Peter B. Best’s research while affiliated with University of Pretoria and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (197)


Fig. 1. The external features of a landed dwarf minke whale showing the distinctive white shoulder/flipper patch. (Photo H. Kato)
Sightings of dwarf minke whales in the Southern Hemisphere during the SOWER cruises
  • Article
  • Full-text available

April 2024

·

24 Reads

IWC Journal of Cetacean Research and Management

Hidehiro Kato

·

Koji Matsuoka

·

Gen Nakamura

·

Peter B. Best

This paper examines sightings of dwarf minke whales during the SOWER cruises. A total of 12 sightings were made between 1994/95 and 2003/04, across a relatively wide latitude (37°S–62°S) but limited longitude, between IWC Management Area III (0–70°E) and V (130°E–170°W), with no sightings in Area I (0–60°W) or II (60°W–120°W). Despite this low number of sightings, most were close to the Antarctic Convergence at 58°S–65°S. There may be some seasonality in their southbound migration.

Download

Baleen whale microsatellite panel for individual identification and parentage assignment in Mysticeti

April 2024

·

145 Reads

Global Ecology and Conservation

·

·

Lutz Bachmann

·

[...]

·


Population structure of pygmy (Kogia breviceps) and dwarf (Kogia sima) sperm whales in the Southern Hemisphere may reflect foraging ecology and dispersal patterns

November 2023

·

155 Reads

·

5 Citations

Little is known about the biology of pygmy (Kogia breviceps) and dwarf (K. sima) sperm whales as these animals are difficult to observe in the wild. However, both species strand frequently along the South African, Australian and New Zealand coastlines, providing samples for these otherwise inaccessible species. The use of DNA samples from tissue and DNA extracted from historical material, such as teeth and bone, allowed a first analysis of the population structure of both species in the Southern Hemisphere.


Multiplex oligo-nucleotide panels for mysticete species.
Universal baleen whale microsatellite panel for individual identification and power to detect parentage

April 2023

·

184 Reads

·

2 Citations

Highly polymorphic single tandem repeat loci (STR, also known as microsatellite loci) remain a familiar, cost efficient class of markers for genetic analyses in ecology, behavior and conservation. We characterize a new universal set of ten STR loci (from 28 potential candidate loci) in seven baleen whale species, which are optimized for PCR amplification in two multiplex reactions along with a Y chromosome marker for sex determination. The optimized, universal set of STR loci provides an ideal starting point for new studies in baleen whales aimed at individual-based and population genetic studies, and facilitates data sharing among research groups. Data from the new STR loci were combined with genotypes from other published STR loci to assess the power to assign parentage (paternity) using exclusion in four species: fin whales, humpback whales, blue whales and bowhead whales. We argue that parentage studies should present a power analysis to demonstrate that the specific data are sufficiently informative to assign parentage with statistical rigor.


Mortalities of southern right whales (Eubalaena australis) and related anthropogenic factors in South African waters, 1999–2019

November 2022

·

116 Reads

·

2 Citations

IWC Journal of Cetacean Research and Management

The southern right whale (Eubalaena australis; SRW) population in South Africa’s coastal waters has experienced marked changes since 2009, including altered feeding and migration behaviour, and decreased calving success. At the same time, anthropogenic activities in the area have increased. Based on this, an update on SRW mortalities and related anthropogenic factors is warranted. Building on the published information of Best et al. (2001a), data were collated on all SRW mortalities as well as non‐fatal ship‐strikes and entanglements along the South African coast between 1999 and 2019. A total of 97 SRW mortalities were recorded, including three that did not result in a stranding, of which the majority were classified as calves of the year. Most of these occurred on the Western Cape coast between the months of July to November, coinciding with the seasonal presence of the species in South African coastal waters. Eleven of these mortalities could be attributed to ship‐strikes whereas three mortalities related to entanglements. A total of 98 non‐fatal incidents, including 16 ship‐strikes and 82 entanglements with SRWs, were recorded in South Africa between 1999 and 2019. Ship‐strikes occurred mainly around the area of Cape Town harbour. Entanglements occurred mainly in rock‐lobster gear and bather‐protection nets in the Western Cape and KwaZulu‐Natal provinces respectively, although the latter did not occur between 2015–2019 attributable to the replacement of over 70% of the nets by drumlines, and the removal of the remaining nets during whale season. In general, the incidence of SRW mortalities and entanglements decreased post‐2007, coinciding with the decreased presence of SRWs along the South African coast. Available data show a relatively low rate of fatal entanglements and ship‐strikes, although this may be underestimated due to the opportunistic nature of the collated data. In view of the population growth rate and the increased anthropogenic activities in South African coastal waters, continued and improved monitoring (e.g. through a more systematic reporting system) of these incidents is crucial to ensure accurate knowledge‐based management decisions in the future. Possible mitigation measures aimed at reducing anthropogenic interactions are mooted.



Figure 2. Haplotype network of southern right whale mtDNA control region (381 bp) showing the position of Chile-Peru sample (indicated by dashed purple arrow) and South Georgia (Islas Georgias del Sur) samples (red block arrows) in the broader southern right whale haplotype network.
Figure 4. GENEPLOT of southern right whale microsatellite genotypes showing LGP for South Atlantic and Indo-Pacific reference populations, with South Georgia (Islas Georgias del Sur) and Chile-Peru query samples. The thick central diagonal line indicates an equal posterior probability for both reference populations; a point lying on that line has the same LGP with respect to both reference populations. The thin diagonal lines indicate where the genotype probability (the inverse-log of the LGP) for one population is 10 times greater than it is for the other population. Also shown are the 1% quantiles: only 1% of genotypes that could arise from the given population are estimated to have LGPs below this line. The marginal plots show the home (dashed line) and away (solid line) profiles of LGPs within each reference population, with rug plots indicating the LGPs of the query samples on each axis. Bottom margin -home: South Atlantic; away: Indo-Pacific. Left margin -home: Indo-Pacific; away: South Atlantic.
Summary of microsatellite and mtDNA diversity statistics for southern right whale winter nursery/socializing (W) and summer feeding (S) grounds
Pairwise genetic differentiation indices between South Atlantic sampling sites with (A) mtDNA table showing ϕ ST (top right), F ST (bottom left quadrant) and (B) microsatellites showing Jost's D (top right) and F ST (bottom left quadrant)
Estimates of genetic differentiation between the Indo-Pacific and South Atlantic wintering grounds and the SG feeding ground, with (A) mtDNA table showing ϕ ST (top right), F ST (bottom left quadrant) and (B) microsatellites showing Jost's D (top right) and F ST (bottom left quadrant)
Genetic diversity and connectivity of southern right whales (Eubalaena australis) found in the Brazil and Chile-Peru wintering grounds and the South Georgia (Islas Georgias del Sur) feeding ground *** This paper is open access: https://academic.oup.com/jhered/article/111/3/263/5826886 ***

April 2020

·

586 Reads

·

30 Citations

Journal of Heredity

As species recover from exploitation, continued assessments of connectivity and population structure are warranted to provide information for conservation and management. This is particularly true in species with high dispersal capacity, such as migratory whales, where patterns of connectivity could change rapidly. Here we build on a previous long-term, large-scale collaboration on southern right whales (Eubalaena australis) to combine new (nnew) and published (npub) mitochondrial (mtDNA) and microsatellite genetic data from all major wintering grounds and, uniquely, the South Georgia (Islas Georgias del Sur: SG) feeding grounds. Specifically, we include data from Argentina (npub mtDNA/microsatellite=208/46), Brazil (nnew mtDNA/microsatellite=50/50), South Africa (nnew mtDNA/microsatellite=66/77, npub mtDNA/microsatellite=350/47), Chile-Peru (nnew mtDNA/microsatellite=1/1), the Indo-Pacific (npub mtDNA/microsatellite=769/126), and SG (npub mtDNA/microsatellite=8/0, nnew mtDNA/microsatellite=3/11) to investigate the position of previously unstudied habitats in the migratory network: Brazil, SG and Chile-Peru. These new genetic data show connectivity between Brazil and Argentina, exemplified by weak genetic differentiation and the movement of one genetically identified individual between the South American grounds. The single sample from Chile-Peru had a mtDNA haplotype previously only observed in the Indo-Pacific and had a nuclear genotype that appeared admixed between the Indo-Pacific and South Atlantic, based on genetic clustering and assignment algorithms. The SG samples were clearly South Atlantic, and were more similar to the South American than the South African wintering grounds. This study highlights how international collaborations are critical to provide context for emerging or recovering regions, like the SG feeding ground, as well as those that remain critically endangered, such as Chile-Peru.


Figure 1: Location of southern right whale sampling sites including wintering grounds A. Chile; B. Brazil; C. Argentina; D. South Africa; E. Australia; F. New Zealand subantarctic and summer feeding ground G. South Georgia.
Figure 4: Geneplot showing log genotype probabilities (LGP) for South Atlantic and Indo-Pacific reference and South Georgian and Chilean query southern right whale microsatellite genotypes. The thick centre diagonal line indicates an equal posterior probability for both reference populations; a point lying on that line has the same LGP with respect to both reference populations. The thin diagonal lines indicate where the genotype probability (the inverse-log of the LGP) for one population is 10 times greater than it is for the other population. Also shown are the 1% quantiles; only 1% of all possible genotypes that could arise from the given population would have LGPs below this line. The bottom graph shows the fit of possible South Atlantic (dashed line) and Indo-Pacific (solid line) individuals with respect to the South Atlantic population; the left graph shows the fit of possible Indo-Pacific (dashed line) and South Atlantic (solid line) individuals with respect to the Indo-Pacific population.
GENETIC DIVERSITY AND CONNECTIVITY OF SOUTHERN RIGHT WHALES (EUBALAENA AUSTRALIS) FOUND IN THE CHILEAN WINTERING GROUND AND SOUTH GEORGIA/ISLAS GEORGIAS DEL SUR FEEDING GROUND

January 2019

·

92 Reads

·

2 Citations

Southern right whale (Eubalaena australis) population structure can be viewed as a migratory network of winter calving/socialising and summer feeding grounds. Here we investigate the position of the Chile-Peru wintering ground (n = 1) and the South Georgia feeding ground (n = 15) in the broader migratory network, using mitochondrial DNA (mtDNA) and nuclear microsatellite data (nDNA) from all major wintering grounds. This includes new data from Brazil (n = 60) and South Africa (n = 88), as well as published data from across the species’ circumpolar distribution (nDNA = 222; mtDNA = 1327). The single sample from Chile-Peru had a mtDNA haplotype previously only observed in the Indo-Pacific and had a nuclear genotype that appeared admixed between the Indo-Pacific and South Atlantic, based on genetic clustering and assignment algorithms. The South Georgia samples were clearly South Atlantic, based on both genetic differentiation and clustering analyses. As a group, South Georgia was more similar to the Southwest Atlantic wintering grounds (Brazil, Argentina) than to the South African wintering ground, and showed significant genetic differentiation from the latter. However, the weak genetic differentiation amongst the South Atlantic wintering grounds meant that population assignment methods were unable to resolve the likely winter association of the South Georgia samples. This may be overcome using additional loci and/or by limiting comparisons to nursery areas within wintering grounds.



Fig. 1. Major ocean currents and summer sea ice conditions before and after the PleistoceneHolocene transition. (A-B) Simplified depiction of the major surface ocean currents in the Southern Ocean and North Atlantic Ocean. (C-D) Contemporary summer sea and land ice coverage. (E-F) Inferred summer sea and land ice coverage during the LGM.
Fig. 2. Estimated temporal trends of í µí¼½ (as proxy for baleen whale and prey abundances) during the Pleistocene and Holocene (1-30 kya). (A & D) Baleen whale species, (B & E) prey species. Note the different scales of the values on the vertical axis in genetic diversity (í µí¼ƒ). Horizontal axis denotes the time in thousands of years ago (kya). (C & F) Historical surface air temperature relative to present temperature (SATRTP) in degrees Celsius (°C). NE-NA: Northeastern North Atlantic (NA), SE-NA: Southeastern NA. W-NA: Western NA. (G) Graphic depiction of the bottom-up control of the demographic response of baleen whales during the Pleistocene-Holocene transition suggested by the results of this study. Red-and light blue-shaded areas indicate the LGM.
Fig. 3. Estimated relative change in abundance for baleen whales and prey during the Pleistocene and Holocene. (A) Baleen whales and (B) prey species. Circles represent the median point estimates of í µí¼ƒ in each species. Dotted lines indicate the geometric mean of í µí¼ƒ (estimated from all point estimates). The numbers with an x (e.g., 7.5x) indicate the relative change in í µí¼ƒ (∆í µí¼ƒ) at one thousand years ago (kya) relative to 21 kya.
Strong and lasting impacts of past global warming on baleen whale and prey abundance

December 2018

·

1,273 Reads

·

3 Citations

The demography of baleen whales and their prey during the past 30 thousand years was assessed to understand the effects of past rapid global warming on marine ecosystems. Mitochondrial and genome-wide DNA sequence variation in eight baleen whale and seven prey species revealed strong, ocean-wide demographic changes that were correlated with changes in global temperatures and regional oceanographic conditions. In the Southern Ocean baleen whale and prey abundance increased exponentially and in apparent synchrony, whereas changes in abundance varied among species in the more heterogeneous North Atlantic Ocean. The estimated changes in whale abundance correlated with increases in the abundance of prey likely driven by reductions in sea-ice cover and an overall increase in primary production. However, the specific regional oceanographic environment, trophic interactions and species ecology also appeared to play an important role. Somewhat surprisingly the abundance of baleen whales and prey continued to increase for several thousand years after global temperatures stabilized. These findings warn of the potential for dramatic, long-term effects of current climate changes on the marine ecosystem. One Sentence Summary The effects of past global warming on marine ecosystems were drastic, system-wide and long-lasting.


Citations (57)


... New Zealand is world renowned for its frequent live cetacean stranding events. Two of the most common species to strand in this region are long-finned pilot whales (Globicephala melas edwardii) and pygmy sperm whales (Kogia breviceps) (Betty 2019;Plön et al. 2023). Due to the low survival likelihood and negative welfare impacts, dependent animals found stranded alone or with deceased mothers are considered non-viable for rescue in New Zealand, as stated in the Department of Conservation Te Papa Atawhai (DOC) Standard Operating Procedures (Boren 2012;Boys et al. 2022a). ...

Reference:

Evaluation of ballistics euthanasia applied to stranded cetaceans using ethological and post-mortem computed tomography assessment
Population structure of pygmy (Kogia breviceps) and dwarf (Kogia sima) sperm whales in the Southern Hemisphere may reflect foraging ecology and dispersal patterns
  • Citing Chapter
  • November 2023

... Along the south-western cape of South Africa, the Mammal Research Institute Whale Unit (MRIUW), University of Pretoria, reported 62 cetacean stranding events over the study period. An additional 550 collective records of southern right whale strandings from South Africa (Vermeulen et al., 2021) were unfortunately not made available for analysis, except for five submitted by MRIUW. Out of the 62 cetacean stranding events reported by MRIUW, two were not included in the present analysis, because latitude/longitude data were not available, nor identifiable geographical landmarks. ...

Mortalities of southern right whales (Eubalaena australis) and related anthropogenic factors in South African waters, 1999 – 2019.

... Extracted DNA was re-suspended in 1x TE buffer (10mM Tris-HCl, 1mM EDTA, pH 8.0). The genotypes were determined at 20 microsatellite loci, using the following oligonucleotide primers: EV001, EV037 and EV094 [49], GATA028, GATA098, GATA417, and TAA023 [50], GT011 [51], GT023, GT211, GT271, GT310, and GT575 [52], AC087 and CA234 [53], GATA25072, GATA43950, GATA5947654, GATA6063318, GATA91083 [54]. Samples were genotyped in multiplex PCR reactions, using the MM2X™ Multiplex kit Plus (Qiagen Inc.) in 5µL reaction volumes. ...

Universal baleen whale microsatellite panel for individual identification and power to detect parentage

... Unlike tail flukes, dorsal fins are always exposed during surfacings; however, the extent to which photographic quality or distinctiveness affects the ability to match dorsal fins of humpback whales is unknown. A recent examination of individually identified humpback whales that feed around Saldanha Bay on the west coast of South Africa (Barendse et al. 2010a), showed that capture-recapture data from different identification features resulted in abundance estimates that varied considerably, and that estimates based on tail flukes (TF) were consistently lower than those derived from left and right dorsal fins (LDF, RDF) and microsatellites (MS) (Barendse et al. 2010b). These results suggested that fewer animals in the area tended to exhibit fluking-up behaviour, or that there was an apparent difficulty in obtaining fluke pictures during boat intercepts, thus reducing the overall number of whales identified by this feature. ...

Photo identification of humpback whales Megaptera novaeangliae off West South Africa (Breeding Stock B2), and a preliminary (sub-) population estimate

... NARW samples were selected from across the species' range and SRW genomes were sampled from winter calving grounds in Peninsula Valdes, Argentina (n = 9) and summer feeding grounds off the coast of South Georgia (n = 1). Note that both microsatellite loci and mitochondrial gene fragment analyses show that SRW sampled from South Georgia during the summer are genetically indistinguishable from SRW from Argentina (Carroll et al. 2020). In addition, whole genome analyses show no population stratification across NARW (Crossman, Fontaine, and Frasier 2023). ...

Genetic diversity and connectivity of southern right whales (Eubalaena australis) found in the Brazil and Chile-Peru wintering grounds and the South Georgia (Islas Georgias del Sur) feeding ground *** This paper is open access: https://academic.oup.com/jhered/article/111/3/263/5826886 ***

Journal of Heredity

... Meyer-Gutbrod and Greene (2018) demonstrate how North Atlantic right whales continue to use calving grounds off the coasts of Florida and Georgia whilst their feeding grounds move northwards in response to warmer waters, and the migration between feeding and nursery grounds continues to lengthen with detrimental impacts on the reproduction rates on right whale populations. Cabrera et al. (2018) analysed the demography of baleen whales and their prey during the past 30,000 years to understand the effects of past rapid global warming on marine ecosystems. Mitochondrial and genome-wide DNA sequence variation in eight baleen whale and seven prey species revealed strong, ocean-wide demographic changes that were correlated with changes in global temperatures and regional oceanographic conditions. ...

Strong and lasting impacts of past global warming on baleen whale and prey abundance

... Instead, the very short life span of NARW almost certainly results from the well-documented anthropogenic and ecological factors that greatly increase the mortality hazard across age classes (13)(14)(15). NARWs experience their lowest annual mortality hazard in their fifth year of life. In that year, they have an expected 2.56% chance of dying. ...

The recovery of North Atlantic right whales, Eubalaena glacialis , has been constrained by human-caused mortality

... Bryde's whales are often misidentified as other species, and their taxonomy has yet to be well resolved (Smultea et al., 2010). Further studies of the phylogenetic relationships between geographically isolated populations of Bryde's whales, by means of differences in behavior, vocalization, and mitochondrial DNA, are required to avoid conservation risks to genetically distinct populations, such as those now faced by Rice's whale (Constantine et al., 2018;Penry et al., 2018). Aside from the issues regarding taxonomy and population abundance of isolated stocks, relatively little is known regarding the swimming behavior, migratory habits, vocalizations, and the current population trend of Bryde's whales (Constantine et al., 2018;Helble et al., 2024;Penry et al., 2016). ...

Phylogenetic relationships in southern African Bryde’s whales inferred from mitochondrial DNA: further support for subspecies delineation between the two allopatric populations

Conservation Genetics

... If incomplete lineage sorting is not the sole underlying cause of the observed polyphyly inferred from the mitochondrial genomes, introgression may have contributed to the observed polyphyly (with respect to oceanic origin) inferred from the mitochondrial genomes in fin whales (Pamilo and Nei 1988;Maddison 1997). Past paleoclimatic cycles may have facilitated secondary contact between otherwise isolated oceanic populations (Bérubé et al. 1998;Palsbøll et al. 2007;Alter et al. 2012Alter et al. , 2015Carroll et al. 2019;Cabrera et al. 2022). During glacial periods, inter-oceanic gene flow was likely elevated when the ranges of baleen whales were contracted towards lower latitudes (Bérubé et al. 1998;Carroll et al. 2019;Cabrera et al. 2022). ...

Incorporating non-equilibrium dynamics into demographic history inferences of a migratory marine species
  • Citing Article
  • May 2018

Heredity

... tively, can be found inhabiting the waters off the South African coast (Constantine et al., 2018;Penry et al., 2016). ...

A conservation assessment of Balaenoptera edeni. In Child MF, Roxburgh L, Do Linh San E, Raimondo D, Davies-Mostert HT, editors. The Red List of Mammals of South Africa, Swaziland and Lesotho. South African National Biodiversity Institute and Endangered Wildlife Trust, South Africa.