A certain type of deep‐sea sediment exhibits very high content of rare earth elements and yttrium (REY) and is therefore expected to serve as a novel resource for these industrially essential metals. In this paper, we statistically analyzed the bulk chemical composition of deep‐sea sediments collected from the western North Pacific Ocean. By applying independent component analysis to the multielemental data set, we extracted three independent components (ICs) that can be interpreted as the influence of Mn‐oxides (IC1), REY‐enriched biogenic calcium phosphate (IC2), and possibly a diagenetic effect involving Cu enrichment (IC3) on bulk sediment geochemistry. Subsequently, we selected representative samples based on the independent component analysis result, and implemented Sr–Nd–Pb isotopic analyses of bulk sediments. The results indicate that the extremely REY‐rich mud characterized by IC2 inherits the geochemical signature of deep Pacific seawater, whereas the non‐REY‐rich mud with less diagenetic alterations, characterized by IC3, implies an influence of terrigenous dust probably from the Taklimakan desert–Chinese loess plateau. IC1 may reflect the variation in sedimentation rates. Characteristic downhole variations of IC1 and IC3 scores imply the presence of hiatus and/or erosion of the sediment column across the REY content peak. The putative cause is an enhanced bottom current, which can physically separate coarse biogenic calcium phosphate grains with very high REY content and thus produce an extremely REY‐enriched sediment layer.

Deep-sea sediments with total rare-earth elements and yttrium (ΣREY) concentrations exceeding 400 ppm, which are termed REY-rich mud, are widely distributed in the world oceans. Specifically, deep-sea sediments within the Japanese exclusive economic zone (EEZ) surrounding Minamitorishima Island in the western North Pacific have attracted significant attention as a new REY resource, because they contain REY-enriched layers exceeding 2000 ppm of ΣREY. However, neither the sediments deeper than 15 m below the seafloor (mbsf) nor those outside the Minamitorishima EEZ have ever been studied. Recently, a number of distinct geochemical features which are aligned in stratigraphic order were recognized in these sediments, based on multi-elemental composition data. Chemostratigraphy enables us to laterally correlate three REY peaks among apparently featureless pelagic clays. Here, we apply chemostratigraphic correlation to 19 new cores collected from the northern Pigafetta Basin and several small basins within the Marcus-Wake Seamounts. This study revealed that the REY-enriched layers occur at greater depths than the piston core length in a wider area than previously investigated (e.g., ~20.5 mbsf at Ocean Drilling Program Site 801A). This finding suggests that the depositional environments in these areas were basically similar, although local geographic conditions could have affected the continuity of REY peaks.

The origin of deep-sea sediments in the western North Pacific Ocean, which are significantly enriched in rare-earth elements and yttrium (REY), and its paleoceanographic implications have been poorly constrained. Here, we investigated stratigraphic variations in the chemical compositions and textures of ferromanganese (Fe–Mn) micronodules separated from western North Pacific sediments. The characteristics of the micronodules of an extremely REY-rich mud layer vary from almost purely diagenetic to relatively hydrogenetic. This indicates the abundant supply of organic matter to the sediment together with fish debris that accumulates REY at the onset of the REY-enrichment of the mud, followed by the exposure of the seafloor to oxic water masses during the latter half of the formation of the REY-rich mud. These results support a previously proposed formation mechanism based on which enhanced bottom water currents caused pelagic fish proliferation via the upwelling of nutrients and fish debris was physically sorted and selectively accumulated on the seafloor. After the main REY-enrichment, the micronodules exhibit varying diagenetic signatures, suggesting changes in the bottom current intensities after the main REY-enrichment. However, the bulk REY contents do not increase. This implies that a sufficient increase in the fish productivity is an essential factor affecting the formation of REY-rich mud.

Deep‐sea sediments around Minamitorishima Island in the western North Pacific Ocean record the depositional environment in the central to western North Pacific since the late Cretaceous. Previous studies on the bulk chemical composition of deep‐sea sediments in this area have revealed that the sediment column can be divided into five chemostratigraphic units with at least three intercalated layers enriched in rare‐earth elements. However, the end‐member components and their changes in abundance, which indicate compositional variation, as well as the environmental factors affecting them, remain unclear. Here, we report the bulk chemistry, including newly analyzed ⁸⁷Sr/⁸⁶Sr ratios of the sediments, seafloor Mn nodules, and fish teeth collected from the deep‐sea basin around Minamitorishima Island, to identify the end‐member components of the sediments. Our results suggest that the pelagic sediments in the study area are mainly composed of terrigenous components, hydrogenous Mn oxides, biogenic calcium phosphate, and volcanic materials. The combination of Sr isotope modeling and bulk chemistry revealed that the input of volcanic materials has increased twice, which might be Izu‐Bonin‐Mariana tephras of the latest Eocene to Oligocene explosive volcanism at the later event but is unclear at the earlier event. The provenance of terrigenous materials has changed from North America to East Asia. The bulk sediment chemostratigraphy around Minamitorishima Island could have resulted not only from the local environmental changes in the pelagic realm, but also from volcanism around the Pacific Ocean and the northwestward movement of the area due to the Pacific plate motion.