Contributors | Affiliation | Role |
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Lopanik, Nicole | Georgia Institute of Technology (GA Tech) | Principal Investigator |
Lim-Fong, Grace | Randolph-Macon College | Co-Principal Investigator |
Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Distribution of benthic invertebrates along the East Coast, USA from latitudes 38.61283 to 29.753272.
Samples were collected by hand using a 15x15 cm grid placed randomly on submerged area of floating dock, and identified by eye. For some colonial organisms (sponges, hydroids, tunicates, bryozoans), enumeration was challenging. Zeros indicate no animals in that group were found in that sample.
Temperature was measured with a digital thermometer, and salinity with a refractometer at the time of collection.
We have analyzed the proportions at differing latitudes and performed regression analysis with various factors (latitude, longitude, temperature, salinity) using SPSS Statistics 24.
BCO-DMO Processing:
- copied date, location name, location code, lat, lon, temp, and sal to each relevant row (was only included the first row for each sample set);
- created location_descrip column for more detailed location place name;
- modified parameter names;
- moved "Total" to the "Grid" column;
- removed commas and apostrophes from place names; replaced spaces with underscores;
- replaced blanks with "nd" (no data).
File |
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invert_dist.csv (Comma Separated Values (.csv), 64.17 KB) MD5:13066356a8522518992f187ccf5fb2f7 Primary data file for dataset ID 719556 |
Parameter | Description | Units |
date | Date of collection, formatted as mm/dd/yyyy | unitless |
location | Location samples collected | unitless |
location_descrip | Specific area within location where samples were collected | unitless |
location_code | Location code | unitless |
Latitude | Latitude of location | decimal degrees |
Longitude | Longitude of location | decimal degrees |
temp | Water temperature | degrees Celsius |
salinity | Water salinity | parts per thousand |
grid_num | Sampling effort replicate | unitless |
sponge_random | Random sponge count | unitless |
sponge_orange | Orange sponge count | unitless |
sponge_yellow | Yellow sponge count | unitless |
sponge_purp_gray | Purple/gray sponge count | unitless |
sponge_pink | Pink sponge count | unitless |
sponge_green | Green sponge count | unitless |
spong_orange_encr | Orange encr. sponge count | unitless |
Anemone | Anemone count | unitless |
hydroid | Hydroid count | unitless |
hydroid_tubularia | Hydroid (tubularia) count | unitless |
crab | Crab count | unitless |
barnacle | Barnacle count | unitless |
oyster | Oyster count | unitless |
mussel | Mussel count | unitless |
snail | Snail count | unitless |
nudibranch | Nudibranch count | unitless |
limpet | Limpet count | unitless |
worm_red | Red worm count | unitless |
worm_green | Green worm count | unitless |
tubeworm | Tubeworm count | unitless |
ragworm | Ragworm count | unitless |
tunicate_orange | Orange tunicate count | unitless |
tunicate_black | Black tunicate count | unitless |
molgula | Molgula count | unitless |
styela | Styela count | unitless |
ecteinascidia_like_tunicate | Ecteinascidia-like tunicate count | unitless |
white_tunicate_clavelina | White tunicate/clavelina count | unitless |
clear_tunicate | Clear tunicate count | unitless |
stalked_tunicate | Stalked tunicate count | unitless |
encrusting_bryozoan | Encrusting bryozoan count | unitless |
bugula_sp | Bugula sp. count | unitless |
B_neritina | B. neritina count | unitless |
total_count | Total count | unitless |
sponge_tot | Total sponge count (counts summed by taxonomic grouping) | unitless |
anemone_tot | Total anemone count (counts summed by taxonomic grouping) | unitless |
hydroid_tot | Total hydroid count (counts summed by taxonomic grouping) | unitless |
barnacle_tot | Total barnacle count (counts summed by taxonomic grouping) | unitless |
oyster_tot | Total oyster count (counts summed by taxonomic grouping) | unitless |
mussel_tot | Total mussel count (counts summed by taxonomic grouping) | unitless |
other_mollusk_tot | Total other mollusk count (counts summed by taxonomic grouping) | unitless |
worm_tot | Total worm count (counts summed by taxonomic grouping) | unitless |
colonial_tun_tot | Total colonial tunicate count (counts summed by taxonomic grouping) | unitless |
solitary_tun_tot | Total solitary tunicate count (counts summed by taxonomic grouping) | unitless |
encr_bry_tot | Total encrusting bryozoan count (counts summed by taxonomic grouping) | unitless |
B_stolon_tot | Total B. stolon count (counts summed by taxonomic grouping) | unitless |
B_neritina_tot | Total B. neritina count (counts summed by taxonomic grouping) | unitless |
total | Total of counts summed by taxonomic grouping | unitless |
total_minus_bry | Total of counts summed by taxonomic grouping minus the bryozoans | unitless |
sponge_prop | sponge_tot as a proportion | unitless |
anemone_prop | anemone_tot as a proportion | unitless |
hydroid_prop | hydroid_tot as a proportion | unitless |
barnacle_prop | barnacle_tot as a proportion | unitless |
oyster_prop | oyster_tot as a proportion | unitless |
mussel_prop | mussel_tot as a proportion | unitless |
other_mollusk_prop | other_mullusk_tot as a proportion | unitless |
worm_prop | worm_tot as a proportion | unitless |
colonial_tun_prop | colonial_tun_tot as a proportion | unitless |
solitary_tun_prop | solitary_tun_tot as a proportion | unitless |
encr_bry_prop | encr_bry_tot as a proportion | unitless |
B_stolon_prop | B_stolon_tot as a proportion | unitless |
B_neritina_prop | B_neritina_tot as a proportion | unitless |
total_prop | Total of proportions | unitless |
sponge_minus_bry_prop | Sponge proportion after removing bryozoan counts | unitless |
anemone_minus_bry_prop | Anemone proportion after removing bryozoan counts | unitless |
hydroid_minus_bry_prop | Hydroid proportion after removing bryozoan counts | unitless |
barnacle_minus_bry_prop | Barnacle proportion after removing bryozoan counts | unitless |
mollusks_minus_bry_prop | Mollusks proportion after removing bryozoan counts | unitless |
worm_minus_bry_prop | Worm proportion after removing bryozoan counts | unitless |
tunicates_minus_bry_prop | Tunicates proportion after removing bryozoan counts | unitless |
total_minus_bry_prop | Total of proportions after removing bryozoan counts | unitless |
Dataset-specific Instrument Name | |
Generic Instrument Name | digital thermometer |
Generic Instrument Description | An instrument that measures temperature digitally. |
Dataset-specific Instrument Name | |
Generic Instrument Name | Refractometer |
Generic Instrument Description | A refractometer is a laboratory or field device for the measurement of an index of refraction (refractometry). The index of refraction is calculated from Snell's law and can be calculated from the composition of the material using the Gladstone-Dale relation.
In optics the refractive index (or index of refraction) n of a substance (optical medium) is a dimensionless number that describes how light, or any other radiation, propagates through that medium. |
Recent research has shown that microorganisms can be very important to their eukaryotic hosts, by providing nutrition or contributing to host defense against enemies, such as pathogens or predators. In many cases, however, hosting a bacterial symbiont imposes a physiological cost on the host organism, resulting in reduced growth or reproduction in the presence of the symbiont. Further, these costs may be more pronounced in some habitats than others, causing natural selection to act in eliminating symbiont-containing hosts from the population. In this project, the investigators are studying the relationship between the marine bryozoan invertebrate, Bugula neritina, and its uncultured symbiont. The symbiont produces natural products with activity against cancer, Alzheimer's disease, and HIV. Interestingly, these compounds also are distasteful and protect larvae from predators, indicating that this symbiotic relationship is defensive in nature. Along the East Coast of the US, the investigators have found a much higher proportion of individuals that have the defensive symbiont at lower latitudes, while the symbiont is absent in individuals collected at higher latitudes. This pattern is consistent with the theory that higher predation pressure exists at lower latitudes. Other environmental factors, such as temperature, can also vary over a wide geographical area, and may also play a role in influencing the relationship. In this project, the investigators will evaluate the ecological and environmental parameters that influence the distribution of a defensive symbiont, including predation pressure and temperature. Defensive symbionts represent another level of ecological complexity, and likely play an important role in structuring marine communities. This study will provide insight into how environmental factors can influence host-symbiont interactions and drive partner co-evolution. Furthermore, the bioactive products have pharmaceutical potential, and understanding how environmental factors influence the relationship between B. neritina and its symbiont may improve bioprospecting for novel compounds that could be developed into drugs.
In this research, the investigators will determine the ecological and environmental parameters that influence the distribution of a defensive symbiont in the marine bryozoan, Bugula neritina. The goal of this research is to determine the mechanism that results in the defensive endosymbiont being restricted to hosts that inhabit lower latitudes. This pattern of symbiont distribution could be the result of differing levels of costs and benefits at different latitudes: where predation pressure is low, the costs of hosting the symbiont outweigh the benefits, and aposymbiotic individuals outcompete their symbiotic conspecifics. In areas of higher predation, the defensive benefit outweighs the cost, and symbiotic individuals have higher survival rates than their undefended, aposymbiotic conspecifics. An alternative, but not mutually exclusive hypothesis, is that symbiont growth is inhibited at higher latitudes, where it is not as beneficial, and growth is induced in areas of higher predation. Specific goals are to determine if (1) a biogeographical cline in predation pressure corresponds to a gradient of symbiont frequency associating with the host, (2) symbiotic hosts have a higher fitness at low latitudes, and aposymbiotic hosts have a higher fitness at high latitudes, and (3) symbiont growth is promoted at low latitudes and inhibited at high latitudes. A combination of field and laboratory-based experiments will be conducted using ecological and molecular biology techniques. Bioactive compounds produced by symbionts of marine invertebrates can mediate multi-trophic interactions and potentially influence benthic community structure. There has been almost no research, however, on how ecological and environmental parameters influence the distribution of marine defensive endosymbionts.
Related Reference:
Linneman J, Paulus D, Lim-Fong G, Lopanik NB (2014) Latitudinal Variation of a Defensive Symbiosis in the Bugula neritina (Bryozoa) Sibling Species Complex. PLoS ONE 9(10): e108783. doi:10.1371/journal.pone.0108783
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |