
and thus can be found in continental waters and estuaries.
For example, they can swim far up into large rivers and
have been found in lakes in South America, Africa, and
Southeast Asia (Harrison and Dulvy 2014).
Pristis pristis is morphologically characterized by the
rst dorsal n located in front of the origin of the pelvic
ns, the presence, in all stages of growth, of the lower
lobe of the caudal n, and by having a shorter and wider
rostrum than the other species of Pristis (Faria et al.
2013). Recent studies have shown that P. perotteti from
the Atlantic Ocean and P. microdon from the western
Indo-Pacic Ocean are synonyms of P. pristis. This euro-
haline species, as currently dened, has a circumtropical
geographic distribution with 4 genetically dierentiated
populations: eastern Pacic, western Atlantic, eastern
Atlantic, and western Indo-Pacic Ocean (Faria et al.
2013).
NOTES ON GEOGRAPHIC DISTRIBUTION
262 Check List 13 (4)
Apparently, populations of P. pristis have been
reduced considerably from their former abundances
throughout their range (Carlson et al. 2013a). According
to Carlson et al. (2013a), the eastern Pacic population
was formerly distributed from the Gulf of Mexico to
Peru, but until 2013 only a few records existed from the
Pacic coast of Nicaragua, Panama and Colombia. There-
fore, Carlson et al. (2013a) argued that there had been a
considerable population decline based on the retraction
of the extent of occurrence of ≥ 80% over a 3-generation
period. A major threat to P. pristis in the eastern Pacic
is the decline of mangrove habitats that are utilized as
nurseries, for reproduction, and feeding grounds. Other
pervasive threats are longline sheries for sharks and
coastal gillnets (Carlson et al. 2013a). Consequently, the
International Union for Conservation of Nature listed this
species and all other sawsh species as Critically Endan-
gered (Kyne et al. 2013). Pristis pristis is also included in
Appendix 1 of the Convention on International Trade in
Endangered Species of Wild Fauna and Flora, as well as
in Appendix 1 of the Convention on the Conservation of
Migratory Species of Wild Animals (CMS).
In Peru, occurrence data on sawshes are relatively
scarce. Until 1920, P. pristis was not reported in Peru,
but Nichols and Murphy (1922) mentioned that sher-
men already knew of it there. Chirichigno and Cornejo
(2001) listed the genus Pristis from Peruvian waters and
reported 2 species: P. microdon and Pristis pectinatus (a
synonymous of P. pectinata). Chirichigno and Cornejo
(2001) mentioned that both of these species occur in
Tumbes, northern Peru; however, the report of P. pecti-
natus by Chirichigno and Cornejo (2001) was likely a
misidentication of P. pristis, because we now know that
P. pectinata only occurs in the Atlantic Ocean (Carlson
et al. 2013b). In addition, there is undated photographic
evidence showing sawsh specimens captured in Cabo
Blanco and Punta Sal (Fig. 1) (Dr Matthew McDavitt
pers. comm.). The most recent reports for Pristis species
Figure 1. Map showing the locations of Pristis pristis recorded in Peru. Circles are previous reports of landings: mouth of the Tumbes River
(Chirichigno and Cornejo 2001), Punta Sal and Cabo Blanco (McDavitt pers. comm. 2016). Squares show new landing reports: Caleta La Cruz
(2014) and Cancas (2015), both in the Department of Tumbes. Map created using Maptool (Seaturtle.org 2002).
Mendoza et al. | Sawsh in Peru 263
in Peru come from information collected by researchers
from the Instituto del Mar del Peru between 1996 and
2005 in the Tumbes Region (Llanos et al. 2010), but
these reports are without specic information. However,
an author of this report (Carlos Inga, pers. comm.) men-
tioned that sawsh remains were observed only up to the
1990s.
Nonetheless, until a decade ago the international sci-
entic community thought that sawshes did not occur
in Peru (Compagno and Cook 1995, Compagno and
Cook 2005). Following Faria et al. (2013), who included
P. pristis from Peru based on previous works listing the
species in Peruvian waters, subsequent scientic and
technical publications also listed this species from Peru
but without more precise distributional data and cited
it as a historical distribution given the absence of con-
rmed records for more than 10 years. As a result, many
researchers believed that the species had been extirpated
from Peru (Carlson et al. 2013a, Dulvy et al. 2014, Har-
rison and Dulvy 2014).
According to shermen from Cancas and Caleta La
Cruz (Fig. 1), sawshes used to be abundant along the
north coast of Peru, but due to overshing, they have now
almost disappeared. Overshing was driven by the high
valued in Peru of sawsh teeth using in cockghting as
articial spurs tted to the birds’ feet as a competitive
advantage during ghts (McDavitt 2014). In addition,
sawshes are not protected by the Peruvian legislation,
so the capture and commercialization of this species is
not illegal.
The objective of this study was to update the presence
of P. pristis in Peru by reporting 2 recent records.
Methods
The area of interest is located along the coast of the depart-
ment of Tumbes (Fig. 1), in the Guayaquil ecoregion of
the Tropical East Pacic Marine Province (Spalding et
al. 2007). The coastline of Tumbes includes 2 mangrove
systems that are fed by the waters of the Tumbes and
Zarumilla rivers (Angulo 2014).
On 22 January 2014, 1 specimen of P. pristis was inci-
dentally captured in our nets during commercial shing (by
Wilmer Gonzales Cherres) and taken to the landing site at
La Cruz, Tumbes (Fig. 1, Table 1). The sawsh was caught
at dawn with a gillnet o Playa Hermosa. It was later
butchered and its teeth were sold (Table 1). This specimen
measured approximately 350 cm in total length (TL), the
rostrum 100 cm, and the body without rostrum weighed
146 kg (Fig. 2). The specimen was a gravid female, con-
taining yellow and spherical eggs similar to those of the
Pacic Angel Shark, Squatina californica Ayres, 1859.
On 14 February 2015 (9:00 h), we received a call
from a shermen informing us that a sawsh was being
brought alive to the Cancas dock in the district of Canoas
de Punta Sal, Tumbes (Fig. 1, Table 1). The rst author
moved to the site and at 11:00 h the boat arrived with
the specimen. It measured approximately 6 m TL, but
the sex could not be determined (Fig. 3). The sh was
incidentally caught by the boat during a gillnet sh-
ing trip in front of El Bravo beach (Fig. 1). Once at the
dock, shermen Richard Pingo Antón, Luis Pingo Antón,
Baltazar Fiestas Querevalu, and Tomas Pingo Chiroque
called the authorities to decide what to do with the saw-
sh since they were unfamiliar with the regulation on
its capture, but they knew that it was a rare nd. They
decided to release the individual, which was carried out
in the presence of the Director of the Regional Direc-
torate of Production of Tumbes (DIREPRO Tumbes), a
representative of the General Directorate of Coast Guard
(DICAPI), and A. Mendoza, a representative of our non-
prot organization ecOceánica, all who signed the Act of
Liberation drafted by DIREPRO Tumbes. The individual
was released at 12:40 h on the same day.
Results
Both specimens were identied as P. pristis (Figs. 2, 3)
based on the following combination of distinctive char-
acters: origin of the rst dorsal n anterior to the pelvic
n origin and presence of a lower caudal n lobe (Faria et
al. 2014).The specic identication of the specimens also
was conrmed using photographs by the sawsh special-
ist Dr Peter Kyne, from Charles Darwin University.
Discussion
In Peru, the last year that sawshes were observed was
1999 (Carlos Inga pers. comm.). Since then, a couple of
publications reported the presence of sawshes in Peru
based on Chirichigno and Cornejo (2001). The National
Action Plan for the Conservation and Management of
Sharks, Rays and Related Species in Peru (PRODUCE
2014) mentions 2 species of Pristidae but without
Table 1. New records of Pristis pristis in Peru including capture data and the fate of the individuals.
Date Landing site Latitude Longitude Size TL cm Sex Fate
January 22, 2014 La Cruz, Tumbes –3.6362 –80.5996 350 female Dead, teeth sold
February 14, 2015 Cancas, Tumbes –3.9445 –80.9400 600 unknown Liberated alive
Figure 2. Sawsh landed dead at La Cruz, Tumbes, on 22 January
2014.
264 Check List 13 (4)
specifying them. The other publication is a revised list
of Chondrichthyans in Peru (Cornejo et al. 2015), which
included P. pristis and P. pectinata. Given that the inclu-
sion of this species in PRODUCE (2014) and Cornejo et
al. (2015) are the result of literature reviews and are not
based on eld surveys, the documentation here of 2 new
specimens provide the rst empirical records of P. pristis
in Peru since 1999.
These records demonstrate that P. pristis is not extir-
pated from Peru, and they highlight the need to identify
and protect critical habitats that could contribute to sawsh
conservation. There is additional anecdotal information.
On 2 March 2017, a new specimen was captured in a gill-
net and landed dead in Mancora (J. Guerrero Chinchay,
Mancora Dock Manager, pers. comm). The 3 reports of
P. pristis are from the same area where Chirichigno and
Cornejo (2001) had earlier reported it (Fig. 1). The spatial
distribution of this species in Peru would seem to extend
from the Ecuadorian border to Cabo Blanco (Fig. 1).
The capture of a specimen of P. pristis in the Pacic
waters of southern Ecuador was also reported in July
2014. The individual (506 cm TL) was landed in the port
of Santa Rosa de Salinas (Universidad Laica Eloy Alfaro
de Manabi 2014). This record shows that this species is
not extirpated from Ecuador either, and would suggest that
there is still a small extant population between southern
Ecuador and northern Peru, an area where river mouths
form mangrove estuaries. These data, coupled with pre-
vious reports from Nicaragua, Panama and Colombia
(Carlson et al. 2013a) give support to the premise that the
distribution of this species is continuous from northern
Peru to Nicaragua.
The size at sexual maturity of P. pristis is 300 cm for
females and 280–300 cm for males (Dulvy et al. 2014).
Therefore, the 2 observations in Peru, and 1 in Ecuador,
suggest that this part of the Eastern Pacic, adjacent to
mangroves, is used by adults and reproductively active
females. Moreover, it is possible that the better-preserved
mangrove habitats of northern Peru could be preferred
by sawsh in the southeast Pacic. On the other hand, the
seasonality of the 3 encounters in Peru (late January to
early March) may imply that the presence of this species
in Peru represents a seasonal migration from its core area
in Central America as postulated by Kyne et al. (2014).
However, the observation in July of the individual in
Ecuador is not in agreement with the seasonal migration
hypothesis. In this regard, more research is needed to
understand the habitat use and phenology of this species.
Gillnets are a major threat to the survival of sawshes
as all 3 individuals recorded recently in Peru were cap-
tured using this gear. As we have observed in the eld,
many shers in northern Peru set their nets at night and
check them in the morning, leaving them long periods
unattended. This practice can have deleterious collateral
impacts as they capture non-target species that will likely
drown, be depredated, or suer post-release mortality
from stress.
Now that P. pristis is conclusively known not to be
locally extinct in Peru, there is a need for further research
on this species, to put the sawsh on the agenda of the
Peruvian government, to promote their conservation
through environmental education, and to seek national
legislation to give the species full legal protection.
Acknowledgements
To the shermen from Cancas: Richard Pingo Antón,
Luis Pingo Antón, Baltazar Fiestas Querevalu, and Tomas
Pingo Chiroque for liberated the specimen found in front
of Playa Hermosa. To Dr Matthew T. McDavitt for the
historic photographic material. To Dr Peter Kyne for the
verication of the specimens as Pristis pristis and for
providing literature. To Lisa E. Poser and Catherine M.
McClellan for providing edits that improved the manu-
script.
Authors’ Contributions
AM, WGC and RM collected the data, AM and SK wrote
the text.
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... This individual, which was ca. 5 m in total length, was taken to the fishing port of Salinas, Santa Elena Province, and then released (Rosas-Luis 2021). In Peru, recent reports of largetooth sawfish have been rare, but their captures by fishers in northern Peru were documented in 2014, 2015, and 2017, confirming that the species is still occasionally encountered in this region (Mendoza et al. 2017, Cabanillas-Torpoco et al. 2020. ...
... In addition, this study provides encouraging evidence that largetooth sawfish persist in Ecuador and northern Peru and that they were once a commonly encountered species on the coasts of both countries. Furthermore, continued observations of sawfish by fishers in recent decades suggest that rather than being occasional or seasonal visitors to the Peruvian coast as had previously been suggested (Mendoza et al. 2017), sawfish were present year-round, at least historically. Enforcement and efforts to discourage the capture and retention of accidental catch of sawfish are required; for example, through the development of alternative livelihoods in communities interacting with sawfishes (e.g. ...
... 6 m total length). Both landings occurred in Tumbes Department and the sawfish caught in 2015 was released alive (Mendoza et al. 2017). ...
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Sawfish conservation is a critical concern, yet insufficient baseline data on their presence and status has hindered conservation efforts at national and regional levels. Between 2015 and 2017, interviews were conducted in fishing communities in Ecuador and Peru to assess the historical and current status of largetooth sawfish Pristis pristis . Interviews with cockfighting practitioners in Peru aimed to gauge the use and demand for cockfighting spurs made from sawfish rostral teeth. Our study confirmed the presence of largetooth sawfish in the waters of both countries. Importantly, some fishermen are aware of the value of rostral teeth, which may influence their decisions not to release sawfish alive. Of the interviewees (n = 188), a majority (88%) reported a perceived decline in sawfish abundance during their lifetimes. In this region, as in other sawfish habitats, bycatch and habitat loss pose significant threats. To address these challenges, potential actions include strategic conservation planning, reinforced national and international trade regulations, education campaigns targeting the cockfighting community, public outreach initiatives, and the live release of sawfish specimens. These efforts can enhance the conservation status of largetooth sawfish, particularly in a region isolated from other persisting populations that potentially harbours vital genetic diversity. Furthermore, safeguarding sawfish contributes to the implementation of national instruments like the National Action Plans for Sharks in both countries. Neglecting these threats could perpetuate sawfish capture and mortality in a region where local populations are already severely depleted, elevating the risk of regional extinction. Prioritizing sawfish conservation is imperative to prevent further decline and preserve their ecological importance.
... No recent biological or ecological information exists for P. pristis in Colombia and Panamá, since it is an extremely rare species in the area and therefore difficult to assess and research. The species is known to be locally extinct in 27 of the 75 countries where it was historically present (Faria et al. 2013, Dulvy et al. 2016, Mendoza et al. 2017. In its native Caribbean range, P. pristis is thought to be locally extinct (Gómez-Rodríguez et al. 2014). ...
... Locations highlighted in the interviews are characterised by high coverage of mangrove forests and low human population density. Recent studies in the eastern tropical Pacific region have also documented sawfish sightings between 2013 and 2018 in areas of dense protected mangrove forest, such as the Térraba-Sierpe National Wetlands in Costa Rica (Valerio-Vargas & Espinoza 2019) and the Tumbes region in northern Perú (Mendoza et al. 2017). These findings align with recent research that showed ha bitat availability, differential fishing pressure, and proximity to mangrove areas as factors strongly involved in sawfish residency, habitat suitability, and probability of local extinction (Yan et al. 2021). ...
... shells, tannins, charcoal, fish) since pre-Columbian times (López-Angarita et al. 2016), yet only since the emergence of gill nets as a common fishing gear in nearshore areas would human−sawfish interactions have become more frequent. Elsewhere in the region, gill nets have been identified as a major threat to sawfish , Mendoza et al. 2017, and in areas heavily fished with this gear, there is evidence of the historical reduction of their populations, such as the Gulf of Nicoya in Costa Rica (Valerio-Vargas & Espinoza 2019). Interestingly, the database analysed for the northern Chocó region in Colombia includes data from a participatory monitoring program between 2010 and 2013, in an area that has restricted the use of nets since 2008 (Díaz & Galeano 2016). ...
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Freshwater fish communities in Ecuador exhibit some of the highest levels of diversity and endemism in the Neotropics. Unfortunately, aquatic ecosystems in the country are under serious threat and conditions are deteriorating. In 2018–19, the government of Ecuador sponsored a series of workshops to examine the conservation status of Ecuador's freshwater fishes. Concerns were identified for 35 species, most of which are native to the Amazon region, and overfishing of Amazonian pimelodid catfishes emerged as a major issue. However, much of the information needed to make decisions across fish groups and regions was not available, hindering the process and highlighting the need for a review of the conservation threats to Ecuador's freshwater fishes. Here, we review how the physical alteration of rivers, deforestation, wetland and floodplain degradation, agricultural and urban water pollution, mining, oil extraction, dams, overfishing, introduced species and climate change are affecting freshwater fishes in Ecuador. Although many of these factors affect fishes throughout the Neotropics, the lack of data on Ecuadorian fish communities is staggering and highlights the urgent need for more research. We also make recommendations, including the need for proper enforcement of existing environmental laws, restoration of degraded aquatic ecosystems, establishment of a national monitoring system for freshwater ecosystems, investment in research to fill gaps in knowledge, and encouragement of public engagement in citizen science and conservation efforts. Freshwater fishes are an important component of the cultural and biological legacy of the Ecuadorian people. Conserving them for future generations is critical.
... Where detailed presence or absence data are missing, conservation plans are often built based upon community knowledge of sawfish catches, with opportunistic collection of size and catch data where samples are available (Leeney & Poncelet, 2015;Jabado et al., 2017;Mendoza et al., 2017;Haque, Leeney & Biswas, 2020;L opez-Angarita et al., 2021). While historical data may not reflect the current state of the population, it increasingly plays a role in planning and management within marine science, as conservation often requires an understanding of both historical range and current information to define conservation goals (M añez et al., 2014). ...
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• The ecology of endangered and rare species can be difficult to study owing to their low abundances and legal limits on scientist’s ability to catch, sample, and track them. This is particularly true of sawfish (family Pristidae), whose numbers have declined precipitously, placing all five species on the IUCN Red List of Threatened Species worldwide. Best known for their distinctive, toothed rostrum, the ecology, movement and life-history of sawfish are poorly understood. • Sawfish rostral teeth are modified placoid scales, which grow continuously throughout the life of the fish. This continuous growth, combined with their stable calcified makeup, makes sawfish rostral teeth a potential source of temporal records of chemical and isotopic changes through the life of the fish. • Rostral teeth are often preserved in museums and as curios, potentially providing a source of life-history data to inform conservation actions without the need for field study, or as an important compliment to it. This is the first study to recover temporally explicit chemical data from sawfish rostral teeth. • Using archived samples of largetooth sawfish (Pristis pristis) we show that multiple chemical tracers can be recovered from sawfish rostral teeth, and that these tracers can be used to understand movement across salinity gradients. We further show that sawfish rostral teeth contain repeated structures and indistinct banding which could potentially be used for ageing or growth analysis of fish.
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Sawfishes (Pristidae) have been severely impacted by coastal development and unregulated fisheries and are considered Critically Endangered by the IUCN Red List. Environmental DNA (eDNA) analyses have shown potential for monitoring elasmobranch species, with various studies focusing on using species-specific approaches to detect Pristis species. However positive detection using existing probes has not been confirmed in some geographic regions where they would be expected. Here, we aimed to test whether mutations at key sites have been detrimental to species-specific detection of P. pristis (Linnaeus, 1758) using the existing probe set. To test this hypothesis mitogenomes were assembled that were found to follow the typical pattern of vertebrate mitogenomic organization. Phylogenetic trees showed similar topologies and confirmed geographic mitochondrial variation in P. pristis. Mismatches for the published 12S species-specific probe set for P. pristis were identified that prevent amplification of positive control samples from Brazil. However, ddPCR detection of the positive control was possible using a newly designed species-specific probe set. This study highlights how geographical variation can severely impact the success of generally applying species-specific detection systems developed based on data from only one geographical region. The new mitogenomes and species-specific probe set developed here may also contribute to improving the potential to map and monitor these Critically Endangered species across the globe.
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The first updated and comprehensive checklist of Chondrichthyes from the southeast Pacific off Peru, based on the revision of scientific literature, is presented. The group of Chondrichthyes in the Peruvian coast is composed of 115 species that include 66 species of sharks, 43 species of batoids, and six species of chi-maeras. We present nine new records and one recent discovery obtained from secondary sources. For some species, we also compiled the extensions in the geographic distributions.
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Sawfish are arguably the world's most imperilled marine fishes. All five species are classified as highly threatened with extinction: three are Critically Endangered (smalltooth sawfish Pristis pectinata , largetooth sawfish Pristis pristis, and green sawfish Pristis zijsron ); two are Endangered (narrow sawfish Anoxypristis cuspidata , and dwarf sawfish Pristis clavata ). Sawfishes are threatened primarily due to a combination of their low intrinsic rates of population increase, high catchability in fisheries, and high value. Sawfishes are among the world's largest marine fishes, and they are caught by a wide range of fishing gears owing to their tooth‐studded rostra being easily entangled. Sawfish fins are some of the most valuable for shark fin soup, and their rostra have long been traded as curios. In addition, they inhabit shallow coastal waters, estuaries, and rivers of the tropics and subtropics, down to a maximum depth rarely exceeding 100 m and are associated with threatened mangrove and seagrass habitats. Historically, sawfishes were distributed in the coastal waters of 90 countries and territories. Over the past century, their geographic distribution has been greatly diminished. For example, the smalltooth sawfish is now found in <20% of its former range. Globally, sawfishes are now entirely absent from 20 countries; 43 countries have lost at least one species. Sawfishes are legally protected, to some degree, in 16 of the 90 range states. These safeguards encompass, on average, 81% of their Extant distribution; however, the quality and breadth of protection varies dramatically across countries and species. Smalltooth sawfish currently has the least amount of such coverage of only half (49%) of Extant distribution. The global conservation strategy specifies actions to protect sawfish and their habitats. Such actions are urgently warranted to avoid global extinction and to restore robust populations for the benefit of coastal ecosystem function and biodiversity. © 2014 The Authors. Aquatic Conservation: Marine and Freshwater Ecosystems published by John Wiley & Sons, Ltd.
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The conservation and sustainable use of marine resources is a highlighted goal in a growing number of national and international policy agendas. Unfortunately, efforts to assess progress, as well as to strategically plan and prioritize new marine conservation measures, have been hampered by the lack of a detailed and comprehensive biogeographic system to classify the oceans. Here we report on a new global system for coast and shelf areas – the Marine Ecoregions of the World (MEOW) – a nested system of 12 realms, 62 provinces and 232 ecoregions. This system provides considerably better spatial resolution than previous global systems, while preserving many common elements, and can be cross-referenced to many regional biogeographic classifications. The designation of terrestrial ecoregions has revolutionized priority setting and planning for land conservation; we anticipate similar benefits from the creation of a coherent and credible marine system.
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Sawfishes are among the most endangered of all elasmobranch species, a factor fostering considerable worldwide interest in the conservation of these animals. However, conservation efforts have been hampered by the confusing taxonomy of the group and the poor state of knowledge about the family's geographical population structure. Based on historical taxonomy, external morphology, and mitochondrial DNA sequences (NADH‐2), we show here that, globally, the sawfish comprise five species in two genera: Pristis pristis (circumtropical), Pristis clavata (east Indo‐West Pacific), Pristis pectinata (Atlantic), Pristis zijsron (Indo‐West Pacific), and Anoxypristis cuspidata (Indo‐West Pacific, except for East Africa and the Red Sea). This improved understanding will have implications for the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), International Union for Conservation of Nature (IUCN) Red List assessments, and endangered species laws and regulations in several countries. Furthermore, based on both or either of NADH‐2 and the number of rostral teeth per side, we show that populations of P. pristis, P. pectinata, P. zijsron, and A. cuspidata exhibit significant geographic structuring across their respective ranges, meaning that regional‐level conservation will be required. Finally, the NADH‐2 gene may serve as a marker for the identification of rostra and fins involved in illegal trade. © 2012 The Linnean Society of London
Pristis pristis (Eastern Pacific subpopulation)
  • J Carlson
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Pristis pectinata. The IUCN Red List of Threatened Species
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Carlson J, Wiley T, Smith K (2013b) Pristis pectinata. The IUCN Red List of Threatened Species 2013: e.T18175A43398238. http:// dx.doi.org/10.2305/iucn.uk.2013-1.rlts.t18175a43398238.en. Accessed on: 2016-1-22.
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Order Rajiformes, batoids, suborder Pristoidei, sawfishes
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