Science topic

Biological Oceanography - Science topic

Biological Oceanography is the study of life in the oceans - the quantity, productivity, and geographic distribution of marine life.
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I have a netCDF4 (.nc) file having ocean SST data, with coordinates (lat, lon, time). I want to predict and plot maps for the future. How can I do this using python?
Please recommend a python code for time series forecasting based on this approach.
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This is not a programming question. It's a time-series question. Imagine measuring temperature in your back yard every hour for a day. You could use that to make predictions, but they might not be very useful, because weather changes from day to day. So, you need more than a day. Maybe you measure for 3 days. That would be better. But maybe those were 3 warm days, which are followed by 3 cool days. Etc.
Depending on your background, you might start by reading books on time-series analysis. Then move on to books about ocean physics. And then climate physics. You will soon see that statistical prediction is a weak approach, and that dynamical models are required. That takes you from the domain of reading and plotting with python to the domain of building PhD-level scientific and computing skills. The latter go way beyond plotting with python; you'll need to deploy supercomputers to run models that were took many person-decades to develop and take person-years to learn to run. Oh, and the end result will be a model prediction that will not agree with other model predictions to within the error bars we want for climate prediction.
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How can I convert plankton concentration (micro, nano, pico) from mg/m3 into mol/m3
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@Kunal Madkaiker I see, that information was missing from your question. To do that, you could start with this one: Behrenfeld, M.J.; Boss, E.; Siegel, D.A.; Shea, D.M. Carbon-based ocean productivity and phytoplankton physiology from space. Glob. Biogeochem. Cycles 2005, 19.
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Artificial intelligence (AI) is a rapidly advancing tool. It is heavily reliant on programming languages, data manipulation and analysis. As colleagues in the field of oceanography, I would like to know your opinions on the use of AI in this field. Furthermore, I would appreciate any recommendations for publications that could support your viewpoints.
It is important to be transparent about the limitations in terms of programming for the diferent subfields of oceanography, such as physical, chemical, biological, ecosystemic, and geological; how the incorporation of AI may lead to new disparities in scientific research; and how careful you would be with the use of these tools.
Thanks for your times!
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Sebastian E. Cornejo-Guzmán AI is becoming an increasingly significant tool in oceanography because of its ability to handle and analyze vast volumes of data rapidly and efficiently. It is crucial to highlight, however, that the application of AI in oceanography may result in research inequities, since certain subfields may have more resources and skills to deploy AI-based methodologies than others. Furthermore, it is critical to be open about the limitations of AI in each sector and to utilize the technology with caution, ensuring that the findings are accurate and dependable.
There are several papers that explore the application of AI in oceanography, some of which are as follows:
  • "Deep Learning in Oceanography: A Review" by B. Kostas et al. (2019)
  • "Artificial Intelligence in Oceanography: Challenges and Opportunities" by J. Chen et al. (2019)
  • "The Role of Artificial Intelligence in Oceanography and Marine Affairs" by S. J. Kim et al. (2018)
These papers can give more thorough information on the application of AI in oceanography, including possible advantages and problems.
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I am masters student and I will be studying micro plastics on a river system in the UK.  I have only found one location that sells Manta nets in USA but I was wondering if anyone knew of one to buy or borrow in the UK.  
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KC Denmark A/S is a global supplier of equipment. They have a range of Manta nets complete with accessories such as digital flow meters. I have just received a quotation from then.
You may consider visiting their website.
Regards
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I am working on fish ecology in an Indian estuary. However, proper identification of species belonging to Mugilidae is very difficult particularly of the genus Mugil and Liza. Most of the references available (FAO identification sheets and some Indian keys) differentiate the species based on the premaxillae shape which is difficult to ascertain in juveniles of the family. Also the family is highly dynamic with many new or updated genus and species. So, are there any recent comprehensive taxonomic keys available for the family from the Eastern or Western Indian Ocean regions?
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Hope for u always success
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Currently, microplastics (MPs) occurence researches in coastal and marine animals are performed in huge amounts, but their results concerning MPs abundances are not always given with the same unity.
  • From what I can tell from studies I read, most provide data using MPs/individual. There are some studies that sample in pools, and then, after ending samplings, calculate the MPs/individual data. It would be an issue if we compare MPs/individual data of two different studies: one that sampled in each individual and another that sampled in pools?
  • Should a specific study provide just the MPs/individual data? I think this study it would be sort of incomplete, considering that this data would not totally reflect the abundance of animals with different sizes, weights, and possibly ages, etc.
  • What is the best approach between other unities, such as MPs/g of the whole sample, MPs/g of their dry or wet weight? That are some formulas to convert samples weight for dry and/or wet. This is applicable for MPs?
I know much of that depends on the study's biological samples, and objectives, but I would enjoy reading researchers opinion about it.
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Dear Victor
Mostly expressed as items/m3, but you use another unites according to your specified work too!
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I am working on MODIS-SST, I need SST in situ data and water column data, Please guide me in this.
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Imran AHMED Khan, Apart from the Coriolis ARGO products, I would recommend using US-GODAE ARGO data. Please, go to the following links:
To answer your questions, the Argo data are very useful with a careful choice based on the quality flags.
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I do not have the PAR data. Fluorescence can be detected from dead particles too, but can it be utilized to get an idea about the euphotic depth.
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Have a look at our paper, "Resolving the Euphotic Zone," Deep-Sea Research I, vol. 83, pp. 45-50. We propose that the biological compensation depth is roughly equivalent to the depth of the base of the fluorescence maximum.
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I have downloaded one EO-1 Hyperion image, removed the bad bands, de-stripped the image using THOR De-striping in ENVI and applied the atmospheric correction using FLAASH in ENVI. Now I have the surface reflectance data in my hand. I need to apply some bio-optical algorithm for ocean colour application (IOP and Bathymetry Retrieval). For that I need the Remote Sensing Reflectance as an input. How can I get Remote Sensing Reflectance (Rrs) from Surface Reflectance? What are the procedures?
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Hello. This paper can help you with the answer to your question.
Poddar, S.; Chacko, N.; Swain, D. Estimation of chlorophyll-a in northern coastal bay of bengal using landsat-8 OLI and sentinel-2 MSI sensors. Front. Mar. Sci. 2019, 6, 598.
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I have CTD and Chlorophyll data for an upwelling location from two different years (Aug 2017 and Aug 2018). What should I be looking at to get an idea about the age of upwelled waters?
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Hi Saumya,
Here are some clues with regard to your question.
Radiocarbon (14C) in dissolved inorganic carbon in the ocean can trace the age of ocean water relative to the atmosphere and provide insight into climate‐driven changes in ocean circulation since the last glaciation.
The surface waters of the modern ocean are not in 14C isotopic equilibrium with the atmosphere. A steady state balance exists between the slow invasion of atmospheric 14C into surface waters following production in the atmosphere and the aging of isolated interior water (marked by the decay of 14C over time) with the subsequent cycling of those waters back to the mixed layer. These dynamics result in an age difference between surface waters and the atmosphere termed the reservoir age.
I think you can follow the approach outlined above to determine a possible age difference between your 2017 and 2018 water samples. Evidently you will have to apply a good statistical test to determine whether a difference in reservoir age is statistically significantly different. This requires a very accurate estimate of the variability (or standard deviation) on your reservoir age measurements. Furthermore, two samples in time are not enough to elicit a trend in reservoir age I am afraid. For this type of analysis you need more sampling in function of time (years).
Lots of success.
Frank
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Which grab type would you suggest for sampling marine benthic macroinvertebrates in sandy substrate or maerl? We would like to use it in coastal samplings, often in recreational boats carrying a small winch, by one or two people. So, it shouldn’t be very heavy, and the ideal surface would be around 0.05m2.
In our lab we have a 30-years old Ponar grab (9”x9”) that needs to be replaced. Every time we tried using this specific grab, it had serious issues sampling sufficiently any substrate than mud. In muddy sediments it was capable to collect almost full volumes of samples. However, both in the description from Wildco and references (e.g. Elliot & Drake, 1981), Ponar grab is suggested as the ideal type for sampling coarse material. So, I wonder if the issues in our Ponar are due to old age or maybe poor maintenance.
Has any of you had trouble sampling coarse material with a Ponar grab? Would you suggest another type for this substrate?
Thank you in advance for any suggestions.
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Van-Veen grab 1/40 m2
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This is in relation to the sampling done at various stations along a cruise track at different times of the day. The surface temperature would be affected by the time of the day it was sampled. How can I eliminate that difference to look at the trend?
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Working with time-of-day as a factor will be a challenge because I assume your sampling times are random randomly spaced. That means you might be better off fitting for a trend plus some model of diurnal variation. The problem is that latter can take many functional forms, depending on solar forcing, whether there is nighttime convection, and so on.
I would advise starting by regressing to a formula that has a trend, plus both a sine() and a cosine() with period one day. (Using both sin and cos lets you find the phase, but still in a linear regression, which is easier to deal with than a nonlinear one, unless you are experienced.) Then add a twice-daily harmonic. Then add a thrice-daily harmonic. By comparing the results you may start to learn how the diurnal variation is affecting your estimate of the trend.
I would start with artificial data, so you can test the accuracy. AIC or other methods should be used to avoid overfitting. (If you don't know what AIC means, you ought to give yourself some time to learn elementary stats, before trying anything complicated with your data.)
Whether you will see a linear trend is questionable. I've never seen such a simple pattern in ocean data. So you might want to start by fitting this sort of sequence of diurnal models, then removing the diurnal signal, and then simply plotting the results, rather than expecting a trend.
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I am wondering if storing biological samples in ethanol is acceptable, if these organisms are to later be tested for their mercury concentration. 
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Thank you both so much for the feedback. It is very appreciated. 
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I will be increasing T by 2C every few days and need a heater that can do this accurately for a few gallons of seawater
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Tubular Immersion heaters are best option. It can be designed to based on Tank dimensions n with a suitable control System ( Panel). We make such heaters.
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Seto Inland Sea, the largest semi-enclosed sea in Japan,
Some researchers provide the M2, S2, K1, Ovalues of the main strait of the Seto Inland Sea, Some provide the mean surface current of the whole Seto Inland Sea, which one or someone else is the best descriptor of the current speed? I want to investigate the influence of current (speed) on water stability and red tide occurrence. 
Thank you!
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For the residual current speed, you need to take out the tides and analyze the sub-tidal velocities. sub-tidal velocities can be obtained by low-pass filtering your original raw time series. You can also use Tidal harmonic analysis packages like t_tide  to find the tidal velocities and remove it.
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This far the species are identified as:
1. Diadema setosum
2. Sarcophyton sp
3. Heteractis magnifica 
4. Red Mushoom / Stone ? - what is the latin name?
5. some kind of sponge?
6. seastar
7. Zebrasoma scopas 
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6 is definitely an asterina star. Hard to elucidate a species in a photograph. That is a common "pest" in the aquarium hobby. Some are known to feed on crustose coralline algae, while others will feed on zoanthids. 
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Is there a consensus on the optimal concentration of glutaraldehyde for the preservation of marine phytoplankton?  I typically use 1%, but notice that other researchers use from 0.1% to 3%.
I am interested in maintaining as many taxonomic features as possible for LM and SEM with the lowest concentration of glutaraldehyde that is acceptable, since I don't like working with this chemical at sea. I typically work in low chlorophyll high nutrient areas of the Southern Ocean, but may find sea-ice blooms from time to time.
I appreciate you thoughts and recommendations :).
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HI.
usually working stock of 10% then between 1% and 2% is where I have usually gone. I have a paper which I used as a good reference for marine samples, ya no lugols, as the colour issue and also the degradation with diatom frustules getting broken down. My lowest would be 1% pretty smelly still, but I make it on board ship in fume hood then you can pre-spike vials keep it in the fridge and then out samples back into the fridge after sample is added, I hope that helps? Ya more is better than less. Also remember that lugols does colour the organelles so harder to identify, much better to use glut.
I hope this helps, let me know if you need the paper?
Di
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i have been collected my samples from Persian gulf, hard bottom, that they were attached to a soft coral.
i think it is a Ophiothrix sp, but i cant identify it in species level
if you know its name, please send me a reference
thanks a lot
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Definitely not Ophiolepis. Ophiotrichidae is correct and I think it is Ophiopsammium not Ophiothela but needs to be verified with literature and close examination.
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Found in a marine plankton sample
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scale of butterfly
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Many gastropods are predators that drill or bore through their prey's body covering (shell, exoskeleton, etc.) using a combination of radular scraping and chemical dissolution. Examples I know well include moon snails (Euspira (= Lunatia) spp. (Naticidae)), "whelks" (e.g., Nucella spp. (Muricidae), Buccinum spp. (Buccinidae)), but I suspect there are many others.
I am gathering information on gastropods that feed in this way, and would like to assemble a list of as many (or all) species that do so as possible. There is a lot of literature on fossil borehole/drilling predation, but I am interested in EXTANT species. Are there any good resources (reviews, book chapters, etc.) that might present such a list? Are there other taxa within the Gastropods beside the Muricidae, Naticidae, and Buccinidae that contain boring/drilling predatory species?  Just how many gastropods do this?
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Hi Brady, find a comprehensive list of boring gastropods in the Table 2 of this paper by Michal Kowalewski
You may obtain a decent estimate of the total recent species diversity of each family (and global georeferenced occurrences) at the Ocean Biogeographic Information System
Best regards
Marcelo
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working on sparids diet i'm looking for a site or link for identification of preys mainly:
-crustacean, annelids, fish, echinoderms, algae...etc
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All very good advice!  I dissected flounder juveniles and knew what species the single eyeballs in the gut were from.  I was able to infer how many of that species had been ingested! Good Luck!
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I am checking the biological production rate in a particular season and hence studying seasonal variability. 
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Dear Samiran,
2. For chlorophyll check http://oceancolor.gsfc.nasa.gov/cms/
Rgds.
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These are formations found in the pump house of a salt work near Port Elizabeth, South Africa. The amber-like yellowish-brown substance inside the formation is hard at the edges but still soft in the middle. What is it and what is likely to produce it?
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I've also been trying to figure out what the formations are. Adding onto the possible cyanobacteria answer, Nostoc pruniforme heterocysts (Mare's eggs) are formed in fresh water environments but there may be similar nitrogen fixing cyanobacteria formations in saline or hypersaline environments; purely a guess but would be interested to find out.
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Hi! Everyone,
Could someone help me in identifying the brittle star in attached photo. It was collected  from massive coral colonies mostly Porites spp and Cyphastrea spp in Kuwait, Arabian  Gulf.
Thanks! in advance.
Best Regards,
M. Nithyanandan
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Thanks! Dave,
I will do the needful and try to get hold of Clark, 1938.
Best Regards,
Anand.
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I found them from low saline condition of Cochin back water system. Initially I thought both could be species of Staurastrum/ Actinastrum (green algae). But I cant find out the specimen (b). Kindly help me to identify.
Thank you.
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1) Staurastrum
2) Eunotia
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How to rear Macrobrachium rosenbergii larvae? Whether 1 or 2 litre plastic containers are enough? What will be the preferred feed at diff. stages?
Kindly advise me on this
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Hello,
This depends upon the number of larvae you are intended to rear together. If you rear them individually 50 or even 20 ml per larva could be enough. Anyway, be sure that oxygen concentration remains at a hight level according to temperature.
As for food, you may use Artemia  nauplii for the first stages, may be larger Artemia larvae later.
Cordially
Auguste
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the images was attached 
salinity of the collected water  is 4 ppt, almost freshwater resource.
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Rajan:
You have not provided magnification. Still upper two forms show affinity with Spirogyra and lower one with Pediastrum.
Best
Syed
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Plotting real tidal data from different regions and different tidal reference stations, it is clear that some tidal datums often have the same relative position.
Trivial examples are the relative positions of the Lowest High Water (LHW) and the Highest High Water (HHW); or of the Mean Lower High Water (MLHW) and the Mean Higher High Water (MHHW) in a semidiurnal cycle.
However, the relative position of some other datums does not appear as trivial, especially when considering the neap-spring synodic cycle.
For example, the Lowest High Water Neap (LHWN) can be lower or higher than the Highest Low Water Neap (HLWN), i.e. the range of the neap high tide can overlap or not with the range of the neap low tide. Another example is the relative position of MLHW and the Mean High Water Neap (MHWN).
I wonder if there is any classification of tidal regimes that describes these types of patterns, that is or might be related to geographic areas, or ecological patterns.
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I've read that SST fronts stimulate biological productivity (e.g. Woodson and Litvin 2015, PNAS). But my question is how strong of a SST front is needed to significantly enhance productivity? Of course this will be dependent on a number of factors, but what is a rough estimate? Will a front with 1 ℃ SST change be relevant? Or is this only found with much bigger gradients (e.g. 10 ℃ change)?
I'm particularly interested in the application of this question in the Gulf of California, Mexico.
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Particularmente en el Golfo de California ocurren demasiados procesos de diferente índole que resultan en frentes superficiales de temperatura. En el norte la mezcla de marea genera frentes térmicos de hasta 3 grados en el archipielago central, y frentes más difusos en el alto golfo. En el sur del golfo los procesos predominantes que generan frentes son la surgencia en invierno/primavera y los remolinos en verano, En la boca por otro lado la interacción con la corriente de California y el agua tropical generan frentes de masas de agua.
Entonces, todo el golfo es susceptible a los procesos de mesoescala, pero hablar de un frente superficial, sin tomar en cuenta su origen, dificulta evaluar en que medida promueve el aumento de la productividad.
Particularly in the Gulf of California too many different kinds processes resulting in surface temperature fronts. In the north, tidal mixing generates thermal fronts up to 3 degrees in the central archipelago, and more diffuse fronts in the upper gulf. In the southern Gulf, predominant processes that generate fronts are upwelling in winter / spring and eddys in summer. In the mouth, interaction with the California current and tropical water, and gulf water generate fronts throughout the year.
Then, the entire Gulf is susceptible to mesoscale processes, but talk of a surface front, regardless of its origin, difficult to assess to what extent promotes increased productivity.
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Can anyone help me to identify this DINO?
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Dear Jackson, thanks for your attention. I suspect it's C. helix or C. convolutum, but I am not sure, I will try to establish pure culture and do 28s LSU DNA to confirm it.
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I found this species under the rock by attaching firmly. Its almost around 7-8 cm long. Collected along the coast of southern Tamilnadu. The body was so soft feels like worm. Help me to identify this.
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Dear Nandha,
I think it is white sea cucumber probably Eupentacta quinquesemita.
Best regards
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I use sea surface temperature (SST) from satellites to assess marine mammal and sea turtle bycatch, habitat, and distribution. Recently the primary SST data source that we had been using (Pathfinder SST) has not been updated. So, we are looking for a new satellite SST source. Websites such as JPL's PO.DAAC (http://podaac.jpl.nasa.gov/) have added lot of choices in the last few years for different SST products, many of which blend data from multiple satellites and often interpolate to fill in areas that would other wise be missing data due to cloud cover. Can anyone suggest which data product would be best? We would prefer products with <= 4km resolution that go back a few years, if not many years. One source that seems promising is the G1 SST (http://podaac.jpl.nasa.gov/dataset/JPL_OUROCEAN-L4UHfnd-GLOB-G1SST), though it would be great if it went back further in time. If anyone could offer advice as to which data products are likely to be the most accurate, I would greatly appreciate it.
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I suggest you MODIS SST. You can refer to the following publication for investigation and validation of MODIS SST:
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Hi, I would like to know if any has some insights about colonial stage conservation of P. pouchetii at long term. I stored seawater samples with lugol at 4C for above a year. I was wondering if the colonies could have been disrupted over time. Thank you!
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I would be pretty certain that the integrity of the colonies are not preserved, certainly not over that time. Even if "Psedulogols" are used as this mixture of glutaraldehyde and lugs are often called. Instead the best you can do is live samples in a FlowCam, or put them on a filter and freeze (Estep et al)
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I'm trying to determine some preliminary distribution info for a few soft coral species that may cross over from temperate to tropical waters.  I'm particularly interested in Telesto sanguinea, Leptagorgia virgulata, L. hebes. Have you seen them further south than mid-Florida and if so where did you locate them? Also, have you seen them in the Gulf of Mexico?
Thanks!
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You may wish to check out NOAA's Deep-Sea Coral & Sponge Data Portal.  
The map portal (click on the map) has a data query tab, where you can enter a scientific name.  While most of the records are currently from US waters, there are quite a few records from elsewhere in the Caribbean (mostly from the Smithsonian's National Museum of Natural History).  Our database focuses on species that occur deeper than 50 m, so it may not capture some of the species you are interested in.
There are records of Telesto sanguinea from the Florida Keys and the Gulf of Mexico.
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For modelling of species distribution in North Sea waters, I am looking for the best source for high resolution gridded oceanographic data for the North Sea. Since the North Sea is a small sea, I think the smallest resolution available is best.
Currently I am downloading the MARSPEC dataset (http://www.marspec.org), which seems one of the highest resolutions available (ESRI raster grids at a 30 arc-second spatial resolution). But they only offer derivations of Bathymetry, Sea Surface Salinity and SS Temperature. I also want to use current velocity and organic matter content (e.g. detritus or POM) in my model.
Can anybody advise me on what source to use?
Other sources I looked at are:
http://www.oracle.ugent.be/ - This is on a much lower resolution than my intended modelling resolution of 1,000x1,000 m.
http://www.aquamaps.org - This has an even lower resolution.
Edit (16-08-2015): http://marine.copernicus.eu - This does offer high resolution data sets for ocean colour (e.g. Chlorophyll content or DOM) but sets on other variables are all >7km.
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Hi Joop,
A new publication just appeared
Monthly maps of optimally interpolated in situ hydrography in the North
Sea from 1948 to 2013 by Núñez-Riboni and Akimova in Journal of Marine Systems 151, 15-34
Possibly this is useful to you.
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I am on a study regarding the impact of unregulated fishing practices on stock and biology of yellowfin tuna. I understand biological assessments are used to tell whether or not a body of water can support survival and reproduction of fish. 
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Although this is not strictly my area of expertise, I am currently involved in a aquatic study that consists of a biological characterization in the vicinity of a water intake structure.  To begin with, such factors as bathymetry, prevailing weather, currents, air/water temperature, and insolation obviously play a significant role. Remotely sensed and bathymetric data may help give a general picture of physical conditions over a large area, which could then be used to identify possible sample locations and design a sampling plan.  The approach in general is to assess the habitat - water quality parameters (temperature, dissolved oxygen, pH, salinity/conductivity, and turbidity/Secchi depth), as well as the presence of structure or vegetation - along with sampling of the biological communities present, both plankton and nekton, and in near-shore cases, perhaps even benthic communities, to evaluate the number and diversity of species present. One goal of this sampling is to obtain, if possible, eggs, larvae and/or juvenile organisms to evaluate reproductive activity.  For this reason sampling might need to be undertaken at various times and locations throughout the year to obtain a complete picture of the fishery and spawning patterns.  The species data collected are then statistically evaluated to determine richness, evenness, calculate net productivity, etc.   A good place to start is by reviewing the literature for your fishery or comparable fisheries or species to see the specific approaches and techniques used, as what I have described is a very high-level overview.  Studying a pelagic species like tuna poses challenges, but a skilled fisheries or marine biologist/ecologist could also give you a more detailed (i.e. site-specific) approach tailored to your particular needs.
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How can I get a complete identification key of Zooplanktons ?
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It depends on the zoogeographical region, freshwater or brackish or salt. General keys are based on the most typical (in author's opinion) species. In first approximation such general keys can be used, but you should support tham by specialised keys, e.g. with regional or world fauna books. In post soviets countries f. ins.  when identifying Rotifers we use normally perfect Kutikova book, when have to do with Chidoridae – Smirnov Fauna of the world (1971) (in Russian). As well, Cyclopoidea by Monchenko, Harpacticoidea by Borutzky etc. So, you should define more accurately you interest.
Andrey
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This jellyfish was caught in the eastern central Atlantic in depths between 100 and 600 meters. There was just individual of it. Can anybody identify it?
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I agree with the other comments as it does look like Pelagia noctiluca and it does not have a sedentary life history stage.  So finding it well offshore is very likely. Its nematocysts can penetrate human skin and can leave a weal.  This is a further test! hope this helps. Dan
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These are copepod grazing experiments, where the particle size spectra and abundance were measured with a coulter counter particle counter in initial samples, and final control (no grazer) and treatment (with grazers) bottles.  
This is a new area for me, any help is greatly appreciated. 
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Aha, I misunderstood. Some do test that, you could e.g. make a t test between grazed and control treatments. But i usually do not. Maybe I would if there is no clear grazing effect to be able to state "no significant grazing" Regarding the shrinking I would not worry for short (over night?) incubations. But several common colony forming species do split up in response to copepod grazing. E.g Skeletonema (Bergkvist et al 2012 L&O) Phaeocystis (Long et al 2007 PNAS), and Alexandrium Selander et al 2011 PNAS). At least for Skeletonema and Alexandrium the response typically takes longer than an over night grazing experiment to develop fully. If you do total bio volume it should not matter anyway, the cells are still there. So this probably added more confusion than solution, but I think normally stats is not necessary to prove grazing in a grazing experiment, rather to prove differences in grazing between treatments, prey etc. Best wishes /Erik
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If trapezoidal integration method is used, it provides value with units of mg/m2 (which is per area) but I need to know is there any way to get chlorophyll value for entire water column in terms of mg/m3 (which is per volume)? 
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using  the published methods of chlorophyll determination , such as the method of Holden(1965), the results are given in mg per liter. It is very simple to convert these values as follows:mg per cubic meter =0.001mg per liter.
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This "jelly ball" has been saw twice floating in shallow marine waters in Sicily (Mediterranean Sea). Someone suggested that it might be a damaged jelly umbrella but the evident bilateral symmetry suggests that it should not be a jellyfish. Hence the "damaged jellyfish umbrella" seems improbable. It might possibly be part of an organism or even an ooteca (mollusk ooteca?). What's your idea about?
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No doubt, this is what remains of a scyphozoan jellyfish Chrysaora hysoscella. Probably it has experienced a turtle bite! Keep it in ethanol, we are working on this species, please!! Grazie, Luigi
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VGPM- Vertically Generalized Production Model
SeaBAM model
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I might suggest some absorption-based approaches, especially for coastal area, here are two examples:
Smyth, T. J., G. H. Tilstone and S. B. Groom (2005). "Integration of radiative transfer into satellite models of ocean primary production." J. Geophys. Res. 110: C0014.
Barnes, M. K., G. H. Tilstone, T. Smyth, D. J. Suggett, R. Astoreca, C. Lancelot and J. C. Kromkamp (2014). "Absorption-based algorithm of primary production for coastal waters for total and size-fractionated phytoplankton." Mar. Ecol. Prog. Ser. 504: 73-89.
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I am mostly interested in species identification. Maybe there is some general book about the biological diversity with photos and drawings?
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I have sea surface temperature data from model (numeric model) and in situ measurement (logger). I would like to know quality of my model compare to in situ data. What kind of methods I must used?
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Dear Eko,
I forgot to mention in my last response, a good tool to present the results of your comparison (if you do not already know the method), is to use the Taylor diagram (Taylor, 2001: JGR 106D7, 7183-7192).
(Here also you can contact me for further details at guy.caniaux@meteo.fr)
Best
G.C.
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What are Spatial and seasonal differences in the diet of sedentary annelida polychaeta of Mediterranean sea?
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In addition with the previous comment from Florian, the feeding guilds defined by Fauchald and Jumars were recently updated.
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The distribution of annelid species is based on what? Are there documents on this research?
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Have a look there:
QUIROZ-MARTINEZ, B., FRANÇOIS G. SCHMITT, F.G., DAUVIN, J.C., DEWARUMEZ, J.M., FOVEAU, A. & GARCIA, C.. Distribution patterns of annelid polychaetes species from the continental shelf (0-200 m) in the North Sea, English Channel, Irish Sea and Outer Bristol Channel. Italian Journal of Zoology 78(S1), 324- 332.
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If we have remarkable decrease in fish production, what are the priority suggestions to take? 
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Thanks for your collaborations
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Please help me  know this
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Indeed, those are extended tentacles. The pink indicates damage and that regeneration (growth) is going on. Species: Fungia fungites.
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Can I have information or links on ecology and biological study of the polychaete species of the Algerian coast, and I would like to have some literature on invasive species and endemic to the Mediterranean Sea. Grazie
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Buongiorno F. Kies.
Bakalem A. Diversité de la macrofaune des sables fins de la côte algérienne.
Rebzani-Zahaf C. & al. Cycle annuel du peuplement macrobenthique du port d'Alger.http://archimer.ifremer.fr/doc/00093/20458/18130.pdf
Rouabah A. & Rouabah L. Biodiversité et complexe Perinereis cultrifera Grube (Pelure) : un exemple de spéciation.
Buona fortuna e successo.
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Could you suggest any information or links on the ecology and biology of rivers of the Mediterranean sea, especially North Africa (Algeria)
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The University of Aix Marseille in France are working on the modelling and monitoring of the Po River in the mediterranean sea in the French coast. But I know they have data from the Italian and the rivers from Spain. A good contact point could be: the Dr. Christian Grenz
best regards
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I am working on using  normal Digital camera (gopro, CanonSX230) to capture aerial images and analyze it to be able to identify various benthic organism in tropical marine water. Am a little new to the process, can anyone walk me through a simple approach. 
Sample image attached
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Hola Emmanuel, I have done extensive work in this area (we made an atlas for the entire coastline of Mauritius; mapped seagrass in Florida; intertidal vegetation in both Canadian coasts, and other projects), BUT we used our compact airborne spectrographic imager (CASI); yet, some of the methods might be useful to you.
Asier's points are good, but we found that using unsupervised classification provided better results. Normally, unless you know with some degree of certainty the composition of your study area, or you cannot account for its diversity (and have all the required end members). Having said that, if what you want is to identify certain "classes", the rule image generated from the supervised (we use mostly S.A.M.) gives you nice spatial probabilities.
I advocate for unsupervised, creating a lot of output classes, and then use clear criteria for manual groupings.
I can send you some papers if you want; let me know! and best of luck.
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I am working with phylogeny of venus clams, and there are some weeks I am trying to keep contact with any researcher from Senagal or Nigeria. I need go there to examine some Pitar species to put in my morphological matrix. Unfortunatelly, all my efforts failed. 
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I know this person in Senegal, hope this helps :
Dr Marc BOUVY
Directeur de recherche IRD
Directeur adjoint UMR 5119, Ecologie des Systèmes marins côtiers (ECOSYM)
Université Montpellier II, Place Eugène Bataillon
Case 093, F - 34095 Montpellier cedex 5, FRANCE
+33 (0) 4 67 14 41 28 (tel)
+33 (0) 4 67 14 37 19 (fax)
+33 (0) 6 13 53 24 02 (port)
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From your knowledge and opinion, what are the most efficient protocols (in term of cost and information quality) to monitor the good environment status of marine benthos (hard substrate) in your marine region and why?
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Evaluation of stress index, where both opportunistic and sensitive species are present in the matrix
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I am correlating pCO2 with fluorescence in the Western basin of the Mediterranean Sea. This basin is oligotrophic, but in the spring blooms can occur. I was expecting during this season the pCO2 to decrease due to the biological activity, but the correlation coefficient is positive. What could be the cause behind that?
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I do not agree with what Alastair has said, pCO2 depends on pH of the water, it is other way around, pH of the sea water is dependent on pCO2. moreover, blooms can be also limited by CO2 in the oceans if not having constitute CCM. an increase in pH has been observed many times with enhancement in phytoplankton biomass. However, I agree with the last part of your answer. and also what Koji has mentioned. This is possible that for warming or upwelling, significant amount of CO2 is added up to the surface water and there could be simultaneous uptake also by phytoplankton and enhancement of fluorescence. However, the net increase in CO2 could be more and hence positively correlating with the fluorescence. In the Oligotrophic condition under high solar light there can be photo-inhibition leading to net heterotrophy and can may not uptake considerable amount of pCO2. As Koji said, phytoplankton stock is also important.
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Maybe you have already seen this paper of Morabito et al. 2013, they found that ocean acidification affected the osmotic swelling etc of nematocysts. That would hamper their capacity for food capture. This is a really interesting, and devastating, effect that has received very little attention.
Morabito et al. 2013. Sea Water Acidification Affects Osmotic Swelling, Regulatory Volume Decrease and Discharge in Nematocytes of the Jellyfish. Cellular Physiology and Biochemistry 32(suppl 1): 77-85.
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It’s an incredibly interesting question, Susanna. We’ve known for many decades and across a fairly wide body of literature that pH affects the discharge of nematocysts: in some cases, this is inhibitory, while in other cases this is stimulatory. Most of this work has been done in the context of first aid for things that sting us, rather than on the subtler shifts that could alter an organism’s ability to survive. But given everything we know about nematocysts, it seems completely plausible to me that yes, OA could conceivably alter the discharge of nematocysts. In fact, I would go so far as to say it would be surprising if it didn’t. It’s just an educated guess – certainly the research needs to be performed! Man, this is exciting!
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I currently identify zooplankton to broad categories such as Echinoderm.  I would like to start identifying the echinoderms further to class, but am concerned about being able to tell the difference between the bipinnaria and auricularia larvae.  I understand that the main difference is that the bipinnaria larvae have two ciliary bands whereas the auricualria have only one. Can you see this readily with a stereoscope?  Is there another way to differentiate the two?
Thanks!
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Hello Nicole,
in bipinnaria larvae (=Asteroidea) there is no trace of calcitic skeletal elements or ossicles ... in auricularia larvae (=Holothuroidea) there are calcitic skeletal elements (1: undiferentiated mesh work = Holothuriidae or Stichopodidae; 2: small wheels = Synaptidae) ...
You can check this easily in using a light microscope with a polarizer (in switching between plane- and cross-polarized light) ... calcite is normally colourless/transparent, but has a strong (so-called) double refraction and will appear (with crossed nicols=cross-polarized light) pinkish to greenish white under the microscope (if present).
For other detailed characteristics you may read: "Atlas of Marine Invertebrate Larvae" (2002) ... p. 499ff. (Asteroidea), p. 513ff. (Holothuroidea) ...
Best wishes,
Mike
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These specimens are collected from North Norway. As I know there is more than one Mytilus species and it is hard to identify those from photos. Here are some of the photos of the specimens collected.
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Hi Lennart
I agree with Andrey; Arctica islandica.
I think the mussels are Mytilus edulis, one is extremely distorted.
One of the best bivalve guides for NW Europe is http://naturalhistory.museumwales.ac.uk/britishbivalves/Browse_taxa.php
Click the “here” button to get all species displayed.
If you want a particular species just type its name into Google (or other search engine) followed by the Welsh word for museum “amgueddfa” and you will be directed to the page.
Give it a try with “Arctica islandica amgueddfa”;  it should come top of the list.
 Plate 1 shows an adult, more circular than yours which are not full size, and young ones of various sizes. They darken with age (they can live to over 500 years old). The Norwegian name for it is still used in Orkney, same pronunciation, different spelling: Ku shell.
A useful facebook group for help with identifying marine molluscs is https://www.facebook.com/groups/british.marine.mollusca/ It has members from Norway to Portugal.
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Dear Fellows,
I have identified some of plankton but because I am new in this field, I need your correction as an expert in phycology. 
Thank you so much in advanced !
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you images are not clear for identification
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Hi Friends,
I found this sample(which is attached) along with the phytoplankton samples collected. Suggest me weather its a kind of plankton or some other thing. If its a plankton help me to identify its name.   
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I am fairly sure that it is a cycloid fish scale, as others have suggested. We frequently encounter them in plankton-net samples. They (1) get knocked off of fish that are caught by the plankton net and (2) exist in sediment largely as the result of predation events; sedimented scales may be easily re-suspended into the water column, where they may be collected by plankton nets.
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We found from a recent study on a number of small groups that they appeared to orientate North (hinges South) and wondered if anyone else had come across this? 
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Hi both,  that's great thanks I'll get in touch with them.
Cheers
Kate
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I'm trying to reconstruct the productivity changes in the southeastern Arabian Sea, during the last glacial period. The foraminiferal proxies suggest an increased glacial productivity in this region. I want to understand the physical forcing, responsible for high surface primary productivity in this region during the last glacial period.
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My co-authors and I provide a partial review of the impact of changing glacial winds on the Agulhas Retroflexion during the LGM in this paper. We discuss the impact of variation in regional winds on marine production and coastal currents off West Africa. The results should help you to hypothesize changes you may see in the Indian coastal currents for comparison with your study.
You can also review the chapter from my dissertation work on the California Current during the LGM for comparison. Primary production can be enhanced by several processes in addition to the Fe hypothesis noted in the prior answer. For example, increased offshore Ekman transport, or increased Ekman pumping via enhanced wind stress curl will increase the nutrient flux to the surface ocean, thereby potentially increasing primary and by inference secondary production.
D Nof, V Zharkov, J Ortiz, N Paldor, W Arruda, E Chassignet, The arrested Agulhas    retroflection, Journal of Marine Research 69 (4-6), 4-6, 2011
J Ortiz, A Mix, S Hostetler, M Kashgarian, The California Current of the last glacial maximum: Reconstruction at 42 N based on multiple proxies, Paleoceanography, 12, 191-206, 1997
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Found it on Pachacamac island, near to the central coast of Perú. It was caught last Friday. A female had 6 spotted-young sharks to a litter. My doubt is that females were plain-coloured and the others had tenuous black spots.
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Jesús, Triakis megalopterus is confined to the South African coast (of the Atlantic and Indian oceans).
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Turbid water generally affect the biodiversity badly.
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Well I guess, a phytoplankton bloom increases turbidity, especially in eutrophic waters. And the other way of the causal chain is also possible, in waters with high sediment induced turbidity, phytoplankton may be affected. However, I think submerged macrophytes are generally more affected by turbidity than phytoplankton.
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I would like to get an idea of the depth of light penetration using calibrated chl fluorescence (and transmittance if necessary) depth profiles. Casts were performed before dawn yielding poor PAR profiles.
Is there an up to date version of the Morel 1988 equation: Ctot = 4910*Ze-1.34?
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Hi Nicolas,
you can use the model of morel (1988) and take a look to Morel and Maritorrena (2001) for updated parameterizations.
Besides, you can use standard models for IOPs in case 1 waters, see for instance this publication by André morel which give a good summary of all these relationships (MOrel, 2009), and then calculate Kd as a function of IOPs using MOrel and Loisel (1998) pour each wavelenghts to get Ed at each wavelenght, and integrate over the visible domain.
hope it helps
hubert
Morel, A., and S. Maritorena (2001). Bio-optical properties of oceanic waters: A reappraisal. Journal of Geophysical research, 106, 7763-7780
Morel, A. and J.F. Berthon (1989). Surface pigments, algal biomass profiles, and potential production of the euphotic layer: Relationships reinvestigated in view of remote-sensing applications, Limnology and Oceanography, 34, 1545-1562.
Morel, A. (1988). Optical modeling of the upper ocean in relation to its biogenous matter content (case 1 water), Journal of Geophysical Research, 93, 10,749-10,768.
Morel, A. and H. Loisel (1998). Apparent optical properties of oceanic water: Dependence on the molecular scattering contribution. Applied Optics, 37, 4765-4774.
Morel, A. (2009). Are the empirical relationships describing the bio-optical properties of case 1 waters consistent and internally compatible? Journal of Geophysical Research, 114, C01016, doi:10.1029/2008JC004803.
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Saint-Petersburg State University (Russian Federation) would like to organize some collaboration programs with Universities and researches from Egypt in the fields of Marine biology, Biology, Oceanography. Please contact Dr. Nikolay Maximovich (https://www.researchgate.net/profile/Nikolay_Maximovich) or me during next 3-4 days. Now we just collecting the information about the people and institutions interested in this question.
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Dear Colleagues,
    This idea is really great and we would be glad to join. During summer 2014 we organised our local "The North Pacific biodiversity study summer school at Vostok Marine station in Vladivostok (Russia). This school could offer some initiative for cooperation. We have scientists who could provide classes in the fields of molecular systematics, botany, hydrobiology, cultivation of marine invertebrates and so on. There are the boats, diving service, any kinds of equipments and accomodation that could serve sutisfactory to provide good qulity of research and study. Please, add us into the list of colleaguies who would like to get information and start discussion.
Contact Dr. Arkadiy Reunov (arkadiy_reunov@mail.ru).
Best regards,
Arkadiy
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 Can anyone help understand the seasonal growth patterns and biology of Codium tenue?
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Thank you so much for the info! I appreciate the help and input.
Is there any studies which investigated the optimal temp and other environmental conditions for C. tenue
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We have encountered what appears to be two different marine plants and what could be an encrusting sponge in the southern waters of the Red Sea, Saudi Arabia, near Jizan in 3-5m depths. The general hard substrate consists of rubble and coralline algae. Does anyone have an idea what these species might be? The unidentified species are marked in the attached picture. Thanks for your help.
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Ok Holger,
Nice to read that you already found the connection between Stolonoids and Fronds on that Sargassum species.
Cheers
Ricardo Haroun 
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Survey shows new species have been seen.
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as far as i know, no studies were conducted on this topic.
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My future PhD work will be devoted to research of coccolithophorid blooms (Emiliania huxleyi) using remote sensing algorithms. So at some point I will need to validate these algorithms by comparing results with some in situ measurements, which were done in the Arctic seas. Are there any sources or data bases of in situ measurements which I can use for my work?
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SeaBASS and NESDIS would be good places to look. SeaBASS had some in situ pigment data (multiple methods) and corresponding satellite data in my region (Gulf of Mexico).
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I have some cultured cyanobacteria , and I want to know if it is truly planktonic or not.
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benthic or planktonic none of them has relationship with water movement to show there property. its all about the presence or abscence of the gas vacuole in youger culture gas vacuoles are prominent but as it gets old n ratio of protein to carbohdrate changes its buoyancy reduces. Some times it might be the genetical rearrangements that might lead to loss of buoyancy. Please check the attached papers.
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We got results of nitrogen fixation by unicellular cyanobacteria in an eutrophic estuary. In an eutrophic estuary they have enough nutrients available for their metabolism, so they do not have the need for nitrogen fixation. However, even under these circumstance they continue with nitrogen fixation. What is the reason for this?
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Well its a known fact that cyanobacteria can fix nitrogen. But in eutrophic waterbodies they have to compete with other algal species to bloom. At this stage, cyanobacteria can not risk to loose their energy in Nitrogen fixation, rather they use the available nitrogen source to increase their biomass rapidly.
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I have fish data collected with bottom trawl on a narrow continental shelf, covered with patches of mud, sand and gravel, extension more tham 100 km. The slope begins about the depth of 40-50 m. My data are from the 10, 25 and 50-55 m isobaths. I am in Northeast Brazil.
Would it be a mistake to analyse all the species surveyed, without excluding the small pelagic species, since the trawls are designed to collect the demersal ones?
I name “small pelagic species” the clupeids, engraulids, pristigasterids, sphyraenids, stromateids, young carangids. The fish are concentrated mainly in the shore areas, in terms of species richness, number and weight.
Do you know some book or papers dealing with this subject?
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I agree with Freedman!
At the same time, I am also concerned about the ecosystem that stretches over 100 Km, over which you have used a bottom trawler and cleared off the bottom dwellers living in there.
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There are so many approaches to measure NEP (e.g. statistical, biogeochemical, remote sensing etc.). How is NEP associated to carbon sequestration?
Biologically fixed carbon could be retained by the system at a varying scale (from seconds to 1000s of years). Which one can be considered as real sequestration?
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For my studies, I define NEP as primary production above and beyond metabolic needs of the primary producers (or all primary carbon that can be consumed or lost in the system). NEP can then be utilized by primary consumers or enter the detrital part of the system. I then breakdown the detrital pathway as detrital consumption or export out of the system. After all of these terms have been taken into account the residual carbon (NEP) should enter the remaining path....burial. This is the pool that can be considered sequestered given a defined timeframe. Very over simplified, but this sheds some light on my hierarchy.
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I want to know the reason.
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Thanks Maljkovic, I found the answer in this paper.
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I'm writing a paper on the impact of the dominating currents (Brazil, Malvinas/Falkland) on the distribution of microbes on the Patagonian Shelf. I could not find any information on bacteria bulk parameters (numbers, biomass, growth, respiration, enzymes) in the media. Does anybody in the community know more about this or is it really a black box?
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Dr Paulo Abreu from Federal University of Rio Grande (docpca@furg.br) has collected and counted bacteria along a cruise track from subtropical southern Brazilian waters, crossing all frontal systems down to Antarctic waters. Samples were collected out of the Argentinian shelf (but nearby). The data were never published. Contact him to check this informati9on and how he may help you
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I want to analyze the interaction between fish abundance with environment variables. Does anyone have experience using subsurface data (sst, salinity, etc)? Where can I download this kind of data?
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One should be very careful just downloading climatological data sets, because these are generally constructed from measurements/observations taken at different times. Some of the climatological data sets offer seasonal fields. However also in this case, these are usually constructed by merging measurements from different field campaigns into a data set.
So it dependent on your question if climatological data sets are adequate.
If you stay within a certain region and if you are only interested in the relationship between properties changing substantially with the seasons than climatological data with the temporal resolution of months or seasons might be OK.
If you want to compare different regions climatological data sets might be OK too.
If you want to analyze however at a fixed location the temporal evolution against time aka changing climatological variables climatological fields alone are not sufficient. Here you need some additional information, like real measurement.
Coming to reanalysis data. These are a leap forward to have a consistent picture of ocean process and the relation between different properties. Even if real observations are the input data for the reanalysis, they can differ at certain location significantly. So you have to validate if reanalysis data reproduce the regional or local conditions.
If you want to study a certain region in the ocean, you might ask the responsible local authorities who might monitor the particular region. However it can sometimes be a big hassle to get the data in your hands.
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I am interested in your experience in setting up regular monitoring of phytoplankton production in marine ecosystems: are data sets available either with high frequency or more classical methods?
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High frequency sampling in the water column is essential to understand energy processes both in the pelagic and in the benthic communities. They have been overlooked because are expensive and time consuming, but we have to make the effort to do it if we want to have a clearer picture of the system funcioning. However, to asses the health of an ecosystem you have, in my opinion, to integrate, and short time cycles, high frequency sampling may no be the answer you need. In coastal ecosystems, sediment traps and some variables of the benthic fauna may be better to understand changes through the time and make robust spatial comparisons.
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As I am not able to find Survey manual for tropical marine resources book by English et al online.
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send an email address and I will get a student to make a pdf of the section, We will then upload a full copy to the tracc-borneo.org website and research gate
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Is it appropriate to use methods normally used for benthic communities such as nMDS or RDA, and to treat samples (e.g. monthly samples) as locations in analyses of benthic communities? Which method is recommended for phytoplankton? What should I be aware of?
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If you just want to examine year-to-year patterns this is an example using Nonmetric Multidimensional Scaling (NMS):
Peperzak L (2010) An objective procedure to remove observer-bias from phytoplankton time-series. J Sea Res 63:152-156.
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This is regarding my research work on accumulation of sediments on corals, so can this be done.
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Yes,that's possible,provided the speed of current is not too high & the particle size is not too small.What happens is sediments do accumulate when 1) the substratum is rough (as in case of corals) & 2) rate is more during the NIL tide.By NIL tide I mean the time in between the very last fag end of low tide & beginning of high tide & vice-versa.Though in tide tables it is usually given that ,say, a high tide stops at time X & the low tide starts soon after,but in fields it has been observed that there is a time lag of say 30 to 45 minutes- when the sea water is quite still,after which water actually starts moving.It's at this time the sediment rate is more.
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I am doing some research on side effects of coral reef extinction on human society, and I'd like to use some examples to clarify the importance of extinction.
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I am not a specialist, but I immediately thought about the Brachiopoda ("lamp shells"), since they were very abundant filter-feeding, reef-building organisms during the Paleozoic era, and now most of the species are extinct and their niches, occupied by unrelated phyla. I've found very few in my field sampling expeditions, but their abundance, diversity and even size in the fossil record always amazed me.
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This answer should have different perspective other than lowering of pH.
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Thank you so much all for help.
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Does anyone have any protocol on how can I get the SST and Chl-a values using RS? How do I extract information from satellite data?
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I would suggest using MODIS or VIIRS. You may download all data from NASA's Ocean Biology Processing Group webpage for free. There is also a software package named SeaDAS that can easily do what you need. Notice that if you download Level 2 images you already have such parameters estimated, you just need to project them using SeaDAS or other similar software. For further help, feel free to contact.
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Also I want to know the minimum diameter and length of the corer.
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Hi Ghosh,
vertical profiling of marine faunal distribution such as macro, meiobenthos depth strata varies, here see the tables some of the previous studies
Depth strata Location Reference
0-1, 1-5, 5-10, 10-20 cm Arabian Sea Witte, 2000
0-2, 2-5, 5-10 cm Off Cape Lookout Blake, 1976
0-2, 2-5, 5-10 and 10-15 cm Douro estuary, Portugal Mucha et al., 2004
0-2, 2-5, 5-10, 10-15, 15-20,
20-25, 25-30 Central Indian Ocean Basin Pavithran et al., 2009
0-2, 2-4, 4-6, 6-8, 8-10 Intertidal benthic organisms off Goa Ingole et al., 2006
Coming to the diameter of the core
Plexiglass core tube diameter Location Reference
10cm length and 4.5 cm diam
0-5, 5-10 cm depth strata Some Rivers of the East Coast of India Ansari et al., 1982
0-2, 2-4, 4-6, 6-8, 8-10 Kakinada Bay and backwater, East Coast of India Vijayakumar et al., 1991
2cm sections Western and Central Indian Ocean Basin Parulekar et al., 1992
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What is the difference between pbopt and pbmax?
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PBmax is physiological parameter and PBopt is oceanographic property. In order to obtain PBmax, you need to incubate "same" phytoplankton community (either from sea or culture) with different light condition. On the other hand, to obtain PBopt, samples from different layers are incubated at each light condition.
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If you are out on a field trip (for a couple of weeks away from the lab) and are collecting water samples for culture analysis, what is the best way to store the samples before analysis? I will not have a proper lab to access, and the bacteria in the water will grow if I just store them in the fridge.
I had thought to filter the samples onto membranes, but not to place the membranes onto agar until I got back to the lab?
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if your water samples are not too much, you may freeze them after adding 28% glycerol (1:1 v/v) to the water samples. This will keep your bacterial cell walls intact.
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The ocean is like a carbon dioxide basin because this is where CO2 present in the atmosphere is absorbed. This is causing this body of water to become acidic greatly threatening marine life, which may eventually kill them.
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As is generally the case with anthropogenic disturbances to ecosystems, ocean acidification will have winners and losers: some populations of marine organisms will adapt, while others will go extinct. A recent study by Parker et al. (2012) provides relevant evidence in this respect. They found that exposing adult oysters to elevated CO2 during reproductive conditioning had positive carry-over effects. Larvae spawned from adults exposed to elevated CO2 were larger and developed faster, but displayed similar survival compared with larvae spawned from adults exposed to ambient CO2. Importantly, this happened just across one generation, which is not enough for natural selection.
Parker LM, Ross PM, O’Connor WA, Borysko L, Raftos DA, Pörtner H (2012) Adult exposure influences offspring response to ocean acidification in oysters. Global Change Biology 18:82–92. DOI: 10.1111/j.1365-2486.2011.02520.x
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I need some literature about this topic.
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Thank you Dola for you information.
Best regards!
Erick
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I am attempting to make sense of some d15N-POM data collected at two different stations in open ocean and I have a question. I have nutrient data from both stations and I've been asked to use that and the POM d15N values to determine whether incomplete utilization of nitrate produced the lower d15n values observed at one of my stations.
I know that plotting POM d15N values against fractional nitrate utilization values should allow me to determine the answer to this question and I've found all the related equations in the literature, but i'm unclear how to determine values for the fractional utilization of nitrate. As far as I can tell, it is calculated by subtracting the "final" nitrate concentration from the initial concentration, but as this study was not a time series, I have absolutely no idea what the initial nitrate concentration might have been.
Is it reasonable to use the average sub-thermocline [NO3] as the initial value or is there some other way to do this?
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Hi Rebecca,
I dont know exactly how to answer the question!.. but for surface waters the following explanation I can think of...
1. Use your nutrient data. DIN and DIP to be more precisely..and find out the N*. Probably it may give an idea if the decrease in d15N-PON was due to active nitrogen fixation or not!!.. If nitrogen fixation is taking place, that means nitrate poor conditions prevailed at the time of sampling (normally).
2. But, your question "incomplete nitrate utilization produced d15N values (you did not mention high or low)" seems to be tricky.
3. In the point 1 i tried to look at your question in relation to nitrogen fixation in the open sea. As far as open ocean conditions are concerned, nitrate concentration is always low!.. and question does'nt arise about incomplete utilization. Again, N* values can tell you about whether P was in excess at that time, which in turn show that nitrate limiting conditions prevailed! (so nitrogen fixers grow).. If you have phytoplankton data then you can confirm it.
Vinayak
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How far do such productions show seasonality?
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Hi , Dola Bhattacharjee
Several factors controls the diversity, distribution of microphytobenthos in a particular area say for example sediment grain size, available organic carbon, overlaying water salinity and temperature, natural suspended sediment loads influence light penetration and ambient primary production, local currents that affect the sediment grain size and food availability for filter feeders as well as other factors. Generally shallow areas are influenced by numerous factors on a daily and even hourly basis from changing tides, currents, salinity, and associated factors. Although the deeper or off shore are not exposed to such dramatic changes with time. Many of these natural perturbations are lead to pronounced gradients the biomass, density and diversity of estuarine microphytobenthic communities.
Have a look here some related literature on the influence of sediment on the distribution/ assemblage pattern of microphytobenthos.
1) Maclntyre et al., 1996. Microphytobethos: the ecological role of the secret garden un-investigated shallow water marine habitats. Distribution abundance and primary production. Estaries 19: 186-201
2) Jesus, B., Mendes, C.R., Brotes, V., Paterson, D.M., (2006), Effects of sediment type on microphytobenthos vertical distribution. Expermental Marine biolog y and ecology 332: 60-74
3) Jesus, B., Brotes, V., Ribeiro, L., Mendes, C.R., Cartaxana, P., and Paterson, D.M., (2009), Adaptations of microphytobenthos assemblages to sediment type and tidal position, Continental Shelf Research 29: 1624-1634.
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I would like to know the mechanism of the effect of salinity over biological activities, like productivity, uptake, etc.
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I ,m not sure of your research question. If you are interested in the response of a species community response to its contribution to nitrogen cycling within an estuary then understanding how the species community is affected by by salinity dynamics within the various zones of the estuary is important. However, this is a different question to how salinity dynamics characteristic of an estuary at different time scales affect the nitrogen cycling dynamics of a community that has evolved over the appropriate time scale within estuarine zones. I other words salinity and its variance for that zone with respect to the turnover times of the microbiological community and its affect on the sediment redox , maybe a longer response time, may affect the efficiency of one of the nitrogen cycling processes e.g denitrification, or nitrogen fixation, . The issue then becomes a matter of scale, seasonal and and weekly salinity variability and changes to those parameters due to land use and climate change
Scale is every thing in ecology as its increasingly being realised
All the best
Barry
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I am having some problems deciding which type of regression to use, OLS or RMA. I find support for each one with my dataset and goals. I am regressing nitricline depth against C:Chl ratios. The thoughts for using RMA are that there is error in both measurements and the objective is to possibly define a mutual and codependent underlying the interaction between X and Y (Sprent, 1966). However, the thoughts for using OLS are X (NC) is being used to predict Y (C:Chl) (Smith, 1994), the purpose of the regression is to understand the range of Y values at a given X, and the error in X is << than error in Y. Any thoughts would be helpful.
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Andrew, I thought I'd chime in late with another good reference on the matter. One thing to consider if you went with RMA or other Type II is that you can regress both y on X and x on Y in order to establish bounds on your model.
McArdle, B.H. Lines, models, and errors: Regression in the field. Limonology and Oceanography 48, 1363-1366 (2003).
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Live condition of benthic diatom without preservation under freezing temperature.
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Thank u mam
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I am currently working on my thesis, which attempts to create a transparent exopolymer particle (TEP) cycle for a mesocosm. Part of creating the cycle is identifying sources and sinks of TEP. From background reading I know that both phytoplankton and bacteria are capable of producing TEP, though bacterial contribution is usually low. Thus far I have been unable to find a means of differentiating a bacterial produced from phytoplankton produced TEP that does not involve a highly complex, time consuming, or expensive method. Is there a proxy that could be used to differentiate, or a more simple method I can be pointed toward?
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Have you looked into any of the radioisotope (e.g. triateted leucine, C14) or stable isotope methods for tracing organic matter through microbial food webs? If you have a scintillation counter on hand and some means of effectively quantifying DOC/POC, the former could be used. I seems as if the best approach would be to find a means to quantify total TEP, then one of the microbial contributors (phyto or bact) and figure the other out by difference.