Posted on May 28, 2002

The Exploitative History and Present Status of Marine Mammals in Barbados, W.I.

Joel Creswell
Environmental Studies Program
Macalester College
1600 Grand Ave., St. Paul, MN 55105-1899
jecreswell2000@yahoo.com


Abstract

Marine mammal exploitation in Barbados was different in nature and intensity than that of the surrounding islands, yet its impact on local whale stocks was similar: severe reduction.  Yankee whalers were present in the area as early as 1765, and a shore whaling industry developed in 1867, relying heavily on Yankee influences.  The success of the shore whaling industry peaked around the turn of the 20th century with catches as high as 36 whales per year, but the population crashed shortly after that, and the industry shut down in 1920.  The end of the Barbadian whale fishery is similar to that of Grenada’s, Trinidad’s, and Bequia’s.  Although the whaling industry at each place developed under different influences, used different equipment and methods, and operated in a different time period, each one was shut down due to a lack of whales caused by over-exploitation.

There is no historical or current record of dolphin exploitation, although several different species are present in the area.  There is no reliable evidence than manatees were ever present in the area, due mainly to the island’s outlying position from the arc of southeast Caribbean islands.

Present exploitation is limited to very rare incidental catches of dolphins in fishing nets.  Barbados is under pressure, however, to join the International Whaling Commission in order to promote commercial whaling.  The resumption of commercial whaling, the financial feasibility of which is questionable, would seriously threaten the conservation status of Barbados’ marine mammals.

Introduction

A common problem among ecologists is the assumption that the ecosystems they study were in pristine condition at the time they were first described in scientific literature.  When trying to quantify or describe the human impact on these systems, they use these first scientific descriptions as a baseline.  They should know better than any, however, that ecosystems are dynamic systems, constantly in a state of change.  Thus the concept of a pristine or baseline ecosystem is somewhat normative.  In addition to the changes ecosystems undergo in the absence of human influence, many have been subject to a particularly high degree of alteration since the beginning of human history, which is far older than the science of ecology.  What many ecologists suffer from, then, is a narrowness of focus: they only consult ecological sources when conducting research, thus neglecting a wealth of historical information that could account for gaps in scientific understanding.  This is changing, however.  As several recent papers demonstrate (Jackson, 1997; Romero et al., 1999; Jackson, 2001), looking at environmental issues from an historical perspective is becoming an increasingly popular way to gain insight into the pre-scientific use and exploitation of resources.

Historical studies are increasingly pointing to the idea that marine mammals in the Caribbean may be victims of neoextinctions (Mitchell, 1975; Mitchell and Reeves, 1983; Romero and Hayford, 2000; Reeves et al., 2001; Romero et al., 2002a; Romero et al., 2002b).  Because of the availability of historical, social, political, economic, and ecological information from post-Columbian times, neoextinctions in the Caribbean are relatively easy to study.  A key example of such an extinction is the local extirpation of the West Indian manatee (Trichecus manatus manatus) in most Caribbean islands since the arrival of Columbus (Marsh and Lefebvre, 1994).

Aside from the manatee, the exploitative histories of only few marine mammal species in the Caribbean have been studied.  In light of the exploitation known to have taken place, including aboriginal utilization, Yankee whaling, shore whaling industries, and dolphin fisheries, it is important to study the history of these animals, not only to ascertain the impacts of human activity, but also to better understand their present status.  The better their status is understood, the better-informed governments will be when making conservation decisions and managing populations.  This factor is particularly important, as there is pressure on several southeast Caribbean nations to join the International Whaling Commission (IWC) in order to support a return to commercial whaling (Anonymous, 2001b).

This paper aims to document the past and present utilization and exploitation of marine mammals in Barbados, and to ascertain the present status of local populations.  It complements a growing body of similar research in other parts of the southeastern Caribbean including Venezuela (Romero et al., 2001), Trinidad and Tobago (Reeves et al., 2001; Romero et al., 2002a), and Grenada (Romero and Hayford, 1999; Romero et al., 2002b).  All information presented will be analyzed in this historical context and compared to other countries, in an attempt to paint as complete a picture as possible of the exploitative history of marine mammals in this region.

Figure 1

Figure 1: Map of the island of Barbados, West Indies.

 

 

Figure 2

Figure 2:  A map of the Caribbean island chain.

Methods

This paper is largely based on field and archival studies conducted in Barbados from 24 to 7 April 2002.  We visited all known possible locations of whaling sites, all of them along the northern half of the west coast (Figure 1).  We interviewed local fishers about present locations and frequencies of marine mammal sightings in the following towns: Half Moon Fort, Six Men’s Bay, Weston, Holetown, Payne’s Bay, Bridgetown, Oistins, and Silver Sands (just west of Oistins).  Fishers were all asked where they fish, whether they see whales or dolphins while fishing, what types of each they see (they were asked to describe them rather than name species), how often they see each species, what time of year each species is seen, and how close to shore each species goes.  Caribbean terminology for marine species was used.  Thus when a fisher mentioned a “porpoise,” dolphin was recorded.  When “dolphins” were mentioned, it was assumed that fishers were discussing the dolphin fish, also known as dorado and Mahi Mahi (Coryphaena spp.).  “Blackfish” was interpreted as pilot whales (Globicephela spp.).  When a dolphin species was described as “Flipper,” bottlenose dolphin (Tursiops truncatus) was recorded.

We visited the Barbados Museum and Historical Society’s museum and library, the National Library Service, the National Archives, the Fisheries Division, the library of the University of the West Indies, Cave Hill Campus, and the West Indies Collection of the same library.  In addition, we examined the private collection of Mr. Charles, Mr. Elmer, and Ms. Ina Jordan.  At each place, we examined every available publication, record, or object related to marine mammals.  All pertinent items were photocopied, scanned, photographed, or noted.

Results and Discussion

Historical Account

Environment

Barbados is a small southeastern Caribbean island (Figure 1), 430 square km in size.  It is geologically distinct from the majority of Caribbean islands (Figure 2), which are volcanic and form an arc stretching from Venezuela to Cuba.  Barbados and Tobago, approximately 320 km to the south, are the only two islands that form a different island arc that is tectonic in origin (Watts, 1987) (Figure 3).  As a result of its formation, most of the bedrock in Barbados is biogenic limestone, which originated on the ocean floor.  The topography has been heavily altered by above-ground and subterranean freshwater flows, creating a large number of Karst caves and gullies.

There is archaeological evidence of prehistoric sperm whale and dolphin presence in Barbados, but none of humpback whales (Ray, 1964; Wing, 2000).  Humpbacks are mentioned in the earliest accounts of whaling around the island, however, showing that a population existed prior to the beginning of human exploitation (Anonymous, 1857-1858; Anonymous, 1862-1864; Anonymous, 1864-1866).  Like any marine species, a humpback remains have to be deposited on shore in order for them to be easily accessible to archaeologists.  Thus the lack of archaeological records for humpbacks is most likely the result of a low stranding rate.

Humpback whales migrate to the Caribbean in the late winter and spring months from their northern feeding grounds.  They spend their time in the Caribbean breeding and calving. 

Figure 3

Figure 3:  A map of the Caribbean islands showing the primary and secondary island arcs, based on on Watts (1987).

Humpbacks in the West Indies have been shown to have migrated from the Gulf of Maine, Newfoundland, the Gulf of St. Lawrence, Greenland, Iceland, and Norway (Martin et al., 1984; Clapham and Mattila, 1990; Stevick et al., 1999, Clapham, 2002).  The most heavily used breeding grounds in the Caribbean include Silver Bank, Navidad Bank, and Samana Bay, all in the Dominican Republic, as well as Mona Passage in Puerto Rico, and Virgin Bank (Smith et al., 1999).  By far the most popular among these sites are Silver and Navidad Banks, which may host as many as 85 percent of western North Atlantic breeding humpbacks (Winn et al., 1975).  The abundance of humpbacks further south in the Caribbean, among the Windward Islands, is low, probably the combined effect of Yankee and shore whaling in those areas.

Katona and Beard (1990) estimated the current size of the western North Atlantic humpback whale population to be between 2,888 and 8,122 (95% CI) individuals.  Whitehead’s (1982) estimate for the same group places the population between 2,000 and 6,000 individuals.  He also estimated that the peak population of humpbacks on Silver, Navidad, and Mouchoir Banks to be 2,000-3,500 individuals.  The population in these areas peaks in the winter months, when humpbacks are in the Caribbean breeding and calving.  Winn et al. (1975) estimates that 85 percent of breeding humpbacks are on these banks during the breeding season, which means that relatively few are distributed throughout the Lesser Antilles.  If Whitehead’s (1982) maximum estimate of peak population on Silver, Navidad, and Mouchoir Banks is correct (3,500 individuals), then at most, only around 620 animals inhabit the entire remainder of the Caribbean.

Humpbacks reproduce at a low rate, with females giving birth to only one calf at a time and with an inter-birth interval of 2 years, on average (Clapham, 2002).  They also exhibit a strong mother-calf bond, something which was easy for whalers to exploit.  If a humpback calf is struck or injured, its mother will stay with it as long as it is alive.  Likewise, the calf will not abandon a wounded mother.  This means that, in most cases, when either member of a mother-calf pair was attacked, usually both were killed.  Species exhibiting this trait are more susceptible to hunting pressures than others for this reason (Oldfield, 1988).

Unlike humpback whales, very little is known about the stock structure and migratory patterns of sperm whales.  Like humpbacks, they have a worldwide distribution, but their migratory patterns are not as clear.  Some groups of sperm whales follow a somewhat regular migration pattern of moving north in the summer and south in the winter, but these are mainly in mid-latitudes.  There is no clear seasonal pattern in the tropics (Whitehead, 2002).  There is significant evidence, however, that there is a single North Atlantic stock (Dufault et al., 1999), which includes the sperm whales present in the Caribbean.

Rice (1989) estimated that the pre-whaling North Atlantic sperm whale population consisted of 330,000 individuals, about 12 percent of his estimated worldwide population.  His estimate of the current North Atlantic population is 190,000 individuals, 10 percent of his estimated world total.  These animals range throughout the Caribbean, spending most of their time in areas where the water depth is greater than 1,000 m.  They tend to concentrate themselves in areas approximately 1,000 km across, which are often associated with islands where the depth increases quickly from the coast (Whitehead, 2002; Dufault, et al., 1999).  One such area, in which sperm whales are relatively highly concentrated, is Dominica, where they reach densities of up to .55 whales per square kilometer (Gordon et al., 1998).  There are few records for sperm whales around Barbados in scientific literature (Wing, 2000), and none in the whaling logbooks reviewed for this paper (Anonymous, 1857-1858; Anonymous, 1862-1864; Anonymous, 1864-1866) or in the much more extensive sample reviewed by Townsend (1935).  Swartz et al. (2001) spent a total of four days in Barbados on a recent visual and acoustic survey of the Caribbean, and recorded no sightings of sperm whales.

Sperm whales, like humpbacks, have low fecundity, with females not reaching sexual maturity until age nine, and with a gestation period of 14-16 months.  Calves are born singly (Whitehead, 2002).  Sperm whales also exhibit a strong mother-calf bond, such that the pair will stay close together even if one is struck by whalers.  Thus, like humpbacks, when one member of a sperm whale mother-calf pair is killed, the other is usually killed also (Oldfield, 1988).  The combined result of these characteristics is a low rate of recovery from hunting pressures, like humpbacks.

Unlike whales and dolphins, there is no evidence that manatees ever inhabited Barbados.  There is one record of a sighting of a live manatee on the island, but it is unreliable, as it is not accompanied by any description, and is not consistent with the majority of the literature on the subject (Schomburgk, 1848).  The lack of manatees probably has to do with Barbados’ location outside the primary arc of Caribbean islands (Figure 3).  Because it is far away from its neighbors, and far east of most of them, it would be difficult for a manatee to migrate.  The dominant wind and ocean currents in the latitudes of the Lesser Antilles move from east to west.  In addition, manatees are not long-distance swimmers, and are dependent on shallow-water ecosystems for feeding.  Thus any migrating manatee would not only have to travel a long distance to reach Barbados, it would have to do so against the dominant wind and ocean currents, and without feeding for the duration of the journey (Rouse, 1964).

Although present conditions would not support manatee migration, it is possible that at some point in the manatee’s history in the southeastern Caribbean, the oceanography of the area was better suited to long-distance movements.  For example, at the end of the last glacial maximum (21,000 YBP), sea levels around Barbados are believed to have been 120 m lower than today (Peltier, 2002).  This would have enlarged Barbados’ land area, and would have created shallow-water habitat closer to the island’s nearest neighbors.  However, this would only have moved the shallow water surrounding Barbados several kilometers closer to the primary island arc.  Thus, unless wind and ocean currents moved from west to east at the end of the last glacial maximum, it is unlikely that manatees would have been able to migrate to Barbados at that time either.  Despite the fact that Barbados has some suitable manatee habitat, such as the Constitution River in Bridgetown, there is no evidence that a manatee population was ever established there.

Barbados is one of very few Caribbean islands for which there are no records of manatees (Lefebvre et al., 2001).  In addition to Barbados, this group includes Montserrat, Dominica, Nevis, San Eustatius, Saba, St. Bartholomew, St. Martin, Anguilla, and Tobago (Romero, 2002).  All of these islands except for Barbados, Tobago, Montserrat, and Dominica are very small and have no freshwater, and thus no manatee habitat.  Montserrat is volcanic, and has a long history of cataclysmic eruptions, so it is possible that there were once manatees there that were wiped out.  Tobago, like Barbados did not have manatees due to its location outside the primary arc of islands.

Manatees were wiped out from all of the Caribbean islands between Puerto Rico and Trinidad, due largely to hunting (Lefebvre et al., 2001).  There are several reasons for this.  Manatees are an easy target for hunters, being large, slow-moving, docile, and inhabiting shallow waters.  They also have a significant amount of fat, making their meat highly nutritious.  They have a low fecundity, with gestation lasting up to 400 days, calves born singly, and an inter-birth interval of 2.5 to 3 years (Husar, 1977).  In addition, females do not reproduce for the first time until they are 6-10 years old.  The combined effect of these characteristics is that manatees have little ability to recover from hunting pressures on their populations (Jackson, 2001).

Human History

The name Barbados comes from a name given to the island by a Portuguese mariner sailing to Brazil.  He named it Las Barbudos, meaning “the bearded ones,” after the bearded fig trees he saw growing in abundance there (Sinckler, 1914).  There is some controversy over whether the name refers to the fig trees or whether it was given in reference to a bearded race of Indians inhabiting the island.  The fig tree theory is generally more accepted, however, as the first official seal of the island bears the picture of a bearded fig tree.  Whether or not bearded fig trees were actually seen by early mariners passing Barbados is uncertain.  Although the trees do exist in Barbados, they are not extremely common.  A more likely explanation of what the early sailors saw is various different species of trees with Spanish moss (Thilandsia usneoides) growing on them, which makes them appear similar to bearded fig trees (Aldemaro Romero, 2002, personal communication).

The first known human inhabitants of the island were Amerindians, the Arawak, who were named for their language group.  They migrated northward through the Lesser Antilles (the southeast Caribbean island arc, stretching from Venezuela to Puerto Rico, Figure 2) from South America around 1,750 Years Before the Present (YPB).  This first group of Arawak is known as the Saladoid, and is distinguished from other Arawak groups by its pottery style.  Another Arawak group, the Barrancoid, was less vigorous in the West Indies than the Saladoid, and is known to have reached Trinidad sometime later.  The most prominent Barrancoid settlements are in the Dominican Republic, although there is evidence of Barrancoid presence throughout the Lesser Antilles (Rouse, 1964).

Barbados’ next settlers, the Carib, were another Amerindian group.  They began colonizing the Lesser Antilles around 1,000 YBP, following the same route as the Arawak, and, in most cases, driving them northward as they migrated.  Some evidence suggests, however, that Barbados was home to a mixed population of Caribs and Arawaks, possibly the result of the Carib killing Arawak men and marrying the women (Rouse, 1964; Watts, 1987).  The Carib reached Barbados around 800 YBP.  The island was consecutively inhabited by these two Amerindian groups for a total of about 1250 years.  Their presence in Barbados ended sometime around 1500, when the Spanish arrived to capture and enslave the Carib (Sinckler, 1914; Rouse and Cruxent, 1963; Tree, 1972).  Columbus discovered Cubagua’s pearl beds in 1498, and large-scale exploitation of them, involving the use of Amerindian slaves from neighboring islands as divers, began shortly thereafter (Romero et al., 1999).  In addition, the Spanish Cédula (royal decree) of 1511 allowed Caribs to be taken as slaves to work in the mines of Puerto Rico (Tree, 1972).  Thus Caribs were taken as slaves to meet Spain’s rising labor demand in the region, which resulted in Barbados being uninhabited from 1500 until the early 17th century.

Much of Arawak and Carib subsistence and culture in the Lesser Antilles was based on marine organisms.  The vast majority of Amerindian settlements on the island were in coastal areas, and much of the waste found in their middens was the remains of marine organisms. Animal protein made up around 33 percent of the caloric yield of the Arawak diet, and probably a similar percentage of the Carib diet.  Fish provided 47 percent of that animal protein.  Fishing was done near the shoreline, using nets as well as hook and line (Watts, 1987).

In addition to fish, on some islands, marine mammals made up a portion of the Carib and Arawak diet.  There are records of manatee bones in Arawak middens on many southeast Caribbean islands, and although an exhibit at the Barbados Museum and Historical Society mentions findings of manatee bones in Barbados, this claim is not supported by the literature.  In other areas, manatee flesh was eaten, and the bones were used to make tools, ornaments, and musical instruments.  They were easy to capture, given their slow speed and shallow water, often inland habitat.  A single manatee yielded an average of around 440 kg of meat, plus some fat, making it an excellent, easily exploitable food source.  They were hunted from canoes, using harpoons with floats and ropes attached (Rouse, 1948; McKillop, 1985; Watts, 1987).

Sperm whale bones have been found in Amerindian middens in Barbados and Tortola, Virgin Islands (Wing, 2000).  There is no evidence, however, that they were ever hunted by Arawaks or Caribs.  Neither group had sufficient technology to pursue large whales in the open ocean (Watts, 1987; Sutty, 1995).  These bones most likely came from stranded animals that the Indians utilized.  Thus sperm whales were not an important part of the Amerindian subsistence, as they were only utilized when the rare opportunity arose.  This means that manatees were the only marine mammal to make up a regular part of the Amerindian diet.  Because these were not present in Barbados, the marine mammal utilization of the Arawak and Carib there was almost zero.

During the hiatus in human habitation, between when the Carib were removed and the arrival of the British, the only visitors to Barbados were the Portuguese, whose ships stopped there to replenish freshwater supplies on the journey to and from Brazil.  The main lasting effect they had on the island was the introduction of pigs, which were left behind by Pedro á Campos, a Portuguese sailor, in 1563, for breeding purposes, so that they could eventually provide food for passing sailors (Sinckler, 1914).  They established quite a successful feral population, and eventually, the island became a supply point for meat as well as fresh water.  The pigs were still present when the British first arrived in 1625, but there is no feral pig population in Barbados today.

The British established a colony in Barbados in 1627 (Sinckler, 1914) and governed the island until 1966, when it was granted independence.  Under British rule, Barbados was cleared for agriculture and became a major producer of sugar.  By the middle of the 17th century, African slaves, brought over to work on sugar cane plantations, vastly outnumbered British residents.  It is descendents of these Africans who make up the majority of the population today.  There are similar stories behind the ethnic makeup of most of the other Caribbean islands.

Yankee Whaling

Under British rule, Bridgetown became a busy port and Barbados a regular stop on the routes of many cargo, passenger, and whale ships.  At the peak of the shipping industry, several ships were arriving at and departing from Bridgetown every day (Anonymous, 1839).  Although the whaling vessels’ purpose in going to Barbados was to replenish supplies and recruit crew members, and was not specifically to look for whales, humpbacks are described by the ships’ record keepers as “plentiful,” just outside Bridgetown Harbor (Anonymous, 1857-1858; Anonymous, 1862-1864; Anonymous, 1864-1866).  Thus whales were often taken in Barbados waters.  There is even a record of a bull humpback whale being taken in Carlisle Bay (Figure 1), by the Bark Messenger on 19 March 1859 (Anonymous, 1959).

The Yankee whalers used boats to catch and kill whales.  When a whale was spotted from on board the ship, rowboats would be lowered to pursue it.  They would strike it with a harpoon attached to a rope, the purpose of which was to catch, but not necessarily kill the whale.  Generally, after it was struck, the whale would either take the boat on a wild chase at the surface, or would sound (dive deeply), out of self-defense.  Once the animal was tired enough to be approached by the boat again, it would be killed using a lance, similar to that in Figure 4, which would sometimes contain explosives, so that it would kill the animal quickly.

Once dead, the whale was dragged to the ship, where it was fastened to the hull with chains.  The jaw and head were cut off and raised up to the deck, and then cutting stages were lowered, so that the whale could be flensed (have its blubber cut off) while still in the water.  The blubber was taken into the ship through hatches, and boiled down to oil on deck.  Once cooled, the oil was casked and stored (Ellis, 2002).

The blubber oil and spermaceti brought in by the whaling industry was in high demand for a number of uses.  Blubber oil was yielded by both sperm whales and humpbacks, but spermaceti was only found in sperm whales, and indeed, the name “sperm whale” is shortened from its earlier name, “spermaceti whale.”  Spermaceti was thus named because of the resemblance it bears to semen, its roots being sperma, Latin for sperm, and ceti, Latin for whale.  The primary use of the blubber oil and spermaceti was as lamp fuel.  Spermaceti was also used to make candles.  Other uses included high-pressure lubricant, an ingredient in hydraulic fluid, ink, detergent, cosmetics, as a tanning agent for leather, and a degreaser for wool.  By the time the whaling industry was in decline, several substitutes for whale oil had been developed, the most popular of which were petroleum products and jojoba oil (Rice, 2002).

The two species of whale most heavily hunted in the southeastern Caribbean were the humpback and the sperm whale.  Because these are migratory and have a worldwide distribution, we cannot assess the impact of Yankee whaling on Barbadian or Caribbean whale stocks, but instead the impact of whaling in Barbados waters on the entire North Atlantic populations of humpback and sperm whales.  Pre-whaling estimates of population sizes exist only for sperm whales, not for humpbacks, and the sperm whale estimates are for the entire North Atlantic.  Thus we cannot measure the exact impact of whaling on these stocks, but we can look at present numbers and make estimates of the impact based on evidence in whaling logbooks and literature sources.

Although the size and geographic distribution of the pre-whaling humpback population is not known, the current southeastern Caribbean population estimate of 620 whales would have been able to support a sizeable whaling industry for over a century.  This claim is supported by Mitchell and Reeves’ (1983) estimate that, between 1866 and 1887, Yankee whalers killed 2,421 humpbacks in the Caribbean.  This is a kill rate of 115 whales per year.  At that rate, a population of 620 whales would have been wiped out in 5.5 years.  This means that the pre-whaling humpback population in the Caribbean must have been substantially larger than it is today.  These data support the fact that humpbacks’ ability to recover from heavy whaling pressure is low.  No humpbacks have been hunted in the Caribbean for the better part of a century, yet their population remains low.

It is interesting to note that relatively little effort was devoted by Yankee Whalers to humpbacking in sites in the Greater Antilles that are known to have high abundances of the whales today.  Places such as Samana Bay and Mona Passage were all but ignored by whale ships, despite the fact that the occasional whaler had extraordinary success in these waters.  The whalers preferred locations in the Windward Islands such as Bequia, St. Lucia, and Trinidad, all places in which humpbacks are presently scarce (Reeves et al., 2002).  This suggests that whale populations in the southeastern Caribbean were once much higher, perhaps as high as the populations in Samana Bay and Mona Passage today, but that they were greatly reduced by whaling.  By the same logic, the lack of whaling in the Greater Antilles offers the most likely explanation of their current high abundance in that area.

At the peak of the American whaling effort, in the 1830’s, about 5,000 sperm whales per year were being killed by whalers, worldwide (Whitehead, 2002).  In addition, during the 18th century, at times, there were as many as 25 ships were in the West Indies hunting whales (Duerden, 1901).  According to Rice’s (1989) estimates of a pre-whaling North Atlantic population of 330,000 and a post-whaling population of 190,000, this group of sperm whales lost 45 percent of its members as a result of whaling.  According to Goode (1884), “There is no reason to doubt that Sperm Whales were at one time, nearly two centuries back, as abundant in the North Atlantic as in more recent years in the North Pacific.  The vigorous prosecution of the whale fishery since the early part of the eighteenth century by American vessels has had much to do with their present scarcity.”  Exactly how much of this whaling took place in the Caribbean, however, is not known.  According to Townsend (1935), sperm whaling in the West Indies was practiced to a limited extent, and only between February and May.  It is unlikely that sperm whales were hunted in Barbadian waters, due to the fact that they were not sighted by whaling ships in the area.

Sperm whaling declined in the latter half of the 19th century, due mainly to the introduction of substitutes for sperm whale products, but also somewhat to the depletion of the stock (Whitehead, 2002).  The depletion of the sperm whale stock, however, was not as severe as that of the humpback whale stock.  This can be seen in the population numbers, as the highest current estimate of the North Atlantic humpback population is 8,122, while the estimate of the sperm whale population in the same area is 190,000.  The difference in the level of exploitation can also be seen in the fact that sperm whaling was resumed after the end of the Yankee industry (although not by American ships) around the 1940's, with catches of up to 30,000 whales per year (Whitehead, 2002).  Humpback whaling was never resumed after it ended in the early 20th century.

Shore Whaling

The first record of a whale being taken in Barbados by a shore-based whaler is from 1813, and the whale is described as a “Grampus,” more commonly known as Risso’s Dolphin (Grampus griseus) (Schomburgk, 1848).  Based on its dimensions, however, Mitchell and Reeves (1983) believe it to be a young humpback.  Regardless, however, this date marks the beginning of shore whaling in Barbados, although a commercial whaling industry did not begin operation until 1867 (Reeves et al., 2002).

Barbados’ shore whaling industry was started by former crew members of Yankee whaling ships.  Ever since 1765, when the first New England whaling ships visited the West Indies and the Caribbean, whalers would recruit Barbadians to join their crews when they stopped at Bridgetown (Hohman, 1928).  These Yankee Whalers frequented Barbados, which was the central supply port to ships in the West Indies in the 18th and 19th centuries (Goode, 1887; Hughes, 1961).  Death and desertion of crew members was not uncommon on whaling ships, so there was often a need to recruit locals when the ships stopped for supplies.  Some of these Barbadians who had worked on whaling ships returned home after the voyages, having gained the necessary skills to hunt whales, and started their own operations (Rathjen and Sullivan, 1970; Caldwell and Caldwell, 1971; Adams, 1994).  This is similar to the origins of shore whaling in Bequia (Adams, 1971) and Grenada (Romero and Hayford, 2000), but quite different from that of Trinidad (Romero et al., 2002a), which developed its shore whaling operations independently from foreign influence.  This is also quite different from Venezuela, whose only shore-based marine mammal exploitation is a dolphin fishery (Romero et al., 1997).

There were three shore whaling stations in Barbados.  The first, which operated from 1867 to 1920, was in Speightstown (Figure 1) and was owned by Mr. C. H. P. Jordan at the end of its operation.  The original owner is not known (Brown, 1942).  The second was also in Speightstown, located immediately next to Mr. Jordan’s, and was owned by Allan O’N. Skinner prior to being shut down (Elmer Jordan, 2002, personal communication).  The third was in Holetown (Figure 1) and began operation in 1869 (Reeves et al., 2002), under the ownership of Mr. A. Archer (Caldwell and Caldwell, 1971).

Barbadian shore whaling, unlike Yankee ship-based whaling, was largely opportunistic.  The shore whalers set out to capture a whale only after it had been spotted from shore first, as opposed to the American whaling ships, which sailed all over the world in search of whales.  When a whale was spotted, the whaling crew would set out in boats to pursue it.  The boats used were 7.62 to 9.14 m (25 to 30 ft.) long, rigged with sails as well as oars, and each had a crew of 14.  The oars were used for maximum steering and control when pursuing a whale, and the sails at other times.  They would use a harpoon to capture the whale and an explosive lance, known as the bomb lance, to kill it (Figures 4 and 5).  They would then jump into the water and sew its mouth shut, to prevent it from filling with water and sinking.  Rather than hauling it aboard a ship at this point, they would drag it ashore, alongside the Speightstown jetty in Speightstown or on the beach in Holetown, for flensing (Figure 6).  The whale would be flensed on the beach and the blubber would then be boiled in copper kettles, of the same design as those used to boil sugar cane juice in the production of sugar (Figures 7-9).  Indeed, the boilers used by the Jordan whaling station in Speightstown were sold to a sugar factory after the station closed (Brown, 1942; Bair, 1962; Yates, 1998; Elmer Jordan, 2002, personal communication). 

Figure 4

Figure 4: A dismantled bomb lance, belonging to Charles Jordan.

  Figure 5

Figure 5: A whaling gun, from which the bomb-lance was shot, belonging to Charles Jordan.  Being demonstrated by Aldemaro Romero.

Figure 6

Figure 6: The Speightstown jetty, circa 1911.

Figure 7

Figure 7: A copper boiler used by the C.H.P. Jordan whaling station in Speightstown, currently belonging to Elmer Jordan, top view.

Figure 8

Figure 8: A copper boiler used by the C.H.P. Jordan whaling station in Speightstown, currently belonging to Elmer Jordan, bottom view.

Figure 9

Figure 9: A sugar-boiling house, with a boiler similar to those used in the whaling industry pictured in the foreground, date unknown.

Once it had been boiled down, the oil was put in barrels, it was exported to England (Yates, 1998) and Canada (Geoffrey O’N. Skinner, 2002, personal communication).  The bones were ground and used to make fertilizer.  The meat was sold locally for consumption, and was reportedly very nourishing and preferred to beef, and was “used as a food by the negroes” (Skinner, 1914).  The baleen plates were used to make brooms.  In these different ways, the entire whale carcass was used, although the main generator of profit for the whaling operation was the oil (Anonymous, 1959).

After the closure of the Speightstown whaling station owned by C.H.P. Jordan in 1920, rather than being sold or converted to fishing vessels, the two whale boats that remained at that time were taken to Grenada.  Ernest Greaves, the last whaler employed at the Jordan station, operated in Grenada, using those boats, from 1920 to 1923.  He found ample whales there, but apparently, the tide was too strong to run under sail, so he sold the boats there and went to work for the Norwegian whale fishery on Glover Island, a small island off Grenada’s south coast.  Thus there is a direct connection between the Barbadian and Grenadian whale fisheries, although the whaling methods employed by the Norwegians in Grenada do not show signs of Barbadian influence (Marsland, 1925; Brown, 1942; Romero and Hayford, 2000).

The opportunistic nature of the Barbadian shore-based whale fishery is similar to that of Trinidad, but very different from Grenada and Bequia.  In Grenada, Norwegian whalers actively sought whales in ships (Marsland, 1925), while in Bequia, spotters on shore would look for whales and signal crews out on whale boats using mirrors (Adams, 1971).  This is because of the scope of the industry in each country.  In Barbados and Trinidad, whaling operations were owned by local business families, and were one of several ventures in which each family was involved (Elmer Jordan, 2002, personal communication; Romero et al., 2002a).  Whaling was not their primary source of income.  In Grenada, although the first whaling venture was started up by a local banker as a side business, a Norwegian whaling company soon became involved, and considerable capital was invested.  Whaling was the primary business of the people running this operation.  By 1925, two ships were cruising the waters of Grenada in search of whales, full time, with a third ship added to the effort in 1926 (Romero and Hayford, 2000).

The boats used in Barbados are different from those used anywhere else in the southeastern Caribbean.  Trinidad used pirogues, small, wooden fishing boats, which were oar-powered.  These had a crew of six rowers and one harpooner in the bow (Romero et al., 2002a).  Bequia used 7.62-7.92 m (25-26 ft.) open sailing boats, modeled after those built in Nantucket.  These had a crew of six, including the harpooner and the captain (Adams, 1971).  The boats in Grenada were modern Norwegian whaling ships, which were steam-powered, unlike the oar-powered boats of the neighboring countries, cruised at a speed of 11 knots, and could tow up to five whales (Marsland, 1925).  They could be operated by a relatively small crew, as they did not need rowers.  The large crew and medium size of the Barbadian boats makes them substantially different from any others in the area, demonstrating that the whaling industries of many neighboring southeast Caribbean countries had little contact with each other.

The whaling stations in Barbados are also different from those in other Caribbean countries.  The Barbadian stations consisted of a shack in which whaling gear was stored.  There were no permanent buildings.  All of the operations of the whaling industry that took place on shore were carried out on the beach (Elmer Jordan, 2002, personal communication).  This is similar to the construction of stations in Bequia.  The Bequia stations had a small shed for storing blubber and a small structure that supported their boiling kettles, but no buildings of substantial size (Adams, 1971).  These stand in stark contrast to Grenada, whose station on Glover Island was a two-story building with a concrete chute for dragging whales up to a flensing platform (Romero and Hayford, 2000).  In between Grenada and Barbados in terms of technological advancement were the stations in Trinidad.  These were one-story buildings with no structures to assist with bringing whales onto the beach, as whales were flensed in the water (Reeves et al., 2001; Romero et al., 2002a).  Thus the Barbadian stations were the most primitive of the three types found in the southeastern Caribbean.

In Trinidad’s and Bequia’s whaling industries, there are reports of sharks attacking whale carcasses and eating the blubber (de Verteuil, 1858; Adams, 1971).  The economic losses due to sharks were significant enough that Trinidadian whaling stations employed men with axes to kill sharks and Bequia whalers would lance sharks from the whale boats while whales were being brought ashore.  Although there are similar reports of sharks attacking whale carcasses in Barbados (Elmer Jordan, 2002, personal communication), the Barbadian operations never employed anyone to kill the sharks.  In fact, the whalers could reportedly walk through the water in the midst of the frenzied sharks and not be harmed.

There were wide fluctuations in oil production over the duration of the industry, however, the average annual production between 1889, the first year production rose about 100 barrels, and 1902, described as the last successful season, was 289 barrels per year (Figure 10).  According to Bair (1962), 10-20 whales were killed per year during the peak of the industry, presumably during this time span (Figure 11).  Based on Mitchell and Reeves’ (1983) estimate that the average humpback whale yields 25 barrels of oil, the average number of whales taken per year between 1889 and 1902 is 11.6.  This estimate is based entirely on whales processed by the Barbadian shore whaling industry.  Mitchell and Reeves include in their paper methods of factoring in the number of humpbacks killed but not recovered, including whales killed but lost, struck but lost, struck and lost with major wounds, struck and lost with whaling gear still attached, and the number of calves orphaned.  Without detailed catch data, however, such as the whaling logbooks Mitchell and Reeves used, it is impossible to accurately estimate this loss factor.  Like in the American humpback fishery, on which Mitchell and Reeves’ analysis is based, there was no doubt a loss factor in the Barbadian shore fishery, but lost whales were not recorded.  It is certain, however, that, due to losses, the number of whales landed is lower than the total number of whales killed.  The total number of whales killed in the Barbadian shore whaling industry, based on Blue Book data and Schomburgk (1848), is 187.  

Figure 10

Figure 10: Total number of barrels of whale oil exported from Barbados and its total value (in British pounds).  Based on Blue Books for Barbados.

Figure 11

Figure 11: Total number of whales landed annually, based Blue Book data and an estimate that one whale yields 25 barrels (Mitchell and Reeves, 1983).

The Barbadian whale oil export market exhibited a normal economic relationship between supply and demand (Figure 10).  The value of oil remained relatively constant at low levels of production, but when production increased dramatically, the price of oil dropped substantially.  Other than the one-year peak in 1907, the price of whale oil in the 20th century never returned to its previous high value.  Indeed at the peak of production, in 1901, the price per barrel dropped below £1.  The fact that the price per barrel remains relatively low after the peak suggests that the market was saturated in those years.  It also suggests that the demand for whale oil was decreasing, which it was in the early 20th century, as people began to substitute alternatives for whale products.  The same factor contributed to the demise of Trinidad’s whaling industry.  From the 1870's onward, there was an overproduction of whale oil and kerosene was being used as lamp fuel, instead of whale oil.  Thus the price for whale oil plummeted (Romero et al., 2002a)

There was often significant competition between the stations in Speightstown over whales.  Because the stations were next to each other, they both saw whales at essentially the same time and would race to be the first one to strike it.  In 1904, the government passed the Fisheries Regulation Act, updating all of Barbados’ fishing regulations and consolidating them into a single bill (Appendix II).  This included laws governing competition between whaling boats from different operations, probably as a response to quarrels between the two stations.  These laws include provisions that establish ownership of a whale by the first boat that strikes it and the ownership of a mother by a boat that strikes her calf, and vice versa.  They even detail how profits and expenses are to be split if two boats happen to strike the same whale (Archer and Fergusson, 1944).

A similar law exists in St. Vincent and the Grenadines, governing the whale fishery at Bequia.  Written only a few years earlier than the Barbados law, in 1887, the “Whalers Ordinance of 1887” lays out many of the same rules as the Fisheries Regulation Act.  The Whalers Ordinance was the result not only of quarreling, but also of hostile behavior between whaling companies, such as boats ramming each other and whalers scaring whales away to prevent their competitors from catching them (Adams, 1971; Beck, 1986).

The fact that there were two whaling stations in one place, scouting and competing for the same whales, probably means that a relatively high percentage of the whales that passed Speightstown during the years of the stations’ operation were taken.  If a whale were passing along the west coast, heading south, the chances of it making it past the two stations and Speightstown and another at Holetown, 7 km south (Figure 1), would have been slim.  This intensity of whaling is probably the most important contributor to the vast reduction in humpback whale populations passing along Barbados’ west coast.

The most common explanation for the end of the Barbadian whaling industry is related to the intensity of the whaling on the west coast.  The argument is simply that the whale stock was depleted and did not recover.  This is the explanation given by Earnest Greaves, the “last survivor” of the Speightstown whaling industry (Brown, 1942).  He remembers 1902 to be the last really successful whaling season.  Elmer Jordan agrees that whaling stopped because the whales were depleted (Appendix III).  The export data support this (Figure 10).  In 1902, 405 barrels were produced.  This is the middle of a sharp drop from the absolute peak in production, in 1901, when 919 barrels were produced.  The decline ended in 1904 with only 12 barrels being produced.  Although production increased again in 1906, to 250 barrels, it never returned to its high levels of the turn of the century.

These production data provide further support for the premise that the whaling industry ended due to depletion of the whale stock.  As figure 10 shows, despite minor oscillations, the production curve gradually increases from the first year records were kept, 1876, until the peak in production in 1901.  After 1901, it falls sharply and never recovers.  Another small peak in 1906 is followed by decline and 10 consecutive years of no production whatsoever, after which the industry shut down.  This trend suggests that as the intensity of whaling increased, the whale population became less able to recover and was eventually eliminated.

A further factor supporting the hypothesis that whaling ended because the whales were eliminated comes from a look at migratory patterns and whaling histories of other Caribbean countries.  Because some whales migrated across the entire Caribbean Sea, from north to south and back, to their preferred breeding and calving grounds, they would pass many islands on the way.  Any whale killed by a whaling operation may be one that had already reached its destination and was resting in its winter habitat, or it may be one that was en route to another area.  This means that whales traveling as far south as Barbados would have been at risk from several whaling operations before even entering Barbadian waters.  Thus the whaling industry in Bequia, which was in operation at the same time as the one in Barbados, may have impacted Barbados’ whale stocks.  Likewise, Barbadian whaling probably influenced Trinidad’s whale stocks.

This experience in Barbados is similar to that of Grenada and Trinidad.  Grenada followed a similar trend of increasing production, but on a much shorter time scale than Barbados.  Large-scale whaling in Grenada took place for only seven years, from 1920 to 1926.  The peak in production was in 1925, when 105 whales were taken.  The following year, 72 whales were taken, and by 1927, not a single whale was taken, and the industry was dismantled.  The decline in whale populations is cited as a major reason behind the end of Grenada’s industry.  Trinidad’s production did not take off as fast as Grenada’s.  The island’s first whaling station opened around 1826, and by 1830, 14 or 15 whales had been killed.  Between 1830 and 1862 between 20 and 35 whales per year were captured.  Then, around 1865, commercial whaling ceased.  The local extinction of humpback whales, the primary species exploited, is cited as the primary reason behind the cessation of whaling (Romero and Hayford, 2000; Romero, et al., 2002b).

Another explanation as to why fewer and fewer whales were returning to Barbados had to do with a structural change in the sugar industry.  In the late 19th century, when shore whaling began, there were 200-300 sugarcane-grinding windmills and boiling houses around the island, one at each plantation.  In the early 20th century, those windmills and boiling houses closed down as growers began sending their cane to factories to be processed.  When boiling houses were numerous, many people claimed that the sweet smell of cane juice could be smelled 20 miles out at sea.  They believed that this smell brought the whales close to shore, and that once the factories were built, the smell was no longer strong enough to attract the whales, which is why they stopped coming (Stoute, 1975).  This explanation is unlikely, due to the fact that both toothed and baleen whales, such as the sperm and the humpback, respectively, have an underdeveloped and probably nonfunctional sense of smell (Edinger, 1955; Wartzok and Ketten, 1999).

Present Status

Present threats to marine mammals in Barbados are limited to incidental catch in fishing nets, and the paucity of incidental catch reports suggests that this is minimal (Christopher Parker, 2002, personal communication).  The primary use of nets by Barbadian fishers is to catch flying fishes (Chelipogon spp., Cypselurus comatus, Exocoetus spp., Hirundichthys spp., Oxyporhamphus micropterus, Parexocoetus brachypterus, Prognichthys gibbifrons), for which 41-45mm mesh gill nets are used.  The nets are between 10-30m long and 3m deep.  These potentially put at least three species of cetaceans at risk: the bottlenose dolphin, short-finned pilot whale, and unidentified species of spotted dolphins (Vidal et al., 1994).

The low abundance of marine mammals in Barbados’ waters is similar to the situation in Grenada and Trinidad (Romero et al., 2000).  Populations in both of these islands were heavily impacted by their whaling industries, resulting in very few present-day sightings.  Trinidad does not have any whale or dolphin watching enterprises, and Grenada has only two.  The lack of major industries in this area could be due as much to both islands’ lack of a serious tourist industry, however, as to a lack of marine mammals.  And although it is significant that Grenada has whale and dolphin watching businesses, since Trinidad and Barbados do not, it is important to note that the operations target local resident populations of dolphins and sperm whales, neither of which were heavily commercially exploited, like the humpback.  Trinidad has a small population of manatees, which tourists are sometimes allowed to visit, but they are confined to a small swamp on private land along the central east coast of the island.  Sightings of marine mammals in both places, like in Barbados, are limited primarily to those made by fishers, who spend a significant amount of time on the water.

In sharp contrast to Barbados, Tobago, St. Vincent, Bequia, and St. Lucia all have large numbers of marine mammals in their waters, and sightings are common.  Tobago even has a dolphin watching tour company serving its small but growing tourism.  St. Vincent and the Grenadines and St. Lucia have enough marine mammals present even to carry support small whaling operations (Hoyt, 1994).  They are the only two Caribbean countries that have whaling allowances from the International Whaling Commission.  St. Lucia has an allowance of two humpbacks per year, and St. Vincent and the Grenadines has an aboriginal whaling allowance of three humpbacks per year (Agard and Gobin, 2000).

Marine mammals are not a common sight in the waters around Barbados.  This is evidenced by the fact that there are no dolphin and whale watching operations for tourists, despite the fact that tourism is the largest contributor to the national economy (Pariser, 2000).  Many Barbadians are not aware that there are whales and dolphins in their waters.  According to reports from fishers, however, dolphins and whales, mostly bottlenose and humpback, are present (Appendix III).  The bottlenose dolphins are present year-round, but do not often get closer to shore than a few miles.  The humpbacks go close to land, sometimes as close as 200 or 300 m, but are a seasonal presence, with most of them passing Barbados from March through May.  There are also occasional reports from fishers of sightings of other species, such as sperm whales, killer whales (Orcinus orca), and pygmy sperm whales (Kogia breviceps).  There are literature records for Cuvier’s beaked whale (Ziphius cavirostris), short-finned pilot whale (Globicephela macrorhynchus), bottlenose dolphin, spotted dolphin (Stenella frontalis), Stenella spp., sperm whales, humpback whales, bowhead whales (Balaena mysticetus), Risso’s dolphin, and common dolphin (Delphinus delphis) in Barbados (Caldwell et al., 1971; Swartz et al., 2001).

Barbados’ lack of a whale or dolphin watching industry is probably the result of two factors.  First, based on fishers’ reports, dolphins are never seen closer than 1.6 km from shore, and the majority of sightings are several kilometers out.  This means that boats would have to travel several miles to reach an area where dolphins could be seen, which would make tours long and expensive.  Also, once they are several kilometers away from the shore, boats would have to search a very large area to find dolphins.  Thus the likelihood that any individual tour would see any dolphins is not high enough to make the venture profitable (Best, 1999).

The second factor is that the majority of the whales in the area are migratory.  Although they pass close to shore, they are only present a few months out of the year.  In addition, no individual pod of whales spends a significant amount of time in one area.  Because Barbados is merely a point along their migratory pathway, they do not stop there for long periods of time.  Thus the likelihood of seeing a whale on any given tour is also too low to support a tourist operation.

Some argue that instead of attempting to pursue whale and dolphin watching, it would be more economically feasible for Barbados and several other southeast Caribbean countries to resume whaling.  The main proponents of this idea are Grenada, Dominica, Antigua, St. Kitts and Nevis, St. Lucia, and St. Vincent and the Grenadines.  They argue that the IWC’s international ban on whaling is not supported by sufficient scientific data, but is rather a form of “Eco-Posturing” (Alleyne, 2001).  They, along with China, Japan, and Norway, are attempting to form a pro-whaling voting bloc within the IWC to pass a resolution allowing what they call sustainable use of marine resources.  Their primary opponents, Australia, New Zealand, the United States, Britain, France, Brazil, Germany, Monaco, Italy and Mexico, base management decisions for whale stocks on much more grave population assessments, and thus feel justified in banning whaling (Alleyne, 2001; Anonymous, 2001a).

Japan’s main interest in the issue lies in the fact that it is one of the few countries that has continued to whale since the IWC whaling moratorium in 1986.  Japan has been operating under a permit that allows whaling for scientific purposes, however, much of the meat from the whales taken ends up in supermarkets.  The whales actually being taken also differ from what Japan reports to the IWC.  A recent genetic study of whale meat in Japanese supermarkets showed that such species as sperm whales, killer whales, dolphins, porpoises, fin whales (Balaenoptera physalus), sei whales (Balaenoptera borealis), Bryde’s whales (Balaenoptera edeni), blue whales (Balaenoptera musculus), gray whales (Eschrichtius robustus), and humpback whales are among those captured.  Japan’s scientific whaling permit only allows for the capture of minke whales (Balaenoptera acutorostrata), and these must be taken in pelagic waters, but many of the species found in supermarkets, minke whales included, appear to have come from the genetically unique Sea of Japan (Baker et al., 2000).

Although Barbados is not a member of the IWC, it is involved in the issue as it has the option of joining at any time.  Barbados also received money from Japan to upgrade its disaster emergency mechanism, a move many see as Barbados selling its vote.  Japan has taken similar action in the six southeast Caribbean countries who are currently IWC members, building fishing complexes.  Although Japan has been accused of attempting to buy votes, it denies any foul play.  Likewise all of the countries that have accepted aid from Japan deny that their vote is for sale. (Ally and Peltier, 2001; Anonymous, 2001b).

Conclusions

Patterns of marine mammal exploitation in Barbados are different from those of the neighboring countries, such as Trinidad and Tobago, St. Vincent and the Grenadines, Grenada, and Venezuela.  Although they all share similarities, several factors make Barbados’ exploitative history distinct from the rest of them.  For example, while Barbados’, Bequia’s, and Grenada’s whaling industries developed under heavy foreign influence, Venezuela’s and Trinidad’s developed relatively independently.  Another example of differences among the different countries is the type of boat used.  Barbados used what were essentially converted fishing boats.  Grenada used relatively similar boats that were copies of those used by Yankee whale ships.  Grenada had technologically advanced steam ships.  Venezuela used simple wooden skiffs.  Trinidad used wooden pirogues, another type of converted fishing boat.

Thus, despite their geographical closeness and many shared historical events (visits by Columbus, presence of Arawak and Carib Indians, visits from Spanish and Portuguese trading and slave ships), each country has taken a distinct path in the exploitation of its marine mammals.  One common trend, with the possible exception of Bequia, is that every island has largely depleted its whale stocks, especially humpback whales.  Bequia has an abundant population of pilot whales, large enough to support its small whaling operation, but that population continues to be reduced by whaling (Caldwell et al., 1971).  has been greatly reduced by the country’s over 100 years of whaling or not.

Acknowledgments

This research was generously funded by the Macalester College Environmental Studies Program.  The following individuals provided me with valuable information: Mr. Elmer Jordan, Mr. Charles Jordan, Ms. Ina Jordan; Dr. Christopher Parker, Fisheries Division, Barbados; Dr. Julia Horrocks, Biology Department, University of the West Indies, Cave Hill; and numerous local fishers.  Ms. Karen Solomon provided indispensable assistance with materials at the Barbados National Library Service.  Aaron Albertson dedicated countless time and energy to securing inter-library loan material.  I would like to thank Anna Payden for generously donating her time to create the maps, and for her moral support throughout the research and writing process.  I would also like to extend my thanks to my thesis committee, Peter Vaughan, Environmental Studies Program, Macalester College; and Donald Siniff, Department of Ecology, Evolution, and Behavior, University of Minnesota; for their time and valuable feedback, and Aldemaro Romero, Environmental Studies Program, Macalester College; for his indispensable advice, feedback, assistance with field work, and mentorship throughout this process.

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Appendices

Appendix I:  Transcript of a videotape interview with Elmer Jordan, son of Percy Jordan, last owner of the C.H.P. Jordan whaling station in Speightstown.

Appendix II:  The Fisheries Regulation Act of 1904, Part III: Whaling. Source: Archer and Fergusson (1944).

Appendix III:  Records of marine mammal sightings based on interviews with fishers.


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