This document provides a final report on estimating the abundance of blue whales off the US West Coast using photo identification from 2004-2006. 481 unique blue whales were identified from coastal surveys during this period. Additionally, 38 whales were identified from broad-scale ship surveys and 7 from fine-scale surveys. Mark-recapture analysis estimated the blue whale population at 2,842, higher than previous estimates, though with high uncertainty. Abundance estimates using different methods tended to increase over time, though fluctuated substantially.
This document summarizes a study that estimated the seasonal abundance and distribution of cetaceans off the coast of Southern California using data from 16 quarterly ship-based surveys between 2004-2008. The surveys covered an area of 238,494 km2 from nearshore waters to 700 km offshore. Abundance estimates were determined for the 11 most commonly encountered species based on 693 encounters, and were calculated separately for summer-fall and winter-spring periods as well as for shallow (<2000.5 m) and deep (≥2000.5 m) waters. Density estimates showed seasonal variations by depth for some species, with the highest densities generally occurring in summer-fall in shallow waters for species like blue whales and common dolphins.
Population structure, fecundity and morphological characteristics of M. vollenhovenii were studied around Lower Volta River, Ghana subject to dirt of information on this prawn species around the study location. The most prominent morphological characteristics already documented for identification of this species was rostrum bearing 13-15 continuous teeth dorsally and 4-5 teeth on its ventral part. These morphological traits formed the principal components for identification in this study. Results showed that morphological traits on second pereiopods such as presence of spines, spinules, teeth borne within the fingers, and dense projections of setae-like features on telson and uropod were observed relevant for identification purposes. Other results revealed that maximum total length recorded in this study (150-155mm) was higher than total length ranges (≤125mm) documented for this species in earlier studies. Consequently, two adult’s classes of prawns were identified (old adult class 81-120mm; and young adults 31-80mm) and older class was observed to be more in catches than the younger prawns. Absolute fecundity revealed that oocytes estimation varied with respect to seasons, ages of prawns and body sizes of specimens examined. In conclusion, this study observed that M. vollenhovenii fishery is operating in a sustainable manner at the time of this study around the study location.
Delineation and biogeography of semipelagic spotted eagle raysStephenBergacker
This study aimed to evaluate population structure and biogeography in spotted eagle rays using genetic analysis. Two species delineation methods, ABGD and GMYC, supported the existence of three spotted eagle ray species: A. laticeps, A. narinari, and A. ocellatus. A. ocellatus populations were highly structured with distinct populations in the Arabian Sea, South Africa, and other Indo-Pacific regions. Historical analysis suggested an origin in the Tethys Sea with subsequent radiation into current biogeographic regions separated by barriers like ocean currents.
Poster Distributional Pattern of IchthyofaunaVinciusCorra19
The document analyzes the distribution patterns of freshwater fish species in the Chacoan Sub-region of South America using panbiogeography. 38 generalized tracks and 4 nodes were identified for families of Characiforms, Siluriforms, Gymnotiforms and Cyprinodontiforms. The fish distribution patterns matched previously described patterns (A, B, C) found in other taxa, suggesting congruent biogeographic histories among groups in the region.
Evidence for morphological evolutionary stasis in a Middle Miocene Inselbergs...AndressaCabral18
This study examines the phylogeny, biogeography, and taxonomy of the Barbacenia group of plants found on inselbergs in the Atlantic Forest region. Phylogenetic analysis recovered two major clades of Barbacenia, one containing species endemic to Atlantic Forest inselbergs and the other containing species from campo rupestre rocky grasslands. Divergence time estimates indicate the diversification of Barbacenia likely occurred in the Middle Miocene. Ancestral area reconstruction supports the Atlantic Forest and Cerrado as the areas of origin. The inselberg endemic clade exhibits low morphological diversity and long-term morphological stasis, possibly due to niche conservatism and geographical isolation on the mountain tops.
Exploration of the Ecological Niche of Chacoan Species in Environmental SpaceAlejandro Manuel Ferreiro
This document explores the ecological niches of four species predominantly found in the Chaco region - Bulnesia sarmientoi, Calomys callosus, Leptodactylus bufonius, and Tolypeutes matacus - by modeling their niches in environmental space. It finds that L. bufonius and T. matacus have broader niches while B. sarmientoi and C. callosus have narrower niches. Additionally, all species' niches show some overlap, with an area of environmental space where all four species' niches overlap. Modeling species' niches in environmental space provides new insights into the biogeography of species in the Chaco
Assessment of coral reefs damaged due to MV Pazifik ran aground in the Sape S...Yayasan TERANGI
Assessment of coral reefs damaged due to MV Pazifik ran aground in the Sape Strait using an aerial photography approach and species distribution modeling
This document summarizes a study that estimated the seasonal abundance and distribution of cetaceans off the coast of Southern California using data from 16 quarterly ship-based surveys between 2004-2008. The surveys covered an area of 238,494 km2 from nearshore waters to 700 km offshore. Abundance estimates were determined for the 11 most commonly encountered species based on 693 encounters, and were calculated separately for summer-fall and winter-spring periods as well as for shallow (<2000.5 m) and deep (≥2000.5 m) waters. Density estimates showed seasonal variations by depth for some species, with the highest densities generally occurring in summer-fall in shallow waters for species like blue whales and common dolphins.
Population structure, fecundity and morphological characteristics of M. vollenhovenii were studied around Lower Volta River, Ghana subject to dirt of information on this prawn species around the study location. The most prominent morphological characteristics already documented for identification of this species was rostrum bearing 13-15 continuous teeth dorsally and 4-5 teeth on its ventral part. These morphological traits formed the principal components for identification in this study. Results showed that morphological traits on second pereiopods such as presence of spines, spinules, teeth borne within the fingers, and dense projections of setae-like features on telson and uropod were observed relevant for identification purposes. Other results revealed that maximum total length recorded in this study (150-155mm) was higher than total length ranges (≤125mm) documented for this species in earlier studies. Consequently, two adult’s classes of prawns were identified (old adult class 81-120mm; and young adults 31-80mm) and older class was observed to be more in catches than the younger prawns. Absolute fecundity revealed that oocytes estimation varied with respect to seasons, ages of prawns and body sizes of specimens examined. In conclusion, this study observed that M. vollenhovenii fishery is operating in a sustainable manner at the time of this study around the study location.
Delineation and biogeography of semipelagic spotted eagle raysStephenBergacker
This study aimed to evaluate population structure and biogeography in spotted eagle rays using genetic analysis. Two species delineation methods, ABGD and GMYC, supported the existence of three spotted eagle ray species: A. laticeps, A. narinari, and A. ocellatus. A. ocellatus populations were highly structured with distinct populations in the Arabian Sea, South Africa, and other Indo-Pacific regions. Historical analysis suggested an origin in the Tethys Sea with subsequent radiation into current biogeographic regions separated by barriers like ocean currents.
Poster Distributional Pattern of IchthyofaunaVinciusCorra19
The document analyzes the distribution patterns of freshwater fish species in the Chacoan Sub-region of South America using panbiogeography. 38 generalized tracks and 4 nodes were identified for families of Characiforms, Siluriforms, Gymnotiforms and Cyprinodontiforms. The fish distribution patterns matched previously described patterns (A, B, C) found in other taxa, suggesting congruent biogeographic histories among groups in the region.
Evidence for morphological evolutionary stasis in a Middle Miocene Inselbergs...AndressaCabral18
This study examines the phylogeny, biogeography, and taxonomy of the Barbacenia group of plants found on inselbergs in the Atlantic Forest region. Phylogenetic analysis recovered two major clades of Barbacenia, one containing species endemic to Atlantic Forest inselbergs and the other containing species from campo rupestre rocky grasslands. Divergence time estimates indicate the diversification of Barbacenia likely occurred in the Middle Miocene. Ancestral area reconstruction supports the Atlantic Forest and Cerrado as the areas of origin. The inselberg endemic clade exhibits low morphological diversity and long-term morphological stasis, possibly due to niche conservatism and geographical isolation on the mountain tops.
Exploration of the Ecological Niche of Chacoan Species in Environmental SpaceAlejandro Manuel Ferreiro
This document explores the ecological niches of four species predominantly found in the Chaco region - Bulnesia sarmientoi, Calomys callosus, Leptodactylus bufonius, and Tolypeutes matacus - by modeling their niches in environmental space. It finds that L. bufonius and T. matacus have broader niches while B. sarmientoi and C. callosus have narrower niches. Additionally, all species' niches show some overlap, with an area of environmental space where all four species' niches overlap. Modeling species' niches in environmental space provides new insights into the biogeography of species in the Chaco
Assessment of coral reefs damaged due to MV Pazifik ran aground in the Sape S...Yayasan TERANGI
Assessment of coral reefs damaged due to MV Pazifik ran aground in the Sape Strait using an aerial photography approach and species distribution modeling
Investigation of Groundwater Potential and Aquifer Protective Capacity of Par...Premier Publishers
The aim of this study was to investigate groundwater potential and aquifer protective capacity of an area behind the College of Science, Federal University of Petroleum Resources, Effurun-Warri area of Delta State, Nigeria. The data was acquired using ABEM SAS 4000 Terrameter and processed using IPI2win and Interpex software. Five Vertical Electrical Soundings were carried out with maximum current electrode separation (AB) of 120 m. The VES curves generated from the data revealed HKH curve type for VES 1 and VES 2, KQH curve for VES 3 and KH curve for VES 4 and 5. Five resistivity layers were identified for VES 1 - 3 while four resistivity layers were identified for VES 4 – 5. Analysis and interpretation of VES data obtained from the study area showed VES 3, VES 4 and VES 5 to be most appropriate locations to be explored for borehole development due to low resistivity of the weathered/fractured aquiferous layers coupled with the relatively high thicknesses of the weathered layers. However, all the aquifers in the VES locations are poorly protected due to the very low aquifer protective capacity parameters in the VES locations.
This document summarizes observations of squid launching into the air and flying using rocket propulsion. High-speed photographs of Sthenoteuthis pteropus off the coast of Brazil were analyzed and showed squid accelerating in air at 265 body lengths per second squared, three times faster than their acceleration in water. Their air velocity of 37 body lengths per second was also almost four times faster than in water. Fin flaps appear to develop in squids at the same size they begin exhibiting flight behaviors, supporting hypotheses that flaps function as ailerons while flying. The document compares squid flight mechanics and energetics to swimming and discusses how flight may benefit squid migration and predator avoidance.
Historical biogeography and diversification in Sisyrinchium (Iridaceae) Verônica Thode
This document summarizes a study on the historical biogeography and diversification of the plant genus Sisyrinchium. The study used a densely sampled dated phylogeny of 103 Sisyrinchium species and 13 outgroups along with 8 molecular markers and 9,000 occurrence records to address: 1) When and where Sisyrinchium colonized the New World and 2) Which geological and climatic factors influenced diversification patterns. Key results included Sisyrinchium originating in the mid-Miocene (12.7 Ma) in South America and diversifying during the Pliocene and Pleistocene, with dispersal to Central and North America earlier than the closure of the Panama Isthmus. Diversification
Magpali et al (2020) Adaptive evolution of hearing genes in echolocating dolp...Letícia Magpali
Candidate poster for presentation at the I Meeting of Systematics, Biogeography and Evolution (SBE), in the category Phylogenomics and molecular evolution.
Magpali, L.; Freitas, L.; Ramos, E. K. S.; de Souza, E. M. S.; Nery, M. F.
University of Campinas / Biology Institute, Brazil
Berrow et al. 2014. Deployment of Passive Acoustic Monitoring Equipment in th...Ryan Wilson-Parr
This document provides a summary of a cruise conducted in May 2014 that had three main objectives:
1) Deploy passive acoustic monitoring equipment at three sites in the Porcupine Seabight region to monitor cetaceans.
2) Conduct visual surveys for cetaceans and seabirds while transiting to and from the monitoring locations.
3) Collect CTD data at each of the three sites where acoustic monitoring equipment was deployed to record temperature, depth, and salinity.
The cruise aimed to add to the body of knowledge on cetacean and seabird distributions in the Porcupine Seabight, an important habitat.
Island biogeography in continental areas: inferring dispersal based on distri...Oscar Mahecha
This document summarizes a study on the distribution patterns of Pronophilina butterflies in the northern Andean massifs. The study applied island biogeography methods to examine dispersal between the mountain ranges. It found that the elevation at which mountain ranges touch was a better predictor of species affinities and richness between ranges than horizontal distance alone. This implies dispersal occurred through past ecological corridors rather than isolated jumps. The analysis provides indirect evidence on past vertical movements of vegetation zones and is a valuable tool for paleoecologists.
Phylogeography and genetic diversity of Baetodes huaico (EPHEMEROPTERA: BAETI...jcgjuancruz
The document analyzes genetic variability and phylogeographic patterns in the mayfly species Baetodes huaico based on mitochondrial DNA sequences. Two main results are:
1) A median-joining network identified two divergent haplogroups separated by 12 mutations. Haplogroup I shows a star-like pattern centered around the common and widespread haplotype 5, suggesting a population expansion effect.
2) Haplogroup II has lower genetic diversity and is located farther south, being more differentiated from Haplogroup I. Southern populations of B. huaico appear more isolated, possibly due to different ecosystem barriers restricting gene flow.
Aspects of the biology of african moony, monodactylus sebae from badagry cree...Alexander Decker
The document summarizes a study on the biology of the African moony fish (Monodactylus sebae) in Badagry Creek, Lagos, Nigeria. A total of 267 fish were collected from May 2012 to April 2013. The fish lengths ranged from 56-163 mm and weights ranged from 5.6-151.7 g. The length-weight relationship showed negative allometric growth. The condition factor was higher in females than males. The sex ratio was approximately 1:1 male to female.
Atkinson et al 2015 Length-weight Emerald shinerThomas Simon
This document summarizes a study that examined the length-weight relationships of Emerald Shiners (Notropis atherinoides) in the western basin of Lake Erie. The study analyzed 400 Emerald Shiners collected from coastal and open water habitats to determine relationships between length (total length and standard length) and weight for males and females. It found strong positive correlations between length and weight for both sexes. It also found that length-weight relationships were significantly influenced by sex and habitat. The study identified three age classes and observed differences in length ranges between age classes and sexes.
GEOGRAPHIC ISOLATION OF Hypostomus cordovae (SILURIFORMES, LORICARIIDAE) IN A...YaninaFlorenciaBrioc
This study examines the population genetic structure of Hypostomus cordovae, a bottom-dwelling fish endemic to Argentina. The researchers sequenced the mitochondrial DNA control region of individuals from 14 localities across exorheic (flowing out to sea) and endorheic (internal draining) basins. They found 6 distinct haplotypes. Isolation-by-distance explained 29% of genetic variability, while isolation-by-barrier between exorheic and endorheic basins explained 53% of variability. Periodic drying of rivers likely fragmented populations, leading to genetic differentiation over time through prolonged isolation of fragmented basins.
Diatom biogeography: distribution of the Luticola species found in Iguazú Nat...JulinSimonato
The document summarizes a study on the diatom genus Luticola found in Iguazú National Park in Argentina. 18 Luticola species were identified from samples collected at 8 sites within the park. Most species had Neotropical or tropical distributions, while 2 were cosmopolitan and 2 had disjunct distributions. The results indicate high diatom diversity and endemism within the park and add to understanding biogeography patterns of the genus in South America.
Alison Gould is a Ph.D. candidate in Ecology and Evolutionary Biology at the University of Michigan. Her research focuses on the evolutionary ecology of bioluminescent symbioses between marine organisms. She has over 10 publications on topics including the life history of luminous reef fish and copepods. Gould has received numerous awards and grants including an NSF DDIG. She has taught several courses and mentored many undergraduate researchers.
Evidence of mangrove ecosystems during the Late Miocene? of southern South Am...Eli Moya
This document summarizes a study that discovered fossil wood related to mangrove environments in southern South America during the Late Miocene. The fossil, named Mangroveoxylon areniensis, was found in Entre Ríos, Argentina. It shares anatomical characteristics most similar to the genus Conocarpus, particularly Conocarpus erectus, a species associated with mangroves. This suggests mangrove ecosystems existed further south than previously thought during this time period. Associated fossils of oysters that attach to mangrove tree roots also support the presence of mangroves. This discovery provides the first evidence of a coastal marine environment in this region during the Late Miocene, indicating tropical conditions extended further south than today.
Supporting evidence for a cryptic species within the Neotropical freshwater f...Izabela Mendes
Presentation by Izabela Santos Mendes for the I Virtual Meeting of Systematics, Biogeography and Evolution (SBE).
Authors: Izabela Santos Mendes, Bruno Francelino de Melo, Daniel Fonseca Teixeira, Júnio Damasceno Souza, Daniel Cardoso Carvalho.
Geophysics of overburden moving geophysics gtom exploration to application Dr Lendy Spires
This document summarizes the objectives and results of a geophysics field school in Africa over 10 years that trained students in practical geophysical techniques. The school focused on solving problems typically encountered in mining exploration, such as estimating overburden thickness and mapping dykes, faults and ore bodies. Methods taught included magnetic, seismic, ground penetrating radar and resistivity surveys. The surveys successfully mapped dykes and structures and estimated overburden depths, demonstrating the value of integrated geophysical techniques for mine planning applications. Over 10 years the program trained many African students.
The document summarizes a shellfish study conducted in July and August 2009 to assess the impact of a proposed marina expansion. Sampling methods included grab samples to analyze juvenile clam populations and clam raking to examine adult clams. Of 28 juvenile sampling sites, only 1 juvenile clam was found, indicating a density of 0.04 clams/sq ft across the study area. For adult clams, 62 were found across 18 sampling sites via raking 719.82 sq ft, indicating a density of 0.086 clams/sq ft. Most of the study area did not support a viable clam population based on NJ standards. The study concludes the proposed expansion area is generally not suitable clam
1. The study presents new specimens of three species of armadillos from the Quebrada de los Colorados Formation in northwest Argentina.
2. The specimens represent two previously known species - Pucatherium parvum and Parutaetus punaensis - as well as a new species.
3. While the low number of species prevents formalizing a new cingulate association, the two unequivocally identified species have not been reported in other formations, suggesting some regional differentiation during the middle Eocene.
Oh my teeth! Odontocetes feeding methods diversification in the early MioceneMariana Viglino
Dolgopolis kinchikafiforo is a new genus and species of toothless river dolphin from the early Miocene of Patagonia that used capture-suction feeding. Analysis of the skull and mandibles indicates it was a member of Platanistoidea, an early group of toothed whales that showed diversity in feeding methods during the Miocene. While Platanistoidea declined later in the Miocene, their initial radiation was associated with varied morphologies and ecological strategies including different feeding styles like the capture-suction seen in D. kinchikafiforo.
This document summarizes a study on the rockfish resources of the south central California coast. Researchers from California Polytechnic State University placed observers on party boats from 2003-2005 to record catch data by species, including catch per unit effort and mean size. They supplemented this with historical catch data from 1980-1998 from the California Department of Fish and Game and Pacific Gas & Electric. The study aims to analyze population trends over the past 25 years for various rockfish species in the region and compare sizes over time. Preliminary results found fluctuating catch rates but no consistent declining trends, except for bocaccio rockfish. Mean sizes were generally above maturity levels.
This document examines the potential effects of Hurricane Katrina on Atlantic bottlenose dolphin reproduction in the Mississippi Sound. It finds that approximately two years after the hurricane, calf encounter rates and the percentage of calves observed significantly increased. This suggests reproduction increased. The increase is likely due to a combination of factors from the hurricane, including increased fish abundance from decreased fishing, fewer boats disturbing dolphins, and more reproductively active females after the storm led to calf losses.
Investigation of Groundwater Potential and Aquifer Protective Capacity of Par...Premier Publishers
The aim of this study was to investigate groundwater potential and aquifer protective capacity of an area behind the College of Science, Federal University of Petroleum Resources, Effurun-Warri area of Delta State, Nigeria. The data was acquired using ABEM SAS 4000 Terrameter and processed using IPI2win and Interpex software. Five Vertical Electrical Soundings were carried out with maximum current electrode separation (AB) of 120 m. The VES curves generated from the data revealed HKH curve type for VES 1 and VES 2, KQH curve for VES 3 and KH curve for VES 4 and 5. Five resistivity layers were identified for VES 1 - 3 while four resistivity layers were identified for VES 4 – 5. Analysis and interpretation of VES data obtained from the study area showed VES 3, VES 4 and VES 5 to be most appropriate locations to be explored for borehole development due to low resistivity of the weathered/fractured aquiferous layers coupled with the relatively high thicknesses of the weathered layers. However, all the aquifers in the VES locations are poorly protected due to the very low aquifer protective capacity parameters in the VES locations.
This document summarizes observations of squid launching into the air and flying using rocket propulsion. High-speed photographs of Sthenoteuthis pteropus off the coast of Brazil were analyzed and showed squid accelerating in air at 265 body lengths per second squared, three times faster than their acceleration in water. Their air velocity of 37 body lengths per second was also almost four times faster than in water. Fin flaps appear to develop in squids at the same size they begin exhibiting flight behaviors, supporting hypotheses that flaps function as ailerons while flying. The document compares squid flight mechanics and energetics to swimming and discusses how flight may benefit squid migration and predator avoidance.
Historical biogeography and diversification in Sisyrinchium (Iridaceae) Verônica Thode
This document summarizes a study on the historical biogeography and diversification of the plant genus Sisyrinchium. The study used a densely sampled dated phylogeny of 103 Sisyrinchium species and 13 outgroups along with 8 molecular markers and 9,000 occurrence records to address: 1) When and where Sisyrinchium colonized the New World and 2) Which geological and climatic factors influenced diversification patterns. Key results included Sisyrinchium originating in the mid-Miocene (12.7 Ma) in South America and diversifying during the Pliocene and Pleistocene, with dispersal to Central and North America earlier than the closure of the Panama Isthmus. Diversification
Magpali et al (2020) Adaptive evolution of hearing genes in echolocating dolp...Letícia Magpali
Candidate poster for presentation at the I Meeting of Systematics, Biogeography and Evolution (SBE), in the category Phylogenomics and molecular evolution.
Magpali, L.; Freitas, L.; Ramos, E. K. S.; de Souza, E. M. S.; Nery, M. F.
University of Campinas / Biology Institute, Brazil
Berrow et al. 2014. Deployment of Passive Acoustic Monitoring Equipment in th...Ryan Wilson-Parr
This document provides a summary of a cruise conducted in May 2014 that had three main objectives:
1) Deploy passive acoustic monitoring equipment at three sites in the Porcupine Seabight region to monitor cetaceans.
2) Conduct visual surveys for cetaceans and seabirds while transiting to and from the monitoring locations.
3) Collect CTD data at each of the three sites where acoustic monitoring equipment was deployed to record temperature, depth, and salinity.
The cruise aimed to add to the body of knowledge on cetacean and seabird distributions in the Porcupine Seabight, an important habitat.
Island biogeography in continental areas: inferring dispersal based on distri...Oscar Mahecha
This document summarizes a study on the distribution patterns of Pronophilina butterflies in the northern Andean massifs. The study applied island biogeography methods to examine dispersal between the mountain ranges. It found that the elevation at which mountain ranges touch was a better predictor of species affinities and richness between ranges than horizontal distance alone. This implies dispersal occurred through past ecological corridors rather than isolated jumps. The analysis provides indirect evidence on past vertical movements of vegetation zones and is a valuable tool for paleoecologists.
Phylogeography and genetic diversity of Baetodes huaico (EPHEMEROPTERA: BAETI...jcgjuancruz
The document analyzes genetic variability and phylogeographic patterns in the mayfly species Baetodes huaico based on mitochondrial DNA sequences. Two main results are:
1) A median-joining network identified two divergent haplogroups separated by 12 mutations. Haplogroup I shows a star-like pattern centered around the common and widespread haplotype 5, suggesting a population expansion effect.
2) Haplogroup II has lower genetic diversity and is located farther south, being more differentiated from Haplogroup I. Southern populations of B. huaico appear more isolated, possibly due to different ecosystem barriers restricting gene flow.
Aspects of the biology of african moony, monodactylus sebae from badagry cree...Alexander Decker
The document summarizes a study on the biology of the African moony fish (Monodactylus sebae) in Badagry Creek, Lagos, Nigeria. A total of 267 fish were collected from May 2012 to April 2013. The fish lengths ranged from 56-163 mm and weights ranged from 5.6-151.7 g. The length-weight relationship showed negative allometric growth. The condition factor was higher in females than males. The sex ratio was approximately 1:1 male to female.
Atkinson et al 2015 Length-weight Emerald shinerThomas Simon
This document summarizes a study that examined the length-weight relationships of Emerald Shiners (Notropis atherinoides) in the western basin of Lake Erie. The study analyzed 400 Emerald Shiners collected from coastal and open water habitats to determine relationships between length (total length and standard length) and weight for males and females. It found strong positive correlations between length and weight for both sexes. It also found that length-weight relationships were significantly influenced by sex and habitat. The study identified three age classes and observed differences in length ranges between age classes and sexes.
GEOGRAPHIC ISOLATION OF Hypostomus cordovae (SILURIFORMES, LORICARIIDAE) IN A...YaninaFlorenciaBrioc
This study examines the population genetic structure of Hypostomus cordovae, a bottom-dwelling fish endemic to Argentina. The researchers sequenced the mitochondrial DNA control region of individuals from 14 localities across exorheic (flowing out to sea) and endorheic (internal draining) basins. They found 6 distinct haplotypes. Isolation-by-distance explained 29% of genetic variability, while isolation-by-barrier between exorheic and endorheic basins explained 53% of variability. Periodic drying of rivers likely fragmented populations, leading to genetic differentiation over time through prolonged isolation of fragmented basins.
Diatom biogeography: distribution of the Luticola species found in Iguazú Nat...JulinSimonato
The document summarizes a study on the diatom genus Luticola found in Iguazú National Park in Argentina. 18 Luticola species were identified from samples collected at 8 sites within the park. Most species had Neotropical or tropical distributions, while 2 were cosmopolitan and 2 had disjunct distributions. The results indicate high diatom diversity and endemism within the park and add to understanding biogeography patterns of the genus in South America.
Alison Gould is a Ph.D. candidate in Ecology and Evolutionary Biology at the University of Michigan. Her research focuses on the evolutionary ecology of bioluminescent symbioses between marine organisms. She has over 10 publications on topics including the life history of luminous reef fish and copepods. Gould has received numerous awards and grants including an NSF DDIG. She has taught several courses and mentored many undergraduate researchers.
Evidence of mangrove ecosystems during the Late Miocene? of southern South Am...Eli Moya
This document summarizes a study that discovered fossil wood related to mangrove environments in southern South America during the Late Miocene. The fossil, named Mangroveoxylon areniensis, was found in Entre Ríos, Argentina. It shares anatomical characteristics most similar to the genus Conocarpus, particularly Conocarpus erectus, a species associated with mangroves. This suggests mangrove ecosystems existed further south than previously thought during this time period. Associated fossils of oysters that attach to mangrove tree roots also support the presence of mangroves. This discovery provides the first evidence of a coastal marine environment in this region during the Late Miocene, indicating tropical conditions extended further south than today.
Supporting evidence for a cryptic species within the Neotropical freshwater f...Izabela Mendes
Presentation by Izabela Santos Mendes for the I Virtual Meeting of Systematics, Biogeography and Evolution (SBE).
Authors: Izabela Santos Mendes, Bruno Francelino de Melo, Daniel Fonseca Teixeira, Júnio Damasceno Souza, Daniel Cardoso Carvalho.
Geophysics of overburden moving geophysics gtom exploration to application Dr Lendy Spires
This document summarizes the objectives and results of a geophysics field school in Africa over 10 years that trained students in practical geophysical techniques. The school focused on solving problems typically encountered in mining exploration, such as estimating overburden thickness and mapping dykes, faults and ore bodies. Methods taught included magnetic, seismic, ground penetrating radar and resistivity surveys. The surveys successfully mapped dykes and structures and estimated overburden depths, demonstrating the value of integrated geophysical techniques for mine planning applications. Over 10 years the program trained many African students.
The document summarizes a shellfish study conducted in July and August 2009 to assess the impact of a proposed marina expansion. Sampling methods included grab samples to analyze juvenile clam populations and clam raking to examine adult clams. Of 28 juvenile sampling sites, only 1 juvenile clam was found, indicating a density of 0.04 clams/sq ft across the study area. For adult clams, 62 were found across 18 sampling sites via raking 719.82 sq ft, indicating a density of 0.086 clams/sq ft. Most of the study area did not support a viable clam population based on NJ standards. The study concludes the proposed expansion area is generally not suitable clam
1. The study presents new specimens of three species of armadillos from the Quebrada de los Colorados Formation in northwest Argentina.
2. The specimens represent two previously known species - Pucatherium parvum and Parutaetus punaensis - as well as a new species.
3. While the low number of species prevents formalizing a new cingulate association, the two unequivocally identified species have not been reported in other formations, suggesting some regional differentiation during the middle Eocene.
Oh my teeth! Odontocetes feeding methods diversification in the early MioceneMariana Viglino
Dolgopolis kinchikafiforo is a new genus and species of toothless river dolphin from the early Miocene of Patagonia that used capture-suction feeding. Analysis of the skull and mandibles indicates it was a member of Platanistoidea, an early group of toothed whales that showed diversity in feeding methods during the Miocene. While Platanistoidea declined later in the Miocene, their initial radiation was associated with varied morphologies and ecological strategies including different feeding styles like the capture-suction seen in D. kinchikafiforo.
This document summarizes a study on the rockfish resources of the south central California coast. Researchers from California Polytechnic State University placed observers on party boats from 2003-2005 to record catch data by species, including catch per unit effort and mean size. They supplemented this with historical catch data from 1980-1998 from the California Department of Fish and Game and Pacific Gas & Electric. The study aims to analyze population trends over the past 25 years for various rockfish species in the region and compare sizes over time. Preliminary results found fluctuating catch rates but no consistent declining trends, except for bocaccio rockfish. Mean sizes were generally above maturity levels.
This document examines the potential effects of Hurricane Katrina on Atlantic bottlenose dolphin reproduction in the Mississippi Sound. It finds that approximately two years after the hurricane, calf encounter rates and the percentage of calves observed significantly increased. This suggests reproduction increased. The increase is likely due to a combination of factors from the hurricane, including increased fish abundance from decreased fishing, fewer boats disturbing dolphins, and more reproductively active females after the storm led to calf losses.
This document summarizes a study that used photographic identification to assess site fidelity of grey whales in Bahía Magdalena, Mexico. Researchers photographed grey whales from 2011 and compared the photos to catalogs from 1998-2010. Only two whales were resighted, one from 2003 and one from 2004. No whales were resighted within 2011. The results indicate low site fidelity among grey whales in the bay. More research is needed to better understand short-term movement patterns.
AGU 2012 Conference, San Francisco, CA
Student Oral Presenter
• Presented at the American Geophysical Union (AGU) on “Validating Annual Growth Bands of Deep Sea
Corals from the Gulf of Mexico and Southeastern United States”.
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1. FINAL REPORT
ABUNDANCE OF BLUE WHALES OFF THE US WEST COAST USING PHOTO
IDENTIFICATION
Conducted under PO Order No.: AB133F06SE3906
from
Southwest Fisheries Science Center
8604 La Jolla Shores Drive
La Jolla, CA 92037
Prepared by
John Calambokidis
Annie Douglas
Erin Falcone
Lisa Schlender
Cascadia Research
218½ W Fourth Ave.
Olympia, WA 98501
September 2007
2. INTRODUCTION
Blue whales (Balaenoptera musculus) are considered endangered and their populations were
depleted by whaling throughout most of their range. Blue whales feed off California from May
through November (Dohl et al. 1983) and migrate to waters off Mexico and Central America in
winter and spring (Calambokidis et al. 1990, Stafford et al. 1999, Mate et al. 1999, Chandler et
al. 1999). Photographic identification of blue whales has revealed that animals identified off
California have been seen as far north as the Queen Charlotte Islands (Calambokidis et al. 2004)
and the Gulf of Alaska and as far south as the Costa Rica Dome (Chandler et al. 1999).
Blue whales occur in both coastal and offshore waters of the US West Coast. Accurate
estimates of blue whale abundance off California using capture-recapture methods have only been
possible when at least one representative sample is obtained from surveys systematically covering
both inshore and offshore waters (Calambokidis and Barlow 2004). This is because a portion of the
blue whale population feeds offshore beyond the reach of small-boat surveys. Although there is
interchange between inshore and offshore areas, there is not complete mixing. To avoid
heterogeneity of capture probabilities which would bias capture-recapture estimates, past estimates
have relied on at least one sample coming from identifications obtained during systematic ship
surveys covering both coastal and offshore waters, similar to that obtained by Southwest Fisheries
Science Center (SWFSC) on the Collaborative Survey of Cetacean Abundance and the Pelagic
Ecosystem (CSCAPE) cruise in 2005 (Forney 2007).
OBJECTIVES AND GENERAL APPROACH
The primary objective of the research was to obtain a new estimate of blue whale
abundance. To achieve this we sought to:
1. Obtain a large and representative sample of blue whale identifications from coastal
waters and, where possible, offshore waters of the West Coast in 2006 to supplement that
already available for past years.
2. Compare identification photographs obtained during 2005 CSCAPE systematic surveys
with those available from dedicated photo-ID surveys.
3. Generate an abundance estimate of blue whales for the 2004-2006 period using mark-
recapture, where the non-systematic identifications gathered from 2004 to 2006 are
treated as one sample and those obtained on the CSCAPE cruise as a second independent
sample.
4. Compare this estimate with the three similarly obtained estimates during the last 15 years
to evaluate potential trends in blue whale abundance.
2
3. METHODS
Survey effort
A major focus of our field effort was to obtain as large a sample of photographic
identifications as possible with broad geographic and temporal coverage. Strategies for achieving
this included: 1) conduct small boat operations in many different areas, 2) cover large areas both
offshore and inshore, 3) effectively sample large concentrations of whales, and 4) achieve broad
temporal coverage. We achieved these objectives with a combination of dedicated small boats
surveys, opportunistic identifications during our other field research, and identifications from
other opportunistic sources.
We conducted dedicated photo-identification surveys off California, Oregon, and
Washington in the summer and fall of 2004 to 2006 (Table 1). These were primarily conducted
between June and November. Timing and exact locations of these surveys were based on
weather patterns and anticipated whale abundance based on sighting reports and historical data.
The primary vessels employed in these dedicated photo-identification surveys were three 5.3-
5.9m rigid-hull inflatables equipped with outboard engines operated by Cascadia Research and
used extensively in our past photo-identification research. Vessels covered up to 200 nmi/day
and operated up to 50 nmi offshore. The boats were transported from one region to another by
trailer.
Cascadia Research also conducted a number of other research efforts off the coast of
California, Oregon, and Washington that provided additional opportunities to obtain identification
photographs. These included efforts to tag and track humpback and blue whales, monitoring of
marine mammals of areas in conjunction with acoustic monitoring, surveys conducted as part of
collaborations with Channel Islands and Olympic Coast National Marine Sanctuaries, effort
associated with the SPLASH project (in 2004 and 2005), and effort associated with underwater
filming of blue whales. A number of other more opportunistic platforms were used to obtain
additional identification photographs. The most extensive contribution of opportunistic photographs
came from our collaboration with the Channel Islands Naturalist Corps as well as whale watch
operations out of Monterey Bay and San Francisco Bay.
Photographic identification from ship surveys
A critical part of the mark-recapture estimates for blue whales was the systematic
identifications obtained in conjunction with broad-scale SWFSC marine mammal ship surveys.
Key samples for the current study were the identifications obtained during the 2005 CSCAPE
surveys covering waters out to 300 nmi off California, Oregon, and Washington. Additional fine-
scale survey effort was completed during CSCAPE 2005 in waters of four West Coast National
Marine Sanctuaries, providing additional blue whale identifications in nearshore waters.
Data analyses
All photographs were judged using a three-tier quality criterion. This score, along with
associated sighting information (date, latitude, longitude), was entered into the identification
database for analysis. Identification photographs of suitable quality were internally compared to
3
4. identify resightings (and remove duplicates) of animals for each year. Each individual was then
compared to Cascadia’s historical catalog (archived photographs) of all blue whales identified
off northern Baja, California, Oregon and Washington. Individual whales identified each year
that did not match past years and which were of suitable quality were assigned a new unique
identification number and added to the catalog annually.
Estimates of humpback and blue whale abundance were made using several capture-
recapture methods (Calambokidis and Barlow 2004). The primary methods were two-sample
Petersen capture-recapture estimates (Chapman modification for sampling without replacement)
conducted using the identifications obtained in different pairs of samples including: 1) pairs of
adjacent years as the two samples, 2) identifications from the systematic broad-scale and fine-
scale ship surveys in 2005 as one sample and the second sample from the coastal surveys for the
3-year surrounding period (2004-2006), 3) all identifications in the year of the SWFSC survey as
one sample and identifications from the year before and after as the second sample. An unbiased
estimate of blue whale abundance using the two-sample Petersen estimate requires that all
animals in the population have an equal probability of being photographed in at least one of the
samples. The second sample does not have to meet this criterion as long as it is independent of
the first sample. This approach of using the identifications from the systematic ship surveys as
the one representative sample provided reliable estimates of blue whale abundance for similar
surveys in the past (Calambokidis and Barlow 2004, Calambokidis and Steiger 1995, Barlow and
Calambokidis 1995). We also used a multi-year open population model (Jolly-Seber) to examine
rates of natality and mortality for the population using the Model A (standard Jolly-Seber) from
the Program Jolly.
RESULTS AND DISCUSSION
Identifications of 481 different blue whales were obtained on dedicated photo-ID surveys
and opportunistic surveys mostly in coastal waters from Northern Baja to Oregon from 2004 to
2006 (Table 1). Photographs of both sides were not obtained for all individuals potentially
preventing reconciliation of some individuals. The systematic broad-scale surveys during
CSCAPE 2005 obtained identifications of 38 blue whales and the fine-scale CSCAPE surveys
conducted in sanctuary waters added an additional 7 individuals (there were no resightings of the
same animal between the broad-scale and fine-scale surveys). Resightings of only four whales
were made between the 2004-2006 coastal effort and those obtained on the CSCAPE broad-scale
surveys (3 and 2 matches isolated by left or right sides, respectively). Inclusion of the seven
identifications on the CSCAPE fine-scale surveys into the CSCAPE sample raised the number of
matches to the coastal effort to six (Table 1).
The locations of blue whale identifications by survey type for 2004 to 2006 are shown in
Figure 1. There was a fairly dramatic geographic separation between identifications from the
coastal surveys and those from the CSCAPE surveys, especially the broad-scale survey lines.
Identifications from the CSCAPE broad-scale surveys came mostly from offshore areas (Figure
1). Tracklines from the CSCAPE cruise (Figure 2, Forney 2007) indicate a tendency for
incomplete transect lines nearshore due to poor weather and there were some difficulties
launching a small to get photo-IDs due to concern about fog or other logistics during some of the
encounters near shore (Forney, pers. com.).
4
5. Table 1. Summary of number of unique blue whales photographically identified in different
surveys during 2004 to 2006 in the eastern North Pacific and matches between collections.
Survey Any side L side R side
CSCAPE systematic - 2005 38 29 34
CSCAPE Fine scale - 2005 7 6 4
Coastal effort N Baja to Washington - 2004-
2006 481 352 365
Other (AK, BC, Sea of Cortez) 21 15 13
Matches
CSCAPE Broad scale vs. Fine scale and coastal 4 3 2
All CSCAPE to Coastal 6 5 3
31
33
35
37
39
41
43
45
47
‐132 ‐130 ‐128 ‐126 ‐124 ‐122 ‐120 ‐118 ‐116 ‐114
CSCAPE‐systematic
CSCAPE‐fine scale
CRC‐Opport
ID connections
Figure 1. Locations of identifications of blue whales from 2004 to 2006 from both CSCAPE and
coastal surveys. Dashed lines connect resightings of the same individual.
5
6. The few matches between the CSCAPE broad-scale surveys and those on the coastal
surveys came from CSCAPE identifications made closer to shore. Although there were high
numbers of blue whale sightings in some inshore parts of the CSCAPE surveys, especially in the
southern-most area (Figure 2), CSCAPE fine-scale surveys yielded few identifications overall (7
total by either a right or left side).
Figure 2. CSCAPE effort and blue whale sightings on CSCAPE broad-scale surveys (left panel)
and fine-scale surveys (right panels) in 2005 (from Forney 2007).
To calculate blue whale abundance estimates using the 2005 CSCAPE effort we decided
to pool the small number of identifications from the fine-scale effort in with the identifications
obtained in the broad-scale CSCAPE surveys. This was done to help balance the small number
of identifications obtained from CSCAPE in coastal waters and also to improve the available
sample size. The small number of identifications from the fine-scale surveys (7) only slightly
altered the predominant offshore distribution of the identifications obtained from the greater
CSCAPE broad-scale survey effort.
Petersen mark-recapture estimates using all CSCAPE as one sample and the coastal effort
for 2004-2006 as another, yielded higher estimates of abundance than previous similar
6
7. calculations for 1991 to 2001 (Table 2). With the small sample sizes and few matches (5 and 3
for left and right sides, respectively), the estimates were variable and had fairly high CVs (0.34
and 0.42). The average of the two sides was 2,842, higher than the 2,000 blue whales estimated
for 1991 to 1993 but not out of line given the high CVs with these estimates.
Table 2. Petersen mark-recapture estimates of blue whale abundance using survey type as
samples. CSCAPE surveys were used as the first sample and identifications from the more shore-
based effort in the 3-year period surrounding the systematic survey as the other sample.
Samples used Left sides Right sides Mean
n1 n2 m Est. CV1 n1 n2 m Est. CV1
Pooled years using survey type as samples
1991-93 all qualities 61 293 8 2,024 0.29 74 289 10 1,976 0.26 2,000
1995-97 all qualities 43 350 7 1,930 0.30 34 361 7 1,583 0.29 1,756
2000-2002 all qualities 20 452 5 1,585 0.32 24 474 5 1,978 0.33 1,781
2004-2006 all qualitites 35 352 5 2,117 0.34 38 365 3 3,568 0.42 2,842
We also examined abundance using Petersen mark-recapture with pairs of samples using
all the identifications from the year with the systematic survey (2005) as one sample and all
identifications from the adjacent years as the other sample (Table 3). The combined
identifications from both the coastal effort and ship surveys in 2005 represent the most complete
and thorough effort of any year. These estimates were lower than those obtained using only the
systematic effort and showed a steady increase from 816 in 1991-93 to 1,428 in 2004-06.
Table 3. Summary of Petersen mark-recapture estimates for blue whales off California and W.
Baja Mexico. Sample 1 consists of all the identified whales from the year of the SWFSC
systematic ship surveys and n2 is from coastal small-boat work in the adjacent years. The
number of matches or recaptures (m) are indicated. Coefficients of variation (CV) are based on
analytical formulae.
n1 (systematic yr) n2 (adjacent yrs)
Period Year n1 Years n2 m Est. CV
1991-93 1992 281 1991 & 1993 193 66 816 0.09
1995-97 1996 183 1995 & 1997 368 56 1,190 0.10
2000-2002 2001 286 2000 & 2002 449 99 1,291 0.07
2004-2006 2005 179 2004 & 2006 388 48 1,428 0.11
Estimates based on all pairs of years regardless of whether they included a systematic
survey also tended to show a general increasing trend in abundance (Table 4). While CVs were
generally low for these estimates (because they made use of the entire annual samples), the
estimates tended to fluctuate over a fairly wide range from 755 to 1,739 with highest estimates in
recent years (2003 to 2006).
Abundance estimates were similar using the Jolly-Seber open population model (Table
5). Annual abundance estimates ranged from 617 to 1,543. While the range and some of the
fluctuations was similar to the results from some of the Petersen models that used adjacent years
as samples, the Jolly-Seber did not show as clear a trend toward increasing abundance. Estimates
of annual rate of mortality/emigration averaged 0.91 (SE = 0.012) and number of
7
8. births/immigration averaged 149 (SE=12), however, there was a high degree of variation among
annual estimates that often exceeded levels that were biologically reasonable for blue whales.
Table 4. Annual estimates of abundance of blue whales using adjacent annual years for the
region from northern Baja to Washington with no selection by quality or side.
Sample 1 Sample 2
Period Year Ident. n Year Ident. n Match Est. CV
1991-92 1991 113 76 1992 674 281 26 803 0.14
1992-93 1992 674 281 1993 214 125 46 755 0.10
1993-94 1993 214 125 1994 433 211 20 1,271 0.18
1994-95 1994 433 211 1995 373 228 40 1,183 0.13
1995-96 1995 373 228 1996 297 183 34 1,203 0.14
1996-97 1996 297 183 1997 322 181 35 929 0.13
1997-98 1997 322 181 1998 404 228 54 757 0.10
1998-99 1998 404 228 1999 416 177 47 848 0.11
1999-2000 1999 416 177 2000 348 182 41 775 0.12
2000-01 2000 348 182 2001 573 286 51 1,009 0.11
2001-02 2001 573 286 2002 535 310 61 1,439 0.10
2002-03 2002 535 310 2003 537 292 67 1,339 0.09
2003-04 2003 537 292 2004 265 189 31 1,739 0.15
2004-05 2004 265 189 2005 310 179 27 1,220 0.16
2005-06 2005 310 179 2006 427 217 24 1,569 0.17
n-Number of unique individuals in sample used in mark-recapture estimate
Est.-Estimated abundance
CV-Coeficient of variation based on Chapman
Table 5. Results of Jolly-Seber mark-recapture open population model using all identifications
with years as samples. Output is from program Jolly based on Model A (full Jolly-Seber).
Period PHI
SE(PHI
) M SE'(M) N SE(N) p SE(p) B SE(B)
1991 0.778 0.071
1992 1.038 0.077 59 4.0 617 95 0.440 0.071 198 146
1993 0.853 0.071 326 24.1 839 107 0.147 0.022 393 129
1994 0.987 0.069 345 19.0 1,108 120 0.188 0.023 450 177
1995 0.841 0.061 485 28.4 1,543 167 0.146 0.018 -84 152
1996 0.859 0.058 541 29.5 1,214 115 0.150 0.017 -45 101
1997 1.057 0.071 554 26.0 998 79 0.181 0.018 94 86
1998 0.816 0.060 672 36.3 1,148 87 0.198 0.019 -14 64
1999 0.875 0.062 627 33.3 923 68 0.191 0.019 156 64
2000 1.048 0.073 601 30.1 964 73 0.188 0.019 105 69
2001 0.905 0.072 703 37.9 1,115 77 0.256 0.022 281 71
2002 0.957 0.100 734 46.5 1,290 101 0.240 0.022 92 76
2003 0.851 0.132 833 73.9 1,327 131 0.220 0.024 331 110
2004 0.832 0.183 807 107.7 1,459 215 0.129 0.021 -16 99
2005 753 137.7 1,199 230 0.149 0.030
MEAN 0.907 0.0125 574 15 1,125 37 0.202 0.008 149 12
8
9. Abundance estimates that used all the identifications in a year or combination of years as
a sample showed fairly good agreement with each other both in terms of their average values and
some of the patterns of annual variation (Figure 3). The estimates that used the systematic
surveys as a single sample and the bracketing 3-year period as the other sample consistently
showed higher estimates than the other methods although the value of this difference varied,
with the 1991 to 1993 and 2004 to 2006 estimates differing the most.
-
500
1,000
1,500
2,000
2,500
3,000
1991 1993 1995 1997 1999 2001 2003 2005 2007
Year
Estimatedabundance
Petersen w/ Syst vs Coastal in 3 yr
Petersen w/ Syst yr vs. adjacent
Petersen w/ all IDs for adjacent years
Jolly-Seber all IDs all years
Figure 3. Comparison of abundance estimates using different mark-recapture models (Tables 2-
5).
Identifications were not obtained consistently in the same locations among years, and
therefore may explain some of the observed patterns in abundance. In the early 1990s the coastal
effort was more concentrated in specific areas with primary effort in specific areas off central
California (Farallons and Monterey Bay) and southern California (Santa Barbara Channel). The
consistency of some of this annual effort may have caused a higher rate of heterogeneity of
capture probabilities and hence tended to bias these annual estimates downward. Our overall
effort was more broadly geographically distributed in later years and also tended to vary from
year to year potentially reducing the bias from geographic heterogeneity. The single high
estimate using CSCAPE in 2005 as one sample may just be the result of variation from small
sample size with the possible influence of this sample not tending to be truly geographically
9
10. representative as in past years. The high proportion of identifications from offshore areas in 2005
may have lead to the reduced matches and causing an upward bias to this estimate.
We report mark-recapture abundance estimates of blue whales showing a stable or
possibly increasing abundance, which is in sharp contrast to estimates generated from line-
transect survey efforts off the US West Coast and derived from the same systematic surveys used
here for the mark-recapture estimates. Barlow and Forney (2007) report a dramatic decline in
estimated blue whale density and abundance off the US West Coast between the surveys
conducted in 1992 and 1996 and those in 2001 and 2005. This was after an apparent increase in
blue whale numbers off California between 1979/80 and 1991 (Barlow 1994). There was
agreement between estimates of abundance of blue whales from line transects and those from
mark-recapture in the 1990s indicated the vast majority of the blue whale population being
estimated by mark-recapture was present off the US West Coast during the Summer-Fall line-
transect surveys (Calambokidis and Barlow 2004). The decline in the line-transect estimates but
not the mark-recapture estimates for the surveys from 2001 to 2005, and the resultant differences
in estimates of abundance in recent years is likely the result of a significant number of blue
whales now spending portions of the Summer-Fall outside the area systematically surveyed off
the US West Coast. If blue whales reduced their time inside the survey area by being present
only part of the season or only in some years, they would still be available to be identified and
therefore included in the mark-recapture estimates but might be missed by line-transect surveys
(effectively lowering their apparent density and hence abundance).
There have been several indications of blue whale use of areas outside of the US West
Coast in recent years. Calambokidis et al. (in prep.) report sightings of blue whales off British
Columbia and in the Gulf of Alaska, both areas where blue whales were heavily hunted during
whaling (Rice 1963, 1974, Gregr and Trites 2001) but where blue whales had only very rarely
been seen during the 1990s. In our surveys in 2006, we found large numbers of blue whales both
in the summer and fall using waters off northern Baja California just south of the US/Mexico
border, an adjacent area that would have not been included in the line-transect surveys.
There have been indications of changes in krill abundance off California that could be
altering the availability of prey for blue whales and causing a shift in distribution. Roemmich and
McGowan (1995) reported declines in plankton abundance off California. Seabirds also provide an
indicator of krill and ocean conditions (Hyrenbach and Veit 2003). Sydeman et al (2006) reported
breeding failure in Cassin’s auklet, a krill-feeding seabird, off northern California and the
apparent shift of these animals to southern California in response to reduced krill abundance they
attributed to an anomalous atmospheric condition. In our research on humpback whales off
California, we have noted an increase in the proportion of humpback whales feeding on fish
rather than krill in recent years compared to the 1990s (Cascadia Research, unpubl, data).
Because of their more limited diet, blue whales would not have the same option to switch prey
and instead would have to adapt to changes in prey availability by shifting feeding locations.
Given the evidence that blue whales during whaling days were mostly taken off British
Columbia and Alaska, it is possible that blue whale are returning to those habitats used
historically.
10
11. ACKNOWLEDGMENTS
Many people helped with the Cascadia blue whale field work between 2004 and 2006,
including Todd Chandler, Sherwin Cotler, Jeff Jacobson, Erin Oleson, and Greg Schorr. Oregon
State University provided identifications from their tagging efforts. Volunteers with the Channel
Islands Naturalist Corps coordinated by the Channel Islands National Marine Sanctuary provided
identifications obtained during whale-watch operations in the Santa Barbara Channel and we
thank all the participants in that program especially Shauna Bingham, Josh Kaye-Carr, and Clare
Fritzsche. The identification from the SWFSC CSCAPE 2005 surveys was critical to the data we
report, we especially thank the SWFSC ship observers especially Holly Fearnbach, Laura Morse,
Cornelia Oedekoven as well as the overall coordinator, Karin Forney. Additional opportunistic
identifications of blue whales for 2004 to 2006 were received from Charles Stinchomb, Dave
Anderson, Eric Martin, Peggy Stap, Bernardo Alps, Eric Zimmerman, Kate Thomas, Michael H.
Smith, Maddalena Bearzi, Scot Anderson, Ski Laniewicz, and Michuru Ogino. Photographic
matching was conducted with the help of Ulrike Wolf, Veronica Iriarte, Randy Lumper, Alexis
Rudd, and Amber Klimek. Support for some of the field effort came from Michiru Ogino,
Southwest Fisheries Science Center, Olympic Coast National Marine Sanctuary, Channel Islands
National Marine Sanctuary, and Fisheries and Oceans Canada. Support for the overall analysis
came from Southwest Fisheries Science Center (coordinated by Jay Barlow). Comments on the
draft report were provided by Jay Barlow, Karin Forney, and Gretchen Steiger.
11
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