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	<title>sea temperature &#8211; Science</title>
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	<title>sea temperature &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Clouds, Winds and Warm Water Set the Clock for Coral Breeding in Panama</title>
		<link>https://scienmag.com/clouds-winds-and-warm-water-set-the-clock-for-coral-breeding-in-panama/</link>
		
		<dc:creator><![CDATA[Violet Maxwell]]></dc:creator>
		<pubDate>Fri, 02 Oct 2026 11:02:10 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[coral reef conservation and climate change]]></category>
		<category><![CDATA[coral reefs]]></category>
		<category><![CDATA[coral reproduction]]></category>
		<category><![CDATA[Coral reproductive timing]]></category>
		<category><![CDATA[coral spawning environmental cues]]></category>
		<category><![CDATA[coral spawning synchronization]]></category>
		<category><![CDATA[differences in coral reproductive strategies]]></category>
		<category><![CDATA[eastern Pacific]]></category>
		<category><![CDATA[effects of winds and warm water on corals]]></category>
		<category><![CDATA[gametogenesis]]></category>
		<category><![CDATA[Gulf of Panamá]]></category>
		<category><![CDATA[Gulf of Panamá coral species]]></category>
		<category><![CDATA[impact of climate variability on coral reproduction]]></category>
		<category><![CDATA[Intertropical Convergence Zone]]></category>
		<category><![CDATA[Intertropical Convergence Zone influence]]></category>
		<category><![CDATA[long-term coral reproductive studies]]></category>
		<category><![CDATA[PAR]]></category>
		<category><![CDATA[Pavona gigantea]]></category>
		<category><![CDATA[photoperiod]]></category>
		<category><![CDATA[Psammocora stellata]]></category>
		<category><![CDATA[reef-building coral biology]]></category>
		<category><![CDATA[satellite climate data coral research]]></category>
		<category><![CDATA[sea temperature]]></category>
		<category><![CDATA[seasonal coral reproductive cycles]]></category>
		<category><![CDATA[upwelling]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=227351</guid>

					<description><![CDATA[A decades-long study in the Gulf of Panamá shows that seasonal shifts in wind, cloud cover, light and temperature, driven by the Intertropical Convergence Zone, control when two key reef-building corals develop gametes.]]></description>
										<content:encoded><![CDATA[<p>On the reefs of the Gulf of Panamá, two of the region&#8217;s most important reef-building corals keep their reproductive calendars in strikingly different ways, and a new long-term study has finally worked out what sets the timing. By combining decades of histological observations with satellite-derived climate data, researchers found that the annual migration of the Intertropical Convergence Zone, the great band of low pressure and heavy rain that sweeps across the equatorial eastern Pacific, effectively orchestrates when these corals make gametes. The work, published in Discover Oceans, is the first in a series examining how local environmental conditions shape the sexual reproduction of corals across this under-studied corner of the ocean.</p>
<p>The study focused on two species with very different biologies. Pavona gigantea is a hermaphroditic, massive coral that contributes substantially to reef frameworks across the eastern Pacific, while Psammocora stellata is a small, nodular, free-living species with separate male and female colonies. Both are broadcast spawners, releasing gametes into the water column, and both had previously been shown to reproduce over extended periods, an anomaly among corals that is often attributed to their equatorial position. What remained unclear was which environmental signals actually govern the initiation and cessation of gamete development in a region where the climate swings between a cool, windy upwelling season and a warm, wet season.</p>
<p>To answer that question, the team drew on gametogenesis records collected between 1985 and 1993 from colonies at Taboga and Saboga Islands in the Gulf of Panamá, part of a monitoring program begun after the catastrophic 1982–83 El Niño bleaching event devastated eastern Pacific reefs. Coral fragments collected by scuba were fixed, decalcified, stained and examined under a compound microscope to detect the presence of male or female gametes at any stage of development. Monthly percentages of reproductive samples were then regressed against a suite of environmental variables: reef temperature, precipitation, cloud cover, wind speed, wind direction, photosynthetically active radiation (PAR), insolation and photoperiod, using generalized linear mixed models and a principal component analysis to handle the strong correlations among these factors.</p>
<p>The results reveal two species marching to different drummers. Pavona produced gametes from January through August, with peak activity between May and August, and its reproduction was most strongly associated with photoperiod and the rate of temperature change. Psammocora, by contrast, bred from May to December and showed a strong association with nearly every warm-wet season variable tested, with sea temperature and insolation exerting the strongest statistical effects. Critically, all reproductive samples of Psammocora appeared only once mean monthly reef temperature had reached 27.8 degrees Celsius, suggesting a clear thermal threshold for this species, whereas Pavona tolerated a much broader temperature range and even produced gametes at low frequency during the coolest months.</p>
<p>Perhaps the most surprising finding concerns light. Coral gametogenesis in both species was negatively associated with PAR and positively associated with cloud cover, implying that excessive solar radiation, rather than its absence, may limit reproduction in this equatorial setting. PAR values in the Gulf of Panamá peaked at roughly 108 to 118 watts per square meter during the upwelling season, when skies are clear and reproductive activity is minimal, while the greatest reproductive activity occurred when PAR had fallen to between 88 and 97 watts per square meter under thick wet-season cloud. The authors suggest that heavy cloud cover may shield the corals&#8217; symbiotic algae from damaging radiation near the equator, where photoinhibition is a real risk, and note that on-reef light measurements will be needed to confirm this interpretation.</p>
<p>Wind emerged as another key player, both through its speed and its direction. Most Pavona colonies carried gametes only when mean monthly wind speeds dropped to around 5 meters per second or below, and reproduction in both species surged as the strong northerly trade winds that drive seasonal upwelling relaxed in April and May. Wind direction proved an even better predictor than speed: when winds blew steadily from the north during the cool season, reproduction was nominal in Pavona and absent in Psammocora, but as winds swung away from north in May, gamete production began. A later shift toward westerly and southwesterly winds in August and September coincided with the end of Pavona&#8217;s breeding season, while Psammocora continued until winds returned to the north in January.</p>
<p>Overlaying all the environmental curves revealed something remarkable: nearly every factor the team measured, including temperature, precipitation, cloud cover, wind speed, insolation and PAR, converges at a critical transition in mid-April, just after the March equinox, when the Intertropical Convergence Zone moves in and the dry season gives way to the wet. A second, looser convergence occurs in November and December as conditions swing back. The researchers describe these intersections as reproductive &#8216;sweet spots&#8217; that predict when gamete development starts, accelerates or stops. Psammocora&#8217;s entire breeding season fits neatly between the two transitions, while Pavona initiates gametogenesis at the second transition into the dry season, when rising insolation appears to matter more than falling temperature.</p>
<p>The study also highlights how these corals manage to reproduce at all in such a marginal habitat. Unusually cold water during upwelling, sometimes dipping below 20 degrees Celsius, suppresses reproduction and can even threaten survival, yet Pavona appears better equipped to cope, possibly by feeding on the plankton blooms that upwelling generates with its large polyps and extensible tentacles. Psammocora, with its small polyps, may compensate through a fast, opportunistic strategy, producing gametes rapidly throughout the warm season and maintaining abundant populations across varied habitats. Neither species produces buoyant egg-sperm bundles like corals elsewhere, an adaptation the authors suggest may protect fertilization success from the sudden salinity drops caused by intense seasonal rainfall.</p>
<p>Why does this matter now? Understanding the timing and environmental triggers of coral sexual reproduction is essential for predicting how reefs can recover from bleaching and mortality events, and for designing rehabilitation and conservation programs that work with, rather than against, natural reproductive rhythms. Eastern Pacific corals have already endured repeated El Niño-driven catastrophes, and their populations remain small and vulnerable. As ocean warming accelerates a global reef decline, knowing which species can breed under which conditions, and when, offers a practical tool for restoration planning. The authors argue that seasonal transitions, those &#8216;sweet spots&#8217; where the region&#8217;s climate pivots, provide a usable predictor of reproductive activity that managers can apply directly. Future papers in the series will extend this approach to other equatorial eastern Pacific sites, helping to identify which coral species are most resilient to the thermal extremes and ENSO-driven variability that define life on these remarkable, and imperiled, reefs.</p>
<p><strong>Subject of Research:</strong> Environmental drivers of coral reproductive phenology in the equatorial eastern Pacific</p>
<p><strong>Article Title:</strong> Environmental conditions and Equatorial Eastern Pacific coral reproductive phenology in the Gulf of Panamá (Pavona gigantea and Psammocora stellata)</p>
<p><strong>Article References:</strong> Colley, S. B., Maté, J. L., Danos, D., &amp; Glynn, P. W. (2026). Environmental conditions and Equatorial Eastern Pacific coral reproductive phenology in the Gulf of Panamá (Pavona gigantea and Psammocora stellata). <em>Discover Oceans, 3</em>(1), Article 26. <a href="https://doi.org/10.1007/s44289-026-00122-8" rel="noopener noreferrer">https://doi.org/10.1007/s44289-026-00122-8</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44289-026-00122-8" rel="noopener noreferrer">10.1007/s44289-026-00122-8</a></p>
<p><strong>Keywords:</strong> coral reproduction, gametogenesis, Gulf of Panamá, Intertropical Convergence Zone, Pavona gigantea, Psammocora stellata, upwelling, photoperiod, PAR, sea temperature, coral reefs, eastern Pacific</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">227351</post-id>	</item>
		<item>
		<title>Male Loggerhead Turtles Reveal Hidden Dive Secrets Across the Mediterranean</title>
		<link>https://scienmag.com/male-loggerhead-turtles-reveal-hidden-dive-secrets-across-the-mediterranean/</link>
		
		<dc:creator><![CDATA[Sloane Callahan]]></dc:creator>
		<pubDate>Wed, 23 Sep 2026 23:00:23 +0000</pubDate>
				<category><![CDATA[Climate]]></category>
		<category><![CDATA[Argos telemetry]]></category>
		<category><![CDATA[breeding and foraging habitats of loggerheads]]></category>
		<category><![CDATA[bycatch]]></category>
		<category><![CDATA[Caretta caretta]]></category>
		<category><![CDATA[conservation]]></category>
		<category><![CDATA[conservation strategies for marine reptiles]]></category>
		<category><![CDATA[diving behaviour]]></category>
		<category><![CDATA[effects of climate change on sea turtle habitats]]></category>
		<category><![CDATA[elusive male sea turtle studies]]></category>
		<category><![CDATA[Fisheries Management]]></category>
		<category><![CDATA[impact of fishing gear on sea turtles]]></category>
		<category><![CDATA[Kyparissia Bay]]></category>
		<category><![CDATA[Loggerhead sea turtle behavior]]></category>
		<category><![CDATA[loggerhead turtle]]></category>
		<category><![CDATA[male sea turtle migration patterns]]></category>
		<category><![CDATA[marine animal tracking technology]]></category>
		<category><![CDATA[Mediterranean marine conservation]]></category>
		<category><![CDATA[Mediterranean Sea]]></category>
		<category><![CDATA[Mediterranean sea turtle population dynamics]]></category>
		<category><![CDATA[satellite tracking]]></category>
		<category><![CDATA[satellite tracking of marine animals]]></category>
		<category><![CDATA[sea temperature]]></category>
		<category><![CDATA[thermocline]]></category>
		<category><![CDATA[underwater depth and temperature preferences]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=211046</guid>

					<description><![CDATA[Satellite-tagged adult male loggerhead turtles from Greece spent most of their lives in shallow water, altered their diving around thermoclines and switched to multi-hour dives as winter waters cooled.]]></description>
										<content:encoded><![CDATA[<p>For decades, scientists studying the Mediterranean&#8217;s loggerhead sea turtles have focused overwhelmingly on females, because nesting beaches make them easy to find and monitor. Males, which never come ashore after maturity, have remained an enigma, particularly when it comes to how they use the vertical world beneath the waves. Now, a team led by Alan F. Rees of Turtles from Above, working with colleagues from Greek conservation institutions, has shed light on this hidden life. By attaching satellite tags to three breeding adult males captured in Kyparissia Bay, Greece, the largest loggerhead breeding aggregation in the Mediterranean, the researchers followed the turtles to their distant foraging grounds while continuously recording the depths they occupied and the temperatures they experienced. The results, published in Discover Conservation, offer the most detailed picture yet of how adult male loggerheads distribute themselves through the water column, and the findings carry direct consequences for reducing one of the species&#8217; greatest threats: accidental capture in fishing gear.</p>
<p>The technical challenge of studying diving animals at sea is formidable. Sea turtles are air-breathing reptiles, and although they can remain submerged for extended periods, they must return to the surface to breathe. That dependency means they occupy much of the vertical space in coastal and neritic habitats, putting them in harm&#8217;s way wherever fishing gear is set, from surface longlines to bottom trawls. The lungs of a turtle play a dual role, storing oxygen and controlling buoyancy, which shapes how the animals dive and rest. To untangle these behaviours, the team used Wildlife Computers SPLASH10-385 C transmitters, instruments capable of logging depth at 0.1 metre resolution and temperature to within 0.1 degrees Celsius at five-second intervals. The onboard data were compressed and transmitted in hour-long snapshots through the low-bandwidth Argos satellite system, with tags limited to 250 transmissions per day, producing a stream of time-series depth and temperature records spanning the turtles&#8217; migrations.</p>
<p>The three turtles, labelled I, J and K, were captured in May 2023 in Kyparissia harbour using the established turtle rodeo technique. To guarantee that only actively breeding adult males were tagged, the researchers targeted individuals observed mounted upon or attempting to mount other turtles, a reliable behavioural indicator of breeding males. Once ashore, each turtle&#8217;s carapace was sanded, cleaned with acetone and fitted with an epoxy-and-fibreglass transmitter attachment. The tags then recorded each animal&#8217;s post-breeding movements: turtle I migrated east into the northern Aegean Sea near Thasos Island, turtle K settled in the Argolic Gulf on the eastern Peloponnese, and turtle J travelled north through the Ionian Sea before establishing two sequential foraging sites in the Adriatic. Transmission durations ranged from 98 days for turtle I to an impressive 547 days for turtle J, the only individual tracked long enough to reveal a full seasonal cycle.</p>
<p>The depth data revealed a striking pattern: despite differences in destination, all three turtles overwhelmingly favoured shallow water. Turtle I spent 98.6 percent of its time shallower than 10 metres and over 99 percent shallower than 20 metres. Turtle K and turtle J were more adventurous, spending 55.3 and 62.3 percent of their time above 10 metres respectively, yet both still exceeded 99 percent of their time within the top 80 metres. Even turtle J, the deepest diver of the trio, which twice plunged beyond 200 metres, reaching 201.5 metres in August 2023 and a remarkable 288 metres in September 2023, spent 95 percent of its life above 70 metres. For fisheries managers, this is the crucial message: turtles concentrate their lives in narrow vertical bands, and gear positioned away from those bands is far less likely to intercept them.</p>
<p>Temperature proved to be a powerful driver of behaviour. Summer sea surface temperatures peaked near 29 degrees Celsius in July and August, and the turtles registered short-term spikes well above ambient values, occasionally approaching 45 degrees, which the authors interpret as surface basking rather than true water temperature. More intriguing were the thermal structures the turtles swam through. The time-series data captured shallow thermoclines at around 9 metres and deeper ones near 35 metres, and when a distinct deep thermocline was present, the turtles altered their diving, executing multi-depth dives that clearly separated warmer shallow phases from colder deep phases. Turtle J lived in waters with a notable deep thermocline for more than 30 consecutive days, sometimes rising above the boundary to hold steady at about 30 metres for 20 to 30 minutes, behaviour that may represent warming up after foraging in colder water below, or movement along the seafloor between thermal layers. Such responses to thermoclines have never previously been reported for Mediterranean sea turtles.</p>
<p>Daily rhythms also shaped the animals&#8217; vertical lives. During warm periods, the turtles showed classic diel patterns: relatively active, erratic diving by day and longer, quieter resting dives at night, or in some cases the reverse, with one turtle performing nocturnal resting dives at 30 metres and deeper daytime dives beyond 70 metres. These patterns likely reflect shifts between nocturnal refuge and daytime foraging, though the available tracking resolution cannot fully separate behavioural change from movement between sites. The study classified the dives using a standard lettered nomenclature for sea turtle dive profiles: steady Type A dives suggesting rest, variable-bottom Type B dives indicating activity, Type E profiles associated with thermoclines, and the rare Type C plunge, a rapid straight descent followed by an immediate ascent, exemplified by turtle J&#8217;s 288-metre excursion. The purpose of such extreme dives remains uncertain; comparable dives elsewhere have been interpreted as exploratory, navigational or prey-searching, but the authors candidly note that without direct observation, much interpretation rests on what they describe as speculation and guesswork.</p>
<p>Winter transformed the picture entirely. As waters cooled through November into April, turtle J, the only animal still transmitting, shifted to spending far more time at depth, with dives regularly exceeding one hour and the longest, repeated dives surpassing three hours between 19 and 21 February 2024, with no clear day-night rhythm. This is consistent with cold-induced dormancy: cooler water slows reptilian metabolism, reducing oxygen demand and allowing extraordinary breath-holding. Loggerheads are the champions of cheloniid endurance, with reported winter dives of up to 614 minutes. Yet a subtle finding complicates the dormancy story. Even when diving deeper than 50 metres in midwinter, turtle J rarely encountered water below about 15 degrees Celsius, recording values below that threshold on only three days, with a minimum of 14.2 degrees. The 15-degree mark has long been proposed as a trigger for overwintering behaviour in sea turtles, though empirical support has been lacking, and the authors note that deeper waters are thermally buffered from surface variability, a stability visible even in slight nocturnal thermal inversions where the surface was about one degree cooler than the water below.</p>
<p>The conservation implications are immediate and practical. Fishing activity in the Mediterranean is estimated to catch around 132,000 turtles annually, killing roughly 44,000 as bycatch or through entanglement in lost ghost gear. Because turtle depth use varies with season and temperature, the authors argue that management tools such as depth limits and soak-time restrictions should evolve dynamically with seasonal sea temperatures rather than remaining static. In colder months, quiescent turtles resting on the seafloor become especially vulnerable to bottom trawling, while in warmer periods most of a turtle&#8217;s time is spent in the top few metres, suggesting that deeper-set nets and hooks could dramatically reduce encounters. Similar depth-based strategies have informed longline management in the Pacific, and tracking of loggerheads from Crete has already suggested that setting gear below 5 metres could cut bycatch, though outcomes remain untested. Beyond fisheries, knowing what fraction of time turtles spend at the surface is essential for correcting aerial and boat survey counts for availability bias, adjustments that can inflate abundance estimates nearly twentyfold.</p>
<p>There is also an unexpected bonus: the turtles themselves are ocean observers. Their tags returned depth-linked temperature profiles reaching down to about 80 metres, echoing findings from loggerheads in the northwest Atlantic, and such animal-borne data can refine remotely sensed sea-surface temperature products and contribute to climate forecasting. The authors acknowledge the limits of their study; with winter data from a single individual, they deliberately avoided quantitative analysis, and two of the three tags stopped transmitting early, probably dislodged or damaged rather than a sign of turtle injury. But the 2,426 hours of paired depth and temperature data from turtle J alone demonstrate what is possible. Future work with more tracked males and finer-scale sensors should disentangle the effects of temperature, season, time of day and seabed depth on behaviour, enabling better predictions of how these animals will redistribute their lives as the Mediterranean warms. For now, the message from three roaming males is clear: protect the narrow, shallow, temperature-shaped band where they actually live, and one of the sea&#8217;s most iconic survivors gains a fighting chance.</p>
<p><strong>Subject of Research:</strong> Depth use and thermal environment of adult male Mediterranean loggerhead sea turtles tracked by satellite</p>
<p><strong>Article Title:</strong> Depth use and thermal environment of adult male Mediterranean loggerhead sea turtles</p>
<p><strong>Article References:</strong> Rees, A. F., Batzios, P., Dendrinos, P., Dimalexis, T., Mikoniatis, G., Paxinos, O., &amp; Vavassis, Y. (2026). Depth use and thermal environment of adult male Mediterranean loggerhead sea turtles. <em>Discover Conservation, 3</em>(1), Article 22. <a href="https://doi.org/10.1007/s44353-026-00091-1" rel="noopener noreferrer">https://doi.org/10.1007/s44353-026-00091-1</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44353-026-00091-1" rel="noopener noreferrer">10.1007/s44353-026-00091-1</a></p>
<p><strong>Keywords:</strong> loggerhead turtle, Caretta caretta, Mediterranean Sea, satellite tracking, diving behaviour, thermocline, bycatch, fisheries management, Kyparissia Bay, sea temperature, conservation, Argos telemetry</p>
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